Endangered and Threatened Wildlife and Plants; Proposed Rule to List Five Foreign Bird Species in Colombia and Ecuador, South America, under the Endangered Species Act, 32308-32349 [E9-15826]
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Federal Register / Vol. 74, No. 128 / Tuesday, July 7, 2009 / Proposed Rules
Information Relay Service (FIRS) at 800877-8339.
SUPPLEMENTARY INFORMATION:
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[FWS-R9-IA-2009-12; 96100-1671-9FLS–B6]
RIN 1018–AV75
Endangered and Threatened Wildlife
and Plants; Proposed Rule to List Five
Foreign Bird Species in Colombia and
Ecuador, South America, under the
Endangered Species Act
AGENCY: Fish and Wildlife Service,
Interior.
ACTION: Proposed rule.
SUMMARY: We, the U.S. Fish and
Wildlife Service (Service), propose to
list as endangered four species of birds
from Colombia — the blue-billed
curassow (Crax alberti), the brownbanded antpitta (Grallaria milleri), the
Cauca guan (Penelope perspicax), and
the gorgeted wood-quail (Odontophorus
strophium) — and one bird species from
Ecuador — the Esmeraldas woodstar
(Chaetocercus berlepschi) — as
endangered under the Endangered
Species Act of 1973, as amended (Act)
(16 U.S.C. 1531 et seq.). This proposal,
if made final, would extend the Act’s
protection to these species. The Service
seeks data and comments from the
public on this proposed rule.
DATES: We will accept comments
received or postmarked on or before
September 8, 2009. We must receive
requests for public hearings, in writing,
at the address shown in the ADDRESSES
section by August 21, 2009.
ADDRESSES: You may submit comments
by one of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• U.S. mail or hand-delivery: Public
Comments Processing, Attn: RIN 1018AV75; Division of Policy and Directives
Management; U.S. Fish and Wildlife
Service; 4401 N. Fairfax Drive, Suite
222; Arlington, VA 22203.
We will post all comments on https://
www.regulations.gov . This generally
means that we will post any personal
information you provide us (see the
Public Comments section below for
more information).
FOR FURTHER INFORMATION CONTACT:
Douglas Krofta, Chief, Branch of Listing,
Endangered Species Program, U.S. Fish
and Wildlife Service, 4401 N. Fairfax
Drive, Room 420, Arlington, VA 22203;
telephone 703-358-2105; facsimile 703358-1735. If you use a
telecommunications device for the deaf
(TDD), you may call the Federal
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Public Comments
We intend that any final action
resulting from this proposal will be as
accurate and as effective as possible.
Therefore, we request comments or
suggestions on this proposed rule. We
are particularly seek comments
concerning:
(1) Biological, commercial trade, or
other relevant data concerning any
threats (or lack thereof) to these species
and regulations that may be addressing
those threats.
(2) Additional information concerning
the taxonomy, range, distribution, and
population size of these species,
including the locations of any
additional populations of these species.
(3) Any information on the biological
or ecological requirements of these
species.
(4) Current or planned activities in the
areas occupied by these species and
possible impacts of these activities on
these species.
(5) Any information concerning the
effects of climate change on these
species or their habitats.
You may submit your comments and
materials concerning this proposed rule
by one of the methods listed in the
ADDRESSES section. We will not
consider comments sent by e-mail or fax
or to an address not listed in the
ADDRESSES section.
If you submit a comment via https://
www.regulations.gov, your entire
comment—including any personal
identifying information—will be posted
on the website. If you submit a
hardcopy comment 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 comments 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, Endangered Species Program,
4401 N. Fairfax Drive, Room 420,
Arlington, VA 22203; telephone 703358-2171.
Background
Section 4(b)(3)(A) of the Act requires
us to make a finding (known as a ‘‘90–
day finding’’) on whether a petition to
add, remove, or reclassify a species from
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the list of endangered or threatened
species has presented substantial
information indicating that the
requested action may be warranted. To
the maximum extent practicable, the
finding shall be made within 90 days
following receipt of the petition and
published promptly in the Federal
Register. If we find that the petition has
presented substantial information
indicating that the requested action may
be warranted (a positive finding),
section 4(b)(3)(A) of the Act requires us
to commence a status review of the
species if one has not already been
initiated under our internal candidate
assessment process. In addition, section
4(b)(3)(B) of the Act requires us to make
a finding within 12 months following
receipt of the petition on whether the
requested action is warranted, not
warranted, or warranted but precluded
by higher-priority listing actions (this
finding is referred to as the ‘‘12–month
finding’’). Section 4(b)(3)(C) of the Act
requires that a finding of warranted but
precluded for petitioned species should
be treated as having been resubmitted
on the date of the warranted-butprecluded finding, and is, therefore,
subject to a new finding within 1 year
and subsequently thereafter until we
publish a proposal to list or a finding
that the petitioned action is not
warranted. The Service publishes an
annual notice of resubmitted petition
findings (annual notice) for all foreign
species for which listings were
previously found to be warranted but
precluded.
Previous Federal Action
On November 24, 1980, we received
a petition (1980 petition) from Dr.
Warren B. King, Chairman of the
International Council for Bird
Preservation (ICBP), to add 60 foreign
bird species to the list of Threatened
and Endangered Wildlife (50 CFR
17.11(h)), including two species from
Colombia (the Cauca guan and the
gorgeted wood-quail) that are the subject
of this proposed rule. In response to the
1980 petition, we published a positive
90–day finding on May 12, 1981 (46 FR
26464), to initiate a status review for 58
foreign species, noting that 2 of the
species identified in the petition were
already listed under the Act. On January
20, 1984 (49 FR 2485), we published a
12–month finding within an annual
review on pending petitions and
description of progress on all species
petition findings addressed therein. In
that notice, we found that all 58 foreign
bird species from the 1980 petition were
warranted but precluded by higherpriority listing actions. On May 10,
1985, we published the first annual
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notice (50 FR 19761), in which we
continued to find that listing all 58
foreign bird species from the 1980
petition was warranted but precluded.
In our next annual notice, published on
January 9, 1986 (51 FR 996), we found
that listing 54 species from the 1980
petition, including the two Colombian
species mentioned above, continued to
be warranted but precluded, whereas
new information caused us to find that
listing four other species in the 1980
petition was no longer warranted. We
published additional annual notices on
the remaining 54 species included in
the 1980 petition on July 7, 1988 (53 FR
25511); December 29, 1988 (53 FR
52746); and November 21, 1991 (56 FR
58664), in which we indicated that the
Cauca guan and the gorgeted woodquail, along with the remaining species
in the 1980 petition, continued to be
warranted but precluded.
On May 6, 1991, we received a
petition (1991 petition) from Alison
Stattersfield, of ICBP, to add 53 species
of foreign birds to the list of Endangered
and Threatened Wildlife, including the
blue-billed curassow and the brownbanded antpitta, from Colombia, and
Esmeraldas woodstar, from Ecuador. In
response to the 1991 petition, we
published a positive 90–day finding on
December 16, 1991 (56 FR 65207), for all
53 species and announced the initiation
of a status review. On March 28, 1994
(59 FR 14496), we published a 12–
month finding on the 1991 petition,
along with a proposed rule to list 30
African birds under the Act (15 each
from the 1980 petition and 1991
petition). In that document, we
announced our finding that listing the
remaining 38 species from the 1991
petition, including the blue-billed
curassow and the brown-banded
antpitta, from Colombia, and
Esmeraldas woodstar, from Ecuador,
was warranted but precluded by higherpriority listing actions. On January 12,
1995 (60 FR 2899), we reiterated the
warranted-but-precluded status of the
remaining species from the 1991
petition. We made subsequent
warranted but precluded findings for all
outstanding foreign species from the
1980 and 1991 petitions, including all
five of the Colombian and Ecuadorian
bird species that are the subject of this
proposed rule, as published in our
annual notices of review (ANOR) on
May 21, 2004 (69 FR 29354), and April
23, 2007 (72 FR 20184).
Per the Service’s listing priority
guidelines (September 21, 1983; 48 FR
43098), we identified the listing priority
numbers (LPNs) (ranging from 1 to 12)
for all outstanding foreign species in our
2007 ANOR (72 FR 20184), published
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on April 23, 2007. In that notice, the
five species included in this proposed
rule were designated with an LPN of 2,
and it was determined that their listing
continued to be warranted but
precluded because of other listing
activity. A listing priority of 2 indicates
that the subject species face imminent
threats of high magnitude. With the
exception of LPN 1, which addresses
monotypic genera that face imminent
threats of high magnitude, category 2
represents the Service’s highest priority.
On July 29, 2008 (73 FR 44062), we
published in the Federal Register a
notice announcing our annual petition
findings for foreign species (2008
ANOR). In that notice, we announced
that listing was warranted for 30 foreign
bird species, including the five species
that are the subject of this proposed
rule. The five species were selected
from the list of warranted-but-precluded
species because of their LPN, their
similarity of habitat, and the similarity
of threats to these species. Combining
species that face similar threats within
the same general geographic area into
one proposed rule allows us to
maximize our limited staff resources,
thus increasing our ability to complete
the listing process for warranted-butprecluded species.
Species Information and Factors
Affecting the Species
Section 4 of the Act (16 U.S.C. 1533),
and its implementing regulations at 50
CFR part 424, set forth the procedures
for adding species to the Federal Lists
of Endangered and Threatened Wildlife
and Plants. A species may be
determined to be an endangered or
threatened species due to one or more
of the five factors described in section
4(a)(1) of the Act. The five factors are:
(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; and (E) other natural or
manmade factors affecting its continued
existence.
Under the Act, we may determine a
species to be endangered or threatened.
An endangered species is defined as a
species that is in danger of extinction
throughout all or a significant portion of
its range. A threatened species is
defined as a species that is likely to
become an endangered species within
the foreseeable future throughout all or
a significant portion of its range.
Therefore, we evaluated the best
available scientific and commercial
information on each species under the
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five listing factors to determine whether
they met the definition of endangered or
threatened.
Below is a species-by-species analysis
of these five factors using the best
available scientific and commercial
information to determine whether the
species meet the definition of
endangered or threatened. The species
are considered in alphabetical order,
beginning with the Colombian species:
blue-billed curassow, brown-banded
antpitta, Cauca guan, gorgeted woodquail, and followed by the Ecuadorian
species: the Esmeraldas woodstar.
Colombian Bird Species
I. Blue-Billed Curassow (Crax alberti)
Species Description
The blue-billed curassow, endemic to
Colombia, is a large (82-92 centimeters
(cm) (32-36 inches (in)), tree-dwelling
member of the Cracid family (Cracidae)
(Collar et al. 1992, p. 154; del Hoyo
1994, p. 361; Salaman et al. 2001, p.
183). The species is locally known as
´
´
‘‘Paujıl de pico azul’’ or ‘‘Pavon
Colombiano’’ and is also referred to in
English as the blue-knobbed curassow
(Cuervo 2002, p. 138; United Nations
Environment Programme – World
Conservation Monitoring Centre (UNEPWCMC) 2008c, p. 1). In older literature,
the species is referred to as Prince
Albert’s curassow (Throp 1964, p. 124).
The blue-billed curassow is described as
mainly black with blue at the base of its
bill. The male has a white-plumaged
crissum (the area under the tail),
whereas the female has a black and
white crest and black and white barring
on her wings (BirdLife International
(BLI) 2007d, p. 1; Throp 1964, p. 124).
Taxonomy
The species was first taxonomically
described by Fraser in 1852 and placed
in the family Cracidae.
Habitat and Life History
Blue-billed curassows prefer
undisturbed, heterogeneous primary
forests in the humid lowlands of the
Sierra Nevada de Santa Marta
Mountains at elevations up to 1,200
meters (m) (3,937 feet (ft)) (Collar et al.
1992, p. 154; del Hoyo 1994, p. 361;
Salaman et al. 2001, p. 183). The bluebilled curassow requires a large home
range of primary tropical forest (Cuervo
2002, pp. 138-140). The species will
rarely cross narrow deforested corridors,
such as those caused by roads or oil
pipelines, and will not cross large open
areas between forest fragments (Cuervo
and Salaman 1999, p. 7). The species is
described as being trusting of humans
(del Hoyo 1994, p. 336).
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This terrestrial bird feeds mostly on
fruit and leaves, and sometimes feeds
upon worms and carrion. It plays an
important role in dispersing seeds and
regenerating tropical forests (BLI 2007d,
p. 1; Brooks 2006, p. 17; Brooks and
Strahl 2000, pp. 5-8; Cuervo and
Salaman 1999, p. 8).
Cracids are also slow to reproduce,
with a replacement rate of at least 6
years (Silva and Strahl 1991, p. 50).
Curassows reach sexual maturity in
their second year (Throp 1964, p. 130).
Blue-billed curassows form
monogamous pairs that share
responsibilities for young (Cuervo and
Salaman 1999, p. 9; Todd et al. 2008).
The breeding season begins in December
and goes through March (Cuervo and
Salaman 1999, p. 8). During the mating
season, the male blue-billed curassows
makes ‘‘booming’’ calls that can be
heard 500 m (0.31 mi) away (OchoaQuintero et al. 2005, pp. 42, 44). Large
nests made of sticks and leaves are built
in dense lianas (woody vines) (Cuervo
and Salaman 1999, p. 8). The typical
blue-billed curassow clutch size is 1-2
large white eggs, which is a low clutch
size relative to other Galliformes (del
Hoyo 1994, p. 336; Throp 1964, p. 130),
and young are hatched in July after an
approximately 29–day incubation
period (del Hoyo 1994, p. 361; Hilty and
Brown 1986, p. 129; Throp 1964, p.
131). In captivity, curassows are longlived species (Todd et al. 2008, p.7).
Throp (1964, p. 132) recorded a bluebilled curassow still laying eggs at 20
years of age. However, in the wild, one
generation is considered to be 10 years
(Cuervo 2002, p. 141).
Historical Range and Distribution
The blue-billed curassow historically
occurred in northern Colombia, from the
base of the Sierra Nevada de Santa
Marta (in the northern Departments of
Magdalena La Guijaira, and Cesar), west
´
to the Sinu valley (Department of
´
´
Cordoba), through the Rıo Magdalena
(through the Departments (from south to
north) of Huila, Tolima, Caldas,
Antioquia, Santander, Bolivar,
Magdalena, and La Guajira) (BLI 2007a,
p. 1; Cuervo and Salaman 1999, p. 7; del
Hoyo 1994, p. 361). The species’ historic
range encompassed an area of
approximately 106,700 square
kilometers (km2) (41,197 square miles
(mi2)) (Cuervo 2002, p. 141). There were
no confirmed observations of blue-billed
curassows between 1978 and 1997
(Brooks and Gonzalez-Garcia 2001, p.
183), and surveys conducted in 1998
failed to locate any males (BLI 2007d, p.
3) (as detailed under Factor B, below),
prompting researchers to believe the
species to be extinct in the wild (del
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Hoyo 1994, p. 361). However, a series of
reported observations made in 1993
were confirmed in the year 2000
(Cuervo 2002, pp. 136-137).
Current Range and Distribution
The current range of the blue-billed
curassow is estimated to be a 2,090-km2
(807-mi2) area (BLI 2007d, p. 2) of
fragmented, disjunct, and isolated
tropical moist and humid lowlands and
´
premontane forested foothills in the Rıo
Magdalena and lower Cauca Valleys of
the Sierra Nevada de Santa Marta
Mountains. The species may be found at
elevations up to 1,200 m (3,937 ft)
(Collar et al. 1992, p. 154; Cuervo and
Salaman 1999, p. 7; del Hoyo 1994, p.
361; Donegan and Huertas 2005, p. 29;
Salaman et al. 2001, p. 183), but it is
more commonly found below 600 m
(del Hoyo 1994, p. 361). Little
information is available on the size of
the forest fragments in which the
species has been observed. However,
researchers conducting fieldwork in the
´
Department of Antioquıa in 1999 and
2001 noted that the patch sizes varied
from 3 km2 (1.2 mi2) to 10 km2 (3.9 mi2)
in size (Ochoa-Quintero et al. 2005, p.
46).
In 1993, sightings were reported in
´
the northern Departments of Cordoba (at
´
La Terretera, near Alto Sinu) and
´
´
Bolıvar (in the Serranıa de San Jacinto
(San Jacinto Mountains)) (Williams, in
litt., as cited in BLI 2007d, p. 2).
Additional observations were made in
the northernmost Department of La
Guajira in 2003 (in the Valle de San
Salvador Valley) (Strewe and Navarro
2003, p. 32). More recently, individuals
have been observed in the tropical
forests of the central Departments of
´
´
Antioquıa (on the slopes of the Serranıa
´
de San Lucas and Bajo Cauca-Nechı
Regional Reserve area), the Departments
´
of Santander and Boyaca (on the slopes
´
of the Serranıa de las Quinchas), and in
the southeastern Department of Cauca
(in northeastern and lower Cauca
Valley) (BLI 2007d, p. 2; Cuervo 2002,
pp. 135-138; Donegan and Huertas 2005,
p. 29; Ochoa-Quintero et al. 2005, p. 43˜
4; Uruena et al. 2006, p. 42). Experts
consider the most important refuges for
´
this species to be: (1) Serranıa de San
´
Lucas (Antioquıa); (2) Paramillo
´
´
National Park (Antioquıa and Cordoba
´
Departments); (3) Bajo Cauca-Nechı
´
Regional Reserve (Antioquıa and
´
´
Cordoba Departments); and, (4) Serranıa
de las Quinchas Bird Reserve
´
(Santander and Boyaca Departments)
(BLI 2007d, p. 3; Cuervo 2002, p. 139).
These refugia are discussed under
Factor A, below.
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Population Estimates
There is little information on
population numbers for the various
reported locations of the species, and
political instability within the country
makes it difficult to know the exact
population size of this species (Houston
Zoo 2008). In 2002, Cuervo (2002, p.
´
141) considered the Serranıa de las
´
Quinchas and Serranıa de San Lucas
populations to be the stronghold of the
species. However, surveys in 2003 led
´
researchers to believe that Serranıa de
las Quinchas serves as the species’
stronghold (BLI 2007d, pp. 2, 5-6). In
´
2003, the population at Serranıa de las
´
Quinchas (Boyaca Department) location
was estimated to be between 250 and
1,000 birds. The only other information
on the subpopulation level is a report
from Strewe and Navarro (2003, p. 32),
based on field studies conducted
between 2000 and 2001, that hunting
had nearly extirpated the blue-billed
curassow from a site in San Salvador (La
Guijara) (Factor B).
Using the International Union for
Conservation of Nature and Natural
Resources (IUCN) categories, the bluebilled curassow population was
estimated according to IUCN criteria to
be more than 1,000 but fewer than 2,500
in 1994 (BLI 2007d, p. 2). In 2001,
Brooks and Gonzalez-Garcia (2001, p.
184) estimated the total population to be
much fewer than 2,000 individuals. In
2002, it was estimated that the species
had lost 88 percent of its habitat and
half of its population within the last
three generations, or 30 years (Cuervo
2002, p. 141). Local reports indicate an
overall declining trend characterized by
recent rapid declines of all
subpopulations (BLI 2007d, p. 1; Cuervo
2002, p. 138; Strahl et al. 1995, p.25).
For further information on population
size, see Factor E, below.
Conservation Status
The blue-billed curassow is identified
as a critically endangered species under
Colombian law (EcoLex 2002, p. 12).
The species is considered one of the
most threatened cracids by the IUCN
Cracid Specialist Group. The species is
categorized by the IUCN as ‘Critically
Endangered,’ with habitat loss as a
primary threat (BLI 2004b, p. 1; Cuervo
2002, p. 141; del Hoyo 1994 p. 340;
˜
Strahl et al. 1995, pp. 4-5; Uruena et al.
2006, pp. 41-2).
