Center for Biological Diversity v. Ross ( 2022 )


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  •                            UNITED STATES DISTRICT COURT
    FOR THE DISTRICT OF COLUMBIA
    CENTER FOR BIOLOGICAL
    DIVERSITY, et al.,
    Plaintiffs,
    v.                                        Civil Action No. 18-112 (JEB)
    GINA RAIMONDO, in her official capacity
    as Secretary of Commerce, et al.,
    Defendants,
    and
    MAINE LOBSTERMEN’S
    ASSOCIATION, et al.,
    Defendant-Intervenors.
    MEMORANDUM OPINION
    The lives of our vast oceans may appear timeless. Indeed, at the end of Moby-Dick, “the
    great shroud of the sea rolled on as it rolled five thousand years ago.” Not so, however, for many
    creatures who live there, including its greatest leviathans. For example, just around 370 North
    Atlantic right whales remain in existence. For centuries, these whales were imperiled by
    excessive hunting, but today the greatest human-caused threat comes from entanglement in
    fishing gear.
    Much of that gear is dropped into the ocean by crews fishing for lobster. Since the gear
    harms right whales, the Endangered Species Act requires that before Defendant National Marine
    Fisheries Service authorizes the fisheries under its management, it must issue a Biological
    Opinion finding that the fishery operations will not jeopardize the continued existence of the
    1
    right whale. As part of such a “no-jeopardy” BiOp, NMFS must issue an “incidental take
    statement” (ITS) authorizing the number, if any, of anticipated future killings or injuries of right
    whales.
    This Court has already once found a previous version of NMFS’s BiOp invalid for lack
    of an ITS and sent the agency back to the drawing board. In 2021, the Service released a new
    BiOp addressing how lobster and crab fishing off the Atlantic coast would affect the dwindling
    right-whale population. In this most recent BiOp, NMFS concluded that the fisheries under
    review would not jeopardize the continued existence of the whale despite acknowledging the
    expected potential harm to the species. In reaching this determination, the Service included an
    ITS in which it authorized no lethal taking of the whales, even though it projected that, at least in
    the near future, nearly three whales could be killed annually. NMFS, in consultation with a
    variety of stakeholders, and as mandated by the Marine Mammal Protection Act, also released a
    Final Rule that amended the specific rules that constituted the Atlantic Large Whale Take
    Reduction Plan.
    Three conservation groups have renewed their suit against the Department of Commerce,
    of which NMFS is a part. They argue that the new BiOp still does not satisfy the ESA and
    MMPA’s requirements, just as the Final Rule flunks the MMPA’s. Although the Court will not
    reach every shortcoming that Plaintiffs allege, it concurs that NMFS violated the ESA by failing
    to satisfy the MMPA’s “negligible impact” requirement before setting the authorized level of
    lethal take in its ITS. NMFS also breached the time requirements mandated by the MMPA in the
    2021 Final Rule. The Court will thus hold the 2021 Biological Opinion and the 2021 Final Rule
    to be invalid.
    2
    Cognizant of the potential effects of this ruling on the lobster industry — and on the
    economies of Maine and Massachusetts — and given the highly complex statutory and
    regulatory environment that this case involves, the Court orders no remedy here. Instead, it will
    offer the parties the opportunity for further briefing to articulate alternatives the Court may
    select.
    I.        Background
    The Court starts by laying out the framework of the two statutes most relevant to this case
    — the Marine Mammal Protection Act and the Endangered Species Act — before describing the
    factual and procedural background. As will be explained in more depth below, Plaintiffs’
    Complaints rely on the ESA, the MMPA, and the Administrative Procedure Act for different
    counts.
    Within this statutory scheme, NMFS plays an important role, as it is the agency within
    the Department of Commerce that “is responsible for the stewardship of the nation’s ocean
    resources and their habitat.” NOAA FISHERIES, About Us, https://bit.ly/3Nd7HP1 (last accessed
    June 22, 2022). This work includes implementing fishery-management plans and working to
    protect endangered marine species. See Oceana, Inc. v. Raimondo, 
    35 F.4th 904
    , 906 (D.C. Cir.
    2022). The American lobster and Jonah Crab fisheries fall under NMFS’s auspices as the
    Service adopts and implements “regulations compatible with the interstate fishery management
    plans” required by statute. See ECF No. 216-3 (Joint Appendix Vol. 3 “JA3”) at ECF p. 80.
    This implementation process includes “a federal permitting process for fishermen harvesting
    lobster in federal waters,” which are waters over three nautical miles from the shore extending to
    around two hundred nautical miles. See ECF No. 198-1 (State of Maine Cross-MSJ) at 4; see
    also 
    16 U.S.C. § 5103
     (requirements for state-federal cooperation in managing Atlantic coastal
    3
    fisheries). State waters, conversely, lie in the three nautical miles closest to shore. See ECF No.
    188-1 (Pls. MSJ) at 13. NMFS also issues and implements regulations under plans designed to
    reduce the killing and injury of certain marine mammals, including right whales. See 
    16 U.S.C. § 1387
    (f).
    A. Statutory Framework
    1. Marine Mammal Protection Act
    The MMPA was passed in 1972 in acknowledgment of the fact that “certain species and
    population stocks of marine mammals are, or may be, in danger of extinction or depletion as a
    result of man’s activities” and “should be protected and encouraged to develop to the greatest
    extent feasible commensurate with sound policies of resource management.” 
    16 U.S.C. § 1361
    (1) & (6). To that end, the Act “generally prohibits any individual from ‘taking’ a marine
    mammal.” Winter v. NRDC, 
    555 U.S. 7
    , 15 (2008). The MMPA defines to “take” as “to harass,
    hunt, capture, or kill, or attempt to harass, hunt, capture, or kill any marine mammal.” 
    16 U.S.C. § 1362
    (13); see also 
    50 C.F.R. § 216.3
     (explaining that “[t]ak[ing]” also includes “the doing of
    any other negligent or intentional act which results in disturbing or molesting a marine
    mammal”).
    Although the MMPA places “a moratorium on the taking and importation of marine
    mammals,” 
    16 U.S.C. § 1371
    (a), there are “several enumerated exceptions.” In re Polar Bear
    Endangered Species Act Listing and Section 4(d) Rule Litig., 
    720 F.3d 354
    , 357 (D.C. Cir.
    2013). Two in particular govern the incidental taking of marine mammals “in the course of
    commercial fishing operations” under the MMPA. See 
    16 U.S.C. § 1371
    (a)(2); see also 140
    Cong. Rec. 8609, 8761 (April 26, 1994) (statement of Senator Stevens that “in the case of
    threatened or endangered marine mammals, both section 101(a)(5)(E) and section 118 apply”).
    4
    Section 101(a)(5)(E)(i) permits the taking incidental to commercial fishing operations “of
    marine mammals from a species or stock designated as depleted because of its listing as an
    endangered species or threatened species” under the ESA if certain elements are satisfied. See
    
    16 U.S.C. § 1371
    (a)(5)(E)(i). Such taking may be allowed for a period of three years only if
    “after notice and opportunity for public comment,” NMFS finds that “the incidental mortality
    and serious injury from commercial fisheries will have a negligible impact on such species or
    stock.” 
    Id.
     § 1371(a)(5)(E)(i)(I) (emphasis added). Negligible impact, in this context, is “an
    impact resulting from [a] specified activity that cannot be reasonably expected to, and is not
    reasonably likely to, adversely affect the species or stock through effects on annual rates of
    recruitment or survival.” 
    50 C.F.R. § 216.103
    . This negligible impact will be one significant
    issue here. Section 101(a)(5)(E) also requires that a species-recovery plan be developed or be in
    process and that any monitoring program, vessel registration, or take-reduction plan required
    under section 118 of the MMPA be in place. See 
    16 U.S.C. § 1371
    (a)(5)(E)(i)(II)–(III).
    Section 118, meanwhile, imposes additional requirements governing the taking of marine
    mammals incidental to commercial fishing. For example, the Secretary must “develop and
    implement a take reduction plan designed to assist in the recovery or prevent the depletion of
    each strategic stock which interacts with [the relevant] commercial fisher[ies].” 
    Id.
     § 1387(f)(1).
    These take-reduction plans are developed by take-reduction teams and must include
    information on the number of animals being killed or seriously injured annually, recommended
    measures to reduce M/SI (mortality and serious injury) takings, and dates for achieving these
    goals. Id. §§ 1387(f)(4)–(f)(6). In this case, the plan is entitled the Atlantic Large Whale Take
    Reduction Plan (ALWTRP) and seeks to lower the incidental entanglement of several types of
    large whales, including right whales, in fishing gear. The MMPA requires that “[t]he immediate
    5
    goal of a take reduction plan . . . be to reduce, within 6 months of its implementation, the
    incidental mortality or serious injury of marine mammals incidentally taken in the course of
    commercial fishing operations to levels less than the potential biological removal level” for that
    marine mammal stock. Id. § 1387(f)(2). The potential biological removal (PBR) level is “the
    maximum number of animals, not including natural mortalities, that may be removed from a
    marine mammal stock while allowing that stock to reach or maintain its optimum sustainable
    population.” 
    50 C.F.R. § 229.2
    . The six-month deadline is another focus of the controversy
    here. Additionally, the “long-term goal” of a take-reduction plan is “to reduce, within 5 years of
    its implementation, the incidental mortality or serious injury of marine mammals incidentally
    taken in the course of commercial fishing operations to insignificant levels approaching a zero
    mortality and serious injury rate, taking into account the economics of the fishery, the
    availability of existing technology, and existing State or regional fishery management plans.” 
    16 U.S.C. § 1387
    (f)(2). A take-reduction plan must be amended “as necessary to meet the
    requirements of” the MMPA. 
    Id.
     § 13887(f)(7)(F).
    2. Endangered Species Act
    The ESA was passed in 1973 “to halt and reverse the trend toward species extinction,
    whatever the cost.” Nat’l Ass’n of Home Builders v. U.S. Fish and Wildlife Serv., 
    786 F.3d 1050
    , 1052 (D.C. Cir. 2015) (quoting Tenn. Valley Auth. v. Hill, 
    437 U.S. 153
    , 184 (1978)).
    The most salient of the Act’s provisions for this case are those ensuring that proposed federal
    actions will not threaten endangered species and that appropriate consultations occur to address
    such risks. Section 7(a)(2) of the ESA, for instance, states that “[e]ach Federal agency shall . . .
    insure that any action authorized, funded, or carried out by such agency . . . is not likely to
    jeopardize the continued existence of any endangered species.” 
    16 U.S.C. § 1536
    (a)(2). To
    6
    carry out this task, the accompanying regulations state that “[e]ach Federal agency shall review
    its actions at the earliest possible time to determine whether any action may affect listed
    species.” 
    50 C.F.R. § 402.14
    (a). If that is the case, the relevant agency (known as the “action
    agency” because it is the one proposing the action) must consult with a “consulting agency,”
    which conducts the expert analysis on how the proposed action will affect the survival of the
    relevant endangered species and the effects on its habitat. Id.; Conservation Law Found. v. Ross,
    
