Endangered and Threatened Wildlife and Plants; Review of Foreign Species That Are Candidates for Listing as Endangered or Threatened; Annual Notification of Findings on Resubmitted Petitions; Annual Description of Progress on Listing Actions, 71457-71471 [2016-24931]
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Federal Register / Vol. 81, No. 200 / Monday, October 17, 2016 / Proposed Rules
for the relevant maintenance period
with mobile source emissions at the
levels of the MVEBs.
jstallworth on DSK7TPTVN1PROD with PROPOSALS
C. What is a safety margin?
A ‘‘safety margin’’ is the difference
between the attainment level of
emissions (from all sources) and the
projected level of emissions (from all
sources) in the maintenance plan. As
noted in Table 11, the emissions in the
Cleveland area are projected to have
safety margins of 117.22 TPSD for NOX
and 28.48 TPSD for VOC in 2030 (the
total net change between the attainment
year, 2014, emissions and the projected
2030 emissions for all sources in the
Cleveland area). Similarly, there is a
safety margin of 89.24 TPSD for NOX
and 11.61 TPSD for VOC in 2020. Even
if emissions reached the full level of the
safety margin, the counties would still
demonstrate maintenance since
emission levels would equal those in
the attainment year.
As shown in Table 12 above, Ohio is
allocating a portion of that safety margin
to the mobile source sector. Specifically,
in 2020, Ohio is allocating 5.07 TPSD
and 8.03 TPSD of the VOC and NOX
safety margins, respectively. In 2030,
Ohio is allocating 4.02 TPSD and 5.72
TPSD of the VOC and NOX safety
margins, respectively. Ohio EPA is not
requesting allocation to the MVEBs of
the entire available safety margins
reflected in the demonstration of
maintenance. In fact, the amount
allocated to the MVEBs represents only
a small portion of the 2020 and 2030
safety margins. Therefore, even though
the State is requesting MVEBs that
exceed the projected on-road mobile
source emissions for 2020 and 2030
contained in the demonstration of
maintenance, the increase in on-road
mobile source emissions that can be
considered for transportation
conformity purposes is well within the
safety margins of the ozone maintenance
demonstration. Further, once allocated
to mobile sources, these safety margins
will not be available for use by other
sources.
VI. Proposed Actions
EPA is proposing to determine that
the Cleveland area has met the
requirements for redesignation under
section 107(d)(3)(E) of the CAA. EPA is
thus proposing to approve Ohio’s
request to change the legal designation
of the Cleveland area from
nonattainment to attainment for the
2008 ozone standard. EPA is also
proposing to approve, as a revision to
the Ohio SIP, the state’s maintenance
plan for the area. The maintenance plan
is designed to keep the Cleveland area
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in attainment of the 2008 ozone NAAQS
through 2030. Finally, EPA finds
adequate and is proposing to approve
the newly-established 2020 and 2030
MVEBs for the Cleveland area.
VII. Statutory and Executive Order
Reviews
Under the CAA, redesignation of an
area to attainment and the
accompanying approval of a
maintenance plan under section
107(d)(3)(E) are actions that affect the
status of a geographical area and do not
impose any additional regulatory
requirements on sources beyond those
imposed by state law. A redesignation to
attainment does not in and of itself
create any new requirements, but rather
results in the applicability of
requirements contained in the CAA for
areas that have been redesignated to
attainment. Moreover, the Administrator
is required to approve a SIP submission
that complies with the provisions of the
CAA and applicable Federal regulations.
42 U.S.C. 7410(k); 40 CFR 52.02(a).
Thus, in reviewing SIP submissions,
EPA’s role is to approve state choices,
provided that they meet the criteria of
the CAA. Accordingly, this action
merely approves state law as meeting
Federal requirements and does not
impose additional requirements beyond
those imposed by state law. For that
reason, this action:
• Is not a significant regulatory action
subject to review by the Office of
Management and Budget under
Executive Orders 12866 (58 FR 51735,
October 4, 1993) and 13563 (76 FR 3821,
January 21, 2011);
• Does not impose an information
collection burden under the provisions
of the Paperwork Reduction Act (44
U.S.C. 3501 et seq.);
• Is certified as not having a
significant economic impact on a
substantial number of small entities
under the Regulatory Flexibility Act (5
U.S.C. 601 et seq.);
• Does not contain any unfunded
mandate or significantly or uniquely
affect small governments, as described
in the Unfunded Mandates Reform Act
of 1995 (Pub. L. 104–4);
• Does not have Federalism
implications as specified in Executive
Order 13132 (64 FR 43255, August 10,
1999);
• Is not an economically significant
regulatory action based on health or
safety risks subject to Executive Order
13045 (62 FR 19885, April 23, 1997);
• Is not a significant regulatory action
subject to Executive Order 13211 (66 FR
28355, May 22, 2001);
• Is not subject to requirements of
Section 12(d) of the National
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71457
Technology Transfer and Advancement
Act of 1995 (15 U.S.C. 272 note) because
application of those requirements would
be inconsistent with the CAA; and
• Does not provide EPA with the
discretionary authority to address, as
appropriate, disproportionate human
health or environmental effects, using
practicable and legally permissible
methods, under Executive Order 12898
(59 FR 7629, February 16, 1994).
In addition, the SIP is not approved
to apply on any Indian reservation land
or in any other area where EPA or an
Indian tribe has demonstrated that a
tribe has jurisdiction. In those areas of
Indian country, this rule does not have
tribal implications as specified by
Executive Order 13175 (65 FR 67249,
November 9, 2000), because
redesignation is an action that affects
the status of a geographical area and
does not impose any new regulatory
requirements on tribes, impact any
existing sources of air pollution on
tribal lands, nor impair the maintenance
of ozone NAAQS in tribal lands.
List of Subjects in 40 CFR Part 52
Environmental protection, Air
pollution control, Incorporation by
reference, Intergovernmental relations,
Oxides of nitrogen, Ozone, Volatile
organic compounds.
Dated: October 5, 2016.
Robert A. Kaplan,
Acting Regional Administrator, Region 5.
[FR Doc. 2016–24914 Filed 10–14–16; 8:45 am]
BILLING CODE P
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS–HQ–ES–2016–0072;
4500030115]
Endangered and Threatened Wildlife
and Plants; Review of Foreign Species
That Are Candidates for Listing as
Endangered or Threatened; Annual
Notification of Findings on
Resubmitted Petitions; Annual
Description of Progress on Listing
Actions
Fish and Wildlife Service,
Interior.
ACTION: Notification of review.
AGENCY:
In this Candidate Notice of
Review of Foreign Species (CNOR–FS),
we present an updated list of plant and
animal species foreign to the United
States that we regard as candidates for
addition to the Lists of Endangered and
SUMMARY:
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Threatened Wildlife and Plants under
the Endangered Species Act of 1973, as
amended. Identification of candidate
species can assist conservation planning
efforts by providing advance notice of
potential listings and awareness of
species’ status. Even if we subsequently
list a candidate species, the early notice
provided here could result in more
options for species management and
recovery by prompting measures to
alleviate threats to the species.
DATES: We will accept information on
any of the species in this Candidate
Notice of Review of Foreign Species at
any time.
ADDRESSES: Document availability: This
CNOR–FS and supporting
documentation, including more detailed
information on these candidate species
and the references cited, is available on
the Internet at https://
www.regulations.gov at Docket No.
FWS–HQ–ES–2016–0072. Please submit
any new information, materials,
comments, or questions on this CNOR–
FS and the supporting documentation to
the Falls Church, VA, address listed in
FOR FURTHER INFORMATION CONTACT
below.
FOR FURTHER INFORMATION CONTACT:
jstallworth on DSK7TPTVN1PROD with PROPOSALS
Chief, Branch of Foreign Species,
Ecological Services Program, U.S. Fish
and Wildlife Service, 5275 Leesburg
Pike, MS: ES, Falls Church, VA 22041–
3808; telephone 703–358–2171. If you
use a telecommunications device for the
deaf (TDD), call the Federal Information
Relay Service (FIRS) at 800–877–8339.
SUPPLEMENTARY INFORMATION:
Executive Summary
This CNOR–FS summarizes the status
and threats that we evaluated in order
to determine that species qualify as
candidates, to assign a listing priority
number (LPN) to each species, and to
determine whether a species should be
removed from candidate status.
Additional material that we relied on for
each candidate species is available in
supporting documentation on the
Internet at https://www.regulations.gov at
Docket No. FWS–HQ–ES–2016–0072
Twenty foreign species are current
candidates for listing. This document
includes our findings on resubmitted
petitions and describes our progress in
revising the Lists of Endangered and
Threatened Wildlife and Plants (Lists)
during the period April 25, 2013,
through April 7, 2016. Based on our
review, we find that 19 species continue
to warrant listing, but their listing
remains precluded by higher-priority
proposals to determine whether other
species are an endangered species or a
threatened species. We are removing
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one candidate from the list due to
recovery, and we are adding a species
that was originally considered to be one
taxon but has recently been determined
to be two full species. Additionally, in
this CNOR–FS, we have assigned a
listing priority number (LPN) to the new
candidate species and have changed the
LPNs for three candidate species.
Background
The Endangered Species Act of 1973,
as amended (Act) (16 U.S.C. 1531 et
seq.), requires that we identify species
of wildlife and plants that are
endangered or threatened based on the
best available scientific and commercial
information. As defined in section 3 of
the Act, an endangered species is any
species that is in danger of extinction
throughout all or a significant portion of
its range, and a threatened species is
any species that is likely to become an
endangered species within the
foreseeable future throughout all or a
significant portion of its range. Through
the Federal rulemaking process, we add
species that meet these definitions to
the List of Endangered and Threatened
Wildlife at 50 CFR 17.11 or the List of
Endangered and Threatened Plants at 50
CFR 17.12 (List). Candidate taxa are
those taxa for which we have sufficient
information on file relating to biological
vulnerability and threats to support a
proposal to list the taxa as endangered
or threatened, but for which preparation
and publication of a proposed rule is
precluded by higher-priority proposals
to determine whether any species is an
endangered species or a threatened
species. We may identify a species as a
candidate for listing after we have
conducted an evaluation of its status—
either on our own initiative, or in
response to a petition we have received.
Under section 4(b)(3)(A) of the Act,
when we receive a petition to add a
species or to remove a species from the
List we must determine within 90 days,
to the maximum extent practicable,
whether the petition presents
substantial scientific or commercial
information indicating that the
petitioned action may be warranted (90day finding). Section 4(b)(3)(B) requires
that, within 12 months after receiving
any petition that contains substantial
scientific or commercial information
indicating that listing an animal or plant
species may be warranted, we make one
of the following findings (12-month
finding): (1) Not warranted; (2)
warranted; or (3) warranted, but the
immediate proposal of a regulation
implementing the petitioned action is
precluded by other pending proposals to
determine whether species are
endangered or threatened species
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(warranted but precluded), and
expeditious progress is being made to
add or remove qualified species from
the List (See Preclusion and Expeditious
Progress below).
In accordance with section
4(b)(3)(C)(i) of the Act, when, in
response to a petition, we find that
listing a species is warranted but
precluded, we must make a new 12month finding annually until we
publish a proposed rule to list the
species or make a determination that
listing is not warranted. These
subsequent 12-month findings are
referred to as ‘‘resubmitted’’ petition
findings. This CNOR–FS contains our
resubmitted petition findings for foreign
species previously described in the
Annual Notice of Review published
April 25, 2013 (78 FR 24604).
We maintain this list of candidates for
a variety of reasons:
(1) To notify the public that these
species are facing threats to their
survival;
(2) to provide advance knowledge of
potential listings;
(3) to provide information that may
stimulate and guide conservation efforts
that will remove or reduce threats to
these species and possibly make listing
unnecessary;
(4) to request input from interested
parties to help us identify those
candidate species that may not require
protection under the Act or additional
species that may require the Act’s
protections; and
(5) to request necessary information
for setting priorities for preparing listing
proposals. We strongly encourage
collaborative conservation efforts for
candidate species. For additional
information regarding such assistance,
see FOR FURTHER INFORMATION CONTACT.
On September 21, 1983, we published
guidance for assigning a listing priority
number (LPN) for each candidate
species (48 FR 43098). Guidelines for
such a priority-ranking guidance system
are required under section 4(h)(3) of the
Act (15 U.S.C. 1533(h)(3)). Using this
guidance, we assign each candidate an
LPN of 1 to 12, depending on the
magnitude of threats, immediacy of
threats, and taxonomic status; the lower
the LPN, the higher the listing priority
(that is, a species with an LPN of 1
would have the highest listing priority).
As explained below, we first categorize
based on the magnitude of the threat(s),
then by the immediacy of the threat(s),
and finally by taxonomic status.
Under this priority-ranking system,
magnitude of threat can be either ‘‘high’’
or ‘‘moderate to low.’’ This criterion
helps ensure that the species facing the
greatest threats to their continued
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existence receive the highest listing
priority. It is important to recognize that
all candidate species face threats to their
continued existence, so the magnitude
of threats is in relative terms. When
evaluating the magnitude of the threat(s)
facing the species, we consider
information such as: the number of
populations and/or extent of range of
the species affected by the threat(s); the
biological significance of the affected
population(s), the life-history
characteristics of the species and its
current abundance and distribution; and
whether the threats affect the species in
only a portion of its range.
As used in our priority ranking
system, immediacy of threat is
categorized as either ‘‘imminent’’ or
‘‘nonimminent.’’ It is not a measure of
how quickly the species is likely to
become extinct if the threats are not
addressed; rather, immediacy is based
on when the threats will begin. If a
threat is currently occurring or likely to
occur in the very near future, we
classify the threat as imminent.
Determining the immediacy of threats
helps ensure that species facing actual,
identifiable threats are given priority for
listing proposals over those for which
threats are only potential or species that
are intrinsically vulnerable to certain
types of threats, but are not known to be
presently facing such threats.
Our priority-ranking system has three
categories for taxonomic status: Species
that are the sole members of a genus;
full species (in genera that have more
than one species); and subspecies and
distinct population segments of
vertebrate species (DPSs). The result of
the ranking system is that we assign
each candidate a listing priority number
of 1 to 12. For example, if the threats are
of high magnitude, with immediacy
classified as imminent, the listable
entity is assigned an LPN of 1, 2, or 3
based on its taxonomic status (i.e., a
species that is the only member of its
genus would be assigned to the LPN 1
category, a full species to LPN 2, and a
subspecies or DPS would be assigned to
LPN 3). In summary, the LPN ranking
system provides a basis for making
decisions about the relative priority for
preparing a proposed rule to list a given
species. Each species included in this
CNOR–FS is one for which we have
sufficient information to prepare a
proposed rule to list, because it is in
danger of extinction or likely to become
endangered within the foreseeable
future throughout all or a significant
portion of its range.
For more information on the process
and standards used in assigning LPNs,
a copy of the guidance is available at:
https://www.fws.gov/endangered/esa-
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library/pdf/1983_LPN_Policy_FR_
pub.pdf. A rationale for the
determination of the magnitude and
imminence of threat(s) and assignment
of the LPN is presented in this CNOR–
FS. For more information on the LPN
assigned to a particular species, see the
supporting documentation at https://
www.regulations.gov at Docket No.
FWS–HQ–ES–2016–0072.
Request for Information
With this CNOR–FS, we request
additional information for the 20 taxa
whose listings are warranted but
precluded by higher-priority proposals
to determine whether any species is an
endangered or threatened species. We
will consider this information in
preparing listing documents or future
resubmitted petition findings for these
20 taxa. This information will also help
us to monitor the status of the taxa and
conserve them. We request the
submission of any further information
on the species in this CNOR–FS as soon
as possible, or whenever it becomes
available. We especially seek
information:
(1) Indicating that we should remove
a taxon from consideration for listing;
(2) Documenting threats to any of the
included taxa;
(3) Describing the immediacy or
magnitude of threats facing these taxa;
(4) Identifying taxonomic or
nomenclatural changes for any of the
taxa; or
(5) Noting any mistakes, such as
errors in the indicated historical ranges.
You may submit your information
concerning this CNOR–FS in general or
for any of the species included in this
CNOR–FS as described in ADDRESSES.
Previous Publications
We called our previous reviews of
foreign species an ‘‘Annual Notice of
Review,’’ or ‘‘ANOR.’’ In this review, we
use the term ‘‘Candidate Notice of
Review of Foreign Species (CNOR–FS)’’
to better align with terminology and
processes used for our Candidate Notice
of Review of native species—meaning
those species native to the United
States.
Nineteen of the species discussed in
this CNOR–FS are the result of three
separate petitions submitted to the U.S.
Fish and Wildlife Service (Service) to
list a number of foreign bird and
butterfly species as endangered or
threatened under the Act. We received
petitions to list the 13 foreign bird
species included in this CNOR–FS on
November 24, 1980, and May 6, 1991.
We found the petitions presented
substantial scientific or commercial
information indicating that listing these
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71459
13 species may be warranted on May 12,
1981 and December 16, 1991,
respectively (46 FR 26464 and 56 FR
65207), and first identified them as
candidates on May 21, 2004 (69 FR
2935). On January 10, 1994, we received
a petition to list seven butterfly species
as endangered or threatened, and we
found the petition presented substantial
scientific or commercial information
indicating that listing these species may
be warranted on May 10, 1994 (59 FR
24117). On December 7, 2004, we
identified five of the seven butterflies as
candidates and two were determined to
be ‘‘not warranted’’ (69 FR 70580). Our
most recent ANOR was published on
April 25, 2013 (78 FR 24604). Our
current revised CNOR–FS supersedes all
previous ANORs/Notices.
Status Assessment of Foreign Candidate
Species and Findings on Resubmitted
Petitions
Since the publication of our previous
ANOR on April 25, 2013 (78 FR 24604),
we reviewed the available information
on candidate species to determine
whether listing remains warranted for
each species and, if so, reevaluated the
relative LPN assigned to each species.
We also evaluated the need to
emergency list any of these species,
particularly species with high listing
priority numbers (i.e., species with
LPNs of 1, 2, or 3). This review ensures
that we focus conservation efforts on
those species at greatest risk first. In
addition to reviewing foreign candidate
species since publication of the last
ANOR, we have worked on numerous
findings in response to petitions to list
species and on proposed and final
determinations for rules to list, delist, or
downlist species under the Act. Some of
these findings and determinations have
been completed and published in the
Federal Register, while work on others
is still under way (see Preclusion and
Expeditious Progress section, below, for
details).
The current number of foreign species
that are candidates for listing is 20.
Based on our current review, we find
that one species (the Codfish Island
fernbird) has recovered and no longer
warrants listing; therefore, we removed
this species from the candidate list. We
also find that the southern helmeted
curassow is actually two species, the
southern helmeted or horned curassow
endemic to Bolivia (Pauxi unicornis)
and the Sira curassow endemic to Peru
(Pauxi koepckeae). Thus, we find that
20 species continue to warrant listing,
but their listing remains precluded by
higher-priority proposals to determine
whether any species is an endangered
species or a threatened species. Lastly,
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we have assigned an LPN of 2 for the
Sira curassow and have changed the
LPNs for the Brasilia tapaculo, the
Harris’ mimic swallowtail butterfly, and
the fluminense swallowtail butterfly.
This CNOR–FS summarizes the
current status of, and threats to, the 20
species we previously determined
qualified as candidates (78 FR 24604;
April 25, 2013). It also serves to
reevaluate the assigned listing priority
number given any changes in taxonomy
or threats, and includes our findings on
resubmitted petitions for 20 foreign
species. We have considered all of the
new information that we have obtained
since the previous finding, and we have
reviewed in accordance with our Listing
Priority Guidance the LPN of each taxon
for which proposed listing continues to
be warranted but precluded. Based on
our review of the best available
scientific and commercial information,
with this CNOR–FS, we are removing
one species from the candidate list due
to recovery and we are adding an
additional species to the list, the Sira
curassow (Pauxi koepckeae), which was
determined to be a separate species from
the petitioned southern helmeted
curassow (Pauxi unicornis).
We emphasize that we are not
proposing these species for listing, but
we do anticipate developing and
publishing proposed listing rules for
these species in the future, with the
objective of making expeditious
progress in addressing all 20 of these
foreign species within a reasonable
timeframe.
Table 1 provides a summary of all
updated determinations of the 20 taxa in
our review. The column labeled
‘‘Priority’’ indicates the LPN. Following
the scientific name of each taxon (third
column) is the family designation
(fourth column) and the common name,
if one exists (fifth column). The sixth
column provides the known historical
range for the taxon. The avian species in
table 1 are listed taxonomically.
TABLE 1—SPECIES IN 2016 CANDIDATE NOTICE OF REVIEW OF FOREIGN SPECIES
[C = Candidate (listing is warranted but precluded); Rc = Removing candidate from the list (listing is no longer warranted]
Status
Scientific name
Category
Family
Common name
Historical range
Priority
Birds
C ..............
2
Pauxi unicornis ..................
Cracidae ............................
C
C
C
C
..............
..............
..............
..............
2
2
8
8
Pauxi koepckeae ...............
Rallus semiplumbeus ........
Porphyrio hochstetteri .......
Haematopus chathamensis
Cracidae ............................
Rallidae ..............................
Rallidae ..............................
Haematopodidae ...............
southern helmeted
curassow.
Sira curassow ....................
´
Bogota rail .........................
takahe ................................
Chatham oystercatcher .....
Bolivia.
C ..............
C ..............
C ..............
8
8
8
Cyanoramphus malherbi ...
Eunymphicus uvaeensis ....
Dryocopus galeatus ...........
Psittacidae .........................
Psittacidae .........................
Picidae ...............................
orange-fronted parakeet ....
Uvea parakeet ...................
helmeted woodpecker .......
C ..............
C ..............
C ..............
Rc ............
2
2
8
....................
Dendrocopos noguchii .......
Aulacorhynchus huallagae
Scytalopus novacapitalis ...
