Endangered and Threatened Wildlife and Plants; Reclassifying the Golden Conure From Endangered to Threatened With a Section 4(d) Rule, 45073-45087 [2018-19153]
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Federal Register / Vol. 83, No. 172 / Wednesday, September 5, 2018 / Proposed Rules
overlap, or conflict with any other Federal
rules. There are no known significant
alternative approaches to the proposed rule
that would meet the applicable requirement.
requirements and financial terms (e.g.,
fees or payment terms) differ between a
lease and a rental agreement.
The Regulatory Secretariat Division
has submitted a copy of the IRFA to the
Chief Counsel for Advocacy of the Small
Business Administration. A copy of the
IRFA may be obtained from the
Regulatory Secretariat Division. DoD,
GSA and NASA invite comments from
small business concerns and other
interested parties on the expected
impact of this rule on small entities.
DoD, GSA, and NASA will also
consider comments from small entities
concerning the existing regulations in
subparts affected by this rule consistent
with 5 U.S.C. 610. Interested parties
must submit such comments separately
and should cite 5 U.S.C. 610 (FAR Case
2017–017) in correspondence.
§ 7.401
VII. Paperwork Reduction Act
The proposed rule does not contain
any information collection requirements
that require the approval of the Office of
Management and Budget under the
Paperwork Reduction Act (44 U.S.C.
chapter 35).
List of Subjects in 48 CFR Part 7
Government procurement.
Dated: August 30, 2018.
William F. Clark,
Director, Office of Government-wide
Acquisition Policy, Office of Acquisition
Policy, Office of Government-wide Policy.
Therefore, DoD, GSA, and NASA are
proposing to amend 48 CFR part 7 as set
forth below:
[Amended]
2. Amend section 7.401 by removing
from paragraph (a)(3) ‘‘rental payments’’
and adding ‘‘lease, or other periodic
payments, however described,’’ in its
place.
■ 3. Amend section 7.403 by revising
the section heading and paragraph (b),
and adding paragraph (c) to read as
follows:
■
§ 7.403 General Services Administration
assistance and OMB Guidance.
*
*
*
*
*
(b) Agencies may request information
from the following GSA office: GSA
FAS National Customer Service Center
by phone at 1–800–488–3111 or by
email at ncsccustomer.service@gsa.gov.
Additional information to assist with
deciding whether to purchase or lease
equipment is available at https://
www.gsa.gov/acquisition/purchasingprograms/gsa-schedules/list-of-gsaschedules/schedule-51-vhardwaresuperstore/equipment-rental-andleasing.
(c) See Special Guidance for Leasepurchase Analysis (Section 13 of OMB
Circular A–94, also see 8.c.(2)) at
https://www.whitehouse.gov/sites/
whitehouse.gov/files/omb/circulars/
A94/a094.pdf and OMB Circular A–11
Appendix B Budgetary Treatment of
Lease-Purchases and Leases of Capital
Assets at https://www.whitehouse.gov/
wp-content/uploads/2018/06/app_
b.pdf.
[FR Doc. 2018–19177 Filed 9–4–18; 8:45 am]
PART 7—ACQUISITION PLANNING
BILLING CODE 6820–EP–P
1. The authority citation for part 7
continues to read as follows:
■
DEPARTMENT OF THE INTERIOR
Authority: 40 U.S.C. 121(c); 10 U.S.C.
chapter 137; and 51 U.S.C. 20113.
Fish and Wildlife Service
2. Revise section 7.400 to read as
follows:
■
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§ 7.400
50 CFR Part 17
Scope of subpart.
This subpart provides guidance
pertaining to the decision to acquire
equipment by lease or purchase. It
applies to both the initial acquisition of
equipment and the renewal or extension
of existing equipment leases. The term
‘‘lease’’, as used in this subpart, applies
to both the lease and rental of
equipment. While there are some
differences between renting and leasing
in many industries, there is no standard
distinction between both renting and
leasing that spans across all industries.
Rental agreements are typically for
shorter periods of time than lease
agreements. Additionally, maintenance
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[Docket No. FWS–HQ–ES–2015–0019;
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RIN 1018–BC78
Endangered and Threatened Wildlife
and Plants; Reclassifying the Golden
Conure From Endangered to
Threatened With a Section 4(d) Rule
Fish and Wildlife Service,
Interior.
ACTION: Proposed rule.
AGENCY:
We, the U.S. Fish and
Wildlife Service (Service), announce a
12-month finding on a petition to delist
or downlist the golden conure under the
SUMMARY:
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Endangered Species Act of 1973, as
amended (Act). The golden conure is a
psittacine bird (parrots, parakeets,
macaws, cockatoos, and others) endemic
to the south Amazon Basin in Brazil.
After review of the best available
scientific and commercial information,
we find that listing the golden conure as
a threatened species is warranted.
Accordingly, we propose to list it as a
threatened species with a rule issued
under section 4(d) of the Act. If we
finalize this rule as proposed, it would
reclassify the golden conure from
endangered to threatened on the List of
Endangered and Threatened Wildlife
(List). Additionally, we are proposing to
update the List to reflect the latest
scientifically accepted taxonomy and
nomenclature for the species as
Guaruba guarouba, golden conure.
DATES: We will accept comments
received or postmarked on or before
November 5, 2018. Comments submitted
electronically using the Federal
eRulemaking Portal (see ADDRESSES,
below) must be received by 11:59 p.m.
Eastern Time on the closing date. We
must receive requests for public
hearings, in writing, at the address
shown in FOR FURTHER INFORMATION
CONTACT by October 22, 2018.
ADDRESSES: You may submit comments
by one of the following methods:
(1) Electronically: Go to the Federal
eRulemaking Portal: https://
www.regulations.gov. In the Search box,
enter FWS–HQ–ES–2015–0019, which
is the docket number for this
rulemaking. Then, click on the Search
button. On the resulting page, in the
Search panel on the left side of the
screen, under the Document Type
heading, click on the Proposed Rules
link to locate this document. You may
submit a comment by clicking on
‘‘Comment Now!’’
(2) By hard copy: Submit by U.S. mail
or hand-delivery to: Public Comments
Processing, Attn: FWS–HQ–ES–2015–
0019; U.S. Fish and Wildlife Service,
MS: BPHC, 5275 Leesburg Pike, Falls
Church, VA 22041–3803.
We request that you send comments
only by the methods described above.
We will post all comments on https://
www.regulations.gov. This generally
means that we will post any personal
information you provide us (see Public
Comments, below, for more
information).
FOR FURTHER INFORMATION CONTACT: Don
Morgan, Chief, Branch of Delisting and
Foreign Species, Ecological Services,
U.S. Fish and Wildlife Service, MS: ES,
5275 Leesburg Pike, Falls Church, VA
22041–3803; telephone, 703–358–2171.
If you use a telecommunications device
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for the deaf (TDD), call the Federal
Relay Service at 800–877–8339.
SUPPLEMENTARY INFORMATION:
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Information Requested
Public Comments
We intend that any final action
resulting from this proposed rule will be
based on the best scientific and
commercial data available and be as
accurate and as effective as possible.
Therefore, we request comments and
information from other concerned
governmental agencies, the scientific
community, industry, or any other
interested parties concerning this
proposed rule. We particularly seek
comments concerning:
(1) Reasons why we should or should
not reclassify the golden conure from an
endangered species to a threatened
species under the Act (16 U.S.C. 1531 et
seq.).
(2) The golden conure’s biology,
range, and population trends, including:
(a) Biological or ecological
requirements of the species, including
habitat requirements for feeding,
breeding, and sheltering;
(b) Genetics and taxonomy;
(c) Historical and current range,
including distribution patterns;
(d) Historical and current population
levels, and current and projected trends;
and
(e) Past and ongoing conservation
measures for the species, its habitat, or
both.
(3) Factors that may affect the
continued existence of the species,
which may include:
(a) Habitat modification or destruction
(e.g., information regarding future rates
of deforestation or other forms of habitat
loss or degradation within the known
range of the golden conure);
(b) Overutilization, including
information regarding illegal collection
and trade;
(c) Disease or predation;
(d) The inadequacy of existing
regulatory mechanisms; or
(e) Other natural or manmade factors
affecting the species’ continued
existence.
(4) Biological, commercial trade, or
other relevant data concerning any
threats (or lack thereof) to this species
and existing regulations that may be
addressing those threats.
(5) Information on the locations of any
additional or newly discovered
populations of this species. See
Appendix B in the species status
assessment report (SSA) for a list of
known localities used by the golden
conure (available under Docket No.
FWS–HQ–ES–2015–0019 on https://
www.regulations.gov.
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(6) Information on the number of
captive-bred golden conures in Brazil.
(7) Information regarding current or
future rates of deforestation in the
Brazilian Amazon as they may correlate
to current or projected gross domestic
product (GDP) in that country.
(8) The appropriateness of the
conservation measures proposed under
section 4(d) of the Act, including those
that would allow the import and export
of certain golden conures into and from
the United States and certain acts in
interstate commerce without a permit
under the Act.
Please include sufficient information
with your submission (such as
electronic copies of scientific journal
articles or other publications, preferably
in English) to allow us to verify any
scientific or commercial information
you include.
Please note that submissions merely
stating support for or opposition to the
action under consideration without
providing supporting information,
although noted, will not be considered
in making a determination, as section
4(b)(1)(A) of the Act directs that
determinations as to whether any
species is an endangered or threatened
species must be made ‘‘solely on the
basis of the best scientific and
commercial data available.’’
You may submit your comments and
materials concerning this proposed rule
by one of the methods listed in
ADDRESSES. We request that you send
comments only by the methods
described in ADDRESSES.
If you submit information via https://
www.regulations.gov, your entire
submission—including any personal
identifying information—will be posted
on the website. If your submission is
made via a hardcopy that includes
personal identifying information, you
may request at the top of your document
that we withhold this information from
public review. However, we cannot
guarantee that we will be able to do so.
We will post all hardcopy submissions
on https://www.regulations.gov.
Comments and materials we receive,
as well as supporting documentation we
used in preparing this proposed rule,
will be available for public inspection
on https://www.regulations.gov, or by
appointment, during normal business
hours, at the U.S. Fish and Wildlife
Service, Headquarters Office (see FOR
FURTHER INFORMATION CONTACT).
Public Hearing
Section 4(b)(5)(E) of the Act provides
for a public hearing on this proposal, if
requested within 45 days of the date of
publication of this proposed rule.
Requests must be sent to the address
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shown in FOR FURTHER INFORMATION
and received by the date
specified in DATES.
CONTACT
Peer Review
The purpose of peer review is to
ensure that our reclassification
determination is based on scientifically
sound data, assumptions, and analyses.
In accordance with our joint policy on
peer review published in the Federal
Register on July 1, 1994 (59 FR 34270),
and our August 22, 2016, memorandum
updating and clarifying the role of peer
review of listing actions under the Act,
we sought the expert opinions of five
appropriate specialists regarding the
SSA report that informed this proposed
rule. The peer reviewers have expertise
in (1) the life history of the golden
conure, (2) birds of the Amazon, and (3)
the effects of habitat degradation and
deforestation on Amazonian birds. We
received responses from four of the five
peer reviewers, which we took into
account in our SSA and this proposed
rule. Their comments and suggestions
can be found online at https://
www.fws.gov/endangered/improving_
ESA/peer_review_process.html. We
invite any additional comments from
the peer reviewers on the proposed rule
during the public comment period on
this proposed rule (see DATES, above);
all comments received from peer
reviewers will be available, along with
other public comments, in the docket
for this proposed rule at https://
www.regulations.gov under Docket No.
FWS–HQ–ES–2015–0019.
Previous Federal Actions
On May 22, 1975, the Fund for
Animals, Inc., petitioned us to list 216
taxa of plants and animals, including
the ‘‘golden parakeet,’’ as an endangered
species pursuant to the Act. On
September 26, 1975, we proposed to list
the ‘‘golden parakeet (Aratinga
guaruba)’’ as endangered (40 FR 44329).
On June 14, 1976 (41 FR 24062), we
finalized the listing as endangered.
On August 21, 2014, we received a
petition from the American Federation
of Aviculture, Inc. (AFA), requesting
that the golden conure be removed from
the List or reclassified as a threatened
species. The AFA also requested that if
we determined that downlisting to
threatened status was warranted, we
develop a rule under section 4(d) of the
Act (also called a 4(d) rule) that would
allow for import and export of certain
golden conures into and from the
United States, and interstate commerce
of the species under certain
circumstances.
On April 10, 2015, we published in
the Federal Register (80 FR 19259), a
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90-day finding for the 2014 petition,
concluding that the petition provided
substantial information indicating the
petitioned action may be warranted, and
we initiated a status review for this
species.
On July 29, 2017, the AFA filed a
complaint under the Act to compel the
Service to issue a 12-month finding
regarding the AFA’s petition, pursuant
to 16 U.S.C. 1533(b)(3)(B). On November
6, 2017, the AFA and the Service
entered into a settlement agreement
whereby the Service agreed to submit a
12-month finding for the golden conure
to the Federal Register for publication
no later than September 1, 2018. This
proposed rule constitutes the 12-month
finding and our 5-year status review for
the golden conure.
Background
Species Status Assessment (SSA) Report
for the Golden Conure
A thorough review of the taxonomy,
life history, ecology, and overall
viability of the golden conure is
presented in the SSA Report (Service
2018; available at Docket No. FWS–HQ–
ES–2015–0019 on https://
www.regulations.gov). The following
discussion is a summary of the
information and analyses from the SSA
Report.
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Current Conservation Status
The golden conure is currently listed
as endangered under the Act (41 FR
24062; June 14, 1976) and the species is
considered ‘‘Vulnerable’’ at the national
level in Brazil (MMA 2014, p. 122). The
International Union for the
Conservation of Nature (IUCN) recently
reclassified the species from endangered
to vulnerable because its population is
estimated to be larger than previously
thought (Bird Life International (BLI)
2017, unpaginated). IUCN’s
‘‘vulnerable’’ listing acknowledges that
the species nevertheless has a small
estimated population that is expected to
experience a rapid decline over the next
three generations due to habitat loss and
limited pressure from poaching (BLI
2017, unpaginated). The species is also
included in Convention on International
Trade in Endangered Species of Wild
Fauna and Flora (CITES) Appendix I
(CITES 2018a, unpaginated). CITES is
an international treaty for the
conservation of wild fauna and flora
subject to trade; species on CITES
Appendix I are considered threatened
with extinction and international trade
is permitted only under exceptional
circumstances, which generally
precludes commercial trade (CITES
2016, unpaginated).
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Species Description
The golden conure is a large, 34centimeter (13-inch), macaw-like bird
with striking yellow plumage and green
flight feathers (Laranjeiras 2011a,
unpaginated; Parr and Juniper 2010, p.
436). The sexes are similar in
appearance, but in first-year juveniles
the yellow color is variably streaked
with green—most often on the back of
the head, nape and chest (Forshaw
2017, p. 223; Laranjeiras 2011a,
unpaginated; Reynolds 2003, p. 10).
Taxonomy
The golden conure was first
documented in 1788 (ITIS 2017,
unpaginated) and was later noted in the
manuscripts of European explorers to
Brazil in the 18th and 19th centuries
(Yamashita 2003, p. 38). It was
originally placed in its own (monotypic)
genus Guaruba, then subsequently
placed in the genus Aratinga by some
authors (Peters 1937; Pinto 1978;
Forshaw 1989, as cited in Tavares et al.
2004, p. 239), while others placed it in
the genus Conurus (Salvadori 1891;
Miranda Ribeiro 1920, as cited in
Tavares et al. 2004, p. 239).
Researchers have since noted that its
behaviors, including reproduction and
vocalization, differ markedly from those
of Aratinga species and have
recommended that the golden conure’s
scientific name be returned to the
monotypic genus Guaruba (Laranjeiras
2011a, unpaginated; Sick 1990, p. 112).
Additionally, recent genetic analyses
indicate that the golden conure is more
closely related to the red-shouldered
macaw (Diopsittaca nobilis) and the
blue-crowned parakeet (Thectocercus
acuticaudatus) (Uranto´wka and
Mackiewicz 2017, entire), than to the
Aratinga parakeets (Tavares et al. 2004,
pp. 230, 236–237, 239). Therefore, the
golden conure is recognized as Guaruba
guarouba by (1) the Integrated
Taxonomic Information System (ITIS
2017, unpaginated); (2) the Brazilian
Ornithological Records Committee
(Piacentini et al. 2015, p. 163); (3)
Taxonomy of Birds of the World
(Clements et al. 2017, unpaginated); and
(4) Birdlife International (BLI 2017,
unpaginated). Based upon our review of
the best available information, we
recognize the golden conure as a valid
full species in the monotypic genus
Guaruba and we are proposing to
correct its scientific name to Guaruba
guarouba on the Federal List of
Endangered and Threatened Wildlife
(see Proposed Technical Correction,
below).
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Abundance and Distribution
In general, the golden conure is
relatively poorly studied and
information on local abundance and
distribution of populations throughout
the range is limited (Laranjeiras 2011b,
p. 303). An earlier global population
estimate (i.e., from 2010 and earlier)
indicated fewer than 2,500 individuals
remained, but a 2011 estimate signaled
the global population contained 10,875
individuals within 174,000 square
kilometers (km2) (67,182 square miles
(mi2)) of suitable habitat (Laranjeiras
2011b, p. 311). This estimate was
derived using: (1) Occurrence data
obtained after 1987, that extended the
species’ known range considerably to
the southwest; (2) a density estimate
calculated from a conure survey in
western Para´ in 2007 (Laranjeiras 2011b,
p. 311); and (3) estimates of suitable
habitat within the known area of
occurrence from a habitat modeling
study in 2009 (Laranjeiras and CohnHaft 2009). However, because the
golden conure has a patchy distribution
and is poorly studied, more survey work
would be required to produce better
estimates.
The species’ current known range
includes portions of the following four
states in Brazil (noted from east to west):
(1) The western part of Maranha˜o; (2)
the central region of Para´; (3) the
extreme southeast of Amazonas; and (4)
the northeastern portion of Rondoˆnia
(Laranjeiras 2011a, unpaginated).
Additionally, the species was recorded
in a fifth state, the northern portion of
Mato Grosso, in the 1990s (Lo 1995,
entire), but there have been no recent
sightings in that area (Moura in litt.
2018; BLI 2016, p. 2; Laranjeiras 2011a,
unpaginated; Laranjeiras and Cohn-Haft
2009, p. 3; Albertani et al. 1997, p. 135).
The species’ historical range once
extended farther eastward (to more
eastern portions of the states of Para´ and
Maranha˜o), but the habitat there was
mostly deforested in the 1970s and
1980s (Laranjeiras and Cohn-Haft 2009,
p. 5). The golden conure is believed to
be extirpated from these regions (BLI
2017, unpaginated; BLI 2016, p. 3;
Laranjeiras and Cohn-Haft 2009, p. 5),
which represented approximately 30 to
35 percent of the historical range
(Laranjeiras 2011a, unpaginated;
Laranjeiras and Cohn-Haft 2009, p. 8).
The species is limited to regions
where extensive stands of tall
Amazonian rainforest are still present
(Oren and Novaes 1986, p. 331).
Although the species can tolerate some
disturbance in the forest, the golden
conure is absent from landscapes with
advanced deforestation; flocks
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disappear seasonally from the
fragmented landscapes, indicating that
they require intact forest (Laranjeiras
2011a, unpaginated).
The best estimate of the geographic
distribution of the golden conure is
based on recent records and habitat
modeling (see Service 2018, Figures 5
and 6, pp. 19–20; Laranjeiras 2011b, p.
311; Laranjeiras and Cohn-Haft 2009,
entire). The total current range of the
golden conure is estimated to be no
more than 340,000 km2 (131,275 mi2)
(Laranjeiras and Cohn-Haft 2009, p. 3).
The species’ distribution within this
range is not continuous and is described
as patchy—possibly associated with the
distribution of specific nesting or food
resources (Laranjeiras 2008, as cited in
Laranjeiras and Cohn-Haft 2009, p. 6).
The estimated suitable habitat for the
golden conure within this range is
174,000 km2 (67,182 mi2) (Laranjeiras
2011b, p. 311). However, parrots can
cross great gaps and are capable of
flying long distances (Lees and Peres
2009, pp. 284, 286); thus, it is possible
that some of the recent records of the
golden conure that extended the range
represent vagrant groups (Moura in litt.
2018). Because the species has a patchy
distribution within its range,
extrapolation of densities to estimate the
global population is problematic, and
population estimates throughout the
range are needed (Laranjeiras 2011a,
unpaginated).
Habitat
The golden conure lives in in Brazil’s
lower Amazon basin, in an area south of
the Amazon River, east of the Madeira
River, and north of the Brazilian Shield
(Laranjeiras and Cohn-Haft 2009, p. 9).
The Brazilian Shield is a region formed
of Precambrian crystalline rocks that
may be exposed or covered by layers of
sedimentary rocks (Buckup 2011, p.
203). The species occupies primary (old
growth) terra firme (unflooded)
rainforest on undulating landscapes in
the lowlands at elevation at or under
300 meters (984 feet) (Sick 1997, as
cited by Laranjeiras 2011a,
unpaginated). However, the species has
also has been recorded in the regrowth
of secondary forests and in igapo´
(seasonally flooded) forests while
feeding (Laranjeiras 2011a, unpaginated,
citing several sources; Laranjeiras
2011b, pp. 308–309; Oren and Noveas
1986, p. 332; Laranjeiras 2008a, as cited
in Laranjeiras 2011a, unpaginated). The
majority of golden conure groups appear
to be resident (i.e., non-migratory), even
in the post-reproductive period
(Laranjeiras 2008, as cited in Forshaw
2017, p. 226; Laranjeiras 2011a,
unpaginated; Yamashita 2003, p. 38).
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The golden conure uses large, old
growth, hardwood trees (Yamashita
2003, p. 38) for cavity nesting (Oren and
Novaes 1986, pp. 333–334). In most
cases, the species uses the same tree for
nesting and roosting (BLI 2016, p. 4;
Laranjeiras 2011a, unpaginated;
Yamashita 2003, p. 38). Most known
nest and roost cavities have been found
high in tall, standing, dead trees within
a small, disturbed (cleared) area
adjacent to continuous forest. The
golden conure seems to prefer using
isolated trees (i.e., some distance from a
neighboring tree) for nesting likely
because isolated trees provide better
protection against terrestrial or arboreal
predators (Laranjeiras 2011a,
unpaginated; Kyle 2005, p. 3). To date,
we are aware of 7 different species of
hardwood trees used for nesting
(Laranjeiras 2011b, p. 308; Silveira and
Belmonte in press, unpaginated; Oren
and Novaes 1986, p. 333; Lima et al.
2014, p. 323) and more than 28 species
of fruiting trees used for feeding
(Service 2018, pp. 10, 60–61).