    422 F. Supp. 3d 12
    , 16–17 (D.D.C. Oct. 28, 2019). This consulting agency is either the U.S.
    Fish and Wildlife Service or the National Marine Fisheries Service. United States Fish &
    Wildlife Serv. v. Sierra Club, Inc., 
    141 S. Ct. 777
    , 784 (2021). Here, both the “action agency”
    and the “consulting agency” were divisions of NMFS, with the former being NMFS’s
    Sustainable Fisheries Division, and the latter its Protected Resources Division. See JA3 at ECF
    p. 8; 
    id.
     at ECF p. 80 (when NMFS itself is “proposing an action[,] . . . the agency must conduct
    intra-service consultation”).
    The aim of this process is for the consulting agency to assess whether the action will
    violate section 7(a)(2)’s prohibition on jeopardizing the continued existence of endangered and
    threatened species. The process culminates in a “biological opinion” to be issued by the
    “consulting agency,” not the agency proposing the action. See 
    50 C.F.R. § 402.14
    (e). “In
    formulating a Biological Opinion, FWS and NMFS must ‘use the best scientific and commercial
    data available.’” Oceana, Inc. v. Pritzker, 
    75 F. Supp. 3d 469
    , 475 (D.D.C. 2014) (citing 
    16 U.S.C. § 1536
    (a)(2)). The BiOp issued can either be “a ‘jeopardy’ biological opinion” or “a ‘no
    jeopardy’ biological opinion” depending on whether the action under review is “likely to
    jeopardize the continued existence of a listed species” or harm a “critical habitat.” 
    16 U.S.C. § 402.14
    (h)(1)(iv). “[I]f a ‘jeopardy’ biological opinion is issued, the agency must either
    7
    implement the reasonable and prudent alternatives [proposed by the consulting agency],
    terminate the action altogether, or seek an exemption” for their project. United States Fish &
    Wildlife Serv., 141 S. Ct. at 784; see also 
    50 C.F.R. § 402.15
    .
    In this case, the 2021 BiOp issued by the Protected Resources Division was a “no
    jeopardy” biological opinion. See JA3 at ECF p. 162. When a “no jeopardy” BiOp issues — or
    when there are reasonable and prudent alternatives to the proposed action — a project may
    proceed, but the BiOp must include what is known as an “incidental take statement” addressing
    certain elements of the project’s potential to “take” a species. See 
    50 C.F.R. § 402.14
    (i). Much
    like the MMPA, the ESA defines to “take” as “to harass, harm, pursue, hunt, shoot, wound, kill,
    trap, capture, or collect, or to attempt to engage in any such conduct.” 
    16 U.S.C. § 1532
    (19); see
    also 
    50 C.F.R. § 222.102
     (definition also includes “significant habitat modification or
    degradation which actually kills or injures fish or wildlife by significantly impairing essential
    behavioral patterns, including, breeding, spawning, rearing, migrating, feeding or sheltering”).
    The information that an agency must produce regarding “take” is laid out below:
    If after consultation under subsection (a)(2), the Secretary concludes
    that —
    (A) the agency action will not violate such subsection [i.e.,
    through a no-jeopardy BiOp], or offers reasonable and
    prudent alternatives which the Secretary believes would not
    violate such subsection;
    (B) the taking of an endangered species or a threatened
    species incidental to the agency action will not violate such
    subsection; and
    (C) if an endangered species or threatened species of a
    marine mammal is involved, the taking is authorized
    pursuant to section 1371(a)(5) of [the MMPA, discussed
    below];
    the Secretary shall provide the Federal agency and the applicant
    concerned, if any, with a written statement that —
    (i) specifies the impact of such incidental taking on the
    species,
    8
    (ii) specifies those reasonable and prudent measures that the
    Secretary considers necessary or appropriate to minimize
    such impact,
    (iii) in the case of marine mammals, specifies those measures
    that are necessary to comply with section 1371(a)(5) of [the
    MMPA] with regard to such taking, and
    (iv) sets forth the terms and conditions (including, but not
    limited to, reporting requirements) that must be complied
    with by the Federal agency or applicant (if any), or both, to
    implement the measures specified under clauses (ii) and (iii).
    