Bowdleria punctata wilsoni
Picidae ...............................
Ramphastidae ...................
Rhinocryptidae ...................
Sylviidae ............................
Okinawa woodpecker ........
yellow-browed toucanet .....
Brasilia tapaculo ................
Codfish Island fernbird ......
C ..............
C ..............
C ..............
2
8
6
Zosterops luteirostris .........
Tangara peruviana ............
Strepera graculina crissalis
Zosteropidae ......................
Thraupidae ........................
Cracticidae .........................
Ghizo white-eye .................
black-backed tanager ........
Lord Howe Island pied
currawong.
Peru.
Colombia.
New Zealand.
Chatham Islands, New
Zealand.
New Zealand.
Uvea, New Caledonia.
Argentina, Brazil, Paraguay.
Okinawa Island, Japan.
Peru.
Brazil.
Codfish Island, New Zealand.
Solomon Islands.
Brazil.
Lord Howe Island, New
South Wales.
Papilionidae .......................
Harris’ mimic swallowtail ...
Brazil.
Invertebrates (Butterflies)
3
C ..............
2
C ..............
C ..............
C ..............
jstallworth on DSK7TPTVN1PROD with PROPOSALS
C ..............
Papilionidae .......................
Jamaican kite swallowtail ..
Jamaica.
2
2
Mimoides (= Eurytides or
Graphium) lysithous
harrisianus.
Protographium (= Eurytides
or Graphium or
Neographium or
Protesilaus) marcellinus.
Parides ascanius ...............
Parides hahneli ..................
Papilionidae .......................
Papilionidae .......................
Brazil.
Brazil.
8
Teinopalpus imperialis .......
Papilionidae .......................
Fluminense swallowtail ......
Hahnel’s Amazonian swallowtail.
Kaiser-i-Hind swallowtail ...
Colorado delta clam ..........
Mexico.
Bhutan, China, India, Laos,
Myanmar, Nepal, Thailand, Vietnam.
Mollusc
C ..............
2
Mulinia coloradoensis ........
We will continue to monitor the
status of these species as new
information becomes available (see
Monitoring, below). Our review of new
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Mactridae ...........................
information will determine if a change
in status is warranted, including the
need to emergency list any species or
change the LPN of any of the species. In
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the following sections, we describe our
findings for the individual species. The
summaries are based on information
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contained in our files, including any
petitions we received.
New Candidates
Sira curassow (Pauxi koepckeae)—We
added the Sira curassow as a new
candidate species. In previous ANORs,
we evaluated two bird subspecies under
the genus Pauxi, the southern helmeted
curassow or horned curassow (P.
unicornis unicornis) from Bolivia and
the Sira curassow (P. unicornis
koepckeae) from Peru. The ranges of the
two curassows are separated by
approximately 2,000 kilometers (km)
(1,243 miles (mi)). In 2014, BirdLife
International’s (BLI) Taxonomic
Working Group evaluated all nonpasserines (non-perching birds),
including the southern helmeted
curassow, applying quantitative criteria
for species delimitation, using a scoring
system to examine differences in
morphology, vocalizations, ecology, and
geographical relationships—the results
of which elevated both of these
subspecies to species: P. unicornis and
P. koepckeae. Although BLI and
International Union for the
Conservation of Nature (IUCN) now
recognize these as full species, the
Integrated Taxonomic Information
System (ITIS) continues to recognize P.
unicornis as a full species with P.
unicornis unicornis and P. unicornis
koepckeae as subspecies. Based upon
review of the available information, we
consider these two curassows (P.
unicornis and P. koepckeae) as valid,
full species. Therefore, we have
expanded our review to include the Sira
curassow (P. koepckeae), and have
added the Sira curassow to table 1. More
information on Sira curassow is
provided below and in the supporting
documents for this CNOR–FS.
The Sira curassow is a game bird that
is known only from the Cerros del Sira
region of Peru. Size and coloration are
similar to the southern helmeted
curassow, but the Sira curassow has a
shorter and rounder pale-blue casque (a
horn-like bony appendage above the
bill) that is flattened against the head.
The Sira curassow inhabits cloud-forest
habitat (a type of rainforest that occurs
on high mountains in the tropics) at
elevations from 1,100 to 1,450 meters
(m) (3,609–4,757 feet (ft)) and above.
Although historical population data
are lacking, the population is currently
estimated at fewer than 250 mature
individuals and is declining. The
primarily cause of the decline is
ongoing hunting by local communities.
Additionally, the Sira curassow’s
habitat is being degraded by subsistence
agriculture, forest clearing, road
building, and associated rural
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development. Although the Sira
curassow is legally protected in a large
portion of its range in El Sira Communal
Reserve, illegal hunting still occurs
there. The species is classified as
critically endangered on the IUCN Red
List. It is not threatened by international
trade, and it is not listed in any
appendices of the Convention on
International Trade in Endangered
Species of Wild Fauna and Flora
(CITES). In the previous ANOR, both the
southern helmeted curassow and the
Sira curassow had an LPN of 2. Now
that the Sira curassow, Pauxi
koepckeae, is a valid, distinct species,
we have reevaluated the species and
conclude that an LPN of 2 continues to
be accurate. The Sira curassow does not
represent a monotypic genus. It faces
threats that are high in magnitude based
on its small estimated population and
limited range. The few locations where
it is believed to exist continue to face
pressure from hunting and habitat loss.
The best scientific information available
indicates that the population decline
will continue in the future. Because the
species is experiencing significant
population declines and ongoing habitat
loss and degradation, we have assigned
an LPN of 2 to reflect imminent threats
of high magnitude.
Listing Priority Changes in Candidates
We reviewed the LPNs for all
candidate species and are changing the
LPNs for the following three species
discussed below. More information on
these species may be found in the
supporting documents for this CNOR–
FS.
Birds
Brasilia tapaculo (Scytalopus
novacapitalis)—The Brasilia tapaculo is
a small, secretive ground-dwelling bird
with limited flight ability. The tapaculo
is found in gallery-forest habitat that is
a smaller component of the wider
tropical savanna or ‘‘Cerrado’’ of the
´
Central Goias Plateau of Brazil. Gallery
forests are narrow fringes of thick
streamside vegetation that occur on the
edges of rivers and streams at elevations
of approximately 800–1,000 m (2,625–
3,281 ft). The Brasilia tapaculo is
described as ‘‘rare,’’ but the population
size is unknown. Despite a lack of data
on population trends, declines are
suspected to be occurring, owing to
habitat loss and degradation in the
Cerrado. It is known to occur in six
protected areas and has been found on
private land next to protected areas.
Protected areas are limited in extent and
size. Only 1.2 percent of the Cerrado is
in protected areas and those protected
areas are not distributed evenly across
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the region. Additionally, there are few
protected areas of more than 25,000
hectares (61,776 acres).
The primary threat to the species is
loss and degradation of its habitat. The
Cerrado is the largest, most diverse, and
possibly most threatened tropical
savanna in the world. Land in the
Cerrado is currently being converted to
soybean and rice plantations. At current
rates, the remaining natural habitat in
the Cerrado is predicted to be converted
to other uses by 2030. The tapaculo’s
gallery-forest habitat has been less
affected by clearing for agriculture than
the surrounding Cerrado. However,
larger impacts to the Cerrado are certain
to affect gallery forests; erosion and
deterioration of streams is increasing,
and wetland drainage and the diversion
of water for irrigation and annual
burning of adjacent grasslands is
expected to limit the availability and
extent of suitable habitat for the Brasilia
tapaculo.
The Brazilian national authority on
wildlife, Instituto Chico Mendes de
Conservacao da Biodiversidade
¸˜
(ICMBio), categorizes Brasilia tapaculo
as endangered based on severe
fragmentation of populations and
continued decline in habitat. The IUCN
Red List categorizes the species as ‘‘Near
Threatened.’’ It is not threatened by
international trade and is not listed in
any appendices of CITES.
In the previous ANOR, we assigned
the Brasilia tapaculo an LPN of 11. After
reevaluating the available information,
we find that a change to an LPN of 8 is
appropriate. The Brasilia tapaculo does
not represent a monotypic genus. The
threat to the species is of moderate
magnitude and is imminent. The species
has a fairly wide geographic range but
is endemic to the Cerrado and strongly
associated with gallery forests, a very
small component of the Cerrado. The
drastic conversion of the Cerrado is
ongoing. The populations currently
appear to be found only in or next to a
handful of protected areas and most of
these areas are small. The species is
reported as rare, even in protected areas.
Thus, based on review of the best
available scientific and commercial
information, the LPN has been changed
from 11 to 8 to reflect imminent threats
of moderate magnitude.
Invertebrates (Butterflies)
Harris’ mimic swallowtail (Mimoides
lysithous harrisianus)—The Harris’
mimic swallowtail is a subspecies that
inhabits the restinga (sand forest)
habitats of the coastal Atlantic Forest of
Brazil. It historically occurred in
southern Espirito Santo State and along
the coast of the State of Rio de Janeiro,
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Brazil. More recent records are from
three locations in the State of Rio de
Janeiro, but we could not find recent
population information for the
subspecies.
Habitat destruction has been the main
threat and is ongoing. Based on a
number of estimates, 88 to 95 percent of
the area historically covered by tropical
forests within the Atlantic Forest biome
has been converted or severely degraded
as the result of human activities. In
addition to the overall loss and
degradation of its habitat, the remaining
tracts of its habitat are severely
fragmented. Habitat loss due to sea-level
rise may also affect this coastal
subspecies, and losses may be
compounded by an increased demand
by humans to use remaining land for
housing and infrastructure.
Another factor affecting this butterfly
is collection. In previous ANORs we
suspected that collection may be a
stressor for this species but have now
noted sale of the subspecies on the
internet. The Harris’ mimic swallowtail
is on the list of Brazilian fauna
threatened with extinction, and
collection and trade of the subspecies is
prohibited. However, we recently found
three online advertisements for the
Harris’ mimic swallowtail at prices
ranging from 990 to 1,950 Euros each
(approximately 1,118 to 2,182 U.S.
dollars (USD)) indicating that illegal
collection and trade may be occurring
and demand for this butterfly is high.
Harris’ mimic swallowtail is not
currently on the IUCN Red list, although
it was identified as a ‘‘Threatened and
Extinct Subspecies’’ in the family
Papilionidae in the 1994 IUCN Red List.
The subspecies has not been formally
considered for listing in the appendices
to CITES. It is also not regulated on the
annexes to European Union Wildlife
Trade Regulations.
In the previous ANOR, the Harris’
mimic swallowtail was assigned an LPN
of 6. After reevaluating the threats to
this species, we have determined that a
change to an LPN of 3 is appropriate.
Harris’ mimic swallowtail is a
subspecies that is not within a
monotypic genus. Although the beststudied colony has maintained a stable
and viable size for nearly two decades,
there is limited recent information on
status. Threats are high in magnitude
due to the existence of only a few, small
fragmented colonies, and the potential
for catastrophic events such as severe
tropical storms, fire or introduction of a
new disease or predator. Additionally,
although the subspecies is protected by
Brazilian law and the colonies are
located within protected areas, the high
price advertised online for specimens
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indicates that there is demand for the
subspecies, likely from illegal
collection. Because the population is
very small and limited to only three
known colonies, removal of individuals
from the remaining small, fragmented
colonies could, in combination with
other stressors, contribute to local
extirpations. We find these threats are of
high magnitude and based on the best
available information, we have changed
the LPN from 6 to 3 to reflect imminent
threats of high magnitude for this
subspecies.
Fluminense swallowtail (Parides
ascanius)—The fluminense swallowtail
(Parides ascanius) also inhabits the
restinga (sand forest) habitats of the
coastal Atlantic Forest of Brazil within
the State of Rio de Janeiro. The overall
number of populations reported for the
species has declined from ‘‘fewer than
20 colonies’’ in 1994 to 8 in 2015.
Genetic analysis of the eight remaining
populations is consistent with
metapopulation dynamics (a group of
separate populations that has some level
of mixing) with low genetic diversity
and trending towards increased
isolation of these populations from
urban development. Habitat loss,
degradation, and fragmentation are the
principal threats to this species. The
species occupies highly specialized
habitat and requires large areas to
maintain a viable colony. Only one of
the eight known populations is
presently found within a large protected
area (Poco das Antas Biological
¸
Reserve), and the majority of the
remaining populations are on smaller,
fragmented parcels with limited or no
protections. Collection and commercial
exploitation (see Harris’ mimic
swallowtail above) were also identified
as possible factors affecting the
fluminense swallowtail. The species is
located near urban areas and is easy to
capture. The impact of illegal collection
to the fluminense swallowtail is
difficult to assess, but removal of
individuals from the remaining small,
fragmented populations could, in
combination with other stressors,
contribute to local extirpations.
The fluminense swallowtail butterfly
was the first invertebrate to be officially
noted on the list of Brazilian animals
threatened with extinction in 1973. It
has been classified as ‘‘Vulnerable’’ by
the IUCN Red List since 1983, although
it is now marked as ‘‘Needs Updating.’’
The species is currently categorized by
Brazil as ‘‘Imperiled.’’ It has not been
formally considered for listing in the
appendices to CITES. However, it is
listed on annex B of the European
Union Trade Regulation.
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In the previous ANOR, the fluminense
swallowtail was assigned an LPN of 5.
After reevaluating the factors affecting
the fluminense swallowtail and its
population decline, we have determined
that a change in the listing priority
number to 2 is appropriate. The
fluminense swallowtail does not
represent a monotypic genus. The
overall number of populations recorded
for the species has declined and most of
the remaining populations are small and
fragmented. The species is currently
affected by habitat destruction, which is
high in magnitude and imminence.
Despite the conservation measures in
place, some of the remaining small
populations may be impacted by illegal
collection. On the basis of this new
information, we have changed the LPN
for the fluminense swallowtail from 5 to
2.
Candidate Removals
Codfish Island fernbird (Bowdleria
punctata wilsoni)—We have evaluated
the threats to the Codfish Island fernbird
(Bowdleria punctata wilsoni) and
considered factors that, individually
and in combination, currently or
potentially could pose a risk to the
species and its habitat. After a review of
the best available scientific and
commercial data, we conclude that
listing this species under the Act is not
warranted because it is not likely to
become an endangered species within
the foreseeable future throughout all or
a significant portion of its range.
Therefore, we no longer consider the
Codfish Island fernbird to be a
candidate species for listing. We will
continue to monitor the status of this
species and to accept additional
information and comments concerning
this finding. We will reconsider our
determination in the event that we
gather new information that indicates
that the threats are of a considerably
greater magnitude or imminence than
identified through assessments of
information contained in our files, as
summarized below. More information
on this species may be found in the
supporting documents for this CNOR–
FS.
The Codfish Island fernbird is a small,
insect-eating songbird native to Codfish
Island, New Zealand. Codfish Island is
a nature reserve, located 3 km (1.8 mi)
off the northwest coast of Stewart
Island. The subspecies was also
successfully introduced to Putauhinu
Island, approximately 40 km south of
Codfish Island, in the late 1990s. The
Codfish Island fernbird is secretive, and
its main habitat is the pakihi, which
consists of dense vegetation 0.9 to 2.1 m
(3 to 7 ft) high. Fernbirds will also
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occupy forest habitats as long as rat
populations are absent. Fernbirds are
poor fliers that typically scramble
through vegetation, though they
occasionally fly short distances.
At its lowest point, in the early 1970s,
the population was estimated to be less
than 100 individuals. Although there is
no current estimate of the size of the
Codfish Island fernbird population, the
population on Codfish Island as of 2007
was believed to be ‘‘several hundred,’’
with an additional 200–300 birds on
Putauhinu Island, based on incidental
encounter rates in the various habitats.
Populations on both islands appear to
have expanded into all available
habitats and appear to be stable and
secure. Historically, Codfish Island
fernbird populations were greatly
reduced in number due to predation by
Polynesian rats and weka (Gallirallus
australis), a flightless woodhen that is
endemic to New Zealand. Codfish
Island’s native vegetation was also
modified by the introduced Australian
brush-tailed possum (Trichosurus
vulpecula). These threats have now
been eliminated through intensive
eradication efforts. The Codfish Island
fernbird population has rebounded
strongly with the removal of nonnative
predators in the 1980s and 1990s.
Additionally, forest habitat is now
regenerating, and the fernbird has
successfully recolonized and expanded
its range on Codfish Island. With the
introduction of the fernbird to a second
island that is free of nonnative
predators, the primary threats to the
species have been eliminated.
Neither the IUCN nor BLI have
assessed the status of this subspecies.
The New Zealand Department of
Conservation (NZDOC) categorizes the
Codfish Island fernbird as a rangerestricted island endemic that is
‘‘naturally uncommon.’’ It is not listed
in any appendices of CITES.
In the previous ANOR, the Codfish
Island fernbird was assigned an LPN of
12. After reevaluating the available
information, we find that this
subspecies no longer warrants listing.
Although it is an island endemic that is
restricted in range, the primary threat to
the species—nonnative predators—has
been removed, and the population has
responded and expanded throughout its
known historical range on Codfish
Island, occupying all available habitats.
In addition, conservation efforts by
NZDOC have resulted in the
establishment of a second population on
Putauhinu island that is free of
nonnative predators, and that
population has expanded and appears to
be secure. Finally, the two islands
occupied by the Codfish Island fernbird
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have restricted access, such that
reestablishment of nonnative predators
is extremely unlikely. In the unlikely
event of nonnative predators
reappearing on either island, NZDOC
has a proven track-record of success in
eradicating mammalian predators from
these islands. Therefore, we have
determined that this subspecies no
longer warrants listing and are removing
it from the candidate list.
Findings for Petitioned Candidate
Species
Birds
Southern helmeted curassow (Pauxi
unicornis)—Like the Sira curassow (see
above), the Southern helmeted curassow
is a game bird with a distinctive paleblue horn-like appendage, or casque,
above its bill. The southern helmeted
curassow is known only from central
Bolivia on the eastern slope of the
Andes, where large portions of its
habitat are in National Parks. The
species inhabits dense, humid, foothill
and lower montane forest and adjacent
evergreen forest at altitudes between
450 and 1,500 m (1,476 to 4,921 ft).
The total population of southern
helmeted curassow is estimated to be
between 1,500 and 7,500 individuals
and is declining. Hunting is believed to
be the primary threat to the species,
followed by habitat loss and
degradation. Although the National
Parks have been important for the
preservation of the species, financial
and human resources needed to protect
park resources are limited. Within the
Parks, there are human settlements and
ongoing encroachment, including illegal
logging operations and forest clearing
for farming. Rural development and
road building limit the species’ ability
to disperse. Range reductions due to
climate change are also predicted for the
southern helmeted curassow, when
warming temperatures may cause the
species to shift its distribution upslope
and outside of protected National Parks.
The southern helmeted curassow is
classified as critically endangered on
the IUCN Red List. Trade has not been
noted internationally, and the species is
not listed in any appendices of CITES.
The species is listed in annex D of the
European Union Trade Regulations.
In the previous ANOR, the southern
helmeted curassow was assigned an
LPN of 2. After reevaluating the threats
to the species, we have determined that
no change in the LPN is warranted. The
southern helmeted curassow does not
represent a monotypic genus. It faces
threats that are high in magnitude based
on its small, limited range. The few
locations where it is believed to exist
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continue to face pressure from hunting
and habitat loss and destruction, and
population decline will likely continue.
Because the species is experiencing
ongoing significant population declines
and habitat loss, we have made no
change to the LPN of 2, which reflects
imminent threats of high magnitude.
´
Bogota rail (Rallus semiplumbeus)—
´
The Bogota rail is found in the East
Andes of Colombia, South America. It is
a medium-sized nonmigratory rail
largely restricted to areas at elevations
from 2,500–4,000 m (8,202–13,123 ft) in
´
and surrounding Bogota, Columbia, on
´
´
the Ubate-Bogota Plateau. This region
formerly supported vast marshes and
swamps, but few lakes with suitable
habitat for the rail remain. The species
is secretive, and wetland habitats most
frequently used by rail are fringed by
dense vegetation-rich shallows. The
´
current population size of the Bogota
rail is estimated between 1,000 and
2,499 mature individuals and is thought
to be declining. The primary threat to
the rail is habitat loss and degradation.
Approximately 8 million people live in
´
the City of Bogota and 11 million in the
larger metro area. The wetlands have
experienced a 97-percent loss in
historical extent with few suitably
vegetated marshes remaining.
Additionally, road building may result
in further colonization and human
interference, including introduction of
nonnative species in previously stable
´
wetland environments. The Bogota rail
is listed as endangered at the global and
national level by IUCN. Trade does not
appear to be of concern at the
international level, and the species is
not listed in any appendices of CITES.
´
In the previous ANOR, the Bogota rail
was assigned an LPN of 2. After
reevaluating the threats to this species,
we have determined that no change in
the LPN for the species is needed. The
´
Bogota rail does not represent a
monotypic genus. It faces threats that
are high in magnitude due to the
pressures on the species’ habitat. Its
range is very small and is rapidly
contracting because of widespread
habitat loss and degradation. Although
´
portions of the Bogota rail’s range occur
in protected areas, most of the savanna
wetlands are unprotected. The
population is small and is believed to be
rapidly declining. The factors affecting
the species are ongoing, and are,
therefore, imminent. Thus, the LPN
remains at 2 to reflect imminent threats
of high magnitude.
Takahe (Porphyrio hochstetteri)—The
takahe is a large flightless bird in the
rail family. The takahe was once
widespread in the forest and grassland
ecosystems of New Zealand. It was
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thought to be extinct until it was
rediscovered in the Murchison
Mountains on the South Island of New
Zealand in 1948. In addition to its
native range on the mainland, the
takahe has been introduced to offshore
islands and mainland sanctuaries.
