U.2. REGULATORY FRAMEWORK

The basic framework for controlling air pollutants in the United States is mandated by the 1970 Clean Air Act (CAA) and its amendments, Environmental Protection Agency (EPA) regulations, including the 1999 Regional Haze Regulations, and state and local air quality regulations. The CAA addresses criteria air pollutants, state and national ambient air quality standards for criteria air pollutants, and the Prevention of Significant Deterioration (PSD) program. The Regional Haze Regulations address visibility impairment. EPA regulations address ambient air quality standards for criteria pollutants, emission control technology, air quality monitoring, and State Implementation Plan (SIP) development (which may include air quality modeling), and air quality related value (AQRV) analyses related to regional haze.

Ambient Air Quality Constituents

Air pollutants addressed in this study include criteria pollutants, hazardous air pollutants (HAP), and sulfur and nitrogen compounds, which could cause visibility impairment or atmospheric deposition impacts.

Criteria Pollutants

Criteria pollutants are those for which national standards of concentration have been established. Ambient air concentrations of these constituents greater than the standards represent a risk to human health. Criteria pollutants include carbon monoxide (CO), nitrogen dioxide (NO2), sulfur dioxide (SO2), ozone (O3), particulate matter (PM10, PM2.5), and lead, each of which is listed below.

Carbon Monoxide.

CO is an odorless, colorless gas formed during any combustion process, such as operation of engines, fireplaces, and furnaces. High concentrations of CO affect the oxygen-carrying capacity of the blood and can lead to unconsciousness and asphyxiation. Wildfires are natural sources of CO.

Nitrogen Dioxide.

NO2 is a red-brown gas formed during the operation of internal combustion engines or other burning processes. Such processes emit a mixture of nitrogen gases, collectively called nitrogen oxides (NOx). NOx can contribute to brown cloud conditions and can convert to ammonium nitrate particles and nitric acid, which can cause visibility impairment and acid rain. Bacterial action in soil can be a natural source of nitrogen compounds.

Sulfur Dioxide.

SO2 forms during combustion from trace levels of sulfur in coal or diesel fuel. It can convert to ammonium sulfate and sulfuric acid, which can cause visibility impairment and acid rain. Volcanoes are natural sources of SO2. Anthropogenic sources include refineries and power plants.

Ozone.

O3 is a gas that generally is not emitted directly into the atmosphere, but is formed from the chemical reactions of NOx and volatile organic compound (VOC) emissions. As stated above, internal combustion engines are the main source of NOx, while sources of VOCs include, but are not limited to, leaks from oil and gas development operations (“fugitive” emissions), paint, varnish, and various types of vegetation. The faint acrid smell common after thunderstorms is caused by ozone formation caused by lightning. Ozone is a strong oxidizing chemical that can burn lungs and eyes, as well as damage plants.

Particulate Matter.

Particulate matter (e.g., soil particles, hair, pollen) are essentially small particles suspended in the air that settle to the ground slowly and may be re-suspended if disturbed. Separate allowable concentration levels for particulate matter are based on the relative size of the particle:

Lead.

Before the widespread use of unleaded fuel in automobiles, lead particles were emitted from automobile tailpipes. Lead is not considered in this RMP and EIS because no proposed projects are expected to emit lead. The lead standard also will not be addressed in this appendix because lead is not a current concern; it will, however, be considered in future projects. Lead is also generally not considered in site specific environmental analysis for similar reasons.

Hazardous Air Pollutants

Although HAPs, including N-hexane, ethylbenzene, toluene, xylene, formaldehyde, and benzene, do not have ambient air quality standards, the EPA has issued reference concentrations for evaluating the inhalation risk for cancerous and noncancerous health impacts, known as reference concentrations for chronic inhalation.

The EIS associated with the Bighorn Basin RMP is a National Environmental Policy Act (NEPA) document and not a regulatory document, but the Record of Decision (ROD) is binding and a “public record” (see 40 Code of Federal Regulations [CFR] 1505.2). In addition, there are regulatory issues that should be taken into account in preparing this EIS and ensuing project-specific EISs. Actual regulation of HAPs is achieved through compliance with the applicable maximum achievable control technology (MACT) standards and not through ambient air quality standards. Regulatory agencies implement control through Section 112 programs, specifically Section 112(g) case-by-case MACT determinations based on 40 CFR Part 63, Subpart B, and Section 112(d) MACT emission standards.