    16 U.S.C. § 1536
    (b)(4).
    This section creates two sets of requirements for the written incidental-take statement.
    First, there are antecedent conditions laid out in subsections (A) through (C) that must be
    satisfied before an agency can even issue an ITS. Second, there are certain elements that the ITS
    must include, which are articulated in 
    16 U.S.C. § 1536
    (b)(4)(i)–(iv). See also 
    50 C.F.R. § 402.14
    (i). Of the most relevance here is the third antecedent condition to issuing an ITS: that
    an agency cannot do so unless the amount of projected incidental take from the project is
    authorized under section 101(a)(5) of the Marine Mammal Protection Act, which, as earlier
    discussed, requires that the taking have no more than a negligible impact on the species. See 
    16 U.S.C. §§ 1536
    (b)(4)(C), 1371(a)(5); see also 
    50 C.F.R. § 402.14
    (i)(1) (requiring an ITS “[i]n
    those cases where the [expert agency] concludes that an action (or the implementation of any
    reasonable and prudent alternatives) and the resultant incidental take of listed species will not
    violate section 7(a)(2) and, in the case of marine mammals, where the taking is authorized
    pursuant to section 101(a)(5) of the Marine Mammal Protection Act of 1972”).
    Overall, ITSs serve several functions. Since the ESA makes it unlawful to “take” a
    species except in certain circumstances, an ITS “constitutes a permit authorizing the action
    agency to ‘take’ the endangered or threatened species” up to the level specified in the ITS “so
    long as [the action agency] respects the” terms and conditions with which the ITS states it must
    9
    comply. Bennett v. Spear, 
    520 U.S. 154
    , 170 (1997). Additionally, “[i]f the amount or extent of
    taking specified in the incidental take statement is exceeded,” then an agency must reinitiate
    Section 7 consultations, another long-standing issue at play in this case. See 
    50 C.F.R. § 402.16
    (a)(1).
    B. Factual and Procedural History
    Well before the elaborate scheme of environmental protections just described was
    enacted, the North Atlantic right whale was so named because it was the right whale to hunt.
    The species has thus long been in peril. Indeed, it has been listed as endangered since 1970,
    predating even the passage of the ESA. See JA3 at ECF p. 101. Although the right-whale
    population has fluctuated over time, new scientific evidence in 2017 showed that its numbers had
    been declining for nearly a decade. See ECF 202-2 (Fed. Dfts. Cross-MSJ) at 9. As of January
    2019, the population was estimated at 368, a considerable drop from 481 just eight years prior.
    See JA3 at ECF p. 103. There are likely even fewer today. See Pls. MSJ at 3 (citing New
    England Aquarium, North Atlantic Right Whale Consortium Report Card, https://bit.ly/3t6FbqS
    (last visited June 3, 2022)). Given these limited numbers, “even one additional death a year
    increases the odds that the right whale will go extinct.” District 4 Lodge of the Int’l Ass’n of
    Machinists and Aerospace Workers Local Lodge 207 v. Raimondo, 
    18 F.4th 38
    , 41 (1st Cir.
    2021).
    Although a variety of factors have precipitated this decline, “the two major known human
    causes of mortality are vessel strikes and entanglement in fishing gear.” JA3 at ECF p. 104.
    Between 2010 and 2018, there were 107 entanglements of the North Atlantic right whale, nearly
    half of which resulted in mortality or serious injury. 
    Id.
     at ECF p. 119. Vertical-line fishing gear
    poses a particular threat to the whales, as they can become trapped in ropes stretching down from
    10
    the water’s surface to the ocean floor. Among the types of vertical-line fishing gear are trap/pot
    gear, used for catching lobsters and Jonah crabs, and gillnets, which are used to catch various
    types of fish. Ctr. for Biological Diversity v. Ross, No. 18-112, 
    2020 WL 1809465
    , at *5
    (D.D.C. Apr. 9, 2020) (CBD I). Of the two, entanglement in trap/pot gear is far deadlier for right
    whales. See JA3 at ECF p. 122.
    1. Case Background
    As will be explained below, this case has washed up on this Court’s shores several times.
    Plaintiffs — the Center for Biological Diversity, Defenders of Wildlife, and Conservation Law
    Foundation — first sued in January 2018 challenging the 2014 BiOp and subsequent agency
    action. See ECF No. 1 (Compl.). Although four claims were initially raised, the case was
    resolved on only one of them — namely, the fact that the 2014 BiOp did not include an ITS and
    included instead only a numerical trigger for how many right whales would need to be killed
    before ESA section 7 consultations would be reinitiated. In April 2020, this Court found that
    “the Service’s failure to include an ITS in its 2014 BiOp,” despite the relatively high rate of
    lethal take anticipated, was “about as straightforward a violation of the ESA as they come.”
    CBD I, 
    2020 WL 1809465
    , at *10. It thus “declare[d] the 2014 BiOp to be invalid under the
    Endangered Species Act.” 
    Id.
     In a subsequent Opinion in August 2020, the Court addressed the
    appropriate remedy. Because NFMS was already in the process of amending the Atlantic Large
    Whale Take Reduction Plan and crafting a new Biological Opinion, this Court vacated the 2014
    BiOp, but held that relief should be stayed until May 31, 2021, to allow for completion of those
    two documents. Ctr. for Biological Diversity v. Ross, 
    480 F. Supp. 3d 236
    , 240 (D.D.C. 2020)
    (CBD II). Amendments to the ALWTRP are issued through the notice-and-comment rulemaking
    11
    process, while the BiOp analyzes the effect that the consulting agency projects that particular
    actions will have on threatened species.
    2. 2021 BiOp and Incidental Take Statement
    On May 27, 2021, NMFS issued its new Biological Opinion. See JA3 at ECF p. 75. This
    2021 BiOp authorized fishing in an “action area” encompassing federal waters in which “ten
    fisheries operate” between Maine and Key West, Florida. See JA3 at ECF p. 93; 
    id.
     at ECF p. 85
    (proposed action is authorization of ten fisheries). This area spans the American portion of the
    North Atlantic right whales’ habitat; true to their name, these whales “are primarily found in the
    western North Atlantic, from their calving grounds in lower latitudes off the coast of the
    southeastern United States to their feeding grounds in higher latitudes off the coast of New
    England and Nova Scotia.” 
    Id.
     at ECF p. 102. Given climate change, however, the whales’
    habitat has shifted northward as of late following the movement of their main food sources —
    zooplankton and copepods — to cooler waters. 
    Id.
     at ECF p. 119; see also Fed. Dfts. Cross-MSJ
    at 8–9.
    Within the scope of the 2021 BiOp’s analysis — in addition to the authorization of
    fisheries — was a proposal developed to reduce the lethal taking of North Atlantic right whales
    to near zero by 2030 under a four-part scheme. See Fed. Dfts. Cross-MSJ at 18. This proposal is
    known as the North Atlantic Right Whale Conservation Framework for Federal Fisheries in the
    Greater Atlantic Region (the Framework). See JA3 at ECF p. 86.
    Even accounting for the effects of this Framework, however, NMFS still projects in the
    2021 BiOp that the population of right whales will continue to decline during the coming decade.
    In particular, it estimates that even after implementation of the modifications in the Final Rule
    proposed to the ALWTRP, several right whales will be killed or severely injured annually in
    12
    trap/pot fisheries and gillnets. An estimated 2.69 entanglements per year leading to mortality or
    serious injury (M/SI incidents) for right whales are expected to occur in federal fisheries in 2022,
    although this rate will gradually decline to 2.61 in 2023–2025 and to 0.136 per year by 2030.
    See JA3 at ECF p. 146. Of these entanglements, 2.56 would occur from the trap/pot fisheries
    associated with lobstering and crabbing until 2025. 
    Id.
     Although these rates of M/SI
    entanglement are still below the average of 4.7 per year between 2010 and 2018 (4.57 of which
    were in trap/pot gear), 
    id.,
     they nonetheless remain well above the right whale’s potential
    biological removal level (PBR) at least for the next few years. Currently for right whales that
    level is just 0.8 M/SI per year. See 
    86 Fed. Reg. 51,970
    , 51,971 (Sept. 17, 2021).
    Despite these findings, the 2021 BiOp nonetheless “conclude[s] that right whale
    entanglements due to the operation of the federal fisheries will not result in an appreciable
    reduction in the likelihood of survival and recovery of North Atlantic right whales compared to
    the no federal fishery scenario.” JA3 at ECF p. 162. As a result, it determined that “the
    proposed action, including the implementation of the Framework, is not likely to jeopardize the
    continued existence of North Atlantic right whales.” 
    Id.
     Additionally, in the ITS accompanying
    the BiOp, NMFS states that it is “authorizing zero lethal take of these whales because the lethal
    incidental take of ESA-listed whales has not been authorized under section 101(a)(5) of the
    MMPA.” 
    Id.
     at ECF p. 165. The ITS also includes an “exemption for non-lethal take of North
    Atlantic [right whales]” of up to 9.14% of the species’ population. 
    Id.
     at ECF pp. 165–66. If
    either the lethal or non-lethal take threshold is exceeded, then consultations must be reinitiated
    under section 7 of the ESA. 
    Id.
     at ECF p. 165.
    NMFS does acknowledge, however, that “further efforts are necessary to reduce
    interactions between authorized federal fisheries and large whales in order to achieve the
    13
    MMPA’s goal of insignificant levels of incidental mortality and serious injury of marine
    mammals approaching a zero mortality and serious injury rate” and that it will continue to work
    towards the “zero mortality goal” through the Framework. 
    Id.
     The ITS, which clearly reflects
    the expenditure of considerable effort by NMFS, also includes reasonable and prudent measures,
    monitoring protocols, and other features aimed at minimizing incidental take. 
    Id.
     at ECF pp.
    167–173.
    3. 2021 Final Rule
    In September 2021, NMFS released the Final Rule amending the Atlantic Large Whale
    Take Reduction Plan. See 
    86 Fed. Reg. 51,970
    . The changes in this rule represent the first
    phase of the Framework discussed above. See JA3 at ECF p. 88.
    The ALWTRP was issued in 1997 in fulfillment of NMFS’s obligations under section
    118 of the MMPA. 
    Id.
     at ECF p. 185. It is the product of consultations by the Take Reduction
    Team (TRT), which consists of “representatives from the fishing industry, state and Federal
    resource management agencies, the scientific community, and conservation organizations,”
    including Plaintiffs, and was first convened in 1996. See Fed. Dfts. Cross-MSJ at 9. The
    ALWTRP has been amended over time to meet the conservation needs of right whales, including
    most recently in the 2021 Final Rule, which arose from a reinitiation of consultation by the TRT
    members in 2017. 
    Id.
     (discussing need to reconvene TRT in wake of “unusual mortality event”
    for right whales). The 2021 Final Rule creates two new seasonal restricted areas for fishing and
    expands others. See 
    86 Fed. Reg. 52,019
    –23. The Rule also includes new requirements on
    trap/pot gear to reduce the potential harm from entanglements, including by preventing buoy
    lines from floating on the surface, reducing the number of lines that can be placed per trawl, and
    14
    requiring the insertion of weak links that will break more easily if a whale becomes entangled.
    Id. at 52,017–19. These changes went into effect last month.
    This new Rule comes into play against the backdrop of the importance of lobster fishing
    to the economies of several states along the Atlantic seaboard. In particular, in coastal Maine,
    “the lobster supply chain has an economic impact . . . of $1 billion annually” and benefits
    numerous fishermen and their families. See Maine Cross-MSJ at 11; see also ECF No. 206
    (Massachusetts Lobstermen’s Association’s Opposition (MALA Opp.)) at 9–11 (discussing
    economic and labor effects of trap/pot fishing on coastal Massachusetts communities).
    C. Current Suit
    Despite all of the efforts incorporated in the new 2021 BiOp and the Final Rule amending
    the ALWTRP, Plaintiffs remain dissatisfied. They thus filed an Amended Complaint in
    September 2021. See ECF No. 171 (Am. Compl.). In total, Plaintiffs now raise six claims: they
    believe that the final two counts from their original 2018 Complaint remain live, and they present
    four new causes of action in the Amended Complaint. For the sake of consistency with the
    parties, the original numbering of these claims is maintained. The extant counts are thus: III) the
    BiOp violates the ESA by allowing for the unpermitted take of North Atlantic right whales; IV)
    NMFS’s actions violate the MMPA and APA because the required “negligible impact” finding
    has not been made under section 101(a)(5)(E) of the MMPA; V) the BiOp is unlawful under the
    APA and ESA because it fails to consider the full effects of the agency action by focusing on too
    limited a geographic area and too large a time span; VI) NMFS has failed to issue a lawful
    incidental-take statement for the right whales in contravention of the APA and ESA; VII) the
    Final Rule violates the APA and MMPA as it does not “reduce right whale mortality and serious
    injury to below PBR within six months,” as required under 
    16 U.S.C. § 1387
    (f); and VIII) the
    15
    Court should compel NMFS to address its “ongoing failure to reduce right whale mortality and
    serious injury in the lobster fishery to below PBR within the timeline mandated by the MMPA,”
    as failure to do so is an unreasonable delay under the APA. See Compl., ¶¶ 130–39 (Counts III–
    IV); Am. Compl., ¶¶ 130–56 (Counts V–VIII).
    Finally, the parties involved remain nearly the same as in this case’s earlier iterations. In
    addition to the Maine Lobstermen’s Association and the Massachusetts Lobstermen’s
    Association, who were both Defendant-Intervenors initially, the State of Maine and the Maine
    Lobstering Union have now intervened as well. See ECF Nos. 98 (Maine Lobstering Union’s
    Motion to Intervene) and 172 (Maine’s Motion to Intervene).
    II.    Legal Standard
    Plaintiffs, Federal Defendants, the State of Maine, and the Maine Lobstermen’s
    Association have all cross-moved for summary judgment. The APA provides the standard of
    review for Plaintiffs’ claims, although some are brought under the APA and MMPA, others
    invoke the APA and the ESA, and one names the ESA alone. Nat’l Ass’n of Home Builders v.
    Norton, 
    415 F.3d 8
    , 13 (D.C. Cir. 2005) (APA provides standard of review in ESA cases);
    NRDC v. Evans, 
    279 F. Supp. 2d 1129
    , 1142 (N.D. Cal. 2003) (“[A]ctions challenged under the
    MMPA are reviewed under the APA . . . .”).
    “[W]hen a party seeks review of agency action under the APA [before a district court], . . .
    the district judge sits as an appellate tribunal.” Rempfer v. Sharfstein, 
    583 F.3d 860
    , 865 (D.C.
    Cir. 2009) (alteration in original) (quoting Am. Bioscience, Inc. v. Thompson, 
    269 F.3d 1077
    ,
    1083 (D.C. Cir. 2001)). In other words, “[t]he entire case on review is a question of law.” 
    Id.
    (quoting Marshall Cty. Health Care Auth. v. Shalala, 
    988 F.2d 1221
    , 1226 (D.C. Cir. 1993)).
    16
    The APA requires courts to “hold unlawful and set aside agency action, findings, and
    conclusions” that are “arbitrary, capricious, an abuse of discretion, or otherwise not in
    accordance with law.” 
    5 U.S.C. § 706
    (2)(A). Such “arbitrary and capricious” review applies to
    Counts IV, VI, and VII in this case, which are the ones the Opinion examines. Agency action is
    arbitrary and capricious if, for example, the agency “entirely failed to consider an important
    aspect of the problem, offered an explanation for its decision that runs counter to the evidence
    before the agency, or is so implausible that it could not be ascribed to a difference in view or the
    product of agency expertise.” Motor Vehicle Mfrs. Ass’n of U.S., Inc. v. State Farm Mut. Auto.
    Ins. Co., 
    463 U.S. 29
    , 43 (1983). “‘The scope of review [in an APA case] is narrow and a court
    is not to substitute its judgment for that of the agency,’ provided the agency has ‘examine[d] the
    relevant data and articulate[d] a satisfactory explanation for its action including a rational
    connection between the facts found and the choice made.’” Airmotive Eng’g Corp. v. FAA, 
    882 F.3d 1157
    , 1159 (D.C. Cir. 2018) (second and third alterations in original) (quoting State Farm,
    
