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Performance Evaluation Studies on Wastewater Laboratories (Renewal)

OMB: 2080-0021

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Information Collection Request for

Performance Evaluation Studies on Wastewater Laboratories









November 2016














Prepared by:

U. S. Environmental Protection Agency

Office of Enforcement and Compliance Assurance

Office of Compliance

Monitoring, Assistance, and Media Programs Division

Water Branch

1200 Pennsylvania Ave., NW

Washington, D.C. 20460

TABLE OF CONTENTS


1 IDENTIFICATION OF THE INFORMATION COLLECTION 1

1(a) Title and Number of the Information Collection 1

1(b) Short Characterization 1

2 NEED FOR AND USE OF THE COLLECTION 2

2(a) Need/Authority for the Collection 2

2(b) Practical Utility/Users of the Data 2

3 NONDUPLICATION, CONSULTATIONS, AND OTHER COLLECTION CRITERIA 3

3(a) Non-duplication 3

3(b) Public Notice Required Prior to ICR Submission to OMB 3

3(c) Consultations 3

3(d) Effects of Less Frequent Collection 4

3(e) General Guidelines 4

3(f) Confidentiality 4

3(g) Sensitive Questions 4

4 THE RESPONDENTS AND THE INFORMATION REQUESTED 5

4(a) Respondents and SIC/NAICS Codes 5

4(b) Information Needed 5

4(b)(i) Data items 5

4(b)(ii) Respondent Activities 5

5 THE INFORMATION COLLECTED – AGENCY ACTIVITIES, COLLECTION METHODOLOGY AND INFORMATION MANAGEMENT 7

5(a) Agency Activities 7

5(b) Collection Methodology and Management 7

5(c) Small Entity Flexibility 7

5(d) Collection Schedule 7

6 ESTIMATING THE BURDEN AND COST OF THE COLLECTION 8

6(a) Estimating Respondent Burden 8

6(b) Estimating Respondent Costs 9

6(b)(i) Respondent Labor 9

6(b)(ii) Respondent Operation and Maintenance Costs 10

6(b)(iii) Capital/Startup Operating and Maintenance (O&M) Costs 11

6(c) Estimating Agency Burden and Costs 11

6(d) Estimating the Respondent Universe and Total Burden and Costs 12

6(e) Bottom Line Burden Hours and Cost Tables 12

6(f) Reasons for Change in Burden 12

6(g) Burden Statement 13

APPENDIX A: LIST OF CHEMISTRY & MICROBIOLOGY ANALYTES AND WET TEST METHODS 14

APPENDIX B: LIST OF TOP CHEMISTRY & MICROBIOLOGY ANALYTES AND WET TEST METHODS AND TIMES FOR ANALYZING 16



1 IDENTIFICATION OF THE INFORMATION COLLECTION

1(a) Title and Number of the Information Collection

Performance Evaluation Studies of Wastewater Laboratories (Renewal). OMB Control No. 2080-0021, EPA ICR No. 0234.12.

1(b) Short Characterization

This is a request to renew an existing Information Collection Request (ICR) to support the collection of Proficiency Testing (PT) data on the performance of laboratories that conduct discharge analyses for the Discharge Monitoring Report – Quality Assurance (DMR-QA) study program. This request will replace the expiring ICR (Performance Evaluation Studies of Water and Wastewater Laboratories (OMB Control No. 2080-0021, EPA ICR No. 0234.11). This ICR refers only to DMR-QA. Therefore, the figures for burdens only support DMR-QA. EPA is requesting a standard three-year clearance for this ICR.


The National Pollutant Discharge Elimination System (NPDES) program is implemented by the United States Environmental Protection Agency (EPA) and the states that EPA has authorized to implement the program. In accordance with terms and conditions of NPDES permits, chemical monitoring data for wastewater are submitted from a variety of laboratories to the appropriate NPDES permitting authority every year. EPA and states must rely on these results when carrying out permitting, compliance, and enforcement activities. In order to provide an objective demonstration that these laboratories are submitting reliable information, the subject Performance Evaluation (PE) studies were developed. Participation in the DMR-QA studies is mandatory for major dischargers and selected minor dischargers under the NPDES permitting program. Major municipal dischargers are defined as facilities designed to discharge at least 1 million gallons of wastewater per day, service a population of at least 10,000, or have a discharge that causes significant water quality impacts. Non-municipal major facilities are defined as major facilities based on a numerical rating system that evaluates their significance using criteria such as toxic pollutant potential, flow volume and water quality factors. Minor dischargers are selected to monitor the analytes/toxics discharged by the facility.


EPA formerly administered and prepared test standards for the DMR-QA program as part of the Agency’s mandate to assure the quality of environmental monitoring data submitted by NPDES permit holders (permittees). Preparation, distribution and grading of the test standards have now been privatized to lessen EPA’s burden in carrying out this mandate. Private sector companies manufacture and distribute test samples to contract and in-house laboratories, and are known as Proficiency Testing (PT) providers. The laboratories submit their analytical results to the PT Providers for evaluation. The PT Providers evaluate the submitted data and send the graded results back to the laboratories. These laboratories then forward copies of their graded data to their permittee clients, who will review the results and forward the data to their designated certifying/enforcement authorities. Providers also send electronic copies of the graded results to the designated certifying/enforcement authorities and to EPA. Graded results include the names and addresses of the laboratories, analytes tested, concentration of the analytes, and the acceptance criteria and evaluations.