Any source that emits or has the potential to emit 10 tons per year or more of any HAP or 25 tons per year or more of any combination of HAPs is considered a major source and will require a Title V, Part 70, operating permit review and permit. This may include either a case-by-case 112(g) MACT determination, if the source is new or has had major modifications and no applicable MACT emission standard has been promulgated, or compliance with an applicable MACT emission standard. Specific regulations that may apply in the Planning Area include 40 CFR Part 63 Subpart HH, National Emission Standards for Hazardous Air Pollutants From Oil and Natural Gas Production Facilities; 40 CFR Part 63 Subpart HHH, National Emission Standards for Hazardous Air Pollutants From Natural Gas Transmission and Storage Facilities; and 40 CFR Part 63 Subpart ZZZ, National Emission Standards for Hazardous Air Pollutants for Stationary Reciprocating Internal Combustion Engines. This last regulation, new in 2004, affects source categories using reciprocating engines for gas compression. HAP emissions are associated with industrial activities, such as oil and gas operations, refineries, paint shops, dry cleaning facilities, and woodworking shops. Because this analysis is qualitative, no specific analyses of either short- or long-term HAP impacts are made.

Atmospheric Deposition Constituents

Sulfur and nitrogen compounds that can be deposited in terrestrial and aquatic ecosystems include nitric acid, nitrate, ammonium, and sulfate. Nitric acid and nitrate are not emitted directly into the air, but form in the atmosphere from industrial and automotive emissions of NOx. Sulfate is formed in the atmosphere from industrial emission of SO2. Deposition of nitric acid, nitrate, and sulfate can adversely affect plant growth, soil chemistry, lichens, aquatic environments, and petroglyphs. Ammonium is primarily associated with feedlots and agricultural fertilization. Ammonium deposits can affect terrestrial and aquatic vegetation. Although deposition may be beneficial as a fertilizer, it can adversely affect the timing of plant growth and dormancy. Although this analysis will be qualitative, future specific projects will require quantitative analyses using the criteria listed below.

Wyoming and National Ambient Air Quality Standards

Wyoming Ambient Air Quality Standards (WAAQS) and National Ambient Air Quality Standards (NAAQS) are health-based standards that identify maximum limits for criteria air pollutant concentrations at all locations to which the public has access. The WAAQS and NAAQS are legally enforceable standards. Concentrations above the WAAQS and NAAQS represent a risk to human health that by law, require public safeguards be implemented. State standards must be at least as protective of human health as federal standards, and may be more restrictive than the federal standards as allowed by the CAA. The EPA has developed standards for each pollutant for a specific averaging time (See Table U-1). Short averaging times (1, 8, and 24 hours) address short-tem exposure, while the annual standards address long-term exposure.

Table U.1. National and Wyoming Ambient Air Quality Standards

Pollutant

Averaging Time

NAAQS

WAAQS

(ppm)

(ppb)

(µg/m3)

(ppm)

(ppb)

(µg/m3)

Carbon Monoxide
(CO)

1 hour1

35

35,000

40,000

35

35,000

40,000

8 hour1

9

9,000

10,000

9

9,000

10,000

Nitrogen Dioxide
(NO2)

1 hour2

0.10

100

188.7

N/A

N/A

N/A

Annual(Arithmetic Mean)

0.053

53

100

0.053

53

100

Ozone (O3)

8 hour3

0.075

75

147

0.075

75

147

PM10

24 hour4

N/A

N/A

150

N/A

N/A

150

Annual

N/A

N/A

N/A

N/A

N/A

50

PM2.5

24 hour5

N/A

N/A

35

N/A

N/A

65

Annual6

N/A

N/A

15

N/A

N/A

15

Sulfur Dioxide (SO2)

1 hour7

0.075

75

195

N/A

N/A

N/A

3 hour

N/A

N/A

N/A

0.5

500

1,300

24 hour1

0.140

140

365

0.099

99

260

Annual(Arithmetic Mean)

0.031

31

80

0.023

23

60

1Not to be exceeded more than once per year.

2To attain this standard, the 3-year average of the 98th percentile of 1-hour concentrations at each monitor within an area must not exceed 100 ppb.

3To attain this standard, the 3-year average of the fourth-highest daily maximum 8-hour average ozone concentrations measured at each monitor within an area over each year must not exceed 75 ppb.

4Not to be exceeded more than once per year on average over 3 years.

5To attain this standard, the 3-year average of the 98th percentile of 24-hour concentrations at each population-oriented monitor within an area must not exceed 35 µg/m3.

6To attain this standard, the 3-year average of the weighted annual mean PM2.5 concentrations from single or multiple community-oriented monitors must not exceed 15.0 µg/m3.

7To attain this standard, the 3-year average of the 98th percentile of 1-hour concentrations at each monitor within an area must not exceed 100 ppb.