    463 U.S. at 43
    ). While the court “may not supply a reasoned basis for the agency’s action that
    the agency itself has not given, [it] will uphold a decision of less than ideal clarity if the agency’s
    path may reasonably be discerned.” Bowman Transp., Inc. v. Ark.-Best Freight Sys., Inc., 
    419 U.S. 281
    , 285–86 (1974) (citation omitted) (citing SEC v. Chenery Corp., 
    332 U.S. 194
    , 196
    (1947); then citing Colo. Interstate Gas Co. v. FPC, 
    324 U.S. 581
    , 595 (1945)). It is only these
    “certain minimal standards of rationality” to which a reviewing court holds an agency. Nat’l
    Env’t. Dev. Ass’n’s Clean Air Project v. EPA, 
    686 F.3d 803
    , 810 (D.C. Cir. 2012) (quoting
    Ethyl Corp. v. EPA, 
    541 F.2d 1
    , 36–37 (D.C. Cir. 1976) (en banc)).
    When reviewing an agency’s interpretation of a law it administers, a court must apply the
    principles of Chevron U.S.A., Inc. v. Natural Resources Defense Council, Inc., 
    467 U.S. 837
    17
    (1984). See Se. Ala. Med. Ctr. v. Sebelius, 
    572 F.3d 912
    , 916 (D.C. Cir. 2009). Under Chevron,
    the first step is to “examine the statute de novo, ‘employing traditional tools of statutory
    construction.’” Nat’l Ass’n of Clean Air Agencies v. EPA, 
    489 F.3d 1221
    , 1228 (D.C. Cir.
    2007) (quoting Chevron, 
    467 U.S. at
    843 n.9); see also Mount Royal Joint Venture v.
    Kempthorne, 
    477 F.3d 745
    , 754 (D.C. Cir. 2007) (court begins by “applying customary rules of
    statutory interpretation”). “If the intent of Congress is clear, that is the end of the matter; for the
    court, as well as the agency, must give effect to the unambiguously expressed intent of
    Congress.” Chevron, 
    467 U.S. at
    842–43; see also Eagle Broadcasting Group, Ltd. v. FCC, 
    563 F.3d 543
    , 552 (D.C. Cir. 2009) (if the “search for the plain meaning of the statute . . . yields a
    clear result, then Congress has expressed its intention as to the question, and deference is not
    appropriate”) (internal citation and quotations omitted); Ark. Dairy Coop. Ass’n, Inc. v. U.S.
    Dep’t of Agric., 
    573 F.3d 815
    , 829 (D.C. Cir. 2009) (no deference due where agency’s
    construction is “contrary to clear congressional intent”).
    If, however, “the statute is silent or ambiguous with respect to the specific issue,”
    Chevron, 
    467 U.S. at 843
    , the analysis proceeds to “determine the deference, if any, [the court]
    owe[s] the agency’s interpretation of the statute.” Mount Royal Joint Venture, 
    477 F.3d at 754
    .
    Under this step, “[i]f Congress has explicitly left a gap for the agency to fill, there is an express
    delegation of authority to the agency to elucidate a specific provision of the statute by regulation.
    Such legislative regulations are given controlling weight unless they are arbitrary, capricious, or
    manifestly contrary to the statute.” Chevron, 
    467 U.S. at
    843–44. Where a “legislative
    delegation to an agency on a particular question is implicit rather than explicit,” 
    id. at 844
    , a
    court must uphold any “‘reasonable interpretation made by the administrator’ of that agency.”
    18
    Am. Paper Inst., Inc. v. EPA, 
    996 F.2d 346
    , 356 (D.C. Cir. 1993) (quoting Chevron, 
    467 U.S. at 844
    ).
    In this case, however, the Court can terminate its analysis at step one of Chevron, as the
    intent of Congress with respect to the relevant sections of the MMPA and ESA is clear. NMFS,
    moreover, never invokes Chevron deference for its interpretations.
    III.    Analysis
    Despite the numerous claims and statutes at play, the Court need only reach two issues to
    resolve this case because those are enough to find the 2021 Final Rule and 2021 BiOp invalid.
    First, it addresses whether the incidental-take statement accompanying the 2021 BiOp
    appropriately authorized zero lethal take of the North Atlantic right whale despite not satisfying
    the relevant sections of the MMPA and ESA. Second, it turns to whether the 2021 Final Rule
    amending the Atlantic Large Whale Take Reduction Plan met certain requirements laid out in the
    MMPA. Although neither question is an easy cruise, the Court ultimately determines that each
    action cannot stand.
    A. Lethal Take
    Plaintiffs’ allegations of infirmities in the lethal-take portion of the ITS accompanying
    the 2021 BiOp arise in two counts — one regarding the MMPA and another the ESA. First, they
    claim in Count IV of their original Complaint that NMFS’s BiOp violates the MMPA and APA
    by allowing for the “unauthorized take” of right whales since the Service “authorize[d] operation
    of the fishery” without first making the findings required under the MMPA. See Compl.,
    ¶¶ 130–39. Although Count IV was originally brought in the context of the 2014 BiOp,
    Plaintiffs have maintained that it remains live given that they believe that the 2021 BiOp also did
    not include a valid ITS. See ECF No. 141 (Plaintiffs’ Motion to Enforce Opinions and Orders)
    19
    at 17. Additionally, in Count VI of the Amended Complaint, Plaintiffs allege that the 2021 BiOp
    has not met the conditions necessary “[t]o authorize incidental take under the ESA” for an
    endangered marine mammal and that the BiOp “fails to include a lawful ITS for th[e] anticipated
    lethal take of right whales.” Am. Compl., ¶¶ 140, 143.
    Diving into these two counts requires an understanding of what has occurred before. In a
    prior Opinion this Court concluded that NMFS had violated the ESA by failing to issue an ITS at
    all when the taking of an endangered species was anticipated. CBD I, 
    2020 WL 1809465
    , at *8.
    At that time, the Service recognized that under the ESA it was required “to find that any take
    would not violate § 101(a)(5) of the MMPA” and it “had been ‘unable to [so] find.’” Id.
    (alteration in original) (internal citations omitted). Thus, “[f]aced with the choice of issuing no
    BiOp (and therefore closing the lobster fishery) or issuing a BiOp without an ITS, NMFS
    reasonably chose the latter.” ECF No. 82 (NMFS 2019 Cross-MSJ) at 3. Now, NMFS faces the
    same dilemma but has tried a new approach. Rather than not issuing an ITS, it has published one
    in which it authorized zero lethal take of right whales but still did not first satisfy the
    requirements of section 101(a)(5). As will be explained in depth below, this approach still leaves
    NMFS out to sea for several reasons.
    1. Antecedent “negligible impact” requirement
    The Court first anchors its reasoning more firmly in the statutory and regulatory
    requirements that underlie its conclusion. As described above, NMFS must “[f]ormulate a
    statement concerning incidental take, if such take is reasonably certain to occur,” and it has done
    so. See 
    50 C.F.R. § 402.14
    (g)(7); JA3 at ECF p. 164–65. Before issuing an ITS for an
    “endangered species or threatened species of a marine mammal,” moreover, the relevant agency
    must find that “the taking is authorized pursuant to” section 101(a)(5) of the MMPA, as codified
    20
    at 
    16 U.S.C. § 1371
    (a)(5). See 
    16 U.S.C. § 1536
    (b)(4); see also 
    50 C.F.R. § 402.14
     (biological
    opinion must include incidental-take statement when incidental take is “authorized pursuant to
    section 101(a)(5) of the Marine Mammal Protection Act of 1972”). The text of the ESA makes
    clear that this is an antecedent requirement, stating that “[i]f . . . the Secretary concludes that”
    “the taking is authorized” under the MMPA, then “the Secretary shall provide” an ITS. See 
    16 U.S.C. § 1536
    (b)(4) (emphasis added).
    Section 101(a)(5) of the MMPA, meanwhile, permits the Secretary of Commerce to
    “allow the incidental, but not the intentional, taking [by U.S. vessels or validly permitted vessels]
    . . . of marine mammals” from an endangered or threatened species only if the Secretary
    determines, among other elements, that “the incidental mortality and serious injury from
    commercial fisheries will have a negligible impact on such species or stock.” 
    16 U.S.C. § 1371
    (a)(5)(E)(i) (emphasis added). The need for such a finding is consistent with the MMPA’s
    overall aim of reducing M/SI rates for marine mammals to near zero. See, e.g., 
    16 U.S.C. § 1387
    (a)(1) (goal of zero M/SI rate by May 2001); 
    16 U.S.C. § 1371
    (a)(2) (aiming for
    incidental M/SI rates to be “reduced to insignificant levels approaching a zero mortality and
    serious injury rate”). Under the 2021 BiOp projections, however, “the incidental mortality and
    serious injury from commercial fisheries” will not have “a negligible impact” on the right-whale
    population in coming years, as NMFS projects that levels of M/SI take from trap/pot gear in
    federal fisheries will in fact exceed the potential biological replacement level for right whales
    until 2030.
    Unable to satisfy the negligible-impact threshold, but nonetheless having been instructed
    to issue an ITS, NMFS found itself in rough waters. It decided to “authoriz[e] zero lethal take of
    these whales because the lethal incidental take of ESA-listed whales has not been authorized
    21
    under section 101(a)(5) of the MMPA.” JA3 at ECF p. 165. NMFS maintains that this “is
    entirely consistent with the ESA, the MMPA, and pertinent caselaw.” ECF No. 214 (Fed. Dfts.
    Reply) at 12. Defendant-Intervenors echo this argument, explaining that “NMFS’s approach . . .
    reasonably balances its obligations to comply with both this Court’s order” in April 2020 to issue
    an ITS and the requirements of MMPA section 101(a)(5)(E), which NMFS cannot currently
    meet. See ECF No. 204-1 (Maine Lobstermen’s Association’s (MELA) Cross-MSJ) at 23; see
    also Maine Cross-MSJ at 22–23. Plaintiffs, however, rejoin that “NMFS cannot simply cite its
    inability to comply with the MMPA as an excuse for violating the ESA by failing to issue the
    required ITS for anticipated lethal take.” Pls. MSJ at 26.
    The Court agrees with the conservation groups. The ESA does not provide for such a
    workaround if taking cannot be authorized under section 101(a)(5)(E). Prior to issuing an ITS,
    NMFS was required to work with stakeholders to develop a plan under which the level of M/SI
    take was not “reasonably likely to[. . .] adversely affect the species or stock through effects on
    annual rates of recruitment or survival.” 
    50 C.F.R. § 216.103
    . Exactly how NMFS should have
    achieved this goal is a matter of some dispute. The Service finds itself caught between the devil
    and the deep blue sea given that the low numbers of right whales mean that almost any action
    will have more than a “negligible impact” on the species. Plaintiffs, however, maintain that
    “Congress gave NMFS all the authority it needed to bring right whale M/SI in the lobster fishery
    to the point of negligible impact through the Plan amendments.” ECF No. 210 (Pls. Reply/Opp.)
    at 15. The Maine Lobstermen’s Association, meanwhile, argues that had NMFS “objectively
    evaluated” take from the American lobster fishery, rather than projecting a “hypothetical ‘worst
    case scenario,’” it might “very well have been able to issue an incidental take authorization under
    MMPA Section 101(a)(5)(E).” MELA Cross-MSJ at 23; see also Maine Lobstermen’s
    22
    Association v. National Marine Fisheries Service, No. 21-2509, ECF No. 1-1 (Complaint),
    ¶¶ 54–91. Potential fixes are an issue for another day.
    For now, it is clear that NMFS did not satisfy the antecedent “negligible impact”
    requirement, and it cannot make up for its failure to do so by setting the level of lethal take
    authorized at zero. See, e.g., Wash. Toxics Coal. v. EPA, 
    413 F.3d 1024
    , 1032 (9th Cir. 2005)
    (“[A]n agency cannot escape its obligation to comply with the ESA merely because it is bound to
    comply with another statute that has consistent, complementary objectives.”); see also CBD I,
    