EPA is required to conduct this ICR analysis because more than nine non-Federal entities will be asked to respond to this data request. Because state agencies use the resulting data for their own laboratory certification/enforcement programs and are not reporting any information from the PT studies to EPA, they do not incur any burden under this ICR. In addition, cost and burden to PT Providers are not considered in this ICR because the vendor costs associated with this program are accounted for in the pricing of their standards (i.e., the costs incurred by the Providers is factored into the cost of the PT standards).


The total annual burden and labor costs incurred by the 5,700 permittees associated with this ICR are estimated to be 37,620 hours and $5,113,983 per year over the 3-year ICR period (calendar years 2017-2019). EPA estimates that it takes 6.6 hours and costs $897.19 per year per respondent to comply with this requirement. Respondent labor costs are linked with the time it takes to read and understand the annual DMR-QA announcement sent by EPA, plan activities, analyze PT standards, report information to the PT Providers, and maintain records. Respondent operation and maintenance (O&M) costs are associated with purchasing the PT standards. No costs or burdens to PT Providers or state regulatory agencies are associated with this ICR.


2 NEED FOR AND USE OF THE COLLECTION

2(a) Need/Authority for the Collection

Laboratory Performance Evaluation (PE) studies are designed to fulfill the need to monitor the quality of analytical data for select critical analytes within major point-source discharge samples. Results from the PE studies over time have generally shown a slow but regular improvement in average performance by the laboratories producing the monitored data. By helping laboratories identify and correct analytical problems, the PE studies are also responsible for documented improvement in this data.


The Clean Water Act, and the related regulations in 40 CFR part 136, require extensive analysis of water and wastewater samples by EPA, state, local government and private laboratories, to maintain ambient water quality and control point-source discharges. EPA uses this data as the basis for many important decisions, including policy and regulation development, compliance and enforcement determinations, and program development. The data quality depends heavily upon the availability of capable laboratory analyses at all levels and reliability must be ensured.

2(b) Practical Utility/Users of the Data

States and laboratory personnel will use the results of these studies to identify problems associated with laboratory analysis and substandard facility discharges. This will improve the quality of water data in critical monitoring areas and the quality of facility discharges returned to the environment. These studies have demonstrated that problems exist and arise periodically with dischargers and water testing laboratories. Without future studies, many such problems will go unrecognized and unresolved. Results from the DMR-QA studies are used to highlight NPDES facilities and laboratories with apparent analytical problems that should be inspected on-site by state regulatory personnel. Results from the PT studies are used by state personnel as a major part of the basis for certifying laboratories to produce required regulatory data and as a basis for potential regulatory enforcement.

3 NONDUPLICATION, CONSULTATIONS, AND OTHER COLLECTION CRITERIA

3(a) Non-duplication

Data and results from other federally sponsored water quality programs, such as the Water Pollution (WP) program, can be used to fulfill obligations under the DMR-QA as long as the laboratories meet the condition that they perform the PE sample analyses between January 1st and the last day of the DMR-QA study. The DMR-QA study commences on or around March 15th, and concludes on or around July 1st of each year.


As of January 1, 2016, EPA has granted full or partial waivers to 17 states to use their state laboratory certification program in lieu of their permittees participating in DMR-QA. Five of these waivers have been granted since the last ICR was renewed in March 2014.

3(b) Public Notice Required Prior to ICR Submission to OMB

In compliance with the Paperwork Reduction Act, a notice of this Information Collection Request ICR was published in the Federal Register on July 6, 2016 (81 FR 44017). No comments were received.

3(c) Consultations

The DMR-QA has been administered by the EPA for over 35 years. The Office of Research and Development initiated and administered the program until the responsibility was assigned to the Office of Enforcement and Compliance Assurance (OECA). OECA will consider any comments received and make appropriate adjustments to the program.


The seven PT Providers are accredited by the American Association for Laboratory Accreditation (A2LA), and ANAB, the ANSI-ASQ National Accreditation Board. A2LA is a nonprofit, non-governmental, public service, membership society. The mission of A2LA is to provide comprehensive services in laboratory accreditation and laboratory-related training. The list of PT Providers accredited by A2LA is available at http://www.nelac-institute.org/ptproviders.php. ANAB is a non-profit, non-governmental organization that provides accreditation services to public- and private-sector organizations and is jointly owned by the American National Standards Institute and the American Society for Quality. ANAB provides accreditation for ISO/IEC 17043 for proficiency testing providers. The list of PT Providers accredited by ANAB is available at http://search.anab.org/search-accredited-companies.aspx.


