216-RICR-50-05-1
A. Wherever used in these Regulations the following terms shall be construed as follows:
24. “Connection” means the water service line connecting a structure to the water distribution line. In the absence of data on the number of service connections, the population served divided by 2.5 shall be used as the default value.
a. The following are excluded from the “connection” component of the PWS definition:
(1) A connection to a system that delivers water through constructed conveyances other than pipes is excluded from consideration as a “connection” under three (3) circumstances:
(CC) Where the Director determines that the water provided for drinking, cooking, and bathing is treated (centrally or by point of entry) by the provider, a pass-through entity, or the user to achieve the equivalent level of protection provided by the applicable national primary drinking water regulations.
37. “Diatomaceous earth filtration” means a process resulting in substantial particulate removal in which:
63. “Groundwater under the direct influence of surface water” means any water beneath the surface of the ground with:
87. “Noncompliance”, “Nonconformance”, “Failure to comply” and “Violation” each mean any act or failure to act which constitutes or results in or from:
103. “Public water system” or “PWS” means a system for the provision to the public of water for human consumption through pipes or other constructed conveyances, if such system has at least fifteen (15) service connections or regularly serves at least twenty-five (25) individuals daily at least sixty (60) days out of the year. Such term includes:
122. “Special irrigation district” means an irrigation district in existence prior to May 18, 1994 that provides primarily agricultural service through a piped water system with only incidental residential or similar use where the system or the residential or similar users of the system if the Director determines that:
A. This Part applies to any PWS unless a PWS meets all of the following conditions:
B. General Requirements
C. Licensing Requirement
1. Applicability
2. License Application
3. License Fees
4. Denial of License
5. Suspension or Revocation of a License
6. Renewal of License
g. Penalties for Late Renewals
8. PWS Contact Information
A. Proposed New Water Sources
B. In the case of a proposed gravel packed or gravel developed (stratified drift) well, within the area as specified below, the site plans shall show pertinent information including, but not limited to, locations of existing or proposed sewage disposal systems, and any other existing or proposed potential sources of pollution including, but not limited to, those listed in § 1.23 of this Part.
C. In the case of a proposed drilled (bedrock) or driven well, within a radius dependent on the proposed pumping rate as specified in the following table “Wellhead Protection Area Radius for Bedrock Wells”, but not less than 1,750 feet, the site plan shall show pertinent information including, but not limited to, the location of existing and proposed sewage disposal systems and any other existing or proposed potential sources of pollution including but not limited to those listed in § 1.23 of this Part. Generally, the land within two hundred (200) feet of such wells shall be reserved for protection of the water quality of the well, and shall be delineated on the site plan by a topographic mapping of the two hundred (200) foot area to an appropriate scale. This distance may be modified at the discretion of the Director taking into consideration such factors as the volume and type of waste material to be disposed or stored in close proximity to the land area reserved for protection of the well, the depth below grade to impervious formation, the depth below grade to the water table, the type of soil in the area, or any other factors the Director deems pertinent.
1. Wellhead Protection Area Radius for Bedrock Wells.
| Pumping Rate (gpm) | Radius (ft) | Pumping Rate (gpm) | Radius (ft) |
| = 10 | 1750 | 23 | 2411 |
| 11 | 1820 | 24 | 2440 |
| 12 | 1872 | 25 | 2466 |
| 13 | 1920 | 30 | 2568 |
| 14 | 1965 | 35 | 2638 |
| 15 | 2008 | 40 | 2689 |
| 16 | 2087 | 45 | 2729 |
| 17 | 2153 | 50 | 2760 |
| 18 | 2211 | 60 | 2806 |
| 19 | 2261 | 70 | 2875 |
| 20 | 2305 | 80 | 2985 |
| 21 | 2344 | 90 | 3068 |
| 22 | 2380 | 100 | 3133 |
2. gpm = gallons per minute. For pumping rates not provided below, the Wellhead Protection Area Radius shall be calculated using the formula below in accordance with Rhode Island Department of Environmental Management Groundwater Quality Rules:
J. All newly constructed or reconstructed wells shall perform the following procedures and testing prior to final approval:
L. Well Construction
2. Well Grouting (Sealing)
a. All wells must be sealed in a manner that protects the water-bearing formations from contamination from surface runoff and subsurface contaminants. When sealing the annular space, a grout seal mixture shall be utilized which will:
d. When using cement grout as the sealing material in a well, it must meet one of the following requirements:
e. When using bentonite grout as the sealing method in a well, it must meet the following requirements and be mixed and added by manufacturer’s specification:
3. The pump installation, piping arrangements, other appurtenances, and well house details at wells which serve as the source of supply for a PWS, shall meet the following requirements.
5. Well Performance Test.
d. The test shall provide for continuous pumping at +/- five percent (5%) of the design.
e. The following data shall be submitted to the Director:
f. A report shall be submitted which provides recordings and graphic evaluation of the following.
M. Approval of Reconstructed Water Sources
1. Proposed Reconstructed Water Sources
6. Well Abandonment and Decommissioning
A. No new water treatment works or water storage or pumping facilities shall be constructed or such existing works or facilities substantially altered until design plans, engineering calculations, pumping test data, water quality testing results, component specifications, and any other information necessary to demonstrate compliance with this Part, prepared by a professional engineer registered in accordance with R.I. Gen. Laws Chapter 5-8, and a plan for operation and maintenance, have been approved by the Director. Such plans shall also be provided in electronic format compatible with the Department’s computer software. The design of water treatment works, water storage or water pumping facilities should reflect the guidance contained in Recommended Standards for Water Works: Policies for the Review and Approval of Plans and Specifications for Public Water Supplies, incorporated by reference in § 1.24(A) of this Part, where applicable. These facilities shall also be installed and constructed in accordance with applicable American Water Works Association (AWWA) Standards with reference to materials used and construction procedures to be followed. Exceptions from this requirement may be granted by the Director.
2. Only products which meet the standards adopted in or pursuant to this Section shall be used by a supplier of water in a public water supply. Certification that a product meets the standards adopted pursuant to this Section by an organization having a third-party certification program accredited by American National Standards Institute, the American Association for Laboratory Accreditation, or the International Accreditation Service, Inc. or equivalent to test and certify products shall be prima facie evidence that a product meets the standards.
| Product Type | Standard |
| Drinking Water Treatment Chemicals | 60 |
| Pipes and Related Products | 61 |
| Protective (Barrier) Materials | 61 |
| Joining and Sealing Materials | 61 |
| Process Media | 61 |
| Mechanical Devices | 61 |
| Plumbing Devices | 61 |
3. NSF Standards have also been developed for certain Drinking Water Treatment Units. Units meeting these criteria may be considered for approval, if deemed appropriate by the Director.
| Product Type | Standard |
| Cation Exchange Water Softeners | 44 |
| Drinking Water Distillation Systems | 62 |
F. Use of Non-Centralized Treatment Devices
1. Criteria and procedures for PWS using point-of-entry devices.
d. Effective technology must be properly applied under a plan approved by the Director and the microbiological safety of the water must be maintained.
(2) NSF Standards have been developed for certain point of entry and point of use treatment systems. Certification of compliance with these standards shall be considered adequate certification of performance. Units meeting these standards may be considered for approval, if deemed appropriate by the Director.
| Product Type | Standard |
| Drinking Water Treatment Units – Aesthetic Effects | 42 |
| Drinking Water Treatment Units – Health Effects | 53 |
| Reverse Osmosis Drinking Water Treatment Systems | 58 |
| Ultraviolet Microbiological Water Treatment Systems | 55 |
| Shower Filtration Systems – Aesthetic Effects | 177 |
| Microbiological Water Purifiers | P231 |
G. Use of Bottled Water or Point of Use Treatment Devices. PWS shall not use bottled water or point-of-use devices to achieve compliance with an MCL. Bottled water or point-of-use devices may be used on a temporary basis to avoid an unreasonable risk to health, and only with prior approval of the Director.
B. The treatment technique requirements consist of installing and properly operating water treatment processes which reliably achieve:
C. A § 1.6 PWS is considered to be in compliance with the requirements of § 1.6.1(B) of this Part, if:
F. Recycle Provisions: All § 1.6 PWS that employ conventional filtration or direct filtration treatment and that recycle spent filter backwash water, thickener supernatant, or liquids from dewatering processes must meet the requirements in §§ 1.6.1(F)(1) and 1.6.8(D) of this Part.
1. Treatment Technique Requirement. Any PWS that recycles spent filter backwash water, thickener supernatant, or liquids from dewatering processes must return these flows through the processes of a PWS's existing conventional or direct filtration system as defined in 40 C.F.R. § 141.2 or at an alternate location approved by the Director.
D. Source Water Quality Conditions:
E. Site Specific Conditions:
1. Compliance
2. The PWS must maintain a watershed control program which minimizes the potential for contamination by Giardia lamblia cysts, Cryptosporidium oocysts and viruses in the source water. During the onsite inspection (discussed in § 1.6.2(F)(3) of this Part), the adequacy of a watershed control program will be determined by the Director. The adequacy of a program to limit potential contamination by Giardia lamblia cysts, Cryptosporidium oocysts, and viruses must include, but not be limited to, the following measures:
c. The extent to which the PWS has maximized land ownership and/or controlled land use within the watershed. At a minimum, the watershed control program must:
3. The PWS must be subject to an annual on-site inspection to assess the watershed control program and disinfection treatment process. A report of the on-site inspection summarizing all findings must be prepared every year. The on-site inspection must indicate to the Director's satisfaction that the watershed control program and disinfection treatment process are adequately designed and maintained. The on-site inspection will include but not be limited to:
F. Treatment Technique Violations
2. A PWS that has not installed filtration is in violation of a treatment technique requirement if:
b. The PWS is identified as a source of a waterborne disease outbreak.
E. Disinfection Requirements for PWS That Do Not Provide Filtration
1. The disinfection treatment must be sufficient to ensure at least 99.9 percent (3-log) inactivation of Giardia lamblia cysts and 99.99 percent (4-log) inactivation of viruses, every day the PWS serves water to the public, except any one (1) day each month. Each day a PWS serves water to the public, the PWS must calculate the CT value(s) from the PWS's treatment parameters, using the procedure specified in §§ 1.6.6(A)(3) and (4) of this Part, and determine whether this value is sufficient to achieve the specified inactivation rates for Giardia lamblia cysts and viruses.
2. The disinfection system must have either:
b. Automatic shut-off of delivery of water to the distribution system whenever there is less than 0.2 mg/L of residual disinfectant concentration in the water.
4. The residual disinfectant concentration in the distribution system, measured as total chlorine, combined chlorine or chlorine dioxide as specified in § 1.6.5 of this Part, cannot be undetectable in more than five (5) percent of the samples each month, for any two (2) consecutive months that the PWS serves water to the public.
a. Water in the distribution system with a heterotrophic bacteria concentration less than or equal to 500/ml measured as heterotrophic plate count (HPC) as specified in § 1.6.5 of this Part, is deemed to have a detectable disinfectant residual for purposes of determining compliance with this requirement. Thus, the value “V” in the following formula cannot exceed 5 percent in one (1) month for any two (2) consecutive months:
F. Disinfection Requirements for PWS Which Provide Filtration. Each PWS that provides filtration treatment must provide disinfection treatment as follows:
1. The disinfection treatment must be sufficient to ensure that the total treatment processes of that system achieve at least 99.9 percent (3-log) inactivation and/or removal of Giardia lamblia cysts and at least 99.99 percent (4-log) inactivation and/or removal of viruses as determined by the Director every day the PWS serves water to the public, except any one (1) day each month. At least 0.5 log (68.4 percent) must be achieved by chemical disinfection. Each day a PWS serves water to the public, the PWS must calculate the CT value(s) from the PWS’s treatment parameters, using the procedure specified in § 1.6.6(A)(3) and (4) of this Part and determine whether this value is sufficient to achieve the specified inactivation rates for Giardia lamblia cysts and viruses. In lieu of Tables 1.1-1.6, 2.1, and 3.1 in § 1.6.8 of this Part for 99.9 percent inactivation, Tables C-1 through C-13 of the 1999 EPA Disinfection Profiling and Benchmarking Guidance Manual may be used for different percent inactivation requirements such as 68.4 percent (0.5-log).
2. The disinfection system must have either:
b. Automatic shut-off of delivery of water to the distribution system whenever there is less than 0.2 mg/L of residual disinfectant concentration in the water.
4. The residual disinfectant concentration in the distribution system, measured as total chlorine, combined chlorine, or chlorine dioxide, as specified in § 1.6.5 of this Part, cannot be undetectable in more than five (5) percent of the samples each month, for any two (2) consecutive months that the PWS serves water to the public.
G. Disinfection Profiling and Benchmarking
1. A § 1.6 community or non-transient, non-community PWS that serves fewer than ten thousand (10,000) people must develop a disinfection profile, a graphical representation of a PWS's level of Giardia lamblia or virus inactivation measured during the course of a year, under the provisions of §§ 1.6.3(G)(1), (2) and (3) of this Part, unless the Director determines that it is unnecessary. At the Director’s discretion, a § 1.6 PWS that serves at least ten thousand (10,000) people may also be required to develop a disinfection profile. If the Director requires a PWS serving at least ten thousand (10,000) people to develop a profile, the Director shall specify procedures for developing that profile.
2. Disinfection Profile Criteria
a. Any § 1.6 PWS serving fewer than ten thousand (10,000) people that meets the criteria in § 1.6.3(G)(1)(b) of this Part must develop a disinfection profile of its disinfection practice for a period of up to one (1) year. The Director may approve the use of a more representative data set for disinfection profiling than the data set required under §§ 1.6.3(G)(2)(a)(1) and (G)(3) of this Part.
(1) PWS must collect data for several parameters from the plant, specified in §§ 1.6.3(G)(2)(a)(1)(AA) through (DD) of this Part, once per week on the same calendar day over twelve (12) consecutive calendar months to determine the total logs of inactivation for each day of operation, based on the CT99.9 values in Tables 1.1-1.6, 2.1 and 3.1 in § 1.6.8 of this Part, as appropriate, through the entire treatment plant. PWS serving between five hundred (500) and nine hundred ninety-nine (9,999) persons must begin to collect data no later than July 1, 2003. PWS serving fewer than five hundred (500) persons must begin to collect data no later than January 1, 2004. The PWS must monitor the parameters listed in §§ 1.6.3(G)(2)(a)(1)(AA) through (DD) of this Part, necessary to determine the total inactivation ratio, using analytical methods in §§ 1.6.5 and 1.21 of this Part.
3. Developing a Disinfection Profile
4. Disinfection Benchmark
a. A § 1.6 PWS serving less than ten thousand (10,000) people that is required to develop a disinfection profile under the provisions of § 1.6.3(G)(1) of this Part, must develop a Disinfection Benchmark as described in §§ 1.6.3(G)(4)(c) and (d) of this Part and provide the benchmark to the Director if the PWS decides to make a significant change to its disinfection practice. A § 1.6 PWS serving at least ten thousand (10,000) people that is required to develop a disinfection profile under the provisions of § 1.6.3(G)(1) of this Part, must develop a Disinfection Benchmark using procedures specified by the Director if the PWS decides to make a significant change to its disinfection practice. All PWS must consult with the Director for approval prior to making such changes. Significant changes to disinfection practice are:
b. PWS must submit the following information to the Director as part of the consultation and approval process:
c. Any PWS that is modifying its disinfection practice must calculate its disinfection benchmark using the procedures specified in §§ 1.6.3(G)(4)(c)(1) through (2) of this Part.
d. A PWS that uses chloramines, ozone or chlorine dioxide for primary disinfection must calculate the disinfection benchmark from the data collected for viruses to develop the disinfection profile in addition to the Giardia lamblia disinfection benchmark calculated under § 1.6.3(G)(4)(c) of this Part. This viral benchmark must be approved by the Director and must be calculated in the same manner used to calculate the Giardia lamblia disinfection benchmark in § 1.6.3(G)(4)(c) of this Part.
B. Conventional Filtration Treatment or Direct Filtration:
1. PWS that use conventional filtration or direct filtration that do not meet all of the criteria listed in 40 C.F.R. § 141.71 for avoiding filtration must meet the turbidity requirements listed in §§ 1.6.4(B)(1)(a), (b) and (c) of this Part below:
C. Slow Sand Filtration
D. Diatomaceous Earth Filtration
E. Other Filtration Technologies. A PWS may use a filtration technology not listed in 40 C.F.R. § 141.73 or § 1.6.4 of this Part, if it demonstrates to the Director, using pilot plant studies or other means, that the alternative filtration technology, in combination with disinfection treatment that meets the requirements of 40 C.F.R. §§ 141.72 and 141.73, consistently achieves ninety-nine percent (99%) removal of Cryptosporidium oocysts, 99.9 percent removal and/or inactivation of Giardia lamblia cysts and 99.99 percent removal and/or inactivation of viruses. Upon completion of the demonstration, the Director will determine the 95th percentile turbidity value (not to exceed one (1) NTU) and the maximum turbidity value (not to exceed five (5) NTU) based on the demonstration.
A. Only the analytical method(s) specified in this Section, or otherwise approved by the Director, may be used to demonstrate compliance with the requirements of §§ 1.6.2, 1.6.3, or 1.6.4 of this Part.
B. The following procedures shall be performed in accordance with the methods listed.
9. Indigo Method for determination of Ozone in water, as set forth in § 1.21 of this Part.
A. A PWS that uses a surface water source and does not provide filtration treatment must begin monitoring, as specified in this Section, unless the Director has determined that filtration is required in writing, in which case the Director may specify alternative monitoring requirements, until filtration is in place. A PWS that uses a groundwater source under the direct influence of surface water and does not provide filtration treatment must begin monitoring as specified in this Section six (6) months after the Director determines that the groundwater source is under the direct influence of surface water, unless the Director has determined that filtration is required in writing.
1. Fecal coliform or total coliform density measurements, as required by § 1.6.2(E) of this Part, must be performed on representative source water samples immediately prior to the first or only point of disinfectant application. The PWS must sample for fecal or total coliforms at the following minimum frequency each week the PWS serves water to the public:
| PWS Size (Persons Served) | Samples/Week (samples must be taken on separate days) |
| <500 | 1 |
| 501 to 3,300 | 2 |
| 3,301 to 10,000 | 3 |
| 10,001 to 25,000 | 4 |
| >25,000 | 5 |
3. The total inactivation ratio for each day that the PWS is in operation must be determined based on the CT99.9 values in Tables 1.1-1.6, 2.1 and 3.1 in § 1.6.8 of this Part, as appropriate. The parameters necessary to determine the total inactivation ratio must be monitored as follows:
4. The total inactivation ratio must be calculated as follows:
a. If the PWS uses only one (1) point of disinfectant application, the PWS may determine the total inactivation ratio based on either of the following two (2) methods:
(2) Successive CTcalc/CT99.9 values representing sequential inactivation ratios are determined between the point of disinfectant application and a point before or at the first customer during peak hourly flow. Under this alternative, the following method must be used to calculate the total inactivation ratio:
5. The residual disinfectant concentration of the water entering the distribution system must be monitored continuously using analytical methods specified in § 1.21 of this Part, and the lowest value must be recorded each day. In the event of system monitoring failure, grab sampling may be conducted every four (4) hours, for no more than five (5) working days.
a. PWS serving three thousand three hundred (3,300) or fewer persons may take grab samples in lieu of continuous monitoring on an ongoing basis at the frequencies prescribed below:
| PWS Size by Population | Samples/day (The day's samples cannot be taken at the same time. The sampling intervals are subject to the Director's review and approval) |
| <501 | 1 |
| 501 to 1,000 | 2 |
| 1,001 to 2,500 | 3 |
| 2,501 to 3,300 | 4 |
6. The residual disinfectant concentration must be measured at least at the same points in the distribution system and at the same time as total coliforms are sampled, as specified in §§ 1.16.4 and 1.17.1 of this Part. The Director may allow a PWS which uses both a surface water source or a groundwater source under direct influence of surface water, and a groundwater source to take disinfectant residual samples at points other than the total coliform sampling points, if the Director determines that such points are more representative of treated (disinfected) water quality within the distribution system.
a. Heterotrophic bacteria, measured as HPC as specified in § 1.6.5(B)(3) of this Part, may be measured in lieu of residual disinfectant concentration except as specified in § 1.8.5(C)(1) of this Part.
A. A PWS that uses a surface water source or a groundwater source under the influence of surface water and provides filtration treatment must monitor in accordance with this Section:
1. Turbidity
a. Representative Filtered Effluent Turbidity Requirements
b. Individual Filter Turbidity Requirements
(1) § 1.6 PWS that use conventional or direct filtration must conduct continuous monitoring of turbidity for each individual filter in the system. The following requirements apply to continuous turbidity monitoring:
3. The residual disinfectant concentration of the water entering the distribution system, and throughout the distribution system, must be monitored as indicated in §§ 1.6.6(A)(5) and (6) of this Part.
A. A PWS that uses a surface water source and does not provide filtration treatment must report the following information monthly to the Director unless the Director has determined that filtration is required in writing, in which case the Director may specify alternate reporting requirements as appropriate until filtration is in place. A PWS that uses a groundwater source under the direct influence of surface water and does not provide filtration treatment must report monthly to the Director, the following information beginning no later than six (6) months after the Director determines that the groundwater source is under the direct influence of surface water:
1. Source water quality information must be reported to the Director within ten (10) days after the end of each month the PWS serves water to the public. Information that must be reported:
2. Disinfection information must be reported to the Director within ten (10) days after the end of each month the PWS serves water to the public. Information that must be reported:
h. The following information on the samples taken in the distribution system in conjunction with total coliform monitoring specified in § 1.6.3 of this Part.
i. A PWS need not report the data listed in §§ 1.6.8(A)(2)(a) and (c) through (f) of this Part, if all data listed in §§ 1.6.8(A)(2)(a) through (h) of this Part, remain on file at the PWS and the Director determines that:
5. Each PWS, upon discovering that a waterborne disease outbreak potentially attributable to that PWS has occurred, must report that occurrence to the Director as soon as possible, but no later than the end of the next business day.
B. § 1.6 PWS that provide filtration treatment must report monthly to the Director the following information in §§ 1.6.8(B)(1) through (4) of this Part, unless otherwise stated.
1. Turbidity requirements: Turbidity measurements as required by §§ 1.6.4 and 1.6.7 of this Part, must be reported within ten (10) days after the end of each month the PWS serves water to the public. Information that must be reported includes:
3. Disinfection information must be reported to the Director within ten (10) days after the end of each month and must include all items specified in §§ 1.6.8(A)(2)(a) through (h) and 1.6.8(A)(5) of this Part.
4. Individual filter effluent follow-up actions: For all PWS, reporting to the Director is required by the 10th of the following month for exceedance listed in §§ 1.6.8(B)(4)(a) through (d) of this Part, unless otherwise stated. PWS that use lime softening may apply to the Director for alternative exceedance levels for the levels specified in §§ 1.6.8(B)(4)(a) through (d) of this Part, if they can demonstrate that higher turbidity levels in individual filters are due to lime carryover only and not due to degraded filter performance.
c. If the individual filter effluent turbidity (or for PWS serving fewer than 10,000, the CFE turbidity of PWSs with two (2) filters that monitor CFE in lieu of individual filters) exceeded 1.0 NTU in two (2) consecutive 15-minute readings for three (3) consecutive months, the PWS must report the filter number, the turbidity measurement, and the date(s) on which the exceedance occurred. In addition, the PWS must conduct a self-assessment of the filter(s) within fourteen (14) days of the exceedance unless a CPE as specified in § 1.6.8(B)(4)(d) of this Part, was required. PWS with two (2) filters that monitor combined filter effluent in lieu of individual filters must conduct a self-assessment on both filters. The PWS must report the date the filter self-assessment was triggered and the date it was completed by the 10th of the following month or fourteen (14) days after the self-assessment was triggered only if the self-assessment was triggered during the last four (4) days of the month. The self-assessment must consist of at least the following components:
D. Recycle Provisions:
1. Reporting. A PWS must notify the Director if the PWS recycles spent filter backwash water, thickener supernatant, or liquids from dewatering processes. This notification must include, at a minimum, the information specified in §§ 1.6.8(D)(1)(a) and (b) of this Part.
2. Recordkeeping. The PWS must collect and retain on file recycle flow information specified in §§ 1.6.8(D)(2)(a) through (f) of this Part, for review and evaluation by the Director.
f. Data on the physical dimensions of the equalization and/or treatment units, typical and maximum hydraulic loading rates, type of treatment chemicals used and average dose and frequency of use, and frequency at which solids are removed, if applicable.
| Table 1.1 CT values (CT99.9) for 99.9 percent inactivation of giardia lamblia cysts by free chlorine at 0.5°C or lower1 | |||||||
| Residual (mg/L) | pH | ||||||
| <6.0 | 6.5 | 7.0 | 7.5 | 8.0 | 8.5 | <9.0 | |
| <0.4 | 137 | 163 | 195 | 237 | 277 | 329 | 390 |
| 0.6 | 141 | 168 | 200 | 239 | 286 | 342 | 407 |
| 0.8 | 145 | 172 | 205 | 246 | 295 | 354 | 422 |
| 1.0 | 148 | 176 | 210 | 253 | 304 | 365 | 437 |
| 1.2 | 152 | 180 | 215 | 259 | 313 | 376 | 451 |
| 1.4 | 155 | 184 | 221 | 266 | 321 | 387 | 464 |
| 1.6 | 157 | 189 | 226 | 273 | 329 | 397 | 477 |
| 1.8 | 162 | 193 | 231 | 279 | 338 | 407 | 489 |
| 2.0 | 165 | 197 | 236 | 286 | 346 | 417 | 500 |
| 2.2 | 169 | 201 | 242 | 297 | 353 | 426 | 511 |
| 2.4 | 172 | 205 | 247 | 298 | 361 | 435 | 522 |
| 2.6 | 175 | 209 | 252 | 304 | 368 | 444 | 533 |
| 2.8 | 178 | 213 | 257 | 310 | 375 | 452 | 543 |
| 3.0 | 181 | 217 | 261 | 316 | 382 | 460 | 552 |
| 1 These CT values achieve greater than a 99.99 percent inactivation of viruses. CT values between the indicated pH values may be determined by interpolation. CT values between the indicated temperatures of different tables may be determined by linear interpolation. If no interpolation is used, use the CT99.9 value at the lower temperature and at the higher pH. |
| Table 1.2 CT values (CT99.9) for 99.9 percent inactivation of giardia lamblia cysts by free chlorine at 0.5°C1 | |||||||
| Free Residual (mg/L) | pH | ||||||
| <6.0 | 6.5 | 7.0 | 7.5 | 8.0 | 8.5 | <9.0 | |
| <0.4 | 97 | 117 | 139 | 166 | 198 | 236 | 279 |
| 0.6 | 100 | 120 | 143 | 171 | 204 | 244 | 291 |
| 0.8 | 103 | 122 | 146 | 175 | 210 | 252 | 301 |
| 1.0 | 105 | 125 | 149 | 179 | 216 | 260 | 312 |
| 1.2 | 107 | 127 | 152 | 183 | 221 | 267 | 320 |
| 1.4 | 109 | 130 | 155 | 187 | 227 | 274 | 329 |
| 1.6 | 111 | 132 | 158 | 192 | 232 | 281 | 337 |
| 1.8 | 114 | 135 | 162 | 196 | 238 | 287 | 345 |
| 2.0 | 116 | 138 | 165 | 200 | 243 | 294 | 353 |
| 2.2 | 118 | 140 | 169 | 204 | 248 | 300 | 361 |
| 2.4 | 120 | 143 | 172 | 209 | 253 | 306 | 368 |
| 2.6 | 122 | 146 | 175 | 213 | 258 | 312 | 375 |
| 2.8 | 124 | 148 | 178 | 217 | 263 | 318 | 382 |
| 3.0 | 126 | 151 | 182 | 221 | 268 | 324 | 389 |
| 1 These CT values achieve greater than a 99.99 percent inactivation of viruses. CT values between the indicated pH values may be determined by interpolation. CT values between the indicated temperatures of different tables may be determined by linear interpolation. If no interpolation is used, use the CT99.9 value at the lower temperature and at the higher pH. |
| Table 1.3 CT values (CT99.9) for 99.9 percent inactivation of giardia lamblia cysts by free chlorine at 10.0°C1 | |||||||
| Free Residual (mg/L) | pH | ||||||
| <6.0 | 6.5 | 7.0 | 7.5 | 8.0 | 8.5 | <9.0 | |
| <0.4 | 73 | 88 | 104 | 125 | 149 | 177 | 209 |
| 0.6 | 75 | 90 | 107 | 128 | 153 | 183 | 218 |
| 0.8 | 78 | 92 | 110 | 131 | 158 | 189 | 226 |
| 1.0 | 79 | 94 | 112 | 134 | 162 | 195 | 234 |
| 1.2 | 80 | 95 | 114 | 137 | 166 | 200 | 240 |
| 1.4 | 82 | 98 | 116 | 140 | 170 | 206 | 247 |
| 1.6 | 83 | 99 | 119 | 144 | 174 | 211 | 253 |
| 1.8 | 86 | 101 | 122 | 147 | 179 | 215 | 259 |
| 2.0 | 87 | 104 | 124 | 150 | 182 | 221 | 265 |
| 2.2 | 89 | 105 | 127 | 153 | 186 | 225 | 271 |
| 2.4 | 90 | 107 | 129 | 157 | 190 | 230 | 276 |
| 2.6 | 92 | 110 | 131 | 160 | 194 | 234 | 281 |
| 2.8 | 93 | 111 | 134 | 163 | 197 | 239 | 287 |
| 3.0 | 95 | 113 | 137 | 166 | 201 | 243 | 292 |
| 1 These CT values achieve greater than a 99.99 percent inactivation of viruses. CT values between the indicated pH values may be determined by interpolation. CT values between the indicated temperatures of different tables may be determined by linear interpolation. If no interpolation is used, use the CT99.9 value at the lower temperature and at the higher pH. |
| Table 1.4 CT values (CT99.9) for 99.9 percent inactivation of giardia lamblia cysts by free chlorine at 15.0°C1 | |||||||
| Free Residual (mg/L) | pH | ||||||
| <6.0 | 6.5 | 7.0 | 7.5 | 8.0 | 8.5 | <9.0 | |
| <0.4 | 49 | 59 | 70 | 83 | 99 | 118 | 140 |
| 0.6 | 50 | 60 | 72 | 86 | 102 | 122 | 146 |
| 0.8 | 52 | 61 | 73 | 88 | 105 | 126 | 151 |
| 1.0 | 53 | 63 | 75 | 90 | 108 | 130 | 156 |
| 1.2 | 54 | 64 | 76 | 92 | 111 | 134 | 160 |
| 1.4 | 55 | 65 | 78 | 94 | 114 | 137 | 165 |
| 1.6 | 56 | 66 | 79 | 96 | 116 | 141 | 169 |
| 1.8 | 57 | 68 | 81 | 98 | 119 | 144 | 173 |
| 2.0 | 58 | 69 | 83 | 100 | 122 | 147 | 177 |
| 2.2 | 59 | 70 | 85 | 102 | 124 | 150 | 181 |
| 2.4 | 60 | 72 | 86 | 105 | 127 | 153 | 184 |
| 2.6 | 61 | 73 | 88 | 107 | 129 | 156 | 188 |
| 2.8 | 62 | 74 | 89 | 109 | 132 | 159 | 191 |
| 3.0 | 63 | 76 | 91 | 111 | 134 | 162 | 195 |
| 1 These CT values achieve greater than a 99.99 percent inactivation of viruses. CT values between the indicated pH values may be determined by interpolation. CT values between the indicated temperatures of different tables may be determined by linear interpolation. If no interpolation is used, use the CT99.9 value at the lower temperature and at the higher pH. |
| Table 1.5 CT values (CT99.9) for 99.9 percent inactivation of giardia lamblia cysts by free chlorine at 20.0°C1 | |||||||
| Free Residual (mg/L) | pH | ||||||
| <6.0 | 6.5 | 7.0 | 7.5 | 8.0 | 8.5 | <9.0 | |
| <0.4 | 36 | 44 | 52 | 62 | 74 | 89 | 105 |
| 0.6 | 38 | 45 | 54 | 64 | 77 | 92 | 109 |
| 0.8 | 39 | 46 | 55 | 66 | 79 | 95 | 113 |
| 1.0 | 39 | 47 | 56 | 67 | 81 | 98 | 117 |
| 1.2 | 40 | 48 | 57 | 69 | 83 | 100 | 120 |
| 1.4 | 41 | 49 | 58 | 70 | 85 | 103 | 123 |
| 1.6 | 42 | 50 | 59 | 72 | 87 | 105 | 126 |
| 1.8 | 43 | 51 | 61 | 74 | 89 | 108 | 129 |
| 2.0 | 44 | 52 | 62 | 75 | 91 | 110 | 132 |
| 2.2 | 44 | 53 | 63 | 77 | 93 | 113 | 135 |
| 2.4 | 45 | 54 | 65 | 78 | 95 | 115 | 138 |
| 2.6 | 46 | 55 | 66 | 80 | 97 | 117 | 141 |
| 2.8 | 47 | 56 | 67 | 81 | 99 | 119 | 143 |
| 3.0 | 47 | 57 | 68 | 83 | 101 | 122 | 146 |
| 1 These CT values achieve greater than a 99.99 percent inactivation of viruses. CT values between the indicated pH values may be determined by interpolation. CT values between the indicated temperatures of different tables may be determined by linear interpolation. If no interpolation is used, use the CT99.9 value at the lower temperature and at the higher pH. |
| Table 1.6 CT values (CT99.9) for 99.9 percent inactivation of giardia lamblia cysts by free chlorine at 25°C1 and higher | |||||||
| Free Residual (mg/L) | pH | ||||||
| <6.0 | 6.5 | 7.0 | 7.5 | 8.0 | 8.5 | <9.0 | |
| <0.4 | 24 | 29 | 35 | 42 | 50 | 59 | 70 |
| 0.6 | 25 | 30 | 36 | 43 | 51 | 61 | 73 |
| 0.8 | 26 | 31 | 37 | 44 | 53 | 63 | 75 |
| 1.0 | 26 | 31 | 37 | 45 | 54 | 65 | 78 |
| 1.2 | 27 | 32 | 38 | 46 | 55 | 67 | 80 |
| 1.4 | 27 | 33 | 39 | 47 | 57 | 69 | 82 |
| 1.6 | 28 | 33 | 40 | 48 | 58 | 70 | 84 |
| 1.8 | 29 | 34 | 41 | 49 | 60 | 72 | 86 |
| 2.0 | 29 | 35 | 41 | 50 | 61 | 74 | 88 |
| 2.2 | 30 | 35 | 42 | 51 | 62 | 75 | 90 |
| 2.4 | 30 | 36 | 43 | 52 | 63 | 77 | 92 |
| 2.6 | 31 | 37 | 44 | 53 | 65 | 78 | 94 |
| 2.8 | 31 | 37 | 45 | 54 | 66 | 80 | 96 |
| 3.0 | 32 | 38 | 46 | 55 | 67 | 81 | 97 |
| 1 These CT values achieve greater than a 99.99 percent inactivation of viruses. CT values between the indicated pH values may be determined by interpolation. CT values between the indicated temperatures of different tables may be determined by linear interpolation. If no interpolation is used, use the CT99.9 value at the lower temperature and at the higher pH. |
| Table 2.1 CT values (CT99.9) for 99.9 percent inactivation of giardia lamblia cysts by chlorine dioxide and ozone1 | ||||||
| Free Residual (mg/L) | Temperature | |||||
| 1°C | 5°C | 10°C | 15°C | 20°C | >25°C | |
| Chlorinedioxide | 63 | 26 | 23 | 19 | 15 | 11 |
| Ozone | 2.0 | 1.9 | 1.4 | 0.95 | 0.72 | 0.46 |
| 1 These CT values achieve greater than 99.99 percent inactivation of viruses. CT values between the indicated temperatures may be determined by linear interpolation. If no interpolation is used, use the CT99.9 value at the lower temperature for determining CT99.9 values between indicated temperatures. |
| Table 3.1 CT values (CT99.9) for 99.9 percent inactivation of giardia lamblia cysts by chloramines1 Temperature | |||||
| <1°C | 5°C | 10°C | 15°C | 20°C | >25°C |
| 2.0 | 1.9 | 1.4 | 0.95 | 0.72 | 0.46 |
1 These values are for pH values of 6 to 9. These CT values may be assumed to achieve greater than 99.99 percent inactivation of viruses only if chlorine is added and mixed in the water prior to the addition of ammonia. If this condition is not met, the system must demonstrate, based on on-site studies or other information, as approved by the State, that the system is achieving at least 99.99 percent inactivation of viruses. CT values between the indicated temperatures may be determined by linear interpolation. If no interpolation is used, use the CT99.9 value at the lower temperature for determining CT99.9 values between indicated temperatures.
A. General Requirements
2. Applicability. The requirements of § 1.6.9 of this Part apply to all PWS subject to § 1.6 of this Part, which are PWS supplied by a surface water source and PWS supplied by a groundwater source under the direct influence of surface water.
3. Requirements. PWS subject to § 1.6.9 of this Part, must comply with the following requirements:
B. Source Water Monitoring
1. Initial Round of Source Water Monitoring. PWS must conduct the following monitoring on the schedule in § 1.6.9(B)(3) of this Part unless they meet the monitoring exemption criteria in § 1.6.9(B)(4) of this Part.
c. Filtered PWS serving fewer than 10,000 people must sample their source water for E. coli at least once every two weeks for twelve (12) months.
d. Filtered PWS serving fewer than 10,000 people must sample their source water for Cryptosporidium at least twice per month for twelve (12) months or at least monthly for twenty-four (24) months if they meet one of the following, based on monitoring conducted under § 1.6.9(B)(1)(c) of this Part:
3. Monitoring Schedule. PWS must begin the monitoring required in §§ 1.6.9(B)(1) and (2) of this Part, no later than the month beginning with the date listed in the table below:
| SOURCE WATER MONITORING STARTING DATES TABLE | ||
| PWS that serve: | Must begin the first round of source water monitoring no later than the month beginning: | And must begin the second round of source water monitoring no later than the month beginning: |
| (1) At least 100,000 people | (i) October 1, 2006. | (ii) April 1, 2015 |
| (2) From 50,000 to 99,999 people | (i) April 1, 2007 | (ii) October 1, 2015 |
| (3) From 10,000 to 49,999 people | (i) April 1, 2008 | (ii) October 1, 2016 |
| (4) Fewer than 10,000 and monitor for E. coli (applies only to filtered PWS) | (i) October 1, 2008 | (ii) October 1, 2017 |
| (5) Fewer than 10,000 and monitor for Cryptosporidium (applies to filtered PWS that meet the conditions of § 1.6.9(B)(1)(d) of this Part and unfiltered PWS) | (i) April 1, 2010 | (ii) April 1, 2019 |
4. Monitoring Avoidance
5. Plants Operating Only Part of The Year. PWS with treatment plants that must comply with § 1.6 of this Part and that operate for only part of the year must conduct source water monitoring in accordance with § 1.6.9 of this Part, but with the following modifications:
6. New Sources. A PWS that begins using a new source of surface water or GWUDI after the PWS is required to begin monitoring under § 1.6.9(B)(3) of this Part, must monitor the new source on a schedule the Director approves. Source water monitoring must meet the requirements of this § 1.6.9 of this Part. The PWS must also meet the bin classification and Cryptosporidium treatment requirements of §§ 1.6.9(K) and (L) or (M) of this Part, as applicable, for the new source on a schedule the Director approves.
C. Sampling Schedules
1. PWS required to conduct source water monitoring under § 1.6.9(B) of this Part, must submit a sampling schedule that specifies the calendar dates when the PWS will collect each required sample.
b. PWS serving at least 10,000 people must submit their sampling schedule for the initial round of source water monitoring under § 1.6.9(B)(1) of this Part, to EPA electronically.
2. PWS must collect samples within two (2) days before or two (2) days after the dates indicated in their sampling schedule (i.e., within a five-day period around the schedule date) unless one of the conditions of §§ 1.6.9(C)(2)(a) or (b) of this Part applies.
b. If a PWS is unable to report a valid analytical result for a scheduled sampling date due to equipment failure, loss of or damage to the sample, failure to comply with the analytical method requirements, including the quality control requirements in § 1.6.9(E) of this Part, or the failure of an approved laboratory to analyze the sample, then the PWS must collect a replacement sample.
D. Sampling Locations
2. PWSs must collect source water samples prior to chemical treatment, such as coagulants, oxidants, and disinfectants, unless the PWS meets the condition of § 1.6.9(D)(2)(a) of this Part.
4. Bank Filtration
5. Multiple Sources. PWSs with plants that use multiple water sources, including multiple surface water sources and blended surface water and groundwater sources, must collect samples as specified in §§ 1.6.9(D)(5)(a) or (b) of this Part. The use of multiple sources during monitoring must be consistent with routine operational practice.
b. If a sampling tap where the sources are combined prior to treatment is not available, PWSs must collect samples at each source near the intake on the same day and must follow either §§ 1.6.9(D)(5)(b)(1) or (2) of this Part, for sample analysis.
E. Analytical Methods
1. Cryptosporidium. PWSs must analyze for Cryptosporidium using Method 1623: Cryptosporidium and Giardia in Water by Filtration/IMS/FA, 2005, United States Environmental Protection Agency, EPA-815-R-05-002 or Method 1622: Cryptosporidium in Water by Filtration/IMS/FA, 2005, United States Environmental Protection Agency, EPA-815-R-05-001, which are incorporated by reference.
b. Matrix spike (MS) samples, as required by the methods in § 1.6.9(E)(1) of this Part, must be spiked and filtered by a laboratory approved for Cryptosporidium analysis under § 1.6.9(F) of this Part.
2. E. coli. PWSs must use methods for enumeration of E. coli in source water approved in § 1.21 of this Part.
F. Approved Laboratories
G. Reporting Source Water Monitoring Results
2. All PWSs serving at least 10,000 people must report the results from the initial source water monitoring required under § 1.6.9(B)(1) of this Part, to EPA electronically.
5. PWSs must report the applicable information in §§ 1.6.9(G)(5)(a) and (b) of this Part, for the source water monitoring required under § 1.6.9(B) of this Part.
a. PWSs must report the following data elements for each Cryptosporidium analysis:
(7) Number of oocysts counted.
b. PWSs must report the following data elements for each E. coli analysis:
H. Grandfathering Previously Collected Data
1. PWSs may comply with the initial source water monitoring requirements of § 1.6.9(B)(1) of this Part, by grandfathering sample results collected before the PWS is required to begin monitoring (i.e., previously collected data). To be grandfathered, the sample results and analysis must meet the criteria in this Section and the Director must approve.
3. Cryptosporidium Sample Analysis. The analysis of Cryptosporidium samples must meet the criteria in this paragraph.
a. Laboratories analyzed Cryptosporidium samples using one of the analytical methods in §§ 1.6.9(H)(3)(a)(1) through (6) of this Part.
5. Sampling Frequency. Cryptosporidium samples were collected no less frequently than each calendar month on a regular schedule, beginning no earlier than January 1999. Sample collection intervals may vary for the conditions specified in §§ 1.6.9(C)(2)(a) and (b) of this Part, if the PWS provides documentation of the condition when reporting monitoring results.
6. Reporting Monitoring Results for Grandfathering. PWSs that request to grand-father previously collected monitoring results must report the following information by the applicable dates listed in this paragraph. PWSs serving at least 10,000 people must report this information to EPA unless the Director approves reporting to the Director rather than EPA. PWSs serving fewer than 10,000 people must report this information to the Director.
b. PWSs must report previously collected monitoring results for grandfathering, along with the associated documentation listed in §§ 1.6.9(H)(6)(b)(1) through (4) of this Part, no later than two months after the applicable date listed in § 1.6.9(B)(3) of this Part.
I. Requirements When Making a Significant Change in Disinfection Practice
1. Following the completion of initial source water monitoring under § 1.6.9(B)(1) of this Part, a PWS that plans to make a significant change to its disinfection practice, as defined in § 1.6.9(I)(2) of this Part, must develop disinfection profiles and calculate disinfection benchmarks for Giardia lamblia and viruses as described in § 1.6.9(J) of this Part. Prior to changing the disinfection practice, the PWS must notify the Director and must include in this notice the information in §§ 1.6.9(I)(1)(a) through (c) of this Part.
2. Significant changes to disinfection practice are defined as follows:
J. Developing the Disinfection Profile and Benchmark
2. PWSs with a single point of disinfectant application prior to the entrance to the distribution PWS must conduct the monitoring in §§ 1.6.9(J)(2)(a) through (d) of this Part. PWSs with more than one point of disinfectant application must conduct the monitoring in §§ 1.6.9(J)(2)(a) through (d) of this Part, for each disinfection segment. PWSs must monitor the parameters necessary to determine the total inactivation ratio, using analytical methods in § 1.21 of this Part.
3. In lieu of conducting new monitoring under § 1.6.9(J)(2) of this Part, PWSs may elect to meet the requirements of §§ 1.6.9(J)(3)(a) or (b) of this Part.
4. PWSs must calculate the total inactivation ratio for Giardia lamblia as specified in §§ 1.6.9(J)(4)(a) through (c) of this Part.
a. PWSs using only one point of disinfectant application may determine the total inactivation ratio for the disinfection segment based on either of the methods in §§ 1.6.9(J)(4)(a)(1) or (2) of this Part.
5. PWSs must use the procedures specified in §§ 1.6.9(J)(5)(a) and (b) of this Part to calculate a disinfection benchmark.
K. Bin Classification for Filtered PWSs
2. Procedures
3. Filtered PWSs must determine their initial bin classification from the following table and using the Cryptosporidium bin concentration calculated under §§ 1.6.9(K)(1) and (2) of this Part:
| BIN CLASSIFICATION TABLE FOR FILTERED PWS | ||
| For PWS that are: | With a Cryptosporidium bin concentration of (Based on calculations in § 1.6.9(K)(1) or (2) of this Part, as applicable) | The bin classification is |
| Required to monitor for Cryptosporidium under § 1.6.9(B) of this Part | Cryptosporidium < 0.075 oocyst/L | Bin 1 |
| 0.075 oocysts/L = Cryptosporidium < 1.0 oocysts/L | Bin 2 | |
| 1.0 oocysts/L = Cryptosporidium < 3.0 oocysts/L | Bin 3 | |
| Cryptosporidium = 3.0 oocysts/L | Bin 4 | |
| Serving fewer than 10,000 people and NOT required to monitor for Cryptosporidium under § 1.6.9(B)(1)(d) of this Part. | NA | Bin 5 |
5. Filtered PWSs must report their initial bin classification under § 1.6.9(K)(3) of this Part, to the Director for approval no later than six (6) months after the PWS is required to complete initial source water monitoring based on the schedule in § 1.6.9(B)(3) of this Part.