When rediscovered in 1948, it was
estimated that the takahe population
consisted of 100 to 300 birds; in 2013,
the population was estimated at 227
adult birds. Several factors have
historically led to the species’ decline,
including hunting, competition from
introduced herbivores (animals that feed
on plants), and predators such as
weasels and the weka, a flightless
woodhen that is endemic to New
Zealand. Currently, weasel predation
appears to be the most significant of
these threats. Weasel trapping is an
effective tool at slowly increasing
survival and reproductive output of
takahe; however, control efforts do not
completely eliminate the threat. Takahe
is a long-lived bird, potentially living
between 14 and 20 years, and has a low
reproductive rate, with clutches
consisting of one to three eggs. Severe
weather in the Murchison Mountains
(cold winters and high snowfall) may
also be a limiting factor to the takahe.
The population of takahe remains very
small and has low genetic diversity
relative to other species. The NZDOC is
currently attempting to manage further
loss of genetic diversity through
translocations. Additionally, NZDOC
has implemented a captive-breeding and
release program to supplement the
mainland population and has
established several reserve populations
on islands and fenced mainland sites;
these actions are having a positive effect
on population growth. The takahe is
listed as endangered on the IUCN Red
List, and New Zealand considers it to be
a nationally critical species. It is not
listed in any appendices of CITES as
international trade is not a concern.
In the previous ANOR, the takahe was
assigned an LPN of 8. After reevaluating
the threats to the takahe, we have
determined that no change in the
classification of the magnitude and
imminence of threats to the species is
warranted at this time. The takahe does
not represent a monotypic genus.
Although it has a small population,
limited suitable habitat, and may
experience inbreeding depression,
because the NZDOC is actively involved
in measures to aid the recovery of the
species, we find the threats are
moderate in magnitude. Despite
conservation efforts, the threats are
ongoing and, therefore, imminent. Lack
of suitable habitat and predation,
combined with the takahe’s small
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population size and naturally low
reproductive rate, are threats to this
species that are moderate in magnitude.
Thus, the LPN remains at 8 to reflect
imminent threats of moderate
magnitude.
Chatham oystercatcher (Haematopus
chathamensis)—The Chatham
oystercatcher is native to the Chatham
Island group located 860 km (534 mi)
east of mainland New Zealand. The
species breeds along the coastline of
four islands in the chain: Chatham, Pitt,
Rangatira, and Mangere. The Chatham
oystercatcher is found mainly along
rocky shores, including wide volcanic
rock platforms and occasionally on
sandy or gravelly beaches.
The Chatham oystercatcher is the
rarest oystercatcher in the world, with a
recent population estimate of 309 birds.
The species has experienced a three-fold
increase in its population since the first
reliable census was conducted in 1987.
Most of this increase occurred during a
period of intensive management,
especially predator control, from 1998
through 2004. The Chatham
oystercatcher is listed as nationally
critical by the NZDOC. It is classified as
‘‘Endangered’’ on the IUCN Red List and
is not listed in any appendices of CITES.
Predation of eggs and chicks, and to
a lesser extent of adults, is thought to be
the main impediment to the Chatham
oystercatcher population. Although
Mangere and Rangatira nature reserves
are free of all mammalian predators,
nonnative mammalian predators inhabit
Chatham and Pitt Islands. Feral cats are
the most common predator on eggs.
Other documented predators include
gulls (Larus spp.), the native brown skua
(Catharacta antarctica), weka, and
domestic dogs. Nest destruction and
disturbance by humans and livestock
are also noted threats. Habitat loss and
degradation has occurred from
introductions of nonnative Marram
grass (Ammophila arenaria) in the early
1900s to re-vegetate destabilized dunes.
The dense marram grass is unsuitable
for Chatham oystercatcher nesting.
Consequently, the Chatham
oystercatcher is forced to nest closer to
shore, where nests are vulnerable to
tides and storm surges; up to 50 percent
of eggs are lost in some years. Rising sea
levels associated with climate change
will likely affect future nesting success.
In the previous ANOR, the Chatham
oystercatcher was assigned an LPN of 8.
After reevaluating the threats to this
species, we have determined that no
change in the classification of the
magnitude and imminence of threats to
the species is warranted. The Chatham
oystercatcher does not represent a
monotypic genus. The current
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population estimate is very small, and
the species has a limited range, but
NZDOC has taken measures to recover
the species and the population is slowly
growing. However, threats (predation,
trampling, low population numbers, and
loss of eggs due to storm surges) are
ongoing and, thus, are imminent. The
LPN remains an 8 to reflect imminent
threats of moderate magnitude.
Orange-fronted parakeet
(Cyanoramphus malherbi)—The orangefronted parakeet was once well
distributed on the South Island of
mainland New Zealand and a few
offshore islands. It is now considered
the rarest parakeet in New Zealand.
Remaining naturally occurring
populations are restricted to limited
range (30 km (18.6 mi)) of four areas of
subalpine mature beech forests
(Nothofagus spp.), on the South Island.
Orange-fronted parakeets have also been
released onto four predator-free islands
where breeding has been confirmed.
The species’ range contracted when
its population was severely reduced in
the late 1800s and early 1900s for
unknown reasons. Information on
current population status is mixed, but
optimistic. The population experienced
another crash in 1990–2000 following
rat invasions. The population is still
small and has declined over the last
decade with estimates between 290 and
690 individuals in early 2013. The 2013
estimates indicated further declines on
the mainland and, during a 14-year
period (approximately three
generations), a reduction in the number
of mature birds. More recently, the
global population is reported as
increasing due to successful
translocations to predator-free islands
and control of predators in its range on
the South Island.
The most prominent factors affecting
the species on the mainland are
predation by nonnative mammals such
as weasels and rats (Rattus spp.), as well
as habitat destruction. Habitat loss and
degradation has affected large areas of
native forest on the mainland. In
addition, silviculture (care and
cultivation) of beech forests in the past
had removed mature trees with nest
cavities needed by the parakeet. The
species’ habitat is also degraded by
introduced herbivores that alter forest
structure in a way that reduces the
available feeding habitat for the
parakeet. Lastly, Beak and Feather
Disease Virus (BFDV) is a potential
threat to this species. The disease was
discovered in wild native birds in New
Zealand in 2008 (e.g., the red-fronted
parakeet, Cyanoramphus
novaezelandiae) though it has not been
documented in the orange-fronted
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parakeet. Infected birds either develop
immunity, die within a couple of weeks,
or become chronically infected. Chronic
infections result in feather loss and
deformities of beak and feathers.
In the previous ANOR, the orangefronted parakeet was assigned an LPN of
8. After reevaluating the factors affecting
the species, we have determined that no
change in the classification of the
magnitude of threats to the species is
warranted because NZDOC is actively
managing the species. The orangefronted parakeet does not represent a
monotypic genus. Although the species’
available suitable nesting habitat in
beech forests is extremely limited,
translocations have taken place and
seem to be successful. However, the
population is still small and vulnerable
to several threats despite management
efforts that may have stabilized the
population (albeit at small numbers).
Small populations may also be
vulnerable to stochastic events,
including disease outbreaks such as
BFDV. We find that the threats to this
species are still imminent; thus, the LPN
remains at 8 to reflect imminent threats
of moderate magnitude.
Uvea parakeet (Eunymphicus
uvaeensis)—The Uvea parakeet is a
relatively large, green parakeet found on
the small atoll of Uvea, located
approximately 1,500 km (932 mi) east of
Australia in the Loyalty Archipelago,
New Caledonia (a territory of France).
The entire island of Uvea is considered
an Important Bird Area by BirdLife
International which works with
communities to combine conservation
with sustainable livelihoods. To date,
however, we are unaware of any
designated reserves or provincial parks.
Uvea parakeets were introduced to the
adjacent island of Lifou (to establish a
second population) in 1925 and 1963,
but these introductions failed. The
species occupies both the north and
south end of Uvea Island. The species
primarily uses older (old-growth) forest
habitats and nests in the cavities of
living Syzygium and Mimusops trees.
Their exclusive use of tree cavities for
nesting may be a limiting factor. In
1977, the Uvea parakeet population was
estimated to be between 500 to 800
individuals. More recent analyses
provided two population estimates of
approximately 1,730 birds with varying
confidence intervals.
Historically, the primary threat to this
species was the capture of juveniles for
the pet trade, which involved cutting
open nesting cavities to extract
nestlings; this practice renders the holes
unsuitable for future nesting. Since
restrictions have been put into place
and the species has been more closely
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monitored, it appears that nest poaching
is no longer occurring such that it
significantly affects this species, and the
population has increased. Other
identified threats to the species include:
Habitat degradation and conversion,
loss of nesting cavities to bees, loss of
habitat through climate change, and the
potential for introduction of nonnative
predators. Artificial nests are being
installed to increase available nesting
sites; however, Uvea parakeets have not
yet used the artificial nests provided.
Uvea is a low-elevation and relatively
flat island. Climate change (and
associated sea-level rise) will likely
result in loss of forest habitat or
important food species and is
considered a substantial threat to the
persistence of Uvea parakeets. The
limited occupied range of the species
(only 34 km2 (13 mi2)) in a few
fragmented patches on Uvea, amplifies
this threat. Uvea parakeet is listed as
‘‘Endangered’’ on the IUCN Red List. It
is listed in appendix I of CITES and
annex A of the European Union Trade
Regulations.
In the previous ANOR, the Uvea
parakeet was assigned an LPN of 8.
After reevaluating the threats to this
species, we have determined that no
change in the classification of the
magnitude and imminence of threats to
the species is warranted. The Uvea
parakeet does not represent a monotypic
genus. The Uvea parakeet has a limited
distribution on a single small island
with limited remaining old-growth
forest on which the bird depends for
nesting cavities. The population has
increased in size due to conservation,
education, a ban on commercial trade,
and a reduction in poaching; however,
several threats (including habitat loss,
loss of nesting cavities and effects from
climate change) are still present and
ongoing and, therefore, imminent. The
LPN remains an 8 to reflect imminent
threats of moderate magnitude.
Helmeted woodpecker (Dryocopus
galeatus)—The helmeted woodpecker is
a fairly small woodpecker native to
regions of southern Brazil, eastern
Paraguay, and northeastern Argentina.
Its characteristic habitat is expansive,
well-preserved southern Atlantic Forest
in both lowland and montane areas from
sea level up to elevations of 1,000 m
(3,280 ft). It is believed to prefer mature
(old-growth) trees in tropical and
subtropical semi-deciduous forests as
well as in mixed deciduous-coniferous
forests.
The helmeted woodpecker’s
population is believed to have declined
sharply between 1945 and 2000 in
conjunction with the clearing of mature
forest habitat and is currently estimated
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at 400–8,900 individuals. Although
forest clearing has recently slowed, and
the species occurs in at least 17
protected areas throughout its range,
habitat degradation continues and the
population is still believed to be
declining. The principal threat to the
helmeted woodpecker is loss,
degradation, and fragmentation of its
Atlantic forest habitat. Competition for
nest cavities is also likely a limiting
factor. The helmeted woodpecker is one
of the rarest woodpecker in the
Americas. It is listed as endangered in
Brazil and as vulnerable by the IUCN. It
is not listed in any appendices of CITES.
In the previous ANOR, the helmeted
woodpecker was assigned an LPN of 8.
After reevaluating the available
information, we find that no change in
the LPN for the helmeted woodpecker is
warranted. The helmeted woodpecker
does not represent a monotypic genus.
The magnitude of threats to the species
is moderate because the species’ range
is fairly large. The threats are imminent
because the forest habitat upon which
the species depends is still being altered
and degraded. An LPN of 8 continues to
be accurate for this species.
Okinawa woodpecker (Dendrocopos
noguchii syn. Sapheopipo noguchii)—
The Okinawa woodpecker is a relatively
large woodpecker found on Okinawa
Island, Japan. The species prefers
undisturbed, mature, subtropical
evergreen broadleaf forests. It currently
occurs within the forested areas in the
northern part of the island, generally in
the Yambaru forest, and in some
undisturbed forested in coastal areas.
Most of the older forests that support
the species are within the Jungle
Warfare Training Center (formerly, the
Northern Training Area), part of the
United States Marine Corps installation
on Okinawa Island.
The Okinawa woodpecker is
considered one of the world’s rarest
woodpecker species. Current population
estimates are between 100 and 390
individuals and declining.
Habitat destruction and fragmentation
was a significant threat. As of 2001, only
40 km2 (15 mi2) of suitable habitat was
available for this species. While most of
the habitat loss appears to have ceased,
the Okinawa woodpecker still suffers
from limited suitable habitat and a small
population size. This situation makes it
vulnerable to extinction from disease
and natural disasters such as typhoons.
In addition, the species is vulnerable to
introduced predators such as feral dogs
and cats, Javan mongoose (Herpestes
javanicus), and weasels (Mustela itatsi).
The species is listed as critically
endangered on the IUCN Red List. It is
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legally protected in Japan. It is not listed
in any appendices of CITES.
In the previous ANOR, the Okinawa
woodpecker was assigned an LPN of 2.
After reevaluating the available
information, we find that no change in
the LPN is warranted. The Okinawa
woodpecker does not represent a
monotypic genus. Threats to the species
are of high magnitude due to the
scarcity of old-growth habitat, upon
which the species is dependent. Its
population is very small and is believed
to still be declining, and species with
fragmented habitat in combination with
small population sizes may be at greater
risk of extinction due to synergistic
effects. The threats to the species are
ongoing and imminent and high in
magnitude due to its restricted
population size, past habitat loss, and
endemism. The LPN for this species
remains a 2 to reflect imminent threats
of high magnitude.
Yellow-browed toucanet
(Aulacorhynchus huallagae)—The
yellow-browed toucanet has a small
range on the east slope of the Andes of
north-central Peru at elevations of
2,000–2,600 m (6,562–8,530 ft). The
toucanet occurs in humid montane
forests. The population status is not
well known because of the
inaccessibility of its habitat, but is
estimated at 600–1,500 mature
individuals. Habitat loss and
destruction from deforestation for
agriculture has been widespread in the
region and is suspected to be the main
threat, although deforestation appears to
have occurred mainly below the
altitudinal range of this toucanet. Gold
mining and manufacturing also are
common in the region. The yellowbrowed toucanet is described as scarce
wherever found, and ongoing
population declines resulting from
habitat loss are assumed. It is classified
as endangered on the IUCN Red List and
is not listed in any CITES appendices.
In the previous ANOR, the yellowbrowed toucanet was assigned an LPN
of 2. After reevaluating the available
information, we find that no change in
the classification of the magnitude and
imminence of threats to the species is
warranted at this time. The yellowbrowed toucanet does not represent a
monotypic genus. The estimated
population is small with a restricted
range. The magnitude of threats to the
habitat remains high, and its population
is likely declining. The LPN remains a
2 to reflect imminent threats of high
magnitude.
Ghizo white-eye (Zosterops
luteirostris)—The Ghizo white-eye is a
small passerine (perching) bird. It is
endemic to the small island of Ghizo in
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the Solomon Islands in the South
Pacific Ocean, east of Papua New
Guinea. The total range of the Ghizo
white-eye is estimated to be less than 35
km2 (13.5 mi2), of which less than 1 km2
(0.39 mi2) is the old-growth forest that
the species apparently prefers.
Little information is available about
this species and its habitat. It is locally
common in old-growth forest patches
and less common elsewhere. The
species has been observed in a variety
of habitats on the island, but it is
unknown whether sustainable
populations can exist outside of forested
habitats. The population is estimated to
be between 250 and 999 mature
individuals and is suspected to be
declining due to habitat degradation,
particularly since a tsunami hit the
island in 2007. Habitat loss appears to
be the main threat. As of 2012, the
human population on the island was
7,177 and growing rapidly, and there
has been prolific growth in informal
human settlements and temporary
housing on Ghizo, which may be
adversely affecting the Ghizo white-eye
and its habitat. Areas around Ghizo
Town, which previously supported the
species, have been further degraded
since the town was devastated by the
2007 tsunami, and habitat was found
less likely able to support the species in
2012. The species is also affected by
conversion of forested areas to
agricultural uses. The old-growth forest
on Ghizo is still under pressure from
clearance for local use as timber,
firewood, and gardens, as are the areas
of secondary growth, which are already
suspected to be suboptimal habitat for
this species.
The population of this species is
believed to be declining and, given its
fragmented habitat in combination with
small population sizes, may be at greater
risk of extinction due to synergistic
effects. The IUCN Red List classifies this
species as endangered. It is not listed in
any appendices of CITES, and this
species is not in international trade.
In the previous ANOR, the Ghizo
white-eye was assigned an LPN of 2.
After reevaluating the available
information, we find that no change in
the LPN for this species is warranted.
The Ghizo white-eye does not represent
a monotypic genus. It faces threats that
are high in magnitude due to declining
suitable habitat and its small, declining
population size. The best available
information indicates that forest
clearing is occurring at a pace that is
rapidly denuding the habitat;
secondary-growth forest continues to be
converted to agricultural purposes.
Further, the human population on the
small island is likely contributing to the
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reduction in old-growth forest for local
uses such as gardens and timber. These
threats to the species are ongoing, of
high magnitude, and imminent. Thus,
based on the best available scientific
and commercial information, the LPN
remains a 2 for this species.
Black-backed tanager (Tangara
peruviana)—The black-backed tanager
is endemic to the coastal Atlantic Forest
region of southeastern Brazil. It has been
found in the coastal states of Espirito
`
˜
Santo, Rio de Janeiro, Sao Paulo, Parana,
Santa Catarina, and Rio Grande do Sul.
The species is generally restricted to the
sand-forest ‘‘restinga’’ habitat, which is
a coastal component habitat of the
greater Atlantic Forest complex.
Restingas are herbaceous, shrubby
coastal sand-dune habitats. The blackbacked tanager is primarily found in
undisturbed habitat but has also been
observed in secondary (or secondgrowth) forests. It has also been
observed visiting gardens and orchards
of houses close to forested areas. Within
suitable habitat, the black-backed
tanager is generally not considered rare.
The population estimate is between
2,500 to 10,000 mature individuals.
Populations currently appear small and
fragmented and are believed to be
declining.
The primary factor affecting this
species is the rapid and widespread loss
of habitat, mainly to urban expansion
and beachfront development. Its habitat
is under pressure from the intense
development that occurs in coastal
areas, particularly south of Rio de
Janeiro. In addition to the overall loss
and degradation of its habitat, the
remaining tracts of its habitat are
severely fragmented. The black-backed
tanager’s remaining suitable habitat in
´
the areas of Rio de Janeiro and Parana
have largely been destroyed, and habitat
loss and degradation will likely increase
in the future. Additionally, although
small portions of this species’ range
occur in six protected areas, protections
appear limited. Sea-level rise may also
affect this species, which inhabits
coastal areas. Habitat loss due to sealevel rise may be compounded by an
increased demand by humans to use
remaining land for housing and
infrastructure. These factors affecting
the black-backed tanager’s remaining
habitat are ongoing due to the
challenges that Brazil faces to balance
its competing development and
environmental priorities. The blackbacked tanager is classified as
vulnerable by the IUCN. It is not listed
in any appendices of CITES. It is listed
as vulnerable in Brazil.
In the previous ANOR, the blackbacked tanager was assigned an LPN of
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8. After reevaluating the available
information, we have determined that
no change in the LPN for this species is
warranted at this time. The blackbacked tanager does not represent a
monotypic genus. This species is
protected under Brazil’s National
Environmental Policy Act (Law 6.938 of
1981), and several other laws
implementing protection for fauna.
Despite these laws, its habitat continues
to diminish. We find that threats
(primarily habitat loss) to the species are
moderate in magnitude due to the
species’ fairly large range, its existence
in protected areas, and apparent
flexibility in diet and habitat suitability.
Threats are imminent because the
species is at risk due to ongoing and
widespread loss of habitat due to
beachfront and related development.
Therefore, an LPN of 8 remains valid for
this species.
Lord Howe Island pied currawong
(Strepera graculina crissalis)—The Lord
Howe Island pied currawong is a fairly
large crow-like bird, endemic to Lord
Howe Island, New South Wales,
Australia. Lord Howe Island is a small
island northeast of Sydney, Australia,
with 28 smaller islets and rocks. The
Lord Howe pied currawong occurs
throughout the island but is most
numerous in the mountainous areas on
the southern end. It has also been
recorded to a limited extent on the
Admiralty Islands, located 1 km (0.6 mi)
north of Lord Howe Island.
Approximately 75 percent of Lord Howe
Island, plus all outlying islets and rocks
within the Lord Howe Island group, are
protected under the Permanent Park
Preserve, which has similar status to
that of a national park. The Lord Howe
Island pied currawong breeds in
rainforests and palm forests, particularly
along streams.
The best current population estimate
in 2005 and 2006 indicated that there
were approximately 200 individuals.
The Lord Howe Island pied currawong
exists as a small isolated population,
which makes it vulnerable to stochastic
events. The potential for an introduction
of other exotic predators to this island
ecosystem has also been identified as an
issue for this species. In addition to its
small population size, direct
persecution (via shootings) by humans
in retaliation for predation on domestic
and endemic birds has been
documented. The incidence of shootings
has declined since the 1970s, when
conservation efforts on Lord Howe
Island began, but occasional shootings
were still occurring as of 2007.
Because the Lord Howe pied
currawong often preys on small rodents,
it may be subject to nontarget poisoning
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during ongoing rat-baiting programs.
Experimental efforts to develop
techniques to house the birds in aviaries
while rat-baiting programs take place
show promise for protecting the species
during these eradication efforts. The
subspecies’ status is not addressed by
IUCN. It is not listed in any appendices
of CITES as trade is not an issue for this
taxon. The New South Wales
Threatened Species Conservation Act of
1995 lists the Lord Howe pied
currawong as ‘‘Vulnerable’’ due to its
extremely limited range and its small
population size.