In preparation of this ICR, EPA contacted the seven PT Providers and three responded (PT Provider contact information can be found on Page 6 of EPA Form 6400-01 [OMB 2080-0021], which is included as an attachment to this ICR package). The PT Providers were asked to provide input on the estimated time burden for respondents as well as the fees which laboratories need to pay for samples provided by the PT Providers. The PT Providers that responded indicated that it costs $305 to $772 per laboratory for chemical/microbiological samples. EPA chose to use the conservative high end estimate of $772 per laboratory for the purposes of estimating ICR costs to respondents. For Whole Effluent Toxicity (WET) tests, the range was $1,100 to $2,374 per laboratory, and the high-end estimate of $2,374 was used. It should be noted that this is the cost that both in-house and contract laboratories pay, and this is passed on to the permittee. Therefore, if a lab is contracted by several permittees, then EPA considers that the cost will be distributed evenly among the permittees. However, if a permittee employs an in-house laboratory, the permittee is burdened with the entire cost of obtaining samples as well as the labor costs of the laboratory. Since the ratio of in-house and contract laboratories is unknown, an average was obtained for all laboratories and a ratio of 0.633 laboratories per permittee was used. This ratio is the same as used in the 2013 ICR. Using this ratio, the cost of obtaining samples is estimated to be $488.68 per permittee for chemical/microbiological tests and $1,502.74 for WET tests.


3(d) Effects of Less Frequent Collection

The current frequency for the DMR-QA is judged to be the minimum needed to assess the accuracy of data production required by discharge permits. Under DMR-QA, laboratories producing data are expected to demonstrate adequate analytical proficiency once per year for each analyte they test routinely for their NPDES permittee clients. Collecting water quality data less than once per year to measure the accuracy of laboratory work would potentially delay corrective actions required by the permittee and therefore compromise discharge water quality.

3(e) General Guidelines

This ICR was prepared in accordance with the October 2009 version of the ICR Handbook developed by EPA's Office of Environmental Information, Office of Information Collection, Collection Strategies Division. The ICR Handbook provides the most current instructions for ICR preparation to ensure compliance with the 1995 Paperwork Reduction Act (PRA) Amendments and OMB's implementing guidelines.


EPA believes participation in these studies is a reasonable requirement for all laboratories routinely producing data to satisfy NPDES permit requirements. Providing PE samples to the responsible NPDES permitting authorities assures that permittees’ laboratories are testing the analytes using methods specified by the permit.

3(f) Confidentiality

This information collection does not require respondents to disclose confidential information.

3(g) Sensitive Questions

No questions of a sensitive nature are included in any of the information collection requirements outlined in this ICR.


4 THE RESPONDENTS AND THE INFORMATION REQUESTED

4(a) Respondents and SIC/NAICS Codes

Respondents in DMR-QA studies are NPDES permittees designated by the EPA region or state with permitting responsibility and the laboratories doing chemical/microbiological analysis and whole-effluent toxicity testing for these major dischargers. These respondents are most likely from the following SIC and NAICS codes:



CATEGORY

SIC NUMBERS

NAICS NUMBERS

Manufacturers

2011 through 3999   

311611

Water Supply Systems

4941

22131

Sewerage Systems

4952

22132

Water Testing Laboratories

8734

54194

4(b) Information Needed

4(b)(i) Data items

In all laboratory PE studies, the data result from analyses of synthetic samples that contain known amounts of specific compounds, usually dissolved in reagent water. In DMR-QA studies, the compounds are those of primary interest with regard to the monitoring requirements in the NPDES permits. All studies also collect sufficient data to properly identify and characterize the respondents. Each respondent reports only data for that portion of the study analytes for which they wish to be certified or as directed by the responsible regulatory official.

4(b)(ii) Respondent Activities

The primary burden involves analyzing and reporting results for relevant study samples according to instructions. About 5,700 respondents participated in the 2016 DMR-QA study. EPA projects that this number of respondents will remain relatively static for the next ICR period.


The DMR-QA program requires major permittees to submit results annually, and minor permittees are selected for participation by the DMR-QA state coordinators. The fluctuation of major permit holders and the selection process at the state level causes the exact number of permittees to vary each year. A percentage of these permittees do all the work onsite themselves, using in-house laboratories. The remaining permittees contract at least some of the analysis to commercial laboratories. The commercial laboratory may do work for many permittees; the DMR-QA results would then be sent to these permittees. Therefore, there are fewer labs than permittees. However, EPA does not have data on how many in-house laboratories and contract laboratories are used, as permit holders may choose to have commercial or in-house laboratories perform the analyses. Furthermore, EPA does not track how many laboratories participated in one or more studies or how many permittees participated in only chemistry and microbiology and those that also participated in WET testing. EPA is estimating the “maximum” impact of the DMR-QA program on the regulated community. EPA will assume that all 5,700 permittees will fulfill requirements for the top 10 chemistry and microbiology analytes and the top 10 WET test methods. EPA believes this ICR may overestimate the burden because not all permittees are required to perform WET testing. (See Appendix B for a list of the top 10 chemistry and microbiology analytes and the top 10 WET test methods).


To calculate the burden incurred on laboratories performing PE samples, EPA used a ratio of 0.633 laboratories per NPDES permittee. This ratio was calculated based on data procured by four PT Providers in 2006. EPA assumes that the ratio of laboratories per permittee has not changed significantly since the last ICR was approved. Based on this ratio (0.633 laboratories per NPDES permittee) and that there are 5,700 permittees participating in the DMR-QA, EPA estimates there are a total of 3,608 laboratories performing PE studies under DMR-QA. To provide an estimate of respondent burden for the WET testing portion of DMR-QA, EPA determined that an average of 4.77% of all laboratories participating in DMR-QA perform WET PE tests, or 172 laboratories. This percentage is also based on the information from the four providers received in 2006. EPA is not estimating the burden for the PT Providers, because this burden is internalized in the cost of obtaining PE samples from the PT Providers.