L. Filtered PWS Additional Cryptosporidium Treatment Requirements
2. Filtered PWSs must use one or more of the treatment and management options listed in § 1.6.9(O) of this Part, termed the microbial toolbox, to comply with the additional Cryptosporidium treatment required in § 1.6.9(L)(1) of this Part.
| If the PWS bin classification is | And the PWS uses the following filtration treatment in full compliance with § 1.5 of this Part (as applicable), then the additional Cryptosporidium treatment requirements are | |||
| (A) | Conventional filtration treatment (including softening) | Direct filtration | Slow sand or diatomaceous earth filtration | Alternative technologies |
| Bin 1 | No additional treatment | No additional treatment | No additional treatment | No additional treatment |
| Bin 2 | 1-log treatment | 1.5-log treatment | 1-log treatment | As determined by the Director such that the total Cryptosporidium removal and inactivation is at least 4.0-log. |
| Bin 3 | 2-log treatment | 2.5-log treatment | 2-log treatment | As determined by the Director such that the total Cryptosporidium removal and inactivation is at least 5.0-log. |
| Bin 4 | 2.5-log treatment | 3-log treatment | 2.5-log treatment | As determined by the Director such that the total Cryptosporidium removal and inactivation is at least 5.5-log. |
M. Unfiltered PWS Cryptosporidium Treatment Requirements
1. Determination of Mean Cryptosporidium Level
2. Cryptosporidium Inactivation Requirements. Unfiltered PWSs must provide the level of inactivation for Cryptosporidium specified in this paragraph, based on their mean Cryptosporidium levels as determined under § 1.6.9(M)(1) of this Part and according to the schedule in § 1.6.9(N) of this Part.
3. Inactivation Treatment Technology Requirements. Unfiltered PWSs must use chlorine dioxide, ozone, or UV as described in § 1.6.9(T) of this Part, to meet the Cryptosporidium inactivation requirements of this Section.
N. Schedule for Compliance with Cryptosporidium Treatment Requirements
3. Cryptosporidium treatment compliance dates
| CRYPTOSPORIDIUM TREATMENT COMPLIANCE DATES TABLE | |
| PWS that serve: | Must comply with Cryptosporidium treatment requirements no later than (the Director may allow up to an additional two years for complying with the treatment requirement for systems making capital improvements): |
| a. At least 100,000 people | April 1, 2012 |
| b. From 50,000 to 99,999 people | October 1, 2012 |
| c. From 10,000 to 49,999 people | October 1, 2013 |
| d. Fewer than 10,000 people | October 1, 2014 |
O. Microbial Toolbox Options for Meeting Cryptosporidium Treatment Requirements
1. PWSs receive the treatment credits listed in the table in § 1.6.9(O)(2) of this Part by meeting the conditions for microbial toolbox options described in §§ 1.6.9(P) through 1.6.9(T) of this Part.
2. The following table summarizes options in the microbial toolbox:
| MICROBIAL TOOLBOX SUMMARY TABLE: OPTIONS, TREATMENT CREDITS AND CRITERIA | |
| Toolbox Option | Cryptosporidium treatment credit with design and implementation criteria |
| Source Protection and Management Toolbox Options | |
| (1) Watershed control program | 0.5-log credit for Director-approved program comprising required elements, annual program status report to Director, and regular watershed survey. Unfiltered PWSs are not eligible for credit. Specific criteria are in § 1.6.9(P)(1) of this Part. |
| (2) Alternative source/intake management | No prescribed credit. PWSs may conduct simultaneous monitoring for treatment bin classification at alternative intake locations or under alternative intake management strategies. Specific criteria are in § 1.6.9(P)(2) of this Part. |
| Toolbox Option | Cryptosporidium treatment credit with design and implementation criteria |
| Pre-Filtration Toolbox Options | |
| (3) Presedimentation basin with coagulation | 0.5-log credit during any month that presedimentation basins achieve a monthly mean reduction of 0.5-log or greater in turbidity or alternative Director-approved performance criteria. To be eligible, basins must be operated continuously with coagulant addition and all plant flow must pass through basins. Specific criteria are in § 1.6.9(Q)(1) of this Part. |
| (4) Two-stage lime softening | 0.5-log credit for two-stage softening where chemical addition and hardness precipitation occur in both stages. All plant flow must pass through both stages. Single-stage softening is credited as equivalent to conventional treatment. Specific criteria are in § 1.6.9(Q)(2) of this Part. |
| (5) Bank filtration | 0.5-log credit for 25-foot setback; 1.0-log credit for 50-foot setback; aquifer must be unconsolidated sand containing at least 10 percent fines; average turbidity in wells must be less than 1 NTU. PWSs using wells followed by filtration when conducting source water monitoring must sample the well to determine bin classification and are not eligible for additional credit. Specific criteria are in § 1.6.9(Q)(3) of this Part. |
| Treatment Performance Toolbox Options | |
| (6) Combined filter performance | 0.5-log credit for combined filter effluent turbidity less than or equal to 0.15 NTU in at least 95 percent of measurements each month. Specific criteria are in § 1.6.9(R)(1) of this Part. |
| (7) Individual filter performance | 0.5-log credit (in addition to 0.5-log combined filter performance credit) if individual filter effluent turbidity is less than or equal to 0.15 NTU in at least 95 percent of samples each month in each filter and is never greater than 0.3 NTU in two consecutive measurements in any filter. Specific criteria are in § 1.6.9(R)(2) of this Part. |
| (8) Demonstration of performance | Credit awarded to unit process or treatment train based on a demonstration to the Director with a Director-approved protocol. Specific criteria are in § 1.6.9(R)(3) of this Part. |
| Toolbox Option | Cryptosporidium treatment credit with design and implementation criteria |
| Additional Filtration Toolbox Options | |
| (9) Bag or cartridge filters (individual filters) | Up to 2-log credit based on the removal efficiency demonstrated during challenge testing with a 1.0-log factor of safety. Specific criteria are in § 1.6.9(S)(1) of this Part. |
| (10) Bag or cartridge filters (in series) | Up to 2.5-log credit based on the removal efficiency demonstrated during challenge testing with a 0.5-log factor of safety. Specific criteria are in § 1.6.9(S)(1) of this Part. |
| (11) Membrane filtration | Log credit equivalent to removal efficiency demonstrated in challenge test for device if supported by direct integrity testing. Specific criteria are in § 1.6.9(S)(2) of this Part. |
| (12) Second stage filtration | 0.5-log credit for second separate granular media filtration stage if treatment train includes coagulation prior to first filter. Specific criteria are in § 1.6.9(S)(3) of this Part. |
| (13) Slow sand filters | 2.5-log credit as a secondary filtration step; 3.0-log credit as a primary filtration process. No prior chlorination for either option. Specific criteria are in § 1.6.9(S)(4) of this Part. |
| Inactivation Toolbox Options | |
| (14) Chlorine dioxide | Log credit based on measured CT in relation to CT table. Specific criteria in § 1.6.9(T)(2) of this Part. |
| (15) Ozone | Log credit based on measured CT in relation to CT table. Specific criteria in § 1.6.9(T)(2) of this Part. |
| (16) UV | Log credit based on validated UV dose in relation to UV dose table; reactor validation testing required to establish UV dose and associated operating conditions. Specific criteria in § 1.6.9(T)(4) of this Part. |
P. Source Toolbox Components
1. Watershed Control Program. PWSs receive 0.5-log Cryptosporidium treatment credit for implementing a watershed control program that meets the requirements of this Section.
b. PWSs must submit to the Director a proposed watershed control plan no later than one year before the applicable treatment compliance date in § 1.6.9(N) of this Part. The Director must approve the watershed control plan for the PWS to receive watershed control program treatment credit. The watershed control plan must include the elements in §§ 1.6.9(P)(1)(b)(1) through (4) of this Part.
e. PWSs must complete the actions in §§ 1.6.9(P)(1)(e)(1) through (3) of this Part to maintain the 0.5-log credit.
(2) Undergo a watershed sanitary survey every three years for community PWS and every five years for noncommunity PWS and submit the survey report to the Director. The survey must be conducted according to the Director’s guidelines and by persons the Director approves.
2. Alternative Source
Q. Pre-Filtration Treatment Toolbox Components
1. Presedimentation. PWSs receive 0.5-log Cryptosporidium treatment credit for a presedimentation basin during any month the process meets the criteria in this paragraph.
c. The presedimentation basin must achieve the performance criteria in §§ 1.6.9(Q)(1)(c)(1) or (2) of this Part.
3. Bank Filtration. PWSs receive Cryptosporidium treatment credit for bank filtration that serves as pretreatment to a filtration plant by meeting the criteria in this paragraph. PWSs using bank filtration when they begin source water monitoring under § 1.6.9(B)(1) of this Part must collect samples as described in § 1.6.9(D)(4) of this Part, and are not eligible for this credit.
g. Bank Filtration Demonstration of Performance. The Director may approve Cryptosporidium treatment credit for bank filtration based on a demonstration of performance study that meets the criteria in this paragraph. This treatment credit may be greater than 1.0-log and may be awarded to bank filtration that does not meet the criteria in §§ 1.6.9(Q)(3)(a) through (e) of this Part.
R. Treatment Performance Toolbox Components
2. Individual filter performance. PWSs using conventional filtration treatment or direct filtration treatment receive 0.5-log Cryptosporidium treatment credit, which can be in addition to the 0.5-log credit under § 1.6.9(R)(1) of this Part, during any month the PWS meets the criteria in this paragraph. Compliance with these criteria must be based on individual filter turbidity monitoring as described in § 1.6.7 of this Part, as applicable.
c. Any PWS that has received treatment credit for individual filter performance and fails to meet the requirements of §§ 1.6.9(R)(2)(a) or (b) of this Part during any month does not receive a treatment technique violation under § 1.6.9(L)(3) of this Part, if the Director determines the following:
3. Demonstration of Performance. The Director may approve Cryptosporidium treatment credit for drinking water treatment processes based on a demonstration of performance study that meets the criteria in this paragraph. This treatment credit may be greater than or less than the prescribed treatment credits in § 1.6.9(L) or §§ 1.6.9(Q) through (T) of this Part, and may be awarded to treatment processes that do not meet the criteria for the prescribed credits.
S. Additional Filtration Toolbox Components
1. Bag and Cartridge Filters. PWSs receive Cryptosporidium treatment credit of up to 2.0-log for individual bag or cartridge filters and up to 2.5-log for bag or cartridge filters operated in series by meeting the criteria in §§ 1.6.9(S)(1)(a) through (j) of this Part. To be eligible for this credit, PWSs must report the results of challenge testing that meets the requirements of §§ 1.6.9(S)(1)(b) through (i) of this Part to the Director. The filters must treat the entire plant flow taken from a § 1.6 source.
d. The maximum feed water concentration that can be used during a challenge test must be based on the detection limit of the challenge particulate in the filtrate (i.e., filtrate detection limit) and must be calculated using the following equation:
g. Removal efficiency of a filter must be determined from the results of the challenge test and expressed in terms of log removal values using the following equation:
2. Membrane Filtration
a. PWSs receive Cryptosporidium treatment credit for membrane filtration that meets the criteria of this paragraph. Membrane cartridge filters that meet the definition of membrane filtration in § 1.2 of this Part are eligible for this credit. The level of treatment credit a PWS receives is equal to the lower of the values determined under §§ 1.6.9(S)(2)(a)(1) and (2) of this Part.
b. Challenge Testing. The membrane used by the PWS must undergo challenge testing to evaluate removal efficiency, and the PWS must report the results of challenge testing to the Director. Challenge testing must be conducted according to the criteria in §§ 1.6.9(S)(2)(b)(1) through (7) of this Part. PWSs may use data from challenge testing conducted prior to January 5, 2006 if the prior testing was consistent with the criteria in §§ 1.6.9(S)(2)(b)(1) through (7) of this Part.
(3) The maximum feed water concentration that can be used during a challenge test is based on the detection limit of the challenge particulate in the filtrate and must be determined according to the following equation:
(5) Removal efficiency of a membrane module must be calculated from the challenge test results and expressed as a log removal value according to the following equation:
c. Direct Integrity Testing. PWSs must conduct direct integrity testing in a manner that demonstrates a removal efficiency equal to or greater than the removal credit awarded to the membrane filtration process and meets the requirements described in §§ 1.6.9(S)(2)(c)(1) through (6) of this Part. A direct integrity test is defined as a physical test applied to a membrane unit in order to identify and isolate integrity breaches (i.e., one or more leaks that could result in contamination of the filtrate).
(3) The direct integrity test must have a sensitivity sufficient to verify the log treatment credit awarded to the membrane filtration process by the Director, where sensitivity is defined as the maximum log removal value that can be reliably verified by a direct integrity test. Sensitivity must be determined using the approach in either §§ 1.6.9(S)(2)(c)(3)(AA) or (BB) of this Part as applicable to the type of direct integrity test the PWS uses.
(AA) For direct integrity tests that use an applied pressure or vacuum, the direct integrity test sensitivity must be calculated according to the following equation:
(BB) For direct integrity tests that use a particulate or molecular marker, the direct integrity test sensitivity must be calculated according to the following equation:
d. Indirect Integrity Monitoring. PWSs must conduct continuous indirect integrity monitoring on each membrane unit according to the criteria in §§ 1.6.9(S)(2)(d)(1) through (5) of this Part. Indirect integrity monitoring is defined as monitoring some aspect of filtrate water quality that is indicative of the removal of particulate matter. A PWS that implements continuous direct integrity testing of membrane units in accordance with the criteria in §§ 1.6.9(S)(2)(c)(1) through (5) of this Part is not subject to the requirements for continuous indirect integrity monitoring. PWSs must submit a monthly report to the Director summarizing all continuous indirect integrity monitoring results triggering direct integrity testing and the corrective action that was taken in each case.
T. Inactivation Toolbox Components
1. Calculation of CT Values
2. CT Values for Chlorine Dioxide and Ozone.
a. PWSs receive the Cryptosporidium treatment credit listed in this table by meeting the corresponding chlorine dioxide CT value for the applicable water temperature, as described in § 1.6.9(T)(1) of this Part.
| CT Values (mg·min/L) for Cryptosporidium Inactivation by Chlorine Dioxide8 | |||||||||||
| Log credit | Water Temperature, ºC | ||||||||||
| = 0.5 | 1 | 2 | 3 | 5 | 7 | 10 | 15 | 20 | 25 | 30 | |
| (i) 0.25 | 159 | 153 | 140 | 128 | 107 | 90 | 69 | 45 | 29 | 19 | 12 |
| (ii) 0.5 | 319 | 305 | 279 | 256 | 214 | 180 | 138 | 89 | 58 | 38 | 24 |
| (iii) 1.0 | 637 | 610 | 558 | 511 | 429 | 360 | 277 | 179 | 116 | 75 | 49 |
| (iv) 1.5 | 956 | 915 | 838 | 767 | 643 | 539 | 415 | 268 | 174 | 113 | 73 |
| (v) 2.0 | 1275 | 1220 | 1117 | 1023 | 858 | 719 | 553 | 357 | 232 | 150 | 98 |
| (vi) 2.5 | 1594 | 1525 | 1396 | 1278 | 1072 | 899 | 691 | 447 | 289 | 188 | 122 |
| (vii) 3.0 | 1912 | 1830 | 1675 | 1534 | 1286 | 1079 | 830 | 536 | 347 | 226 | 147 |
| 8 Systems may use this equation to determine log credit between the indicated values: Log credit = (0.001506 x (1.09116)Temp) x CT. |
b. PWSs receive the Cryptosporidium treatment credit listed in this table by meeting the corresponding ozone CT values for the applicable water temperature, as described in § 1.6.9(T)(1) of this Part.
| CT Values (mg·min/L) for Cryptosporidium Inactivation by Ozone9 | |||||||||||
| Log credit | Water Temperature, ºC | ||||||||||
| = 0.5 | 1 | 2 | 3 | 5 | 7 | 10 | 15 | 20 | 25 | 30 | |
| (i) 0.25 | 6.0 | 5.8 | 5.2 | 4.8 | 4.0 | 3.3 | 2.5 | 1.6 | 1.0 | 0.6 | 0.39 |
| (ii) 0.5 | 12 | 12 | 10 | 9.5 | 7.9 | 6.5 | 4.9 | 3.1 | 2.0 | 1.2 | 0.78 |
| (iii) 1.0 | 24 | 23 | 21 | 19 | 16 | 13 | 9.9 | 6.2 | 3.9 | 2.5 | 1.6 |
| (iv) 1.5 | 36 | 35 | 31 | 29 | 24 | 20 | 15 | 9.3 | 5.9 | 3.7 | 2.4 |
| (v) 2.0. | 48 | 46 | 42 | 38 | 32 | 26 | 20 | 12 | 7.8 | 4.9 | 3.1 |
| (vi) 2.5 | 60 | 58 | 52 | 48 | 40 | 33 | 25 | 16 | 9.8 | 6.2 | 3.9 |
| (vii) 3.0 | 72 | 69 | 63 | 57 | 47 | 39 | 30 | 19 | 12 | 7.4 | 4.7 |
| 9 Systems may use this equation to determine log credit between the indicated values: Log credit = (0.0397 x (1.09757)Temp) x CT. |
4. Ultraviolet Light. PWSs receive Cryptosporidium, Giardia lamblia, and virus treatment credits for ultraviolet (UV) light reactors by achieving the corresponding UV dose values shown in § 1.6.9(T)(4)(a) of this Part. PWSs must validate and monitor UV reactors as described in §§ 1.6.9(T)(4)(b) and (c) of this Part to demonstrate that they are achieving a particular UV dose value for treatment credit.
a. UV Dose Table. The treatment credits listed in this table are for UV light at a wavelength of 254 nm as produced by a low-pressure mercury vapor lamp. To receive treatment credit for other lamp types, PWSs must demonstrate an equivalent germicidal dose through reactor validation testing, as described in § 1.6.9(T)(4)(b) of this Part. The UV dose values in this table are applicable only to post-filter applications of UV in filtered PWSs and to unfiltered PWSs.
| UV Dose Table for Cryptosporidium, Giardia lamblia, and Virus Inactivation Credit | |||
| Log credit | Cryptosporidium UV dose (mJ/cm2) | Giardia lamblia UV dose (mJ/cm2) | Virus UV dose (mJ/cm2) |
| (i) 0.5 | 1.6 | 1.5 | 39 |
| (ii) 1.0 | 2.5 | 2.1 | 58 |
| (iii) 1.5 | 3.9 | 3.0 | 79 |
| (iv) 2.0 | 5.8 | 5.2 | 100 |
| (v) 2.5. | 8.5 | 7.7 | 121 |
| (vi) 3.0 | 12 | 11 | 143 |
| (vii) 3.5 | 15 | 15 | 163 |
| (viii) 4.0 | 22 | 22 | 186 |
b. Reactor Validation Testing. PWSs must use UV reactors that have undergone validation testing to determine the operating conditions under which the reactor delivers the UV dose required in § 1.6.9(T)(4)(a) of this Part (i.e., validated operating conditions).
c. Reactor Monitoring
U. Reporting Requirements
5. PWSs must report to the Director in accordance with the following table for any microbial toolbox options used to comply with treatment requirements under §§ 1.6.9(L) or 1.6.9(M) of this Part. Alternatively, the Director may approve a PWS to certify operation within required parameters for treatment credit rather than reporting monthly operational data for toolbox options.
MICROBIAL TOOLBOX REPORTING REQUIREMENTS | ||
| Toolbox option | PWSs must submit the following information | On the following schedule |
| (1) Watershed control program (WCP) | (i) Notice of intention to develop a new or continue an existing watershed control program | No later than two (2) years before the applicable treatment compliance date in § 1.6.9(N) of this Part. |
| (ii) Watershed control plan | No later than one (1) year before the applicable treatment compliance date in § 1.6.9(N) of this Part. | |
| (iii) Annual watershed control program status report | Every twelve (12) months, beginning one (1) year after the applicable treatment compliance date in § 1.6.9(N) of this Part. | |
| (iv) Watershed sanitary survey report | For community PWS, every three (3) years beginning three (3) years after the applicable treatment compliance date in § 1.6.9(N) of this Part. For noncommunity PWS, every five (5) years beginning five (5) years after the applicable treatment compliance date in § 1.6.9(N) of this Part. | |
| (2) Alternative source/intake management | Verification that PWS has relocated the intake or adopted the intake withdrawal procedure reflected in monitoring results | No later than the applicable treatment compliance date in § 1.6.9(N) of this Part. |
| (3) Presedimentation | Monthly verification of the following: (i) Continuous basin operation (ii) Treatment of 100% of the flow (iii) Continuous addition of a coagulant (iv) At least 0.5-log mean reduction of influent turbidity or compliance with alternative State-approved performance criteria. | Monthly reporting within ten (10) days following the month in which the monitoring was conducted, beginning on the applicable treatment compliance date in § 1.6.9(N) of this Part. |
| (4) Two-stage lime softening | Monthly verification of the following: (i) Chemical addition and hardness precipitation occurred in two separate and sequential softening stages prior to filtration (ii) Both stages treated 100% of the plant flow. | Monthly reporting within ten (10) days following the month in which the monitoring was conducted, beginning on the applicable treatment compliance date in § 1.6.9(N) of this Part. |
| (5) Bank filtration | (i) Initial demonstration of the following: (A) Unconsolidated, predominantly sandy aquifer (B) Setback distance of at least 25 ft. (0.5-log credit) or 50 ft. (1.0-log credit). | No later than the applicable treatment compliance date in § 1.6.9(N) of this Part. |
| (ii) If monthly average of daily max turbidity is greater than 1 NTU then PWS must report result and submit an assessment of the cause. | Report within thirty (30) days following the month in which the monitoring was conducted, beginning on the applicable treatment compliance date in § 1.6.9(N) of this Part. | |
| (6) Combined filter performance | Monthly verification of combined filter effluent (CFE) turbidity levels less than or equal to 0.15 NTU in at least 95 percent of the 4-hour CFE measurements taken each month. | Monthly reporting within ten (10) days following the month in which the monitoring was conducted, beginning on the applicable treatment compliance date in § 1.6.9(N) of this Part. |
| (7) Individual filter performance | Monthly verification of the following: (i) Individual filter effluent (IFE) turbidity levels less than or equal to 0.15 NTU in at least 95 percent of samples each month in each filter (ii) No individual filter greater than 0.3 NTU in two consecutive readings 15 minutes apart | Monthly reporting within ten (10) days following the month in which the monitoring was conducted, beginning on the applicable treatment compliance date in § 1.6.9(N) of this Part. |
| (8) Demonstration of performance | (i) Results from testing following a State approved protocol. | No later than the applicable treatment compliance date in § 1.6.9(N) of this Part. |
| (ii) As required by the State, monthly verification of operation within conditions of State approval for demonstration of performance credit. | Within ten (10) days following the month in which monitoring was conducted, beginning on the applicable treatment compliance date in § 1.6.9(N) of this Part. | |
| (9) Bag filters and cartridge filters | (i) Demonstration that the following criteria are met: (A) Process meets the definition of bag or cartridge filtration; (B) Removal efficiency established through challenge testing that meets criteria in this subpart. | No later than the applicable treatment compliance date in § 1.6.9(N) of this Part. |
| (ii) Monthly verification that 100% of plant flow was filtered | Within ten (10) days following the month in which monitoring was conducted, beginning on the applicable treatment compliance date in § 1.6.9(N) of this Part. | |
| (10) Membrane filtration | (i) Results of verification testing demonstrating the following: (A) Removal efficiency established through challenge testing that meets criteria in this subpart; (B) Integrity test method and parameters, including resolution, sensitivity, test frequency, control limits, and associated baseline. | No later than the applicable treatment compliance date in § 1.6.9(N) of this Part. |
| (ii) Monthly report summarizing the following: (A) All direct integrity tests above the control limit; (B) If applicable, any turbidity or alternative state approved indirect integrity monitoring results triggering direct integrity testing and the corrective action that was taken. | Within ten (10) days following the month in which monitoring was conducted, beginning on the applicable treatment compliance date in § 1.6.9(N) of this Part. | |
| (11) Second stage filtration | Monthly verification that 100% of flow was filtered through both stages and that first stage was preceded by coagulation step. | Within ten (10) days following the month in which monitoring was conducted, beginning on the applicable treatment compliance date in § 1.6.9(N) of this Part. |
| (12) Slow sand filtration (as secondary filter) | Monthly verification that both a slow sand filter and a preceding separate stage of filtration treated 100% of flow from § 1.6 sources. | Within ten (10) days following the month in which monitoring was conducted, beginning on the applicable treatment compliance date in § 1.6.9(N) of this Part. |
| (13) Chlorine dioxide | Summary of CT values for each day as described in § 1.6.9(T) of this Part. | Within ten (10) days following the month in which monitoring was conducted. |
| (14) Ozone | Summary of CT values for each day as described in § 1.6.9(T) of this Part. | Within ten (10) days following the month in which monitoring was conducted. |
| (15) UV | (i) Validation test results demonstrating operating conditions that achieve required UV dose. | No later than the applicable treatment compliance date in § 1.6.9(N) of this Part. |
| (ii) Monthly report summarizing the percentage of water entering the distribution system that was not treated by UV reactors operating within validated conditions for the required dose as specified in § 1.6.9(T)(4) of this Part. | Within ten (10) days following the month in which monitoring was conducted, beginning on the applicable treatment compliance date in § 1.6.9(N) of this Part. |
V. Recordkeeping Requirements
W. Requirements to Respond to Significant Deficiencies Identified in Sanitary Surveys Performed by the Director
1. For the purposes of this Section, a “sanitary survey,” as conducted by the Director, includes but is not limited to, an onsite review of the water source(s) (identifying sources of contamination by using results of source water assessments or other relevant information where available), facilities, equipment, operation, maintenance, and monitoring compliance of a PWS to evaluate the adequacy of the PWS, its sources and operations and the distribution of safe drinking water. The sanitary survey must include an evaluation of the applicable components listed in § 1.6.9(W)(1)(a) through (h):
4. PWSs must correct significant deficiencies identified in sanitary survey reports according to the schedule approved by the Director, or if there is no approved schedule, according to the schedule reported under § 1.6.9(W)(3) above if such deficiencies are within the control of the PWS.
A. Maximum Contaminant Levels (MCLs) for Algal Toxins
B. Source Water Surveillance
C. Bloom Severity
2. Severe Bloom (meets any of the following):
3. Moderate Bloom (meets any of the following):
4. Minor Bloom (meets any of the following):
D. Algal Bloom Response Actions
1. The decision to continue observation, conduct screening or proceed to algal toxin monitoring shall be determined on a case by case basis after considering the following factors:
2. The following table shall be used when determining proper response action.
| Bloom Severity | Likelihood of being drawn into the intake | Advanced Treatment | Action |
| Severe | More likely | Not in use or not working properly | Monitor for toxins weekly and observe daily |
| Severe | More likely | In use | Monitor for toxins weekly and observe daily |
| Severe | Less likely | Not in use or not working properly | Screen weekly and observe daily |
| Severe | Less likely | In use | Screen weekly and observe daily |
| Moderate | More likely | Not in use or not working properly | Monitor for Toxins weekly and observe daily |
| Moderate | More likely | In use | Screen weekly and observe daily |
| Moderate | Less likely | Not in use or not working properly | Screen weekly and observe daily |
| Moderate | Less likely | In use | Observe daily |
| Minor | More likely | Not in use or not working properly | Screen weekly and observe daily |
| Minor | More likely | In use | Observe daily |
| Minor | Less likely | Not in use or not working properly | Observe daily |
| Minor | Less likely | In use | Observe daily |
3. Cyanobacteria Screening
b. The PWS shall conduct screening at a minimum frequency of once per week while any of the following conditions occur:
c. Sample Location
4. Algal Toxin Monitoring
a. PWS shall conduct algal toxin monitoring when any of the following conditions occur:
c. Sample Locations
5. Response to Algal Toxin MCL Exceedance
a. If any algal toxin exceeds the MCL listed in § 1.6.10(A) of this Part in any routine weekly samples collected at the finished water sampling point, the PWS shall:
b. Consecutive PWS receiving water from a surface water PWS.
c. Revised cyanobacteria screening or algal toxin monitoring frequency.
d. Monitoring extension
(3) Examples of potential logistical problems include, but are not limited to:
6. Harmful Algal Blooms – Treatment
b. All § 1.6 PWS shall develop and submit to the Director written treatment optimization protocols. The protocols shall include treatment adjustments that will be made under various raw and finished water conditions. In developing the protocols, the PWS shall review and optimize existing treatment for algal toxins, considering effective strategies for algal toxin treatment such as:
c. The treatment optimization protocols shall be submitted to the Director in accordance with the following timelines:
d. A PWS shall comply with all of the following when monitoring conducted in accordance with this Section indicates algal toxin concentrations exceed the MCL in a sample collected at the raw water sampling point more than once within a consecutive twelve-month period, or when algal toxins are detected in a sample collected at a finished water sampling point or a distribution sampling point:
7. Public Notification and Data Reporting
b. A PWS which has exceeded the MCL for an algal toxin in finished water must notify the public in accordance with § 1.16.6 of this Part Tier 1 public noticing requirements and as indicated below, using the standard health effects language of § 1.16.8 of this Part.
| Tier 1 Public Notice Use Restrictions | Microcystin µg/L | Anatoxin-a µg/L | Cylindro-spermopsin µg/L | Saxitoxin µg/L |
| DO NOT DRINK WARNING | 0.3-20 | 20-300 | 1-20 | 0.2-3 |
| DO NOT USE WARNING | >20 | >300 | >20 | >3 |
A. Applicability and Effective Dates
C. Lead and Copper Action Levels
3. The 90th percentile lead and copper levels shall be computed as follows:
D. Corrosion Control Treatment Requirements
K. Failure to comply with the applicable requirements of §§ 1.7.1 through 1.7.12 of this Part, including requirements established by the Director pursuant to these provisions, shall constitute a violation of this Part.
A. PWS shall complete the applicable corrosion control treatment requirements described in § 1.7.3 of this Part, by the deadlines established in this Section.
B. A PWS is deemed to have optimized corrosion control and is not required to complete the applicable corrosion control treatment steps identified in this Section if the PWS satisfies one (1) of the criteria specified in §§ 1.7.2(B)(1) through (3) of this Part. Any such PWS deemed to have optimized corrosion control under this paragraph, and which has treatment in place, shall continue to operate and maintain optimal corrosion control treatment and meet any requirements that the Director determines appropriate to ensure optimal corrosion control treatment is maintained.
2. Any PWS may be deemed by the Director to have optimized corrosion control treatment if the PWS demonstrates to the satisfaction of the Director that it has conducted activities equivalent to the corrosion control steps applicable to such PWS under this Section. If the Director makes this determination, the Director shall provide the PWS with written notice explaining the basis for his decision and shall specify the water quality control parameters representing optimal corrosion control in accordance with § 1.7.3(G) of this Part. PWS deemed to have optimized corrosion control under this paragraph shall operate in compliance with the Director-designated optimal water quality control parameters in accordance with § 1.7.3(H) of this Part, and continue to conduct lead and copper tap and water quality parameter sampling in accordance with §§ 1.7.7(D)(3) and 1.7.8(E) of this Part, respectively. A PWS shall provide the Director with the following information in order to support a determination under this paragraph:
3. Any PWS is deemed to have optimized corrosion control if it submits results of tap water monitoring conducted in accordance with § 1.7.7 of this Part and source water monitoring conducted in accordance with § 1.7.9 of this Part that demonstrates for two (2) consecutive six-month monitoring periods that the difference between the 90th percentile tap water lead level computed under § 1.7.1(C)(3) of this Part, and the highest source water lead concentration, is less than the Practical Quantitation Level for lead specified in § 1.7.10(A)(1)(b) of this Part.
D. Treatment Steps and Deadlines for Large PWSs. Except as provided in §§ 1.7.2(B)(2) and (3) of this Part, large PWSs shall complete the following corrosion control treatment steps (described in the referenced portions of §§ 1.7.3, 1.7.7, and 1.7.8 of this Part) by the indicated dates.
E. Treatment Steps and Deadlines for Small and Medium-size PWS. Except as provided in § 1.7.2(B) of this Part, small and medium-size PWS shall complete the following corrosion control treatment steps (described in the referenced portions of §§ 1.7.3, 1.7.7 and 1.7.8 of this Part) by the indicated time periods.
2. Step 2: Within twelve (12) months after the end of the monitoring period during which a PWS exceeds the lead or copper action level, the Director may require the PWS to perform corrosion control studies (§ 1.7.3(C) of this Part). If the Director does not require the PWS to perform such studies, the Director shall specify optimal corrosion control treatment (§ 1.7.3(E) of this Part) within the following time frames:
8. Step 8: The PWS shall operate in compliance with the Director-designated optimal water quality control parameters (§ 1.7.3(H) of this Part) and continue to conduct tap sampling (§§ 1.7.7(D)(3) and 1.7.8(E) of this Part).
D. Performance of Corrosion Control Studies
1. Any PWS performing corrosion control studies shall evaluate the effectiveness of each of the following treatments, and, if appropriate, combinations of the following treatments to identify the optimal corrosion control treatment for that PWS:
3. The PWS shall measure the following water quality parameters in any tests conducted under this paragraph before and after evaluating the corrosion control treatments listed above:
4. The PWS shall identify all chemical or physical constraints that limit or prohibit the use of a particular corrosion control treatment and document such constraints with at least one (1) of the following:
E. Designation of Optimal Corrosion Control Treatment
G. Review of Treatment and Specification of Optimal Water Quality Control Parameters. The Director shall evaluate the results of all lead and copper tap samples and water quality parameter samples submitted by the PWS and determine whether the PWS has properly installed and operated the optimal corrosion control treatment designated by the Director in § 1.7.3(E) of this Part. Upon reviewing the results of tap water and water quality parameter monitoring by the PWS, both before and after the PWS installs optimal corrosion control treatment, the Director shall designate:
H. Continued Operation and Monitoring. All PWS optimizing corrosion control shall continue to operate and maintain optimal corrosion control treatment, including maintaining water quality parameters at or above minimum values or within ranges designated by the Director under § 1.7.3(G) of this Part, in accordance with this paragraph for all samples collected under §§ 1.7.8(E) through (G) of this Part. Compliance with the requirements of this paragraph shall be determined every six (6) months, as specified under § 1.7.8(E) of this Part. A PWS is out of compliance with the requirements of this paragraph for a six-month period if it has excursions for any Director- specified parameter on more than nine (9) days during the period. An excursion occurs whenever the daily value for one or more of the water quality parameters measured at a sampling location is below the minimum value or outside the range designated by the Director. Daily values are calculated as follows. The Director has the discretion to delete results of obvious sampling errors from this calculation.
I. Modification of the Director's Treatment Decisions. Upon his or her own initiative or in response to a request by a PWS or other interested party, the Director may modify his or her determination of the optimal corrosion control treatment under § 1.7.3(E) of this Part or optimal water quality control parameters under § 1.7.3(G) of this Part. A request for modification by a PWS or other interested party shall be in writing, explain why the modification is appropriate and provide supporting documentation. The Director may modify his or her determination where s/he concludes that such change is necessary to ensure that the PWS continues to optimize corrosion control treatment. A revised determination shall be made in writing, set forth the new treatment requirements, explain the basis for the Director's decision and provide an implementation schedule for completing the treatment modifications.
B. Deadlines for Completing Source Water Treatment Steps
C. Description of Source Water Treatment Requirements
6. Modification of Treatment Decisions. Upon his or her own initiative or in response to a request by a PWS or other interested party, the Director may modify his or her determination of the source water treatment under § 1.7.4(C)(2) of this Part, or maximum permissible lead and copper concentrations for finished water entering the distribution system under § 1.7.4(C)(4) of this Part. A request for modification by a PWS or other interested party shall be in writing, explain why the modification is appropriate and provide supporting documentation. The Director may modify his or her determination where s/he concludes that such change is necessary to ensure that the PWS continues to minimize lead and copper concentrations in source water. A revised determination shall be made in writing, set forth the new treatment requirements, explain the basis for the Director's decision, and provide an implementation schedule for completing the treatment modifications.
B. A PWS shall replace annually at least seven (7) percent of the initial number of lead service lines in its distribution system. The initial number of lead service lines is the number of lead lines in place at the time the replacement program begins. The PWS shall identify the initial number of lead service lines in its distribution system, including an identification of the portion(s) owned by the PWS, based upon a materials evaluation, including the evaluation required under § 1.7.7(A) of this Part, and relevant legal authorities (e.g., contracts, local ordinances) regarding the portion owned by the PWS. The first year of lead service line replacement shall begin on the first day following the end of the monitoring period in which the action level was exceeded under § 1.7.5(A) of this Part. If monitoring is required annually or less frequently, the end of the monitoring period is September 30 of the calendar year in which the sampling occurs. If the Director has established an alternate monitoring period, then the end of the monitoring period will be the last day of that period.
D. A PWS shall replace that portion of the lead service line that it owns. In cases where the PWS does not own the entire lead service line, the PWS shall notify the owner of the line, or the owner's authorized agent, that the PWS will replace the portion of the service line that it owns and shall offer to replace the owner’s portion of the line. A PWS is not required to bear the cost of replacing the privately-owned portion of the line, nor is it required to replace the privately-owned portion where the owner chooses not to pay the cost of replacing the privately-owned portion of the line, or where replacing the privately-owned portion would be precluded by the State, local or common law. A PWS that does not replace the entire length of the service line also shall complete the following tasks.
G. To demonstrate compliance with §§ 1.7.5(A) through (D) of this Part, a PWS shall report to the Director the information specified in § 1.7.11(F) of this Part.
B. Content of Written Public Education Materials
1. Community PWS and non-transient non-community PWS. PWS must include the following elements in printed materials (e.g., brochures and pamphlets) in the same order as listed below. In addition, language in §§ 1.7.6(B)(1)(a) through (b) and 1.7.6(B)(1)(f) of this Part must be included in the materials, exactly as written, except for the text in brackets in these paragraphs for which the PWS must include PWS-specific information. Any additional information presented by a PWS must be consistent with the information below and be in plain language that can be understood by the general public. PWS must submit all written public education materials to the Director prior to delivery. The Director may require the PWS to obtain approval of the content of written public materials prior to delivery.
c. Sources of Lead
d. Discuss the steps the consumer can take to reduce their exposure to lead in drinking water.
2. Community PWS. In addition to including the elements specified in § 1.7.6(B)(1) of this Part, community PWS must:
C. Delivery of Public Education Materials
2. A community PWS that exceeds the lead action level on the basis of tap water samples collected in accordance with § 1.7.7 of this Part, and that is not already conducting public education tasks under this Section, must conduct the public education tasks under this Section within sixty (60) days after the end of the monitoring period in which the exceedance occurred:
b. Contact customers who are most at risk by delivering education materials that meet the content requirements of § 1.7.6(B) of this Part, to local public health agencies even if they are not located within the PWS's service area, along with an informational notice that encourages distribution to all the organization's potentially affected customers or community PWS's users. The PWS must contact the local public health agencies directly by phone or in person. The local public health agencies may provide a specific list of additional community based organizations serving target populations, which may include organizations outside the service area of the PWS. If such lists are provided, PWSs must deliver education materials that meet the content requirements of § 1.7.6(B) of this Part, to all organizations on the provided lists.
(1) Contact customers who are most at risk by delivering materials that meet the content requirements of § 1.7.6(A) of this Part, to the following organizations listed in §§ 1.7.6(C)(2)(b)(1)(AA) through (FF) of this Part that are located within the water PWS's service area, along with an informational notice that encourages distribution to all the organization's potentially affected customers or community PWS's users:
(2) Make a good faith effort to locate the following organizations within the service area and deliver materials that meet the content requirements of § 1.7.6(B) of this Part to them, along with an informational notice that encourages distribution to all potentially affected customers or users. The good faith effort to contact at-risk customers may include requesting a specific contact list of these organizations from the local public health agencies, even if the agencies are not located within the PWS's service area:
f. In addition to §§ 1.7.6(C)(2)(a) through (e) of this Part, PWSs must implement at least three activities from one or more categories listed below. The educational content and selection of these activities must be determined in consultation with the Director.
3. As long as a community PWS exceeds the action level, it must repeat the activities pursuant to § 1.7.6(C)(2) of this Part as described in §§ 1.7.6(C)(3)(a) through (d) of this Part.
4. Within 60 days after the end of the monitoring period in which the exceedance occurred (unless it already is repeating public education tasks pursuant to § 1.7.6(C)(5) of this Part), a non- transient non-community PWS shall deliver the public education materials specified by § 1.7.6(B) of this Part, as follows:
7. A community PWS may apply to the Director, in writing (unless the Director has waived the requirement for prior Director approval), to use only the text specified in § 1.7.6(B)(1) of this Part in lieu of the text in §§ 1.7.6(B)(1) and (B)(2) of this Part and to perform the tasks listed in §§ 1.7.6(C)(4) and (5) of this Part in lieu of the tasks in §§ 1.7.6(C)(2) and (3) of this Part, if:
8. A community PWS serving 3,300 or fewer people may limit certain aspects of their public education programs as follows:
E. Notification of Results
3. Content. The consumer notice must include the results of lead tap water monitoring for the tap that was tested, an explanation of the health effects of lead, list steps consumers can take to reduce exposure to lead in drinking water and contact information for the water utility. The notice must also provide the maximum contaminant level goal and the action level for lead and the definitions for these two terms as contained in the following text:
4. Delivery. The consumer notice must be provided to persons served at the tap that was tested, either by mail or by another method approved by the Director. For example, upon approval by the Director, a non-transient non-community PWS could post the results on a bulletin board in the facility to allow users to review the information. The PWS must provide the notice to customers at sample taps tested, including consumers who do not receive water bills.
A. Sample Site Location
2. A PWS shall use the information on lead, copper and galvanized steel that is required when conducting a materials evaluation (presence of lead from piping, solder, caulking, interior home plumbing, copper from piping and alloys, service lines, and home plumbing, and galvanized piping, service lines and home plumbing within the distribution system.) When an evaluation of the information collected pursuant to the above is insufficient to locate the requisite number of lead and copper sampling sites that meet the targeting criteria in § 1.7.7(A)(2)(a) of this Part, the PWS shall review the sources of information listed below in order to identify a sufficient number of sampling sites. In addition, the PWS shall seek to collect such information where possible in the course of its normal operations (e.g., checking service line materials when reading water meters or performing maintenance activities):
3. The sampling sites selected for a community PWS's sampling pool (“tier 1 sampling sites”) shall consist of single family structures that:
4. Any community PWS with insufficient tier 1 sampling sites shall complete its sampling pool with “tier 2 sampling sites”, consisting of buildings, including multiple- family residences that:
6. The sampling sites selected for a non-transient, non-community PWS (“tier 1 sampling sites”) shall consist of buildings that:
B. Sample Collection Methods
3. Each service line sample shall be one (1) liter in volume and have stood motionless in the lead service line for at least six (6) hours. Lead service line samples shall be collected in one (1) of the following three (3) ways:
C. Number of Samples. PWS shall collect at least one (1) sample during each monitoring period specified in § 1.7.7(D) of this Part, from the number of sites listed in the first column (“standard monitoring”) of the table in this paragraph. A PWS conducting reduced monitoring under § 1.7.7(D)(4) of this Part, shall collect at least one (1) sample from the number of sites specified in the second column (“reduced monitoring”) of the table in this paragraph during each monitoring period specified in § 1.7.7(D)(4) of this Part. Such reduced monitoring sites shall be representative of the sites required for standard monitoring. A PWS that has fewer than five drinking water taps, that can be used for human consumption meeting the sample site criteria of § 1.7.7(A) of this Part to reach the required number of sample sites listed in § 1.7.7(C) of this Part, must collect at least one sample from each tap and then must collect additional samples from those taps on different days during the monitoring period to meet the required number of sites. Alternatively, the Director may allow these PWS to collect a number of samples fewer than the number of sites specified in § 1.7.7(C) of this Part, provided that 100 percent of all taps that can be used for human consumption are sampled. The Director must approve this reduction of the minimum number of samples in writing based on a request from the PWS or onsite verification by the Director. The Director may specify sampling locations when a PWS is conducting reduced monitoring. The table is as follows:
| System Size (# of People Served) | Number of Sites (Standard Monitoring) | Number of Sites (Reduced Monitoring) |
| >100,000 | 100 | 50 |
| 10,001-100,000 | 60 | 30 |
| 3,301 to 10,000 | 40 | 20 |
| 501 to 3,300 | 20 | 10 |
| 101 to 500 | 10 | 5 |
| <100 | 5 | 5 |
D. Timing of Monitoring
1. Initial Tap Sampling. The first six-month monitoring period for small, medium-size, and large PWS shall begin on the following dates:
b. All small and medium-size PWS shall monitor during each six-month monitoring period until:
| System Size (# People Served) | First Six-Month Monitoring Period Begins On |
| >50,000 | January 1, 1992 |
| 3,301 to 50,000 | July 1, 1992 |
| <3,300 | July 1, 1993 |
2. Monitoring after Installation of Corrosion Control and Source Water Treatment
4. Reduced Monitoring
d. A PWS that reduces the number and frequency of sampling shall collect these samples from representative sites included in the pool of targeted sampling sites identified in § 1.7.7(A) of this Part. PWSs sampling annually or less frequently shall conduct the lead and copper tap sampling during the months of June, July, August or September unless the Director has approved a different sampling period in accordance with § 1.7.7(D)(4)(d)(1) of this Part.
g. Any PWS subject to the reduced monitoring frequency that fails to meet the lead action level during any four (4) month monitoring period or that fails to operate at or above the minimum value or within the range of values for the water quality parameters specified by the Director under § 1.7.3(G) of this Part, for more than nine (9) days in any six (6) month period specified in § 1.7.8(E) of this Part, shall conduct tap water sampling for lead and copper at the frequency specified in § 1.7.7(D)(3) of this Part, collect the number of samples specified for standard monitoring under § 1.7.7(C) of this Part, and shall resume monitoring for water quality parameters within the distribution system in accordance with § 1.7.8(E) of this Part. This standard tap water sampling shall begin no later than the six (6) month period beginning January 1 of the calendar year following the lead action level exceedance or water quality parameter excursion. Such a PWS may resume reduced monitoring for lead and copper at the tap and for water quality parameters within the distribution system under the following conditions:
F. Invalidation of Lead or Copper Tap Water Samples. A sample invalidated under this paragraph does not count toward determining lead or copper 90th percentile levels under § 1.7.1(C)(3) of this Part or toward meeting the minimum monitoring requirements of § 1.7.7(C) of this Part.
