Endangered and Threatened Wildlife and Plants; Threatened Species Status With Section 4(d) Rule for Pyramid Pigtoe, 49989-50011 [2021-19091]
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Federal Register / Vol. 86, No. 170 / Tuesday, September 7, 2021 / Proposed Rules
United States contains, at most, less
than 1 percent of the worldwide jaguar
habitat, and has no resident population
of jaguars (Rosemont 2020, p. 9). This
information relates to the status of the
species and does not address whether or
not Unit 3 allows for the normal
demographic function and possible
range expansion of the Northwestern
Recovery Unit. The petition also states
that removal of the northern Santa Rita
Mountains and Subunit 4b represents a
very small percentage of the total
critical habitat—about 6.5 percent—that
would be removed by the petitioned
action and will not prevent the
remaining critical habitat from
functioning as intended for the support
of the Northwest Recovery Unit
(Rosemont 2020, pp. 13–14). The
recovery function and value of critical
habitat for the jaguar within the United
States is to contribute to the species’
persistence and, therefore, overall
conservation by identifying areas that
support some individuals during
dispersal movements, that contain small
patches of habitat (perhaps in some
cases with a few resident jaguars), and
that allow for cyclic expansion and
contraction of the nearest core area and
breeding population in the
Northwestern Recovery Unit (79 FR
12572, March 5, 2014, p. 79 FR 12574).
Removal of the northern Santa Rita
Mountains would withdraw areas that
currently provide the physical and
biological features of jaguar critical
habitat and in which confirmed jaguar
detections occurred between 2012 and
2015 (U.S. Fish and Wildlife Service
2016, p. 295). In addition, removal of
Subunit 4b eliminates half of the
available connections to Mexico for Unit
4 (specifically to Subunit 4a), which is
a unit in which the same jaguar that
occupied the Santa Rita Mountains
(Unit 3) was detected in 2011. The
petition does not explain why these
areas are no longer essential other than
to assert that most critical habitat units
would be unaffected, and that impacts
to Unit 3 and Unit 4 would be minor
and would not prevent the units from
functioning as intended. This assertion
does not demonstrate that changes have
occurred to these areas such that the
function they provide to jaguars, and the
reason for which they were designated
as critical habitat, is compromised.
Therefore, the petition does not provide
substantial scientific information that
the northern Santa Rita Mountains in
Unit 3 and all of Subunit 4b no longer
function as critical habitat and are not
essential in allowing for the normal
demographic function and possible
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range expansion of the Northwestern
Recovery Unit.
The petition discusses the 2013
biological opinion for the Rosemont
Copper Mine, which was overturned by
a court decision (Ctr. for Biological
Diversity at 873), and our 2019
amendments to the regulations at 50
CFR 424.12 in its request to revise
critical habitat for jaguars. We reviewed
the petition’s argument and find that
these documents are not relevant to the
question of whether the petition
contained substantial information to
support the removal of areas from
critical habitat. Neither line of
discussion speaks to whether the areas
petitioned for removal contain the
physical or biological features essential
to the conservation of the species or
provides information that these features
do not require special management
considerations or protection (50 CFR
424.14(e)(4).
Based on our review of the petition
and sources cited in the petition, we
find that the petition does not present
substantial scientific or commercial
information indicating the petitioned
action may be warranted for the jaguar.
Because the petition does not present
substantial information indicating that
revision of critical habitat for jaguar may
be warranted, we do not intend to
proceed with any such revision.
However, we ask that the public submit
to us any new information that becomes
available concerning this species’
habitat at any time by contacting the
person listed under FOR FURTHER
INFORMATION CONTACT, above.
References Cited
A complete list of references cited in
this document is available on the
internet at https://www.regulations.gov
and upon request from the Arizona
Ecological Services Field Office (see FOR
FURTHER INFORMATION CONTACT).
Authors
The primary authors of this document
are the staff members of the Arizona
Ecological Services Field Office (see FOR
FURTHER INFORMATION CONTACT).
Authority
The authority for this action is the
Endangered Species Act of 1973, as
amended (16 U.S.C. 1531 et seq.).
Martha Williams,
Principal Deputy Director, Exercising the
Delegated Authority of the Director, U.S. Fish
and Wildlife Service.
[FR Doc. 2021–19062 Filed 9–3–21; 8:45 am]
BILLING CODE 4333–15–P
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49989
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS–R4–ES–2021–0092;
FF09E21000 FXES11110900000 212]
RIN 1018–BF43
Endangered and Threatened Wildlife
and Plants; Threatened Species Status
With Section 4(d) Rule for Pyramid
Pigtoe
Fish and Wildlife Service,
Interior.
ACTION: Proposed rule.
AGENCY:
We, the U.S. Fish and
Wildlife Service (Service), announce our
12-month finding on a petition to list
the pyramid pigtoe (Pleurobema
rubrum), a freshwater mussel species
from Alabama, Arkansas, Kentucky,
Louisiana, Mississippi, Ohio,
Oklahoma, Tennessee, and Virginia, as
an endangered or threatened species
under the Endangered Species Act of
1973, as amended (Act). After a review
of the best available scientific and
commercial information, we find that
listing the species is warranted.
Accordingly, we propose to list the
pyramid pigtoe as a threatened species
with a rule issued under section 4(d) of
the Act (‘‘4(d) rule’’). If we finalize this
rule as proposed, it would add this
species to the List of Endangered and
Threatened Wildlife and extend the
Act’s protections to the species.
DATES: We will accept comments
received or postmarked on or before
November 8, 2021. Comments submitted
electronically using the Federal
eRulemaking Portal (see ADDRESSES,
below) must be received by 11:59 p.m.
Eastern Time on the closing date. We
must receive requests for a public
hearing, in writing, at the address
shown in FOR FURTHER INFORMATION
CONTACT by October 22, 2021.
ADDRESSES: You may submit comments
by one of the following methods:
(1) Electronically: Go to the Federal
eRulemaking Portal: https://
www.regulations.gov. In the Search box,
enter the docket number or RIN for this
rulemaking (presented above in the
document headings). For best results, do
not copy and paste either number;
instead, type the docket number or RIN
into the Search box using hyphens.
Then, click on the Search button. On the
resulting page, in the panel on the left
side of the screen, under the Document
Type heading, check the Proposed Rule
box to locate this document. You may
SUMMARY:
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submit a comment by clicking on
‘‘Comment.’’
(2) By hard copy: Submit by U.S. mail
to: Public Comments Processing, Attn:
FWS–R4–ES–2021–0092, U.S. Fish and
Wildlife Service, MS: PRB/3W, 5275
Leesburg Pike, Falls Church, VA 22041–
3803.
We request that you send comments
only by the methods described above.
We will post all comments on https://
www.regulations.gov. This generally
means that we will post any personal
information you provide us (see
Information Requested, below, for more
information).
FOR FURTHER INFORMATION CONTACT:
Janet Mizzi, Field Supervisor, U.S. Fish
and Wildlife Service, Asheville
Ecological Services Field Office, 160
Zillicoa St, Asheville, NC 28801;
telephone 828–258–3939. Persons who
use a telecommunications device for the
deaf (TDD) may call the Federal Relay
Service at 800–877–8339.
SUPPLEMENTARY INFORMATION:
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Executive Summary
Why we need to publish a rule. Under
the Endangered Species Act of 1973, as
amended (Act; 16 U.S.C. 1531 et seq.),
if we determine that a species is an
endangered or threatened species
throughout all or a significant portion of
its range, we are required to promptly
publish a proposal in the Federal
Register and make a determination on
our proposal within 1 year, unless, due
to substantial disagreement regarding
the sufficiency or accuracy of the
available data, we extend the 1-year
period for no more than 6 months to
solicit additional data. To the maximum
extent prudent and determinable, we
must designate critical habitat for any
species that we determine to be an
endangered or threatened species under
the Act. Listing a species as an
endangered or threatened species can
only be completed by issuing a rule.
What this document does. We
propose to list the pyramid pigtoe as a
threatened species with a rule under
section 4(d) of the Act. If made final,
this action would add the species to the
List of Endangered and Threatened
Wildlife in title 50 of the Code of
Federal Regulations (CFR) at 50 CFR
17.11(h) and add specific provisions
pertaining to the pyramid pigtoe to 50
CFR 17.45.
The basis for our action. Under the
Act, we may determine that a species is
an endangered or threatened species
because of any of five factors: (A) The
present or threatened destruction,
modification, or curtailment of its
habitat or range; (B) overutilization for
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commercial, recreational, scientific, or
educational purposes; (C) disease or
predation; (D) the inadequacy of
existing regulatory mechanisms; or (E)
other natural or manmade factors
affecting its continued existence. We
have determined that threats to the
pyramid pigtoe include habitat
degradation or loss from a variety of
sources (e.g., dams and other barriers,
resource extraction); degraded water
quality from chemical contamination
and erosion from development,
agriculture, and mining operations;
direct mortality from dredging; residual
impacts (reduced population size) from
historical harvest; and the proliferation
of invasive, nonnative species. These
threats also compound the negative
effects associated with the species’
small population size.
Section 4(a)(3) of the Act requires the
Secretary of the Interior (Secretary) to
designate critical habitat concurrent
with listing to the maximum extent
prudent and determinable. Section
3(5)(A) of the Act defines critical habitat
as (i) the specific areas within the
geographical area occupied by the
species, at the time it is listed, on which
are found those physical or biological
features (I) essential to the conservation
of the species and (II) which may
require special management
considerations or protections; and (ii)
specific areas outside the geographical
area occupied by the species at the time
it is listed, upon a determination by the
Secretary that such areas are essential
for the conservation of the species.
Section 4(b)(2) of the Act states that the
Secretary must make the designation on
the basis of the best scientific data
available and after taking into
consideration the economic impact, the
impact on national security, and any
other relevant impacts of specifying any
particular area as critical habitat.
Critical habitat is not currently
determinable. However, critical habitat
is prudent, and we intend to propose
critical habitat for the species within 1
year of publishing this rule, after
acquiring the information to determine
the areas warranting critical habitat
designation.
Information Requested
We intend that any final action
resulting from this proposed rule will be
based on the best scientific and
commercial data available and be as
accurate and as effective as possible.
Therefore, we request comments or
information from other governmental
agencies, Native American Tribes, the
scientific community, industry, or any
other interested parties concerning this
proposed rule.
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We particularly seek comments
concerning:
(1) The species’ biology, range, and
population trends, including:
(a) Biological or ecological
requirements of the species, including
habitat requirements for feeding,
breeding, and sheltering;
(b) Genetics and taxonomy;
(c) Historical and current range,
including distribution patterns;
(d) Historical and current population
levels, and current and projected trends;
and
(e) Past and ongoing conservation
measures for the species, its habitat, or
both.
(2) Factors that may affect the
continued existence of the species,
which may include habitat modification
or destruction, overutilization, disease,
predation, the inadequacy of existing
regulatory mechanisms, or other natural
or manmade factors.
(3) Biological, commercial trade, or
other relevant data concerning any
threats (or lack thereof) to this species
and existing regulations that may be
addressing those threats.
(4) Additional information concerning
the historical and current status, range,
distribution, and population size of this
species, including the locations of any
additional populations of this species.
(5) Information on regulations that are
necessary and advisable to provide for
the conservation of the pyramid pigtoe
and that the Service can consider in
developing a 4(d) rule for the species. In
particular, information concerning the
extent to which we should include any
of the section 9 prohibitions in the 4(d)
rule or whether we should consider any
additional exceptions from the
prohibitions in the 4(d) rule.
(6) Which areas would be appropriate
as critical habitat for the species and
why areas should or should not be
proposed for designation as critical
habitat in the future.
(7) Specific information on:
(a) The amount and distribution of
habitat for pyramid pigtoe that should
be considered for proposed critical
habitat;
(b) What may constitute ‘‘physical or
biological features essential to the
conservation of the species within the
geographical range currently occupied
by the species’’;
(c) Where these features are currently
found;
(d) Whether any of these features may
require special management
considerations or practices;
(e) What areas that are currently
occupied and contain features essential
to the conservation of the species
should be included in the designation
and why; and
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(f) What unoccupied areas are
essential for the conservation of the
species and why.
Please include sufficient information
with your submission (such as scientific
journal articles or other publications) to
allow us to verify any scientific or
commercial information you include.
Please note that submissions merely
stating support for, or opposition to, the
action under consideration without
providing supporting information,
although noted, will not be considered
in making a determination, as section
4(b)(1)(A) of the Act directs that
determinations as to whether any
species is an endangered or a threatened
species must be made ‘‘solely on the
basis of the best scientific and
commercial data available.’’
You may submit your comments and
materials concerning this proposed rule
by one of the methods listed in
ADDRESSES. We request that you send
comments only by the methods
described in ADDRESSES.
If you submit information via https://
www.regulations.gov, your entire
submission—including any personal
identifying information—will be posted
on the website. If your submission is
made via a hardcopy that includes
personal identifying information, you
may request at the top of your document
that we withhold this information from
public review. However, we cannot
guarantee that we will be able to do so.
We will post all hardcopy submissions
on https://www.regulations.gov.
Comments and materials we receive,
as well as supporting documentation we
used in preparing this proposed rule,
will be available for public inspection
on https://www.regulations.gov.
Because we will consider all
comments and information we receive
during the comment period, our final
determinations may differ from this
proposal. Based on the new information
we receive (and any comments on that
new information), we may conclude that
the species is endangered instead of
threatened, or we may conclude that the
species does not warrant listing as either
an endangered species or a threatened
species. In addition, we may change the
parameters of the prohibitions or the
exceptions to those prohibitions in the
4(d) rule if we conclude it is appropriate
in light of comments and new
information received. For example, we
may expand the prohibitions to include
prohibiting take associated with
additional activities if we conclude that
those additional activities are not
compatible with conservation of the
species. Conversely, we may establish
additional exceptions to the
prohibitions in the final rule if we
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conclude that the activities would
facilitate or are compatible with the
conservation and recovery of the
species.
Public Hearing
Section 4(b)(5) of the Act provides for
a public hearing on this proposal, if
requested. Requests must be received by
the date specified in DATES. Such
requests must be sent to the address
shown in FOR FURTHER INFORMATION
CONTACT. We will schedule a public
hearing on this proposal, if requested,
and announce the date, time, and place
of the hearing, as well as how to obtain
reasonable accommodations, in the
Federal Register and local newspapers
at least 15 days before the hearing. For
the immediate future, we will provide
these public hearings using webinars
that will be announced on the Service’s
website, in addition to the Federal
Register. The use of these virtual public
hearings is consistent with our
regulations at 50 CFR 424.16(c)(3).
Previous Federal Actions
In our 1989 Animal Notice of Review
(a notice identifying animal taxa that are
native to the United States and being
considered for addition to the List of
Endangered and Threatened Wildlife),
we categorized the pyramid pigtoe
(which we referred to as ‘‘pink pigtoe’’)
as a taxon not meeting the Act’s legal
definition of a species, based on our
taxonomic understanding of information
in published scientific literature at that
time (54 FR 554, January 6, 1989). While
taxonomic uncertainty remains
regarding some populations identified
as pyramid pigtoe, the species is
recognized as valid in current scientific
literature (see Background, below). On
April 20, 2010, we received a petition
from the Center for Biological Diversity
(CBD), Alabama Rivers Alliance, Clinch
Coalition, Dogwood Alliance, Gulf
Restoration Network, Tennessee Forests
Council, and West Virginia Highlands
Conservancy to list 404 aquatic,
riparian, and wetland species, including
the pyramid pigtoe (referred to as ‘‘pink
pigtoe’’ in our National Domestic Listing
Workplan) as endangered or threatened
species under the Act. On September
27, 2011, we published our
determination that the petition
contained substantial information
indicating listing may be warranted (76
FR 59836). On April 17, 2019, CBD filed
a complaint challenging the Service’s
failure to complete 12-month findings
for these species within the statutory
deadline. The Service and CBD reached
a stipulated settlement agreement
whereby the Service agreed to deliver a
12-month finding for the pyramid pigtoe
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to the Office of the Federal Register by
August 31, 2021.
Supporting Documents
A species status assessment (SSA)
team prepared an SSA report for the
pyramid pigtoe. The SSA team was
composed of Service biologists, in
consultation with other species experts.
The SSA report represents a
compilation of the best scientific and
commercial data available concerning
the status of the species, including the
impacts of past, present, and future
factors (both negative and beneficial)
affecting the species. In accordance with
our joint policy on peer review
published in the Federal Register on
July 1, 1994 (59 FR 34270), and our
August 22, 2016, memorandum
updating and clarifying the role of peer
review of listing actions under the Act,
we sought the expert opinions of three
appropriate specialists regarding the
SSA. We received two responses. We
also received SSA report reviews from
one Federal agency and five State
agency partners, including scientists
with expertise in aquatic ecology,
freshwater mussel biology, taxonomy,
and conservation. In addition, more
than 50 individuals at Federal or State
agencies, colleges or universities, or
consultants provided data used in the
SSA report.
I. Proposed Listing Determination
Background
A thorough review of the taxonomy,
life history, and ecology of the pyramid
pigtoe (Pleurobema rubrum) is
presented in the SSA report (version
1.0; Service 2021, pp. 19–36).
The pyramid pigtoe is a freshwater
mussel, reddish to chestnut brown in
color, with a smooth periostracum
(outer shell surface) that darkens with
age (Watters et al. 2009, p. 233).
Juveniles may have green rays that
typically disappear with age. The shell
is thick, triangular, and medium-sized
(up to 3.6 inches (in) (91 millimeters
(mm)) (Williams et al. 2008, p. 564). It
has a shallow sulcus (depressed
channel) and high anteriorly directed
beak that is elevated above the hinge
line (Stansbery 1967, p. 3).
The pyramid pigtoe is found in
medium to large rivers, in a mixture of
sand, gravel, and cobble substrates. It
currently occurs in Kentucky,
Tennessee, Virginia, Ohio, Alabama,
Oklahoma, Arkansas, Mississippi, and
Louisiana. It is considered extirpated
from Pennsylvania, West Virginia,
Indiana, Illinois, Wisconsin, Minnesota,
Iowa, Kansas, and Missouri. Extant
populations of pyramid pigtoe occur in
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the Arkansas-White-Red, Lower
Mississippi, Missouri, and Ohio River
regions (Hydrologic Unit Code 2 scale,
Seaber et al. 1987, pp. 3–4), and it is
extirpated from the Missouri and Upper
Mississippi River regions (Figure 1).
Relying on fish hosts for successful
reproduction, the pyramid pigtoe has a
complex life cycle similar to other
mussels. In general, mussels are either
male or female, but differences between
sexes in shell shape are subtle (Haag
2012, p. 54). Males release sperm into
the water column, which is taken in by
the female through the incurrent
aperture, where water enters the mantle
cavity. The sperm fertilize eggs in the
suprabranchial chamber (located above
the gills) as ova are passed from the
gonad to the marsupia (Yokley 1972, p.
357). Developing larvae remain in the
gill chamber until they mature (called
glochidia) and are ready for release.
Once released, the glochidia draw
nutrients from fish hosts and develop
into juvenile mussels, dropping from
the hosts weeks to months after initial
attachment. Only a few glochidia reach
the free-living juvenile stage, and
mortality rates for the glochidial stage
have been estimated at 99 percent,
making this a critical phase in the life
history of freshwater mussels (Jansen et
al. 2001, p. 211).
Rangewide Distribution of Pyramid Pigtoe
Extant Basins
Extirpated Basins
E:23. Arkansas-White-Red
-Mlssot1ri
~ Lower Mississippi
-
1 inch = 864 Kilometers
Upper Mississippi
1 inch = 537 miles
~Ohio
F:: 1Tennessee
A
The pyramid pigtoe is a short-term
brooder and has been recorded as gravid
in the Cumberland River in May, June,
and July (Gordon and Layzer 1989, p.
50). Host fish species are minnows of
the family Cyprinidae and genera
Cyprinella, Erimystax, Lythrurus, and
Notropis (Culp et al. 2009, p. 19).
Similar to other species in its tribe,
Pleurobemini (taxonomic rank above
genus and below family), the pyramid
pigtoe targets drift-feeding minnow
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species by releasing glochidia contained
in packets called conglutinates (Haag
2012, p. 163). Following release from
the female mussel, the semi-buoyant
conglutinates drift in the water column
where they are targeted by sight-feeding
minnows (Culp et al, 2009, p. 21).
A relatively long-lived species, the
pyramid pigtoe has a lifespan that likely
averages 20 to 30 years, based on
observations of the closely related Ohio
pigtoe and round pigtoe (Slater 2018, p.
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35; Watters et al. 2009, p. 299). Given
the longevity of closely related species,
it possibly lives up to 40–45 years in
some locations (Ostby and Beaty 2016,
p. 117).
The pyramid pigtoe exhibits a
preference for sand and gravel in rivers
but also may be found in coarse sand in
larger rivers (Gordon and Layzer 1989,
p. 31). They can be found at depths less
than 3 ft (1 m) but in large rivers can
be found commonly at depths of 13 to
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Figure 1. Rangewide distribution of pyramid pigtoe.
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20 ft (4 to 6 m) or greater (Parmalee and
Bogan 1998, p. 193; Williams et al.
2008, p. 566). Adult freshwater mussels
within the genus Pleurobema are
suspension-feeders that filter water and
nutrients to eat. Mussels may shift to
deposit feeding, though reasons for this
are poorly known and may depend on
flow conditions or temperature. Their
diet consists of a mixture of algae,
bacteria, detritus, and microscopic
animals (Gatenby et al. 1996, p. 606;
Strayer et al. 2004, p. 430). It has also
been surmised that dissolved organic
matter may be a significant source of
nutrition (Strayer et al. 2004, p. 431).
The pyramid pigtoe (Pleurobema
rubrum) belongs to a complex of four
morphologically similar species, which
includes the Ohio pigtoe (P. cordatum),
rough pigtoe (P. plenum) and round
pigtoe (P. sintoxia). Since its original
description as a species (Rafinesque
1820, p. 314), Pleurobema rubrum has
undergone several scientific name
changes, due to its widespread
distribution, variability in shell shape
and size throughout its range, and
similarity in morphological characters
to other closely related species.
Additionally, based on shell characters
alone, the pyramid pigtoe has been
periodically considered a subspecies of
the Ohio pigtoe (Ortmann 1911, p. 331).
Since its initial description in 1820, the
pyramid pigtoe has sometimes been
referred to as pink pigtoe by commercial
shell harvesters and biologists.
However, the common name applied to
the species in the scientific literature
and in the Integrated Taxonomic
Information System is pyramid pigtoe.
Genetic studies to clarify the
taxonomic relationships among
Pleurobema indicate potential
differences between pyramid pigtoe
populations occupying separate river
drainages. Mitochondrial DNA samples
from two specimens of pyramid pigtoe
indicated the Duck River, Tennessee,
specimen was genetically distinct from
the St. Francis River, Arkansas,
specimen (Campbell et al. 2005, p. 143).
These same data were included in
subsequent phylogenetic studies
focused on Fusconaia (Burdick and
White 2007, p. 372) and Pleurobema
(Campbell et al. 2008, p. 714; Campbell
and Lydeard 2012b, p. 27) with similar
results. Phylogeographic structuring has
been observed between pyramid pigtoe
from the Ouachita and St. Francis
drainages in Arkansas that may
represent species-level variation
(Christian et al. 2008, p. 9; Harris et al.
2009, p. 74). Additionally, an analysis
that included all previously published
and new data representing a broad
sampling across Pleurobemini revealed
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that pyramid pigtoe and round pigtoe
may represent a single species, with two
out of three species delineation models
indicating one lineage present in
specimens identified as round pigtoe
and pyramid pigtoe (Inoue et al. 2018,
p. 694). However, one of the three
models indicated separate lineages of
the two species. While there is some
uncertainty in the taxonomic identity of
populations referred to as pyramid
pigtoe, especially those outside the
Ohio, Cumberland, and Tennessee
basins, our SSA report analyzed the
status of the single species currently
recognized by the scientific community
(Williams et al. 2017, p. 42; Graf and
Cummings 2021, p. 19).
Regulatory and Analytical Framework
Regulatory Framework
Section 4 of the Act (16 U.S.C. 1533)
and its implementing regulations (50
CFR part 424) set forth the procedures
for determining whether a species is an
endangered species or a threatened
species. The Act defines an endangered
species as a species that is ‘‘in danger
of extinction throughout all or a
significant portion of its range’’ and a
threatened species as a species that is
‘‘likely to become an endangered
species within the foreseeable future
throughout all or a significant portion of
its range.’’ The Act requires that we
determine whether any species is an
endangered species or a threatened
species because of any of the following
factors:
(A) The present or threatened
destruction, modification, or
curtailment of its habitat or range;
(B) Overutilization for commercial,
recreational, scientific, or educational
purposes;
(C) Disease or predation;
(D) The inadequacy of existing
regulatory mechanisms; or
(E) Other natural or manmade factors
affecting its continued existence.
These factors represent broad
categories of natural or human-caused
actions or conditions that could have an
effect on a species’ continued existence.
In evaluating these actions and
conditions, we look for those that may
have a negative effect on individuals of
the species, as well as other actions or
conditions that may ameliorate any
negative effects or may have positive
effects.
We use the term ‘‘threat’’ to refer in
general to actions or conditions that are
known to or are reasonably likely to
negatively affect individuals of a
species. The term ‘‘threat’’ includes
actions or conditions that have a direct
impact on individuals (direct impacts),
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as well as those that affect individuals
through alteration of their habitat or
required resources (stressors). The term
‘‘threat’’ may encompass—either
together or separately—the source of the
action or condition or the action or
condition itself.
However, the mere identification of
any threat(s) does not necessarily mean
that the species meets the statutory
definition of an ‘‘endangered species’’ or
a ‘‘threatened species.’’ In determining
whether a species meets either
definition, we must evaluate all
identified threats by considering the
expected response by the species, and
the effects of the threats—in light of
those actions and conditions that will
ameliorate the threats—on an
individual, population, and species
level. We evaluate each threat and its
expected effects on the species, then
analyze the cumulative effect of all of
the threats on the species as a whole.
We also consider the cumulative effect
of the threats in light of those actions
and conditions that will have positive
effects on the species, such as any
existing regulatory mechanisms or
conservation efforts. The Secretary
determines whether the species meets
the definition of an ‘‘endangered
species’’ or a ‘‘threatened species’’ only
after conducting this cumulative
analysis and describing the expected
effect on the species now and in the
foreseeable future.
The Act does not define the term
‘‘foreseeable future,’’ which appears in
the statutory definition of ‘‘threatened
species.’’ Our implementing regulations
at 50 CFR 424.11(d) set forth a
framework for evaluating the foreseeable
future on a case-by-case basis. The term
‘‘foreseeable future’’ extends only so far
into the future as the Service can
reasonably determine that both the
future threats and the species’ responses
to those threats are likely. In other
words, the foreseeable future is the
period of time in which we can make
reliable predictions. ‘‘Reliable’’ does not
mean ‘‘certain’’; it means sufficient to
provide a reasonable degree of
confidence in the prediction. Thus, a
prediction is reliable if it is reasonable
to depend on it when making decisions.
It is not always possible or necessary
to define foreseeable future as a
particular number of years. Analysis of
the foreseeable future uses the best
scientific and commercial data available
and should consider the timeframes
applicable to the relevant threats and to
the species’ likely responses to those
threats in view of its life-history
characteristics. Data that are typically
relevant to assessing the species’
biological response include species-
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specific factors such as lifespan,
reproductive rates or productivity,
certain behaviors, and other
demographic factors.
Analytical Framework
The SSA report documents the results
of our comprehensive biological review
of the best scientific and commercial
data regarding the status of the species,
including an assessment of the potential
threats to the species. The SSA report
does not represent a decision by the
Service on whether the species should
be proposed for listing as an endangered
or threatened species under the Act.
However, it does provide the scientific
basis that informs our regulatory
decisions, which involve the further
application of standards within the Act
and its implementing regulations and
policies. The following is a summary of
the key results and conclusions from the
SSA report; the full SSA report can be
found at Docket FWS–R4–ES–2021–
0092 on https://www.regulations.gov and
at https://www.fws.gov/Asheville/.
To assess pyramid pigtoe viability, we
used the three conservation biology
principles of resiliency, redundancy,
and representation (Shaffer and Stein
2000, pp. 306–310). Briefly, resiliency
supports the ability of the species to
withstand environmental and
demographic stochasticity (for example,
wet or dry, warm or cold years),
redundancy supports the ability of the
species to withstand catastrophic events
(for example, droughts, large pollution
events), and representation supports the
ability of the species to adapt over time
to long-term changes in the environment
(for example, climate changes). In
general, the more resilient and
redundant a species is and the more
representation it has, the more likely it
is to sustain populations over time, even
under changing environmental
conditions. Using these principles, we
identified the species’ ecological
requirements for survival and
reproduction at the individual,
population, and species levels, and
described the beneficial and risk factors
influencing the species’ viability.
