Endangered and Threatened Wildlife; 90-Day Finding on a Petition To List the Whitespotted Eagle Ray as Threatened or Endangered Under the Endangered Species Act, 28707-28713 [2024-08340]
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Federal Register / Vol. 89, No. 77 / Friday, April 19, 2024 / Proposed Rules
ray, and if we determine the
whitespotted eagle ray warrants listing
as a threatened species, we promulgate
a protective regulation under section
4(d) of the ESA. The petition is available
online (see ADDRESSES).
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
50 CFR Parts 223 and 224
[Docket No. 240212–0044; RTID 0648–
XR130]
Endangered and Threatened Wildlife;
90-Day Finding on a Petition To List
the Whitespotted Eagle Ray as
Threatened or Endangered Under the
Endangered Species Act
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Notification of 90-day petition
finding.
AGENCY:
We, NMFS, announce a 90day finding on a petition under the
Endangered Species Act (ESA) to list the
whitespotted eagle ray (Aetobatus
narinari) as a threatened or endangered
species and to designate critical habitat
concurrent with the listing. We find that
the petition does not present substantial
scientific or commercial information
indicating that the petitioned action
may be warranted.
DATES: These findings were made on
April 19, 2024.
ADDRESSES: Copies of the petition and
related materials are available from the
NMFS website at https://www.fisheries.
noaa.gov/national/endangered-speciesconservation/negative-90-day-findings.
FOR FURTHER INFORMATION CONTACT:
Adrienne Lohe, NMFS Office of
Protected Resources, (301) 427–8442,
adrienne.lohe@noaa.gov.
SUPPLEMENTARY INFORMATION:
SUMMARY:
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Background
On April 6, 2023, we received a
petition from the Defend Them All
Foundation to list the whitespotted
eagle ray, Aetobatus narinari, as a
threatened or endangered species under
the ESA and to designate critical habitat
concurrent with the listing. The petition
asserts that this species is threatened by
four of the five ESA section 4(a)(1)
factors: (1) present or threatened
destruction, modification, or
curtailment of its habitat or range; (2)
overutilization for commercial and
recreational purposes; (3) inadequacy of
existing regulatory mechanisms; and (4)
other natural or manmade factors. The
petition requests that if the species is
listed as threatened or endangered, we
promulgate a regulation under section
4(e) of the ESA for species similar in
appearance to the whitespotted eagle
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ESA Statutory, Regulatory, and Policy
Provisions and Evaluation Framework
Section 4(b)(3)(A) of the ESA of 1973,
as amended (16 U.S.C. 1531 et seq.),
requires, to the maximum extent
practicable, that within 90 days of
receipt of a petition to list a species as
threatened or endangered, the Secretary
of Commerce make a finding on whether
that petition presents substantial
scientific or commercial information
indicating that the petitioned action
may be warranted, and to promptly
publish such finding in the Federal
Register (16 U.S.C. 1533(b)(3)(A)). When
it is found that substantial scientific or
commercial information in a petition
indicates the petitioned action may be
warranted (a ‘‘positive 90-day finding’’),
we are required to promptly commence
a review of the status of the species
concerned during which we will
conduct a comprehensive review of the
best available scientific and commercial
information. In such cases, we conclude
the review with a finding as to whether,
in fact, the petitioned action is
warranted within 12 months of receipt
of the petition (16 U.S.C. 1533(b)(3)(B)).
Because the finding at the 12-month
stage is based on a more thorough
review that encompasses all the best
available information, as compared to
the narrow scope of review at the 90-day
stage, a ‘‘may be warranted’’ finding
does not prejudge the outcome of the
status review.
Under the ESA, a listing
determination may address a species,
which is defined to also include
subspecies and any vertebrate distinct
population segment (DPS) that
interbreeds when mature (16 U.S.C.
1532(16)). A joint NMFS–U.S. Fish and
Wildlife Service (USFWS) (jointly, ‘‘the
Services’’) policy clarifies the Services’
interpretation of the phrase ‘‘distinct
population segment’’ for the purposes of
listing, delisting, and reclassifying a
species under the ESA (61 FR 4722,
February 7, 1996). A species,
subspecies, or DPS is ‘‘endangered’’ if it
is in danger of extinction throughout all
or a significant portion of its range, and
‘‘threatened’’ if it is likely to become
endangered within the foreseeable
future throughout all or a significant
portion of its range (ESA sections 3(6)
and 3(20), respectively, 16 U.S.C.
1532(6) and (20)). Pursuant to the ESA
and our implementing regulations, we
determine whether species are
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threatened or endangered based on any
one or a combination of the following
five ESA section 4(a)(1) factors: (1) the
present or threatened destruction,
modification, or curtailment of habitat
or range; (2) overutilization for
commercial, recreational, scientific, or
educational purposes; (3) disease or
predation; (4) inadequacy of existing
regulatory mechanisms to address
identified threats; or (5) any other
natural or manmade factors affecting the
species’ existence (16 U.S.C. 1533(a)(1),
50 CFR 424.11(c)).
ESA-implementing regulations issued
jointly by NMFS and USFWS (50 CFR
424.14(h)(1)(i)) define ‘‘substantial
scientific or commercial information’’ in
the context of reviewing a petition to
list, delist, or reclassify a species as
‘‘credible scientific or commercial
information in support of the petition’s
claims such that a reasonable person
conducting an impartial scientific
review would conclude that the action
proposed in the petition may be
warranted.’’ Conclusions drawn in the
petition without the support of credible
scientific or commercial information
will not be considered ‘‘substantial
information.’’ In accordance with 50
CFR 424.14(h)(1)(ii), in reaching the
initial (90-day) finding on the petition,
we will consider the information
described in subsections 50 CFR
424.14(c), (d), and (g) (if applicable).
Our determination as to whether the
petition provides substantial scientific
or commercial information indicating
that the petitioned action may be
warranted will depend in part on the
degree to which the petition includes
the following types of information: (1)
information on current population
status and trends and estimates of
current population sizes and
distributions, both in captivity and the
wild, if available; (2) identification of
the factors under section 4(a)(1) of the
ESA that may affect the species and
where these factors are acting upon the
species; (3) whether and to what extent
any or all of the factors alone or in
combination identified in section 4(a)(1)
of the ESA may cause the species to be
an endangered species or threatened
species (i.e., the species is currently in
danger of extinction or is likely to
become so within the foreseeable
future), and, if so, how high in
magnitude and how imminent the
threats to the species and its habitat are;
(4) information on adequacy of
regulatory protections and effectiveness
of conservation activities by states as
well as other parties, that have been
initiated or that are ongoing, that may
protect the species or its habitat; and (5)
a complete, balanced representation of
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the relevant facts, including information
that may contradict claims in the
petition. See 50 CFR 424.14(d).
If the petitioner provides
supplemental information before the
initial finding is made and states that it
is part of the petition, the new
information, along with the previously
submitted information, is treated as a
new petition that supersedes the
original petition, and the statutory
timeframes will begin when such
supplemental information is received.
See 50 CFR 424.14(g).
We may also consider information
readily available at the time the
determination is made (50 CFR
424.14(h)(1)(ii)). We are not required to
consider any supporting materials cited
by the petitioner if the petitioner does
not provide electronic or hard copies, to
the extent permitted by U.S. copyright
law, or appropriate excerpts or
quotations from those materials (e.g.,
publications, maps, reports, letters from
authorities). See 50 CFR 424.14(c)(6).
The ‘‘substantial scientific or
commercial information’’ standard must
be applied in light of any prior reviews
or findings we have made on the listing
status of the species that is the subject
of the petition (50 CFR 424.14(h)(1)(iii)).
Where we have already conducted a
finding on, or review of, the listing
status of that species (whether in
response to a petition or on our own
initiative), we will evaluate any petition
received thereafter seeking to list, delist,
or reclassify that species to determine
whether a reasonable person conducting
an impartial scientific review would
conclude that the action proposed in the
petition may be warranted despite the
previous review or finding. Where the
prior review resulted in a final agency
action—such as a final listing
determination, 90-day not-substantial
finding, or 12-month not-warranted
finding—a petitioned action will
generally not be considered to present
substantial scientific and commercial
information indicating that the action
may be warranted unless the petition
provides new information or analysis
not previously considered.
At the 90-day finding stage, we do not
conduct additional research, and we do
not solicit information from parties
outside the agency to help us in
evaluating the petition. We will accept
the petitioners’ sources and
characterizations of the information
presented if they appear to be based on
accepted scientific principles, unless we
have specific information in our files
that indicates the petition’s information
is incorrect, unreliable, obsolete, or
otherwise irrelevant to the requested
action. Information that is susceptible to
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more than one interpretation or that is
contradicted by other available
information will not be dismissed at the
90-day finding stage, so long as it is
reliable and a reasonable person
conducting an impartial scientific
review would conclude it supports the
petitioners’ assertions. In other words,
conclusive information indicating the
species may meet the ESA’s
requirements for listing is not required
to make a positive 90-day finding. We
will not conclude that a lack of specific
information alone necessitates a
negative 90-day finding if a reasonable
person conducting an impartial
scientific review would conclude that
the unknown information itself suggests
the species may be at risk of extinction
presently or within the foreseeable
future.
To make a 90-day finding on a
petition to list a species, we evaluate
whether the petition presents
substantial scientific or commercial
information indicating the subject
species may be either threatened or
endangered, as defined by the ESA.
First, we evaluate whether the
information presented in the petition, in
light of the information readily available
in our files, indicates that the petitioned
entity constitutes a ‘‘species’’ eligible for
listing under the ESA. Next, we evaluate
whether the information indicates that
the species faces an extinction risk such
that listing, delisting, or reclassification
may be warranted; this may be indicated
in information expressly discussing the
species’ status and trends, or in
information describing impacts and
threats to the species. We evaluate any
information on specific demographic
factors pertinent to evaluating
extinction risk for the species (e.g.,
population abundance and trends,
productivity, spatial structure, age
structure, sex ratio, diversity, current
and historical range, habitat integrity or
fragmentation), and the potential
contribution of identified demographic
risks to extinction risk for the species.
We then evaluate the potential links
between these demographic risks and
the causative impacts and threats
identified in section 4(a)(1).
Information presented on impacts or
threats should be specific to the species
and should reasonably suggest that one
or more of these factors may be
operative threats that act or have acted
on the species to the point that it may
warrant protection under the ESA.