Biology
The golden conure is frugivorous
(fruit-eating), and its diet varies
throughout the year and across its
distribution (Laranjeiras 2011a,
unpaginated). The species eats whole
fruit, seeds, pulp, buds and flowers,
nectar, and peels; it will also feed on
cultivated plants such as corn (Zea
mays) and mangoes (Mangifera indica)
(Laranjeiras 2011b, pp. 308–309; Oren
and Noveas 1986, p. 332).
Breeding and nesting take place
during the wet months, generally from
November or December through April
(Forshaw 2017, p. 227; Laranjeiras
2011a, unpaginated; Oren and Novaes
1986, p. 332). The social structure and
breeding behavior of the golden conure
appear to be unique from that of other
members of the parrot family in that the
species engages in communal broodrearing. The golden conure remains in
flocks made up of family groups or clans
(averaging 10 individuals) (Laranjeiras
2011a, unpaginated), and individuals in
the group (referred to as ‘‘reproductive
helpers’’) assist in rearing the young.
Most other large parrots are believed to
incubate and rear young in pairs
(Albertani et al. 1997, pp. 135–136).
The golden conure’s communal
brood-rearing includes the use of one or
two uncommon reproductive strategies
where the flock is either made up of (1)
multiple related nesting pairs with
reproductive helpers (Oren and Novaes
1986, p. 333), or (2) a single leading pair
with juveniles from different
generations acting as helpers (Reynolds
2003, p. 12; Oren and Novaes 1986, p.
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333). Nest protection seems to be an
important part of communal broodrearing, and a group will vigorously
defend the nest in response to potential
competitors or predators (Forshaw 2017,
p. 228; Laranjeiras 2008a, as cited in
Laranjeiras 2011a, unpaginated).
Most of the information regarding
development of the young is from
captive birds. Eggs hatch within 28 to 30
days (Arndt 1996, as cited by Forshaw
2017, p. 227; Laranjeiras 2011a,
unpaginated; Oren and Novaes 1986, p.
333). Nestlings reach adult size in about
60 days (Laranjeiras 2011a,
unpaginated) and fledge at
approximately 55–60 days post hatch
(Arndt 1996, as cited by Forshaw 2017,
p. 227). The post-reproductive period,
when first year juveniles can be seen in
the flocks at feeding sites in the wild, is
from March or April to July or August
(Laranjeiras 2011b, p. 304; Oren and
Novaes 1986, p. 332).
First-year juveniles always stay with
the family group and can be easily
identified by their green-streaked
plumage (Yamashita 2003, p. 38).
Juveniles attain adult plumage in a molt
when they are about 1 year old
(Laranjeiras 2011a, unpaginated).
Fledged chicks and juveniles will beg
for food from foraging adults (Kyle 2005,
p. 4). Annual survival information is
limited, but first-year juveniles
represent no more than 13 percent of the
individuals in flocks (Laranjeiras 2008a,
as cited in Laranjeiras 2011a,
unpaginated). In some areas (e.g., in
eastern Para´, where trapping for the
illegal pet trade has occurred), the
percentage of observed first-year
juveniles in the flocks was zero
(Reynolds 2003 as cited by Laranjeiras
2011b, p. 309).
In captivity, adults reach sexual
maturity at about 3 years of age (Oren
and Novaes 1986, p. 333), with the
average age for successful breeding
occurring between 6 and 8 years
(Reynolds, 2003, p. 12). Lifespan for the
golden conure in the wild is not known,
although the generation length was
estimated as 7.4 years (BLI 2016,
unpaginated) and the maximum age
recorded for the species in captivity was
60 years with a median age of 14 years
(calculated using adults ≥4 years; n =
190) (Young et al. 2011, p. 35).
Information is lacking on the species’
carrying capacity, birth rates, nesting
success, and home range (broadly
defined as confined areas where
individuals conduct their day-to-day
activities (Boitani and Fuller 2000, p.
65).
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Summary of Factors Affecting the
Species
A species is an ‘‘endangered species’’
for purposes of the Act if it is in danger
of extinction throughout all or a
significant portion of its range and is a
‘‘threatened species’’ if it is likely to
become an endangered species within
the foreseeable future throughout all or
a significant portion of its range. Section
4 of the Act and its implementing
regulations (50 CFR part 424) set forth
the procedures for listing species,
reclassifying species, or removing
species from listed status. A species
may be determined to be an endangered
or threatened species due to one or more
of the five listing factors described in
section 4(a)(1) of the Act: (A) The
present or threatened destruction,
modification, or curtailment of its
habitat or range; (B) overutilization for
commercial, recreational, scientific, or
educational purposes; (C) disease or
predation; (D) the inadequacy of
existing regulatory mechanisms; or (E)
other natural or manmade factors
affecting its continued existence. A
species may be removed from listed
status (i.e., ‘‘delisted’’) or reclassified on
the same basis. Our analysis of threats
is an evaluation of both the threats
currently facing the species and the
threats that are reasonably likely to
affect the species in the foreseeable
future without the Act’s protections.
In our analysis, we considered
conservation measures (primarily the
use of protected areas) as part of the
current condition and projected future
scenarios to evaluate viability of the
species (Service 2018, pp. 42–47). We
generally define viability as the ability
the golden conure to sustain
populations in natural ecosystems and
disturbed habitats over time. Using the
SSA framework, we considered what
the species needs to maintain viability
by evaluating the species in terms of
resiliency, redundancy, and
representation (Wolf et al. 2015, entire).
For further information on viability, see
the SSA Report (https://
www.regulations.gov at Docket No.
FWS–HQ–ES–2015–0019).
When we listed the golden conure as
endangered in 1976, the species was
perceived to be declining in numbers
due to any one the following factors, or
a combination of all three factors: The
present or threatened destruction,
modification, or curtailment of its
habitat or range (Factor A);
overutilization of the species for
commercial, recreational, scientific, or
educational purposes (Factor B); or the
inadequacy of existing regulatory
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mechanisms (Factor D) (41 FR 24062;
June 14, 1976).
The golden conure presently faces the
most risk from loss and degradation of
its habitat from deforestation originating
from multiple anthropogenic activities
(Factor A) (BLI 2016, p. 4; IBAMA 2003
and SEMA 2007, as cited by Laranjeiras
2011a, unpaginated; Collar 1992, p. 5).
Habitat loss and degradation is likely to
be intensified by synergistic effects
associated with the consequences of
climate change (Staal et al. 2015, p. 2)
(Factor E). Climate projections include
increased temperatures, dryer
conditions, and more extreme weather
(including droughts), which have the
potential to stress trees and cause tree
mortality (Fearnside 2009, pp. 1003,
1005). These conditions also increase
the unintentional spread of fires, further
contributing to deforestation (Fearnside
2009, p. 1005). Additionally, the golden
conure is still being illegally collected
and traded within Brazil, at some
unknown level, for the live pet bird
trade (Factor B). These threats and other
potential stressors are discussed in
detail in the SSA Report and are
summarized below.
Habitat Loss—Deforestation
Large-scale deforestation in the
Amazon has occurred since the 1970s
and 1980s concurrent with the growth
of Brazil’s economy (GFA 2017,
unpaginated). The Brazilian Amazon is
approximately the size of Western
Europe, and as of 2016, an area the size
of France has been lost to deforestation
(Fearnside 2017a, pp. 1, 3).
Approximately 30 to 35 percent of the
golden conure’s range has already been
lost to deforestation, primarily in the
eastern states of Para´ and Maranha˜o
(Laranjeiras 2011a, unpaginated;
Laranjeiras and Cohn-Haft 2009, p. 8),
and another 23 to 30 percent of the
golden conure’s habitat is predicted to
be lost within 22 years or three
generations (Bird et al. 2011 Appendix
S1),
The golden conure’s range partially
overlaps what is known as the ‘‘arc of
deforestation,’’ an area in the
southeastern Amazon where rates of
deforestation and forest fragmentation
have been the highest (Prioste et al.
2012, p. 701; Laranjeiras 2011a,
unpaginated; Laranjeiras and Cohn-Haft
2009, p. 8). After a long period of
deforestation in the Amazon, rates
dropped dramatically during the years
from 2005 to 2011 (Alves et al. 2017, p.
76; Fearnside 2017b, p. 1; Prodes 2017,
unpaginated; Hochstetler and Viola
2012, p. 759)). Deforestation declined
from an annual average of about 21,000
km2 (8,108 mi2) per year for the 5-year
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period between 2000 to 2004—to 7,000
km2 (2,703 mi2) in 2009 (Petherick 2013,
p. 8; Hochstetler and Viola 2012, p.
759).
Despite these declines, the total area
deforested in Brazil’s Amazon has risen
steadily since deforestation rates were
first measured in 1988 (IPAM 2017, p.
7 using PRODES 2017 data). More
recently, deforestation rates are
increasing again (Fearnside 2017b, p. 1;
IPAM 2017, p. 15; Biderman and
Nogueron 2016, unpaginated), as global
demand for agricultural commodities
continues to rise (Brando et al. 2016,
abstract), and the ‘‘arc of deforestation’’
could continue to be a hotspot (Alves et
al. 2017, p. 76).
An area does not have to be mostly
deforested to lose value as suitable
habitat for forest-dependent species
such as the golden conure. Deforestation
itself creates isolation of remnant forest
patches and forest edge effects (Barlow
et al. 2016, p. 144; Ewers and Didham
2006, pp. 123–124). Edge effects
decrease habitat quality within
remaining patches and the functional
connectivity between them (Zurita et al.
2012, p. 504, citing many sources).
Additionally, disturbance within the
forest remnant, such as selective logging
and increased fires, changes forest
structure and species composition,
generally reducing biodiversity (Barlow
et al. 2016, p. 144).
Forest habitat degradation and
fragmentation typically begin with road
construction and subsequent human
settlement. Activities resulting from
human settlement include: (1) An
increased network of unofficial roads;
(2) logging; (3) crop production and
cattle ranching; (4) increased fires; and
(4) further infrastructure development,
including more roads, dams and
hydroelectric projects, and mining (GFA
2018a, b, c, and d, unpaginated; GFA
2017, unpaginated; Sonter et al. 2017,
entire; Barber et al. 2014, entire; BLI
2016, unpaginated; Yamashita 2003, p.
38).
Roads have a major effect on Amazon
deforestation. Deforestation is much
higher near roads (including unofficial
roads) and rivers (Barber et al. 2014,
entire). Nearly 95 percent of all
deforestation occurred within 5.5 km
(3.4 mi) of roads or 1 km (0.6 mi) of
rivers (Barber et al. 2014, pp. 203, 205,
208). Unofficial roads are rapidly
expanding in the region and contribute
to further degradation, including
logging, new colonization, forest
fragmentation, and increased fire risk
(Barber et al. 2014, p. 203).
Logging in the Amazon was once
restricted to areas bordering major rivers
but the construction of highways and
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strategic access roads, coupled with the
depletion of hardwood stocks in the
south of Brazil, made logging an
important, growing industry (Verı´ssimo
et al. 1992, p. 170). Logging operations
typically occur on private lands claimed
by ranchers, land speculators, and
squatters who sell extraction rights to
logging companies (GFA 2018a and b,
unpaginated). After logging, the land
may be clear-cut and burned, in
preparation for crops (Reynolds 2003, p.
10). Burning makes nutrient-deficient
land temporarily nutrient-rich, but it
will only yield crops for a few years,
creating a cycle of more land clearing
(Reynolds 2003, p. 10). Revenues from
timber sales are also used to finance
conversion of the land to cattle ranching
(GFA 2018a, unpaginated). Although the
Brazilian forest code requires private
landowners in the Amazon to maintain
80 percent of their land as forest, the
code has been poorly enforced (GFA
2018b, unpaginated), and full
compliance has not been achieved
(Azevedo et al. 2017, entire; see
Conservation Measures and Regulatory
Mechanisms, below).
Logging on public lands is allowed
via concessions where logging
companies are granted logging rights for
a fee (GFA 2018a, unpaginated). The
concession system typically requires
practices that minimize effects to the
forest (e.g., rotation of harvest,
minimum-tree-size standards, and
targets for long-term sustainable yield)
(GFA 2018a, unpaginated). However,
the concession system is not currently
working as intended and illegal logging
in public protected areas remains a
serious threat, particularly logging of
mahogany (Swietenia macrophylla) (BLI
2016, p. 5), a CITES Appendix II species
(CITES 2018b). CITES Appendix II
includes species that are not necessarily
threatened with extinction, but for
which trade must be controlled to avoid
uses that are incompatible with their
survival (CITES 2016, unpaginated). An
example of illegal logging is that which
occurs in Jamari National Forest, an area
that is poorly protected and faces
pressures from loggers, squatters, and
poachers (Forshaw 2017, p. 224, F.
Olmos in litt. 1999 as cited in BLI 2016,
p. 5).
Also, as of 2010, Brazil had only
leased a small amount of private
concession forest, and instead, had
announced plans to sell large forest
tracts (GFA 2018a, unpaginated). If
these lands were to become privately
owned, they would be subject to Brazil’s
forest code and up to 20 percent could
be legally deforested. Additionally,
although selective logging and
requirements for minimum tree sizes are
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intended to minimize effects to the
forest, logging of larger trees is likely to
have a greater effect on the golden
conure because the species uses larger,
older trees for its nesting and roosting
(Yamashita 2003, p. 38).
Expanding crop production and
ranching are also major drivers of
deforestation in the Amazon basin. Soy
beans only grew in temperate climates
until agricultural research generated
new varieties that grow in the tropics.
These innovations, coupled with the
application of fertilizer, allowed for the
expansion of soy farming into the
Amazon beginning in the 1970s (GFA
2018c, unpaginated). Soy beans are
primarily used for cattle feed, and in
1990s and early 2000s, high demand for
beef created a ‘‘soy-cattle pasture
deforestation dynamic,’’ where soy
production replaced existing cattle
pasture, and forced new deforestation
into the Amazon for cattle ranching
(GFA 2018c, unpaginated). In 2006, the
soy industry, in response to pressure
from consumers, retailers, and
nongovernment organizations, instituted
a soy moratorium in Brazil’s Amazon.
The agreement curbs forest clearing for
soy by blocking farms that violate the
agreement from selling to companies
that signed the soy moratorium (Gibbs et
al. 2015, p. 377). In the 2 years
preceding the moratorium,
approximately 30 percent of soy
expansion occurred through
deforestation rather than by replacement
of pasture or other previously cleared
lands; by 2014, just 1 percent of soy
expansion was responsible for
deforestation in Brazil’s Amazon (Gibbs
et al. 2015, p. 377). The soy moratorium
was renewed indefinitely in 2016, or
until it is no longer needed (Patin˜o
2016, unpaginated).
Cattle ranching is the largest cause of
deforestation in every Amazon country
and is responsible for about 80 percent
of current deforestation rates (GFA
2018d, unpaginated). Brazil is the
largest beef exporter in the world,
supplying about one quarter of the
world market (GFA 2018d,
unpaginated). Brazil’s Amazon supports
about 200 million head of cattle on
approximately 450,000 km2 (173,746
mi2) of deforested land (GFA 2018d,
unpaginated). Cattle from the Amazon
are mostly sold in the domestic markets
because some of the Amazon states have
not been cleared for the presence of
foot-and-mouth disease (Fearnside
2017b, p. 14). Beginning in 1998, states
in the south (non-Amazonian) were
certified as free of foot-and-mouth
disease (Kaimowitz et al. 2004, as cited
by Fearnside 2017b, p. 14). The growing
export market for beef from these
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southern states has indirectly increased
the demand for Amazon beef for the
domestic market (Fearnside 2017b, p.
14). In 2015 and 2016, new markets for
Brazilian beef were opened up via
agreements with Russia, the United
States, and China (Fearnside 2017b, p.
14). The Chinese market, in particular,
has significant potential demand for
both beef and leather, with China being
the world’s largest manufacturer of
shoes (Fearnside 2017b, p. 16).
Conversion of native forest for the
cultivation of palm plantations for the
production of palm oil is an emerging
agricultural use in the region that is
likely to further reduce the amount of
habitat available to golden conure. Palm
oil is in high demand and the industry
is highly profitable (Lees et al. 2015, p.
2). Increased palm oil production has
the potential to create thousands of new
jobs and raise regional standards of
living in Brazil (Lees et al. 2015, p. 2).
The Brazilian government plans to
increase biofuel production in the next
decade, driven primarily by demands
for fuel (ethanol and biodiesel) (Villela
et al. 2014, p. 273). Palm oil production
has been touted as a ‘‘green fuel’’ from
both a biodiversity and a climate change
perspective because degraded lands
(e.g., abandoned cattle pastures and
mining areas) can be used for
plantations (Lees et al. 2015, p. 2).
However, a recent study of regional
avian biodiversity in palm oil
plantations concluded that they are as
detrimental to avian biodiversity as
other forms of agriculture such as cattle
pasture (Lees et al. 2015, entire).
Therefore, any native forest converted to
palm plantations will result in habitat
loss for the golden conure, and any
degraded land that is planted for palm
oil will not have the opportunity to
regenerate or be restored to suitable
habitat for the species.
Increased fire risk results from human
settlement and the activities noted
above (Barber et al. 2014, p. 203) (see
Projected Effects from Climate Change,
below). Although use of fire for land
management is now common in rural
Amazonia (Malhi et al. 2008, p. 171),
wildfires in the tropical forests of the
Amazon were rare over the past
millennia, and the trees are not adapted
for fire (Fearnside 2009, p. 1005).
Amazonian trees have thin bark, and
fire heats the cambium under the bark
at the base of the trunk, causing the tree
to die (Fearnside 2009, p. 1005) and
further contributing to deforestation.
Hydroelectric dams are also a major
contributor to deforestation in the
Amazon. Areas affected by dams
include both the area flooded by the
dam and effects from the increased
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human settlement around the dam (GFA
2018e, unpaginated). Brazil is the
second-largest producer of
hydroelectricity in the world (after
China), and hydropower supplies about
75 percent of Brazil’s electricity (GFA
2018e, unpaginated; Fearnside 2017c,
unpaginated). Numerous dams are
under construction or planned in the
Amazon basin. For example, the Belo
Monte ‘‘mega dam’’ on the Xingu River,
flooded 673 km2 (260 mi2) of lowlands
and forest, and blocked 1,609 km (1,000
mi) of the Xingu River (Fearnside 2017c,
unpaginated). Recently the Brazilian
Government announced an end to the
construction of mega dams in the
Amazon (Branford 2018, unpaginated),
but smaller dams within the golden
conure’s range are still under
construction or planned (GFA 2018e,
unpaginated; Fearnside 2017c,
unpaginated; Nobre et al. 2016, p.
10763).
Mining for minerals also contributes
to deforestation of the Amazon. In
Brazil, mining has grown from 1.6
percent of GDP in 2000, to 4.1 percent
in 2011, and is projected to increase by
a factor of 3 to 5 by 2030 (Brasil
Ministe´rio de Minas e Energia 2010, as
cited by Ferreira et al. 2014, p. 706). In
Brazil’s Amazon, mining leases,
exploration permits, and concessions
collectively encompass 1.65 million
km2 (0.64 million mi2) of land, with
about 60 percent located in the Amazon
forest (Departamento Nacional de
Produc¸a˜o Mineral 2012, as cited in
Sonter et al. p. 1). Although mining is
rapidly expanding in the region, to date,
the environmental approval process for
new mines or the expansion of existing
projects does not consistently evaluate
for off-lease effects of these projects,
including the indirect or cumulative
impacts to the surrounding forest
(Sonter et al. 2017, p. 1). The total offlease effects of mining-induced
deforestation can be 12 times greater
than that from the leases alone (Sonter
et al. 2017, p. 2).
Deforestation Rates and Gross Domestic
Product
Annual deforestation rates in the
Brazilian Amazon have always varied,
but have generally been correlated with
national economic growth as measured
by GDP (Petherick 2013 p.7; Hochstetler
and Viola 2012, p. 759). However,
beginning in 2005, measures of
deforestation and GDP have separated or
‘‘decoupled’’ (Lapola et al. 2014, p. 27;
Petherick 2013 p.7). The Amazon
experienced dramatic reductions in
annual average rates of deforestation
from almost 21,000 km2 (8,108 mi2)
between 2000 and 2004—to about 7,000
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km2 (2,703 mi2) in 2009 and 2010
(Prodes 2017, unpaginated; Petherick
2013, p. 8; Hochstetler and Viola 2012,
p. 759) and 6,418 km2 (2,478 mi2) in
2011 (Prodes 2017, unpaginated).
During this same period, Brazil’s GDP
rose steadily, indicating strong,
sustained growth from an export
commodity boom (Petherick 2013 p.7;
Hochstetler and Viola 2012, pp. 759–
760).
The decoupling has been attributed to
a number of factors with no clear
consensus on which factor has been the
most effective (Moutinho 2015, p. 2).
Contributing factors include government
strategies and policies for forest
conservation (Assunc¸a˜o et al. 2012, p.
697) such as: (1) The expansion of
protected areas, which reduced the
supply of unclaimed forest land
(Nepstad et al. 2014, p. 1118); (2) an
effort that began in 2007 to blacklist the
worst deforesters; and (3) efforts to
monitor and control municipalities with
high levels of illegal deforestation
through sanctions and restricted access
to credit (Moutinho 2015, p. 3;
Assunc¸a˜o et al. 2012, p. 698).
Reductions in deforestation have also
been attributed to market and social
forces, such as decreases in the price of
agricultural commodities (including soy
and beef) in 2005 (Fearnside 2017b, p.
1; Assunc¸a˜o et al. 2012, entire) and the
2006 soy moratorium (Gibbs et al. 2015,
pp. 377–378). Importantly, increased
soy production from 2006 to 2010 was
due to agricultural intensification
practices (Lapola et al. 2014, p. 28) and
expansion into previously cleared land
in the Amazon (Nepstad et al. 2014, p.
1121). Eventually cleared land that is
suitable for soy production will become
scarce, likely increasing deforestation
pressure on the Amazon (Nepstad et al.
2014, p. 1121). Although GDP is not
presently a good predictor of Amazon
deforestation (Fearnside 2017b, p. 14),
as global population and food demands
continue to rise (Beckman et al. 2017, p.
i; Brando et al. 2016, abstract), it is
possible that these measures could more
closely correlate in the future.
Brazil is one of the countries that
currently has comparatively low
productivity levels and is projected to
grow faster as it catches up with more
developed countries (Guardian 2012,
unpaginated). Brazil is expected to
remain among the top ten economies as
rated by GDP based on purchasing
power parity (GDP PPP) by 2050 (PWC
Global 2016). GDP PPP measures the
relative purchasing power of different
countries’ currencies over the same
types of goods and services, allowing for
more accurate comparison of living
standards (Euromonitor International
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2013, unpaginated). Forecasts vary for
Brazil’s GDP PPP, with one forecast
predicting that GDP PPP will rise
steadily through 2050 (PWC Global
2016, unpaginated), while a more recent
forecast predicts that GDP PPP will
stagnate then drop after about 2050
(Knoema 2018, unpaginated). Therefore,
if deforestation rates were to correlate
more closely with GDP PPP in the
future, in one scenario deforestation
rates would steadily rise, and in the
other scenario, deforestation rates
would stabilize and then decline after
about 2050.