The SSA process can be categorized
into three sequential stages. During the
first stage, we evaluated the individual
species’ life-history needs. The next
stage involved an assessment of the
historical and current condition of the
species’ demographics and habitat
characteristics, including an
explanation of how the species arrived
at its current condition. The final stage
of the SSA involved making predictions
about the species’ responses to positive
and negative environmental and
anthropogenic influences. Throughout
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all of these stages, we used the best
available information to characterize
viability as the ability of a species to
sustain populations in the wild over
time. We use this information to inform
our regulatory decision.
Summary of Biological Status and
Threats
In this discussion, we review the
biological condition of the species and
its resources, and the threats that
influence the species’ current and future
condition, in order to assess the species’
overall viability and the risks to that
viability.
Species Needs
We assessed the best available
information to identify the physical and
biological needs to support individual
fitness at all life stages for the pyramid
pigtoe. Full descriptions of all needs are
available in chapter 4 of the SSA report
(Service 2021, pp. 29–36), which can be
found in docket number FWS–R4–ES–
2021–0092 on https://
www.regulations.gov, and on our
internet site https://www.fws.gov/
Asheville/. To maintain viability,
individual pyramid pigtoes need clean
flowing water, appropriate water quality
and temperatures (parameters listed in
Service 2021, p. 29), low levels of
sedimentation, and food and nutrients.
Pyramid pigtoe habitat is in rivers with
natural flow regimes. Perturbations that
disrupt natural flow patterns (e.g.,
dams) have a negative influence on
pyramid pigtoe and host fish resilience.
Pyramid pigtoe habitat must have
adequate flow to deliver oxygen, enable
passive reproduction, and deliver food.
At the population and species
(rangewide) level, the pyramid pigtoe
needs habitat connectivity and positive
demographic attributes (population
density and growth rate, age class
structure, recruitment) to maintain
viability (Service 2021, pp. 32–33).
Dendritic, or branched, orientation of
stream systems can enhance
metapopulation persistence compared
to linear or two-dimensional systems
(Fagan 2002, p. 3,243). Tributary
connection to river mainstems allows
movement of host fishes and helps
facilitate dispersal and colonization of
appropriate habitat patches by mussels.
A high degree of connection between
habitat patches and occupied reaches is
necessary, because mussels are heavily
dependent on gene exchange and host
fish movement and dispersal within
river corridors to maintain viable
populations (Newton et al. 2008, p.
425).
Fragmentation of stream habitat
results in barriers to host fish
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movement, which in turn, influences
mussel distributions, increasing the
likelihood and compounding the
significance of local extirpation events
(Fagan 2002, p. 3,248). The pyramid
pigtoe and other mussel species that use
small host fishes, such as minnows and
shiners (family Cyprinidae), are more
susceptible to impacts from habitat
fragmentation. This is due to increasing
distance between suitable habitat
patches and low likelihood of small host
fish swimming over that distance as
compared to large host fishes (Vaughn
2012, p. 7). Barriers to movement can
cause isolated or patchy distributions of
mussels, which may limit both genetic
exchange and recolonization (Jones et
al. 2006, p. 528).
Mussel abundance in a given river
reach is a product of the number of
mussel beds (aggregations of freshwater
mussels) and the density of mussels
within those beds. Healthy pyramid
pigtoe populations have numerous
individuals, with multiple age classes,
and exhibit regular recruitment of new
age classes. For pyramid pigtoe
populations to be resilient, there must
be multiple mussel beds of sufficient
density such that local stochastic events
do not eliminate the bed(s), allowing the
mussel bed and the overall local
population within a river reach to
recover from any one event. A dendritic
distribution (branching, such that there
is not a line connecting a single
upstream and downstream aggregation)
over a large area also helps buffer
against stochastic events that may
impact populations. Mussels do not
actively seek mates; rather, males
release sperm into the water column,
where it drifts until a female takes it in
(Moles and Layzer 2008, p. 212).
Therefore, successful individual
reproduction and population viability
require sufficient numbers of female
mussels downstream of sufficient
numbers of male mussels; higher
density (number of mussels per unit
area) increases the likelihood of
fertilization.
Threats
We have determined that past and
current threats to the pyramid pigtoe
include habitat degradation or loss from
a variety of sources (e.g., dams and other
barriers, resource extraction); degraded
water quality from chemical
contamination and erosion from
development, agriculture, and mining
operations; direct mortality from
dredging; residual impacts (reduced
population size) from historical harvest;
and the proliferation of invasive,
nonnative species. Cumulatively, these
threats also contribute to the negative
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effects associated with the species’
small population size in certain areas.
The following discussions include
evaluations of three current threats and
associated sources that are affecting the
pyramid pigtoe and its habitat: (1)
Habitat (including water quality)
degradation or loss, (2) invasive and
nonnative species, and (3) negative
effects associated with small population
size (Service 2021, pp. 51–83). We also
considered impacts from climate
change, but found no evidence linking
climate change impacts to the current
status of the pyramid pigtoe. We note
that overutilization (commercial mussel
harvest) was a threat historically and
likely reduced the size of many
populations such that they have not
recovered to historical abundance
levels, but it is not currently a threat. In
addition, potential impacts from
disease, parasites, and predation, as
well as potential impacts to host
species, were evaluated but were found
to have minimal effects on viability of
the pyramid pigtoe based on current
knowledge (Service 2021, pp. 78–79).
Although not a widespread threat,
disease is likely affecting at least one
population of pyramid pigtoe: The
Clinch River mussel assemblage, which
includes a pyramid pigtoe population,
has recently undergone a die-off that is
associated with a novel densovirus
(Richard et al. 2020, entire). Finally, we
also considered effects associated with
enigmatic population declines
(unexplained die-offs of large numbers
of mussels over a short period of time),
which have been documented in fresh
water river mussel populations since the
1960s; despite speculation and repeated
aquatic organism surveys and water
quality monitoring, the causes of these
events are largely unknown (Haag 2019,
p. 43).
49995
Predominant threats affecting each
pyramid pigtoe population are listed in
Table 1. Based on threat information in
the literature or State Wildlife Action
Plans, we categorized the threat level as
low, moderate, or high depending on
their magnitude and immediacy:
• Low—Threats to aquatic fauna far
enough removed in time or space that
they are currently exerting minimal
influence on mussel populations.
• Moderate—Multiple threats linked
to negative effects on mussels are
present. Some threats currently acting
on mussel habitat, reducing resource
needs, and limiting recruitment and
population growth.
• High—Multiple threats linked to
negative effects on mussels are present
and have been acting cumulatively on
mussel habitat, prohibiting sustained
recruitment and population growth.
TABLE 1—CURRENT THREATS AND LEVEL OF THREAT TO THE PYRAMID PIGTOE BY RIVER BASIN AND POPULATION
[Adapted and modified from SSA report, Service 2021, pp. 157–164]
Population
Threat level
category
Threats
OHIO RIVER BASIN
Muskingum River ......................
High ................
Upper Green River ....................
Low .................
Barren River ..............................
Moderate ........
Middle Green River ...................
Moderate ........
Lower Green River ....................
Moderate ........
Cumberland River .....................
High ................
Hydropower development; impoundment; dredging; population isolation; past commercial
harvest.
Impoundment; habitat loss and water quality degradation; resource extraction; past commercial harvest.
Impoundment; habitat loss and water quality degradation; resource extraction; past commercial harvest.
Impoundment; habitat loss and water quality degradation; resource extraction; past commercial harvest.
Impoundment; habitat loss and water quality degradation; resource extraction; past commercial harvest.
Habitat fragmentation, hypolimnetic discharges.
TENNESSEE RIVER BASIN
Holston River ............................
Clinch River ...............................
High ................
Moderate ........
Paint Rock River .......................
Low .................
Tennessee River (Wheeler Reservoir).
Tennessee River (Pickwick
Reservoir).
Tennessee River (Kentucky
Reservoir).
Upper Duck River .....................
High ................
Habitat fragmentation, hypolimnetic discharges.
Development; agricultural activities; dams; overharvest historically; contaminants; resource
extraction; degraded water quality; enigmatic die-offs.
Habitat loss through channel maintenance (snag removal); habitat fragmentation and population isolation due to impoundment; agriculture.
Impoundment; habitat degradation from flow releases; past commercial harvest.
High ................
Impoundment; dredging; navigation impacts; past commercial harvest.
High ................
Impoundment; dredging and navigation impacts; agriculture.
Moderate ........
Lower Duck River .....................
Moderate ........
Development; agricultural activities; water quality degradation; impoundments; fragmented
populations.
Development and water quality degradation.
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ARKANSAS-WHITE-RED BASIN
Petit Jean River ........................
Eleven Point River ....................
Little River .................................
Moderate ........
Low .................
Moderate ........
Agriculture; habitat loss and water quality degradation.
Habitat loss and water quality degradation; agricultural effects.
Impoundment, habitat loss, and water quality degradation.
LOWER MISSISSIPPI BASIN
Lower Black River .....................
Lower St. Francis River ............
Tyronza River ............................
White River ...............................
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Moderate ........
High ................
High ................
Moderate ........
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Agriculture, habitat loss, and water
Agriculture, habitat loss, and water
Agriculture, habitat loss, and water
Impoundment, resource extraction,
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quality degradation.
quality degradation.
quality degradation.
habitat loss, and water quality degradation.
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TABLE 1—CURRENT THREATS AND LEVEL OF THREAT TO THE PYRAMID PIGTOE BY RIVER BASIN AND POPULATION—
Continued
[Adapted and modified from SSA report, Service 2021, pp. 157–164]
Population
Threat level
category
Upper Ouachita River ...............
Little Missouri River ..................
Ouachita River ..........................
Upper Saline River ....................
Moderate
Moderate
Moderate
Moderate
........
........
........
........
Lower Saline River ....................
Moderate ........
Bayou Bartholomew ..................
Lower Ouachita River ...............
Big Sunflower River ..................
Hushpuckna River .....................
Bogue Phalia .............................
Little Sunflower River ................
Sunflower River .........................
Sandy Bayou .............................
Big Black River .........................
High
High
High
High
High
High
High
High
High
................
................
................
................
................
................
................
................
................
Habitat Degradation or Loss
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Threats
Development and Urbanization
Development and urbanization
activities that may contribute to
pyramid pigtoe habitat degradation or
loss, including reduced water quality,
occur throughout the species’ range. The
term ‘‘development’’ refers to
urbanization of the landscape, including
(but not limited to) land conversion for
residential, commercial, and industrial
uses and the accompanying
infrastructure. The effects of
urbanization may include alterations to
water quality, water quantity, and
habitat (both in-stream and streamside)
(Ren et al. 2003, p. 649; Wilson 2015, p.
424). Urban development can lead to
increased variability in streamflow,
typically increasing the extent and
volume of water entering a stream after
a storm and decreasing the time it takes
for the water to travel over the land
before entering the stream (Giddings et
al. 2009, p. 1). Deleterious effects on
streams (i.e., water collection on
impervious surfaces that rapidly flows
into storm drains and local streams),
including those that may be occupied by
the pyramid pigtoe, include:
• Water Quantity: Storm drains
deliver large volumes of water to
streams much faster than would
naturally occur, often resulting in
flooding and bank erosion that reshapes
the channel and causes substrate
instability, resulting in destabilization
of bottom sediments. Increased, highvelocity discharges can cause pyramid
pigtoe to become stressed, displaced, or
killed by fast-moving water and the
debris and sediment carried in it.
• Water Quality: Pollutants (e.g.,
gasoline, oil drips, fertilizers) that
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Impoundment, navigation, habitat loss, and water quality degradation.
Agriculture, habitat loss, and water quality degradation.
Impoundment, navigation, habitat loss, and water quality degradation.
Impoundment, navigation; agriculture; resource extraction; habitat loss and water quality
degradation.
Impoundment, navigation, agriculture, resource extraction, habitat loss, and water quality
degradation.
Agriculture, habitat loss and water quality degradation.
Impoundment; navigation; habitat loss and water quality degradation.
Agriculture; habitat loss and water quality degradation.
Impoundment; agriculture; navigation; habitat loss and water quality degradation.
Impoundment; agriculture; navigation; habitat loss and water quality degradation.
Impoundment; agriculture; navigation; habitat loss and water quality degradation.
Impoundment; agriculture; navigation; habitat loss and water quality degradation.
Impoundment; agriculture; navigation; habitat loss and water quality degradation.
Impoundment; agriculture, habitat loss and water quality degradation.
accumulate on impervious surfaces may
be washed directly into streams during
storm events thereby directing killing
pyramid pigtoe individuals.
• Water Temperature: During warm
weather, rain that falls on impervious
surfaces becomes superheated and can
stress or kill pyramid pigtoe individuals
when it enters streams.
Water infrastructure to support
development, including water supply,
reclamation, and wastewater treatment,
results in pollution or contaminant
discharges to streams. Right of way
(ROW) crossings for waterlines and
other utility lines also affect stream
habitats. Direct impacts from utility
crossings include direct exposure or
crushing of individuals, sedimentation,
and flow disturbance. The most
significant cumulative impact involves
cleared ROWs that result in direct
runoff and increased stream temperature
at the crossing locations. Maintenance
or clearing of ROWs may entail
herbicide applications that subsequently
enter streams via stream runoff.
Most populations of pyramid pigtoe
in urban areas with large human
populations have been diminished or
lost. Secondary impacts resulting from
development, such as the increased
contaminant introduction, stream
disturbance caused by impervious
surfaces, barrier construction, and forest
conversion to other land use types such
as agriculture or urban uses are likely
acting cumulatively on the species.
Increased human population growth
projections indicate urban sprawl (a
current process) will affect pyramid
pigtoe populations in the Tennessee and
Ohio basins (Terando et al. 2014, p. 7;
Tayyebi et al. 2015, p. 110). In the
Upper and Lower Duck River MUs, the
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species is currently impacted by rapid
development encroaching from the city
of Nashville and nearby smaller urban
areas such as Columbia, TN (TWRA
2016, p. 15). The pyramid pigtoe
population in the Muskingum River is
downstream of the Tuscarawas River,
which has been severely degraded by
industrial development that continues
to affect water quality (Hoggarth 1994,
p. 3; Haefner and Simonson 2018, p. 1).
Threats to the pyramid pigtoe from
development are partly mitigated by
Federal lands. Several locations where
the pyramid pigtoe occurs in water
bodies located on or immediately
adjacent to Federal lands receive some
indirect benefits to viability such as lack
of urbanization and land development
pressure. These include the Pond Creek
Refuge in Arkansas (Arkansas-WhiteRed basin) as well as Upper Ouachita,
Felsenthal, and White River Refuges
(Lower Mississippi basin), and Wheeler
Refuge (Tennessee Basin) that are
adjacent to large rivers where the
pyramid pigtoe occurs. Mammoth Cave
National Park also provides a level of
localized protection against
development pressures for the pyramid
pigtoe population in the upper Green
River, Kentucky (Ohio Basin).
On private lands, the Saline-CaddoOuachita Programmatic Safe Harbor
Agreement and Candidate Conservation
Agreement with Assurances programs
are voluntary conservation programs
that support ongoing stewardship for
imperiled species, including the
pyramid pigtoe. Large tracts of private
land in the upper Saline and Ouachita
River systems adjacent to streams and
upland areas are covered under these
programs. These lands are mostly
upstream of pyramid pigtoe sites
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(Service 2015, p. 6) but could have a
positive indirect long-term benefit to the
species by reducing sediment and
pollutant runoff and improving water
quality downstream. Some private lands
in pyramid pigtoe MUs also are
managed for conservation through The
Nature Conservancy (TNC) programs in
the upper Green River in Kentucky, the
upper Clinch/Powell River, Tennessee
and Virginia, the Saline River in
Arkansas, and the Paint Rock River in
Alabama. In these watersheds, TNC has
a few riparian inholdings that are
protected from developments. In
addition, within these watersheds, TNC
implements community-based and
partner-oriented projects to address
aquatic species and instream habitat
conservation by restoring and protecting
streambanks and riparian zones.
Various small, isolated parcels of
State land (e.g., State parks, State
forests, wildlife management areas)
along MUs where the pyramid pigtoe
occurs also provide a conservation
benefit as a buffer to development.
However, vast tracks of riparian lands in
the range of the pyramid pigtoe are
privately owned, without conservation
programs, and the prevalence of
privately owned lands along rivers is
comparatively much larger than the
species’ occurrence on public lands.
Limited overlap of the species’ range
with public lands and private lands
with conservation programs diminishes
their ability to protect the species,
because the habitat protection benefits
these lands provide are at significant
risk of being negated by detrimental
activities upstream or immediately
downstream.
Transportation
Transportation-related impacts
include both road development and
river navigation. Road development
increases impervious surfaces as well as
land clearing and habitat fragmentation.
Roads are generally associated with
negative effects on the biotic integrity of
aquatic ecosystems, including changes
in surface water temperatures and
patterns of runoff, sedimentation,
adding heavy metals (especially lead),
salts, organics, and nutrients to stream
systems (Trombulak and Frissell 2000,
p. 18).
With regard to river navigation,
dredging and channelization activities
(as a means of maintaining waterways)
have altered riverine habitats
nationwide (Ebert 1993, p. 157).
Channelization affects many physical
characteristics of streams through
accelerated erosion, increased bedload,
reduced depth, decreased habitat
diversity, geomorphic instability, and
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riparian canopy loss (Hartfield 1993, p.
139). All of these impacts contribute to
loss of habitat for the pyramid pigtoe
and host fishes. Increases in turbulence,
suspended and deposited sediments,
and turbidity resulting from river
transportation and associated activities
may affect mussel feeding and
respiration (Aldridge et al. 1987, p. 25).
In addition to dredging and channel
maintenance, impacts associated with
barge traffic, which includes
construction of fleeting areas, mooring
cells, docking facilities, and propeller
wash, also destroy and disrupt mussel
habitat (see Miller et al. (1989, pp. 48–
49) as an example for disturbance from
barges).
Transportation-related impacts across
the range of the pyramid pigtoe include
(but are not limited to) the following
examples:
• Extensive stream channelization
and snag removal has severely affected
the freshwater mussel fauna and habitat
in the Paint Rock River system,
including the lower reaches of Estill
Fork and Hurricane Creek (Ahlstedt
1995–96, p. 65). Even if active
channelization activities are not
currently occurring in rivers and
streams occupied by the pyramid pigtoe,
impacts of past actions can have
permanent effects (Haag and Cicerello
2016, p. 60; Hubbard et al. 1993, p. 142;
Watters 2000, p. 274).
• Commercial navigation previously
took place in the lower Green and
Barren Rivers, where navigation dams
remain but are not in operation. Past
dredging and navigation affected mussel
beds in the mainstem Cumberland
River, which has the last remaining
population of pyramid pigtoe in the
Cumberland River system (Hubbs 2012,
p. 9).
• Currently, all three of the Tennessee
River mainstem pyramid pigtoe MUs are
likely affected to some extent by
channel maintenance and navigation
operations, due to their clustered
distribution and proximity to navigation
dams.
• Two navigation dams are operated
on the Ouachita River, which is
maintained by the Corps as a waterway,
and affect three MUs.
Contaminants
Contaminants contained in point and
non-point discharges can degrade water
and substrate quality and adversely
impact mussel populations. The effects
of contaminants such as metals,
chlorine, and ammonia are profound on
juvenile mussels (Bartsch et al. 2003, p.
2,566; Augspurger et al. 2003, p. 2,571).
Juvenile mussels may readily ingest
contaminants bound to sediment
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49997
particles (Newton and Cope 2007, p.
276). These contaminants also affect
mussel glochidia, which are very
sensitive to some toxicants (Goudreau et
al. 1993, p. 221; Jacobson et al. 1997, p.
2,386; Valenti et al. 2005, p. 1,243).
High levels of suspended solids alone
(without bound contaminants) can
result in mussel reproductive failure or
low fertilization rates of long-term
brooders, such as species of the genus
Pleurobema (Gascho-Landis and
Stoeckel 2015, p. 229).
Current State regulations regarding
pollutants are designed to be protective
of aquatic organisms; however,
freshwater mussels may be more
susceptible to some pollutants than the
test organisms commonly used in
bioassays. Additionally, water quality
criteria may not incorporate data
available for freshwater mussels (March
et al. 2007, pp. 2,066–2,067). A
multitude of bioassays conducted on 16
mussel species (summarized by
Augspurger et al. 2007, pp. 2,025–2,028)
show that freshwater mollusks are more
sensitive than previously believed to
some chemical pollutants, including
chlorine, ammonia, copper, fungicides,
and herbicide surfactants. Nickel and
chloride were toxic to federally
threatened mussel species at levels
below the current criteria and are
sensitive to sodium dodecyl sulfate
(SDS), a surfactant commonly used in
household detergents, for which water
quality criteria do not currently exist
(Gibson 2015, p. 80, p. 90; Gibson et al.
2018, pp. 247–250). None of the States
in the range of the pyramid pigtoe have
fully adopted the Environmental
Protection Agency’s 2013 recommended
ammonia criteria for freshwater
mollusks (78 FR 52192, August 22,
2013).
Contaminant inputs (including
sediments) to pyramid pigtoe habitat
stem from multiple threats, including
urbanization, resource extraction,
agriculture, and channel maintenance
for navigation, diminishing water
quality in many areas of the four basins
where the species occurs. Examples of
contaminant-related impacts in the
range of the pyramid pigtoe include (but
are not limited to) the following:
• Long-term declines and extirpation
of mussels from reaches of the Upper
Clinch MU in Virginia attributed, in
part, to copper and zinc contamination
originating from wastewater discharges
at coal-fired power plants (Price et al.
2014, p. 12; Zipper et al. 2014, p. 9).
Coal plants also are located on the
Lower Green and Cumberland-Old
Hickory MUs.
• Heavy metals toxicity to mussels
has been documented in the
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Muskingum, Upper Clinch, and all
Tennessee River MUs (Havlik and
Marking 1987, pp. 4–9).
• A chemical spill from a tanker truck
accident flowed into the Upper Clinch
MU in Virginia and eliminated
approximately 18,000 individuals of
several mussel species (Jones et al. 2001,
p. 20; Schmerfeld 2006, p. 12),
including approximately 750
individuals of three federally listed
species (Schmerfeld 2006, p. 12). A
catastrophic chemical spill in 1999
affected approximately 10 miles of the
Ohio River and resulted in the loss of an
estimated 1 million mussels, including
two federally listed species (Butler
2005, p. 24).
State and Federal water quality
programs provide a level of protection
to the pyramid pigtoe from
development, agriculture, and river
navigation activities by regulating storm
water and point source (end of pipe)
discharges to streams. Section 401 of the
Federal Clean Water Act (CWA; 33
U.S.C. 1251 et seq.) requires that an
applicant for a Federal license or permit
provide a certification that any
discharges from the facility will not
degrade water quality or violate waterquality standards, including those
established by States. Section 404 of the
CWA establishes a program to regulate
the discharge of dredged and fill
material into waters of the United
States. Under the CWA, permits to fill
wetlands and culvert, bridge, or realign
streams or water features are issued by
the U.S. Army Corps of Engineers.
Current State regulations regarding
pollutants are designed to be protective
of aquatic organisms; however, as
discussed above, freshwater mussels
may be more susceptible to some
pollutants than the aquatic biota for
which water quality criteria are
currently established.
Despite existing authorities such as
the CWA, pollutants continue to impair
the water quality in areas of the pyramid
pigtoe’s range. State and Federal
regulatory mechanisms have helped
reduce the negative effects of point
source discharges since the 1970s, yet
these regulations are difficult to
implement and enforce. Although new
water quality criteria are under
development that will take into account
more sensitive aquatic species, most
current criteria do not. It is expected
that several years will be needed to
implement new water quality criteria
throughout the species’ range.
Agriculture
Agricultural activities occur across
the range of the pyramid pigtoe and are
a factor in its historical decline and
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localized extirpations. The advent of
intensive row crop agricultural practices
corresponds with freshwater mussel
declines, and species extirpations, in
the eastern United States (Peacock et al.
2005, p. 550). Nutrient enrichment and
water withdrawals, threats commonly
associated with agricultural activities,
may be localized and limited in scope,
and have the potential to affect
individual pyramid pigtoe mussels.
However, chemical control using
pesticides may have broader impacts.
Pesticides, including herbicides,
fungicides, and insecticides as well as
their surfactants and adjuvants, are
highly toxic to juvenile and adult
freshwater mussels (Bringolf et al. 2007,
p. 2,092) and deleterious if not properly
applied to agricultural operations.
Waste from confined animal feeding and
commercial livestock operations is
another potential source of
contaminants that come from
agricultural runoff. The concentrations
of these contaminants from fields or
pastures may be at levels that can affect
an entire population, especially given
the highly fragmented distribution of
the pyramid pigtoe.
Agencies such as the Natural
Resources Conservation Service (NRCS)
and the Soil and Water Conservation
Districts provide technical and financial
assistance to farmers and private
landowners. Additionally, county
resource development councils and
university agricultural extension
services disseminate information on the
importance of minimizing land use
impacts, specifically agriculture, on
aquatic resources. These programs help
identify opportunities for conservation
through projects such as exclusion
fencing and alternate water supply
sources, which help decrease nutrient
inputs and water withdrawals and help
keep livestock off stream banks and
shorelines, reducing erosion. However,
the overall effectiveness of these
programs over a large scale is unknown
given the pyramid pigtoe’s wide
distribution and varying agricultural
intensities in its range.
Dams and Barriers
Whether for flood control,
hydropower, river navigation, or as
abandoned mill structures, dams and
their impoundments are one of the most
pervasive threats to pyramid pigtoe
rangewide: 26 of 35 populations and all
4 major basins in the species’ range are
affected (Table 1). Dams have many
impacts on stream ecosystems, and the
effects of impoundments and barriers on
aquatic habitats and freshwater mussels
are relatively well-documented (Watters
2000, p. 261). Extinction and extirpation
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of many North American freshwater
mussels can be traced to impoundment
and inundation of riffle habitats in all
major river basins of the central and
eastern United States (Haag 2009, p.
107). Reductions in the diversity and
abundance of mussels are primarily
attributed to habitat shifts, alteration
and disruption of connectivity, and
diminished water quality as a result of
reservoir construction (Neves et al.
1997, p. 63). The survival and
reproductive success of mussels are
influenced upstream of dams as flowing
waters change to impounded waters,
with increased depths and buildup of
sediments, decreased dissolved oxygen,
and drastic alteration of resident fish
assemblages. Downstream of dams,
biotic and physical habitat conditions
provided by natural flow regimes are
altered by minimal releases or scouring
flows, seasonal dissolved oxygen
depletion, and reduced or increased
water temperatures. The number of fish
species is greatly reduced where
coldwater flow (hypolimnetic discharge)
is released. Additionally, dams fragment
habitat, limiting dispersal of mussels on
their fish hosts, which leads to genetic
isolation of mussel populations.
Resource Extraction
Predominant resource extraction
threats in the range of the pyramid
pigtoe stem from mining (primarily coal
but including other mineral resources)
and oil and gas exploration. Activities
associated with coal mining and oil and
gas drilling can contribute chemical
pollutants to streams. Acid mine
drainage is created from the oxidation of
iron-sulfide minerals such as pyrite,
forming sulfuric acid (Sams and Beer
2000, p. 3). This acid mine drainage
may be associated with high
concentrations of aluminum,
manganese, zinc, and other constituents
(Tennessee Department of Environment
and Conservation (TDEC) 2014, p. 72).
The metals, and the high acidity
typically associated with acid mine
drainage, can be acutely and chronically
toxic to aquatic life (Jones 1964, p. 96).
Implementation of the Surface Mining
Control and Reclamation Act of 1977
(SMCRA; 30 U.S.C. 1201 et seq.) has
significantly reduced acid mine
drainage from new coal mines; however,
un-reclaimed areas mined prior to the
SMCRA continue to generate acid mine
drainage in portions of the pyramid
pigtoe’s range. Direct impacts to the
pyramid pigtoe from acid mine drainage
in most occupied river reaches are
unlikely because coal mining sites tend
to be adjacent to smaller headwater
streams, but mining pollutants can be
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transferred downstream to pyramid
pigtoe habitats.
Surface mining has been identified as
a source of impairment for
approximately 775 mi (1,247 km) of
streams in Kentucky (Kentucky
Department for Environmental
Protection 2014, p. 66). Weathering of
soils and rock broken apart to access
coal seams typically increases
alkalinity, total dissolved solids,
salinity, and sedimentation and alters
hydrology and physical habitat of
streams receiving surface mine drainage,
impacting fish and aquatic invertebrate
communities (e.g., Bernhardt and
Palmer 2011, pp. 42–49; Linberg et al.
2011, entire; Hopkins and Roush 2013,
pp. 585–586; Hitt and Chambers 2014,
p. 923; Hitt et al. 2016, pp. 47–53).
Mining continues to impair water
quality in streams in the Cumberland
Plateau and Central Appalachian
regions of Tennessee and Kentucky
(TDEC 2014, p. 62), which contain
portions of the Tennessee and
Cumberland River basins, and is the
primary source of low pH impairment of
376 mi (605 km) of rivers in Tennessee
(TDEC 2014, p. 53). Coal mining has
resulted in discharges of industrial and
mine wastes from coal mines and coal
processing facilities in the Clinch and
Powell Rivers (Ahlstedt et al. 2016, p.