    2020 WL 1809465
    , at *9 (“[T]he ESA and accompanying regulations . . . require that the ITS
    find that any take resulting from the proposed agency action will . . . no[t] run afoul of
    § 101(a)(5) of the MMPA.”). If the action under review could not be authorized under the
    MMPA, then the agency “was obligated to revise its action to ensure any anticipated take would
    be lawfully authorized and appropriately minimized” to meet the antecedent requirement. See
    Pls. Reply/Opp. at 15. This alone means that the BiOp cannot survive.
    2. Discrepancy between anticipated take and authorized take
    The flaws in NMFS’s attempt to work around the MMPA’s “negligible impact”
    requirement are further laid bare by the fact that this approach yields a discrepancy between the
    number of lethal takes the ITS authorizes (zero) and the number of M/SI takes that the 2021
    BiOp projects will occur, especially in the early years of the Framework. See JA3 at ECF p. 166
    (setting lethal take at zero). Between 2022 and 2025 — during the first two phases of the
    Framework — NMFS anticipates that on average 2.56 M/SI incidents involving right whales will
    occur every year in trap/pot fisheries. Id. at ECF p. 146; Fed. Dfts. Cross-MSJ at 23. This
    period includes the implementation of the 2021 Final Rule amending the ALWTRP. The M/SI
    rates will improve over time, falling to an average rate of 0.136 M/SI incidents annually by 2030.
    23
    See JA3 at ECF p. 146. Although the Court commends NMFS for the significant reduction in
    M/SI incidents that this represents compared to years past, 2.56 M/SI incidents remains quite a
    bit more than the zero authorized under the BiOp. Id.
    Defendants wave away this discrepancy on the ground that “the ESA does not preclude
    NMFS from authorizing less than the estimated amount of take in an ITS” and cite cases in
    which the level of lethal take authorized was zero. See Fed. Dfts. Cross-MSJ at 24 & n.10; see
    also ECF No. 197 (Maine Lobstermen’s Union (MLU) Opp.) at 25–26. They are correct in the
    abstract that an agency certainly can issue an ITS that sets the rate of lethal take at zero. Pub.
    Emps. for Env’t Resp. v. Beaudreau, 
    25 F. Supp. 3d 67
    , 115 n.26 (D.D.C. 2014); Town of
    Superior v. U.S. Fish & Wildlife Serv., 
    913 F. Supp. 2d 1087
    , 1143 (D. Colo. 2012). When that
    happens, however, it is in circumstances where the agency does not anticipate that any lethal take
    will in fact occur. See, e.g., Beaudreau, 25 F. Supp. 3d at 114, 115 n. 26 (explaining that NMFS
    must set an authorized lethal-take level even if it “determined that [incidental] take [of right
    whales] would not occur” and whale strike had never occurred in the area, but that “[t]o be sure,
    ‘[t]hat limit may be zero; that is, a valid [incidental take statement] may exempt no take.’”
    (alterations in original) (quoting Town of Superior v. U.S. Fish & Wildlife Serv., 
    913 F. Supp. 2d 1087
    , 1143 (D. Colo. 2012)); WildEarth Guardians v. U.S. Forest Serv., No. 19-203, 
    2020 WL 2239975
    , at *1, *4 (D. Idaho May 7, 2020) (setting lethal-take level at zero when there was
    “remote” possibility of lethal taking of grizzly bear); see also Pls. Reply/Opp. at 16–17.
    Even outside the zero-lethal-take context, the level of take an ITS authorizes will usually
    roughly correspond to the amount of take actually anticipated. See, e.g., Mayo v. Jarvis, 
    177 F. Supp. 3d 91
    , 142 (D.D.C. 2016), amended, 
    203 F. Supp. 3d 31
     (D.D.C. 2016) (allowing
    incidental take of 3–4 bears based on projection from past data that 1.5 bears might be taken in
    24
    remaining action period); Oceana, Inc., 75 F. Supp. 3d at 493 (take limits for loggerhead turtles
    set by NMFS at the number of turtles estimated to be taken by dredge and trawl annually in
    BiOp); Defs. of Wildlife v. Dep’t of Navy, 
    733 F.3d 1106
    , 1112–13 (11th Cir. 2013) (explaining
    that ESA amended to include an ITS that would “specify[] the amount or extent
    of anticipated take”). Indeed, the last time this case was before the Court, NMFS set the lethal-
    take “reinitiation trigger” intended to substitute for an ITS at 3.25 since the 2014 BiOp
    concluded that “the lobster fishery ha[d] the potential to seriously injure or kill an average of
    3.25 right whales per year.” Compare ECF No. 88-6 (2020 Joint Appendix Volume 6) at ECF p.
    83 (noting M/SI entanglement level), with 
    id.
     at ECF p. 209 (setting reinitiation trigger). The
    regulations governing incidental-take statements also suggest a correspondence between the level
    of authorized take and the level of anticipated take. See 
    50 C.F.R. § 402.14
    (i)(1)(i) (ITS can use
    proxy to specify “the amount or extent of anticipated take” as long as ITS “sets a clear standard
    for determining when the level of anticipated take has been exceeded”).
    NMFS recognizes this contradiction but explains that because it “could not authorize the
    anticipated level of take,” it “was not able to issue an ITS authorizing, under the ESA, that level
    of anticipated take,” and instead its only option was “to issue a zero take ITS.” Fed. Dfts. Reply
    at 12. In other words, the Service agrees that, as a result of zero lethal take being authorized, if
    “a single lethal take or pro-rated M/SI is assigned to the federal fisheries considered in the 2021
    BiOp (including the lobster fishery), NMFS must reinitiate ESA Section 7 consultation.” Fed.
    Dfts. Cross-MSJ at 12; see also JA3 at ECF p. 166 n.391 (saying same).
    As a matter of pure practicality, this initially appears to make some sense. An ITS by
    regulation is a mechanism to ensure that consultations restart when “during the course of the
    action the amount or extent of incidental taking . . . is exceeded.” 
    50 C.F.R. § 402.14
    (i)(4).
    25
    Additionally, “the Incidental Take Statement functions as a safe harbor provision” for incidental
    killing of an endangered species. Ariz. Cattle Growers’ Ass’n v. U.S. Fish & Wildlife, Bureau
    of Land Mgmt., 
    273 F.3d 1229
    , 1239 (9th Cir. 2001). If lethal take is set at zero, then there is no
    safe harbor. If the goal is to protect right whales, then creating no safe harbor is clearly
    preferable to authorizing the actual anticipated take of two per year.
    The reinitiation-of-consultation requirement, however, is more limited than NMFS’s
    briefing suggests. If a new consultation begins, the Service is not required to “issue a new
    Biological Opinion [arising from that consultation] before the agency action may continue.”
    Env’t Prot. Info. Ctr. v. Simpson Timber Co., 
    255 F.3d 1073
    , 1076 (9th Cir. 2001); see Oceana
    v. Bureau of Ocean Energy Mgmt., 
    37 F. Supp. 3d 147
    , 175 n. 26 (D.D.C. 2014) (this Circuit
    does not require new BiOp to be issued pursuant to reinitiation of consultation before project
    may proceed, as Ninth Circuit caselaw on this “appear[s] in dicta and the relevant quotes are
    dropped in the legal standard sections with no explanation or citation whatsoever”); Defs. of
    Wildlife v. Bureau of Ocean Energy Mgmt., 
    684 F.3d 1242
    , 1253 (11th Cir. 2012) (cessation of
    action during consultation does not derive from ESA). Given that anticipated levels of M/SI take
    for right whales exceed zero in the coming years, it seems likely that whales will continue to be
    killed during the consultations.
    Yet NMFS never specifies whether and under what conditions activity in the American
    lobster fishery would go forward during the reinitiation-of-consultation period. Merely requiring
    that consultations restart if “a single lethal take or pro-rated M/SI is assigned to the federal
    fisheries,” Fed. Dfts. Cross-MSJ at 12, cannot loose NMFS from the net of its statutory
    obligations under the MMPA. Such a plan does not ensure that the action has a “negligible
    impact” on right whales or even that the lethal take of right whales in federal fisheries will
    26
    actually be zero, since a killing could occur in the midst of renewed consultations. To thus claim
    to authorize zero lethal take while in fact anticipating that such take will continue to occur “runs
    counter to the evidence before the agency” and is arbitrary and capricious. State Farm, 
    463 U.S. at 43
    .
    3. Judicial estoppel
    Last, NMFS maintains that Plaintiffs are judicially estopped from arguing that the 2021
    ITS unlawfully sets the incidental-lethal-take level at zero because “[i]n prior summary judgment
    filings, Plaintiffs urged the Court to find that NMFS should have done in the 2014 BiOp exactly
    what it did here” in so setting lethal take. See Fed. Dfts. Cross-MSJ at 26. NMFS further claims
    that this Court in a prior Opinion relied on Plaintiffs’ urging to set lethal take at zero, as did
    NMFS in formulating the 2021 BiOp. Id. at 27; see also CBD II, 480 F. Supp. 3d at 246
    (discussing potential of zero-lethal-take ITS).
    “[J]udicial estoppel ‘is an equitable doctrine invoked by a court at its discretion,’” with
    the intention of “prevent[ing] ‘improper use of judicial machinery’” by letting a party adopt a
    position contrary to what it has argued in a previous case. New Hampshire v. Maine, 
    532 U.S. 742
    , 750 (2001) (quoting first Russell v. Rolfs, 
    893 F.2d 1033
    , 1037 (9th Cir. 1990), then
    Konstantinidis v. Chen, 
    626 F.2d 933
    , 938 (D.C. Cir. 1980)). Courts look to “at least three
    questions . . . in deciding whether to apply judicial estoppel: (1) Is a party’s later position clearly
    inconsistent with its earlier position? (2) Has the party succeeded in persuading a court to accept
    that party’s earlier position, so that judicial acceptance of an inconsistent position in a later
    proceeding would create the perception that either the first or the second court was misled? [and]
    (3) Will the party seeking to assert an inconsistent position derive an unfair advantage or impose
    an unfair detriment on the opposing party if not estopped?” Moses v. Howard Univ. Hosp., 606
    