In the previous ANOR, the Lord Howe
pied currawong was assigned an LPN of
6. After reevaluating the threats to the
Lord Howe pied currawong, we have
determined that no change in the LPN
representing the magnitude and
imminence of threats to the subspecies
is warranted. The Lord Howe pied
currawong does not represent a
monotypic genus. It faces threats that
are high in magnitude due to a
combination of factors including its
extremely small population size, and
nontarget poisoning. Despite
conservation efforts, the population of
the Lord Howe pied currawong has
remained small. Species with small
population sizes such as these may be
at greater risk of extinction due to
synergistic effects of factors affecting
this species. However, because
conservation efforts for the species have
been implemented, and the species is
being closely managed and monitored,
we find that the threats are
nonimminent. Thus, based on the best
available information, the LPN remains
at 6 to reflect nonimminent threats of
high magnitude.
Invertebrates (Butterflies)
Jamaican kite swallowtail
(Protographium marcellinus, syn.
Eurytides)—The Jamaican kite
swallowtail is a small blue-green and
black butterfly endemic to Jamaica. The
species occurs in limestone forest
containing its only known larval host
plant, Oxandra lanceolata. There is no
known estimate of population size. The
Jamaican kite swallowtail was
historically locally abundant. Presently
it maintains low population levels with
occasional strong flight seasons with
higher numbers. There is only one
known breeding site in the eastern coast
town of Rozelle, in St. Thomas Parish,
near Kingston (Jamaica’s capital).
However, researchers now believe that
there are likely other breeding sites—
one potential site being Jamaica’s
Cockpit Country, a remote and rugged
forested region in the west-central
portion of the island.
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Habitat loss, degradation, and
fragmentation are considered to be the
primary factors affecting the Jamaican
kite swallowtail. Additionally, the
species is vulnerable due to its small
population size and limited distribution
on the island. After centuries of a high
rate of deforestation, the island lost
much of its original forest. Eight percent
of the total land area of Jamaica is
natural forest with minimal human
disturbance. In Rozelle, habitat
modification for agricultural and
industrial purposes such as mining has
diminished this species’ habitat. Most of
the damage took place decades ago, but
small farming still occurs there. The
rugged terrain of the Cockpit Country
has hindered large-scale exploitation of
resources in the interior, but the
periphery and surrounding plains are
badly degraded. Major threats identified
for the Cockpit Country include:
Mining, forest conversion, nonnative
invasive species, solid-waste disposal,
incompatible agricultural practices, and
collecting. Additionally, bauxite mining
for aluminum production is an
important economic activity for Jamaica
and is a large contributor to
deforestation. Jamaica’s location in the
hurricane belt increases its vulnerability
to natural environmental events.
Although the Jamaican Wildlife
Protection Act of 1994 carries steep
fines and penalties, illegal collection
(see Harris’ mimic swallowtail above) is
a potential threat for the Jamaican kite
swallowtail. The butterfly has been
noted for sale on the internet as recently
as 2015 for 150 Euros (164 USD). The
species is classified as vulnerable on the
IUCN Red List and IUCN indicates that
this assessment needs updating. It is not
is not listed in any appendices of CITES
nor is it listed on annex B of the
European Union Trade Regulations.
In the previous ANOR, the Jamaican
kite swallowtail was assigned an LPN of
2. After reevaluating the factors affecting
the Jamaican kite swallowtail, we have
determined that no change in LPN is
warranted. The Jamaican kite
swallowtail does not represent a
monotypic genus. Although alternate
breeding sites are likely, the only
documented site and the presumed core
population for this species is in one
location that is vulnerable to stochastic
environmental events such as
hurricanes. Although Jamaica has taken
regulatory steps to preserve native
swallowtail habitat, plans for
conservation of two vital areas for the
butterfly (Rozelle and the Cockpit
Country) have not been implemented.
Based on our reevaluation of the threats
to this species, the LPN remains a 2 to
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reflect imminent threats of high
magnitude.
Hahnel’s Amazonian swallowtail
(Parides hahneli)—Hahnel’s Amazonian
swallowtail is a large black and yellow
butterfly endemic to Brazil. It is known
from three locations along the
tributaries of the middle and lower
Amazon River basin in the states of
´
Amazonas and Para. Its preferred habitat
is old sand strips (stranded beaches)
that are overgrown with dense scrub
vegetation or forest found close to the
major rivers. Hahnel’s Amazonian
swallowtail is described as very scarce
and extremely localized in association
with its specialized habitat and its larval
host plant. Population size and trends
are not known for this species.
However, habitat alteration (e.g., for
dam construction and waterway crop
transport) and destruction (e.g., clearing
for agriculture and cattle grazing) are
´
ongoing in Para and Amazonas where
this species is found. Researchers are
concerned that potential harmful
impacts from habitat alterations are
taking place before the butterfly can be
better studied and its ecological needs
can be understood.
Collection (see Harris’ mimic
swallowtail above) is also a potential
threat for Hahnel’s Amazonian
swallowtail. The species has been
collected for commercial trade and may
also be reared for trade. Locations in the
wild have been kept secret given the
high value of this butterfly to collectors.
Two specimens of Hahnel’s Amazonian
swallowtail were recently noted in
online sales from locations in the
United States (500 USD) and Germany
(approximately 166 USD). Hahnel’s
Amazonian swallowtail is described as
data deficient by the IUCN Red List. The
species is listed as endangered on the
´
State of Para’s list of threatened species,
but it is not listed by the State of
Amazonas or by Brazil. Hahnel’s
Amazonian swallowtail is not listed in
any appendices of CITES. However, it is
listed on annex B of the European
Union Trade Regulations.
In our previous ANOR, the Hahnel’s
Amazonian swallowtail was assigned an
LPN of 2. After reevaluating the threats
to the Hahnel’s Amazonian swallowtail,
we have determined that no change in
the LPN is warranted. This swallowtail
does not represent a monotypic genus.
It faces threats that are high in
magnitude and imminence due to its
small endemic population, and limited
and decreasing availability of its highly
specialized habitat. Habitat alteration
and destruction (e.g., dam construction,
waterway crop transport, clearing for
agriculture, and cattle grazing) are
´
ongoing in Para and Amazonas where
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the butterfly is found. These threats are
high in magnitude due to the species’
highly localized and specialized habitat
requirements. Potential impacts from
collection are unknown but could, in
combination with other stressors,
contribute to local extirpations. Based
on a reevaluation of the threats, the LPN
remains a 2 to reflect imminent threats
of high magnitude.
Kaiser-i-Hind swallowtail
(Teinopalpus imperialis)—The Kaiser-iHind swallowtail is native to Himalayan
regions of Bhutan, China, India, Laos,
Myanmar, Nepal, Thailand, and
Vietnam. Although it has a relatively
large range, it is restricted to higher
elevations and occurs only locally
within this range. This species occurs at
altitudes of 1,500 to 3,050 m (4,921 to
10,000 ft) above sea level, in
undisturbed (primary) broad-leavedevergreen forests or montane deciduous
forests. Adults fly up to open hilltops
above the forests to mate, where males
will often defend mating territories.
Larval host-plants are limited to
Magnolia and Daphne spp., and in some
regions the Kaiser-i-Hind swallowtail is
strictly monophagous, only using a
single species of Magnolia as a host
plant. Despite the species’ widespread
distribution, populations are described
as being very local and never abundant.
Even early accounts of the species
described it as being a very rare
occurrence. Habitat destruction is
believed to negatively affect this
species, which prefers undisturbed
high-altitude forests. In China and India,
the Kaiser-i-Hind swallowtail
populations are affected by habitat
modification and destruction due to
commercial and illegal logging. In
Nepal, the species is affected by habitat
disturbance and destruction resulting
from mining, wood collection for use as
fuel, deforestation, collection of fodders
and fiber plants, forest fires, invasion of
bamboo species into the oak forests,
agriculture, and grazing animals. In
Vietnam, the forest habitat is reportedly
declining. The Forest Ministry in Nepal
considers habitat destruction to be a
critical threat to all biodiversity,
including the Kaiser-i-Hind swallowtail.
Comprehensive information on the rate
of degradation of Himalayan forests
containing the Kaiser-i-Hind butterfly is
not available, but habitat loss is
consistently reported as one of the
primary ongoing threats to the species
there.
Collection for commercial trade is
also regarded as a threat to the species.
The Kaiser-i-Hind swallowtail is highly
valued and has been collected and
traded despite various prohibitions.
Although it is difficult to assess the
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potential impacts from collection, it is
possible that collection in combination
with other stressors could contribute to
local extirpations of small populations.
Since 1996, the Kaiser-i-Hind
swallowtail has been categorized on the
IUCN Red List as ‘‘Lower Risk/near
threatened,’’ but IUCN indicates that
this assessment needs updating. The
Kaiser-i-Hind swallowtail has been
listed in CITES appendix II since 1987.
Additionally, the Kaiser-i-Hind
swallowtail is listed on annex B of the
European Union Trade Regulations.
After reevaluating the threats to this
species, we have determined that no
change in its LPN of 8 is appropriate.
The Kaiser-i-Hind swallowtail does not
represent a monotypic genus. The
current factors, habitat destruction and
illegal collection, are moderate in
magnitude due to the species’ wide
distribution and to various protections
in place within each country. We find
that the threats are imminent due to
ongoing habitat destruction and high
market value for specimens. Based on
our reassessment of the threats, we have
retained an LPN of 8 to reflect imminent
threats of moderate magnitude.
Findings for Non-Petitioned Candidate
Species
Molluscs
Colorado delta clam (Mulinia
coloradoensis)—The Colorado Delta
clam is a relatively large, approximately
30 mm (1.2 in) average length, estuarine
bivalve, once abundant at the head of
the Gulf of California in the Colorado
River estuary in Mexico prior to the
construction of dams on the Colorado
River. Live individuals of the clam were
not observed anywhere in the wild
between 1968 and 1998, despite
extensive studies of bottom-dwelling
fauna in the region. In 1998, a small
relict population was discovered at Isla
Montague, Mexico, at the mouth of the
Colorado River Delta, and this
population represents the extent of the
species’ currently known range. The
clam is found in low intertidal mud at
depths of about 7 cm (2.75 in) beneath
the sediment and is a suspension-feeder.
Freshwater inflow is critical to the
species’ survival because brackish water
(a mix of salt and fresh water) is an
important component of its habitat and
life history. We are unaware of precise
estimates of the population size for the
Colorado Delta clam, but a 90-percent
decline since dam construction has been
suggested.
Habitat loss and degradation are
considered to be the primary factors
affecting the Colorado Delta clam.
Additionally, the species is now
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vulnerable due to its small population
size and limited distribution. Dams and
diversions along the Colorado River
have greatly affected the estuarine
environment, decreasing freshwater,
nutrient and sediment inflow. The
Colorado Delta clam may have
experienced a greater than 90-percent
reduction in its occupied range caused
by the decrease in freshwater flow to the
estuary.
Agricultural return flow from the
Mexicali Valley, coupled with aquifer
inflow, is a very important freshwater
source ensuring the maintenance of the
estuarine environment in the Delta and
the continued survival of the clam. In
2009, the U.S. completed lining of the
All-American Canal to prevent water
loss via seepage. Prior to lining, water
seepage from the All-American Canal
was an important source of recharge to
the Mexicali Valley aquifer. The AllAmerican Canal lining is predicted to
reduce total recharge to the Mexicali
Valley aquifer, which will reduce the
freshwater inflow into the Delta.
Additionally, predicted increases in
drought and warmer temperatures
associated with climate change will
contribute to deterioration of the clam’s
habitat by further curtailing freshwater
inflow and favoring nonnative invasive
aquatic species to the detriment of
native species like the Colorado Delta
clam. The species has not been assessed
for the IUCN Red List. It is not
threatened by international trade, and it
is not listed in any appendices of CITES.
In the previous ANOR, the Colorado
Delta clam was assigned an LPN of 2.
After reevaluating the factors affecting
the clam, we have determined that no
change in LPN is warranted. The
Colorado Delta clam does not represent
a monotypic genus. The available
evidence indicates that Colorado delta
clam is now restricted to one relict
population at Isla Montague at the
mouth of the Colorado River delta. Its
habitat is currently affected by the
ongoing and continuing (i.e., imminent)
loss of freshwater input into the Delta.
Furthermore, the available information
indicates that loss of freshwater will
likely worsen in the near- and long-term
future. Since habitat containing the
entire range of the species may be
rendered unsuitable within the near
future, we find that threats are of high
magnitude. Therefore, we find the
Colorado delta clam is subject to highmagnitude imminent threats, and we
retain an LPN of 2 for this species.
Preclusion and Expeditious Progress
To make a finding that a particular
action is warranted but precluded, the
Service must make two determinations:
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(1) That the immediate proposal and
timely promulgation of a final
regulation is precluded by pending
listing proposals and (2) that
expeditious progress is being made to
add qualified species to either of the
lists and to remove species from the lists
(16 U.S.C. 1533(b)(3)(B)(iii)). A listing
proposal is precluded if the Service
does not have sufficient resources
available to complete the proposal,
because there are competing demands
for those resources, and the relative
priority of those competing demands is
higher. Thus, in any given fiscal year
(FY), multiple factors dictate whether it
will be possible to undertake work on a
listing proposal regulation or whether
publication of such a proposal is
precluded by higher-priority listing
actions, including: (1) The amount of
resources available for completing the
listing function; (2) the estimated cost of
completing the proposed listing; and (3)
the Service’s workload and
prioritization of the proposed listing in
relation to other actions.
The resources available for listing
actions are determined through the
annual Congressional appropriations
process. The appropriation for the
Listing Program is available to support
work involving the following listing
actions: Proposed and final listing rules;
90-day and 12-month findings on
petitions to add species to the Lists of
Endangered and Threatened Wildlife
and Plants (Lists) or to change the status
of a species from threatened to
endangered; annual determinations on
prior ‘‘warranted-but-precluded’’
petition findings as required under
section 4(b)(3)(C)(i) of the Act; critical
habitat petition findings; proposed and
final rules designating critical habitat;
and litigation-related, administrative,
and program-management functions
(including preparing and allocating
budgets, responding to Congressional
and public inquiries, and conducting
public outreach regarding listing and
critical habitat).
The work involved in preparing
various listing documents can be
extensive and may include, but is not
limited to: Gathering and assessing the
best scientific and commercial data
available and conducting analyses used
as the basis for our decisions; writing
and publishing documents; and
obtaining, reviewing, and evaluating
public comments and peer review
comments on proposed rules and
incorporating relevant information into
final rules. The number of listing
actions that we can undertake in a given
year also is influenced by the
complexity of those listing actions; that
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71469
is, more complex actions generally are
more costly.
We cannot spend more than is
appropriated for the Listing Program
without violating the Anti-Deficiency
Act (see 31 U.S.C. 1341(a)(1)(A)). In
addition, in FY 1998 and for each fiscal
year since then, Congress has placed a
statutory cap on funds that may be
expended for the Listing Program, equal
to the amount expressly appropriated
for that purpose in that fiscal year. This
cap was designed to prevent funds
appropriated for other functions under
the Act (for example, recovery funds for
removing species from the Lists), or for
other Service programs, from being used
for Listing Program actions (see House
Report 105–163, 105th Congress, 1st
Session, July 1, 1997).
Prior to FY 2012, there was no
distinction in appropriations for listing
domestic and foreign species. However,
in an effort to balance foreign species
listing commitments with other Listing
Program responsibilities, effective FY
2012 and for each fiscal year since then,
the Service’s Listing Program budget has
included a foreign species subcap
providing that funding is not to exceed
a specified amount for implementation
of subsections (a), (b), (c), and (e) of
section 4 of the Act for species that are
not indigenous to the United States (see
Conference Report 112–331, 112th
Congress, 1st session, Dec. 15, 2011).
Thus, through the listing program cap
and the foreign species subcap,
Congress has determined the amount of
money available for foreign species
listing activities, including petition
findings and listing determinations.
In FY 2016, the Service had
$1,504,000 that could be used for listing
actions for foreign species. This funding
supports work in the following
categories: Compliance with court
orders and court-approved settlement
agreements requiring that petition
findings or listing determinations be
completed by a specific date; section 4
(of the Act) listing actions with absolute
statutory deadlines; essential litigationrelated, administrative, and listing
program-management functions; and
high-priority listing actions for some of
our candidate species.
In addition, available staff resources
are also a factor in determining which
high-priority species are provided with
funding. The Branch of Foreign Species
may, depending on available staff
resources, work on species described
within this CNOR–FS with an LPN of 2
or 3, and when appropriate, species
with a lower priority if they overlap
geographically or have the same threats
as the species with the high priority.
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Based on the prioritization factors
mentioned above, we continue to find
that proposals to list the candidate
species included in this CNOR–FS are
all precluded by higher-priority listing
actions. Because the actions in table 2
below are either the subject of a courtapproved settlement agreement or
subject to an absolute statutory deadline
and, thus, are higher priority than work
on proposed listing determinations for
the 20 species described above,
publication of proposed rules for these
20 species is precluded.
TABLE 2—PENDING ESA FOREIGN SPECIES LISTING ACTIONS
Species
Action
Actions Subject to Court Order/Settlement Agreement
All have been completed (See table 3 below for these specific actions).
Actions With Statutory Deadlines
Scarlet macaw ................................................................................................................................................................
Virgin Islands coqui ........................................................................................................................................................
Hyacinth macaw .............................................................................................................................................................
Peary, and Dolphin and Union caribou ..........................................................................................................................
3 Aral Sea sturgeon species ..........................................................................................................................................
3 East Asian sturgeon species .......................................................................................................................................
11 tarantula species .......................................................................................................................................................
4 Persian sturgeon species ............................................................................................................................................
Ridgway’s hawk eagle ....................................................................................................................................................
15 bat species ................................................................................................................................................................
Emperor penguin ............................................................................................................................................................
Flores hawk-eagle ..........................................................................................................................................................
Three-toed pygmy sloth ..................................................................................................................................................
Egyptian tortoise .............................................................................................................................................................
Golden conure ................................................................................................................................................................
2 Australian parakeet species ........................................................................................................................................
Flat-tailed tortoise ...........................................................................................................................................................
Spider tortoise .................................................................................................................................................................
7 pangolin species ..........................................................................................................................................................
African elephant ..............................................................................................................................................................
Long-tailed chinchilla ......................................................................................................................................................
As explained above, a determination
that listing is warranted but precluded
must also demonstrate that expeditious
progress is being made to add and
remove qualified species to and from
the Lists. As with our ‘‘precluded’’
finding, the evaluation of whether
progress in adding qualified species to
the Lists has been expeditious is a
function of the resources available for
listing and the competing demands for
those funds. Our expeditious progress
Final listing determination.
12-month petition finding.
Final listing determination.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
Final listing determination.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
12-month petition finding.
for foreign species since publication of
our previous ANOR, published on April
25, 2013 (78 FR 24604), to October 17,
2016, includes preparing and publishing
the following:
TABLE 3—ESA FOREIGN SPECIES LISTING ACTIONS PUBLISHED SINCE THE PREVIOUS ANOR WAS PUBLISHED ON APRIL
25, 2013
Publication date
Species
Action
6/5/2013 ............
Scimitar-horned oryx, dama gazelle, and addax ..
6/12/2013 ..........
6/25/2013 ..........
9/11/2013 ..........
Chimpanzee ..........................................................
Broad-snouted caiman ..........................................
Southern white rhino .............................................
9/24/2013 ..........
10/3/2013 ..........
10/29/2013 ........
11/19/2013 ........
Ten sturgeon species ...........................................
Blue-throated macaw ............................................
Five birds from Columbia and Ecuador ................
˜
Vicuna in Argentina, Bolivia, Chile, Ecuador, and
Peru.
Eleven tarantula species .......................................
Straight-horned markhor .......................................
12-month petition findings; delisting not warranted.
12-month petition finding and proposed rule ........
Final rule; threatened with special rule .................
Interim rule: Threatened due to similarity of appearance.
90-day finding; initiation of status review .............
Final rule: Endangered .........................................
Final rule; endangered ..........................................
Notice of initiation of 5-year review ......................
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12/3/2013 ..........
12/5/2013 ..........
1/22/2014 ..........
5/20/2014 ..........
6/9/2014 ............
6/24/2014 ..........
6/24/2014 ..........
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Fifteen foreign bats, emperor penguin, Flores
hawk-eagle, Ridgway’s hawk, and Virgin Is´
lands coquı.
Southern white rhino .............................................
Flat-tailed tortoise, spider tortoise, and pygmy
three-toed sloth.
Philippine cockatoo and yellow-crested cockatoo
White cockatoo .....................................................
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78 FR 33790–33797
78 FR 35201–35217
78 FR 38162–38190
78 FR 55649–55656
78
78
78
78
FR
FR
FR
FR
58507–58510
61208–61219
64692–64733
69436–69437
90-day findings; initiation of status reviews ..........
Proposed rule revision; Threatened with special
rule.
90-day findings; initiation of status reviews ..........
78 FR 72622–72625
78 FR 73173–73185
Affirmation of interim rule as final rule: Threatened due to similarity of appearance.
90-day findings; initiation of status reviews ..........
79 FR 28847–28849
79 FR 32900–32903
Final rule; endangered ..........................................
Final rule; threatened with special rule .................
79 FR 35870–35900
79 FR 35870–35900
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TABLE 3—ESA FOREIGN SPECIES LISTING ACTIONS PUBLISHED SINCE THE PREVIOUS ANOR WAS PUBLISHED ON APRIL
25, 2013—Continued
Publication date
Species
Action
10/7/2014 ..........
10/29/2014 ........
4/10/2015 ..........
Straight-horned markhor .......................................
African lion ............................................................
Egyptian tortoise, golden conure, and long-tailed
chinchilla.
Chimpanzee ..........................................................
Honduran emerald hummingbird ..........................
Great green and military macaw ..........................
Lion—Panthera leo leo .........................................
Lion—Panthera leo melanochaita .........................
