Environmental Defense Fund v. U.S. Environmental Protection Agency

CourtDistrict Court, D. Montana
DecidedJanuary 27, 2021
Docket4:21-cv-00003
StatusUnknown

This text of Environmental Defense Fund v. U.S. Environmental Protection Agency (Environmental Defense Fund v. U.S. Environmental Protection Agency) is published on Counsel Stack Legal Research, covering District Court, D. Montana primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Environmental Defense Fund v. U.S. Environmental Protection Agency, (D. Mont. 2021).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF MONTANA GREAT FALLS DIVISION

ENVIRONMENTAL DEFENSE FUND;

MONTANA ENVIRONMENTAL 4:21-cv-03-BMM INFORMATION CENTER; and CITIZENS

FOR CLEAN ENERGY,

ORDER Plaintiffs,

vs.

U.S. ENVIRONMENTAL PROTECTION AGENCY; and ANDREW R. WHEELER, in his official capacity as Administrator of the U.S. Environmental Protection Agency,

Defendants.

INTRODUCTION Environmental Defense Fund (“EDF”), Montana Environmental Information Center (“MEIC”), and Citizens for Clean Energy (“CCE”) (collectively, “Plaintiffs”) brought this action against the U.S. Environmental Protection Agency (“EPA”) and Andrew R. Wheeler in his official capacity as Administrator of EPA (“Federal Defendants”) to challenge an EPA rulemaking. (Doc. 1). Plaintiffs allege two counts: that the final rule itself was unlawful; and that EPA’s decision to make the final rule effective on publication was unlawful. (Doc. 1 at 10–13). Plaintiffs filed a Motion to Expedite their Motion for Partial Summary Judgment. (Doc. 7). Plaintiffs also filed concurrently a Motion for Partial

Summary Judgment centered on the effective date count. (Doc. 8). Plaintiffs seek an order declaring unlawful and setting aside EPA’s decision to make the final rule effective immediately and declaring that the final rule should remain ineffective

until 30 days from its publication date. (Doc. 8 at 1–2; Doc. 9 at 3–4). Plaintiffs proposed an expedited briefing schedule for their summary judgment motion. (Doc. 7 at 3). Federal Defendants disagreed with the justification for expedited resolution, but asserted they would “nevertheless agree with the

briefing schedule set forth” in Plaintiffs’ motion. (Doc. 16 at 1). The Court granted the Motion to Expedite. (Doc. 18). The Motion for Partial Summary Judgment proves fully briefed and ripe. (Docs. 8, 9, 24, 27).

BACKGROUND Factual Background President Richard Nixon established EPA in 1970 “to make a coordinated attack on the pollutants which debase the air we breathe, the water we drink, and

the land that grows our food.” Reorganization Plan No. 3 of 1970 (July 9, 1970). William D. Ruckelshaus, the first EPA Administrator, further elaborated that EPA has a “broad responsibility for research, standard-setting, monitoring and enforcement with regard to five environmental hazards: air and water pollution, solid waste disposal, radiation, and pesticides.” EPA’s First Administrator on Establishment of EPA, Press Release (Dec. 16, 1970).

EPA’s mission remains “to protect human health and the environment.” EPA achieves that mission through the implementation of these core environmental laws: the Clean Air Act (“CAA”), 42 U.S.C. §§ 7401–7671q; the Clean Water Act

(“CWA”), 33 U.S.C. §§ 1251–1387; the Safe Drinking Water Act (“SDWA”), 42 U.S.C. §§ 300f–300j-26; the Toxic Substances Control Act (“TSCA”), 15 U.S.C. §§ 2601–2697; the Emergency Planning and Community Right-to-Know Act (“EPCRA”), 42 U.S.C. §§ 11001–11050; and the Federal Insecticide, Fungicide,

and Rodenticide Act (“FIFRA”), 7 U.S.C. §§ 136–136y, among others. EPA implements these substantive environmental statutes by establishing quantitative limits and standards to protect public health and the environment.

Congress directed EPA through those statutes to use the “latest,” “generally accepted,” and “best available” science to inform the agency’s decisions. For one example, the CAA requires EPA to establish science-based standards to control air pollution to protect public health and welfare. See 42 U.S.C. § 7401(b)(1); Am.

Lung Ass’n v. Envtl. Prot. Agency, No. 19-1140, 2021 WL 162579, at *25–*26 (D.C. Cir. Jan. 19, 2021) (describing the purpose and history of the CAA). EPA sets air pollution standards known as air quality criteria that must

“accurately reflect the latest scientific knowledge.” 42 U.S.C. § 7408(a)(2). EPA must consider “all identifiable effects [of air pollutants] on public health and welfare” and “include information” on certain science-based factors “to the extent

practicable” when it establishes air quality criteria. Id. EPA must then use these criteria to adopt National Ambient Air Quality Standards (“NAAQS”) at levels requisite to protect public health with an adequate margin of safety. See id. §

7409(b). The CAA further requires EPA to evaluate health risks and effects of hazardous air pollutants (“HAPs”) and to set emission standards to reduce such risks using science-based considerations. See id. § 7412. As part of the residual risk requirements, EPA also must investigate and report on “the actual health

effects with respect to persons living in the vicinity of sources,” and “any available epidemiological or other health studies” regarding the effects of HAPs. Id. § 7412(f)(1)(C).

EPA relies on a wide range of scientific research to implement its standards and rules. Such research includes epidemiological studies that use dose-response data to link exposure to a pollutant, contaminant, or substance to a public health or environmental harm. Some of these epidemiological studies—particularly studies

that examine small populations or populations with unique health challenges—use data that includes confidential medical or other personally identifiable information. Such information could be used to identify study participants. Federal law

generally prohibits public disclosure of these data to protect the privacy of those who participated in those studies. See, e.g., Health Insurance Portability and Accountability Act (“HIPAA”) Privacy Rules, 45 C.F.R. Parts 160 and 164,

Subparts A & E (establishing safeguards to protect the privacy of personal health information, and setting limits and conditions on the uses and disclosures that may be made of such information without patient authorization); 21st Century Cures

Act, 42 U.S.C. § 241 (requiring government agencies to provide a certificate of confidentiality to protect the privacy of individuals participating in certain research); Privacy Act of 1974, 5 U.S.C. § 552a (precluding disclosure of personally identifiable information or records by government agencies except in

very limited enumerated circumstances). As a result, public health researchers frequently make confidential the data that underlies their findings. The scientific community has developed

methodologies, such as peer review, to validate the result of studies even when the underlying data remains unavailable publicly. See Jeremy Berg, Philip Campbell, Veronique Kiermer, Natasha Raikhel & Deborah Sweet, Joint Statement on EPA Proposed Rule and Public Availability of Data, Nature (Apr. 30, 2018). EPA long

has relied on these proven review mechanisms to ensure that the public health studies that underly regulatory decisions prove scientifically valid. The D.C.

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