    27 F.3d 789
    , 798 (D.C. Cir. 2010). In this case the answer to each of these questions is no for the
    reasons that follow. The Court thus finds that Plaintiffs are not foreclosed from opposing the
    zero-lethal-take ITS accompanying the 2021 BiOp.
    This determination bears some elaboration. Considering the first of the three judicial-
    estoppel questions, Plaintiffs’ current position is not “clearly inconsistent” with the arguments
    that they made in their 2019 summary-judgment briefing. At that time, the conservation groups
    posited that the reinitiation trigger that NMFS included in lieu of an ITS in the 2014 BiOp was
    not equivalent to an ITS. In particular, they noted the discrepancy between the fact that the 2014
    BiOp “stated that while no take was authorized [as it could not be under the MMPA], . . . the
    trigger would only be met if multiple right whales were killed or seriously injured.” ECF No. 83
    (Pls. 2019 Reply/Opp.) at 16. They argued that setting the reinitiation trigger at 3.25 right
    whales annually was tantamount to authorizing incidental take. 
    Id.
     at 16–17. In contrast, had
    NMFS really not authorized any incidental lethal take as claimed, it “could have set the trigger at
    zero, such that reinitiation of consultation would have been immediately triggered if a right
    whale was taken.” 
    Id.
     at 17 (citing to Beaudreau, 25 F. Supp. 3d at 115 n.26 for proposition that
    trigger could be set at zero). Nowhere in that brief, however, did Plaintiffs argue that setting the
    reinitiation trigger at zero could supersede the requirement that, before issuing an ITS, NMFS
    find that the action would have no more than a “negligible impact” on the right-whale
    population. See, e.g., Pls. 2019 Reply/Opp. at 16 (maintaining argument that NMFS’s only
    “course of action” was “to work internally to” satisfy section 101(a)(5)(E) requirement).
    Plaintiffs’ current arguments do not contradict their earlier position. Now, they put
    forward two points with respect to the zero-lethal-take finding: 1) NMFS still has not
    “authorize[d] . . . incidental take pursuant to MMPA section 101(a)(5)(E)” as it must before
    28
    issuing an ITS; and 2) the 2021 BiOp is invalid as it “anticipates that lethal take of right whales
    will continue to occur in the federal lobster fishery, [but] the ITS purports to authorize ‘zero
    lethal take.’” Pls. MSJ at 24. Plaintiffs’ 2019 and 2022 positions are consistent in that both
    maintain the view that NMFS has implicitly authorized lethal take of right whales even as it says
    that it is not doing so. The only difference is that the form that this implicit authorization takes is
    now different from that in the prior case where no ITS was issued at all.
    This Court also did not “accept [Plaintiffs’] earlier position” in its 2020 remedies
    Opinion. Moses, 606 F.3d at 798; cf. Fed. Dfts. Cross-MSJ at 27. The Court there addressed
    Beaudreau, 
    25 F. Supp. 3d 67
    , as an example of a case that “the agency cite[d] . . . in which
    courts declined to vacate a BiOp for ITS-related shortcomings.” CBD II, 480 F. Supp. 3d at 246
    (emphasis added). Notably, the Court did not find Beaudreau persuasive because in that case
    there was in fact “little practical difference between having an ITS and not,” as “the agency had
    suggested that given the unlikelihood of any take, the acceptable level of incidental take might
    well be zero.” Id. The Court’s statements can hardly be read as “adopting Plaintiffs’ position”
    that a “zero take ITS would have passed muster,” Fed. Dfts. Cross-MSJ at 27, since they do not
    endorse setting lethal take at zero in circumstances different from those in Beaudreau — such as
    those of the 2014 or 2021 BiOps, both of which “forecasted a considerable level of right-whale
    take.” CBD II, 480 F. Supp. 3d at 246. Additionally, the Court did not consider arguments
    about authorizing zero lethal take at all in its April 2020 Opinion finding the 2014 BiOp
    unlawful because it lacked an ITS entirely.
    Finally, NMFS asserts that if Plaintiffs are not estopped, it “would be prejudiced because
    it took Plaintiffs’ views into account when drafting the 2021 BiOp.” Fed. Dfts Cross-MSJ at 27.
    Although the Court cannot know everything that NMFS may have considered in drafting the
    29
    2021 BiOp, nothing in the record indicates that the Service relied on the statements in Plaintiffs’
    2019 brief regarding zero-lethal-take ITSs. Indeed, the only record cite that NMFS provides to
    support this position has nothing to do with the lobster fishery. See Fed. Dfts. Cross-MSJ at 27;
    Fed. Dfts. Reply at 14 (both citing to JA3 at ECF p. 83). Although the administrative record
    reflects that NMFS was aware of various court decisions, including the deadline imposed in this
    Court’s August 2020 remedies Opinion, there is no reference to a court decision or comment
    from Plaintiffs supporting a zero-lethal-take ITS for right whales. See, e.g., JA3 at ECF p. 12
    (noting “court-ordered” May 31, 2021, deadline imposed in August 2020 opinion); id. at ECF pp.
    56 & 85 (noting various court decisions in for-the-record feedback to comments received on
    draft 2021 BiOp). Plaintiffs, moreover, submitted comments on the draft BiOp on February 19,
    2021, in which they criticized the document for “fail[ing] to include a proper incidental take
    statement” and observed that the draft BiOp in fact projected lethal take of right whales. See
    JA3 at ECF pp. 415, 460. There is thus nothing in the record to suggest that NMFS relied on
    Plaintiffs’ or this Court’s prior statements in such a way that allowing Plaintiffs’ current
    arguments to go forward would impose an “unfair detriment on the opposing party.” Moses, 606
    F.3d at 798. Defendants’ arguments, consequently, catch no wind.
    B. Six-Month Time Requirement
    In Count VII of their Amended Complaint, Plaintiffs also maintain that the 2021 Final
    Rule amending the ALWTRP violates the MMPA and APA for a separate reason: it fails to meet
    timing requirements enshrined in the former statute. See Pls. MSJ at 29–34. Section 118 of the
    MMPA states that “[f]or any stock in which incidental mortality and serious injury from
    commercial fisheries exceeds the potential biological removal level[,] . . . the plan shall include
    measures the Secretary expects will reduce, within 6 months of the plan’s implementation, such
    30
    mortality and serious injury to a level below the potential biological removal level.” 
    16 U.S.C. § 1387
    (f)(5)(A) (emphasis added). This six-month timeframe comes after language earlier in the
    same section explaining thus:
    The immediate goal of a take reduction plan for a strategic stock
    shall be to reduce, within 6 months of its implementation, the
    incidental mortality or serious injury of marine mammals
    incidentally taken in the course of commercial fishing operations to
    levels less than the potential biological removal level established for
    that stock under section 1386 of this title. The long-term goal of the
    plan shall be to reduce, within 5 years of its implementation, the
    incidental mortality or serious injury of marine mammals
    incidentally taken in the course of commercial fishing operations to
    insignificant levels approaching a zero mortality and serious injury
    rate, taking into account the economics of the fishery, the
    availability of existing technology, and existing State or regional
    fishery management plans.
    
    Id.
     § 1387(f)(2) (emphasis added).
    Plaintiffs argue that the 2021 Rule flunks the six-month requirement because the level of
    M/SI incidents for North Atlantic right whales currently exceeds PBR and the BiOp and the Rule
    project that the number of M/SI incidents in federal fisheries will average above 2.6 annually
    through 2025, which continues to exceed the PBR level. See JA3 at ECF p. 146 (analyzing M/SI
    incident rate in Phase 1, which is the current rulemaking action); 
    86 Fed. Reg. 51,993
     (noting
    that right-whale PBR level is 0.8 per year); see also Pls. MSJ at 30. Indeed, the projected M/SI
    incident rate will not fall below the PBR level until Phase 4 of the Framework, eight years after
    implementation of the 2021 Final Rule. See JA3 at ECF p. 146 (M/SI incident rate falls to
    0.136). Although NMFS does dispute these facts from the administrative record, it asserts two
    main arguments in response: 1) the six-month requirement applies only to the 1997 initial take-
    reduction plan, not to subsequent amendments such as those in the Final Rule; and 2) the
    31
    requirement is an aspirational goal, not a mandatory duty. See Fed. Dfts. Cross-MSJ at 30–37.
    Looking at each of these positions separately leaves the Court unconvinced.
    1. Applicability to plan amendments
    The Court examines first the question of whether the six-month time requirement applies
    only to the initial take-reduction plan or to subsequent amendments as well. This question, in
    turn, implicates whether Plaintiffs have challenged the correct agency action and, if not, whether
    they have lost their chance to do so.
    NMFS maintains that the time requirement applies only to the initial plan and that this
    Court so held in a prior Opinion. See Fed. Dfts. Cross-MSJ at 31; see also MELA Cross-MSJ at
    36–37. Defendants note that in section 118, “Congress clearly demarcated the two types of
    action: first, a plan, and, subsequently, plan amendments.” Fed. Dfts. Cross-MSJ at 31; compare
    