Projected Effects From Climate Change
Changes in Brazil’s climate and
associated changes to the landscape are
likely to result in additional habitat loss
for the golden conure. Across Brazil,
temperatures are projected to increase
and precipitation to decrease (Barros
and Albernaz 2014, p. 811; Carabine and
Lemma 2014, p. 11). The 2013
Intergovernmental Panel on Climate
Change (IPCC) predicted that by 2100,
South America will experience
temperature increases ranging from 1.7
to 6.7 degrees Celsius (°C) (3.06 to 12.06
degrees Fahrenheit (°F)) under the
medium and high emission scenarios
and 1.0 to 1.5 °C (1.8 to 2.7 °F) under
a low emissions scenario (Carabine and
Lemma 2014, p. 10; Magrin et al. 2014,
p. 1502). Projected changes in
precipitation in South America vary by
region, with rainfall reductions in the
Amazon estimated with medium
confidence (about a 5 out of 10 chance)
(IPCC 2018, unpaginated; Carabine and
Lemma 2014, p. 11; Magrin et al. 2014,
p. 1502).
Downscaled models, based, in part,
on the earlier (2007) IPCC data, predict
more severe changes, with the greatest
warming and drying occurring over the
Amazon rainforest, particularly after
2040 (Marengo et al. 2011, pp. 8, 15, 27,
39, 48; Fe´res et al. 2009, p. 2). Estimates
of temperature changes in the Amazon
by the end of the 21st century (2090–
2099) are 2.2 °C (4 °F) under a low
greenhouse gas emission scenario and
4.5 °C (8 °F) under a high-emission
scenario (Marengo et al. 2011, p. 27).
Increased temperatures of these
amounts put the Amazon region at a
high risk of forest loss and more
frequent wildfires (Magrin et al. 2007, p.
596). Some leading global circulation
models indicate that extreme weather
events, such as droughts, will increase
in frequency or severity due to global
warming. As a result, droughts in
Amazonian forests could become more
frequent in the future (Marengo et al.
2011, p. 48). For example, the 2005
drought in Amazonia was a 1-in-20-year
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event; however, those conditions may
become a 1-in-2-year event by 2025, and
a 9-in-10-year event by 2060 (Marengo
et al. 2011, p. 28). Deforestation is
greater under drought conditions due to
more risk of fires (Marengo et al. 2011,
p. 16).
A number of large-scale drivers of
environmental change (i.e., land-use
change from deforestation and climate
changes due to global warming) are
operating simultaneously and
interacting nonlinearly in the Amazon
(Nobre et al. 2016, p. 10759). Thus, the
risks to golden conure from
deforestation will likely be intensified
by synergistic effects associated with
climate change (Staal et al. 2015, p. 2).
The Amazon’s rainforest may have two
‘‘tipping points’’: (1) A temperature
increase of 4.0 °C (7.2 14;°F); or (2)
deforestation exceeding 40 percent
(Nobre et al. 2016, p. 10759). Once
exceeded, these tipping points could
cause large-scale shifts in the vegetation
to a savanna (i.e., ‘‘savannization’’)
mostly in the southern and eastern
Amazon (Nobre et al. 2016, p. 10759)
within the golden conure’s range.
Similarly, a recent study that
considered only the effects from global
warming (i.e., absent deforestation)
predicted that by the end of this
century, some areas of rainforest will be
replaced by deciduous forest and
grassland in a moderate emissions
scenario (RCP 4.5) and by all grassland
in the high emissions scenario (RCP 8.5)
(Lyra et al. 2016, entire). Although the
projected outcomes of models are not
definitive, any terra firme forest habitat
that shifts from rainforest to other
habitat types (e.g., savanna) would
result in loss of habitat for the golden
conure.
Illegal Collection and Trade
The golden conure is highly prized as
an aviary bird and has been extensively
trapped for both the domestic and
international pet trade in the past (BLI
2016, p. 5; Alves et al. 2013, p. 60;
Laranjeiras 2011a, unpaginated;
Yamashita 2003, p. 38; Snyder et al.
2000, p. 132; Collar 1992, p. 304; Oren
and Novaes 1986, pp. 329, 334–335).
The international trade of wild
neotropical parrots was significantly
reduced during the 1990s due to (1)
tighter enforcement of CITES
regulations, (2) stricter measures under
European Union legislation, (3)
adoption of the Wild Bird Conservation
Act (WBCA; 16 U.S.C. 4901 et seq.) in
the United States, and (4) adoption of
national legislation in various other
countries (Snyder et al. 2000, p. 99).
Although an illegal international trade
of the golden conure for the pet trade
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occurred in the past, there is little
evidence that this practice is continuing
(Laranjeiras 2011a, unpaginated;
Silveira and Belmonte 2005 in press,
unpaginated). In contrast, the illegal
domestic market for the species is still
occurring at some level (Silveira and
Belmonte in press, unpaginated).
Historically, keeping birds was an
important part of local indigenous
tradition and culture (Carvalho 1951
and Cascudo 1973, as cited by Alves et
al. 2013, p. 54). Young golden conures
were taken from the wild to raise as pets
and for feathers, but now they are also
sold to bird traders (Oren and Novaes
1986, p. 335). Much of the area
occupied by the golden conure is poor,
and selling the birds for the domestic
pet trade provides an extra source of
income (Yamashita 2003, p. 39).
There are mixed reports regarding the
degree to which illegal capture of
golden conures from the wild
(‘‘poaching’’) is still occurring. The
Brazilian Institute of Environment and
Renewable Natural Resources (IBAMA)
has licensed and regulated bird breeding
in an effort to reduce poaching (Alves et
al. 2013, p. 61). As a result, several
sources believe poaching is no longer a
major concern for the species because
trade is thought to mostly be from the
substantial captive population, and thus
does not significantly affect the wild
population (Silveira in litt. 2012, Lees in
litt. 2013, in BLI 2016, p. 5). Additional
captive populations exist outside Brazil.
There are CITES-registered captivebreeding operations for golden conures
in the United Kingdom and the
Philippines.
However, some level of illegal capture
and trade of the species is still
occurring. For example, in 2016,
approximately 57 golden conures were
seized in Brazil (IBAMA 2017 as cited
by Lima in litt. 2018). We have no
seizure data from any other years, and
this number may represent a year where
seizures were high, but it demonstrates
that domestic trafficking is occurring
(Lima in litt. 2018). Captive rearing may
not be a practical alternative to illegal
trade, particularly in low-income areas
because the price of commercially bred
birds is approximately 10 times higher
than wild-caught individuals (Renctas
2001, as cited in Alves et al. 2013, p. 61;
Machado 2002, as cited in Alves et al.
2010, p. 155).
Additionally, oversight of domestic
wildlife-breeding facilities in Brazil is
limited (Alves et al. 2010, entire), and
many wild bird species declared to be
captive-bred are actually born in the
wild and traded under fraudulent
documentation (Alves et al. 2013, p. 61).
Although each Brazilian state has a
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wildlife center responsible for
managing, licensing, and inspecting all
categories of breeders, traders, and zoos
(Kuhnen and Kanaan 2014, p. 125),
most centers lack resources and funding
(Padrone 2004, as cited in Kuhnen and
Kanaan 2014, p. 125). Also, there are not
enough inspections at market places and
commercial breeding facilities to fight
illegal domestic trade (Alves et al. 2010,
pp. 154–155).
The United States is a major importer
of pet birds, yet relatively little trade in
the golden conure has been observed.
We reviewed all records of legal and
intercepted illegal trade in the CITES
annual trade records submitted by the
U.S. Fish and Wildlife Service from
1981 to 2016. During this 35-year
period, 54 live golden conures were
imported into the United States and 26
were exported (UNEP–WCMC 2018,
unpaginated). One record of illegal trade
was reported in 1981, and involved the
unlawful importation of a single animal
from Brazil. Overall, the U.S. trade in
the golden conure has been relatively
low compared with other pet birds.
Other Potential Stressors
Other potential stressors to the golden
conure include hunting and persecution
(Factor B), and predation or disease
(Factor C). The species is likely still
hunted at low levels as a food source,
and for feathers, and birds that raid
crops may be shot by farmers (Oren and
Novaes 1986, p. 335). However, we have
no information about the rate that these
activities may be occurring or the extent
to which they may be affecting
populations. Similarly, we have no
information regarding diseases that may
affect golden conures in the wild.
Golden conures, including eggs and
nestlings, are prey to a variety of native
predators, including toucans (Oren and
Novaes 1986, p. 334; Forshaw 2017, p.
228), raptors (Laranjeiras 2008a, as cited
in Laranjeiras 2011a, unpaginated;
Silveira and Belmonte in press,
unpaginated), monkeys, snakes, and the
tayra (Eira barbara), an omnivorous
weasel (Oren and Novaes 1986, p. 334).
However, we have no information
regarding the rates predation on the
golden conure from these predators and
how that may be affecting the conure.
Conservation Measures and Regulatory
Mechanisms
The golden conure is considered
‘‘Vulnerable’’ at the national level in
Brazil (MMA 2014, p. 122). Like other
wildlife species, conures and their
nests, shelters, and breeding grounds are
protected by Brazilian environmental
laws (Clayton 2011, p. 4; Environmental
Crimes law of Brazil (1999) as cited in
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MSU 2018, unpaginated; Official List of
Brazilian Endangered Animal Species
Order No. 1.522/1989 as cited in
ECOLEX 2018; CFRB 2010, p. 150; Law
No. 5.197/1967 as cited in LatinLawyer
2018, unpaginated). Additionally,
several Brazilian laws are designed to
protect forests. Destruction and damage
of forest reserves, cutting trees in forest
reserves, and causing fire in forests,
among other actions, without
authorization are prohibited (Clayton
2011, p. 5; Law No. 9.605/1998 as cited
in LatinLawyer 2018, unpaginated).
Protected areas have been emphasized
as the best hope for the golden conure’s
survival (e.g., in the Tapajos River
region and the Gurupi Biological
Preserve) (Laranjeiras and Cohn-Haft
2009, pp. 1, 8; Silveira and Belmonte in
press, unpaginated). The species occurs
in nine areas recently designated as
Important Bird Areas (IBAs) in Brazil
(BLI 2018a–h, unpaginated; Lima et al.
2014, p. 318; Laranjeiras 2011a,
unpaginated; Devenish et al. 2009, pp.
104–106). IBAs are places of
international significance for the
conservation of birds and other
biodiversity (BLI 2018i, unpaginated).
Levels of protection at IBAs vary from
fully protected to no protections (BLI
2018i, unpaginated). For example, the
Gurupi IBA has partial protection while
the Caxiuana˜/Portel IBA has none
(Service 2018, pp. 68–70; BLI 2018b,
unpaginated; Devenish et al. 2009, pp.
104–106). Additionally, the species’
predicted range overlaps with numerous
other protected areas, also having
various levels of protection (Service
2018, pp. 68–70; Laranjeiras and CohnHaft 2009, p. 8).
Various regulatory mechanisms (Law
No. 11.516, Act No. 7.735, and Decree
No. 78, as cited in ECOLEX 2018,
unpaginated) and Law 6.938/1981
(LatinLawyer 2018, unpaginated) direct
Brazil’s federal and state agencies to
promote the protection of lands and
govern the formal establishment and
management of protected areas to
promote conservation of the country’s
natural resources. These mechanisms
generally aim to protect imperiled
wildlife and plant species, genetic
resources, overall biodiversity, and
native ecosystems on federal, state, and
privately owned lands (e.g., Law No.
9.985, Law No. 11.132, Resolution No.
4, and Decree No. 1.922, as cited in
ECOLEX 2018, unpaginated).
Protected Areas: Protected areas have
traditionally formed the backbone of
forest conservation in the Amazon
Basin, and they still remain a vital
conservation strategy (GFA 2018f,
unpaginated). Brazil has the largest
protected area network in the world.
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The National Protected Areas System
(Federal Act 9.985/2000, as cited in
LatinLawyer 2018, unpaginated) was
established in 2000, and covers nearly
2.2 million km2 (0.8 million mi2) or 12.4
percent of the global total (WDPA, 2012
as cited by Ferreira et al. 2014, p. 706).
This extensive network of protected
areas is intended to (1) preserve priority
biodiversity conservation areas, (2)
establish biodiversity corridors, and (3)
protect portions of the 23 Amazonian
ecoregions identified by World Wildlife
Fund (Rylands and Brandon 2005, pp.
612, 615; Silva, 2005, entire). Brazil’s
Protected Areas may be categorized as
‘‘strictly protected’’ or ‘‘sustainable use’’
based on their overall management
objectives. Strictly protected areas
include national parks, biological
reserves, ecological stations, natural
monuments, and wildlife refuges
protected for educational and
recreational purposes and scientific
research. Protected areas of sustainable
use (national forests, environmental
protection areas, areas of relevant
ecological interest, extractive reserves,
fauna reserves, sustainable development
reserves, and private natural heritage
reserves) allow for different types and
levels of human use with conservation
of biodiversity as a secondary objective.
By 2006, 1.8 million km2 (0.7 million
mi2), or approximately 45 percent of
Brazil’s Amazonian tropical forest, was
under some level of protection as
federal or state managed land, or
designated as indigenous reserve
(managed by indigenous communities)
(Barber et al. 2014, p. 204). Of this, 19.2
percent was strictly protected areas, and
30.6 percent was comprised of federal
and state sustainable use area, with
indigenous reserves making up the
remainder (Barber et al. 2014, p. 204).
Indigenous lands are legally
recognized areas where indigenous
peoples have perpetual rights of access,
use, withdrawal, management, and
exclusion over the land and associated
resources (GFW 2018, unpaginated).
Indigenous communities sustainably
use their forest land, and large-scale
deforestation is prohibited (Barber et al.
2014, p. 204). Indigenous communities
practice shifting cultivation, trade nontimber forest products, and occasionally
allow selective logging (GFA 2018g,
unpaginated; Schwartzman and
Zimmerman 2005, p. 721).
To date, the golden conure has been
found in numerous protected areas or
IBAs, with a total area of approximately
154,673 km2 (51,719 mi2) (Service 2018,
pp 68–70). However, not all of the area
represented contains suitable habitat for
the species and several of the IBAs (39
percent) presently have no protection
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(61,864 km2 (23,866 mi2). An additional
26 percent of IBAs presently have just
partial protection (40,582 km2 (15,669
mi2) (Service 2018, pp 68–70).
Despite significant efforts to designate
and establish protected areas, funding
and resources are limited and adequate
enforcement of these areas is
challenging. For example, the conure
occurs in Jamari National Forest, which
is poorly protected and faces pressures
from loggers, squatters, and poachers
(Forshaw 2017, p. 224, F. Olmos in litt.
1999 as cited in BLI 2016, p. 5).
Forest Code: Brazil’s forest code was
created in 1965, and was subsequently
changed in the 1990s via a series of
presidential decrees (Soares-Filho et al.
2014, p. 363). As of 2001, the forest code
required landowners in the Amazon to
conserve native vegetation on their rural
properties by setting aside what is
called a ‘‘legal reserve’’ of 80 percent of
their property (i.e., with 20 percent
available to be harvested) (Soares-Filho
et al. 2014, p. 363). The forest code
severely restricted deforestation on
private properties but proved
challenging to enforce, and full
compliance has not been achieved (GFA
2018b, unpaginated; Azevedo et al.
2017, entire; Soares-Filho et al. 2014, p.
363). For instance, the lack of registered
property boundaries made it difficult to
link deforestation to particular land
owners, and the majority of
deforestation from 2002 to 2009 (about
69 percent) occurred on properties
whose boundaries were not publicly
registered (Azevedo et al. 2017, p.
7653).
In late 2012, a new forest code was
approved that reduces restoration
requirements by providing amnesty for
previous illegal deforestation by smaller
property holders (Soares-Filho et al.
2014, p. 363). Under the older forest
code, legal reserves that were illegally
deforested were required to be restored
at the landowner’s expense. The new
forest code forgives the legal reserve
debt of small properties (up to 440
hectares (1,087 acres)) (Soares-Filho et
al. 2014, p. 363). Although the 2012
forest code reduced the restoration
requirements, it also introduced
measures that strengthen conservation
including addressing (1) fire
management, (2) forest carbon, and (3)
payments for ecosystem services
(Soares-Filho et al. 2014, p. 363).
Additionally, the new forest code
created an Environmental Reserve
Quota where quota surplus on one
property may be used to offset a legal
reserve debt on another property within
the same biome; this could create a
market for forested lands, adding
monetary value to native vegetation and
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potentially abating up to 56 percent of
legal reserve debt (Soares-Filho et al.
2014, p. 363). Proponents of the new
forest code believe that it will act as an
effective barrier to agricultural
development, while others believe that
amnesty will lead to the perception that
illegal deforesters are unlikely to be
prosecuted or could be forgiven in
future land reforms (Soares-Filho et al.
2014, pp. 363–364).
Legal Captive Rearing and Trade:
IBAMA has licensed and regulated
breeding of native bird species,
including golden conure, in an effort to
reduce poaching (Alves et al. 2013, p.
61). The captive population of golden
conures in Brazil is believed to be about
600 birds (Prioste et al. 2013, p. 146),
and one breeder reported that in 8 years
she reared nearly 600 birds (Weinzettl,
in litt. 2015). Therefore, there is reason
to believe that the captive population of
golden conures in Brazil is at least 600
birds or larger. Additional captive
populations of golden conures exist as
CITES-registered captive-breeding
operations in the United Kingdom and
the Philippines. Although we have no
further information on these programs,
the captive rearing of golden conures in
Brazil is believed to have reduced the
incidence of poaching of young golden
conures from the wild (Silveira in litt.
2012, Lees in litt. 2013, as cited in BLI
2016, p. 5).
Reintroduction: Captive rearing and
reintroduction efforts have contributed
to the recovery of other parrots in
Central and South America but we
know of only one attempt to reintroduce
the golden conure to an area where it
had been extirpated. The species was
extirpated from the Bele´m region of Para´
in 1848 (Moura et al. 2014, p. 5). In
2017, researchers reintroduced the
golden conure to this area (at Utinga
State Park in Bele´m) (globo.com 2018,
unpaginated). The project includes a
post-release monitoring component
(Moura in litt. 2018), but it is too soon
to know whether or not the
reintroduction has been successful.
Additional Regulatory Mechanisms:
‘‘Reducing Emissions from Deforestation
and Forest Degradation’’ (REDD) is a
‘‘payment for ecological services’’
initiative that creates a financial value
for the carbon stored in forests (GFA
2018h, unpaginated). The program
offers incentives to developing countries
to reduce emissions from forested lands
and invest in low-carbon paths to
sustainable development (GFA 2018h,
unpaginated). REDD plus (REDD+) goes
one step further by including objectives
for (1) biodiversity conservation, (2)
sustainable management of forests, and
(3) improvements to forest governance
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and local livelihoods (GFA 2018h,
unpaginated). Brazil is one of the most
advanced countries in the world in
REDD+ planning and maintains an
‘‘Amazon Fund,’’ which receives
compensation for reductions in
deforestation. To date, the Norwegian
government is the major donor and
lesser donors include the government of
Germany and the Brazilian oil company
Petrobras (GFA 2018h, unpaginated).
The successful funding and
implementation of REDD+ is expected
to reduce rates of deforestation in
Brazil’s Amazon rainforest and would
likely benefit the golden conure and its
habitat. However, the initiative is in its
early stages and is being hampered by
numerous issues, particularly
unresolved land-tenure problems (May
et al. 2018, p. 44).
The golden conure is protected under
CITES, an international agreement
between member governments to ensure
that the international trade of CITESlisted plant and animal species is legal
and does not threaten species’ survival.
Under this treaty, CITES Parties
(member countries or signatories)
regulate the import, export, and reexport of specimens, parts, and products
of CITES-listed plant and animal
species. Brazil is a Party to CITES. Trade
in CITES-listed plants and animals must
be authorized through a licensing
system of permits and certificates that
are provided by the designated CITES
Management Authority of each CITES
Party. CITES includes three Appendices
that list species meeting specific
criteria. Depending on the Appendix in
which they are listed, species are
subject to various permitting
requirements.
The golden conure is listed in CITES
Appendix I and receives the highest
degree of protection. Species listed in
this Appendix are those that are
threatened with extinction and which
are, or may be, affected by trade.
Commercial trade in Appendix I
wildlife species is strictly prohibited,
except in limited circumstances
provided by the treaty. However,
commercial international trade may be
allowed in certain circumstances where
animals have been produced by CITESregistered captive-breeding operations.
Trade in specimens from registered
operations may be treated as if they
were listed in CITES Appendix II,
although they remain Appendix I listed
specimens. Each shipment requires the
issuance of both CITES export and
import documents. There are two
CITES-registered captive-breeding
operations for the golden conure: one in
the United Kingdom and the other in
the Philippines. The United States may
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also allow non-commercial trade in this
species on a case-by-case basis for
approved purposes such as scientific,
zoological, and educational activities.
Two other laws in the United States
apart from the Act provide protection
from the illegal import of wild-caught
birds into the United States: the Wild
Bird Conservation Act (WBCA) and the
Lacey Act (18 U.S.C. 42; 16 U.S.C. 3371
et seq.). The WBCA was enacted in
1992, to ensure that exotic bird species
are not harmed by international trade
and to encourage wild bird conservation
programs in countries of origin. Under
the WBCA and our implementing
regulations (50 CFR 15.11), it is
unlawful to import into the United
States any exotic bird species listed
under CITES except under certain
circumstances. We may issue permits to
allow import of listed birds for scientific
research, zoological breeding or display,
cooperative breeding, or personal pet
purposes when the applicant meets
certain criteria (50 CFR 15.22–15.25).
The Lacey Act was originally passed
in 1900, and was the first Federal law
protecting wildlife. Today, it provides
civil and criminal penalties for the
illegal trade of animals and plants.
Under the Lacey Act, in part, it is
unlawful to (1) import, export,
transport, sell, receive, acquire, or
purchase any fish, or wildlife taken,
possessed, transported, or sold in
violation of any law, treaty, or
regulation of the United States or in
violation of any Indian tribal law; or (2)
import, export, transport, sell, receive,
acquire, or purchase in interstate or
foreign commerce any fish or wildlife
taken, possessed, transported, or sold in
violation of any law or regulation of any
State or in violation of any foreign law.
Therefore, for example, because the take
of wild-caught golden conures would be
in violation of Brazil’s wildlife law, the
subsequent import of the species would
be in violation of the Lacey Act.