N/A not applicable

NAAQS National Ambient Air Quality Standards

WAAQS Wyoming Ambient Air Quality Standards

PM2.5 particulate matter less than 2.5 microns in diameter

PM10 particulate matter less than 10 microns in diameter

ppm parts per million

ppb parts per billion

µg/m3 micrograms per cubic meter


Prevention of Significant Deterioration

The goal of the PSD program is to ensure that air quality in areas with clean air does not significantly deteriorate, while a margin for future industrial growth is maintained. Major stationary sources are governed by the PSD program, which is unlikely to apply to BLM sources in the Planning Area with the exception of gas compressor stations. Under the PSD program, each area in the United States is classified by the air quality in that region according to the following system:

PSD Class I Areas. Areas with pristine air quality, such as wilderness areas, national parks, and some Native American reservations, are accorded the strictest protection. Only very small incremental increases in pollutant concentrations are allowed in order to maintain the very clean air quality in these areas.

PSD Class II Areas. Essentially, all areas that are not designated as Class I are designated as Class II. Moderate incremental increases in pollutant concentrations are allowed, although the concentrations are not allowed to reach the concentrations set by Wyoming and federal standards (WAAQS and NAAQS).

PSD Class III Areas. No areas have been designated yet as Class III. A larger incremental increase in pollutant concentrations would be allowed, up to the applicable WAAQS and NAAQS.

The incremental increases allowed for specific pollutants in Class I and Class II areas can be found in the Wyoming Air Quality Standards and Regulations (Wyoming DEQ 2004). Comparisons of potential PM10, NO2, and SO2 concentrations with PSD increments are intended to evaluate a threshold of concern only and do not represent a regulatory PSD increment consumption analysis. Regulatory PSD increment consumption analyses are solely the responsibility of the State of Wyoming, which has been granted primacy (with EPA oversight) under the CAA. In project-specific EISs, the BLM does not expect that a PSD analysis will be performed; rather, the PSD standards are used as a reference only to give the public a better understanding of the level of potential impact.

Regional Haze Regulations

Visibility impairment in the form of regional haze obscures the clarity, color, texture, and form of what we see. Haze-causing pollutants (mostly fine particles) are directly emitted into the atmosphere or are formed when gases emitted into the air form particles as they are carried downwind. Emissions from human-caused and natural sources can be carried great distances, contributing to regional haze. The Wyoming Department of Environmental Quality (DEQ)–Air Quality Division (AQD) originally submitted its Regional Haze SIP in accordance with 40 CFR, Part 51.309, in December 2003. This SIP emphasized reductions in SO2 emissions with a goal of improving visibility on the Colorado Plateau. Since its submission, EPA revised 40 CFR, Parts 51.308 and 309 based on legal actions, and a revised 309 SIP was submitted by Wyoming DEQ in November 2008. A draft supplemental revision to the 309 SIP was prepared in August 2009 and is currently under review.

The EPA developed regional haze regulations in response to the CAA amendments of 1977 and 1990. These regulations are intended to maintain visibility on the least-impaired days and to improve visibility on the most-impaired days in mandatory federal Class I areas across the United States, so that visibility in these areas is returned to natural conditions by the year 2064. These regulations require states to submit a regional haze SIP and progress reports to demonstrate reasonable progress toward the 2064 goal. Additional information on the analysis performed in the EIS is found in Section 6 Emissions Calculations.

Applicability to the Planning Area

Air pollution impacts are limited by local, state, tribal, and federal air quality regulations, standards, and implementation plans established under the CAA and administered by the Wyoming DEQ AQD with oversight from the EPA. Air quality regulations require that proposed new, or modified existing, air pollutant emission stationary sources (including oil and gas compression facilities) undergo a permitting review before their construction can begin. Therefore, the Wyoming DEQ AQD has the primary authority and responsibility to review permit applications and to require emission permits, fees, and control devices before construction or start of operation. Fugitive dust and exhaust from construction activities, along with air pollutants emitted during operation (for example, well operations, booster and pipeline compressor engines associated with natural gas wells), are potential causes of air quality impacts. These issues are more likely to generate public concern where natural gas development activities occur near residential areas or near sensitive Class I and Class II areas.

The United States Forest Service (USFS), the National Park Service, and the United States Fish and Wildlife Service (USFWS), located throughout Wyoming, also have expressed concerns about potential atmospheric deposition (acid rain) and visibility impacts within downwind PSD Class I and PSD Class II sensitive areas under their administrations.