    16 U.S.C. § 1387
    (f)(7)(E) (describing how often take-reduction team should meet “to monitor
    the implementation of the final take reduction plan”), with 
    id.
     § 1387(f)(7)(F) (“The Secretary
    shall amend the take reduction plan and implementing regulations as necessary to meet the
    requirements of this section.”). They then point to the text, which states that “the plan shall
    include measures” that reduce M/SI below the PBR level within six months; there is no mention
    of later amendments. See 
    16 U.S.C. § 1387
    (f)(5)(A); see also 
    16 U.S.C. § 1387
    (f)(2) (also
    referring to plan, not the amendments). If it is the case that the time requirement applies only to
    the initial plan, then the only relevant action would be the original 1997 Atlantic Large Whale
    Take Reduction Plan, not the various amendments, and the statute of limitations period to
    challenge the 1997 Plan would have closed.
    For starters, the Court is not bound by dicta from its August 2020 remedies Opinion.
    That Opinion stated that “it is not obvious to the Court that Plaintiffs’ cited statutory deadlines
    32
    apply to amendments to existing take-reduction plans; it is possible to read them as applying
    only to the initial plan developed by a Team after it is constituted.” CBD II, 480 F. Supp. 3d at
    248; see also Fed. Dfts. Cross-MSJ at 31 (noting this point). There, the Court was addressing the
    slightly different issue of whether “the agency’s proposed timeline [was] out of compliance with
    the” MMPA’s deadlines for when NMFS had to publish proposed rules after receiving the Take
    Reduction Team’s proposed plan. CBD II, 480 F. Supp. 3d at 248. While the Court
    acknowledges the similarity of the two issues, it did not box itself into a particular interpretation
    in its earlier Opinion. It merely said that “it [was] not obvious” that the deadline applied to plan
    amendments as well. Id. Upon further consideration, it now concludes that application to plan
    amendments is in fact the better reading.
    The amendment process for a take-reduction plan directs NMFS that it “shall amend the
    take reduction plan and implementing regulations as necessary to meet the requirements of this
    section,” meaning section 118. See 
    16 U.S.C. § 1387
    (f)(7)(F). This language implies that all
    amendments must be designed to meet section 118’s requirements, including the requirement
    that the plan “include measures” that the agency “expects will reduce” M/SI to a level below that
    of PBR “within 6 months of the plan’s implementation.” 
    Id.
     § 1387(f)(5)(A); Pls. Reply/Opp. at
    24. This reading is consistent with the legislative history of section 118, which was introduced
    during the 1994 amendments to the MMPA. See Cares Cmty. Health v. Dep’t of Health & Hum.
    Servs., 
    944 F.3d 950
    , 957 (D.C. Cir. 2019) (in construing statute, court “look[s] to the
    ‘traditional tools of statutory interpretation — text, structure, purpose, and legislative history”)
    (quoting In re Sealed Case, 
    932 F.3d 915
    , 928 (D.C. Cir. 2019)). The House Report
    accompanying the amendments explains that “[t]he goal of these [take-reduction] plans is to
    reduce incidental lethal takes resulting from commercial fishing operations to levels less than the
    33
    potential biological removal level” and that a “[f]ailure of a plan to meet these goals shall result
    in a revision of the plan and promulgation of regulations necessary to achieve that goal.” H.R.
    Rep. No. 103-439 (1994) at 37. This stated legislative purpose aligns with the most natural
    reading of Section 1387(f)(7)(F) — namely, that any later revisions of a take-reduction plan must
    fulfill the time-related goals of the initial plan. Indeed, given the emphasis on reaching zero
    mortality and lowering levels of take throughout section 118 and the MMPA overall, it would
    make little sense for the statute to have created a regime where if an agency fails to reduce take
    under its initial plan, it is then absolved from needing to try to reach that goal within a specified
    timeframe in later amendments. See Pls. Reply/Opp. at 26. This cannot be what Congress
    intended.
    This reading is further supported by the treatment of take-reduction plans as evolving
    documents to which amendments are made over time. See, e.g., 
    86 Fed. Reg. 51,970
     (“[t]his
    final rule implements modifications to the Atlantic Large Whale Take Reduction Plan” and
    describing series of modifications made through amendments); see also ECF No. 216-2 (Joint
    Appendix Volume 2) at ECF p. 9 (Section 7 consultation letter on 2021 Final Rule stating, “The
    proposed action is NMFS’s implementation of the Plan, which requires gear regulations for U.S.
    fixed gear fisheries.”) (emphasis added). NMFS itself has even acknowledged that the six-month
    and five-year timeframes can apply to amendments. In a final rule amending the implementing
    regulations of the ALWTRP in 2007, the Service stated, “The MMPA provides that the
    immediate goal of a take reduction plan is to reduce incidental mortality and serious injury of
    marine mammals taken in the course of commercial fishing to levels less than the PBR level and
    the long-term goal is to reduce such incidental mortality and serious injury to insignificant levels
    34
    approaching a zero rate. These regulatory changes are necessary to attain these goals.” 
    72 Fed. Reg. 57,104
    , 57,122 (October 5, 2007).
    The fact that the original ALWTRP also included measures “expected to achieve the
    necessary take reductions within 6 months” does not undermine the conclusion that time
    requirements apply to plan amendments as well. See 
    62 Fed. Reg. 39,157
    , 39,159 (July 22,
    1997); see also MELA Cross-MSJ at 34. Both the original plan and the amendments face the
    same constraints, which is why the Court also does not find it prohibitive that Plaintiffs argue
    elsewhere that NMFS should have met the long-term goal of bringing right whale M/SI in
    commercial fisheries to “insignificant levels approaching a zero” within five years of the original
    promulgation of the ALWTRP in 1997. See Pls. MSJ at 35. Such a claim does not imply that
    Plaintiffs think that only the original take-reduction plan is subject to a timeframe requirement;
    rather, it suggests that both the original plan and subsequent amendments needed to meet the
    criterion.
    Last, the Court addresses Defendants’ argument that Plaintiffs’ six-month claim is barred
    under the six-year statute of limitations for bringing an action against the United States. See 
    28 U.S.C. § 2401
    (a); Fed. Dfts. Cross-MSJ at 32; MELA Cross-MSJ at 36. This issue merits some
    scrutiny because “[u]nlike an ordinary statute of limitations, § 2401(a) is a jurisdictional
    condition attached to the government’s waiver of sovereign immunity, and as such must be
    strictly construed.” Peri & Sons Farms, Inc. v. Acosta, 
    374 F. Supp. 3d 63
    , 70–71 (D.D.C.
    2019). The six-year statute-of-limitations period “set by § 2401(a) begins to run when ‘the right
    of action first accrues.’” Alaska Cmty. Action on Toxics v. EPA, 
    943 F. Supp. 2d 96
    , 102
    (D.D.C. 2013) (quoting 
    28 U.S.C. § 2401
    (a)). “A cause of action against an administrative
    agency ‘first accrues,’ within the meaning of § 2401(a), as soon as (but not before) the person
    35
    challenging the agency action can institute and maintain a suit in court.” Id. (quoting Spannaus
    v. Dep’t of Justice, 
    824 F.2d 52
    , 56 (D.C. Cir. 1987)).
    NMFS argues that Plaintiffs’ claims are time barred because the cause of action first
    began to accrue in 1997 when the ALWTRP was implemented, and the six years would have
    then elapsed in 2003. See Fed Dfts. Cross-MSJ at 32. In so contending, Defendants rely on
    Alaska Community Action on Toxics, a case in which the plaintiffs challenged the agency action
    of publishing a new schedule listing products eligible to be used for oil discharge. See 943 F.
    Supp. 2d at 100–01. The underlying decision that those plaintiffs were arguing against, however,
    was the agency’s choice not to list “waters and quantities for use” regarding such oil-dispersant
    products. Id. at 104. That decision had been made decades earlier in a final rule. Id. (dismissing
    case as barred by statute of limitations given decision made 30 years prior).
    For the reasons just discussed, however, the amendments to the 2021 Final Rule were a
    new administrative action, and the statute-of-limitations question is thus not implicated because
    Plaintiffs’ six-year period to bring a challenge restarted with the Final Rule’s issuance. This
    leaves Plaintiffs well within their allotted time.
    If anything, the contrast between the Final Rule amending the ALWTRP and the routine
    publication of the product list in Alaska Community Action on Toxics shows why the better
    reading of 
    16 U.S.C. § 1387
    (f)(5) encompasses the plan amendments and thus triggers a reset of
    the statute of limitations. There, the district court explained that the product schedule did not
    result from a robust process, and “[n]othing about that decision [not to list waters or use
    quantities] has changed in the nearly thirty years since it was made.” 943 F. Supp. 2d at 104. In
    contrast, the 2021 Final Rule was released only after full notice-and-comment rulemaking, and
    “a complex process involving multiple stakeholders” and “many hours of complicated
    36
    discussions and negotiations,” as NMFS has previously informed this Court. See ECF No. 111
    (Fed. Dfts. Remedy Response Brief) at 8. That process resulted in a rule altering significant
    aspects of operations in the American lobster fishery, including the types of equipment that
    lobstermen can use and what areas are open for fishing. It is not just “implement[ing] the
    decisions [the agency] made ‘long ago’” but making new decisions entirely. See Peri & Sons
    Farms, Inc., 374 F. Supp. 3d at 73 (quoting Alaska Cmty. Action on Toxics, 943 F. Supp. 2d at
    105).
    In a final effort, NMFS argues in its Reply that Plaintiffs have waived the statute-of-
    limitations point by failing to respond to Federal Defendants’ argument on this score. See Fed.
    Dfts. Reply at 15. A court can treat “specific arguments as conceded” when a “party fails to
    respond to arguments in opposition papers.” Dinkel v. MedStar Health, 
    880 F. Supp. 2d 49
    , 58
    (D.D.C. 2012) (internal quotation marks and citations omitted). Here, however, Plaintiffs do
    briefly address this issue as it applies to the TRP amendments. See Pls. Reply/Opp. at 23. More
    importantly, they devote three pages of their Reply to addressing why the six-month timeline
    applies to the TRP amendments as well as to the original plan. This argument is closely
    intertwined with the statute-of-limitations issue since a finding for Plaintiffs on this issue vitiates
    a § 2401 claim. Id. at 23–27. The argument was thus not waived.
    2. Obligation vs. goal
    Defendants also argue that section 118 “spoke advisedly” in creating a goal of reducing
    M/SI incidents below PBR within six months but did not mandate an absolute deadline. See Fed.
    Dfts. Cross-MSJ at 32–33; MELA Cross-MSJ. at 35–36; MALA Opp. at 22–23. In particular,