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Summary of Factors Affecting the BlueBilled Curassow
A. The Present or Threatened
Destruction, Modification, or
Curtailment of the Habitat or Range
The blue-billed curassow prefers
undisturbed, heterogeneous forests and
is rarely found in secondary or even
slightly disturbed forests (Cuervo and
Salaman 1999, p. 7). The blue-billed
curassow occur today in several disjunct
locations along a much-restricted part of
its historic distribution (Brooks and
Gonzalez-Garcia 2001, p. 183; Collar et
al. 1992, pp. 61-62; Cuervo and Salaman
1999, p. 7). Researchers note that the
blue-billed curassow requires large
territories, but there is little information
as to the actual size of the remaining
forest fragments (Cuervo and Salaman
1999, p. 7). In 1999 and 2001,
researchers conducting fieldwork in the
´
Department of Antioquia noted that the
patch sizes in which the species were
observed or heard varied from 3 km2
(1.2 mi2) to 10 km2 (3.9 mi2) in size
(Ochoa-Quintero et al. 2005, p. 46).
Since the 1990s, the species has been
´
observed in the Departments of Cordoba
´
(at La Terretera, near Alto Sinu, 1993)
´
´
and Bolıvar (in the Serranıa de San
Jacinto, 1993) (Williams in litt., as cited
in BLI 2007d, p. 2); La Guajira (in the
Valle de San Salvador Valley, 2003)
(Strewe and Navarro 2003, p. 32);
´
´
Antioquıa (on the slopes of the Serranıa
´
de San Lucas and Bajo Cauca-Nechı
Regional Reserve area, 1999 and 2001)
(Ochoa-Quintero et al. 2005, p. 43-44);
´
Santander and Boyaca (on the slopes of
´
the Serranıa de las Quinchas); and
Cauca (in northeastern and lower Cauca
Valley) (BLI 2007d, p. 2; Cuervo 2002,
pp. 135-138; Donegan and Huertas 2005,
˜
p. 29; Uruena et al. 2006, p. 42).
Deforestation rates and patterns:
Primary forest habitats throughout
Colombia have undergone extensive
˜
deforestation. Vina et al. (2004, pp. 123124) used satellite imagery to analyze
deforestation rates and patterns along
the Colombian-Ecuadorian Border (in
the Departments of Putumayo and
Sucumbios, respectively), finding that,
from 1973 to 1996, a total of 829 km2
(320 mi2) of tropical forests within the
study area were converted to other uses.
This corresponds to a nearly one-third
total loss of primary forest habitat, or a
nearly 2 percent mean annual rate of
deforestation within the study area.
During the study, the area within
Colombia experienced a three-timeslarger annual rate of loss than that in
Ecuador, due to more intense pressures
from human colonization and illegal
˜
crop cultivation (Vina et al. 2004, p.
124). The human population within the
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area increased from approximately
50,000 to over 250,000 people during
the 23–year period (Perz et al. 2005, pp.
26-28). A similar phenomenon occurred
´
in the Rıo Magdalena Valley, which
coincides with the species’ historic
range as well as its disjunct and
´
restricted current range. The Rıo
Magdalena runs from south to north
approximately 1,540 km (950 mi)
through western Colombia and served as
the main waterway connecting coffee
(Coffea spp.) plantations to the ports on
the Western Colombian coast in the
1920s, when the river was reportedly
plagued by occasional droughts and
erosion. In the 1930s, a railway was
´
completed along much of the Rıo
Magdalena Valley; this infrastructural
improvement contributed to a growth in
several industries, including coffee
´
(throughout the Rıo Magdalena valley),
bananas (Musa spp.) (Magdalena
Department), and oil fields (Santander
Department) (Ocampo and Botero 2000,
pp. 76-78). Deforestation and habitat
loss throughout the lowland forests
across northern Colombia over the past
100 years contributed to the increasing
rarity of the species, and extirpated the
species from a large portion of its
previous range by the 1980s (Brooks and
Gonzalez-Garcia 2001, p. 183; Collar et
al. 1992, pp. 61-62; Cuervo and Salaman
1999, p. 7).
In a similar study specific to the
western Andean Amazon area of
Colombia (in the Departments of
Arauca, Casemere, Meta, Vichada,
´
Amazonas, Caqueta, Guainia, Guaviare,
´
Putumayo, and Vaupes), deforestation
between 1980 and 1990 totaled 52,320
km2 (20,201 mi2) (Perz et al. 2005, pp.
26-28). The most recent reports indicate
that habitat loss is ongoing and may be
accelerating. Between the years 1990
and 2005, Colombia lost a total of 7,920
km2 (3,058 mi2) of primary forest (Butler
2006a, pp. 1-3; Food and Agriculture
Organization of the United Nations
(FAO) 2003a, p. 1). Researchers have
observed that road building and other
infrastructure improvements in
previously remote forested areas have
increased accessibility and facilitated
further habitat destruction, exploitation,
´
and human settlement (Alvarez 2005, p.
´
´
2042; Cardenas and Rodrıguez Becerra
2004, pp. 125-130; Etter et al. 2006, p.
˜
1; Hunter 1996, p. 158-159; Vina et al.
2004, pp. 118-119). In Antioquia, cattle
ranches are extensive in areas where the
blue-billed curassow occurs; cattle
ranching is considered a less laborintensive land use, meaning that more
people need to turn to alternative
sources of income generation, such as
cultivation or extractive industries
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32311
(Melo and Ochoa 2004, as cited in
´
˜
Uruena et al. 2006, p. 42). In Serranıa
de las Quinchas, the economy is based
principally on timber extraction,
˜
agriculture, and cattle ranching (Uruena
and Quevedo unpubl. data 2004, as
˜
cited in Uruena et al. 2006, p. 47). These
activities contribute to further habitat
fragmentation and reduction. In terms of
habitat destruction, an influx of settlers
displaced from the Departments of
Antioquia, Tolima, and Cundinamarca,
due to violence and public disorder in
these Departments, are the principal
threat to the mountainous regions in
˜
these Departments (Uruena et al. 2006,
p. 42).
The decline in blue-billed curassow
population numbers (see Population
estimates, above) is inextricably linked
to habitat loss. The blue-billed curassow
became increasingly rare during the
20th Century, as much of the lowerelevation forests in their historic range
´
´
of the Rıo Magdalena and Rıo Cauca
Valleys were deforested, forcing the
blue-billed curassow to move to higher
elevations (Cuervo and Salaman 1999,
p. 8). By the 1980s, the species had
disappeared from a large portion of its
previous range (Collar et al. 1992, pp.
61-62), which historically encompassed
approximately 106,700 km2 (41,197 mi2)
(Cuervo 2002, p. 141). In 2002, it was
estimated that, within the three prior
generations (30 years), the species had
lost 88 percent of its original habitat and
that the remaining suitable habitat had
been reduced to 13,300 km2 (5135 m2)
(Cuervo 2002, p. 141). The current range
of the blue-billed curassow is estimated
to be 2,090 km2 (807 mi2) (BLI 2007d,
p.2) (see also ‘‘Small Population Size,’’
Factor E).
Deforestation and fragmentation
caused by human encroachment are
ongoing throughout the blue-billed
´
curassow’s range, including: Antioquıa
´
(on the slopes of the Serranıa de San
´
Lucas and Bajo Cauca-Nechı Regional
´
Reserve area); Santander and Boyaca
Departments (on the slopes of the
´
Serranıa de las Quinchas); and in the
southeastern Department of Cauca (in
northeastern and lower Cauca Valley),
where timber extraction and mining
˜
continue (Uruena et al. 2006, p. 42).
Human activities that are contributing to
habitat loss include: forest clearing for
subsistence agriculture, cash crops
´
(such as coffee), and grazing (Alvarez
´
2005, p. 2042; BLI 2007d, p. 3; Cardenas
´
and Rodrıguez Becerra 2004, p. 355;
Oldham and Massey 2002, pp. 9-12;
˜
Uruena et al. 2006, p. 42); habitat
alteration, human population
displacement, and hunting as a result of
´
armed conflict (Alvarez 2001, p. 305;
´
Alvarez 2003, pp. 51-52); habitat
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destruction and alteration as a result of
´
fire (Alvarez 2005, p. 2041; Moreno et
al. 2006, p. 1); habitat loss for dams and
reservoir development (Cuervo 2002, p.
139; Kreger 2005, pp.5-6); illicit crop
cultivation (such as the coca plant
´
(Erythroxylum coca)) (Alvarez 2001, pp.
´
1086-1087; Alvarez 2007, pp. 133-135;
´
´
Cardenas and Rodrıguez Becerra 2004,
p. 355; Oldham and Massey 2002, pp. 912); gold mining activities (Cuervo 2002,
p. 139); habitat pollution due to oil
´
development and distribution (Alvarez
´
´
2005, p. 2041; Cardenas and Rodrıguez
Becerra 2004, p. 355); and increased
access and habitat destruction resulting
from road development (Cuervo 2002,
pp. 139-140). Roads create barriers to
animal movements, expose animals to
traffic hazards, and increase human
access into habitat, thus facilitating
further exploitation and habitat
destruction (Hunter 1996, 158-159).
Local human populations have recently
settled in forested areas that previously
provided habitat for blue-billed
curassows. This human settlement is
accelerating habitat loss and
fragmentation with only 5 percent of the
species’ restricted range now covered by
forest (Brooks and Gonzalez-Garcia
2001, pp. 183-184), and is leaving only
fragmented, disjunct, and isolated
populations in the remaining four or
five patches of tropical humid and
´
premontane forests (Alvarez 2003, p. 51;
Brooks and Strahl 2000, pp. 14-15;
Collar et al. 1994, pp. 61-62; Cuervo and
Salaman 1999, p. 7; Donegan and
Huertas 2005, p. 29).
Illegal drugs and their eradication:
The cultivation of illegal crops
(including coca) poses additional threats
to the environment beyond encouraging
the destruction of montane forests
(Balslev 1993, p. 3). Van Schoik and
Schulberg (1993, p. 21) noted that coca
crop production destroys the soil
quality by causing the soil to become
more acidic, which depletes the soil
nutrients and ultimately impedes the
regrowth of secondary forests in
abandoned fields. Although Colombia
continues to be the leading coca bush
producer (United Nations Office of
Drugs and Crime (UNODC) et al. 2007,
p. 7), since 2003, cocaine cultivation has
remained stable at about 800 km2 (309
mi2) of land under cultivation (UNODC
et al. 2007, p. 8). This stabilization of
production is partially attributed to
alternative development projects that
were implemented between 1999 and
2004 to encourage pursuits other than
illegal crop cultivation (UNODC et al.
2007, p. 77). This is also attributed to
heightened eradication efforts. Between
2002 and 2004, aerial spraying occurred
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over more than 1,300 km2 (502 mi2)
annually, peaking in 2004, when 1,360
km2 (525 mi2) of illicit crops were
sprayed (UNODC and the Government
of Colombia (GOC) 2005, p. 11). In 2006,
eradication efforts were undertaken on
over 2,130 km2 (822 mi2) of land, which
included sraying of 1,720 km2 (664 mi2)
and manual eradication on the
remaining land. Eradication efforts
undertaken in 2006 occurred over an
area 2.7 times greater than the net
cultivation area (UNODC et al. 2007, p.
8). Drug eradication efforts in Colombia
have further degraded and destroyed
primary forest habitat by using
nonspecific aerial herbicides to destroy
´
illegal crops (Alvarez 2005, p. 2042; BLI
´
´
2007d, p. 3; Cardenas and Rodrıguez
Becerra 2004, p. 355; Oldham and
Massey 2002, pp. 9-12). Herbicide
spraying has introduced harmful
chemicals into blue-billed curassow
habitat and has led to further
destruction of the habitat by forcing
illicit growers to move to new,
previously untouched forested areas
´
´
(Alvarez 2002, pp. 1088-1093; Alvarez
´
2005, p. 2042; Alvarez 2007, pp. 133´
143; BLI 2007d, p. 3; Cardenas and
´
Rodrıguez Becerra 2004, p. 355; Oldham
and Massey 2002, pp. 9-12). Between
1998 and 2002, cultivation of illicit
crops increased by 21 percent each year,
with a concomitant increase in
deforestation of formerly pristine areas
´
of approximately 60 percent (Alvarez
2002, pp. 1088-1093).
Effects of habitat fragmentation: A
study conducted on the effects of habitat
fragmentation on Andean birds within
western Colombia determined two
primary conditions that increased a
species’ vulnerability to habitat
fragmentation and susceptibility to local
extirpation and extinction: (1) species
that were located at the upper or lower
limit of their altitudinal or geographical
distribution (as is the case for the bluebilled curassow, which formerly
occupied the now-cleared lower
elevation forests and is relegated to
isolated forest fragments within its
current range), and (2) species that were
large fruit-eating birds with limited
distributions and narrow habitat
preferences (also traits of the blue-billed
´
curassow) (Kattan and Alvarez-Lopez
1996, pp. 5-6). The study also
determined that 31 percent of the
historical bird populations in western
Colombia had become extinct or locally
extirpated by 1990, largely as a result of
habitat fragmentation from deforestation
and human encroachment (Kattan and
´
Alvarez-Lopez 1996, p. 5; Kattan et al.
1994, p. 141). The most direct physical
consequence of habitat fragmentation is
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loss of habitat heterogeneity; habitat
heterogeneity is a characteristic
preferred by the blue-billed curassow
(see Habitat and Life History, above)
´
(Kattan and Alvarez-Lopez 1996, p. 6).
Local reports indicate an overall
declining trend characterized by recent
rapid declines of all the populations of
blue-billed curassows (BLI 2007d, p. 1;
Cuervo 2002, p. 138; Strahl et al. 1995,
p. 25). Moreover, the ability of the bluebilled curassow to repopulate an
isolated patch of suitable habitat
following decline or extirpation is
highly unlikely due to the species’ small
overall population size, its tendency to
avoid degraded habitats, and the large
distances between the remaining
primary forest fragments in addition to
the species’ reticence to cross large areas
of open habitat (Cuervo and Salaman
1999, p. 7; Hanski 1998, pp. 45-46).
In addition to the direct detrimental
effect of habitat loss, blue-billed
curassows and other cracids are
susceptible to indirect effects of habitat
disturbance and fragmentation (Brooks
and Strahl 2000, p. 10; Silva and Strahl
1991, p. 38). A study conducted in
northwestern Colombia suggests that
habitat destruction and fragmentation
may increase a species’ vulnerability to
´
predation (Arango-Velez and Kattan
1997, pp. 140-142) (Factor C). Habitat
fragmentation, in combination with
growing numbers of human settlements,
has made the species’ habitat more
accessible and more vulnerable to
hunting (Factor B) and predation (Factor
C). Habitat loss also compounds the
species’ decline in population numbers
(estimated to be between 1,000 and
2,500 individuals) (BLI 2004b, p. 1) (see
Factor E, Small population size).
Refugia: Several areas within the
blue-billed curassow’s current range are
designated as national parks or other
types of preserves, including Tayrona
and Sierra Nevada de Santa Marta
´
National Parks (both in Antioquıa
Department) (Cuervo 2002, p. 140) and
´
the Colorados Sanctuary (Bolıvar
Department), which protects part of the
´
Serranıa de San Jacinto (BLI 2007d, pp.
˜
2-3; Uruena et al. 2006, p. 42). Experts
consider the most important refuges for
this species, containing the largest
remaining areas of suitable habitat, to be
in the following areas (arranged
geographically, from north to south): (1)
´
Serranıa de San Lucas, (2) Paramillo
´
National Park, (3) Bajo Cauca-Nechı
´
Regional Reserve, and (4) El Paujıl Bird
Reserve (BLI 2007d, p. 3; Cuervo 2002,
˜
p. 139-140; Uruena et al. 2006, p. 42),
four of the five locations where the
species has been observed in the 21st
Century (see Current Range, above). The
habitat within these refugia underserves
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the needs of the species for various
reasons (including past and ongoing
habitat destruction and incomplete
habitat inclusion), as enumerated below.
In addition, inadequate regulatory
mechanisms hamper protection of the
species and its habitat (Factor D).
´
´
(1) Serranıa de San Lucas (Antioquıa)
is not a protected area, but is one of the
largest remaining tracts of forest that is
the least disturbed (WWF 2001b, p. 1).
Even so, only a few isolated forest
patches survive above 1,000 m (3,280 ft)
´
in the northern lowlands (Antioquia
Department) (Donegan and Salaman
1999, p. 4). Ongoing pressures on this
habitat include human encroachment
for natural resources, colonization,
ranching, logging, and crop production,
as well as pollution of the Magdelena
and Cauca Rivers (WWF 2001b, p. 3). In
1996, there was a gold rush that led to
deforestation for logging, settlements,
conversion to agriculture, and coca
production (BLI 2007d, p 3). Using
satellite imagery and fieldwork, Cuervo
(2002, p. 140) determined that
deforestation on the eastern slopes of
´
the Serranıa de San Lucas was extensive
between 1995 and 1996. In 2005,
highway construction was underway as
part of a national plan to connect the
East Andes, the West Andes, and the
Pacific ports, including roadbuilding
´
through the Serranıa de San Lucas and
´
adjacent lowlands (Alvarez 2005, p.
2042). Because the species prefers
pristine habitat, this ongoing habitat
alteration negatively impacts the
integrity of this location and the
survival of the species therein.
(2) The Paramillo National Park
´
´
(Antioquıa and Cordoba Departments),
created in 1977, encompasses an area
4600 km2 (1776 mi2) in size and
includes moist and cloud forest habitats
(Corantioquia 2008, p. 1). However, it
only protects the upper elevational limit
of the habitat occupied by the species,
where the species is rarer (Cuervo 2002,
p. 140). This Park is inhabited by an
´
indigenous community (Embera), for
whom the Park was created. Farmers
also inhabit the interior regions of the
Park (BLI 2007a, p. 1-2). The areas to the
south of the Park have undergone
intense habitat disturbance from
logging, drug crop production, and
inundation from flooding caused by the
´
construction of the Urra Dam (Cuervo
2002, p. 139). Deforestation has
occurred throughout a large portion of
the Park’s buffer zone as well as in the
extreme southern reaches within Park
boundaries (Cuervo 2002, p. 140).
Between 2003 and 2004, cocaine
cultivation within the Paramillo
National Park went from 1.1km2 to 4.6
km2 (UNODC and GOC 2005, p. 45). The
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´
´
Urra Dam was constructed on the Sinu
´
River between 1993 and 1998; the Sinu
River Valley was part of the blue-billed
curassows’ historic range (BirdLife
International (BLI) 2007a, p. 1; Cuervo
and Salaman 1999, p. 7; del Hoyo 1994,
p. 361). The reservoir flooded the area
and led to displacement of human
populations and other habitat
alterations, including fish kills caused
by blocked spawning and migratory
routes (NGO Working Group on Export
Development Canada 2003, p.31).
´
(3) The Bajo Cauca-Nechı Regional
´
´
Reserve (Antioquıa and Cordoba
Departments), created in 1999, is
located within a large tract (450 km2
(174 mi2)) of forested land at an
elevation of 800 m (2,625 ft). Bajo Cauca
is the second most populated region in
the Department of Antioquia. Logging is
important in this region, and the
Reserve allows commercial exploitation
´
of wood (Fundacion Viztaz 2007, p. 2).
Surveys are scant in this area, which is
believed to be home to many species as
yet unidentified by science (Cuervo
2002, p. 137; Donegan and Salaman
1999, p. 12). Although the Reserve
provides suitable habitat for the species,
and the blue-billed curassow is
presumed to inhabit this area, it has not
been confirmed within the Reserve (BLI
2007d, p. 3).
´
(4) El Paujıl Bird Reserve (Santander
´
and Boyaca Departments) is a private
´
reserve established in Serranıa de las
Quinchas (WorldTwitch Colombia 2004,
´
p.3). In the early 1990s, the Serranıa de
´
las Quinchas (Boyaca Department,
central Colombia) was considered one of
the last remaining well-preserved cloud
forests and the largest tract of lowland
wet forest in the region, with up to 500
km2 (193 mi2) of forest remaining.