Similarly, under the Lacey Act, it is
unlawful to import, export, transport,
sell, receive, acquire, or purchase
specimens of these species traded
contrary to CITES.
Summary of Biological Status and
Threats
The best scientific and commercial
information available indicates that the
golden conure is more widespread and
abundant than believed at the time of
listing as endangered (BLI 2017,
unpaginated; Bird et al. 2011, Appendix
S1; Laranjeiras 2011b, p. 311;
Laranjeiras and Cohn-Haft 2009, pp. 1,
3) and that the threat from poaching for
the pet trade (Factor B) has diminished
(Silveira in litt. 2012, Lees in litt. 2013,
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in BLI 2016, p. 5; Snyder et al. 2000, p.
99) but is still occurring at some
unknown level. The global population is
estimated at 10,875 individuals within
174,000 km2 (67,182 mi2) of suitable
habitat across a range of approximately
340,000 km2 (131,275 mi2) (Laranjeiras
2011b, p. 311; Laranjeiras and CohnHaft 2009, pp. 1, 3). Nevertheless, the
population is regarded as small, and is
believed to declining (BLI 2016, p. 1)
primarily due to loss and degradation of
its habitat from deforestation (Factor A)
(BLI 2016, p. 4; IBAMA 2003 and SEMA
2007, as cited by Laranjeiras 2011a,
unpaginated; Collar 1992, p. 5).
Although rates of deforestation have
declined in recent decades, they are
increasing again (Alves et al. 2017, p.
76; Fearnside 2017b, p. 1; IPAM 2017,
p. 15;Prodes 2017, unpaginated;
Biderman and Nogueron 2016,
unpaginated) and are projected to
continue to increase (Bird et al. 2011,
entire; Soares-Filho et al. 2006, p. 520)
as the global demand for agricultural
commodities continues to rise (Brando
et al. 2016, abstract). Risks from
deforestation will likely be intensified
by synergistic effects associated with
climate change (Staal et al. 2015, p. 2)
(Factor E). Climate projections include
increased temperatures, dryer
conditions, and more frequent extreme
weather (including droughts), which
have the potential to stress trees and
cause tree mortality (Fearnside 2009,
pp. 1003, 1005). These conditions also
increase the unintentional spread of
fires, further contributing to
deforestation (Fearnside 2009, p. 1005).
Deforestation itself can cause regional
shifts in the climate and is likely to
operate together with the effects of
climate change to negatively alter
rainforest habitat. Although there are
uncertainties in the various models, and
projected outcomes are not definitive,
any terra firme forest habitat that shifts
from rainforest to other habitat types
(e.g., savanna) would no longer be
available to the golden conure.
Although an illegal international trade
of the golden conure occurred in the
past, there is little evidence that this
practice is continuing (Laranjeiras
2011a, unpaginated; Silveira and
Belmonte 2005 in press, unpaginated).
In contrast, the golden conure continues
to face an unknown level of pressure
from poaching and illegal trade within
Brazil (Factor B) (Silveira and Belmonte
in press, unpaginated), particularly in
poorer areas (Silveira and Belmonte in
press, unpaginated; Alves et al. 2013, p.
61). Captive golden conure breeding
programs in Brazil have helped to limit
poaching of wild golden conures
(Silveira in litt. 2012, Lees in litt. 2013,
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in BLI 2016, p. 5). However, poaching
of young conures for the illicit domestic
pet trade in Brazil has the potential to
negatively affect golden conure
populations, especially if individuals
are being collected from small or
fragmented populations. Populationlevel effects could operate
synergistically with effects from habitat
loss or degradation to the further
detriment of the species.
Although existing conservation efforts
and regulatory mechanisms appear to be
substantial (e.g., Brazil has the largest
protected area network in the world), at
this time they do not adequately
ameliorate threats to the golden conure
(Factor D). Despite significant efforts to
preserve the rainforest in Brazil’s
Amazon basin, enforcement has proven
to be challenging, and full compliance
has not been achieved. Habitat loss due
to deforestation is ongoing and is
predicted to continue, resulting in
global population declines of the golden
conure (BLI 2016, p. 1; Bird et al. 2011
Appendix S1).
Proposed Determination of Species
Status
Section 4 of the Act (16 U.S.C. 1533),
and its implementing regulations at 50
CFR part 424, set forth the procedures
for determining whether a species is an
endangered species or threatened
species and should be included on the
Federal Lists of Endangered and
Threatened Wildlife and Plants (listed).
The Act defines an endangered species
as any species that is ‘‘in danger of
extinction throughout all or a significant
portion of its range’’ and a threatened
species as any species ‘‘that is likely to
become endangered throughout all or a
significant portion of its range within
the foreseeable future.’’ Under section
4(a)(1) of the Act, we determine whether
a species is an endangered species or
threatened species because of any one or
a combination of the following: (A) The
present or threatened destruction,
modification, or curtailment of its
habitat or range; (B) overutilization for
commercial, recreational, scientific, or
educational purposes; (C) disease or
predation; (D) the inadequacy of
existing regulatory mechanisms; or (E)
other natural or manmade factors
affecting its continued existence.
Determination of Status Throughout All
of Its Range
As required by section 4(a)(1) of the
Act, we conducted a review of the status
of the golden conure and assessed the
five factors to evaluate whether the
species is endangered or threatened
throughout all of its range. We
examined the best scientific and
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commercial information available
regarding the past, present, and future
threats faced by the golden conure. We
reviewed information presented in the
2014 petition, information available in
our files, information gathered through
our 90-day finding in response to the
petition, information gathered in our
status review, and other available
published and unpublished
information.
In considering what factors may
constitute threats, we must look beyond
the mere exposure of the species to the
factor to determine whether the species
responds to the factor in a way that
causes actual impacts to the species. If
there is exposure to the factor, but no
response, or only a positive response,
that factor is not a threat. If there is
exposure and the species responds
negatively, the factor may be a threat
and we then attempt to determine if it
may drive or contribute to the risk of
extinction of the species such that the
species warrants listing as an
endangered or threatened species as
those terms are defined by the Act.
When we listed the golden conure as
endangered in 1976, the species was
perceived to be declining in numbers
due to either Factor A, Factor B, or
Factor D, or a combination of all three
factors (41 FR 24062; June 14, 1976). At
present, the best scientific and
commercial information available on the
range and abundance of the species
indicates that the species is more
widespread and abundant than
previously believed and that the threat
from overutilization for the pet trade
(Factor B) has diminished (Silveira in
litt. 2012, Lees in litt. 2013, in BLI 2016,
p. 5; Snyder et al. 2000, p. 99). Habitat
modeling studies have estimated that
there are approximately 10,875
individuals within 174,000 km2 (67,182
mi2) of suitable habitat across a range of
approximately 340,000 km2 (131,275
mi2) (Laranjeiras 2011b, p. 311;
Laranjeiras and Cohn-Haft 2009, pp. 1,
3).
Tighter enforcement of CITES, stricter
European Union legislation, adoption of
the WBCA in the United States, and
adoption of national legislation in other
countries have all helped to
significantly curtail illegal international
trade (Snyder et al. 2000, p. 99). In
addition, government-authorized
captive breeding programs in Brazil are
thought to have curtailed the illegal
domestic trade (Silveira in litt. 2012,
Lees in litt. 2013, in BLI 2016, p. 5).
Thus, after assessing the best available
information and as a result of the
aforementioned information, we
conclude the golden conure is not
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currently in danger of extinction
throughout its range.
As described below, we next
considered whether the golden conure
is likely to become in danger of
extinction throughout its range within
the foreseeable future. The term
‘‘foreseeable future’’ describes the extent
to which we can reasonably rely on
predictions about the future in making
determinations about the future
conservation status of the species. The
golden conure has already lost 30 to 35
of its historical range (Laranjeiras 2011a,
unpaginated; Laranjeiras and Cohn-Haft
2009, p. 8). We expect both the species’
global population and its habitat to
decline an additional 23 to 30 percent
in 22 years (Service 2018, pp. 42–46;
Bird et al. 2011 Appendix S1).
Additionally, habitat loss and
degradation is likely to be intensified by
synergistic effects associated with the
consequences of climate change (Service
2018, pp. 42–46; Staal et al. 2015, p. 2).
There is a strong likelihood of warming
to at least 1.5 to 2.0 °C (3.6 °F) in Latin
America by the end of the Century
(Carabine and Lemma 2014, p. 8), and
downscaled estimates for the Amazon
over the same time period (i.e., by the
end of the Century) indicate
temperature increases of 2.2 °C (4 °F)
under a low greenhouse gas emission
scenario and 4.5 °C (8 °F) under a highemission scenario (Marengo et al. 2011,
p. 27). Increased temperatures of these
amounts put the Amazon region at a
high risk of forest loss and more
frequent wildfires (Magrin et al. 2007, p.
596). Downscaled models, based, in
part, on the earlier (2007) IPCC data,
predict severe changes (increased
warming and drying) over the Amazon
rainforest, particularly after 2040
(Marengo et al. 2011, pp. 8, 15, 27, 39,
48; Fe´res et al. 2009, p. 2). Additionally,
some leading global-circulation models
indicate that extreme weather events,
such as droughts, will increase in
frequency, with drought becoming a 9in-10-year event, by 2060 (Marengo et
al. 2011, p. 28) further contributing to
deforestation due to more risk from fires
(Marengo et al. 2011, p. 16). Therefore,
based on the best available data, we
assessed foreseeable future to be 22 to
42 years (or approximately three to six
generations of the golden conure). We
based the lower end of this range (22
years) on the peer-reviewed work by
Bird et al. 2011, relating to deforestation
and declines in the population. We
based the upper end of this range (42
years) on peer-reviewed studies
predicting effects from climate change
(such as drought) on deforestation after
about 2040 to 2060 (Marengo et al. 2011,
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pp. 8, 15, 27, 28, 39, 48; Fe´res et al.
2009, p. 2). We conclude that it is
reasonable to rely on the predictions
made in these peer-reviewed studies in
making determinations about the future
conservation status of the golden
conure.
Although the golden conure is now
known to be more widespread and
abundant than previously thought, the
species remains relatively rare. It occurs
only within the southern basin of
Brazil’s Amazon, and much of this area
is in the ‘‘arc of deforestation’’ and is
threatened by loss and degradation of its
rainforest habitat from deforestation.
Effects from deforestation are
exacerbated by the projected effects
from climate change. Additionally, even
though government-authorized captive
breeding programs in Brazil are thought
to have curtailed the illegal domestic
trade, some unknown level of illegal
collection and trade is ongoing,
particularly within Brazil (Silveira and
Belmonte in press, unpaginated).
Existing regulatory mechanisms and
conservation efforts do not currently
adequately ameliorate threats to the
golden conure (Factor D). The factors
identified above continue to affect the
golden conure such that it is likely to
become in danger of extinction within
the foreseeable future throughout all of
its range. Based on the best available
scientific studies and information
assessing land-use trends, lack of
enforcement of laws, predicted
landscape changes under climatechange scenarios, and predictions about
how those threats may impact the
golden conure, we conclude that the
species is likely to be in danger of
extinction in the foreseeable future
throughout all of its range. Accordingly,
we find that the golden conure meets
the definition of a ‘‘threatened species’’
under the Act, and we are proposing to
list the golden conure as threatened
throughout its range.
Species Act’s Definitions of
‘‘Endangered Species and ‘‘Threatened
Species’’ (79 FR 37578; July 1, 2014)
(SPR Policy), if a species warrants
listing throughout all of its range, no
portion of the species’ range can be a
‘‘significant’’ portion of its range.
Significant Portion of Its Range
Under the Act and our implementing
regulations, a species warrants listing if
it is endangered or threatened. The Act
defines ‘‘endangered species’’ as any
species that is in danger of extinction
throughout all or a significant portion of
its range (16 U.S.C. 1532(6)), and
‘‘threatened species’’ as any species that
is likely to become an endangered
species within the foreseeable future
throughout all or a significant portion of
its range (16 U.S.C. 1532(20)). Because
we have determined that the golden
conure is threatened throughout all of
its range, under the Final Policy on
Interpretation of the Phrase ‘‘Significant
Portion of Its Range’’ in the Endangered
Import and Export
The proposed 4(d) rule imposes a
prohibition on imports and exports (by
incorporating 50 CFR 17.31), but creates
exceptions for certain golden conures.
Shipments of captive specimens (i.e.,
not taken from the wild) may include
live and dead golden conures and parts
and products, including the import and
export of personal pets and research
samples. The proposed 4(d) rule would
adopt the existing conservation
regulatory requirements of CITES and
the WBCA as the appropriate regulatory
provisions for the import and export of
these golden conure specimens.
This 4(d) rule proposes to allow a
person to import or export, into and
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Proposed 4(d) Rule
When a species is listed as
endangered, certain actions are
prohibited under section 9 of the Act
and our regulations at 50 CFR 17.21.
These include, among others,
prohibitions on take within the United
States, within the territorial seas of the
United States, or upon the high seas;
import; export; and shipment in
interstate or foreign commerce in the
course of a commercial activity.
Exceptions to the prohibitions for
endangered species may be granted in
accordance with section 10 of the Act
and our regulations at 50 CFR 17.22.
The Act does not specify particular
prohibitions and exceptions to those
prohibitions for threatened species.
Instead, under section 4(d) of the Act,
the Secretary of the Interior, as well as
the Secretary of Commerce depending
on the species, was given the discretion
to issue such regulations as deemed
necessary and advisable to provide for
the conservation of such species. The
Secretary also has the discretion to
prohibit by regulation with respect to
any threatened species any act
prohibited under section 9(a)(1) of the
Act. For the golden conure, the Service
is exercising our discretion to propose a
rule under section 4(d) of the Act. If this
proposed rule is adopted, we will
incorporate all prohibitions and
provisions of 50 CFR 17.31 and 17.32,
except that import and export of certain
golden conures into and from the
United States and certain acts in
interstate commerce will be allowed
without a permit under the Act, as
explained below.
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from the United States, captive
specimens, without a permit issued
under the Act, provided that the export
is authorized under CITES and the
import is authorized under CITES and
the WBCA. The import would require a
CITES document issued by the foreign
Management Authority indicating a
source code of ‘‘C’’, ‘‘D’’, or ‘‘F.’’
Exporters of captive birds would need to
provide a signed and dated statement
from the breeder of the bird, along with
documentation that identifies the source
of their breeding stock in order to obtain
a CITES export permit from the U.S.
Fish and Wildlife Service’s Division of
Management Authority. Exporters of
captive-bred birds must provide a
signed and dated statement from the
breeder of the bird confirming its
captive-bred status, and documentation
on the source of the breeder’s breeding
stock. The source codes of C, D, and F
for CITES permits and certificates are as
follows:
• Source Code C: Animals bred in
captivity in accordance with Resolution
Conf. 10.16 (Rev.), as well as parts and
derivatives thereof, exported under the
provisions of Article VII, paragraph 5 of
the Convention.
• Source Code D: Appendix I animals
bred in captivity for commercial
purposes in operations included in the
Secretariat’s Register, in accordance
with Resolution Conf. 12.10 (Rev.
CoP15), and Appendix I plants
artificially propagated for commercial
purposes, as well as parts and
derivatives thereof, exported under the
provisions of Article VII, paragraph 4, of
the Convention.
• Source Code F: Animals born in
captivity (F1 or subsequent generations)
that do not fulfill the definition of ‘‘bred
in captivity’’ in Resolution Conf. 10.16
(Rev.), as well as parts and derivatives
thereof.
The proposed 4(d) rule would not
allow any U.S. import or export of
golden conures that are taken from the
wild; such birds must continue to meet
the requirements of 50 CFR 17.31 and
17.32, including obtaining a permit
under the Act, with the following
exception. This 4(d) rule proposes to
allow a person to import or export a
wild golden conure specimen if the
specimen was held in captivity prior to
the date the species was listed in CITES
Appendix I (i.e., prior to the date that
CITES entered into force on July 1,
1975, with ‘‘golden parakeet’’ (i.e., the
golden conure) listed in Appendix I)
and provided that it meets all the
requirements of CITES and WBCA. If a
specimen was taken from the wild and
held in captivity prior to that date (July
1, 1975), the exporter would need to
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provide documentation as part of the
application for a U.S. CITES
preconvention certificate. Examples of
documentation may include: (1) A copy
of the original CITES permit indicating
when the bird was removed from the
wild, (2) veterinary records, or (3)
museum specimen reports.
Additionally, consistent with the 4(d)
regulations for other species in the
parrot family at 50 CFR 17.41 (c), the
prohibitions on take would apply and
the 4(d) rule would require a permit
under the Act for any activity that could
take a golden conure. Our regulations at
50 CFR 17.3 establish that take, when
applied to captive wildlife, does not
include generally accepted animal
husbandry practices, breeding
procedures, or provisions of veterinary
care for confining, tranquilizing, or
anesthetizing, when such practices are
not likely to result in injury to the
wildlife.
We assessed the conservation needs of
the golden conure in light of the broad
protections provided to the species
under CITES and the WBCA. As noted
above in Summary of Factors Affecting
the Species, some level of poaching for
illegal trade of golden conures is
occurring within Brazil (Silveira and
Belmonte in press, unpaginated) but
there is little evidence that this practice
occurs at the international level
(Laranjeiras 2011a, unpaginated;
Silveira and Belmonte 2005 in press,
unpaginated). The best available
commercial data indicate that tighter
enforcement of CITES, stricter European
Union legislation, adoption of the
WBCA in the United States, and
adoption of national legislation in other
countries have all helped to
significantly curtail illegal international
trade (Snyder et al. 2000, p. 99).
Therefore, illegal international trade is
not likely to be occurring at levels that
negatively affect the golden conure
population. Additionally, legal
international trade of the species is not
currently occurring at levels that affect
the golden conure population.
Therefore, we find that the import and
export requirements of the proposed
4(d) rule provide the necessary and
advisable conservation measures that
are needed for this species. This
proposed 4(d) rule, if made final, would
streamline the permitting process for
these types of activities by deferring to
existing laws that are protective of
golden conures in the course of import
and export.
Interstate Commerce
Under the proposed 4(d) rule, a
person may deliver, receive, carry,
transport, or ship a golden conure in
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45085
interstate commerce in the course of a
commercial activity, or sell or offer to
sell in interstate commerce a golden
conure without a permit under the Act.
At the same time, the prohibitions on
take under 50 CFR 17.21 would apply
under this proposed 4(d) rule, and any
interstate commerce activities that could
incidentally take golden conure or
otherwise constitute prohibited acts in
foreign commerce would require a
permit under 50 CFR 17.32.
Between 1981 and 2016, persons
within the United States imported 54
golden conures and exported 26; all
were reported as live captive-bred birds
except two exported birds that
originated from an unknown source and
one imported bird seized upon import
(UNEP–WCMC 2018, unpaginated;
Service 2018, p. 33). These imports and
exports were made for commercial,
captive-breeding, zoological, and
personal purposes (UNEP–WCMC 2018,
unpaginated; Service 2018, p. 33). We
have no information to indicate that
interstate commerce activities in the
United States are associated with threats
to the golden conure or would
negatively affect any efforts aimed at the
recovery of wild populations of the
species. Therefore, because (1) acts in
interstate commerce within the United
States have not been found to threaten
the golden conure, (2) the species is
otherwise protected in the course of
interstate and foreign commercial
activities under the take provisions set
forth at 50 CFR 17.31, and (3)
international trade of this species
appears to be effectively regulated under
CITES, we find this proposed 4(d) rule
contains all the prohibitions and
authorizations necessary and advisable
for the conservation of the golden
conure.
Proposed Technical Correction
Sections 50 CFR 17.11(c) and 17.12(b)
of Title 50 of the Code of Federal
Regulations direct us to use the most
recently accepted scientific name of any
wildlife or plant species, respectively,
that we have determined to be an
endangered or threatened species. The
golden conure currently appears on the
List as the ‘‘golden parakeet’’ (Aratinga
guarouba). However, in this proposed
rule, we refer to the species by the
common name ‘‘golden conure’’ and,
based on the best available scientific
information regarding the species’
taxonomy, we use the scientific name
Guaruba guarouba. Both ‘‘golden
conure’’ and ‘‘golden parakeet’’ are
common names associated with
Guaruba guarouba. We find that the
best available scientific information
available supports the designation of the
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golden conure to its own genus
(Guaruba). Therefore, we propose to
update the List to reflect this change in
the scientific name for golden conure.
The basis for this taxonomic change is
supported by published studies in peerreviewed journals (e.g., Uranto´wka and
Mackiewicz 2017, entire; Tavares et al.
2004, pp. 230, 236–237, 239; Sick 1990,
p. 112). Accordingly, we propose to
correct the scientific name of the species
under section 4 of the Act (16 U.S.C.
1531 et seq.) by changing the name as
currently listed (i.e., golden parakeet
(Aratinga guarouba)) to the corrected
species name (i.e., golden conure or
golden parakeet (Guaruba guarouba)).
We note that we are not required to
propose such a technical correction and
can generally make such a change in a
direct final rule. We determined it more
efficient, however, to include the
technical correction in this proposal.
Effects of This Rule
If this proposed rule is made final, it
would revise 50 CFR 17.11(h) to
reclassify the golden conure from
endangered to threatened on the List of
Endangered and Threatened Wildlife.
Additionally, if the proposed 4(d) rule
is adopted in a final rule, the Service
will incorporate all prohibitions and
provisions of 50 CFR 17.31 and 17.32,
except that import and export of certain
golden conures into and from the
United States and certain acts in
interstate commerce will be allowed
without a permit under the Act. In
addition, if the proposed taxonomic
change is made final, we will revise the
List of Endangered and Threatened
Wildlife to change the species’ scientific
name to Guaruba guarouba, and its
common name to golden conure
(=golden parakeet).
Common name
Required Determinations
Clarity of the Rule
We are required by Executive Orders
12866 and 12988 and by the
Presidential Memorandum of June 1,
1998, to write all rules in plain
language. This means that each rule we
publish must:
(1) Be logically organized;
(2) Use the active voice to address
readers directly;
(3) Use clear language rather than
jargon;
(4) Be divided into short sections and
sentences; and
(5) Use lists and tables wherever
possible.
If you feel that we have not met these
requirements, send us comments by one
of the methods listed in ADDRESSES. To
better help us revise the rule, your
comments should be as specific as
possible. For example, you should tell
us the numbers of the sections or
paragraphs that are unclearly written,
which sections or sentences are too
long, the sections where you feel lists or
tables would be useful, etc.
National Environmental Policy Act (42
U.S.C. 4321 et seq.)
We have determined that we do not
need to prepare an environmental
assessment, as defined under the
authority of the National Environmental
Policy Act of 1969, in connection with
regulations adopted under section 4(a)
of the Endangered Species Act. We
published a notice outlining our reasons
for this determination in the Federal
Register on October 25, 1983 (48 FR
49244).