Scarlet-chested parakeet and turquoise parakeet
African elephant, Chinese pangolin, giant ground
pangolin, Indian pangolin, long-tailed pangolin,
Philippine pangolin, Sunda pangolin, tree pangolin.
Scarlet macaw ......................................................
Final rule: Threatened with special rule ...............
Proposed rule: Threatened with special rule ........
90-day findings; initiation of status reviews ..........
79 FR 60365–60379
79 FR 64472–64502
80 FR 19259–19263
Final rule; endangered ..........................................
Final rule; endangered ..........................................
Final rule; endangered ..........................................
Final rule; endangered ..........................................
Final rule; threatened with special rule .................
Reopening of the public comment period .............
90-day findings; initiation of status reviews ..........
80
80
80
80
80
81
81
Revised proposed listing rule ...............................
81 FR 20302–20316
6/16/2015 ..........
7/29/2015 ..........
10/2/2015 ..........
12/23/2015 ........
12/23/2015 ........
1/21/2016 ..........
3/16/2016 ..........
4/7/2016 ............
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Our expeditious progress also
includes work on pending listing
actions described above in our
‘‘precluded finding,’’ but for which
decisions had not been completed at the
time of this publication. After taking
into consideration the limited resources
available for listing foreign species, the
competing demands for those funds,
and the completed work catalogued in
the tables above, we find that we are
making expeditious progress to add
qualified species to the Lists in FY 2016.
We have endeavored to make our
listing actions as efficient and timely as
possible, given the requirements of the
relevant law and regulations, and
constraints relating to workload and
personnel. We are continually
considering ways to streamline
processes or achieve economies of scale,
such as by publishing related actions
together.
Monitoring
Section 4(b)(3)(C)(iii) of the Act
requires us to ‘‘implement a system to
monitor effectively the status of all
species’’ for which we have made a
warranted-but-precluded 12-month
finding, and to ‘‘make prompt use of the
[emergency listing] authority [under
section 4(b)(7)] to prevent a significant
risk to the well-being of any such
species.’’ For foreign species, the
Service’s ability to gather information to
monitor species is limited. The Service
welcomes all information relevant to the
status of these species, because we have
no ability to gather data in foreign
countries directly and cannot compel
another country to provide information.
Thus, this CNOR–FS plays a critical role
in our monitoring efforts for foreign
species.
With each CNOR–FS, we request
information on the status of the species
included in the CNOR–FS. Information
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18:20 Oct 14, 2016
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and comments on the annual findings
can be submitted at any time. We review
all new information received through
this process as well as any other new
information we obtain using a variety of
methods. We collect information
directly from range countries by
correspondence, from peer-reviewed
scientific literature, unpublished
literature, scientific meeting
proceedings, and CITES documents
(including species proposals and reports
from scientific committees). We also
obtain information through the permitapplication processes under CITES, the
Act, and the Wild Bird Conservation Act
(16 U.S.C. 4901 et seq.). We also consult
with the IUCN species specialist groups
and staff members of the U.S. CITES
Scientific and Management Authorities,
and the Division of International
Conservation; and we attend scientific
meetings, when possible, to obtain
current status information for relevant
species. As previously stated, if we
identify any species for which
emergency listing is appropriate, we
will make prompt use of the emergency
listing authority under section 4(b)(7) of
the Act.
References Cited
A list of the references used to
develop this CNOR–FS is available at
https://www.regulations.gov at Docket
No. FWS–HQ–ES–2016–0072.
Authors
This Candidate Notice of Review of
Foreign Species was primarily authored
by staff of the Branch of Foreign Species
and Jesse D’Elia, Ecological Services
Program, U.S. Fish and Wildlife Service.
Authority
This Candidate Notice of Review of
Foreign Species is published under the
authority of the Endangered Species Act
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FR pages
FR
FR
FR
FR
FR
FR
FR
34500–34525
45086–45097
59976–60021
80000–80056
80000–80056
3373–3374
14058–14072
of 1973, as amended (16 U.S.C. 1531 et
seq.).
Dated: September 29, 2016.
Stephen Guertin,
Acting Director, U.S. Fish and Wildlife
Service.
[FR Doc. 2016–24931 Filed 10–14–16; 8:45 am]
BILLING CODE 4333–15–P
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
50 CFR Part 622
[Docket No. 160510416–6416–01]
RIN 0648–BG06
Fisheries of the Caribbean, Gulf of
Mexico, and South Atlantic; Reef Fish
Fishery of the Gulf of Mexico;
Yellowtail Snapper Management
Measures
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Proposed rule; request for
comments.
AGENCY:
NMFS proposes to implement
management measures described in a
framework action to the Fishery
Management Plan for the Reef Fish
Resources of the Gulf of Mexico (FMP),
as prepared by the Gulf of Mexico (Gulf)
Fishery Management Council (Gulf
Council). If implemented, this proposed
rule would revise the yellowtail snapper
commercial and recreational fishing
year and remove the requirement to use
circle hooks for the commercial harvest
of yellowtail snapper in the Gulf
exclusive economic zone (EEZ) south of
Cape Sable, Florida. The purpose of this
SUMMARY:
E:\FR\FM\17OCP1.SGM
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Agencies
[Federal Register Volume 81, Number 200 (Monday, October 17, 2016)]
[Proposed Rules]
[Pages 71457-71471]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-24931]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-HQ-ES-2016-0072; 4500030115]
Endangered and Threatened Wildlife and Plants; Review of Foreign
Species That Are Candidates for Listing as Endangered or Threatened;
Annual Notification of Findings on Resubmitted Petitions; Annual
Description of Progress on Listing Actions
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Notification of review.
-----------------------------------------------------------------------
SUMMARY: In this Candidate Notice of Review of Foreign Species (CNOR-
FS), we present an updated list of plant and animal species foreign to
the United States that we regard as candidates for addition to the
Lists of Endangered and
[[Page 71458]]
Threatened Wildlife and Plants under the Endangered Species Act of
1973, as amended. Identification of candidate species can assist
conservation planning efforts by providing advance notice of potential
listings and awareness of species' status. Even if we subsequently list
a candidate species, the early notice provided here could result in
more options for species management and recovery by prompting measures
to alleviate threats to the species.
DATES: We will accept information on any of the species in this
Candidate Notice of Review of Foreign Species at any time.
ADDRESSES: Document availability: This CNOR-FS and supporting
documentation, including more detailed information on these candidate
species and the references cited, is available on the Internet at
https://www.regulations.gov at Docket No. FWS-HQ-ES-2016-0072. Please
submit any new information, materials, comments, or questions on this
CNOR-FS and the supporting documentation to the Falls Church, VA,
address listed in FOR FURTHER INFORMATION CONTACT below.
FOR FURTHER INFORMATION CONTACT: Chief, Branch of Foreign Species,
Ecological Services Program, U.S. Fish and Wildlife Service, 5275
Leesburg Pike, MS: ES, Falls Church, VA 22041-3808; telephone 703-358-
2171. If you use a telecommunications device for the deaf (TDD), call
the Federal Information Relay Service (FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Executive Summary
This CNOR-FS summarizes the status and threats that we evaluated in
order to determine that species qualify as candidates, to assign a
listing priority number (LPN) to each species, and to determine whether
a species should be removed from candidate status. Additional material
that we relied on for each candidate species is available in supporting
documentation on the Internet at https://www.regulations.gov at Docket
No. FWS-HQ-ES-2016-0072
Twenty foreign species are current candidates for listing. This
document includes our findings on resubmitted petitions and describes
our progress in revising the Lists of Endangered and Threatened
Wildlife and Plants (Lists) during the period April 25, 2013, through
April 7, 2016. Based on our review, we find that 19 species continue to
warrant listing, but their listing remains precluded by higher-priority
proposals to determine whether other species are an endangered species
or a threatened species. We are removing one candidate from the list
due to recovery, and we are adding a species that was originally
considered to be one taxon but has recently been determined to be two
full species. Additionally, in this CNOR-FS, we have assigned a listing
priority number (LPN) to the new candidate species and have changed the
LPNs for three candidate species.
Background
The Endangered Species Act of 1973, as amended (Act) (16 U.S.C.
1531 et seq.), requires that we identify species of wildlife and plants
that are endangered or threatened based on the best available
scientific and commercial information. As defined in section 3 of the
Act, an endangered species is any species that is in danger of
extinction throughout all or a significant portion of its range, and a
threatened species is any species that is likely to become an
endangered species within the foreseeable future throughout all or a
significant portion of its range. Through the Federal rulemaking
process, we add species that meet these definitions to the List of
Endangered and Threatened Wildlife at 50 CFR 17.11 or the List of
Endangered and Threatened Plants at 50 CFR 17.12 (List). Candidate taxa
are those taxa for which we have sufficient information on file
relating to biological vulnerability and threats to support a proposal
to list the taxa as endangered or threatened, but for which preparation
and publication of a proposed rule is precluded by higher-priority
proposals to determine whether any species is an endangered species or
a threatened species. We may identify a species as a candidate for
listing after we have conducted an evaluation of its status--either on
our own initiative, or in response to a petition we have received.
Under section 4(b)(3)(A) of the Act, when we receive a petition to
add a species or to remove a species from the List we must determine
within 90 days, to the maximum extent practicable, whether the petition
presents substantial scientific or commercial information indicating
that the petitioned action may be warranted (90-day finding). Section
4(b)(3)(B) requires that, within 12 months after receiving any petition
that contains substantial scientific or commercial information
indicating that listing an animal or plant species may be warranted, we
make one of the following findings (12-month finding): (1) Not
warranted; (2) warranted; or (3) warranted, but the immediate proposal
of a regulation implementing the petitioned action is precluded by
other pending proposals to determine whether species are endangered or
threatened species (warranted but precluded), and expeditious progress
is being made to add or remove qualified species from the List (See
Preclusion and Expeditious Progress below).
In accordance with section 4(b)(3)(C)(i) of the Act, when, in
response to a petition, we find that listing a species is warranted but
precluded, we must make a new 12-month finding annually until we
publish a proposed rule to list the species or make a determination
that listing is not warranted. These subsequent 12-month findings are
referred to as ``resubmitted'' petition findings. This CNOR-FS contains
our resubmitted petition findings for foreign species previously
described in the Annual Notice of Review published April 25, 2013 (78
FR 24604).
We maintain this list of candidates for a variety of reasons:
(1) To notify the public that these species are facing threats to
their survival;
(2) to provide advance knowledge of potential listings;
(3) to provide information that may stimulate and guide
conservation efforts that will remove or reduce threats to these
species and possibly make listing unnecessary;
(4) to request input from interested parties to help us identify
those candidate species that may not require protection under the Act
or additional species that may require the Act's protections; and
(5) to request necessary information for setting priorities for
preparing listing proposals. We strongly encourage collaborative
conservation efforts for candidate species. For additional information
regarding such assistance, see FOR FURTHER INFORMATION CONTACT.
On September 21, 1983, we published guidance for assigning a
listing priority number (LPN) for each candidate species (48 FR 43098).
Guidelines for such a priority-ranking guidance system are required
under section 4(h)(3) of the Act (15 U.S.C. 1533(h)(3)). Using this
guidance, we assign each candidate an LPN of 1 to 12, depending on the
magnitude of threats, immediacy of threats, and taxonomic status; the
lower the LPN, the higher the listing priority (that is, a species with
an LPN of 1 would have the highest listing priority). As explained
below, we first categorize based on the magnitude of the threat(s),
then by the immediacy of the threat(s), and finally by taxonomic
status.
Under this priority-ranking system, magnitude of threat can be
either ``high'' or ``moderate to low.'' This criterion helps ensure
that the species facing the greatest threats to their continued
[[Page 71459]]
existence receive the highest listing priority. It is important to
recognize that all candidate species face threats to their continued
existence, so the magnitude of threats is in relative terms. When
evaluating the magnitude of the threat(s) facing the species, we
consider information such as: the number of populations and/or extent
of range of the species affected by the threat(s); the biological
significance of the affected population(s), the life-history
characteristics of the species and its current abundance and
distribution; and whether the threats affect the species in only a
portion of its range.
As used in our priority ranking system, immediacy of threat is
categorized as either ``imminent'' or ``nonimminent.'' It is not a
measure of how quickly the species is likely to become extinct if the
threats are not addressed; rather, immediacy is based on when the
threats will begin. If a threat is currently occurring or likely to
occur in the very near future, we classify the threat as imminent.
Determining the immediacy of threats helps ensure that species facing
actual, identifiable threats are given priority for listing proposals
over those for which threats are only potential or species that are
intrinsically vulnerable to certain types of threats, but are not known
to be presently facing such threats.
Our priority-ranking system has three categories for taxonomic
status: Species that are the sole members of a genus; full species (in
genera that have more than one species); and subspecies and distinct
population segments of vertebrate species (DPSs). The result of the
ranking system is that we assign each candidate a listing priority
number of 1 to 12. For example, if the threats are of high magnitude,
with immediacy classified as imminent, the listable entity is assigned
an LPN of 1, 2, or 3 based on its taxonomic status (i.e., a species
that is the only member of its genus would be assigned to the LPN 1
category, a full species to LPN 2, and a subspecies or DPS would be
assigned to LPN 3). In summary, the LPN ranking system provides a basis
for making decisions about the relative priority for preparing a
proposed rule to list a given species. Each species included in this
CNOR-FS is one for which we have sufficient information to prepare a
proposed rule to list, because it is in danger of extinction or likely
to become endangered within the foreseeable future throughout all or a
significant portion of its range.
For more information on the process and standards used in assigning
LPNs, a copy of the guidance is available at: https://www.fws.gov/endangered/esa-library/pdf/1983_LPN_Policy_FR_pub.pdf. A rationale for
the determination of the magnitude and imminence of threat(s) and
assignment of the LPN is presented in this CNOR-FS. For more
information on the LPN assigned to a particular species, see the
supporting documentation at https://www.regulations.gov at Docket No.
FWS-HQ-ES-2016-0072.
Request for Information
With this CNOR-FS, we request additional information for the 20
taxa whose listings are warranted but precluded by higher-priority
proposals to determine whether any species is an endangered or
threatened species. We will consider this information in preparing
listing documents or future resubmitted petition findings for these 20
taxa. This information will also help us to monitor the status of the
taxa and conserve them. We request the submission of any further
information on the species in this CNOR-FS as soon as possible, or
whenever it becomes available. We especially seek information:
(1) Indicating that we should remove a taxon from consideration for
listing;
(2) Documenting threats to any of the included taxa;
(3) Describing the immediacy or magnitude of threats facing these
taxa;
(4) Identifying taxonomic or nomenclatural changes for any of the
taxa; or
(5) Noting any mistakes, such as errors in the indicated historical
ranges.
You may submit your information concerning this CNOR-FS in general
or for any of the species included in this CNOR-FS as described in
ADDRESSES.
Previous Publications
We called our previous reviews of foreign species an ``Annual
Notice of Review,'' or ``ANOR.'' In this review, we use the term
``Candidate Notice of Review of Foreign Species (CNOR-FS)'' to better
align with terminology and processes used for our Candidate Notice of
Review of native species--meaning those species native to the United
States.
Nineteen of the species discussed in this CNOR-FS are the result of
three separate petitions submitted to the U.S. Fish and Wildlife
Service (Service) to list a number of foreign bird and butterfly
species as endangered or threatened under the Act. We received
petitions to list the 13 foreign bird species included in this CNOR-FS
on November 24, 1980, and May 6, 1991. We found the petitions presented
substantial scientific or commercial information indicating that
listing these 13 species may be warranted on May 12, 1981 and December
16, 1991, respectively (46 FR 26464 and 56 FR 65207), and first
identified them as candidates on May 21, 2004 (69 FR 2935). On January
10, 1994, we received a petition to list seven butterfly species as
endangered or threatened, and we found the petition presented
substantial scientific or commercial information indicating that
listing these species may be warranted on May 10, 1994 (59 FR 24117).
On December 7, 2004, we identified five of the seven butterflies as
candidates and two were determined to be ``not warranted'' (69 FR
70580). Our most recent ANOR was published on April 25, 2013 (78 FR
24604). Our current revised CNOR-FS supersedes all previous ANORs/
Notices.
Status Assessment of Foreign Candidate Species and Findings on
Resubmitted Petitions
Since the publication of our previous ANOR on April 25, 2013 (78 FR
24604), we reviewed the available information on candidate species to
determine whether listing remains warranted for each species and, if
so, reevaluated the relative LPN assigned to each species. We also
evaluated the need to emergency list any of these species, particularly
species with high listing priority numbers (i.e., species with LPNs of
1, 2, or 3). This review ensures that we focus conservation efforts on
those species at greatest risk first. In addition to reviewing foreign
candidate species since publication of the last ANOR, we have worked on
numerous findings in response to petitions to list species and on
proposed and final determinations for rules to list, delist, or
downlist species under the Act. Some of these findings and
determinations have been completed and published in the Federal
Register, while work on others is still under way (see Preclusion and
Expeditious Progress section, below, for details).
The current number of foreign species that are candidates for
listing is 20. Based on our current review, we find that one species
(the Codfish Island fernbird) has recovered and no longer warrants
listing; therefore, we removed this species from the candidate list. We
also find that the southern helmeted curassow is actually two species,
the southern helmeted or horned curassow endemic to Bolivia (Pauxi
unicornis) and the Sira curassow endemic to Peru (Pauxi koepckeae).
Thus, we find that 20 species continue to warrant listing, but their
listing remains precluded by higher-priority proposals to determine
whether any species is an endangered species or a threatened species.
Lastly,
[[Page 71460]]
we have assigned an LPN of 2 for the Sira curassow and have changed the
LPNs for the Brasilia tapaculo, the Harris' mimic swallowtail
butterfly, and the fluminense swallowtail butterfly.
This CNOR-FS summarizes the current status of, and threats to, the
20 species we previously determined qualified as candidates (78 FR
24604; April 25, 2013). It also serves to reevaluate the assigned
listing priority number given any changes in taxonomy or threats, and
includes our findings on resubmitted petitions for 20 foreign species.
We have considered all of the new information that we have obtained
since the previous finding, and we have reviewed in accordance with our
Listing Priority Guidance the LPN of each taxon for which proposed
listing continues to be warranted but precluded. Based on our review of
the best available scientific and commercial information, with this
CNOR-FS, we are removing one species from the candidate list due to
recovery and we are adding an additional species to the list, the Sira
curassow (Pauxi koepckeae), which was determined to be a separate
species from the petitioned southern helmeted curassow (Pauxi
unicornis).
We emphasize that we are not proposing these species for listing,
but we do anticipate developing and publishing proposed listing rules
for these species in the future, with the objective of making
expeditious progress in addressing all 20 of these foreign species
within a reasonable timeframe.
Table 1 provides a summary of all updated determinations of the 20
taxa in our review. The column labeled ``Priority'' indicates the LPN.
Following the scientific name of each taxon (third column) is the
family designation (fourth column) and the common name, if one exists
(fifth column). The sixth column provides the known historical range
for the taxon. The avian species in table 1 are listed taxonomically.
Table 1--Species in 2016 Candidate Notice of Review of Foreign Species
[C = Candidate (listing is warranted but precluded); Rc = Removing candidate from the list (listing is no longer
warranted]
----------------------------------------------------------------------------------------------------------------
Status
------------------------------- Scientific name Family Common name Historical range
Category Priority
----------------------------------------------------------------------------------------------------------------
Birds
----------------------------------------------------------------------------------------------------------------
C................ 2 Pauxi unicornis.... Cracidae........... southern helmeted Bolivia.
curassow.
C................ 2 Pauxi koepckeae.... Cracidae........... Sira curassow..... Peru.
C................ 2 Rallus semiplumbeus Rallidae........... Bogot[aacute] rail Colombia.
C................ 8 Porphyrio Rallidae........... takahe............ New Zealand.
hochstetteri.
C................ 8 Haematopus Haematopodidae..... Chatham Chatham Islands,
chathamensis. oystercatcher. New Zealand.
C................ 8 Cyanoramphus Psittacidae........ orange-fronted New Zealand.
malherbi. parakeet.
C................ 8 Eunymphicus Psittacidae........ Uvea parakeet..... Uvea, New
uvaeensis. Caledonia.
C................ 8 Dryocopus galeatus. Picidae............ helmeted Argentina, Brazil,
woodpecker. Paraguay.
C................ 2 Dendrocopos Picidae............ Okinawa woodpecker Okinawa Island,
noguchii. Japan.
C................ 2 Aulacorhynchus Ramphastidae....... yellow-browed Peru.
huallagae. toucanet.
C................ 8 Scytalopus Rhinocryptidae..... Brasilia tapaculo. Brazil.
novacapitalis.
Rc............... ........... Bowdleria punctata Sylviidae.......... Codfish Island Codfish Island,
wilsoni. fernbird. New Zealand.
C................ 2 Zosterops Zosteropidae....... Ghizo white-eye... Solomon Islands.
luteirostris.
C................ 8 Tangara peruviana.. Thraupidae......... black-backed Brazil.
tanager.
C................ 6 Strepera graculina Cracticidae........ Lord Howe Island Lord Howe Island,
crissalis. pied currawong. New South Wales.
----------------------------------------------------------------------------------------------------------------
Invertebrates (Butterflies)
----------------------------------------------------------------------------------------------------------------
C................ 3 Mimoides (= Papilionidae....... Harris' mimic Brazil.
Eurytides or swallowtail.
Graphium)
lysithous
harrisianus.
C................ 2 Protographium (= Papilionidae....... Jamaican kite Jamaica.
Eurytides or swallowtail.
Graphium or
Neographium or
Protesilaus)
marcellinus.
C................ 2 Parides ascanius... Papilionidae....... Fluminense Brazil.
swallowtail.
C................ 2 Parides hahneli.... Papilionidae....... Hahnel's Amazonian Brazil.
swallowtail.
C................ 8 Teinopalpus Papilionidae....... Kaiser-i-Hind Bhutan, China,
imperialis. swallowtail. India, Laos,
Myanmar, Nepal,
Thailand,
Vietnam.