Within a decade, the forest had
dwindled to 120 km2 (46 mi2)
(WorldTwitch Colombia 2004, p. 3). In
2002, the largest known subpopulation
of blue-billed curassow was located in
´
the Serranıa de las Quinchas and
became regarded as the stronghold of
´
the species (BLI 2007d, p. 2). El Paujıl
Bird Reserve was created in 2004
specifically to protect the blue-billed
curassow and its habitat (BLI 2007b, p.
2). Comprising 10 km2 (3.9 mi2) of
lowland tropical forest up to elevations
of 700 m (2297 ft), the Reserve includes
suitable habitat for the species.
However, collection of eggs and chicks
are ongoing within the region (Cuervo
˜
2002, p. 139; Uruena et al. 2006, p. 42)
(Factor B), and there are questions as to
the effectiveness of this Reserve to
protect the species (Factor D).
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32313
Summary of Factor A
The blue-billed curassow prefers
undisturbed habitat, and the remaining
small populations are limited to four or
five small, disjunct, and isolated areas
in seven different Departments. Within
the past three generations, or 30 years,
the species is estimated to have lost 88
percent of its habitat and half of its
population. Deforestation and
conversion of primary forests for human
settlements and agriculture has led to
habitat fragmentation throughout the
species’ range and to isolation of
remaining populations. Habitat loss and
fragmentation were factors in the
species’ historical decline (over the past
50 years) and caused localized
extirpations, and continue to be factors
negatively affecting the blue-billed
curassow in the wild. Human
encroachment into the species’
preferred primary forest habitat has
resulted in habitat alteration and
disturbance activities that have caused
declines in the blue-billed curassow
population. Cultivation of illegal drug
crops, such as cocaine, leads to further
deforestation and alters soil
compositions, hindering regeneration of
abandoned fields. In addition, drug
eradication programs involving the
aerial spraying of non-specific
herbicides lead to further environmental
degradation and destruction of primary
forest habitat. Three of the four most
important refugia continue to undergo
habitat destruction, and regulatory
mechanisms are inadequate to mitigate
the primary threats to this species
´
(Factor D). A private refuge, the El Paujıl
Bird Reserve, was formed to protect the
blue-billed curassow and its habitat,
which includes a large amount of
suitable habitat, but may be lacking in
its ability to adequately protect the
species (Factors B and D). Habitat
fragmentation contributes to the species’
vulnerability to hunting (discussed
under Factor B) and predation
(discussed under Factor C) by increasing
human and predator access to the
habitat. The species’ historic range,
which encompassed approximately
106,700 km2 (41,197 mi2), has been
reduced to 2,090 km2 (807 mi2). Experts
estimate that 88 percent of this habitat
loss has occurred within the last three
generations, or 30 years. Habitat
destruction and fragmentation of the
remaining primary forest habitat is
expected to continue, as human
encroachment and associated activities
continue within the blue-billed
curassow’s range. Therefore, we find
that the present destruction,
modification, and curtailment of habitat
E:\FR\FM\07JYP3.SGM
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are threats to the blue-billed curassow
throughout all of its range.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
Blue-billed curassows are hunted by
indigenous people and local residents
for subsistence, sport, trade, and
entertainment (Brooks and GonzalezGarcia 2001, p. 183; Brooks and Strahl
2000, p. 10; Cuervo and Salaman 1999,
˜
p. 9; Throp 1964, p. 127; Uruena et al.
2006, p. 42). Cracids, including the
blue-billed curassow, are considered
particularly vulnerable to hunting
pressures and are among those species
most rapidly depleted by hunting
(Redford 1992, p. 419). Several factors
contribute to the species’ vulnerability
to hunting and collection: their large
size, ease of location during the
breeding season, trusting nature, and
low productivity (1-2 eggs) relative to
other Galliformes (del Hoyo 1994, p.
336). Cracids are also slow to reproduce,
with a replacement rate of at least 6
years (Silva and Strahl 1991, p. 50),
which makes it difficult for the species
to rebound from hunting pressures.
Hunting affects the blue-billed
curassow in all life stages. In 1999,
´
hunters in Antioquıo (where the bluebilled curassow is known on the slopes
´
of the Serranıa de San Lucas and Bajo
´
Cauca-Nechı Regional Reserve area)
reported killing as many as 20 bluebilled curassows within the prior 20
years (Donegan and Salaman 1999, p.
21). In 2004, it was reported that
hunting had abated somewhat, because
productive hunting grounds had become
too remote from villages and because
the communities have access to
domestic meat (Melo and Ochoa 2004,
˜
as cited in Uruena et al. 2006, p. 42).
However, both eggs and chicks continue
to be collected in some areas (such as
´
Serranıa de las Quinchas, where El
´
Paujıl Reserve is located) to be sold at
local markets (Cuervo 2002, p. 139;
˜
Uruena et al. 2006, p. 42), despite
measures to protect the species from
collection (Factor D). In 1999, live
trapped birds (typically chicks) sold for
up to US$100 (greater than the average
monthly income) (Donegan and
Salaman 1999, p. 21). These birds are
either consumed or maintained as
captive animals. The blue-billed
curassow, as well as other cracids (e.g.,
chachalacas (Ortalis spp.) and guans
(Penelope spp.)) serve as a major source
of protein for indigenous people and
attract a great deal of ecotourism
(Brooks and Strahl 2000, p. 8). People
colonizing forested areas capture
juvenile birds as pets and hold them in
captivity in fenced yards or in cages
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(Cuervo and Salaman 1999, p. 8;
Donegan and Salaman 1999, p. 21).
Indigenous people also collect feathers
and other body parts of curassows for
rituals, ornamentation, arrowheads, and
for sale to tourists (Silva and Strahl
1991, p. 38).
Most hunting occurs during the
mating season, when males are more
easily located by their booming mating
calls (Cuervo and Salaman 1999, p. 9;
del Hoyo 1994, p. 336), which can be
heard from up to 500 m (0.31 mi) away
(Ochoa-Quintero et al. 2005, pp. 42, 44).
The direct take of males leads to
disequilibrium of sex ratios for this
species, which forms monogamous pairs
(Cuervo and Salaman 1999, p. 9; Todd
et al. 2008), and it also leads to the
disruption of mating activities (Cuervo
and Salaman 1999, p. 9; del Hoyo 1994,
p. 336). Researchers attribute hunting
pressure as the cause for the near
extinction of the blue-billed curassow
population in the San Salvador Valley
(Strewe and Navarro 2003, p. 32).
Researchers also attribute to hunting the
absence of blue-billed curassows from
parts of its historical range where
suitable habitat (primary forest) still
exists to hunting (Brooks and Strahl
2000, p. 10). In 1998, for instance, no
males were observed during field
surveys, prompting researchers to
conclude that hunting continued to be
a serious risk to the species (BLI 2007d,
p. 3).
Habitat fragmentation and
concomitant human encroachment
(Factor A) have made the species’
habitat more accessible and more
vulnerable to hunting. A study
conducted in French Guiana provided a
quantitative estimate of the effect of
hunting on a related cracid species, the
black curassow (Crax alector) (del Hoyo
1994, p. 336). The black curassow has
similar habitat requirements
(undisturbed primary tropical to
subtropical humid forest at 0-1,400 m
(0-4600 ft) elevation) as the blue-billed
curassow (BLI 2007e). The estimated
population density of black curassows
in non-hunted areas was between 7 and
9 birds per 1 km2 (0.4 mi2); in areas with
intermittent hunting, the numbers fell to
between 0.5 and 2.25 birds; and in areas
where hunting was regular, numbers fell
to between 0.5 and 0.73 birds (del Hoyo
1994, p. 336). We believe that the effects
of hunting on the blue-billed curassow
would result in similar population
reductions based on its similarity of
habitat requirements and life history
traits.
In 1988, Colombia listed the bluebilled curassow in Appendix III of the
Convention on International Trade in
Endangered Species of Wild Fauna and
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Sfmt 4702
Flora (CITES) (UNEP-WCMC 2008c). An
Appendix-III listing requires that: (1) the
listing range country (in this case,
Colombia) must issue an export permit
for all exports of the species; (2)
specimens for these exports must be
legally obtained; (3) live specimens
must be transported such that risk of
injury, damage, and cruelty are
minimized; (4) exports from any other
range countries require a certificate of
origin; and (5) re-exports require a reexport certificate issued by the country
of re-export (UNEP-WCMC 2008a).
According to the World Conservation
Monitoring Centre (WCMC), a total of 12
live birds have been traded
internationally since 1990 (UNEPWCMC 2008e). This trade included
imports of two individuals into the
United States and five birds into Mexico
in the early 1990s. Therefore,
commercial international trade in wild
specimens over the past 20 years has not
been extensive.
The remaining CITES-documented
trade has consisted of exports of
captive-bred specimens from the United
States to Colombia and Belgium. The
blue-billed curassow has been collected
from the wild for use in zoos and in
captive-breeding programs, both
domestically and abroad. A small
number of birds have been collected by
the Cali Zoo and Santa Fe de Medellin
Zoo in Colombia (Cuervo 2002, p. 142),
and small collections are held in the
United States, including the Houston
Zoo and San Diego Zoo, as well as in
Japan and Mexico (Brooks and Strahl
2000, p. 15; Cuervo 2002, p. 142). The
Cali and Houston Zoo collections are
being used for captive breeding, which
we consider vital to conserving and
recovering this species (Factor E).
International trade for zoos and captivebreeding purposes does not contribute
to the endangerment of the species. We
believe that this limited amount of
international trade, controlled via
CITES, is not a threat to the species.
Summary of Factor B
The blue-billed curassow is hunted
and collected from the wild at all life
stages throughout its current range.
Blue-billed curassow eggs and chicks
are collected for food and sale in local
markets, or are often captured and held
in captivity as pets or as a future food
source. Hunting results in the direct
removal of eggs, juveniles, and adults
from the population. Blue-billed
curassows are slow to reproduce,
produce a low clutch size, and exhibit
a poor replacement rate (see Habitat and
Life History). Hunting can destroy pair
bonds and remove potentially
reproductive adults from the breeding
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pool. The species is particularly
vulnerable to hunting and collection
pressures due to the ease in locating this
large bird during its breeding season.
The majority of hunting occurs during
the mating season, when males are
heard calling for females, leading to
disproportionate hunting of males.
Hunting disturbances during the
breeding season disrupt breeding
activities, further compounding the
threats associated with hunting
mortalities. There are continued reports
of hunting pressures on the species;
these pressures have been and continue
to be compounded by ongoing human
encroachment into previously
undisturbed forests (Factor A). Hunting
and collection negatively affect the
global population of the blue-billed
curassow, due to its small population
size and fragmented distribution.
Hunting, combined with habitat
fragmentation (Factor A), increases the
possibility of local extirpation since the
blue-billed curassow is unlikely to reoccupy an area that has been depleted
through hunting because it avoids
crossing large, open areas between
habitat fragments (see Factor E,
Likelihood to Disperse). Therefore, we
find that hunting, collection, and
associated disturbances are threats to
the blue-billed curassow.
C. Disease or Predation
Disease: We are unaware of
information regarding disease or the
potential for significant disease
outbreaks in the blue-billed curassow.
As a result, we do not consider disease
to be a threat to the species.
Predation: According to Delacour and
Amadon (1973), predators of cracids
include snakes (suborder Serpentes),
foxes (family Canidae), wild cats (Felis
silvestris), feral dogs (Canus lupus
familiaris), and raptors (order
´
Falconiformes). Arango-Velez and
Kattan (1997, pp. 137-143) studied nest
predation rates on Andean birds within
fragmented forest habitats of
northwestern Colombia. Although not
specific to the blue-billed curassow, the
study focused on understory nesting
birds with similar nesting habits and in
forest fragment sizes similar to where
the blue-billed curassow is currently
´
found (Arango-Velez and Kattan 1997,
p. 138). The study found that nest
predation by generalist predators is
more prevalent in smaller, isolated
forest patches. However, in the study,
increased predation in smaller habitat
fragments could not be solely attributed
to the ‘‘edge effect,’’ whereby smaller
patch sizes facilitate predators’ access
and ability to capture prey throughout
the fragments. Rather, reduced habitat
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patch sizes caused a shift from larger to
smaller predators, which tended to prey
upon the eggs and juveniles of
understory birds, rendering grounddwelling birds such as blue-billed
curassows particularly susceptible
´
(Arango-Velez and Kattan 1997, pp. 140142). Other studies concerning the
effects of habitat fragmentation on avian
predation show similar results (Hoover
et al. 1995, p. 151; Keyser 2002, p. 186;
Keyser et al. 1998, p. 991; Renjifo 1999,
p. 1133; Wilcove 1985, p. 1214). Gibbs
(1991, p. 157) found that a larger
proportion of ground-nests and elevated
nests were predated in patches smaller
than 1 km2 (0.39 mi2) and that groundnesting birds were predated more
heavily than elevated-nesting birds. In
addition to the importance of patch size
for influencing the level of predation,
the composition of the areas
surrounding the patch is also important
´
(Arango-Velez and Kattan 1997, p. 141).
For instance, in lowland Costa Rica, the
edge effect (where predation is greater at
the edge of forest patches than in the
interior of the patch) was greatest in
forest patches bordered by secondary
growth than by pasture (Gibbs 1991, p.
157).
Summary of Factor C
Snakes, foxes, feral cats, feral dogs,
and raptors are all predators of cracids.
Predation results in the direct removal
of eggs, juveniles, and adults from the
population. Blue-billed curassows are
slow to reproduce, produce a low clutch
size, and exhibit a poor replacement rate
(see Habitat and Life History). Predation
can destroy pair bonds and remove
potentially reproductive adults from the
breeding pool. Studies on similar
species in similar Andean habitats
indicate that vulnerability to predation
by generalist predators increases with
increased habitat fragmentation and
smaller patch sizes. Predation
exacerbates the genetic complications
associated with the species’ small
population size (Factor E). Because of
the species’ small population size and
inability to recolonize isolated habitat
fragments (Factor E), predation renders
the species vulnerable to local
extirpation. Therefore, we find that
predation, compounded by ongoing
habitat destruction (Factor A) and
hunting (Factor B), is a threat to the
blue-billed curassow.
D. The Inadequacy of Existing
Regulatory Mechanisms
Regulatory mechanisms may provide
species-specific or habitat-specific
protections. An evaluation of the
adequacy of regulatory mechanisms
within Colombia to mitigate or remove
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the threats to the blue-billed curassow is
provided below, beginning with speciesspecific and followed by habitat-specific
protection mechanisms.
The Colombian government has
enacted and ratified numerous domestic
and international laws, decrees, and
resolutions for managing and conserving
wildlife and flora (Matallana-T. 2005, p.
121). Colombian Law No. 99 of 1993
(Creating the Ministry of the
Environment and Renewable Natural
Resources and organizing the National
Environmental System (SINA)) sets out
the principles governing environmental
policy in Colombia, and provides that
the country’s biodiversity be protected
and used primarily in a sustainable
manner (EcoLex 1993, p. 2). Resolution
No. 584 of 2002 (Species that are
endangered wildlife in the national
territory) provides a list of Colombian
wildlife and flora that are considered
threatened. Threatened is defined as
those species whose natural populations
are at risk of extinction, as their habitat,
range, or ecosystems that support them
have been affected by either natural
causes or human actions. Threatened
species are further categorized as
critically endangered, endangered, or
vulnerable. A critically endangered
species (CR) is one that faces a very high
probability of extinction in the wild in
the immediate future, based on a drastic
reduction of its natural populations and
a severe deterioration of its range; an
endangered species (EN) is one that has
a high probability of extinction in the
wild in the near future, based on a
declining trend of its natural
populations and a deterioration of its
range; and a vulnerable species (VU) is
one that is not in imminent danger of
extinction in the near future, but it
could be if natural population trends
continue downward and deterioration of
its range continues (EcoLex 2002, p. 10).
The blue-billed curassow is
considered a critically endangered
species under Colombian law pursuant
to paragraph 23 of Article 5 of Law No.
99, as outlined in Resolution No. 584
(EcoLex 2002, p. 12). This status confers
certain protections upon the species.
Resolution No. 849 of 1973 ([Laws
governing] commercial hunting of
´
saınos, boas, anacondas and birds
throughout the country) and Resolution
No. 787of 1977 ([Laws governing] sport
hunting of mammals, birds and reptiles
of wildlife), regulate and prohibit
commercial and sport hunting of all
wild bird species, respectively, except
those specifically identified by the
Ministry of the Environment or
otherwise permitted (EcoLex 1973, p.1;
EcoLex 1977, p. 3). Because of its status
as a critically endangered species, the
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Ministry of the Environment does not
permit the blue-billed curassow to be
hunted commercially or for sport.
Neither Resolution prohibits subsistence
hunting. As discussed under Factor B,
commercial and sport hunting are not
threats to this species, but subsistence
hunting continues to threaten the
species throughout its range, including
within protected areas. Thus, these
Resolutions are ineffective at reducing
the existing threat of subsistence
hunting to the blue-billed curassow.
Additional efforts to protect the
species from subsistence hunting are
´
inadequate. Within El Paujıl Reserve, for
instance, there are penalties for shooting
or trapping the species (BLI 2007d, p. 3).
However, as recently as 2006, it was
reported that both chicks and eggs
´
continued to be collected in the Serranıa
de las Quinchas region, where the
Reserve is located, for domestic use and
for sale at local markets (Cuervo 2002,
˜
p. 139; Uruena et al. 2006, p. 42) (Factor
B). Thus, private efforts to protect the
species from hunting appear to be
inadequate within a region where
national laws are ineffective at
protecting the species from such take.
The blue-billed curassow is listed in
Appendix III of CITES (see Factor B).
CITES is an international treaty among
174 nations, including Colombia (which
became a Party in 1981) and the United
States (which became a Party in 1975)
(UNEP-WCMC 2008a, p. 1). In the
United States, CITES is implemented
through the U.S. Endangered Species
Act (Act). The Act designates the
Secretary of the Interior as the Scientific
and Management Authorities to
implement the treaty, with all functions
carried out by the Service. Under this
treaty, countries work together to ensure
that international trade in animal and
plant species is not detrimental to the
survival of wild populations, by
regulating the import, export, re-export,
and introduction from the sea of CITESlisted animal and plant species (USFWS
2008, p. 1). As discussed under Factor
B, we do not consider commercial
international trade to be a threat
impacting the blue-billed curassow.
Colombia has numerous laws and
regulations pertaining to forests and
forestry management, including: the
Forestry Law of 1959 (Law 2 – [On]
forest economy [of the] nation and
conservation [of] renewable natural
resources) (EcoLex 1959); the Forestry
Code of 1974 (Decree 2,811 – National
code of renewable natural resources and
protection of the environment) (Faolex
1974), and the forest plan of 1996
(Decree 1,791 – Forest Improvement
Plan) (Faolex 1996). A new forest law
was developed and approved in 2006
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(Law No. 1,021, General [Forestry] Law).
The new law seeks to: (1) further
promote forest plantations and create
financial mechanisms for investments,
(2) provide for rigorous control and
expanded sustainable use of natural
forests, (3) and regulate and further
develop forest concessions in the
country (International Tropical Timber
Organization (ITTO) 2006, p. 218).
However, the ITTO considers the
Colombian forestry sector to be lacking
in law enforcement and on-the-ground
control of forest resources, with no
specific standards for large-scale
forestry production, no forestry
concession policies, and a lack of
transparency in the application of the
various laws regulating wildlife and
their habitats (ITTO 2006, p. 222).