Respondents (permittees) will participate in the following activities:


      1. Read Instructions: Each of the 5,700 respondents will read the instructions provided by EPA.


      1. Plan Activities: Each of the 5,700 respondents will incur burden to plan activities associated with the PT studies.


      1. Analyze Chemistry and Microbiology Analytes: EPA assumes that all 5,700 respondents will participate in the PT studies for microbiology, trace metals, demands, minerals, nutrients, and miscellaneous chemical analytes as required by respondents’ permits. EPA assumes that 3,608 in-house and contract laboratories will do the work for the 5,700 permittees.


      1. Analyze WET: EPA assumes that all 5,700 permittees will participate in the PT studies for WET. It is assumed that 172 in-house and contract laboratories will do the work for the 5,700 permittees.


      1. Report Results: Each of the 5,700 respondents will incur burden to report its study results to the PT Provider.


      1. Maintain Records: Each of the 5,700 respondents will incur burden to maintain records associated with the PT study.

5 THE INFORMATION COLLECTED – AGENCY ACTIVITIES, COLLECTION METHODOLOGY AND INFORMATION MANAGEMENT

5(a) Agency Activities

EPA provides general program management support, develops guidance and maintains oversight of state DMR-QA activities, as well as oversight of the PT Providers and participating laboratories on an as-needed basis.

5(b) Collection Methodology and Management

EPA notifies the permittee of their requirement to participate in the relevant PE program annually. The permittee’s in-house or contract laboratory will then select an accredited private PT Provider to provide them with the appropriate samples. The testing facility will then send the analysis data of these samples to the PT Provider. The permittee will use the form approved by OMB to report DMR-QA results. This form will be available in two formats: a hard copy that will be part of the announcement which is mailed annually and an online PDF form, available on the EPA website. This PDF form can be filled out and then printed for submission. The PT Provider will send evaluations of the submitted data back to the permittee and the designated certifying/enforcement authority. PT Providers may also send summary data in electronic form to EPA for archiving.

5(c) Small Entity Flexibility

The major requirement under Small Business Regulatory Enforcement Fairness Act (SBREFA) is a regulatory flexibility analysis of all rules that have a "significant economic impact on a substantial number of small entities." Since this data request is not part of a rule, this ICR is not subject to SBREFA.

5(d) Collection Schedule

EPA determines the requirements for the frequency that a permittee must demonstrate proficiency by passing a PE study. The study typically starts on or around March 15th and ends on or around July 1st. The participating permittees’ in-house/contract laboratories demonstrate their proficiency by passing a PE study conducted by an accredited PT Provider for a fee. The PT Provider must submit the results of each study to the participating laboratories. The permittees must then request the participating laboratories to forward the graded results that were transmitted by the PT Provider, and in turn, the permittee must submit the graded results to the appropriate regional or state DMR-QA coordinator.

In summary: each participating in-house or contract laboratory must report test results to the PT Provider once a year. The PT Provider must submit the results of all studies they conduct to the participating laboratories. The permittees must then require the laboratories to forward them the graded results the laboratories received from the PT Provider. The permittees then submit a copy of the graded results to the appropriate regional or state DMR-QA coordinator. Participating permittees must re-qualify for each analyte it reports one year from the last certification that it received.


6 ESTIMATING THE BURDEN AND COST OF THE COLLECTION

This section describes the estimated average annual burden and costs for the information collection activities for PT studies that will be conducted by laboratories. For this data submission, PT Providers, state agencies and EPA have no burden and costs. The Agency's burden and cost estimates are outlined in Section 6(c).


To estimate the costs, EPA made assumptions about the burden associated with activities that would likely be needed to fulfill the request. EPA emphasizes that the per-respondent estimates represent the average annual burden and cost over the 3-year period covered by this ICR (2017-2019). Some respondents may incur higher costs and some will fall below the average. EPA made the assumption that all respondents perform all the tests included in this analysis. As a result, the burden is assumed to be a high estimate.


Burden and costs are not distinguished by categorized entities, public (federal, state and local government dischargers) and private (commercial, industrial and others) sectors, because EPA currently does not track this information.

6(a) Estimating Respondent Burden

The average annual respondent burden (in labor hours) for permittees is shown in Table 6.1. PT Providers conduct the studies, removing this burden from EPA. Participating laboratories receive samples from the PT Provider and return test results to the PT Providers. The PT Providers evaluate the data and send reports to the laboratories. The total burden on the laboratories is 37,620 hours, with an average of 6.6 hours per respondent (37,620 total hours divided by 5,700 permittees). This estimate includes burden for participating laboratories to read instructions, plan activities, analyze samples, submit data to the PT Providers, and maintain records.


EPA assumes that the respondent burden will be divided among three labor categories: manager, chemist, and records clerk. The labor associated with each of the ICR activities are discussed in more detail below.


  • Read Instructions: EPA assumes that each of the 5,700 respondents will require 0.5 hours to read the instructions provided by EPA. The burden will be divided between a manager and chemist. Sample instructions and forms can be found in the DMR-QA Study 36 package included in the docket.