1. The Director may invalidate a lead or copper tap water sample if at least one (1) of the following conditions is met:
4. The PWS must collect replacement samples for any samples invalidated under this Section if, after the invalidation of one (1) or more samples, the PWS has too few samples to meet the minimum requirements of § 1.7.7(C) of this Part. Any such replacement samples must be taken as soon as possible, but no later than twenty (20) days after the date the Director invalidates the sample or by the end of the applicable monitoring period, whichever occurs later. Replacement samples taken after the end of the applicable monitoring period shall not also be used to meet the monitoring requirements of a subsequent monitoring period. The replacement samples shall be taken at the same locations as the invalidated samples or, if that is not possible, at locations other than those already used for sampling during the monitoring period.
B. General Requirements
1. Sample Collection Methods
2. Number of Samples
a. PWS shall collect two (2) tap samples for applicable water quality parameters during each monitoring period specified under §§ 1.7.8(C) through (F) of this Part.
| System Size (# People Served) | # of Sites for Water Quality Parameters |
| >100,000 | 25 |
| 10,001-100,000 | 10 |
| 3,301 to 10,000 | 3 |
| 501 to 3,300 | 2 |
| 101 to 500 | 1 |
| <100 | 1 |
C. Initial Sampling. All large PWS shall measure the applicable water quality parameters as specified below at taps and at each entry point to the distribution system during each six-month monitoring period specified in § 1.7.7(D)(1) of this Part. All small and medium-size PWS shall measure the applicable water quality parameters at the locations specified below during each six-month monitoring period specified in § 1.7.7(D)(1) of this Part, during which the PWS exceeds the lead or copper action level.
1. At taps:
D. Monitoring after Installation of Corrosion Control. Any large PWS which installs optimal corrosion control treatment pursuant to § 1.7.2(D)(4) of this Part, shall measure the water quality parameters at the locations and frequencies specified below during each six-month monitoring period specified in § 1.7.7(D)(2)(a) of this Part. Any small or medium-size PWS which installs optimal corrosion control treatment shall conduct such monitoring during each six-month monitoring period specified in § 1.7.7(D)(2)(b) of this Part, in which the PWS exceeds the lead or copper action level.
1. At taps, two (2) samples for:
2. Except as provided in § 1.7.8(D)(3) of this Part, at each entry point to the distribution system, at least one (1) sample no less frequently than every two (2) weeks (bi-weekly) for:
F. Reduced Monitoring.
1. Any PWS that maintains the range of values for the water quality parameters reflecting optimal corrosion control treatment during each of two (2) consecutive six-month monitoring periods under § 1.7.8(E) of this Part shall continue monitoring at the entry point(s) to the distribution system as specified in § 1.7.8(D)(2) of this Part. Such PWS may collect two (2) tap samples for applicable water quality parameters from the following reduced number of sites during each six-month monitoring period.
| System Size (# People Served) | Reduced # of Sites for Water Quality Parameters |
| >100,000 | 10 |
| 10,001 to 100,000 | 7 |
| 3,301 to 10,000 | 3 |
| 501 to 3,300 | 2 |
| 101 to 500 | 1 |
| <100 | 1 |
2. Any PWS that maintains the range of values for the water quality parameters reflecting optimal corrosion control treatment specified by the Director under § 1.7.3(G) of this Part, during three (3) consecutive years of monitoring may reduce the frequency with which it collects the number of tap samples for applicable water quality parameters specified in § 1.7.8(F)(1) of this Part, from every six (6) months to annually. This sampling begins during the calendar year immediately following the end of the monitoring period in which the third consecutive year of six-month monitoring occurs. Any PWS that maintains the range of values for the water quality parameters reflecting optimal corrosion control treatment specified by the Director under § 1.7.3(G) of this Part during three (3) consecutive years of annual monitoring under this paragraph may reduce the frequency with which it collects the number of tap samples for applicable water quality parameters specified in § 1.7.8(F)(1) of this Part from annually to every three (3) years. This sampling begins no later than the third calendar year following the end of the monitoring period in which the third consecutive year of monitoring occurs.
G. Additional Monitoring by PWS. The results of any monitoring conducted in addition to the minimum requirements of this Section shall be considered by the PWS and the Director in making any determinations (i.e., determining concentrations of water quality parameters) under this Section or § 1.7.3 of this Part.
| Summary of Monitoring Requirements For Water Quality Parameters1 | |||
| Monitoring Period | Parameters2 | Location | Frequency |
| Initial Monitoring | pH, alkalinity, orthophosphate or silica3, calcium, conductivity, temperature | Taps and at entry point(s) to distribution system | Every six (6) months |
| After Installation of Corrosion Control | pH, alkalinity, orthophosphate or silica3, calcium4 | Taps | Every six (6) months |
| pH, alkalinity dosage rate and concentration (if alkalinity adjusted as part of corrosion control), inhibitor dosage rate and inhibitor residual5 | Entry point(s) to distribution system | No less frequently than every two (2) weeks | |
| After Director Specifies Parameter Values For Optimal Corrosion Control | pH, alkalinity, orthophosphate or silica3, calcium4 | Taps | Every six (6) months |
| pH, alkalinity dosage rate and concentration (if alkalinity adjusted as part of corrosion control), inhibitor dosage rate and inhibitor residual5 | Entry point(s) to distribution system | No less frequently than every two (2) weeks | |
| Reduced Monitoring | pH, alkalinity, orthophosphate or silica3, calcium4 | Taps | Every six (6) months, annually7 or every three (3) years8 reduced number of sites |
| pH, alkalinity dosage rate and concentration (if alkalinity adjusted as part of corrosion control), inhibitor dosage rate and inhibitor residual5 | Entry point(s) to distribution system | No less frequently than every two (2) weeks | |
| 1 Table is for illustrative purposes; consult the text of this Section for precise regulatory requirements.2 Small and medium-size systems have to monitor for water quality parameters only during monitoring periods in which the system exceeds the lead or copper action level.3 Orthophosphate must be measured only when an inhibitor containing a phosphate compound is used. Silica must be measured only when an inhibitor containing silicate compound is used.4 Calcium must be measured only when calcium carbonate stabilization is used as part of corrosion control.5 Inhibitor dosage rates and inhibitor residual concentrations (orthophosphate or silica) must be measured only when an inhibitor is used.6 Ground water systems may limit monitoring to representative locations throughout the system.7 Water systems may reduce frequency of monitoring for water quality parameters at the tap from every six (6) months to annually if they have maintained the range of values for water quality parameters reflecting optimal corrosion control during 3 consecutive years of monitoring.8 Water systems may further reduce the frequency of monitoring for water quality parameters at the tap from annually to once every 3 years if they have maintained the range of values for water quality parameters reflecting optimal corrosion control during 3 consecutive years of annual monitoring. Water systems may accelerate to triennial monitoring for water quality parameters at the tap if they have maintained 90th percentile lead levels less than or equal to 0.005 mg/L, 90th percentile copper levels less than or equal to 0.65 mg/L, and the range of water quality parameters designated by the Director under § 1.7.3 of this Part as representing optimal corrosion control during two (2) consecutive six-month monitoring periods. |
A. Sample Location, Collection Methods, and Number of Samples
1. A PWS that fails to meet the lead or copper action level on the basis of tap samples collected in accordance with § 1.7.7 of this Part, shall collect lead and copper source water samples in accordance with the following requirements regarding sample location, number of samples, and collection methods:
d. The Director may reduce the total number of samples which must be analyzed by allowing the use of compositing. Compositing of samples must be done by certified laboratory personnel. Composite samples from a maximum of five (5) samples are allowed, provided that if the lead concentration in the composite sample is greater than or equal to 0.001 mg/L or the copper concentration is greater than or equal to 0.160 mg/L, then either:
D. Monitoring Frequency after the Director Specifies Maximum Permissible Source Water Levels or Determines That Source Water Treatment Is Not Needed
1. A PWS shall monitor at the frequency specified below in cases where the Director specifies maximum permissible source water levels under § 1.7.4(C)(4) of this Part, or determines that the PWS is not required to install source water treatment under § 1.7.4(C)(2) of this Part.
E. Reduced Monitoring Frequency
1. A PWS using only groundwater may reduce the monitoring frequency for lead and/or copper in source water to once during each nine-year compliance cycle (as that term is defined in § 1.2 of this Part) provided that the samples are collected no later than every ninth calendar year and if the PWS meets one (1) of the following criteria:
2. A PWS using surface water (or a combination of surface water and groundwater) may reduce the monitoring frequency in § 1.7.9(D)(1) of this Part, to once during each nine-year compliance cycle (as that term is defined in § 1.2 of this Part) provided that the samples are collected no later than every ninth calendar year and if the PWS meets one (1) of the following criteria:
3. A PWS that uses a new source of water is not eligible for reduced monitoring for lead and/or copper until concentrations in samples collected from the new source during three (3) consecutive monitoring periods are below the maximum permissible lead and copper concentrations specified by the Director in § 1.7.4(B)(5) of this Part.
A. Analyses for lead, copper, pH, conductivity, calcium, alkalinity, orthophosphate, silica, and temperature shall be conducted with the methods in § 1.21 of this Part.
1. Analyses under this Section shall only be conducted by certified laboratories using the methods specified in § 1.21 of this Part. Analyses for pH and temperature shall be conducted using methods specified in § 1.21 of this Part by a party approved by the Director. To obtain certification to conduct analyses for lead and copper, laboratories must:
b. Achieve quantitative acceptance limits as follows:
4. All copper levels measured between the PQL and the MDL must be either reported as measured or they can be reported as one-half the PQL (0.025 mg/L). All levels below the copper MDL must be reported as zero.
B. Reporting Requirements for Tap Water Monitoring for Lead and Copper and for Water Quality Parameter Monitoring
1. Except as provided in § 1.7.11(B)(1)(g) of this Part, a PWS shall report the information specified below for all tap water samples specified in § 1.7.7 of this Part and for all water quality parameter samples specified in § 1.7.8 of this Part within the first ten (10) days following the end of each applicable monitoring period specified in §§ 1.7.7 and 1.7.8 of this Part (i.e., every six-months, annually, every 3 years, or every 9 years). For monitoring periods with a duration less than six (6) months, the end of the monitoring period is the last date samples can be collected during that period as specified in §§ 1.7.7 and 1.7.8 of this Part.
2. For a non-transient non-community PWS, or a community PWS meeting the criteria of § 1.7.6(C)(7) of this Part, that does not have enough taps that can provide first-draw samples, the PWS must either:
C. Source Water Monitoring Reporting Requirements
D. Corrosion Control Treatment Reporting Requirements. By the applicable dates under § 1.7.2 of this Part, PWS shall report the following information:
E. Source Water Treatment Reporting Requirements. By the applicable dates in § 1.7.4 of this Part, PWS shall provide the following information to the Director:
F. Lead Service Line Replacement Reporting Requirements. PWS shall report the following information to the Director to demonstrate compliance with the requirements of § 1.7.5 of this Part:
2. No later than twelve (12) months after the end of a monitoring period in which a PWS exceeds the lead action level in sampling referred to in § 1.7.5(A) of this Part, and every twelve (12) months thereafter, the PWS shall demonstrate to the Director in writing that the PWS has either:
3. The annual letter submitted to the Director under paragraph § 1.7.11(F)(2) of this Part of this Section shall contain the following information:
G. Public Education Program Reporting Requirements
1. Any PWS that is subject to the public education requirements in § 1.7.6 of this Part, shall, within ten (10) days after the end of each period in which the PWS is required to perform public education tasks in accordance with § 1.7.6(C) of this Part, send written documentation to the Director that contains:
I. Reporting of 90th Percentile Lead and Copper Concentrations Where the Director Calculates a PWS’s 90th Percentile Concentration. A PWS is not required to report the 90th percentile lead and copper concentrations measured from among all lead and copper tap water samples collected during each monitoring period, as required by § 1.7.11(B)(1)(d) of this Part, if:
2. The PWS has provided the following information to the Director by the date specified in § 1.7.11(I)(1) of this Part:
3. The Director has provided the results of the 90th percentile lead and copper calculations, in writing, to the PWS before the end of the monitoring period.
A. The maximum contaminant levels (MCLs) for disinfection byproducts are as follows:
| Disinfection Byproduct | MCL (mg/L) |
| Total Trihalomethanes (TTHM) | 0.080 |
| Haloacetic Acids (five) (HAA5) | 0.060 |
| Bromate | 0.010 |
| Chlorite | 1.0 |
B. Compliance dates
1. Community PWS and non-transient, non-community PWS. § 1.6 PWS must comply with this Section as follows:
C. Best Technology, Treatment Techniques, or Other Means for Achieving Compliance
1. The following are identified as the best technology, treatment techniques, or other means available for achieving compliance with the maximum contaminant levels for disinfection byproducts identified in § 1.8.1(A) of this Part:
2. The following are identified as the best technology, treatment techniques, or other means available for achieving compliance with the maximum contaminant levels for TTHM and HAA5 identified in § 1.8.1(A) of this Part for all PWS that disinfect their source water:
3. The following are identified as the best technology, treatment techniques, or other means available for achieving compliance with the maximum contaminant levels for TTHM and HAA5 identified in § 1.8.1(A) of this Part, for consecutive PWS and applies only to the disinfected water that consecutive PWS buy or otherwise receive:
a. TTHM and HAA5:
(2) Systems serving less than 10,000: Improved distribution system and storage tank management to reduce residence time.
A. Maximum residual disinfectant levels (MRDLs) are as follows:
B. Compliance Dates
C. The following are identified as the best technology, treatment techniques, or other means available for achieving compliance with the maximum residual disinfectant levels identified in § 1.8.2(A) of this Part: control of treatment processes to reduce disinfectant demand and control of disinfection treatment processes to reduce disinfectant levels.
A. The requirements of § 1.8 of this Part constitute the State of Rhode Island primary drinking water regulations.
C. Control of Disinfectant Residuals. Notwithstanding the MRDLs in § 1.8.2 of this Part, PWS may increase residual disinfectant levels in the distribution system of chlorine or chloramines (but not chlorine dioxide) to a level and for a time necessary to protect public health, to address specific microbiological contamination problems caused by circumstances such as, but not limited to, distribution line breaks, storm run-off events, source water contamination events, or cross-connection events.
A. General
B. Disinfection Byproducts
C. Disinfectant Residuals
D. Additional Analytical Methods. PWS required to analyze parameters not included in §§ 1.8.4(B) and (C) of this Part must use the following methods. A party approved by EPA or the Director must measure these parameters.
6. Magnesium. All methods allowed in § 1.21 of this Part for measuring magnesium.
A. General Requirements
B. Monitoring Requirements for Disinfection Byproducts
1. TTHMs and HAA5
a. Routine monitoring. PWS must monitor at the frequency indicated in the following table. Multiple wells drawing water from a single aquifer may be considered one (1) treatment plant for determining the minimum number of samples required, with Director approval in accordance with criteria developed by the Director:
| Routine Monitoring Frequency for TTHM and HAA5 | ||
| Type Of PWS | Minimum Monitoring Frequency | Sample Location in The Distribution System |
| § 1.6 PWS serving at least 10,000 persons. | Four (4) water samples per quarter per treatment plant. | At least 25 percent of all samples collected each quarter at locations representing maximum residence time. Remaining samples taken at locations representative of at least average residence time in the distribution system and representing the entire distribution system, taking into account number of persons served, different sources of water, and different treatment methods. If a PWS elects to sample more frequently than the minimum required, at least twenty-five percent (25%) of all samples collected each quarter (including those taken in excess of the required frequency) must be taken at locations that represent the maximum residence time of the water in the distribution system. The remaining samples must be taken at locations representative of at least average residence time in the distribution system. |
| § 1.6 PWS serving from 500 to 9,999 persons. | One (1) water sample per quarter per treatment plant. | Locations representing maximum residence time. |
| § 1.6 PWS serving fewer than 500 persons. | One (1) sample per year per treatment plant during month of warmest water temperature. | Locations representing maximum residence time. If the sample (or average of annual samples, if more than one (1) sample is taken) exceeds the MCL, the PWS must increase monitoring to one (1) sample per treatment plant per quarter, taken at a point reflecting the maximum residence time in the distribution system, until the PWS meets criteria in § 1.8.5(B)(1)(d) of this Part. |
| PWS using only groundwater not under direct influence of surface water using chemical disinfectant and serving at least 10,000 persons. | One (1) water sample per quarter per treatment plant. | Locations representing maximum residence time. |
| PWS using only groundwater not under direct influence of surface water using chemical disinfectant and serving fewer than 10,000 persons. | One (1) water sample per year per treatment plant during month of warmest water temperature. | Locations representing maximum residence time. If the sample (or average of annual samples, if more than one (1) sample is taken) exceeds the MCL, the PWS must increase monitoring to one (1) sample per treatment plant per quarter, taken at a point reflecting the maximum residence time in the distribution system, until the PWS meets criteria in § 1.8.5(B)(1)(d) of this Part. |
b. PWS may reduce monitoring, except as otherwise provided, in accordance with the following table:
| Reduced Monitoring Frequency for TTHM and HAA5 | ||
| If You Are A… | You May Reduce Monitoring If You Have Monitored At Least One (1) Year And Your… | To This Level |
| § 1.6 PWS serving at least 10,000 persons which has a source water annual average TOC level, before any treatment, =4.0 mg/L. | TTHM annual average =0.040 mg/L and HAA5 annual average =0.030 mg/L. | One (1) sample per treatment plant per quarter at distribution system location reflecting maximum residence time. |
| § 1.6 PWS serving from 500 to 9,999 persons which has a source average TOC level, before any treatment, =4.0 mg/L. | TTHM annual average =0.040 mg/L and HAA5 =0.030 mg/L. | One (1) sample per treatment plant per year at distribution system location reflecting maximum residence time during month of warmest water temperature. NOTE: Any § 1.6 PWS serving fewer than 500 persons may not reduce its monitoring to less than one (1) sample per treatment plant per year. |
| PWS using only groundwater not under direct influence of surface water using chemical disinfectant and serving at least 10,000 persons. | TTHM annual average =0.040 mg/L and HAA5 annual average =0.030 mg/L. | One (1) sample per treatment plant per year at distribution system location reflecting maximum residence time during month of warmest water temperature. |
| PWS using only groundwater not under direct influence of surface water using chemical disinfectant and serving fewer than 10,000 persons. | TTHM annual average =0.040 mg/L and HAA5 distribution annual average =0.030 mg/L for two (2) consecutive years OR TTHM annual average =0.020 mg/L and HAA5 annual average =0.015 mg/L for one (1) year. | One (1) sample per treatment plant per three-year monitoring cycle at PWS location reflecting maximum residence time during month of warmest water temperature, with the three-year cycle beginning on January 1 following quarter in which PWS qualifies for reduced monitoring. |
2. Chlorite. Community and non-transient, non-community PWS using chlorine dioxide, for disinfection or oxidation, must conduct monitoring for chlorite.
a. Routine Monitoring
c. Reduced monitoring
3. Bromate
b. Reduced monitoring
C. Monitoring Requirements for Disinfectant Residuals
1. Chlorine and Chloramines
2. Chlorine Dioxide
D. Monitoring Requirements for Disinfection Byproduct Precursors (DBPP)
F. Monitoring Plans. Each PWS required to monitor under this subpart must develop and implement a monitoring plan. The PWS must maintain the plan and make it available for inspection by the Director and the general public no later than thirty (30) days following the applicable compliance dates in § 1.8.3 of this Part. All § 1.6 PWSs serving more than 3,300 people must submit a copy of the monitoring plan to the Director no later than the date of the first report required under § 1.8.7 of this Part. The Director may also require the plan to be submitted by any other PWS. After review, the Director may require changes in any plan elements. The plan must include at least the following elements.
3. If approved by the Director for monitoring as a consecutive PWS, or if providing water to a consecutive PWS, the sampling plan must reflect the entire distribution system.
A. General Requirements
B. Disinfection Byproducts
1. TTHMs and HAA5
C. Disinfectant Residuals
1. Chlorine and Chloramines
2. Chlorine Dioxide
D. Disinfection Byproduct Precursors (DBPP). Compliance must be determined as specified by § 1.8.8(C) of this Part. PWS may begin monitoring to determine whether Step 1 TOC removals can be met twelve (12) months prior to the compliance date for the PWS. This monitoring is not required and failure to monitor during this period is not a violation. However, any PWS that does not monitor during this period, and then determines in the first twelve (12) months after the compliance date that it is not able to meet the Step 1 requirements in § 1.8.8(B)(2) of this Part, and must therefore apply for alternate minimum TOC removal (Step 2) requirements, is not eligible for retroactive approval of alternate minimum TOC removal (Step 2) requirements as allowed pursuant to § 1.8.8 (B)(3) of this Part, and is in violation. PWS may apply for alternate minimum TOC removal (Step 2) requirements any time after the compliance date. For PWS required to meet Step 1 TOC removals, if the value calculated under § 1.8.8 of this Part, is less than 1.00, the PWS is in violation of the treatment technique requirements and must notify the public pursuant to § 1.16.6 of this Part, in addition to reporting to the Director pursuant to § 1.8.7 of this Part.
B. Disinfection Byproducts. PWS must report the information specified in the following table:
| If you are a | You must report (The Director may choose to perform calculations and determine whether the MCL was exceeded, in lieu of having the PWS report that information) |
| (1) PWS monitoring for TTHMs and HAA5 under the requirements of § 1.8.5(B) of this Part, on a quarterly or more frequent basis. | (i) The number of samples taken during the last quarter. (ii) The location, date, and result of each sample taken during the last quarter. (iii) The arithmetic average of all samples taken in the last quarter. (iv) The annual arithmetic average of the quarterly arithmetic averages of this Section for the last four (4) quarters. (v) Whether, based on § 1.8.6(B)(1) of this Part, the MCL was violated |
| (2) PWS monitoring for TTHMs and HAA5 under the requirements of § 1.8.5(B) less frequently than quarterly (but as least annually). | (i) The number of samples taken during the last year. (ii) The location, date, and result of each sample taken during the last monitoring period. (iii) The arithmetic average of all samples taken over the last year. (iv) Whether, based on § 1.8.6(B)(1) of this Part, the MCL was violated. |
| (3) PWS monitoring for TTHMs and HAA5 under the requirements of § 1.8.5(B) of this Part, less frequently than annually. | (i) The location, date, and result of each sample taken. (ii) Whether, based on § 1.8.6(B)(1) of this Part, the MCL was violated. |
| (4) PWS monitoring for chlorite under the requirements of § 1.8.5 (B) of this Part. | (i) The number of entry point samples taken each month for the last 3 months. (ii) The location, date, and result of each sample (both entry point and distribution system) taken during the last quarter. (iii) For each month in the reporting period, the arithmetic average of all samples taken in each three (3) samples set taken in the distribution system. (iv) Whether, based on § 1.8.6(B)(3) of this Part, the MCL was violated, in which month, and how many times it was violated each month. |
| (5) PWS monitoring for bromate under the requirements of § 1.8.5(B) of this Part. | (i) The number of samples taken during the last quarter. (ii) The location, date, and result of each sample taken during the last quarter. (iii) The arithmetic average of the monthly arithmetic averages of all samples taken in the last year. (iv) Whether, based on § 1.8.6(B)(2) of this Part, the MCL was violated. |
C. Disinfectants. PWS must report the information specified in the following table:
| If you are a | You must report (The Director may choose to perform calculations and determine whether the MRDL was exceeded, in lieu of having the PWS report that information) |
| (1) PWS monitoring for chlorine or chloramines under the requirements of § 1.8.5(C) of this Part. | (i) The number of samples taken during each month of the last quarter. (ii) The month arithmetic average of all samples taken in each month for the last 12 months. (iii) The arithmetic average of the monthly averages for the last 12 months. (iv) Whether, based on § 1.8.6(C)(1) of this Part, the MRDL was violated. |
| (2) PWS monitoring for chlorine dioxide under the requirements of § 1.8.5(C) of this Part. | (i) The dates, result, and locations of samples taken during the last quarter. (ii) Whether, based on § 1.8.6(C)(2) of this Part, the MRDL was violated. (iii) Whether the MRDL was exceeded in any two (2) consecutive daily samples and whether the resulting violation was acute or nonacute. |
D. Disinfection Byproduct Precursors and Enhanced Coagulation or Enhanced Softening. PWSs must report the information specified in the following table:
| If you are a | You must report (The Director may choose to perform calculations and determine whether the treatment technique was met, in lieu of having the PWS report that information) |
| (1) PWS monitoring monthly or quarterly for TOC under the requirements of § 1.8.5(D) of this Part and required to meet the enhanced coagulation or enhanced softening requirements in §§ 1.8.8(B)(2) or (3) of this Part. | (i) The number of paired (source water and treated water) samples taken during the last quarter. (ii) The location, date, and results of each paired sample and associated alkalinity taken during the last quarter. (iii) For each month in the reporting period that paired samples were taken, the arithmetic average of the percent reduction of TOC for each paired sample and the required TOC percent removal. (iv) Calculations for determining compliance with the TOC percent removal requirements, as provided in § 1.8.8(C)(1) of this Part. (v) Whether the PWS is in compliance with the enhanced coagulation or enhanced softening percent removal requirements in § 1.8.8(B) of this Part for the last four (4) quarters. |
| (2) PWS monitoring monthly or quarterly for TOC under the requirements of § 1.8.5(D) of this Part and meeting one (1) or more of the alternative compliance criteria in §§ 1.8.8(A)(2) or (3) of this Part. | (i) The alternative compliance criterion that the PWS is using. (ii) The number of paired samples taken during the last quarter. (iii) The location, date, and result of each paired sample and associated alkalinity taken during the last quarter. (iv) The running annual arithmetic average based on monthly averages (or quarterly samples) of source water TOC for PWS meeting a criterion in §§ 1.8.8(A)(2)(a) or (c) or of treated water TOC for PWS meeting the criterion in § 1.8.8(A)(2)(b) of this Part. (v) The running annual arithmetic average based on monthly averages (or quarterly samples) of source water SUVA for PWS meeting the criterion in § 1.8.8(A)(2)(e) or of treated water SUVA for PWS meeting the criterion in § 1.8.8(A)(2)(f) of this Part. (vi) The running annual average of source water alkalinity for PWS meeting the criterion in § 1.8.8(A)(2)(c) and of treated water alkalinity for PWS meeting the criterion in § 1.8.8(A)(3)(a) of this Part. (vii) The running annual average for both TTHM and HAA5 for PWS meeting the criterion in §§ 1.8.8(A)(2)(c) or (d) of this Part. (viii) The running annual average of the amount of magnesium hardness removal (as CaCO3, in mg/L) for PWS meeting the criterion in § 1.8.8(A)(3)(b) of this Part. (ix) Whether the PWS is in compliance with the particular alternative compliance criterion in §§ 1.8.8(A)(2) or (3) of this Part. |
A. Applicability
2. Alternative Compliance Criteria for Enhanced Coagulation and Enhanced Softening Systems. § 1.6 PWS using conventional filtration treatment may use the alternative compliance criteria in §§ 1.8.8(A)(2)(a) through (f) of this Part to comply with this Section in lieu of complying with § 1.8.8(B) of this Part. PWS must still comply with monitoring requirements in § 1.8.5(D) of this Part.
3. Additional Alternative Compliance Criteria for Softening Systems. PWS practicing enhanced softening that cannot achieve the TOC removals required by § 1.8.8(B)(2) of this Part may use the alternative compliance criteria in §§ 1.8.8(A)(3)(a) and (b) of this Part in lieu of complying with § 1.8.8(B) of this Part. PWS must still comply with monitoring requirements in § 1.8.5(D) of this Part.
B. Enhanced Coagulation and Enhanced Softening Performance Requirements
2. Required Step 1 TOC reductions, indicated in the following table, are based upon specified source water parameters measured in accordance with § 1.8.4(D) of this Part. PWS practicing softening are required to meet the Step 1 TOC reductions in the far-right column (Source water alkalinity >120 mg/L) for the specified source water TOC.
| Step 1 Required Removal of TOC by Enhanced Coagulation and Enhanced Softening for § 1.5 PWSs Using Conventional Treatment. | |||
| PWS meeting at least one (1) of the conditions in §§ 1.8.8(A)(2)(a) through (f) of this Part are not required to operate with enhanced coagulation.Softening systems meeting one (1) of the alternative compliance criteria in § 1.8.8(A)(3) of this Part are not required to operate with enhanced softening. | |||
| Source-water TOC, mg/L | Source-water alkalinity, mg/L as CaCO3 (in percentages) | ||
| 0-60 | >60-120 | >120 (PWS practicing softening must meet the TOC removal requirements in this column) | |
| >2.0-4.0 | 35.0 | 25.0 | 15.0 |
| >4.0-8.0 | 45.0 | 35.0 | 25.0 |
| >8.0 | 50.0 | 40.0 | 30.0 |
4. Alternate Minimum TOC Removal (Step 2) Requirements. Applications made to the Director by enhanced coagulation systems for approval of alternate minimum TOC removal (Step 2) requirements under § 1.8.8(B)(3) of this Part must include, at a minimum, results of bench- or pilot-scale testing conducted under § 1.8.8(B)(4)(a) of this Part. The submitted bench- or pilot-scale testing must be used to determine the alternate enhanced coagulation level.
b. Bench- or pilot-scale testing of enhanced coagulation must be conducted by using representative water samples and adding 10 mg/L increments of alum (or equivalent amounts of ferric salt) until the pH is reduced to a level less than or equal to the enhanced coagulation Step 2 target pH shown in the following table:
| Enhanced Coagulation Step 2 Target pH | |
| Alkalinity (mg/L as CaCO3) | Target pH |
| 0-60 | 5.5 |
| >60-120 | 6.3 |
| >120-240 | 7.0 |
| >240 | 7.5 |
C. Compliance Calculations
1. § 1.6 PWS other than those identified in §§ 1.8.8(A)(2) or (3) of this Part must comply with requirements contained in §§ 1.8.8(B)(2) or (3) of this Part. PWS must calculate compliance quarterly, beginning after the PWS has collected twelve (12) months of data, by determining an annual average using the following method:
2. PWS may use the provisions in §§ 1.8.8(C)(2)(a) through (e) of this Part in lieu of the calculations in §§ 1.8.8(C)(1)(a) through (e) of this Part, to determine compliance with TOC percent removal requirements.
D. Treatment Technique Requirements for DBP Precursors. The following are identified as treatment techniques to control the level of disinfection byproduct precursors in drinking water treatment and distribution systems. For § 1.6 PWS using conventional treatment, enhanced coagulation or enhanced softening.
A. General Requirements
3. Schedule
a. You must comply with the requirements of § 1.8.9 of this Part on the schedule in the table below.
| If you serve this population | You must submit your standard monitoring plan or system specific study plan (If, within 12 months after the date identified in this column, the Director does not approve your plan or notify you that it has not yet completed its review, you may consider the plan that you submitted as approved. You must implement that plan and you must complete standard monitoring or a system specific study no later than the date identified in the third column) or 40/30 certification (You must submit your 40/30 certification under § 1.8.9(D) of this Part by the date indicated) to the Director by or receive very small system waiver from Director | You must complete your standard monitoring system specific study by | You must submit your IDSE report Director by (If, within three months after the date identified in this column (nine months after the date identified in this column if you must comply on the schedule in § 1.8.9(A)(3)(a) of this Part, the Director does not approve your IDSE report or notify you that it has not yet completed its review, you may consider the report that you submitted as approved and you must implement the recommended § 1.8.10 of this Part monitoring as required) |
| Systems that are not part of a combined distribution system and systems that serve the largest population in the combined distribution system | |||
| (i) Greater than or equal to 100,000 | October 1, 2006 | September 30, 2008 | January 1, 2009 |
| (ii) 50,000-99,999 | April 1, 2007 | March 31, 2009 | July 1, 2009 |
| (iii) 10,000-49,999 | October 1, 2007 | September 30, 2009 | January 1, 2010 |
| (iv) Less than 10,000 (CWS only) | April 1, 2008 | March 31, 2010 | July 1, 2010 |
| Other systems that are part of a combined distribution system | |||
| (v) Wholesale system or consecutive system | At the same time as the system with the earliest compliance date in the combined distribution system |
4. You must conduct standard monitoring that meets the requirements in § 1.8.9(B) of this Part, or a system specific study that meets the requirements in § 1.8.9(C) of this Part, or certify to the Director that you meet 40/30 certification criteria under § 1.8.9(D) of this Part, or qualify for a very small system waiver under § 1.8.9(E) of this Part.
B. Standard Monitoring
1. Standard Monitoring Plan. Your standard monitoring plan must comply with §§ 1.8.9(B)(1)(a) through (d) of this Part. You must prepare and submit your standard monitoring plan to the Director according to the schedule in § 1.8.9(A)(3) of this Part.
2. Standard Monitoring
a. You must monitor as indicated in the table below. You must collect dual sample sets at each monitoring location. One sample in the dual sample set must be analyzed for TTHM. The other sample in the dual sample set must be analyzed for HAA5. You must conduct one monitoring period during the peak historical month for TTHM levels or HAA5 levels or the month of warmest water temperature. You must review available compliance, study, or operational data to determine the peak historical month for TTHM or HAA5 levels or warmest water temperature.
| Source Water Type | Population Size Category | Monitoring periods and frequency of sampling | Distribution system monitoring locations18 | ||||
| Total per monitoring period | Near entry points | Average residence time | High TTHM locations | High HAA5 locations | |||
| < 500 consecutive systems | One (during peak historical month)19 | 2 | 1 | …… | 1 | ||
| < 500 non- consecutive systems | ........................ | 2 | …… | …… | 1 | 1 | |
| 500-3,300 consecutive systems | Four (every 90 days) | 2 | 1 | …… | 1 | ||
| 500-3,300 non- consecutive systems | ........................ | 2 | …… | …… | 1 | 1 | |
| 3,301-9,999 | ........................ | 4 | …… | 1 | 2 | 1 | |
| 10,000-49,999 | Six (every 60 days) | 8 | 1 | 2 | 3 | 2 | |
| 50,000-249,999 | ........................ | 16 | 3 | 4 | 5 | 4 | |
| 250,000-999,999 | ........................ | 24 | 4 | 6 | 8 | 6 | |
| 1,000,000-4,999,999 | ........................ | 32 | 6 | 8 | 10 | 8 | |
| = 5,000,000 | ........................ | 40 | 8 | 10 | 12 | 10 | |
| Ground Water: | |||||||
| < 500 consecutive systems | One (during peak historical month)19 | 2 | 1 | ………. | 1 | ||
| < 500 non- consecutive systems | ........................ | 2 | …. | ………. | 1 | 1 | |
| 500-9,999 | Four (every 90 days) | 2 | …. | ………. | 1 | 1 | |
| 10,000-99,999 | ........................ | 6 | 1 | 1 | 2 | 2 | |
| 1,000,000-4,999,999 | ........................ | 8 | 1 | 1 | 3 | 3 | |
| = 5,000,000 | ........................ | 12 | 2 | 2 | 4 | 4 | |
| 18 A dual sample set (i.e., a TTHM and an HAA5 sample) must be taken at each monitoring location during each monitoring period19 The peak historical month is the month with the highest TTHM or HAA5 levels or the warmest water temperature. |
b. You must take samples at locations other than the existing § 1.8 of this Part monitoring locations. Monitoring locations must be distributed throughout the distribution system.
3. IDSE Report. Your IDSE report must include the elements required in §§ 1.8.9(B)(3)(a) through (d) of this Part. You must submit your IDSE report to the Director according to the schedule in § 1.8.9(A)(3) of this Part.
C. System Specific Studies
1. System Specific Study Plan. Your system specific study plan must be based on either existing monitoring results as required under § 1.8.9(C)(1)(a) of this Part or modeling as required under § 1.8.9(C)(1)(b) of this Part. You must prepare and submit your system specific study plan to the Director according to the schedule in § 1.8.9(A)(3) of this Part.
a. Existing Monitoring Results. You may comply by submitting monitoring results collected before you are required to begin monitoring under § 1.8.9(A)(3) of this Part. The monitoring results and analysis must meet the criteria in §§ 1.8.9(C)(1)(a)(1) and (2) of this Part.
(1) Minimum Requirements
(BB) The monitoring locations and frequency must meet the conditions identified in this paragraph [§ 1.8.9(C)(1)(a)(1)(BB) of this Part]. Each location must be sampled once during the peak historical month for TTHM levels or HAA5 levels or the month of warmest water temperature for every 12 months of data submitted for that location. Monitoring results must include all § 1.8 of this Part compliance monitoring results plus additional monitoring results as necessary to meet minimum sample requirements.
| System Type | Population Size Category | Number of Monitoring Locations | Number of Samples | |
| TTHM | HAA5 | |||
| § 1.6 | ||||
| < 500 | 3 | 3 | 3 | |
| 500-3,300 | 3 | 9 | 9 | |
| 3,301-9,999 | 6 | 36 | 36 | |
| 10,000-49,999 | 12 | 72 | 72 | |
| 50,000-249,999 | 24 | 144 | 144 | |
| 250,000-999,999 | 36 | 216 | 216 | |
| 1,000,000-4,999,999 | 48 | 288 | 288 | |
| = 5,000,000 | 60 | 300 | 300 | |
| Ground Water: | ||||
| < 500 | 3 | 3 | 3 | |
| 500-9,999 | 3 | 9 | 9 | |
| 10,000-99,999 | 12 | 48 | 48 | |
| 1,000,000-4,999,999 | 18 | 72 | 72 | |
| = 5,000,000 | 24 | 96 | 96 |
(2) Reporting Monitoring Results. You must report the information in this paragraph [§ 1.8.9(C)(1)(a)(2) of this Part].
b. Modeling. You may comply through analysis of an extended period simulation hydraulic model. The extended period simulation hydraulic model and analysis must meet the criteria in this paragraph, § 1.8.9(C)(1)(b) of this Part.
(1) Minimum Requirements.
(BB) The model must represent the criteria listed in §§ 1.8.9(C)(1)(b)(1)(BB)(i) through (ix) of this Part.
(2) Reporting Modeling. Your system specific study plan must include the information in this paragraph [§ 1.8.9(C)(1)(b)(2) of this Part].
2. IDSE Report. Your IDSE report must include the elements required in §§ 1.8.9(C)(2)(a) through (f) of this Part. You must submit your IDSE report according to the schedule in § 1.8.9(A)(3) of this Part.
D. 40/30 Certification
1. Eligibility. You are eligible for 40/30 certification if you had no TTHM or HAA5 monitoring violations under § 1.8 of this Part, and no individual sample exceeded 0.040 mg/L for TTHM or 0.030 mg/L for HAA5 during an eight-consecutive calendar quarter period beginning no earlier than the date specified in the table below.
| If your 40/30 certification is due | Then your eligibility for 40/30 certification is based on eight consecutive calendar quarters of § 1.8 of this Part compliance monitoring results beginning no earlier than (unless you are on reduced monitoring under § 1.8 of this Part and were not required to monitor during the specified period. If you did not monitor during the specified period, you must base your eligibility on compliance samples taken during the 12 months preceding the specified period) |
| (1) October 1, 2006 | January 2004 |
| (2) April 1, 2007 | January 2004 |
| (3) October 1, 2007 | January 2005 |
| (4) April 1, 2008 | January 2005 |
2. 40/30 Certification
E. Very Small System Waivers
F. Stage 2 (§ 1.8.10) Compliance Monitoring Location Recommendations
2. You must select the number of monitoring locations specified in the table below. You will use these recommended locations as § 1.8.10 of this Part routine compliance monitoring locations, unless the Director requires different or additional locations. You should distribute locations throughout the distribution system to the extent possible.
| Source Water Type | Population Size Category | Monitoring Frequency | Distribution system monitoring location | |||
| Total per monitoring period | Highest TTHM locations | Highest HAA5 locations | Existing § 1.8 locations | |||
| § 1.6 | Less than 500 | Per year | 2 | 1 | 1 | |
| 500-3,300 | Per quarter | 2 | 1 | 1 | ||
| 3,301-9,999 | Per quarter | 2 | 1 | 1 | ||
| 10,000-49,999 | Per quarter | 4 | 2 | 2 | 1 | |
| 50,000-249,999 | Per quarter | 8 | 3 | 3 | 2 | |
| 250,000-999,999 | Per quarter | 12 | 5 | 5 | 3 | |
| 1,000,000-4,999,999 | Per quarter | 16 | 6 | 6 | 4 | |
| Greater than or equal to 5,000,000 | Per quarter | 20 | 8 | 7 | 5 | |
| Ground Water | Less than 500 | Per year | 2 | 1 | 1 | |
| 500-9,999 | Per year | 2 | 1 | 1 | ||
| 10,000-99,999 | Per quarter | 4 | 2 | 1 | 1 | |
| 1,000,000-4,999,999 | Per quarter | 6 | 3 | 2 | 1 | |
| Greater than or equal to 5,000,000 | Per quarter | 8 | 3 | 3 | 2 |
3. You must recommend § 1.8.10 compliance monitoring locations based on standard monitoring results, system specific study results, and § 1.8 of this Part compliance monitoring results. You must follow the protocol in §§ 1.8.9(F)(3)(a) through (h) of this Part. If required to monitor at more than eight locations, you must repeat the protocol as necessary. If you do not have existing § 1.8 of this Part compliance monitoring results or if you do not have enough existing § 1.8 of this Part compliance monitoring results, you must repeat the protocol, skipping the provisions of §§ 1.8.9(F)(3)(c) and (g) of this Part, as necessary, until you have identified the required total number of monitoring locations.
5. Your recommended schedule must include § 1.8.10 of this Part monitoring during the peak historical month for TTHM and HAA5 concentration, unless the Director approves another month. Once you have identified the peak historical month, and if you are required to conduct routine monitoring at least quarterly, you must schedule § 1.8.10 of this Part compliance monitoring at a regular frequency of every 90 days or fewer.
A. General Requirements
3. Schedule. You must comply with the requirements in this subpart on the schedule in the following table based on your PWS type.
| If you are this type of PWS | You must comply with § 1.8.10 of this Part monitoring by: (The Director may grant up to an additional twenty-four (24) months for compliance with MCLs and operational evaluation levels if you require capital improvements to comply with an MCL.) |
| PWS that are not part of a combined distribution system and PWS that serve the largest population in the combined distribution system | |
| a. PWS serving = 100,000 | April 1, 2012 |
| b. PWS serving 50,000-99,999 | October 1, 2012 |
| c. PWS serving 10,000-49,999 | October 1, 2013 |
| d. PWS serving < 10,000 | October 1, 2013 if no Cryptosporidium monitoring is required under § 1.6.9(B)(1)(d) of this Part, orOctober 1, 2014 if Cryptosporidium monitoring is required under §§ 1.6.9(B)(1)(d) or (f) of this Part |
| Other PWS that are part of a combined distribution system | |
| e. Consecutive PWS or wholesale PWS | At the same time as the PWS with the earliest compliance date in the combined distribution system |
| f. Your monitoring frequency is specified in § 1.8.10(B)(1)(b) of this Part.(1)If you are required to conduct quarterly monitoring, you must begin monitoring in the first full calendar quarter that includes the compliance date in the table in § 1.8.10(A)(3) of this Part.(2)If you are required to conduct monitoring at a frequency that is less than quarterly, you must begin monitoring in the calendar month recommended in the IDSE report prepared under §§ 1.8.9(B) or 1.8.9(C) of this Part or the calendar month identified in the § 1.8.10 monitoring plan developed under § 1.8.10(C) of this Part, no later than twelve (12) months after the compliance date in this table. | |
| g. If you are required to conduct quarterly monitoring, you must make compliance calculations at the end of the fourth calendar quarter that follows the compliance date and at the end of each subsequent quarter (or earlier if the LRAA calculated based on fewer than four quarters of data would cause the MCL to be exceeded regardless of the monitoring results of subsequent quarters). If you are required to conduct monitoring at a frequency that is less than quarterly, you must make compliance calculations beginning with the first compliance sample taken after the compliance date. | |
| h. For the purpose of the schedule in § 1.8.10(A)(3) of this Part, the Director may determine that the combined distribution system does not include certain consecutive PWS based on factors such as receiving water from a wholesale PWS only on an emergency basis or receiving only a small percentage and small volume of water from a wholesale PWS. The Director may also determine that the combined distribution system does not include certain wholesale PWS based on factors such as delivering water to a consecutive PWS only on an emergency basis or delivering only a small percentage and small volume of water to a consecutive PWS. |
4. Monitoring and Compliance
B. Routine Monitoring
1. Monitoring
b. You must monitor at no fewer than the number of locations identified in the table below.
| Source Water Type | Population Size Category | Monitoring Frequency | Distribution system monitoring location per monitoring period |
| § 1.6 | Less than 500 | Per year | 2 |
| 500-3,300 | Per quarter | 2 | |
| 3,301-9,999 | Per quarter | 2 | |
| 10,000-49,999 | Per quarter | 4 | |
| 50,000-249,999 | Per quarter | 8 | |
| 250,000-999,999 | Per quarter | 12 | |
| 1,000,000-4,999,999 | Per quarter | 16 | |
| Greater than or equal to 5,000,000 | Per quarter | 20 | |
| Ground Water | Less than 500 | Per year | 2 |
| 500-9,999 | Per year | 2 | |
| 10,000-99,999 | Per quarter | 4 | |
| 1,000,000-4,999,999 | Per quarter | 6 | |
| Greater than or equal to 5,000,000 | Per quarter | 8 |
C. Monitoring Plan
1. You must develop and implement a monitoring plan to be kept on file for Director and public review. The monitoring plan must contain the elements in §§ 1.8.10(C)(1)(a) through (d) of this Part and be complete no later than the date you conduct your initial monitoring under this subpart.