8). Direct impacts to the pyramid pigtoe
from acid mine drainage or total
dissolved solids in most occupied river
reaches are unlikely because coal
mining sites tend to be adjacent to
smaller headwater streams, but
associated mining pollutants (fine
sediments, metals, and salts) can be
transferred downstream to medium and
large river pyramid pigtoe habitats
(Bernhardt and Palmer, 2011 p. 46).
Natural gas extraction in the
Appalachians, including the
Cumberland River basin, has negatively
affected water quality through
accidental spills and discharges, as well
as increased sedimentation due to
development of road construction,
pipeline, drill pad construction, as well
as tree removal required to clear the
construction areas (Vidic et al. 2013, p.
6). Disposal of insufficiently treated
brine wastewater, more saline than
seawater, has specifically been found to
adversely affect freshwater mussels
(Patnode et al. 2015, p. 62). Potential
threats from natural gas and oil
exploration are also a concern in the
White River basin.
Instream sand and alluvial gravel
mining has been implicated in the
destruction of mussel populations
(Hartfield 1993, p. 138). Negative
impacts associated with gravel mining
include stream channel modifications
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such as altered habitat, disrupted flow
patterns, and sediment transport (Hubbs
et al. 2006, p. 170). Additionally, water
quality modifications including
increased turbidity, reduced light
penetration, increased temperature, and
increased sedimentation result from
gravel mining. Commercial sand and
gravel mining and dredging directly
affects the pyramid pigtoe in the
Tennessee River, specifically within the
Lower Tennessee–Beech MU (Hubbs et
al. 2006, p. 170). The Lower
Cumberland Old Hickory MU has also
been affected by gravel mining and
dredging in the past (Sickel 1982, p. 4)
that has resulted in permanent
alteration of substrates and hydraulic
patterns, contributing to habitat loss for
freshwater mussels.
Invasive and Nonnative Species
Invasive and nonnative species in the
range of the pyramid pigtoe include the
Asian clam, zebra mussel, black carp,
and the plant species, hydrilla. These
nonnative species impact the pyramid
pigtoe through competitive interactions,
water quality degradation, predation,
and habitat alteration.
The Asian clam, found throughout the
range of the pyramid pigtoe, alters
benthic substrates, may filter native
mussel sperm or glochidia, competes
with native species for limited
resources, and causes ammonia spikes
in surrounding water when dying off en
masse (Scheller 1997, p. 2). A typical
settlement of the Asian clam occurs
with a population density ranging from
100 to 200 clams per square meter,
which may not be detrimental to native
unionids; however, populations can
grow as large as 3,000 clams per square
meter, which would influence both food
resources and competition for space for
the pyramid pigtoe.
Within the range of the pyramid
pigtoe, the zebra mussel occurs in the
Ohio, Tennessee, and Arkansas-WhiteRed River basins. Native mussels, such
as the pyramid pigtoe, are negatively
affected by zebra mussels through direct
colonization, reduction of available
habitat, changes in the biotic
environment, or a reduction in food
sources (MacIsaac 1996, p. 292). One of
the direct consequences of the invasion
of zebra mussels is the local extirpation
of native freshwater mussel populations
from (1) attachment to the shells of
native mussels, which can kill them
(zebra mussels are sessile, and cling to
hard surfaces); (2) affecting vertical and
lateral movements of native mussels,
due to heavy infestations, which can
prevent valve closure; and (3)
outcompeting native mussels and other
filter-feeding invertebrates for food. This
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problem has been particularly acute in
the Ohio and Tennessee River systems.
Densities of zebra mussels attained
17,000 per square meter in the
Tennessee River below Wilson Dam in
2017, although recent survey efforts
indicate a decline from that population
explosion (Garner 2018, pers. comm.).
The black carp, which feeds on
mollusks, is listed as ‘‘injurious’’ under
the Lacey Act and occurs in the Ohio,
Tennessee, Lower Mississippi and
Arkansas-White-Red basins where it
overlaps populations of the pyramid
pigtoe. It is highly likely that this
nonnative fish will negatively impact
native aquatic communities by direct
predation, thus reducing populations of
native mussels (Nico et al. 2005, p. 193).
Because black carp attain a large size
and have a lifespan reportedly over 15
years, they have the potential to cause
significant harm to native mollusks by
predation on multiple age classes (Nico
et al. 2005, p. 77).
In addition to negative impacts of
nonnative animals, the invasive
nonnative plant hydrilla can affect
native mussels by covering spawning
areas for native fish, which may be hosts
for glochidia, and can cause significant
reductions in stream oxygen levels
(Colle et al. 1987, p. 410). Hydrilla is
widespread in the Ohio, Cumberland,
and Tennessee River systems. In
general, invasive aquatic plants grow
uncontrolled and can cause habitat to
fill in, affect flow dynamics, and
increase water temperature,
exacerbating drought impacts in stream
habitats (Colle et al. 1987, p. 416).
The Aquatic Nuisance Species (ANS)
Task Force, co-chaired by the Service
and the National Oceanic and
Atmospheric Administration (NOAA),
encourages State and interstate planning
entities to develop management plans
describing detection and monitoring
efforts of aquatic nuisance and
nonnative species, prevention efforts to
stop their introduction and spread, and
control efforts to reduce their impacts.
Management plan approval by the ANS
Task Force is required to obtain funding
under Section 1204 of the ANS
Prevention and Control Act. Each state
within the range of the pyramid pigtoe
has either a plan approved by or
submitted to the ANS Task Force, or a
plan under development. These plans
have been effective in terms of raising
awareness at the state level of the
severity of ecological damage that nonnative and nuisance species are capable
of, but many are in early stages of
implementation. Although laws and
efforts are in place which may be
effective in controlling or diminishing
non-native and invasive species, these
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organisms are a current and future
threat to the pyramid pigtoe throughout
its range.
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Small Population Size
Historically, an extensive, largely
contiguous pyramid pigtoe population
occurred through much of the eastern
half of the United States, and there were
limited barriers preventing genetic
interchange among river systems. With
the completion of hundreds of dams in
the 1900s, many large-river pyramid
pigtoe populations were lost, resulting
in isolation of tributary populations.
The population size of a long-lived
species, such as the pyramid pigtoe,
may take decades to decline to
extirpation post-impoundment. At best,
limited post-impoundment recruitment
may be occurring in the isolated
pyramid pigtoe populations, indicating
that these small populations are not
likely viable long term.
Currently, the pyramid pigtoe exhibits
several traits that reduce population
viability, including small population
size and low fecundity at many
locations compared to other mussels.
Smaller population size puts the species
at greater risk of extirpation from
stochastic events (e.g., drought) or
anthropomorphic changes and
management activities that affect
habitat. In addition, smaller populations
may have reduced genetic diversity, be
less genetically fit, and more susceptible
to disease during extreme
environmental conditions (Frankham
1996, p. 1,505). Moreover, small and
isolated populations are at higher risk of
further loss of genetic variation due to
genetic drift, thereby lessening the
affected species’ ability to adapt to a
continuously changing environment.
Lastly, the relatively low fecundity,
coupled with low juvenile survivorship,
limit the pyramid pigtoe’s ability to
withstand and recover from population
losses. While several populations of
pyramid pigtoe are at risk of extirpation
due to their small size, other
populations are large enough and
sufficiently connected within their MU
that they are regularly recruiting new
cohorts. Therefore, small population
size is a population-level threat but not
currently a species-level or rangewide
threat.
Changing Climate Conditions
Climate change threats for freshwater
mussels include alteration of natural
stream flow and water temperature
regimes as drought, precipitation, and
temperature patterns shift. Population
discontinuity and isolation is possible
due to the dynamics in range shifts of
mussels and their host fishes as a result
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of warming climates, based on lifehistory traits (Archambault et al. 2018,
p. 880). However, the mechanisms
behind these shifts and how they alter
population connectivity and gene flow
are uncertain, and there is no evidence
linking climate change impacts
specifically to the current status of the
pyramid pigtoe.
Cumulative/Synergistic Effects
Collectively, threats to the pyramid
pigtoe have acted on the species to
reduce the number of historical
populations and fragment and reduce
the size of extant populations.
Currently, 15 of the 35 extant
populations are small in size,
represented by fewer than 10
individuals observed over the past 20
years. Factors such as low effective
population size, genetic isolation,
relatively low levels of fecundity and
recruitment, and limited juvenile
survival could affect the ability of these
species to maintain current population
levels and to rebound if a reduction in
population occurs (e.g., through
predation, toxic releases or spills, or
poor environmental conditions that
inhibit successful reproduction).
Additionally, fragmentation (i.e., the
breaking apart of habitat segments,
independent of habitat loss (Fahrig
2003; p. 299)) and isolation contribute
to the extinction risk that mussel
populations face from stochastic events
(see Haag 2012, pp. 336–338).
Throughout the range of the pyramid
pigtoe, impoundments fragment and
isolate populations from one another,
prevent dispersal, which reduces gene
flow (Vaughn 2012, p. 6; Service 2018,
pp. 59–60; Service 2019, p. 74), and
compound other threats, such as the
introduction of contaminants and
pollution resulting from mining, oil and
gas exploration, agricultural runoff, and
untreated or poorly treated wastewater
discharges.
Current Conditions
Current (and future) conditions are
described using the following categories
that characterize the overall condition
(resiliency) of the pyramid pigtoe
populations:
• High—Population with more than
50 individuals reported since 2000,
distributed over a more or less
contiguous river or stream of at least 31
miles (mi) (50 kilometers (km)) in
length, with evidence of recent
recruitment. Water quality and habitat
conditions remain optimal for
recruitment, and multiple age classes
are represented. Populations are not
linearly distributed and occur in more
than one stream within the river system.
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• Medium—small restricted
populations (10 to 50 individuals
reported since 2000) generally
distributed over a more or less
contiguous length of river or stream of
at least 6.2 mi (10 km) but less than 31
mi (50 km)), with some level of age class
structure, but vulnerable to existing
threats. Appropriate substrates are
generally maintained with instream
flows that mimic natural conditions.
Water quality and habitat degradation
may occur but not at a level that
negatively affects both the density and
extent of a population.
• Low—very small and highly
restricted populations (fewer than 10
individuals reported since 2000),
distributed over less than 6.2 mi (10 km)
of river or stream, with little to no
evidence of age class structure (only
older individuals observable). Loss of
mussel habitat or water quality
degradation within the formerly
occupied river or stream reach has been
measured or observed, and imminent
threats are documented. Population is
linearly distributed and geographically
restricted and is not likely to withstand
stochastic events.
We assessed resiliency and
redundancy based on management units
(MUs) defined at the hydrologic unit
code (HUC) scale (Seaber et al. 1987,
entire; U.S. Geological Survey 2018,
entire). Management units consisted of
HUC–8 regions, which are analogous to
medium-sized river basins across the
United States. An MU consisting of a
linear reach of stream could harbor one
population or, if it contained a large gap
in the species’ distribution as a result of
an impoundment or physiographic
boundary, more than one population. If
multiple tributaries were occupied
(dendritic distribution) each tributary
within the MU was considered to
represent a population. A majority of
MUs contained one population, given
that the pyramid pigtoe occurs only in
large or medium-sized rivers and not
smaller tributaries.
Representation was assessed at the
larger HUC–2 region (major basin) scale,
and representation units were
delineated to capture the variation in
adaptive traits and genetic diversity. See
chapter 2 in the SSA report for further
explanation of the analysis methodology
(Service 2021, pp. 20–22). Each major
basin contains unique physiographic
provinces and ecoregions. Therefore, the
populations within each major basin
may harbor basin-specific adaptive traits
and as such species representation has
been reduced from six basins to four
basins. Historical connectivity between
the major basins has been lost due
habitat degradation and construction of
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impoundments and there is no
opportunity for exchange of beneficial,
or adaptive, genes between the basins.
The pyramid pigtoe’s current range
extends over nine States, including
Alabama, Arkansas, Kentucky,
Louisiana, Mississippi, Ohio,
Oklahoma, Tennessee, and Virginia. The
species is considered extirpated in
Indiana, Illinois, Iowa, Kansas,
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Minnesota, Missouri, Pennsylvania,
West Virginia, and Wisconsin. Its
current range is within four major HUC–
2 regions (the Arkansas-White-Red,
Lower Mississippi, Ohio, and Tennessee
River regions, Figure 1). It is extirpated
in the Missouri and Upper Mississippi
River HUC–2 regions. Overall, the
pyramid pigtoe formerly occupied at
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least 135 MUs but currently occurs in 28
MUs (Figure 2). Known populations
have declined in number, from 151
historically to 35 today. Currently, 15
MUs have low resiliency, 9 MUs have
medium resiliency, and 4 MUs have
high resiliency (Table 2, in Future
Conditions).
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Rangewide Distribution of Pyramid Pigtoe
~ Extant Management Units
1111 Extirpated Management Units
1 inch = 353 Kilometers
1 inch= 219 miles
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Future Conditions
In the SSA report, we forecast the
pyramid pigtoe’s response to plausible
future scenarios of environmental
conditions. The future scenarios project
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the range in magnitude and scope of
threats into the future. Uncertainty is
inherent in any risk assessment, so we
must consider plausible conditions to
make our determinations. When
assessing the future, viability is not a
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specific state, but rather a continuous
measure of the likelihood that the
species will sustain populations over
time.
The scenarios described in the SSA
report represent two possible future
conditions. Under scenario 1, the threat
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Figure 2. Extant and extirpated MUs (HUC-8) of pyramid pigtoe across its entire
historical and current range.
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levels remain unchanged (threats
continue to act on the species at the
current rate), whereas under scenario 2
the threat levels increase. Both scenarios
project existing regulatory mechanisms
and voluntary conservation measures
benefiting the species remaining in
place. We did not analyze a scenario
whereby threat levels lessen because the
primary threats that have fragmented
and isolated populations will persist.
Developed areas, large dams, and most
of the small and retired dams affecting
the species will remain in place.
We included climate change in our
future scenarios as a factor that would
add to the negative impacts of the
primary threats on the species’ habitat.
Climate change is expected to alter the
natural flow regime through increased
drought and flooding worsening
desiccation, scour, and sedimentation in
each MU. However, in our analysis the
influence of climate change, as a
secondary threat, does not alter the
projected future viability of any
population or management unit. Those
future outcomes are driven by the
primary threats of habitat alteration or
loss, nonnative invasive species, and the
effects of small population size.
Using the scenarios, we project the
pyramid pigtoe’s viability over 20 to 30
years. We selected this duration because
the species is slow growing and longlived and has relatively low fecundity;
long-term trend information on pyramid
pigtoe abundance and threats is not
available across the species’ range to
contribute to meaningful alternative
timeframes.
Future resiliency of pyramid pigtoe
populations depends on the extent to
which the species’ needs are met for
water quality, flow, substrate suitability,
abundance and distribution of host fish
species, and habitat connectivity. We
projected the expected future resiliency
of each population based on how events
likely to occur under each scenario
would affect the species’ resource
needs. Future resiliency of each
population is classified as high,
medium, low, or very low. Where
multiple populations occur within an
MU, the MU condition is the average of
the population condition classifications;
however, there are no management units
where the population classifications
vary (i.e., all populations within the MU
have the same classification). These
projections are informed by
development planning documents, peerreviewed literature, vetting of initial
condition ranking by mussel experts,
and our best professional judgment.
Very low condition populations will
become extirpated; low condition
populations will become functionally
extirpated (no recruitment); medium
condition populations will exhibit
limited recruitment and be linearly
distributed and thus will have impaired
ability to recover from disturbances and
will be vulnerable to catastrophic
events; and high condition populations
will consistently recruit and be
distributed over long distances and in
connected mainstem and tributary river
reaches (see SSA report for detailed
future condition category definitions,
Service 2021, pp. 84–85).
Our analysis shows that whether
threats remain constant or increase into
the future, all 35 populations are
expected to experience negative changes
to their important habitat requisites or
resource needs, and the condition of
many of the populations would decrease
(Table 2). Under scenario 1, we expect
23 populations will be in low or very
low condition and 9 in medium
condition, with no to little resiliency,
respectively. The remaining 3
populations occurring within the Saline
or Upper Ouachita Rivers, where the
impact of impoundments is not as
severe as elsewhere in the species’
range, are expected to maintain a high
condition. Under scenario 2, we expect
31 populations to be either functionally
extirpated (low condition) or extirpated
(very low condition) and 4 to be in
medium condition. With increasing
threat levels, the population condition
of the Saline and Upper Ouachita Rivers
decline, and, thus, within 20 to 30 years
no high condition populations remain.
TABLE 2—SUMMARY OF PYRAMID PIGTOE CURRENT MUSSEL POPULATION SIZE, EXTENT, THREAT LEVEL, AND
PROJECTED FUTURE CONDITIONS. ONLY OVERALL CONDITION IS LISTED FOR FUTURE SCENARIOS
Future condition
Contiguous population
(occupied river)
Management unit
Population
size
Population
extent
Current
condition
Threat level
Scenario
1
I
Scenario
2
OHIO BASIN
Muskingum ...............................
Upper Green ............................
Barren ......................................
Middle Green ...........................
Lower Green ............................
Lower Cumberland-Old Hickory
Lake.
Muskingum River .....................
Upper Green River ..................
Barren River .............................
Middle Green River ..................
Lower Green River ..................
Cumberland River (Old Hickory
Reservoir) Cordell Hull
Tailwater.
Small .............
Large ............
Small .............
Medium .........
Small .............
Medium .........
Small .............
Large ............
Small .............
Medium .........
Small .............
Small .............
High ..............
Low ...............
Mod ...............
Mod ...............
Mod ...............
High ..............
Low ...............
High ..............
Med ...............
Med ...............
Low ...............
Low ...............
Very Low ......
Medium .........
Medium .........
Medium .........
Low ...............
Very Low ......
Very Low.
Medium.
Low.
Low.
Very Low.
Very Low.
TENNESSEE BASIN
Holston .....................................
Upper Clinch ............................
Wheeler Lake ...........................
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Pickwick Lake ..........................
Lower Tennessee-Beech .........
Upper Duck ..............................
Lower Duck ..............................
Holston River ...........................
Clinch River .............................
Paint Rock River ......................
Tennessee River (Wheeler
Reservoir) Guntersville
Tailwater.
Tennessee River (Pickwick
Reservoir) Wilson Tailwater.
Tennessee River (Kentucky
Reservoir) Pickwick
Tailwater.
Upper Duck River ....................
Lower Duck River ....................
Small .............
Medium .........
Small .............
Medium .........
Small .............
Medium .........
Small .............
Small .............
High ..............
Mod ...............
Mod ...............
High ..............
Low
Med
Low
Low
...............
...............
...............
...............
Very Low ......
Low ...............
Low ...............
Low ...............
Very Low.
Low.
Very Low.
Very Low.
Medium .........
Medium .........
High ..............
Low ...............
Low ...............
Low.
Small .............
Small .............
High ..............
Low ...............
Low ...............
Low.
Large ............
Large ............
Medium .........
Small .............
Mod ...............
Mod ...............
Med ...............
Med ...............
Medium .........
Low ...............
Low.
Very Low.
Mod ...............
Low ...............
Low ...............
Low ...............
Low ...............
Low ...............
Very Low.
Very Low.
ARKANSAS–WHITE–RED BASIN
Petit Jean .................................
Eleven Point .............................
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Eleven Point River ...................
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Small .............
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Small .............
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TABLE 2—SUMMARY OF PYRAMID PIGTOE CURRENT MUSSEL POPULATION SIZE, EXTENT, THREAT LEVEL, AND
PROJECTED FUTURE CONDITIONS. ONLY OVERALL CONDITION IS LISTED FOR FUTURE SCENARIOS—Continued
Future condition
Management unit
Contiguous population
(occupied river)
Population
size
Population
extent
Threat level
Current
condition
Lower Little ...............................
Little River ................................
Medium .........
Small .............
Mod ...............
Low ...............
Scenario
1
Scenario
2
ILow ............... I Very Low.
LOWER MISSISSIPPI BASIN
Lower Black .............................
Lower St. Francis .....................
Middle White ............................
Upper Ouachita ........................
Little Missouri ...........................
Lower Ouachita-Smackover .....
Upper Saline ............................
Lower Saline ............................
Bayou Bartholomew .................
Lower Ouachita-Bayou De
Loutre.
Big Sunflower ...........................
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Lower Big Black .......................
Lower Black River ....................
St. Francis River ......................
Tyronza River ..........................
Middle White River ..................
Upper Ouachita River ..............
Little Missouri River .................
Lower Ouachita River
(Smackover).
Upper Saline River ..................
Lower Saline River ..................
Bayou Bartholomew .................
Lower Ouachita River (Bayou
De Loutre).
Hushpuckna River ...................
Bogue Phalia ...........................
Little Sunflower River ...............
Sunflower River .......................
Sandy Bayou ...........................
Big Sunflower River .................
Big Black River ........................
The viability implications associated
with the expected change in population
conditions can be discerned at the MU
and HUC–2 scales. Under scenario 1, we
expect 3 MUs (11 percent) remain in
high condition; 9 MUs (32 percent), in
medium condition; 12 MUs (43
percent), in low condition; and 4 (14
percent), in very low condition.
Therefore, the species’ ability to
withstand natural environmental
variation and threats will be greatly
limited. Loss of the three MUs reduces
the species’ distribution, increasing its
risk to catastrophic events. The pyramid
pigtoe will continue to be represented in
the Ohio, Tennessee, and Lower
Mississippi basins, but reduced to six
States (as compared to the current nine
States) occupied by the species.
Representation will be lost from the
Arkansas-White-Red basin, as all of its
MUs are expected to be in low
condition. It will take many years
(potentially beyond the 20- to 30-year
timeframe analyzed), for full evaluation
of the species’ response to any current
beneficial actions, such as removal of
Lock and Dam 6 on the Green River, or
the safe harbor agreements and
candidate conservation agreements with
assurances in the Upper Ouachita and
Upper Saline Rivers.
Under scenario 2, none of the MUs are
expected to be in high condition, 4 (14
percent) are in medium condition, 11
(39 percent) are in low condition, and
13 (46 percent) are in very low
condition. Given no MUs will be in high
condition, the species’ ability to
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Small .............
Medium .........
Medium .........
Small .............
Large ............
Large ............
Medium .........
Small .............
Small .............
Large ............
Small .............
Large ............
Medium .........
Medium .........
Mod ...............
High ..............
High ..............
Mod ...............
Mod ...............
Mod ...............
Mod ...............
Low ...............
Med ...............
Med ...............
Low ...............
High ..............
Med ...............
Med ...............
Low ...............
Medium .........
Medium .........
Low ...............
High ..............
Medium .........
Medium .........
Very Low.
Low.
Low.
Very Low.
Medium.
Low.
Low.
Large ............
Large ............
Large ............
Medium .........
Large ............
Large ............
Large ............
Medium .........
Mod ...............
High ..............
High ..............
High ..............
High ..............
High ..............
Med ...............
Low ...............
High ..............
High ..............
Medium .........
Low ...............
Medium.
Medium.
Low.
Low.
Small .............
Small .............
Small .............
Medium .........
Small .............
Medium .........
Small .............
Small
Small
Small
Large
Small
Large
Small
High
High
High
High
High
High
High
Med
Med
Med
Med
Med
Med
Low
Low ...............
Low ...............
Low ...............
Low ...............
Low ...............
Low ...............
Very Low ......
Very
Very
Very
Very
Very
Very
Very
.............
.............
.............
............
.............
............
.............
..............
..............
..............
..............
..............
..............
..............
withstand natural environmental
variation and threats will be
substantially limited. Redundancy will
also be substantially reduced with no
high condition MUs remaining and the
expected loss of 13 (46 percent) MUs.
Loss of the species from the ArkansasWhite-Red basin, with no high
condition MUs in any basin, and
potential extirpation of the species from
the States of Virginia, Ohio, Oklahoma,
and Mississippi will substantially
reduce the species’ genetic diversity,
thereby decreasing its ability to adapt to
changing environmental conditions.
We note that, by using the SSA
framework to guide our analysis of the
scientific information documented in
the SSA report, we have not only
analyzed individual effects on the
species, but we have also analyzed their
potential cumulative effects. We
incorporate the cumulative effects into
our SSA analysis when we characterize
the current and future condition of the
species. To assess the current and future
condition of the species, we undertake
an iterative analysis that encompasses
and incorporates the threats
individually and then accumulates and
evaluates the effects of all the factors
that may be influencing the species,
including threats and conservation
efforts. Because the SSA framework
considers not just the presence of the
factors, but to what degree they
collectively influence risk to the entire
species, our assessment integrates the
cumulative effects of the factors and
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...............
...............
...............
...............
...............
...............
...............
Low.
Low.
Low.
Low.
Low.
Low.
Low.
replaces a standalone cumulative effects
analysis.
Conservation Efforts and Regulatory
Mechanisms
As discussed under Threats, Federal
and State lands and water quality
regulations afford the pyramid pigtoe
and its habitats some protection from
land development, industrial, and
transportation activities. Additionally,
laws intended to reduce the threat of
nonnative species are in place. Many
populations of the pyramid pigtoe were
extirpated or reduced prior to
development of modern conservation
programs and regulatory mechanisms.
As such, historical threats no longer
present on the landscape impart a
legacy effect (small population size or
degraded habitat) on some current
populations. Further, some water
quality regulations have not been fully
adopted or consistently applied across
the species’ range. Therefore, despite
the existing regulatory mechanisms in
place, the combined threats and impacts
of actions that occurred prior to the
implementation of these regulatory
mechanisms continue to negatively
affect the pyramid pigtoe.
Determination of Pyramid Pigtoe Status
Section 4 of the Act (16 U.S.C. 1533)
and its implementing regulations (50
CFR part 424) set forth the procedures
for determining whether a species meets
the definition of an endangered species
or a threatened species. The Act defines
an endangered species as a species ‘‘in
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danger of extinction throughout all or a
significant portion of its range’’ and a
threatened species as a species ‘‘likely
to become an endangered species within
the foreseeable future throughout all or
a significant portion of its range.’’ The
Act requires that we determine whether
a species meets the definition of an
endangered species or a threatened
species because of any of the following
factors: (A) The present or threatened
destruction, modification, or
curtailment of its habitat or range; (B)
overutilization for commercial,
recreational, scientific, or educational
purposes; (C) disease or predation; (D)
the inadequacy of existing regulatory
mechanisms; or (E) other natural or
manmade factors affecting its continued
existence.
Status Throughout All of Its Range
Historically, the pyramid pigtoe
occurred within 151 populations and
136 MUs, in 6 basins across 18 States
(Figure 2). Currently, the species occurs
within 35 populations and 28 MUs, in
4 basins across 9 States, which
represents a 77 percent reduction of its
historically occupied populations. Of
the extant MUs, 4 are highly resilient,
while 9 and 15 have medium and low
resiliency, respectively. The threats
leading to its current condition include
past and ongoing habitat degradation or
loss (Factor A), residual impacts from
past harvest and overutilization (Factor
B), and ongoing competition, predation,
and habitat alteration from invasive,
nonnative species (Factor E).
Collectively, these threats reduce
population abundance, thereby
precipitating negative genetic and
demographic effects associated with
small population size (Factor E) within
some of the smaller populations.
Although downtrends from historical
numbers are evident and declines are
likely to continue, four high resilient
MUs are distributed across two of the
four occupied major river basins. These
four MUs provide for current
representation and redundancy of the
species. Thus, after assessing the best
available information, we conclude that
the pyramid pigtoe is not in danger of
extinction throughout all of its range.
We, therefore, proceed with determining
whether the pyramid pigtoe is likely to
become endangered within the
foreseeable future throughout all of its
range.
The best available information
suggests that the threats currently acting
upon the pyramid pigtoe will continue
into the foreseeable future. In areas
experiencing human population and
land development growth, these threats
(e.g., water quality and habitat
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degradation) are reasonably expected to
increase over time, further reducing the
species’ resiliency, redundancy, and
representation. Our foreseeable future
(20 to 30 years) reflects the period of
time over which we can reliably predict
both the threats to the pyramid pigtoe
and the pyramid pigtoe’s response to
those threats based on the best available
information. Within the foreseeable
future, even if threats were to remain at
current levels and not increase, 23 of the
35 populations are projected to become
extirpated or functionally extirpated
(Table 2). Additionally, with no change
in threat levels, the condition of one of
the four high resilient populations will
decline to medium resiliency and the
remaining three high resilient
populations would be confined to a
single basin. At the MU scale, only 3 of
the 28 extant MUs remain in high
condition, with 17 MUs projected to
become extirpated or functionally
extirpated within 20 to 30 years. If
threats increase, 19 populations will
likely be extirpated within 20 to 30
years, leading to only 4 MUs persisting.
These MUs will have limited
recruitment potential and restricted
distribution, thus impairing the species’
ability to recover from disturbances and
increasing its vulnerability to
catastrophic events. In summary, threats
currently acting on the species are likely
to persist or increase in the foreseeable
future, resulting in zero to three high
resilient populations in one of its six
historical major basins and resulting in
a high risk of impacts from a single
catastrophe or stochastic events. Thus,
after assessing the best available
information, we conclude that the
pyramid pigtoe is likely to become in
danger of extinction within the
foreseeable future throughout all of its
range.