References Cited
A complete list of references cited in
this rulemaking is available on the
Scientific name
*
*
Where listed
*
Status
internet at https://www.regulations.gov
under Docket No. FWS–HQ–ES–2015–
0019 or upon request (see FOR FURTHER
INFORMATION CONTACT). Authors
The primary authors of this proposed
rule are the staff members of the Branch
of Delisting and Foreign Species,
Ecological Services Program, U.S. Fish
and Wildlife Service.
List of Subjects in 50 CFR Part 17
Endangered and threatened species,
Exports, Imports, Reporting and
recordkeeping requirements, Wildlife.
Proposed Regulation Promulgation
Accordingly, we propose to amend
part 17, subchapter B of chapter I, title
50 of the Code of Federal Regulations,
as set forth below:
PART 17—ENDANGERED AND
THREATENED WILDLIFE AND PLANTS
1. The authority citation for part 17
continues to read as follows:
■
Authority: 16 U.S.C. 1361–1407; 1531–
1544; and 4201–4245, unless otherwise
noted.
2. Amend § 17.11(h), the List of
Endangered and Threatened Wildlife,
by:
■ a. Removing the entry for ‘‘Parakeet,
golden’’ under BIRDS; and
■ b. Adding an entry for ‘‘Conure,
golden (=golden parakeet)’’ in
alphabetical order under BIRDS to read
as follows:
■
§ 17.11 Endangered and threatened
wildlife.
*
*
*
(h) * * *
*
*
Listing citations and applicable rules
*
*
*
*
BIRDS
*
*
Conure, golden, (=golden parakeet).
*
*
Guaruba
guarouba.
*
*
3. Amend § 17.41 by revising
paragraph (c) introductory text and
paragraph (c)(2)(ii) introductory text,
and by adding paragraph (c)(2)(ii)(D) to
read as follows:
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■
§ 17.41
*
*
Special rules—birds.
*
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*
*
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*
T
*
*
*
41 FR 24062, 6/14/1976; [Federal Register citation of final
rule]; 50 CFR 17.41(c) 4d.
*
*
(c) The following species in the parrot
family: Salmon-crested cockatoo
(Cacatua moluccensis), yellow-billed
parrot (Amazona collaria), white
cockatoo (Cacatua alba), and the golden
conure (Guaruba guarouba).
*
*
*
*
*
(2) * * *
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*
*
(ii) Specimens held in captivity prior
to certain dates: You must provide
documentation to demonstrate that the
specimen was held in captivity prior to
the applicable date specified in
paragraphs (c)(2)(ii)(A), (B), (C), or (D) of
this section. Such documentation may
include copies of receipts, accession or
veterinary records, CITES documents, or
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wildlife declaration forms, which must
be dated prior to the specified dates.
*
*
*
*
*
(D) For golden conures: July 1, 1975
(the date CITES entered into force with
the ‘‘golden parakeet’’ (i.e., the golden
conure) listed in Appendix I).
*
*
*
*
*
Dated: August 3, 2018.
James W. Kurth,
Deputy Director, U.S. Fish and Wildlife
Service, Exercising the Authority of the
Director, U.S. Fish and Wildlife Service.
[FR Doc. 2018–19153 Filed 9–4–18; 8:45 am]
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Agencies
[Federal Register Volume 83, Number 172 (Wednesday, September 5, 2018)]
[Proposed Rules]
[Pages 45073-45087]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-19153]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-HQ-ES-2015-0019; 4500090024]
RIN 1018-BC78
Endangered and Threatened Wildlife and Plants; Reclassifying the
Golden Conure From Endangered to Threatened With a Section 4(d) Rule
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), announce a
12-month finding on a petition to delist or downlist the golden conure
under the Endangered Species Act of 1973, as amended (Act). The golden
conure is a psittacine bird (parrots, parakeets, macaws, cockatoos, and
others) endemic to the south Amazon Basin in Brazil. After review of
the best available scientific and commercial information, we find that
listing the golden conure as a threatened species is warranted.
Accordingly, we propose to list it as a threatened species with a rule
issued under section 4(d) of the Act. If we finalize this rule as
proposed, it would reclassify the golden conure from endangered to
threatened on the List of Endangered and Threatened Wildlife (List).
Additionally, we are proposing to update the List to reflect the latest
scientifically accepted taxonomy and nomenclature for the species as
Guaruba guarouba, golden conure.
DATES: We will accept comments received or postmarked on or before
November 5, 2018. Comments submitted electronically using the Federal
eRulemaking Portal (see ADDRESSES, below) must be received by 11:59
p.m. Eastern Time on the closing date. We must receive requests for
public hearings, in writing, at the address shown in FOR FURTHER
INFORMATION CONTACT by October 22, 2018.
ADDRESSES: You may submit comments by one of the following methods:
(1) Electronically: Go to the Federal eRulemaking Portal: https://www.regulations.gov. In the Search box, enter FWS-HQ-ES-2015-0019,
which is the docket number for this rulemaking. Then, click on the
Search button. On the resulting page, in the Search panel on the left
side of the screen, under the Document Type heading, click on the
Proposed Rules link to locate this document. You may submit a comment
by clicking on ``Comment Now!''
(2) By hard copy: Submit by U.S. mail or hand-delivery to: Public
Comments Processing, Attn: FWS-HQ-ES-2015-0019; U.S. Fish and Wildlife
Service, MS: BPHC, 5275 Leesburg Pike, Falls Church, VA 22041-3803.
We request that you send comments only by the methods described
above. We will post all comments on https://www.regulations.gov. This
generally means that we will post any personal information you provide
us (see Public Comments, below, for more information).
FOR FURTHER INFORMATION CONTACT: Don Morgan, Chief, Branch of Delisting
and Foreign Species, Ecological Services, U.S. Fish and Wildlife
Service, MS: ES, 5275 Leesburg Pike, Falls Church, VA 22041-3803;
telephone, 703-358-2171. If you use a telecommunications device
[[Page 45074]]
for the deaf (TDD), call the Federal Relay Service at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Information Requested
Public Comments
We intend that any final action resulting from this proposed rule
will be based on the best scientific and commercial data available and
be as accurate and as effective as possible. Therefore, we request
comments and information from other concerned governmental agencies,
the scientific community, industry, or any other interested parties
concerning this proposed rule. We particularly seek comments
concerning:
(1) Reasons why we should or should not reclassify the golden
conure from an endangered species to a threatened species under the Act
(16 U.S.C. 1531 et seq.).
(2) The golden conure's biology, range, and population trends,
including:
(a) Biological or ecological requirements of the species, including
habitat requirements for feeding, breeding, and sheltering;
(b) Genetics and taxonomy;
(c) Historical and current range, including distribution patterns;
(d) Historical and current population levels, and current and
projected trends; and
(e) Past and ongoing conservation measures for the species, its
habitat, or both.
(3) Factors that may affect the continued existence of the species,
which may include:
(a) Habitat modification or destruction (e.g., information
regarding future rates of deforestation or other forms of habitat loss
or degradation within the known range of the golden conure);
(b) Overutilization, including information regarding illegal
collection and trade;
(c) Disease or predation;
(d) The inadequacy of existing regulatory mechanisms; or
(e) Other natural or manmade factors affecting the species'
continued existence.
(4) Biological, commercial trade, or other relevant data concerning
any threats (or lack thereof) to this species and existing regulations
that may be addressing those threats.
(5) Information on the locations of any additional or newly
discovered populations of this species. See Appendix B in the species
status assessment report (SSA) for a list of known localities used by
the golden conure (available under Docket No. FWS-HQ-ES-2015-0019 on
https://www.regulations.gov.
(6) Information on the number of captive-bred golden conures in
Brazil.
(7) Information regarding current or future rates of deforestation
in the Brazilian Amazon as they may correlate to current or projected
gross domestic product (GDP) in that country.
(8) The appropriateness of the conservation measures proposed under
section 4(d) of the Act, including those that would allow the import
and export of certain golden conures into and from the United States
and certain acts in interstate commerce without a permit under the Act.
Please include sufficient information with your submission (such as
electronic copies of scientific journal articles or other publications,
preferably in English) to allow us to verify any scientific or
commercial information you include.
Please note that submissions merely stating support for or
opposition to the action under consideration without providing
supporting information, although noted, will not be considered in
making a determination, as section 4(b)(1)(A) of the Act directs that
determinations as to whether any species is an endangered or threatened
species must be made ``solely on the basis of the best scientific and
commercial data available.''
You may submit your comments and materials concerning this proposed
rule by one of the methods listed in ADDRESSES. We request that you
send comments only by the methods described in ADDRESSES.
If you submit information via https://www.regulations.gov, your
entire submission--including any personal identifying information--will
be posted on the website. If your submission is made via a hardcopy
that includes personal identifying information, you may request at the
top of your document that we withhold this information from public
review. However, we cannot guarantee that we will be able to do so. We
will post all hardcopy submissions on https://www.regulations.gov.
Comments and materials we receive, as well as supporting
documentation we used in preparing this proposed rule, will be
available for public inspection on https://www.regulations.gov, or by
appointment, during normal business hours, at the U.S. Fish and
Wildlife Service, Headquarters Office (see FOR FURTHER INFORMATION
CONTACT).
Public Hearing
Section 4(b)(5)(E) of the Act provides for a public hearing on this
proposal, if requested within 45 days of the date of publication of
this proposed rule. Requests must be sent to the address shown in FOR
FURTHER INFORMATION CONTACT and received by the date specified in
DATES.
Peer Review
The purpose of peer review is to ensure that our reclassification
determination is based on scientifically sound data, assumptions, and
analyses. In accordance with our joint policy on peer review published
in the Federal Register on July 1, 1994 (59 FR 34270), and our August
22, 2016, memorandum updating and clarifying the role of peer review of
listing actions under the Act, we sought the expert opinions of five
appropriate specialists regarding the SSA report that informed this
proposed rule. The peer reviewers have expertise in (1) the life
history of the golden conure, (2) birds of the Amazon, and (3) the
effects of habitat degradation and deforestation on Amazonian birds. We
received responses from four of the five peer reviewers, which we took
into account in our SSA and this proposed rule. Their comments and
suggestions can be found online at https://www.fws.gov/endangered/improving_ESA/peer_review_process.html. We invite any additional
comments from the peer reviewers on the proposed rule during the public
comment period on this proposed rule (see DATES, above); all comments
received from peer reviewers will be available, along with other public
comments, in the docket for this proposed rule at https://www.regulations.gov under Docket No. FWS-HQ-ES-2015-0019.
Previous Federal Actions
On May 22, 1975, the Fund for Animals, Inc., petitioned us to list
216 taxa of plants and animals, including the ``golden parakeet,'' as
an endangered species pursuant to the Act. On September 26, 1975, we
proposed to list the ``golden parakeet (Aratinga guaruba)'' as
endangered (40 FR 44329). On June 14, 1976 (41 FR 24062), we finalized
the listing as endangered.
On August 21, 2014, we received a petition from the American
Federation of Aviculture, Inc. (AFA), requesting that the golden conure
be removed from the List or reclassified as a threatened species. The
AFA also requested that if we determined that downlisting to threatened
status was warranted, we develop a rule under section 4(d) of the Act
(also called a 4(d) rule) that would allow for import and export of
certain golden conures into and from the United States, and interstate
commerce of the species under certain circumstances.
On April 10, 2015, we published in the Federal Register (80 FR
19259), a
[[Page 45075]]
90-day finding for the 2014 petition, concluding that the petition
provided substantial information indicating the petitioned action may
be warranted, and we initiated a status review for this species.
On July 29, 2017, the AFA filed a complaint under the Act to compel
the Service to issue a 12-month finding regarding the AFA's petition,
pursuant to 16 U.S.C. 1533(b)(3)(B). On November 6, 2017, the AFA and
the Service entered into a settlement agreement whereby the Service
agreed to submit a 12-month finding for the golden conure to the
Federal Register for publication no later than September 1, 2018. This
proposed rule constitutes the 12-month finding and our 5-year status
review for the golden conure.
Background
Species Status Assessment (SSA) Report for the Golden Conure
A thorough review of the taxonomy, life history, ecology, and
overall viability of the golden conure is presented in the SSA Report
(Service 2018; available at Docket No. FWS-HQ-ES-2015-0019 on https://www.regulations.gov). The following discussion is a summary of the
information and analyses from the SSA Report.
Current Conservation Status
The golden conure is currently listed as endangered under the Act
(41 FR 24062; June 14, 1976) and the species is considered
``Vulnerable'' at the national level in Brazil (MMA 2014, p. 122). The
International Union for the Conservation of Nature (IUCN) recently
reclassified the species from endangered to vulnerable because its
population is estimated to be larger than previously thought (Bird Life
International (BLI) 2017, unpaginated). IUCN's ``vulnerable'' listing
acknowledges that the species nevertheless has a small estimated
population that is expected to experience a rapid decline over the next
three generations due to habitat loss and limited pressure from
poaching (BLI 2017, unpaginated). The species is also included in
Convention on International Trade in Endangered Species of Wild Fauna
and Flora (CITES) Appendix I (CITES 2018a, unpaginated). CITES is an
international treaty for the conservation of wild fauna and flora
subject to trade; species on CITES Appendix I are considered threatened
with extinction and international trade is permitted only under
exceptional circumstances, which generally precludes commercial trade
(CITES 2016, unpaginated).
Species Description
The golden conure is a large, 34-centimeter (13-inch), macaw-like
bird with striking yellow plumage and green flight feathers
(Laranjeiras 2011a, unpaginated; Parr and Juniper 2010, p. 436). The
sexes are similar in appearance, but in first-year juveniles the yellow
color is variably streaked with green--most often on the back of the
head, nape and chest (Forshaw 2017, p. 223; Laranjeiras 2011a,
unpaginated; Reynolds 2003, p. 10).
Taxonomy
The golden conure was first documented in 1788 (ITIS 2017,
unpaginated) and was later noted in the manuscripts of European
explorers to Brazil in the 18th and 19th centuries (Yamashita 2003, p.
38). It was originally placed in its own (monotypic) genus Guaruba,
then subsequently placed in the genus Aratinga by some authors (Peters
1937; Pinto 1978; Forshaw 1989, as cited in Tavares et al. 2004, p.
239), while others placed it in the genus Conurus (Salvadori 1891;
Miranda Ribeiro 1920, as cited in Tavares et al. 2004, p. 239).
Researchers have since noted that its behaviors, including
reproduction and vocalization, differ markedly from those of Aratinga
species and have recommended that the golden conure's scientific name
be returned to the monotypic genus Guaruba (Laranjeiras 2011a,
unpaginated; Sick 1990, p. 112). Additionally, recent genetic analyses
indicate that the golden conure is more closely related to the red-
shouldered macaw (Diopsittaca nobilis) and the blue-crowned parakeet
(Thectocercus acuticaudatus) (Urant[oacute]wka and Mackiewicz 2017,
entire), than to the Aratinga parakeets (Tavares et al. 2004, pp. 230,
236-237, 239). Therefore, the golden conure is recognized as Guaruba
guarouba by (1) the Integrated Taxonomic Information System (ITIS 2017,
unpaginated); (2) the Brazilian Ornithological Records Committee
(Piacentini et al. 2015, p. 163); (3) Taxonomy of Birds of the World
(Clements et al. 2017, unpaginated); and (4) Birdlife International
(BLI 2017, unpaginated). Based upon our review of the best available
information, we recognize the golden conure as a valid full species in
the monotypic genus Guaruba and we are proposing to correct its
scientific name to Guaruba guarouba on the Federal List of Endangered
and Threatened Wildlife (see Proposed Technical Correction, below).
Abundance and Distribution
In general, the golden conure is relatively poorly studied and
information on local abundance and distribution of populations
throughout the range is limited (Laranjeiras 2011b, p. 303). An earlier
global population estimate (i.e., from 2010 and earlier) indicated
fewer than 2,500 individuals remained, but a 2011 estimate signaled the
global population contained 10,875 individuals within 174,000 square
kilometers (km\2\) (67,182 square miles (mi\2\)) of suitable habitat
(Laranjeiras 2011b, p. 311). This estimate was derived using: (1)
Occurrence data obtained after 1987, that extended the species' known
range considerably to the southwest; (2) a density estimate calculated
from a conure survey in western Par[aacute] in 2007 (Laranjeiras 2011b,
p. 311); and (3) estimates of suitable habitat within the known area of
occurrence from a habitat modeling study in 2009 (Laranjeiras and Cohn-
Haft 2009). However, because the golden conure has a patchy
distribution and is poorly studied, more survey work would be required
to produce better estimates.
The species' current known range includes portions of the following
four states in Brazil (noted from east to west): (1) The western part
of Maranh[atilde]o; (2) the central region of Par[aacute]; (3) the
extreme southeast of Amazonas; and (4) the northeastern portion of
Rond[ocirc]nia (Laranjeiras 2011a, unpaginated). Additionally, the
species was recorded in a fifth state, the northern portion of Mato
Grosso, in the 1990s (Lo 1995, entire), but there have been no recent
sightings in that area (Moura in litt. 2018; BLI 2016, p. 2;
Laranjeiras 2011a, unpaginated; Laranjeiras and Cohn-Haft 2009, p. 3;
Albertani et al. 1997, p. 135).
The species' historical range once extended farther eastward (to
more eastern portions of the states of Par[aacute] and
Maranh[atilde]o), but the habitat there was mostly deforested in the
1970s and 1980s (Laranjeiras and Cohn-Haft 2009, p. 5). The golden
conure is believed to be extirpated from these regions (BLI 2017,
unpaginated; BLI 2016, p. 3; Laranjeiras and Cohn-Haft 2009, p. 5),
which represented approximately 30 to 35 percent of the historical
range (Laranjeiras 2011a, unpaginated; Laranjeiras and Cohn-Haft 2009,
p. 8).
The species is limited to regions where extensive stands of tall
Amazonian rainforest are still present (Oren and Novaes 1986, p. 331).
Although the species can tolerate some disturbance in the forest, the
golden conure is absent from landscapes with advanced deforestation;
flocks
[[Page 45076]]
disappear seasonally from the fragmented landscapes, indicating that
they require intact forest (Laranjeiras 2011a, unpaginated).
The best estimate of the geographic distribution of the golden
conure is based on recent records and habitat modeling (see Service
2018, Figures 5 and 6, pp. 19-20; Laranjeiras 2011b, p. 311;
Laranjeiras and Cohn-Haft 2009, entire). The total current range of the
golden conure is estimated to be no more than 340,000 km\2\ (131,275
mi\2\) (Laranjeiras and Cohn-Haft 2009, p. 3). The species'
distribution within this range is not continuous and is described as
patchy--possibly associated with the distribution of specific nesting
or food resources (Laranjeiras 2008, as cited in Laranjeiras and Cohn-
Haft 2009, p. 6). The estimated suitable habitat for the golden conure
within this range is 174,000 km\2\ (67,182 mi\2\) (Laranjeiras 2011b,
p. 311). However, parrots can cross great gaps and are capable of
flying long distances (Lees and Peres 2009, pp. 284, 286); thus, it is
possible that some of the recent records of the golden conure that
extended the range represent vagrant groups (Moura in litt. 2018).
Because the species has a patchy distribution within its range,
extrapolation of densities to estimate the global population is
problematic, and population estimates throughout the range are needed
(Laranjeiras 2011a, unpaginated).
Habitat
The golden conure lives in in Brazil's lower Amazon basin, in an
area south of the Amazon River, east of the Madeira River, and north of
the Brazilian Shield (Laranjeiras and Cohn-Haft 2009, p. 9). The
Brazilian Shield is a region formed of Precambrian crystalline rocks
that may be exposed or covered by layers of sedimentary rocks (Buckup
2011, p. 203). The species occupies primary (old growth) terra firme
(unflooded) rainforest on undulating landscapes in the lowlands at
elevation at or under 300 meters (984 feet) (Sick 1997, as cited by
Laranjeiras 2011a, unpaginated). However, the species has also has been
recorded in the regrowth of secondary forests and in igap[oacute]
(seasonally flooded) forests while feeding (Laranjeiras 2011a,
unpaginated, citing several sources; Laranjeiras 2011b, pp. 308-309;
Oren and Noveas 1986, p. 332; Laranjeiras 2008a, as cited in
Laranjeiras 2011a, unpaginated). The majority of golden conure groups
appear to be resident (i.e., non-migratory), even in the post-
reproductive period (Laranjeiras 2008, as cited in Forshaw 2017, p.
226; Laranjeiras 2011a, unpaginated; Yamashita 2003, p. 38).
The golden conure uses large, old growth, hardwood trees (Yamashita
2003, p. 38) for cavity nesting (Oren and Novaes 1986, pp. 333-334). In
most cases, the species uses the same tree for nesting and roosting
(BLI 2016, p. 4; Laranjeiras 2011a, unpaginated; Yamashita 2003, p.
38). Most known nest and roost cavities have been found high in tall,
standing, dead trees within a small, disturbed (cleared) area adjacent
to continuous forest. The golden conure seems to prefer using isolated
trees (i.e., some distance from a neighboring tree) for nesting likely
because isolated trees provide better protection against terrestrial or
arboreal predators (Laranjeiras 2011a, unpaginated; Kyle 2005, p. 3).
To date, we are aware of 7 different species of hardwood trees used for
nesting (Laranjeiras 2011b, p. 308; Silveira and Belmonte in press,
unpaginated; Oren and Novaes 1986, p. 333; Lima et al. 2014, p. 323)
and more than 28 species of fruiting trees used for feeding (Service
2018, pp. 10, 60-61).
Biology
The golden conure is frugivorous (fruit-eating), and its diet
varies throughout the year and across its distribution (Laranjeiras
2011a, unpaginated). The species eats whole fruit, seeds, pulp, buds
and flowers, nectar, and peels; it will also feed on cultivated plants
such as corn (Zea mays) and mangoes (Mangifera indica) (Laranjeiras
2011b, pp. 308-309; Oren and Noveas 1986, p. 332).
Breeding and nesting take place during the wet months, generally
from November or December through April (Forshaw 2017, p. 227;
Laranjeiras 2011a, unpaginated; Oren and Novaes 1986, p. 332). The
social structure and breeding behavior of the golden conure appear to
be unique from that of other members of the parrot family in that the
species engages in communal brood-rearing. The golden conure remains in
flocks made up of family groups or clans (averaging 10 individuals)
(Laranjeiras 2011a, unpaginated), and individuals in the group
(referred to as ``reproductive helpers'') assist in rearing the young.
Most other large parrots are believed to incubate and rear young in
pairs (Albertani et al. 1997, pp. 135-136).
The golden conure's communal brood-rearing includes the use of one
or two uncommon reproductive strategies where the flock is either made
up of (1) multiple related nesting pairs with reproductive helpers
(Oren and Novaes 1986, p. 333), or (2) a single leading pair with
juveniles from different generations acting as helpers (Reynolds 2003,
p. 12; Oren and Novaes 1986, p. 333). Nest protection seems to be an
important part of communal brood-rearing, and a group will vigorously
defend the nest in response to potential competitors or predators
(Forshaw 2017, p. 228; Laranjeiras 2008a, as cited in Laranjeiras
2011a, unpaginated).