D. Reduced Monitoring
1. You may reduce monitoring to the level specified in the table below any time the LRAA is = 0.040 mg/L for TTHM and = 0.030 mg/L for HAA5 at all monitoring locations. You may only use data collected under the provisions of §§ 1.8.5 or 1.8.10 of this Part to qualify for reduced monitoring. In addition, the source water annual average TOC level, before any treatment, must be = 4.0 mg/L at each treatment plant treating surface water or groundwater under the direct influence of surface water, based on monitoring conducted under either §§ 1.8.5(B)(1)(c) or 1.8.5(D) of this Part.
| Source Water Type | Population Size Category | Monitoring Frequency | Distribution system monitoring location per monitoring period |
| § 1.6 | Less than 500 | Monitoring may not be reduced | |
| 500-3,300 | Per year | 1 TTHM and 1 HAA5 sample: one at the location and during the quarter with the highest TTHM single measurement, one at the location and during the quarter with the highest HAA5 single measurement; 1 dual sample set per year if the highest TTHM and HAA5 measurements occurred at the same location and quarter | |
| 3,301-9,999 | Per year | 2 dual sample sets: one at the location and during the quarter with the highest TTHM single measurement, one at the location and during the quarter with the highest HAA5 single measurement | |
| 10,000-49,999 | Per quarter | 2 dual sample sets at the locations with the highest TTHM and highest HAA5 LRAAs | |
| 50,000-249,999 | Per quarter | 4 dual sample sets at the locations with the two highest TTHM and two highest HAA5 LRAAs | |
| 250,000-999,999 | Per quarter | 6 dual sample sets at locations with the three highest TTHM and three highest HAA5 LRAAs | |
| 1,000,000-4,999,999 | Per quarter | 8 dual sample sets at the locations with the four highest TTHM and four highest HAA5 LRAAs | |
| Greater than or equal to 5,000,000 | Per quarter | 10 dual sample sets at the locations with the five highest TTHM and five highest HAA5 LRAAs | |
| Ground Water | Less than 500 | Every third year | 1 TTHM and 1 HAA5 sample: one at the location and during the quarter with the highest TTHM single measurement, one at the location and during the quarter with the highest HAA5 single measurement; 1 dual sample set per year if the highest TTHM and HAA5 measurements occurred at the same location and quarter |
| 500-9,999 | Per year | 1 TTHM and 1 HAA5 sample: one at the location and during the quarter with the highest TTHM single measurement, one at the location and during the quarter with the highest HAA5 single measurement; 1 dual sample set per year if the highest TTHM and HAA5 measurements occurred at the same location and quarter | |
| 10,000-99,999 | Per year | 2 dual sample sets: one at the location and during the quarter with the highest TTHM single measurement, one at the location and during the quarter with the highest HAA5 single measurement | |
| 1,000,000-4,999,999 | Per quarter | 2 dual sample sets at the locations with the highest TTHM and highest HAA5 LRAAs | |
| Greater than or equal to 5,000,000 | Per quarter | 4 dual sample sets at the locations with the two highest TTHM and two highest HAA5 LRAAs |
F. Conditions Requiring Increased Monitoring
G. Operational Evaluation Levels
2. If you exceed the operational evaluation level, you must conduct an operational evaluation and submit a written report of the evaluation to the Director no later than 90 days after being notified of the analytical result that causes you to exceed the operational evaluation level. The written report must be made available to the public upon request.
a. Your operational evaluation must include an examination of PWS treatment and distribution operational practices, including storage tank operations, excess storage capacity, distribution system flushing, changes in sources or source water quality, and treatment changes or problems that may contribute to TTHM and HAA5 formation and what steps could be considered to minimize future exceedances.
H. Requirements for Remaining on Reduced TTHM and HAA5 Monitoring Based on Stage 1 Results
I. Requirements for Remaining on Increased TTHM and HAA5 Monitoring Based on Stage 1 Results
J. Reporting and Recordkeeping Requirements
1. Reporting
a. You must report the following information for each monitoring location to the Director within 10 days of the end of any quarter in which monitoring is required:
b. If you are a § 1.6 PWS seeking to qualify for or remain on reduced TTHM/HAA5 monitoring, you must report the following source water TOC information for each treatment plant that treats surface water or groundwater under the direct influence of surface water to the Director within 10 days of the end of any quarter in which monitoring is required:
A. Any person maintaining a PWS shall operate and maintain the water supply facilities so that the water furnished to the public is safe and potable.
B. Avoidance of Contamination in Tanks. Any person who is furnished water from a PWS and maintains a tank supplied only by such water shall have such tank so constructed and maintained to prevent contaminants from gaining access to the tank interior.
B. It is the responsibility of the PWS to register all existing or proposed connections between the PWS and any other water supply with the Director on or before January 1, 1992 or as they are proposed or discovered, whichever is later.
A. Applicability
B. Cross-Connections
C. Required Plan Components
1. Each plan must be prepared in accordance with current State approved guidance and shall include, at a minimum, the following ten elements:
d. Administration. Planning and implementation of the program, determination of level of hazard, and suitable timetables for:
e. Required Records
f. Enforcement Policy
g. Quality Assurance and Control
h. Templates
i. Public Education
j. Response
D. Approved References
1. The development and implementation of cross-connection control programs must reflect the guidance provided in the most recently published editions of references such as, but not limited to, those listed below:
E. Training and Certification of Personnel
1. Any individual conducting work or tests on a backflow preventer, surveying for cross-connections, or drafting (reviewing and approving) plans/programs must hold a current certification from a program recognized by the Director, appropriate to the responsibilities and skill required.
a. Two (2) functional classes of certification are recognized: Inspector/Tester and Surveyor.
F. Approved Backflow Preventers
G. Certification of Plan Compliance
1. Submission of cross-connection control plans to the Director is not required. All community and non-transient, non-community PWS shall certify to the Director that their plan meets or exceeds the requirements of this Regulation in accordance with the following schedule:
H. Dual-Sources
I. Transfer of Real Estate
J. Yearly Reporting
1. All PWS required to comply with this Part must provide an annual report to the Director on forms provided by the Director. The report shall cover January 1st through December 31st and be submitted to the Director no later than January 15th of the following year.
A. All community and non-transient non-community PWS with populations 1,000 or greater must maintain a written flushing schedule, procedure, and log which shall be made available to the Director upon request.
D. Dewatering: An unsafe condition occurs when the pressure in the entire system, or any significant portion of a system has no pressure as indicated by either no water, or a trickle of water at the fixtures; or if the pressure at a well pressure tank is less than 20 psi. The Director must be notified within twenty-four (24) hours when these conditions occur. Once pressure is re-established, the system must be disinfected in accordance with AWWA standards and samples of the distribution system must be taken. Until results indicate an absence of bacteria in the system, the public water system must operate under a precautionary boil water notice.
C. Non-transient, non-community PWS that supply water to schools, day care facilities, institutions or medical facilities must provide auxiliary power in accordance with this Part by April 1, 2021.
A. All owners of PWSs or their designee shall provide notification as to the status of the PWS to the Director in the event of an emergency. Such notifications shall include, at a minimum, the following:
2. If the PWS is not operable:
D. All public notification requirements as found in this Part shall be adhered to in the event of an emergency.
B. Transient non-community PWS shall develop emergency response plans and certify to the Director that the plan meets or exceeds the requirements of § 1.9.9 of this Part by December 1, 2020.
1. Required Plan Components
b. The PWS emergency response plan shall include, without limitation:
C. Community and non-transient, non-community PWS shall develop emergency response plans and certify to the Director that the plan meets or exceeds the requirements of § 1.9.9 of this Part. Approved emergency response plans under R.I. Gen. Laws § 46-15.3-5.1, Water Supply Systems Management Plans, are considered to be in compliance with this requirement. PWS serving populations of 10,000 or fewer shall develop emergency response plans and certify to the Director by July 1, 2020. PWS serving populations greater than or equal to 10,001 shall develop emergency response plans and certify to the Director by January 1, 2020.
1. Required Plan Components
b. The PWS emergency response plan shall include, without limitation:
4. Plan Certification. Each PWS shall certify in writing to the Director that the PWS has completed such plan and that the plan is in compliance with the requirements of this Part.
C. Notification to consumers
B. It is the responsibility of the PWS to collect, have analyzed, and report the results of all water quality samples required by this Part. Samples must be collected in accordance with a written sample siting plan. These plans are subject to the Director's review and revision.
A. Except where a shorter period is specified in this Part, the supplier of water shall report to the Director the results of any test measurement or analysis required by this Part within:
3. For priority results, no later than twenty-four (24) hours after the results are known, or the next business day if State offices are closed, in accordance with the rules and regulations for Certifying Analytical Laboratories (Part 60-05-5 of this Title). Priority results include:
4. The compliance sampling report, containing the sampling results for microbiological contaminants, inorganic compounds, volatile organic compounds, synthetic organic compounds, PFAS, radionuclides and lead and copper analyses, shall be prepared in a format prescribed by and on forms available from and submitted to the Director at the following address:
| Rhode Island Department of Health |
| Center for Drinking Water Quality |
| 3 Capitol Hill, Room 209 |
| Providence, R.I. 02908 |
H. Failure to comply with the requirements of §§ 1.11.1 through 1.11.2 of this Part results in a reporting violation of this Part, with the exception of § 1.11.2(A)(3) of this Part, which is a violation of the rules and regulations for Certifying Analytical Laboratories (Part 60-05-5 of this Title). §§ 1.11.1 through 1.11.2 of this Part are not subject to the public notice requirements of § 1.16.6 of this Part except as specified in §§ 1.16.4 and 1.17.1 of this Part.
A. Any owner or operator of a PWS subject to the provisions of this Part shall retain on its premises or at a convenient location near its premises the following records:
1. Records of microbiological analyses and turbidity analyses made pursuant to this Part shall be kept for not less than five (5) years. Records of chemical analyses made pursuant to this Part shall be kept for not less than ten (10) years. Actual laboratory reports may be kept, or data may be transferred to tabular summaries, provided that the following information is included:
A. Scope
B. Applicability
C. General Requirements
1. PWSs subject to this Section must comply with the following requirements:
D. Compliance Date
1. Groundwater systems must comply, unless otherwise noted, with the requirements of this Section.
C. The sanitary survey must include an evaluation of the applicable components listed in §§ 1.13.2(C)(1) through (8) of this Part:
8. Operator compliance with Director requirements.
A. Triggered Source Water Monitoring
1. General Requirements
a. A groundwater system must conduct triggered source water monitoring if the conditions identified in §§ 1.13.3(A)(1)(a)(1) and (2) of this Part exist.
2. Sampling Requirements
a. A groundwater system must collect, within twenty-four (24) hours of notification of the total coliform-positive sample, at least one groundwater source sample from each groundwater source in use at the time the total coliform-positive sample was collected under §§ 1.16.4(A) and 1.17.1(A) of this Part, except as provided in § 1.13.3(A)(2)(a)(2) of this Part.
3. Additional Requirements
4. Consecutive and Wholesale PWSs
b. In addition to the other requirements of § 1.13.3(A) of this Part, a wholesale groundwater system must comply with §§ 1.13.3(A)(4)(b)(1) and (2) of this Part.
5. Exceptions to The Triggered Source Water Monitoring Requirements
a. A groundwater system is not required to comply with the source water monitoring requirements of § 1.13.3(A) of this Part, if either of the following conditions exists:
B. Assessment Source Water Monitoring
1. If directed by the Director, groundwater systems must conduct assessment source water monitoring that meets Director-determined requirements for such monitoring. A groundwater system conducting assessment source water monitoring may use a triggered source water sample collected under § 1.13.3(A)(2) of this Part to meet the requirements of § 1.13.3(B) of this Part. Director-determined assessment source water monitoring requirements may include:
C. Analytical Methods
D. Invalidation of a Fecal Indicator-Positive Groundwater Source Sample
1. A groundwater system may obtain Director invalidation of a fecal indicator-positive groundwater source sample collected under § 1.13.3(A) of this Part, only under the conditions specified in §§ 1.13.3(D)(1)(a) and (b) of this Part.
E. Sampling Location
F. New Sources
G. Public Notification
H. Monitoring Violations
1. Failure to meet the requirements of §§ 1.13.3(A) through (F) of this Part is a monitoring violation and requires the groundwater system to provide public notification under § 1.16.6(D) of this Part.
A. Groundwater Systems with Significant Deficiencies or Source Water Fecal Contamination.
5. Within one hundred and twenty (120) days (or earlier if directed by the Director) of receiving written notification from the Director of a significant deficiency, written notice from a laboratory that a groundwater source sample collected under § 1.13.3(A)(3) of this Part, was found to be fecal indicator-positive, or direction from the Director that a fecal indicator-positive sample collected under §§ 1.13.3(A)(2), 1.13.3(A)(4), or 1.13.3(B) of this Part requires corrective action, the groundwater system must either:
b. Be in compliance with a Director-approved corrective action plan and schedule subject to the conditions specified in §§ 1.13.4(A)(5)(b)(1) and (2) of this Part.
6. Corrective Action Alternatives
a. Groundwater systems that meet the conditions of §§ 1.13.4(A)(1) or (2) of this Part must implement one or more of the following corrective action alternatives:
7. Special Notice to The Public of Significant Deficiencies or Source Water Fecal Contamination.
b. In addition to the applicable public notification requirements of § 1.16.6(B) of this Part, a non-community groundwater system that receives notice from the Director of a significant deficiency must inform the public served by the PWS in a manner approved by the Director of any significant deficiency that has not been corrected within twelve (12) months of being notified by the Director, or earlier if directed by the Director. The PWS must continue to inform the public annually until the significant deficiency is corrected. The information must include:
B. Compliance Monitoring
2. New Groundwater Sources. A groundwater system that places a groundwater source in service after November 30, 2009, that is not required to meet the source water monitoring requirements of this Section because the PWS provides at least 4-log treatment of viruses (using inactivation, removal, or a Director-approved combination of 4-log virus inactivation and removal) before or at the first customer for the groundwater source must comply with the requirements of §§ 1.13.4(B)(2)(a), (b) and (c) of this Part.
3. Monitoring Requirements. A groundwater system subject to the requirements of §§ 1.13.4(A), (B)(1) or (B)(2) of this Part must monitor the effectiveness and reliability of treatment for that groundwater source before or at the first customer as follows:
a. Chemical Disinfection
b. Membrane Filtration. A groundwater system that uses membrane filtration to meet the requirements of this Section must monitor the membrane filtration process in accordance with all Director-specified monitoring requirements and must operate the membrane filtration in accordance with all Director-specified compliance requirements. A groundwater system that uses membrane filtration is in compliance with the requirement to achieve at least 4-log removal of viruses when:
c. Alternative Treatment
(1) A groundwater system that uses a Director-approved alternative treatment to meet the requirements of this subpart by providing at least 4- log treatment of viruses (using inactivation, removal, or a Director-approved combination of 4-log virus inactivation and removal) before or at the first customer must:
C. Discontinuing Treatment
D. Failure to meet the monitoring requirements of § 1.13.4(B) of this Part is a monitoring violation and requires the groundwater system to provide public notification under § 1.16.6(D) of this Part.
A. A groundwater system with a significant deficiency is in violation of the treatment technique requirement if, within one hundred and twenty (120) days (or earlier if directed by the Director) of receiving written notice from the Director of the significant deficiency, the PWS:
B. Unless the Director invalidates a fecal indicator-positive groundwater source sample under § 1.13.3(D) of this Part, a groundwater system is in violation of the treatment technique requirement if, within 120 days (or earlier if directed by the Director) of meeting the conditions of §§ 1.13.4(A)(1) or (2) of this Part, the PWS:
D. A groundwater system must give public notification under § 1.16.6(C) of this Part for the treatment technique violations specified in §§ 1.13.5(A), (B) and (C) of this Part.
A. Reporting
1. In addition to the requirements of § 1.11 of this Part, a groundwater system regulated under this Section must provide the following information to the Director:
B. Recordkeeping
1. In addition to the requirements of § 1.11 of this Part, a groundwater system regulated under this Section must maintain the following information in its records:
e. For PWSs, including wholesale PWSs, that are required to perform compliance monitoring under § 1.13.4(B) of this Part:
B. Variances pursuant to 42 U.S.C. § 300g.4 may be granted as follows:
1. The Director may grant variances from an applicable national primary drinking water regulation to a PWS which, because of characteristics of the raw water sources which are reasonably available to the PWS, cannot meet the requirements respecting the maximum contaminant levels of such drinking water regulation. A variance may be issued to a PWS on condition that the PWS install the best technology, treatment techniques, or other means, which the Director finds are available (taking costs into consideration) and based upon an evaluation satisfactory to the Director that indicates that alternative sources of water are not reasonably available to the PWS. Before the Director may grant a variance under § 1.15.1(B)(1) of this Part, the Director must find that the variance will not result in an unreasonable risk to health. If the Director grants a PWS a variance under § 1.15.1(B)(1) of this Part, the Director shall prescribe at the time the variance is granted, a schedule for:
5. For such variance issued under this Subparagraph, the Director
b. If the Director prescribes a schedule pursuant to § 1.15.1(B)(1) of this Part requiring compliance with a contaminant level for which the variance is granted later than five (5) years from the date of issuance of the variance the Director must:
6. General Provisions for Small Systems Variances
c. Requirements to receive a small system variance
d. Regulatory requirements for a small system variance
(2) A small system variance under § 1.15 of this Part, is otherwise only available for compliance with a requirement specifying a maximum contaminant level or treatment technique for a contaminant with respect to which:
e. No small system variance can be granted by the Director until the later of the following:
f. Responsibilities of the PWS, Director, and the Administrator in ensuring that sufficient information is available and for evaluation of a small system variance application
(2) Based upon an application for a small system variance and other information, and before a small system variance may be proposed under this subpart, the Director must find and document the following:
(BB) The PWS cannot afford to comply, in accordance with the affordability criteria established by the Director, with the national primary drinking water regulation for which a small system variance is sought, including by:
(EE) The terms and conditions of the small system variance, as developed through compliance with § 1.15.1(B)(6)(g) of this Part, ensure adequate protection of human health, considering the following:
g. Terms and conditions of a small system variance
(2) The terms and conditions of a small system variance issued under this subpart must include, at a minimum, the following requirements:
(CC) Any other terms or conditions that are necessary to ensure adequate protection of public health, which may include:
(3) The Director must establish a schedule for the PWS to comply with the terms and conditions of the small system variance which must include, at a minimum, the following requirements:
(DD) Compliance with the terms and conditions of the small system variance as soon as practicable but not later than three (3) years after the date on which the small system variance is granted. The Director may allow up to two (2) additional years if the Director determines that additional time is necessary for the PWS to:
h. Public Participation
(1) Required public notice prior to issuance of small system variance
(AA) At least fifteen (15) days before the date of proposal, and at least thirty (30) days prior to a public meeting to discuss the proposed small system variance, the Director, or PWS as directed by the Director, must provide notice to persons served by the PWS. For billed customers, identified in § 1.15.1(B)(1) of this Part, this notice must include the information listed in § 1.15.1(B)(3) of this Part. For other persons regularly served by the system, identified in § 1.15.1(B)(2) of this Part, the notice shall include the information identified in § 1.15.1(B)(4) of this Part. Notice must be provided to all persons served by:
(CC) The notice in §§ 1.15.1(B)(1) and (2) of this Part, must include, at a minimum, the following:
(2) Public Meeting Requirements for proposal of a small variance system
(BB) At the time of the public meeting, the Director must prepare and make publicly available, in addition to the information listed in § 1.15.1(B)(6)(h)(1)(CC) of this Part, either:
(3) Obtaining EPA review of a small system variance proposed by the Director
(BB) The Administrator must respond to a petition filed by any person served by the PWS and determine whether to object to the small system variance no later than sixty (60) days after the receipt of the petition.
(4) Administrator objections to a proposed small system variance or overturn of a granted small system variance for a PWS serving 3,300 or fewer persons
(5) EPA action necessary when the Director proposes to grant a small system variance to a PWS serving a population of more than 3,300 and fewer than 10,000 persons
C. Exemptions Pursuant to 42 U.S.C. § 300g.5 of the Safe Drinking Water Act
1. Exemptions may be granted by the Director from any requirement respecting a maximum contaminant level or any treatment technique requirement, or from both, of an applicable national primary drinking water regulation upon a finding that:
2. If the Director grants a PWS an exemption under § 1.15.1(C)(1) of this Part, the exemption shall include a schedule which includes the items listed in this Paragraph. Before a schedule prescribed by the Director pursuant to this Subsection may take effect, the Director shall provide notice and opportunity for a public hearing on the schedule.
a. The Director shall prescribe, at the time the exemption is granted, a schedule for:
b. A schedule prescribed pursuant to this Subsection for a PWS granted an exemption under § 1.15.1(C)(1) of this Part shall require the following:
(2) No exemption shall be granted unless the PWS establishes that the PWS is taking all practicable steps to meet the standard; and
4. The Director must document all findings that are required under 42 U.S.C. § 300g.5 of the Act:
a. Before finding that management and restructuring changes cannot be made, the Director must consider the following measures, and the availability of State Revolving Loan Fund assistance, or any other Federal or State program, that is reasonably likely to be available within the period of the exemption to implement these measures:
b. The Director must consider the availability of an alternative source of water, including the feasibility of partnerships with neighboring PWSs, as identified by the PWS or by the Director consistent with the Capacity Development Strategy.
A. Exceptions to § 1.15.2 of this Part, with respect to the MCL for total coliforms can be granted if the PWS can demonstrate to the Director that:
4. No problem in the operation or maintenance of the distribution system exists.
A. Community PWS and non-transient, non-community PWS shall be required to install and/or use any treatment method identified in §§ 1.16.1(R), 1.16.2(C) and 1.16.5(H) of this Part as a condition for granting a variance except as provided in § 1.15.3(A)(1) of this Part. If, after the PWS’s installation of the treatment method, the PWS cannot meet the MCL, that PWS shall be eligible for a variance.
2. If the Director determines that a treatment method identified in § 1.15.3(B)(1) of this Part is technically feasible, the PWS will be required to install and/or use that treatment method in connection with a compliance schedule. The Director's determination shall be based upon studies by the PWS and other relevant information.
C. In requiring the use of a point-of-entry device as a condition for granting an exemption from the treatment requirements for lead and copper under §§ 1.7.4 or 1.7.5 of this Part, the Director must be assured that use of the device will not cause increased corrosion of lead and copper bearing materials located between the device and the tap that could increase contaminant levels at the tap.
A. At the discretion of the Director, nitrate levels not to exceed twenty (20) mg/l may be allowed in a non-community PWS if the supplier of water demonstrates to the satisfaction of the Director that:
A. Community PWS shall conduct monitoring to determine compliance with the MCLs specified in this Section.
1. Monitoring shall be conducted as follows:
2. The Director may reduce the total number of samples which must be analyzed by allowing the use of compositing. Composite samples from a maximum of five (5) samples are allowed, provided that the detection limit of the method used for analysis is less than one-fifth of the MCL. Compositing of samples must be done in the laboratory.
B. The frequency of monitoring conducted to determine compliance with the maximum contaminant level for asbestos specified in § 1.16.1 of this Part shall be conducted as follows:
3. The Director may grant a waiver based on a consideration of the following factors:
C. The frequency of monitoring conducted to determine compliance with the maximum contaminant levels in § 1.16.1 of this Part, for antimony, arsenic, barium, beryllium, cadmium, chromium, cyanide, fluoride, mercury, nickel, thallium and selenium shall be as follows:
5. In determining the appropriate reduced monitoring frequency, the Director shall consider:
D. All PWS (community; non-transient, non-community; and transient, non-community PWS) shall monitor to determine compliance with the maximum contaminant level for nitrate in § 1.16.1 of this Part.
E. All PWS (community; non-transient, non-community; and transient, non-community PWS) shall monitor to determine compliance with the maximum contaminant level for nitrite in § 1.16.1 of this Part.
F. Confirmation Samples
I. Compliance with § 1.16.1 of this Part, shall be determined based on the analytical result(s) obtained at each sampling point.
J. Sample collection and analyses for the purpose of determining compliance with arsenic shall be conducted using the requirements specified in § 1.21 of this Part.
O. Mechanical Fluoride Adjustment - Monitoring Frequency and Reporting Requirements
P. Monitoring Protocol for Sodium. Each community PWS will sample each of its active sources at the entry point of the source into the distribution system, following any treatment provided to one (1) or more sources of water, as follows:
R. BAT for Inorganic Contaminants. The following are hereby identified as the best technology, treatment technique, or other means available for achieving compliance with the maximum contaminant level for inorganic contaminants identified in this Part, except fluoride:
| BAT For Inorganic Contaminants Listed in § 1.16.1 | |
| Chemical Name | BAT(s) |
| Antimony | 2,7 |
| Arsenic 4,5 | 1,2,5,6,7,9,126 |
| Asbestos | 2,3,8 |
| Barium | 5,6,7,9 |
| Beryllium | 1,2,5,6,7 |
| Cadmium | 2,5,6,7 |
| Chromium | 2,5,62,7 |
| Cyanide | 5,7,10 |
| Mercury | 21,4,61,71 |
| Nickel | 5,6,7 |
| Nitrate | 5,7,9 |
| Nitrite | 5,7 |
| Selenium | 1,23,6,7,9 |
| Thallium | 1,5 |
S. The Director hereby identifies in the following table the affordable technology, treatment technique, or other means available to PWS serving 10,000 persons or fewer for achieving compliance with the maximum contaminant level for arsenic effective January 23, 2006:
| Small System Compliance Technologies (SSCTS)1 for Arsenic2 | |
| Small System Compliance Technology | Affordable for listed small system categories3 |
| Activated Alumina (centralized) | All size categories |
| Activated Alumina (Point-of-Use)4 | All size categories |
| Coagulation/Filtration5 | 501–3,300, 3,301–10,000 |
| Coagulation-assisted Microfiltration | 501–3,300, 3,301–10,000 |
| Electrodialysis reversal6 | 501–3,300, 3,301–10,000 |
| Enhanced coagulation/filtration | All size categories |
| Enhanced lime softening (pH> 10.5) | All size categories |
| Ion Exchange | All size categories |
| Lime Softening5 | 501–3,300, 3,301–10,000 |
| Oxidation/Filtration7 | All size categories |
| Reverse Osmosis (centralized)6 | 501–3,300, 3,301–10,000 |
| Reverse Osmosis (Point-of-Use)4 | All size categories |
| 1 Section 1412(b)(4)(E)(ii) of SDWA specifies that SSCTs must be affordable and technically feasible for small systems.2 SSCTs for Arsenic V. Pre-oxidation may be required to convert Arsenic III to Arsenic V.3 The Act (ibid.) specifies three (3) categories of small systems: (i) those serving 25 or more, but fewer than 501,(ii) those serving more than 500, but fewer than 3,301, and (iii) those serving more than 3,300, but fewer than 10,001.4 When POU or POE devices are used for compliance, programs to ensure proper long-term operation, maintenance, and monitoring must be provided by the water system to ensure adequate performance.5 Unlikely to be installed solely for arsenic removal. May require pH adjustment to optimal range if high removals are needed.6 Technologies reject a large volume of water—may not be appropriate for areas where water quantity may be an issue.7 To obtain high removals, iron to arsenic ratio must be at least 20:1 |
A. Maximum Contaminant Levels for Synthetic Organic Contaminants
5. Monitoring Frequency:
7. The Director may grant a waiver after evaluating the following factor(s): Knowledge of previous use (including transport, storage, or disposal) of the contaminant within the watershed or zone of influence of the PWS. If a determination by the Director reveals no previous use of the contaminant within the watershed or zone of influence, a waiver may be granted. If previous use of the contaminant is unknown or it has been used previously, then the following factors shall be used to determine whether a waiver is granted.
8. If an organic contaminant listed in § 1.16.2(A) of this Part is detected (as defined by § 1.16.2(A)(18) of this Part) in any sample, then:
11. The Director may reduce the total number of samples a PWS must analyze by allowing the use of compositing. Composite samples from a maximum of five (5) sampling points are allowed, provided that the detection limit of the method used for analysis is less than one-fifth of the MCL. Compositing of samples must be done in the laboratory and analyzed within fourteen (14) days of sample collection.
12. Compliance with § 1.16.2(A) of this Part shall be determined based on the analytical results obtained at each sampling point. If one (1) sampling point is in violation of an MCL, the PWS is in violation of the MCL.
18. Detection as used in this Paragraph shall be defined as greater than or equal to the following concentrations for each contaminant.
| Contaminant | Detection limit (mg/L) |
| Alachlor | 0.0002 |
| Aldicarb | 0.0005 |
| Aldicarb sulfoxide | 0.0005 |
| Aldicarb sulfone | 0.0008 |
| Atrazine | 0.0001 |
| Benzo[a]pyrene | 0.00002 |
| Carbofuran | 0.0009 |
| Chlordane | 0.0002 |
| Dalapon | 0.001 |
| Dibromochloropropane (DBCP) | 0.00002 |
| Di (2-ethylhexyl) adipate | 0.0006 |
| Di (2-ethylhexyl) phthalate | 0.0006 |
| Dinoseb | 0.0002 |
| Diquat | 0.0004 |
| 2,4-D | 0.0001 |
| Endothall | 0.009 |
| Endrin | 0.00001 |
| Ethylene dibromide (EDB) | 0.00001 |
| Glyphosate | 0.006 |
| Heptachlor | 0.00004 |
| Heptachlor epoxide | 0.00002 |
| Hexachlorobenzene | 0.0001 |
| Hexachlorocyclopentadiene | 0.0001 |
| Lindane | 0.00002 |
| Methoxychlor | 0.0001 |
| Oxamyl | 0.002 |
| Picloram | 0.0001 |
| Polychlorinated biphenyls (PCBs) (as decachlorobiphenyl) | 0.0001 |
| Pentachlorophenol | 0.00004 |
| Simazine | 0.00007 |
| Toxaphene | 0.001 |
| 2,3,7,8-TCDD (Dixon) | 0.000000005 |
| 2,4,5-TP (Silvex) | 0.0002 |
| Contaminant | MCL (mg/L) |
| Alachlor | 0.002 |
| Aldicarb | reserved |
| Aldicarb sulfoxide | reserved |
| Aldicarb sulfone | reserved |
| Altrazine | 0.003 |
| Carbofuran | 0.04 |
| Chlordane | 0.002 |
| Dibromochloropropane | 0.0002 |
| 2,4-D | 0.07 |
| Ethylene dibromide | 0.00005 |
| Heptachlor | 0.0004 |
| Heptachlor epoxide | 0.0002 |
| Lindane | 0.0002 |
| Methoxychlor | 0.04 |
| Polychlorinated biphenyls | 0.0005 |
| Pentachlorophenol | 0.001 |
| Toxaphene | 0.003 |
| 2,4,5-TP | 0.05 |
| Benzo[a]pyrene | 0.0002 |
| Dalapon | 0.2 |
| Di(2-ethylhexyl) adipate | 0.4 |
| Di(2-ethylhexyl) phthalate | 0.006 |
| Dinoseb | 0.007 |
| Diquat | 0.02 |
| Endothall | 0.1 |
| Endrin | 0.002 |
| Glyphosate | 0.7 |
| Hexacholorbenzene | 0.001 |
| Hexachlorocyclopentadiene | 0.05 |
| Oxamyl (Vydate) | 0.2 |
| Picloram | 0.5 |
| Simazine | 0.004 |
| 2,3,7,8-TCDD (Dioxin) | 3x10-8 |
B. Volatile Organic Chemicals. Maximum contaminant levels for certain volatile organic chemicals:
22. Beginning with the initial compliance period, analysis of the contaminants listed in §§ 1.16.2(B)(1) through (21) of this Part, for the purpose of determining compliance with the maximum contaminant level shall be conducted as follows:
h. The Director may grant a waiver after evaluating the following factor(s):
(2) If previous use of the contaminant is unknown or it has been used previously, then the factors below shall be used to determine whether a waiver is granted.
k. If a contaminant listed in §§ 1.16.2(B)(2) through (21) of this Part is detected at a level exceeding 0.0005 mg/L in any sample, then:
n. The Director may reduce the total number of samples a PWS must analyze by allowing the use of compositing. Composite samples from a maximum of five (5) sampling points are allowed provided that the detection limit of the method used for analysis is less than one-fifth of the MCL. Compositing of samples must be done in the laboratory and analyzed within fourteen (14) days of sample collection.
o. Compliance with §§ 1.16.2(B)(1) through (21) of this Part, shall be determined based on the analytical results obtained at each sampling point. If one (1) sampling point is in violation of an MCL, the PWS is in violation of the MCL.
C. Best Available Technologies (BAT) for Organic Contaminants. The following table identifies granular activated carbon (GAC), packed tower aeration (PTA), or oxidation (OX), anion exchange resin (AER), or reverse osmosis (RO) as the best technology, treatment technique, or other means available for achieving compliance with the maximum contaminant level for organic contaminants identified in §§ 1.16.2(A), (B) and (E) of this Part:
| BAT FOR ORGANIC CONTAMINANTS LISTED IN § 1.16.2(A), (B), and (E) | ||||||
| CAS No. | CONTAMINANT | GAC | PTA | OX | AER | RO |
| 15972-60-8 | Alachlor | X | ||||
| 116-06-3 | Aldicarb | X | ||||
| 1646-88-4 | Aldicarb sulfone | X | ||||
| 1646-87-3 | Aldicarb sulfoxide | X | ||||
| 1912-24-9 | Atrazine | X | ||||
| 71-43-2 | Benzene | X | X | |||
| 50-32-8 | Benzo[a]pyrene | X | ||||
| 1563-66-2 | Carbofuran | X | ||||
| 56-23-5 | Carbon tetrachloride | X | X | |||
| 57-74-9 | Chlordane | X | ||||
| 75-99-0 | Dalapon | X | ||||
| 94-75-7 | 2,4-D | X | ||||
| 103-23-1 | Di(2-ethylhexyl) adipate | X | X | |||
| 117-81-7 | Di (2-ethylhexyl) phthalate | X | ||||
| 96-12-8 | Dibromochloropropane (DBCP) | X | X | |||
| 95-50-1 | o-Dichlorobenzene | X | X | |||
| 106-46-7 | para-Dichlorobenzene | X | X | |||
| 107-06-2 | 1,2-Dichloroethane | X | X | |||
| 75-35-4 | 1,1-Dichloroethylene | X | X | |||
| 156-59-2 | cis-1,2-Dichloroethylene | X | X | |||
| 156-60-5 | trans-1,2-Dichloroethylene | X | X | |||
| 75-09-2 | Dichloromethane | X | ||||
| 78-87-5 | 1,2-Dichloropropane | X | X | |||
| 88-85-7 | Dinoseb | X | ||||
| 85-00-7 | Diquat | X | ||||
| 145-73-3 | Endothall | X | ||||
| 72-20-8 | Endrin | X | ||||
| 100-41-4 | Ethylbenzene | X | X | |||
| 106-93-4 | Ethylene Dibromide (EDB) | X | X | |||
| 1071-83-6 | Gylphosate | X | ||||
| 76-44-8 | Heptachlor | X | ||||
| 1024-57-3 | Heptachlor epoxide | X | ||||
| 118-74-1 | Hexachlorobenzene | X | ||||
| 77-47-3 | Hexachlorocyclopentadiene | X | X | |||
| 58-89-9 | Lindane | X | ||||
| 72-43-5 | Methoxychlor | X | ||||
| 108-90-7 | Monochlorobenzene | X | X | |||
| 23135-22-0 | Oxamyl (Vydate) | X | ||||
| 87-86-5 | Pentachlorophenol | X | ||||
| 335-76-2 | Perfluorodeconoic Acid (PFDA) | X1 | X1 | X1 | ||
| 375-85-9 | Perfluoroheptanoic Acid (PFHpA) | X1 | X1 | X1 | ||
| 355-46-4 | Perfluorohexane sulfonate (PFHxS) | X1 | X1 | X1 | ||
| 375-95-1 | Perfluorononoic Acid (PFNA) | X1 | X1 | X1 | ||
| 1763-23-1 | Perfluorooctane sulfonate (PFOS) | X1 | X1 | X1 | ||
| 335-67-1 | Perfluorooctanoic Acid (PFOA) | X1 | X1 | X1 | ||
| 1918-02-1 | Picloram | X | ||||
| 1336-36-3 | Polychlorinated biphenyls (PCB) | X | ||||
| 122-34-9 | Simazine | X | ||||
| 100-42-5 | Styrene | X | X | |||
| 1746-01-6 | 2,3,7,8-TCDD (Dioxin) | X | ||||
| 127-18-4 | Tetrachloroethylene | X | X | |||
| 108-88-3 | Toluene | X | X | |||
| 8001-35-2 | Toxaphene | X | ||||
| 93-72-1 | 2,4,5-TP (Silvex) | X | ||||
| 120-82-1 | 1,2,4-Trichlorobenzene | X | X | |||
| 71-55-6 | 1,1,1-Trichloroethane | X | X | |||
| 79-00-5 | 1,1,2-Trichloroethane | X | X | |||
| 79-01-6 | Trichloroethylene | X | X | |||
| 75-01-4 | Vinyl chloride | X | ||||
| 1330-20-7 | Xylene | X | X | |||
| 1 Best available technology for per- and -polyfluoroalkyl substances are granular activated carbon, anion exchange resin, reverse osmosis or an equally efficient technology approved by the Director. |
D. Treatment Techniques for Acrylamide and Epichlorohydrin. Each PWS must certify annually in writing to the Director (using third party or manufacturer's certification) that when acrylamide and epichlorohydrin are used in drinking water systems, the combination (or product) of dose and monomer level does not exceed the levels specified as follows:
E. State Requirements for Total Per- and Polyfluoroalkyl Substances (PFAS)
1. The MCL for Total PFAS shall be 0.000020 mg/L (ppm), or 20 ng/L (ppt). Total PFAS shall mean the sum of the six (6) PFAS listed in the following table:
| Contaminant | Total PFAS MCL (mg/L) |
| Perfluorodeconoic Acid (PFDA) | 0.000020 |
| Perfluoroheptanoic Acid (PFHpA) | |
| Perfluorohexane sulfonate (PFHxS) | |
| Perfluorononoic Acid (PFNA) | |
| Perfluorooctane sulfonate (PFOS) | |
| Perfluorooctanoic Acid (PFOA) |
6. Monitoring Frequency
b. Commencement of Initial Monitoring: PWSs with one (1) or more samples taken at each sampling point as part of R.I. Gen. Laws § 46-32-2 or previously submitted to the Department with a laboratory minimum reporting limit of no greater than 0.000002 mg/L (2 ng/L) shall conduct initial sampling as described in §§ 1.16.2(E)(6)(b)(1) - (3) of this Part. The Director may allow the grandfathering of previously-submitted monitoring data as described in § 1.16.2(E)(6)(b)(4) of this Part.
7. If any of the six (6) PFAS listed in § 1.16.2(E)(1) of this Part is detected (as defined by § 1.16.2(E)(18) of this Part) in any sample, then:
9. Unless otherwise directed by the Director prior to September 18, 2024 in a consent agreement executed pursuant to R.I. Gen. Laws § 46-32-2(d), a PWS that violates the requirements of § 1.16.2(E) of this Part as determined by § 1.16.2(E)(10) of this Part is subject to the following:
10. Compliance with § 1.16.2(E) of this Part shall be determined based on the analytical results obtained at each sampling point. If one (1) sampling point is in violation of an MCL, the PWS is in violation of the MCL. A PWS in violation of § 1.16.2(E) of this Part as determined by § 1.16.2(E)(10) of this Part must follow the return-to-compliance provisions of § 1.16.2(E)(9) of this Part.
12. PWSs which are conducting monthly monitoring as specified in § 1.16.2(E)(7)(b) of this Part after sampling results in a detection (as defined by § 1.16.2(E)(18) of this Part), and the average of such detection and an associated confirmation sample exceeds the MCL, shall provide interim consumer notice of the exceedance in accordance with §§ 1.16.6(C)(2), and (3), 1.16.2(E)(10)(d), and 1.16.2(E)(13) of this Part as soon as practical and no later than thirty (30) days after receipt of the confirmation sample results from the laboratory. The PWS shall then continue to monitor monthly as specified in § 1.16.2(E)(7)(b) to determine compliance with the MCL.
13. Interim consumer notice as required by § 1.16.2(E)(12) of this Part shall contain the following content:
18. Detection as used in § 1.16.2(E)(18) of this Part shall be defined as greater than or equal to the following concentration of any of the six (6) PFAS listed in § 1.16.2(E)(1) of this Part.
| Contaminant | PFAS Detection limit (mg/L) |
| Perfluorodeconoic Acid (PFDA) | 0.0000020 |
| Perfluoroheptanoic Acid (PFHpA) | 0.0000020 |
| Perfluorohexane sulfonate (PFHxS) | 0.0000020 |
| Perfluorononanoic Acid (PFNA) | 0.0000020 |
| Perfluorooctane sulfonate (PFOS) | 0.0000020 |
| Perfluorooctanoic Acid (PFOA) | 0.0000020 |
19. All new PWS or PWS that use a new source of water that begin operation after September 18, 2024 must comply with the provisions of § 1.16.2(E) of this Part, except for the initial monitoring requirements in § 1.16.2(E)(6)(b). All new PWS or PWS that use a new source of water that begin operation after September 18, 2024 must demonstrate compliance with the MCL in § 1.16.2(E) of this Part within a period of time specified by the Director.
A. Applicability
D. A PWS that uses surface water or groundwater under the direct influence of surface water, as defined in § 1.2 of this Part, and does not practice filtration in compliance with § 1.6.4 of this Part, must collect at least one (1) sample near the first service connection each day the turbidity level of the source water measured as specified in § 1.6 of this Part, exceeds 1 NTU. This sample must be analyzed for the presence of total coliforms. When one (1) or more turbidity measurements in any day exceed 1 NTU, the PWS must collect this coliform sample within twenty-four (24) hours of the first exceedance, unless the Director determines that the PWS, for logistical reasons outside of the PWS's control cannot have the sample analyzed within thirty (30) hours of collection. Sample results from this coliform monitoring must be included in determining compliance with the MCL for total coliforms in § 1.16.4 of this Part.
A. Revised Total Coliform Rule (RTCR)
2. Community PWS must continue to monitor according to the total coliform monitoring schedules that were in effect on March 31, 2016, unless any of the conditions for increased monitoring in §§ 1.16.4(A)(12)(a) through (b) and 1.16.4(A)(14)(b) of this Part are triggered, or unless otherwise directed by the Director.
a. Community PWS serving 1,000 or fewer people using only groundwater.
3. General
4. Routine Monitoring. The purpose of coliform and E. coli monitoring is to determine if the protective barriers that keep coliform bacteria out of the PWS have been breached or compromised.
a. Sample Siting Plans
(6) The plan must include all primary sampling locations and repeat sampling locations within 5 service connections upstream of each identified primary site and within 5 service connections downstream of each identified primary site.
b. The monitoring frequency for total coliforms for PWS is based on population served by the PWS as follows:
| Total Coliform Monitoring Frequency for PWS | |
| Population Served | Minimum Number of Samples per Month |
| 25 to 1,000 (Includes PWS which have at least 15 service connections, but serve fewer than 25 persons) | 1 (Some GW PWS may be allowed to sample quarterly based on TCR/RTCR transition and/or § 1.16.4(A)(11) of this Part) |
| 1,001 to 2,500 | 2 |
| 2,501 to 3,300 | 3 |
| 3,301 to 4,100 | 4 |
| 4,101 to 4,900 | 5 |
| 4,901 to 5,800 | 6 |
| 5,801 to 6,700 | 7 |
| 6,701 to 7,600 | 8 |
| 7,601 to 8,500 | 9 |
| 8,501 to 12,900 | 10 |
| 12,901 to 17,200 | 15 |
| 17,201 to 21,500 | 20 |
| 21,501 to 25,000 | 25 |
| 25,001 to 33,000 | 30 |
| 33,001 to 41,000 | 40 |
| 41,001 to 50,000 | 50 |
| 50,001 to 59,000 | 60 |
| 59,001 to 70,000 | 70 |
| 70,001 to 83,000 | 80 |
| 83,001 to 96,000 | 90 |
| 96,001 to 130,000 | 100 |
| 130,001 to 220,000 | 120 |
| 220,001 to 320,000 | 150 |
| 320,001 to 450,000 | 180 |
| 450,001 to 600,000 | 210 |
| 600,001 to 780,000 | 240 |
| 780,001 to 970,000 | 270 |
| 970,001 to 1,230,000 | 300 |
| 1,230,001 to 1,520,000 | 330 |
| 1,520,001 to 1,850,000 | 360 |
| 1,850,001 to 2,270,000 | 390 |
| 2,270,001 to 3,020,000 | 420 |
| 3,020,001 to 3,960,000 | 450 |
| 3,960,001 or more | 480 |
d. A PWS that uses surface water or groundwater under the direct influence of surface water, as determined by the Director, and does not practice filtration in compliance with § 1.6 of this Part must:
5. Analytical Methodology. Coliform organism examinations shall be made in accordance with § 1.21 of this Part.
6. Maximum Contaminant Level Goals (MCLGs) and Maximum Contaminant Levels (MCLs) and Treatment Technique (TT) Triggers for Microbiological Contaminants
a. MCLGs for the following contaminants are as indicated in the following table:
| Contaminant | MCLG |
| Giardia lamblia | Zero |
| Viruses | Zero |
| Legionella | Zero |
| Total coliforms (including fecal coliforms and Escherichia coli) | Zero |
| Cryptosporidium | Zero |
| Escherichia coli (E. coli) | Zero |
c. A coliform treatment technique (TT) trigger is based on total coliform and/or E. coli monitoring results. The following constitutes a (TT) trigger.
f. A PWS must take at least the minimum number of required samples even if the PWS has had an E. coli MCL violation or has exceeded the coliform treatment technique triggers.
g. Special purpose samples such as those taken to determine whether disinfection practices are sufficient following pipe placement, replacement, or repair, must not be used to determine whether the coliform treatment technique trigger has been exceeded and shall not be used to determine the E. coli MCL or TT for total coliforms.
h. The following constitutes a violation of the E. coli MCL:
j. The following constitute the best technology treatment techniques, or other means available for achieving compliance with the E. coli MCL and TT requirements.
7. Assessments and Corrective Action
c. The PWS must conduct the assessment consistent with any State directives that tailor specific assessment elements with respect to the size and type of the PWS and the size, type, and characteristics of the distribution system.
d. Level 1 Assessments
(5) When sanitary defects are identified during the assessment the PWS must complete corrective actions by one of the following timeframes:
(CC) Timeframes determined by the Director and communicated to the PWS upon review of the assessment form and consultation with the PWS.
(10) Consultation
e. Level 2 Assessments
(7) When sanitary defects are identified during the assessment, the PWS must complete corrective actions by one of the following timeframes:
(12) Consultation
8. Repeat Monitoring
a. If a routine sample is total coliform-positive (TC+), the PWS must collect a set of repeat samples for each total coliform positive within twenty-four (24) hours of being notified of the positive result as follows:
e. The PWS may propose alternative repeat monitoring locations that are expected to better represent pathways of contamination into the distribution system; however, this proposal must be submitted for inclusion in the PWS’s sample plan prior to any routine total coliform-positive results.
g. PWS must identify repeat monitoring locations in the sample siting plan.
h. The Director may review, revise, and approve, as appropriate, repeat sampling proposed by PWS under §§ 1.16.4(A)(8)(e)(1) and (2) of this Part.
l. If one (1) or more repeat sample in the set is total coliform-positive, the PWS must collect an additional set of repeat samples as described in this Section.
n. PWS on quarterly monitoring schedules must take a minimum of three (3) additional routine samples the month following a total coliform–positive (TC+) routine or repeat sample.