Status Throughout a Significant Portion
of Its Range
Under the Act and our implementing
regulations, a species may warrant
listing if it is in danger of extinction or
likely to become so in the foreseeable
future throughout all or a significant
portion of its range. The court in Center
for Biological Diversity v. Everson, 2020
WL 437289 (D.D.C. Jan. 28, 2020)
(Center for Biological Diversity), vacated
the aspect of the Final Policy on
Interpretation of the Phrase ‘‘Significant
Portion of Its Range’’ in the Endangered
Species Act’s Definitions of
‘‘Endangered Species’’ and ‘‘Threatened
Species’’ (79 FR 37578; July 1, 2014)
that provided that the Service does not
undertake an analysis of significant
portions of a species’ range if the
species warrants listing as threatened
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50005
throughout all of its range. Therefore,
we proceed to evaluating whether the
species is endangered in a significant
portion of its range—that is, whether
there is any portion of the species’ range
for which both (1) the portion is
significant and (2) the species is in
danger of extinction in that portion.
Depending on the case, it might be more
efficient for us to address the
‘‘significance’’ question or the ‘‘status’’
question first. We can choose to address
either question first. Regardless of
which question we address first, if we
reach a negative answer with respect to
the first question that we address, we do
not need to evaluate the other question
for that portion of the species’ range.
Following the court’s holding in
Center for Biological Diversity, we now
consider whether there are any
significant portions of the species’ range
where the species is in danger of
extinction now (i.e., endangered). In
undertaking this analysis for the
pyramid pigtoe, we choose to address
the status question first—we consider
information pertaining to the geographic
distribution of both the species and the
threats that the species faces to identify
any portions of the range where the
species is endangered.
For the pyramid pigtoe, we
considered whether the threats are
geographically concentrated in any
portion of the species’ range at a
biologically meaningful scale. We
examined the following threats: Habitat
degradation or loss, invasive and
nonnative species, and negative effects
associated with small population size,
including cumulative effects. Habitat
degradation or loss, including
diminished water quality, is a threat in
all four basins occupied by the pyramid
pigtoe, although the contribution by
source (e.g., agriculture, urbanization,
mining, dredging) varies. Invasive or
nonnative species also is a threat in
each occupied basin. Lastly, large
populations (number of individuals)
occur in three of the four basins, and
medium populations occur in all four
basins.
We examined the Arkansas-WhiteRed basin (the only basin not containing
any large populations) to determine if
there is a concentration of threats
because, of the three populations in the
basin, two have a moderate threat level
and one has a low threat level. All three
of these populations are in a low current
condition, and two of the three
populations have small numbers of
individuals. Thus, the cumulative
effects of small population size with the
other identified threats may be
concentrated in this basin.
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We then evaluated whether the
Arkansas-White-Red basin may be
biologically important to the overall
species’ viability, i.e., significant. This
basin contains 3 of the 35 (8.6 percent)
pyramid pigtoe populations. By length
of river, the populations combined
occupy about 5 percent of the species’
range. Therefore, the populations in the
Arkansas-White-Red basin minimally
contribute to the overall viability of the
species.
The pyramid pigtoe occurs in similar
habitats across the four basins it
occupies and does not use unique
observable environmental
characteristics attributable to any of the
basins. The Arkansas-White-Red basin
populations occur in stream habitat
with substrate types and water quality
similar to the other basins where the
pyramid pigtoe performs the important
life-history functions of breeding,
feeding, and sheltering. The basin does
not act as a refugium for the species or
as an important spawning ground. In
addition, the water quality is similar
throughout the species’ range, with
impaired water quality occurring in all
four basins. Because the pyramid pigtoe
occurs in similar aquatic habitats, the
Arkansas-White-Red basin population
exhibits similar habitat use as
populations in the remainder of the
range.
Overall, we found no substantial
information that would indicate the
Arkansas-White-Red basin is a portion
of the range that may be significant in
terms of its overall contribution to the
species’ resiliency, redundancy, and
representation, or that it is significant in
terms of high-quality habitat or habitat
that is otherwise important for the
species’ life history. Additionally,
within each of the other three basins (or
portions of the range) there was no
concentration of threats that would
indicate the species is facing elevated
threats in those portions. As a result, we
determined there is no portion of the
pyramid pigtoe’s range that constitutes
a significant portion of the range where
the species is currently endangered.
Accordingly, we determine that the
species is likely to become in danger of
extinction within the foreseeable future
throughout all of its range. This is
consistent with the courts’ holdings in
Desert Survivors v. Department of the
Interior, No. 16–cv–01165–JCS, 2018
WL 4053447 (N.D. Cal. Aug. 24, 2018),
and Center for Biological Diversity v.
Jewell, 248 F. Supp. 3d, 946, 959 (D.
Ariz. 2017).
Determination of Status
Our review of the best available
scientific and commercial information
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indicates that the pyramid pigtoe meets
the definition of a threatened species.
Therefore, we propose to list the
pyramid pigtoe as a threatened species
in accordance with sections 3(20) and
4(a)(1) of the Act.
Available Conservation Measures
Conservation measures provided to
species listed as endangered or
threatened species under the Act
include recognition, recovery actions,
requirements for Federal protection, and
prohibitions against certain practices.
Recognition through listing results in
public awareness, and conservation by
Federal, State, Tribal, and local
agencies, private organizations, and
individuals. The Act encourages
cooperation with the States and other
countries and calls for recovery actions
to be carried out for listed species. The
protection required by Federal agencies
and the prohibitions against certain
activities are discussed, in part, below.
The primary purpose of the Act is the
conservation of endangered and
threatened species and the ecosystems
upon which they depend. The ultimate
goal of such conservation efforts is the
recovery of these listed species, so that
they no longer need the protective
measures of the Act. Section 4(f) of the
Act calls for the Service to develop and
implement recovery plans for the
conservation of endangered and
threatened species. The recovery
planning process involves the
identification of actions that are
necessary to halt or reverse the species’
decline by addressing the threats to its
survival and recovery. The goal of this
process is to restore listed species to a
point where they are secure, selfsustaining, and functioning components
of their ecosystems.
Recovery planning consists of
preparing draft and final recovery plans,
beginning with the development of a
recovery outline and making it available
to the public following a final listing
determination. The recovery outline
guides the immediate implementation of
urgent recovery actions and describes
the process to be used to develop a
recovery plan. Revisions of the plan
may be done to address continuing or
new threats to the species, as new
substantive information becomes
available. The recovery plan also
identifies recovery criteria for review of
when a species may be ready for
reclassification from endangered to
threatened (‘‘downlisting’’) or removal
from protected status (‘‘delisting’’), and
methods for monitoring recovery
progress. Recovery plans also establish
a framework for agencies to coordinate
their recovery efforts and provide
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estimates of the cost of implementing
recovery tasks. Recovery teams
(composed of species experts, Federal
and State agencies, nongovernmental
organizations, and stakeholders) are
often established to develop recovery
plans. When completed, the recovery
outline, draft recovery plan, and the
final recovery plan will be available on
our website (https://www.fws.gov/
endangered), or from our Asheville
Field Office (see FOR FURTHER
INFORMATION CONTACT).
Implementation of recovery actions
generally requires the participation of a
broad range of partners, including other
Federal agencies, States, Tribes,
nongovernmental organizations,
businesses, and private landowners.
Examples of recovery actions include
habitat restoration (e.g., restoration of
native vegetation), research, captive
propagation and reintroduction, and
outreach and education. The recovery of
many listed species cannot be
accomplished solely on Federal lands
because their range may occur primarily
or solely on non-Federal lands. To
achieve recovery of these species
requires cooperative conservation efforts
on private, State, and Tribal lands.
If this species is listed, funding for
recovery actions will be available from
a variety of sources, including Federal
budgets, State programs, and cost-share
grants for non-Federal landowners, the
academic community, and
nongovernmental organizations. In
addition, pursuant to section 6 of the
Act, the States of Alabama, Arkansas,
Kentucky, Louisiana, Mississippi, Ohio,
Oklahoma, Tennessee, and Virginia
would be eligible for Federal funds to
implement management actions that
promote the protection or recovery of
the pyramid pigtoe. Information on our
grant programs that are available to aid
species recovery can be found at: https://
www.fws.gov/grants.
Although the pyramid pigtoe is only
proposed for listing under the Act at
this time, please let us know if you are
interested in participating in recovery
efforts for this species. Additionally, we
invite you to submit any new
information on this species whenever it
becomes available and any information
you may have for recovery planning
purposes (see FOR FURTHER INFORMATION
CONTACT).
Section 7(a) of the Act requires
Federal agencies to evaluate their
actions with respect to any species that
is proposed or listed as an endangered
or threatened species and with respect
to its critical habitat, if any is
designated. Regulations implementing
this interagency cooperation provision
of the Act are codified at 50 CFR part
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402. Section 7(a)(4) of the Act requires
Federal agencies to confer with the
Service on any action that is likely to
jeopardize the continued existence of a
species proposed for listing or result in
destruction or adverse modification of
proposed critical habitat. If a species is
listed subsequently, section 7(a)(2) of
the Act requires Federal agencies to
ensure that activities they authorize,
fund, or carry out are not likely to
jeopardize the continued existence of
the species or destroy or adversely
modify its critical habitat. If a Federal
action may affect a listed species or its
critical habitat, the responsible Federal
agency must enter into consultation
with the Service.
Federal agency actions within the
species’ habitat that may require
conference, consultation, or both as
described in the preceding paragraph
include management and any other
landscape-altering activities on Federal
lands administered by the following:
(1) U.S. Army Corps of Engineers
(channel dredging and maintenance;
dam projects including flood control,
navigation, hydropower, bridge projects,
stream restoration, and Clean Water Act
permitting).
(2) U.S. Department of Agriculture,
including the Natural Resources
Conservation Service and Farm Service
Agency (technical and financial
assistance for projects) and the Forest
Service (aquatic habitat restoration, fire
management plans, fire suppression,
fuel reduction treatments, forest plans,
mining permits).
(3) U.S. Department of Energy
(renewable and alternative energy
projects).
(4) Federal Energy Regulatory
Commission (interstate pipeline
construction and maintenance, dam
relicensing, and hydrokinetics).
(5) U.S. Department of Transportation
(highway and bridge construction and
maintenance).
(6) U.S. Fish and Wildlife Service
(issuance of section 10 permits for
enhancement of survival, habitat
conservation plans, and safe harbor
agreements; National Wildlife Refuge
planning and refuge activities; Partners
for Fish and Wildlife program projects
benefiting these species or other listed
species; Wildlife and Sportfish
Restoration program sportfish stocking).
(7) Environmental Protection Agency
(water quality criteria, permitting).
(8) Tennessee Valley Authority (flood
control, navigation, hydropower, and
land management for the Tennessee
River system).
(9) Office of Surface Mining
Reclamation and Enforcement (land
resource management plans, mining
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permits, oil and natural gas permits,
abandoned mine land projects, and
renewable energy development).
(10) National Park Service (aquatic
habitat restoration, fire management
plans, fire suppression, fuel reduction
treatments, land management plans,
mining permits).
It is our policy, as published in the
Federal Register on July 1, 1994 (59 FR
34272), to identify to the maximum
extent practicable at the time a species
is listed, those activities that would or
would not constitute a violation of
section 9 of the Act. The intent of this
policy is to increase public awareness of
the effect of a proposed listing on
proposed and ongoing activities within
the range of the species proposed for
listing. The discussion below regarding
protective regulations under section 4(d)
of the Act complies with our policy.
II. Proposed Rule Issued Under Section
4(d) of the Act
Background
Section 4(d) of the Act contains two
sentences. The first sentence states that
the Secretary shall issue such
regulations as he deems necessary and
advisable to provide for the
conservation of species listed as
threatened. The U.S. Supreme Court has
noted that statutory language like
‘‘necessary and advisable’’ demonstrates
a large degree of deference to the agency
(see Webster v. Doe, 486 U.S. 592
(1988)). Conservation is defined in the
Act to mean the use of all methods and
procedures which are necessary to bring
any endangered species or threatened
species to the point at which the
measures provided pursuant to the Act
are no longer necessary. Additionally,
the second sentence of section 4(d) of
the Act states that the Secretary may by
regulation prohibit with respect to any
threatened species any act prohibited
under section 9(a)(1), in the case of fish
or wildlife, or section 9(a)(2), in the case
of plants. Thus, the combination of the
two sentences of section 4(d) provides
the Secretary with wide latitude of
discretion to select and promulgate
appropriate regulations tailored to the
specific conservation needs of the
threatened species. The second sentence
grants particularly broad discretion to
the Service when adopting the
prohibitions under section 9.
The courts have recognized the extent
of the Secretary’s discretion under this
standard to develop rules that are
appropriate for the conservation of a
species. For example, courts have
upheld rules developed under section
4(d) as a valid exercise of agency
authority where they prohibited take of
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50007
threatened wildlife, or include a limited
taking prohibition (see Alsea Valley
Alliance v. Lautenbacher, 2007 U.S.
Dist. Lexis 60203 (D. Or. 2007);
Washington Environmental Council v.
National Marine Fisheries Service, 2002
U.S. Dist. Lexis 5432 (W.D. Wash.
2002)). Courts have also upheld 4(d)
rules that do not address all of the
threats a species faces (see State of
Louisiana v. Verity, 853 F.2d 322 (5th
Cir. 1988)). As noted in the legislative
history when the Act was initially
enacted, ‘‘once an animal is on the
threatened list, the Secretary has an
almost infinite number of options
available to him with regard to the
permitted activities for those species. He
may, for example, permit taking, but not
importation of such species, or he may
choose to forbid both taking and
importation but allow the transportation
of such species’’ (H.R. Rep. No. 412,
93rd Cong., 1st Sess. 1973).
Exercising this authority under
section 4(d), we have developed a
proposed rule that is designed to
address the pyramid pigtoe’s
conservation needs. Although the
statute does not require us to make a
‘‘necessary and advisable’’ finding with
respect to the adoption of specific
prohibitions under section 9, we find
that this rule as a whole satisfies the
requirement in section 4(d) of the Act to
issue regulations deemed necessary and
advisable to provide for the
conservation of the pyramid pigtoe.
As discussed above under Summary
of Biological Status and Threats, we
have concluded that the pyramid pigtoe
is likely to become in danger of
extinction within the foreseeable future
primarily due to declines in water
quality, alteration and deterioration of
instream habitats, fragmentation and
isolation of populations, and nonnative
species. These threats, which are
expected to be exacerbated by continued
urbanization and land development,
were central to our assessment of the
future viability of the pyramid pigtoe.
The provisions of this proposed 4(d)
rule would promote conservation of the
pyramid pigtoe by encouraging
management of the landscape in ways
that meet the conservation needs of the
pyramid pigtoe and are consistent with
land management considerations. The
provisions of this proposed rule are one
of many tools that we would use to
promote the conservation of the
pyramid pigtoe. This proposed 4(d) rule
would apply only if and when we make
final the listing of the pyramid pigtoe as
a threatened species.
Section 7(a)(2) of the Act requires
Federal agencies, including the Service,
to ensure that any action they fund,
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authorize, or carry out is not likely to
jeopardize the continued existence of
any endangered species or threatened
species or result in the destruction or
adverse modification of designated
critical habitat of such species. In
addition, section 7(a)(4) of the Act
requires Federal agencies to confer with
the Service on any agency action which
is likely to jeopardize the continued
existence of any species proposed to be
listed under the Act or result in the
destruction or adverse modification of
proposed critical habitat.
If a Federal action may affect a listed
species or its critical habitat, the
responsible Federal agency (action
agency) must enter into consultation
with us. Examples of actions that are
subject to the section 7 consultation
process are actions on State, Tribal,
local, or private lands that require a
Federal permit or that involve some
other Federal action such as funding,
like those listed above under Available
Conservation Measures. Federal actions
not affecting listed species or critical
habitat—and actions on State, Tribal,
local, or private lands that are not
federally funded, authorized, or carried
out by a Federal agency—do not require
section 7 consultation.
This obligation does not change in
any way for a threatened species with a
species-specific 4(d) rule. Actions that a
Federal agency determines ‘‘may affect’’
listed species or critical habitat continue
to require consultation and actions that
are ‘‘likely to adversely affect’’ a species
require formal consultation and the
formulation of a biological opinion.
Provisions of the Proposed 4(d) Rule
This proposed 4(d) rule would
provide for the conservation of the
pyramid pigtoe by prohibiting the
following activities, except as otherwise
authorized or permitted: Importing or
exporting; take; possession and other
acts with unlawfully taken specimens;
delivering, receiving, transporting, or
shipping in interstate or foreign
commerce in the course of commercial
activity; or selling or offering for sale in
interstate or foreign commerce.
As discussed above under Summary
of Biological Status and Threats,
multiple factors are affecting the status
of the pyramid pigtoe. A range of
activities have the potential to affect the
pyramid pigtoe, including declines in
water quality, alteration and
deterioration of instream habitats,
fragmentation and isolation of
populations, and nonnative species.
These threats, which are expected to
continue due to land development for
urbanization, agriculture, and resource
extraction, channel navigation, and dam
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operations were central to our
assessment of the future viability of the
pyramid pigtoe. Therefore, we prohibit
actions resulting in the incidental take
of the pyramid pigtoe by altering or
degrading its habitat.
Under the Act, ‘‘take’’ means to
harass, harm, pursue, hunt, shoot,
wound, kill, trap, capture, or collect, or
to attempt to engage in any such
conduct. Some of these provisions have
been further defined in regulations at 50
CFR 17.3. Take can result knowingly or
otherwise, by direct and indirect
impacts, intentionally or incidentally.
Regulating incidental and/or intentional
take would help preserve the species’
remaining populations, slow their rate
of decline, and decrease synergistic,
negative effects from other stressors.
We may issue permits to carry out
otherwise prohibited activities,
including those described above,
involving threatened wildlife under
certain circumstances. Regulations
governing permits are codified at 50
CFR 17.32. With regard to threatened
wildlife, a permit may be issued for the
following purposes: For scientific
purposes, to enhance propagation or
survival, for economic hardship, for
zoological exhibition, for educational
purposes, for incidental taking, or for
special purposes consistent with the
purposes of the Act. The statute also
contains certain exemptions from the
prohibitions, which are found in
sections 9 and 10 of the Act.
The proposed 4(d) rule would also
provide for the conservation of the
species by allowing exceptions for take
associated with actions and activities
that, while they may have some
minimal level of disturbance to pyramid
pigtoe, are not expected to negatively
impact conservation and recovery
efforts for the species. The proposed
exceptions to these prohibitions include
incidental take associated with (1)
conservation efforts by the Service or
State wildlife agencies, (2) channel
restoration projects, (3) bank restoration
projects, and (4) take necessary to aid a
sick or injured specimen, or to salvage
a dead specimen.
The first exception is for conservation
and restoration efforts for pyramid
pigtoe by the Service or State wildlife
agencies, and including, but not limited
to, collection of broodstock, tissue
collection for genetic analysis, captive
propagation, and subsequent stocking
into unoccupied areas within the
historical range of the species. We
recognize the special and unique
relationship with our State natural
resource agency partners in contributing
to conservation of listed species. State
agencies often possess scientific data
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and valuable expertise on the status and
distribution of endangered, threatened,
and candidate species of wildlife and
plants. State agencies, because of their
authorities and their close working
relationships with local governments
and landowners, are in a unique
position to assist the Service in
implementing all aspects of the Act. In
this regard, section 6 of the Act provides
that the Service shall cooperate to the
maximum extent practicable with the
States in carrying out programs
authorized by the Act. Therefore, any
qualified employee or agent of a State
conservation agency that is a party to a
cooperative agreement with the Service
in accordance with section 6(c) of the
Act, who is designated by his or her
agency for such purposes, would be able
to conduct activities designed to
conserve the pyramid pigtoe that may
result in otherwise prohibited take
without additional authorization.
The second and third exceptions are
for channel and bank restoration
projects for creation of natural,
physically stable, ecologically
functioning streams, taking into
consideration connectivity with
floodplain and groundwater aquifers.
These exceptions include a requirement
that bank restoration projects require
planting appropriate native vegetation,
including woody species appropriate for
the region and habitat. We also propose
language that would require surveys and
relocation prior to commencement of
restoration actions for pyramid pigtoe
that would otherwise be negatively
affected by the actions. We reiterate that
these actions and activities may have
some minimal level of take of pyramid
pigtoe, but any such take is expected to
be rare and insignificant and is not
expected to negatively impact
conservation and recovery efforts.
Rather, we expect they would have a net
beneficial effect on the species. Across
the species’ range, instream habitats
have been degraded physically by
sedimentation and by direct and
indirect channel disturbance. The
habitat restoration activities in the
proposed 4(d) rule are intended to
improve habitat conditions for the
species in the long term.
Finally, the proposed 4(d) rule would
allow take of pyramid pigtoe without a
permit by any employee or agent of the
Service or a State conservation agency
designated by the agency for such
purposes and when acting in the course
of their official duties if such action is
necessary to aid a sick or injured
specimen, or to salvage a dead specimen
which may be useful for scientific
study. In addition, Federal and State
wildlife law enforcement officers,
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working in coordination with Service
field office personnel, may possess,
deliver, carry, transport, or ship
pyramid pigtoe taken in violation of the
Act as necessary.
Nothing in this proposed 4(d) rule
would change in any way the recovery
planning provisions of section 4(f) of the
Act, the consultation requirements
under section 7 of the Act, or the ability
of the Service to enter into partnerships
for the management and protection of
the pyramid pigtoe. However,
interagency cooperation may be further
streamlined through planned
programmatic consultations for the
species between Federal agencies and
the Service, where appropriate. We ask
the public, particularly State agencies
and other interested stakeholders that
may be affected by the proposed 4(d)
rule, to provide comments and
suggestions regarding additional
guidance and methods that the Service
could provide or use, respectively, to
streamline the implementation of this
proposed 4(d) rule (see Information
Requested, above).
III. Critical Habitat
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Prudency Determination
Section 4(a)(3) of the Act, as
amended, and implementing regulations
(50 CFR 424.12) require that, to the
maximum extent prudent and
determinable, the Secretary shall
designate critical habitat at the time the
species is determined to be an
endangered or threatened species. Our
regulations (50 CFR 424.12(a)(1)) state
that the Secretary may, but is not
required to, determine that a
designation would not be prudent in the
following circumstances:
(i) The species is threatened by taking
or other human activity and
identification of critical habitat can be
expected to increase the degree of such
threat to the species;
(ii) The present or threatened
destruction, modification, or
curtailment of a species’ habitat or range
is not a threat to the species, or threats
to the species’ habitat stem solely from
causes that cannot be addressed through
management actions resulting from
consultations under section 7(a)(2) of
the Act;
(iii) Areas within the jurisdiction of
the United States provide no more than
negligible conservation value, if any, for
a species occurring primarily outside
the jurisdiction of the United States;
(iv) No areas meet the definition of
critical habitat; or
(v) The Secretary otherwise
determines that designation of critical
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habitat would not be prudent based on
the best scientific data available.
As discussed earlier in this document,
there is currently no imminent threat of
collection or vandalism identified under
Factor B for this species, and
identification and mapping of critical
habitat is not expected to initiate any
such threat. In our SSA and proposed
listing determination for the pyramid
pigtoe, we determined that the present
or threatened destruction, modification,
or curtailment of habitat or range is a
threat to the pyramid pigtoe and that
those threats in some way can be
addressed by section 7(a)(2)
consultation measures. The species
occurs wholly in the jurisdiction of the
United States, and we are able to
identify areas that meet the definition of
critical habitat. Therefore, because none
of the circumstances enumerated in our
regulations at 50 CFR 424.12(a)(1) have
been met and because there are no other
circumstances the Secretary has
identified for which this designation of
critical habitat would be not prudent,
we have determined that the
designation of critical habitat is prudent
for the pyramid pigtoe.
Critical Habitat Determinability
Having determined that designation is
prudent, under section 4(a)(3) of the Act
we consider whether critical habitat for
the pyramid pigtoe is determinable. Our
regulations at 50 CFR 424.12(a)(2) state
that critical habitat is not determinable
when one or both of the following
situations exist:
(i) Data sufficient to perform required
analyses are lacking, or
(ii) The biological needs of the species
are not sufficiently well known to
identify any area that meets the
definition of ‘‘critical habitat.’’
For the pyramid pigtoe, the species’
needs are sufficiently well known.
However, there is some uncertainty
regarding the taxonomic identity of
populations outside the Ohio,
Cumberland, and Tennessee River
basins (see Background), which is
currently under investigation using
different genetic markers than assessed
thus far. Results of this taxonomic
investigation, which may more
accurately delineate the species’
occupied range, are likely to be
completed and submitted to a peerreviewed journal within 1 year. In
addition to this taxonomic investigation
that may better determine critical
habitat areas, a careful assessment of the
economic impacts that may occur due to
a critical habitat designation is ongoing,
and we are in the process of acquiring
the necessary information to perform
that assessment. Because the
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50009
information sufficient to perform a
required analysis of the impacts of the
designation is lacking, we find
designation of critical habitat for the
pyramid pigtoe to be not determinable
at this time. The Act allows the Service
an additional year to publish a critical
habitat designation that is not
determinable at the time of listing (16
U.S.C. 1533(b)(6)(C)(ii)).
Required Determinations
Clarity of the Rule
We are required by Executive Orders
12866 and 12988 and by the
Presidential Memorandum of June 1,
1998, to write all rules in plain
language. This means that each rule we
publish must:
(1) Be logically organized;
(2) Use the active voice to address
readers directly;
(3) Use clear language rather than
jargon;
(4) Be divided into short sections and
sentences; and
(5) Use lists and tables wherever
possible.
If you feel that we have not met these
requirements, send us comments by one
of the methods listed in ADDRESSES. To
better help us revise the rule, your
comments should be as specific as
possible. For example, you should tell
us the numbers of the sections or
paragraphs that are unclearly written,
which sections or sentences are too
long, the sections where you feel lists or
tables would be useful, etc.
National Environmental Policy Act (42
U.S.C. 4321 et seq.)
It is our position that, outside the
jurisdiction of the U.S. Court of Appeals
for the Tenth Circuit, we do not need to
prepare environmental analyses
pursuant to the National Environmental
Policy Act (NEPA; 42 U.S.C. 4321 et
seq.) in connection with regulations
adopted pursuant to section 4(a) of the
Act. We published a notice outlining
our reasons for this determination in the
Federal Register on October 25, 1983
(48 FR 49244). This position was upheld
by the U.S. Court of Appeals for the
Ninth Circuit (Douglas County v.
Babbitt, 48 F.3d 1495 (9th Cir. 1995),
cert. denied 516 U.S. 1042 (1996)).
Government-to-Government
Relationship With Tribes
In accordance with the President’s
memorandum of April 29, 1994
(Government-to-Government Relations
with Native American Tribal
Governments; 59 FR 22951), Executive
Order 13175 (Consultation and
Coordination with Indian Tribal
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Governments), and the Department of
the Interior’s manual at 512 DM 2, we
readily acknowledge our responsibility
to communicate meaningfully with
recognized Federal Tribes on a
government-to-government basis. In
accordance with Secretarial Order 3206
of June 5, 1997 (American Indian Tribal
Rights, Federal-Tribal Trust
Responsibilities, and the Endangered
Species Act), we readily acknowledge
our responsibilities to work directly
with Tribes in developing programs for
healthy ecosystems, to acknowledge that
Tribal lands are not subject to the same
controls as Federal public lands, to
remain sensitive to Indian culture, and
to make information available to Tribes.
There are no Tribal lands within or
adjacent to known pyramid pigtoe
occupied habitat. We will coordinate
with Tribes whose lands are close to
pyramid pigtoe populations.
Common name
*
CLAMS
*
Pleurobema
rubrum.
*
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List of Subjects in 50 CFR Part 17
Endangered and threatened species,
Exports, Imports, Reporting and
recordkeeping requirements,
Transportation.
Accordingly, we propose to amend
part 17, subchapter B of chapter I, title
Status
T ...........
Special rules—snails and clams.
*
*
*
*
(e) Pyramid pigtoe (Pleurobema
rubrum).
(1) Prohibitions. The following
prohibitions that apply to endangered
wildlife also apply to the pyramid
pigtoe. Except as provided under
paragraph (e)(2) of this section and
§§ 17.4 and 17.5, it is unlawful for any
person subject to the jurisdiction of the
United States to commit, to attempt to
commit, to solicit another to commit, or
cause to be committed, any of the
following acts in regard to this species:
(i) Import or export, as set forth at
§ 17.21(b) for endangered wildlife.
(ii) Take, as set forth at § 17.21(c)(1)
for endangered wildlife.
(iii) Possession and other acts with
unlawfully taken specimens, as set forth
at § 17.21(d)(1) for endangered wildlife.
Jkt 253001
1. The authority citation for part 17
continues to read as follows:
■
Authority: 16 U.S.C. 1361–1407; 1531–
1544; and 4201–4245, unless otherwise
noted.
2. Amend § 17.11(h) by adding an
entry for ‘‘Pigtoe, pyramid’’ to the List
of Endangered and Threatened Wildlife
in alphabetical order under Clams to
read as set forth below:
■
§ 17.11 Endangered and threatened
wildlife.
*
*
*
(h) * * *
*
*
*
*
*
*
*
*
[Federal Register citation when published as a final rule]; 50 CFR
17.45(e); 4d.