  • Plan Activities: EPA assumes that the manager of each laboratory will require 0.5 hours to plan activities associated with the PT studies. The burden will be divided between a manager and chemist.


  • Analyze Chemistry and Microbiology Analytes: A total of 5,700 permittees are expected to use a total of 3,608 laboratories (a ratio of 0.633 laboratories for every permittee). Analysis is assumed to require approximately 2.1 hours to analyze PT standards for the top 10 analytes. All hours will be incurred by a chemist. See Appendix B for these tests and the estimated time for an analysis. These estimates assume that the laboratory is adding a DMR-QA sample to the normal processing that occurs in the laboratory using an already calibrated instrument/process.


  • Analyze WET: A biologist or project manager constructs the test chambers and records organism mortality (morbidity) of test organisms while a chemist analyzes the water chemistry. Biologists and chemists are assumed to require 2.4 hours to analyze PT standards for WET. It is assumed that 172 laboratories do this work for all 5,700 permittees. These estimates assume that the laboratory is adding a DMR-QA sample to the normal processing that occurs in the laboratory using an already calibrated instrument/process.


  • Report Results: EPA assumes that each of the 5,700 respondents will require 1.0 hours to report the results of the study to the PT Provider. The burden will be divided between a manager and records clerk.


  • Maintain Records: EPA assumes that a records clerk in each of the 5,700 laboratories will require 0.1 hours to maintain the files from the PT study.


Table 6.1 Estimated Annual Respondent Burdens for Proficiency Testing

Collection Activities

Annual # Respondents1

Burden

Manager

Chemist2

Record Clerk

Total Burden (hours/year)

hours /year

hours /year

hours /year

Per Respondent

All Respondents

Read Instructions

5,700

0.2

0.3

0

0.5

2,850

Plan activities

5,700

0.2

0.3

0

0.5

2,850

Analyze Chemistry/Microbiology

5,700

0

2.1

0

2.1

11,970

Analyze WET

5,700

0

2.4

0

2.4

13,680

Report Results

5,700

0.3

0

0.7

1

5,700

Maintain Records

5,700

0

0

0.1

0.1

570

Total

5,700

 

 

 

 

37,620

Total Annual # Responses:

5,700

Avg. Labor (hours) per Respondent:

6.6


1 In 2016 it is estimated that 5,700 NPDES permittees participated in the DMR-QA program. Most of the permittees participate in the Chemistry/Microbiology component. A smaller amount of permittees also participates in WET analysis. It is estimated that 4.77% of all labs participate in the WET analysis.

2 Refer to Appendix B for analysis times for Chemistry/Microbiology analytes and WET methods.

6(b) Estimating Respondent Costs

Table 6.2 shows the total annual average costs for laboratories over the 3-year ICR period. Average annual labor costs for all 5,700 permittees are estimated to be $1,919,931. Average annual O&M costs are estimated to be $3,194,052. EPA estimates each laboratory will incur an annual average labor plus non-labor cost of $885.24 for this data collection effort (see Table 6.2).

6(b)(i) Respondent Labor

The labor cost was arrived at by estimating the amount of labor required to participate on an annual basis in the DMR-QA study. Labor costs are based on information provided by the U.S. Department of Labor Statistics, May 2015, National Industry Specific Occupational Employment and Wage Estimate. The labor categories include a manager at an hourly rate of $57.77, a data entry clerical person at an hourly rate of $18.26, and a skilled technician or chemist to conduct the measurements at an hourly rate of $34.26. Table 6.2 lists the estimated burden and costs for labor related to each activity. The annual respondent labor cost, for all 5,700 respondents is estimated to be $1,919,931 for 37,620 hours. The labor costs take into account benefits/ compensation in addition to salary. EPA relies on the Bureau of Labor Statistics to estimate the benefits/compensation to be 30.7% of total compensation for management positions, 28.3% of total compensation for office positions, and 32.3% of total compensations for natural resource positions. See Table 6.2 for references.

6(b)(ii) Respondent Operation and Maintenance Costs

Operation and Maintenance (O&M) costs for laboratories include all costs related to providing personnel with the space, equipment and materials necessary to perform the tasks required by this ICR. Since laboratories are driven by their compliance monitoring requirements to purchase the analytical instrumentation and computers and not by this ICR, no capital costs are considered to be associated with this ICR. Only the costs associated with purchasing the PT standards is appropriate for consideration in this category.


Permittees may participate in the PT studies for some or all of the chemistry and microbiology analytes and WET test methods (refer to Appendix A for a list of chemistry and microbiology analytes and WET test methods). The cost of the PE samples varies with the costs for the chemical, microbiological, and WET testing required for each calendar year. This is complicated by the fact that the participants in any given study need not analyze all of the samples available for that study, only the ones that are required by their permits. EPA estimated a cost of $885.24 per laboratory based on feedback from PT Providers who did an analysis of the average cost of buying PE samples.


Because EPA does not have sufficient information to estimate how many analytes are contained in the PT samples sent to each laboratory, EPA assumes that a single PT sample contains standards for the top ten analytes for chemistry and microbiology and the top 10 WET test methods, based on information from the PT Providers. Therefore, laboratories participating in the chemistry and microbiology PT study are assumed to receive and run analyses for 10 analytes. Similarly, those participating in the PT study for WET would receive samples for each of 10 WET test methods. EPA estimates the costs of obtaining PT samples to be $885.24 per laboratory and $560.36 per permittee (respondent). Average annual O&M costs (fees for PE samples) for the respondents is estimated to be $3,194,052.