Most of the information regarding development of the young is from
captive birds. Eggs hatch within 28 to 30 days (Arndt 1996, as cited by
Forshaw 2017, p. 227; Laranjeiras 2011a, unpaginated; Oren and Novaes
1986, p. 333). Nestlings reach adult size in about 60 days (Laranjeiras
2011a, unpaginated) and fledge at approximately 55-60 days post hatch
(Arndt 1996, as cited by Forshaw 2017, p. 227). The post-reproductive
period, when first year juveniles can be seen in the flocks at feeding
sites in the wild, is from March or April to July or August
(Laranjeiras 2011b, p. 304; Oren and Novaes 1986, p. 332).
First-year juveniles always stay with the family group and can be
easily identified by their green-streaked plumage (Yamashita 2003, p.
38). Juveniles attain adult plumage in a molt when they are about 1
year old (Laranjeiras 2011a, unpaginated). Fledged chicks and juveniles
will beg for food from foraging adults (Kyle 2005, p. 4). Annual
survival information is limited, but first-year juveniles represent no
more than 13 percent of the individuals in flocks (Laranjeiras 2008a,
as cited in Laranjeiras 2011a, unpaginated). In some areas (e.g., in
eastern Par[aacute], where trapping for the illegal pet trade has
occurred), the percentage of observed first-year juveniles in the
flocks was zero (Reynolds 2003 as cited by Laranjeiras 2011b, p. 309).
In captivity, adults reach sexual maturity at about 3 years of age
(Oren and Novaes 1986, p. 333), with the average age for successful
breeding occurring between 6 and 8 years (Reynolds, 2003, p. 12).
Lifespan for the golden conure in the wild is not known, although the
generation length was estimated as 7.4 years (BLI 2016, unpaginated)
and the maximum age recorded for the species in captivity was 60 years
with a median age of 14 years (calculated using adults >=4 years; n =
190) (Young et al. 2011, p. 35). Information is lacking on the species'
carrying capacity, birth rates, nesting success, and home range
(broadly defined as confined areas where individuals conduct their day-
to-day activities (Boitani and Fuller 2000, p. 65).
[[Page 45077]]
Summary of Factors Affecting the Species
A species is an ``endangered species'' for purposes of the Act if
it is in danger of extinction throughout all or a significant portion
of its range and is a ``threatened species'' if it is likely to become
an endangered species within the foreseeable future throughout all or a
significant portion of its range. Section 4 of the Act and its
implementing regulations (50 CFR part 424) set forth the procedures for
listing species, reclassifying species, or removing species from listed
status. A species may be determined to be an endangered or threatened
species due to one or more of the five listing factors described in
section 4(a)(1) of the Act: (A) The present or threatened destruction,
modification, or curtailment of its habitat or range; (B)
overutilization for commercial, recreational, scientific, or
educational purposes; (C) disease or predation; (D) the inadequacy of
existing regulatory mechanisms; or (E) other natural or manmade factors
affecting its continued existence. A species may be removed from listed
status (i.e., ``delisted'') or reclassified on the same basis. Our
analysis of threats is an evaluation of both the threats currently
facing the species and the threats that are reasonably likely to affect
the species in the foreseeable future without the Act's protections.
In our analysis, we considered conservation measures (primarily the
use of protected areas) as part of the current condition and projected
future scenarios to evaluate viability of the species (Service 2018,
pp. 42-47). We generally define viability as the ability the golden
conure to sustain populations in natural ecosystems and disturbed
habitats over time. Using the SSA framework, we considered what the
species needs to maintain viability by evaluating the species in terms
of resiliency, redundancy, and representation (Wolf et al. 2015,
entire). For further information on viability, see the SSA Report
(https://www.regulations.gov at Docket No. FWS-HQ-ES-2015-0019).
When we listed the golden conure as endangered in 1976, the species
was perceived to be declining in numbers due to any one the following
factors, or a combination of all three factors: The present or
threatened destruction, modification, or curtailment of its habitat or
range (Factor A); overutilization of the species for commercial,
recreational, scientific, or educational purposes (Factor B); or the
inadequacy of existing regulatory mechanisms (Factor D) (41 FR 24062;
June 14, 1976).
The golden conure presently faces the most risk from loss and
degradation of its habitat from deforestation originating from multiple
anthropogenic activities (Factor A) (BLI 2016, p. 4; IBAMA 2003 and
SEMA 2007, as cited by Laranjeiras 2011a, unpaginated; Collar 1992, p.
5). Habitat loss and degradation is likely to be intensified by
synergistic effects associated with the consequences of climate change
(Staal et al. 2015, p. 2) (Factor E). Climate projections include
increased temperatures, dryer conditions, and more extreme weather
(including droughts), which have the potential to stress trees and
cause tree mortality (Fearnside 2009, pp. 1003, 1005). These conditions
also increase the unintentional spread of fires, further contributing
to deforestation (Fearnside 2009, p. 1005). Additionally, the golden
conure is still being illegally collected and traded within Brazil, at
some unknown level, for the live pet bird trade (Factor B). These
threats and other potential stressors are discussed in detail in the
SSA Report and are summarized below.
Habitat Loss--Deforestation
Large-scale deforestation in the Amazon has occurred since the
1970s and 1980s concurrent with the growth of Brazil's economy (GFA
2017, unpaginated). The Brazilian Amazon is approximately the size of
Western Europe, and as of 2016, an area the size of France has been
lost to deforestation (Fearnside 2017a, pp. 1, 3). Approximately 30 to
35 percent of the golden conure's range has already been lost to
deforestation, primarily in the eastern states of Par[aacute] and
Maranh[atilde]o (Laranjeiras 2011a, unpaginated; Laranjeiras and Cohn-
Haft 2009, p. 8), and another 23 to 30 percent of the golden conure's
habitat is predicted to be lost within 22 years or three generations
(Bird et al. 2011 Appendix S1),
The golden conure's range partially overlaps what is known as the
``arc of deforestation,'' an area in the southeastern Amazon where
rates of deforestation and forest fragmentation have been the highest
(Prioste et al. 2012, p. 701; Laranjeiras 2011a, unpaginated;
Laranjeiras and Cohn-Haft 2009, p. 8). After a long period of
deforestation in the Amazon, rates dropped dramatically during the
years from 2005 to 2011 (Alves et al. 2017, p. 76; Fearnside 2017b, p.
1; Prodes 2017, unpaginated; Hochstetler and Viola 2012, p. 759)).
Deforestation declined from an annual average of about 21,000 km\2\
(8,108 mi\2\) per year for the 5-year period between 2000 to 2004--to
7,000 km\2\ (2,703 mi\2\) in 2009 (Petherick 2013, p. 8; Hochstetler
and Viola 2012, p. 759).
Despite these declines, the total area deforested in Brazil's
Amazon has risen steadily since deforestation rates were first measured
in 1988 (IPAM 2017, p. 7 using PRODES 2017 data). More recently,
deforestation rates are increasing again (Fearnside 2017b, p. 1; IPAM
2017, p. 15; Biderman and Nogueron 2016, unpaginated), as global demand
for agricultural commodities continues to rise (Brando et al. 2016,
abstract), and the ``arc of deforestation'' could continue to be a
hotspot (Alves et al. 2017, p. 76).
An area does not have to be mostly deforested to lose value as
suitable habitat for forest-dependent species such as the golden
conure. Deforestation itself creates isolation of remnant forest
patches and forest edge effects (Barlow et al. 2016, p. 144; Ewers and
Didham 2006, pp. 123-124). Edge effects decrease habitat quality within
remaining patches and the functional connectivity between them (Zurita
et al. 2012, p. 504, citing many sources). Additionally, disturbance
within the forest remnant, such as selective logging and increased
fires, changes forest structure and species composition, generally
reducing biodiversity (Barlow et al. 2016, p. 144).
Forest habitat degradation and fragmentation typically begin with
road construction and subsequent human settlement. Activities resulting
from human settlement include: (1) An increased network of unofficial
roads; (2) logging; (3) crop production and cattle ranching; (4)
increased fires; and (4) further infrastructure development, including
more roads, dams and hydroelectric projects, and mining (GFA 2018a, b,
c, and d, unpaginated; GFA 2017, unpaginated; Sonter et al. 2017,
entire; Barber et al. 2014, entire; BLI 2016, unpaginated; Yamashita
2003, p. 38).
Roads have a major effect on Amazon deforestation. Deforestation is
much higher near roads (including unofficial roads) and rivers (Barber
et al. 2014, entire). Nearly 95 percent of all deforestation occurred
within 5.5 km (3.4 mi) of roads or 1 km (0.6 mi) of rivers (Barber et
al. 2014, pp. 203, 205, 208). Unofficial roads are rapidly
expanding in the region and contribute to further degradation,
including logging, new colonization, forest fragmentation, and
increased fire risk (Barber et al. 2014, p. 203).
Logging in the Amazon was once restricted to areas bordering major
rivers but the construction of highways and
[[Page 45078]]
strategic access roads, coupled with the depletion of hardwood stocks
in the south of Brazil, made logging an important, growing industry
(Ver[iacute]ssimo et al. 1992, p. 170). Logging operations typically
occur on private lands claimed by ranchers, land speculators, and
squatters who sell extraction rights to logging companies (GFA 2018a
and b, unpaginated). After logging, the land may be clear-cut and
burned, in preparation for crops (Reynolds 2003, p. 10). Burning makes
nutrient-deficient land temporarily nutrient-rich, but it will only
yield crops for a few years, creating a cycle of more land clearing
(Reynolds 2003, p. 10). Revenues from timber sales are also used to
finance conversion of the land to cattle ranching (GFA 2018a,
unpaginated). Although the Brazilian forest code requires private
landowners in the Amazon to maintain 80 percent of their land as
forest, the code has been poorly enforced (GFA 2018b, unpaginated), and
full compliance has not been achieved (Azevedo et al. 2017, entire; see
Conservation Measures and Regulatory Mechanisms, below).
Logging on public lands is allowed via concessions where logging
companies are granted logging rights for a fee (GFA 2018a,
unpaginated). The concession system typically requires practices that
minimize effects to the forest (e.g., rotation of harvest, minimum-
tree-size standards, and targets for long-term sustainable yield) (GFA
2018a, unpaginated). However, the concession system is not currently
working as intended and illegal logging in public protected areas
remains a serious threat, particularly logging of mahogany (Swietenia
macrophylla) (BLI 2016, p. 5), a CITES Appendix II species (CITES
2018b). CITES Appendix II includes species that are not necessarily
threatened with extinction, but for which trade must be controlled to
avoid uses that are incompatible with their survival (CITES 2016,
unpaginated). An example of illegal logging is that which occurs in
Jamari National Forest, an area that is poorly protected and faces
pressures from loggers, squatters, and poachers (Forshaw 2017, p. 224,
F. Olmos in litt. 1999 as cited in BLI 2016, p. 5).
Also, as of 2010, Brazil had only leased a small amount of private
concession forest, and instead, had announced plans to sell large
forest tracts (GFA 2018a, unpaginated). If these lands were to become
privately owned, they would be subject to Brazil's forest code and up
to 20 percent could be legally deforested. Additionally, although
selective logging and requirements for minimum tree sizes are intended
to minimize effects to the forest, logging of larger trees is likely to
have a greater effect on the golden conure because the species uses
larger, older trees for its nesting and roosting (Yamashita 2003, p.
38).
Expanding crop production and ranching are also major drivers of
deforestation in the Amazon basin. Soy beans only grew in temperate
climates until agricultural research generated new varieties that grow
in the tropics. These innovations, coupled with the application of
fertilizer, allowed for the expansion of soy farming into the Amazon
beginning in the 1970s (GFA 2018c, unpaginated). Soy beans are
primarily used for cattle feed, and in 1990s and early 2000s, high
demand for beef created a ``soy-cattle pasture deforestation dynamic,''
where soy production replaced existing cattle pasture, and forced new
deforestation into the Amazon for cattle ranching (GFA 2018c,
unpaginated). In 2006, the soy industry, in response to pressure from
consumers, retailers, and nongovernment organizations, instituted a soy
moratorium in Brazil's Amazon. The agreement curbs forest clearing for
soy by blocking farms that violate the agreement from selling to
companies that signed the soy moratorium (Gibbs et al. 2015, p. 377).
In the 2 years preceding the moratorium, approximately 30 percent of
soy expansion occurred through deforestation rather than by replacement
of pasture or other previously cleared lands; by 2014, just 1 percent
of soy expansion was responsible for deforestation in Brazil's Amazon
(Gibbs et al. 2015, p. 377). The soy moratorium was renewed
indefinitely in 2016, or until it is no longer needed (Pati[ntilde]o
2016, unpaginated).
Cattle ranching is the largest cause of deforestation in every
Amazon country and is responsible for about 80 percent of current
deforestation rates (GFA 2018d, unpaginated). Brazil is the largest
beef exporter in the world, supplying about one quarter of the world
market (GFA 2018d, unpaginated). Brazil's Amazon supports about 200
million head of cattle on approximately 450,000 km\2\ (173,746 mi\2\)
of deforested land (GFA 2018d, unpaginated). Cattle from the Amazon are
mostly sold in the domestic markets because some of the Amazon states
have not been cleared for the presence of foot-and-mouth disease
(Fearnside 2017b, p. 14). Beginning in 1998, states in the south (non-
Amazonian) were certified as free of foot-and-mouth disease (Kaimowitz
et al. 2004, as cited by Fearnside 2017b, p. 14). The growing export
market for beef from these southern states has indirectly increased the
demand for Amazon beef for the domestic market (Fearnside 2017b, p.
14). In 2015 and 2016, new markets for Brazilian beef were opened up
via agreements with Russia, the United States, and China (Fearnside
2017b, p. 14). The Chinese market, in particular, has significant
potential demand for both beef and leather, with China being the
world's largest manufacturer of shoes (Fearnside 2017b, p. 16).
Conversion of native forest for the cultivation of palm plantations
for the production of palm oil is an emerging agricultural use in the
region that is likely to further reduce the amount of habitat available
to golden conure. Palm oil is in high demand and the industry is highly
profitable (Lees et al. 2015, p. 2). Increased palm oil production has
the potential to create thousands of new jobs and raise regional
standards of living in Brazil (Lees et al. 2015, p. 2). The Brazilian
government plans to increase biofuel production in the next decade,
driven primarily by demands for fuel (ethanol and biodiesel) (Villela
et al. 2014, p. 273). Palm oil production has been touted as a ``green
fuel'' from both a biodiversity and a climate change perspective
because degraded lands (e.g., abandoned cattle pastures and mining
areas) can be used for plantations (Lees et al. 2015, p. 2). However, a
recent study of regional avian biodiversity in palm oil plantations
concluded that they are as detrimental to avian biodiversity as other
forms of agriculture such as cattle pasture (Lees et al. 2015, entire).
Therefore, any native forest converted to palm plantations will result
in habitat loss for the golden conure, and any degraded land that is
planted for palm oil will not have the opportunity to regenerate or be
restored to suitable habitat for the species.
Increased fire risk results from human settlement and the
activities noted above (Barber et al. 2014, p. 203) (see Projected
Effects from Climate Change, below). Although use of fire for land
management is now common in rural Amazonia (Malhi et al. 2008, p. 171),
wildfires in the tropical forests of the Amazon were rare over the past
millennia, and the trees are not adapted for fire (Fearnside 2009, p.
1005). Amazonian trees have thin bark, and fire heats the cambium under
the bark at the base of the trunk, causing the tree to die (Fearnside
2009, p. 1005) and further contributing to deforestation.
Hydroelectric dams are also a major contributor to deforestation in
the Amazon. Areas affected by dams include both the area flooded by the
dam and effects from the increased
[[Page 45079]]
human settlement around the dam (GFA 2018e, unpaginated). Brazil is the
second-largest producer of hydroelectricity in the world (after China),
and hydropower supplies about 75 percent of Brazil's electricity (GFA
2018e, unpaginated; Fearnside 2017c, unpaginated). Numerous dams are
under construction or planned in the Amazon basin. For example, the
Belo Monte ``mega dam'' on the Xingu River, flooded 673 km\2\ (260
mi\2\) of lowlands and forest, and blocked 1,609 km (1,000 mi) of the
Xingu River (Fearnside 2017c, unpaginated). Recently the Brazilian
Government announced an end to the construction of mega dams in the
Amazon (Branford 2018, unpaginated), but smaller dams within the golden
conure's range are still under construction or planned (GFA 2018e,
unpaginated; Fearnside 2017c, unpaginated; Nobre et al. 2016, p.
10763).
Mining for minerals also contributes to deforestation of the
Amazon. In Brazil, mining has grown from 1.6 percent of GDP in 2000, to
4.1 percent in 2011, and is projected to increase by a factor of 3 to 5
by 2030 (Brasil Minist[eacute]rio de Minas e Energia 2010, as cited by
Ferreira et al. 2014, p. 706). In Brazil's Amazon, mining leases,
exploration permits, and concessions collectively encompass 1.65
million km\2\ (0.64 million mi\2\) of land, with about 60 percent
located in the Amazon forest (Departamento Nacional de
Produ[ccedil][atilde]o Mineral 2012, as cited in Sonter et al. p. 1).
Although mining is rapidly expanding in the region, to date, the
environmental approval process for new mines or the expansion of
existing projects does not consistently evaluate for off-lease effects
of these projects, including the indirect or cumulative impacts to the
surrounding forest (Sonter et al. 2017, p. 1). The total off-lease
effects of mining-induced deforestation can be 12 times greater than
that from the leases alone (Sonter et al. 2017, p. 2).
Deforestation Rates and Gross Domestic Product
Annual deforestation rates in the Brazilian Amazon have always
varied, but have generally been correlated with national economic
growth as measured by GDP (Petherick 2013 p.7; Hochstetler and Viola
2012, p. 759). However, beginning in 2005, measures of deforestation
and GDP have separated or ``decoupled'' (Lapola et al. 2014, p. 27;
Petherick 2013 p.7). The Amazon experienced dramatic reductions in
annual average rates of deforestation from almost 21,000 km\2\ (8,108
mi\2\) between 2000 and 2004--to about 7,000 km\2\ (2,703 mi\2\) in
2009 and 2010 (Prodes 2017, unpaginated; Petherick 2013, p. 8;
Hochstetler and Viola 2012, p. 759) and 6,418 km\2\ (2,478 mi\2\) in
2011 (Prodes 2017, unpaginated). During this same period, Brazil's GDP
rose steadily, indicating strong, sustained growth from an export
commodity boom (Petherick 2013 p.7; Hochstetler and Viola 2012, pp.
759-760).
The decoupling has been attributed to a number of factors with no
clear consensus on which factor has been the most effective (Moutinho
2015, p. 2). Contributing factors include government strategies and
policies for forest conservation (Assun[ccedil][atilde]o et al. 2012,
p. 697) such as: (1) The expansion of protected areas, which reduced
the supply of unclaimed forest land (Nepstad et al. 2014, p. 1118); (2)
an effort that began in 2007 to blacklist the worst deforesters; and
(3) efforts to monitor and control municipalities with high levels of
illegal deforestation through sanctions and restricted access to credit
(Moutinho 2015, p. 3; Assun[ccedil][atilde]o et al. 2012, p. 698).
Reductions in deforestation have also been attributed to market and
social forces, such as decreases in the price of agricultural
commodities (including soy and beef) in 2005 (Fearnside 2017b, p. 1;
Assun[ccedil][atilde]o et al. 2012, entire) and the 2006 soy moratorium
(Gibbs et al. 2015, pp. 377-378). Importantly, increased soy production
from 2006 to 2010 was due to agricultural intensification practices
(Lapola et al. 2014, p. 28) and expansion into previously cleared land
in the Amazon (Nepstad et al. 2014, p. 1121). Eventually cleared land
that is suitable for soy production will become scarce, likely
increasing deforestation pressure on the Amazon (Nepstad et al. 2014,
p. 1121). Although GDP is not presently a good predictor of Amazon
deforestation (Fearnside 2017b, p. 14), as global population and food
demands continue to rise (Beckman et al. 2017, p. i; Brando et al.
2016, abstract), it is possible that these measures could more closely
correlate in the future.
Brazil is one of the countries that currently has comparatively low
productivity levels and is projected to grow faster as it catches up
with more developed countries (Guardian 2012, unpaginated). Brazil is
expected to remain among the top ten economies as rated by GDP based on
purchasing power parity (GDP PPP) by 2050 (PWC Global 2016). GDP PPP
measures the relative purchasing power of different countries'
currencies over the same types of goods and services, allowing for more
accurate comparison of living standards (Euromonitor International
2013, unpaginated). Forecasts vary for Brazil's GDP PPP, with one
forecast predicting that GDP PPP will rise steadily through 2050 (PWC
Global 2016, unpaginated), while a more recent forecast predicts that
GDP PPP will stagnate then drop after about 2050 (Knoema 2018,
unpaginated). Therefore, if deforestation rates were to correlate more
closely with GDP PPP in the future, in one scenario deforestation rates
would steadily rise, and in the other scenario, deforestation rates
would stabilize and then decline after about 2050.
Projected Effects From Climate Change
Changes in Brazil's climate and associated changes to the landscape
are likely to result in additional habitat loss for the golden conure.
Across Brazil, temperatures are projected to increase and precipitation
to decrease (Barros and Albernaz 2014, p. 811; Carabine and Lemma 2014,
p. 11). The 2013 Intergovernmental Panel on Climate Change (IPCC)
predicted that by 2100, South America will experience temperature
increases ranging from 1.7 to 6.7 degrees Celsius ([deg]C) (3.06 to
12.06 degrees Fahrenheit ([deg]F)) under the medium and high emission
scenarios and 1.0 to 1.5 [deg]C (1.8 to 2.7[emsp14][deg]F) under a low
emissions scenario (Carabine and Lemma 2014, p. 10; Magrin et al. 2014,
p. 1502). Projected changes in precipitation in South America vary by
region, with rainfall reductions in the Amazon estimated with medium
confidence (about a 5 out of 10 chance) (IPCC 2018, unpaginated;
Carabine and Lemma 2014, p. 11; Magrin et al. 2014, p. 1502).
Downscaled models, based, in part, on the earlier (2007) IPCC data,
predict more severe changes, with the greatest warming and drying
occurring over the Amazon rainforest, particularly after 2040 (Marengo
et al. 2011, pp. 8, 15, 27, 39, 48; F[eacute]res et al. 2009, p. 2).
Estimates of temperature changes in the Amazon by the end of the 21st
century (2090-2099) are 2.2 [deg]C (4[emsp14][deg]F) under a low
greenhouse gas emission scenario and 4.5 [deg]C (8[emsp14][deg]F) under
a high-emission scenario (Marengo et al. 2011, p. 27). Increased
temperatures of these amounts put the Amazon region at a high risk of
forest loss and more frequent wildfires (Magrin et al. 2007, p. 596).