*
Frm 00081
PART 17—ENDANGERED AND
THREATENED WILDLIFE AND PLANTS
*
*
(iv) Interstate or foreign commerce in
the course of commercial activity, as set
forth at § 17.21(e) for endangered
wildlife.
(v) Sale or offer for sale, as set forth
at § 17.21(f) for endangered wildlife.
(2) Exceptions from prohibitions. In
regard to this species, you may:
(i) Conduct activities as authorized by
a permit under § 17.32.
(ii) Take, as set forth at § 17.21(c)(3)
and (4) for endangered wildlife.
(iii) Take as set forth at § 17.31(b).
(iv) Take incidental to an otherwise
lawful activity caused by:
(A) Channel restoration projects that
create natural, physically stable,
ecologically functioning streams (or
stream and wetland systems). These
projects can be accomplished using a
variety of methods, but the desired
outcome is a natural channel with low
shear stress (force of water moving
against the channel); bank heights that
enable reconnection to the floodplain;
connection of surface and groundwater
systems, resulting in perennial flows in
the channel; riffles and pools composed
of existing soil, rock, and wood instead
of large imported materials; low
compaction of soils within adjacent
riparian areas; and inclusion of riparian
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50 of the Code of Federal Regulations,
as set forth below:
Listing citations and applicable rules
*
*
*
20:17 Sep 03, 2021
The primary authors of this proposed
rule are the staff members of the Fish
and Wildlife Service’s Species
Assessment Team and the Asheville
Ecological Services Field Office.
*
Wherever found ..
3. As proposed to be added at 83 FR
51570 (Oct. 11, 2018), and amended at
85 FR 44821 (July 24, 2020), 85 FR
59487 (Sept. 22, 2020), 85 FR 61384
(Sept. 29, 2020), and 86 FR 47916
(August 26, 2021), § 17.45 is further
amended by adding paragraph (e) to
read as follows:
VerDate Sep<11>2014
Authors
*
■
§ 17.45
A complete list of references cited in
this rulemaking is available on the
internet at https://www.regulations.gov
and upon request from the Asheville
Ecological Services Field Office (see FOR
FURTHER INFORMATION CONTACT).
Where listed
*
*
Pigtoe, pyramid ..
*
Scientific name
References Cited
Fmt 4702
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*
*
wetlands. Streams reconstructed in this
way would offer suitable habitats for the
pyramid pigtoe and contain stable
channel features, such as pools, glides,
runs, and riffles, which could be used
by the species and its host fish for
spawning, rearing, growth, feeding,
migration, and other normal behaviors.
Prior to commencement of restoration
actions, surveys to determine presence
of the pyramid pigtoe must be
performed, and, if any pyramid pigtoe
are located, in coordination with the
local Service field office, they must be
relocated prior to project
implementation and monitored postimplementation. To qualify under this
exemption, a channel restoration project
must satisfy all Federal, State, and local
permitting requirements.
(B) Bank restoration projects that use
bioengineering methods to replace
preexisting, bare, eroding stream banks
with vegetated, stable stream banks,
thereby reducing bank erosion and
instream sedimentation and improving
habitat conditions for the species.
Following these bioengineering
methods, stream banks may be
stabilized using native species live
stakes (live, vegetative cuttings inserted
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or tamped into the ground in a manner
that allows the stake to take root and
grow), native species live fascines (live
branch cuttings, usually willows, bound
together into long, cigar-shaped
bundles), or native species brush
layering (cuttings or branches of easily
rooted tree species layered between
successive lifts of soil fill). Bank
restoration projects would require
planting appropriate native vegetation,
including woody species appropriate for
the region and habitat. These methods
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will not include the sole use of quarried
rock (rip-rap) or the use of rock baskets
or gabion structures. Prior to
commencement of bank stabilization
actions, surveys to determine presence
of pyramid pigtoe must be performed,
and, if any pyramid pigtoe are located,
in coordination with the local Service
field office, they must be relocated prior
to project implementation and
monitored post-implementation. To
qualify under this exemption, a bank
restoration project must satisfy all
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Federal, State, and local permitting
requirements.
(v) Possess and engage in other acts
with unlawfully taken wildlife, as set
forth at § 17.21(d)(2) for endangered
wildlife.
Martha Williams,
Principal Deputy Director, Exercising the
Delegated Authority of the Director, U.S. Fish
and Wildlife Service.
[FR Doc. 2021–19091 Filed 9–3–21; 8:45 am]
BILLING CODE 4333–15–P
E:\FR\FM\07SEP1.SGM
07SEP1
Agencies
[Federal Register Volume 86, Number 170 (Tuesday, September 7, 2021)]
[Proposed Rules]
[Pages 49989-50011]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-19091]
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DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R4-ES-2021-0092; FF09E21000 FXES11110900000 212]
RIN 1018-BF43
Endangered and Threatened Wildlife and Plants; Threatened Species
Status With Section 4(d) Rule for Pyramid Pigtoe
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Proposed rule.
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SUMMARY: We, the U.S. Fish and Wildlife Service (Service), announce our
12-month finding on a petition to list the pyramid pigtoe (Pleurobema
rubrum), a freshwater mussel species from Alabama, Arkansas, Kentucky,
Louisiana, Mississippi, Ohio, Oklahoma, Tennessee, and Virginia, as an
endangered or threatened species under the Endangered Species Act of
1973, as amended (Act). After a review of the best available scientific
and commercial information, we find that listing the species is
warranted. Accordingly, we propose to list the pyramid pigtoe as a
threatened species with a rule issued under section 4(d) of the Act
(``4(d) rule''). If we finalize this rule as proposed, it would add
this species to the List of Endangered and Threatened Wildlife and
extend the Act's protections to the species.
DATES: We will accept comments received or postmarked on or before
November 8, 2021. Comments submitted electronically using the Federal
eRulemaking Portal (see ADDRESSES, below) must be received by 11:59
p.m. Eastern Time on the closing date. We must receive requests for a
public hearing, in writing, at the address shown in FOR FURTHER
INFORMATION CONTACT by October 22, 2021.
ADDRESSES: You may submit comments by one of the following methods:
(1) Electronically: Go to the Federal eRulemaking Portal: https://www.regulations.gov. In the Search box, enter the docket number or RIN
for this rulemaking (presented above in the document headings). For
best results, do not copy and paste either number; instead, type the
docket number or RIN into the Search box using hyphens. Then, click on
the Search button. On the resulting page, in the panel on the left side
of the screen, under the Document Type heading, check the Proposed Rule
box to locate this document. You may
[[Page 49990]]
submit a comment by clicking on ``Comment.''
(2) By hard copy: Submit by U.S. mail to: Public Comments
Processing, Attn: FWS-R4-ES-2021-0092, U.S. Fish and Wildlife Service,
MS: PRB/3W, 5275 Leesburg Pike, Falls Church, VA 22041-3803.
We request that you send comments only by the methods described
above. We will post all comments on https://www.regulations.gov. This
generally means that we will post any personal information you provide
us (see Information Requested, below, for more information).
FOR FURTHER INFORMATION CONTACT: Janet Mizzi, Field Supervisor, U.S.
Fish and Wildlife Service, Asheville Ecological Services Field Office,
160 Zillicoa St, Asheville, NC 28801; telephone 828-258-3939. Persons
who use a telecommunications device for the deaf (TDD) may call the
Federal Relay Service at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Executive Summary
Why we need to publish a rule. Under the Endangered Species Act of
1973, as amended (Act; 16 U.S.C. 1531 et seq.), if we determine that a
species is an endangered or threatened species throughout all or a
significant portion of its range, we are required to promptly publish a
proposal in the Federal Register and make a determination on our
proposal within 1 year, unless, due to substantial disagreement
regarding the sufficiency or accuracy of the available data, we extend
the 1-year period for no more than 6 months to solicit additional data.
To the maximum extent prudent and determinable, we must designate
critical habitat for any species that we determine to be an endangered
or threatened species under the Act. Listing a species as an endangered
or threatened species can only be completed by issuing a rule.
What this document does. We propose to list the pyramid pigtoe as a
threatened species with a rule under section 4(d) of the Act. If made
final, this action would add the species to the List of Endangered and
Threatened Wildlife in title 50 of the Code of Federal Regulations
(CFR) at 50 CFR 17.11(h) and add specific provisions pertaining to the
pyramid pigtoe to 50 CFR 17.45.
The basis for our action. Under the Act, we may determine that a
species is an endangered or threatened species because of any of five
factors: (A) The present or threatened destruction, modification, or
curtailment of its habitat or range; (B) overutilization for
commercial, recreational, scientific, or educational purposes; (C)
disease or predation; (D) the inadequacy of existing regulatory
mechanisms; or (E) other natural or manmade factors affecting its
continued existence. We have determined that threats to the pyramid
pigtoe include habitat degradation or loss from a variety of sources
(e.g., dams and other barriers, resource extraction); degraded water
quality from chemical contamination and erosion from development,
agriculture, and mining operations; direct mortality from dredging;
residual impacts (reduced population size) from historical harvest; and
the proliferation of invasive, nonnative species. These threats also
compound the negative effects associated with the species' small
population size.
Section 4(a)(3) of the Act requires the Secretary of the Interior
(Secretary) to designate critical habitat concurrent with listing to
the maximum extent prudent and determinable. Section 3(5)(A) of the Act
defines critical habitat as (i) the specific areas within the
geographical area occupied by the species, at the time it is listed, on
which are found those physical or biological features (I) essential to
the conservation of the species and (II) which may require special
management considerations or protections; and (ii) specific areas
outside the geographical area occupied by the species at the time it is
listed, upon a determination by the Secretary that such areas are
essential for the conservation of the species. Section 4(b)(2) of the
Act states that the Secretary must make the designation on the basis of
the best scientific data available and after taking into consideration
the economic impact, the impact on national security, and any other
relevant impacts of specifying any particular area as critical habitat.
Critical habitat is not currently determinable. However, critical
habitat is prudent, and we intend to propose critical habitat for the
species within 1 year of publishing this rule, after acquiring the
information to determine the areas warranting critical habitat
designation.
Information Requested
We intend that any final action resulting from this proposed rule
will be based on the best scientific and commercial data available and
be as accurate and as effective as possible. Therefore, we request
comments or information from other governmental agencies, Native
American Tribes, the scientific community, industry, or any other
interested parties concerning this proposed rule.
We particularly seek comments concerning:
(1) The species' biology, range, and population trends, including:
(a) Biological or ecological requirements of the species, including
habitat requirements for feeding, breeding, and sheltering;
(b) Genetics and taxonomy;
(c) Historical and current range, including distribution patterns;
(d) Historical and current population levels, and current and
projected trends; and
(e) Past and ongoing conservation measures for the species, its
habitat, or both.
(2) Factors that may affect the continued existence of the species,
which may include habitat modification or destruction, overutilization,
disease, predation, the inadequacy of existing regulatory mechanisms,
or other natural or manmade factors.
(3) Biological, commercial trade, or other relevant data concerning
any threats (or lack thereof) to this species and existing regulations
that may be addressing those threats.
(4) Additional information concerning the historical and current
status, range, distribution, and population size of this species,
including the locations of any additional populations of this species.
(5) Information on regulations that are necessary and advisable to
provide for the conservation of the pyramid pigtoe and that the Service
can consider in developing a 4(d) rule for the species. In particular,
information concerning the extent to which we should include any of the
section 9 prohibitions in the 4(d) rule or whether we should consider
any additional exceptions from the prohibitions in the 4(d) rule.
(6) Which areas would be appropriate as critical habitat for the
species and why areas should or should not be proposed for designation
as critical habitat in the future.
(7) Specific information on:
(a) The amount and distribution of habitat for pyramid pigtoe that
should be considered for proposed critical habitat;
(b) What may constitute ``physical or biological features essential
to the conservation of the species within the geographical range
currently occupied by the species'';
(c) Where these features are currently found;
(d) Whether any of these features may require special management
considerations or practices;
(e) What areas that are currently occupied and contain features
essential to the conservation of the species should be included in the
designation and why; and
[[Page 49991]]
(f) What unoccupied areas are essential for the conservation of the
species and why.
Please include sufficient information with your submission (such as
scientific journal articles or other publications) to allow us to
verify any scientific or commercial information you include.
Please note that submissions merely stating support for, or
opposition to, the action under consideration without providing
supporting information, although noted, will not be considered in
making a determination, as section 4(b)(1)(A) of the Act directs that
determinations as to whether any species is an endangered or a
threatened species must be made ``solely on the basis of the best
scientific and commercial data available.''
You may submit your comments and materials concerning this proposed
rule by one of the methods listed in ADDRESSES. We request that you
send comments only by the methods described in ADDRESSES.
If you submit information via https://www.regulations.gov, your
entire submission--including any personal identifying information--will
be posted on the website. If your submission is made via a hardcopy
that includes personal identifying information, you may request at the
top of your document that we withhold this information from public
review. However, we cannot guarantee that we will be able to do so. We
will post all hardcopy submissions on https://www.regulations.gov.
Comments and materials we receive, as well as supporting
documentation we used in preparing this proposed rule, will be
available for public inspection on https://www.regulations.gov.
Because we will consider all comments and information we receive
during the comment period, our final determinations may differ from
this proposal. Based on the new information we receive (and any
comments on that new information), we may conclude that the species is
endangered instead of threatened, or we may conclude that the species
does not warrant listing as either an endangered species or a
threatened species. In addition, we may change the parameters of the
prohibitions or the exceptions to those prohibitions in the 4(d) rule
if we conclude it is appropriate in light of comments and new
information received. For example, we may expand the prohibitions to
include prohibiting take associated with additional activities if we
conclude that those additional activities are not compatible with
conservation of the species. Conversely, we may establish additional
exceptions to the prohibitions in the final rule if we conclude that
the activities would facilitate or are compatible with the conservation
and recovery of the species.
Public Hearing
Section 4(b)(5) of the Act provides for a public hearing on this
proposal, if requested. Requests must be received by the date specified
in DATES. Such requests must be sent to the address shown in FOR
FURTHER INFORMATION CONTACT. We will schedule a public hearing on this
proposal, if requested, and announce the date, time, and place of the
hearing, as well as how to obtain reasonable accommodations, in the
Federal Register and local newspapers at least 15 days before the
hearing. For the immediate future, we will provide these public
hearings using webinars that will be announced on the Service's
website, in addition to the Federal Register. The use of these virtual
public hearings is consistent with our regulations at 50 CFR
424.16(c)(3).
Previous Federal Actions
In our 1989 Animal Notice of Review (a notice identifying animal
taxa that are native to the United States and being considered for
addition to the List of Endangered and Threatened Wildlife), we
categorized the pyramid pigtoe (which we referred to as ``pink
pigtoe'') as a taxon not meeting the Act's legal definition of a
species, based on our taxonomic understanding of information in
published scientific literature at that time (54 FR 554, January 6,
1989). While taxonomic uncertainty remains regarding some populations
identified as pyramid pigtoe, the species is recognized as valid in
current scientific literature (see Background, below). On April 20,
2010, we received a petition from the Center for Biological Diversity
(CBD), Alabama Rivers Alliance, Clinch Coalition, Dogwood Alliance,
Gulf Restoration Network, Tennessee Forests Council, and West Virginia
Highlands Conservancy to list 404 aquatic, riparian, and wetland
species, including the pyramid pigtoe (referred to as ``pink pigtoe''
in our National Domestic Listing Workplan) as endangered or threatened
species under the Act. On September 27, 2011, we published our
determination that the petition contained substantial information
indicating listing may be warranted (76 FR 59836). On April 17, 2019,
CBD filed a complaint challenging the Service's failure to complete 12-
month findings for these species within the statutory deadline. The
Service and CBD reached a stipulated settlement agreement whereby the
Service agreed to deliver a 12-month finding for the pyramid pigtoe to
the Office of the Federal Register by August 31, 2021.
Supporting Documents
A species status assessment (SSA) team prepared an SSA report for
the pyramid pigtoe. The SSA team was composed of Service biologists, in
consultation with other species experts. The SSA report represents a
compilation of the best scientific and commercial data available
concerning the status of the species, including the impacts of past,
present, and future factors (both negative and beneficial) affecting
the species. In accordance with our joint policy on peer review
published in the Federal Register on July 1, 1994 (59 FR 34270), and
our August 22, 2016, memorandum updating and clarifying the role of
peer review of listing actions under the Act, we sought the expert
opinions of three appropriate specialists regarding the SSA. We
received two responses. We also received SSA report reviews from one
Federal agency and five State agency partners, including scientists
with expertise in aquatic ecology, freshwater mussel biology, taxonomy,
and conservation. In addition, more than 50 individuals at Federal or
State agencies, colleges or universities, or consultants provided data
used in the SSA report.
I. Proposed Listing Determination
Background
A thorough review of the taxonomy, life history, and ecology of the
pyramid pigtoe (Pleurobema rubrum) is presented in the SSA report
(version 1.0; Service 2021, pp. 19-36).
The pyramid pigtoe is a freshwater mussel, reddish to chestnut
brown in color, with a smooth periostracum (outer shell surface) that
darkens with age (Watters et al. 2009, p. 233). Juveniles may have
green rays that typically disappear with age. The shell is thick,
triangular, and medium-sized (up to 3.6 inches (in) (91 millimeters
(mm)) (Williams et al. 2008, p. 564). It has a shallow sulcus
(depressed channel) and high anteriorly directed beak that is elevated
above the hinge line (Stansbery 1967, p. 3).
The pyramid pigtoe is found in medium to large rivers, in a mixture
of sand, gravel, and cobble substrates. It currently occurs in
Kentucky, Tennessee, Virginia, Ohio, Alabama, Oklahoma, Arkansas,
Mississippi, and Louisiana. It is considered extirpated from
Pennsylvania, West Virginia, Indiana, Illinois, Wisconsin, Minnesota,
Iowa, Kansas, and Missouri. Extant populations of pyramid pigtoe occur
in
[[Page 49992]]
the Arkansas-White-Red, Lower Mississippi, Missouri, and Ohio River
regions (Hydrologic Unit Code 2 scale, Seaber et al. 1987, pp. 3-4),
and it is extirpated from the Missouri and Upper Mississippi River
regions (Figure 1).
Relying on fish hosts for successful reproduction, the pyramid
pigtoe has a complex life cycle similar to other mussels. In general,
mussels are either male or female, but differences between sexes in
shell shape are subtle (Haag 2012, p. 54). Males release sperm into the
water column, which is taken in by the female through the incurrent
aperture, where water enters the mantle cavity. The sperm fertilize
eggs in the suprabranchial chamber (located above the gills) as ova are
passed from the gonad to the marsupia (Yokley 1972, p. 357). Developing
larvae remain in the gill chamber until they mature (called glochidia)
and are ready for release. Once released, the glochidia draw nutrients
from fish hosts and develop into juvenile mussels, dropping from the
hosts weeks to months after initial attachment. Only a few glochidia
reach the free-living juvenile stage, and mortality rates for the
glochidial stage have been estimated at 99 percent, making this a
critical phase in the life history of freshwater mussels (Jansen et al.
2001, p. 211).
[GRAPHIC] [TIFF OMITTED] TP07SE21.021
The pyramid pigtoe is a short-term brooder and has been recorded as
gravid in the Cumberland River in May, June, and July (Gordon and
Layzer 1989, p. 50). Host fish species are minnows of the family
Cyprinidae and genera Cyprinella, Erimystax, Lythrurus, and Notropis
(Culp et al. 2009, p. 19). Similar to other species in its tribe,
Pleurobemini (taxonomic rank above genus and below family), the pyramid
pigtoe targets drift-feeding minnow species by releasing glochidia
contained in packets called conglutinates (Haag 2012, p. 163).
Following release from the female mussel, the semi-buoyant
conglutinates drift in the water column where they are targeted by
sight-feeding minnows (Culp et al, 2009, p. 21).
A relatively long-lived species, the pyramid pigtoe has a lifespan
that likely averages 20 to 30 years, based on observations of the
closely related Ohio pigtoe and round pigtoe (Slater 2018, p. 35;
Watters et al. 2009, p. 299). Given the longevity of closely related
species, it possibly lives up to 40-45 years in some locations (Ostby
and Beaty 2016, p. 117).
The pyramid pigtoe exhibits a preference for sand and gravel in
rivers but also may be found in coarse sand in larger rivers (Gordon
and Layzer 1989, p. 31). They can be found at depths less than 3 ft (1
m) but in large rivers can be found commonly at depths of 13 to
[[Page 49993]]
20 ft (4 to 6 m) or greater (Parmalee and Bogan 1998, p. 193; Williams
et al. 2008, p. 566). Adult freshwater mussels within the genus
Pleurobema are suspension-feeders that filter water and nutrients to
eat. Mussels may shift to deposit feeding, though reasons for this are
poorly known and may depend on flow conditions or temperature. Their
diet consists of a mixture of algae, bacteria, detritus, and
microscopic animals (Gatenby et al. 1996, p. 606; Strayer et al. 2004,
p. 430). It has also been surmised that dissolved organic matter may be
a significant source of nutrition (Strayer et al. 2004, p. 431).
The pyramid pigtoe (Pleurobema rubrum) belongs to a complex of four
morphologically similar species, which includes the Ohio pigtoe (P.
cordatum), rough pigtoe (P. plenum) and round pigtoe (P. sintoxia).
Since its original description as a species (Rafinesque 1820, p. 314),
Pleurobema rubrum has undergone several scientific name changes, due to
its widespread distribution, variability in shell shape and size
throughout its range, and similarity in morphological characters to
other closely related species. Additionally, based on shell characters
alone, the pyramid pigtoe has been periodically considered a subspecies
of the Ohio pigtoe (Ortmann 1911, p. 331). Since its initial
description in 1820, the pyramid pigtoe has sometimes been referred to
as pink pigtoe by commercial shell harvesters and biologists. However,
the common name applied to the species in the scientific literature and
in the Integrated Taxonomic Information System is pyramid pigtoe.
Genetic studies to clarify the taxonomic relationships among
Pleurobema indicate potential differences between pyramid pigtoe
populations occupying separate river drainages. Mitochondrial DNA
samples from two specimens of pyramid pigtoe indicated the Duck River,
Tennessee, specimen was genetically distinct from the St. Francis
River, Arkansas, specimen (Campbell et al. 2005, p. 143). These same
data were included in subsequent phylogenetic studies focused on
Fusconaia (Burdick and White 2007, p. 372) and Pleurobema (Campbell et
al. 2008, p. 714; Campbell and Lydeard 2012b, p. 27) with similar
results. Phylogeographic structuring has been observed between pyramid
pigtoe from the Ouachita and St. Francis drainages in Arkansas that may
represent species-level variation (Christian et al. 2008, p. 9; Harris
et al. 2009, p. 74). Additionally, an analysis that included all
previously published and new data representing a broad sampling across
Pleurobemini revealed that pyramid pigtoe and round pigtoe may
represent a single species, with two out of three species delineation
models indicating one lineage present in specimens identified as round
pigtoe and pyramid pigtoe (Inoue et al. 2018, p. 694). However, one of
the three models indicated separate lineages of the two species. While
there is some uncertainty in the taxonomic identity of populations
referred to as pyramid pigtoe, especially those outside the Ohio,
Cumberland, and Tennessee basins, our SSA report analyzed the status of
the single species currently recognized by the scientific community
(Williams et al. 2017, p. 42; Graf and Cummings 2021, p. 19).
Regulatory and Analytical Framework
Regulatory Framework
Section 4 of the Act (16 U.S.C. 1533) and its implementing
regulations (50 CFR part 424) set forth the procedures for determining
whether a species is an endangered species or a threatened species. The
Act defines an endangered species as a species that is ``in danger of
extinction throughout all or a significant portion of its range'' and a
threatened species as a species that is ``likely to become an
endangered species within the foreseeable future throughout all or a
significant portion of its range.'' The Act requires that we determine
whether any species is an endangered species or a threatened species
because of any of the following factors:
(A) The present or threatened destruction, modification, or
curtailment of its habitat or range;
(B) Overutilization for commercial, recreational, scientific, or
educational purposes;
(C) Disease or predation;
(D) The inadequacy of existing regulatory mechanisms; or
(E) Other natural or manmade factors affecting its continued
existence.
These factors represent broad categories of natural or human-caused
actions or conditions that could have an effect on a species' continued
existence. In evaluating these actions and conditions, we look for
those that may have a negative effect on individuals of the species, as
well as other actions or conditions that may ameliorate any negative
effects or may have positive effects.
We use the term ``threat'' to refer in general to actions or
conditions that are known to or are reasonably likely to negatively
affect individuals of a species. The term ``threat'' includes actions
or conditions that have a direct impact on individuals (direct
impacts), as well as those that affect individuals through alteration
of their habitat or required resources (stressors). The term ``threat''
may encompass--either together or separately--the source of the action
or condition or the action or condition itself.
However, the mere identification of any threat(s) does not
necessarily mean that the species meets the statutory definition of an
``endangered species'' or a ``threatened species.'' In determining
whether a species meets either definition, we must evaluate all
identified threats by considering the expected response by the species,
and the effects of the threats--in light of those actions and
conditions that will ameliorate the threats--on an individual,
population, and species level. We evaluate each threat and its expected
effects on the species, then analyze the cumulative effect of all of
the threats on the species as a whole. We also consider the cumulative
effect of the threats in light of those actions and conditions that
will have positive effects on the species, such as any existing
regulatory mechanisms or conservation efforts. The Secretary determines
whether the species meets the definition of an ``endangered species''
or a ``threatened species'' only after conducting this cumulative
analysis and describing the expected effect on the species now and in
the foreseeable future.
The Act does not define the term ``foreseeable future,'' which
appears in the statutory definition of ``threatened species.'' Our
implementing regulations at 50 CFR 424.11(d) set forth a framework for
evaluating the foreseeable future on a case-by-case basis. The term
``foreseeable future'' extends only so far into the future as the
Service can reasonably determine that both the future threats and the
species' responses to those threats are likely. In other words, the
foreseeable future is the period of time in which we can make reliable
predictions. ``Reliable'' does not mean ``certain''; it means
sufficient to provide a reasonable degree of confidence in the
prediction. Thus, a prediction is reliable if it is reasonable to
depend on it when making decisions.
It is not always possible or necessary to define foreseeable future
as a particular number of years. Analysis of the foreseeable future
uses the best scientific and commercial data available and should
consider the timeframes applicable to the relevant threats and to the
species' likely responses to those threats in view of its life-history
characteristics. Data that are typically relevant to assessing the
species' biological response include species-
[[Page 49994]]
specific factors such as lifespan, reproductive rates or productivity,
certain behaviors, and other demographic factors.
Analytical Framework
The SSA report documents the results of our comprehensive
biological review of the best scientific and commercial data regarding
the status of the species, including an assessment of the potential
threats to the species. The SSA report does not represent a decision by
the Service on whether the species should be proposed for listing as an
endangered or threatened species under the Act. However, it does
provide the scientific basis that informs our regulatory decisions,
which involve the further application of standards within the Act and
its implementing regulations and policies. The following is a summary
of the key results and conclusions from the SSA report; the full SSA
report can be found at Docket FWS-R4-ES-2021-0092 on https://www.regulations.gov and at https://www.fws.gov/Asheville/.
To assess pyramid pigtoe viability, we used the three conservation
biology principles of resiliency, redundancy, and representation
(Shaffer and Stein 2000, pp. 306-310). Briefly, resiliency supports the
ability of the species to withstand environmental and demographic
stochasticity (for example, wet or dry, warm or cold years), redundancy
supports the ability of the species to withstand catastrophic events
(for example, droughts, large pollution events), and representation
supports the ability of the species to adapt over time to long-term
changes in the environment (for example, climate changes). In general,
the more resilient and redundant a species is and the more
representation it has, the more likely it is to sustain populations
over time, even under changing environmental conditions. Using these
principles, we identified the species' ecological requirements for
survival and reproduction at the individual, population, and species
levels, and described the beneficial and risk factors influencing the
species' viability.
The SSA process can be categorized into three sequential stages.
During the first stage, we evaluated the individual species' life-
history needs. The next stage involved an assessment of the historical
and current condition of the species' demographics and habitat
characteristics, including an explanation of how the species arrived at
its current condition. The final stage of the SSA involved making
predictions about the species' responses to positive and negative
environmental and anthropogenic influences. Throughout all of these
stages, we used the best available information to characterize
viability as the ability of a species to sustain populations in the
wild over time. We use this information to inform our regulatory
decision.
Summary of Biological Status and Threats
In this discussion, we review the biological condition of the
species and its resources, and the threats that influence the species'
current and future condition, in order to assess the species' overall
viability and the risks to that viability.
Species Needs
We assessed the best available information to identify the physical
and biological needs to support individual fitness at all life stages
for the pyramid pigtoe. Full descriptions of all needs are available in
chapter 4 of the SSA report (Service 2021, pp. 29-36), which can be
found in docket number FWS-R4-ES-2021-0092 on https://www.regulations.gov, and on our internet site https://www.fws.gov/Asheville/. To maintain viability, individual pyramid pigtoes need
clean flowing water, appropriate water quality and temperatures
(parameters listed in Service 2021, p. 29), low levels of
sedimentation, and food and nutrients. Pyramid pigtoe habitat is in
rivers with natural flow regimes. Perturbations that disrupt natural
flow patterns (e.g., dams) have a negative influence on pyramid pigtoe
and host fish resilience. Pyramid pigtoe habitat must have adequate
flow to deliver oxygen, enable passive reproduction, and deliver food.