Table 6.2 Estimated Annual Respondent Costs for Proficiency Testing

Collection Activities

Labor Cost 1

Non-Labor Cost

Labor Plus Non-Labor

Manager 2

Chemist 3

Record Clerk 4

Labor Costs

Cost of Standards per PT Analysis5

Average Labor plus Non-Labor Costs

at $83.36/hr

at $50.61/hr

at $25.47/
hr

per Respondent

All Respondents

per Respondent

All Respondents

per Respondent

All Respondents

Read Instructions

$16.67

$15.18

$0.00

$31.85

$181,545

$0

$0

$31.85

$181,545

Plan activities

$16.67

$15.18

$0.00

$31.85

$181,545

$0

$0

$31.85

$181,545

Analyze Chemistry and Microbiology

$0.00

$106.28

$0.00

$106.28

$605,796

$488.68

$2,785,476

$594.96

$3,391,272

Analyze WET

$0.00

$121.46

$0.00

$121.46

$692,322

$71.68

$408,576

$193.14

$1,100,898

Report Results

$25.01

$0.00

$17.83

$42.84

$244,188

$0

$0

$42.84

$244,188

Maintain Records

$0.00

$0.00

$2.55

$2.55

$14,535

$0

$0

$2.55

$14,535

Total

 

 

 

$336.83

$1,919,931

$560.36

$3,194,052

$897.19

$5,113,983

1 Median salaries from U.S. Bureau of Labor Statistics (BLS), May 2015, National Industry Specific Occupational Employment and Wage Estimates (http://www.bls.gov/oes/). As a percentage of total compensation, BLS estimates benefits to be 30.7% for management positions, 32.3% for natural resource positions and 28.3% for office positions. (Employer Costs for Employee Compensation, December 2015, Table 5, http://www.bls.gov/news.release/archives/ecec_03102016.htm.)

2 BLS, Natural Science Manager 11-9121 ($57.77/hr, median salary only--see Footnote 1).

3 BLS, Chemist 19-2031 ($34.26/hr, median salary only--see Footnote 1).

4 BLS, Information and Record Clerk 43-4199 ($18.26/hr, median salary only--see Footnote 1).

5 Based upon estimated cost of $772 per chemistry/microbiology laboratory and $2,374 per WET laboratory. Includes a factor of 0.633 labs per respondent. WET analysis is multiplied by 0.0477 since only 4.77% of all labs perform WET tests. Therefore, the average cost spread out over all respondents is $2,374 * 0.633 * 0.0477 = $71.68.

6(b)(iii) Capital/Startup Operating and Maintenance (O&M) Costs

There are no Capital/Startup costs associated with this information collection. The annual Operating and Maintenance costs associated with this ICR are estimated to be $560.36 per respondent.

6(c) Estimating Agency Burden and Costs

EPA’s role is advisory and involves program management only. The burden to the Agency, other than the time required to put together the annual announcement and printing and mailing costs of the annual announcement, is low. On average, 3,000 announcements are printed annually to send out to permittees, PT Providers, state and regional coordinators as well as spare copies. This annual average is also a conservative estimate because in 2013 EPA began distributing announcements by e-mail when possible. The annual burden is estimated below:


  • Maintaining records of active participants in the program: 80 hours

  • Putting together the annual announcement and answering questions: 480 hours (40 hours/month)

  • Cost of printing 3,000 announcements: $1,920

  • Cost of mailing announcements: $3,360

  • Total annual burden and cost to EPA: 560 hours and $5,280

6(d) Estimating the Respondent Universe and Total Burden and Costs

The respondents for this ICR are major and select minor NPDES permittees. Some or all permittees in states that have received EPA waivers from the DMR-QA program may not be required to participate. Permittees who participate may use contract laboratories to perform the work, but the burden is considered to be upon the permittees, since they bear the costs of labor and operations & maintenance. As itemized in section 6(b), the annual respondent burden is 6.6 hours and $897.19 per participant. The total annual respondent burden is 37,620 hours and $5,113,983 for 5,700 participants. Currently, there are 7 PT Providers. PT Providers’ burdens are not assessed in this ICR because their cost burden for this ICR is part of the estimated PE sample cost burden for the laboratories. Burden and costs to EPA is minimal, being limited to the drafting of the annual announcement and printing/mailing costs, which come to a total of 560 hours and $5,280 on an annual basis.

6(e) Bottom Line Burden Hours and Cost Tables

The bottom line burden hours and costs for this ICR are shown in Table 6.3. This includes the burden and costs to the 5,700 respondents that are affected by this ICR.