Resource management in Colombia is
highly decentralized. Resources are
managed within local municipalities by
one of 33 Autonomous Regional
Corporations known as CARs
´
(Corporaciones Autonomas Regionales)
(Matallana-T. 2005, p. 121). CARs are
corporate bodies of a public nature,
endowed with administrative and
financial autonomy to manage the
environment and renewable natural
resources (Law 99 of 1993). The bluebilled curassow is currently known to
occur within seven different
Departments, each of which is managed
by a separate local entity. These
corporations grant concessions, permits,
and authorizations for forest harvesting
(ITTO 2006, p. 219). Forty percent of
Colombia’s public resources are
managed by local municipalities,
making Colombia one of the most
decentralized countries in terms of
forestry management in Latin America
(Matallana-T. 2005, p. 121). Monitoring
of resource use and forest development
authorized by these corporations is
conducted mostly by local
nongovernmental organizations.
Governmental institutions responsible
for oversight appear to be
underresourced and unable to maintain
an effective presence in the field (ITTO
2006, p. 222). Consequently, there is no
vehicle for overall coordination of
species management for
multijurisdictional species such as the
blue-billed curassow. The private
Proaves-Colombia Foundation plans to
generate a national strategy for the
conservation of the blue-billed curassow
through the project, ‘‘Saving the Bluebilled Curassow’’ (Quevedo et al. 2005,
˜
as cited in Uruena et al. 2006, p. 42). In
2004, this project evaluated and
´
prioritized threats in Serranıa de las
Quinchas region (Machado 2004, as
˜
cited in Uruena et al. 2006, p. 42),
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assessed population density and
˜
structure (Arias 2005, as cited in Uruena
et al. 2006, p. 42), studied habitat use
´
and behavioral aspects in Paujıl de Pico
˜
Bird Reserve (Uruena 2005, as cited in
˜
Uruena et al. 2006, p. 42), and promoted
an environmental education campaign
´
and the creation of El Paujıl Bird
˜
Reserve (Uruena and Quevedo 2005, as
˜
cited in Uruena et al. 2006, p. 42).
However, a national strategy for the
conservation of blue-billed curassows is
not currently in place, and it is unclear
if or when it will be enacted, and
whether the Colombian government will
adopt the strategy. Therefore, we are
unable to determine that this
conservation strategy will mitigate
threats to the blue-billed curassow.
Currently there are approximately 49
nationally recognized protected areas in
Colombia (Matallano-T. 2005, p. 121).
The five most common categories of
habitat protection are: (1) National
Natural Park (an area whose ecosystems
have not been substantially altered by
human exploitation or occupation, and
where plant and animal species, or
complex geomorphological landscapes
have historical, cultural, scientific,
educational, aesthetic, or recreational
value); (2) Wildlife Sanctuary for Fauna
and Flora (an area dedicated to preserve
species or communities of wildlife, and
to conserve genetic resources of
wildlife); (3) National Natural Reserve
(an area that preserves flora and fauna
and is established for the study of its
natural wealth); (4) Panoramic Park (a
parcel of land of panoramic, cultural or
natural value preserved for education
and relaxation); and (5) Unique National
Area (a rare or unique ecosystem)
(Matallano-T. 2005, p. 121). Several
areas considered to be important refuges
for the blue-billed curassow are
protected areas and are managed by
autonomous corporations, including: (1)
The Paramillo National Natural Park
´
´
(Antioquıa and Cordoba Departments)
´
and (2) The Bajo Cauca–Nechı Regional
´
´
Natural Reserve (Antioquıa and Cordoba
Departments) (BLI 2007d, p. 3; Cuervo
2002, p. 139), both of which are
managed by Corantioquia (Corantioquia
2008, p. 1).
(1) The Paramillo National Natural
´
´
Park (Antioquıa and Cordoba
Departments) is a large Park, but no
protective measures have been
implemented to curb human impacts on
the habitat and species by the
indigenous and farming residents
within the park (BLI 2007a, pp. 1-2; BLI
2007d, p. 3) (Factor A). Cocaine
cultivation is occurring within the Park
boundaries (UNODC and GOC 2005, p.
´
45). Dam construction on the Sinı River,
part of the species’ historic range (BLI
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2007a, p. 1; Cuervo and Salaman 1999,
p. 7; del Hoyo 1994, p. 361), has caused
ongoing flooding in the area since its
completion in 1998 (Cuervo 2002, p.
139; NGO Working Group on Export
Development Canada 2003, p. 31). Thus,
the designation of this area as a Park has
not mitigated human-induced habitat
destruction (Factor A).
´
(2) The Bajo Cauca-Nechı Regional
´
´
Natural Reserve (Antioquıa and Cordoba
Departments) encompasses suitable
habitat for the blue-billed curassow, but
the species has not been confirmed
within the Reserve (BLI 2007d, p. 3).
Nonetheless, it is notable that this
Reserve, which is designated to preserve
and research flora and fauna, allows
´
logging (Fundacion Viztaz 2007, p. 2).
Thus, should the species be located
therein, this Reserve’s designation as a
preserve would not mitigate the threat
from habitat destruction (Factor A).
´
The privately-owned El Paujıl Bird
Preserve, which was established
specifically to protect the blue-billed
curassow and its habitat (BLI 2007d, p.
2) (Factor A), has measures in place to
penalize shooting or trapping the
species (BLI 2007d, p. 3). However, egg
and chick collection are ongoing within
´
the Serranıa de las Quinchas area,
where the private reserve is located
(Factor B). Aside from the Paramillo
National Park, which includes habitat in
the upper elevational limit of the bluebilled curassow’s preferred range
(Cuervo 2002, p. 140), no effective
protective measures have been
undertaken (BLI 2007d, p. 2; Brooks and
Gonzalez-Garcia 2001, p. 183) such that
the regulatory mechanisms in place in
these protected areas do not mitigate
habitat destruction, which is a primary
risk factor for this species (Factor A).
Thus, these protected areas do not
provide sufficient protections to
mitigate the effects from habitat loss
(Factor A) or reduce threats from
hunting and collection (Factor B).
Summary of Factor D
Colombia has numerous laws and
regulatory mechanisms intended to
protect and manage wildlife and their
habitats. The blue-billed curassow is
considered critically endangered under
Colombian law and lives within several
managed forests or protected areas.
However, on-the-ground enforcement of
existing wildlife protection and forestry
laws and oversight of the local
jurisdictions implementing and
regulating activities are ineffective at
mitigating the primary threats to the
blue-billed curassow. As discussed for
Factor A, habitat destruction,
degradation, and fragmentation
continue throughout the existing range
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32317
Small Population Size: Deforestation
and habitat loss throughout the bluebilled curassow’s historic range has
resulted in fragmented, disjunct, and
isolated populations in the remaining
four or five patches of tropical humid
and premontane forests and caused
regional extirpations of the blue-billed
curassow (Brooks and Gonzalez-Garcia
2001, p. 183; Collar et al. 1992, pp. 6162; Cuervo and Salaman 1999, p. 7). It
is estimated that the largest
´
subpopulation (in the Serranıa de las
´
Quinchas, Boyaca Department) contains
between 250 and 999 birds (BLI 2007d,
p. 2), and that the total population is
much fewer than 2,000 individuals
(Brooks and Gonzalez-Garcia 2001, p.
184). Cuervo (2002, p. 141) estimated
that the species had lost more than half
of its population over the last three
generations, or 30 years. Further, it is
estimated that, at the current rate of
decline, the blue-billed curassow could
lose up to 79 percent of its current
population within the next 10 years and
could be extinct within the next three
generations, or 30 years (BLI 2007d, p.
3; Cuervo 2002, p. 141).
E. Other Natural or Manmade Factors
The blue-billed curassow’s restricted
Affecting the Continued Existence of the and fragmented range, combined with
Species
its small population size (Cuervo 2002,
p. 138; Cuervo and Salaman 1999, p. 7;
Three additional factors affect the
del Hoyo 1994, p. 361), makes the
blue-billed curassow: its limited ability
species particularly vulnerable to the
to disperse to unoccupied habitat, the
threat of adverse genetic effects and
species’ small population size and
susceptible to extinction through
captive-breeding programs.
natural or manmade events that destroy
Likelihood to Disperse: The blueindividuals and their habitat (BLI
billed curassow exhibits several
2007d, pp. 1-2; Brooks and Gonzalezcharacteristics that make it unlikely that Garcia 2001, pp. 185-190; Cuervo 2002,
the species would disperse into isolated p. 140). Meta-population analysis
habitat fragments to repopulate
involves the study of the dynamics of an
extirpated patches of suitable habitat.
entire population by studying
The blue-billed curassow requires a
movements within local populations
large home range of primary tropical
(Hanski 1998, p. 41). ‘‘A metaforest (Cuervo 2002, pp. 138-140). The
population composed of extinctionhabitat patches within the blue-billed
prone local populations in a small patch
curassow’s current range are described
network is necessarily more threatened
by researchers as fragmented, disjunct,
than are meta-populations in large and
and isolated (Collar et al. 1992, p. 154;
well connected networks’’ (Hanski 1998,
Cuervo and Salaman 1999, p. 7; del
p. 42). Considering that not all blueHoyo 1994, p. 361; Donegan and
billed curassow individuals in a
Huertas 2005, p. 29; Salaman et al. 2001, population are breeding at any one time,
p. 183). The species will rarely cross
the actual number of individuals
narrow deforested corridors, such as
contributing to population growth will
those caused by roads or oil pipelines,
be a smaller number than the total
and it will not cross large open areas
number of individuals.
between forest fragments (Cuervo and
Small population sizes render species
Salaman 1999, p. 7). In addition to the
vulnerable to any of several risks,
species’ small overall population size
including loss of genetic variation,
(see below), researchers believe it is
inbreeding depression, and
unlikely that the blue-billed curassow
accumulation of deleterious genes.
would repopulate an isolated patch of
Inbreeding can have individual or
suitable habitat following decline or
population-level consequences either by
extirpation of the species from that
increasing the phenotypic expression
patch (Cuervo and Salaman 1999, p. 7;
(the outward appearance or observable
Hanski 1998, pp. 45-46) (see Factor E,
structure, function, or behavior of a
Captive Breeding Program).
living organism) of recessive,
of the blue-billed curassow. As
discussed for Factor B, uncontrolled
hunting and commercial use of the bluebilled curassow are ongoing and
continue to negatively affect the
continued existence of the species.
Moreover, the lack of a species
conservation strategy and the
decentralized management of natural
resources in Colombia provide no
overall coordination in the conservation
for species such as the blue-billed
curassow, which ranges in multiple
jurisdictions. Despite ongoing work
toward developing a national
conservation strategy for the species, it
has not yet been developed, it is not
known whether it will be formally
adopted by the Government of
Colombia, and we are unable to
determine that the strategy will be
effective in reducing the threats to this
species on a local or rangewide basis.
Therefore, we find that the existing
regulatory mechanisms currently in
place for the blue-billed curassow do
not reduce or remove the factors
threatening the species.
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deleterious alleles or by reducing the
overall fitness of individuals in the
population (Charlesworth and
Charlesworth 1987, p. 238; Shaffer 1981,
p. 131). Small, isolated populations of
wildlife species are also susceptible to
demographic problems (Shaffer 1981, p.
131), which may include reduced
reproductive success of individuals and
chance disequilibrium of sex ratios.
Chance disequilibrium of sex ratios
would be further exacerbated by
preferential hunting of male birds
(Factor B). This species’ risk of
extinction is further compounded by
ongoing collection of eggs and chicks,
and by hunting-related disturbances that
may disrupt breeding pairs (Factor B).
Once a population is reduced below a
certain number of individuals, it tends
to rapidly decline towards extinction
(Franklin 1980, pp. 147-148; Gilpin and
´
Soule 1986, p. 25; Holsinger 2000, pp.
´
64-65; Soule 1987, p.181).
Captive-Breeding Program: A captivebreeding program is being developed
within the species’ range (see Current
Range and Distribution, above)by
´
Fundacion Ecolombia, based at the
Wildlife Rehabilitation Centre in Los
´
Farallones (Antioquıa Department,
Colombia). The captive-held population
includes three males and two females.
The program has met with little success
because attempts to breed the species in
captivity have been unsuccessful to date
(two sterile eggs laid in 2003 and none
since). The species is historically known
to be a poor breeder in captivity (Throp
1964, p. 127). The program is exploring
artificial insemination for future
breeding (Wildlife Protection
Foundation (WPF) 2007, p. 2). The
Houston Zoo, however, which has
maintained cracids since the 1960s, has
bred the species for 30 years and has
successfully raised at least 10 bluebilled curassows in captivity (Houston
Zoo 2008, p. 2; Todd et al. 2008, p. 1).
The Houston Zoo also conducts
outreach and breeding research. While
this has resulted in limited exports of
captive-bred birds for scientific
purposes (i.e., to zoos; see also Factor
B), the number of birds in captivity has
dropped worldwide. In addition, the
number of specimens originally
imported into the United States was
small (Houston Zoo 2008, p. 2), which
would limit their conservation value for
reintroduction into the wild. Thus, the
captive breeding program is not
currently contributing to reintroduction,
but serves a conservation value by
providing specimens for zoos that
conduct outreach and breeding research.
Further, reintroduction would appear to
be important for recovery of this species
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because the species is not likely to
disperse into or repopulate suitable
habitat on its own.
Summary of Factor E
The blue-billed curassow’s small
population size increases its
vulnerability to genetic risks associated
with small population sizes that
negatively impact the species’ long-term
viability and increase the possibility of
localized extirpations of the remaining
fragmented populations. Further, the
species is unlikely to repopulate areas of
suitable habitat from which a
subpopulation has been extirpated
because it avoids crossing the disturbed
areas that separate the remaining
suitable habitat for this species. Rangecountry attempts at captive breeding
have been unsuccessful, and the stock
in U.S. captive-breeding programs is
limited; therefore, the captive-breeding
program is not contributing to
reintroduction of the species in the wild
and so is not currently mitigating the
problem of small population size.
Therefore, we believe that, in
combination with the risks to the
species from habitat destruction (Factor
A), hunting (Factor B), and predation
(Factor C), the blue-billed curassow is
vulnerable to localized extirpation or
extinction from which the species
would be unable to recover, due it its
small population size and apparent
inability to repopulate fragmented,
isolated habitats such as those currently
present within this species’ range.
Status Determination for the Blue-Billed
Curassow
The five primary factors that threaten
the survival of the blue-billed curassow
are: (1) habitat destruction,
fragmentation, and degradation (Factor
A); (2) overexploitation due to hunting
and collecting of eggs and chicks (Factor
B); (3) predation (Factor C); (4)
inadequacy of regulatory mechanisms to
reduce the threats to the species (Factor
D); and (5) small population size and
isolation of remaining populations
(Factor E).
The direct loss of habitat through
widespread deforestation and
conversion of primary forests to human
settlement and agricultural uses has led
to the fragmentation of habitat
throughout the range of the blue-billed
curassow and isolation of the remaining
populations (Factor A). The species’
historic range, which encompassed
approximately 106,700 km2 (41,197
mi2), has been reduced to 2,090 km2
(807 mi2). Experts estimate that 88
percent of this habitat loss has occurred
within the last three generations, or 30
years. The best available information
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indicates that the species’ population
was reduced by 50 percent in the 30
years prior to 2002 and that ongoing
habitat destruction and degradation are
continuing at a rate that would lead to
the extinction of the blue-billed
curassow in the next 30 years if
measures are not taken to ameliorate the
loss of habitat. Thus, habitat loss poses
an imminent threat of extinction and is
a factor that currently endangers the
species.
The blue-billed curassow is hunted or
collected, whole or in parts, in all life
stages (eggs, juveniles, adults, feathers,
and other body parts) throughout its
current range by both indigenous people
and by local settlers for both sustenance
and sport; for domestic use in rituals;
and for sale to tourists (Factor B).
Several life-history traits of the species
contribute to its vulnerability to hunting
and collection: its large size, ease of
location during breeding season,
trusting nature, low productivity (1-2
eggs), and a replacement rate of 6 years
(taking an individual of the species an
average of 6 years to replace itself).
Adults are hunted mainly during the
breeding season, when males are most
vulnerable and more easily located by
their loud mating calls that are audible
at long distances. The direct take of
males disrupts sex ratios in this species,
which forms monogamous pairs, and
this take also disrupts mating activities.
Hunting pressure has caused severe
depletion or near extirpation in portions
of its historical range, despite the
continued availability of suitable habitat
(primary forest). The effects of hunting
are exacerbated by ongoing habitat
fragmentation (Factor A), which
increases accessibility into the species’
habitat, rendering it more vulnerable to
hunting. Concomitantly, increased
conversion of primary forest habitat has
encouraged further human settlement
within the blue-billed curassow’s
habitat. Hunting poses an imminent
threat of extinction and is a factor that
currently endangers the species.
Blue-billed curassows are vulnerable
to predation by generalist predators,
including snakes, foxes, feral cats, feral
dogs, and raptors (Factor C). Habitat
fragmentation (Factor A) contributes to
this vulnerability, because research
indicates that predation increases with
increased habitat fragmentation and
smaller patch sizes. Predation leads to
the direct removal of eggs, juveniles,
and adults from the population,
exacerbating risks associated with the
species’ small population size (see
below). Predation can destroy pair
bonds and remove potentially
reproductive adults from the breeding
pool. The blue-billed curassow is slow
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to reproduce and produces a low clutch
size, and predation exacerbates this
species’ already poor replacement rate
(see Habitat and Life History).
The threats from habitat destruction,
hunting, and predation are compounded
by the species’ small population size
(Factor E). The blue-billed curassow’s
population has been reduced by 50
percent within the last 30 years. The
species’ low population estimate of
fewer than 2,000 individuals, combined
with its restricted, fragmented, and
isolated habitat, makes the species
particularly vulnerable to numerous
human factors (e.g., agricultural
development, armed conflict, fire, dams
and reservoir development, increased
human settlement, illicit drug
production and control, mining
activities, oil development and
distribution, and road development).
Further, the species’ reticence to cross
large open areas makes it unlikely that
the species would repopulate suitable
habitat in remaining isolated forest
patches that are separated by large
distances, all of which put the species
at a risk of extinction.
Finally, despite numerous laws and
regulatory mechanisms (Factor D) to
administer and manage wildlife and
their habitats, on-the-ground
enforcement of these laws and oversight
of the local jurisdictions implementing
and regulating activities within the
species’ habitat are inadequate to
mitigate the effects of habitat loss
(Factor A) and hunting (Factor B).
Habitat destruction and hunting
continues within the species’ range and,
´
aside from El Paujıl Bird Preserve, no
other areas provide effective protective
measures for protecting the blue-billed
curassow from ongoing hunting or its
habitat from ongoing destruction.
We have carefully assessed the best
available scientific and commercial
information regarding the past, present,
and potential future threats faced by the
blue-billed curassow. We consider the
ongoing threats to the blue-billed
curassow, habitat destruction (Factor A),
hunting (Factor B), and predation
(Factor C), exacerbated by the species’
small population size and limited
dispersal ability (Factor E), and
compounded by inadequate regulatory
mechanisms to mitigate these threats
(Factor D), to be equally present and of
the same magnitude throughout the
species’ entire current range. Based on
this information, we determine that the
blue-billed curassow is endangered
throughout its range. Therefore, we are
proposing to list the blue-billed
curassow as an endangered species.
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II. Brown-Banded Antpitta (Grallaria
milleri)
Species Description
The brown-banded antpitta is a
member of the Ground-Antbird Family
(Formicariidae), is approximately 18 cm
(7 in) long from bill to tail, and endemic
to the west slope of the central Andes
of Colombia (Krabbe and Schulenberg
¨
2003, p. 682; Fjeldsa and Krabbe 1990,
p. 414; Hilty and Brown 1986, p. 422).
The species is locally known as
´
‘‘Tororoi’’ (Beltran and Kattan 2002).
This bird is a uniform dark brown, with
a dingy white throat and underbelly.
Taxonomy
The brown-banded antpitta was first
taxonomically described by Chapman in
1911 and placed in the Ground-Antbird
Family (Formicariidae). The type
specimen (the actual specimen that was
first described by Chapman) was
´
obtained from Laguneta (Quindıo
´
Department) (Beltran and Kattan 2002,
p. 327). Laguneta is, therefore, referred
to as the ‘‘type locality.’’