At the population and species (rangewide) level, the pyramid pigtoe
needs habitat connectivity and positive demographic attributes
(population density and growth rate, age class structure, recruitment)
to maintain viability (Service 2021, pp. 32-33). Dendritic, or
branched, orientation of stream systems can enhance metapopulation
persistence compared to linear or two-dimensional systems (Fagan 2002,
p. 3,243). Tributary connection to river mainstems allows movement of
host fishes and helps facilitate dispersal and colonization of
appropriate habitat patches by mussels. A high degree of connection
between habitat patches and occupied reaches is necessary, because
mussels are heavily dependent on gene exchange and host fish movement
and dispersal within river corridors to maintain viable populations
(Newton et al. 2008, p. 425).
Fragmentation of stream habitat results in barriers to host fish
movement, which in turn, influences mussel distributions, increasing
the likelihood and compounding the significance of local extirpation
events (Fagan 2002, p. 3,248). The pyramid pigtoe and other mussel
species that use small host fishes, such as minnows and shiners (family
Cyprinidae), are more susceptible to impacts from habitat
fragmentation. This is due to increasing distance between suitable
habitat patches and low likelihood of small host fish swimming over
that distance as compared to large host fishes (Vaughn 2012, p. 7).
Barriers to movement can cause isolated or patchy distributions of
mussels, which may limit both genetic exchange and recolonization
(Jones et al. 2006, p. 528).
Mussel abundance in a given river reach is a product of the number
of mussel beds (aggregations of freshwater mussels) and the density of
mussels within those beds. Healthy pyramid pigtoe populations have
numerous individuals, with multiple age classes, and exhibit regular
recruitment of new age classes. For pyramid pigtoe populations to be
resilient, there must be multiple mussel beds of sufficient density
such that local stochastic events do not eliminate the bed(s), allowing
the mussel bed and the overall local population within a river reach to
recover from any one event. A dendritic distribution (branching, such
that there is not a line connecting a single upstream and downstream
aggregation) over a large area also helps buffer against stochastic
events that may impact populations. Mussels do not actively seek mates;
rather, males release sperm into the water column, where it drifts
until a female takes it in (Moles and Layzer 2008, p. 212). Therefore,
successful individual reproduction and population viability require
sufficient numbers of female mussels downstream of sufficient numbers
of male mussels; higher density (number of mussels per unit area)
increases the likelihood of fertilization.
Threats
We have determined that past and current threats to the pyramid
pigtoe include habitat degradation or loss from a variety of sources
(e.g., dams and other barriers, resource extraction); degraded water
quality from chemical contamination and erosion from development,
agriculture, and mining operations; direct mortality from dredging;
residual impacts (reduced population size) from historical harvest; and
the proliferation of invasive, nonnative species. Cumulatively, these
threats also contribute to the negative
[[Page 49995]]
effects associated with the species' small population size in certain
areas.
The following discussions include evaluations of three current
threats and associated sources that are affecting the pyramid pigtoe
and its habitat: (1) Habitat (including water quality) degradation or
loss, (2) invasive and nonnative species, and (3) negative effects
associated with small population size (Service 2021, pp. 51-83). We
also considered impacts from climate change, but found no evidence
linking climate change impacts to the current status of the pyramid
pigtoe. We note that overutilization (commercial mussel harvest) was a
threat historically and likely reduced the size of many populations
such that they have not recovered to historical abundance levels, but
it is not currently a threat. In addition, potential impacts from
disease, parasites, and predation, as well as potential impacts to host
species, were evaluated but were found to have minimal effects on
viability of the pyramid pigtoe based on current knowledge (Service
2021, pp. 78-79). Although not a widespread threat, disease is likely
affecting at least one population of pyramid pigtoe: The Clinch River
mussel assemblage, which includes a pyramid pigtoe population, has
recently undergone a die-off that is associated with a novel densovirus
(Richard et al. 2020, entire). Finally, we also considered effects
associated with enigmatic population declines (unexplained die-offs of
large numbers of mussels over a short period of time), which have been
documented in fresh water river mussel populations since the 1960s;
despite speculation and repeated aquatic organism surveys and water
quality monitoring, the causes of these events are largely unknown
(Haag 2019, p. 43).
Predominant threats affecting each pyramid pigtoe population are
listed in Table 1. Based on threat information in the literature or
State Wildlife Action Plans, we categorized the threat level as low,
moderate, or high depending on their magnitude and immediacy:
Low--Threats to aquatic fauna far enough removed in time
or space that they are currently exerting minimal influence on mussel
populations.
Moderate--Multiple threats linked to negative effects on
mussels are present. Some threats currently acting on mussel habitat,
reducing resource needs, and limiting recruitment and population
growth.
High--Multiple threats linked to negative effects on
mussels are present and have been acting cumulatively on mussel
habitat, prohibiting sustained recruitment and population growth.
Table 1--Current Threats and Level of Threat to the Pyramid Pigtoe by River Basin and Population
[Adapted and modified from SSA report, Service 2021, pp. 157-164]
----------------------------------------------------------------------------------------------------------------
Population Threat level category Threats
----------------------------------------------------------------------------------------------------------------
OHIO RIVER BASIN
----------------------------------------------------------------------------------------------------------------
Muskingum River......................... High....................... Hydropower development; impoundment;
dredging; population isolation; past
commercial harvest.
Upper Green River....................... Low........................ Impoundment; habitat loss and water
quality degradation; resource
extraction; past commercial harvest.
Barren River............................ Moderate................... Impoundment; habitat loss and water
quality degradation; resource
extraction; past commercial harvest.
Middle Green River...................... Moderate................... Impoundment; habitat loss and water
quality degradation; resource
extraction; past commercial harvest.
Lower Green River....................... Moderate................... Impoundment; habitat loss and water
quality degradation; resource
extraction; past commercial harvest.
Cumberland River........................ High....................... Habitat fragmentation, hypolimnetic
discharges.
----------------------------------------------------------------------------------------------------------------
TENNESSEE RIVER BASIN
----------------------------------------------------------------------------------------------------------------
Holston River........................... High....................... Habitat fragmentation, hypolimnetic
discharges.
Clinch River............................ Moderate................... Development; agricultural activities;
dams; overharvest historically;
contaminants; resource extraction;
degraded water quality; enigmatic die-
offs.
Paint Rock River........................ Low........................ Habitat loss through channel maintenance
(snag removal); habitat fragmentation
and population isolation due to
impoundment; agriculture.
Tennessee River (Wheeler Reservoir)..... High....................... Impoundment; habitat degradation from
flow releases; past commercial harvest.
Tennessee River (Pickwick Reservoir).... High....................... Impoundment; dredging; navigation
impacts; past commercial harvest.
Tennessee River (Kentucky Reservoir).... High....................... Impoundment; dredging and navigation
impacts; agriculture.
Upper Duck River........................ Moderate................... Development; agricultural activities;
water quality degradation; impoundments;
fragmented populations.
Lower Duck River........................ Moderate................... Development and water quality
degradation.
----------------------------------------------------------------------------------------------------------------
ARKANSAS-WHITE-RED BASIN
----------------------------------------------------------------------------------------------------------------
Petit Jean River........................ Moderate................... Agriculture; habitat loss and water
quality degradation.
Eleven Point River...................... Low........................ Habitat loss and water quality
degradation; agricultural effects.
Little River............................ Moderate................... Impoundment, habitat loss, and water
quality degradation.
----------------------------------------------------------------------------------------------------------------
LOWER MISSISSIPPI BASIN
----------------------------------------------------------------------------------------------------------------
Lower Black River....................... Moderate................... Agriculture, habitat loss, and water
quality degradation.
Lower St. Francis River................. High....................... Agriculture, habitat loss, and water
quality degradation.
Tyronza River........................... High....................... Agriculture, habitat loss, and water
quality degradation.
White River............................. Moderate................... Impoundment, resource extraction, habitat
loss, and water quality degradation.
[[Page 49996]]
Upper Ouachita River.................... Moderate................... Impoundment, navigation, habitat loss,
and water quality degradation.
Little Missouri River................... Moderate................... Agriculture, habitat loss, and water
quality degradation.
Ouachita River.......................... Moderate................... Impoundment, navigation, habitat loss,
and water quality degradation.
Upper Saline River...................... Moderate................... Impoundment, navigation; agriculture;
resource extraction; habitat loss and
water quality degradation.
Lower Saline River...................... Moderate................... Impoundment, navigation, agriculture,
resource extraction, habitat loss, and
water quality degradation.
Bayou Bartholomew....................... High....................... Agriculture, habitat loss and water
quality degradation.
Lower Ouachita River.................... High....................... Impoundment; navigation; habitat loss and
water quality degradation.
Big Sunflower River..................... High....................... Agriculture; habitat loss and water
quality degradation.
Hushpuckna River........................ High....................... Impoundment; agriculture; navigation;
habitat loss and water quality
degradation.
Bogue Phalia............................ High....................... Impoundment; agriculture; navigation;
habitat loss and water quality
degradation.
Little Sunflower River.................. High....................... Impoundment; agriculture; navigation;
habitat loss and water quality
degradation.
Sunflower River......................... High....................... Impoundment; agriculture; navigation;
habitat loss and water quality
degradation.
Sandy Bayou............................. High....................... Impoundment; agriculture; navigation;
habitat loss and water quality
degradation.
Big Black River......................... High....................... Impoundment; agriculture, habitat loss
and water quality degradation.
----------------------------------------------------------------------------------------------------------------
Habitat Degradation or Loss
Development and Urbanization
Development and urbanization activities that may contribute to
pyramid pigtoe habitat degradation or loss, including reduced water
quality, occur throughout the species' range. The term ``development''
refers to urbanization of the landscape, including (but not limited to)
land conversion for residential, commercial, and industrial uses and
the accompanying infrastructure. The effects of urbanization may
include alterations to water quality, water quantity, and habitat (both
in-stream and streamside) (Ren et al. 2003, p. 649; Wilson 2015, p.
424). Urban development can lead to increased variability in
streamflow, typically increasing the extent and volume of water
entering a stream after a storm and decreasing the time it takes for
the water to travel over the land before entering the stream (Giddings
et al. 2009, p. 1). Deleterious effects on streams (i.e., water
collection on impervious surfaces that rapidly flows into storm drains
and local streams), including those that may be occupied by the pyramid
pigtoe, include:
Water Quantity: Storm drains deliver large volumes of
water to streams much faster than would naturally occur, often
resulting in flooding and bank erosion that reshapes the channel and
causes substrate instability, resulting in destabilization of bottom
sediments. Increased, high-velocity discharges can cause pyramid pigtoe
to become stressed, displaced, or killed by fast-moving water and the
debris and sediment carried in it.
Water Quality: Pollutants (e.g., gasoline, oil drips,
fertilizers) that accumulate on impervious surfaces may be washed
directly into streams during storm events thereby directing killing
pyramid pigtoe individuals.
Water Temperature: During warm weather, rain that falls on
impervious surfaces becomes superheated and can stress or kill pyramid
pigtoe individuals when it enters streams.
Water infrastructure to support development, including water
supply, reclamation, and wastewater treatment, results in pollution or
contaminant discharges to streams. Right of way (ROW) crossings for
waterlines and other utility lines also affect stream habitats. Direct
impacts from utility crossings include direct exposure or crushing of
individuals, sedimentation, and flow disturbance. The most significant
cumulative impact involves cleared ROWs that result in direct runoff
and increased stream temperature at the crossing locations. Maintenance
or clearing of ROWs may entail herbicide applications that subsequently
enter streams via stream runoff.
Most populations of pyramid pigtoe in urban areas with large human
populations have been diminished or lost. Secondary impacts resulting
from development, such as the increased contaminant introduction,
stream disturbance caused by impervious surfaces, barrier construction,
and forest conversion to other land use types such as agriculture or
urban uses are likely acting cumulatively on the species. Increased
human population growth projections indicate urban sprawl (a current
process) will affect pyramid pigtoe populations in the Tennessee and
Ohio basins (Terando et al. 2014, p. 7; Tayyebi et al. 2015, p. 110).
In the Upper and Lower Duck River MUs, the species is currently
impacted by rapid development encroaching from the city of Nashville
and nearby smaller urban areas such as Columbia, TN (TWRA 2016, p. 15).
The pyramid pigtoe population in the Muskingum River is downstream of
the Tuscarawas River, which has been severely degraded by industrial
development that continues to affect water quality (Hoggarth 1994, p.
3; Haefner and Simonson 2018, p. 1).
Threats to the pyramid pigtoe from development are partly mitigated
by Federal lands. Several locations where the pyramid pigtoe occurs in
water bodies located on or immediately adjacent to Federal lands
receive some indirect benefits to viability such as lack of
urbanization and land development pressure. These include the Pond
Creek Refuge in Arkansas (Arkansas-White-Red basin) as well as Upper
Ouachita, Felsenthal, and White River Refuges (Lower Mississippi
basin), and Wheeler Refuge (Tennessee Basin) that are adjacent to large
rivers where the pyramid pigtoe occurs. Mammoth Cave National Park also
provides a level of localized protection against development pressures
for the pyramid pigtoe population in the upper Green River, Kentucky
(Ohio Basin).
On private lands, the Saline-Caddo-Ouachita Programmatic Safe
Harbor Agreement and Candidate Conservation Agreement with Assurances
programs are voluntary conservation programs that support ongoing
stewardship for imperiled species, including the pyramid pigtoe. Large
tracts of private land in the upper Saline and Ouachita River systems
adjacent to streams and upland areas are covered under these programs.
These lands are mostly upstream of pyramid pigtoe sites
[[Page 49997]]
(Service 2015, p. 6) but could have a positive indirect long-term
benefit to the species by reducing sediment and pollutant runoff and
improving water quality downstream. Some private lands in pyramid
pigtoe MUs also are managed for conservation through The Nature
Conservancy (TNC) programs in the upper Green River in Kentucky, the
upper Clinch/Powell River, Tennessee and Virginia, the Saline River in
Arkansas, and the Paint Rock River in Alabama. In these watersheds, TNC
has a few riparian inholdings that are protected from developments. In
addition, within these watersheds, TNC implements community-based and
partner-oriented projects to address aquatic species and instream
habitat conservation by restoring and protecting streambanks and
riparian zones.
Various small, isolated parcels of State land (e.g., State parks,
State forests, wildlife management areas) along MUs where the pyramid
pigtoe occurs also provide a conservation benefit as a buffer to
development. However, vast tracks of riparian lands in the range of the
pyramid pigtoe are privately owned, without conservation programs, and
the prevalence of privately owned lands along rivers is comparatively
much larger than the species' occurrence on public lands. Limited
overlap of the species' range with public lands and private lands with
conservation programs diminishes their ability to protect the species,
because the habitat protection benefits these lands provide are at
significant risk of being negated by detrimental activities upstream or
immediately downstream.
Transportation
Transportation-related impacts include both road development and
river navigation. Road development increases impervious surfaces as
well as land clearing and habitat fragmentation. Roads are generally
associated with negative effects on the biotic integrity of aquatic
ecosystems, including changes in surface water temperatures and
patterns of runoff, sedimentation, adding heavy metals (especially
lead), salts, organics, and nutrients to stream systems (Trombulak and
Frissell 2000, p. 18).
With regard to river navigation, dredging and channelization
activities (as a means of maintaining waterways) have altered riverine
habitats nationwide (Ebert 1993, p. 157). Channelization affects many
physical characteristics of streams through accelerated erosion,
increased bedload, reduced depth, decreased habitat diversity,
geomorphic instability, and riparian canopy loss (Hartfield 1993, p.
139). All of these impacts contribute to loss of habitat for the
pyramid pigtoe and host fishes. Increases in turbulence, suspended and
deposited sediments, and turbidity resulting from river transportation
and associated activities may affect mussel feeding and respiration
(Aldridge et al. 1987, p. 25). In addition to dredging and channel
maintenance, impacts associated with barge traffic, which includes
construction of fleeting areas, mooring cells, docking facilities, and
propeller wash, also destroy and disrupt mussel habitat (see Miller et
al. (1989, pp. 48-49) as an example for disturbance from barges).
Transportation-related impacts across the range of the pyramid
pigtoe include (but are not limited to) the following examples:
Extensive stream channelization and snag removal has
severely affected the freshwater mussel fauna and habitat in the Paint
Rock River system, including the lower reaches of Estill Fork and
Hurricane Creek (Ahlstedt 1995-96, p. 65). Even if active
channelization activities are not currently occurring in rivers and
streams occupied by the pyramid pigtoe, impacts of past actions can
have permanent effects (Haag and Cicerello 2016, p. 60; Hubbard et al.
1993, p. 142; Watters 2000, p. 274).
Commercial navigation previously took place in the lower
Green and Barren Rivers, where navigation dams remain but are not in
operation. Past dredging and navigation affected mussel beds in the
mainstem Cumberland River, which has the last remaining population of
pyramid pigtoe in the Cumberland River system (Hubbs 2012, p. 9).
Currently, all three of the Tennessee River mainstem
pyramid pigtoe MUs are likely affected to some extent by channel
maintenance and navigation operations, due to their clustered
distribution and proximity to navigation dams.
Two navigation dams are operated on the Ouachita River,
which is maintained by the Corps as a waterway, and affect three MUs.
Contaminants
Contaminants contained in point and non-point discharges can
degrade water and substrate quality and adversely impact mussel
populations. The effects of contaminants such as metals, chlorine, and
ammonia are profound on juvenile mussels (Bartsch et al. 2003, p.
2,566; Augspurger et al. 2003, p. 2,571). Juvenile mussels may readily
ingest contaminants bound to sediment particles (Newton and Cope 2007,
p. 276). These contaminants also affect mussel glochidia, which are
very sensitive to some toxicants (Goudreau et al. 1993, p. 221;
Jacobson et al. 1997, p. 2,386; Valenti et al. 2005, p. 1,243). High
levels of suspended solids alone (without bound contaminants) can
result in mussel reproductive failure or low fertilization rates of
long-term brooders, such as species of the genus Pleurobema (Gascho-
Landis and Stoeckel 2015, p. 229).
Current State regulations regarding pollutants are designed to be
protective of aquatic organisms; however, freshwater mussels may be
more susceptible to some pollutants than the test organisms commonly
used in bioassays. Additionally, water quality criteria may not
incorporate data available for freshwater mussels (March et al. 2007,
pp. 2,066-2,067). A multitude of bioassays conducted on 16 mussel
species (summarized by Augspurger et al. 2007, pp. 2,025-2,028) show
that freshwater mollusks are more sensitive than previously believed to
some chemical pollutants, including chlorine, ammonia, copper,
fungicides, and herbicide surfactants. Nickel and chloride were toxic
to federally threatened mussel species at levels below the current
criteria and are sensitive to sodium dodecyl sulfate (SDS), a
surfactant commonly used in household detergents, for which water
quality criteria do not currently exist (Gibson 2015, p. 80, p. 90;
Gibson et al. 2018, pp. 247-250). None of the States in the range of
the pyramid pigtoe have fully adopted the Environmental Protection
Agency's 2013 recommended ammonia criteria for freshwater mollusks (78
FR 52192, August 22, 2013).
Contaminant inputs (including sediments) to pyramid pigtoe habitat
stem from multiple threats, including urbanization, resource
extraction, agriculture, and channel maintenance for navigation,
diminishing water quality in many areas of the four basins where the
species occurs. Examples of contaminant-related impacts in the range of
the pyramid pigtoe include (but are not limited to) the following:
Long-term declines and extirpation of mussels from reaches
of the Upper Clinch MU in Virginia attributed, in part, to copper and
zinc contamination originating from wastewater discharges at coal-fired
power plants (Price et al. 2014, p. 12; Zipper et al. 2014, p. 9). Coal
plants also are located on the Lower Green and Cumberland-Old Hickory
MUs.
Heavy metals toxicity to mussels has been documented in
the
[[Page 49998]]
Muskingum, Upper Clinch, and all Tennessee River MUs (Havlik and
Marking 1987, pp. 4-9).
A chemical spill from a tanker truck accident flowed into
the Upper Clinch MU in Virginia and eliminated approximately 18,000
individuals of several mussel species (Jones et al. 2001, p. 20;
Schmerfeld 2006, p. 12), including approximately 750 individuals of
three federally listed species (Schmerfeld 2006, p. 12). A catastrophic
chemical spill in 1999 affected approximately 10 miles of the Ohio
River and resulted in the loss of an estimated 1 million mussels,
including two federally listed species (Butler 2005, p. 24).
State and Federal water quality programs provide a level of
protection to the pyramid pigtoe from development, agriculture, and
river navigation activities by regulating storm water and point source
(end of pipe) discharges to streams. Section 401 of the Federal Clean
Water Act (CWA; 33 U.S.C. 1251 et seq.) requires that an applicant for
a Federal license or permit provide a certification that any discharges
from the facility will not degrade water quality or violate water-
quality standards, including those established by States. Section 404
of the CWA establishes a program to regulate the discharge of dredged
and fill material into waters of the United States. Under the CWA,
permits to fill wetlands and culvert, bridge, or realign streams or
water features are issued by the U.S. Army Corps of Engineers. Current
State regulations regarding pollutants are designed to be protective of
aquatic organisms; however, as discussed above, freshwater mussels may
be more susceptible to some pollutants than the aquatic biota for which
water quality criteria are currently established.
Despite existing authorities such as the CWA, pollutants continue
to impair the water quality in areas of the pyramid pigtoe's range.
State and Federal regulatory mechanisms have helped reduce the negative
effects of point source discharges since the 1970s, yet these
regulations are difficult to implement and enforce. Although new water
quality criteria are under development that will take into account more
sensitive aquatic species, most current criteria do not. It is expected
that several years will be needed to implement new water quality
criteria throughout the species' range.
Agriculture
Agricultural activities occur across the range of the pyramid
pigtoe and are a factor in its historical decline and localized
extirpations. The advent of intensive row crop agricultural practices
corresponds with freshwater mussel declines, and species extirpations,
in the eastern United States (Peacock et al. 2005, p. 550). Nutrient
enrichment and water withdrawals, threats commonly associated with
agricultural activities, may be localized and limited in scope, and
have the potential to affect individual pyramid pigtoe mussels.
However, chemical control using pesticides may have broader impacts.
Pesticides, including herbicides, fungicides, and insecticides as well
as their surfactants and adjuvants, are highly toxic to juvenile and
adult freshwater mussels (Bringolf et al. 2007, p. 2,092) and
deleterious if not properly applied to agricultural operations. Waste
from confined animal feeding and commercial livestock operations is
another potential source of contaminants that come from agricultural
runoff. The concentrations of these contaminants from fields or
pastures may be at levels that can affect an entire population,
especially given the highly fragmented distribution of the pyramid
pigtoe.
Agencies such as the Natural Resources Conservation Service (NRCS)
and the Soil and Water Conservation Districts provide technical and
financial assistance to farmers and private landowners. Additionally,
county resource development councils and university agricultural
extension services disseminate information on the importance of
minimizing land use impacts, specifically agriculture, on aquatic
resources. These programs help identify opportunities for conservation
through projects such as exclusion fencing and alternate water supply
sources, which help decrease nutrient inputs and water withdrawals and
help keep livestock off stream banks and shorelines, reducing erosion.
However, the overall effectiveness of these programs over a large scale
is unknown given the pyramid pigtoe's wide distribution and varying
agricultural intensities in its range.
Dams and Barriers
Whether for flood control, hydropower, river navigation, or as
abandoned mill structures, dams and their impoundments are one of the
most pervasive threats to pyramid pigtoe rangewide: 26 of 35
populations and all 4 major basins in the species' range are affected
(Table 1). Dams have many impacts on stream ecosystems, and the effects
of impoundments and barriers on aquatic habitats and freshwater mussels
are relatively well-documented (Watters 2000, p. 261). Extinction and
extirpation of many North American freshwater mussels can be traced to
impoundment and inundation of riffle habitats in all major river basins
of the central and eastern United States (Haag 2009, p. 107).
Reductions in the diversity and abundance of mussels are primarily
attributed to habitat shifts, alteration and disruption of
connectivity, and diminished water quality as a result of reservoir
construction (Neves et al. 1997, p. 63). The survival and reproductive
success of mussels are influenced upstream of dams as flowing waters
change to impounded waters, with increased depths and buildup of
sediments, decreased dissolved oxygen, and drastic alteration of
resident fish assemblages. Downstream of dams, biotic and physical
habitat conditions provided by natural flow regimes are altered by
minimal releases or scouring flows, seasonal dissolved oxygen
depletion, and reduced or increased water temperatures. The number of
fish species is greatly reduced where coldwater flow (hypolimnetic
discharge) is released. Additionally, dams fragment habitat, limiting
dispersal of mussels on their fish hosts, which leads to genetic
isolation of mussel populations.
Resource Extraction
Predominant resource extraction threats in the range of the pyramid
pigtoe stem from mining (primarily coal but including other mineral
resources) and oil and gas exploration. Activities associated with coal
mining and oil and gas drilling can contribute chemical pollutants to
streams. Acid mine drainage is created from the oxidation of iron-
sulfide minerals such as pyrite, forming sulfuric acid (Sams and Beer
2000, p. 3). This acid mine drainage may be associated with high
concentrations of aluminum, manganese, zinc, and other constituents
(Tennessee Department of Environment and Conservation (TDEC) 2014, p.
72). The metals, and the high acidity typically associated with acid
mine drainage, can be acutely and chronically toxic to aquatic life
(Jones 1964, p. 96). Implementation of the Surface Mining Control and
Reclamation Act of 1977 (SMCRA; 30 U.S.C. 1201 et seq.) has
significantly reduced acid mine drainage from new coal mines; however,
un-reclaimed areas mined prior to the SMCRA continue to generate acid
mine drainage in portions of the pyramid pigtoe's range. Direct impacts
to the pyramid pigtoe from acid mine drainage in most occupied river
reaches are unlikely because coal mining sites tend to be adjacent to
smaller headwater streams, but mining pollutants can be
[[Page 49999]]
transferred downstream to pyramid pigtoe habitats.
Surface mining has been identified as a source of impairment for
approximately 775 mi (1,247 km) of streams in Kentucky (Kentucky
Department for Environmental Protection 2014, p. 66). Weathering of
soils and rock broken apart to access coal seams typically increases
alkalinity, total dissolved solids, salinity, and sedimentation and
alters hydrology and physical habitat of streams receiving surface mine
drainage, impacting fish and aquatic invertebrate communities (e.g.,
Bernhardt and Palmer 2011, pp. 42-49; Linberg et al. 2011, entire;
Hopkins and Roush 2013, pp. 585-586; Hitt and Chambers 2014, p. 923;
Hitt et al. 2016, pp. 47-53). Mining continues to impair water quality
in streams in the Cumberland Plateau and Central Appalachian regions of
Tennessee and Kentucky (TDEC 2014, p. 62), which contain portions of
the Tennessee and Cumberland River basins, and is the primary source of
low pH impairment of 376 mi (605 km) of rivers in Tennessee (TDEC 2014,
p. 53). Coal mining has resulted in discharges of industrial and mine
wastes from coal mines and coal processing facilities in the Clinch and
Powell Rivers (Ahlstedt et al. 2016, p. 8). Direct impacts to the
pyramid pigtoe from acid mine drainage or total dissolved solids in
most occupied river reaches are unlikely because coal mining sites tend
to be adjacent to smaller headwater streams, but associated mining
pollutants (fine sediments, metals, and salts) can be transferred
downstream to medium and large river pyramid pigtoe habitats (Bernhardt
and Palmer, 2011 p. 46).
Natural gas extraction in the Appalachians, including the
Cumberland River basin, has negatively affected water quality through
accidental spills and discharges, as well as increased sedimentation
due to development of road construction, pipeline, drill pad
construction, as well as tree removal required to clear the
construction areas (Vidic et al. 2013, p. 6). Disposal of
insufficiently treated brine wastewater, more saline than seawater, has
specifically been found to adversely affect freshwater mussels (Patnode
et al. 2015, p. 62). Potential threats from natural gas and oil
exploration are also a concern in the White River basin.
Instream sand and alluvial gravel mining has been implicated in the
destruction of mussel populations (Hartfield 1993, p. 138). Negative
impacts associated with gravel mining include stream channel
modifications such as altered habitat, disrupted flow patterns, and
sediment transport (Hubbs et al. 2006, p. 170). Additionally, water
quality modifications including increased turbidity, reduced light
penetration, increased temperature, and increased sedimentation result
from gravel mining. Commercial sand and gravel mining and dredging
directly affects the pyramid pigtoe in the Tennessee River,
specifically within the Lower Tennessee-Beech MU (Hubbs et al. 2006, p.
170). The Lower Cumberland Old Hickory MU has also been affected by
gravel mining and dredging in the past (Sickel 1982, p. 4) that has
resulted in permanent alteration of substrates and hydraulic patterns,
contributing to habitat loss for freshwater mussels.