Some leading global circulation models indicate that extreme weather
events, such as droughts, will increase in frequency or severity due to
global warming. As a result, droughts in Amazonian forests could become
more frequent in the future (Marengo et al. 2011, p. 48). For example,
the 2005 drought in Amazonia was a 1-in-20-year
[[Page 45080]]
event; however, those conditions may become a 1-in-2-year event by
2025, and a 9-in-10-year event by 2060 (Marengo et al. 2011, p. 28).
Deforestation is greater under drought conditions due to more risk of
fires (Marengo et al. 2011, p. 16).
A number of large-scale drivers of environmental change (i.e.,
land-use change from deforestation and climate changes due to global
warming) are operating simultaneously and interacting nonlinearly in
the Amazon (Nobre et al. 2016, p. 10759). Thus, the risks to golden
conure from deforestation will likely be intensified by synergistic
effects associated with climate change (Staal et al. 2015, p. 2). The
Amazon's rainforest may have two ``tipping points'': (1) A temperature
increase of 4.0 [deg]C (7.2 14;[deg]F); or (2) deforestation exceeding
40 percent (Nobre et al. 2016, p. 10759). Once exceeded, these tipping
points could cause large-scale shifts in the vegetation to a savanna
(i.e., ``savannization'') mostly in the southern and eastern Amazon
(Nobre et al. 2016, p. 10759) within the golden conure's range.
Similarly, a recent study that considered only the effects from
global warming (i.e., absent deforestation) predicted that by the end
of this century, some areas of rainforest will be replaced by deciduous
forest and grassland in a moderate emissions scenario (RCP 4.5) and by
all grassland in the high emissions scenario (RCP 8.5) (Lyra et al.
2016, entire). Although the projected outcomes of models are not
definitive, any terra firme forest habitat that shifts from rainforest
to other habitat types (e.g., savanna) would result in loss of habitat
for the golden conure.
Illegal Collection and Trade
The golden conure is highly prized as an aviary bird and has been
extensively trapped for both the domestic and international pet trade
in the past (BLI 2016, p. 5; Alves et al. 2013, p. 60; Laranjeiras
2011a, unpaginated; Yamashita 2003, p. 38; Snyder et al. 2000, p. 132;
Collar 1992, p. 304; Oren and Novaes 1986, pp. 329, 334-335). The
international trade of wild neotropical parrots was significantly
reduced during the 1990s due to (1) tighter enforcement of CITES
regulations, (2) stricter measures under European Union legislation,
(3) adoption of the Wild Bird Conservation Act (WBCA; 16 U.S.C. 4901 et
seq.) in the United States, and (4) adoption of national legislation in
various other countries (Snyder et al. 2000, p. 99). Although an
illegal international trade of the golden conure for the pet trade
occurred in the past, there is little evidence that this practice is
continuing (Laranjeiras 2011a, unpaginated; Silveira and Belmonte 2005
in press, unpaginated). In contrast, the illegal domestic market for
the species is still occurring at some level (Silveira and Belmonte in
press, unpaginated).
Historically, keeping birds was an important part of local
indigenous tradition and culture (Carvalho 1951 and Cascudo 1973, as
cited by Alves et al. 2013, p. 54). Young golden conures were taken
from the wild to raise as pets and for feathers, but now they are also
sold to bird traders (Oren and Novaes 1986, p. 335). Much of the area
occupied by the golden conure is poor, and selling the birds for the
domestic pet trade provides an extra source of income (Yamashita 2003,
p. 39).
There are mixed reports regarding the degree to which illegal
capture of golden conures from the wild (``poaching'') is still
occurring. The Brazilian Institute of Environment and Renewable Natural
Resources (IBAMA) has licensed and regulated bird breeding in an effort
to reduce poaching (Alves et al. 2013, p. 61). As a result, several
sources believe poaching is no longer a major concern for the species
because trade is thought to mostly be from the substantial captive
population, and thus does not significantly affect the wild population
(Silveira in litt. 2012, Lees in litt. 2013, in BLI 2016, p. 5).
Additional captive populations exist outside Brazil. There are CITES-
registered captive-breeding operations for golden conures in the United
Kingdom and the Philippines.
However, some level of illegal capture and trade of the species is
still occurring. For example, in 2016, approximately 57 golden conures
were seized in Brazil (IBAMA 2017 as cited by Lima in litt. 2018). We
have no seizure data from any other years, and this number may
represent a year where seizures were high, but it demonstrates that
domestic trafficking is occurring (Lima in litt. 2018). Captive rearing
may not be a practical alternative to illegal trade, particularly in
low-income areas because the price of commercially bred birds is
approximately 10 times higher than wild-caught individuals (Renctas
2001, as cited in Alves et al. 2013, p. 61; Machado 2002, as cited in
Alves et al. 2010, p. 155).
Additionally, oversight of domestic wildlife-breeding facilities in
Brazil is limited (Alves et al. 2010, entire), and many wild bird
species declared to be captive-bred are actually born in the wild and
traded under fraudulent documentation (Alves et al. 2013, p. 61).
Although each Brazilian state has a wildlife center responsible for
managing, licensing, and inspecting all categories of breeders,
traders, and zoos (Kuhnen and Kanaan 2014, p. 125), most centers lack
resources and funding (Padrone 2004, as cited in Kuhnen and Kanaan
2014, p. 125). Also, there are not enough inspections at market places
and commercial breeding facilities to fight illegal domestic trade
(Alves et al. 2010, pp. 154-155).
The United States is a major importer of pet birds, yet relatively
little trade in the golden conure has been observed. We reviewed all
records of legal and intercepted illegal trade in the CITES annual
trade records submitted by the U.S. Fish and Wildlife Service from 1981
to 2016. During this 35-year period, 54 live golden conures were
imported into the United States and 26 were exported (UNEP-WCMC 2018,
unpaginated). One record of illegal trade was reported in 1981, and
involved the unlawful importation of a single animal from Brazil.
Overall, the U.S. trade in the golden conure has been relatively low
compared with other pet birds.
Other Potential Stressors
Other potential stressors to the golden conure include hunting and
persecution (Factor B), and predation or disease (Factor C). The
species is likely still hunted at low levels as a food source, and for
feathers, and birds that raid crops may be shot by farmers (Oren and
Novaes 1986, p. 335). However, we have no information about the rate
that these activities may be occurring or the extent to which they may
be affecting populations. Similarly, we have no information regarding
diseases that may affect golden conures in the wild.
Golden conures, including eggs and nestlings, are prey to a variety
of native predators, including toucans (Oren and Novaes 1986, p. 334;
Forshaw 2017, p. 228), raptors (Laranjeiras 2008a, as cited in
Laranjeiras 2011a, unpaginated; Silveira and Belmonte in press,
unpaginated), monkeys, snakes, and the tayra (Eira barbara), an
omnivorous weasel (Oren and Novaes 1986, p. 334). However, we have no
information regarding the rates predation on the golden conure from
these predators and how that may be affecting the conure.
Conservation Measures and Regulatory Mechanisms
The golden conure is considered ``Vulnerable'' at the national
level in Brazil (MMA 2014, p. 122). Like other wildlife species,
conures and their nests, shelters, and breeding grounds are protected
by Brazilian environmental laws (Clayton 2011, p. 4; Environmental
Crimes law of Brazil (1999) as cited in
[[Page 45081]]
MSU 2018, unpaginated; Official List of Brazilian Endangered Animal
Species Order No. 1.522/1989 as cited in ECOLEX 2018; CFRB 2010, p.
150; Law No. 5.197/1967 as cited in LatinLawyer 2018, unpaginated).
Additionally, several Brazilian laws are designed to protect forests.
Destruction and damage of forest reserves, cutting trees in forest
reserves, and causing fire in forests, among other actions, without
authorization are prohibited (Clayton 2011, p. 5; Law No. 9.605/1998 as
cited in LatinLawyer 2018, unpaginated).
Protected areas have been emphasized as the best hope for the
golden conure's survival (e.g., in the Tapajos River region and the
Gurupi Biological Preserve) (Laranjeiras and Cohn-Haft 2009, pp. 1, 8;
Silveira and Belmonte in press, unpaginated). The species occurs in
nine areas recently designated as Important Bird Areas (IBAs) in Brazil
(BLI 2018a-h, unpaginated; Lima et al. 2014, p. 318; Laranjeiras 2011a,
unpaginated; Devenish et al. 2009, pp. 104-106). IBAs are places of
international significance for the conservation of birds and other
biodiversity (BLI 2018i, unpaginated). Levels of protection at IBAs
vary from fully protected to no protections (BLI 2018i, unpaginated).
For example, the Gurupi IBA has partial protection while the
Caxiuan[atilde]/Portel IBA has none (Service 2018, pp. 68-70; BLI
2018b, unpaginated; Devenish et al. 2009, pp. 104-106). Additionally,
the species' predicted range overlaps with numerous other protected
areas, also having various levels of protection (Service 2018, pp. 68-
70; Laranjeiras and Cohn-Haft 2009, p. 8).
Various regulatory mechanisms (Law No. 11.516, Act No. 7.735, and
Decree No. 78, as cited in ECOLEX 2018, unpaginated) and Law 6.938/1981
(LatinLawyer 2018, unpaginated) direct Brazil's federal and state
agencies to promote the protection of lands and govern the formal
establishment and management of protected areas to promote conservation
of the country's natural resources. These mechanisms generally aim to
protect imperiled wildlife and plant species, genetic resources,
overall biodiversity, and native ecosystems on federal, state, and
privately owned lands (e.g., Law No. 9.985, Law No. 11.132, Resolution
No. 4, and Decree No. 1.922, as cited in ECOLEX 2018, unpaginated).
Protected Areas: Protected areas have traditionally formed the
backbone of forest conservation in the Amazon Basin, and they still
remain a vital conservation strategy (GFA 2018f, unpaginated). Brazil
has the largest protected area network in the world. The National
Protected Areas System (Federal Act 9.985/2000, as cited in LatinLawyer
2018, unpaginated) was established in 2000, and covers nearly 2.2
million km\2\ (0.8 million mi\2\) or 12.4 percent of the global total
(WDPA, 2012 as cited by Ferreira et al. 2014, p. 706). This extensive
network of protected areas is intended to (1) preserve priority
biodiversity conservation areas, (2) establish biodiversity corridors,
and (3) protect portions of the 23 Amazonian ecoregions identified by
World Wildlife Fund (Rylands and Brandon 2005, pp. 612, 615; Silva,
2005, entire). Brazil's Protected Areas may be categorized as
``strictly protected'' or ``sustainable use'' based on their overall
management objectives. Strictly protected areas include national parks,
biological reserves, ecological stations, natural monuments, and
wildlife refuges protected for educational and recreational purposes
and scientific research. Protected areas of sustainable use (national
forests, environmental protection areas, areas of relevant ecological
interest, extractive reserves, fauna reserves, sustainable development
reserves, and private natural heritage reserves) allow for different
types and levels of human use with conservation of biodiversity as a
secondary objective.
By 2006, 1.8 million km\2\ (0.7 million mi\2\), or approximately 45
percent of Brazil's Amazonian tropical forest, was under some level of
protection as federal or state managed land, or designated as
indigenous reserve (managed by indigenous communities) (Barber et al.
2014, p. 204). Of this, 19.2 percent was strictly protected areas, and
30.6 percent was comprised of federal and state sustainable use area,
with indigenous reserves making up the remainder (Barber et al. 2014,
p. 204).
Indigenous lands are legally recognized areas where indigenous
peoples have perpetual rights of access, use, withdrawal, management,
and exclusion over the land and associated resources (GFW 2018,
unpaginated). Indigenous communities sustainably use their forest land,
and large-scale deforestation is prohibited (Barber et al. 2014, p.
204). Indigenous communities practice shifting cultivation, trade non-
timber forest products, and occasionally allow selective logging (GFA
2018g, unpaginated; Schwartzman and Zimmerman 2005, p. 721).
To date, the golden conure has been found in numerous protected
areas or IBAs, with a total area of approximately 154,673 km\2\ (51,719
mi\2\) (Service 2018, pp 68-70). However, not all of the area
represented contains suitable habitat for the species and several of
the IBAs (39 percent) presently have no protection (61,864 km\2\
(23,866 mi\2\). An additional 26 percent of IBAs presently have just
partial protection (40,582 km\2\ (15,669 mi\2\) (Service 2018, pp 68-
70).
Despite significant efforts to designate and establish protected
areas, funding and resources are limited and adequate enforcement of
these areas is challenging. For example, the conure occurs in Jamari
National Forest, which is poorly protected and faces pressures from
loggers, squatters, and poachers (Forshaw 2017, p. 224, F. Olmos in
litt. 1999 as cited in BLI 2016, p. 5).
Forest Code: Brazil's forest code was created in 1965, and was
subsequently changed in the 1990s via a series of presidential decrees
(Soares-Filho et al. 2014, p. 363). As of 2001, the forest code
required landowners in the Amazon to conserve native vegetation on
their rural properties by setting aside what is called a ``legal
reserve'' of 80 percent of their property (i.e., with 20 percent
available to be harvested) (Soares-Filho et al. 2014, p. 363). The
forest code severely restricted deforestation on private properties but
proved challenging to enforce, and full compliance has not been
achieved (GFA 2018b, unpaginated; Azevedo et al. 2017, entire; Soares-
Filho et al. 2014, p. 363). For instance, the lack of registered
property boundaries made it difficult to link deforestation to
particular land owners, and the majority of deforestation from 2002 to
2009 (about 69 percent) occurred on properties whose boundaries were
not publicly registered (Azevedo et al. 2017, p. 7653).
In late 2012, a new forest code was approved that reduces
restoration requirements by providing amnesty for previous illegal
deforestation by smaller property holders (Soares-Filho et al. 2014, p.
363). Under the older forest code, legal reserves that were illegally
deforested were required to be restored at the landowner's expense. The
new forest code forgives the legal reserve debt of small properties (up
to 440 hectares (1,087 acres)) (Soares-Filho et al. 2014, p. 363).
Although the 2012 forest code reduced the restoration requirements, it
also introduced measures that strengthen conservation including
addressing (1) fire management, (2) forest carbon, and (3) payments for
ecosystem services (Soares-Filho et al. 2014, p. 363).
Additionally, the new forest code created an Environmental Reserve
Quota where quota surplus on one property may be used to offset a legal
reserve debt on another property within the same biome; this could
create a market for forested lands, adding monetary value to native
vegetation and
[[Page 45082]]
potentially abating up to 56 percent of legal reserve debt (Soares-
Filho et al. 2014, p. 363). Proponents of the new forest code believe
that it will act as an effective barrier to agricultural development,
while others believe that amnesty will lead to the perception that
illegal deforesters are unlikely to be prosecuted or could be forgiven
in future land reforms (Soares-Filho et al. 2014, pp. 363-364).
Legal Captive Rearing and Trade: IBAMA has licensed and regulated
breeding of native bird species, including golden conure, in an effort
to reduce poaching (Alves et al. 2013, p. 61). The captive population
of golden conures in Brazil is believed to be about 600 birds (Prioste
et al. 2013, p. 146), and one breeder reported that in 8 years she
reared nearly 600 birds (Weinzettl, in litt. 2015). Therefore, there is
reason to believe that the captive population of golden conures in
Brazil is at least 600 birds or larger. Additional captive populations
of golden conures exist as CITES-registered captive-breeding operations
in the United Kingdom and the Philippines. Although we have no further
information on these programs, the captive rearing of golden conures in
Brazil is believed to have reduced the incidence of poaching of young
golden conures from the wild (Silveira in litt. 2012, Lees in litt.
2013, as cited in BLI 2016, p. 5).
Reintroduction: Captive rearing and reintroduction efforts have
contributed to the recovery of other parrots in Central and South
America but we know of only one attempt to reintroduce the golden
conure to an area where it had been extirpated. The species was
extirpated from the Bel[eacute]m region of Par[aacute] in 1848 (Moura
et al. 2014, p. 5). In 2017, researchers reintroduced the golden conure
to this area (at Utinga State Park in Bel[eacute]m) (globo.com 2018,
unpaginated). The project includes a post-release monitoring component
(Moura in litt. 2018), but it is too soon to know whether or not the
reintroduction has been successful.
Additional Regulatory Mechanisms: ``Reducing Emissions from
Deforestation and Forest Degradation'' (REDD) is a ``payment for
ecological services'' initiative that creates a financial value for the
carbon stored in forests (GFA 2018h, unpaginated). The program offers
incentives to developing countries to reduce emissions from forested
lands and invest in low-carbon paths to sustainable development (GFA
2018h, unpaginated). REDD plus (REDD+) goes one step further by
including objectives for (1) biodiversity conservation, (2) sustainable
management of forests, and (3) improvements to forest governance and
local livelihoods (GFA 2018h, unpaginated). Brazil is one of the most
advanced countries in the world in REDD+ planning and maintains an
``Amazon Fund,'' which receives compensation for reductions in
deforestation. To date, the Norwegian government is the major donor and
lesser donors include the government of Germany and the Brazilian oil
company Petrobras (GFA 2018h, unpaginated). The successful funding and
implementation of REDD+ is expected to reduce rates of deforestation in
Brazil's Amazon rainforest and would likely benefit the golden conure
and its habitat. However, the initiative is in its early stages and is
being hampered by numerous issues, particularly unresolved land-tenure
problems (May et al. 2018, p. 44).
The golden conure is protected under CITES, an international
agreement between member governments to ensure that the international
trade of CITES-listed plant and animal species is legal and does not
threaten species' survival. Under this treaty, CITES Parties (member
countries or signatories) regulate the import, export, and re-export of
specimens, parts, and products of CITES-listed plant and animal
species. Brazil is a Party to CITES. Trade in CITES-listed plants and
animals must be authorized through a licensing system of permits and
certificates that are provided by the designated CITES Management
Authority of each CITES Party. CITES includes three Appendices that
list species meeting specific criteria. Depending on the Appendix in
which they are listed, species are subject to various permitting
requirements.
The golden conure is listed in CITES Appendix I and receives the
highest degree of protection. Species listed in this Appendix are those
that are threatened with extinction and which are, or may be, affected
by trade. Commercial trade in Appendix I wildlife species is strictly
prohibited, except in limited circumstances provided by the treaty.
However, commercial international trade may be allowed in certain
circumstances where animals have been produced by CITES-registered
captive-breeding operations. Trade in specimens from registered
operations may be treated as if they were listed in CITES Appendix II,
although they remain Appendix I listed specimens. Each shipment
requires the issuance of both CITES export and import documents. There
are two CITES-registered captive-breeding operations for the golden
conure: one in the United Kingdom and the other in the Philippines. The
United States may also allow non-commercial trade in this species on a
case-by-case basis for approved purposes such as scientific,
zoological, and educational activities.
Two other laws in the United States apart from the Act provide
protection from the illegal import of wild-caught birds into the United
States: the Wild Bird Conservation Act (WBCA) and the Lacey Act (18
U.S.C. 42; 16 U.S.C. 3371 et seq.). The WBCA was enacted in 1992, to
ensure that exotic bird species are not harmed by international trade
and to encourage wild bird conservation programs in countries of
origin. Under the WBCA and our implementing regulations (50 CFR 15.11),
it is unlawful to import into the United States any exotic bird species
listed under CITES except under certain circumstances. We may issue
permits to allow import of listed birds for scientific research,
zoological breeding or display, cooperative breeding, or personal pet
purposes when the applicant meets certain criteria (50 CFR 15.22-
15.25).
The Lacey Act was originally passed in 1900, and was the first
Federal law protecting wildlife. Today, it provides civil and criminal
penalties for the illegal trade of animals and plants. Under the Lacey
Act, in part, it is unlawful to (1) import, export, transport, sell,
receive, acquire, or purchase any fish, or wildlife taken, possessed,
transported, or sold in violation of any law, treaty, or regulation of
the United States or in violation of any Indian tribal law; or (2)
import, export, transport, sell, receive, acquire, or purchase in
interstate or foreign commerce any fish or wildlife taken, possessed,
transported, or sold in violation of any law or regulation of any State
or in violation of any foreign law. Therefore, for example, because the
take of wild-caught golden conures would be in violation of Brazil's
wildlife law, the subsequent import of the species would be in
violation of the Lacey Act. Similarly, under the Lacey Act, it is
unlawful to import, export, transport, sell, receive, acquire, or
purchase specimens of these species traded contrary to CITES.
Summary of Biological Status and Threats
The best scientific and commercial information available indicates
that the golden conure is more widespread and abundant than believed at
the time of listing as endangered (BLI 2017, unpaginated; Bird et al.
2011, Appendix S1; Laranjeiras 2011b, p. 311; Laranjeiras and Cohn-Haft
2009, pp. 1, 3) and that the threat from poaching for the pet trade
(Factor B) has diminished (Silveira in litt. 2012, Lees in litt. 2013,
[[Page 45083]]
in BLI 2016, p. 5; Snyder et al. 2000, p. 99) but is still occurring at
some unknown level. The global population is estimated at 10,875
individuals within 174,000 km\2\ (67,182 mi\2\) of suitable habitat
across a range of approximately 340,000 km\2\ (131,275 mi\2\)
(Laranjeiras 2011b, p. 311; Laranjeiras and Cohn-Haft 2009, pp. 1, 3).
Nevertheless, the population is regarded as small, and is believed to
declining (BLI 2016, p. 1) primarily due to loss and degradation of its
habitat from deforestation (Factor A) (BLI 2016, p. 4; IBAMA 2003 and
SEMA 2007, as cited by Laranjeiras 2011a, unpaginated; Collar 1992, p.
5).
Although rates of deforestation have declined in recent decades,
they are increasing again (Alves et al. 2017, p. 76; Fearnside 2017b,
p. 1; IPAM 2017, p. 15;Prodes 2017, unpaginated; Biderman and Nogueron
2016, unpaginated) and are projected to continue to increase (Bird et
al. 2011, entire; Soares-Filho et al. 2006, p. 520) as the global
demand for agricultural commodities continues to rise (Brando et al.
2016, abstract). Risks from deforestation will likely be intensified by
synergistic effects associated with climate change (Staal et al. 2015,
p. 2) (Factor E). Climate projections include increased temperatures,
dryer conditions, and more frequent extreme weather (including
droughts), which have the potential to stress trees and cause tree
mortality (Fearnside 2009, pp. 1003, 1005). These conditions also
increase the unintentional spread of fires, further contributing to
deforestation (Fearnside 2009, p. 1005). Deforestation itself can cause
regional shifts in the climate and is likely to operate together with
the effects of climate change to negatively alter rainforest habitat.
Although there are uncertainties in the various models, and projected
outcomes are not definitive, any terra firme forest habitat that shifts
from rainforest to other habitat types (e.g., savanna) would no longer
be available to the golden conure.