9. E. coli Testing
10. Invalidation of Samples
b. The Director will invalidate a total coliform-positive sample and document same in writing only if:
(2) The Director determines that the total coliform-positive sample resulted from a domestic or other non-distribution system plumbing problem.
(3) The Director has substantial grounds to believe that a total coliform-positive result is due to a circumstance or condition which does not reflect water quality in the distribution system.
d. If a laboratory invalidates a sample because of such interference, the PWS must collect another sample from the same location as the original sample within twenty-four (24) hours of being notified of the interference problem, and have it analyzed for the presence of total coliforms.
11. Reduced Monitoring
a. A groundwater community PWS serving 1,000 or fewer people may reduce its routine monitoring (1 sample per month) to 1 sample per quarter if it meets the following criteria:
(6) In addition, the PWS must meet at least one of the following criteria:
12. Return to Routine Monitoring for Community PWS
b. The PWS must continue monthly monitoring until it meets the reduced monitoring requirements in § 1.16.4(A)(13) of this Part.
13. Return to Reduced Monitoring After Being Triggered to Increased Monitoring for Community PWS.
a. A groundwater community PWS serving 1,000 or fewer people must meet the following criteria in order to return to routine quarterly monitoring after being triggered to increased monitoring:
14. Sanitary Surveys
15. Violation Types
a. E. coli MCL Violation. A PWS is in violation of the MCL for E. coli when any of the following conditions occur:
b. Treatment Technique Violation. The following are treatment technique violations:
c. Monitoring Violation. The following are monitoring violations:
d. Reporting Violation. The following are reporting violations:
16. Reporting Requirements
a. In addition to the general reporting requirements found at § 1.11 of this Part, the following apply to § 1.16.4 of this Part:
c. A community PWS must report the following in its Consumer Confidence Report (CCR):
(2) Level 1 or Level 2 assessment language.
A. Monitoring and Compliance Requirements for Gross Alpha Particle Activity, Radium- 226, Radium-228 and Uranium
1. Community PWS must conduct initial monitoring to determine compliance with §§ 1.16.5(B) and (C) of this Part, by December 31, 2007. For the purposes of monitoring for gross alpha particle activity, radium-226, radium-228, and uranium in drinking water, “detection limit” is defined as in § 1.21 of this Part.
a. Applicability and sampling location for existing community PWS or sources.
b. Applicability and sampling location for new community PWS or sources
2. Initial Monitoring. PWSs must conduct initial monitoring for gross alpha particle activity, radium-226, radium-228, and uranium as follows:
b. Grandfathering of Data: The Director may allow historical monitoring data collected at a sampling point to satisfy the initial monitoring requirements for that sampling point, for the following situations:
3. Reduced Monitoring. The Director may allow community PWS to reduce the future frequency of monitoring from once every three (3) years to once every six (6) or nine (9) years at each sampling point, based on the following criteria.
B. Maximum Contaminant Level for Gross Alpha Particle Activity and Radium-226 and Radium-228
| Contaminant | Picocuries per Liter (pCi/l) |
| Radium-226 and Radium-228 Combined (The combined radium-226 and radium-228 value is determined by the addition of the results of the analysis for radium-226 and the analysis for radium-228) | 5 |
| Gross alpha particle activity (Including radium-226 but excluding radon and uranium) | 15 |
D. Maximum Contaminant Level for Manmade Beta Particle and Photon Emitters. The average annual concentration of manmade beta particle and photon emitters shall not meet or exceed an annual dose equivalent to the total body or any internal organ of 4 millirems/year.
2. If two (2) or more radionuclides are present, the sum of their annual dose equivalent to the total body or to any internal organ shall not exceed 4 mrem/year.
| Table A. Average Annual Concentrations Assumed to Produce a Total Body or Any Internal Organ Dose of 4 millirem/year | ||
| Radionuclide | Critical Organ | pCi/l |
| Tritium | Total body | 20,000 |
| Strontium-90 | Bone marrow | 8 |
E. Monitoring and Compliance Requirements for Beta Particle and Photon Radioactivity. For the purposes of monitoring for beta particle and photon radioactivity in drinking water, “detection limit” is defined as in § 1.21 of this Part. To determine compliance with the maximum contaminant levels in § 1.16.5(D) of this Part for beta particle and photon radioactivity, a PWS must monitor at a frequency as follows:
1. Community PWS (both surface and groundwater) designated by the Director as vulnerable must sample for beta particle and photon radioactivity. PWSs must collect quarterly samples for beta emitters and annual samples for tritium and strontium-90 at each entry point to the distribution system (hereafter called a sampling point), beginning within one (1) quarter after being notified by the Director. PWSs already designated by the Director must continue to sample until the Director reviews and either reaffirms or removes the designation.
2. Community PWS (both surface and groundwater) designated by the Director as utilizing waters contaminated by effluents from nuclear facilities must sample for beta particle and photon radioactivity. PWSs must collect quarterly samples for beta emitters and iodine-131 and annual samples for tritium and strontium-90 at each entry point to the distribution system (hereafter called a sampling point), beginning within one (1) quarter after being notified by the Director. PWSs already designated by the Director as PWSs using waters contaminated by effluents from nuclear facilities must continue to sample until the Director reviews and either reaffirms or removes the designation.
F. General Monitoring and Compliance Requirements for Radionuclides.
3. Compliance: Compliance with §§ 1.16.5(B) through (D) of this Part will be determined based on the analytical result(s) obtained at each sampling point. If one (1) sampling point is in violation of an MCL, the PWS is in violation of the MCL.
H. Best Available Technologies (BATs) for Radionuclides. The Director hereby identifies as indicated in the following table the best technology available for achieving compliance with the maximum contaminant levels for combined radium-226 and -228, uranium, gross alpha particle activity and beta particle and photon radioactivity.
| Table B. BAT for Combined Radium-226 and Radium-228, Uranium, Gross Alpha Particle Activity, and Beta Particle and Photon Radioactivity | |
| Contaminant | BAT |
| 1. Combined radium-226 and radium-228 | Ion exchange, reverse osmosis, lime softening |
| 2. Uranium | Ion exchange, reverse osmosis, lime softening, coagulation/filtration |
| 3. Gross alpha particle activity (excluding Radon and Uranium) | Reverse osmosis |
| 4. Beta particle and photon radioactivity | Ion exchange, reverse osmosis |
I. Small Systems Compliance Technologies List for Radionuclides
| Table C. List of Small Systems Compliance Technologies for Radionuclides and Limitations to Use. | |||
| Unit Technologies | Limitations (see footnotes) | Operator Skill Level Required1 | Raw Water Quality Range and Considerations1 |
| 1. Ion exchange (IE) | (a) | Intermediate | All ground waters |
| 2. Point of use (POU2) IE | (b) | Basic | All ground waters |
| 3. Reverse osmosis (RO) | (c) | Advanced | Surface waters usually require pre-filtration |
| 4. POU2 RO | (b) | Basic | Surface waters usually require pre-filtration |
| 5. Lime softening | (d) | Advanced | All waters |
| 6. Green sand filtration | (e) | Basic | |
| 7. Co-precipitation with Barium sulfate | (f) | Intermediate to Advanced | Ground waters with suitable water quality |
| 8. Electrodialysis/ electrodialysis reversal | Basic to Intermediate | All ground waters | |
| 9. Pre-formed hydrous Manganese oxide filtration | (g) | Intermediate | All ground waters |
| 10.Activated alumina | (a), (h) | Advanced | All ground waters; competing anion concentrations may affect regeneration frequency. |
| 11.Enhanced coagulation/ filtration | (i) | Advanced | Can treat a wide range of water qualities |
| 1 National Research Council (NRC). Safe Water from Every Tap: Improving Water Service to Small Communities. National Academy Press. Washington, D.C. 1997.2 A POU, or ‘‘point-of-use’’ technology is a treatment device installed at a single tap used for the purpose of reducing contaminants in drinking water at that one (1) tap. POU devices are typically installed at the kitchen tap. See the April 21, 2000 NODA for more details.Limitations Footnotes:Technologies for Radionuclides:a The regeneration solution contains high concentrations of the contaminant ions. Disposal options should be carefully considered before choosing this technology.b When POU devices are used for compliance, programs for long-term operation, maintenance and monitoring must be provided by water utility to ensure proper performance.c Reject water disposal options should be carefully considered before choosing this technology. See other RO limitations described in the SWTR Compliance Technologies Table.d The combination of variable source water quality and the complexity of the water chemistry involved may make this technology too complex for small surface water systems.e Removal efficiencies can vary depending on water quality.f This technology may be very limited in application to small systems. Since the process requires static mixing, detention basins, and filtration, it is most applicable to systems with sufficiently high sulfate levels that already have a suitable filtration treatment train in place.g This technology is most applicable to small systems that already have filtration in place.h Handling of chemicals required during regeneration and pH adjustment may be too difficult for small systems without an adequately trained operator.i Assumes modification to a coagulation/filtration process already in place. |
| Table D. Compliance Technologies by System Size Category for Radionuclide NPDWR’s | |||
| Compliance Technologies1 for System Size Categories (population served) | |||
| Contaminant | 25-500 | 501-3,300 | 3,300-10,000 |
| 1. Combined radium-226 and radium-228 | 1, 2, 3, 4, 5, 6, 7, 8, 9 | 1, 2, 3, 4, 5, 6, 7, 8, 9 | 1, 2, 3, 4, 5, 6, 7, 8, 9 |
| 2. Gross alpha particle activity | 3, 4 | 3, 4 | 3, 4 |
| 3. Beta particle activity and photon activity | 1, 2, 3, 4 | 1, 2, 3, 4 | 1, 2, 3, 4 |
| 4. Uranium | 1, 2, 4, 10, 11 | 1, 2, 3, 4, 5, 10, 11 | 1, 2, 3, 4, 5, 10, 11 |
| Note: 1 Numbers correspond to those technologies found listed in Table C of § 16.5(i) above. |
A. General Public Notification Requirements
1. Each owner or operator of a PWS (community PWS, non-transient, non-community PWS and transient non-community PWS) must give notice for all violations of state public drinking water regulations (SDWR) and national primary drinking water regulations (NPDWR) and for other situations, as listed in Table 1 and § 1.16.7 of this Part. The term “SDWR and NPDWR violations” is used in this Part to include violations of the maximum contaminant level (MCL), maximum residual disinfection level (MRDL), treatment technique (TT), monitoring requirements and testing procedures in this Part. § 1.16.7 of this Part identifies the tier assignment for each specific violation or situation requiring a public notice. § 1.16.6 of this Part details some specific instances in which special public notice is required and the associated requirements for such notice; however, those instances are not exclusive of other violations or situations that the Director may determine require special public notice. The Director has discretion to determine other violations and situations that require a public notice and the appropriate tier of public notice for such violation or situation.
a. Table 1 to § 1.16.6(A) of this Part – Violation Categories and Other Situations Requiring a Public Notice
| (1)SDWR and NPDWR violations: |
| (i)Failure to comply with an applicable maximum contaminant level (MCL) or maximum residual disinfectant level (MRDL). |
| (ii)Failure to comply with a prescribed treatment technique (TT). |
| (iii)Failure to perform water quality monitoring, as required by the drinking water regulations. |
| (iv)Failure to comply with testing procedures as prescribed by a drinking water regulation. |
| (2)Variance and exemptions under sections 1415 and 1416 of SDWA: |
| (i)Operation under a variance or an exemption. |
| (ii)Failure to comply with the requirements of any schedule that has been set under a variance or exemption. |
| (3)Special public notices: |
| (i)Occurrence of a waterborne disease outbreak or other waterborne emergency. |
| (ii)Exceedance of the nitrate MCL by non-community water systems (NCWS), where granted permission by the Director under § 15.5 of this Part. |
| (iii)Exceedance of the secondary maximum contaminant level (SMCL) for fluoride. |
| (iv)Availability of unregulated contaminant monitoring data. |
| (v)Other violations and situations determined by the Director to require a public notice under this subpart, not already listed in § 1.16.7 of this Part. |
2. Public notice requirements are divided into three (3) tiers, to take into account the seriousness of the violation or situation and of any potential adverse health effects that may be involved. The public notice requirements for each violation or situation listed in Table 1 of this Section are determined by the tier to which it is assigned. Table 2 of this Section provides the definition of each tier. § 1.16.7 of this Part identifies the tier assignment for each specific violation or situation.
a. Table 2 to § 1.16.6(A) of this Part– Definition of Public Notice Tiers
| (1)Tier 1 Public Notice – required for SDWR and NPDWR violations and situations with significant potential to have serious adverse effects on human health as a result of short-term exposure. |
| (2)Tier 2 Public Notice – required for all other SDWR and NPDWR violations and situations with potential to have serious adverse effects on human health. |
| (3)Tier 3 Public Notice – required for all other SDWR and NPDWR violations and situations not included in Tier 1 and Tier 2. |
3. Persons required to be notified:
B. Tier 1 Public Notice–Form, Manner and Frequency of Notice
1. Table 1 of this Section lists the violation categories and other situations requiring a Tier 1 public notice. § 1.16.7 of this Part identifies the tier assignment for each specific violation or situation.
| Table 1 to § 1.16.6(B) of this Part– Violation Categories and Other Situations Requiring a Tier 1 Public Notice |
| (1) Violation of the E. Coli MCL (as specified in § 1.16.4(A)(6)(h) of this Part); |
| (2) Violation of the MCL for nitrate, nitrite, or total nitrate and nitrite, as defined in § 1.16.1 of this Part, or when the PWS fails to take a confirmation sample within 24 hours of the PWS's receipt of the first sample showing an exceedance of the nitrate or nitrite MCL, as specified in § 1.16.1(F)(2) of this Part; |
| (3) Exceedance of the nitrate MCL by non-community PWS, where permitted to exceed the MCL by the Director under § 1.15.5 of this Part, as required under § 1.16.6(I) of this Part; |
| (4) Violation of the MRDL for chlorine dioxide, as defined in § 1.8.2(A) of this Part, when one (1) or more samples taken in the distribution system the day following an exceedance of the MRDL at the entrance of the distribution system exceed the MRDL, or when the PWS does not take the required samples in the distribution system, as specified in § 1.8.6(C)(2)(a) of this Part; |
| (5) Violation of the turbidity MCL under § 1.16.3 of this Part, where the Director determines after consultation that a Tier 1 notice is required or where consultation does not take place within 24 hours after the PWS learns of the violation; |
| (6) Violation of the Surface Water Treatment Rule (SWTR), Interim Enhanced Surface Water Treatment Rule (IESWTR), or Long Term 1 Interim Enhanced Surface Water Treatment Rule (LT1ESWTR), § 1.6 of this Part, treatment technique requirements resulting from a single exceedance of the maximum allowable turbidity limit (as identified in § 1.16.7 of this Part), where the Director determines after consultation that a Tier 1 notice is required or where consultation does not take place within 24 hours after the PWS learns of the violation; |
| (7) Occurrence of a waterborne disease outbreak, as defined in § 1.2 of this Part, or other waterborne emergency (such as a failure or significant interruption in key water treatment processes, a natural disaster that disrupts the water supply or distribution system, or a chemical spill or unexpected loading of possible pathogens into the source water that significantly increases the potential for drinking water contamination); |
| (8) Detection of E. coli, enterococci, or coliphage in source water samples as specified in §§ 1.13.3(A) and (B) of this Part; |
| (9) Other violations or situations with significant potential to have serious adverse effects on human health as a result of short-term exposure, as determined by the Director either in § 1.16.7 of this Part or on a case-by-case basis. |
2. PWSs must:
3. PWSs must provide the notice within twenty-four (24) hours in a form and manner reasonably calculated to reach all persons served. The form and manner used by the PWS are to fit the specific situation, but must be designed to reach residential, transient and non-transient users of the PWS. In order to reach all persons served, PWS are to use, at a minimum, one (1) or more of the following forms of delivery:
C. Tier 2 Public Notice-Form, Manner, and Frequency of Notice
1. Table 1 of this Section lists the violation categories and other situations requiring a Tier 2 public notice. § 1.16.7 of this Part identifies the tier assignment for each specific violation or situation.
| Table 1 to § 1.16.6(C) of this Part– Violation Categories and Other Situations Requiring a Tier 2 Public Notice |
| (1) All violations of the MCL, MRDL and treatment technique requirements, except where a Tier 1 notice is required under § 1.16.6(B)(1) of this Part or where the Director determines that a Tier 1 notice is required; |
| (2) Violations of the monitoring and testing procedure requirements, where the Director determines that a Tier 2 rather than a Tier 3 public notice is required, taking into account potential health impacts and persistence of the violation; and |
| (3) Failure to comply with the terms and conditions of any variance or exemption in place. |
| (4) Failure to take corrective action or failure to maintain at least 4-log treatment of viruses (using inactivation, removal, or a State-approved combination of 4-log virus inactivation and removal) before or at the first customer under § 1.13.4(A) of this Part. |
| (5) Other violations or situations with potential to have serious adverse effects on human health, as determined by the Director in § 1.16.7 of this Part or on a case-by-case basis. |
2. Tier 2 Public Notice
c. For the turbidity violations specified in this Paragraph, PWSs must consult with the Director as soon as practical but no later than twenty-four (24) hours after the PWS learns of the violation, to determine whether a Tier 1 public notice under § 1.16.6(B)(1) of this Part is required to protect public health. When consultation does not take place within the 24-hour period, the PWS must distribute a Tier 1 notice of the violation within the next twenty-four (24) hours (i.e., no later than 48 hours after the PWS learns of the violation), following the requirements under § 1.16.6(B) of this Part and consultation with the Director is required for:
3. PWSs must provide the initial public notice and any repeat notices in a form and manner that is reasonably calculated to reach persons served in the required time period. The form and manner of the public notice may vary based on the specific situation and type of PWS, but it must at a minimum meet the following requirements:
a. Unless directed otherwise by the Director in writing, community PWS must provide notice by:
b. Unless directed otherwise by the Director in writing, non-community PWS must provide notice by:
D. Tier 3 Public Notice–Form, Manner, and Frequency of Notice
1. Table 1 of this Section lists the violation categories and other situations requiring a Tier 3 public notice. § 1.16.7 of this Part identifies the tier assignment for each specific violation or situation.
| Table 1 to § 1.16.6(D) of this Part– Violation Categories and Other Situations Requiring a Tier 3 Public Notice |
| (1) Monitoring violations, except where a Tier 1 notice is required under § 1.16.6(B) of this Part or where the Director determines that a Tier 2 notice is required; |
| (2) Failure to comply with a testing procedure established in this Part, except where a Tier 1 notice is required under § 1.16.6(B)(1) of this Part or where the Director determines that a Tier 2 notice is required; |
| (3) Operation under a variance granted under 42 U.S.C. § 300g4 or an exemption granted under 42 U.S.C. § 300g5 of the Safe Drinking Water Act; |
| (4) Availability of unregulated contaminant monitoring results, as required under § 1.16.6(G) of this Part; and |
| (5) Exceedance of the fluoride secondary maximum contaminant level (SMCL), as required under § 1.16.6(H) of this Part. |
| (6) Recordkeeping violations as defined in this Part; and |
| (7) Failure to comply with reporting requirements as defined under § 1.16.4(A)(16) of this Part. |
| (8) Other SDWR and NPDWR violations and situations not included in Tier 1 and Tier 2, as determined by the Director either in § 1.16.7 of this Part or on a case-by-case basis. |
2. Notification Timeframe
3. A PWS must provide the initial notice and any repeat notices in a form and manner that is reasonably calculated to reach persons served in the required time period. The form and manner of the public notice may vary based on the specific situation and type of PWS, but it must at a minimum meet the following requirements:
a. Unless directed otherwise by the Director in writing, community PWS must provide notice by:
b. Unless directed otherwise by the Director in writing, non-community PWS must provide notice by:
4. In what situations, may the Consumer Confidence Report be used to meet the Tier 3 public notice requirements? For community PWS, the Consumer Confidence Report (CCR) required under § 1.16.11 of this Part may be used as a vehicle for the initial Tier 3 public notice and all required repeat notices, as long as:
E. Content of the Public Notice
1. When a PWS violates a SDWR or NPDWR or has a situation requiring public notification, each public notice must include the following elements:
2. Elements that must be included in the public notice for a PWS operating under a variance or exemption
a. If a PWS has been granted a variance or an exemption, the public notice must contain:
3. Public notice presentation requirements:
a. Each public notice required by § 1.16.6 of this Part:
b. Each public notice required by § 1.16.6 of this Part must comply with multilingual requirements, as follows:
4. PWSs are required to include the following standard language in their public notice:
d. A report that contains information regarding a Level 1 or Level 2 Assessment required under § 1.16.4 of this Part must include the applicable definitions:
F. Notice to New Billing Units or New Customers
G. Special Notice of the Availability of Unregulated Contaminant Monitoring Results
H. Special Notice for Exceedance of 2 mg/L Fluoride
I. Special Notice for Nitrate Exceedances Above MCL by Non-Community PWS, where Granted Permission by the Director under § 1.15.5 of this Part.
J. Notice by Director on Behalf of the PWS
L. Special notice for repeated failure to conduct monitoring of the source water for Cryptosporidium and for failure to determine bin classification or mean Cryptosporidium level.
4. The notice must contain the following language, including the language necessary to fill in the blanks.
c. Each special notice must also include a description of what the PWS is doing to correct the violation and when the PWS expects to return to compliance or resolve the situation.
| SDWR AND NPDWR VIOLATIONS AND OTHER SITUATIONS REQUIRING PUBLIC NOTICE | ||||
| MCL/MRDL/TT violations2 | Monitoring, reporting & testing procedure violations | |||
| Contaminant | Tier of public notice required | Citation | Tier of public notice required | Citation |
| I. Violations of SDWR and NPDWR3 | ||||
| A. Microbiological Contaminants | ||||
| 1. Total coliform | N/A | N/A | 3 | 1.16.4 |
| 2. E. Coli | 1 | 1.16.4(A)(15)(a) | 1, 34 | 1.16.4(A)(15)(d)(2) |
| 3. PWS fails to conduct a required Level 1 or 2 assessment within 10 or 30 days, respectively, of learning of the trigger as defined in § 1.16.4 of this Part, or in accordance with a schedule approved by the Director (TT). | 2 | 1.16.4(A)(15)(b)(1) | 3 | 1.16.4(A)(15)(d)(1) |
| 4. PWS fails to correct any sanitary defect found through either a Level 1 or 2 assessment within 30 days of learning of the trigger or in accordance with a schedule approved by the Director (TT). | 2 | 1.16.4(A)(15)(b)(3) | 3 | 1.16.4(A)(15)(d)(1) |
| 5. Seasonal PWS fails to complete state-approved start-up procedures prior to serving water to the public (TT). | 2 | 1.16.4(A)(15)(b)(2) | 3 | 1.16.4(A)(15)(d)(3) |
| 6. Surface Water Treatment Rule violations, other than violations resulting from single exceedance of max. allowable turbidity level (TT). | 2 | 1.6–1.6.8 | 3 | 1.6.5 |
| 7. Interim Enhanced Surface Water Treatment Rule violations, other than violations resulting from single exceedance of max. turbidity level (TT) | 27 | 1.6.11.6.21.6.3(G)1.6.4(B)1.6.4(E) | 3 | 1.6.3(G)1.6.7(A)(1)(b)1.6.8(B)(1) |
| 8. Filter Backwash Recycling Rule violations | 2 | 1.6.1(F)1.6.8(D) | 3 | 1.6.1(F)1.6.8(D) |
| 9. Long Term 1 Enhanced Surface Water Treatment Rule violations | 2 | 1.6.11.6.21.6.3(G)1.6.4(B)1.6.4(E) | 3 | 1.6.3(G)1.6.7(A)(1)(b)1.6.8(B)(4) |
| 10. Long Term 2 Enhanced Surface Water Treatment Rule violations | 2 | 1.6.9(K) – 1.6.9(T) | 222, 3 | 1.6.9(B) – 1.6.9(F) and 1.6.9(I) – 1.6.9(J) |
| 11. Groundwater Rule violations | 2 | 1.13.5 | 3 | 1.13.3(H), 1.13.4(D) |
| B. Inorganic Chemicals (IOCs) | ||||
| 1. Antimony | 2 | 1.16.1 | 3 | 1.16.1 |
| 2. Arsenic | 2 | 1.16.11.16.1(J)(4)8 | 3 | 1.16.1(A) and (C)11 |
| 3. Asbestos (fibers >10 mm) | 2 | 1.16.1 | 3 | 1.16.1 |
| 4. Barium | 2 | 1.16.1 | 3 | 1.16.1 |
| 5. Beryllium | 2 | 1.16.1 | 3 | 1.16.1 |
| 6. Cadmium | 2 | 1.16.1 | 3 | 1.16.1 |
| 7. Chromium (total) | 2 | 1.16.1 | 3 | 1.16.1 |
| 8. Cyanide | 2 | 1.16.1 | 3 | 1.16.1 |
| 9. Fluoride | 2 | 1.16.1 | 3 | 1.16.1 |
| 10. Mercury (inorganic) | 2 | 1.16.1 | 3 | 1.16.1 |
| 11. Nitrate | 1 | 1.16.1 | 1, 312 | 1.16.1 |
| 12. Nitrite | 1 | 1.16.1 | 1, 312 | 1.16.1 |
| 13. Total Nitrate and Nitrite | 1 | 1.16.1 | 3 | 1.16.1 |
| 14. Selenium | 2 | 1.16.1 | 3 | 1.16.1 |
| 15. Thallium | 2 | 1.16.1 | 3 | 1.16.1 |
| C. Lead and Copper Rule (Action Level for lead is 0.015 mg/L, for copper is 1.3 mg/L) | ||||
| 1. Lead and Copper Rule (TT) | 2 | 1.7.1- 1.7.6 | 3 | 1.7.7-1.7.11 |
| D. Synthetic Organic Chemicals (SOCs) | ||||
| 1. 2,4-D | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 2. 2,4,5-TP (Silvex) | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 3. Alachlor | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 4. Atrazine | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 5. Benzo(a)pyrene (PAHs) | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 6. Carbofuran | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 7. Chlordane | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 8. Dalapon | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 9. Di (2-ethylhexyl) adipate | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 10. Di (2-ethylhexyl) phthalate | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 11. Dibromochloropropane | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 12. Dinoseb | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 13. Dioxin (2,3,7,8-TCDD) | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 14. Diquat | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 15. Endothall | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 16. Endrin | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 17. Ethylene dibromide | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 18. Glyphosate | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 19. Heptachlor | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 20. Heptachlor epoxide | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 21. Hexachlorobenzene | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 22. Hexachlorocyclo-pentadiene | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 23. Lindane | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 24. Methoxychlor | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 25. Oxamyl (Vydate) | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 26. Pentachlorophenol | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 27. Picloram | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 28. Polychlorinated biphenyls (PCBs) | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 29. Simazine | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| 30. Total Per- and Polyfluoroalkyl Substances (PFAS) | 221 | 1.16.2(E) | 3 | 1.16.2(E) |
| 31. Toxaphene | 2 | 1.16.2(A) | 3 | 1.16.2(A) |
| E. Volatile Organic Chemicals (VOCs) | ||||
| 1. Benzene | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 2. Carbon tetrachloride | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 3. Chlorobenzene (monochlorobenzene) | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 4. o-Dichlorobenzene | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 5. p-Dichlorobenzene | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 6. 1,2-Dichloroethane | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 7. 1,1-Dichloroethylene | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 8. cis-1,2-Dichloroethylene | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 9. trans-1,2-Dichloroethylene | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 10. Dichloromethane | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 11. 1,2-Dichloropropane | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 12. Ethylbenzene | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 13. Styrene | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 14. Tetrachloroethylene | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 15. Toluene | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 16. 1,2,4-Trichlorobenzene | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 17. 1,1,1-Trichloroethane | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 18. 1,1,2-Trichloroethane | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 19. Trichloroethylene | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 20. Vinyl chloride | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| 21. Xylenes (total) | 2 | 1.16.2(B) | 3 | 1.16.2(B) |
| F. Radioactive Contaminants | ||||
| 1. Beta/photon emitters | 2 | 1.16.5(D) | 3 | 1.16.5 |
| 2. Alpha emitters | 2 | 1.16.5(B) | 3 | 1.16.5 |
| 3. Combined radium (226 & 228) | 2 | 1.16.5(B) | 3 | 1.16.5 |
| 4. Uranium | 29 | 1.16.5(C) | 310 | 1.16.5(A) |
| G. Disinfection Byproducts (DBPs), Byproduct Precursors, Disinfectant Residuals. Where disinfection is used in the treatment of drinking water, disinfectants combine with organic and inorganic matter present in water to form chemicals called disinfection byproducts (DBPs). EPA sets standards for controlling the levels of disinfectants and DBPs in drinking water, including trihalomethanes (THMs) and haloacetic acids (HAAs).13 | ||||
| 1. Total trihalomethanes (TTHMs) | 2 | 1.16.2(A)141.8.1(A) | 3 | 1.16.2(A) |
| 2. Haloacetic Acids (HAA5) | 2 | 1.8.1(A) | 3 | 1.8.5(A)–(B) |
| 3. Bromate | 2 | 1.8.1(A) | 3 | 1.8.5(A)–(B) |
| 4. Chlorite | 2 | 1.8.1(A) | 3 | 1.8.5(A)–(B) |
| 5. Chlorine (MRDL) | 2 | 1.8.2(A) | 3 | 1.8.5(A), (C) |
| 6. Chloramine (MRDL) | 2 | 1.8.2(A) | 3 | 1.8.5(A), (C) |
| 7. Chlorine dioxide (MRDL), where any 2 consecutive daily samples at entrance to distribution system only are above MRDL | 2 | 1.8.2(A)1.8.6(C) | 215, 3 | 1.8.5(A), (C)1.8.6(C)(2) |
| 8. Chlorine dioxide (MRDL), where sample(s) in distribution system the next day are also above MRDL | 116 | 1.8.2(A)1.8.6(C) | 1 | 1.8.5(A), (C)1.8.6(C)(2) |
| 9. Control of DBP precursors– TOC (TT) | 2 | 1.8.8(A)–(B) | 3 | 1.8.5(D) |
| 10. Benchmarking and disinfection profiling | N/A | N/A | 3 | 1.6.3(G) |
| 11. Development of monitoring plan | N/A | N/A | 3 | 1.8.5(C) |
| H. Other Treatment Techniques | ||||
| 1. Acrylamide (TT) | 2 | 1.16.2(D) | N/A | N/A |
| 2. Epichlorohydrin (TT) | 2 | 1.16.2(D) | N/A | N/A |
| II. Unregulated Contaminant Monitoring17 | ||||
| A. Unregulated contaminants | N/A | N/A | 3 | 40 C.F.R. 141-40 |
| B. Nickel | N/A | N/A | 3 | 1.16.1 |
| III. Public Notification for Variances and Exemptions: | ||||
| A. Operation under a variance or exemption | 3 | 1415, 141618 | N/A | N/A |
| B. Violation of conditions of a variance or exemption | 2 | 1415, 1416142.30719 | N/A | N/A |
| IV. Other Situations Requiring Public Notification: | ||||
| A. Fluoride secondary maximum contaminant level (SMCL) exceedance | 3 | 1.16.6(H) | N/A | N/A |
| B. Exceedance of nitrate MCL for non- community PWSs, as allowed by Director | 1 | 1.15.5 | N/A | N/A |
| C. Availability of unregulated contaminant monitoring data | 3 | 1.16.6(G) | N/A | N/A |
| D. Waterborne disease outbreak | 1 | 1.6.2(F)(2)(b) | N/A | N/A |
| E. Other waterborne emergency20 | 1 | N/A | N/A | N/A |
| F. Source Water Sample Positive for GWR Fecal indicators: E. coli, enterococci, or coliphage | 1 | 1.13.3(G) | 3 | 1.13.3 |
| G. Other situations as determined by the Director | 1, 2, 321 | N/A | N/A | N/A |
A. Appendix A – Endnotes
22. Failure to collect three or more samples for Cryptosporidium analysis is a Tier 2 violation requiring special notice as specified in § 1.16.6(L) of this Part. All other monitoring and testing procedure violations are Tier 3.
| STANDARD HEALTH EFFECTS LANGUAGE FOR PUBLIC NOTIFICATION | |||
| Contaminant | MCLG1 mg/L | MCL2 mg/L | Standard health effects language for public notification |
| SDWR and NPDWR | |||
| A.Microbiological Contaminants | |||
| 1a. Total coliform | Zero | See endnote3 | Coliforms are bacteria that are naturally present in the environment and are used as an indicator that other, potentially harmful, bacteria may be present. Coliforms were found in more samples than allowed and this was a warning of potential problems. |
| 1b. E. Coli (RTCR) | Zero | Zero | E. Coli are bacteria whose presence indicates that the water may be contaminated with human or animal wastes. Microbes in these wastes can cause short- term effects, such as diarrhea, cramps, nausea, headaches, or other symptoms. They may pose a special health risk for infants, young children and people with severely compromised immune systems. |
| 1c. Failure to conduct assessments or corrective action related to total coliform. | N/A | TT | Coliforms are bacteria that are naturally present in the environment and are used as an indicator that other, potentially harmful, waterborne pathogens may be present or that a potential pathway exists through which contamination may enter the drinking water distribution system. We found coliforms indicating the need to look for potential problems in water treatment or distribution. When this occurs, we are required to conduct assessments to identify problems and to correct any problems that are found.In addition, the PWS must include one or both of the following statements, as appropriate:1. We failed to conduct the required assessment.2. We failed to correct all identified sanitary defects that were found during the assessment(s). |
| 1d. Failure to conduct a Level 2 assessment or corrective action related to E. coli. | N/A | TT | E. coli are bacteria whose presence indicates that the water may be contaminated with human or animal wastes. Human pathogens in these wastes can cause short-term effects, such as diarrhea, cramps, nausea, headaches, or other symptoms. They may pose a greater health risk for infants, young children, the elderly, and people with severely compromised immune systems. We violated the standard for E. coli, indicating the need to look for potential problems in water treatment or distribution. When this occurs, we are required to conduct a detailed assessment to identify problems and to correct any problems that are found.In addition, include one or both of the following statements, as appropriate:1. We failed to conduct the required assessment.2. We failed to correct all identified sanitary defects that were found during the assessment that we conducted. |
| 1e. Failure to conduct a Level 2 assessment that is triggered by a second Level 1 assessment in the specified timeframe; or take corrective action in this circumstance. | N/A | TT | Coliforms are bacteria that are naturally present in the environment and are used as an indicator that other, potentially harmful, waterborne pathogens may be present or that a potential pathway exists through which contamination may enter the drinking water distribution system. We found coliforms indicating the need to look for potential problems in water treatment or distribution. When this occurs, we are required to conduct assessments to identify problems and to correct any problems that are found.In addition, the PWS must include one or both of the following statements, as appropriate:1. We failed to conduct the required assessment.2. We failed to correct all identified sanitary defects that were found during the assessment(s). |
| 1f. Failure of a seasonal PWS to follow state-approved start-up procedures prior to serving water to the public – including failure to monitor for total coliforms or E. coli | N/A | TT | When this violation includes the failure to monitor for total coliforms or E. coli prior to serving water to the public, the following language from must be included:We are required to monitor your drinking water for specific contaminants on a regular basis. Results of regular monitoring are an indicator of whether or not your drinking water meets health standards. During [compliance period], we “did not monitor or test” or “did not complete all monitoring or testing” for [contaminant(s)], and therefore, cannot be sure of the quality of your drinking water during that time. |
| 1g. Failure of a seasonal PWS to follow state-approved start-up procedures prior to serving water to the public – when monitoring is not required | N/A | TT | If monitoring is not required as part of the start-up procedures or when this violation includes failure to complete other actions, the appropriate elements required for PN under § 1.16.6 of this Part. |
| 1h. Fecal indicators (GWR):i.E. coliii.Enterococciiii.Coliphage | ZeroNoneNone | TTTTTT | Fecal indicators are microbes whose presence indicates that the water may be contaminated with human or animal wastes. Microbes in these wastes can cause short-term health effects, such as diarrhea, cramps, nausea, headaches, or other symptoms. They may pose a special health risk for infants, young children, some of the elderly, and people with severely compromised immune systems. |
| 1i. Groundwater Rule (GWR) TT violations | None | TT | Inadequately treated or inadequately protected water may contain disease-causing organisms. These organisms can cause symptoms such as diarrhea, nausea, cramps, and associated headaches. |
| 2a. Turbidity (MCL4) | None | 1 NTU55 NTU | Turbidity has no health effects. However, turbidity can interfere with disinfection and provide a medium for microbial growth. Turbidity may indicate the presence of disease-causing organisms. These organisms include bacteria, viruses, and parasites that can cause symptoms such as nausea, cramps, diarrhea and associated headaches. |
| 2b. Turbidity (SWTR TT)6 | None | TT7 | Turbidity has no health effects. However, turbidity can interfere with disinfection and provide a medium for microbial growth. Turbidity may indicate the presence of disease-causing organisms. These organisms include bacteria, viruses, and parasites that can cause symptoms such as nausea, cramps, diarrhea and associated headaches. |
| 2c. Turbidity (IESWTR TT and LT1ESWTR TT)8 | None | TT | Turbidity has no health effects. However, turbidity can interfere with disinfection and provide a medium for microbial growth. Turbidity may indicate the presence of disease-causing organisms. These organisms include bacteria, viruses, and parasites that can cause symptoms such as nausea, cramps, diarrhea and associated headaches. |
| B. Surface Water Treatment Rule (SWTR) and Interim Enhanced Surface Water Treatment Rule (IESWTR), Long Term 1 Enhanced Surface Water Treatment Rule (LT1ESWTR) and the Filter Backwash Recycling Rule (FBRR) violations | |||
| 3. Giardia lamblia(SWTR/IESWTR/LT1ESWTR)4. Viruses(SWTR/IESWTR/LT1ESWTR)5. Heterotrophic plate count (HPC) bacteria9(SWTR/IESWTR/LT1ESWTR)6. Legionella(SWTR/IESWTR/LT1ESWTR)7. Cryptosporidium(IESWTR/FBRR/LT1ESWTR) | Zero | TT10 | Inadequately treated water may contain disease-causing organisms. These organisms include bacteria, viruses and parasites which can cause symptoms such as nausea, cramps, diarrhea, and associated headaches. |
| C. Inorganic Chemicals (IOCs) | |||
| 8. Antimony | 0.006 | 0.006 | Some people who drink water containing antimony well in excess of the MCL over many years could experience increases in blood cholesterol and decreases in blood sugar. |
| 9. Arsenic11 | Zero | 0.010 | Some people who drink water containing arsenic in excess of the MCL over many years could experience skin damage or problems with their circulatory system, and may have an increased risk of getting cancer. |
| 10. Asbestos (>10 µm) | 7 MFL12 | 7 MFL | Some people who drink water containing asbestos in excess of the MCL over many years may have an increased risk of developing benign intestinal polyps. |
| 11. Barium | 2 | 2 | Some people who drink water containing barium in excess of the MCL over many years could experience an increase in their blood pressure. |
| 12. Beryllium | 0.004 | 0.004 | Some people who drink water containing beryllium well in excess of the MCL over many years could develop intestinal lesions. |
| 13. Cadmium | 0.005 | 0.005 | Some people who drink water containing cadmium in excess of the MCL over many years could experience kidney damage. |
| 14. Chromium (total) | 0.1 | 0.1 | Some people who use water containing chromium well in excess of the MCL over many years could experience allergic dermatitis. |
| 15. Cyanide | 0.2 | 0.2 | Some people who drink water containing cyanide well in excess of the MCL over many years could experience nerve damage or problems with their thyroid. |
| 16. Fluoride | 4.0 | 4.0 | Some people who drink water containing fluoride in excess of the MCL over many years could get bone disease, including pain and tenderness of the bones. Fluoride in drinking water at half the MCL or more may cause mottling of children's teeth, usually in children less than nine (9) years old. Mottling, also known as dental fluorosis, may include brown staining and/or pitting of the teeth, and occurs only in developing teeth, before they erupt from the gums. |
| 17. Mercury (inorganic) | 0.002 | 0.002 | Some people who drink water containing inorganic mercury well in excess of the MCL over many years could experience kidney damage. |
| 18. Nitrate | 10 | 10 | Infants below the age of six (6) months who drink water containing nitrate in excess of the MCL could become seriously ill and, if untreated, may die. Symptoms include shortness of breath and blue-baby syndrome. |
| 19. Nitrite | 1 | 1 | Infants below the age of six (6) months who drink water containing nitrite in excess of the MCL could become seriously ill and, if untreated, may die. Symptoms include shortness of breath and blue-baby syndrome. |
| 20. Total Nitrate and Nitrite | 10 | 10 | Infants below the age of six (6) months who drink water containing nitrate and nitrite in excess of the MCL could become seriously ill and, if untreated, may die. Symptoms include shortness of breath and blue baby syndrome. |
| 21. Selenium | 0.05 | 0.05 | Selenium is an essential nutrient. However, some people who drink water containing selenium in excess of the MCL over many years could experience hair or fingernail losses, numbness in fingers or toes, or problems with their circulation. |
| 22. Thallium | 0.0005 | 0.002 | Some people who drink water containing thallium in excess of the MCL over many years could experience hair loss, changes in their blood, or problems with their kidneys, intestines, or liver. |
| D. Lead and Copper Rule | |||
| 23. Lead | Zero | TT13 | Infants and children who drink water containing lead in excess of the action level could experience delays in their physical or mental development. Children could show slight deficits in attention span and learning abilities. Adults who drink this water over many years could develop kidney problems or high blood pressure. |
| 24. Copper | 1.3 | TT14 | Copper is an essential nutrient, but some people who drink water containing copper in excess of the action level over a relatively short amount of time could experience gastrointestinal distress. Some people who drink water containing copper in excess of the action level over many years could suffer liver or kidney damage. People with Wilson's Disease should consult their personal doctor. |
| E. Synthetic Organic Compounds (SOCs) | |||
| 25. 2,4-D | 0.07 | 0.07 | Some people who drink water containing the weed killer 2,4-D well in excess of the MCL over many years could experience problems with their kidneys, liver, or adrenal glands. |
| 26. 2,4,5-TP (Silvex) | 0.05 | 0.05 | Some people who drink water containing silvex in excess of the MCL over many years could experience liver problems. |
| 27. Alachlor | Zero | 0.002 | Some people who drink water containing alachlor in excess of the MCL over many years could have problems with their eyes, liver, kidneys, or spleen, experience anemia, or may have an increased risk of getting cancer. |
| 28. Atrazine | 0.003 | 0.003 | Some people who drink water containing atrazine well in excess of the MCL over many years could experience problems with their cardiovascular system or reproductive difficulties. |
| 29. Benzo(a)pyrene (PAHs) | Zero | 0.0002 | Some people who drink water containing benzo(a)pyrene in excess of the MCL over many years may experience reproductive difficulties or may have an increased risk of getting cancer. |
| 30. Carbofuran | 0.04 | 0.04 | Some people who drink water containing carbofuran in excess of the MCL over many years could experience problems with their blood, or nervous or reproductive systems. |
| 31. Chlordane | Zero | 0.002 | Some people who drink water containing chlordane in excess of the MCL over many years could experience problems with their liver, or nervous system, and may have an increased risk of getting cancer. |
| 32. Dalapon | 0.2 | 0.2 | Some people who drink water containing dalapon well in excess of the MCL over many years could experience minor kidney changes. |
| 33. Di (2-ethylhexyl) adipate | 0.4 | 0.4 | Some people who drink water containing di (2- ethylhexyl) adipate well in excess of the MCL over many years could experience general toxic effects or reproductive difficulties. |
| 34. Di(2-ethylhexyl) phthalate | Zero | 0.006 | Some people who drink water containing di (2- ethylhexyl) phthalate in excess of the MCL over many years may have problems with their liver, or experience reproductive difficulties, and may have an increased risk of getting cancer. |
| 35. Dibromochloropropane (DBCP) | Zero | 0.0002 | Some people who drink water containing DBCP in excess of the MCL over many years could experience reproductive difficulties and may have an increased risk of getting cancer. |
| 36. Dinoseb | 0.007 | 0.007 | Some people who drink water containing dinoseb well in excess of the MCL over many years could experience reproductive difficulties. |
| 37. Dioxin (2,3,7,8-TCDD) | Zero | 3 x 10-8 | Some people who drink water containing dioxin in excess of the MCL over many years could experience reproductive difficulties and may have an increased risk of getting cancer. |
| 38. Diquat | 0.02 | 0.02 | Some people who drink water containing diquat in excess of the MCL over many years could get cataracts. |
| 39. Endothall | 0.1 | 0.1 | Some people who drink water containing endothall in excess of the MCL over many years could experience problems with their stomach or intestines. |
| 40. Endrin | 0.002 | 0.002 | Some people who drink water containing endrin in excess of the MCL over many years could experience liver problems. |
| 41. Ethylene dibromide | Zero | 0.00005 | Some people who drink water containing ethylene dibromide in excess of the MCL over many years could experience problems with their liver, stomach, reproductive system, or kidneys, and may have an increased risk of getting cancer. |
| 42. Glyphosate | 0.7 | 0.7 | Some people who drink water containing glyphosate in excess of the MCL over many years could experience problems with their kidneys or reproductive difficulties. |
| 43. Heptachlor | Zero | 0.0004 | Some people who drink water containing heptachlor in excess of the MCL over many years could experience liver damage and may have an increased risk of getting cancer. |
| 44. Heptachlor epoxide | Zero | 0.0002 | Some people who drink water containing heptachlor epoxide in excess of the MCL over many years could experience liver damage, and may have an increased risk of getting cancer. |
| 45. Hexachlorobenzene | Zero | 0.001 | Some people who drink water containing hexachlorobenzene in excess of the MCL over many years could experience problems with their liver or kidneys, or adverse reproductive effects, and may have an increased risk of getting cancer. |
| 46. Hexachlorocyclopentadiene | 0.05 | 0.05 | Some people who drink water containing hexachlorocyclopentadiene well in excess of the MCL over many years could experience problems with their kidneys or stomach. |
| 47. Lindane | 0.0002 | 0.0002 | Some people who drink water containing lindane in excess of the MCL over many years could experience problems with their kidneys or liver. |
| 48. Methoxychlor | 0.04 | 0.04 | Some people who drink water containing methoxychlor in excess of the MCL over many years could experience reproductive difficulties. |
| 49. Oxamyl (Vydate) | 0.2 | 0.2 | Some people who drink water containing oxamyl in excess of the MCL over many years could experience slight nervous system effects. |
| 50. Pentachlorophenol | Zero | 0.001 | Some people who drink water containing pentachlorophenol in excess of the MCL over many years could experience problems with their liver or kidneys, and may have an increased risk of getting cancer. |
| 51. Picloram | 0.5 | 0.5 | Some people who drink water containing picloram in excess of the MCL over many years could experience problems with their liver. |
| 52. Polychlorinated biphenyls (PCBs) | Zero | 0.0005 | Some people who drink water containing PCBs in excess of the MCL over many years could experience changes in their skin, problems with their thymus gland, immune deficiencies, or reproductive or nervous system difficulties, and may have an increased risk of getting cancer. |
| 53. Simazine | 0.004 | 0.004 | Some people who drink water containing simazine in excess of the MCL over many years could experience problems with their blood. |
| 54. Total Per- and Polyfluoroalkyl Substances (PFAS) | 0.000020 | Studies have shown certain PFAS can cause negative health effects, including higher cholesterol levels, lower infant birth weights, weakened immune response, and an increased risk of some cancers, including prostate, kidney, and testicular cancers. | |
| 55. Toxaphene | Zero | 0.003 | Some people who drink water containing toxaphene in excess of the MCL over many years could have problems with their kidneys, liver, or thyroid, and may have an increased risk of getting cancer. |
| F. Volatile Organic Chemicals (VOCs) | |||
| 56. Benzene | Zero | 0.005 | Some people who drink water containing benzene in excess of the MCL over many years could experience anemia or a decrease in blood platelets, and may have an increased risk of getting cancer. |
| 57. Carbon tetrachloride | Zero | 0.005 | Some people who drink water containing carbon tetrachloride in excess of the MCL over many years could experience problems with their liver and may have an increased risk of getting cancer. |
| 58. Chlorobenzene (monochlorobenzene) | 0.1 | 0.1 | Some people who drink water containing chlorobenzene in excess of the MCL over many years could experience problems with their liver or kidneys |
| 59. o-Dichlorobenzene | 0.6 | 0.6 | Some people who drink water containing o- dichlorobenzene well in excess of the MCL over many years could experience problems with their liver, kidneys, or circulatory systems. |
| 60. p-Dichlorobenzene | 0.075 | 0.075 | Some people who drink water containing p- dichlorobenzene in excess of the MCL over many years could experience anemia, damage to their liver, kidneys, or spleen, or changes in their blood. |
| 61. 1,2-Dichloroethane | Zero | 0.005 | Some people who drink water containing 1,2- dichloroethane in excess of the MCL over many years may have an increased risk of getting cancer. |
| 62. 1,1-Dichloroethylene | 0.007 | 0.007 | Some people who drink water containing 1,1- dichloroethylene in excess of the MCL over many years could experience problems with their liver. |
| 63. cis-1,2-Dichloroethylene | 0.07 | 0.07 | Some people who drink water containing cis-1,2-dichloroethylene in excess of the MCL over many years could experience problems with their liver. |
| 64. trans-1,2-Dichloroethylene | 0.1 | 0.1 | Some people who drink water containing trans-1,2-dichloroethylene well in excess of the MCL over many years could experience problems with their liver. |
| 65. Dichloromethane | Zero | 0.005 | Some people who drink water containing dichloromethane in excess of the MCL over many years could have liver problems and may have an increased risk of getting cancer. |
| 66. 1,2-Dichloropropane | Zero | 0.005 | Some people who drink water containing 1,2- dichloropropane in excess of the MCL over many years may have an increased risk of getting cancer. |
| 67. Ethylbenzene | 0.7 | 0.7 | Some people who drink water containing ethylbenzene well in excess of the MCL over many years could experience problems with their liver or kidneys. |
| 68. Styrene | 0.1 | 0.1 | Some people who drink water containing styrene well in excess of the MCL over many years could have problems with their liver, kidneys, or circulatory system. |
| 69. Tetrachloroethylene | Zero | 0.005 | Some people who drink water containing tetrachloroethylene in excess of the MCL over many years could have problems with their liver, and may have an increased risk of getting cancer. |
| 70. Toluene | 1 | 1 | Some people who drink water containing toluene well in excess of the MCL over many years could have problems with their nervous system, kidneys, or liver. |
| 71. 1,2,4-Trichlorobenzene | 0.07 | 0.07 | Some people who drink water containing 1,2,4-trichlorobenzene well in excess of the MCL over many years could experience changes in their adrenal glands. |
| 72. 1,1,1-Trichloroethane | 0.2 | 0.2 | Some people who drink water containing 1,1,1- trichloroethane in excess of the MCL over many years could experience problems with their liver, nervous system, or circulatory system. |
| 73. 1,1,2-Trichloroethane | 0.003 | 0.005 | Some people who drink water containing 1,1,2- trichloroethane well in excess of the MCL over many years could have problems with their liver, kidneys, or immune systems. |
| 74. Trichloroethylene | Zero | 0.005 | Some people who drink water containing trichloroethylene in excess of the MCL over many years could experience problems with their liver and may have an increased risk of getting cancer. |
| 75. Vinyl chloride | Zero | 0.002 | Some people who drink water containing vinyl chloride in excess of the MCL over many years may have an increased risk of getting cancer. |
| 76. Xylenes (total) | 10 | 10 | Some people who drink water containing xylenes in excess of the MCL over many years could experience damage to their nervous system. |
| G. Radioactive Contaminants | |||
| 77. Beta/photon emitters | Zero | 4 mrem/yr15 | Certain minerals are radioactive and may emit forms of radiation known as photons and beta radiation. Some people who drink water containing beta and photon emitters in excess of the MCL over many years may have an increased risk of getting cancer. |
| 78. Alpha emitters (Gross alpha) | Zero | 15 pCi/L17 | Certain minerals are radioactive and may emit a form of radiation known as alpha radiation. Some people who drink water containing alpha emitters in excess of the MCL over many years may have an increased risk of getting cancer. |
| 79. Combined radium (226 & 228) | Zero | 5 pCi/L | Some people who drink water containing radium 226 or 228 in excess of the MCL over many years may have an increased risk of getting cancer. |
| 80. Uranium16 | Zero | 30 µg/L | Some people who drink water containing uranium in excess of the MCL over many years may have an increased risk of getting cancer and kidney toxicity. |
| H. Disinfection Byproducts (DBPs), Byproduct Precursors, and Disinfectant Residuals: Where disinfection is used in the treatment of drinking water, disinfectants combine with organic and inorganic matter present in water to form chemicals called disinfection byproducts (DBPs). EPA also sets standards for controlling the levels of disinfectants and DBPs in drinking water, which include trihalomethanes (THMs) and haloacetic acids (HAAs).18 | |||
| 81. Total trihalomethanes (TTHMs) | N/A | 0.08019,20 | Some people who drink water containing trihalomethanes in excess of the MCL over many years may experience problems with their liver, kidneys, or central nervous system, and may have an increased risk of getting cancer. |
| 82. Haloacetic Acids (HAA5) | N/A | 0.06021 | Some people who drink water containing HAAs in excess of the MCL over many years may have an increased risk of developing cancer. |
| 83. Bromate | Zero | 0.010 | Some people who drink water containing bromate in excess of the MCL over many years may have an increased risk of developing cancer. |
| 84. Chlorite | 0.8 | 1.0 | Some infants and young children who drink water containing chlorite in excess of the MCL could experience nervous system effects. Similar effects may occur in fetuses of pregnant mothers who drink water containing chlorite in excess of the MCL. Some people may experience anemia. |
| 85. Chlorine | 4 (MRDLG)22 | 4.0 (MRDL)23 | Some people who contact drinking water containing chlorine well in excess of the MRDL could experience irritating effects to their eyes and nose. Some people who drink water containing chlorine well in excess of the MRDL could experience stomach discomfort. |
| 86. Chloramines | 4 (MRDLG) | 4.0 (MRDL) | Some people who contact drinking water containing chloramines well in excess of the MRDL could experience irritating effects to their eyes and nose. Some people who drink water containing chloramines well in excess of the MRDL could experience stomach discomfort or anemia. |
| 87a. Chlorine dioxide, where any 2 consecutive daily samples taken at the entrance to the distribution system are above the MRDL | 0.8 (MRDLG) | 0.8 (MRDL) | Some infants and young children who drink water containing chlorine dioxide in excess of the MRDL could experience nervous system effects. Similar effects may occur in fetuses of pregnant mothers who drink water containing chlorine dioxide in excess of the MRDL. Some people may experience anemia.Add for public notification only: The chlorine dioxide violations reported today are the result of exceedances at the treatment facility only, not within the distribution system which delivers water to consumers. Continued compliance with chlorine dioxide levels within the distribution system minimizes the potential risk of these violations to consumers. |
| 87b. Chlorine dioxide, where one (1) or more distribution system sample(s) are above the MRDL | 0.8 (MRDLG) | 0.8 (MRDL) | Some infants and young children who drink water containing chlorine dioxide in excess of the MRDL could experience nervous system effects. Similar effects may occur in fetuses of pregnant mothers who drink water containing chlorine dioxide in excess of the MRDL. Some people may experience anemia.Add for public notification only: The chlorine dioxide violations reported today include exceedances of the EPA standard within the distribution system which delivers water to consumers. Violations of the chlorine dioxide standard within the distribution system may harm human health based on short-term exposures. Certain groups, including fetuses, infants and young children, may be especially susceptible to nervous system effects from excessive chlorine dioxide exposure. |
| 88. Control of DBP precursors (TOC) | None | TT | Total organic carbon (TOC) has no health effects. However, total organic carbon provides a medium for the formation of disinfection by products. These byproducts include trihalomethanes (THMs) and haloacetic acids (HAAs), which may lead to adverse health effects, liver or kidney problems, or nervous system effects, and may lead to an increased risk of getting cancer. |
| I. Other Treatment Techniques | |||
| 89. Acrylamide | Zero | TT | Some people who drink water containing high levels of acrylamide over a long period of time could have problems with their nervous system or blood, and may have an increased risk of getting cancer. |
| 90. Epichlorohydrin | Zero | TT | Some people who drink water containing high levels of epichlorohydrin over a long period of time could experience stomach problems, and may have an increased risk of getting cancer. |
| J. Algal Toxins | |||
| 91. Microcystin | 0.3-1.6 microgram/liter (do not drink)20 micrograms/liter (do not use) | Consuming water containing algal toxins may result in abnormal liver function, diarrhea, vomiting, nausea, numbness or dizziness. Seek medical attention if you feel you have been exposed to algal toxins and are having adverse health effects. Skin contact with contaminated water can cause irritation or rashes. Algal toxins may pose a special health risk for young children, pregnant women, nursing mothers, those with pre-existing liver conditions, people with compromised immune systems, medically fragile individuals and pets. Contact a veterinarian immediately if pets or livestock show signs of illness. | |
| 92. Cylindrospermopsin | 1 microgram/liter (do not drink)20 micrograms/liter (do not use) | Consuming water containing algal toxins may result in abnormal liver function, diarrhea, vomiting, nausea, numbness or dizziness. Seek medical attention if you feel you have been exposed to algal toxins and are having adverse health effects. Skin contact with contaminated water can cause irritation or rashes. Algal toxins may pose a special health risk for young children, pregnant women, people with compromised immune systems, medically fragile individuals and pets. Contact a veterinarian immediately if pets or livestock show signs of illness. | |
| 93. Anatoxin-a | 20 micrograms/liter (do not drink)300 micrograms/liter (do not use) | Consuming water containing algal toxins may result in abnormal liver function, diarrhea, vomiting, nausea, numbness or dizziness. Seek medical attention if you feel you have been exposed to algal toxins and are having adverse health effects. Skin contact with contaminated water can cause irritation or rashes. Algal toxins may pose a special health risk for young children, pregnant women, people with compromised immune systems, medically fragile individuals and pets. Contact a veterinarian immediately if pets or livestock show signs of illness. | |
| 94. Saxitoxin | 0.2 micrograms/liter (do not drink)3 micrograms/liter (do not use) | Consuming water containing algal toxins may result in abnormal liver function, diarrhea, vomiting, nausea, numbness or dizziness. Seek medical attention if you feel you have been exposed to algal toxins and are having adverse health effects. Skin contact with contaminated water can cause irritation or rashes. Algal toxins may pose a special health risk for young children, pregnant women, people with compromised immune systems, medically fragile individuals and pets. Contact a veterinarian immediately if pets or livestock show signs of illness. |