----------------------------------------------------------------------------------------------------------------
Mollusc
----------------------------------------------------------------------------------------------------------------
C................ 2 Mulinia Mactridae.......... Colorado delta Mexico.
coloradoensis. clam.
----------------------------------------------------------------------------------------------------------------
We will continue to monitor the status of these species as new
information becomes available (see Monitoring, below). Our review of
new information will determine if a change in status is warranted,
including the need to emergency list any species or change the LPN of
any of the species. In the following sections, we describe our findings
for the individual species. The summaries are based on information
[[Page 71461]]
contained in our files, including any petitions we received.
New Candidates
Sira curassow (Pauxi koepckeae)--We added the Sira curassow as a
new candidate species. In previous ANORs, we evaluated two bird
subspecies under the genus Pauxi, the southern helmeted curassow or
horned curassow (P. unicornis unicornis) from Bolivia and the Sira
curassow (P. unicornis koepckeae) from Peru. The ranges of the two
curassows are separated by approximately 2,000 kilometers (km) (1,243
miles (mi)). In 2014, BirdLife International's (BLI) Taxonomic Working
Group evaluated all non-passerines (non-perching birds), including the
southern helmeted curassow, applying quantitative criteria for species
delimitation, using a scoring system to examine differences in
morphology, vocalizations, ecology, and geographical relationships--the
results of which elevated both of these subspecies to species: P.
unicornis and P. koepckeae. Although BLI and International Union for
the Conservation of Nature (IUCN) now recognize these as full species,
the Integrated Taxonomic Information System (ITIS) continues to
recognize P. unicornis as a full species with P. unicornis unicornis
and P. unicornis koepckeae as subspecies. Based upon review of the
available information, we consider these two curassows (P. unicornis
and P. koepckeae) as valid, full species. Therefore, we have expanded
our review to include the Sira curassow (P. koepckeae), and have added
the Sira curassow to table 1. More information on Sira curassow is
provided below and in the supporting documents for this CNOR-FS.
The Sira curassow is a game bird that is known only from the Cerros
del Sira region of Peru. Size and coloration are similar to the
southern helmeted curassow, but the Sira curassow has a shorter and
rounder pale-blue casque (a horn-like bony appendage above the bill)
that is flattened against the head. The Sira curassow inhabits cloud-
forest habitat (a type of rainforest that occurs on high mountains in
the tropics) at elevations from 1,100 to 1,450 meters (m) (3,609-4,757
feet (ft)) and above.
Although historical population data are lacking, the population is
currently estimated at fewer than 250 mature individuals and is
declining. The primarily cause of the decline is ongoing hunting by
local communities. Additionally, the Sira curassow's habitat is being
degraded by subsistence agriculture, forest clearing, road building,
and associated rural development. Although the Sira curassow is legally
protected in a large portion of its range in El Sira Communal Reserve,
illegal hunting still occurs there. The species is classified as
critically endangered on the IUCN Red List. It is not threatened by
international trade, and it is not listed in any appendices of the
Convention on International Trade in Endangered Species of Wild Fauna
and Flora (CITES). In the previous ANOR, both the southern helmeted
curassow and the Sira curassow had an LPN of 2. Now that the Sira
curassow, Pauxi koepckeae, is a valid, distinct species, we have
reevaluated the species and conclude that an LPN of 2 continues to be
accurate. The Sira curassow does not represent a monotypic genus. It
faces threats that are high in magnitude based on its small estimated
population and limited range. The few locations where it is believed to
exist continue to face pressure from hunting and habitat loss. The best
scientific information available indicates that the population decline
will continue in the future. Because the species is experiencing
significant population declines and ongoing habitat loss and
degradation, we have assigned an LPN of 2 to reflect imminent threats
of high magnitude.
Listing Priority Changes in Candidates
We reviewed the LPNs for all candidate species and are changing the
LPNs for the following three species discussed below. More information
on these species may be found in the supporting documents for this
CNOR-FS.
Birds
Brasilia tapaculo (Scytalopus novacapitalis)--The Brasilia tapaculo
is a small, secretive ground-dwelling bird with limited flight ability.
The tapaculo is found in gallery-forest habitat that is a smaller
component of the wider tropical savanna or ``Cerrado'' of the Central
Goi[aacute]s Plateau of Brazil. Gallery forests are narrow fringes of
thick streamside vegetation that occur on the edges of rivers and
streams at elevations of approximately 800-1,000 m (2,625-3,281 ft).
The Brasilia tapaculo is described as ``rare,'' but the population size
is unknown. Despite a lack of data on population trends, declines are
suspected to be occurring, owing to habitat loss and degradation in the
Cerrado. It is known to occur in six protected areas and has been found
on private land next to protected areas. Protected areas are limited in
extent and size. Only 1.2 percent of the Cerrado is in protected areas
and those protected areas are not distributed evenly across the region.
Additionally, there are few protected areas of more than 25,000
hectares (61,776 acres).
The primary threat to the species is loss and degradation of its
habitat. The Cerrado is the largest, most diverse, and possibly most
threatened tropical savanna in the world. Land in the Cerrado is
currently being converted to soybean and rice plantations. At current
rates, the remaining natural habitat in the Cerrado is predicted to be
converted to other uses by 2030. The tapaculo's gallery-forest habitat
has been less affected by clearing for agriculture than the surrounding
Cerrado. However, larger impacts to the Cerrado are certain to affect
gallery forests; erosion and deterioration of streams is increasing,
and wetland drainage and the diversion of water for irrigation and
annual burning of adjacent grasslands is expected to limit the
availability and extent of suitable habitat for the Brasilia tapaculo.
The Brazilian national authority on wildlife, Instituto Chico
Mendes de Conserva[ccedil][atilde]o da Biodiversidade (ICMBio),
categorizes Brasilia tapaculo as endangered based on severe
fragmentation of populations and continued decline in habitat. The IUCN
Red List categorizes the species as ``Near Threatened.'' It is not
threatened by international trade and is not listed in any appendices
of CITES.
In the previous ANOR, we assigned the Brasilia tapaculo an LPN of
11. After reevaluating the available information, we find that a change
to an LPN of 8 is appropriate. The Brasilia tapaculo does not represent
a monotypic genus. The threat to the species is of moderate magnitude
and is imminent. The species has a fairly wide geographic range but is
endemic to the Cerrado and strongly associated with gallery forests, a
very small component of the Cerrado. The drastic conversion of the
Cerrado is ongoing. The populations currently appear to be found only
in or next to a handful of protected areas and most of these areas are
small. The species is reported as rare, even in protected areas. Thus,
based on review of the best available scientific and commercial
information, the LPN has been changed from 11 to 8 to reflect imminent
threats of moderate magnitude.
Invertebrates (Butterflies)
Harris' mimic swallowtail (Mimoides lysithous harrisianus)--The
Harris' mimic swallowtail is a subspecies that inhabits the restinga
(sand forest) habitats of the coastal Atlantic Forest of Brazil. It
historically occurred in southern Espirito Santo State and along the
coast of the State of Rio de Janeiro,
[[Page 71462]]
Brazil. More recent records are from three locations in the State of
Rio de Janeiro, but we could not find recent population information for
the subspecies.
Habitat destruction has been the main threat and is ongoing. Based
on a number of estimates, 88 to 95 percent of the area historically
covered by tropical forests within the Atlantic Forest biome has been
converted or severely degraded as the result of human activities. In
addition to the overall loss and degradation of its habitat, the
remaining tracts of its habitat are severely fragmented. Habitat loss
due to sea-level rise may also affect this coastal subspecies, and
losses may be compounded by an increased demand by humans to use
remaining land for housing and infrastructure.
Another factor affecting this butterfly is collection. In previous
ANORs we suspected that collection may be a stressor for this species
but have now noted sale of the subspecies on the internet. The Harris'
mimic swallowtail is on the list of Brazilian fauna threatened with
extinction, and collection and trade of the subspecies is prohibited.
However, we recently found three online advertisements for the Harris'
mimic swallowtail at prices ranging from 990 to 1,950 Euros each
(approximately 1,118 to 2,182 U.S. dollars (USD)) indicating that
illegal collection and trade may be occurring and demand for this
butterfly is high. Harris' mimic swallowtail is not currently on the
IUCN Red list, although it was identified as a ``Threatened and Extinct
Subspecies'' in the family Papilionidae in the 1994 IUCN Red List. The
subspecies has not been formally considered for listing in the
appendices to CITES. It is also not regulated on the annexes to
European Union Wildlife Trade Regulations.
In the previous ANOR, the Harris' mimic swallowtail was assigned an
LPN of 6. After reevaluating the threats to this species, we have
determined that a change to an LPN of 3 is appropriate. Harris' mimic
swallowtail is a subspecies that is not within a monotypic genus.
Although the best-studied colony has maintained a stable and viable
size for nearly two decades, there is limited recent information on
status. Threats are high in magnitude due to the existence of only a
few, small fragmented colonies, and the potential for catastrophic
events such as severe tropical storms, fire or introduction of a new
disease or predator. Additionally, although the subspecies is protected
by Brazilian law and the colonies are located within protected areas,
the high price advertised online for specimens indicates that there is
demand for the subspecies, likely from illegal collection. Because the
population is very small and limited to only three known colonies,
removal of individuals from the remaining small, fragmented colonies
could, in combination with other stressors, contribute to local
extirpations. We find these threats are of high magnitude and based on
the best available information, we have changed the LPN from 6 to 3 to
reflect imminent threats of high magnitude for this subspecies.
Fluminense swallowtail (Parides ascanius)--The fluminense
swallowtail (Parides ascanius) also inhabits the restinga (sand forest)
habitats of the coastal Atlantic Forest of Brazil within the State of
Rio de Janeiro. The overall number of populations reported for the
species has declined from ``fewer than 20 colonies'' in 1994 to 8 in
2015. Genetic analysis of the eight remaining populations is consistent
with metapopulation dynamics (a group of separate populations that has
some level of mixing) with low genetic diversity and trending towards
increased isolation of these populations from urban development.
Habitat loss, degradation, and fragmentation are the principal threats
to this species. The species occupies highly specialized habitat and
requires large areas to maintain a viable colony. Only one of the eight
known populations is presently found within a large protected area
(Po[ccedil]o das Antas Biological Reserve), and the majority of the
remaining populations are on smaller, fragmented parcels with limited
or no protections. Collection and commercial exploitation (see Harris'
mimic swallowtail above) were also identified as possible factors
affecting the fluminense swallowtail. The species is located near urban
areas and is easy to capture. The impact of illegal collection to the
fluminense swallowtail is difficult to assess, but removal of
individuals from the remaining small, fragmented populations could, in
combination with other stressors, contribute to local extirpations.
The fluminense swallowtail butterfly was the first invertebrate to
be officially noted on the list of Brazilian animals threatened with
extinction in 1973. It has been classified as ``Vulnerable'' by the
IUCN Red List since 1983, although it is now marked as ``Needs
Updating.'' The species is currently categorized by Brazil as
``Imperiled.'' It has not been formally considered for listing in the
appendices to CITES. However, it is listed on annex B of the European
Union Trade Regulation.
In the previous ANOR, the fluminense swallowtail was assigned an
LPN of 5. After reevaluating the factors affecting the fluminense
swallowtail and its population decline, we have determined that a
change in the listing priority number to 2 is appropriate. The
fluminense swallowtail does not represent a monotypic genus. The
overall number of populations recorded for the species has declined and
most of the remaining populations are small and fragmented. The species
is currently affected by habitat destruction, which is high in
magnitude and imminence. Despite the conservation measures in place,
some of the remaining small populations may be impacted by illegal
collection. On the basis of this new information, we have changed the
LPN for the fluminense swallowtail from 5 to 2.
Candidate Removals
Codfish Island fernbird (Bowdleria punctata wilsoni)--We have
evaluated the threats to the Codfish Island fernbird (Bowdleria
punctata wilsoni) and considered factors that, individually and in
combination, currently or potentially could pose a risk to the species
and its habitat. After a review of the best available scientific and
commercial data, we conclude that listing this species under the Act is
not warranted because it is not likely to become an endangered species
within the foreseeable future throughout all or a significant portion
of its range. Therefore, we no longer consider the Codfish Island
fernbird to be a candidate species for listing. We will continue to
monitor the status of this species and to accept additional information
and comments concerning this finding. We will reconsider our
determination in the event that we gather new information that
indicates that the threats are of a considerably greater magnitude or
imminence than identified through assessments of information contained
in our files, as summarized below. More information on this species may
be found in the supporting documents for this CNOR-FS.
The Codfish Island fernbird is a small, insect-eating songbird
native to Codfish Island, New Zealand. Codfish Island is a nature
reserve, located 3 km (1.8 mi) off the northwest coast of Stewart
Island. The subspecies was also successfully introduced to Putauhinu
Island, approximately 40 km south of Codfish Island, in the late 1990s.
The Codfish Island fernbird is secretive, and its main habitat is the
pakihi, which consists of dense vegetation 0.9 to 2.1 m (3 to 7 ft)
high. Fernbirds will also
[[Page 71463]]
occupy forest habitats as long as rat populations are absent. Fernbirds
are poor fliers that typically scramble through vegetation, though they
occasionally fly short distances.
At its lowest point, in the early 1970s, the population was
estimated to be less than 100 individuals. Although there is no current
estimate of the size of the Codfish Island fernbird population, the
population on Codfish Island as of 2007 was believed to be ``several
hundred,'' with an additional 200-300 birds on Putauhinu Island, based
on incidental encounter rates in the various habitats. Populations on
both islands appear to have expanded into all available habitats and
appear to be stable and secure. Historically, Codfish Island fernbird
populations were greatly reduced in number due to predation by
Polynesian rats and weka (Gallirallus australis), a flightless woodhen
that is endemic to New Zealand. Codfish Island's native vegetation was
also modified by the introduced Australian brush-tailed possum
(Trichosurus vulpecula). These threats have now been eliminated through
intensive eradication efforts. The Codfish Island fernbird population
has rebounded strongly with the removal of nonnative predators in the
1980s and 1990s. Additionally, forest habitat is now regenerating, and
the fernbird has successfully recolonized and expanded its range on
Codfish Island. With the introduction of the fernbird to a second
island that is free of nonnative predators, the primary threats to the
species have been eliminated.
Neither the IUCN nor BLI have assessed the status of this
subspecies. The New Zealand Department of Conservation (NZDOC)
categorizes the Codfish Island fernbird as a range-restricted island
endemic that is ``naturally uncommon.'' It is not listed in any
appendices of CITES.
In the previous ANOR, the Codfish Island fernbird was assigned an
LPN of 12. After reevaluating the available information, we find that
this subspecies no longer warrants listing. Although it is an island
endemic that is restricted in range, the primary threat to the
species--nonnative predators--has been removed, and the population has
responded and expanded throughout its known historical range on Codfish
Island, occupying all available habitats. In addition, conservation
efforts by NZDOC have resulted in the establishment of a second
population on Putauhinu island that is free of nonnative predators, and
that population has expanded and appears to be secure. Finally, the two
islands occupied by the Codfish Island fernbird have restricted access,
such that reestablishment of nonnative predators is extremely unlikely.
In the unlikely event of nonnative predators reappearing on either
island, NZDOC has a proven track-record of success in eradicating
mammalian predators from these islands. Therefore, we have determined
that this subspecies no longer warrants listing and are removing it
from the candidate list.
Findings for Petitioned Candidate Species
Birds
Southern helmeted curassow (Pauxi unicornis)--Like the Sira
curassow (see above), the Southern helmeted curassow is a game bird
with a distinctive pale-blue horn-like appendage, or casque, above its
bill. The southern helmeted curassow is known only from central Bolivia
on the eastern slope of the Andes, where large portions of its habitat
are in National Parks. The species inhabits dense, humid, foothill and
lower montane forest and adjacent evergreen forest at altitudes between
450 and 1,500 m (1,476 to 4,921 ft).
The total population of southern helmeted curassow is estimated to
be between 1,500 and 7,500 individuals and is declining. Hunting is
believed to be the primary threat to the species, followed by habitat
loss and degradation. Although the National Parks have been important
for the preservation of the species, financial and human resources
needed to protect park resources are limited. Within the Parks, there
are human settlements and ongoing encroachment, including illegal
logging operations and forest clearing for farming. Rural development
and road building limit the species' ability to disperse. Range
reductions due to climate change are also predicted for the southern
helmeted curassow, when warming temperatures may cause the species to
shift its distribution upslope and outside of protected National Parks.
The southern helmeted curassow is classified as critically
endangered on the IUCN Red List. Trade has not been noted
internationally, and the species is not listed in any appendices of
CITES. The species is listed in annex D of the European Union Trade
Regulations.
In the previous ANOR, the southern helmeted curassow was assigned
an LPN of 2. After reevaluating the threats to the species, we have
determined that no change in the LPN is warranted. The southern
helmeted curassow does not represent a monotypic genus. It faces
threats that are high in magnitude based on its small, limited range.
The few locations where it is believed to exist continue to face
pressure from hunting and habitat loss and destruction, and population
decline will likely continue. Because the species is experiencing
ongoing significant population declines and habitat loss, we have made
no change to the LPN of 2, which reflects imminent threats of high
magnitude.
Bogot[aacute] rail (Rallus semiplumbeus)--The Bogot[aacute] rail is
found in the East Andes of Colombia, South America. It is a medium-
sized nonmigratory rail largely restricted to areas at elevations from
2,500-4,000 m (8,202-13,123 ft) in and surrounding Bogot[aacute],
Columbia, on the Ubat[eacute]-Bogot[aacute] Plateau. This region
formerly supported vast marshes and swamps, but few lakes with suitable
habitat for the rail remain. The species is secretive, and wetland
habitats most frequently used by rail are fringed by dense vegetation-
rich shallows. The current population size of the Bogot[aacute] rail is
estimated between 1,000 and 2,499 mature individuals and is thought to
be declining. The primary threat to the rail is habitat loss and
degradation. Approximately 8 million people live in the City of
Bogot[aacute] and 11 million in the larger metro area. The wetlands
have experienced a 97-percent loss in historical extent with few
suitably vegetated marshes remaining. Additionally, road building may
result in further colonization and human interference, including
introduction of nonnative species in previously stable wetland
environments. The Bogot[aacute] rail is listed as endangered at the
global and national level by IUCN. Trade does not appear to be of
concern at the international level, and the species is not listed in
any appendices of CITES.
In the previous ANOR, the Bogot[aacute] rail was assigned an LPN of
2. After reevaluating the threats to this species, we have determined
that no change in the LPN for the species is needed. The Bogot[aacute]
rail does not represent a monotypic genus. It faces threats that are
high in magnitude due to the pressures on the species' habitat. Its
range is very small and is rapidly contracting because of widespread
habitat loss and degradation. Although portions of the Bogot[aacute]
rail's range occur in protected areas, most of the savanna wetlands are
unprotected. The population is small and is believed to be rapidly
declining. The factors affecting the species are ongoing, and are,
therefore, imminent. Thus, the LPN remains at 2 to reflect imminent
threats of high magnitude.
Takahe (Porphyrio hochstetteri)--The takahe is a large flightless
bird in the rail family. The takahe was once widespread in the forest
and grassland ecosystems of New Zealand. It was
[[Page 71464]]
thought to be extinct until it was rediscovered in the Murchison
Mountains on the South Island of New Zealand in 1948. In addition to
its native range on the mainland, the takahe has been introduced to
offshore islands and mainland sanctuaries.
When rediscovered in 1948, it was estimated that the takahe
population consisted of 100 to 300 birds; in 2013, the population was
estimated at 227 adult birds. Several factors have historically led to
the species' decline, including hunting, competition from introduced
herbivores (animals that feed on plants), and predators such as weasels
and the weka, a flightless woodhen that is endemic to New Zealand.
Currently, weasel predation appears to be the most significant of these
threats. Weasel trapping is an effective tool at slowly increasing
survival and reproductive output of takahe; however, control efforts do
not completely eliminate the threat. Takahe is a long-lived bird,
potentially living between 14 and 20 years, and has a low reproductive
rate, with clutches consisting of one to three eggs. Severe weather in
the Murchison Mountains (cold winters and high snowfall) may also be a
limiting factor to the takahe. The population of takahe remains very
small and has low genetic diversity relative to other species. The
NZDOC is currently attempting to manage further loss of genetic
diversity through translocations. Additionally, NZDOC has implemented a
captive-breeding and release program to supplement the mainland
population and has established several reserve populations on islands
and fenced mainland sites; these actions are having a positive effect
on population growth. The takahe is listed as endangered on the IUCN
Red List, and New Zealand considers it to be a nationally critical
species. It is not listed in any appendices of CITES as international
trade is not a concern.
In the previous ANOR, the takahe was assigned an LPN of 8. After
reevaluating the threats to the takahe, we have determined that no
change in the classification of the magnitude and imminence of threats
to the species is warranted at this time. The takahe does not represent
a monotypic genus. Although it has a small population, limited suitable
habitat, and may experience inbreeding depression, because the NZDOC is
actively involved in measures to aid the recovery of the species, we
find the threats are moderate in magnitude. Despite conservation
efforts, the threats are ongoing and, therefore, imminent. Lack of
suitable habitat and predation, combined with the takahe's small
population size and naturally low reproductive rate, are threats to
this species that are moderate in magnitude. Thus, the LPN remains at 8
to reflect imminent threats of moderate magnitude.
Chatham oystercatcher (Haematopus chathamensis)--The Chatham
oystercatcher is native to the Chatham Island group located 860 km (534
mi) east of mainland New Zealand. The species breeds along the
coastline of four islands in the chain: Chatham, Pitt, Rangatira, and
Mangere. The Chatham oystercatcher is found mainly along rocky shores,
including wide volcanic rock platforms and occasionally on sandy or
gravelly beaches.