Although an illegal international trade of the golden conure
occurred in the past, there is little evidence that this practice is
continuing (Laranjeiras 2011a, unpaginated; Silveira and Belmonte 2005
in press, unpaginated). In contrast, the golden conure continues to
face an unknown level of pressure from poaching and illegal trade
within Brazil (Factor B) (Silveira and Belmonte in press, unpaginated),
particularly in poorer areas (Silveira and Belmonte in press,
unpaginated; Alves et al. 2013, p. 61). Captive golden conure breeding
programs in Brazil have helped to limit poaching of wild golden conures
(Silveira in litt. 2012, Lees in litt. 2013, in BLI 2016, p. 5).
However, poaching of young conures for the illicit domestic pet trade
in Brazil has the potential to negatively affect golden conure
populations, especially if individuals are being collected from small
or fragmented populations. Population-level effects could operate
synergistically with effects from habitat loss or degradation to the
further detriment of the species.
Although existing conservation efforts and regulatory mechanisms
appear to be substantial (e.g., Brazil has the largest protected area
network in the world), at this time they do not adequately ameliorate
threats to the golden conure (Factor D). Despite significant efforts to
preserve the rainforest in Brazil's Amazon basin, enforcement has
proven to be challenging, and full compliance has not been achieved.
Habitat loss due to deforestation is ongoing and is predicted to
continue, resulting in global population declines of the golden conure
(BLI 2016, p. 1; Bird et al. 2011 Appendix S1).
Proposed Determination of Species Status
Section 4 of the Act (16 U.S.C. 1533), and its implementing
regulations at 50 CFR part 424, set forth the procedures for
determining whether a species is an endangered species or threatened
species and should be included on the Federal Lists of Endangered and
Threatened Wildlife and Plants (listed). The Act defines an endangered
species as any species that is ``in danger of extinction throughout all
or a significant portion of its range'' and a threatened species as any
species ``that is likely to become endangered throughout all or a
significant portion of its range within the foreseeable future.'' Under
section 4(a)(1) of the Act, we determine whether a species is an
endangered species or threatened species because of any one or a
combination of the following: (A) The present or threatened
destruction, modification, or curtailment of its habitat or range; (B)
overutilization for commercial, recreational, scientific, or
educational purposes; (C) disease or predation; (D) the inadequacy of
existing regulatory mechanisms; or (E) other natural or manmade factors
affecting its continued existence.
Determination of Status Throughout All of Its Range
As required by section 4(a)(1) of the Act, we conducted a review of
the status of the golden conure and assessed the five factors to
evaluate whether the species is endangered or threatened throughout all
of its range. We examined the best scientific and commercial
information available regarding the past, present, and future threats
faced by the golden conure. We reviewed information presented in the
2014 petition, information available in our files, information gathered
through our 90-day finding in response to the petition, information
gathered in our status review, and other available published and
unpublished information.
In considering what factors may constitute threats, we must look
beyond the mere exposure of the species to the factor to determine
whether the species responds to the factor in a way that causes actual
impacts to the species. If there is exposure to the factor, but no
response, or only a positive response, that factor is not a threat. If
there is exposure and the species responds negatively, the factor may
be a threat and we then attempt to determine if it may drive or
contribute to the risk of extinction of the species such that the
species warrants listing as an endangered or threatened species as
those terms are defined by the Act.
When we listed the golden conure as endangered in 1976, the species
was perceived to be declining in numbers due to either Factor A, Factor
B, or Factor D, or a combination of all three factors (41 FR 24062;
June 14, 1976). At present, the best scientific and commercial
information available on the range and abundance of the species
indicates that the species is more widespread and abundant than
previously believed and that the threat from overutilization for the
pet trade (Factor B) has diminished (Silveira in litt. 2012, Lees in
litt. 2013, in BLI 2016, p. 5; Snyder et al. 2000, p. 99). Habitat
modeling studies have estimated that there are approximately 10,875
individuals within 174,000 km\2\ (67,182 mi\2\) of suitable habitat
across a range of approximately 340,000 km\2\ (131,275 mi\2\)
(Laranjeiras 2011b, p. 311; Laranjeiras and Cohn-Haft 2009, pp. 1, 3).
Tighter enforcement of CITES, stricter European Union legislation,
adoption of the WBCA in the United States, and adoption of national
legislation in other countries have all helped to significantly curtail
illegal international trade (Snyder et al. 2000, p. 99). In addition,
government-authorized captive breeding programs in Brazil are thought
to have curtailed the illegal domestic trade (Silveira in litt. 2012,
Lees in litt. 2013, in BLI 2016, p. 5). Thus, after assessing the best
available information and as a result of the aforementioned
information, we conclude the golden conure is not
[[Page 45084]]
currently in danger of extinction throughout its range.
As described below, we next considered whether the golden conure is
likely to become in danger of extinction throughout its range within
the foreseeable future. The term ``foreseeable future'' describes the
extent to which we can reasonably rely on predictions about the future
in making determinations about the future conservation status of the
species. The golden conure has already lost 30 to 35 of its historical
range (Laranjeiras 2011a, unpaginated; Laranjeiras and Cohn-Haft 2009,
p. 8). We expect both the species' global population and its habitat to
decline an additional 23 to 30 percent in 22 years (Service 2018, pp.
42-46; Bird et al. 2011 Appendix S1). Additionally, habitat loss and
degradation is likely to be intensified by synergistic effects
associated with the consequences of climate change (Service 2018, pp.
42-46; Staal et al. 2015, p. 2). There is a strong likelihood of
warming to at least 1.5 to 2.0 [deg]C (3.6[emsp14][deg]F) in Latin
America by the end of the Century (Carabine and Lemma 2014, p. 8), and
downscaled estimates for the Amazon over the same time period (i.e., by
the end of the Century) indicate temperature increases of 2.2 [deg]C
(4[emsp14][deg]F) under a low greenhouse gas emission scenario and 4.5
[deg]C (8[emsp14][deg]F) under a high-emission scenario (Marengo et al.
2011, p. 27). Increased temperatures of these amounts put the Amazon
region at a high risk of forest loss and more frequent wildfires
(Magrin et al. 2007, p. 596). Downscaled models, based, in part, on the
earlier (2007) IPCC data, predict severe changes (increased warming and
drying) over the Amazon rainforest, particularly after 2040 (Marengo et
al. 2011, pp. 8, 15, 27, 39, 48; F[eacute]res et al. 2009, p. 2).
Additionally, some leading global-circulation models indicate that
extreme weather events, such as droughts, will increase in frequency,
with drought becoming a 9-in-10-year event, by 2060 (Marengo et al.
2011, p. 28) further contributing to deforestation due to more risk
from fires (Marengo et al. 2011, p. 16). Therefore, based on the best
available data, we assessed foreseeable future to be 22 to 42 years (or
approximately three to six generations of the golden conure). We based
the lower end of this range (22 years) on the peer-reviewed work by
Bird et al. 2011, relating to deforestation and declines in the
population. We based the upper end of this range (42 years) on peer-
reviewed studies predicting effects from climate change (such as
drought) on deforestation after about 2040 to 2060 (Marengo et al.
2011, pp. 8, 15, 27, 28, 39, 48; F[eacute]res et al. 2009, p. 2). We
conclude that it is reasonable to rely on the predictions made in these
peer-reviewed studies in making determinations about the future
conservation status of the golden conure.
Although the golden conure is now known to be more widespread and
abundant than previously thought, the species remains relatively rare.
It occurs only within the southern basin of Brazil's Amazon, and much
of this area is in the ``arc of deforestation'' and is threatened by
loss and degradation of its rainforest habitat from deforestation.
Effects from deforestation are exacerbated by the projected effects
from climate change. Additionally, even though government-authorized
captive breeding programs in Brazil are thought to have curtailed the
illegal domestic trade, some unknown level of illegal collection and
trade is ongoing, particularly within Brazil (Silveira and Belmonte in
press, unpaginated).
Existing regulatory mechanisms and conservation efforts do not
currently adequately ameliorate threats to the golden conure (Factor
D). The factors identified above continue to affect the golden conure
such that it is likely to become in danger of extinction within the
foreseeable future throughout all of its range. Based on the best
available scientific studies and information assessing land-use trends,
lack of enforcement of laws, predicted landscape changes under climate-
change scenarios, and predictions about how those threats may impact
the golden conure, we conclude that the species is likely to be in
danger of extinction in the foreseeable future throughout all of its
range. Accordingly, we find that the golden conure meets the definition
of a ``threatened species'' under the Act, and we are proposing to list
the golden conure as threatened throughout its range.
Significant Portion of Its Range
Under the Act and our implementing regulations, a species warrants
listing if it is endangered or threatened. The Act defines ``endangered
species'' as any species that is in danger of extinction throughout all
or a significant portion of its range (16 U.S.C. 1532(6)), and
``threatened species'' as any species that is likely to become an
endangered species within the foreseeable future throughout all or a
significant portion of its range (16 U.S.C. 1532(20)). Because we have
determined that the golden conure is threatened throughout all of its
range, under the Final Policy on Interpretation of the Phrase
``Significant Portion of Its Range'' in the Endangered Species Act's
Definitions of ``Endangered Species and ``Threatened Species'' (79 FR
37578; July 1, 2014) (SPR Policy), if a species warrants listing
throughout all of its range, no portion of the species' range can be a
``significant'' portion of its range.
Proposed 4(d) Rule
When a species is listed as endangered, certain actions are
prohibited under section 9 of the Act and our regulations at 50 CFR
17.21. These include, among others, prohibitions on take within the
United States, within the territorial seas of the United States, or
upon the high seas; import; export; and shipment in interstate or
foreign commerce in the course of a commercial activity. Exceptions to
the prohibitions for endangered species may be granted in accordance
with section 10 of the Act and our regulations at 50 CFR 17.22.
The Act does not specify particular prohibitions and exceptions to
those prohibitions for threatened species. Instead, under section 4(d)
of the Act, the Secretary of the Interior, as well as the Secretary of
Commerce depending on the species, was given the discretion to issue
such regulations as deemed necessary and advisable to provide for the
conservation of such species. The Secretary also has the discretion to
prohibit by regulation with respect to any threatened species any act
prohibited under section 9(a)(1) of the Act. For the golden conure, the
Service is exercising our discretion to propose a rule under section
4(d) of the Act. If this proposed rule is adopted, we will incorporate
all prohibitions and provisions of 50 CFR 17.31 and 17.32, except that
import and export of certain golden conures into and from the United
States and certain acts in interstate commerce will be allowed without
a permit under the Act, as explained below.
Import and Export
The proposed 4(d) rule imposes a prohibition on imports and exports
(by incorporating 50 CFR 17.31), but creates exceptions for certain
golden conures. Shipments of captive specimens (i.e., not taken from
the wild) may include live and dead golden conures and parts and
products, including the import and export of personal pets and research
samples. The proposed 4(d) rule would adopt the existing conservation
regulatory requirements of CITES and the WBCA as the appropriate
regulatory provisions for the import and export of these golden conure
specimens.
This 4(d) rule proposes to allow a person to import or export, into
and
[[Page 45085]]
from the United States, captive specimens, without a permit issued
under the Act, provided that the export is authorized under CITES and
the import is authorized under CITES and the WBCA. The import would
require a CITES document issued by the foreign Management Authority
indicating a source code of ``C'', ``D'', or ``F.'' Exporters of
captive birds would need to provide a signed and dated statement from
the breeder of the bird, along with documentation that identifies the
source of their breeding stock in order to obtain a CITES export permit
from the U.S. Fish and Wildlife Service's Division of Management
Authority. Exporters of captive-bred birds must provide a signed and
dated statement from the breeder of the bird confirming its captive-
bred status, and documentation on the source of the breeder's breeding
stock. The source codes of C, D, and F for CITES permits and
certificates are as follows:
Source Code C: Animals bred in captivity in accordance
with Resolution Conf. 10.16 (Rev.), as well as parts and derivatives
thereof, exported under the provisions of Article VII, paragraph 5 of
the Convention.
Source Code D: Appendix I animals bred in captivity for
commercial purposes in operations included in the Secretariat's
Register, in accordance with Resolution Conf. 12.10 (Rev. CoP15), and
Appendix I plants artificially propagated for commercial purposes, as
well as parts and derivatives thereof, exported under the provisions of
Article VII, paragraph 4, of the Convention.
Source Code F: Animals born in captivity (F1 or subsequent
generations) that do not fulfill the definition of ``bred in
captivity'' in Resolution Conf. 10.16 (Rev.), as well as parts and
derivatives thereof.
The proposed 4(d) rule would not allow any U.S. import or export of
golden conures that are taken from the wild; such birds must continue
to meet the requirements of 50 CFR 17.31 and 17.32, including obtaining
a permit under the Act, with the following exception. This 4(d) rule
proposes to allow a person to import or export a wild golden conure
specimen if the specimen was held in captivity prior to the date the
species was listed in CITES Appendix I (i.e., prior to the date that
CITES entered into force on July 1, 1975, with ``golden parakeet''
(i.e., the golden conure) listed in Appendix I) and provided that it
meets all the requirements of CITES and WBCA. If a specimen was taken
from the wild and held in captivity prior to that date (July 1, 1975),
the exporter would need to provide documentation as part of the
application for a U.S. CITES preconvention certificate. Examples of
documentation may include: (1) A copy of the original CITES permit
indicating when the bird was removed from the wild, (2) veterinary
records, or (3) museum specimen reports. Additionally, consistent with
the 4(d) regulations for other species in the parrot family at 50 CFR
17.41 (c), the prohibitions on take would apply and the 4(d) rule would
require a permit under the Act for any activity that could take a
golden conure. Our regulations at 50 CFR 17.3 establish that take, when
applied to captive wildlife, does not include generally accepted animal
husbandry practices, breeding procedures, or provisions of veterinary
care for confining, tranquilizing, or anesthetizing, when such
practices are not likely to result in injury to the wildlife.
We assessed the conservation needs of the golden conure in light of
the broad protections provided to the species under CITES and the WBCA.
As noted above in Summary of Factors Affecting the Species, some level
of poaching for illegal trade of golden conures is occurring within
Brazil (Silveira and Belmonte in press, unpaginated) but there is
little evidence that this practice occurs at the international level
(Laranjeiras 2011a, unpaginated; Silveira and Belmonte 2005 in press,
unpaginated). The best available commercial data indicate that tighter
enforcement of CITES, stricter European Union legislation, adoption of
the WBCA in the United States, and adoption of national legislation in
other countries have all helped to significantly curtail illegal
international trade (Snyder et al. 2000, p. 99). Therefore, illegal
international trade is not likely to be occurring at levels that
negatively affect the golden conure population. Additionally, legal
international trade of the species is not currently occurring at levels
that affect the golden conure population. Therefore, we find that the
import and export requirements of the proposed 4(d) rule provide the
necessary and advisable conservation measures that are needed for this
species. This proposed 4(d) rule, if made final, would streamline the
permitting process for these types of activities by deferring to
existing laws that are protective of golden conures in the course of
import and export.
Interstate Commerce
Under the proposed 4(d) rule, a person may deliver, receive, carry,
transport, or ship a golden conure in interstate commerce in the course
of a commercial activity, or sell or offer to sell in interstate
commerce a golden conure without a permit under the Act. At the same
time, the prohibitions on take under 50 CFR 17.21 would apply under
this proposed 4(d) rule, and any interstate commerce activities that
could incidentally take golden conure or otherwise constitute
prohibited acts in foreign commerce would require a permit under 50 CFR
17.32.
Between 1981 and 2016, persons within the United States imported 54
golden conures and exported 26; all were reported as live captive-bred
birds except two exported birds that originated from an unknown source
and one imported bird seized upon import (UNEP-WCMC 2018, unpaginated;
Service 2018, p. 33). These imports and exports were made for
commercial, captive-breeding, zoological, and personal purposes (UNEP-
WCMC 2018, unpaginated; Service 2018, p. 33). We have no information to
indicate that interstate commerce activities in the United States are
associated with threats to the golden conure or would negatively affect
any efforts aimed at the recovery of wild populations of the species.
Therefore, because (1) acts in interstate commerce within the United
States have not been found to threaten the golden conure, (2) the
species is otherwise protected in the course of interstate and foreign
commercial activities under the take provisions set forth at 50 CFR
17.31, and (3) international trade of this species appears to be
effectively regulated under CITES, we find this proposed 4(d) rule
contains all the prohibitions and authorizations necessary and
advisable for the conservation of the golden conure.
Proposed Technical Correction
Sections 50 CFR 17.11(c) and 17.12(b) of Title 50 of the Code of
Federal Regulations direct us to use the most recently accepted
scientific name of any wildlife or plant species, respectively, that we
have determined to be an endangered or threatened species. The golden
conure currently appears on the List as the ``golden parakeet''
(Aratinga guarouba). However, in this proposed rule, we refer to the
species by the common name ``golden conure'' and, based on the best
available scientific information regarding the species' taxonomy, we
use the scientific name Guaruba guarouba. Both ``golden conure'' and
``golden parakeet'' are common names associated with Guaruba guarouba.
We find that the best available scientific information available
supports the designation of the
[[Page 45086]]
golden conure to its own genus (Guaruba). Therefore, we propose to
update the List to reflect this change in the scientific name for
golden conure.
The basis for this taxonomic change is supported by published
studies in peer-reviewed journals (e.g., Urant[oacute]wka and
Mackiewicz 2017, entire; Tavares et al. 2004, pp. 230, 236-237, 239;
Sick 1990, p. 112). Accordingly, we propose to correct the scientific
name of the species under section 4 of the Act (16 U.S.C. 1531 et seq.)
by changing the name as currently listed (i.e., golden parakeet
(Aratinga guarouba)) to the corrected species name (i.e., golden conure
or golden parakeet (Guaruba guarouba)). We note that we are not
required to propose such a technical correction and can generally make
such a change in a direct final rule. We determined it more efficient,
however, to include the technical correction in this proposal.
Effects of This Rule
If this proposed rule is made final, it would revise 50 CFR
17.11(h) to reclassify the golden conure from endangered to threatened
on the List of Endangered and Threatened Wildlife. Additionally, if the
proposed 4(d) rule is adopted in a final rule, the Service will
incorporate all prohibitions and provisions of 50 CFR 17.31 and 17.32,
except that import and export of certain golden conures into and from
the United States and certain acts in interstate commerce will be
allowed without a permit under the Act. In addition, if the proposed
taxonomic change is made final, we will revise the List of Endangered
and Threatened Wildlife to change the species' scientific name to
Guaruba guarouba, and its common name to golden conure (=golden
parakeet).
Required Determinations
Clarity of the Rule
We are required by Executive Orders 12866 and 12988 and by the
Presidential Memorandum of June 1, 1998, to write all rules in plain
language. This means that each rule we publish must:
(1) Be logically organized;
(2) Use the active voice to address readers directly;
(3) Use clear language rather than jargon;
(4) Be divided into short sections and sentences; and
(5) Use lists and tables wherever possible.
If you feel that we have not met these requirements, send us
comments by one of the methods listed in ADDRESSES. To better help us
revise the rule, your comments should be as specific as possible. For
example, you should tell us the numbers of the sections or paragraphs
that are unclearly written, which sections or sentences are too long,
the sections where you feel lists or tables would be useful, etc.
National Environmental Policy Act (42 U.S.C. 4321 et seq.)
We have determined that we do not need to prepare an environmental
assessment, as defined under the authority of the National
Environmental Policy Act of 1969, in connection with regulations
adopted under section 4(a) of the Endangered Species Act. We published
a notice outlining our reasons for this determination in the Federal
Register on October 25, 1983 (48 FR 49244).
References Cited
A complete list of references cited in this rulemaking is available
on the internet at https://www.regulations.gov under Docket No. FWS-HQ-
ES-2015-0019 or upon request (see FOR FURTHER INFORMATION CONTACT).
Authors
The primary authors of this proposed rule are the staff members of
the Branch of Delisting and Foreign Species, Ecological Services
Program, U.S. Fish and Wildlife Service.
List of Subjects in 50 CFR Part 17
Endangered and threatened species, Exports, Imports, Reporting and
recordkeeping requirements, Wildlife.
Proposed Regulation Promulgation
Accordingly, we propose to amend part 17, subchapter B of chapter
I, title 50 of the Code of Federal Regulations, as set forth below:
PART 17--ENDANGERED AND THREATENED WILDLIFE AND PLANTS
0
1. The authority citation for part 17 continues to read as follows:
Authority: 16 U.S.C. 1361-1407; 1531-1544; and 4201-4245,
unless otherwise noted.
0
2. Amend Sec. 17.11(h), the List of Endangered and Threatened
Wildlife, by:
0
a. Removing the entry for ``Parakeet, golden'' under BIRDS; and
0
b. Adding an entry for ``Conure, golden (=golden parakeet)'' in
alphabetical order under BIRDS to read as follows:
Sec. 17.11 Endangered and threatened wildlife.
* * * * *
(h) * * *
----------------------------------------------------------------------------------------------------------------
Listing citations and
Common name Scientific name Where listed Status applicable rules
----------------------------------------------------------------------------------------------------------------
* * * * * * *
BIRDS
* * * * * * *
Conure, golden, (=golden Guaruba guarouba... Wherever found..... T 41 FR 24062, 6/14/1976;
parakeet). [Federal Register
citation of final
rule]; 50 CFR 17.41(c)
4d.
* * * * * * *
----------------------------------------------------------------------------------------------------------------
0
3. Amend Sec. 17.41 by revising paragraph (c) introductory text and
paragraph (c)(2)(ii) introductory text, and by adding paragraph
(c)(2)(ii)(D) to read as follows:
Sec. 17.41 Special rules--birds.
* * * * *
(c) The following species in the parrot family: Salmon-crested
cockatoo (Cacatua moluccensis), yellow-billed parrot (Amazona
collaria), white cockatoo (Cacatua alba), and the golden conure
(Guaruba guarouba).
* * * * *
(2) * * *
(ii) Specimens held in captivity prior to certain dates: You must
provide documentation to demonstrate that the specimen was held in
captivity prior to the applicable date specified in paragraphs
(c)(2)(ii)(A), (B), (C), or (D) of this section. Such documentation may
include copies of receipts, accession or veterinary records, CITES
documents, or
[[Page 45087]]
wildlife declaration forms, which must be dated prior to the specified
dates.
* * * * *
(D) For golden conures: July 1, 1975 (the date CITES entered into
force with the ``golden parakeet'' (i.e., the golden conure) listed in
Appendix I).
* * * * *
Dated: August 3, 2018.
James W. Kurth,
Deputy Director, U.S. Fish and Wildlife Service, Exercising the
Authority of the Director, U.S. Fish and Wildlife Service.
[FR Doc. 2018-19153 Filed 9-4-18; 8:45 am]
BILLING CODE 4333-15-P