Broad statements about generalized
threats to the species, or identification
of factors that could negatively impact
a species, do not constitute substantial
information indicating that listing may
be warranted. We look for information
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indicating that not only is the particular
species exposed to a factor, but that the
species may be responding in a negative
fashion; then we assess the potential
significance of that negative response.
Many petitions identify risk
classifications made by
nongovernmental organizations, such as
the International Union for
Conservation of Nature (IUCN), the
American Fisheries Society, or
NatureServe, as evidence of extinction
risk for a species. Risk classifications by
other organizations or made under other
Federal or state statutes may be
informative, but such classification
alone will not provide a sufficient
rationale for a positive 90-day finding
under the ESA. For example, as
explained by NatureServe, their
assessments of a species’ conservation
status do not constitute a
recommendation by NatureServe for
listing under the U.S. Endangered
Species Act because NatureServe
assessments have different criteria,
evidence requirements, purposes and
taxonomic coverage than government
lists of endangered and threatened
species, and therefore these two types of
lists should not be expected to coincide
(https://explorer.natureserve.org/
AboutTheData/DataTypes/Conservation
StatusCategories). Additionally, species
classifications under IUCN and the ESA
are not equivalent; data standards,
criteria used to evaluate species, and
treatment of uncertainty are also not
necessarily the same. Thus, when a
petition cites such classifications, we
will evaluate the source of information
that the classification is based upon in
light of the ESA standards on extinction
risk and impacts or threats discussed
above.
Analysis of the Petition
We have reviewed the petition, the
literature cited in the petition, and other
literature and information readily
available in our files. In this section, we
provide a summary of this information
and present our analysis of whether this
information indicates that the petitioned
action may be warranted.
Species Description
The whitespotted eagle ray, A.
narinari, is a large (up to 230
centimeters (cm) disc width (DW))
benthopelagic batoid found in warmtemperate and tropical coastal waters
(Dulvy et al. 2021). The species was
previously thought to have a
circumglobal distribution, although
morphological, parasitological, and
genetic evidence indicates that the
species is limited to the Atlantic, while
eagle rays in the Pacific and Indian
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Oceans constitute separate species
(Sales et al. 2019). The petition cites
Eschmeyer’s Catalog of Fishes (Fricke et
al. 2020) and Dulvy et al. (2021) in its
assertion that the species spans the
western and eastern Atlantic. This
contradicts Sales et al. (2019)’s
conclusion that based on nuclear and
mitochondrial markers, A. narinari is
restricted to the western Atlantic, and
samples from South Africa formed a
monophyletic clade closest to another
species of eagle ray, Aetobatus
ocellatus, found in the Indian Ocean.
Despite the apparent ongoing scientific
debate surrounding the taxonomy of the
whitespotted eagle ray and the genus as
a whole, there is no further discussion
of the taxonomic status of A. narinari in
the petition. The petition asserts that the
whitespotted eagle ray ranges from Cape
Hatteras, North Carolina, to Rio de
Janeiro, Brazil, including the Gulf of
Mexico, the Bahamas, and the Caribbean
Islands, and in the eastern Atlantic,
from Mauritania south to Angola, and
possibly South Africa (Dulvy et al.
2021). We accept the petition’s
characterization of the species’
taxonomy and distribution because the
petition provides recent and reputable
references for this conclusion, and
because we find that a reasonable
person conducting an impartial
scientific review would conclude that
the petitioners’ assertions are reasonably
supported.
Whitespotted eagle rays occur in the
neritic zone from the low-tide mark to
water depths of 60 meters (m), and are
often associated with coral reefs,
lagoons, and estuaries (Cerutti-Pereyra
et al. 2018, Dulvy et al. 2021). They are
highly mobile and display both
migratory and resident behavior
(Bassos-Hull et al. 2014; Sellas et al.
2015; De Groot et al. 2021).
Whitespotted eagle rays are mid-trophic
level predators that forage for
invertebrates (often bivalves,
gastropods, and crustaceans) in the
seabed sediment, serving as bioturbators
(Ajieman et al. 2012; Flowers et al.
2021). The species is often observed as
solitary individuals, but can also be
seen in large aggregations of up to
several hundred individuals (BassosHull et al. 2014; Tagliafico et al. 2012).
Size at maturity has been estimated at
approximately 115–130 cm DW for
males and slightly larger for females
(Arau´jo et al. 2022; Bassos-Hull et al.
2014; Taglifico et al. 2012). Age at
maturity is estimated at 4 to 6 years
(Cerutti-Pereyra et al. 2018).
Whitespotted eagle rays exhibit
matrotrophic viviparity in which
embryos are nourished through uterine
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secretions and born live (Arau´jo et al.
2022). Between one and five young are
produced in each litter after a gestation
period of 12 months (Dulvy et al. 2021).
Generation length for the species is
estimated at 10 years, inferred from the
slightly larger A. ocellatus which has a
generation length of 12 years (Dulvy et
al. 2021).
Population Status and Trends
The petition asserts that the
whitespotted eagle ray has undergone
dramatic population decline, largely
relying on the IUCN Red List
Assessment of the species as
‘‘endangered’’ (Dulvy et al. 2021). This
assessment concludes that the
whitespotted eagle ray ‘‘is suspected’’ to
have experienced a population
reduction of 50–79 percent over the past
three generation lengths (30 years) due
to ‘‘actual and potential levels of fishing
pressure’’ (Dulvy et al. 2021).
Dulvy et al. (2021) use population
trend data from baited remote
underwater videos (BRUVs) in Belize
from 2009–2018 (G. Clementi and D.
Chapman, unpublished data 2019) and
a survey in Mexico spanning 2000–2014
(J–C. Pe´rez Jime´nez unpublished data
2019) to perform Bayesian state-space
population trend analysis over three
generation lengths (30 years). The BRUV
data from Belize indicated an increase
in abundance of 7.5 percent annually,
while data from Mexico indicate a 0.95
percent decrease in abundance annually
over the respective time series.
Additionally, Dulvy et al. (2021) state
that in the southern Gulf of Mexico,
interviews with fishermen indicated
catch declines from 30–40 rays per
night/trip from 1990 to 2000 to 10–15
rays per night/trip in 2019 (CuevasZimbro´n et al. 2011; J–C. Pe´rez Jime´nez
unpublished data 2019, as cited in
Dulvy et al. 2021). Considering the two
available population trend datasets
(Belize 2009–2018 and Mexico 2000–
2014) and extrapolating over three
generation lengths, however, Dulvy et
al. (2021) found an increasing
population trend of 1.32 percent per
year in the Western Central Atlantic.
Outside of these datasets, there is
little information available on
whitespotted eagle ray population
trends. Dulvy et al. (2021) rely on the
assumption that where the species is
known to be targeted in artisanal
fisheries or bycaught in commercial
fisheries (e.g., in Colombia, Venezuela,
the Guianas; see ESA Section 4(a)(1)
Factors), it is experiencing population
declines. In Brazil, personal
communications cited in Dulvy et al
(2021) from 2018 indicate that landings
of the species in gillnets at Pernambuco
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have declined by about 80 percent since
1995, and that the species has also
declined in Sa˜o Paulo, where fishery
monitoring between 1996 and 2002 only
recorded five individuals. Dulvy et al.
(2021) write that because unmanaged
fisheries in Brazil have led to declines
in other species, ‘‘. . . there is no
reason not to suspect that this species
has also been reduced in numbers in
that area.’’ Based on suspected high
exploitation levels and lack of adequate
management, their assessment indicates
that it is ‘‘suspected that this species has
undergone a population reduction of
50–79 percent over the past three
generation lengths (30 years) in the
Atlantic South American part of its
range’’ (Dulvy et al. 2021). It is unclear
whether the personal communications
cited by Dulvy et al. (2021) are based on
time series data or take into account
fishing effort or other factors. Therefore,
it is unknown how accurately this
estimate reflects the abundance of
whitespotted eagle rays across this
region. We find that, based on the
information presented in the petition, a
reasonable person conducting an
impartial scientific review would
conclude that some level of population
decline may be occurring in the
Southwest Atlantic, although there is
not sufficient credible scientific or
commercial information to conclude
that the species has declined by 50–79
percent.
Trends specific to A. narinari are
unavailable in the Eastern Atlantic, and
therefore Dulvy et al. (2021) use
reported catch levels of elasmobranchs
as a proxy for whitespotted eagle ray
population trends here. Dulvy et al.
(2021) report the decline in average
elasmobranch catch per unit effort by 71
percent from 1970–2015 and
simultaneous increase in average
elasmobranch catch by over 250 percent
across the West Africa region, implying
a dramatic increase in fishing effort.
Trends in elasmobranch landings during
this period of increasing fishing effort
are described for individual countries in
the region. In Mauritania, landings
increased by 246 percent over 1992–
2015; since then effort has been stable
and landings continued to increase. In
Senegal, reconstructed landings (which
include an estimate of unreported
landings data, therefore increasing
uncertainty) showed a 30–80 percent
decline from 2001–2016, suggesting
population decline. In Guinea-Bissau,
reconstructed landings declined 22
percent from 2012 to 2016 after rising
since the 1960s. In Cameroon, there has
been a 96 percent decline in
reconstructed landings from 2007–2016
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after rising since the 1960s. There have
been few recent observations of the
species in the Republic of Congo,
Mauritania, Gabon, Senegal, Gambia,
Guinea-Bissau, Sierra Leone, Ghana,
Nigeria, Cameroon or Angola; in certain
cases, this is despite sightings of species
with similar habitat needs and
catchability. However, some
confounding factors are at play; for
example, in Ghana there are few
shallow fishing gears likely to take the
species (Dulvy et al. 2021). Dulvy et al.
(2021) take the above information to
indicate that the species has largely
disappeared from the Eastern Atlantic
part of its range. Dulvy et al. (2021)
conclude ‘‘it is suspected that a
population reduction of more than 80
percent has occurred in the past three
generation lengths (30 years)’’ (Dulvy et
al. 2021). While trends in elasmobranch
catch and fishing effort are concerning,
they do not provide enough speciesspecific evidence for us to conclude that
the whitespotted eagle ray in particular
has followed these same trends. Further,
neither the petition nor Dulvy et al.