Habitat and Life History
The brown-banded antpitta currently
inhabits the humid understory and
forest floor habitats of mid-montane and
cloud forests between 2,400 and 2,600
m (7,874 and 8,530 ft) with high density
of herbaceous plants and shrubs (Krabbe
and Schulenberg 2003, p. 719; Kattan
´
and Beltran 1999, p. 272). The species
has been observed in older (30–year-old)
secondary-growth forest habitats and
alder (Alnus acuminata) plantations
(Cuervo 2002, pp. 326-327; Krabbe and
Schulenberg 2003, p. 719).
Researchers consider antpitta life
histories to be among the least known of
Neotropical bird species (Dobbs et al.
2001, p. 225). The brown-banded
antpitta, as with other antpittas, is a
secretive species, with a low population
density and high habitat specificity
´
(Kattan and Beltran 2002, p. 232).
Antpittas are considered to be nearly
flightless (Krabbe and Schulenberg
2003, p. 698) and their dispersal
capabilities are not well known (Cuervo
2002, p. 327), except that one banded
individual traveled a distance of 0.041
´
km2 (0.02 mi2) (Kattan and Beltran 2002,
p. 234). This ground-dwelling species
´
lives either singly or in pairs (Beltran
and Kattan 2002, p. 327) and has a high
territorial fidelity (Cuervo 2002, p. 327).
It can be seen running along the forest
floor picking up prey (Krabbe and
Schulenberg 2003, p. 719), which
apparently consists of beetles
(Coleoptera spp.) and earthworms.
Nothing is known about the brownbanded antpitta’s reproductive ecology,
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32319
except that its peak reproductive period
´
is between March and May (Beltran and
Kattan 2002, pp. 326-327) and that both
parents feed the young (del Hoyo 2003,
p. 719). Drawing from studies on similar
species, including the Colombian
species, scaled antpitta (Grallaria
guatimalensis) and chestnut-crowned
antpitta (Grallaria ruficapilla), antpittas
tend to nest on fallen logs, on the forks
of tree trunks, or atop the crowns of
low-growing palms, situated at nearly
groundlevel to no higher than 3 m (10
ft) off the ground (Dobbs et al. 2001, p.
226; Wiedenfeld 1982, p. 581). The
typical clutch size for antpittas is
considered to be two eggs (Dobbs et al.
2001, p. 227; Wiedenfeld 1982, p. 581).
Antpitta nests are roughly circular cups,
loosely constructed of dead leaves that
are generally hard to distinguish from
the surroundings (Dobbs et al. 2001, p.
227; Wiedenfeld 1982, p. 581). Antpittas
appear to rely on camouflage, both to
hide the location of their nests
(Wiedenfeld 1982, p. 580), as well as in
response to disturbance, when birds
remain absolutely still to avoid
detection by potential predators (Dobbs
et al. 2001, p. 226).
Historical Range and Distribution
The brown-banded antpitta was
historically known from a single
location, near Laguneta in the central
Andes (centrally located in the
´
Department of Quindıo), which ranges
in altitude from 1,859 m (6,100 ft) in the
surrounding valleys to 3,140 m (10,300
ft) at its highest point (Chapman 1917,
pp. 35-36, 396). In 1917, the valley
leading to Laguneta was described as
gently rising until about 2,530 m (8,300
ft), when the terrain rose steeply up to
2,896 ft (9,500 ft). The vegetation was
described as open, with scattered palms
and little other vegetation until about
2,835 m (9,300 ft), where the forest
began (Chapman 1917, p. 36). At 3,140
m (10,300 ft), the forest was described
as dense with little undergrowth, except
in occasional clearings dominated by
dense shrubs so thick as to be
impenetrable without a knife (Chapman
1917, p. 35). Eleven specimens were
collected between 1911 and 1942; the
species was last observed and
collections were made at the type
´
locality at Laguneta in 1942 (Beltran and
Kattan 2002, p. 325; Collar et al. 1992,
p. 698).
Chapman (1917, p. 36) described the
practice of slash-and-burn agriculture
around Laguneta in 1917, noting that
much of the hillside between 2,530 and
2,835 m (8,300-9,300 ft) was bare and
close-cropped, having been burned and
cleared. By 1994, the forested area
providing habitat for the brown-banded
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antpitta in and around the type locality
near Laguneta had been mostly
destroyed (Collar et al. 1994, p. 136),
and despite subsequent surveys (in
1986, 1988, and 1991), the species was
not observed there. In 1992, researchers
considered the brown-banded antpitta
to be locally extirpated, if not extinct
throughout its range (Collar et al. 1992,
p. 689; Cuervo 2002, pp. 326-327;
´
Kattan and Beltran 1997, pp. 367-369).
Although the brown-banded antpitta
was rediscovered in 1994 (Kattan and
´
Beltran 1997, pp. 367-369), researchers
continue to consider the species to be
locally extinct (extirpated) from its type
´
locality of Laguneta (Quindıo
´
Department) (Beltran 2002 in litt., as
´
cited in Beltran and Kattan, p. 327) due
´
to extensive deforestation (Beltran and
Kattan 2002, p. 327).
Current Range and Distribution
The current range of the brownbanded antpitta is described as humid
understory and forest floors of midmontane and cloud forests, preferring
altitudes between 2,400 and 2,600 m
(7,874 and 8,530 ft), in areas with a high
density of herbs and shrubs (Krabbe and
Schulenberg 2003, p. 719; Kattan and
´
Beltran 1999, p. 272). The current range
is estimated to be 300 km2 (116 mi2)
(BLI 2007f, p. 1). The species is known
today from only three areas in the upper
´
Rıo Magdalena valley. The first area is
the humid forests in the Central Andes
´
of Colombia’s Ucumarı Regional Park
(Risaralda Department), where it was
´
first sighted in 1994 (Kattan and Beltran
1997, pp. 369-370) and recently
´
observed in 2000 (Beltran and Kattan
2002, p. 326). The site is approximately
´
44 km2 (17 mi2) in the Otun River
´
watershed (Kattan and Beltran 1999, p.
273). The second areas is the south-east
´
´
slope of Volcan Tolima in the Rıo Toche
Valley on private land (the house of La
Carbonera) (Tolima Department), where
it was first observed in 1998 and
´
recently observed in 2000 (Beltran and
Kattan 2002, p. 325). This location is
0.05 km2 (0.02 mi2) in size at elevations
ranging from 2,750 to 2,900 m (9,022 to
´
9,514 ft) (Beltran and Kattan 2002, p.
´
326). The third area is the Rıo Blanco
river basin (Caldas Department), where
it was most recently observed in 2000
´
(Beltran and Kattan 2002, p. 326). This
site is a strip of land less than 200 linear
km (124 linear mi) on the Central
Cordilla, between 2,300 and 3,100 m
(7,546 and 10,171 ft) in elevation (BLI
´
2004c, p. 2; Kattan and Beltran 2002, p.
238). Experts consider the most
important refuges for this species to be:
´
(1) the Ucumarı Regional Park
´
(Risaralda Department), (2) the Rıo
´
Toche Valley (Tolima), (3) the Rıo
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15:11 Jul 06, 2009
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Blanco river basin (Caldas Department),
˜
and (4) the Reserve of Canon and
´
Quindıo Departments, where suitable
habitat exists but the species may be
extirpated. These refugia are further
discussed under Factor A, below.
Population Estimates
There have been few quantitative
surveys of the brown-banded antpitta.
Available population information is
provided for the four areas considered
to be important refugia for the species
(as discussed in Factor A). The
´
population located within the Ucumarı
Regional Park has been surveyed twice.
In the first survey, conducted from 1994
to 1997, 11 brown-banded antpittas
were captured and banded. In a
subsequent survey of a 0.17-1-km2´
(0.07-0.62-mi2) area within the Ucumarı
Regional Park during 1995-2000, Kattan
´
and Beltran (2002, p. 232-3) captured
and banded 36 brown-banded antpittas.
Based on these surveys, the
subpopulation within the 0.63 km2 (0.24
mi2) Park was estimated to include up
to 106 individuals, averaging to
approximately 1.3 individuals per 0.01
´
km2 (0.004 mi2) (Kattan and Beltran
´
1997, pp. 367-369; Kattan and Beltran
1999, p. 276). Thus, this subpopulation
contains at least 36, and possibly as
many as 106 individuals.
Qualitative surveys conducted from
´
1998 to 2000 in the Rıo Toche Valley
determined that the brown-banded
´
antpitta is uncommon and local (Beltran
and Kattan 2002, p. 326). One
individual was observed in 1999
´
(Cuervo in litt., as cited in Beltran (2002
p. 326). There is no information on the
estimated population size of brown´
banded antpitta within the Rıo Toche.
Thus, this subpopulation contains at
least one individual, but there is no
estimate of the upper limit of the
population.
´
A census of the population in the Rıo
Blanco river basin was undertaken in
June 2000, within an approximately 5km (3-mi) transect. Researchers inferred
the presence of at least 30 individuals,
based on vocalizations they elicited in
response to recordings of the species’
´
alarm call (Beltran and Kattan 2002, p.
326). There is no information on the
estimated population size of brown´
banded antpitta within the Rıo Blanco
area. Thus, this population may contain
30 individuals, but the upper limit of
the population estimate is unknown.
The species is not currently known to
˜
inhabit the Reserve del Canon del
´
Quindıo. Although the species was
observed there in 1911 and 1942
´
(Beltran and Kattan 2002, p. 325; Collar
et al. 1992, p. 698) and the area contains
suitable habitat, the species has not
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´
been observed there since 1942 (Beltran
and Kattan 2002, p. 235).
The IUCN estimates that the largest
subpopulation contains 424 individuals
(BLI 2007f, p. 4), but it is unclear as to
which subpopulation this estimate
refers. The global population of brownbanded antpitta is estimated by the
IUCN to be larger than 250 individuals,
but not more than 999 birds (BLI 2007f,
p. 1), equating to approximately 338 to
756 individuals (BLI 2007f, p. 4). It is
estimated that the species has lost up to
9 percent of its population in the last 10
years, or 3 generations, and that this rate
of decline will continue over the next 10
years (BLI 2007f, p. 4). Additional
information on the population size of
this species is provided in the
discussion of Factor E, below.
Conservation Status
The brown-banded antpitta is
identified as an endangered species
under Colombian law pursuant to
paragraph 23 of Article 5 of the Law 99
of 1993, as outlined in Resolution No.
584 of 2002 (EcoLex 2002, p. 12). The
IUCN has classified the species as
‘‘Endangered’’ since 1994 because it is
known from very few locations and
occupies a very small range (BLI 2004c,
p. 1).
Summary of Factors Affecting the
Brown-Banded Antpitta
A. The Present or Threatened
Destruction, Modification, or
Curtailment of the Habitat or Range
The brown-banded antpitta inhabits
the humid understory and forest floor
habitats of mid-montane and cloud
forests between 1,800 and 2,600 m
(5,905 and 8,530 ft) that have a high
density of herbs and shrubs (Krabbe and
Schulenberg 2003, p. 719; Kattan and
´
Beltran 1999, p. 272). The current range
is estimated to be 300 km2 (116 mi2)
(BLI 2007f, p. 1), and the species is
known today in only three locations: (1)
´
Urcumaı Regional Park (Kattan and
´
Beltran 1997, pp. 369-370) (Risaralda
Department), (2) the south-east slope of
´
´
Volcan Tolima in the Rıo Toche Valley
´
(Tolima Department), and (3) the Rıo
Blanco catchment (Caldas Department).
These locations are discussed further
under Refugia, below.
Deforestation rates and patterns:
Colombia has experienced extensive
deforestation in the last half of the 20th
Century as a result of habitat conversion
for human settlements, road building,
agriculture, and timber extraction. A
23–year study, from 1973 to 1996,
demonstrated that these activities
reduced the amount of primary forest
cover in Colombia by approximately
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3,605 hectares (ha) (8,908 acres (ac))
annually, representing a nearly onethird total loss of primary forest habitat
˜
(Vina et al. 2004, pp. 123-124).
Beginning in the 1980s, habitat loss
increased dramatically as a result of
influxes of people settling in formerly
pristine areas (Perz et al. 2005, pp. 26˜
28; Vina et al. 2004, p. 124). More recent
studies indicate that the rate of habitat
destruction is accelerating. Between the
years 1990 and 2005, Colombia lost
approximately 52,800 ha (130,471 ac) of
primary forest annually (Butler 2006a,
pp. 1-3; FAO 2003a, p. 1). Human
activities, such as encroachment,
cultivation, grazing, and infrastructural
development, have resulted in extensive
deforestation and environmental
´
degradation of primary forests in the Rıo
Magdalena valley, part of the brownbanded antpitta’s range (Cuervo and
Salaman 1999, p. 8; Ocampo and Botero
2000, pp. 76-78). These studies and
activities in Colombia are described in
greater detail above for the blue-billed
curassow (Factor A, Deforestation Rates
and Patterns).
A study conducted on the effects of
habitat fragmentation on Andean birds
within western Colombia determined
that 31 percent of the historical bird
populations in western Colombia had
become extinct or locally extirpated by
1990, largely as a result of habitat
fragmentation from deforestation and
human encroachment (Kattan and
´
Alvarez-Lopez 1996, p. 5; Kattan et al.
1994, p. 141). Deforestation has led to
local extirpation of the brown-banded
antpitta in its type locality, near
´
Laguneta in the central Andes (Quindıo
Department), where the natural
vegetation has been reduced to 10
´
percent of its former area (Beltran 2002
´
in litt., as cited in Beltran and Kattan,
p. 327). Deforestation continues in midmontane and cloud forests in the
Departments Caldas and Risaralda,
where this species has been observed
(Dolphijn 2005, p. 2). Human
encroachment and ongoing
deforestation throughout this species’
current range are discussed under
Refugia, below.
In addition to the direct detrimental
effect of habitat loss, there are several
indirect effects of habitat disturbance
and fragmentation (Brooks and Strahl
2000, p. 10; Silva and Strahl 1991, p.
38). Roads create barriers to animal
movement, expose animals to traffic
hazards, and increase human access into
habitat, facilitating further exploitation
and habitat destruction (Hunter 1996,
158-159). Researchers have observed
that road building and other
infrastructure improvements in
previously remote forested areas have
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increased accessibility and facilitated
further habitat destruction, exploitation,
´
and human settlement (Alvarez 2005, p.
´
´
2042; Cardenas and Rodrıguez Becerra
2004, pp. 125-130; Etter et al. 2006, p.
˜
1; Hunter 1996, 158-159; Vina et al.
2004, pp. 118-119).
Illegal drugs and their eradication:
Illegal drug crops are cultivated within
the brown-banded antpitta’s range. In
2003, nearly 80 percent of the heroin
entering the United States came from
opium (Papaver somniferum) farms in
the Department of Tolima (Forero and
Weiner 2003, p. 1). Cocaine cultivation
occurs in other parts of the species’
range. In 2003, authorities first detected
cocaine being cultivated in Caldas,
traditionally the center of the
Colombian coffee-growing industry; it
was estimated that less than 1 km2 of
land was under cocaine cultivation
(0.54 km2 (0.21 mi2)). By 2004,
cultivation had risen 563 percent,
covering a 36 km2- (14 mi2-) area
(UNODC and GOC 2005, p. 27). Coca
crops deplete the soil of nutrients,
which hampers regeneration following
abandonment of fields (Van Schoik and
Schulberg 1993, p. 21). Drug eradication
efforts in Colombia have further
degraded and destroyed primary forest
habitat by using nonspecific aerial
herbicides to destroy illegal crops
´
(Alvarez 2005, p. 2042; BLI 2007d, p. 3;
´
´
Cardenas and Rodrıguez Becerra 2004,
p. 355; Oldham and Massey 2002, pp. 912). Herbicide spraying has introduced
harmful chemicals into brown-banded
antpitta habitat and has led to further
destruction of the habitat by forcing
illicit growers to move to new,
previously untouched forested areas
´
´
(Alvarez 2002, pp. 1088-1093; Alvarez
´
2005, p. 2042; Alvarez 2007, pp. 133´
143; BLI 2007d, p. 3; Cardenas and
´
Rodrıguez Becerra 2004, p. 355; Oldham
and Massey 2002, pp. 9-12). Between
1998 and 2002, cultivation of illicit
crops increased by 21 percent each year,
with a concomitant increase in
deforestation of formerly pristine areas
´
of approximately 60 percent (Alvarez
2002, pp. 1088-1093).
Refugia: The most important refugia
for the brown-banded antpitta include:
´
´
(1) Ucumarı Regional Park, (2) the Rıo
´
Toche Valley, (3) the Rıo Blanco
catchment, and (4) Reserva
´
˜
Departamental del Canon del Quindıo.
These refugia are discussed below.
´
(1) Ucumarı Regional Park (Risaralda
Department) covers an area of
approximately 44 km2 (17 mi2) in the
´
Otun River watershed, with elevations
ranging from 1,700 to 2,600m (5,577 to
´
8,530 ft) (Beltran and Kattan 2002, pp.
´
325-326; Kattan and Beltran 1999, p.
273; Kattan et al. 2006, pp. 301-302).
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The brown-banded antpitta prefers
habitat within the upper range limits of
this Park, at altitudes between 2,400 and
2,600 m (7,874 and 8,530 ft) (Krabbe and
Schulenberg 2003, p. 719; Kattan and
´
Beltran 1999, p. 272). Most of the
forested habitat within the park was
cleared in the 1960s for cattle ranching,
leaving the remaining natural forests
only on the steepest slopes (Kattan and
´
Beltran 1999, p. 273). Much of the Park
has been allowed to naturally
regenerate, and plantations of alder
(Alnus acuminata) and ash (Fraxinus
chinensis) are overgrown with natural
´
vegetation (Kattan and Beltran 1997, p.
369). The Park also contains a small area
of private pasturelands (Kattan and
´
Beltran 1997, p. 369), and agricultural
expansion, selective logging, and
firewood collection are ongoing in the
region (BLI 2008a, p. 1).
´
(2) In Rıo Toche Valley (Tolima
Department), on the south-east slope of
´
Volcan Tolima, the brown-banded
antpitta is considered uncommon and
´
local (Beltran and Kattan 2002, p. 326;
´
BLI 2004c, p. 2; Kattan and Beltran
2002, p. 238). This habitat is described
as fragmented, and it is estimated that
the natural cover has been reduced by
15 percent at elevations between 1,900
and 3,200 m (6,234 and 10,499 ft). The
majority of suitable habitat is above
2,200 m (7,218 ft) in elevation, and
´
Kattan and Beltran (2002, p. 238)
consider it to be of sufficient size to
support a population of brown-banded
antpitta, making this an important area
of suitable habitat for the species (p.
327).
´
(3) Rıo Blanco catchment (Caldas
Department) comprises a strip less than
200 km (124 mi) long on the Central
Cordilla, between 2,300 and 3,100 m
´
(7,546 and 10,171 ft) (Beltran and Kattan
2002, p. 325; BLI 2004c, p. 2; Kattan and
´
Beltran 2002, p. 238). The area is
considered to be of sufficient size to
´
support the species (Kattan and Beltran
2002, p. 238). However, the species has
only been observed at this location
´
once, in the year 2000 (Beltran and
Kattan 2002, p. 328).
˜
(4) Reserva Departamental del Canon
´
´
del Quindıo (Quindıo Department): The
Department of Conservation and
´
Management of Alto Quindıo owns and
manages this 56-km2 (22-mi2) reserve,
which ranges in elevation from 2,600 to
4,000 m (ft) (8,530 to 13,123 ft)
´
´
(Corporacion Autonoma Regional del
´
Quindıo 2008). The type locality for the
brown-banded antpitta (Laguneta) is
´
located in the Department of Quindıo
´
(Beltran and Kattan 2002, p. 325).