Invasive and Nonnative Species
Invasive and nonnative species in the range of the pyramid pigtoe
include the Asian clam, zebra mussel, black carp, and the plant
species, hydrilla. These nonnative species impact the pyramid pigtoe
through competitive interactions, water quality degradation, predation,
and habitat alteration.
The Asian clam, found throughout the range of the pyramid pigtoe,
alters benthic substrates, may filter native mussel sperm or glochidia,
competes with native species for limited resources, and causes ammonia
spikes in surrounding water when dying off en masse (Scheller 1997, p.
2). A typical settlement of the Asian clam occurs with a population
density ranging from 100 to 200 clams per square meter, which may not
be detrimental to native unionids; however, populations can grow as
large as 3,000 clams per square meter, which would influence both food
resources and competition for space for the pyramid pigtoe.
Within the range of the pyramid pigtoe, the zebra mussel occurs in
the Ohio, Tennessee, and Arkansas-White-Red River basins. Native
mussels, such as the pyramid pigtoe, are negatively affected by zebra
mussels through direct colonization, reduction of available habitat,
changes in the biotic environment, or a reduction in food sources
(MacIsaac 1996, p. 292). One of the direct consequences of the invasion
of zebra mussels is the local extirpation of native freshwater mussel
populations from (1) attachment to the shells of native mussels, which
can kill them (zebra mussels are sessile, and cling to hard surfaces);
(2) affecting vertical and lateral movements of native mussels, due to
heavy infestations, which can prevent valve closure; and (3)
outcompeting native mussels and other filter-feeding invertebrates for
food. This problem has been particularly acute in the Ohio and
Tennessee River systems. Densities of zebra mussels attained 17,000 per
square meter in the Tennessee River below Wilson Dam in 2017, although
recent survey efforts indicate a decline from that population explosion
(Garner 2018, pers. comm.).
The black carp, which feeds on mollusks, is listed as ``injurious''
under the Lacey Act and occurs in the Ohio, Tennessee, Lower
Mississippi and Arkansas-White-Red basins where it overlaps populations
of the pyramid pigtoe. It is highly likely that this nonnative fish
will negatively impact native aquatic communities by direct predation,
thus reducing populations of native mussels (Nico et al. 2005, p. 193).
Because black carp attain a large size and have a lifespan reportedly
over 15 years, they have the potential to cause significant harm to
native mollusks by predation on multiple age classes (Nico et al. 2005,
p. 77).
In addition to negative impacts of nonnative animals, the invasive
nonnative plant hydrilla can affect native mussels by covering spawning
areas for native fish, which may be hosts for glochidia, and can cause
significant reductions in stream oxygen levels (Colle et al. 1987, p.
410). Hydrilla is widespread in the Ohio, Cumberland, and Tennessee
River systems. In general, invasive aquatic plants grow uncontrolled
and can cause habitat to fill in, affect flow dynamics, and increase
water temperature, exacerbating drought impacts in stream habitats
(Colle et al. 1987, p. 416).
The Aquatic Nuisance Species (ANS) Task Force, co-chaired by the
Service and the National Oceanic and Atmospheric Administration (NOAA),
encourages State and interstate planning entities to develop management
plans describing detection and monitoring efforts of aquatic nuisance
and nonnative species, prevention efforts to stop their introduction
and spread, and control efforts to reduce their impacts. Management
plan approval by the ANS Task Force is required to obtain funding under
Section 1204 of the ANS Prevention and Control Act. Each state within
the range of the pyramid pigtoe has either a plan approved by or
submitted to the ANS Task Force, or a plan under development. These
plans have been effective in terms of raising awareness at the state
level of the severity of ecological damage that non-native and nuisance
species are capable of, but many are in early stages of implementation.
Although laws and efforts are in place which may be effective in
controlling or diminishing non-native and invasive species, these
[[Page 50000]]
organisms are a current and future threat to the pyramid pigtoe
throughout its range.
Small Population Size
Historically, an extensive, largely contiguous pyramid pigtoe
population occurred through much of the eastern half of the United
States, and there were limited barriers preventing genetic interchange
among river systems. With the completion of hundreds of dams in the
1900s, many large-river pyramid pigtoe populations were lost, resulting
in isolation of tributary populations. The population size of a long-
lived species, such as the pyramid pigtoe, may take decades to decline
to extirpation post-impoundment. At best, limited post-impoundment
recruitment may be occurring in the isolated pyramid pigtoe
populations, indicating that these small populations are not likely
viable long term.
Currently, the pyramid pigtoe exhibits several traits that reduce
population viability, including small population size and low fecundity
at many locations compared to other mussels. Smaller population size
puts the species at greater risk of extirpation from stochastic events
(e.g., drought) or anthropomorphic changes and management activities
that affect habitat. In addition, smaller populations may have reduced
genetic diversity, be less genetically fit, and more susceptible to
disease during extreme environmental conditions (Frankham 1996, p.
1,505). Moreover, small and isolated populations are at higher risk of
further loss of genetic variation due to genetic drift, thereby
lessening the affected species' ability to adapt to a continuously
changing environment. Lastly, the relatively low fecundity, coupled
with low juvenile survivorship, limit the pyramid pigtoe's ability to
withstand and recover from population losses. While several populations
of pyramid pigtoe are at risk of extirpation due to their small size,
other populations are large enough and sufficiently connected within
their MU that they are regularly recruiting new cohorts. Therefore,
small population size is a population-level threat but not currently a
species-level or rangewide threat.
Changing Climate Conditions
Climate change threats for freshwater mussels include alteration of
natural stream flow and water temperature regimes as drought,
precipitation, and temperature patterns shift. Population discontinuity
and isolation is possible due to the dynamics in range shifts of
mussels and their host fishes as a result of warming climates, based on
life-history traits (Archambault et al. 2018, p. 880). However, the
mechanisms behind these shifts and how they alter population
connectivity and gene flow are uncertain, and there is no evidence
linking climate change impacts specifically to the current status of
the pyramid pigtoe.
Cumulative/Synergistic Effects
Collectively, threats to the pyramid pigtoe have acted on the
species to reduce the number of historical populations and fragment and
reduce the size of extant populations. Currently, 15 of the 35 extant
populations are small in size, represented by fewer than 10 individuals
observed over the past 20 years. Factors such as low effective
population size, genetic isolation, relatively low levels of fecundity
and recruitment, and limited juvenile survival could affect the ability
of these species to maintain current population levels and to rebound
if a reduction in population occurs (e.g., through predation, toxic
releases or spills, or poor environmental conditions that inhibit
successful reproduction). Additionally, fragmentation (i.e., the
breaking apart of habitat segments, independent of habitat loss (Fahrig
2003; p. 299)) and isolation contribute to the extinction risk that
mussel populations face from stochastic events (see Haag 2012, pp. 336-
338). Throughout the range of the pyramid pigtoe, impoundments fragment
and isolate populations from one another, prevent dispersal, which
reduces gene flow (Vaughn 2012, p. 6; Service 2018, pp. 59-60; Service
2019, p. 74), and compound other threats, such as the introduction of
contaminants and pollution resulting from mining, oil and gas
exploration, agricultural runoff, and untreated or poorly treated
wastewater discharges.
Current Conditions
Current (and future) conditions are described using the following
categories that characterize the overall condition (resiliency) of the
pyramid pigtoe populations:
High--Population with more than 50 individuals reported
since 2000, distributed over a more or less contiguous river or stream
of at least 31 miles (mi) (50 kilometers (km)) in length, with evidence
of recent recruitment. Water quality and habitat conditions remain
optimal for recruitment, and multiple age classes are represented.
Populations are not linearly distributed and occur in more than one
stream within the river system.
Medium--small restricted populations (10 to 50 individuals
reported since 2000) generally distributed over a more or less
contiguous length of river or stream of at least 6.2 mi (10 km) but
less than 31 mi (50 km)), with some level of age class structure, but
vulnerable to existing threats. Appropriate substrates are generally
maintained with instream flows that mimic natural conditions. Water
quality and habitat degradation may occur but not at a level that
negatively affects both the density and extent of a population.
Low--very small and highly restricted populations (fewer
than 10 individuals reported since 2000), distributed over less than
6.2 mi (10 km) of river or stream, with little to no evidence of age
class structure (only older individuals observable). Loss of mussel
habitat or water quality degradation within the formerly occupied river
or stream reach has been measured or observed, and imminent threats are
documented. Population is linearly distributed and geographically
restricted and is not likely to withstand stochastic events.
We assessed resiliency and redundancy based on management units
(MUs) defined at the hydrologic unit code (HUC) scale (Seaber et al.
1987, entire; U.S. Geological Survey 2018, entire). Management units
consisted of HUC-8 regions, which are analogous to medium-sized river
basins across the United States. An MU consisting of a linear reach of
stream could harbor one population or, if it contained a large gap in
the species' distribution as a result of an impoundment or
physiographic boundary, more than one population. If multiple
tributaries were occupied (dendritic distribution) each tributary
within the MU was considered to represent a population. A majority of
MUs contained one population, given that the pyramid pigtoe occurs only
in large or medium-sized rivers and not smaller tributaries.
Representation was assessed at the larger HUC-2 region (major
basin) scale, and representation units were delineated to capture the
variation in adaptive traits and genetic diversity. See chapter 2 in
the SSA report for further explanation of the analysis methodology
(Service 2021, pp. 20-22). Each major basin contains unique
physiographic provinces and ecoregions. Therefore, the populations
within each major basin may harbor basin-specific adaptive traits and
as such species representation has been reduced from six basins to four
basins. Historical connectivity between the major basins has been lost
due habitat degradation and construction of
[[Page 50001]]
impoundments and there is no opportunity for exchange of beneficial, or
adaptive, genes between the basins.
The pyramid pigtoe's current range extends over nine States,
including Alabama, Arkansas, Kentucky, Louisiana, Mississippi, Ohio,
Oklahoma, Tennessee, and Virginia. The species is considered extirpated
in Indiana, Illinois, Iowa, Kansas, Minnesota, Missouri, Pennsylvania,
West Virginia, and Wisconsin. Its current range is within four major
HUC-2 regions (the Arkansas-White-Red, Lower Mississippi, Ohio, and
Tennessee River regions, Figure 1). It is extirpated in the Missouri
and Upper Mississippi River HUC-2 regions. Overall, the pyramid pigtoe
formerly occupied at least 135 MUs but currently occurs in 28 MUs
(Figure 2). Known populations have declined in number, from 151
historically to 35 today. Currently, 15 MUs have low resiliency, 9 MUs
have medium resiliency, and 4 MUs have high resiliency (Table 2, in
Future Conditions).
BILLING CODE 4333-15-P
[[Page 50002]]
[GRAPHIC] [TIFF OMITTED] TP07SE21.022
BILLING CODE 4333-15-C
Future Conditions
In the SSA report, we forecast the pyramid pigtoe's response to
plausible future scenarios of environmental conditions. The future
scenarios project the range in magnitude and scope of threats into the
future. Uncertainty is inherent in any risk assessment, so we must
consider plausible conditions to make our determinations. When
assessing the future, viability is not a specific state, but rather a
continuous measure of the likelihood that the species will sustain
populations over time.
The scenarios described in the SSA report represent two possible
future conditions. Under scenario 1, the threat
[[Page 50003]]
levels remain unchanged (threats continue to act on the species at the
current rate), whereas under scenario 2 the threat levels increase.
Both scenarios project existing regulatory mechanisms and voluntary
conservation measures benefiting the species remaining in place. We did
not analyze a scenario whereby threat levels lessen because the primary
threats that have fragmented and isolated populations will persist.
Developed areas, large dams, and most of the small and retired dams
affecting the species will remain in place.
We included climate change in our future scenarios as a factor that
would add to the negative impacts of the primary threats on the
species' habitat. Climate change is expected to alter the natural flow
regime through increased drought and flooding worsening desiccation,
scour, and sedimentation in each MU. However, in our analysis the
influence of climate change, as a secondary threat, does not alter the
projected future viability of any population or management unit. Those
future outcomes are driven by the primary threats of habitat alteration
or loss, nonnative invasive species, and the effects of small
population size.
Using the scenarios, we project the pyramid pigtoe's viability over
20 to 30 years. We selected this duration because the species is slow
growing and long-lived and has relatively low fecundity; long-term
trend information on pyramid pigtoe abundance and threats is not
available across the species' range to contribute to meaningful
alternative timeframes.
Future resiliency of pyramid pigtoe populations depends on the
extent to which the species' needs are met for water quality, flow,
substrate suitability, abundance and distribution of host fish species,
and habitat connectivity. We projected the expected future resiliency
of each population based on how events likely to occur under each
scenario would affect the species' resource needs. Future resiliency of
each population is classified as high, medium, low, or very low. Where
multiple populations occur within an MU, the MU condition is the
average of the population condition classifications; however, there are
no management units where the population classifications vary (i.e.,
all populations within the MU have the same classification). These
projections are informed by development planning documents, peer-
reviewed literature, vetting of initial condition ranking by mussel
experts, and our best professional judgment. Very low condition
populations will become extirpated; low condition populations will
become functionally extirpated (no recruitment); medium condition
populations will exhibit limited recruitment and be linearly
distributed and thus will have impaired ability to recover from
disturbances and will be vulnerable to catastrophic events; and high
condition populations will consistently recruit and be distributed over
long distances and in connected mainstem and tributary river reaches
(see SSA report for detailed future condition category definitions,
Service 2021, pp. 84-85).
Our analysis shows that whether threats remain constant or increase
into the future, all 35 populations are expected to experience negative
changes to their important habitat requisites or resource needs, and
the condition of many of the populations would decrease (Table 2).
Under scenario 1, we expect 23 populations will be in low or very low
condition and 9 in medium condition, with no to little resiliency,
respectively. The remaining 3 populations occurring within the Saline
or Upper Ouachita Rivers, where the impact of impoundments is not as
severe as elsewhere in the species' range, are expected to maintain a
high condition. Under scenario 2, we expect 31 populations to be either
functionally extirpated (low condition) or extirpated (very low
condition) and 4 to be in medium condition. With increasing threat
levels, the population condition of the Saline and Upper Ouachita
Rivers decline, and, thus, within 20 to 30 years no high condition
populations remain.
Table 2--Summary of Pyramid Pigtoe Current Mussel Population Size, Extent, Threat Level, and Projected Future Conditions. Only Overall Condition Is
Listed for Future Scenarios
--------------------------------------------------------------------------------------------------------------------------------------------------------
Contiguous Future condition
Management unit population Population size Population Threat level Current ---------------------------------
(occupied river) extent condition Scenario 1 Scenario 2
--------------------------------------------------------------------------------------------------------------------------------------------------------
OHIO BASIN
--------------------------------------------------------------------------------------------------------------------------------------------------------
Muskingum.................... Muskingum River. Small........... Small........... High............ Low............ Very Low....... Very Low.
Upper Green.................. Upper Green Large........... Large........... Low............. High........... Medium......... Medium.
River.
Barren....................... Barren River.... Small........... Small........... Mod............. Med............ Medium......... Low.
Middle Green................. Middle Green Medium.......... Medium.......... Mod............. Med............ Medium......... Low.
River.
Lower Green.................. Lower Green Small........... Small........... Mod............. Low............ Low............ Very Low.
River.
Lower Cumberland-Old Hickory Cumberland River Medium.......... Small........... High............ Low............ Very Low....... Very Low.
Lake. (Old Hickory
Reservoir)
Cordell Hull
Tailwater.
--------------------------------------------------------------------------------------------------------------------------------------------------------
TENNESSEE BASIN
--------------------------------------------------------------------------------------------------------------------------------------------------------
Holston...................... Holston River... Small........... Small........... High............ Low............ Very Low....... Very Low.
Upper Clinch................. Clinch River.... Medium.......... Medium.......... Mod............. Med............ Low............ Low.
Wheeler Lake................. Paint Rock River Small........... Small........... Mod............. Low............ Low............ Very Low.
Tennessee River Medium.......... Small........... High............ Low............ Low............ Very Low.
(Wheeler
Reservoir)
Guntersville
Tailwater.
Pickwick Lake................ Tennessee River Medium.......... Medium.......... High............ Low............ Low............ Low.
(Pickwick
Reservoir)
Wilson
Tailwater.
Lower Tennessee-Beech........ Tennessee River Small........... Small........... High............ Low............ Low............ Low.
(Kentucky
Reservoir)
Pickwick
Tailwater.
Upper Duck................... Upper Duck River Large........... Medium.......... Mod............. Med............ Medium......... Low.
Lower Duck................... Lower Duck River Large........... Small........... Mod............. Med............ Low............ Very Low.
--------------------------------------------------------------------------------------------------------------------------------------------------------
ARKANSAS-WHITE-RED BASIN
--------------------------------------------------------------------------------------------------------------------------------------------------------
Petit Jean................... Petit Jean River Small........... Small........... Mod............. Low............ Low............ Very Low.
Eleven Point................. Eleven Point Small........... Small........... Low............. Low............ Low............ Very Low.
River.
[[Page 50004]]
Lower Little................. Little River.... Medium.......... Small........... Mod............. Low............ Low............ Very Low.
--------------------------------------------------------------------------------------------------------------------------------------------------------
LOWER MISSISSIPPI BASIN
--------------------------------------------------------------------------------------------------------------------------------------------------------
Lower Black.................. Lower Black Small........... Small........... Mod............. Low............ Low............ Very Low.
River.
Lower St. Francis............ St. Francis Medium.......... Small........... High............ Med............ Medium......... Low.
River.
Tyronza River... Medium.......... Large........... High............ Med............ Medium......... Low.
Middle White................. Middle White Small........... Small........... Mod............. Low............ Low............ Very Low.
River.
Upper Ouachita............... Upper Ouachita Large........... Large........... Mod............. High........... High........... Medium.
River.
Little Missouri.............. Little Missouri Large........... Medium.......... Mod............. Med............ Medium......... Low.
River.
Lower Ouachita-Smackover..... Lower Ouachita Medium.......... Medium.......... Mod............. Med............ Medium......... Low.
River
(Smackover).
Upper Saline................. Upper Saline Large........... Large........... Mod............. High........... High........... Medium.
River.
Lower Saline................. Lower Saline Large........... Large........... High............ High........... High........... Medium.
River.
Bayou Bartholomew............ Bayou Large........... Large........... High............ Med............ Medium......... Low.
Bartholomew.
Lower Ouachita-Bayou De Lower Ouachita Medium.......... Medium.......... High............ Low............ Low............ Low.
Loutre. River (Bayou De
Loutre).
Big Sunflower................ Hushpuckna River Small........... Small........... High............ Med............ Low............ Very Low.
Bogue Phalia.... Small........... Small........... High............ Med............ Low............ Very Low.
Little Sunflower Small........... Small........... High............ Med............ Low............ Very Low.
River.
Sunflower River. Medium.......... Large........... High............ Med............ Low............ Very Low.
Sandy Bayou..... Small........... Small........... High............ Med............ Low............ Very Low.
Big Sunflower Medium.......... Large........... High............ Med............ Low............ Very Low.
River.
Lower Big Black.............. Big Black River. Small........... Small........... High............ Low............ Very Low....... Very Low.
--------------------------------------------------------------------------------------------------------------------------------------------------------
The viability implications associated with the expected change in
population conditions can be discerned at the MU and HUC-2 scales.
Under scenario 1, we expect 3 MUs (11 percent) remain in high
condition; 9 MUs (32 percent), in medium condition; 12 MUs (43
percent), in low condition; and 4 (14 percent), in very low condition.
Therefore, the species' ability to withstand natural environmental
variation and threats will be greatly limited. Loss of the three MUs
reduces the species' distribution, increasing its risk to catastrophic
events. The pyramid pigtoe will continue to be represented in the Ohio,
Tennessee, and Lower Mississippi basins, but reduced to six States (as
compared to the current nine States) occupied by the species.
Representation will be lost from the Arkansas-White-Red basin, as all
of its MUs are expected to be in low condition. It will take many years
(potentially beyond the 20- to 30-year timeframe analyzed), for full
evaluation of the species' response to any current beneficial actions,
such as removal of Lock and Dam 6 on the Green River, or the safe
harbor agreements and candidate conservation agreements with assurances
in the Upper Ouachita and Upper Saline Rivers.
Under scenario 2, none of the MUs are expected to be in high
condition, 4 (14 percent) are in medium condition, 11 (39 percent) are
in low condition, and 13 (46 percent) are in very low condition. Given
no MUs will be in high condition, the species' ability to withstand
natural environmental variation and threats will be substantially
limited. Redundancy will also be substantially reduced with no high
condition MUs remaining and the expected loss of 13 (46 percent) MUs.
Loss of the species from the Arkansas-White-Red basin, with no high
condition MUs in any basin, and potential extirpation of the species
from the States of Virginia, Ohio, Oklahoma, and Mississippi will
substantially reduce the species' genetic diversity, thereby decreasing
its ability to adapt to changing environmental conditions.
We note that, by using the SSA framework to guide our analysis of
the scientific information documented in the SSA report, we have not
only analyzed individual effects on the species, but we have also
analyzed their potential cumulative effects. We incorporate the
cumulative effects into our SSA analysis when we characterize the
current and future condition of the species. To assess the current and
future condition of the species, we undertake an iterative analysis
that encompasses and incorporates the threats individually and then
accumulates and evaluates the effects of all the factors that may be
influencing the species, including threats and conservation efforts.
Because the SSA framework considers not just the presence of the
factors, but to what degree they collectively influence risk to the
entire species, our assessment integrates the cumulative effects of the
factors and replaces a standalone cumulative effects analysis.
Conservation Efforts and Regulatory Mechanisms
As discussed under Threats, Federal and State lands and water
quality regulations afford the pyramid pigtoe and its habitats some
protection from land development, industrial, and transportation
activities. Additionally, laws intended to reduce the threat of
nonnative species are in place. Many populations of the pyramid pigtoe
were extirpated or reduced prior to development of modern conservation
programs and regulatory mechanisms. As such, historical threats no
longer present on the landscape impart a legacy effect (small
population size or degraded habitat) on some current populations.
Further, some water quality regulations have not been fully adopted or
consistently applied across the species' range. Therefore, despite the
existing regulatory mechanisms in place, the combined threats and
impacts of actions that occurred prior to the implementation of these
regulatory mechanisms continue to negatively affect the pyramid pigtoe.
Determination of Pyramid Pigtoe Status
Section 4 of the Act (16 U.S.C. 1533) and its implementing
regulations (50 CFR part 424) set forth the procedures for determining
whether a species meets the definition of an endangered species or a
threatened species. The Act defines an endangered species as a species
``in
[[Page 50005]]
danger of extinction throughout all or a significant portion of its
range'' and a threatened species as a species ``likely to become an
endangered species within the foreseeable future throughout all or a
significant portion of its range.'' The Act requires that we determine
whether a species meets the definition of an endangered species or a
threatened species because of any of the following factors: (A) The
present or threatened destruction, modification, or curtailment of its
habitat or range; (B) overutilization for commercial, recreational,
scientific, or educational purposes; (C) disease or predation; (D) the
inadequacy of existing regulatory mechanisms; or (E) other natural or
manmade factors affecting its continued existence.
Status Throughout All of Its Range
Historically, the pyramid pigtoe occurred within 151 populations
and 136 MUs, in 6 basins across 18 States (Figure 2). Currently, the
species occurs within 35 populations and 28 MUs, in 4 basins across 9
States, which represents a 77 percent reduction of its historically
occupied populations. Of the extant MUs, 4 are highly resilient, while
9 and 15 have medium and low resiliency, respectively. The threats
leading to its current condition include past and ongoing habitat
degradation or loss (Factor A), residual impacts from past harvest and
overutilization (Factor B), and ongoing competition, predation, and
habitat alteration from invasive, nonnative species (Factor E).
Collectively, these threats reduce population abundance, thereby
precipitating negative genetic and demographic effects associated with
small population size (Factor E) within some of the smaller
populations. Although downtrends from historical numbers are evident
and declines are likely to continue, four high resilient MUs are
distributed across two of the four occupied major river basins. These
four MUs provide for current representation and redundancy of the
species. Thus, after assessing the best available information, we
conclude that the pyramid pigtoe is not in danger of extinction
throughout all of its range. We, therefore, proceed with determining
whether the pyramid pigtoe is likely to become endangered within the
foreseeable future throughout all of its range.
The best available information suggests that the threats currently
acting upon the pyramid pigtoe will continue into the foreseeable
future. In areas experiencing human population and land development
growth, these threats (e.g., water quality and habitat degradation) are
reasonably expected to increase over time, further reducing the
species' resiliency, redundancy, and representation. Our foreseeable
future (20 to 30 years) reflects the period of time over which we can
reliably predict both the threats to the pyramid pigtoe and the pyramid
pigtoe's response to those threats based on the best available
information. Within the foreseeable future, even if threats were to
remain at current levels and not increase, 23 of the 35 populations are
projected to become extirpated or functionally extirpated (Table 2).
Additionally, with no change in threat levels, the condition of one of
the four high resilient populations will decline to medium resiliency
and the remaining three high resilient populations would be confined to
a single basin. At the MU scale, only 3 of the 28 extant MUs remain in
high condition, with 17 MUs projected to become extirpated or
functionally extirpated within 20 to 30 years. If threats increase, 19
populations will likely be extirpated within 20 to 30 years, leading to
only 4 MUs persisting. These MUs will have limited recruitment
potential and restricted distribution, thus impairing the species'
ability to recover from disturbances and increasing its vulnerability
to catastrophic events. In summary, threats currently acting on the
species are likely to persist or increase in the foreseeable future,
resulting in zero to three high resilient populations in one of its six
historical major basins and resulting in a high risk of impacts from a
single catastrophe or stochastic events. Thus, after assessing the best
available information, we conclude that the pyramid pigtoe is likely to
become in danger of extinction within the foreseeable future throughout
all of its range.
Status Throughout a Significant Portion of Its Range
Under the Act and our implementing regulations, a species may
warrant listing if it is in danger of extinction or likely to become so
in the foreseeable future throughout all or a significant portion of
its range. The court in Center for Biological Diversity v. Everson,
2020 WL 437289 (D.D.C. Jan. 28, 2020) (Center for Biological
Diversity), vacated the aspect of the Final Policy on Interpretation of
the Phrase ``Significant Portion of Its Range'' in the Endangered
Species Act's Definitions of ``Endangered Species'' and ``Threatened
Species'' (79 FR 37578; July 1, 2014) that provided that the Service
does not undertake an analysis of significant portions of a species'
range if the species warrants listing as threatened throughout all of
its range. Therefore, we proceed to evaluating whether the species is
endangered in a significant portion of its range--that is, whether
there is any portion of the species' range for which both (1) the
portion is significant and (2) the species is in danger of extinction
in that portion. Depending on the case, it might be more efficient for
us to address the ``significance'' question or the ``status'' question
first. We can choose to address either question first. Regardless of
which question we address first, if we reach a negative answer with
respect to the first question that we address, we do not need to
evaluate the other question for that portion of the species' range.
Following the court's holding in Center for Biological Diversity,
we now consider whether there are any significant portions of the
species' range where the species is in danger of extinction now (i.e.,
endangered). In undertaking this analysis for the pyramid pigtoe, we
choose to address the status question first--we consider information
pertaining to the geographic distribution of both the species and the
threats that the species faces to identify any portions of the range
where the species is endangered.
For the pyramid pigtoe, we considered whether the threats are
geographically concentrated in any portion of the species' range at a
biologically meaningful scale. We examined the following threats:
Habitat degradation or loss, invasive and nonnative species, and
negative effects associated with small population size, including
cumulative effects. Habitat degradation or loss, including diminished
water quality, is a threat in all four basins occupied by the pyramid
pigtoe, although the contribution by source (e.g., agriculture,
urbanization, mining, dredging) varies. Invasive or nonnative species
also is a threat in each occupied basin. Lastly, large populations
(number of individuals) occur in three of the four basins, and medium
populations occur in all four basins.
We examined the Arkansas-White-Red basin (the only basin not
containing any large populations) to determine if there is a
concentration of threats because, of the three populations in the
basin, two have a moderate threat level and one has a low threat level.
All three of these populations are in a low current condition, and two
of the three populations have small numbers of individuals. Thus, the
cumulative effects of small population size with the other identified
threats may be concentrated in this basin.
[[Page 50006]]
We then evaluated whether the Arkansas-White-Red basin may be
biologically important to the overall species' viability, i.e.,
significant. This basin contains 3 of the 35 (8.6 percent) pyramid
pigtoe populations. By length of river, the populations combined occupy
about 5 percent of the species' range. Therefore, the populations in
the Arkansas-White-Red basin minimally contribute to the overall
viability of the species.
The pyramid pigtoe occurs in similar habitats across the four
basins it occupies and does not use unique observable environmental
characteristics attributable to any of the basins. The Arkansas-White-
Red basin populations occur in stream habitat with substrate types and
water quality similar to the other basins where the pyramid pigtoe
performs the important life-history functions of breeding, feeding, and
sheltering. The basin does not act as a refugium for the species or as
an important spawning ground. In addition, the water quality is similar
throughout the species' range, with impaired water quality occurring in
all four basins. Because the pyramid pigtoe occurs in similar aquatic
habitats, the Arkansas-White-Red basin population exhibits similar
habitat use as populations in the remainder of the range.