(2021) provide information on historical
population sizes in the areas with few
recent observations. We find that, based
on the information presented in the
petition, a reasonable person conducting
an impartial scientific review would
conclude that some level of population
decline may be occurring in the Eastern
Atlantic, although there is not sufficient
credible scientific or commercial
information to conclude that the species
has declined by more than 80 percent.
Altogether, Dulvy et al. (2021)
conclude that the whitespotted eagle ray
has undergone a population reduction
of 50–79 percent over the past three
generation lengths across its range.
However, a reasonable person would
conclude that this information is not
supported by credible scientific
information and is therefore unreliable
given the only available quantitative
population data for whitespotted eagle
rays from Belize and Mexico indicate
that the population is increasing there.
Species-specific information on trends
is unavailable from the Southwest
Atlantic, the Eastern Central Atlantic,
and Southeast Atlantic, although Dulvy
et al. (2021) suspect population
reductions in these areas. While
declining elasmobranch landings, few
recorded sightings of the species, and
accounts of reduced catch by artisanal
fishermen are indicative of potential
population declines in these areas, we
are not able to conclude that this
information points to the dramatic
population declines that Dulvy et al.
(2021) infer.
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Outside of the IUCN Red List
Assessment (Dulvy et al. 2021), the
petition discusses just one other
relevant study relating to population
trends for the species. Bassos-Hull et al.
(2014) observed a yearly decrease in
number of whitespotted eagle rays
observed in both aerial and boat-based
surveys in the eastern Gulf of Mexico off
southwest Florida from 2008–2013. The
authors note, however, that without
further study, it is unclear whether this
is due to a true decrease in abundance
over time or other factors such as
sampling bias, a shift in range, or a
clustering phenomenon in the study
area during the 2008–2009 season
(Bassos-Hull et al. 2014).
In all, we do not find that the
information presented in the petition
constitutes credible scientific
information that indicates a dramatic
decrease in whitespotted eagle ray
abundance across its range as asserted
by the petitioners. In fact, the region
with available time-series population
data shows an increasing population
trend for the species. Information
presented in the petition only points to
potential abundance decreases in other
parts of its range with little supporting
information; the principal study the
petition relies on for this assertion is
unreliable because it rests on
unsupported assumptions (i.e., the
assumptions that, where the species is
known to be targeted in artisanal
fisheries or bycaught in commercial
fisheries, it is experiencing population
declines; and that, where elasmobranch
catch rates are declining, the species is
experiencing population declines)
rather than data. Therefore, we do not
find that the petition offers substantial
scientific or commercial information
that would suggest that the species’
current population status and trends
may warrant the petitioned action.
ESA Section 4(a)(1) Factors
The petition asserts that four of the
five factors in section 4(a)(1) of the ESA
are adversely affecting the whitespotted
eagle ray: (A) present or threatened
destruction, modification, or
curtailment of habitat or range; (B)
overutilization for commercial,
recreational, scientific, or educational
purposes; (D) inadequacy of existing
regulatory mechanisms; and (E) other
natural or manmade factors affecting its
continued existence. While the petition
does not state that factor (C), disease or
predation, poses a threat to the species,
it does argue that the species may be
more susceptible to disease in
combination with other stressors. In the
following sections, we discuss the
information presented in the petition,
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viewed in the context of information
readily available in our files where
applicable, regarding threats to this
species.
(A) Present or Threatened Destruction,
Modification, or Curtailment of Habitat
or Range
The petition describes the effect of
destructive fishing practices,
specifically bottom trawling, on coastal
ocean habitats. Although the petition
discusses negative impacts of trawling,
including damage and destruction of
biotic and abiotic seabed structures,
increased water column turbidity,
release of contaminants contained in
seabed sediment, and reduced food
availability for bottom-feeders, the
petition includes no discussion of
specific areas where bottom trawling
activities occur within the range of the
whitespotted eagle ray, or the intensity
of bottom trawling activity. While the
impacts of bottom trawling are
concerning for certain marine habitats
generally, the extent to which
whitespotted eagle rays in particular
may be threatened by such impacts is
not clear based on the information in
the petition.
The petition similarly discusses
impacts of coastal development and
dredging, as well as resulting pollution
and suspension of sediment, on marine
habitats. Suspension of sediment
resulting from dredging can cause
physiological stress and changes in
foraging and predation behavior in
marine fishes (Wenger et al. 2016).
Contaminants released from disturbed
sediment (e.g., metals and persistent
organic pollutants (POPs) such as
polycyclic aromatic hydrocarbons
(PAHs), polychlorinated biphenyls
(PCBs), and
dichlorodiphenyltrichloroethane
(DDT)), have been shown to accumulate
in, and have further negative impacts on
marine fishes, including on the
reproductive success of adults and
development of eggs and larvae (Wenger
et al. 2016). PCBs, DDT and
hexachlorobenzene (HCB) were detected
in whitespotted eagle rays off Australia,
sometimes in high enough
concentrations to cause possible
negative long-term impacts (Cagnazzi et
al. 2019). Without further study,
however, it remains unclear whether
observed contaminant loads lead to
lower survival and/or lower
reproductive success in elasmobranchs
(Cagnazzi et al. 2019). The petition also
asserts that sounds from dredging
activity may cause harm to whitespotted
eagle rays based on a study that found
the sound of boat motors to disturb A.
ocellatus, causing these rays to exhibit
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escape behavior when foraging (Berthe
and Lecchini 2016). It is unclear
whether such disruptions of foraging
behavior would lead to population-level
impacts to A. narinari, or whether noise
from dredging would cause a similar
response; neither of these points are
addressed in the petition. Generally, the
whitespotted eagle ray is vulnerable to
coastal development as it uses shallow,
coastal areas for breeding and feeding
(Dulvy et al. 2021). While coastal
development has the potential to
negatively impact whitespotted eagle
rays, specific information indicating
how and where dredging and
development are impacting the
whitespotted eagle ray’s habitat is not
provided in the petition, and thus the
degree to which the population may be
threatened by this stressor is unclear.
The petition discusses, and provides
references regarding, direct and indirect
impacts of climate change, including
physical and chemical changes to ocean
habitats (e.g., ocean warming and
increasing ocean acidity), changes in
ocean circulation patterns, declines in
primary productivity, range shifts,
increasing occurrences of extreme
weather events and harmful algal
blooms, and physiological and
behavioral impairments in certain
marine fishes. The specific effects of
climate change on ray ecology are
largely unknown, and few studies have
investigated the impacts of climate
change on the whitespotted eagle ray.
Specific impacts that may be of concern
to the whitespotted eagle ray that are
discussed in the petition include
decreased aragonite and calcite
availability due to ocean acidification,
which can hinder the ability of
calcifying organisms such as bivalves
and corals to build their skeletons
(Branch et al. 2013; Kroeker et al. 2013).
This could result in reduced availability
of certain prey species and coral reef
habitat for the whitespotted eagle ray to
utilize. The petition cites Flowers et al.
(2021) in its assertion that range and
habitat shifts may result in negative
effects on ray fitness through decreased
ability to find food, increased predation
risk and increased competition.
However, the same study points out that
vulnerability to climate change varies by
species, and, in certain cases, climate
change may have beneficial outcomes
for rays (Flowers et al. 2021). The
petition also points out that sharks and
rays in particular exhibit thermotaxis, a
behavior that involves moving to waters
of different temperatures throughout the
day. Therefore, beyond large-scale
geographic range shifts that may occur
as a result of climate change, changes in
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such small-scale movements may also
be significant to the fitness and survival
of sharks and rays (Vilmar and Di Santo
2022). In an assessment of shark and ray
behavior in response to gradual
increases in sea surface temperature as
well as acute temperature anomalies
caused by El Nin˜o Southern Oscillation
over 27 years, A. narinari exhibited
significantly increased relative
abundance at higher temperatures in
both cases (Osgood et al. 2021). While
this study took place in the eastern
Pacific and taxonomic revisions have
limited A. narinari to the Atlantic (see
Species Description), the results suggest
that eagle ray species such as A.
narinari could be more tolerant of
temperature extremes than other
elasmobranchs (Osgood et al. 2021).
Although climate change has the
potential to adversely impact the
whitespotted eagle ray, the degree to
which whitespotted eagle ray
individuals or populations have been or
will be affected is unclear. Therefore,
the degree to which climate change
threatens the whitespotted eagle ray is
not clear based on the information in
the petition.
In summary, the petition and the
references cited therein do not comprise
substantial scientific or commercial
information indicating there is present
or threatened destruction, modification,
or curtailment of the whitespotted eagle
ray’s habitat or range such that a
reasonable person conducting an
impartial scientific review would
conclude that listing may be warranted.
(B) Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
The petition identifies overutilization
for commercial purposes as the greatest
threat to the whitespotted eagle ray. The
species is captured as incidental
bycatch and, less commonly, in targeted
fisheries (Tagliafico et al. 2012).
In the Western Central Atlantic,
artisanal fisheries targeting the species
are known to exist (but ‘‘are not well
described’’) in Mexico, Cuba, the
Caribbean coast of Colombia, and
Venezuela (Dulvy et al. 2021). In
Colombia, the whitespotted eagle ray is
taken in gillnet, longline, and trawl
gears (Dulvy et al. 2021). In both
Colombia and Venezuela, artisanal
fisheries are widespread, intense, and
lack management (Dulvy et al. 2021). A
study of the small, directed fishery in
northeastern Venezuela found that
while the time series analyzed (August
2005 to December 2007) is too short to
infer changes in population abundance,
the capture of juvenile, mature, and
pregnant individuals is of concern
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(Tagliafico et al. 2012). An artisanal
fishery targeting A. narinari exists off
the coast of the State of Campeche in the
southern Gulf of Mexico driven by the
traditional consumption of this species
there (Cuevas-Zimbro´n et al. 2011).
According to fishermen interviewed,
catches of A. narinari have declined
over recent decades due to overfishing
of the species as well as its molluscan
prey (Cuevas-Zimbro´n et al. 2011). Data
from Mexico’s National Aquaculture
and Fisheries Commission
(CONAPESCA) indicate that in 2013, A.
narinari was the second-most captured
batoid in the region at about 40 tons
each year (Rodriguez-Santiago et al.
2016). Whitespotted eagle rays have also
been caught as bycatch in shark gillnet
fisheries in the U.S. south Atlantic, and
the petition asserts that they are among
the top bycatch species by abundance in
the observed catches (Trent et al. 1997).