The Chatham oystercatcher is the rarest oystercatcher in the world,
with a recent population estimate of 309 birds. The species has
experienced a three-fold increase in its population since the first
reliable census was conducted in 1987. Most of this increase occurred
during a period of intensive management, especially predator control,
from 1998 through 2004. The Chatham oystercatcher is listed as
nationally critical by the NZDOC. It is classified as ``Endangered'' on
the IUCN Red List and is not listed in any appendices of CITES.
Predation of eggs and chicks, and to a lesser extent of adults, is
thought to be the main impediment to the Chatham oystercatcher
population. Although Mangere and Rangatira nature reserves are free of
all mammalian predators, nonnative mammalian predators inhabit Chatham
and Pitt Islands. Feral cats are the most common predator on eggs.
Other documented predators include gulls (Larus spp.), the native brown
skua (Catharacta antarctica), weka, and domestic dogs. Nest destruction
and disturbance by humans and livestock are also noted threats. Habitat
loss and degradation has occurred from introductions of nonnative
Marram grass (Ammophila arenaria) in the early 1900s to re-vegetate
destabilized dunes. The dense marram grass is unsuitable for Chatham
oystercatcher nesting. Consequently, the Chatham oystercatcher is
forced to nest closer to shore, where nests are vulnerable to tides and
storm surges; up to 50 percent of eggs are lost in some years. Rising
sea levels associated with climate change will likely affect future
nesting success.
In the previous ANOR, the Chatham oystercatcher was assigned an LPN
of 8. After reevaluating the threats to this species, we have
determined that no change in the classification of the magnitude and
imminence of threats to the species is warranted. The Chatham
oystercatcher does not represent a monotypic genus. The current
population estimate is very small, and the species has a limited range,
but NZDOC has taken measures to recover the species and the population
is slowly growing. However, threats (predation, trampling, low
population numbers, and loss of eggs due to storm surges) are ongoing
and, thus, are imminent. The LPN remains an 8 to reflect imminent
threats of moderate magnitude.
Orange-fronted parakeet (Cyanoramphus malherbi)--The orange-fronted
parakeet was once well distributed on the South Island of mainland New
Zealand and a few offshore islands. It is now considered the rarest
parakeet in New Zealand. Remaining naturally occurring populations are
restricted to limited range (30 km (18.6 mi)) of four areas of
subalpine mature beech forests (Nothofagus spp.), on the South Island.
Orange-fronted parakeets have also been released onto four predator-
free islands where breeding has been confirmed.
The species' range contracted when its population was severely
reduced in the late 1800s and early 1900s for unknown reasons.
Information on current population status is mixed, but optimistic. The
population experienced another crash in 1990-2000 following rat
invasions. The population is still small and has declined over the last
decade with estimates between 290 and 690 individuals in early 2013.
The 2013 estimates indicated further declines on the mainland and,
during a 14-year period (approximately three generations), a reduction
in the number of mature birds. More recently, the global population is
reported as increasing due to successful translocations to predator-
free islands and control of predators in its range on the South Island.
The most prominent factors affecting the species on the mainland
are predation by nonnative mammals such as weasels and rats (Rattus
spp.), as well as habitat destruction. Habitat loss and degradation has
affected large areas of native forest on the mainland. In addition,
silviculture (care and cultivation) of beech forests in the past had
removed mature trees with nest cavities needed by the parakeet. The
species' habitat is also degraded by introduced herbivores that alter
forest structure in a way that reduces the available feeding habitat
for the parakeet. Lastly, Beak and Feather Disease Virus (BFDV) is a
potential threat to this species. The disease was discovered in wild
native birds in New Zealand in 2008 (e.g., the red-fronted parakeet,
Cyanoramphus novaezelandiae) though it has not been documented in the
orange-fronted
[[Page 71465]]
parakeet. Infected birds either develop immunity, die within a couple
of weeks, or become chronically infected. Chronic infections result in
feather loss and deformities of beak and feathers.
In the previous ANOR, the orange-fronted parakeet was assigned an
LPN of 8. After reevaluating the factors affecting the species, we have
determined that no change in the classification of the magnitude of
threats to the species is warranted because NZDOC is actively managing
the species. The orange-fronted parakeet does not represent a monotypic
genus. Although the species' available suitable nesting habitat in
beech forests is extremely limited, translocations have taken place and
seem to be successful. However, the population is still small and
vulnerable to several threats despite management efforts that may have
stabilized the population (albeit at small numbers). Small populations
may also be vulnerable to stochastic events, including disease
outbreaks such as BFDV. We find that the threats to this species are
still imminent; thus, the LPN remains at 8 to reflect imminent threats
of moderate magnitude.
Uvea parakeet (Eunymphicus uvaeensis)--The Uvea parakeet is a
relatively large, green parakeet found on the small atoll of Uvea,
located approximately 1,500 km (932 mi) east of Australia in the
Loyalty Archipelago, New Caledonia (a territory of France). The entire
island of Uvea is considered an Important Bird Area by BirdLife
International which works with communities to combine conservation with
sustainable livelihoods. To date, however, we are unaware of any
designated reserves or provincial parks. Uvea parakeets were introduced
to the adjacent island of Lifou (to establish a second population) in
1925 and 1963, but these introductions failed. The species occupies
both the north and south end of Uvea Island. The species primarily uses
older (old-growth) forest habitats and nests in the cavities of living
Syzygium and Mimusops trees. Their exclusive use of tree cavities for
nesting may be a limiting factor. In 1977, the Uvea parakeet population
was estimated to be between 500 to 800 individuals. More recent
analyses provided two population estimates of approximately 1,730 birds
with varying confidence intervals.
Historically, the primary threat to this species was the capture of
juveniles for the pet trade, which involved cutting open nesting
cavities to extract nestlings; this practice renders the holes
unsuitable for future nesting. Since restrictions have been put into
place and the species has been more closely monitored, it appears that
nest poaching is no longer occurring such that it significantly affects
this species, and the population has increased. Other identified
threats to the species include: Habitat degradation and conversion,
loss of nesting cavities to bees, loss of habitat through climate
change, and the potential for introduction of nonnative predators.
Artificial nests are being installed to increase available nesting
sites; however, Uvea parakeets have not yet used the artificial nests
provided. Uvea is a low-elevation and relatively flat island. Climate
change (and associated sea-level rise) will likely result in loss of
forest habitat or important food species and is considered a
substantial threat to the persistence of Uvea parakeets. The limited
occupied range of the species (only 34 km\2\ (13 mi\2\)) in a few
fragmented patches on Uvea, amplifies this threat. Uvea parakeet is
listed as ``Endangered'' on the IUCN Red List. It is listed in appendix
I of CITES and annex A of the European Union Trade Regulations.
In the previous ANOR, the Uvea parakeet was assigned an LPN of 8.
After reevaluating the threats to this species, we have determined that
no change in the classification of the magnitude and imminence of
threats to the species is warranted. The Uvea parakeet does not
represent a monotypic genus. The Uvea parakeet has a limited
distribution on a single small island with limited remaining old-growth
forest on which the bird depends for nesting cavities. The population
has increased in size due to conservation, education, a ban on
commercial trade, and a reduction in poaching; however, several threats
(including habitat loss, loss of nesting cavities and effects from
climate change) are still present and ongoing and, therefore, imminent.
The LPN remains an 8 to reflect imminent threats of moderate magnitude.
Helmeted woodpecker (Dryocopus galeatus)--The helmeted woodpecker
is a fairly small woodpecker native to regions of southern Brazil,
eastern Paraguay, and northeastern Argentina. Its characteristic
habitat is expansive, well-preserved southern Atlantic Forest in both
lowland and montane areas from sea level up to elevations of 1,000 m
(3,280 ft). It is believed to prefer mature (old-growth) trees in
tropical and subtropical semi-deciduous forests as well as in mixed
deciduous-coniferous forests.
The helmeted woodpecker's population is believed to have declined
sharply between 1945 and 2000 in conjunction with the clearing of
mature forest habitat and is currently estimated at 400-8,900
individuals. Although forest clearing has recently slowed, and the
species occurs in at least 17 protected areas throughout its range,
habitat degradation continues and the population is still believed to
be declining. The principal threat to the helmeted woodpecker is loss,
degradation, and fragmentation of its Atlantic forest habitat.
Competition for nest cavities is also likely a limiting factor. The
helmeted woodpecker is one of the rarest woodpecker in the Americas. It
is listed as endangered in Brazil and as vulnerable by the IUCN. It is
not listed in any appendices of CITES.
In the previous ANOR, the helmeted woodpecker was assigned an LPN
of 8. After reevaluating the available information, we find that no
change in the LPN for the helmeted woodpecker is warranted. The
helmeted woodpecker does not represent a monotypic genus. The magnitude
of threats to the species is moderate because the species' range is
fairly large. The threats are imminent because the forest habitat upon
which the species depends is still being altered and degraded. An LPN
of 8 continues to be accurate for this species.
Okinawa woodpecker (Dendrocopos noguchii syn. Sapheopipo
noguchii)--The Okinawa woodpecker is a relatively large woodpecker
found on Okinawa Island, Japan. The species prefers undisturbed,
mature, subtropical evergreen broadleaf forests. It currently occurs
within the forested areas in the northern part of the island, generally
in the Yambaru forest, and in some undisturbed forested in coastal
areas. Most of the older forests that support the species are within
the Jungle Warfare Training Center (formerly, the Northern Training
Area), part of the United States Marine Corps installation on Okinawa
Island.
The Okinawa woodpecker is considered one of the world's rarest
woodpecker species. Current population estimates are between 100 and
390 individuals and declining.
Habitat destruction and fragmentation was a significant threat. As
of 2001, only 40 km\2\ (15 mi\2\) of suitable habitat was available for
this species. While most of the habitat loss appears to have ceased,
the Okinawa woodpecker still suffers from limited suitable habitat and
a small population size. This situation makes it vulnerable to
extinction from disease and natural disasters such as typhoons. In
addition, the species is vulnerable to introduced predators such as
feral dogs and cats, Javan mongoose (Herpestes javanicus), and weasels
(Mustela itatsi). The species is listed as critically endangered on the
IUCN Red List. It is
[[Page 71466]]
legally protected in Japan. It is not listed in any appendices of
CITES.
In the previous ANOR, the Okinawa woodpecker was assigned an LPN of
2. After reevaluating the available information, we find that no change
in the LPN is warranted. The Okinawa woodpecker does not represent a
monotypic genus. Threats to the species are of high magnitude due to
the scarcity of old-growth habitat, upon which the species is
dependent. Its population is very small and is believed to still be
declining, and species with fragmented habitat in combination with
small population sizes may be at greater risk of extinction due to
synergistic effects. The threats to the species are ongoing and
imminent and high in magnitude due to its restricted population size,
past habitat loss, and endemism. The LPN for this species remains a 2
to reflect imminent threats of high magnitude.
Yellow-browed toucanet (Aulacorhynchus huallagae)--The yellow-
browed toucanet has a small range on the east slope of the Andes of
north-central Peru at elevations of 2,000-2,600 m (6,562-8,530 ft). The
toucanet occurs in humid montane forests. The population status is not
well known because of the inaccessibility of its habitat, but is
estimated at 600-1,500 mature individuals. Habitat loss and destruction
from deforestation for agriculture has been widespread in the region
and is suspected to be the main threat, although deforestation appears
to have occurred mainly below the altitudinal range of this toucanet.
Gold mining and manufacturing also are common in the region. The
yellow-browed toucanet is described as scarce wherever found, and
ongoing population declines resulting from habitat loss are assumed. It
is classified as endangered on the IUCN Red List and is not listed in
any CITES appendices.
In the previous ANOR, the yellow-browed toucanet was assigned an
LPN of 2. After reevaluating the available information, we find that no
change in the classification of the magnitude and imminence of threats
to the species is warranted at this time. The yellow-browed toucanet
does not represent a monotypic genus. The estimated population is small
with a restricted range. The magnitude of threats to the habitat
remains high, and its population is likely declining. The LPN remains a
2 to reflect imminent threats of high magnitude.
Ghizo white-eye (Zosterops luteirostris)--The Ghizo white-eye is a
small passerine (perching) bird. It is endemic to the small island of
Ghizo in the Solomon Islands in the South Pacific Ocean, east of Papua
New Guinea. The total range of the Ghizo white-eye is estimated to be
less than 35 km\2\ (13.5 mi\2\), of which less than 1 km\2\ (0.39
mi\2\) is the old-growth forest that the species apparently prefers.
Little information is available about this species and its habitat.
It is locally common in old-growth forest patches and less common
elsewhere. The species has been observed in a variety of habitats on
the island, but it is unknown whether sustainable populations can exist
outside of forested habitats. The population is estimated to be between
250 and 999 mature individuals and is suspected to be declining due to
habitat degradation, particularly since a tsunami hit the island in
2007. Habitat loss appears to be the main threat. As of 2012, the human
population on the island was 7,177 and growing rapidly, and there has
been prolific growth in informal human settlements and temporary
housing on Ghizo, which may be adversely affecting the Ghizo white-eye
and its habitat. Areas around Ghizo Town, which previously supported
the species, have been further degraded since the town was devastated
by the 2007 tsunami, and habitat was found less likely able to support
the species in 2012. The species is also affected by conversion of
forested areas to agricultural uses. The old-growth forest on Ghizo is
still under pressure from clearance for local use as timber, firewood,
and gardens, as are the areas of secondary growth, which are already
suspected to be suboptimal habitat for this species.
The population of this species is believed to be declining and,
given its fragmented habitat in combination with small population
sizes, may be at greater risk of extinction due to synergistic effects.
The IUCN Red List classifies this species as endangered. It is not
listed in any appendices of CITES, and this species is not in
international trade.
In the previous ANOR, the Ghizo white-eye was assigned an LPN of 2.
After reevaluating the available information, we find that no change in
the LPN for this species is warranted. The Ghizo white-eye does not
represent a monotypic genus. It faces threats that are high in
magnitude due to declining suitable habitat and its small, declining
population size. The best available information indicates that forest
clearing is occurring at a pace that is rapidly denuding the habitat;
secondary-growth forest continues to be converted to agricultural
purposes. Further, the human population on the small island is likely
contributing to the reduction in old-growth forest for local uses such
as gardens and timber. These threats to the species are ongoing, of
high magnitude, and imminent. Thus, based on the best available
scientific and commercial information, the LPN remains a 2 for this
species.
Black-backed tanager (Tangara peruviana)--The black-backed tanager
is endemic to the coastal Atlantic Forest region of southeastern
Brazil. It has been found in the coastal states of Espirito Santo, Rio
de Janeiro, S[atilde]o Paulo, Paran[agrave], Santa Catarina, and Rio
Grande do Sul. The species is generally restricted to the sand-forest
``restinga'' habitat, which is a coastal component habitat of the
greater Atlantic Forest complex. Restingas are herbaceous, shrubby
coastal sand-dune habitats. The black-backed tanager is primarily found
in undisturbed habitat but has also been observed in secondary (or
second-growth) forests. It has also been observed visiting gardens and
orchards of houses close to forested areas. Within suitable habitat,
the black-backed tanager is generally not considered rare. The
population estimate is between 2,500 to 10,000 mature individuals.
Populations currently appear small and fragmented and are believed to
be declining.
The primary factor affecting this species is the rapid and
widespread loss of habitat, mainly to urban expansion and beachfront
development. Its habitat is under pressure from the intense development
that occurs in coastal areas, particularly south of Rio de Janeiro. In
addition to the overall loss and degradation of its habitat, the
remaining tracts of its habitat are severely fragmented. The black-
backed tanager's remaining suitable habitat in the areas of Rio de
Janeiro and Paran[aacute] have largely been destroyed, and habitat loss
and degradation will likely increase in the future. Additionally,
although small portions of this species' range occur in six protected
areas, protections appear limited. Sea-level rise may also affect this
species, which inhabits coastal areas. Habitat loss due to sea-level
rise may be compounded by an increased demand by humans to use
remaining land for housing and infrastructure. These factors affecting
the black-backed tanager's remaining habitat are ongoing due to the
challenges that Brazil faces to balance its competing development and
environmental priorities. The black-backed tanager is classified as
vulnerable by the IUCN. It is not listed in any appendices of CITES. It
is listed as vulnerable in Brazil.
In the previous ANOR, the black-backed tanager was assigned an LPN
of
[[Page 71467]]
8. After reevaluating the available information, we have determined
that no change in the LPN for this species is warranted at this time.
The black-backed tanager does not represent a monotypic genus. This
species is protected under Brazil's National Environmental Policy Act
(Law 6.938 of 1981), and several other laws implementing protection for
fauna. Despite these laws, its habitat continues to diminish. We find
that threats (primarily habitat loss) to the species are moderate in
magnitude due to the species' fairly large range, its existence in
protected areas, and apparent flexibility in diet and habitat
suitability. Threats are imminent because the species is at risk due to
ongoing and widespread loss of habitat due to beachfront and related
development. Therefore, an LPN of 8 remains valid for this species.
Lord Howe Island pied currawong (Strepera graculina crissalis)--The
Lord Howe Island pied currawong is a fairly large crow-like bird,
endemic to Lord Howe Island, New South Wales, Australia. Lord Howe
Island is a small island northeast of Sydney, Australia, with 28
smaller islets and rocks. The Lord Howe pied currawong occurs
throughout the island but is most numerous in the mountainous areas on
the southern end. It has also been recorded to a limited extent on the
Admiralty Islands, located 1 km (0.6 mi) north of Lord Howe Island.
Approximately 75 percent of Lord Howe Island, plus all outlying islets
and rocks within the Lord Howe Island group, are protected under the
Permanent Park Preserve, which has similar status to that of a national
park. The Lord Howe Island pied currawong breeds in rainforests and
palm forests, particularly along streams.
The best current population estimate in 2005 and 2006 indicated
that there were approximately 200 individuals. The Lord Howe Island
pied currawong exists as a small isolated population, which makes it
vulnerable to stochastic events. The potential for an introduction of
other exotic predators to this island ecosystem has also been
identified as an issue for this species. In addition to its small
population size, direct persecution (via shootings) by humans in
retaliation for predation on domestic and endemic birds has been
documented. The incidence of shootings has declined since the 1970s,
when conservation efforts on Lord Howe Island began, but occasional
shootings were still occurring as of 2007.
Because the Lord Howe pied currawong often preys on small rodents,
it may be subject to nontarget poisoning during ongoing rat-baiting
programs. Experimental efforts to develop techniques to house the birds
in aviaries while rat-baiting programs take place show promise for
protecting the species during these eradication efforts. The
subspecies' status is not addressed by IUCN. It is not listed in any
appendices of CITES as trade is not an issue for this taxon. The New
South Wales Threatened Species Conservation Act of 1995 lists the Lord
Howe pied currawong as ``Vulnerable'' due to its extremely limited
range and its small population size.
In the previous ANOR, the Lord Howe pied currawong was assigned an
LPN of 6. After reevaluating the threats to the Lord Howe pied
currawong, we have determined that no change in the LPN representing
the magnitude and imminence of threats to the subspecies is warranted.
The Lord Howe pied currawong does not represent a monotypic genus. It
faces threats that are high in magnitude due to a combination of
factors including its extremely small population size, and nontarget
poisoning. Despite conservation efforts, the population of the Lord
Howe pied currawong has remained small. Species with small population
sizes such as these may be at greater risk of extinction due to
synergistic effects of factors affecting this species. However, because
conservation efforts for the species have been implemented, and the
species is being closely managed and monitored, we find that the
threats are nonimminent. Thus, based on the best available information,
the LPN remains at 6 to reflect nonimminent threats of high magnitude.
Invertebrates (Butterflies)
Jamaican kite swallowtail (Protographium marcellinus, syn.
Eurytides)--The Jamaican kite swallowtail is a small blue-green and
black butterfly endemic to Jamaica. The species occurs in limestone
forest containing its only known larval host plant, Oxandra lanceolata.
There is no known estimate of population size. The Jamaican kite
swallowtail was historically locally abundant. Presently it maintains
low population levels with occasional strong flight seasons with higher
numbers. There is only one known breeding site in the eastern coast
town of Rozelle, in St. Thomas Parish, near Kingston (Jamaica's
capital). However, researchers now believe that there are likely other
breeding sites--one potential site being Jamaica's Cockpit Country, a
remote and rugged forested region in the west-central portion of the
island.
Habitat loss, degradation, and fragmentation are considered to be
the primary factors affecting the Jamaican kite swallowtail.
Additionally, the species is vulnerable due to its small population
size and limited distribution on the island. After centuries of a high
rate of deforestation, the island lost much of its original forest.
Eight percent of the total land area of Jamaica is natural forest with
minimal human disturbance. In Rozelle, habitat modification for
agricultural and industrial purposes such as mining has diminished this
species' habitat. Most of the damage took place decades ago, but small
farming still occurs there. The rugged terrain of the Cockpit Country
has hindered large-scale exploitation of resources in the interior, but
the periphery and surrounding plains are badly degraded. Major threats
identified for the Cockpit Country include: Mining, forest conversion,
nonnative invasive species, solid-waste disposal, incompatible
agricultural practices, and collecting. Additionally, bauxite mining
for aluminum production is an important economic activity for Jamaica
and is a large contributor to deforestation. Jamaica's location in the
hurricane belt increases its vulnerability to natural environmental
events. Although the Jamaican Wildlife Protection Act of 1994 carries
steep fines and penalties, illegal collection (see Harris' mimic
swallowtail above) is a potential threat for the Jamaican kite
swallowtail. The butterfly has been noted for sale on the internet as
recently as 2015 for 150 Euros (164 USD). The species is classified as
vulnerable on the IUCN Red List and IUCN indicates that this assessment
needs updating. It is not is not listed in any appendices of CITES nor
is it listed on annex B of the European Union Trade Regulations.