Table 6.3 Bottom Line Burden and Costs for ICR period (2017-2019)

Cost / Burden

Total Across Three ICR Years (2017-2019)

Average Per Year over ICR Years (2017-2019)

Number of Respondents (Permittees)

5,700

5,700

Total Responses

17,100

5,700

Number of Responses per Permittee

3

1

Burden Hours per Permittee

19.8

6.6

Total Burden Hours (all 5,700 Permittees)

112,860

37,620

Per Permittee Labor Costs

$1,010.49

$336.83

Total Labor Costs (all 5,700 Permittees)

$5,759,793

$1,919,931

Per Permittee O&M Costs

$1,681.08

$560.36

Total O&M Costs (all 5,700 Permittees)

$9,582,156

$3,194,052

Total Costs (Labor plus O&M costs for all 5,700 permittees)

$15,341,949

$5,113,983

6(f) Reasons for Change in Burden

Participation in the DMR-QA PE study has increased from an estimated average of 5,509 to 5,700 since the last renewal of this ICR. This is due to increased discretionary selection of NPDES minor permit holders for DMR-QA participation in the most recent year.


Labor and Operation & Maintenance costs have been updated since the previous renewal of this ICR. Labor costs increased modestly due to changes in employee benefit compensation costs and inflation. Non-labor costs for obtaining proficiency test samples also increased, although the total burden hours per respondent remained the same. Operation & Maintenance costs reflect the costs of obtaining PE samples from the PT Providers. The estimated average cost of obtaining PE samples increased from $431.41 to $560.36 per respondent.

6(g) Burden Statement

The average annual respondent burden for each permittee is estimated to be 6.6 hours per response. This estimate includes the total time, effort, or financial resources expended by permittees to gather and report information, and develop and maintain record.


Burden Statement: The annual public reporting and recordkeeping burden for this collection of information is estimated to average 6.6 hours per response. Burden means the total time, effort, or financial resources expended by persons to generate, maintain, retain, or disclose or provide information to or for a Federal agency. This includes the time needed to review instructions; develop, acquire, install, and utilize technology and systems for the purposes of collecting, validating, and verifying information, processing and maintaining information, and disclosing and providing information; adjust the existing ways to comply with any previously applicable instructions and requirements; train personnel to be able to respond to a collection of information; search data sources; complete and review the collection of information; and transmit or otherwise disclose the information. An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. The OMB control numbers for EPA's regulations are listed in 40 CFR part 9 and 48 CFR chapter 15.


To comment on the Agency's need for this information, the accuracy of the provided burden estimates, and any suggested methods for minimizing respondent burden, including the use of automated collection techniques, EPA has established a public docket for this ICR under Docket ID Number EPA-HQ-OECA-2013-0547, which is available for online viewing at www.regulations.gov, or in person viewing at the Enforcement and Compliance Docket in the EPA Docket Center (EPA/DC), EPA West, Room 3334, 1301 Constitution Avenue, NW, Washington, D.C. The EPA Docket Center Public Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through Friday, excluding legal holidays. The telephone number for the Reading Room is (202) 566-1744, and the telephone number for the Enforcement and Compliance Docket is (202) 566-1752. An electronic version of the public docket is available at www.regulations.gov. This site can be used to submit or view public comments, access the index listing of the contents of the public docket, and to access those documents in the public docket that are available electronically. When in the system, select “search,” then key in the Docket ID Number identified above. Also, you can send comments to the Office of Information and Regulatory Affairs, Office of Management and Budget, 725 17th Street, NW, Washington, D.C. 20503, Attention: Desk Officer for EPA. Please include the EPA Docket ID Number EPA-HQ-OECA-2013-0547 and OMB Control Number 2080-0021 in any correspondence.



APPENDIX A: LIST OF CHEMISTRY & MICROBIOLOGY ANALYTES AND WET TEST METHODS

Chemistry and Microbiology Analytes

Microbiology

Trace Metals

Escherichia coli (E. coli)

Aluminum

Fecal Coliform, MF or MPN

Antimony

Total Coliform, MF or MPN

Arsenic

Minerals

Barium

Alkalinity, total (CaCO3)

Beryllium

Chloride

Cadmium

Fluoride

Chromium, total

Hardness, total (CaCO3)

Chromium, hexavalent

Specific conductance (25°C)

Cobalt

Sulfate

Copper

Total Dissolved Solids (180°C)

Iron

Nutrients

Lead

Ammonia (as N)

Manganese

Nitrate (as N)

Mercury

Nitrite (as N)

Mercury (Low Level)

Orthophosphate (as P)

Molybdenum

Total Kjeldahl-Nitrogen (as N)

Nickel

Total Phosphorus (as P)

Selenium

Miscellaneous Analytes

Silver

Non-Filterable Residue (TSS)

Thallium

Oil and Grease

Vanadium

pH

Zinc

Total Cyanide

Demands

Total Phenolics (4-AAP)

5-day Biochemical Oxygen Demand (BOD5)

Total Residual Chlorine

Total Residual Chlorine (Low Level)

5-day Carbonaceous BOD (CBOD5)

Settleable Solids

Chemical Oxygen Demand (COD)

Turbidity

Total Organic Carbon (TOC)


WET Organisms/Test Conditions/End Points

 

 

 

Analyte Number

Organisms/Conditions

End Points

Test Code 13/EPA Method 2000

 

 

754

Fathead minnow (Pimephales promelas) - MHSF 25°C

LC50

Test Code 14/EPA Method 2000

 

 

755

Fathead minnow (Pimephales promelas) - 20% DMW

LC50

Test Code 15/EPA Method 1000

 

 