B. Appendix B – Endnotes
23. MRDL–Maximum residual disinfectant level.
A. List of Acronyms Used in Public Notification Regulations
32. VOC - Volatile Organic Chemical
A. Records of analyses shall be maintained by the water purveyor. The records of each sample analyzed to comply with this Part shall contain the following information:
F. Copies of monitoring plans developed pursuant to this Part shall be kept for the same period of time as the records of analyses taken under the plan are required to be kept under this Section, except as specified elsewhere in this Part.
A. Purpose and Applicability of § 1.16.11 of this Part
B. Compliance Dates
1. Beginning on the effective date of the January 2026 amendments to § 1.16.11 of this Part through December 31, 2026, community PWS must comply with §§ 141.151 through 141.155, as codified in 40 CFR Part 141, subpart O, on July 1, 2023, with the following modifications.
“(d) For the purpose of this subpart, detected means: at or above the levels prescribed by § 141.23(a)(4) for inorganic contaminants, at or above the levels prescribed by § 141.24(f)(7) for the contaminants listed in § 141.61(a), at or above the levels prescribed by § 141.24(h)(18) for the contaminants listed in § 141.61(c), at or above the levels prescribed by § 141.131(b)(2)(iv) for the contaminants or contaminant groups listed in § 141.64, at or above the levels prescribed by § 141.25(c) for radioactive contaminants, and at or above the levels prescribed in § 1.16.2(E)(1) of the Rhode Island Public Drinking Water regulations, 216-RICR-50-05-1 (PDW Regulations) for the PFAS listed in § 1.16.2(E)(1) of the PDW Regulations.”
“(g) Each community PWS which exceeds an algal toxin MCL established in § 1.6.10 of the PDW Regulations in a sample collected at finished water sampling point in a weekly, resample or repeat sample, or a distribution sampling point collected within their own community PWS in accordance with § 1.6.10 of the PDW Regulations shall include the following in the consumer confidence report:
c. Amend appendix A to subpart O, under the Contaminant heading ‘‘Synthetic organic contaminants including pesticides and herbicides:’’, by adding in alphabetical order an entry for ‘‘Total PFAS [Per- and Polyfluoroalkyl Substances] (ppt)’’ to read as follows:
| Appendix A to Subpart O of Part 141—Regulated Contaminants | ||||||
| Contaminant (units) | Traditional MCL in mg/L | To convert for CCR, multiply by | MCL in CCR units | MCLG | Major Sources in Drinking Water | Health effects language |
| * | * | * | * | * | * | * |
| Total PFAS [Per- and Polyfluoroalkyl Substances] (ppt) | 0.000020 | 1,000,000 | 20 | Discharges and/or emissions from industrial, commercial, and manufacturing sources associated with the production or use of PFAS. The application or accidental release of fire-fighting foams (i.e. aqueous film forming foam, AFFF). Wastewater treatment discharges/ residuals and landfill leachate as a result of the use and disposal of products containing these compounds. | Studies have shown certain PFAS can cause negative health effects, including higher cholesterol levels, lower infant birth weights, weakened immune response, and an increased risk of some cancers, including prostate, kidney, and testicular cancers. | |
| * | * | * | * | * | * | * |
5. A community PWS that sells water to another community PWS must deliver the applicable information required in § 1.16.11(C) of this Part, to the buyer PWS:
C. Content of the Reports
2. Information on the source of the water delivered:
a. Each CCR must identify the source(s) of the water delivered by the community PWS by providing information on:
3. Definitions:
a. Each CCR must include the following definitions:
c. A report that contains data on contaminants that EPA regulates using any of the following terms must include the applicable definitions:
d. A CCR that contains information regarding a Level 1 or Level 2 Assessment required under the § 1.16.4(A) of this Part must include the applicable definitions:
e. Systems must use the following definitions for the terms listed below if the terms are used in the CCR unless the system obtains written approval from the state to use an alternate definition:
4. Information on Detected Contaminants:
a. This § 1.16.11(C)(4) of this Part specifies the requirements for information to be included in each CCR for contaminants subject to mandatory monitoring (except Cryptosporidium). It applies to:
c. The data must be derived from data collected to comply with EPA and State monitoring, and analytical requirements during the previous calendar year, or the most recent calendar year before the previous calendar year, except that:
d. For each detected regulated contaminant (listed in § 1.16.12 of this Part), the contaminant data section(s) must contain:
(4) For contaminants subject to an MCL, except turbidity and E. coli, the contaminant data section(s) must contain the highest contaminant level used to determine compliance with the MCL and the range of detected levels, as provided in §§ 1.16.11(C)(4)(d)(4)(AA)-(BB) of this Part. When rounding of results to determine compliance with the MCL is allowed by the regulations, rounding should be done prior to multiplying the results by the factor listed in § 1.16.12 of this Part;
(5) For turbidity
g. For detected unregulated contaminants for which monitoring is required the CCR must present the average and range at which the contaminant was detected. The CCR must include a brief explanation of the reasons for monitoring for unregulated contaminants such as:
5. Information on Cryptosporidium, Radon, and Other Contaminants:
a. If the PWS has performed any monitoring for Cryptosporidium, which indicates that Cryptosporidium may be present in the source water or the finished water, the CCR must include:
b. If the PWS has performed any monitoring for radon which indicates that radon may be present in the finished water, the CCR must include:
c. If the PWS has performed additional monitoring which indicates the presence of other contaminants in the finished water, the PWS is strongly encouraged to report any results which may indicate a health concern. To determine if results may indicate a health concern, it is recommended that PWSs find out if EPA has proposed an NPDWR or issued a health advisory for that contaminant by contacting EPA by calling the Safe Drinking Water Hotline (800-426-4791) or an alternative method identified on the website epa.gov/safewater. Detects above a proposed MCL or health advisory level are considered to indicate possible health concerns. For such contaminants, it is recommended that the CCR include:
6. Compliance with NPDWR: In addition to the requirements of § 1.16.11(C)(4) of this Part, the CCR must note any violation that occurred during the period covered by the report of a requirement listed below, and include a clear and readily understandable explanation of the violation, any potential adverse health effects, and the steps the PWS has taken to correct the violation.
8. Additional Information
a. The CCR must contain a brief explanation regarding contaminants which may reasonably be expected to be found in drinking water including bottled water. This explanation may include the language of §§ 1.16.11(C)(8)(a)(1) through (3) of this Part, or PWSs may use their own comparable language. The CCR also must include the language of § 1.16.11(C)(8)(a)(4) of this Part.
(2) Contaminants are any physical, chemical, biological, or radiological substance or matter in water. Contaminants that may be present in source water include:
f. PWS required to comply with § 1.13 of this Part.
(1) Any groundwater PWS that receives notice from the Director of a significant deficiency or notice from a laboratory of a fecal indicator-positive groundwater source sample that is not invalidated by the Director under § 1.13.3(D) of this Part, must inform its customers of any significant deficiency that is uncorrected at the time of the next reporting period or of any fecal indicator-positive groundwater source sample in the next CCR or 6 month update according to § 1.16.11(E) of this Part. The PWS must continue to inform the public annually until the Director determines that particular significant deficiency is corrected or the fecal contamination in the groundwater source is addressed under § 1.13.4(A) of this Part. Each CCR must include the following elements:
g. PWS required to comply with § 1.16.4 of this Part.
(1) Any PWS required to comply with the Level 1 assessment requirement or a Level 2 assessment requirement that is not due to an E. coli MCL violation must include in the CCR the text found in §§ 1.16.11(C)(8)(g)(1)(AA) through (CC) of this Part as appropriate, filling in the blanks accordingly and the text found in §§ 1.16.11(C)(8)(g)(1)(DD) of this Part, if appropriate. PWS may use an alternative statement with equivalent information for §§ 1.16.11(C)(8)(g)(1)(BB) and (CC) of this Part if approved by the Director.
(DD) Any PWS that has failed to complete all the required assessments or correct all identified sanitary defects, is in violation of the treatment technique requirement and must also include one or both of the following statements, as appropriate:
(3) Systems may use an alternative statement with equivalent information for §§ 1.16.11(D)(8)(g)(2)(AA) through (CC) of this Part, if approved by the Director.
(CC) Any PWS that has failed to complete the required assessment or correct all identified sanitary defects, is in violation of the treatment technique requirement and must also include one or both of the following statements, as appropriate:
(3) If a PWS detects E. coli and has violated the E. coli MCL, in addition to completing the table as required in § 1.16.11(C)(4)(d) of this Part, the PWS must include one or more of the following statements to describe any noncompliance, as applicable:
h. Systems required to comply with § 1.7 of this Part.
(3) The CCR must contain a plainly worded explanation of the corrosion control efforts the system is taking in accordance with § 1.7 of this Part. Corrosion control efforts consist of treatment (e.g., pH adjustment, alkalinity adjustment, or corrosion inhibitor addition) and other efforts contributing to the control of the corrosivity of the water, e.g. monitoring to assess the corrosivity of water. The system may use one of the following templates or use their own explanation that includes equivalent information.
(AA) For systems with Director or EPA-designated Optimal Corrosion Control Treatment:
(BB) For systems without Director or EPA-designated Optimal Corrosion Control Treatment:
D. Required Additional Health Information
2. A PWS that detects arsenic above 0.005 mg/L and up to and including 0.010 mg/L,:
3. A PWS which detects nitrate at levels above five (5) mg/L, but below the MCL:
4. Every CCR must include the following lead-specific information:
5. Each community PWS which exceeds an algal toxin MCL established in § 1.6.10 of this Part in a sample collected at finished water sampling point in a weekly, resample or repeat sample, or a distribution sampling point collected within their own community PWS in accordance with § 1.6.10 of this Part shall include the following in the CCR:
E. Report Delivery, Reporting, and Recordkeeping
1. Each community PWS must deliver a copy of the CCR to each customer.
a. PWS must use, at a minimum, one of the following forms of delivery:
c. For PWS that choose to electronically deliver the CCRs by posting the CCR to a website and providing a notification either by mail or by email:
2. The PWS must make a good faith effort to reach consumers who do not get water bills, using means recommended by the Director. Such effort must be tailored to the consumers who are served by the PWS but are not bill-paying customers, such as renters or workers.: A good faith effort to reach consumers includes a mix of methods to reach the broadest possible range of persons served by the PWS such as, but not limited to: posting the CCRs on the internet; mailing CCRs or postcards with links to the CCRs to all service addresses and/or postal customers; using an opt in notification system to send emails and/or texts with links to the CCRs to interested consumers; advertising the availability of the CCRs in the news media and on social media; publication in a local newspaper or newsletter; posting a copy of the CCR or notice of availability with links (or equivalent such as Quick Response (QR) codes) in public places such as cafeterias or lunch rooms of public buildings; delivery of multiple copies for distribution by single-biller customers such as apartment buildings or large private employers; delivery to community organizations; holding a public meeting to educate consumers on the CCRs.
9. Delivery timing and biannual delivery:
c. PWS required to comply with § 1.16.11(E)(9)(b) of this Part, with a violation or action level exceedance that occurred between January 1 and June 30 of the current year, or have received monitoring results from the required monitoring under the Unregulated Contaminant Monitoring Rule in 40 C.F.R. § 141.40, must include a 6-month update with the second CCR with the following:
F. Summary of CCR contents.
2. PWS must include, at a minimum, the following information in the summary:
3. If applicable, PWS must include the following in the summary:
6. The CCR summary must include the following standard language to encourage the distribution of the CCR to all persons served: Please share this information with anyone who drinks this water (or their guardians), especially those who may not have received this CCR directly (for example, people in apartments, nursing homes, schools, and businesses). You can do this by posting this CCR in a public place or distributing copies by hand, mail, email, or another method.
| Contaminant (units) | Traditional MCL in mg/L | To convert for CCR, multiply by | MCL in CCR units | MCLG | Major sources in drinking water | Health effects language |
| Microbiological contaminants: | ||||||
| Total Coliform Bacteria | TT | TT | N/A | Naturally present in the environment | Use language found in § 1.16.11(C)(8)(g)(1)(AA) | |
| E. Coli | Routine and repeat samples are total coliform-positive and either is E. coli-positive or system fails to take repeat samples following E. coli-positive routine sample or system fails to analyze total coliform-positive repeat sample for E. coli. | Routine and repeat samples are total coliform-positive and either is E. coli-positive or system fails to take repeat samples following E. coli-positive routine sample or system fails to analyze total coliform-positive repeat sample for E. coli. | 0 | Human and animal fecal waste | E. Coli are bacteria whose presence indicates that the water may be contaminated with human or animal wastes. Human pathogens in these wastes can cause short-term effects, such as diarrhea, cramps, nausea, headaches, or other symptoms. They may pose a greater health risk for infants, young children, the elderly, and people with severely compromised immune systems. | |
| Fecal Indicators (enterococci or coliphage) | TT | TT | N/A | Human and animal fecal waste | Fecal indicators are microbes whose presence indicates that the water may be contaminated with human or animal wastes. Microbes in these wastes can cause short-term health effects, such as diarrhea, cramps, nausea, headaches, or other symptoms. They may pose a special health risk for infants, young children, some of the elderly, and people with severely compromised immune systems. | |
| Total organic carbon (ppm) | TT | TT | N/A | Naturally present in the environment | Total organic carbon (TOC) has no health effects. However, total organic carbon provides a medium for the formation of disinfection by products. These byproducts include trihalomethanes (THMs) and haloacetic acids (HAAs). Drinking water containing these byproducts in excess of the MCL may lead to adverse health effects, liver or kidney problems, or nervous system effects, and may lead to an increased risk of getting cancer. | |
| Turbidity (NTU) | TT | TT | N/A | Soil runoff | Turbidity has no health effects. However, turbidity can interfere with disinfection and provide a medium for microbial growth. Turbidity may indicate the presence of disease-causing organisms. These organisms include bacteria, viruses, and parasites that can cause symptoms such as nausea, cramps, diarrhea and associated headaches. | |
| Radioactive contaminantsBeta/photon emitters (mrem/yr.) | 4 mrem/yr. | 4 | 0 | Decay of natural and man-made deposits | Certain minerals are radioactive and may emit forms of radiation known as photons and beta radiation. Some people who drink water containing beta and photon radioactivity in excess of the MCL over many years may have an increased risk of getting cancer. | |
| Alpha emitters (pCi/l) | 15 pCi/l | 15 | 0 | Erosion of natural deposits | Certain minerals are radioactive and may emit a form of radiation known as alpha radiation. Some people who drink water containing alpha emitters in excess of the MCL over many years may have an increased risk of getting cancer. | |
| Combined radium (pCi/l) | 5 pCi/l | 5 | 0 | Erosion of natural deposits | Some people who drink water containing radium 226 or 228 in excess of the MCL over many years may have an increased risk of getting cancer. | |
| Uranium (µg/L) | 0.030 | 1000 | 30 | 0 | Erosion of natural deposits | Some people who drink water containing uranium in excess of the MCL over many years may have an increased risk of getting cancer and kidney toxicity. |
| Inorganic contaminants: | ||||||
| Antimony (ppb) | 0.006 | 1000 | 6 | 6 | Discharge from petroleum refineries; fire retardants; ceramics; electronics; solder | Some people who drink water containing antimony well in excess of the MCL over many years could experience increases in blood cholesterol and decreases in blood sugar. |
| Arsenic (ppb) | 0.010 | 1000 | 10 | 0 | Erosion of natural deposits; Runoff from orchards; Runoff from glass and electronics production wastes | Some people who drink water containing arsenic in excess of the MCL over many years could experience skin damage or problems with their circulatory system, and may have an increased risk of getting cancer. |
| Asbestos (MFL) | 7 MFL | 7 | 7 | Decay of asbestos cement water mains; Erosion of natural deposits | Some people who drink water containing asbestos in excess of the MCL over many years may have an increased risk of developing benign intestinal polyps. | |
| Barium (ppm) | 2 | 2 | 2 | Discharge of drilling wastes; Discharge from metal refineries; Erosion of natural deposits | Some people who drink water containing barium in excess of the MCL over many years could experience an increase in their blood pressure. | |
| Beryllium (ppb) | 0.004 | 1000 | 4 | 4 | Discharge from metal refineries and coal- burning factories; Discharge from electrical, aerospace, and defense industries | Some people who drink water containing beryllium well in excess of the MCL over many years could develop intestinal lesions. |
| Cadmium (ppb) | 0.005 | 1000 | 5 | 5 | Corrosion of galvanized pipes; Erosion of natural deposits; Discharge from metal refineries; Runoff from waste batteries and paints | Some people who drink water containing cadmium in excess of the MCL over many years could experience kidney damage. |
| Chromium (ppb) | 0.1 | 1000 | 100 | 100 | Discharge from steel and pulp mills; Erosion of natural deposits | Some people who use water containing chromium well in excess of the MCL over many years could experience allergic dermatitis. |
| Copper (ppm) | AL=1.3 | AL=1.3 | 1.3 | Corrosion of household plumbing systems; Erosion of natural deposits; Leaching from wood preservatives | Copper is an essential nutrient, but some people who drink water containing copper in excess of the action level over a relatively short amount of time could experience gastrointestinal distress. Some people who drink water containing copper in excess of the action level over many years could suffer liver or kidney damage. People with Wilson's Disease should consult their personal doctor. | |
| Cyanide (ppb) | 0.2 | 1000 | 200 | 200 | Discharge from steel/metal factories Discharge from plastic and fertilizer factories | Some people who drink water containing cyanide well in excess of the MCL over many years could experience nerve damage or problems with their thyroid. |
| Fluoride (ppm) | 4 | 4 | 4 | Erosion of natural deposits; Water additive which promotes strong teeth; Discharge from fertilizer and aluminum factories | Some people who drink water containing fluoride in excess of the MCL over many years could get bone disease, including pain and tenderness of the bones. Fluoride in drinking water at half the MCL or more may cause mottling of children's teeth, usually in children less than nine (9) years old. Mottling, also known as dental fluorosis, may include brown staining and/or pitting of the teeth, and occurs only in developing teeth before they erupt from the gums. | |
| Lead (ppb) | AL=0.015 | 1000 | AL=15 | 0 | Corrosion of household plumbing systems; Erosion of natural deposits | Exposure to lead in drinking water can cause serious health effects in all age groups. Infants and children can have decreases in IQ and attention span. Lead exposure can lead to new learning and behavior problems or exacerbate existing learning and behavior problems. The children of women who are exposed to lead before or during pregnancy can have increased risk of these adverse health effects. Adults can have increased risks of heart disease, high blood pressure, kidney or nervous system problems |
| Mercury [inorganic] (ppb) | 0.002 | 1000 | 2 | 2 | Erosion of natural deposits; Discharge from refineries and factories; Runoff from landfills; Runoff from cropland | Some people who drink water containing inorganic mercury well in excess of the MCL over many years could experience kidney damage. |
| Nitrate (ppm) | 10 | 10 | 10 | Runoff from fertilizer use; Leaching from septic tanks, sewage; Erosion of natural deposits | Infants below the age of six (6) months who drink water containing nitrate in excess of the MCL could become seriously ill and, if untreated, may die. Symptoms include shortness of breath and blue baby syndrome. | |
| Nitrite (ppm) | 1 | 1 | 1 | Runoff from fertilizer use; Leaching from septic tanks, sewage; Erosion of natural deposits | Infants below the age of six (6) months who drink water containing nitrite in excess of the MCL could become seriously ill and, if untreated, may die. Symptoms include shortness of breath and blue baby syndrome. | |
| Selenium (ppb) | 0.05 | 1000 | 50 | 50 | Discharge from petroleum and metal refineries; Erosion of natural deposits; Discharge from mines | Selenium is an essential nutrient. However, some people who drink water containing selenium in excess of the MCL over many years could experience hair or fingernail losses, numbness in fingers or toes, or problems with their circulation. |
| Thallium (ppb) | 0.002 | 1000 | 2 | 0.5 | Leaching from ore-processing sites; Discharge from electronics, glass, and drug factories | Some people who drink water containing thallium in excess of the MCL over many years could experience hair loss, changes in their blood, or problems with their kidneys, intestines, or liver. |
| Synthetic organic contaminants including pesticides and herbicides: | ||||||
| 2,4-D (ppb) | 0.07 | 1000 | 70 | 70 | Runoff from herbicide used on row crops | Some people who drink water containing the weed killer 2, 4-D well in excess of the MCL over many years could experience problems with their kidneys, liver, or adrenal glands. |
| 2,4,5-TP [Silvex] (ppb) | 0.05 | 1000 | 50 | 50 | Residue of banned herbicide | Some people who drink water containing silvex in excess of the MCL over many years could experience liver problems. |
| Acrylamide | TT | TT | 0 | Added to water during sewage/wastewater treatment | Some people who drink water containing high levels of acrylamide over a long period of time could have problems with their nervous system or blood, and may have an increased risk of getting cancer. | |
| Alachlor (ppb) | 0.002 | 1000 | 2 | 0 | Runoff from herbicide used on row crops | Some people who drink water containing alachlor in excess of the MCL over many years could have problems with their eyes, liver, kidneys, or spleen, or experience anemia, and may have an increased risk of getting cancer. |
| Atrazine (ppb) | 0.003 | 1000 | 3 | 3 | Runoff from herbicide used on row crops | Some people who drink water containing atrazine well in excess of the MCL over many years could experience problems with their cardiovascular system or reproductive difficulties. |
| Benzo(a)pyrene [PAH] (nanograms/l) | 0.0002 | 1,000,000 | 200 | 0 | Leaching from linings of water storage tanks and distribution lines | Some people who drink water containing benzo(a)pyrene in excess of the MCL over many years may experience reproductive difficulties and may have an increased risk of getting cancer. |
| Carbofuran (ppb) | 0.04 | 1000 | 40 | 40 | Leaching of soil fumigant used on rice and alfalfa | Some people who drink water containing carbofuran in excess of the MCL over many years could experience problems with their blood, or nervous or reproductive systems. |
| Chlordane (ppb) | 0.002 | 1000 | 2 | 0 | Residue of banned termiticide | Some people who drink water containing chlordane in excess of the MCL over many years could experience problems with their liver or nervous system, and may have an increased risk of getting cancer. |
| Dalapon (ppb) | 0.2 | 1000 | 200 | 200 | Runoff from herbicide used on rights of way | Some people who drink water containing dalapon well in excess of the MCL over many years could experience minor kidney changes. |
| Di(2-ethylhexyl) adipate (ppb) | 0.4 | 1000 | 400 | 400 | Discharge from chemical factories | Some people who drink water containing di (2-ethylhexyl) adipate well in excess of the MCL over many years could experience general toxic effects or reproductive difficulties. |
| Di(2-ethylhexyl) phthalate (ppb). | 0.006 | 1000 | 6 | 0 | Discharge from rubber and chemical factories | Some people who drink water containing di (2-ethylhexyl) phthalate in excess of the MCL over many years may have problems with their liver, or experience reproductive difficulties, and may have an increased risk of getting cancer. |
| Dibromochloropropane (ppt) | 0.0002 | 1,000,000 | 200 | 0 | Runoff/leaching from soil fumigant used on soybeans, cotton, pineapples, and orchards | Some people who drink water containing DBCP in excess of the MCL over many years could experience reproductive problems and may have an increased risk of getting cancer. |
| Dinoseb (ppb) | 0.007 | 1000 | 7 | 7 | Runoff from herbicide used on soybeans and vegetables | Some people who drink water containing dinoseb well in excess of the MCL over many years could experience reproductive difficulties. |
| Diquat (ppb) | 0.02 | 1000 | 20 | 20 | Runoff from herbicide use | Some people who drink water containing diquat in excess of the MCL over many years could get cataracts. |
| Dioxin [2,3,7,8-TCDD] (ppq). | 0.00000003 | 1,000,000, 000 | 30 | 0 | Emissions from waste incineration and other combustion; Discharge from chemical factories | Some people who drink water containing dioxin in excess of the MCL over many years could experience reproductive difficulties and may have an increased risk of getting cancer. |
| Endothall (ppb) | 0.1 | 1000 | 100 | 100 | Runoff from herbicide use | Some people who drink water containing endothall in excess of the MCL over many years could experience problems with their stomach or intestines. |
| Endrin (ppb) | 0.002 | 1000 | 2 | 2 | Residue of banned insecticide | Some people who drink water containing endrin in excess of the MCL over many years could experience liver problems. |
| Epichlorohydrin | TT | TT | 0 | Discharge from industrial chemical factories; An impurity of some water treatment chemicals | Some people who drink water containing high levels of epichlorohydrin over a long period of time could experience stomach problems, and may have an increased risk of getting cancer. | |
| Ethylene dibromide (ppt) | 0.00005 | 1,000,000 | 50 | 0 | Discharge from petroleum refineries | Some people who drink water containing ethylene dibromide in excess of the MCL over many years could experience problems with their liver, stomach, reproductive system, or kidneys, and may have an increased risk of getting cancer. |
| Glyphosate (ppb) | 0.7 | 1000 | 700 | 700 | Runoff from herbicide use | Some people who drink water containing glyphosate in excess of the MCL over many years could experience problems with their kidneys or reproductive difficulties. |
| Heptachlor (ppt) | 0.0004 | 1,000,000 | 400 | 0 | Residue of banned pesticide | Some people who drink water containing heptachlor in excess of the MCL over many years could experience liver damage and may have an increased risk of getting cancer. |
| Heptachlor epoxide (ppt) | 0.0002 | 1,000,000 | 200 | 0 | Breakdown of heptachlor | Some people who drink water containing heptachlor epoxide in excess of the MCL over many years could experience liver damage, and may have an increased risk of getting cancer. |
| Hexachlorobenzene (ppb) | 0.001 | 1000 | 1 | 0 | Discharge from metal refineries and agricultural chemical factories | Some people who drink water containing hexachlorobenzene in excess of the MCL over many years could experience problems with their liver or kidneys, or adverse reproductive effects, and may have an increased risk of getting cancer. |
| Hexachloro-cyclopentadiene (ppb) | 0.05 | 1000 | 50 | 50 | Discharge from chemical factories | Some people who drink water containing hexachlorocyclopentadiene well in excess of the MCL over many years could experience problems with their kidneys or stomach. |
| Lindane (ppt) | 0.0002 | 1,000,000 | 200 | 200 | Runoff/ leaching from insecticide used on cattle, lumber, gardens | Some people who drink water containing lindane in excess of the MCL over many years could experience problems with their kidneys or liver. |
| Methoxychlor (ppb) | 0.04 | 1000 | 40 | 40 | Runoff/ leaching from insecticide used on fruits, vegetables, alfalfa, livestock | Some people who drink water containing methoxychlor in excess of the MCL over many years could experience reproductive difficulties. |
| Oxamyl [Vydate] (ppb) | 0.2 | 1000 | 200 | 200 | Runoff/ leaching from insecticide used on apples, potatoes and tomatoes | Some people who drink water containing oxamyl in excess of the MCL over many years could experience slight nervous system effects. |
| PCBs [Polychlorinated biphenyls] (ppt) | 0.0005 | 1,000,000 | 500 | 0 | Runoff from landfills; Discharge of waste chemicals | Some people who drink water containing PCBs in excess of the MCL over many years could experience changes in their skin, problems with their thymus gland, immune deficiencies, or reproductive or nervous system difficulties, and may have an increased risk of getting cancer. |
| Pentachlorophenol (ppb) | 0.001 | 1000 | 1 | 0 | Discharge from wood preserving factories | Some people who drink water containing pentachlorophenol in excess of the MCL over many years could experience problems with their liver or kidneys, and may have an increased risk of getting cancer. |
| Picloram (ppb) | 0.5 | 1000 | 500 | 500 | Herbicide runoff | Some people who drink water containing picloram in excess of the MCL over many years could experience problems with their liver. |
| Simazine (ppb) | 0.004 | 1000 | 4 | 4 | Herbicide runoff | Some people who drink water containing simazine in excess of the MCL over many years could experience problems with their blood |
| Total PFAS [Per- and Polyfluoroalkyl Substances] (ppt) | 0.000020 | 1,000,000 | 20 | Discharges and/or emissions from industrial, commercial, and manufacturing sources associated with the production or use of PFAS. The application or accidental release of fire-fighting foams (i.e. aqueous film forming foam, AFFF). Wastewater treatment discharges/residuals and landfill leachate as a result of the use and disposal of products containing these compounds. | Studies have shown certain PFAS can cause negative health effects, including higher cholesterol levels, lower infant birth weights, weakened immune response, and an increased risk of some cancers, including prostate, kidney, and testicular cancers. | |
| Toxaphene (ppb) | 0.003 | 1000 | 3 | 0 | Runoff/leaching from insecticide used on cotton and cattle | Some people who drink water containing toxaphene in excess of the MCL over many years could have problems with their kidneys, liver, or thyroid, and may have an increased risk of getting cancer. |
| Volatile organic contaminants: | ||||||
| Benzene (ppb) | 0.005 | 1000 | 5 | 0 | Discharge from factories; Leaching from gas storage tanks and landfills | Some people who drink water containing benzene in excess of the MCL over many years could experience anemia or a decrease in blood platelets, and may have an increased risk of getting cancer. |
| Bromate (ppb) | 0.010 | 1000 | 10 | 0 | By-product of drinking water chlorination | Some people who drink water containing bromate in excess of the MCL over many years may have an increased risk of getting cancer. |
| Carbon tetrachloride (ppb) | 0.005 | 1000 | 5 | 0 | Discharge from chemical plants and other industrial activities | Some people who drink water containing carbon tetrachloride in excess of the MCL over many years could experience problems with their liver and may have an increased risk of getting cancer. |
| Chloramines (ppm) | MRDL = 4 | MRDL = 4 | MRDLG = 4 | Water additive used to control microbes | Some people who use water containing chloramines well in excess of the MRDL could experience irritating effects to their eyes and nose. Some who drink water containing chloramines well in excess of the MRDL could experience stomach discomfort or anemia. | |
| Chlorine (ppm) | MRDL = 4 | MRDL = 4 | MRDLG = 4 | Water additive used to control microbes | Some people who use water containing chlorine well in excess of the MRDL could experience irritating effects to their eyes and nose. Some people who drink water containing chlorine well in excess of the MRDL could experience stomach discomfort. | |
| Chlorite (ppm) | 1 | 1 | 0.8 | By-product of drinking water chlorination | Some infants and young children who drink water containing chlorite in excess of the MCL could experience nervous system effects. Similar effects may occur in fetuses of pregnant women who drink water containing chlorite in excess of the MCL. Some people may experience anemia. | |
| Chlorine dioxide (ppb) | MRDL = .8 | 1000 | MRDL = 800 | MRDLG = 800 | Water additive used to control microbes | Some infants and young children who drink water containing chlorine dioxide in excess of the MRDL could experience nervous system effects. Similar effects may occur in fetuses of pregnant women who drink water containing chlorine dioxide in excess of the MRDL. Some people may experience anemia. |
| Chlorobenzene (ppb) | 0.1 | 1000 | 100 | 100 | Discharge from chemical and agricultural chemical factories | Some people who drink water containing chlorobenzene in excess of the MCL over many years could experience problems with their liver or kidneys. |
| o-Dichlorobenzene (ppb) | 0.6 | 1000 | 600 | 600 | Discharge from industrial chemical factories | Some people who drink water containing o- dichlorobenzene well in excess of the MCL over many years could experience problems with their liver, kidneys, or circulatory systems. |
| p-Dichlorobenzene (ppb) | 0.075 | 1000 | 75 | 75 | Discharge from industrial chemical factories | Some people who drink water containing p- dichlorobenzene in excess of the MCL over many years could experience anemia, damage to their liver, kidneys, or spleen, or changes in their blood. |
| 1,2-Dichloroethane (ppb) | 0.005 | 1000 | 5 | 0 | Discharge from industrial chemical factories | Some people who drink water containing 1,2- dichloroethane in excess of the MCL over many years may have an increased risk of getting cancer. |
| 1,1-Dichloroethylene (ppb) | 0.007 | 1000 | 7 | 7 | Discharge from industrial chemical factories | Some people who drink water containing 1,1- dichloroethylene in excess of the MCL over many years could experience problems with their liver. |
| cis-1,2-Dichloroethylene (ppb) | 0.07 | 1000 | 70 | 70 | Discharge from industrial chemical factories | Some people who drink water containing cis-1,2-dichloroethylene in excess of the MCL over many years could experience problems with their liver. |
| trans-1,2-Dichloroethylene (ppb) | 0.1 | 1000 | 100 | 100 | Discharge from industrial chemical factories | Some people who drink water containing trans-1,2-dichloroethylene well in excess of the MCL over many years could experience problems with their liver. |
| Dichloromethane (ppb) | 0.005 | 1000 | 5 | 0 | Discharge from pharmaceutical and chemical factories | Some people who drink water containing dichloromethane in excess of the MCL over many years could have liver problems and may have an increased risk of getting cancer. |
| 1,2-Dichloropropane (ppb) | 0.005 | 1000 | 5 | 0 | Discharge from industrial chemical factories | Some people who drink water containing 1,2-dichloropropane in excess of the MCL over many years may have an increased risk of getting cancer. |
| Ethylbenzene (ppb) | 0.7 | 1000 | 700 | 700 | Discharge from petroleum refineries | Some people who drink water containing ethylbenzene well in excess of the MCL over many years could experience problems with their liver or kidneys. |
| Haloacetic Acids (HAA) (ppb) | 0.060 | 1000 | 60 | N/A | By-product of drinking water disinfection | Some people who drink water containing haloacetic acids in excess of the MCL over many years may have an increased risk of getting cancer. |
| Styrene (ppb) | 0.1 | 1000 | 100 | 100 | Discharge from rubber and plastic factories; Leaching from landfills | Some people who drink water containing styrene well in excess of the MCL over many years could have problems with their liver, kidneys, or circulatory system. |
| Tetrachloroethylene (ppb) | 0.005 | 1000 | 5 | 0 | Discharge from factories and dry cleaners | Some people who drink water containing tetrachloroethylene in excess of the MCL over many years could have problems with their liver, and may have an increased risk of getting cancer. |
| 1,2,4-Trichlorobenzene (ppb) | 0.07 | 1000 | 70 | 70 | Discharge from textile-finishing factories | Some people who drink water containing 1,2,4-trichlorobenzene well in excess of the MCL over many years could experience changes in their adrenal glands. |
| 1,1,1-Trichloroethane (ppb) | 0.2 | 1000 | 200 | 200 | Discharge from metal degreasing sites and other factories | Some people who drink water containing 1,1,1-trichloroethane in excess of the MCL over many years could experience problems with their liver, nervous system, or circulatory system. |
| 1,1,2-Trichloroethane (ppb) | 0.005 | 1000 | 5 | 3 | Discharge from industrial chemical factories | Some people who drink water containing 1,1,2-trichloroethane well in excess of the MCL over many years could have problems with their liver, kidneys, or immune systems. |
| Trichloroethylene (ppb) | 0.005 | 1000 | 5 | 0 | Discharge from metal degreasing sites and other factories | Some people who drink water containing trichloroethylene in excess of the MCL over many years could experience problems with their liver and may have an increased risk of getting cancer. |
| TTHMs [Total trihalomethanes] (ppb) | 0.10/0.080 | 1000 | 100/80 | N/A | By-product of drinking water chlorination | Some people who drink water containing trihalomethanes in excess of the MCL over many years may experience problems with their liver, kidneys, or central nervous systems, and may have an increased risk of getting cancer. |
| Toluene (ppm) | 1 | 1 | 1 | Discharge from petroleum factories | Some people who drink water containing toluene well in excess of the MCL over many years could have problems with their nervous system, kidneys, or liver. | |
| Vinyl Chloride (ppb) | 0.002 | 1000 | 2 | 0 | Leaching from PVC piping; Discharge from plastics factories | Some people who drink water containing vinyl chloride in excess of the MCL over many years may have an increased risk of getting cancer. |
| Xylenes (ppm) | 10 | 10 | 10 | Discharge from petroleum factories; Discharge from chemical factories | Some people who drink water containing xylenes in excess of the MCL over many years could experience damage to their nervous system. | |
A. Key:
| Detection Limits for Inorganic Contaminants | |||
| Contaminant | MCL (mg/l) | Methodology | Detection limit (mg/l) |
| Antimony | 0.006 | Atomic Absorption; Furnace | 0.003 |
| Atomic Absorption; Platform | 0.00085 | ||
| ICP-Mass Spectrometry | 0.0004 | ||
| Hydride-Atomic Absorption | 0.001 | ||
| Arsenic | 0.0106 | Atomic Absorption; Furnace | 0.001 |
| Atomic Absorption; Platform-Stabilized Temperature | 0.00057 | ||
| Atomic Absorption; Gaseous Hydride | 0.001 | ||
| ICP-Mass Spectrometry | 0.00148 | ||
| Asbestos | 7 MFL1 | Transmission Electron Microscopy | 0.01 MFL |
| Barium | 2 | Atomic Absorption; furnace technique | 0.002 |
| Atomic Absorption; direct aspiration | 0.1 | ||
| Inductively Coupled Plasma | 0.002 (0.001) | ||
| Beryllium | 0.004 | Atomic Absorption; Furnace | 0.0002 |
| Atomic Absorption; Platform | 0.000025 | ||
| Inductively Coupled Plasma2 | 0.0003 | ||
| ICP-Mass Spectrometry | 0.0003 | ||
| Cadmium | 0.005 | Atomic Absorption; furnace technique | 0.0001 |
| Inductively Coupled Plasma | 0.001 | ||
| Chromium | 0.1 | Atomic Absorption; furnace technique | 0.001 |
| Inductively Coupled Plasma | 0.007 (0.001) | ||
| Cyanide | 0.2 | Distillation, Spectrophotometric3 | 0.02 |
| Distillation, Automated, Spectrophotometric3 | 0.005 | ||
| Distillation, Amenable, Spectrophotometric4 | 0.02 | ||
| Distillation, Selective Electrode3, 4 | 0.05 | ||
| UV, Distillation, Spectrophotometric9 | 0.0005 | ||
| Micro Distillation, Flow Injection, Spectrophotometric3 | 0.0006 | ||
| Ligand Exchange with Amperometry4 | 0.0005 | ||
| Fluoride | 4.0 (Primary Std.) | Ion Chromatography | 1.0 |
| 2.0 (Secondary Std.) | Manual Distillation, Color SPADNSManual ElectrodeAutomated ElectrodeAutomated AlizarinCapillary Ion Electrophoresis | 1.01.01.01.01.0 | |
| Mercury | 0.002 | Manual Cold Vapor Technique | 0.002 |
| Automated Cold Vapor Technique | 0.002 | ||
| Nickel | None | Atomic Absorption; Furnace | 0.001 |
| Atomic Absorption; Platform | 0.00065 | ||
| Inductively Coupled Plasma2 | 0.005 | ||
| ICP-Mass Spectrometry | 0.0005 | ||
| Nitrate | 10 (as N) | Manual Cadmium Reduction | 0.01 |
| Automated Hydrazine Reduction | 0.01 | ||
| Automated Cadmium Reduction | 0.05 | ||
| Ion Selective Electrode | 1 | ||
| Nitrate | 10 (as N) | Ion Chromatography | 0.01 |
| Capillary Ion Electrophoresis | 0.076 | ||
| Nitrite | 1 (as N) | Spectrophotometric | 0.01 |
| Automated Cadmium Reduction | 0.05 | ||
| Manual Cadmium Reduction | 0.01 | ||
| Ion Chromatography | 0.004 | ||
| Capillary Ion Electrophoresis | 0.103 | ||
| Selenium | 0.05 | Atomic Absorption; furnace | 0.002 |
| Atomic Absorption; gaseous hydride | 0.002 | ||
| Thallium | 0.002 | Atomic Absorption; Furnace | 0.001 |
| Atomic Absorption; Platform | 0.00075 | ||
| ICP-Mass Spectrometry | 0.0003 | ||
| Selenium | 0.05 | Atomic Absorption; furnace | 0.002 |
| Atomic Absorption; gaseous hydride | 0.002 | ||
| Thallium | 0.002 | Atomic Absorption; Furnace | 0.001 |
| Atomic Absorption; Platform | 0.00075 | ||
| ICP-Mass Spectrometry | 0.0003 | ||
| 1 MFL = million fibers per liter >10 µm.2 Using a 2X preconcentration step as noted in Method 200.7. Lower MDLs may be achieved when using a 4X preconcentration.3 Screening method for total cyanides.4 Measures “free” cyanides when distillation, digestion, or ligand exchange is omitted.5 Lower MDLs are reported using stabilized temperature graphite furnace atomic absorption.6 The value for arsenic is effective January 23, 2006. Unit then, the MCL is 0.05 mg/L.7 The MDL reported for EPA method 200.9 (Atomic Absorption; Platform—Stablized Temperature) was determined using a 2x concentration step during sample digestion. The MDL determined for samples analyzed using direct analyses (i.e., no sample digestion) will be higher. Using multiple depositions, EPA 200.9 is capable of obtaining MDL of 0.0001 mg/L.8 Using selective ion monitoring, EPA Method 200.8 (ICP-MS) is capable of obtaining a MDL of 0.0001 mg/L.9 Measures total cyanides when UV-digestor is used, and “free” cyanides when UV-digestor is bypassed. |
A. Revised Total Coliform Rule (RTCR)
2. Monitoring Requirement
a. Non-community PWS on quarterly monitoring remain on that schedule unless they have an event that triggers increased monitoring.