However, according to information
readily available in our files, which
provides important context for judging
the accuracy and reliability of the
information presented in the petition,
the species hasn’t been observed as
bycatch in this fishery since 2008
(NOAA Fisheries Southeast Fisheries
Science Center, unpublished data). In
all, despite the existence of artisanal
fisheries targeting the whitespotted
eagle ray in this region as well as
interactions with commercial fisheries,
available population data does not
support the conclusion that these
fisheries are causing significant
population declines. Rather, available
data sources indicate an increasing
population trend in the Western Central
Atlantic (see Population Status and
Trends).
In the Southwest Atlantic, artisanal
fisheries and commercial trawl and
longline fisheries along the coast of
South America can be intense and
unmanaged, and the petition asserts this
has led to the disappearance of several
elasmobranch species in the region,
including largetooth sawfish (Pristis
pristis), smalltooth sawfish (Pristis
pectinata), daggernose shark
(Isogomphodon oxyrhynchus), and
smalltail shark (Carcharhinus porosus)
(Dulvy et al. 2021). Although fishing
pressure is heavy and many of the
stocks targeted by artisanal fishermen
are overexploited in this region (Dulvy
et al. 2021), the petition does not
present any information about the
specific fisheries that interact with the
whitespotted eagle ray, or levels of catch
of the whitespotted eagle ray.
In the Eastern Central Atlantic, sharks
are targeted in artisanal fisheries across
much of the region due to demand for
dried salted shark meat (Dulvy et al.
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2021). Specifically, drift gillnets and
demersal set gillnets are used to target
sharks and rays in artisanal fisheries of
Mauritania, Nigeria, Ghana, and
Cameroon (Dulvy et al. 2021).
Population reductions and some local
extinctions of shark and ray species
have been observed in this region as a
result of fishing pressure (Dulvy et al.
2021). The petition states that total
demersal biomass of inshore stocks in
the Gulf of Guinea is estimated to have
declined by 75 percent since 1982 as a
result of destructive fishing practices
(Dulvy et al. 2021). Additionally, the
number of traditional and industrial
fishing boats has significantly increased
since 1950 (Dulvy et al. 2021). Although
poorly managed fishing activity in this
region is having negative impacts on
fish stocks generally, the petition
presents no information relating to the
capture or landings of the whitespotted
eagle ray in particular.
Little information on the impact of
fisheries bycatch on the species was
provided in the petition. A study
examining the physiological responses
of capture on benthopelagic rays,
including A. narinari, showed elevated
lactate and glucose levels lasting the
length of time that the rays were
confined after capture (Rangel et al.
2021). This is indicative of increased
physiological stress, and immediate
release of captured individuals is
recommended (Rangel et al. 2021).
Mortality rates or other sublethal effects
of capture on the whitespotted eagle ray
were not addressed in the petition.
The petition also discusses other
potential sources of overutilization. The
whitespotted eagle ray is popular in
public aquarium displays and is
collected for this purpose (Dulvy et al.
2021). No further information on the
impact of the aquarium trade on the
species is included in the petition. The
petitioners also assert that the species
may be vulnerable to negative
interactions with shellfish farms due to
their molluscan diet. Negative
interactions have been anecdotally
reported in the Northwest Atlantic,
although confirmed interactions
generally take place with eagle rays in
the Indo-Pacific (Dulvy et al. 2021).
In all, while the petition presents
information on fisheries targeting the
whitespotted eagle ray in the Western
Central Atlantic, overutilization does
not appear to be occurring based on
population increases indicated in this
region. The petition does not provide
information specific to fisheries
affecting the whitespotted eagle ray in
the Southwest Atlantic or the Eastern
Atlantic parts of its range, although
fishing pressure is generally high in
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these areas. There is little information
on other potential sources of
overutilization of the species such as the
aquarium trade. Based on information in
the petition and readily available in our
files, overutilization does not appear to
be affecting the species to such a point
that a reasonable person conducting an
impartial scientific review would
conclude that the petitioned action may
be warranted.
(C) Disease or Predation
Disease and predation are not
identified as primary threats to the
species in the petition. Although the
petition asserts that whitespotted eagle
rays may be more susceptible to disease
and parasitic infection in the face of
other stressors, there is no evidence in
the petition indicating that disease or
predation are negatively impacting the
species.
(D) Inadequacy of Existing Regulatory
Mechanisms
According to the petition, current
regulatory mechanisms are inadequate
to protect the whitespotted eagle ray
from threats posed by fisheries.
Generally, the petition states that the
lack of research, monitoring plans,
protected areas, species management,
and education (as determined by Dulvy
et al. 2021) contribute to the species’
decline. In the United States, while
Florida has prohibited the harvest,
possession, landing, purchase, sale, or
exchange of the species in state waters
for over two decades, neighboring states
do not have similar regulatory measures.
The petition cites Dulvy et al. (2021) in
its assertion that similar actions in other
states ‘‘could contribute to the
conservation of the species.’’ The
petition concludes that because harvest
is allowed in nearby state and federal
waters, regulatory measures are
inadequate; however, the petition fails
to discuss why the lack of regulations is
inadequate to address the threats. As
discussed in Population Status and
Trends above, the species has an
increasing population trend in the
Western Central Atlantic and it is not
clear why further regulation would be
needed in this area. Internationally, 13
of the top 20 shark-fishing nations have
completed and implemented National
Plans of Action for elasmobranchs
(Dulvy et al. 2021), and the petition
argues that this leaves whitespotted
eagle rays vulnerable to threats globally.
It is not clear if this statistic is relevant
to the whitespotted eagle ray, or where
in the species’ range regulatory actions
are lacking. Overall, the petition does
not provide substantive information
regarding the existing regulatory
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mechanisms for the species outside of
the United States, or on whether they
are inadequate to manage fisheries for
the species. Unsupported conclusions
are not considered ‘‘substantial
information’’ under our regulations (50
CFR 424.14(h)(1)(i)).
The petition also argues that current
regulatory mechanisms are inadequate
to protect the whitespotted eagle ray
from threats posed by climate change.
While the petition discusses ways in
which domestic and international
regulatory measures are not sufficient to
reduce greenhouse gas emissions, it
remains unclear to what degree climate
change is impacting or will impact the
species in particular, and therefore,
whether additional regulations are
needed to address the impact of climate
change on the species.
Altogether, we find that the
information presented in the petition
does not comprise substantial scientific
or commercial information indicating
inadequacies of existing regulatory
mechanisms such that a reasonable
person conducting an impartial
scientific review would conclude that
listing may be warranted.
(E) Other Natural or Manmade Factors
Affecting Its Continued Existence
Finally, the petition discusses threats
of noise, chemical pollution, plastic
pollution, and human disturbance. We
considered information provided on the
impacts of noise, chemical pollution,
and human disturbance (development
and dredging) under (A) Present or
Threatened Destruction, Modification,
or Curtailment of Habitat or Range,
above. We considered information
provided on the impact of human
disturbance through fisheries bycatch/
entanglement in fishing gear in (B)
Overutilization for commercial,
recreational, scientific, or educational
purposes, above. The petition very
briefly mentions the species’
susceptibility to boat strikes as it
inhabits coastal waters, although,
beyond two individual whitespotted
eagle rays with scars from boat strikes
documented by Bassos-Hull et al.
(2014), the petition does not provide
any discussion of the frequency of, or
impact of, boat strikes on the species.
Ingestion of microplastics has been
shown to result in deleterious effects
such as inflammation, metabolic
disruption, compromised intestinal
function, and behavioral changes in
bony fishes (Pinho et al. 2022).
Microplastics can also absorb POPs and
other contaminants, leading to further
contaminant exposure when ingested
(Pinho et al. 2022). However, no
information is presented in the petition
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on the effect of microplastic ingestion in
batoids. While microplastic ingestion
poses a potential threat to the
whitespotted eagle ray, the
physiological impacts to individual rays
and population-level impacts on
survival and fitness remain
unaddressed. We therefore find that
there is not substantial scientific or
commercial information provided in the
petition indicating that the other natural
or manmade factors named in the
petition are impacting the species to
such a degree that a reasonable person
conducting an impartial scientific
review would conclude that listing may
be warranted.
Management Plan as recommended by
the Mid-Atlantic Fishery Management
Council. This action proposes to set the
2024 Illex squid and 2024–2026 longfin
squid specifications and reaffirms the
2024 chub mackerel and butterfish
specifications. The implementing
regulations for the Mackerel, Squid, and
Butterfish Fishery Management Plan
require us to publish specifications
every fishing year for each of these
species and to provide an opportunity
for public comment. The proposed
specifications are intended to establish
allowable harvest levels that will
prevent overfishing, consistent with the
most recent scientific information.
Petition Finding
DATES:
After thoroughly reviewing the
information presented in the petition in
the context of information readily
available in our files, we conclude the
petition does not present substantial
scientific or commercial information
indicating that the petitioned action
may be warranted.
References Cited
A complete list of all references cited
herein is available upon request (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.).
Dated: April 15, 2024.
Samuel D. Rauch III,
Deputy Assistant Administrator for
Regulatory Programs, National Marine
Fisheries Service.
[FR Doc. 2024–08340 Filed 4–18–24; 8:45 am]
BILLING CODE 3510–22–P
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
50 CFR Part 648
[Docket No. 240408–0102]
RIN 0648–BM79
Fisheries of the Northeastern United
States; 2024–2026 Specifications for
the Atlantic Mackerel, Squid, and
Butterfish Fishery Management Plan
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Proposed rule, request for
comments.
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AGENCY:
NMFS proposes the 2024–
2026 specifications for the Mackerel,
Squid, and Butterfish Fishery
SUMMARY:
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Public comments must be
received by May 20, 2024.
Copies of supporting
documents used by the Mid-Atlantic
Fishery Management Council, including
the draft Supplemental Information
Report (SIR) and the Regulatory
Flexibility Act (RFA) analysis are
available from: Dr. Christopher M.
Moore, Executive Director, Mid-Atlantic
Fishery Management Council, 800 North
State Street, Suite 201, Dover, DE 19901,
telephone (302) 674–2331.
A plain language summary of this
proposed rule is available at https://
www.regulations.gov/docket/NOAANMFS-2023-0154. You may submit
comments on this document, identified
by NOAA–NMFS–2023–0154, by the
following method:
• Electronic Submission: Submit all
electronic public comments via the
Federal e-Rulemaking Portal. Visit
https://www.regulations.gov and
NOAA–NMFS–2023–0154 in the Search
box. Click on the ‘‘Comment’’ icon,
complete the required fields, and enter
or attach your comments.