756

Fathead minnow (Pimephales promelas) - MHSF

NOEC SURVIVAL

808

Fathead minnow (Pimephales promelas) - MHSF

IC25 (ON) GROWTH

810

Fathead minnow (Pimephales promelas) - MHSF

NOEC (ON) GROWTH

Test Code 16/EPA Method 1000

 

 

759

Fathead minnow (Pimephales promelas) - 20% DMW

NOEC SURVIVAL

812

Fathead minnow (Pimephales promelas) - 20% DMW

IC25 (ON) GROWTH

814

Fathead minnow (Pimephales promelas) - 20% DMW

NOEC (ON) GROWTH

Test Code 19/EPA Method 2002

 

 

764

Ceriodaphnia dubia - MHSF 25°C

LC50

Test Code 20/EPA Method 2002

 

 

765

Ceriodaphnia dubia - 20% DMW 25°C

LC50

Test Code 21/EPA Method 1002

 

 

766

Ceriodaphnia dubia - MHSF

NOEC SURVIVAL

767

Ceriodaphnia dubia - MHSF

IC25 REPRODUCTION

768

Ceriodaphnia dubia - MHSF

NOEC REPRODUCTION

Test Code 22/EPA Method 1002

 

 

769

Ceriodaphnia dubia - 20% DMW

NOEC SURVIVAL

770

Ceriodaphnia dubia - 20% DMW

IC25 REPRODUCTION

771

Ceriodaphnia dubia - 20% DMW

NOEC REPRODUCTION

Test Code 32/EPA Method 2021

 

 

788

Daphnia magna - MHSF 25°C

LC50

Test Code 38/EPA Method 2021

 

 

794

Daphnia pulex - MHSF 25°C

LC50

Test Code 42/EPA Method 2007

 

 

798

Mysid (Mysidopsis bahia) - 25°C

LC50

Test Code 43/EPA Method 1007

 

 

799

Mysid (Mysidopsis bahia)

NOEC SURVIVAL

816

Mysid (Mysidopsis bahia)

IC25 (ON) GROWTH

818

Mysid (Mysidopsis bahia)

NOEC (ON) GROWTH

Test Code 44/EPA Method 2006

 

 

803

Inland silverside (Menidia berylina) - 25°C

LC50

Test Code 45/EPA Method 1006

 

 

824

Inland silverside (Menidia berylina)

NOEC SURVIVAL

825

Inland silverside (Menidia berylina)

IC25 (ON) GROWTH

826

Inland silverside (Menidia berylina)

NOEC (ON) GROWTH

Test Code 46/EPA Method 2004

 

 

804

Sheepshead minnow (Cyprinodon variegatus) - 25°C

LC50

Test Code 47/EPA Method 1004

 

 

805

Sheepshead minnow (Cyprinodon variegatus)

NOEC SURVIVAL

820

Sheepshead minnow (Cyprinodon variegatus)

IC25 GROWTH

822

Sheepshead minnow (Cyprinodon variegatus)

NOEC (ON) GROWTH


APPENDIX B: LIST OF TOP CHEMISTRY & MICROBIOLOGY ANALYTES AND WET TEST METHODS AND TIMES FOR ANALYZING


CHEMISTRY/MICROBIOLOGY ANALYTE CHECKLIST



Rank

Analyte

Time (in minutes) for one analysis*





1

pH

10



2

Total Suspended Solids

30



3

Ammonia (as N)

5



4

Total Residual Chlorine

3



5

Biochemical Oxygen Demand (BOD)

45



6

Carbonaceous BOD

45



7

Total Phosphorus as P

10



8

Settleable Solids

10



9

Fecal Coliform (MF)**

30



10

Oil and Grease

15



 

TOTAL (minutes)

203



 

TOTAL (hours)

3.38




* These estimates assume the DMR-QA sample is being added as additional single analyses to an already calibrated instrument/process, and to the normal processing that occurs in the laboratory.


** 24 hours for incubation


2.1 hours per permittee for Chemistry/Microbiology

 



using ratio of 0.633 labs per permittee








WET ORGANISMS/TEST CONDITIONS/END POINTS CHECKLIST


Rank

Analyte

Time (hours) for one analysis***

type of test



1

Fathead minnow - MHSF - NOEC Survival

10

Chronic


2

Fathead minnow - MHSF - NOEC (ON) Growth

10

Chronic


3

Ceriodaphnia - MHSF - NOEC Survival

10

Chronic


4

Fathead minnow - MHSF 25°C - LC50

3

Acute


5

Fathead minnow - MHSF - IC25 (ON) Growth

10

Chronic


6

Ceriodaphnia - MHSF - NOEC Reproduction

10

Chronic


7

Ceriodaphnia - MHSF - IC25 Reproduction

10

Chronic


8

Ceriodaphnia - MHSF 25°C - LC50

3

Acute


9

Fathead minnow - MHSF 20°C - LC50

3

Acute


10

Mysid - 40 fathoms - NOEC Survival

10

Chronic


 

TOTAL (hours)

79

 



*** based on set-up, maintenance, data crunching at conclusion, 10 hr (chronic) also includes daily weighting







50.0 hours for WET analysis per lab using ratio of 0.633 labs per permittee


because only 4.77% of labs do WET analyses, the following number will be used for time burden for WET tests:


2.4 hours for WET analysis




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