´
Beltran and Kattan (2002, pp. 238, 327)
believe that this Reserve comprises
habitat suitable for the brown-banded
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antpitta (as described under Current
Range, above) and represents an
important habitat conservation area for
´
the species (Beltran and Kattan 2002, p.
327). However, the species has not been
´
´
observed in Quindıo since 1942 (Beltran
and Kattan 2002, p. 325; Collar et al.
1992, p. 698) and is considered to be
´
locally extinct there (Beltran 2002 in
´
litt., as cited in Beltran and Kattan 2002,
p. 327).
Nearly all the other forested habitat
below 3,300 m (10,827 ft) in the Central
Andes where the brown-banded antpitta
occurred historically has been
deforested and cleared for agricultural
land use (BLI 2004c, p. 2). The
remaining forests providing suitable
habitat for the brown-banded antpitta
have become fragmented and isolated
and are either surrounded by or being
converted to pasture and agricultural
crops (e.g., coffee plantations, potatoes,
and beans) (BLI 2004c, p. 2).
Approximately 85 percent of forested
habitat at altitudes between 1,900 m
(6,234 ft) and 3,200 m (10,499 ft) has
been converted to other land uses (BLI
2004c, p. 2; Cuervo 2002, p. 327;
Stattersfield et al. 1998, p. 205). In 1998,
forest conversion within the range of the
brown-banded antpitta was projected to
continue (Stattersfield et al. 1998, p.
205). Cuervo (2002, p. 328) estimated
that the available suitable habitat for
this species totals no more than 500 km2
(310 mi2); BirdLife International
estimated that the species currently
occupies an area 300 km2 (116 mi2) in
size (BLI 2007f, p. 1).
Deforestation has greatly affected the
current population size and
distributional range of the brownbanded antpitta (Collar et al. 1992, p.
´
698; Kattan and Beltran 1997, p. 367).
The species was thought to be extinct or
´
on the verge of extinction (Beltran and
Kattan 2002, pp. 326-327; Collar et al.
´
1992, p. 689; Kattan and Beltran 1997,
pp. 367-369), until its rediscovery in
´
1994 (Kattan and Beltran 1997, pp. 367369). The brown-banded antpitta is now
confirmed within three localities,
´
including the Ucumarı Regional Park,
´
´
the Rıo Toche Valley, and the Rıo
Blanco basin. These habitats are
characterized as heterogeneous and
´
fragmented (Beltran and Kattan 2002, p.
´
327; Kattan and Beltran 2002, p. 237).
The species is considered extirpated
´
from its type locality (Beltran 2002 in
´
litt., as cited in Beltran and Kattan, p.
327), despite the existence of suitable
´
habitat (Beltran and Kattan 2002, p.
328), suggesting that the species is
unable to recolonize areas from which it
has been extirpated.
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Summary of Factor A
C. Disease or Predation
The brown-banded antpitta prefers
the humid understory and forest floor
habitats of mid-montane and cloud
forests between 2,400 and 2,600 m
(7,874 and 8,530 ft) and has been
observed in older (30–year-old)
secondary-growth forest habitats and
alder plantations. Habitat destruction,
alteration, conversion, and
fragmentation continue to be factors
affecting the brown-banded antpitta.
The direct loss of habitat through
widespread deforestation and
conversion of primary forests for human
settlement and agricultural uses has led
to the habitat fragmentation throughout
the brown-banded antpitta’s range.
Cultivation of illegal drug crops, such as
cocaine, leads to further deforestation
and alters soil compositions, hindering
regeneration of abandoned fields. In
addition, drug eradication programs
involving the aerial spraying of
nonspecific herbicides lead to further
environmental degradation and
destruction of primary forest habitat.
The current populations are small, very
localized, and limited to a narrow
elevational band that contains
fragmented, disjunct, and isolated
habitat. The species does not appear
capable of recolonizing areas of suitable
habitat that are isolated from extant
locations (see Factor E, Likelihood to
Disperse).
Historically, the species was known
only in one location, near Laguneta,
which had been reduced to 10 percent
of its original vegetative cover by 1994.
Currently, the species’ range is
estimated to be 300 km2. The
destruction and fragmentation of the
remaining primary forested habitat is
expected to continue, with ongoing
human encroachment bringing
increased population pressures and
drug crop production, along with
infrastructural improvements that
facilitate encroachment into previously
inaccessible areas. Therefore, we find
that the present destruction,
modification, and curtailment of habitat
are a threat to the brown-banded
antpitta throughout all of its range.
Disease: We are unaware of
information regarding disease or the
potential for significant disease
outbreaks in the brown-banded antpitta.
As a result, we do not consider disease
to be impacting the status of the species
in the wild.
Predation: Both terrestrial and avian
predators prey upon antpittas, including
the mountain coati (Nasuella olivacea),
tayra (Eira barbara—in the weasel
family), squirrel cuckoo (Piaya cayana),
and crimson-rumped toucanet
(Aulacorhynchus haematopygus) (Dobbs
et al. 2001, p. 231). Brown-banded
antpittas are a ground dwelling, nearly
´
flightless species (Beltran and Kattan
2002, p. 327; Krabbe and Schulenberg
2003, p. 719). Antpittas generally react
non-confrontationally in response to
potential predators, relying on
camouflage as a defense mechanism.
Nesting birds rarely call from atop their
nests (Wiedenfeld 1982, p. 580); they
rely on their cryptic plumage and
remain still to avoid detection when
potential predators approach (Dobbs et
al. 2001, pp. 226, 230). As discussed in
detail above for the blue-billed curassow
(Factor C, Predation), research on
Andean understory nesting birds that
are similar to the ground-dwelling
´
brown-banded antpitta (Beltran and
Kattan 2002, p. 327) indicated that
predation rates increase in isolated and
fragmented forest habitats, especially
smaller forest patches that facilitate
predator access to the understory
´
(Arango-Velez and Kattan 1997, p. 138;
Gibbs 1991, p. 157; Hoover et al. 1995,
p. 151; Keyser et al. 1998, p. 991; Keyser
2002, p. 186; Renjifo 1999, p. 1133;
Wilcove 1985, p. 1214).
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
We are not aware of any information
currently available that addresses the
occurrence of overutilization that may
be causing a decline of the brownbanded antpitta. Therefore, we do not
consider overutilization for commercial,
recreational, scientific, or educational
purposes to be a threat to the brownbanded antpitta.
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Summary of Factor C
Mountain coatis, tayras, squirrel
cuckoos, and crimson-rumped toucanets
are known antpitta predators. Predation
results in the direct removal of eggs,
juveniles, and adults from the
population. The brown-banded antpitta
produces a low clutch size (see Habitat
and Life History), and predation can
remove potentially reproductive adults
from the breeding pool. Moreover,
habitat fragmentation has occurred and
is ongoing throughout the brownbanded antpitta’s range (Factor A).
Studies on similar species in similar
Andean habitats indicate that
vulnerability to predation increases
with increased habitat fragmentation
and smaller patch sizes. The brownbanded antpitta does not have
sophisticated anti-predator response
mechanisms, making this species
particularly vulnerable to an increased
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risk of predation. Predation exacerbates
the genetic complications associated
with the species’ small population size
(Factor E). Because of the species’ small
population size and inability to
recolonize isolated habitat fragments
(Factor E), predation renders the species
vulnerable to local extirpation.
Therefore, we find that predation,
exacerbated by ongoing habitat
destruction (Factor A), is a threat to the
brown-banded antpitta.
D. The Inadequacy of Existing
Regulatory Mechanisms
Regulatory mechanisms may provide
species-specific or habitat-specific
protections. An evaluation of the
adequacy of regulatory mechanisms
within Colombia to mitigate or remove
the threats to the brown-banded antpitta
is provided below, beginning with
species-specific and followed by
habitat-specific protection mechanisms.
Colombia has enacted numerous laws
to protect species and their habitats
(Matallana-T. 2005, p. 121). The brownbanded antpitta is listed as an
endangered species under Colombian
Law 99 of 1993 (EcoLex 1993, p. 2) and
Resolution No. 584 of 2002 (EcoLex
2002, pp. 10, 12). A full description of
these laws and the categorization of
threatened species in Colombia were
provided above, as part of the Factor D
analysis for the blue-billed curassow.
This threat status confers protections
upon the species, including protection
from commercial take under Resolution
No. 849 of 1973 and Resolution No. 787
of 1977 (EcoLex 1973, p.1; EcoLex 1977,
p. 3). Hunting is not a threat to this
species. Therefore, this law is not
effective at reducing the primary threat
to the species—habitat destruction.
Colombia has enacted numerous
forestry laws and forestry management
practices (Law No. 2 (EcoLex 1959);
Decree No. 2,811 (Faolex 1974); Decree
No. 1,791 (Faolex 1996); Law No. 1,021
(EcoLex 2006)). Weaknesses in the
implementation of these laws and the
decentralized nature of Colombian
resource management are described in
detail above for the blue-billed curassow
(Factor D) (ITTO 2006, pp. 218-9, 222;
Matallana-T. 2005, pp. 121-122). The
brown-banded antpitta ranges in
multiple Departments (currently known
in Risaralda, Caldas, and Tolima), all of
which are administered by different
´
autonomous Corporaciones. Habitat
destruction, the primary threat to the
brown-banded antpitta, is ongoing
throughout the species’ range (Factor A).
The lack of a national conservation
strategy for the brown-banded antpitta,
combined with decentralized natural
resource management in Colombia, may
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15:11 Jul 06, 2009
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hamper conservation of the brownbanded antpitta. The existing laws and
the decentralized nature of forestry
management are ineffective at protecting
the brown-banded antpitta and its
habitat even within protected areas
(Brooks and Gonzalez-Garcia 2001, p.
183).
Colombia has several categories of
national habitat protection (Matallana-T.
2005, p. 121-122), which were described
above, as part of the Factor D analysis
for the blue-billed curassow (MatallanaT. 2005, p. 121-122). Of the four areas
identified as refugia for the brownbanded antpitta, two are considered
protected areas under Colombian law:
´
(1) the Ucumarı Regional Park and (2)
´
˜
Reserva del Canon del Quindıo.
´
(1) The Ucumarı Regional Park
(Risaralda Department) is managed by
´
´
the Corporacion Autonoma Regional de
Risaralda (CARDER) (BLI 2008a, p. 3),
with the primary goals of conservation
and ecotourism. The Park is managed
for multiple uses, including agriculture
and cattle grazing (BLI 2008a, p. 1), and
includes recreation and commercial
areas for activities such as camping and
freshwater fishing (CARDER 1995, pp.
3-4). According to the management plan
for the Park that was instituted in 1995,
recreational and commercial activities
are permitted only when they do not
significantly alter the environment
(CARDER 1995, pp. 3-4). However,
according to BirdLife International
(2008a, p. 3), there has been little in the
way of conservation planning, and the
habitat within the protected area
continues to undergo pressures from
agricultural expansion, firewood
collection, and selective cutting.
Consequently, the threat from habitat
destruction (Factor A) is not reduced or
ameliorated.
´
˜
(2) Reserva del Canon del Quindıo
´
(Quindıo Department) is managed by
´
´
the Corporacion Autonoma Regional del
´
Quindıo (2008, p. 1). According to the
management plan for the Department of
´
Quindıo , between
2007 and 2009, forestry planning will
commence for the entire Department
with the goal of completing forest plans
for four different areas within the
Department by the end of 2009. There
is no information to indicate which
areas will be included in this initial
planning development phase. Therefore,
we are unable to determine what
protections may exist for the brownbanded antpitta within this Reserve.
Moreover, as discussed under Factor A,
although this Reserve contains suitable
habitat for the brown-banded antpitta
´
(Beltran and Kattan 2002, p. 328), there
are no known populations of the brown-
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32323
banded antpitta within this Reserve
´
(Beltran and Kattan 2002, p. 325; Collar
et al. 1992, p. 698). Threfore, the threat
from habitat destruction (Factor A) is
not reduced or ameliorated within this
area.
Summary of Factor D
Colombia has numerous laws and
regulatory mechanisms to administer
and manage wildlife and their habitats.
The brown-banded antpitta is listed as
endangered under Colombian law and
lives within forested or protected areas
that are regulated by law. However, onthe-ground enforcement of existing
wildlife protection and forestry laws
and oversight of the local jurisdictions
implementing and regulating activities
are ineffective at mitigating the primary
threat to the brown-banded antpitta. As
discussed for Factor A, habitat
destruction, degradation, and
fragmentation continue throughout the
existing range of the brown-banded
antpitta. Under Colombian law, there
are two protected areas containing
suitable habitat for the brown-banded
antpitta. The species is known to occur
in only one of these areas, wherein
resources are managed for commercial
and recreational uses. Conservation
planning within both areas is lacking, so
that the existence of these protected
areas does not mitigate the threat of
habitat loss. Therefore, we find that the
existing regulatory mechanisms
currently in place are inadequate to
mitigate the primary threats to the
brown-banded antpitta.
E. Other Natural or Manmade Factors
Affecting the Continued Existence of the
Species
Two additional factors affect the
brown-banded antpitta: itslikelihood to
disperse and their small population
size.
Likelihood to Disperse: The brownbanded antpitta exhibits several
characteristics indicative of its
vulnerability to local extirpation and
inability to recolonize previously
inhabited locations, despite the
presence of suitable habitat. This
´
ground-dwelling species (Beltran and
Kattan 2002, p. 327) has a high
territorial fidelity and, although
dispersal capabilities are not wellknown (Cuervo 2002, p. 327) except
those in the banding study by Kattan
´
and Beltran (2002, p. 234), the farthest
known distance traveled by any one
individual bird was 0.041 km2 (0.02
mi2). This suggests that the brownbanded antpitta is unable to repopulate
an isolated patch of suitable habitat
following decline or local extirpation of
that patch (Cuervo and Salaman 1999, p.
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7; Hanski 1998, pp. 45-46). The local
extirpation of this species from its type
´
´
locality in Laguneta, Quindıo (Beltran
and Kattan 2002, p. 327), and the lack
of recolonization despite the existence
˜
of suitable habitat in the Canon del
´
Quindıo Reserve, support the
hypothesis that the species may be
incapable of dispersing to suitable
habitat fragments without human
intervention. To the best of our
knowledge, there are no recovery or
reintroduction programs in place for
this species.
Small Population Size: There have
been few quantitative studies of brownbanded antpitta populations. A total of
48 individuals have been directly
´
observed at two locations (Ucumarı
´
Regional Park and Rıo Toche) (Cuervo
´
in litt., as cited in Beltran 2002 p. 326;
´
Kattan and Beltran 1997, pp. 367-369;
´
Kattan and Beltran 1999, p. 276; Kattan
´
and Beltran 2002, pp. 232-233), 30 have
´
been inferred at one location (Rıo
´
Blanco) (Beltran and Kattan 2002, p.
326), and up to 106 have been predicted
to occur in one subpopulation within
the brown-banded antpitta’s current
´
range (Ucumarı Regional Park) (Kattan
´
and Beltran 1997, pp. 367-369; Kattan
´
and Beltran 1999, p. 276; Kattan and
´
Beltran 2002, pp. 232-233). From work
´
at Ucumarı Regional Park, Kattan and
´
Beltran (1997, pp. 367-369; Kattan and
´
Beltran 1999, p. 276) predicted a
population density of approximately 1.3
individuals per .01 km2 (0.004 mi2).
The IUCN has estimated the brownbanded antpitta’s total population size
to be more than 250 and fewer than 999
adult individuals in a 300-km2 (116-mi2)
area (BLI 2007f, p. 1). However, this is
a categorical approximation based on
the following extrapolation: an expected
average of 2.5 to 5.6 individuals per
square kilometer multiplied by 45
percent of the extent of occurrence (300
km2) (116 mi2) (BLI 2007f, p. 1), leading
to estimated population numbers
between 338 and 756 individuals (BLI
2007f, p. 4). While this density is well
´
within Kattan and Beltran’s (1997, pp.
´
367-369; Kattan and Beltran 1999, p.
276) predicted population density of 1.3
individuals per .01 km2 (116 mi2), it
should be noted that extrapolating
population sizes based on the
availability of suitable habitat may
result in an overestimate for the brownbanded antpitta for several reasons: (1)
the species may not be randomly
distributed within the given habitat; (2)
extrapolation does not take into account
human-induced threats, such as
disturbance or hunting; and (3) not all
individuals within the population are
breeding at any one time, so that the
actual number of individuals
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contributing to population growth will
be a smaller number than the total
number of individuals. In a review by
Jetz et al. (2008, p. 110) of 1,158 wellstudied bird species in Australia, North
America, and southern Africa, Jetz et al.
(2008, p. 115) found that most species
occurred in only 40-70 percent of the
predicted range. They further noted that
narrow-ranging species, such as the
brown-banded antpitta, are particularly
subject to population size
overestimation, because they are
unlikely to be randomly distributed
within the habitat (Jetz et al. 2008, p.
116). Moreover, at-risk species, existing
in declining, fragmented populations (as
is the case for the brown-banded
antpitta) are often absent from suitable
but suboptimal habitat, thus
exacerbating range overestimates (Jetz et
al. 2008, p. 115). For instance, although
suitable habitat exists in the species’
˜
type locality (Laguneta) in the Canon
´
del Quindıo Reserve, the species has not
been observed there since 1942 and is
considered extirpated from this locality
´
(Beltran and Kattan 2002, p. 327; Collar
et al. 1992, p. 698). Thus, the species
appears to be incapable of repopulating
suitable habitat on its own accord
´
(Beltran and Kattan 2002, p. 328; Jetz et
al. 2008, p. 115) and the existence of
suitable habitat does not connote the
presence of the species. This conclusion
´
is supported by Beltran and Kattan
(2002, p. 328), who noted that, out of a
potential habitat of 855 km2 (330 mi2),
the species did not occupy two of the
seven historical localities, prompting
them to reduce the estimated area of
occupancy to no more than 500 km2.
Thus, ground-truthing is essential to
accurate population-size estimations.
The IUCN is reviewing this situation to
improve upon conservation assessments
(Jetz et al. 2008, p. 117), and although
it may be an overestimate, the figure
ranging from 338 to 756 individuals
represents the best information on
population size.
Based on genetic considerations, in
the absence of quantitative studies
specific to this species, a generally
accepted approximation of minimum
viable population size is described by
the 50/500 rule (Shaffer 1981, p. 133;
´
Soule 1980, pp. 160-162). According to
this rule, the minimum viable
population size is defined as the
minimum number of individuals that is
sufficient to respond over time to
unexpected environmental conditions
within the species’ habitat (Shaffer
´
1981, pp. 132-133; Soule 1980, pp. 160162). This rule states that an effective
population size (Ne) of 50 individuals is
the minimum size required to avoid
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imminent risks from inbreeding. Ne
represents the number of animals in a
population that actually contribute to
reproduction, and is often much smaller
than the census, or total number of
individuals in the population (N).
Furthermore, the rule states that the
long-term fitness of a population
requires an Ne of at least 500
individuals, so that it will not lose its
genetic diversity over time and will
maintain an enhanced capacity to adapt
to changing conditions. Therefore, an
analysis of the fitness of this population
would be a good indicator of the
species’ overall survivability. The
available information for 2007 indicates
that the total global population of the
brown-banded antpitta may range
between 338 and 756 individuals (BLI
2007f, p. 4); 338 is above the minimum
effective population size required to
avoid risks from inbreeding (Ne = 50),
and 756 is above the upper threshold for
long-term fitness (Ne = 500).