Instructions: Comments sent by any
other method, to any other address or
individual, or received after the end of
the comment period, may not be
considered by NMFS. All comments
received are a part of the public record
and will generally be posted for public
viewing on https://www.regulations.gov
without change. All personal identifying
information (e.g., name, address, etc.),
confidential business information, or
otherwise sensitive information
submitted voluntarily by the sender will
be publicly accessible. NMFS will
accept anonymous comments (enter ‘‘N/
A’’ in the required fields if you wish to
remain anonymous).
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Louis Forristall, Fishery Management
Specialist, (978) 281–9321.
SUPPLEMENTARY INFORMATION:
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Background
This rule proposes specifications,
which are the combined suite of
commercial and recreational catch
levels established for one or more
fishing years, for longfin and Illex squid,
and reaffirms previously announced
projected specifications for butterfish
and chub mackerel. Section 302(g)(1)(B)
of the Magnuson-Stevens Fishery
Conservation and Management Act
(Magnuson-Stevens Act) states that the
Scientific and Statistical Committee
(SSC) for each regional fishery
management council shall provide its
Council ongoing scientific advice for
fishery management decisions,
including recommendations for
acceptable biological catch (ABC),
preventing overfishing, ensuring
maximum sustainable yield, and
achieving rebuilding targets. The ABC is
a level of catch that accounts for the
scientific uncertainty in the estimate of
the stock’s defined overfishing limit
(OFL).
The regulations implementing the
fishery management plan (FMP) require
the Mid-Atlantic Fishery Management
Council’s (Council) Mackerel, Squid,
and Butterfish Monitoring Committee to
develop specification recommendations
for each species based upon the ABC
advice of the Council’s SSC. The FMP
regulations also require the specification
of annual catch limits (ACL) and
accountability measure (AM) provisions
for butterfish. Both squid species are
exempt from the ACL/AM requirements
because they have a life cycle of less
than one year. In addition, the
regulations require the specification of
domestic annual harvest (DAH), the
butterfish mortality cap in the longfin
squid fishery, and initial optimum yield
(IOY) for both squid species.
On July 27, 2023 (88 FR 48389),
NMFS published a final rule in the
Federal Register implementing the 2023
specifications for the chub mackerel,
butterfish, longfin squid, and Illex squid
fisheries. This included projected 2024
specifications for butterfish and
projected 2024–2025 specifications for
chub mackerel.
The Council’s SSC met in March,
May, and July 2023 to reevaluate the
longfin squid, Illex squid, chub
mackerel, and butterfish 2024
specifications based upon the latest
information. At those meetings, the SSC
concluded that no adjustments to these
species’ ABCs were warranted.
Proposed 2024–2026 Longfin Squid
Specifications
NMFS proposes to maintain the 2023
longfin squid ABC of 23,400 metric tons
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Agencies
[Federal Register Volume 89, Number 77 (Friday, April 19, 2024)]
[Proposed Rules]
[Pages 28707-28713]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-08340]
[[Page 28707]]
=======================================================================
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DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric Administration
50 CFR Parts 223 and 224
[Docket No. 240212-0044; RTID 0648-XR130]
Endangered and Threatened Wildlife; 90-Day Finding on a Petition
To List the Whitespotted Eagle Ray as Threatened or Endangered Under
the Endangered Species Act
AGENCY: National Marine Fisheries Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA), Commerce.
ACTION: Notification of 90-day petition finding.
-----------------------------------------------------------------------
SUMMARY: We, NMFS, announce a 90-day finding on a petition under the
Endangered Species Act (ESA) to list the whitespotted eagle ray
(Aetobatus narinari) as a threatened or endangered species and to
designate critical habitat concurrent with the listing. We find that
the petition does not present substantial scientific or commercial
information indicating that the petitioned action may be warranted.
DATES: These findings were made on April 19, 2024.
ADDRESSES: Copies of the petition and related materials are available
from the NMFS website at https://www.fisheries.noaa.gov/national/endangered-species-conservation/negative-90-day-findings.
FOR FURTHER INFORMATION CONTACT: Adrienne Lohe, NMFS Office of
Protected Resources, (301) 427-8442, [email protected].
SUPPLEMENTARY INFORMATION:
Background
On April 6, 2023, we received a petition from the Defend Them All
Foundation to list the whitespotted eagle ray, Aetobatus narinari, as a
threatened or endangered species under the ESA and to designate
critical habitat concurrent with the listing. The petition asserts that
this species is threatened by four of the five ESA section 4(a)(1)
factors: (1) present or threatened destruction, modification, or
curtailment of its habitat or range; (2) overutilization for commercial
and recreational purposes; (3) inadequacy of existing regulatory
mechanisms; and (4) other natural or manmade factors. The petition
requests that if the species is listed as threatened or endangered, we
promulgate a regulation under section 4(e) of the ESA for species
similar in appearance to the whitespotted eagle ray, and if we
determine the whitespotted eagle ray warrants listing as a threatened
species, we promulgate a protective regulation under section 4(d) of
the ESA. The petition is available online (see ADDRESSES).
ESA Statutory, Regulatory, and Policy Provisions and Evaluation
Framework
Section 4(b)(3)(A) of the ESA of 1973, as amended (16 U.S.C. 1531
et seq.), requires, to the maximum extent practicable, that within 90
days of receipt of a petition to list a species as threatened or
endangered, the Secretary of Commerce make a finding on whether that
petition presents substantial scientific or commercial information
indicating that the petitioned action may be warranted, and to promptly
publish such finding in the Federal Register (16 U.S.C. 1533(b)(3)(A)).
When it is found that substantial scientific or commercial information
in a petition indicates the petitioned action may be warranted (a
``positive 90-day finding''), we are required to promptly commence a
review of the status of the species concerned during which we will
conduct a comprehensive review of the best available scientific and
commercial information. In such cases, we conclude the review with a
finding as to whether, in fact, the petitioned action is warranted
within 12 months of receipt of the petition (16 U.S.C. 1533(b)(3)(B)).
Because the finding at the 12-month stage is based on a more thorough
review that encompasses all the best available information, as compared
to the narrow scope of review at the 90-day stage, a ``may be
warranted'' finding does not prejudge the outcome of the status review.
Under the ESA, a listing determination may address a species, which
is defined to also include subspecies and any vertebrate distinct
population segment (DPS) that interbreeds when mature (16 U.S.C.
1532(16)). A joint NMFS-U.S. Fish and Wildlife Service (USFWS)
(jointly, ``the Services'') policy clarifies the Services'
interpretation of the phrase ``distinct population segment'' for the
purposes of listing, delisting, and reclassifying a species under the
ESA (61 FR 4722, February 7, 1996). A species, subspecies, or DPS is
``endangered'' if it is in danger of extinction throughout all or a
significant portion of its range, and ``threatened'' if it is likely to
become endangered within the foreseeable future throughout all or a
significant portion of its range (ESA sections 3(6) and 3(20),
respectively, 16 U.S.C. 1532(6) and (20)). Pursuant to the ESA and our
implementing regulations, we determine whether species are threatened
or endangered based on any one or a combination of the following five
ESA section 4(a)(1) factors: (1) the present or threatened destruction,
modification, or curtailment of habitat or range; (2) overutilization
for commercial, recreational, scientific, or educational purposes; (3)
disease or predation; (4) inadequacy of existing regulatory mechanisms
to address identified threats; or (5) any other natural or manmade
factors affecting the species' existence (16 U.S.C. 1533(a)(1), 50 CFR
424.11(c)).
ESA-implementing regulations issued jointly by NMFS and USFWS (50
CFR 424.14(h)(1)(i)) define ``substantial scientific or commercial
information'' in the context of reviewing a petition to list, delist,
or reclassify a species as ``credible scientific or commercial
information in support of the petition's claims such that a reasonable
person conducting an impartial scientific review would conclude that
the action proposed in the petition may be warranted.'' Conclusions
drawn in the petition without the support of credible scientific or
commercial information will not be considered ``substantial
information.'' In accordance with 50 CFR 424.14(h)(1)(ii), in reaching
the initial (90-day) finding on the petition, we will consider the
information described in subsections 50 CFR 424.14(c), (d), and (g) (if
applicable).
Our determination as to whether the petition provides substantial
scientific or commercial information indicating that the petitioned
action may be warranted will depend in part on the degree to which the
petition includes the following types of information: (1) information
on current population status and trends and estimates of current
population sizes and distributions, both in captivity and the wild, if
available; (2) identification of the factors under section 4(a)(1) of
the ESA that may affect the species and where these factors are acting
upon the species; (3) whether and to what extent any or all of the
factors alone or in combination identified in section 4(a)(1) of the
ESA may cause the species to be an endangered species or threatened
species (i.e., the species is currently in danger of extinction or is
likely to become so within the foreseeable future), and, if so, how
high in magnitude and how imminent the threats to the species and its
habitat are; (4) information on adequacy of regulatory protections and
effectiveness of conservation activities by states as well as other
parties, that have been initiated or that are ongoing, that may protect
the species or its habitat; and (5) a complete, balanced representation
of
[[Page 28708]]
the relevant facts, including information that may contradict claims in
the petition. See 50 CFR 424.14(d).
If the petitioner provides supplemental information before the
initial finding is made and states that it is part of the petition, the
new information, along with the previously submitted information, is
treated as a new petition that supersedes the original petition, and
the statutory timeframes will begin when such supplemental information
is received. See 50 CFR 424.14(g).
We may also consider information readily available at the time the
determination is made (50 CFR 424.14(h)(1)(ii)). We are not required to
consider any supporting materials cited by the petitioner if the
petitioner does not provide electronic or hard copies, to the extent
permitted by U.S. copyright law, or appropriate excerpts or quotations
from those materials (e.g., publications, maps, reports, letters from
authorities). See 50 CFR 424.14(c)(6).
The ``substantial scientific or commercial information'' standard
must be applied in light of any prior reviews or findings we have made
on the listing status of the species that is the subject of the
petition (50 CFR 424.14(h)(1)(iii)). Where we have already conducted a
finding on, or review of, the listing status of that species (whether
in response to a petition or on our own initiative), we will evaluate
any petition received thereafter seeking to list, delist, or reclassify
that species to determine whether a reasonable person conducting an
impartial scientific review would conclude that the action proposed in
the petition may be warranted despite the previous review or finding.