b. Groundwater non-community PWS serving 1,000 or fewer persons remain on their former TCR schedule unless or until conditions occur as described in §§ 1.16.4(A)(12) and 1.17.1(A)(6) of this Part, or unless otherwise ordered by the Director.
3. Sampling Plan
b. Seasonal PWSs
(2) The seasonal PWS sample plan is not limited to, but must consist of the following:
(BB) A State-approved start up procedure and shut down procedure specific to that PWS, with an annual attestation submitted to the Director prior to that PWS serving water to the public certifying that the startup procedures were followed. An acceptable startup procedure must include but is not limited to the following:
c. Year-Round Non-Community PWSs with Some Infrastructure Dewatering. Non-community PWS that dewater some of their infrastructure and keep only a small area pressurized during the “off season” must demonstrate completion of a state approved start-up procedure for those portions of the PWS that get dewatered and submit a sampling plan to the Director.
(2) The sample plan for year-round non-community PWSs that dewater some of their infrastructure must consist of the following:
(CC) An acceptable startup procedure must include but is not limited to the following:
4. Non-Community PWS Requirements Similar to Community PWS Requirements.
a. The following requirements for PWS found in § 1.16.4 of this Part also apply to non-community PWS:
5. Reduced Monitoring
a. A seasonal groundwater PWS serving 1,000 or fewer people can be eligible for reduced monitoring from monthly to quarterly by having an approved sample site plan meeting all the criteria as stated in § 1.17.1(A)(3) of this Part and it must also meet all of the following:
6. Increased Monitoring for Non-Community PWS
a. A groundwater Non-community PWS serving 1,000 or fewer people, including seasonal PWSs, must increase from quarterly monitoring to monthly monitoring if one of the following occurs:
7. Return to Reduced Monitoring After Being Triggered to Increased Monitoring for Non-Community PWS.
a. A groundwater non-community PWS serving 1,000 or fewer people must meet the following criteria in order to return to quarterly monitoring after being triggered to increased monitoring:
(5) The PWS must be free of sanitary defects
A. Non-transient non-community PWS shall be required to comply with the requirements of §§ 1.7 and 1.16.1 of this Part, with the following exceptions:
B. Nitrate and Nitrite. The maximum contaminant levels for nitrate, nitrite and combined nitrate and nitrite are as follows:
| Contaminant | MCL (mg/L) |
| Nitrate | 10 (as Nitrogen) |
| Nitrite | 1 (as Nitrogen) |
| Total Nitrate and Nitrite | 10 (as Nitrogen) |
D. Analytical Techniques. Nitrate analyses shall be made in accordance with the methods specified in § 1.21 of this Part.
B. The Director may require transient non-community water systems to sample for the contaminants listed in § 1.16.2(E)(1) of this Part if there is knowledge of previous use (including transport, storage, or disposal) of the contaminant or contamination within the watershed or wellhead protection area of the water system. The Director may require corrective action in the event of any exceedance of any MCLs.
A. Non-community PWS shall comply with the requirements of § 1.16.3 of this Part.
A. Non-transient, non-community PWS that serve more than 10,000 persons shall be required to monitor for unregulated contaminants in conformance with 40 C.F.R. § 141.40.
A. Non-community PWS shall comply with the requirements of § 1.16.6 of this Part.
A. Records of analyses performed by the water purveyor shall be maintained by the water purveyor. The records shall contain the following information:
B. Purpose and Goals
C. Policy. This Part promotes a policy of assuring the effective enforcement of the Act as administered by the Director and to deter noncompliance with the rules, regulations, approvals, permits, certification, license and orders adopted pursuant to the Act and of this Part:
2. Assessing administrative penalties, where appropriate, which:
D. Application
F. Preconditions for Assessment of Administrative Penalty. An administrative penalty may be assessed only for a violation or a failure to comply that, at the time it occurred, constituted noncompliance with a legal requirement:
G. Assessment of Administrative Penalty - Penalty Ceiling. No penalty shall exceed the maximum penalty allowed by the Act. The maximum administrative penalty which the Director has the authority to impose under the Act is five thousand dollars ($5,000.00) per violation per day.
2. A penalty may be assessed “per violation”, multiple violations of the same law, rule, regulation, permit approval, certification, license or order are counted as separate violations if any violation:
H. Assessment of Administrative Penalty – Calculation. The amount of the penalty will be calculated based on the factors enumerated below.
1. The penalty may be based on the gravity of the violation. That portion will be calculated according to the “DWQ Penalty Matrix” (See § 1.22 of this Part). The applicable penalty range is reached by first determining the “Type of Violation” and the “Deviation from the Standard” of the alleged violation.
a. “Type of Violation” – refers to the nature of the legal requirement allegedly violated.
b. “Deviation from the Standard” - refers to the degree to which the violation is out of compliance with the legal requirement allegedly violated. The Deviation from the Standard may be determined without consideration of the factors enunciated below in cases of strict liability. In all other cases, the Department's assessment of whether a violation is a minor, moderate or major deviation from the standard is based upon an evaluation of one (1) or more of the following factors except to the extent already considered:
2. The Economic Benefit from Non-Compliance. The penalty shall include an amount intended to offset the economic benefit of non-compliance.
a. Such an amount may include, but not be limited to:
b. The economic benefit portion may not be included in the penalty only if:
I. Assessment of Administrative Penalty – Hearing
A. MICROBIOLOGY
1. Microbiological Testing – Analytical Methodology. Reference for § 1.6 of this Part – Surface Water and Groundwater Under the Influence of Surface Water and §§ 1.16.4 and 1.17 of this Part – Distribution Samples including Storage Facilities and Groundwater Sources Regulation.
c. PWS must conduct total coliform analyses in accordance with one of the analytical methods in the following table.
| Organism | Methodology1 | Citation2 | TCR3 | SWTR3 |
| Total Coliforms:4 Enzyme Substrate Method | Chromogenic Substrate Coliform Test | SM 9223 | X | X |
| ONPG-MUG Test.5 | ||||
| Colisure Test.6 | SM 9223 | X | ||
| Colilert®, Colilert-18® | SM 9223 | X | X | |
| E*Colite® Test.7 | X | |||
| Colitag® Test.8 | X | |||
| Readycult® Coliforms 100 Presence/Absence Test.9 | X | |||
| Total Coliforms:4 Membrane Filter Method | Total Coliforms10 | EPA 1604; SM 9222 A, B, C | X | X |
| m-ColiBlue24® Test.11 | X | |||
| Chromocult® Test.12 | X | |||
| Coliscan® Test.13 | X | X | ||
| The procedures shall be done in accordance with the documents listed below‡:‡ Copies of the documents may be obtained from the sources listed below. Information regarding obtaining these documents can be obtained from the Safe Drinking Water Hotline at (800) 426-4791. Documents may be inspected at EPA's Drinking Water Docket, EPA West, 1301 Constitution Avenue, NW., EPA West, Room B102, Washington DC 20460 [Telephone: (202) 566-2426]; or at the National Archives and Records Administration (NARA).For information on the availability of this material at NARA, call (202) 741–6030, or go to: 1 The Director strongly recommends that laboratories evaluate the false-positive and negative rates for the method(s) they use for monitoring total coliforms. The Director also encourages laboratories to establish false- positive and false-negative rates within their own laboratory and sample matrix (drinking water or source water) with the intent that if the method they choose has an unacceptable false-positive or negative rate, another method can be used. The Director suggests that laboratories perform these studies on a minimum of 5% of all total coliform-positive samples, except for those methods where verification/ confirmation is already required, e.g., the M-Endo and LES Endo Membrane Filter Tests, Standard Total Coliform Fermentation Technique, and Presence-Absence Coliform Test. Methods for establishing false-positive and negative-rates may be based on lactose fermentation, the rapid test for ß-galactosidase and cytochrome oxidase, multi-test identification systems, or equivalent confirmation tests. False-positive and false-negative information is often available in published studies and/or from the manufacturer(s).2 Standard Methods for the Examination of Water and Wastewater, 18th edition (1992), 19th edition (1995), or 20th edition (1998). American Public Health Association, 1015 Fifteenth Street, NW., Washington, DC 20005.3 TCR = Total Coliform Rule; SWTR = Surface Water Treatment Rule4 The time from sample collection to initiation of analysis may not exceed 30 hours. Systems are encouraged but not required to hold samples below 10 ºC during transit.5 The ONPG-MUG Test is also known as the Autoanalysis Collect System.6 A description of the Colisure Test, Feb 28, 1994, may be obtained from IDEXX Laboratories, Inc., One IDEXX Drive, Westbrook, Maine 04092. The Colisure Test may be read after an incubation time of 24 hours.7 A description of the E*Colite®Test, “Presence/Absence for Coliforms and E. Coli in Water,” Dec 21, 1997, is available from Charm Sciences, Inc., 36 Franklin Street, Malden, MA 02148-4120.8 Colitag®product for the determination of the presence/absence of total coliforms and E. coli is described in “Colitag® Product as a Test for Detection and Identification of Coliforms and E. coli Bacteria in Drinking Water and Source Water as Required in National Primary Drinking Water Regulations,” August 2001, available from CPI International, Inc., 5580 Skylane Blvd., Santa Rosa, CA, 95403, telephone (800) 878-7654, Fax (707) 545-79019 The Readycult® Coliforms 100 Presence/Absence Test is described in the document, “Readycult®Coliforms 100 Presence/Absence Test for Detection and Identification of Coliform Bacteria and Escherichla coli in Finished Waters”, November 2000, Version 1.0, available from EM Science (an affiliate of Merck KGgA, Darmstadt Germany), 480 S. Democrat Road, Gibbstown, NJ 08027-1297. Telephone: (800) 222-034210 Method 1604: Total Coliforms and Escherichia coli in Water by Memberane Filtration Using a Simultaneous Detection Technique (MU Medium) (September 1992). MI agar also may be used. Preparation and use of MI agar is set forth in the article, “New medium for the simultaneous detection of total coliform and Escherichia coli in water” by Brenner, K.P., et. al., 1993, Appl. Environ. Microbiol. 59:3534–3544. Also available from the Office of Water Resource Center (RC–4100T), 1200 Pennsylvania Avenue, NW., Washington, DC 20460, EPA/600/J–99/225. Verification of colonies is not required.11 A description of the m-ColiBlue24® Test, Aug 17, 1999, is available from the Hach Company, 100 Dayton Avenue, Ames, IA 50010.12 Membrane Filter Technique using Chromocult® Coliform Agar is described in the document, “Chromocult® Coliform Agar Presence/Absence Membrane Filter Test Method for Detection and Identification of Coliform Bacteria and Escherichla coli in Finished Waters”, November 2000, Version 1.0, available from EM Science (an affiliate of Merck KGgA, Darmstadt Germany), 480 S. Democrat Road, Gibbstown, NJ 08027-1297. Telephone:(800) 222-034213 A description of the Coliscan® test, August 10, 2000, can be obtained from Micrology Laboratories, LLC P.O.Box 340, Goshen, IN 46527-0340 |
d. PWS must conduct analysis of Escherichia coli in accordance with one of the following analytical methods:
2. Invalidation of Samples
b. The Director will invalidate a total coliform-positive sample and document same in writing only if:
d. A laboratory must invalidate a total coliform sample, unless total coliforms are detected, if
3. Analytical Methods for Source Water Monitoring
| Fecal Indicator1 | Methodology | Method Citation |
| E. coli | Colilert3 | 9223B2 |
| Colisure | 9223B2 | |
| Membrane Filter Method with MI Agar | EPA Method 16044 | |
| m-ColiBlue24 Test5 | ||
| E*Colite Test6 | ||
| EC–MUG7 | 9221F2 | |
| NA–MUG7 | 9222G2 | |
| Enterococci | Multiple-Tube Technique | 9230B2 |
| Membrane Filter Technique | 9230C2 | |
| Membrane Filter Technique | EPA Method 16008 | |
| Enterolert9 | ||
| Coliphage | Two-Step Enrichment Presence-Absence | EPA Method 160110 |
| Procedure | ||
| Single Agar Layer Procedure | EPA Method 160211 | |
| 1 The time from sample collection to initiation of analysis may not exceed 30 hours. The ground water system is encouraged but is not required to hold samples below 10 °C during transit.2 Methods are described in Standard Methods for the Examination of Water and Wastewater 20th edition (1998) and copies may be obtained from the American Public Health Association, 1015 Fifteenth Street, NW., Washington, DC 20005-2605.3 Medium is available through IDEXX Laboratories, Inc., One IDEXX Drive, Westbrook, Maine 04092.4 EPA Method 1604: Total Coliforms and Escherichia coli in Water by Membrane Filtration Using a Simultaneous Detection Technique (MI Medium); September 2002, EPA 821-R-02-024. Method is available at http://www.epa.gov/nerlcwww/1604sp02.pdf or from EPA's Water Resource Center (RC–4100T), 1200 Pennsylvania Avenue, NW., Washington, DC 20460.5 A description of the m-ColiBlue24 Test, “Total Coliforms and E. coli Membrane Filtration Method with m- ColiBlue24® Broth,” Method No. 10029 Revision 2, August 17, 1999, is available from Hach Company, 100 Dayton Ave., Ames, IA 50010 or from EPA's Water Resource Center (RC-4100T), 1200 Pennsylvania Avenue, NW., Washington, DC 20460.6 A description of the E*Colite Test, “Charm E*Colite Presence/Absence Test for Detection and Identification of Coliform Bacteria and Escherichia coli in Drinking Water, January 9, 1998, is available from Charm Sciences, Inc., 659 Andover St., Lawrence, MA 01843–1032 or from EPA's Water Resource Center (RC–4100T), 1200 Pennsylvania Avenue, NW., Washington, DC 20460.7 EC-MUG (Method 9221F) or NA-MUG (Method 9222G) can be used for E. coli testing step as described in Appendix I – Section 1 A.(6) after use of Standard Methods 9221 B, 9221 D, 9222 B, or 9222 C.8 EPA Method 1600: Enterococci in Water by Membrane Filtration Using membrane-Enterococcus Indoxyl-ß-D- Glucoside Agar (mEI) EPA 821-R-02-022 (September 2002) is an approved variation of Standard Method 9230C. The method is available at http://www.epa.gov/nerlcwww/1600sp02.pdf or from EPA's Water Resource Center (RC-4100T), 1200 Pennsylvania Avenue, NW., Washington, DC 20460. The holding time and temperature for ground water samples are specified in footnote 1 above, rather than as specified in Section 8 of EPA Method 1600.9 Medium is available through IDEXX Laboratories, Inc., One IDEXX Drive, Westbrook, Maine 04092. Preparation and use of the medium is set forth in the article “Evaluation of Enterolert for Enumeration of Enterococci in Recreational Waters,” by Budnick, G.E., Howard, R.T., and Mayo, D.R., 1996, Applied and Environmental Microbiology, 62:3881-388410 EPA Method 1601: Male-specific (F+) and Somatic Coliphage in Water by Two-step Enrichment Procedure; April 2001, EPA 821-R-01-030. Method is available at http://www.epa.gov/nerlcwww/1601ap01.pdf or from EPA's Water Resource Center (RC-4100T), 1200 Pennsylvania Avenue, NW., Washington, DC 20460.11 EPA Method 1602: Male-specific (F+) and Somatic Coliphage in Water by Single Agar Layer (SAL) Procedure; April 2001, EPA 821-R-01-029. Method is available at http://www.epa.gov/nerlcwww/1602ap01.pdf or from EPA's Water Resource Center (RC-4100T), 1200 Pennsylvania Avenue, NW., Washington, DC 20460. |
4. Cyanobacteria Identification and Counting (Screening) and Algal Toxin Monitoring
B. CHEMISTRY
1. Inorganic Chemistry References for §§ 1.6, 1.7, 1.16.1 and 1.17.2 of this Part.
a. Surface Water Treatment Rule and Ground Water Rule Monitoring
b. Residual Disinfectant Concentration
| Residual | Methodology | SM1 | SM Online2 | Other |
| Free Chlorine | Amperometric Titration | 4500-Cl D | 4500-Cl D | D1253-863 |
| DPD Ferrous Titrimetric | 4500-Cl F | 4500-Cl F | ||
| DPD Colorimetric | 4500-Cl G | 4500-Cl G | ||
| Syringaldazine (FACTS) | 4500-Cl H | 4500-Cl H | ||
| On-line Chlorine Analyzer | EPA 334.05 | |||
| Total Chlorine | Amperometric Titration | 4500-Cl D | 4500-Cl D | D1253-863 |
| Amperometric Titration (low level measurement) | 4500-Cl E | 4500-Cl E | ||
| DPD Ferrous Titrimetric | 4500-Cl F | 4500-Cl F | ||
| DPD Colorimetric | 4500-Cl G | 4500-Cl G | ||
| Iodometric Electrode | 4500-Cl I | 4500-Cl I | ||
| On-line Chlorine Analyzer | EPA 334.05 | |||
| Combined Chlorine (Chloramines) | Amperometric Titration | 4500-Cl D | ||
| Chlorine Dioxide | Amperometric Titration | 4500-ClO2 C | 4500-ClO2 C | |
| DPD Method | 4500-ClO2 D | |||
| Amperometric Titration | 4500-ClO2 E | 4500-ClO2 E | ||
| Ozone | Indigo Method | 4500-O3 B | 4500-O3 B | |
| 1 All the listed methods are contained in the 18th, 19th, and 20th editions of Standard Methods for the Examination of Water and Wastewater, 1992, 1995, and 1998; the cited methods published in any of these three editions may be used. | ||||
| 2 Standard Methods Online are available at http://www.standardmethods.org. The year in which each method was approved by the Standard Methods Committee is designated by the last two digits in the method number. The methods listed are the only online versions that may be used. | ||||
| 3 Annual Book of ASTM Standards, Vol. 11.01, 2004; ASTM International; any year containing the cited version of the method may be used. Copies of this method may be obtained from ASTM International, 100 Barr Harbor Drive, P.O. Box C700 West Conshohocken, PA 19428-2959. | ||||
| 4 EPA Method 327.0, Revision 1.1, “Determination of Chlorine Dioxide and Chlorite Ion in Drinking Water Using Lissamine Green B and Horseradish Peroxidase with Detection by Visible Spectrophotometry,” USEPA, May 2005, EPA 815-R-05-008. Available online at . | ||||
| 5 EPA Method 334.0. “Determination of Residual Chlorine in Drinking Water Using an On-line Chlorine Analyzer.” August 2009. EPA 815-B-09-013. Available at . |
c. Turbidity:
| Parameter | Methodology | Citation1 |
| Turbidity2 | Nephelometric Method | 2130B |
| Nephelometric Method | 180.13 | |
| Great Lakes Instruments | Method 24 | |
| Hach FilterTrak | 101335 |
d. Regulated Inorganic Chemical Monitoring
(1) Methodology
(AA) PWSs conducting analyses of inorganic chemicals as required in §§ 1.7, 1.16.0 and 1.17.0 of this Part, shall conduct these analyses in accordance with one of the following analytical methods or their equivalent as determined by EPA. Criteria for analyzing arsenic, barium, beryllium, cadmium, chromium, copper, lead, nickel, selenium, sodium and thallium with digestion or directly without digestion, and other analytical test procedures are contained in Technical Notes on Drinking Water Methods, EPA-600\R-94-173, October 1994. This document also contains approved analytical test methods which remain available for compliance monitoring until July 1, 1996. These methods will not be available for use after July 1, 1996. This document is available from the National Technical Information Service, NTIS PB95-104766, U.S. Department of Commerce, 5285 Port Royal Road, Springfield, Virginia 22161. The toll-free number is 800-553- 6847.
| Contaminant | Methodology1 | EPA | ASTM2 | Standard methods3 (18th, 19th, Ed.) | Standard methods3 (20th Ed.) | Standard methods online4 | Other |
| 1. Alkalinity | Titrimetric | D1067-92, 02 B | 2320 B | 2320 B | 2320 B-97 | ||
| Electrometric titration | I-1030-855 | ||||||
| 2. Antimony | Inductively Coupled Plasma (ICP)-Mass Spectrometry | 200.86 | |||||
| Hydride-Atomic Absorption | D3697-92, 02. | ||||||
| Atomic Absorption; Platform | 200.96 | ||||||
| Atomic Absorption; Furnace | 3113 B | 3113 B-99 | |||||
| 3. Arsenic7 | Inductively Coupled Plasma8 | 200.76 | 3120 B | 3120 B | 3120 B-99 | ||
| ICP-Mass Spectrometry | 200.86 | ||||||
| Atomic Absorption; Platform | 200.96 | ||||||
| Atomic Absorption; Furnace | D2972-97, 03 C | 3113 B | 3113 B-99 | ||||
| Hydride Atomic Absorption | D2972-97, 03 B | 3114 B | 3114 B-97 | ||||
| 4. Asbestos | Transmission Electron Microscopy | 100.19 | |||||
| Transmission Electron Microscopy | 100.210 | ||||||
| 5. Barium | Inductively Coupled Plasma | 200.76 | 3120 B | 3120 B | 3120 B-99 | ||
| ICP-Mass Spectrometry | 200.86 | ||||||
| Atomic Absorption; Direct | 3111 D | 3111 D-99 | |||||
| Atomic Absorption; Furnace | 3113 B | 3113 B-99 | |||||
| 6. Beryllium | Inductively Coupled Plasma | 200.76 | 3120 B | 3120 B | 3120 B-99 | ||
| ICP-Mass Spectrometry | 200.86 | ||||||
| Atomic Absorption; Platform | 200.96 | ||||||
| Atomic Absorption; Furnace | D3645-97, 03 B | 3113 B | 3113 B-99 | ||||
| 7. Cadmium | Inductively Coupled Plasma | 200.76 | |||||
| ICP-Mass Spectrometry | 200.86 | ||||||
| Atomic Absorption; Platform | 200.96 | ||||||
| Atomic Absorption; Furnace | 3113 B | 3113 B-99 | |||||
| 8. Calcium | EDTA titrimetric | D511-93, 03 B | 3500-Ca D | 3500-Ca B | 3500-Ca B-97 | ||
| Atomic Absorption; Direct Aspiration. | D511-93, 03 A | 3111 B | 3111 B-99 | ||||
| Inductively Coupled Plasma | 200.76 | 3120 B | 3120 B | 3120 B-99 | |||
| Ion Chromatography | D6919-03 | ||||||
| 9. Chromium | Inductively Coupled Plasma | 200.76 | 3120 B | 3120 B | 3120 B-99 | ||
| ICP-Mass Spectrometry | 200.86 | ||||||
| Atomic Absorption; Platform | 200.96 | ||||||
| Atomic Absorption; Furnace | 3113 B | 3113 B-99 | |||||
| 10. Copper | Atomic Absorption; Furnace | D1688-95, 02 C | 3113 B | 3113 B-99 | |||
| Atomic Absorption; Direct Aspiration | D1688–95, 02 A | 3111 B | 3111 B-99 | ||||
| Inductively Coupled Plasma | 200.76 | 3120 B | 3120 B | 3120 B-99 | |||
| ICP-Mass Spectrometry | 200.86 | ||||||
| Atomic Absorption; Platform | 200.96 | ||||||
| 11. Conductivity | Conductance | D1125-95 (Reapproved 1999) A | 2510 B | 2510 B | 2510 B-97 | ||
| 12. Cyanide | Manual Distillation followed by: | D2036-98 A | 4500-CN- C | 4500-CN- C | |||
| Spectrophotometric, Amenable | D2036-98 B | 4500-CN- G | 4500-CN- G | 4500-CN- G-99 | |||
| Spectrophotometric Manual | 4500-CN- E | 4500-CN- E | 4500-CN- E-99 | I-3300-855 | |||
| Spectro-photometric Semi-automated | 335.411 | ||||||
| Selective Electrode | 4500-CN- F | 4500-CN- F | 4500-CN- F-99 | ||||
| UV, Distillation, SpectrophotometricMicro Distillation, Flow Injection, Spectro-photometric.Ligand Exchange and Amperometry14 | D6888-04 | Kelada-0112 QuikChem 10- 204-00-1-X13 OIA-1677,DW15 | |||||
| 13. Fluoride | Ion Chromatography | 300.011, 300.116 | D4327-97, 03 | 4110 B | 4110 B | 4110 B-00 | |
| Manual Distill.; Color. SPADNS | 4500-F- B, D | 4500-F- B, D | 4500-F- B, D-97 | ||||
| Manual Electrode | D1179-93, 99 B | 4500-F- C | 4500-F- C | 4500-F- C-97 | |||
| Automated Electrode | 380–75WE17 | ||||||
| Automated Alizarin | 4500-F- E | 4500-F- E | 4500-F- E-97 | 129–71W17 | |||
| Capillary Ion Electrophoresis | D6508, Rev. 218 | ||||||
| 14. Lead | Atomic Absorption; Furnace | D3559-96, 03 D | 3113 B | 3113 B-99 | |||
| ICP–Mass spectrometry | 200.86 | ||||||
| Atomic Absorption; Platform. | 200.96 | ||||||
| Differential Pulse Anodic Stripping Voltametry | Method 100119 | ||||||
| 15. Magnesium | Atomic Absorption | D511-93, 03 B | 3111 B | 3111 B-99 | |||
| ICP | 200.76 | 3120 B | 3120 B | 3120 B-99 | |||
| Complexation Titrimetric Methods | D511-93, 03 A | ||||||
| Ion Chromatography | D6919-03 | 3500-Mg E | 3500-Mg B | 3500-Mg B-97 | |||
| 16. Mercury | Manual, Cold Vapor | 245.16 | D3223-95, 02 | 3112 B | 3112 B-99 | ||
| Automated, Cold Vapor | 245.220 | ||||||
| ICP–Mass Spectrometry | 200.86 | ||||||
| 17. Nickel | Inductively Coupled Plasma | 200.76 | 3120 B | 3120 B | 3120 B-99 | ||
| ICP–Mass Spectrometry | 200.86 | ||||||
| Atomic Absorption; Platform | 200.96 | ||||||
| Atomic Absorption; Direct | 3111 B | 3111 B-99 | |||||
| Atomic Absorption; Furnace | 3113 B | 3113 B-99 | |||||
| 18. Nitrate | Ion Chromatography | 300.011300.116 | D4327–97, 03 | 4110 B | 4110 B | 4110 B-00 | B-101121 |
| Automated Cadmium Reduction | 353.211 | D3867-90 A | 4500–NO3 -F | 4500–NO3 -F | 4500–NO3 -F-00 | ||
| Ion Selective Electrode | 4500–NO3 -D | 4500–NO3 -D | 4500–NO3 -D-00 | 60122 | |||
| Manual Cadmium Reduction | D3867-90 B | 4500–NO3 -E | 4500–NO3 -E | 4500–NO3 -E-00 | |||
| Capillary Ion Electrophoresis | D6508, Rev. 218 | ||||||
| 19. Nitrite | Ion Chromatography | 300.011300.116 | D4327–97, 03 | 4110 B | 4110 B | 4110 B-00 | B-101121 |
| Automated Cadmium Reduction | 353.211 | D3867-90 A | 4500–NO3 -F | 4500–NO3 -F | 4500–NO3 -F-00 | ||
| Manual Cadmium Reduction | D3867-90 B | 4500–NO3 -E | 4500–NO3 -E | 4500–NO3 -E-00 | |||
| Spectrophotometric | 4500–NO2 -B | 4500–NO2-B | 4500–NO2 -B-00 | ||||
| Capillary Ion Electrophoresis | D6508, Rev. 218 | ||||||
| 20. Ortho-phosphate23 | Colorimetric, Automated, Ascorbic Acid | 365.111 | 4500-P F | 4500-P F | |||
| Colorimetric, ascorbic acid, single reagent | D515-88 A | 4500-P E | 4500-P E | ||||
| Colorimetric Phosphomolybdate | I-1601-855 | ||||||
| Automated-segmented flow | I-2601-905 | ||||||
| Automated Discrete | I-2598-855 | ||||||
| Ion Chromatography | 300.011300.116 | D4327-97, 03 | 4110 B | 4110 B | 4110 B-00 | ||
| Capillary Ion Electrophoresis | D6508, Rev. 218 | ||||||
| 21. pH | Electrometric | 150.1, 150.220 | D1293-95, 99 | 4500-H+ B | 4500-H+ B | 4500-H+ B-00 | |
| 22. Selenium | Hydride-Atomic Absorption | D3859-98, 03 A | 3114 B | 3114 B-97 | |||
| ICP–Mass Spectrometry | 200.86 | ||||||
| Atomic Absorption; Platform | 200.96 | ||||||
| Atomic Absorption; Furnace | D3859-98, 03 A | 3113 B | 3113 B-99 | ||||
| 23. Silica | Colorimetric, Molybdate Blue | I-1700-855 | |||||
| Automated-segmented Flow | I-2700-855 | ||||||
| Colorimetric | D859-94, 00 | ||||||
| Molybdosilicate | 4500-SiO2 D | 4500-SiO2 C | 4500-SiO2 C-97 | ||||
| Heteropoly blue | 4500-SiO2 E | 4500-SiO2 D | 4500-SiO2 D-97 | ||||
| Automated for Molybdate- reactive Silica | 4500-SiO2 F | 4500-SiO2 E | 4500-SiO2 E-97 | ||||
| Inductively Coupled Plasma | 200.76 | 3120 B | 3120 B | 3120 B-99 | |||
| 24. Sodium | Inductively Coupled Plasma | 200.76 | |||||
| Atomic Absorption; Direct Aspiration | 3111 B | 3111 B-99 | |||||
| Ion Chromatography | D6919-03 | ||||||
| 25. Temperature | Thermometric | 2550 | 2550 | 2550-00 | |||
| 26. Thallium | ICP–Mass Spectrometry | 200.86 | |||||
| The procedures shall be done in accordance with the documents listed below. The incorporation by reference of the following documents listed in footnotes 2-6, 9-13, and 15-22 was approved by the Director of the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR Part 51. Copies of the documents may be obtained from the sources listed below. Information regarding obtaining these documents can be obtained from the Safe Drinking Water Hotline at 800-426-4791. Documents may be inspected at EPA's Drinking Water Docket, EPA West, 1301 Constitution Avenue, NW., Room 3334, Washington, DC 20460 (Telephone: 202-566-2426); or at the National Archives and Records Administration (NARA). For information on the availability of this material at NARA, call 202-741-6030, or go to:.1 Because MDLs reported in EPA Methods 200.7 and 200.9 were determined using a 2x preconcentration step during sample digestion, MDLs determined when samples are analyzed by direct analysis (i.e., no sample digestion) will be higher. For direct analysis of cadmium and arsenic by Method 200.7, and arsenic by Method 3120 B, sample preconcentration using pneumatic nebulization may be required to achieve lower detection limits. Preconcentration may also be required for direct analysis of antimony, lead, and thallium by Method 200.9; antimony and lead by Method 3113 B; and lead by Method D3559-90D, unless multiple in-furnace depositions are made.2 Annual Book of ASTM Standards, 1994, 1996, 1999, or 2003, Vols. 11.01 and 11.02, ASTM International; any year containing the cited version of the method may be used. The previous versions of D1688-95A, D1688-95C (copper), D3559-95D (lead), D1293-95 (pH), D1125-91A (conductivity) and D859-94 (silica) are also approved. These previous versions D1688-90A, C; D3559-90D, D1293-84, D1125-91A and D859-88, respectively are located in the Annual Book of ASTM Standards, 1994, Vol. 11.01. Copies may be obtained from ASTM International, 100 Barr Harbor Drive, West Conshohocken, PA 19428.3 Standard Methods for the Examination of Water and Wastewater, 18th edition (1992), 19th edition (1995), or 20th edition (1998). American Public Health Association, 1015 Fifteenth Street, NW., Washington, DC 20005. The cited methods published in any of these three editions may be used, except that the versions of 3111 B, 3111 D, 3113 B and 3114 B in the 20th edition may not be used.4 Standard Methods Online are available at http://www.standardmethods.org. The year in which each method was approved by the Standard Methods Committee is designated by the last two digits in the method number. The methods listed are the only online versions that may be used.5 Method I-2601-90, Methods for Analysis by the U.S. Geological Survey National Water Quality Laboratory--Determination of Inorganic and Organic Constituents in Water and Fluvial Sediment, Open File Report 93-125, 1993; For Methods I-1030-85; I-1601-85; I-1700-85; I-2598-85; I-2700-85; and I-3300-85 See Techniques of Water Resources Investigation of the U.S. Geological Survey, Book 5, Chapter A-1, 3rd edition., 1989; Available from Information Services, U.S. Geological Survey, Federal Center, Box 25286, Denver, CO 80225-0425.6 “Methods for the Determination of Metals in Environmental Samples--Supplement I,'' EPA/600/R-94/111, May 1994. Available at NTIS, PB95-125472.7 If ultrasonic nebulization is used in the determination of arsenic by Methods 200.7, 200.8, or SM 3120 B, the arsenic must be in the pentavalent state to provide uniform signal response. For Methods 200.7 and 3120 B, both samples and standards must be diluted in the same mixed acid matrix concentration of nitric and hydrochloric acid with the addition of 100 µL of 30% hydrogen peroxide per 100 mL of solution. For direct analysis of arsenic with Method 200.8 using ultrasonic nebulization, samples and standards must contain 1 mg/L of sodium hypochlorite.8 Starting January 23, 2006, analytical methods using the ICP-AES technology may not be used because the detection limits for these methods are 0.008 mg/L or higher. This restriction means that the two ICP-AES methods (EPA Method 200.7 and SM 3120 B) approved for use for the MCL of 0.05 mg/L may not be used for compliance determinations for the revised MCL of 0.010 mg/L. However, prior to January 23, 2006, systems may have compliance samples analyzed with these less sensitive methods.9 Method 100.1, “Analytical Method For Determination of Asbestos Fibers in Water,'' EPA/600/4-83/043, EPA, September 1983. Available at NTIS, PB83-260471.10 Method 100.2, ‘‘Determination of Asbestos Structure Over 10-µm In Length In Drinking Water,’’ EPA/600/R–94/134, June 1994. Available at NTIS, PB94– 201902.11 “Methods for the Determination of Inorganic Substances in Environmental Samples,'' EPA/600/R-93/100, August 1993. Available at NTIS, PB94-120821.12 The description for the Kelada-01 Method, “Kelada Automated Test Methods for Total Cyanide, Acid Dissociable Cyanide, And Thiocyanate,'' Revision 1.2, August 2001, EPA 821-B-01-009 for cyanide is available from the National Technical Information Service (NTIS), PB 2001-108275, 5285 Port Royal Road, Springfield, VA 22161. The toll free telephone number is 800-553-6847. Note: A 450-W UV lamp may be used in this method instead of the 550-W lamp specified if it provides performance within the quality control (QC) acceptance criteria of the method in a given instrument. Similarly, modified flow cell configurations and flow conditions may be used in the method, provided that the QC acceptance criteria are met.13 The description for the QuikChem Method 10-204-00-1-X, “Digestion and distillation of total cyanide in drinking and wastewaters using MICRO DIST and determination of cyanide by flow injection analysis,'' Revision 2.1, November 30, 2000, for cyanide is available from Lachat Instruments, 6645 W. Mill Rd., Milwaukee, WI 53218. Telephone: 414-358-4200.14 Sulfide levels below those detected using lead acetate paper may produce positive method interferences. Test samples using a more sensitive sulfide method to determine if a sulfide interference is present, and treat samples accordingly.15 Method OIA-1677, DW “Available Cyanide by Flow Injection, Ligand Exchange, and Amperometry,'' January 2004. EPA-821-R-04-001, Available from ALPKEM, A Division of OI Analytical, P.O. Box 9010, College Station, TX 77842-9010.16 “Methods for the Determination of Organic and Inorganic Compounds in Drinking Water,'' Vol. 1, EPA 815-R-00-014, August 2000. Available at NTIS, PB2000- 106981.17 Industrial Method No. 129-71W, “Fluoride in Water and Wastewater,'' December 1972, and Method No. 380-75WE, “Fluoride in Water and Wastewater,''February 1976, Technicon Industrial Systems. Copies may be obtained from Bran & Luebbe, 1025 Busch Parkway, Buffalo Grove, IL 60089.18 Method D6508, Rev. 2, “Test Method for Determination of Dissolved Inorganic Anions in Aqueous Matrices Using Capillary Ion Electrophoresis and Chromate Electrolyte,'' available from Waters Corp, 34 Maple St, Milford, MA, 01757, Telephone: 508/482-2131, Fax: 508/482-3625.19 The description for Method Number 1001 for lead is available from Palintest, LTD, 21 Kenton Lands Road, P.O. Box 18395, Erlanger, KY 41018. Or from the Hach Company, P.O. Box 389, Loveland, CO 80539.20 “Methods for Chemical Analysis of Water and Wastes,'' EPA/600/4-79/020, March 1983. Available at NTIS, PB84-128677.21 Method B-1011, “Waters Test Method for Determination of Nitrite/Nitrate in Water Using Single Column Ion Chromatography,'' August 1987. Copies may be obtained from Waters Corporation, Technical Services Division, 34 Maple Street, Milford, MA 01757, Telephone: 508/482-2131, Fax: 508/482-3625.22 The procedure shall be done in accordance with the Technical Bulletin 601 “Standard Method of Test for Nitrate in Drinking Water,'' July 1994, PN221890-001, Analytical Technology, Inc. Copies may be obtained from ATI Orion, 529 Main Street, Boston, MA 02129.23 Unfiltered, no digestion or hydrolysis. |
(2) Sampling Protocol
(AA) Sample collection for antimony, arsenic, asbestos, barium, beryllium, cadmium, chromium, cyanide, fluoride, mercury, nickel, nitrate, nitrite, selenium, and thallium under this Section shall be conducted using the sample preservation containers and maximum holding time procedures specified in the table below:
| Contaminant | Preservative1 | Container2 | Time3 |
| Antimony | HNO3 | P or G | 6 months |
| Arsenic | Conc HNO3 to pH <2 | P or G | 6 months |
| Asbestos | 4° C | P or G | 48 hours4 |
| Barium | HNO3 | P or G | 6 months |
| Beryllium | HNO3 | P or G | 6 months |
| Cadmium | HNO3 | P or G | 6 months |
| Chromium | HNO3 | P or G | 6 months |
| Cyanide | 4° C, NaOH | P or G | 14 days |
| Fluoride | None | P or G | 1 month |
| Mercury | HNO3 | P or G | 28 days |
| Nickel | HNO3 | P or G | 6 months |
| Nitrate | 4° C | P or G | 48 hours5 |
| Nitrate-Nitrite6 | H2SO4 | P or G | 28 days |
| Nitrite | 4° C | P or G | 48 hours |
| Selenium | HNO3 | P or G | 6 months |
| Thallium | HNO3 | P or G | 6 months |
| 1 For cyanide determinations samples must be adjusted with sodium hydroxide to pH 12 at the time off collection. When chilling is indicated the sample must be shipped and stored at 4 °C or less. Acidification of nitrate or metals samples may be with a concentrated acid or a dilute (50% by volume) solution of the applicable concentrated acid. Acidification of samples for metals analysis is encouraged and allowed at the laboratory rather than at the time of sampling provided the shipping time and other instructions in Section 8.3 of EPA Methods 200.7 or 200.8 or 200.9 are followed.2 P = plastic, hard or soft; G = glass, hard or soft.3 In all cases samples should be analyzed as soon after collection as possible. Follow additional (if any) information on preservation, containers or holding times that is specified in method.4 Instructions for containers, preservation procedures and holding times as specified in Method 100.2 must be adhered to for all compliance analyses including those conducted with Method 100.1.5 If the sample is chlorinated, the holding time for an unacidified sample kept at 4 °C is extended to 14 days.6 Nitrate-Nitrite refers to a measurement of total nitrate. |
(3) Acceptance Criteria. Analysis under this Section shall only be conducted by laboratories that have been certified by EPA or the Director. To receive certification to conduct analyses for antimony, arsenic, asbestos, barium, beryllium, cadmium, chromium, cyanide, fluoride, mercury, nickel, nitrate, nitrite and selenium and thallium, the laboratory must:
(BB) Acceptance Limits. For each contaminant that has been included in the PE sample and for each method for which the laboratory desires certification achieves quantitative results on the analyses that are within the following acceptance limits:
| Contaminant | Acceptance Limit |
| Antimony | ±30 at =0.006 mg/1 |
| Arsenic1 | ±30 at =0.003 mg/L |
| Asbestos | 2 standard deviations based on study statistics. |
| Barium | ±15% at =0.15 mg/1 |
| Beryllium | ±15% at =0.001 mg/1 |
| Cadmium | ±20% at =0.002 mg/1 |
| Chromium | ±15% at =0.01 mg/1 |
| Cyanide | ±25% at =0.1 mg/1 |
| Fluoride | ±10% at =1 to 10 mg/1 |
| Mercury | ±30% at =0.0005 mg/1 |
| Nickel | ±15% at =0.01 mg/1 |
| Nitrate | ±10% at =0.4 mg/1 |
| Nitrite | ±15% at =0.4 mg/1 |
| Selenium | ±20% at =0.01 mg/1 |
| Thallium | ±30% at =0.002 mg/1 |
| 1 The arsenic acceptance limit criteria became effective January 23, 2006 |
(CC) For samples which include lead and copper and for each method for which the laboratory desires certification achieve quantitative results on the analyses that are within the following acceptance limits:
2. Volatile Organic Chemistry References for §§ 1.16.2, 1.17.3 and 1.17.5 of this Part.
a. Regulated Volatile Organic Chemicals (VOCs)
(1) Methodology
(AA) PWSs conducting analyses of organic chemicals as listed below and as required in §§ 1.16 and 1.17 of this Part shall conduct these analyses in accordance with one (1) of the following analytical methods or their equivalent as determined by EPA:
| Contaminant | Method1 |
| Benzene | 502.2; 524.2 |
| Carbon tetrachloride | 502.2; 524.2; 551.1 |
| Chlorobenzene | 502.2; 524.2 |
| 1,2-Dichlorobenzene | 502.2; 524.2 |
| 1,4-Dichlorobenzene | 502.2; 524.2 |
| 1,2-Dichloroethane | 502.2; 524.2 |
| Cis-Dichloroethylene | 502.2; 524.2 |
| Trans-dichloroethylene | 502.2; 524.2 |
| Dichloromethane | 502.2; 524.2 |
| 1,2-Dichloropropane | 502.2; 524.2 |
| Ethylbenzene | 502.2; 524.2 |
| Styrene | 502.2; 524.2 |
| Tetrachloroethylene | 502.2; 524.2; 551.1 |
| 1,1,1-Trichloroethane | 502.2; 524.2; 551.1 |
| Trichloroethylene | 502.2; 524.2; 551.1 |
| Toluene | 502.2; 524.2 |
| 1,2,4-Trichlorobenzene | 502.2; 524.2 |
| 1,1-Dichloroethylene | 502.2; 524.2 |
| 1,1,2-Trichloroethane | 502.2; 524.2; 551.1 |
| Vinyl chloride | 502.2; 524.2 |
| Xylenes (total) | 502.2; 524.2 |
| 1 Methods 502.2, 524.2 and 551.1 are in Methods for the Determination of Organic Compounds in Drinking Water--Supplement III, EPA/600/R-95-131, August 1995 |
b. Certification Criteria. To receive certification to conduct analyses for the contaminants listed in § 1.21 of this Part above the laboratory must:
(6) To receive certification for vinyl chloride, the laboratory must:
c. Total Trihalomethane Chemistry
(1) Methodology
d. Unregulated Contaminants and Special Monitoring
(1) Unregulated Volatile Organic Contaminants Methodology
e. Compositing of Samples: All samples must be composited in the laboratory and analyzed within fourteen (14) days of sample collection.