    NMFS objects that if “Congress meant to set a deadline, it would have stated ‘the plan shall
    37
    reduce M/SI to the potential biological removal level’ by a particular date. It did not do so.”
    Fed. Dfts. Cross-MSJ at 33. Here, Plaintiffs and NMFS appear to talk past each other.
    Defendants are correct that 
    16 U.S.C. § 1387
    (f)(2) states that “[t]he immediate goal of a
    take reduction plan for a strategic stock shall be to reduce, within 6 months of its
    implementation, the” incidental M/SI of marine mammals to below PBR, and it similarly sets a
    “long-term goal” for M/SI to approach zero over five years. 
    Id.
     (emphasis added). Another
    subsection within Section 118, however, uses the word “shall” in stating that “[f]or any stock in
    which incidental mortality and serious injury from commercial fisheries exceeds the potential
    biological removal level[,] . . . the plan shall include measures the Secretary expects will reduce”
    M/SI incidents below the PBR level within six months. See 
    16 U.S.C. § 1387
    (f)(5)(A)
    (emphasis added). The latter section is the one that Plaintiffs rely on. See Pls. MSJ at 29–30.
    NMFS itself has stated that it is required to reduce M/SI levels for endangered species to below
    the PBR rate within six months in other take-reduction plans. See, e.g., 
    62 Fed. Reg. 39,173
    (explaining in ALWTRP that “the MMPA requires that NMFS produce a plan to reduce serious
    injuries and mortalities to below the PBR level within 6 months”); 
    71 Fed. Reg. 24,776
    , 24,790–
    91 (Apr. 26, 2006) (same in bottlenose-dolphin take-reduction plan); see also Pls. Reply/Opp. at
    28–29.
    Comparison with subsection 118(f)(5)(B) of the MMPA further demonstrates why
    subsection 118(f)(5)(A) sets more than just an aspirational goal. The former, which does not
    apply to the right whales, states that “[f]or any stock in which human-caused mortality and
    serious injury exceeds the potential biological removal level, other than a stock to which
    subparagraph (A) applies,” NMFS must meet the same requirements as in subsection A, with the
    exception that the measures need only reduce M/SI incidents “to the maximum extent
    38
    practicable” within six months. See 
    16 U.S.C. § 1387
    (f)(5)(B); cf. MLU Opp. at 28 (focusing
    only on subsection B to argue that six-month time requirement is intended to be flexible). That
    the text of subsection A contains no such qualifier implies that the six-month requirement in
    subsection B — the one relevant here — in fact does create a concrete target. See Oceana, Inc.
    v. Locke, 
    670 F.3d 1238
    , 1243 (D.C. Cir. 2011) (comparing two sections, one of which
    contained “to the extent practicable” qualifier and noting that for the other subsection, “[w]hen a
    statute commands an agency without qualification to carry out a particular program in a
    particular way, the agency’s duty is clear”); Pls. Reply/Opp. at 27.
    Defendants’ other counterarguments also run aground. In particular, NMFS protests that
    “[i]t would be nonsensical for Congress to have created” an obligation to act within six months
    when that action has “nebulous ending points” since it is measured from the time it is
    “implemented,” which the MMPA leaves undefined. See Fed. Dfts. Cross-MSJ at 33–34. The
    Court, however, agrees with Plaintiffs that Congress’s failure to define implementation is no bar
    here. See Pls. Reply/Opp. at 33. “When a term goes undefined in a statute, [courts] give the
    term its ordinary meaning.” Taniguchi v. Kan Pac. Saipan, 
    566 U.S. 560
    , 566 (2012).
    “Implement” is defined as “to put into practical effect; to carry out.” AMERICAN HERITAGE
    DICTIONARY (3rd ed. 1992). There is clearly some date by which NMFS considers a Plan or Plan
    amendment to have been put into effect, as the agency has stated in rules that it issued, for
    instance, that a “rule will reduce within 6 months of its implementation the bycatch of harbor
    porpoise to below their PBR level.” 
    63 Fed. Reg. 66,464
    , 66,470 (Dec. 2, 1998).
    If the agency really thought that the undefined term “implementation” provided such
    “nebulous ending points,” then its own such statements would be meaningless. Further, even if a
    date is not set in stone against which to assess reductions in M/SI entanglements precisely six
    39
    months after implementation, the relevant date is surely not several years after implementation,
    as the BiOp suggests would occur for the measures in the 2021 Final Rule. Nor is it the case that
    the implementation of the 2021 Final Rule is “not anticipated to conclude for at least ten years,”
    as the Massachusetts Lobstermen’s Association suggests. See MALA Opp. at 23 (citing JA3 at
    ECF p. 87, which lays out dates for implementation of the Framework, not the 2021 Final Rule,
    the latter of which occurs in Phase 1 of the Framework).
    Next, although the Court agrees that of course “M/SI may fluctuate depending on many
    factors” over time and could thus fall above or below the PBR level, these fluctuations do not
    alter the meaning of sections 118(f)(2) or 118(f)(5). Cf. Fed. Dfts. Cross-MSJ at 33. The
    measures that the MMPA requires are ones that “the Secretary expects will reduce” M/SI to
    below the PBR level within six months. See 
    16 U.S.C. § 1387
    (f)(5)(A) (emphasis added). If
    natural changes unexpectedly lead the PBR level to fall within that period, that would not render
    the plan or plan amendments out of compliance as long as they were expected to achieve the goal
    when promulgated. Additionally, “Congress did not direct that a new ‘deadline’ spring to life
    each time a fishery’s impact exceeds PBR.” Fed. Dfts. Cross-MSJ at 33. Congress simply
    directed that NMFS “amend the take reduction plan and implementing regulations as necessary
    to meet the requirements of this section.” 
    16 U.S.C. § 1387
    (f)(7)(F). If, when making those
    amendments, the rate of M/SI incidents is projected to exceed the PBR level, then the
    amendments must include measures to reduce the M/SI rate within six months.
    This requirement is also a good deal more specific than the “goals” in cases that
    Defendant-Intervenors cite. In those, for example, Congress declared “a national goal [of]”
    preventing and remedying visibility impairments from manmade air pollution. Am. Corn
    Growers Ass’n v. EPA, 
    291 F.3d 1
    , 10 (D.C. Cir. 2002) (discussing goal in 42 U.S.C.
    40
    § 7491(a)(1)); see also Nat’l Wildlife Fed’n v. Gorsuch, 
    693 F.2d 156
    , 178 (D.C. Cir. 1982)
    (warning that “[c]aution is always advisable in relying on a general declaration of purpose to
    alter the apparent meaning of a specific provision,” in context of “grand goal” in Clean Water
    Act to eliminate discharge of pollutants into navigable waters by set date in dispute over whether
    permits for discharge of pollutants were required for certain dams); MELA Cross-MSJ at 35
    (citing cases). If anything, the six-month timeframe in section 118 is a step towards fulfilling the
    MMPA’s broader goal of bringing “the incidental mortality or serious injury of marine mammals
    occurring in the course of commercial fishing operations . . . to insignificant levels approaching a
    zero mortality and serious injury rate within 7 years” from the date of the 1994 amendments.
    See 
    16 U.S.C.A. § 1387
    (a). This timeframe is thus more than just a hortatory aim for the
    agency.
    Having concluded that 1) the six-month deadline applies to plan amendments as well as
    to the ALWTRP itself, 2) that NMFS had to include measures expected to reduce M/SI to below
    PBR by that deadline, and 3) that NMFS did not do so, the Court finds that the 2021 Final Rule
    amending the ALWTRP is invalid.
    *       *        *
    So how does the ship’s log now read? As explained in detail above, the crux of the
    problem is that the 2021 BiOp projects that in the coming years the American lobster fishery will
    continue to potentially kill and seriously injure North Atlantic right whales at over three times
    the sustainable rate. This is expected to occur even after the implementation of the 2021 Final
    Rule amending the ALWTRP and even though zero lethal take is authorized. For the reasons
    stated in this Opinion, the Court concludes that NMFS violated the ESA through its failure to
    satisfying the required antecedent in section 101(a)(5)(E) of the MMPA before issuing an ITS.
    41
    The Court also finds that the 2021 Final Rule did not attempt to meet the take-reduction
    measures that it was obligated to under the MMPA within the required timeline. The Court
    therefore declares the 2021 BiOp and 2021 Final Rule invalid. The Court recognizes that this
    may seem a severe result for the lobster industry and NMFS. But no actor here — neither the
    Court nor the Service — operates free from the strict requirements imposed by the MMPA and
    ESA. If the agency “believes [a] statute untoward in some respect, then ‘it should take its
    concerns to Congress,’ for ‘[i]n the meantime it must obey [the statute] as written.’” Oceana,
    Inc., 670 F.3d at 1243 (quoting Natural Res. Def. Council v. EPA, 
    643 F.3d 311
    , 323 (D.C. Cir.
    2011)).
    C. Remedy
    The Court’s findings at this juncture do not dictate that it must immediately shutter the
    American lobster fishery; indeed, it is cognizant of what a weighty blow that would inflict.
    Instead, the Court will order additional briefing as to potential remedies, which may include
    remand with or without vacatur. CBD I, 
    2020 WL 1809465
    , at *10 (doing same); see also Fed.
    Dfts. Cross-MSJ at 44–45 (requesting supplemental briefing). On such a remand, moreover, the
    Service may find that other measures exist to reduce lethal take, or that projected take is in fact
    lower than originally estimated. Remand thus need not be equivalent to a shutdown. For now,
    however, the Court reaches no determination on this question without the benefit of further
    briefing.
    IV.       Conclusion
    For the foregoing reasons, the Court will grant Plaintiffs’ Motion for Summary Judgment
    and deny Defendants’ and Defendant-Intervenors’ corresponding Cross-Motions for Summary
    Judgment. A contemporaneous Order so stating will issue this day.
    42
    /s/ James E. Boasberg
    JAMES E. BOASBERG
    United States District Judge
    Date: July 8, 2022
    43
    

Document Info

Docket Number: Civil Action No. 2018-0112

Judges: Judge James E. Boasberg

Filed Date: 7/8/2022

Precedential Status: Precedential

Modified Date: 7/8/2022

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Arkansas Dairy Cooperative Ass'n v. United States ... , 573 F.3d 815 ( 2009 )

Rempfer v. Sharfstein , 583 F.3d 860 ( 2009 )

Natural Resources Defense Council v. Environmental ... , 643 F.3d 311 ( 2011 )

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Edward Spannaus v. U.S. Department of Justice , 824 F.2d 52 ( 1987 )

National Ass'n of Clean Air Agencies v. Environmental ... , 489 F.3d 1221 ( 2007 )

Marshall County Health Care Authority v. Donna E. Shalala, ... , 988 F.2d 1221 ( 1993 )

American Corn Growers Association v. Environmental ... , 291 F.3d 1 ( 2002 )

Eagle Broadcasting Group, Ltd. v. Federal Communications ... , 563 F.3d 543 ( 2009 )

Mt Royal Joint Vntr v. Kempthorne, Dirk , 477 F.3d 745 ( 2007 )

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