Where the prior review resulted in a final agency action--such as a
final listing determination, 90-day not-substantial finding, or 12-
month not-warranted finding--a petitioned action will generally not be
considered to present substantial scientific and commercial information
indicating that the action may be warranted unless the petition
provides new information or analysis not previously considered.
At the 90-day finding stage, we do not conduct additional research,
and we do not solicit information from parties outside the agency to
help us in evaluating the petition. We will accept the petitioners'
sources and characterizations of the information presented if they
appear to be based on accepted scientific principles, unless we have
specific information in our files that indicates the petition's
information is incorrect, unreliable, obsolete, or otherwise irrelevant
to the requested action. Information that is susceptible to more than
one interpretation or that is contradicted by other available
information will not be dismissed at the 90-day finding stage, so long
as it is reliable and a reasonable person conducting an impartial
scientific review would conclude it supports the petitioners'
assertions. In other words, conclusive information indicating the
species may meet the ESA's requirements for listing is not required to
make a positive 90-day finding. We will not conclude that a lack of
specific information alone necessitates a negative 90-day finding if a
reasonable person conducting an impartial scientific review would
conclude that the unknown information itself suggests the species may
be at risk of extinction presently or within the foreseeable future.
To make a 90-day finding on a petition to list a species, we
evaluate whether the petition presents substantial scientific or
commercial information indicating the subject species may be either
threatened or endangered, as defined by the ESA. First, we evaluate
whether the information presented in the petition, in light of the
information readily available in our files, indicates that the
petitioned entity constitutes a ``species'' eligible for listing under
the ESA. Next, we evaluate whether the information indicates that the
species faces an extinction risk such that listing, delisting, or
reclassification may be warranted; this may be indicated in information
expressly discussing the species' status and trends, or in information
describing impacts and threats to the species. We evaluate any
information on specific demographic factors pertinent to evaluating
extinction risk for the species (e.g., population abundance and trends,
productivity, spatial structure, age structure, sex ratio, diversity,
current and historical range, habitat integrity or fragmentation), and
the potential contribution of identified demographic risks to
extinction risk for the species. We then evaluate the potential links
between these demographic risks and the causative impacts and threats
identified in section 4(a)(1).
Information presented on impacts or threats should be specific to
the species and should reasonably suggest that one or more of these
factors may be operative threats that act or have acted on the species
to the point that it may warrant protection under the ESA. Broad
statements about generalized threats to the species, or identification
of factors that could negatively impact a species, do not constitute
substantial information indicating that listing may be warranted. We
look for information indicating that not only is the particular species
exposed to a factor, but that the species may be responding in a
negative fashion; then we assess the potential significance of that
negative response.
Many petitions identify risk classifications made by
nongovernmental organizations, such as the International Union for
Conservation of Nature (IUCN), the American Fisheries Society, or
NatureServe, as evidence of extinction risk for a species. Risk
classifications by other organizations or made under other Federal or
state statutes may be informative, but such classification alone will
not provide a sufficient rationale for a positive 90-day finding under
the ESA. For example, as explained by NatureServe, their assessments of
a species' conservation status do not constitute a recommendation by
NatureServe for listing under the U.S. Endangered Species Act because
NatureServe assessments have different criteria, evidence requirements,
purposes and taxonomic coverage than government lists of endangered and
threatened species, and therefore these two types of lists should not
be expected to coincide (https://explorer.natureserve.org/AboutTheData/DataTypes/ConservationStatusCategories). Additionally, species
classifications under IUCN and the ESA are not equivalent; data
standards, criteria used to evaluate species, and treatment of
uncertainty are also not necessarily the same. Thus, when a petition
cites such classifications, we will evaluate the source of information
that the classification is based upon in light of the ESA standards on
extinction risk and impacts or threats discussed above.
Analysis of the Petition
We have reviewed the petition, the literature cited in the
petition, and other literature and information readily available in our
files. In this section, we provide a summary of this information and
present our analysis of whether this information indicates that the
petitioned action may be warranted.
Species Description
The whitespotted eagle ray, A. narinari, is a large (up to 230
centimeters (cm) disc width (DW)) benthopelagic batoid found in warm-
temperate and tropical coastal waters (Dulvy et al. 2021). The species
was previously thought to have a circumglobal distribution, although
morphological, parasitological, and genetic evidence indicates that the
species is limited to the Atlantic, while eagle rays in the Pacific and
Indian
[[Page 28709]]
Oceans constitute separate species (Sales et al. 2019). The petition
cites Eschmeyer's Catalog of Fishes (Fricke et al. 2020) and Dulvy et
al. (2021) in its assertion that the species spans the western and
eastern Atlantic. This contradicts Sales et al. (2019)'s conclusion
that based on nuclear and mitochondrial markers, A. narinari is
restricted to the western Atlantic, and samples from South Africa
formed a monophyletic clade closest to another species of eagle ray,
Aetobatus ocellatus, found in the Indian Ocean. Despite the apparent
ongoing scientific debate surrounding the taxonomy of the whitespotted
eagle ray and the genus as a whole, there is no further discussion of
the taxonomic status of A. narinari in the petition. The petition
asserts that the whitespotted eagle ray ranges from Cape Hatteras,
North Carolina, to Rio de Janeiro, Brazil, including the Gulf of
Mexico, the Bahamas, and the Caribbean Islands, and in the eastern
Atlantic, from Mauritania south to Angola, and possibly South Africa
(Dulvy et al. 2021). We accept the petition's characterization of the
species' taxonomy and distribution because the petition provides recent
and reputable references for this conclusion, and because we find that
a reasonable person conducting an impartial scientific review would
conclude that the petitioners' assertions are reasonably supported.
Whitespotted eagle rays occur in the neritic zone from the low-tide
mark to water depths of 60 meters (m), and are often associated with
coral reefs, lagoons, and estuaries (Cerutti-Pereyra et al. 2018, Dulvy
et al. 2021). They are highly mobile and display both migratory and
resident behavior (Bassos-Hull et al. 2014; Sellas et al. 2015; De
Groot et al. 2021). Whitespotted eagle rays are mid-trophic level
predators that forage for invertebrates (often bivalves, gastropods,
and crustaceans) in the seabed sediment, serving as bioturbators
(Ajieman et al. 2012; Flowers et al. 2021). The species is often
observed as solitary individuals, but can also be seen in large
aggregations of up to several hundred individuals (Bassos-Hull et al.
2014; Tagliafico et al. 2012). Size at maturity has been estimated at
approximately 115-130 cm DW for males and slightly larger for females
(Ara[uacute]jo et al. 2022; Bassos-Hull et al. 2014; Taglifico et al.
2012). Age at maturity is estimated at 4 to 6 years (Cerutti-Pereyra et
al. 2018). Whitespotted eagle rays exhibit matrotrophic viviparity in
which embryos are nourished through uterine secretions and born live
(Ara[uacute]jo et al. 2022). Between one and five young are produced in
each litter after a gestation period of 12 months (Dulvy et al. 2021).
Generation length for the species is estimated at 10 years, inferred
from the slightly larger A. ocellatus which has a generation length of
12 years (Dulvy et al. 2021).
Population Status and Trends
The petition asserts that the whitespotted eagle ray has undergone
dramatic population decline, largely relying on the IUCN Red List
Assessment of the species as ``endangered'' (Dulvy et al. 2021). This
assessment concludes that the whitespotted eagle ray ``is suspected''
to have experienced a population reduction of 50-79 percent over the
past three generation lengths (30 years) due to ``actual and potential
levels of fishing pressure'' (Dulvy et al. 2021).
Dulvy et al. (2021) use population trend data from baited remote
underwater videos (BRUVs) in Belize from 2009-2018 (G. Clementi and D.
Chapman, unpublished data 2019) and a survey in Mexico spanning 2000-
2014 (J-C. P[eacute]rez Jim[eacute]nez unpublished data 2019) to
perform Bayesian state-space population trend analysis over three
generation lengths (30 years). The BRUV data from Belize indicated an
increase in abundance of 7.5 percent annually, while data from Mexico
indicate a 0.95 percent decrease in abundance annually over the
respective time series. Additionally, Dulvy et al. (2021) state that in
the southern Gulf of Mexico, interviews with fishermen indicated catch
declines from 30-40 rays per night/trip from 1990 to 2000 to 10-15 rays
per night/trip in 2019 (Cuevas-Zimbr[oacute]n et al. 2011; J-C.
P[eacute]rez Jim[eacute]nez unpublished data 2019, as cited in Dulvy et
al. 2021). Considering the two available population trend datasets
(Belize 2009-2018 and Mexico 2000-2014) and extrapolating over three
generation lengths, however, Dulvy et al. (2021) found an increasing
population trend of 1.32 percent per year in the Western Central
Atlantic.
Outside of these datasets, there is little information available on
whitespotted eagle ray population trends. Dulvy et al. (2021) rely on
the assumption that where the species is known to be targeted in
artisanal fisheries or bycaught in commercial fisheries (e.g., in
Colombia, Venezuela, the Guianas; see ESA Section 4(a)(1) Factors), it
is experiencing population declines. In Brazil, personal communications
cited in Dulvy et al (2021) from 2018 indicate that landings of the
species in gillnets at Pernambuco have declined by about 80 percent
since 1995, and that the species has also declined in S[atilde]o Paulo,
where fishery monitoring between 1996 and 2002 only recorded five
individuals. Dulvy et al. (2021) write that because unmanaged fisheries
in Brazil have led to declines in other species, ``. . . there is no
reason not to suspect that this species has also been reduced in
numbers in that area.'' Based on suspected high exploitation levels and
lack of adequate management, their assessment indicates that it is
``suspected that this species has undergone a population reduction of
50-79 percent over the past three generation lengths (30 years) in the
Atlantic South American part of its range'' (Dulvy et al. 2021). It is
unclear whether the personal communications cited by Dulvy et al.
(2021) are based on time series data or take into account fishing
effort or other factors. Therefore, it is unknown how accurately this
estimate reflects the abundance of whitespotted eagle rays across this
region. We find that, based on the information presented in the
petition, a reasonable person conducting an impartial scientific review
would conclude that some level of population decline may be occurring
in the Southwest Atlantic, although there is not sufficient credible
scientific or commercial information to conclude that the species has
declined by 50-79 percent.