Table U-2 provides a summary of recent air quality conditions for SO2, NO2, ozone, PM10, and PM2.5, taken from measurements for the period 2007-2009 from available monitors located within or nearby the planning area. These include maximum 24 hour and annual averages for SO2 and PM2.5, maximum 1 hour averages for NO2, maximum annual averages for PM10, and the 4th highest 8-hour average ozone concentration for each year, from which the ozone design value is derived. Except for a relatively high measured 24-hour average concentration of PM2.5 at the Lander site, located outside the Planning Area, most concentrations measured during this period are well within the applicable standards. Given the Planning Area’s current attainment status, future development projects that have the potential to emit more than 250 tons per year of any criteria pollutant (or certain listed sources that have the potential to emit more than 100 tons per year) would be required to undergo a site-specific regulatory PSD increment consumption analysis under the federal New Source Review permitting regulations. Development projects that require PSD permits also may be required by the applicable air quality regulatory agencies to incorporate additional emission control measures (including a best available control technology [BACT] analysis and determination) to ensure protection of air quality resources and to demonstrate that the combined impacts of all PSD sources will not exceed the allowable incremental air quality impacts for NO2, PM10, and SO2. Minor sources having emissions below the cutoff rates mentioned above do not require PSD permits; nevertheless, their emissions consume increment. A regulatory PSD increment consumption analysis may be conducted, either as part of a New Source Review or independently. The determination of PSD increment consumption is a legal responsibility of the applicable air quality regulatory agencies, with EPA oversight. In addition, an analysis of cumulative impacts due to all existing sources and the permit applicant’s sources is required during a New Source Review to demonstrate that applicable ambient air quality standards will be met during the operational lifetime of the permit applicant’s operations.

Sources subject to the PSD permit review procedure also are required to demonstrate potential impacts on AQRV. These include visibility impacts, degradation of mountain lakes due to atmospheric deposition (acid rain), and impacts on sensitive flora and fauna in Class I areas. The CAA also provides specific visibility protection procedures for the mandatory federal Class I areas designated by the United States Congress on August 7, 1977, which included wilderness areas greater than 5,000 acres in size, as well as national parks and national memorial parks greater than 6,000 acres in size as of that date.

Table U.2. Recently Observed SO2, NO2, O3, PM10, and PM2.5 Concentrations Within and in the Vicinity of the Planning Area and Applicable Air Quality Standards

Pollutant/Monitoring Site (ID)

Average Time/Measurement

2006

2007

2008

NAAQS

Sulfur Dioxide (SO2) (ppm)

Sheridan – BLM

24 hours

Annual

0.00058

0.00023

0.00052

0.00024

0.00045

0.00018

0.140

0.031

Nitrogen Dioxide (NO2) (ppb)

Thunder Basin Grassland

1 hour

21

14

14

100

Ozone (O2) (ppb)

Thunder Basin

8 hours (4th high)

72

66

62

75

PM10)(μg/m3)

Cody

24 hours

55

91

78

150

Sheridan – Highland Park

24 hours

60

49

27

150

Sheridan – Police Station

24 hours

168

103

99

150

PM2.5)

North Absoraka*

Annual

3.1

2.3

1.8

15

Lander

Annual

7.5

7.6

8.3

15

Thunder Basin*

Annual

4.6

3.9

3.2

15

Buffalo

Annual

3.4+

3.4+

3.6

15

Cloud Peak*

Annual

3.2

2.2

1.9

15

Sheridan – Highland Park

Annual

6.3

5.5

6.0

15

Sheridan – Police Station

Annual

9.5

8.0

8.4

15

Sheridan – BLM

Annual

3.2+

1.7+

1.3

15

North Absoraka*

24 hours

21.2

9.3

5.0

15

Lander

24 hours

34.9

24.2

37.8

35

Thunder Basin*

24 hours

17.8

15.1

6.7

35

Buffalo

24 hours

19+

25+

10

35

Cloud Peak*

24 hours

22

10.1

5.4

35

Sheridan – Highland Park

24 hours

30.5

19.3

25.9

35

Sheridan – Police Station

24 hours

34.8

27.4

38.6

35

Sheridan – BLM

24 hours

25

20

6

35

*Data summaries obtained from Regional Haze Rule computations on the Visibility Information Exchange Web Site (VIEWS) (VIEWS 2009).

+Computed minus 2nd quarter data.

BLM Bureau of Land Management

N/A not available

NAAQS National Ambient Air Quality Standards

PM2.5 particulate matter less than 2.5 microns in diameter

PM10 particulate matter less than 10 microns in diameter

ppb parts per billion

ppm parts per million

µg/m3 micrograms per cubic meter