Overall, we found no substantial information that would indicate
the Arkansas-White-Red basin is a portion of the range that may be
significant in terms of its overall contribution to the species'
resiliency, redundancy, and representation, or that it is significant
in terms of high-quality habitat or habitat that is otherwise important
for the species' life history. Additionally, within each of the other
three basins (or portions of the range) there was no concentration of
threats that would indicate the species is facing elevated threats in
those portions. As a result, we determined there is no portion of the
pyramid pigtoe's range that constitutes a significant portion of the
range where the species is currently endangered. Accordingly, we
determine that the species is likely to become in danger of extinction
within the foreseeable future throughout all of its range. This is
consistent with the courts' holdings in Desert Survivors v. Department
of the Interior, No. 16-cv-01165-JCS, 2018 WL 4053447 (N.D. Cal. Aug.
24, 2018), and Center for Biological Diversity v. Jewell, 248 F. Supp.
3d, 946, 959 (D. Ariz. 2017).
Determination of Status
Our review of the best available scientific and commercial
information indicates that the pyramid pigtoe meets the definition of a
threatened species. Therefore, we propose to list the pyramid pigtoe as
a threatened species in accordance with sections 3(20) and 4(a)(1) of
the Act.
Available Conservation Measures
Conservation measures provided to species listed as endangered or
threatened species under the Act include recognition, recovery actions,
requirements for Federal protection, and prohibitions against certain
practices. Recognition through listing results in public awareness, and
conservation by Federal, State, Tribal, and local agencies, private
organizations, and individuals. The Act encourages cooperation with the
States and other countries and calls for recovery actions to be carried
out for listed species. The protection required by Federal agencies and
the prohibitions against certain activities are discussed, in part,
below.
The primary purpose of the Act is the conservation of endangered
and threatened species and the ecosystems upon which they depend. The
ultimate goal of such conservation efforts is the recovery of these
listed species, so that they no longer need the protective measures of
the Act. Section 4(f) of the Act calls for the Service to develop and
implement recovery plans for the conservation of endangered and
threatened species. The recovery planning process involves the
identification of actions that are necessary to halt or reverse the
species' decline by addressing the threats to its survival and
recovery. The goal of this process is to restore listed species to a
point where they are secure, self-sustaining, and functioning
components of their ecosystems.
Recovery planning consists of preparing draft and final recovery
plans, beginning with the development of a recovery outline and making
it available to the public following a final listing determination. The
recovery outline guides the immediate implementation of urgent recovery
actions and describes the process to be used to develop a recovery
plan. Revisions of the plan may be done to address continuing or new
threats to the species, as new substantive information becomes
available. The recovery plan also identifies recovery criteria for
review of when a species may be ready for reclassification from
endangered to threatened (``downlisting'') or removal from protected
status (``delisting''), and methods for monitoring recovery progress.
Recovery plans also establish a framework for agencies to coordinate
their recovery efforts and provide estimates of the cost of
implementing recovery tasks. Recovery teams (composed of species
experts, Federal and State agencies, nongovernmental organizations, and
stakeholders) are often established to develop recovery plans. When
completed, the recovery outline, draft recovery plan, and the final
recovery plan will be available on our website (https://www.fws.gov/endangered), or from our Asheville Field Office (see FOR FURTHER
INFORMATION CONTACT).
Implementation of recovery actions generally requires the
participation of a broad range of partners, including other Federal
agencies, States, Tribes, nongovernmental organizations, businesses,
and private landowners. Examples of recovery actions include habitat
restoration (e.g., restoration of native vegetation), research, captive
propagation and reintroduction, and outreach and education. The
recovery of many listed species cannot be accomplished solely on
Federal lands because their range may occur primarily or solely on non-
Federal lands. To achieve recovery of these species requires
cooperative conservation efforts on private, State, and Tribal lands.
If this species is listed, funding for recovery actions will be
available from a variety of sources, including Federal budgets, State
programs, and cost-share grants for non-Federal landowners, the
academic community, and nongovernmental organizations. In addition,
pursuant to section 6 of the Act, the States of Alabama, Arkansas,
Kentucky, Louisiana, Mississippi, Ohio, Oklahoma, Tennessee, and
Virginia would be eligible for Federal funds to implement management
actions that promote the protection or recovery of the pyramid pigtoe.
Information on our grant programs that are available to aid species
recovery can be found at: https://www.fws.gov/grants.
Although the pyramid pigtoe is only proposed for listing under the
Act at this time, please let us know if you are interested in
participating in recovery efforts for this species. Additionally, we
invite you to submit any new information on this species whenever it
becomes available and any information you may have for recovery
planning purposes (see FOR FURTHER INFORMATION CONTACT).
Section 7(a) of the Act requires Federal agencies to evaluate their
actions with respect to any species that is proposed or listed as an
endangered or threatened species and with respect to its critical
habitat, if any is designated. Regulations implementing this
interagency cooperation provision of the Act are codified at 50 CFR
part
[[Page 50007]]
402. Section 7(a)(4) of the Act requires Federal agencies to confer
with the Service on any action that is likely to jeopardize the
continued existence of a species proposed for listing or result in
destruction or adverse modification of proposed critical habitat. If a
species is listed subsequently, section 7(a)(2) of the Act requires
Federal agencies to ensure that activities they authorize, fund, or
carry out are not likely to jeopardize the continued existence of the
species or destroy or adversely modify its critical habitat. If a
Federal action may affect a listed species or its critical habitat, the
responsible Federal agency must enter into consultation with the
Service.
Federal agency actions within the species' habitat that may require
conference, consultation, or both as described in the preceding
paragraph include management and any other landscape-altering
activities on Federal lands administered by the following:
(1) U.S. Army Corps of Engineers (channel dredging and maintenance;
dam projects including flood control, navigation, hydropower, bridge
projects, stream restoration, and Clean Water Act permitting).
(2) U.S. Department of Agriculture, including the Natural Resources
Conservation Service and Farm Service Agency (technical and financial
assistance for projects) and the Forest Service (aquatic habitat
restoration, fire management plans, fire suppression, fuel reduction
treatments, forest plans, mining permits).
(3) U.S. Department of Energy (renewable and alternative energy
projects).
(4) Federal Energy Regulatory Commission (interstate pipeline
construction and maintenance, dam relicensing, and hydrokinetics).
(5) U.S. Department of Transportation (highway and bridge
construction and maintenance).
(6) U.S. Fish and Wildlife Service (issuance of section 10 permits
for enhancement of survival, habitat conservation plans, and safe
harbor agreements; National Wildlife Refuge planning and refuge
activities; Partners for Fish and Wildlife program projects benefiting
these species or other listed species; Wildlife and Sportfish
Restoration program sportfish stocking).
(7) Environmental Protection Agency (water quality criteria,
permitting).
(8) Tennessee Valley Authority (flood control, navigation,
hydropower, and land management for the Tennessee River system).
(9) Office of Surface Mining Reclamation and Enforcement (land
resource management plans, mining permits, oil and natural gas permits,
abandoned mine land projects, and renewable energy development).
(10) National Park Service (aquatic habitat restoration, fire
management plans, fire suppression, fuel reduction treatments, land
management plans, mining permits).
It is our policy, as published in the Federal Register on July 1,
1994 (59 FR 34272), to identify to the maximum extent practicable at
the time a species is listed, those activities that would or would not
constitute a violation of section 9 of the Act. The intent of this
policy is to increase public awareness of the effect of a proposed
listing on proposed and ongoing activities within the range of the
species proposed for listing. The discussion below regarding protective
regulations under section 4(d) of the Act complies with our policy.
II. Proposed Rule Issued Under Section 4(d) of the Act
Background
Section 4(d) of the Act contains two sentences. The first sentence
states that the Secretary shall issue such regulations as he deems
necessary and advisable to provide for the conservation of species
listed as threatened. The U.S. Supreme Court has noted that statutory
language like ``necessary and advisable'' demonstrates a large degree
of deference to the agency (see Webster v. Doe, 486 U.S. 592 (1988)).
Conservation is defined in the Act to mean the use of all methods and
procedures which are necessary to bring any endangered species or
threatened species to the point at which the measures provided pursuant
to the Act are no longer necessary. Additionally, the second sentence
of section 4(d) of the Act states that the Secretary may by regulation
prohibit with respect to any threatened species any act prohibited
under section 9(a)(1), in the case of fish or wildlife, or section
9(a)(2), in the case of plants. Thus, the combination of the two
sentences of section 4(d) provides the Secretary with wide latitude of
discretion to select and promulgate appropriate regulations tailored to
the specific conservation needs of the threatened species. The second
sentence grants particularly broad discretion to the Service when
adopting the prohibitions under section 9.
The courts have recognized the extent of the Secretary's discretion
under this standard to develop rules that are appropriate for the
conservation of a species. For example, courts have upheld rules
developed under section 4(d) as a valid exercise of agency authority
where they prohibited take of threatened wildlife, or include a limited
taking prohibition (see Alsea Valley Alliance v. Lautenbacher, 2007
U.S. Dist. Lexis 60203 (D. Or. 2007); Washington Environmental Council
v. National Marine Fisheries Service, 2002 U.S. Dist. Lexis 5432 (W.D.
Wash. 2002)). Courts have also upheld 4(d) rules that do not address
all of the threats a species faces (see State of Louisiana v. Verity,
853 F.2d 322 (5th Cir. 1988)). As noted in the legislative history when
the Act was initially enacted, ``once an animal is on the threatened
list, the Secretary has an almost infinite number of options available
to him with regard to the permitted activities for those species. He
may, for example, permit taking, but not importation of such species,
or he may choose to forbid both taking and importation but allow the
transportation of such species'' (H.R. Rep. No. 412, 93rd Cong., 1st
Sess. 1973).
Exercising this authority under section 4(d), we have developed a
proposed rule that is designed to address the pyramid pigtoe's
conservation needs. Although the statute does not require us to make a
``necessary and advisable'' finding with respect to the adoption of
specific prohibitions under section 9, we find that this rule as a
whole satisfies the requirement in section 4(d) of the Act to issue
regulations deemed necessary and advisable to provide for the
conservation of the pyramid pigtoe.
As discussed above under Summary of Biological Status and Threats,
we have concluded that the pyramid pigtoe is likely to become in danger
of extinction within the foreseeable future primarily due to declines
in water quality, alteration and deterioration of instream habitats,
fragmentation and isolation of populations, and nonnative species.
These threats, which are expected to be exacerbated by continued
urbanization and land development, were central to our assessment of
the future viability of the pyramid pigtoe. The provisions of this
proposed 4(d) rule would promote conservation of the pyramid pigtoe by
encouraging management of the landscape in ways that meet the
conservation needs of the pyramid pigtoe and are consistent with land
management considerations. The provisions of this proposed rule are one
of many tools that we would use to promote the conservation of the
pyramid pigtoe. This proposed 4(d) rule would apply only if and when we
make final the listing of the pyramid pigtoe as a threatened species.
Section 7(a)(2) of the Act requires Federal agencies, including the
Service, to ensure that any action they fund,
[[Page 50008]]
authorize, or carry out is not likely to jeopardize the continued
existence of any endangered species or threatened species or result in
the destruction or adverse modification of designated critical habitat
of such species. In addition, section 7(a)(4) of the Act requires
Federal agencies to confer with the Service on any agency action which
is likely to jeopardize the continued existence of any species proposed
to be listed under the Act or result in the destruction or adverse
modification of proposed critical habitat.
If a Federal action may affect a listed species or its critical
habitat, the responsible Federal agency (action agency) must enter into
consultation with us. Examples of actions that are subject to the
section 7 consultation process are actions on State, Tribal, local, or
private lands that require a Federal permit or that involve some other
Federal action such as funding, like those listed above under Available
Conservation Measures. Federal actions not affecting listed species or
critical habitat--and actions on State, Tribal, local, or private lands
that are not federally funded, authorized, or carried out by a Federal
agency--do not require section 7 consultation.
This obligation does not change in any way for a threatened species
with a species-specific 4(d) rule. Actions that a Federal agency
determines ``may affect'' listed species or critical habitat continue
to require consultation and actions that are ``likely to adversely
affect'' a species require formal consultation and the formulation of a
biological opinion.
Provisions of the Proposed 4(d) Rule
This proposed 4(d) rule would provide for the conservation of the
pyramid pigtoe by prohibiting the following activities, except as
otherwise authorized or permitted: Importing or exporting; take;
possession and other acts with unlawfully taken specimens; delivering,
receiving, transporting, or shipping in interstate or foreign commerce
in the course of commercial activity; or selling or offering for sale
in interstate or foreign commerce.
As discussed above under Summary of Biological Status and Threats,
multiple factors are affecting the status of the pyramid pigtoe. A
range of activities have the potential to affect the pyramid pigtoe,
including declines in water quality, alteration and deterioration of
instream habitats, fragmentation and isolation of populations, and
nonnative species. These threats, which are expected to continue due to
land development for urbanization, agriculture, and resource
extraction, channel navigation, and dam operations were central to our
assessment of the future viability of the pyramid pigtoe. Therefore, we
prohibit actions resulting in the incidental take of the pyramid pigtoe
by altering or degrading its habitat.
Under the Act, ``take'' means to harass, harm, pursue, hunt, shoot,
wound, kill, trap, capture, or collect, or to attempt to engage in any
such conduct. Some of these provisions have been further defined in
regulations at 50 CFR 17.3. Take can result knowingly or otherwise, by
direct and indirect impacts, intentionally or incidentally. Regulating
incidental and/or intentional take would help preserve the species'
remaining populations, slow their rate of decline, and decrease
synergistic, negative effects from other stressors.
We may issue permits to carry out otherwise prohibited activities,
including those described above, involving threatened wildlife under
certain circumstances. Regulations governing permits are codified at 50
CFR 17.32. With regard to threatened wildlife, a permit may be issued
for the following purposes: For scientific purposes, to enhance
propagation or survival, for economic hardship, for zoological
exhibition, for educational purposes, for incidental taking, or for
special purposes consistent with the purposes of the Act. The statute
also contains certain exemptions from the prohibitions, which are found
in sections 9 and 10 of the Act.
The proposed 4(d) rule would also provide for the conservation of
the species by allowing exceptions for take associated with actions and
activities that, while they may have some minimal level of disturbance
to pyramid pigtoe, are not expected to negatively impact conservation
and recovery efforts for the species. The proposed exceptions to these
prohibitions include incidental take associated with (1) conservation
efforts by the Service or State wildlife agencies, (2) channel
restoration projects, (3) bank restoration projects, and (4) take
necessary to aid a sick or injured specimen, or to salvage a dead
specimen.
The first exception is for conservation and restoration efforts for
pyramid pigtoe by the Service or State wildlife agencies, and
including, but not limited to, collection of broodstock, tissue
collection for genetic analysis, captive propagation, and subsequent
stocking into unoccupied areas within the historical range of the
species. We recognize the special and unique relationship with our
State natural resource agency partners in contributing to conservation
of listed species. State agencies often possess scientific data and
valuable expertise on the status and distribution of endangered,
threatened, and candidate species of wildlife and plants. State
agencies, because of their authorities and their close working
relationships with local governments and landowners, are in a unique
position to assist the Service in implementing all aspects of the Act.
In this regard, section 6 of the Act provides that the Service shall
cooperate to the maximum extent practicable with the States in carrying
out programs authorized by the Act. Therefore, any qualified employee
or agent of a State conservation agency that is a party to a
cooperative agreement with the Service in accordance with section 6(c)
of the Act, who is designated by his or her agency for such purposes,
would be able to conduct activities designed to conserve the pyramid
pigtoe that may result in otherwise prohibited take without additional
authorization.
The second and third exceptions are for channel and bank
restoration projects for creation of natural, physically stable,
ecologically functioning streams, taking into consideration
connectivity with floodplain and groundwater aquifers. These exceptions
include a requirement that bank restoration projects require planting
appropriate native vegetation, including woody species appropriate for
the region and habitat. We also propose language that would require
surveys and relocation prior to commencement of restoration actions for
pyramid pigtoe that would otherwise be negatively affected by the
actions. We reiterate that these actions and activities may have some
minimal level of take of pyramid pigtoe, but any such take is expected
to be rare and insignificant and is not expected to negatively impact
conservation and recovery efforts. Rather, we expect they would have a
net beneficial effect on the species. Across the species' range,
instream habitats have been degraded physically by sedimentation and by
direct and indirect channel disturbance. The habitat restoration
activities in the proposed 4(d) rule are intended to improve habitat
conditions for the species in the long term.
Finally, the proposed 4(d) rule would allow take of pyramid pigtoe
without a permit by any employee or agent of the Service or a State
conservation agency designated by the agency for such purposes and when
acting in the course of their official duties if such action is
necessary to aid a sick or injured specimen, or to salvage a dead
specimen which may be useful for scientific study. In addition, Federal
and State wildlife law enforcement officers,
[[Page 50009]]
working in coordination with Service field office personnel, may
possess, deliver, carry, transport, or ship pyramid pigtoe taken in
violation of the Act as necessary.
Nothing in this proposed 4(d) rule would change in any way the
recovery planning provisions of section 4(f) of the Act, the
consultation requirements under section 7 of the Act, or the ability of
the Service to enter into partnerships for the management and
protection of the pyramid pigtoe. However, interagency cooperation may
be further streamlined through planned programmatic consultations for
the species between Federal agencies and the Service, where
appropriate. We ask the public, particularly State agencies and other
interested stakeholders that may be affected by the proposed 4(d) rule,
to provide comments and suggestions regarding additional guidance and
methods that the Service could provide or use, respectively, to
streamline the implementation of this proposed 4(d) rule (see
Information Requested, above).
III. Critical Habitat
Prudency Determination
Section 4(a)(3) of the Act, as amended, and implementing
regulations (50 CFR 424.12) require that, to the maximum extent prudent
and determinable, the Secretary shall designate critical habitat at the
time the species is determined to be an endangered or threatened
species. Our regulations (50 CFR 424.12(a)(1)) state that the Secretary
may, but is not required to, determine that a designation would not be
prudent in the following circumstances:
(i) The species is threatened by taking or other human activity and
identification of critical habitat can be expected to increase the
degree of such threat to the species;
(ii) The present or threatened destruction, modification, or
curtailment of a species' habitat or range is not a threat to the
species, or threats to the species' habitat stem solely from causes
that cannot be addressed through management actions resulting from
consultations under section 7(a)(2) of the Act;
(iii) Areas within the jurisdiction of the United States provide no
more than negligible conservation value, if any, for a species
occurring primarily outside the jurisdiction of the United States;
(iv) No areas meet the definition of critical habitat; or
(v) The Secretary otherwise determines that designation of critical
habitat would not be prudent based on the best scientific data
available.
As discussed earlier in this document, there is currently no
imminent threat of collection or vandalism identified under Factor B
for this species, and identification and mapping of critical habitat is
not expected to initiate any such threat. In our SSA and proposed
listing determination for the pyramid pigtoe, we determined that the
present or threatened destruction, modification, or curtailment of
habitat or range is a threat to the pyramid pigtoe and that those
threats in some way can be addressed by section 7(a)(2) consultation
measures. The species occurs wholly in the jurisdiction of the United
States, and we are able to identify areas that meet the definition of
critical habitat. Therefore, because none of the circumstances
enumerated in our regulations at 50 CFR 424.12(a)(1) have been met and
because there are no other circumstances the Secretary has identified
for which this designation of critical habitat would be not prudent, we
have determined that the designation of critical habitat is prudent for
the pyramid pigtoe.
Critical Habitat Determinability
Having determined that designation is prudent, under section
4(a)(3) of the Act we consider whether critical habitat for the pyramid
pigtoe is determinable. Our regulations at 50 CFR 424.12(a)(2) state
that critical habitat is not determinable when one or both of the
following situations exist:
(i) Data sufficient to perform required analyses are lacking, or
(ii) The biological needs of the species are not sufficiently well
known to identify any area that meets the definition of ``critical
habitat.''
For the pyramid pigtoe, the species' needs are sufficiently well
known. However, there is some uncertainty regarding the taxonomic
identity of populations outside the Ohio, Cumberland, and Tennessee
River basins (see Background), which is currently under investigation
using different genetic markers than assessed thus far. Results of this
taxonomic investigation, which may more accurately delineate the
species' occupied range, are likely to be completed and submitted to a
peer-reviewed journal within 1 year. In addition to this taxonomic
investigation that may better determine critical habitat areas, a
careful assessment of the economic impacts that may occur due to a
critical habitat designation is ongoing, and we are in the process of
acquiring the necessary information to perform that assessment. Because
the information sufficient to perform a required analysis of the
impacts of the designation is lacking, we find designation of critical
habitat for the pyramid pigtoe to be not determinable at this time. The
Act allows the Service an additional year to publish a critical habitat
designation that is not determinable at the time of listing (16 U.S.C.
1533(b)(6)(C)(ii)).
Required Determinations
Clarity of the Rule
We are required by Executive Orders 12866 and 12988 and by the
Presidential Memorandum of June 1, 1998, to write all rules in plain
language. This means that each rule we publish must:
(1) Be logically organized;
(2) Use the active voice to address readers directly;
(3) Use clear language rather than jargon;
(4) Be divided into short sections and sentences; and
(5) Use lists and tables wherever possible.
If you feel that we have not met these requirements, send us
comments by one of the methods listed in ADDRESSES. To better help us
revise the rule, your comments should be as specific as possible. For
example, you should tell us the numbers of the sections or paragraphs
that are unclearly written, which sections or sentences are too long,
the sections where you feel lists or tables would be useful, etc.
National Environmental Policy Act (42 U.S.C. 4321 et seq.)
It is our position that, outside the jurisdiction of the U.S. Court
of Appeals for the Tenth Circuit, we do not need to prepare
environmental analyses pursuant to the National Environmental Policy
Act (NEPA; 42 U.S.C. 4321 et seq.) in connection with regulations
adopted pursuant to section 4(a) of the Act. We published a notice
outlining our reasons for this determination in the Federal Register on
October 25, 1983 (48 FR 49244). This position was upheld by the U.S.
Court of Appeals for the Ninth Circuit (Douglas County v. Babbitt, 48
F.3d 1495 (9th Cir. 1995), cert. denied 516 U.S. 1042 (1996)).
Government-to-Government Relationship With Tribes
In accordance with the President's memorandum of April 29, 1994
(Government-to-Government Relations with Native American Tribal
Governments; 59 FR 22951), Executive Order 13175 (Consultation and
Coordination with Indian Tribal
[[Page 50010]]
Governments), and the Department of the Interior's manual at 512 DM 2,
we readily acknowledge our responsibility to communicate meaningfully
with recognized Federal Tribes on a government-to-government basis. In
accordance with Secretarial Order 3206 of June 5, 1997 (American Indian
Tribal Rights, Federal-Tribal Trust Responsibilities, and the
Endangered Species Act), we readily acknowledge our responsibilities to
work directly with Tribes in developing programs for healthy
ecosystems, to acknowledge that Tribal lands are not subject to the
same controls as Federal public lands, to remain sensitive to Indian
culture, and to make information available to Tribes. There are no
Tribal lands within or adjacent to known pyramid pigtoe occupied
habitat. We will coordinate with Tribes whose lands are close to
pyramid pigtoe populations.
References Cited
A complete list of references cited in this rulemaking is available
on the internet at https://www.regulations.gov and upon request from the
Asheville Ecological Services Field Office (see FOR FURTHER INFORMATION
CONTACT).
Authors
The primary authors of this proposed rule are the staff members of
the Fish and Wildlife Service's Species Assessment Team and the
Asheville Ecological Services Field Office.
List of Subjects in 50 CFR Part 17
Endangered and threatened species, Exports, Imports, Reporting and
recordkeeping requirements, Transportation.
Accordingly, we propose to amend part 17, subchapter B of chapter
I, title 50 of the Code of Federal Regulations, as set forth below:
PART 17--ENDANGERED AND THREATENED WILDLIFE AND PLANTS
0
1. The authority citation for part 17 continues to read as follows:
Authority: 16 U.S.C. 1361-1407; 1531-1544; and 4201-4245,
unless otherwise noted.
0
2. Amend Sec. 17.11(h) by adding an entry for ``Pigtoe, pyramid'' to
the List of Endangered and Threatened Wildlife in alphabetical order
under Clams to read as set forth below:
Sec. 17.11 Endangered and threatened wildlife.
* * * * *
(h) * * *
--------------------------------------------------------------------------------------------------------------------------------------------------------
Common name Scientific name Where listed Status Listing citations and applicable rules
--------------------------------------------------------------------------------------------------------------------------------------------------------
--------------------------------------------------------------------------------------------------------------------------------------------------------
* * * * * * *
Clams
* * * * * * *
Pigtoe, pyramid.................... Pleurobema rubrum.... Wherever found....... T.................... [Federal Register citation when published as a
final rule]; 50 CFR 17.45(e); \4d\.
* * * * * * *
--------------------------------------------------------------------------------------------------------------------------------------------------------
0
3. As proposed to be added at 83 FR 51570 (Oct. 11, 2018), and amended
at 85 FR 44821 (July 24, 2020), 85 FR 59487 (Sept. 22, 2020), 85 FR
61384 (Sept. 29, 2020), and 86 FR 47916 (August 26, 2021), Sec. 17.45
is further amended by adding paragraph (e) to read as follows:
Sec. 17.45 Special rules--snails and clams.
* * * * *
(e) Pyramid pigtoe (Pleurobema rubrum).
(1) Prohibitions. The following prohibitions that apply to
endangered wildlife also apply to the pyramid pigtoe. Except as
provided under paragraph (e)(2) of this section and Sec. Sec. 17.4 and
17.5, it is unlawful for any person subject to the jurisdiction of the
United States to commit, to attempt to commit, to solicit another to
commit, or cause to be committed, any of the following acts in regard
to this species:
(i) Import or export, as set forth at Sec. 17.21(b) for endangered
wildlife.
(ii) Take, as set forth at Sec. 17.21(c)(1) for endangered
wildlife.
(iii) Possession and other acts with unlawfully taken specimens, as
set forth at Sec. 17.21(d)(1) for endangered wildlife.
(iv) Interstate or foreign commerce in the course of commercial
activity, as set forth at Sec. 17.21(e) for endangered wildlife.
(v) Sale or offer for sale, as set forth at Sec. 17.21(f) for
endangered wildlife.
(2) Exceptions from prohibitions. In regard to this species, you
may:
(i) Conduct activities as authorized by a permit under Sec. 17.32.
(ii) Take, as set forth at Sec. 17.21(c)(3) and (4) for endangered
wildlife.
(iii) Take as set forth at Sec. 17.31(b).
(iv) Take incidental to an otherwise lawful activity caused by:
(A) Channel restoration projects that create natural, physically
stable, ecologically functioning streams (or stream and wetland
systems). These projects can be accomplished using a variety of
methods, but the desired outcome is a natural channel with low shear
stress (force of water moving against the channel); bank heights that
enable reconnection to the floodplain; connection of surface and
groundwater systems, resulting in perennial flows in the channel;
riffles and pools composed of existing soil, rock, and wood instead of
large imported materials; low compaction of soils within adjacent
riparian areas; and inclusion of riparian wetlands. Streams
reconstructed in this way would offer suitable habitats for the pyramid
pigtoe and contain stable channel features, such as pools, glides,
runs, and riffles, which could be used by the species and its host fish
for spawning, rearing, growth, feeding, migration, and other normal
behaviors. Prior to commencement of restoration actions, surveys to
determine presence of the pyramid pigtoe must be performed, and, if any
pyramid pigtoe are located, in coordination with the local Service
field office, they must be relocated prior to project implementation
and monitored post-implementation. To qualify under this exemption, a
channel restoration project must satisfy all Federal, State, and local
permitting requirements.
(B) Bank restoration projects that use bioengineering methods to
replace preexisting, bare, eroding stream banks with vegetated, stable
stream banks, thereby reducing bank erosion and instream sedimentation
and improving habitat conditions for the species. Following these
bioengineering methods, stream banks may be stabilized using native
species live stakes (live, vegetative cuttings inserted
[[Page 50011]]
or tamped into the ground in a manner that allows the stake to take
root and grow), native species live fascines (live branch cuttings,
usually willows, bound together into long, cigar-shaped bundles), or
native species brush layering (cuttings or branches of easily rooted
tree species layered between successive lifts of soil fill). Bank
restoration projects would require planting appropriate native
vegetation, including woody species appropriate for the region and
habitat. These methods will not include the sole use of quarried rock
(rip-rap) or the use of rock baskets or gabion structures. Prior to
commencement of bank stabilization actions, surveys to determine
presence of pyramid pigtoe must be performed, and, if any pyramid
pigtoe are located, in coordination with the local Service field
office, they must be relocated prior to project implementation and
monitored post-implementation. To qualify under this exemption, a bank
restoration project must satisfy all Federal, State, and local
permitting requirements.
(v) Possess and engage in other acts with unlawfully taken
wildlife, as set forth at Sec. 17.21(d)(2) for endangered wildlife.
Martha Williams,
Principal Deputy Director, Exercising the Delegated Authority of the
Director, U.S. Fish and Wildlife Service.
[FR Doc. 2021-19091 Filed 9-3-21; 8:45 am]
BILLING CODE 4333-15-P