Given that the global population size
is a qualitative assessment that may be
an overestimate, that the actual number
of breeding pairs is unknown but
smaller than this number, and that the
species exists in subpopulations that are
unlikely to disperse into other locations,
it is beneficial to analyze the fitness of
the subpopulations that have been
quantitatively assessed. The beststudied subpopulation is located within
´
the Ucumarı Regional Park. A total of 47
individuals have been directly observed,
and researchers estimate that the area
may support as many as 106 individuals
´
(Kattan and Beltran 1997, pp. 367-369;
´
Kattan and Beltran 1999, p. 276; Kattan
´
and Beltran 2002, pp. 232-233). Fortyseven is just below the minimum
effective population size required to
avoid risks from inbreeding (Ne = 50
individuals). Moreover, the upper
estimate of 106 individuals (not all of
which will be reproducing) is
approximately one-fifth of the upper
threshold (Ne = 500 individuals)
required for long-term fitness of a
population that will not lose its genetic
diversity over time and will maintain an
enhanced capacity to adapt to changing
conditions. Therefore, we currently
consider the species to be at risk due to
the lack of near- and long-term viability.
Small population sizes render species
vulnerable to genetic risks that can have
individual or population-level
consequences on the genetic level and
can increase the species’ susceptibility
to demographic problems, as explained
in more detail above for the blue-billed
curassow (Factor E, Small Population
Size) (Charlesworth and Charlesworth
1987, p. 238; Shaffer 1981, p. 131). Once
a population is reduced below a certain
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number of individuals, it tends to
rapidly decline towards extinction
(Franklin 1980, pp. 147-148; Gilpin and
´
Soule 1986, p. 25; Holsinger 2000, pp.
´
64-65; Soule 1987, p. 181).
The brown-banded antpitta’s
restricted range, combined with its
small population size (Cuervo and
Salaman 1999, p. 7; Cuervo 2002, p.
138; del Hoyo 1994, p. 361) and low
´
prospect for dispersal (Beltran and
Kattan 2002, p. 326; BLI 2004c, p. 2;
Cuervo and Salaman 1999, p. 7; del
´
Hoyo 1994, p. 361; Kattan and Beltran
´
1997, pp. 369-370; Kattan and Beltran
´
1999, p. 273; Kattan and Beltran 2002,
p. 238) makes the species particularly
vulnerable to the threat of adverse
natural (e.g., genetic, demographic, or
stochastic) and manmade (e.g., habitat
alteration and destruction) events that
destroy individuals and their habitats
(Brooks and Gonzalez-Garcia 2001, pp.
185-190; Holsinger 2000, pp. 64-65;
Primack 1998, pp. 279-308; Young and
Clarke 2000, pp. 361-366).
Summary of Factor E
The brown-banded antpitta’s small
population size increases its
vulnerability to genetic risks associated
with small population sizes that
negatively impact the species’ long-term
viability and increase the possibility of
localized extirpations of the remaining
fragmented populations. Further, the
species is unlikely to repopulate areas of
suitable habitat from which it has been
locally extirpated because it exhibits
high territorial fidelity and has never
repopulated suitable existing habitat
´
within the Department of Quindıo,
where the species’ type locality
(Laguneta) is located and the species has
not been observed since 1942.
Consequently, we believe that, in
combination with the risks to the
species from habitat destruction (Factor
A) and predation (Factor C), the brownbanded antpitta is vulnerable to
localized extirpation or extinction from
which the species would be unable to
recover, due it its small population size
and apparent inability to repopulate
fragmented, isolated habitats such as
that currently present within this
species’ range.
Status Determination for the BrownBanded Antpitta
The four primary factors that threaten
the survival of the brown-banded
antpitta are: (1) habitat destruction,
fragmentation, and degradation (Factor
A); (2) predation (Factor C); (3)
inadequacy of regulatory mechanisms to
reduce the threats to the species (Factor
D); and (4) small population size and
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isolation of remaining populations
(Factor E).
The direct loss of habitat through
widespread deforestation and
conversion of primary forests to human
settlement and agricultural uses has led
to the fragmentation of habitat
throughout the range of the brownbanded antpitta and isolation of the
remaining populations. The species has
been locally extirpated in its type
locality and has experienced a 55
percent reduction of suitable habitat,
and its range is estimated to be 300 km2
(116 mi2).
Brown-banded antpittas are
vulnerable to predation by mountain
coatis, tayras, squirrel cuckoos, and
crimson-rumped toucanets (Factor C).
Habitat fragmentation (Factor A)
contributes to this vulnerability,
because research indicates that
predation increases with increased
habitat fragmentation and smaller patch
sizes. Predation leads to the direct
removal of eggs, juveniles, and adults
from the population, exacerbating risks
associated with the species’ small
population size and the risk of local
extirpation (Factor E). Brown-banded
antpittas, as with other antpittas,
produce a low clutch size (see Habitat
and Life History) and predation can
destroy pair bonds and remove
potentially reproductive adults from the
breeding pool.
The threats from habitat destruction
(Factor A) and predation (Factor C) are
compounded by the species’ small
population size (Factor E). The brownbanded antpitta has undergone a
population decline that is closely
associated with a reduction in range
caused by habitat destruction (Factor A).
The brown-banded antpitta’s small
population size of between 338 and 756
individuals is likely to be an
overestimate based on the fact that
population sizes for narrow-ranging
species are typically overestimated
when based on extent of occurrence.
The species’ subpopulations, one of
which is estimated to include only 46 to
106 individuals, are isolated from each
other. The species’ confirmed absence
from suitable habitat within its historic
range, combined with the species’ high
territorial fidelity, suggests that the
species is incapable of repopulating
suitable habitat without human
intervention. We are unaware of any
reintroduction or recovery programs for
this species. The species’ small
population size increases its
vulnerability to natural and human
factors (e.g., genetic isolation,
agricultural development, increased
human settlement, and road
development) that could lead to local
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extirpation, which the species has
already experienced in its type locality
due to habitat destruction. Within the
last three generations, or 10 years, the
brown-banded antpitta has undergone
up to a 9 percent reduction in
population size and, at the current level
of habitat destruction, this rate of
decline is projected to continue over the
next 10 years. Below a certain number,
species are unable to recover and, given
the small number and isolated nature of
existing populations, such reductions in
numbers could lead to extinction of the
brown-banded antpitta.
Although Colombia has adopted
numerous laws and regulatory
mechanisms to administer and manage
wildlife and their habitats, on-theground enforcement of these laws and
oversight of the local jurisdictions
implementing and regulating activities
are inadequate to address the primary
threat to this species, which is habitat
loss (Factor A). Several populations of
brown-banded antpitta are within
sanctuaries or preserves; however,
habitat destruction and hunting
continues within the areas, and
regulations are not uniformly enforced,
monitoring is limited, and management
plans are not developed or
implemented, resulting in ineffective
protective measures for conservation of
the species.
We have carefully assessed the best
available scientific and commercial
information regarding the past, present,
and potential future threats faced by the
brown-banded antpitta. We consider the
ongoing threats to the brown-banded
antpitta, habitat destruction (Factor A)
and predation (Factor C), exacerbated by
the species’ small population size and
limited dispersal ability (Factor E), and
compounded by inadequate regulatory
mechanisms to mitigate these threats
(Factor D), to be equally present and of
the same magnitude throughout the
species’ entire current range. Based on
this information, we conclude that the
brown-banded antpitta is in danger of
extinction throughout all of its range.
Therefore, we are proposing to list the
brown-banded antpitta as an
endangered species.
III. Cauca Guan (Penelope perspicax)
Species Description
The Cauca guan, a member of the
Cracid family, is endemic to the central
and western slopes of the Andes of
Colombia (Brooks and Strahl 2000, p.
13; Delacour and Amadon 2004, pp.
133-135; Hilty and Brown 1986, p. 125).
It is a large bird, measuring
approximately 76 cm (30 in) in length
(Hilty and Brown 1986, p. 125). The
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species is locally known as ‘‘Pava
Caucana’’ (Renjifo 2002, p. 124; Rios et
al. 2006, p. 17). The Cauca guan is
described as a ‘‘drab’’ brown-gray, with
a chestnut-colored rear part and tail,
and a bright red dewlap (a flap of skin
hanging beneath its lower jaw) (BLI
2007h, p. 1).
which is considered low. Guans remain
paired during the breeding period and
until chicks are 1 year in age; this is
considered a long fledging period (Rios
et al. 2006, p. 17). Cracids are also slow
to reproduce, with a replacement rate of
at least 6 years (Silva and Strahl 1991,
p. 50).
Taxonomy
The Cauca guan was first
taxonomically described by Bangs in
1911 and placed in the Cracidae family
(BLI 2007h, p. 1).
Historical Range and Distribution
The Cauca guan’s historical
distribution included the east slopes of
´
the West Andes and the Cauca, Patıa,
and Dagua Valleys, in the Departments
´
of Cauca, Quindıo, Risaralda, and Valle
de Cauca. The historic range is
estimated to have been approximately
24,900 km2 (9,614 mi2) (Renjifo 2002, p.
128). In the early part of the 20th
Century, the Cauca guan inhabited the
dry forests of the Cauca, Dagua, and
´
Patıa Valleys (Renjifo 2002, p. 128). The
Cauca Valley lies between the central
and western Andes and spans the
Departments of Cauca, Valle de Cauca,
´
Quindıo, and Risaralda (WWF 2001a, p.
1). The Dagua Valley lies on the Pacific
side of the western Andes, in Valle de
Cauca; it is described as an isolated
valley of dry forest that changes in
elevation from 400 to 2,000 m (1,312 to
6,562 ft) and is surrounded at upper
elevations by humid forest to the west
and cloud forest to the north, south, and
´
east (Silva 2003, p. 4). The Patıa Valley
lies between the central and western
Andes in the Department of Cauca, in
southwestern Colombia; it has a mean
altitude of 600-900 m (1,969-2,953 ft)
(WWF 2001c, p. 1). This area was once
covered in wetlands, humid forests, and
dry forests. Today, most of the dry
forests have been eliminated and highly
fragmented, such that continuous forest
exists only above 2,000 m (6,562 ft)
(Renjifo 2002, p. 128).
From the beginning of the 20th
Century through the 1950s, the species
was considered common (BLI 2007h, p.
1; Renjifo 2002, p. 126). Between the
1970s and 1980s, there was extensive
deforestation in the Cauca Valley, and
the species went unobserved during this
time, leading researchers to suspect that
the Cauca guan was either extinct or on
the verge of extinction (Brooks and
Strahl 2000, p. 14; del Hoyo 1994, pp.
337, 349; Hilty 1985, p. 1004; Hilty and
Brown 1986, p. 125). The species was
rediscovered in 1987 (Renjifo 2002, p.
124).
Habitat and Life History
The Cauca guan has been observed in
mature tropical humid forests and in
fragmented secondary forests, forest
edges, and plantations of the exotic
Chinese ash (Fraxinus chinensis) trees
that are located within 1 km (0.62 mi)
of primary forest (Kattan et al. 2006, p.
299; Renjifo 2002, p. 127; Rios et al.
2006, pp. 17-18). Older reports indicate
that the species once inhabited dry
´
forests in the Cauca, Patıa, and Dagua
River valleys (Renjifo 2002, p. 126). The
Cauca guan requires large territories for
foraging (Kattan 2004, p. 11), but today
is relegated mostly to small forest
fragments (Kattan et al. 2006, p. 301).
This species, as with other guans, tends
to aggregate within its habitat, generally
based on resource availability. For
instance, Cauca guans tend to
congregate around fruit trees at certain
times of year. Thus, depending on the
time of year, improper sampling might
tend to overestimate or underestimate
the population (Kattan et al. 2006, p.
305). Cauca guans are reportedly timid
in the presence of humans (Rios et al.
2006, p. 21).
Cauca guans feed mostly on fruit and
leaves (including those of the nonnative Chinese ash trees) and
occasionally on invertebrates and
˜
flowers (Munoz et al. 2006, p. 49;
Renjifo 2002, p. 127; Rios et al. 2006,
pp. 17-18). Although primarily
terrestrial, the species is occasionally
found in the upper stories of forests
obtaining food. Because fruit availability
within a forest is spatially and
temporally variable, guans must
undergo regional movements in pursuit
of fruiting plants. The species is usually
found singly, in pairs, or in groups of up
to six individuals. The largest recorded
gathering of Cauca guans was 30
individuals (Rios et al. 2006, p. 16).
There are two breeding seasons
coinciding with the rainy seasons, one
at the beginning of the year and another
in August (Rios et al. 2006, p. 17). Nests
are circular cups made of leaves and
small branches (Renjifo 2002, p. 127),
and the typical clutch size is two eggs,
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Current Range and Distribution
Today, the Cauca guan inhabits the
eastern and western slopes of the West
and Central Andes Mountain ranges, in
´
the Departments of Cauca, Quindıo,
Risaralda, and Valle de Cauca (BLI
2007h, p. 1; Kattan et al. 2006, pp. 299,
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301; Renjifo 2002, pp. 124-126). Since
1987, most observations of this species
have been at elevations ranging from
1,400 to 2,000 m (4,593 to 6,562 ft)
(Renjifo 2002, pp. 124-125), with an
occasional sighting at altitudes well
below (i.e., 816 m (2,677 ft)) or well
above (i.e., 2,690 m (8,825 ft)) this
˜
altitudinal range (Munoz et al. 2006, p.
54; Renjifo 2002, pp. 124-125; Rios et al.
´
2006, p. 17). The Ucumarı Regional Park
is considered the stronghold of the
species (BLI 2007h, p. 1) (see Population
Estimates).
The habitat consists primarily of
forest fragments, and although
continuous cover remains at elevations
above 2,000 m (6,562 ft) (Kattan et al.
2006, p. 303), researchers have not
ascertained whether the species inhabits
these higher-altitude contiguous forest
areas (Renjifo 2002, p. 129). The current
range of the species totals less than 750
km2 (290 mi2), of which only 560 km2
(216 mi2) is considered suitable habitat
(BLI 2007h, p. 1; Kattan et al. 2006, p.
299; Rios et al. 2006, p.17).
Population Estimates
Cauca guan populations are
characterized as small, ranging from
only tens of individuals or, in rare
instances, hundreds (Renjifo 2002, p.
12). BirdLife International reported that
the largest subpopulation contained an
estimated 50 to 249 individuals;
however, they do not specify to which
population this refers, and these figures
are not found in any of the other
literature regarding population surveys
´
of the Cauca guan. Ucumarı Regional
Park has been considered the stronghold
of the species (BLI 2007h, p. 1). Sixteen
individuals were counted in 1990, and
the species was characterized as
‘‘common’’ in plantations in 1994-1995
(Wege and Long 1995, p. 141). Since
then, there have been scant sightings of
Cauca guan there (Renjifo 2002, p. 125;
Wege and Long 1995, p. 141), including
the observation of one individual in the
Park in 2004 (Scanlon 2004, pp. 1-3).
There have been no population surveys
within the Park to determine the
species’ current population size therein.
Munchique National Natural Park
(Cauca) is considered to be the most
important locality for this species in the
southern portion of its range because of
the extensive remaining forest habitat,
although habitat destruction is ongoing
there (see Factor A). The species was
last recorded in Munchique in 1987, but
has not been confirmed there since
˜
(Kattan et al. 2006, p. 305; Munoz et al.
2006, p. 54; Salaman in litt. 1999, 2000,
as cited in BLI 2007h, p. 2).
Kattan et al. (2006, p. 302) conducted
the only two population surveys in 2000
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˜
and 2001 (Munoz et al. 2006 p. 55).
They estimated population densities at
´
two locations, Otun-Quimbaya Flora
and Fauna Sanctuary (Risaralda) and
Reserva Forestal de Yotoco (Valle de
Cauca), to be 144-264 individuals and
35-61 individuals, respectively (Kattan
et al. 2006, p. 304). Kattan et al. (2006,
p. 302) also examined 10 additional
localities, based on locality data
reported by Renjifo (2002, pp. 124-125).
Visual confirmations were made at only
2 of the 10 localities (Reserva La Sirena
and Chorro de Plata, both in the
Department of Valle de Cauca), where
the extent and occurrence of the
populations have yet to be determined
(Kattan et al. 2006, p. 303). Auditory
confirmations were made at 5 of the 10
localities, including: La Zulia, Chicoral,
Las Brisas, San Antonio, and Planes de
San Rafael (Kattan et al. 2006, p. 302).
In 2006, Kattan (in litt., as cited in
˜
Munoz et al. 2006 p. 55) estimated the
global population to be between 196 and
342 individuals. The IUCN has placed
the Cauca guan in the population
category ranging from 250 to no more
than 1,000 (BLI 2007h, pp. 1, 3).
Overall, the population is considered to
be in decline (BLI 2007h, p. 2; Kattan
2004, p. 6; Renjifo 2002, p. 129).
Conservation Status
The Cauca guan is listed as
endangered under Colombian law
(EcoLex 2002, p. 12). The IUCN
categorizes the species as ‘‘Endangered’’
due to its small, contracted range
composed of widely fragmented patches
of habitat (BLI 2004e, p. 1).
Summary of Factors Affecting the Cauca
Guan
A. The Present or Threatened
Destruction, Modification, or
Curtailment of the Habitat or Range
Historically, Cauca guans were
considered common (BLI 2007h, p. 1;
Renjifo 2002, p. 126). They inhabited
the eastern slopes of the west Andes and
the dry forests of the Cauca, Dagua, and
´
Patıa Valleys, in the Departments of
´
Cauca, Quindıo, and Valle del Cauca
(Renjifo 2002, p. 124) (see Historical
Distribution, above), in a range
extending over approximately 24,900
km2 (9,614 mi2). Extensive habitat
destruction and fragmentation since the
1950s has resulted in an estimated 95
percent range reduction (Chapman
1917, p. 195; Collar et al. 1992, p. 126;
Kattan et al. 2006, p. 299; Renjifo 2002,
pp. 126-127; Rios et al. 2006, p. 17). As
a result, although it prefers mature
tropical humid forests, the Cauca guan
exists primarily in fragmented and
isolated secondary forest remnants,
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forest edges, and in feral plantations of
the exotic Chinese ash trees that are
located within 1 km (0.62 mi) of
primary forest (Kattan et al. 2006, p.
299; Renjifo 2002, p. 127; Rios et al.
2006, pp. 17-18). Its current range is
estimated to be less than 750 km2 (290
mi2), of which only 560 km2 (216 mi2)
is considered suitable habitat (BLI
2007h, p. 2; Kattan et al. 2006, p. 299;
Rios et al. 2006, p. 17). It is estimated
that more than 30 percent of this loss of
habitat has occurred within the last
three generations, or 30 years (Renjifo
2002, p. 129).
Deforestation rates and patterns:
Colombia has experienced extensive
deforestation in the last half of the 20th
Century as a result of habitat conversion
for human settlements, road building,
agriculture, and timber extraction. A
23–year study, from 1973 to 1996,
demonstrated that these activities
reduced the amount of primary forest
cover in Colombia by approximately
3,605 ha (8,908 ac) annually,
representing a nearly one-third total loss
˜
of primary forest habitat (Vina et al.
2004, pp. 123-124). Beginning in the
1980s, habitat loss increased
dramatically as a result of influxes of
people settling in formerly pristine areas
˜
(Perz et al. 2005, pp. 26-28; Vina et al.
2004, p. 124). More recent studies
indicate that the rate of habitat
destruction is accelerating. During the
period 1990-2005, Colombia lost
approximately 52,800 ha (130,471 ac) of
primary forest annually (Butler 2006a,
pp. 1-3; FAO 2003a, p. 1). These studies
and activities are described in greater
detail above, as part of the Factor A
analysis for the blue-billed curassow
(Deforestation Rates and Patterns).
Human-induced deforestation and
environmental degradation have caused
the Cauca guan to shift its range and
elevational distribution to the few
remaining forest remnants. The Cauca
guan was once considered to occur only
on the eastern slopes of the West Andes
´
and Cauca, Patıa, and Dagua Valleys
(Renjifo 2002, p. 128). Today, the
species occurs on the western slopes of
the central and western Andes of
Colombia (BLI 2007h, p. 1; Delacour and
Amadon 2004, p. 135; Kattan et al.
2006, p. 299; Renjifo 2002, p. 124).