Trends specific to A. narinari are unavailable in the Eastern
Atlantic, and therefore Dulvy et al. (2021) use reported catch levels
of elasmobranchs as a proxy for whitespotted eagle ray population
trends here. Dulvy et al. (2021) report the decline in average
elasmobranch catch per unit effort by 71 percent from 1970-2015 and
simultaneous increase in average elasmobranch catch by over 250 percent
across the West Africa region, implying a dramatic increase in fishing
effort. Trends in elasmobranch landings during this period of
increasing fishing effort are described for individual countries in the
region. In Mauritania, landings increased by 246 percent over 1992-
2015; since then effort has been stable and landings continued to
increase. In Senegal, reconstructed landings (which include an estimate
of unreported landings data, therefore increasing uncertainty) showed a
30-80 percent decline from 2001-2016, suggesting population decline. In
Guinea-Bissau, reconstructed landings declined 22 percent from 2012 to
2016 after rising since the 1960s. In Cameroon, there has been a 96
percent decline in reconstructed landings from 2007-2016
[[Page 28710]]
after rising since the 1960s. There have been few recent observations
of the species in the Republic of Congo, Mauritania, Gabon, Senegal,
Gambia, Guinea-Bissau, Sierra Leone, Ghana, Nigeria, Cameroon or
Angola; in certain cases, this is despite sightings of species with
similar habitat needs and catchability. However, some confounding
factors are at play; for example, in Ghana there are few shallow
fishing gears likely to take the species (Dulvy et al. 2021). Dulvy et
al. (2021) take the above information to indicate that the species has
largely disappeared from the Eastern Atlantic part of its range. Dulvy
et al. (2021) conclude ``it is suspected that a population reduction of
more than 80 percent has occurred in the past three generation lengths
(30 years)'' (Dulvy et al. 2021). While trends in elasmobranch catch
and fishing effort are concerning, they do not provide enough species-
specific evidence for us to conclude that the whitespotted eagle ray in
particular has followed these same trends. Further, neither the
petition nor Dulvy et al. (2021) provide information on historical
population sizes in the areas with few recent observations. We find
that, based on the information presented in the petition, a reasonable
person conducting an impartial scientific review would conclude that
some level of population decline may be occurring in the Eastern
Atlantic, although there is not sufficient credible scientific or
commercial information to conclude that the species has declined by
more than 80 percent.
Altogether, Dulvy et al. (2021) conclude that the whitespotted
eagle ray has undergone a population reduction of 50-79 percent over
the past three generation lengths across its range. However, a
reasonable person would conclude that this information is not supported
by credible scientific information and is therefore unreliable given
the only available quantitative population data for whitespotted eagle
rays from Belize and Mexico indicate that the population is increasing
there. Species-specific information on trends is unavailable from the
Southwest Atlantic, the Eastern Central Atlantic, and Southeast
Atlantic, although Dulvy et al. (2021) suspect population reductions in
these areas. While declining elasmobranch landings, few recorded
sightings of the species, and accounts of reduced catch by artisanal
fishermen are indicative of potential population declines in these
areas, we are not able to conclude that this information points to the
dramatic population declines that Dulvy et al. (2021) infer.
Outside of the IUCN Red List Assessment (Dulvy et al. 2021), the
petition discusses just one other relevant study relating to population
trends for the species. Bassos-Hull et al. (2014) observed a yearly
decrease in number of whitespotted eagle rays observed in both aerial
and boat-based surveys in the eastern Gulf of Mexico off southwest
Florida from 2008-2013. The authors note, however, that without further
study, it is unclear whether this is due to a true decrease in
abundance over time or other factors such as sampling bias, a shift in
range, or a clustering phenomenon in the study area during the 2008-
2009 season (Bassos-Hull et al. 2014).
In all, we do not find that the information presented in the
petition constitutes credible scientific information that indicates a
dramatic decrease in whitespotted eagle ray abundance across its range
as asserted by the petitioners. In fact, the region with available
time-series population data shows an increasing population trend for
the species. Information presented in the petition only points to
potential abundance decreases in other parts of its range with little
supporting information; the principal study the petition relies on for
this assertion is unreliable because it rests on unsupported
assumptions (i.e., the assumptions that, where the species is known to
be targeted in artisanal fisheries or bycaught in commercial fisheries,
it is experiencing population declines; and that, where elasmobranch
catch rates are declining, the species is experiencing population
declines) rather than data. Therefore, we do not find that the petition
offers substantial scientific or commercial information that would
suggest that the species' current population status and trends may
warrant the petitioned action.
ESA Section 4(a)(1) Factors
The petition asserts that four of the five factors in section
4(a)(1) of the ESA are adversely affecting the whitespotted eagle ray:
(A) present or threatened destruction, modification, or curtailment of
habitat or range; (B) overutilization for commercial, recreational,
scientific, or educational purposes; (D) inadequacy of existing
regulatory mechanisms; and (E) other natural or manmade factors
affecting its continued existence. While the petition does not state
that factor (C), disease or predation, poses a threat to the species,
it does argue that the species may be more susceptible to disease in
combination with other stressors. In the following sections, we discuss
the information presented in the petition, viewed in the context of
information readily available in our files where applicable, regarding
threats to this species.
(A) Present or Threatened Destruction, Modification, or Curtailment of
Habitat or Range
The petition describes the effect of destructive fishing practices,
specifically bottom trawling, on coastal ocean habitats. Although the
petition discusses negative impacts of trawling, including damage and
destruction of biotic and abiotic seabed structures, increased water
column turbidity, release of contaminants contained in seabed sediment,
and reduced food availability for bottom-feeders, the petition includes
no discussion of specific areas where bottom trawling activities occur
within the range of the whitespotted eagle ray, or the intensity of
bottom trawling activity. While the impacts of bottom trawling are
concerning for certain marine habitats generally, the extent to which
whitespotted eagle rays in particular may be threatened by such impacts
is not clear based on the information in the petition.
The petition similarly discusses impacts of coastal development and
dredging, as well as resulting pollution and suspension of sediment, on
marine habitats. Suspension of sediment resulting from dredging can
cause physiological stress and changes in foraging and predation
behavior in marine fishes (Wenger et al. 2016). Contaminants released
from disturbed sediment (e.g., metals and persistent organic pollutants
(POPs) such as polycyclic aromatic hydrocarbons (PAHs), polychlorinated
biphenyls (PCBs), and dichlorodiphenyltrichloroethane (DDT)), have been
shown to accumulate in, and have further negative impacts on marine
fishes, including on the reproductive success of adults and development
of eggs and larvae (Wenger et al. 2016). PCBs, DDT and
hexachlorobenzene (HCB) were detected in whitespotted eagle rays off
Australia, sometimes in high enough concentrations to cause possible
negative long-term impacts (Cagnazzi et al. 2019). Without further
study, however, it remains unclear whether observed contaminant loads
lead to lower survival and/or lower reproductive success in
elasmobranchs (Cagnazzi et al. 2019). The petition also asserts that
sounds from dredging activity may cause harm to whitespotted eagle rays
based on a study that found the sound of boat motors to disturb A.
ocellatus, causing these rays to exhibit
[[Page 28711]]
escape behavior when foraging (Berthe and Lecchini 2016). It is unclear
whether such disruptions of foraging behavior would lead to population-
level impacts to A. narinari, or whether noise from dredging would
cause a similar response; neither of these points are addressed in the
petition. Generally, the whitespotted eagle ray is vulnerable to
coastal development as it uses shallow, coastal areas for breeding and
feeding (Dulvy et al. 2021). While coastal development has the
potential to negatively impact whitespotted eagle rays, specific
information indicating how and where dredging and development are
impacting the whitespotted eagle ray's habitat is not provided in the
petition, and thus the degree to which the population may be threatened
by this stressor is unclear.
The petition discusses, and provides references regarding, direct
and indirect impacts of climate change, including physical and chemical
changes to ocean habitats (e.g., ocean warming and increasing ocean
acidity), changes in ocean circulation patterns, declines in primary
productivity, range shifts, increasing occurrences of extreme weather
events and harmful algal blooms, and physiological and behavioral
impairments in certain marine fishes. The specific effects of climate
change on ray ecology are largely unknown, and few studies have
investigated the impacts of climate change on the whitespotted eagle
ray. Specific impacts that may be of concern to the whitespotted eagle
ray that are discussed in the petition include decreased aragonite and
calcite availability due to ocean acidification, which can hinder the
ability of calcifying organisms such as bivalves and corals to build
their skeletons (Branch et al. 2013; Kroeker et al. 2013). This could
result in reduced availability of certain prey species and coral reef
habitat for the whitespotted eagle ray to utilize. The petition cites
Flowers et al. (2021) in its assertion that range and habitat shifts
may result in negative effects on ray fitness through decreased ability
to find food, increased predation risk and increased competition.
However, the same study points out that vulnerability to climate change
varies by species, and, in certain cases, climate change may have
beneficial outcomes for rays (Flowers et al. 2021). The petition also
points out that sharks and rays in particular exhibit thermotaxis, a
behavior that involves moving to waters of different temperatures
throughout the day. Therefore, beyond large-scale geographic range
shifts that may occur as a result of climate change, changes in such
small-scale movements may also be significant to the fitness and
survival of sharks and rays (Vilmar and Di Santo 2022). In an
assessment of shark and ray behavior in response to gradual increases
in sea surface temperature as well as acute temperature anomalies
caused by El Ni[ntilde]o Southern Oscillation over 27 years, A.
narinari exhibited significantly increased relative abundance at higher
temperatures in both cases (Osgood et al. 2021). While this study took
place in the eastern Pacific and taxonomic revisions have limited A.
narinari to the Atlantic (see Species Description), the results suggest
that eagle ray species such as A. narinari could be more tolerant of
temperature extremes than other elasmobranchs (Osgood et al. 2021).
Although climate change has the potential to adversely impact the
whitespotted eagle ray, the degree to which whitespotted eagle ray
individuals or populations have been or will be affected is unclear.
Therefore, the degree to which climate change threatens the
whitespotted eagle ray is not clear based on the information in the
petition.