(1) The following procedure must be followed for the compositing samples prior to GC analysis.
(2) The following procedure must be followed for the compositing samples prior to GC/MS analysis.
3. Synthetic Organic Chemistry References for §§ 1.16.2, 1.17.3 and 1.17.5 of this Part.
a. Regulated Synthetic Organic Chemicals (SOCs)
(1) Methodology
(AA) PWSs conducting analyses of the organic chemicals listed below as required in §§ 1.16 and 1.17 of this Part shall conduct these analyses in accordance with one (1) of the following analytical methods or their equivalent as determined by EPA.
| Synthetic Organic Chemicals | ||||
| Contaminant | EPA Method | Standard Methods | ASTM | Other |
| 2,3,7,8-TCDD (dioxin) | 1613 | |||
| 2,4-D3(as acids, salts, and esters) | 515.2, 555, 515.1, 515.3, 515.4 | D5317-93, 98 (Reapproved 2003) | ||
| 2,4,5-TP3 (Silvex) | 515.2, 555, 515.1, 515.3, 515.4 | D5317-93, 98 (Reapproved 2003) | ||
| Alachlor1 | 505, 507, 525.2, 508.1, 551.1 | |||
| Atrazine1 | 505, 507, 525.2, 508.1, 551.1 | Syngenta4AG-625 | ||
| Benzo(a)pyrene | 525.2, 550, 550.1 | |||
| Carbofuran | 531.1, 531.2 | 6610 | ||
| Chlordane | 505, 508, 525.2, 508.1 | |||
| Dalapon | 552.1, 515.1, 552.2, 515.3, 515.4, 552.3 | |||
| Di(2-ethylhexyl) adipate | 506, 525.2 | |||
| Di(2-ethylhexyl) phthalate | 506, 525.2 | |||
| Dibromochloropropane (DBCP) | 504.1, 551.1 | |||
| Dinoseb3 | 515.2, 555, 515.1 | |||
| Diquat | 549.2 | |||
| Endothall | 548.1 | |||
| Endrin | 505, 508, 525.2, 508.1, 551.1 | |||
| Ethylene dibromide (EDB) | 504.1, 551.1 | |||
| Glyphosate | 547 | 6651 | ||
| Heptachlor | 505, 508, 525.2, 508.1, 551.1 | |||
| Heptachlor Epoxide | 505, 508, 525.2, 508.1, 551.1 | |||
| Hexachlorobenzene | 505, 508, 525.2, 508.1, 551.1 | |||
| Hexachlorocyclopentadiene | 505, 525.2, 508, 508.1, 551.1 | |||
| Lindane | 505, 508, 525.2, 508.1, 551.1 | |||
| Methoxychlor | 505, 508, 525.2, 508.1, 551.1 | |||
| Oxamyl | 531.1, 531.2 | 6610 | ||
| PCBs2 (as decachlorobiphenyl) | 508A | |||
| PCBs2 (as Aroclors) | 505, 508, 508.1, 525.2 | |||
| Pentachlorophenol | 515.2, 525.2, 555, 515.1, 515.3, 515.4 | D5317-93, 98 (Reapproved 2003) | ||
| Picloram3 | 515.2, 555, 515.1, 515.3, 515.4 | D5317-93, 98 (Reapproved 2003) | ||
| Simazine1 | 505, 507, 525.2, 508.1, 551.1 | |||
| Toxaphene | 505, 508, 508.1, 525.2 | |||
| Total Trihalomethanes | 502.2, 524.2, 551.1 | |||
| 1 Substitution of the detector specified in Method 505, 507, 508 or 508.1 for the purpose of achieving lower detection limits is allowed as follows. Either an electron capture or nitrogen phosphorous detector may be used provided all regulatory requirements and quality control criteria are met.2 PCBs are qualitatively identified as Aroclors and measured for compliance purposes as decachlorobiphenyl. Users of Method 505 may have more difficulty in achieving the required detection limits than users of Methods 508.1, 525.2 or 5083 Accurate determination of the chlorinated esters requires hydrolysis of the sample as described in EPA Methods 515.1, 515.2, 515.3, 515.4 and 555 and ASTM Method D5317-93.4 This method may not be used for the analysis of atrazine in any system where chlorine dioxide is used for drinking water treatment. In samples from all other systems, any result for atrazine generated by Method AG-625 that is greater than one-half the maximum contaminant level (MCL) (in other words, greater than 0.0015mg/L or 1.5 µg/L) must be confirmed using another approved method for this contaminant and should use additional volume of the original sample collected for compliance monitoring. In instances where a result from Method AG-625 triggers such confirmatory testing, the confirmatory result is to be used to determine compliance. |
(LL) Polychlorinated biphenyls (PCBs) (as decachlorobiphenyl)
(ii) If PCBs (as one (1) of seven (7) Aroclors) are detected (as designated in this Paragraph) in any sample analyzed using Method505 or 508, the PWS shall reanalyze the sample using Method 508A to quantitate PCBs (as decachlorobiphenyl).
| Aroclor | Detection limit (mg/L) |
| 1016 | 0.00008 |
| 1221 | 0.02 |
| 1232 | 0.0005 |
| 1242 | 0.0003 |
| 1248 | 0.0001 |
| 1254 | 0.0001 |
| 1260 | 0.0002 |
(2) Laboratory Criteria
(AA) Analysis under this Section shall only be conducted by laboratories that have received certification by EPA or the State and have met the following conditions. To receive certification to conduct analyses for the contaminants in § 1.21 of this Part (SOC's) above the laboratory must:
(ii) Achieve quantitative results on the analyses that are within the following acceptance limits:
| Contaminant | Acceptance Limits (percent) |
| Alachlor | ±45 |
| Aldicarb | 2 standard deviations |
| Aldicarb sulfoxide | 2 standard deviations |
| Aldicarb sulfone | 2 standard deviations |
| Atrazine | +45 |
| Benzo(a)pyrene | 2 standard deviations |
| Carbofuran | +45 |
| Chlordane | +45 |
| Dalapon | 2 standard deviations |
| Di(2-ethylhexyl)adipate | 2 standard deviations |
| Dibromochloropropane (DBCP) | +40 |
| 2,3,7,8-TCDD (Dioxin) | 2 standard deviations |
| 2,4-D | ±50 |
| 2,4,5-TP (Silvex) | ±50 |
| Di(2-ethylhexyl) phthalate | 2 standard deviations |
| Dinoseb | 2 standard deviations |
| Diquat | 2 standard deviations |
| Endothall | 2 standard deviations |
| Endrin | ±30 |
| Ethylene dibromide (EDB) | ±40 |
| Glyphosate | 2 standard deviations |
| Heptachlor | ±45 |
| Heptachlor epoxide | ±45 |
| Hexachlorobenzene | 2 standard deviations |
| Hexachloro- cyclopentadiene | 2 standard deviations |
| Lindane | ±45 |
| Methoxychlor | ±45 |
| Oxamyl | 2 standard deviations |
| PCBs (as Decachlorobiphenyl) | 0-200 |
| Picloram | 2 standard deviations |
| Pentachlorophenol | ±50 |
| Simazine | 2 standard deviations |
| Toxaphene | ±45 |
(iii) Detection shall be defined as greater than or equal to the following concentrations for each contaminant:
| Contaminant | Detection Limit (mg/L) |
| Alachlor | 0.0002 |
| Aldicarb | 0.0005 |
| Aldicarb sulfoxide | 0.0005 |
| Aldicarb sulfone | 0.0008 |
| Atrazine | 0.0001 |
| Benzo(a)pyrene | 0.00002 |
| Carbofuran | 0.0009 |
| Chlordane | 0.0002 |
| Dalapon | 0.001 |
| 1,2-Dibromo-3-chloropropane (DBCP) | 0.00002 |
| Di(2-ethylhexyl)adipate | 0.0006 |
| Di(2-ethylhexyl)phthalate | 0.0006 |
| 2,4-D | 0.0001 |
| Dinoseb | 0.0002 |
| Diquat | 0.0004 |
| Endothall | 0.009 |
| Endrin | 0.00001 |
| Ethylene dibromide (EDB) | 0.00001 |
| Glyphosate | 0.006 |
| Heptachlor | 0.00004 |
| Heptachlor epoxide | 0.00002 |
| Hexachlorobenzene | 0.0001 |
| Hexachloro-cyclopentadiene | 0.0001 |
| Lindane | 0.00002 |
| Methoxychlor | 0.0001 |
| Oxamyl | 0.002 |
| PCBs (as Decachlorobiphenyl) | 0.0001 |
| Picloram | 0.0001 |
| Pentachlorophenol | 0.00004 |
| Simazine | 0.00007 |
| Toxaphene | 0.001 |
| 2,3,7,8-TCDD (Dioxin) | 0.000000005 |
| 2,4,5-TP (Silvex) | 0.0002 |
4. Radiological Chemistry Reference for § 1.16.5 of this Part.
a. Analysis for the contaminants in Table A shall be conducted to determine compliance with § 1.16.5 of this Part in accordance with the methods in Table A, or their equivalent as approved by the Director, with prior approval by EPA.
| Contaminant | Methodology | TABLE A: Reference (Method of Page Number) | ||||||||
| EPA1 | EPA2 | EPA3 | EPA4 | SM5 | ASTM6 | USGS7 | DOE8 | Other | ||
| Naturally Occurring: | ||||||||||
| Gross alpha9 and beta | Evaporation | 900.0 | p. 1 | 00-01 | p. 1 | 302, 7110 B, 7110 B-00 | R-1120-76 | |||
| Gross alpha9 | Coprecipitation | 00-02 | 7110 C, 7110 C-00 | |||||||
| Radium 226 | Radon emanation | 903.1 | p. 16 | Ra-04 | p. 19 | 305, 7500-Ra C, 7500- Ra C-01 | D3454-97 | R-1141-76 | Ra-04 | NY10 |
| Radiochemical | 903.0 | p. 13 | Ra-03 | 304, 7500-Ra B, 7500-Ra B-01 | D2460-97 | R-1140-76 | GA12 | |||
| Radium 228 | Radiochemical | 904.0 | p. 24 | Ra-05 | p. 19 | 7500-Ra D, 7500-Ra D-01 | R-1142-76 | NY10, NJ11, GA12 | ||
| Uranium13 | Radiochemical | 908.0 | 7500-U B, | |||||||
| 7500-U B-00 | ||||||||||
| Fluorometric | 908.1 | 7500-U C (17th Ed.). | D2907-97 | R-1180-76, R-1181-76 | U-04 | |||||
| ICP-MS | 200.814 | 3125 | D5673-03 | |||||||
| Alpha Spectrometry | 00-07 | p. 33 | 7500-U C (18th, 19th, or 20th Ed.), 7500-U C-00 | D3972-97, 02. | R-1182-76 | U–02 | ||||
| Laser Phosphorimetry | D5174-97, 02 | |||||||||
| Man-Made: | ||||||||||
| Radioactive Cesium | Radiochemical | 901.0 | p. 4 | 7500-Cs B, 7500-Cs B-00 | D2459-72 | R-1111- 76 | ||||
| Gamma Ray Spectrometry | 901.1 | p. 92 | 7120, 7120-97. | D3649-91, 98a | R-1110- 76 | 4.5.2.3 | ||||
| Radioactive Iodine | Radiochemical | 902.0 | p. 6 | 7500-I B,7500-I B-00 | ||||||
| p. 9 | 7500-I C,7500-I C-007500-I D,7500-I D-00 | D3649-91,98a | ||||||||
| Gamma Ray Spectrometry | 901.1 | p. 92 | 7120, 7120-97 | D4785-93,00a | 4.5.2.3 | |||||
| Radioactive Strontium 89, 90 | Radiochemical | 905.0 | p. 29 | Sr-04 | p. 65 | 303, 7500-Sr B,7500-SrB-01 | R-1160- 76 | Sr-01,Sr-02 | ||
| Tritium | Liquid Scintillation | 906.0 | p. 34 | H-02 | p. 87 | 306, 7500-3 H B, 7500-3H B-00 | D4107-91, 98 (Re-approved 2002) | R-1171- 76 | ||
| Gamma Emitters | Gamma Ray Spectrometry | 901.1 | p. 92 | 7120, 7120-97. | D3649-91,98a | R-1110- 76 | Ga-01-R | |||
| 902.0 | 7500Cs B,7500Cs B-00 | D4785-93,00a | ||||||||
| 901.0 | 7500-I B,7500-I B-00 | |||||||||
| The procedures shall be done in accordance with the documents listed below. Copies of the documents may be obtained from the sources listed below. Information regarding obtaining these documents can be obtained from the Safe Drinking Water Hotline at 800–426–4791. Documents may be inspected at EPA's Drinking Water Docket, EPA West, 1301 Constitution Avenue, NW., Room 3334, Washington, DC 20460 (Telephone: 202-566-2426); or at the National Archives and Records Administration (NARA). For information on the availability of this material at NARA, call 202-741-6030, or go to: 1 “Prescribed Procedures for the Measurement of Radioactivity in Drinking Water,” EPA 600/4-80-032, August 1980. Available at the U.S. Department of Commerce, National Technical Information Service (NTIS), 5285 Port Royal Road, Springfield, VA 22161 (Telephone 800-553-6847), PB 80-224744.2 “Interim Radiochemical Methodology for Drinking Water,” EPA 600/4-75-008 (revised), March 1976. Available NTIS, ibid.3 “Radiochemistry Procedures Manual,” EPA 520/5-84-006, December 1987. Available NTIS, ibid.4 “Radiochemical Analytical Procedures for Analysis of Environmental Samples,” March 1979. Available at NTIS, ibid. EMSL LV 053917.5 “Standard Methods for the Examination of Water and Wastewater,'' 13th, 17th, 18th, 19th or 20th edition, 1971, 1989, 1992, 1995, 1998. Available at American Public Health Association, 1015 Fifteenth Street, NW., Washington, DC 20005. Methods 302, 303, 304, 305 and 306 are only in the 13th edition. Methods 7110B, 7500-Ra B, 7500-Ra C, 7500-Ra D, 7500-U B, 7500-Cs B, 7500-I B, 7500-I C, 7500-I D, 7500-Sr B, and 7500-3H B are in the 17th, 18th, 19th and 20th editions. Method 7110 C is in the 18th, 19th and 20th editions. Method 7500-U C Fluorometric Uranium is only in the 17th Edition, and 7500-U C Alpha spectrometry is only in the 18th, 19th and 20th editions. Method 7120 is only in the 19th and 20th editions. Method 3125 is only in the 20th edition. Methods 7110 B-00, 7110 C-00, 7500-Ra B-01, 7500- Ra C-01, 7500-Ra D-01, 7500-U B-00, 7500-U C-00, 7500-I B-00, 7500-I C-00, 7500-I D-00, 7120-97, 7500-Sr B-01, and 7500-3H B-00 are available online athttp://www.standardmethods.org. The year in which each method was approved by the Standard Methods Committee is designated by the last two digits in the method number. The methods listed are the only online versions that may be used.6 Annual Book of ASTM Standards, Vol. 11.01 and 11.02, 2002; ASTM International; any year containing the cited version of the method may be used. Copies of these two volumes and the 2003 version of D 5673-03 may be obtained from ASTM International, 100 Barr Harbor Drive, P.O. Box C700, West Conshohocken, PA 19428-2959.7 “Methods for Determination of Radioactive Substances in Water and Fluvial Sediments,” Chapter A5 in Book 5 of Techniques of Water-Resources Investigations of the United States Geological Survey, 1977. Available at U.S. Geological Survey (USGS) Information Services, Box 25286, Federal Center, Denver, CO 80225-0425.8 “EML Procedures Manual,” 28th (1997) or 27th (1990) Editions, Volumes 1 and 2; either edition may be used. In the 27th Edition Method Ra-04 is listed as Ra-05 and Method Ga-01-R is listed as Sect. 4.5.2.3. Available at the Environmental Measurements Laboratory, U.S. Department of Energy (DOE), 376 Hudson Street, New York, NY 10014-3621.9 Natural uranium and thorium-230 are approved as gross alpha calibration standards for gross alpha with co-precipitation and evaporation methods; americium-241 is approved with co-precipitation methods.10 “Determination of Ra-226 and Ra-228 (Ra-02),” January 1980, Revised June 1982. Available at Radiological Sciences Institute for Laboratories and Research, New York State Department of Health, Empire State Plaza, Albany, NY 12201.11 “Determination of Radium 228 in Drinking Water,'' August 1980. Available at State of New Jersey, Department of Environmental Protection, Division of Environmental Quality, Bureau of Radiation and Inorganic Analytical Services, 9 Ewing Street, Trenton, NJ 08625.12 “The Determination of Radium-226 and Radium-228 in Drinking Water by Gamma-ray Spectrometry Using HPGE or Ge(Li) Detectors,” Revision 1.2, December 2004. Available from the Environmental Resources Center, Georgia Institute of Technology, 620 Cherry Street, Atlanta, GA 30332-0335, USA, Telephone: 404- 894-3776. This method may be used to analyze for radium-226 and radium-228 in samples collected after January 1, 2005 to satisfy the radium-226 and radium-228 monitoring requirements specified at 40 CFR 141.26.13 If uranium (U) is determined by mass, a 0.67 pCi/µg of uranium conversion factor must be used. This conversion factor is based on the 1:1 activity ratio of U-234 and U-238 that is characteristic of naturally occurring uranium.14 “Determination of Trace Elements in Waters and Wastes by Inductively Coupled Plasma-Mass Spectrometry,'' Revision 5.4, which is published in ``Methods for the Determination of Metals in Environmental Samples--Supplement I,” EPA 600-R-94-111, May 1994. Available at NTIS, PB 95-125472. |
b. When the identification and measurement of radionuclides other than those listed in § 1.21(B)(4)(a) of this Part is required, the following references are to be used, except in cases where alternative methods have been approved by the Director.
c. For the purpose of monitoring radioactivity concentrations in drinking water, the required sensitivity of the radio analysis is defined in terms of a detection limit. The detection limit shall be that concentration which can be counted with a precision of plus or minus 100 percent at the 95 percent confidence level (1.96 s where s is the standard deviation of the net counting rate of the sample).
(1) To determine compliance with §§ 1.16.5(B) and 1.16.5(C) of this Part, the detection limit shall not exceed the concentrations in Table B.
| TABLE B Detection Limits for Gross Alpha Particle Activity, Radium 226, Radium 228, and Uranium | |
| Contaminant | Detection Limit |
| Gross alpha particle activity | 3 pCi/l |
| Radium-226 | 1 pCi/l |
| Radium-228 | 1 pCi/l |
| Uranium | 1 µg/L |
(2) To determine compliance with § 1.16.5(D) of this Part, Man-made Beta Particle and Photon Emitters, the detection limits shall not exceed the concentrations listed in Table C.
| TABLE C Detection Limits for Man-made Beta Particle and Photon Emitters | |
| Radionuclide | Detection Limit |
| Tritium | 1,000 pCi/l |
| Strontium-89 | 10 pCi/l |
| Strontium-90 | 2 pCi/l |
| Iodine-131 | 1 pCi/l |
| Cesium-134 | 10 pCi/l |
| Gross beta | 4 pCi/l |
| Other radionuclides | 1/10 of the applicable limit |
5. Disinfectant Residuals, Disinfection Byproducts, and Disinfection Byproduct Precursors References for §§ 1.8.4(A) through (D) of this Part.
a. Incorporation by Reference: The following documents are incorporated by reference: The Director of the Federal Register approves this incorporation by reference in accordance with 5 U.S.C. § 552(a) and 1 C.F.R. Part 51. Copies may be inspected at EPA's Drinking Water Docket, 1301 Constitution Avenue, NW., EPA West, Room B102, Washington, DC 20460, or at the National Archives and Records Administration (NARA). For information on the availability of this material at NARA, call 202-741-6030, or go to:
b. Disinfection Byproducts
(1) Approved Methods for Disinfection Byproduct Compliance Monitoring
| Contaminant & Methodology1 | EPA Method | Standard Method2 | SM Online3 | ASTM Method4 |
| TTHM | ||||
| P&T/GC/ElCD & PID | 502.25 | |||
| P&T/GC/MS | 524.2 | |||
| LLE/GC/ECD | 551.1 | |||
| HAA5 | ||||
| LLE (diazomethane)/GC/ECD | 6251 B6 | 6251 B-94 | ||
| SPE (acidic methanol)/ GC/ECD | 552.16 | |||
| LLE (acidic methanol)/ GC/ECD | 552.2, 552.3 | |||
| Bromate | ||||
| Ion chromatography | 300.1 | D 6581-00 | ||
| Ion chromatography & post column reaction | 317.0 Rev 2.07, 326.07 | |||
| IC/ICP-MS | 321.87,8 | |||
| Chlorite | ||||
| Amperometric titration | 4500-ClO2 E9 | 4500-ClO2 E-009 | ||
| Spectrophotometry | 327.0 Rev 1.19 | |||
| Ion chromatography | 300.0, 300.1, 317.0 | D 6581-00 | ||
| Rev 2.0, 326.0 | ||||
| 1 P&T = purge and trap; GC = gas chromatography; ElCD = electrolytic conductivity detector; PID = photoionization detector; MS = mass spectrometer; LLE = liquid/liquid extraction; ECD = electron capture detector; SPE = solid phase extraction; IC = ion chromatography; ICP-MS = inductively coupled plasma/mass spectrometer.2 19th and 20th editions of Standard Methods for the Examination of Water and Wastewater, 1995 and 1998, respectively, American Public Health Association; either of these editions may be used.3 The Standard Methods Online version that is approved is indicated by the last two digits in the method number which is the year of approval by the Standard Method Committee. Standard Methods Online are available at: http://www.standardmethods.org.4 Annual Book of ASTM Standards, 2001 or any year containing the cited version of the method, Vol 11.01.5 If TTHMs are the only analytes being measured in the sample, then a PID is not required.6 The samples must be extracted within 14 days of sample collection.7 Ion chromatography & post column reaction or IC/ICP-MS must be used for monitoring of bromate for purposes of demonstrating eligibility of reduced monitoring, as prescribed in § 141.132(b)(3)(ii).8 Samples must be preserved at the time of sampling with 50 mg ethylenediamine (EDA)/L of sample and must be analyzed within 28 days.9 Amperometric titration or spectrophotometry may be used for routine daily monitoring of chlorite at the entrance to the distribution system, as prescribed in § 141.132(b)(2)(i)(A). Ion chromatography must be used for routine monthly monitoring of chlorite and additional monitoring of chlorite in the distribution system, as prescribed in § 141.132(b)(2)(i)(B) and (b)(2)(ii). |
(2) Analysis under § 1.8.4 of this Part for disinfection byproducts must be conducted by laboratories that have received certification by EPA or the Director, except as specified under § 1.8.4(B)(3) of this Part. To receive certification to conduct analyses for the DBP contaminants in § 1.8.1(A) of this Part, the laboratory must:
(CC) Beginning April 1, 2007, the laboratory must achieve quantitative results on the PE sample analyses that are within the following acceptance limits:
| DBP | Acceptance Limits (percent of true value) | Comments |
| TTHM | Laboratory must meet all 4 | |
| Chloroform | ±20 | individual THM acceptance limits |
| Bromodichloromethane | ±20 | in order to successfully pass a PE |
| Dibromochloromethane | ±20 | sample for TTHM |
| Bromoform | ±20 | |
| HAA5 | Laboratory must meet the | |
| Monochloroacetic AcidDichloroacetic AcidTrichloroacetic Acid Monobromoacetic AcidDibromoacetic Acid | ±40±40±40±40±40 | acceptance limits for 4 out of 5 of the HAA5 compounds in order to successfully pass a PE sample for HAA5 |
| Chlorite | ±30 | |
| Bromate | ±30 |
(DD) Beginning April 1, 2007, report quantitative data for concentrations at least as low as the ones listed in the following table for all DBP samples analyzed for compliance with § 1.8.4 of this Part:
| DBP | Minimum Reporting Level (mg/L)10 | Comments |
| TTHM11 | ||
| Chloroform | 0.0010 | |
| Bromodichloromethane | 0.0010 | |
| Dibromochloromethane | 0.0010 | |
| Bromoform | 0.0010 | |
| HAA511 | ||
| Monochloroacetic Acid | 0.0020 | |
| Dichloroacetic Acid | 0.0010 | |
| Trichloroacetic Acid | 0.0010 | |
| Monobromoacetic Acid | 0.0010 | |
| Dibromoacetic Acid | 0.0010 | |
| Chlorite | 0.020 | Applicable to monitoring as prescribed |
| in § 141.132 (b)(2)(1)(B) and (b)(2)(ii). | ||
| Bromate | 0.0050 or | Laboratories that use EPA Methods |
| 0.0010 | 317.0 Revision 2.0, 326.0 or 321.8 | |
| must meet a 0.0010 mg/L MRL for | ||
| bromate. | ||
| 10 The calibration curve must encompass the regulatory minimum reporting level (MRL) concentration. Data may be reported for concentrations lower than the regulatory MRL as long as the precision and accuracy criteria are met by analyzing an MRL check standard at the lowest reporting limit chosen by the laboratory. The laboratory must verify the accuracy of the calibration curve at the MRL concentration by analyzing an MRL check standard with a concentration less than or equal to 110% of the MRL with each batch of samples. The measured concentration for the MRL check standard must be ±50% of the expected value, if any field sample in the batch has a concentration less than 5 times the regulatory MRL. Method requirements to analyze higher concentration check standards and meet tighter acceptance criteria for them must be met in addition to the MRL check standard requirement.11 When adding the individual trihalomethane or haloacetic acid concentrations to calculate the TTHM or HAA5 concentrations, respectively, a zero is used for any analytical result that is less than the MRL concentration for that DBP, unless otherwise specified by the Director. |
c. Analysis of Disinfectant Residuals
| Methodology | SM (19th or 20th ed) | SMOnline12 | ASTMMethod | EPA Method | Residual Measured13 | |||
| Free Cl2 | Combined Cl2 | Total Cl2 | ClO2 | |||||
| Amperometric Titration | 4500-Cl D | 4500-Cl D-00 | D 1253-86 (96), 03 | X | X | X | ||
| Low Level Amperometric | 4500-Cl E | 4500-Cl E-00 | X | |||||
| Titration | ||||||||
| DPD Ferrous Titrimetric | 4500-Cl F | 4500-Cl F-00 | X | X | X | |||
| DPD Colorimetric | 4500-Cl G | 4500-Cl G-00 | X | X | X | |||
| Syringaldazine (FACTS) | 4500-Cl H | 4500-Cl H-00 | X | |||||
| Iodometric Electrode | 4500-Cl I | 4500-Cl I-00 | X | |||||
| DPD | 4500-ClO2 D | X | ||||||
| Amperometric Method II | 4500-ClO2 E | 4500- ClO2 E-00 | X | |||||
| Lissamine Green Spectro- photometric | 327.0 Rev 1.1 | X | ||||||
| 12 The Standard Methods Online version that is approved is indicated by the last two digits in the method number which is the year of approval by the Standard Method Committee. Standard Methods Online are available at http://www.standardmethods.org.13 X indicates method is approved for measuring specified disinfectant residual. Free chlorine or total chlorine may be measured for demonstrating compliance with the chlorine MRDL and combined chlorine, or total chlorine may be measured for demonstrating compliance with the chloramine MRDL. |
d. Additional Analytical Methods
(3) Specific Ultraviolet Absorbance (SUVA). In order to determine SUVA, it is necessary to separately measure UV254 and DOC. When determining SUVA, PWSs must use the methods stipulated in § 1.21(B)(5)(d)(3)(AA) of this Part to measure DOC and the method stipulated in § 1.21(B)(5)(d)(3)(BB) of this Part to measure UV254. SUVA must be determined on water prior to the addition of disinfectants/ oxidants by the PWS. DOC and UV254 samples used to determine a SUVA value must be taken at the same time and at the same location.
(BB) Ultraviolet Absorption at 254 nm (UV254). Method 5910 B or 5910 B-00 (Ultraviolet Absorption Method) or EPA Method 415.3 Revision 1.1. UV absorption must be measured at 253.7 nm (may be rounded off to 254 nm). Prior to analysis, UV254 samples must be filtered through a 0.45 m pore-diameter filter. The pH of UV254 samples may not be adjusted. Samples must be analyzed as soon as practical after sampling, not to exceed forty-eight (48) hours.
6.PFAS Chemistry References for § 1.16.2(E) of this Part.
a. Analysis for each contaminant comprising Total PFAS as required in § 1.16.2(E)(1) of this Part shall be conducted using the following methods or their equivalent as approved by the EPA: (i) Method 533 Determination of Per- and Polyfluoroalkyl Substances in Drinking Water by Isotope Dilution Anion Exchange Solid Phase Extraction and Liquid Chromatography/Tandem Mass Spectrometry, (LC-MS/MS), 815-B-19-020, November 2019; or (ii) until April 25, 2027, or (ii) until April 25, 2027, Method 537.1, Version 1.0 “Determination of Selected Per-and Polyfluorinated Alkyl Substances in Drinking Water by Solid Phase Extraction and Liquid Chromatography/Tandem Mass Spectrometry (LC/MS/MS),” EPA/600/R-18/352 November 2018; or (iii) Method 537.1, Version 2.0 “Determination of Selected Per- and Polyfluorinated Alkyl Substances in Drinking Water by Solid Phase Extraction and Liquid Chromatography/Tandem Mass Spectrometry (LC-MS/MS),” EPA/600/R-20/006, March 2020.
(1) Table of Methodology for Total PFAS
| Contaminant | EPA Method |
| Perfluorodeconoic Acid (PFDA) | 533, 537.1 version 1.0 (until April 25, 2027); 537.1, version 2.0 |
| Perfluoroheptanoic Acid (PFHpA) | 533, 537.1 version 1.0 (until April 25, 2027); 537.1, version 2.0 |
| Perfluorohexane sulfonate (PFHxS) | 533, 537.1, version 1.0 (until April 25, 2027); 537.1, version 2.0 |
| Perfluorononoic Acid (PFNA) | 533, 537.1, version 1.0 (until April 25, 2027); 537.1, version 2.0 |
| Perfluorooctane sulfonate (PFOS) | 533, 537.1, version 1.0 (until April 25, 2027); 537.1, version 2.0 |
| Perfluorooctanoic Acid (PFOA) | 533, 537.1, version 1.0 (until April 25, 2027); 537.1, version 2.0 |
(2) Laboratory Criteria
(AA) Analysis under this § 1.21(B)(6)(a) of this Part shall only be conducted by laboratories that have received certification by EPA or the State and have met the following conditions. To receive certification to conduct analyses for the contaminants in § 1.16.2(E)(1) of this Part the laboratory must:
A. The Director has classified this Part into the following three (3) categories for use when assessing Administrative Penalties:
1. Categories*
a. Category I Penalty Range $1,000.00 - $5,000.00/day/violation. These types of violations have a direct impact on public health and will be given a high priority.
(1) Exceeding any MCL including
b. Category II Penalty Range $100.00 - $1,000.00/day/violation. These types of violations/noncompliance also have a direct impact on public health but are mainly noncompliance with technical safeguards.
c. Category III Penalty Range $100.00 - $300.00/day/violation. These types of violations have an indirect impact on public health and are generally related to poor record keeping.
2. Violation of a Department Order is a separate and additional violation from the violation or violations which gave rise to the issuance of the order, and is given a Base Number of $1000.00. No distinction should be made between a unilateral order and a consent order for the purpose of assessing administrative penalties. The above classification is subject to change as the Director gets more experience with the Administrative Penalties regulations.
| DWQ PENALTY MATRIX | ||
| Sections | Public Drinking Water (216-RICR-50-05-01) | Noncompliance Categories |
| 1.1 | Authority | N/A |
| 1.2 | Definitions | N/A |
| 1.3 | Coverage | I |
| Approval Required | I | |
| Right of Entry | II | |
| PWS Contact Information | III | |
| 1.4 | Approval of New Water Sources | I |
| 1.5 | Approval of Treatment Works, Storage, and Pumping Facilities | I |
| 1.6 | Filtration and Disinfection | |
| 1.6.1 General Requirements | I | |
| 1.6.2 Criteria for avoiding filtration | II | |
| 1.6.3 Disinfection | I | |
| 1.6.4 Filtration | I | |
| 1.6.5 Analytical and monitoring requirements | II | |
| 1.6.6 Monitoring requirements for PWSs that do not provide filtration | II | |
| 1.6.7 Monitoring requirements for PWSs using filtration equipment | II | |
| 1.6.8 Reporting and record keeping requirements | III | |
| 1.6.9 Enhanced Treatment for Cryptosporidium | ||
| 1.6.9(A)General Requirements | ||
| 1.6.9(B) Source Water Monitoring | II | |
| 1.6.9(C) Sampling Schedules | II | |
| 1.6.9(D) Sampling Locations | II | |
| 1.6.9(E) Analytical Methods | II | |
| 1.6.9(F) Approved Laboratories | II | |
| 1.6.9(G) Reporting Source Water Monitoring Results | III | |
| 1.6.9(H) Grandfathering Previously Collected Data | II | |
| 1.6.9(I) Requirements When Making a Significant Change in Disinfection Practice | I | |
| 1.6.9(J) Developing the Disinfection Profile and Benchmark | II | |
| 1.6.9(K) Bin Classification for Filtered PWSs | II | |
| 1.6.9(L) Filtered PWS Additional Cryptosporidium Treatment Requirements | I | |
| 1.6.9(M) Unfiltered PWS Cryptosporidium Treatment Requirements | I | |
| 1.6.9(N) Schedule for Compliance with Cryptosporidium Treatment Requirements | I | |
| 1.6.9(O) Microbial Toolbox Options for Meeting Cryptosporidium Treatment Requirements | I | |
| 1.6.9(P) Source Toolbox Components | I | |
| 1.6.9(Q) Pre-Filtration Treatment Toolbox Components | I | |
| 1.6.9(R) Treatment Performance Toolbox Components | I | |
| 1.6.9(S) Additional Filtration Toolbox Components | I | |
| 1.6.9(T) Inactivation Toolbox Components | I | |
| 1.6.9(U) Reporting Requirements | III | |
| 1.6.9(V) Recordkeeping Requirements | III | |
| 1.6.9(W) Requirements to Respond to Significant Deficiencies Identified in Sanitary Surveys Performed by The Director | I | |
| 1.6.10 Algal Toxins | ||
| 1.6.10(A) Maximum Contaminant Levels for Algal Toxins | I | |
| 1.6.10(B) Source Water Surveillance | II | |
| 1.6.10(C) Bloom Severity | III | |
| 1.6.10(D) Algal Bloom Response Actions | II | |
| 1.6.10(D)(6) Harmful Algal Blooms – Treatment | I | |
| 1.6.10(D)(6)(f) Failure to comply with screening and toxin monitoring | II | |
| 1.6.10(D)(7)(a) Failure to complete any screening or monitoring requirements | III | |
| 1.6.10(D)(7)(b) A PWS which has exceeded the MCL for an algal toxin in finished water | I | |
| 1.6.10(D)(7)(e) A PWS which fails to screen or monitor algal toxins must notify the public | III | |
| 1.7 | Control of Lead and Copper | |
| 1.7.1 General requirements | ||
| 1.7.2 Applicability of corrosion control treatment steps to small, medium-size and large PWSs | I | |
| 1.7.3 Description of corrosion control treatment requirements | I | |
| 1.7.4 Source water treatment requirements | I | |
| 1.7.5 Lead service line replacement requirements | I | |
| 1.7.6 Public education and supplemental monitoring requirements | II | |
| 1.7.7 Monitoring requirements for lead and copper in tap water | II | |
| 1.7.8 Monitoring requirements for water quality parameters | II | |
| 1.7.9 Source monitoring requirements for lead and copper in water | II | |
| 1.7.10 Analytical methods | II | |
| 1.7.11 Reporting requirements | III | |
| 1.7.12 Record keeping requirements | III | |
| 1.8 | Disinfectant Residuals, Disinfection Byproducts and Disinfection Byproduct Precursors | II |
| 1.8.1 Maximum Contaminant Levels (MCLs) for Disinfection Byproducts | I | |
| 1.8.2 Maximum Residual Disinfectant Levels | I | |
| 1.8.3 General Requirements | I | |
| 1.8.4 Analytical Requirements | II | |
| 1.8.5 Monitoring Requirements | II | |
| 1.8.6 Compliance Requirements | I | |
| 1.8.7 Reporting and Recordkeeping Requirements | III | |
| 1.8.8 Treatment Techniques for Control of Disinfection Byproducts | I | |
| 1.8.9 Initial Distribution PWS Evaluations | II | |
| 1.8.9(A) General Requirements | ||
| 1.8.9(B) Standard Monitoring | ||
| 1.8.9(C) System Specific Studies | ||
| 1.8.9(D) 40/30 Certification | ||
| 1.8.9(E) Very Small System Waivers | ||
| 1.8.9(F) Stage 2 (§ 1.8.10) Compliance Monitoring Location Recommendations | ||
| 1.8.10 Stage 2 Disinfection Byproducts Requirements | ||
| 1.8.10(A) General requirements | II | |
| 1.8.10(B) Routine monitoring | II | |
| 1.8.10(C) § 1.8.10 monitoring plan | II | |
| 1.8.10(D) Reduced monitoring | II | |
| 1.8.10(E) Additional requirements for consecutive PWSs | II | |
| 1.8.10(F) Conditions requiring increased monitoring | I | |
| 1.8.10(G) Operational evaluation levels | I | |
| 1.8.10(H) Requirements for remaining on reduced TTHM and HAA5 monitoring based on Stage 1 results | II | |
| 1.8.10(I) Requirements for remaining on increased TTHM and HAA5monitoring based on Stage 1 results | II | |
| 1.8.10(J) Reporting and recordkeeping requirements | III | |
| 1.9 | Assurance of Safety in Public Supply | |
| 1.9.2 Contamination of Tanks | I | |
| 1.9.3 Connection Between Distribution Systems | I | |
| 1.9.5 Flushing of Distribution Systems | II | |
| 1.9.6 Minimum Pressure Requirements | II | |
| 1.9.7 Auxiliary Power | II | |
| 1.9.8 Notifications Involving Emergency Events | II | |
| 1.9.9 PWS Emergency Response Plans | II | |
| 1.10 | Correction of Unsafe Conditions | I |
| 1.11 | Reports as to Public Supplies | II |
| 1.11.2 Reporting Requirements | III | |
| 1.11.3 Record Maintenance | III | |
| 1.12 | Certified Laboratories | II |
| 1.13 | Groundwater Microbiology | |
| 1.13.1 General Requirements and Applicability | II | |
| 1.13.2 Sanitary Surveys for Groundwater Systems | I | |
| 1.13.3 Groundwater Source Microbial Monitoring and Analytical Methods | II | |
| 1.13.4 Treatment Technique Requirements for Groundwater Systems | ||
| 1.13.4(A) Groundwater Systems with Significant Deficiencies or Source Water Fecal Contamination | I | |
| 1.13.4(B) Compliance Monitoring | II | |
| 1.13.5 Treatment Technique Violations for Groundwater Systems | I | |
| 1.13.6 Reporting and Recordkeeping for Groundwater Systems | III | |
| 1.14 | Consecutive PWS Monitoring | N/A |
| 1.15 | Variances and Exemptions | N/A |
| 1.16 | Community PWS Requirements | |
| Maximum Contaminant levels for | ||
| 1.16.1 Inorganic Chemicals | I | |
| 1.16.2 Organic Chemicals | I | |
| 1.16.3 Turbidity | I | |
| 1.16.4 Microbiological | I | |
| 1.16.5 Radioactivity | I | |
| Monitoring Requirements, Analytical Techniques, and Monitoring Frequency for §§ 1.16.1, 1.16.2, 1.16.3, 1.16.4, and 1.16.5 | II | |
| 1.16.6 Public Notification | II | |
| 1.16.10 Records | III | |
| 1.16.11 Consumer Confidence Reports | III | |
| 1.17 | Non-Community PWS Requirements | |
| Maximum Contaminant levels for | ||
| 1.17.1 Microbiological | I | |
| 1.17.2 Inorganic Chemicals | I | |
| 17.3 Organic Chemicals | I | |
| 1.17.4 Turbidity | I | |
| Monitoring Requirements, Analytical Techniques and Monitoring Frequency for §§ 1.17.1, 1.17.2, 1.17.3, 1.17.4 and 1.17.5 | II | |
| 1.17.6 Public Notification | II | |
| 1.17.7 Records | III | |
| 1.18 | Fees | N/A |
| 1.19 | Practices and Procedures | N/A |
| 1.20 | Violations, Noncompliance, and Enforcement | I, II or III |
| Other Areas of Non-Compliance | ||
| Violations of approval letter requirements | I | |
| Contamination incidents | I | |
| Non-compliance with administrative orders | I | |
| Non-compliance with administrative consent agreements | I |
I. Calculate Statutory Maximum Penalty
(B) Maximum Penalty __________
II. Calculate Economic Benefit Component
1. Estimate avoided and delayed costs through reasonable methodology.
III. Calculate Gravity Component
6. GRAVITY BASE NUMBER
7. NUMBER OF DAYS (If applicable) __________
8. TOTAL GRAVITY BASE NUMBER
9. PRELIMINARY SETTLEMENT AMOUNT
IV. Adjustment Factors TO TOTAL GRAVITY BASE NUMBER
TOTAL PERCENTAGE ADJUSTMENTS
V. Final Settlement Amount
F. This Part hereby adopts and incorporates by reference certain federal regulations promulgated by the federal Environmental Protection Agency, including those listed in § 1.24(F)(1) of this Part. All references to particular numbered section(s) or portion(s) of such numbered section(s) of 40 C.F.R. means that such numbered section(s) or portion(s) of such section(s) of 40 C.F.R. is or are incorporated by reference, including any cross-references to additional applicable regulations, notes, appendices, and diagrams, except where additions, modifications, or exceptions are specifically stated. When a federal regulation has been incorporated by reference with State additions, modifications, or exceptions, the governing requirements include the State changes in addition to any unchanged portions of the incorporated federal regulation. Any cross-references in other provisions of this Part to a federal regulation that has been incorporated with State changes are to that regulation with the State changes. When federal regulations are incorporated by reference, State terms are substituted for federal terms, to the extent provided in § 1.2 of this Part (Definitions), in addition to the other State changes specified elsewhere in this Part. For example, where the federal regulation refers to the term “primacy agency,” the term “Director,” as defined in § 1.2 of this Part, shall be substituted.