In the previous ANOR, the Jamaican kite swallowtail was assigned an
LPN of 2. After reevaluating the factors affecting the Jamaican kite
swallowtail, we have determined that no change in LPN is warranted. The
Jamaican kite swallowtail does not represent a monotypic genus.
Although alternate breeding sites are likely, the only documented site
and the presumed core population for this species is in one location
that is vulnerable to stochastic environmental events such as
hurricanes. Although Jamaica has taken regulatory steps to preserve
native swallowtail habitat, plans for conservation of two vital areas
for the butterfly (Rozelle and the Cockpit Country) have not been
implemented. Based on our reevaluation of the threats to this species,
the LPN remains a 2 to
[[Page 71468]]
reflect imminent threats of high magnitude.
Hahnel's Amazonian swallowtail (Parides hahneli)--Hahnel's
Amazonian swallowtail is a large black and yellow butterfly endemic to
Brazil. It is known from three locations along the tributaries of the
middle and lower Amazon River basin in the states of Amazonas and
Par[aacute]. Its preferred habitat is old sand strips (stranded
beaches) that are overgrown with dense scrub vegetation or forest found
close to the major rivers. Hahnel's Amazonian swallowtail is described
as very scarce and extremely localized in association with its
specialized habitat and its larval host plant. Population size and
trends are not known for this species. However, habitat alteration
(e.g., for dam construction and waterway crop transport) and
destruction (e.g., clearing for agriculture and cattle grazing) are
ongoing in Par[aacute] and Amazonas where this species is found.
Researchers are concerned that potential harmful impacts from habitat
alterations are taking place before the butterfly can be better studied
and its ecological needs can be understood.
Collection (see Harris' mimic swallowtail above) is also a
potential threat for Hahnel's Amazonian swallowtail. The species has
been collected for commercial trade and may also be reared for trade.
Locations in the wild have been kept secret given the high value of
this butterfly to collectors. Two specimens of Hahnel's Amazonian
swallowtail were recently noted in online sales from locations in the
United States (500 USD) and Germany (approximately 166 USD). Hahnel's
Amazonian swallowtail is described as data deficient by the IUCN Red
List. The species is listed as endangered on the State of Par[aacute]'s
list of threatened species, but it is not listed by the State of
Amazonas or by Brazil. Hahnel's Amazonian swallowtail is not listed in
any appendices of CITES. However, it is listed on annex B of the
European Union Trade Regulations.
In our previous ANOR, the Hahnel's Amazonian swallowtail was
assigned an LPN of 2. After reevaluating the threats to the Hahnel's
Amazonian swallowtail, we have determined that no change in the LPN is
warranted. This swallowtail does not represent a monotypic genus. It
faces threats that are high in magnitude and imminence due to its small
endemic population, and limited and decreasing availability of its
highly specialized habitat. Habitat alteration and destruction (e.g.,
dam construction, waterway crop transport, clearing for agriculture,
and cattle grazing) are ongoing in Par[aacute] and Amazonas where the
butterfly is found. These threats are high in magnitude due to the
species' highly localized and specialized habitat requirements.
Potential impacts from collection are unknown but could, in combination
with other stressors, contribute to local extirpations. Based on a
reevaluation of the threats, the LPN remains a 2 to reflect imminent
threats of high magnitude.
Kaiser-i-Hind swallowtail (Teinopalpus imperialis)--The Kaiser-i-
Hind swallowtail is native to Himalayan regions of Bhutan, China,
India, Laos, Myanmar, Nepal, Thailand, and Vietnam. Although it has a
relatively large range, it is restricted to higher elevations and
occurs only locally within this range. This species occurs at altitudes
of 1,500 to 3,050 m (4,921 to 10,000 ft) above sea level, in
undisturbed (primary) broad-leaved-evergreen forests or montane
deciduous forests. Adults fly up to open hilltops above the forests to
mate, where males will often defend mating territories. Larval host-
plants are limited to Magnolia and Daphne spp., and in some regions the
Kaiser-i-Hind swallowtail is strictly monophagous, only using a single
species of Magnolia as a host plant. Despite the species' widespread
distribution, populations are described as being very local and never
abundant. Even early accounts of the species described it as being a
very rare occurrence. Habitat destruction is believed to negatively
affect this species, which prefers undisturbed high-altitude forests.
In China and India, the Kaiser-i-Hind swallowtail populations are
affected by habitat modification and destruction due to commercial and
illegal logging. In Nepal, the species is affected by habitat
disturbance and destruction resulting from mining, wood collection for
use as fuel, deforestation, collection of fodders and fiber plants,
forest fires, invasion of bamboo species into the oak forests,
agriculture, and grazing animals. In Vietnam, the forest habitat is
reportedly declining. The Forest Ministry in Nepal considers habitat
destruction to be a critical threat to all biodiversity, including the
Kaiser-i-Hind swallowtail. Comprehensive information on the rate of
degradation of Himalayan forests containing the Kaiser-i-Hind butterfly
is not available, but habitat loss is consistently reported as one of
the primary ongoing threats to the species there.
Collection for commercial trade is also regarded as a threat to the
species. The Kaiser-i-Hind swallowtail is highly valued and has been
collected and traded despite various prohibitions. Although it is
difficult to assess the potential impacts from collection, it is
possible that collection in combination with other stressors could
contribute to local extirpations of small populations.
Since 1996, the Kaiser-i-Hind swallowtail has been categorized on
the IUCN Red List as ``Lower Risk/near threatened,'' but IUCN indicates
that this assessment needs updating. The Kaiser-i-Hind swallowtail has
been listed in CITES appendix II since 1987. Additionally, the Kaiser-
i-Hind swallowtail is listed on annex B of the European Union Trade
Regulations.
After reevaluating the threats to this species, we have determined
that no change in its LPN of 8 is appropriate. The Kaiser-i-Hind
swallowtail does not represent a monotypic genus. The current factors,
habitat destruction and illegal collection, are moderate in magnitude
due to the species' wide distribution and to various protections in
place within each country. We find that the threats are imminent due to
ongoing habitat destruction and high market value for specimens. Based
on our reassessment of the threats, we have retained an LPN of 8 to
reflect imminent threats of moderate magnitude.
Findings for Non-Petitioned Candidate Species
Molluscs
Colorado delta clam (Mulinia coloradoensis)--The Colorado Delta
clam is a relatively large, approximately 30 mm (1.2 in) average
length, estuarine bivalve, once abundant at the head of the Gulf of
California in the Colorado River estuary in Mexico prior to the
construction of dams on the Colorado River. Live individuals of the
clam were not observed anywhere in the wild between 1968 and 1998,
despite extensive studies of bottom-dwelling fauna in the region. In
1998, a small relict population was discovered at Isla Montague,
Mexico, at the mouth of the Colorado River Delta, and this population
represents the extent of the species' currently known range. The clam
is found in low intertidal mud at depths of about 7 cm (2.75 in)
beneath the sediment and is a suspension-feeder. Freshwater inflow is
critical to the species' survival because brackish water (a mix of salt
and fresh water) is an important component of its habitat and life
history. We are unaware of precise estimates of the population size for
the Colorado Delta clam, but a 90-percent decline since dam
construction has been suggested.
Habitat loss and degradation are considered to be the primary
factors affecting the Colorado Delta clam. Additionally, the species is
now
[[Page 71469]]
vulnerable due to its small population size and limited distribution.
Dams and diversions along the Colorado River have greatly affected the
estuarine environment, decreasing freshwater, nutrient and sediment
inflow. The Colorado Delta clam may have experienced a greater than 90-
percent reduction in its occupied range caused by the decrease in
freshwater flow to the estuary.
Agricultural return flow from the Mexicali Valley, coupled with
aquifer inflow, is a very important freshwater source ensuring the
maintenance of the estuarine environment in the Delta and the continued
survival of the clam. In 2009, the U.S. completed lining of the All-
American Canal to prevent water loss via seepage. Prior to lining,
water seepage from the All-American Canal was an important source of
recharge to the Mexicali Valley aquifer. The All-American Canal lining
is predicted to reduce total recharge to the Mexicali Valley aquifer,
which will reduce the freshwater inflow into the Delta. Additionally,
predicted increases in drought and warmer temperatures associated with
climate change will contribute to deterioration of the clam's habitat
by further curtailing freshwater inflow and favoring nonnative invasive
aquatic species to the detriment of native species like the Colorado
Delta clam. The species has not been assessed for the IUCN Red List. It
is not threatened by international trade, and it is not listed in any
appendices of CITES.
In the previous ANOR, the Colorado Delta clam was assigned an LPN
of 2. After reevaluating the factors affecting the clam, we have
determined that no change in LPN is warranted. The Colorado Delta clam
does not represent a monotypic genus. The available evidence indicates
that Colorado delta clam is now restricted to one relict population at
Isla Montague at the mouth of the Colorado River delta. Its habitat is
currently affected by the ongoing and continuing (i.e., imminent) loss
of freshwater input into the Delta. Furthermore, the available
information indicates that loss of freshwater will likely worsen in the
near- and long-term future. Since habitat containing the entire range
of the species may be rendered unsuitable within the near future, we
find that threats are of high magnitude. Therefore, we find the
Colorado delta clam is subject to high-magnitude imminent threats, and
we retain an LPN of 2 for this species.
Preclusion and Expeditious Progress
To make a finding that a particular action is warranted but
precluded, the Service must make two determinations: (1) That the
immediate proposal and timely promulgation of a final regulation is
precluded by pending listing proposals and (2) that expeditious
progress is being made to add qualified species to either of the lists
and to remove species from the lists (16 U.S.C. 1533(b)(3)(B)(iii)). A
listing proposal is precluded if the Service does not have sufficient
resources available to complete the proposal, because there are
competing demands for those resources, and the relative priority of
those competing demands is higher. Thus, in any given fiscal year (FY),
multiple factors dictate whether it will be possible to undertake work
on a listing proposal regulation or whether publication of such a
proposal is precluded by higher-priority listing actions, including:
(1) The amount of resources available for completing the listing
function; (2) the estimated cost of completing the proposed listing;
and (3) the Service's workload and prioritization of the proposed
listing in relation to other actions.
The resources available for listing actions are determined through
the annual Congressional appropriations process. The appropriation for
the Listing Program is available to support work involving the
following listing actions: Proposed and final listing rules; 90-day and
12-month findings on petitions to add species to the Lists of
Endangered and Threatened Wildlife and Plants (Lists) or to change the
status of a species from threatened to endangered; annual
determinations on prior ``warranted-but-precluded'' petition findings
as required under section 4(b)(3)(C)(i) of the Act; critical habitat
petition findings; proposed and final rules designating critical
habitat; and litigation-related, administrative, and program-management
functions (including preparing and allocating budgets, responding to
Congressional and public inquiries, and conducting public outreach
regarding listing and critical habitat).
The work involved in preparing various listing documents can be
extensive and may include, but is not limited to: Gathering and
assessing the best scientific and commercial data available and
conducting analyses used as the basis for our decisions; writing and
publishing documents; and obtaining, reviewing, and evaluating public
comments and peer review comments on proposed rules and incorporating
relevant information into final rules. The number of listing actions
that we can undertake in a given year also is influenced by the
complexity of those listing actions; that is, more complex actions
generally are more costly.
We cannot spend more than is appropriated for the Listing Program
without violating the Anti-Deficiency Act (see 31 U.S.C.
1341(a)(1)(A)). In addition, in FY 1998 and for each fiscal year since
then, Congress has placed a statutory cap on funds that may be expended
for the Listing Program, equal to the amount expressly appropriated for
that purpose in that fiscal year. This cap was designed to prevent
funds appropriated for other functions under the Act (for example,
recovery funds for removing species from the Lists), or for other
Service programs, from being used for Listing Program actions (see
House Report 105-163, 105th Congress, 1st Session, July 1, 1997).
Prior to FY 2012, there was no distinction in appropriations for
listing domestic and foreign species. However, in an effort to balance
foreign species listing commitments with other Listing Program
responsibilities, effective FY 2012 and for each fiscal year since
then, the Service's Listing Program budget has included a foreign
species subcap providing that funding is not to exceed a specified
amount for implementation of subsections (a), (b), (c), and (e) of
section 4 of the Act for species that are not indigenous to the United
States (see Conference Report 112-331, 112th Congress, 1st session,
Dec. 15, 2011).
Thus, through the listing program cap and the foreign species
subcap, Congress has determined the amount of money available for
foreign species listing activities, including petition findings and
listing determinations.
In FY 2016, the Service had $1,504,000 that could be used for
listing actions for foreign species. This funding supports work in the
following categories: Compliance with court orders and court-approved
settlement agreements requiring that petition findings or listing
determinations be completed by a specific date; section 4 (of the Act)
listing actions with absolute statutory deadlines; essential
litigation-related, administrative, and listing program-management
functions; and high-priority listing actions for some of our candidate
species.
In addition, available staff resources are also a factor in
determining which high-priority species are provided with funding. The
Branch of Foreign Species may, depending on available staff resources,
work on species described within this CNOR-FS with an LPN of 2 or 3,
and when appropriate, species with a lower priority if they overlap
geographically or have the same threats as the species with the high
priority.
[[Page 71470]]
Based on the prioritization factors mentioned above, we continue to
find that proposals to list the candidate species included in this
CNOR-FS are all precluded by higher-priority listing actions. Because
the actions in table 2 below are either the subject of a court-approved
settlement agreement or subject to an absolute statutory deadline and,
thus, are higher priority than work on proposed listing determinations
for the 20 species described above, publication of proposed rules for
these 20 species is precluded.
Table 2--Pending ESA Foreign Species Listing Actions
------------------------------------------------------------------------
Species Action
------------------------------------------------------------------------
Actions Subject to Court Order/Settlement Agreement
------------------------------------------------------------------------
All have been completed (See table ....................................
3 below for these specific
actions).
------------------------------------------------------------------------
Actions With Statutory Deadlines
------------------------------------------------------------------------
Scarlet macaw..................... Final listing determination.
Virgin Islands coqui.............. 12-month petition finding.
Hyacinth macaw.................... Final listing determination.
Peary, and Dolphin and Union 12-month petition finding.
caribou.
3 Aral Sea sturgeon species....... 12-month petition finding.
3 East Asian sturgeon species..... 12-month petition finding.
11 tarantula species.............. 12-month petition finding.
4 Persian sturgeon species........ 12-month petition finding.
Ridgway's hawk eagle.............. 12-month petition finding.
15 bat species.................... 12-month petition finding.
Emperor penguin................... 12-month petition finding.
Flores hawk-eagle................. 12-month petition finding.
Three-toed pygmy sloth............ 12-month petition finding.
Egyptian tortoise................. 12-month petition finding.
Golden conure..................... 12-month petition finding.
2 Australian parakeet species..... Final listing determination.
Flat-tailed tortoise.............. 12-month petition finding.
Spider tortoise................... 12-month petition finding.
7 pangolin species................ 12-month petition finding.
African elephant.................. 12-month petition finding.
Long-tailed chinchilla............ 12-month petition finding.
------------------------------------------------------------------------
As explained above, a determination that listing is warranted but
precluded must also demonstrate that expeditious progress is being made
to add and remove qualified species to and from the Lists. As with our
``precluded'' finding, the evaluation of whether progress in adding
qualified species to the Lists has been expeditious is a function of
the resources available for listing and the competing demands for those
funds. Our expeditious progress for foreign species since publication
of our previous ANOR, published on April 25, 2013 (78 FR 24604), to
October 17, 2016, includes preparing and publishing the following:
Table 3--ESA Foreign Species Listing Actions Published Since the Previous ANOR Was Published on April 25, 2013
----------------------------------------------------------------------------------------------------------------
Publication date Species Action FR pages
----------------------------------------------------------------------------------------------------------------
6/5/2013.................... Scimitar-horned oryx, 12-month petition 78 FR 33790-33797
dama gazelle, and findings; delisting
addax. not warranted.
6/12/2013................... Chimpanzee............. 12-month petition 78 FR 35201-35217
finding and proposed
rule.
6/25/2013................... Broad-snouted caiman... Final rule; threatened 78 FR 38162-38190
with special rule.
9/11/2013................... Southern white rhino... Interim rule: 78 FR 55649-55656
Threatened due to
similarity of
appearance.
9/24/2013................... Ten sturgeon species... 90-day finding; 78 FR 58507-58510
initiation of status
review.
10/3/2013................... Blue-throated macaw.... Final rule: Endangered 78 FR 61208-61219
10/29/2013.................. Five birds from Final rule; endangered 78 FR 64692-64733
Columbia and Ecuador.
11/19/2013.................. Vicu[ntilde]a in Notice of initiation 78 FR 69436-69437
Argentina, Bolivia, of 5-year review.
Chile, Ecuador, and
Peru.
12/3/2013................... Eleven tarantula 90-day findings; 78 FR 72622-72625
species. initiation of status
reviews.
12/5/2013................... Straight-horned markhor Proposed rule 78 FR 73173-73185
revision; Threatened
with special rule.
1/22/2014................... Fifteen foreign bats, 90-day findings; 79 FR 3559-3562
emperor penguin, initiation of status
Flores hawk-eagle, reviews.
Ridgway's hawk, and
Virgin Islands
coqu[iacute].
5/20/2014................... Southern white rhino... Affirmation of interim 79 FR 28847-28849
rule as final rule:
Threatened due to
similarity of
appearance.
6/9/2014.................... Flat-tailed tortoise, 90-day findings; 79 FR 32900-32903
spider tortoise, and initiation of status
pygmy three-toed sloth. reviews.
6/24/2014................... Philippine cockatoo and Final rule; endangered 79 FR 35870-35900
yellow-crested
cockatoo.
6/24/2014................... White cockatoo......... Final rule; threatened 79 FR 35870-35900
with special rule.
[[Page 71471]]
10/7/2014................... Straight-horned markhor Final rule: Threatened 79 FR 60365-60379
with special rule.
10/29/2014.................. African lion........... Proposed rule: 79 FR 64472-64502
Threatened with
special rule.
4/10/2015................... Egyptian tortoise, 90-day findings; 80 FR 19259-19263
golden conure, and initiation of status
long-tailed chinchilla. reviews.
6/16/2015................... Chimpanzee............. Final rule; endangered 80 FR 34500-34525
7/29/2015................... Honduran emerald Final rule; endangered 80 FR 45086-45097
hummingbird.
10/2/2015................... Great green and Final rule; endangered 80 FR 59976-60021
military macaw.
12/23/2015.................. Lion--Panthera leo leo. Final rule; endangered 80 FR 80000-80056
12/23/2015.................. Lion--Panthera leo Final rule; threatened 80 FR 80000-80056
melanochaita. with special rule.
1/21/2016................... Scarlet-chested Reopening of the 81 FR 3373-3374
parakeet and turquoise public comment period.
parakeet.
3/16/2016................... African elephant, 90-day findings; 81 FR 14058-14072
Chinese pangolin, initiation of status
giant ground pangolin, reviews.
Indian pangolin, long-
tailed pangolin,
Philippine pangolin,
Sunda pangolin, tree
pangolin.
4/7/2016.................... Scarlet macaw.......... Revised proposed 81 FR 20302-20316
listing rule.
----------------------------------------------------------------------------------------------------------------
Our expeditious progress also includes work on pending listing
actions described above in our ``precluded finding,'' but for which
decisions had not been completed at the time of this publication. After
taking into consideration the limited resources available for listing
foreign species, the competing demands for those funds, and the
completed work catalogued in the tables above, we find that we are
making expeditious progress to add qualified species to the Lists in FY
2016.
We have endeavored to make our listing actions as efficient and
timely as possible, given the requirements of the relevant law and
regulations, and constraints relating to workload and personnel. We are
continually considering ways to streamline processes or achieve
economies of scale, such as by publishing related actions together.
Monitoring
Section 4(b)(3)(C)(iii) of the Act requires us to ``implement a
system to monitor effectively the status of all species'' for which we
have made a warranted-but-precluded 12-month finding, and to ``make
prompt use of the [emergency listing] authority [under section 4(b)(7)]
to prevent a significant risk to the well-being of any such species.''
For foreign species, the Service's ability to gather information to
monitor species is limited. The Service welcomes all information
relevant to the status of these species, because we have no ability to
gather data in foreign countries directly and cannot compel another
country to provide information. Thus, this CNOR-FS plays a critical
role in our monitoring efforts for foreign species.
With each CNOR-FS, we request information on the status of the
species included in the CNOR-FS. Information and comments on the annual
findings can be submitted at any time. We review all new information
received through this process as well as any other new information we
obtain using a variety of methods. We collect information directly from
range countries by correspondence, from peer-reviewed scientific
literature, unpublished literature, scientific meeting proceedings, and
CITES documents (including species proposals and reports from
scientific committees). We also obtain information through the permit-
application processes under CITES, the Act, and the Wild Bird
Conservation Act (16 U.S.C. 4901 et seq.). We also consult with the
IUCN species specialist groups and staff members of the U.S. CITES
Scientific and Management Authorities, and the Division of
International Conservation; and we attend scientific meetings, when
possible, to obtain current status information for relevant species. As
previously stated, if we identify any species for which emergency
listing is appropriate, we will make prompt use of the emergency
listing authority under section 4(b)(7) of the Act.
References Cited
A list of the references used to develop this CNOR-FS is available
at https://www.regulations.gov at Docket No. FWS-HQ-ES-2016-0072.
Authors
This Candidate Notice of Review of Foreign Species was primarily
authored by staff of the Branch of Foreign Species and Jesse D'Elia,
Ecological Services Program, U.S. Fish and Wildlife Service.
Authority
This Candidate Notice of Review of Foreign Species is published
under the authority of the Endangered Species Act of 1973, as amended
(16 U.S.C. 1531 et seq.).
Dated: September 29, 2016.
Stephen Guertin,
Acting Director, U.S. Fish and Wildlife Service.
[FR Doc. 2016-24931 Filed 10-14-16; 8:45 am]
BILLING CODE 4333-15-P