In summary, the petition and the references cited therein do not
comprise substantial scientific or commercial information indicating
there is present or threatened destruction, modification, or
curtailment of the whitespotted eagle ray's habitat or range such that
a reasonable person conducting an impartial scientific review would
conclude that listing may be warranted.
(B) Overutilization for Commercial, Recreational, Scientific, or
Educational Purposes
The petition identifies overutilization for commercial purposes as
the greatest threat to the whitespotted eagle ray. The species is
captured as incidental bycatch and, less commonly, in targeted
fisheries (Tagliafico et al. 2012).
In the Western Central Atlantic, artisanal fisheries targeting the
species are known to exist (but ``are not well described'') in Mexico,
Cuba, the Caribbean coast of Colombia, and Venezuela (Dulvy et al.
2021). In Colombia, the whitespotted eagle ray is taken in gillnet,
longline, and trawl gears (Dulvy et al. 2021). In both Colombia and
Venezuela, artisanal fisheries are widespread, intense, and lack
management (Dulvy et al. 2021). A study of the small, directed fishery
in northeastern Venezuela found that while the time series analyzed
(August 2005 to December 2007) is too short to infer changes in
population abundance, the capture of juvenile, mature, and pregnant
individuals is of concern (Tagliafico et al. 2012). An artisanal
fishery targeting A. narinari exists off the coast of the State of
Campeche in the southern Gulf of Mexico driven by the traditional
consumption of this species there (Cuevas-Zimbr[oacute]n et al. 2011).
According to fishermen interviewed, catches of A. narinari have
declined over recent decades due to overfishing of the species as well
as its molluscan prey (Cuevas-Zimbr[oacute]n et al. 2011). Data from
Mexico's National Aquaculture and Fisheries Commission (CONAPESCA)
indicate that in 2013, A. narinari was the second-most captured batoid
in the region at about 40 tons each year (Rodriguez-Santiago et al.
2016). Whitespotted eagle rays have also been caught as bycatch in
shark gillnet fisheries in the U.S. south Atlantic, and the petition
asserts that they are among the top bycatch species by abundance in the
observed catches (Trent et al. 1997). However, according to information
readily available in our files, which provides important context for
judging the accuracy and reliability of the information presented in
the petition, the species hasn't been observed as bycatch in this
fishery since 2008 (NOAA Fisheries Southeast Fisheries Science Center,
unpublished data). In all, despite the existence of artisanal fisheries
targeting the whitespotted eagle ray in this region as well as
interactions with commercial fisheries, available population data does
not support the conclusion that these fisheries are causing significant
population declines. Rather, available data sources indicate an
increasing population trend in the Western Central Atlantic (see
Population Status and Trends).
In the Southwest Atlantic, artisanal fisheries and commercial trawl
and longline fisheries along the coast of South America can be intense
and unmanaged, and the petition asserts this has led to the
disappearance of several elasmobranch species in the region, including
largetooth sawfish (Pristis pristis), smalltooth sawfish (Pristis
pectinata), daggernose shark (Isogomphodon oxyrhynchus), and smalltail
shark (Carcharhinus porosus) (Dulvy et al. 2021). Although fishing
pressure is heavy and many of the stocks targeted by artisanal
fishermen are overexploited in this region (Dulvy et al. 2021), the
petition does not present any information about the specific fisheries
that interact with the whitespotted eagle ray, or levels of catch of
the whitespotted eagle ray.
In the Eastern Central Atlantic, sharks are targeted in artisanal
fisheries across much of the region due to demand for dried salted
shark meat (Dulvy et al.
[[Page 28712]]
2021). Specifically, drift gillnets and demersal set gillnets are used
to target sharks and rays in artisanal fisheries of Mauritania,
Nigeria, Ghana, and Cameroon (Dulvy et al. 2021). Population reductions
and some local extinctions of shark and ray species have been observed
in this region as a result of fishing pressure (Dulvy et al. 2021). The
petition states that total demersal biomass of inshore stocks in the
Gulf of Guinea is estimated to have declined by 75 percent since 1982
as a result of destructive fishing practices (Dulvy et al. 2021).
Additionally, the number of traditional and industrial fishing boats
has significantly increased since 1950 (Dulvy et al. 2021). Although
poorly managed fishing activity in this region is having negative
impacts on fish stocks generally, the petition presents no information
relating to the capture or landings of the whitespotted eagle ray in
particular.
Little information on the impact of fisheries bycatch on the
species was provided in the petition. A study examining the
physiological responses of capture on benthopelagic rays, including A.
narinari, showed elevated lactate and glucose levels lasting the length
of time that the rays were confined after capture (Rangel et al. 2021).
This is indicative of increased physiological stress, and immediate
release of captured individuals is recommended (Rangel et al. 2021).
Mortality rates or other sublethal effects of capture on the
whitespotted eagle ray were not addressed in the petition.
The petition also discusses other potential sources of
overutilization. The whitespotted eagle ray is popular in public
aquarium displays and is collected for this purpose (Dulvy et al.
2021). No further information on the impact of the aquarium trade on
the species is included in the petition. The petitioners also assert
that the species may be vulnerable to negative interactions with
shellfish farms due to their molluscan diet. Negative interactions have
been anecdotally reported in the Northwest Atlantic, although confirmed
interactions generally take place with eagle rays in the Indo-Pacific
(Dulvy et al. 2021).
In all, while the petition presents information on fisheries
targeting the whitespotted eagle ray in the Western Central Atlantic,
overutilization does not appear to be occurring based on population
increases indicated in this region. The petition does not provide
information specific to fisheries affecting the whitespotted eagle ray
in the Southwest Atlantic or the Eastern Atlantic parts of its range,
although fishing pressure is generally high in these areas. There is
little information on other potential sources of overutilization of the
species such as the aquarium trade. Based on information in the
petition and readily available in our files, overutilization does not
appear to be affecting the species to such a point that a reasonable
person conducting an impartial scientific review would conclude that
the petitioned action may be warranted.
(C) Disease or Predation
Disease and predation are not identified as primary threats to the
species in the petition. Although the petition asserts that
whitespotted eagle rays may be more susceptible to disease and
parasitic infection in the face of other stressors, there is no
evidence in the petition indicating that disease or predation are
negatively impacting the species.
(D) Inadequacy of Existing Regulatory Mechanisms
According to the petition, current regulatory mechanisms are
inadequate to protect the whitespotted eagle ray from threats posed by
fisheries. Generally, the petition states that the lack of research,
monitoring plans, protected areas, species management, and education
(as determined by Dulvy et al. 2021) contribute to the species'
decline. In the United States, while Florida has prohibited the
harvest, possession, landing, purchase, sale, or exchange of the
species in state waters for over two decades, neighboring states do not
have similar regulatory measures. The petition cites Dulvy et al.
(2021) in its assertion that similar actions in other states ``could
contribute to the conservation of the species.'' The petition concludes
that because harvest is allowed in nearby state and federal waters,
regulatory measures are inadequate; however, the petition fails to
discuss why the lack of regulations is inadequate to address the
threats. As discussed in Population Status and Trends above, the
species has an increasing population trend in the Western Central
Atlantic and it is not clear why further regulation would be needed in
this area. Internationally, 13 of the top 20 shark-fishing nations have
completed and implemented National Plans of Action for elasmobranchs
(Dulvy et al. 2021), and the petition argues that this leaves
whitespotted eagle rays vulnerable to threats globally. It is not clear
if this statistic is relevant to the whitespotted eagle ray, or where
in the species' range regulatory actions are lacking. Overall, the
petition does not provide substantive information regarding the
existing regulatory mechanisms for the species outside of the United
States, or on whether they are inadequate to manage fisheries for the
species. Unsupported conclusions are not considered ``substantial
information'' under our regulations (50 CFR 424.14(h)(1)(i)).
The petition also argues that current regulatory mechanisms are
inadequate to protect the whitespotted eagle ray from threats posed by
climate change. While the petition discusses ways in which domestic and
international regulatory measures are not sufficient to reduce
greenhouse gas emissions, it remains unclear to what degree climate
change is impacting or will impact the species in particular, and
therefore, whether additional regulations are needed to address the
impact of climate change on the species.
Altogether, we find that the information presented in the petition
does not comprise substantial scientific or commercial information
indicating inadequacies of existing regulatory mechanisms such that a
reasonable person conducting an impartial scientific review would
conclude that listing may be warranted.
(E) Other Natural or Manmade Factors Affecting Its Continued Existence
Finally, the petition discusses threats of noise, chemical
pollution, plastic pollution, and human disturbance. We considered
information provided on the impacts of noise, chemical pollution, and
human disturbance (development and dredging) under (A) Present or
Threatened Destruction, Modification, or Curtailment of Habitat or
Range, above. We considered information provided on the impact of human
disturbance through fisheries bycatch/entanglement in fishing gear in
(B) Overutilization for commercial, recreational, scientific, or
educational purposes, above. The petition very briefly mentions the
species' susceptibility to boat strikes as it inhabits coastal waters,
although, beyond two individual whitespotted eagle rays with scars from
boat strikes documented by Bassos-Hull et al. (2014), the petition does
not provide any discussion of the frequency of, or impact of, boat
strikes on the species.
Ingestion of microplastics has been shown to result in deleterious
effects such as inflammation, metabolic disruption, compromised
intestinal function, and behavioral changes in bony fishes (Pinho et
al. 2022). Microplastics can also absorb POPs and other contaminants,
leading to further contaminant exposure when ingested (Pinho et al.
2022). However, no information is presented in the petition
[[Page 28713]]
on the effect of microplastic ingestion in batoids. While microplastic
ingestion poses a potential threat to the whitespotted eagle ray, the
physiological impacts to individual rays and population-level impacts
on survival and fitness remain unaddressed. We therefore find that
there is not substantial scientific or commercial information provided
in the petition indicating that the other natural or manmade factors
named in the petition are impacting the species to such a degree that a
reasonable person conducting an impartial scientific review would
conclude that listing may be warranted.
Petition Finding
After thoroughly reviewing the information presented in the
petition in the context of information readily available in our files,
we conclude the petition does not present substantial scientific or
commercial information indicating that the petitioned action may be
warranted.
References Cited
A complete list of all references cited herein is available upon
request (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.).
Dated: April 15, 2024.
Samuel D. Rauch III,
Deputy Assistant Administrator for Regulatory Programs, National Marine
Fisheries Service.
[FR Doc. 2024-08340 Filed 4-18-24; 8:45 am]
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