During the latter half of the 20th
Century, much of the lower-elevation
´
forests in the Rıo Cauca Valley, where
the species was observed most often
between 1937 and 1963 (Renjifo 2002, p.
124), were deforested. Habitat
destruction and alteration in the subAndean slopes around the Cauca, Dagua
´
and Patıa Valleys has left only a few
hundred hectares (100 hectares = 1 km2
= 0.39 mi2) of isolated, small,
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fragmented forest remnants, and the
Cauca guan is absent from most of these
fragments (Renjifo 2002, p. 128). The
species has been extirpated from the
Cauca and Dagua Valleys, but may still
´
exist in patches within the Patıa Valley
(Renjifo 2002, p. 128). Beginning in
1989, the species was observed several
times in the Department of Risaralda, in
an area and at elevations that were not
part of the species’ historic range, but
represent the extreme fringe of its
former range (Renjifo 2002, pp. 124-5).
Habitat destruction and alteration, in
addition to shifting the species to the
fringes of its former range, have caused
the Cauca guan to shift in its altitudinal
distribution (Cuervo and Salaman 1999,
p. 8). Nearly all the forested habitat
below 3,300 m (10,827 ft) in the Central
Andes, where the Cauca guan occurs
today, has been deforested and cleared
for agricultural land use, such as
pasture, coffee plantations, potatoes,
and beans (BLI 2004c, p. 2).
Approximately 85 percent of forested
habitat at altitudes between 1,900 m
(6,234 ft) and 3,200 m (10,499 ft) has
been converted to other land uses (BLI
2004c, p. 2; Cuervo 2002, p. 327;
Stattersfield et al. 1998, p. 205). By
´
1994, in Quindıo, extensive
deforestation at elevations between
1,800 and 2,600 m (5,905 and 8,530 ft)
led to the destruction of much of the
Cauca guan’s preferred habitat of mature
humid forests (Collar et al. 1994, p.
136). Prior to the species’ rediscovery in
1987, its altitudinal range was between
1,300 and 2,100 m (4265 and 6890 ft)
(del Hoyo 1994, p. 349; Hilty and Brown
1986, p. 125), with occasional sightings
´
at lower elevations in the Patıa Valley
(between 642 and 650 m (2,106 and
2,133 ft) (Hilty and Brown 1986, p. 125;
Renjifo 2002, pp. 124-125). Since 1987,
the Cauca guan has been observed only
in the remaining and much-restricted
forest remnants of the following
Departments: Cauca (in the years 1987,
´
1989, and 1992), Quindıo (1995 – 1997),
Risaralda (1989, 1995-1997, 2000, 2001),
and Valle de Cauca (1988, 1999, 2000)
(Delacour and Amadon 2004, p. 135;
Kattan et al. 2006, p. 299; Renjifo 2002,
pp. 124-125). Renjifo (2002, pp. 124125) provided detailed observation
records indicating that reports since
1987 ranged in altitude between one
´
sighting at 900 m (2,953 ft) in the Patıa
Valley in 1992, and the rest between
1,350 and 2,690 m (4,429 and 8,825 ft).
˜
In 2006, Munoz et al. (2006, p. 54)
reported the species’ range as being
between 1,200 and 2,600 m (3,937 and
8,530 ft) and Rios et al. (2006, p. 17)
reported the species’ range as 1,0002,500 m (3,281-8,202 ft). These ranges
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are consistent with recent observations
of the species. Kattan et al. (2006, pp.
299, 301) reported its range as 1,0002,000 m (3,281-6,562 ft), noting that
recent sightings at higher elevations
demonstrated that the species has
shifted its altitudinal range, as
deforestation throughout much of
´
Cauca, Dagua, and Patıa Valley has left
only isolated forest fragments remaining
at elevations below 2,000 m (6,562 ft).
Although continuous cover remains in
some locations above 2,000 m (6,562 ft)
(Kattan et al. 2006, p. 303), researchers
are uncertain whether the species
inhabits these areas (Renjifo 2002, p.
129). The mid-montane and cloud
forests in the Department of Risaralda,
where this species was observed as
recently as the year 2000 (Renjifo 2002,
p. 124), continue to undergo
deforestation (Dolphijn 2005, p. 2). In
Cauca, timber extraction and mining are
˜
ongoing (Uruena et al. 2006, p. 42).
Deforestation and habitat alteration are
ongoing throughout the Cauca guan’s
limited range of 560 km2 (216 mi2).
Illegal drugs and their eradication:
Cocaine and opium have been
cultivated throughout the Cauca guan’s
range. The cultivation of illegal crops
(including coca and opium) in Colombia
destroys montane forests (Balslev 1993,
p. 3). Coca production destroys the soil
quality by causing the soil to become
more acidic, which depletes the soil
nutrients and ultimately impedes the
regrowth of secondary forests in
abandoned fields (Van Schoik and
Schulberg 1993, p. 21). As of 2004, the
estimated total amount of land under
cultivation for cocaine equaled 80,000
ha (197,683 ac); 4,000 ha (9,884 ac) of
land are under opium cultivation
(UNODC et al. 2007, pp. 7-8). These
figures include habitat within the Cauca
guan’s range. Between 2003 and 2004,
cocaine cultivation areas decreased from
1,445 to 1,266 ha (3,571 to 3,128 ac) in
Cauca, and increased 22 percent from 37
ha (91 ac) to 45 ha (111 ac) in Valle de
Cauca (UNODC and GOC 2005, p. 15).
At the same time, opium cultivation
decreased in Cauca from 600 ha (1,483
ac) to 450 ha (1,112 ac) (UNODC 2005,
p. 50).
Colombia continues to be the leading
coca bush producer (UNODC et al. 2007,
p. 7). However, since 2003, cocaine
cultivation has remained stable at about
800 km2 (309 mi2) of land under
cultivation (UNODC et al. 2007, p. 8).
This is attributed, in part, to the
implementation of alternative
development projects, which encourage
people to pursue alternative vocations
to planting illegal crops (UNODC et al.
2007, p. 77). In 2004, the United Nations
Office on Drugs and Crime and the
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Government of Colombia reported that
no coca had been cultivated in the
´
Departments of Quindıo and Risaralda
since the year 2000 (UNODC and GOC
2005, p. 48). This was attributed to
alternative development programs being
implemented between 1999 and 2007,
for which US$200,000 was provided to
´
Quindıo and US$800,000 to Risaralda
(UNODC and GOC 2005, p. 48). During
the same period, at least US$12.1
million (mill) was spent in alternative
development programs in Cauca, where
coca production decreased, and another
1.6 mill was spent in Valle de Cauca,
where coca production increased
(UNODC and GOC 2005, p. 48).
This stabilization of the amount of
land under cultivation for illegal drugs
is also attributed to heightened
eradication efforts. Between 2002 and
2004, aerial spraying occurred over
more than 1,300 km2 (502 mi2)
annually, peaking in 2004, when 1,360
km2 (525 mi2) of illicit crops were
sprayed (UNODC and GOC 2005, p. 11).
In 2006, eradication efforts were
undertaken on over 2,130 km2 (822 mi2)
of land, consisting of 1,720 km2 (664
mi2) of land being sprayed and manual
eradication being used on the remaining
land. Eradication efforts undertaken in
2006 occurred over an area representing
2.7 times more land than the net
cultivation area (UNODC et al. 2007, p.
8). In Cauca alone, 1,811 ha (4,475 ac)
of coca fields and 435 ha (1,075 ac) of
opium fields were sprayed or manually
eradicated in 2004 (UNODC 2005, p.
66).
Drug eradication efforts in Colombia
have further degraded and destroyed
primary forest habitat by using
nonspecific aerial herbicides to destroy
´
illegal crops (Alvarez 2005, p. 2042; BLI
´
´
2007d, p. 3; Cardenas and Rodrıguez
Becerra 2004, p. 355; Oldham and
Massey 2002, pp. 9-12). Herbicide
spraying has introduced harmful
chemicals into Cauca guan habitat and
has led to further destruction of the
habitat by forcing illicit growers to move
to new, previously untouched forested
´
areas (Alvarez 2002, pp. 1088-1093;
´ lvarez 2005, p. 2042; Alvarez 2007, pp.
´
A
´
133-143; BLI 2007d, p. 3; Cardenas and
´
Rodrıguez Becerra 2004, p. 355; Oldham
and Massey 2002, pp. 9-12). Between
1998 and 2002, cultivation of illicit
crops increased 21 percent each year,
with a concomitant increase in
deforestation of formerly pristine areas
´
of approximately 60 percent (Alvarez
2002, pp. 1088-1093).
Effects of habitat fragmentation: The
Cauca guan requires large territories for
foraging (Kattan 2004, p. 11), but today
is relegated mostly to small forest
fragments (Kattan et al. 2006, p. 301),
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Sfmt 4702
making it more susceptible to habitat
disturbance, further fragmentation, and
destruction from human activity (Brooks
and Strahl 2000, p. 10; Silva and Strahl
1991, p. 38).
An analysis of the effects of habitat
fragmentation on Andean birds within
western Colombia established that 31
percent of the historical bird
populations in western Colombia had
become extinct or locally extirpated by
1990, largely as a result of habitat
fragmentation from deforestation caused
by human encroachment (Kattan and
´
Alvarez-Lopez 1996, p. 5; Kattan et al.
´
1994, p. 141). Kattan and Alvarez-Lopez
(1996, pp. 5-6) also identified two
conditions that increase a species’
vulnerability to extinction or local
extirpation as a result of habitat
fragmentation: (1) species at the upper
or lower limit of their altitudinal
distribution (which is the case for the
Cauca guan) are more susceptible to
local extirpation and extinction, and (2)
large fruit-eating birds with limited
distributions and narrow habitat
preferences were most vulnerable to
extinction (also the case for the Cauca
guan). Deforestation has eradicated the
Cauca guan from much of its historic
range and has led to local extirpation
(Collar et al. 1994, pp. 61-62; Kattan et
al. 2006, p. 299) in the Cauca and Dagua
Valleys (Renjifo 2002, p. 128), such as
in San Antonio (Valle de Cauca), where
the species has not been observed since
1917 (Renjifo 2002, p. 124). Moreover,
in light of the species’ characteristics,
the Cauca guan is unlikely to repopulate
an isolated patch of suitable habitat
following decline or local extirpation
(see Factor E, Likelihood to Disperse).
The Cauca guan, as with other
cracids, is susceptible to indirect effects
of habitat disturbance and fragmentation
(Silva and Strahl 1991, p. 38; Brooks
and Strahl 2000, p. 10). A study
conducted in northwestern Colombia
demonstrated that habitat destruction
and fragmentation may increase a
species’ vulnerability to predation
´
(Arango-Velez and Kattan 1997, pp. 140142) (Factor C). In addition, habitat
fragmentation, combined with
continuing human encroachment,
increases the species’ vulnerability to
hunting (Factor B). Habitat
fragmentation may affect population
densities by shifting the availability of
resources, such as food (Kattan et al.
2006, p. 305). Habitat fragmentation also
compounds problems for species with
small population sizes, such as the
Cauca guan, which has an estimated
population between 196 and 342
individuals (Kattan in litt., as cited in
˜
Munoz et al. 2006 p. 55) (Factor E).
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Refugia: The Cauca guan has recently
been confirmed in the following
´
locations: (1) Otun-Quimbaya Flora and
Fauna Sanctuary; (2) Reserva La Sirena;
(3) Reserva Forestal de Yotoco; (4)
Chorro de Plata; and (5) Munchique
National Natural Park (Delacour and
Amadon 2004, p. 135; Kattan et al.
2006, p. 299, 305; Renjifo 2002, pp. 124125). These locations are discussed
below.
´
(1) Otun-Quimbaya Flora and Fauna
Sanctuary (Department of Risaralda), a
4.9-km2 (1.9-mi2) reserve in the
Department of Risaralda, contains a
habitat mosaic of old-growth fragments
and regenerating secondary forests,
including abandoned ash plantations
that cover 0.18 km2 (0.07 mi2) (CARDER
´
2000, p. 1; Kattan and Beltran 1997, p.
369; Kattan et al. 2006, p. 303). Most of
the forested habitat in the area was
cleared in the 1960s for cattle ranching,
leaving the remaining natural forests
only on the steepest slopes (Kattan and
´
Beltran 1999, p. 273). In population
surveys conducted by Kattan et al.
(2006, p. 304) in 2000 and 2001, this
subpopulation was estimated to include
between 144 and 264 individuals.
Kattan (2004, pp. 12-13) also advised
´
that the Otun-Quimbaya Sanctuary was
not large enough to provide the space
and resources needed to sustain a viable
Cauca guan population.
This Sanctuary is adjacent to the
´
Ucumarı Regional Park (Kattan et al.
2006, p. 302), which covers an area of
approximately 44 km2 (17 mi2), with
elevations ranging from 1,700 to 2,600
´
m (5,577 to 8,530 ft) (Kattan and Beltran
1999, p. 273; Kattan et al. 2006, pp. 301´
302). Ucumarı Regional Park has been
considered the stronghold of the species
since the late 1990s (BLI 2007h, p. 1)
(see Population Estimates, above). The
largest number of Cauca guan
individuals observed at this site was 16
in 1990 (Wege and Long 1995, p. 141),
and a single individual was sighted in
2004 (Scanlon 2004, pp. 1-3); however,
there have been no population surveys
within the Park to determine the current
population size. Subsistence hunting
was reportedly prevalent within the
Park in the late 1990s (Collar et al. 1992,
p. 60; del Hoyo 1994, p. 349; Strahl et
al. 1995, p. 81) (Factors B and D).
(2) Reserva La Sirena (Valle de Cauca)
is located above 2,000 m (6,562 ft) and
consists of fragmented riparian forest in
various stages of succession (Kattan et
al. 2006, pp. 302-303). Reserva La
Sirena has an environmental education
center, around which are located some
protected areas as well as continuous
forest above 2,000 m (6,562 ft). Visual
confirmation of the Cauca guan was
made in this locality in surveys
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15:11 Jul 06, 2009
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conducted in 2000 and 2001, but the
extent and occurrence of the population
have yet to be determined (Kattan et al.
2006, p. 303).
(3) Reserva Forestal de Yotoco (Valle
de Cauca) is an isolated 5.6-km2 (2.16mi2) reserve on the eastern slopes of the
Western Andes, ranging in altitude from
1,400 to 1,600 m (4,593 to 5,249 ft)
(Kattan et al. 2006, p. 302). In
population surveys conducted by Kattan
et al. (2006, p. 304) in 2000 and 2001,
this subpopulation was estimated to
include between 35 and 61 individuals.
One of the last remaining humid
tropical forests in the Valle de Cauca,
the forest is mostly wellconserved, but
human impacts are evidenced by an
asphalt highway running through the
middle of the Reserve and numerous
footpaths crossing the Reserve to
connect to coffee plantations, which,
along with pasturelands, surround the
forest (BLI 2007h, p. 13).
(4) Chorro de Plata (Valle de Cauca)
is a 2-km2 (0.77-mi2) forest located at
1,200 m (3937 ft) (Kattan et al. 2006, p.
299; Renjifo 2002, p. 302). Visual
confirmation of the Cauca guan was
made in this locality in surveys
conducted in 2000 and 2001, but the
extent and occurrence of the population
have yet to be determined (Kattan et al.
2006, p. 303).
(5) Munchique National Natural Park
(Cauca) is considered an important
locality in the southern portion of the
species’ range, because the species was
historically seen there several times and
because suitable habitat still exists there
(Kattan et al. 2006, pp. 305-306).
However, the Cauca guan has not been
confirmed there since 1987 (Kattan et al.
˜
2006, p. 305; Munoz et al. 2006, p. 54;
Salaman in litt. 1999, 2000, as cited in
BLI 2007h, p. 2) (see Population
Estimates, above). Moreover, the
location of this Park within the Pacific
Region makes it particularly accessible
and vulnerable to exploitation because
of the numerous rivers in this part of the
country, which facilitate movement of
people and products through the region
(Ojeda et al. 2001, pp. 308-309). In the
1960s and 1970s, the harvest of native
‘‘naranjilla’’ or ‘‘lulo’’ fruits (Solanum
quitoense) became an important part of
the local economy, which deterred
logging. However, logging resumed in
the 1980s after a fungal pathogen—
anthracnose (Colletotrichum acutatum)
(Caicedo and Higuera 2007, p. 41)— and
invasion by a lepidopteran pest—tomato
fruit borer (Neoleucinodes elegantalis)
(Eiras and Blackmer 2003, p. 1)—
destroyed the crops (BLI 2006, p. 2).
Human pressures in the Pacific Region
include unsustainable logging,
colonization, and cash crop cultivation
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32329
(Ojeda et al. 2001, pp. 308-309). Efforts
are underway to replant lulo fruit trees
to encourage a sustainable local
economy, enhance local involvement in
conservation, and provide technical
skills for integrated pest management.
However, logging is ongoing within the
Park, and human population pressures
and associated deforestation, as well as
dam construction, are ongoing in the
area (BLI 2007h, p. 2).
There are several areas of suitable
habitat in which the Cauca guan has not
been observed, but that could serve as
important potential habitat for the
species (see Factor E, Likelihood to
Disperse), including: (1) Bosques del
´
˜
Oriente del Risaralda, (2) Canon del Rıo
Barbas y Bremen, (3) Finca la Betulia
Reserva la Patasola,and (4) Reserva
´
Natural Cajibıo. These areas are
described below.
(1) Bosques del Oriente del Risaralda
(Risaralda): This 23 km2 (8.9 mi2) forest
is located on the western slopes of the
Central Andes, in eastern Risaralda. It
ranges in altitude between 1,300 and
3,800 m (5,905 and 12,467 ft). This highaltitude forest is important for the
hydrology in lower-elevation areas,
´
including the Otun-Quimbaya Flora and
Fauna Sanctuary (Department of
Risaralda), where the Cauca guan has
been observed. The forest has been
recovering from deforestation for the
past 30 years and includes a contiguous
patch of montane and premontane forest
over 85 percent of the area. About 15
percent of the land is zoned for grazing
and agriculture, leading to ongoing
degradation of these deforested areas,
along with conversion for human
settlements within the forest (BLI
2007h, p. 6).
´
˜
(2) Canon del Rıo Barbas y Bremen
(Risaralda): This 51-km2 (20-mi2) forest
is located on the western slopes of the
Central Andes. It ranges in altitude
between 1,600 and 2,100 m (5,249 and
6890 ft). This area includes most of the
Reserva Forestal Bremen (BLI 2007h, p.
9), where the Cauca guan was observed
several times between 1995 and 1997
(Renjifo 2002, pp. 124-125). The Bremen
Forest Reserve was established in the
1970s to protect important waterways
and is protected within the regional
system of protected areas in the coffeegrowing region. Today, the Bremen
forest is comprised of 3.4 km2 (1.31 mi2)
of natural forest and 4.2 km2 (1.62 mi2)
of exotic plantation forests, which are
now being allowed to regenerate to
natural forest. A sustainable forestry
management plan was implemented in
1996, and plans are underway to
connect the isolated forest patches
˜
within the Canon. Currently, the forest
´
˜
patches within the Canon del Rıo Barbas
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y Bremen are surrounded by cattle
ranches and tree plantations, primarily
including eucalyptus (Eucalyptus spp.)
and Mexican weeping pine (Pinus
patula). There is no further information
on the progress of this project.
Currently, the forests located within the
˜
Canon are isolated from each other, and
urbanization, agricultural activities, and
deforestation are ongoing within the
area. The forest is also in close
proximity to a main highway in the
region—the highway between Armenia
˜
and Pereira. A survey of the Canon in
2003 did not reconfirm the presence of
the Cauca guan within this area (BLI
2007h, p. 9).
(3) Finca la Betulia Reserva la
´
Patasola (Quindıo): This 17-km2 (7-mi2)
forest is located on the western slopes
of the Central Andes. It ranges in
altitude between 2,050 and 2,600 m
(6,726 and 8,530 ft). Most of this
Reserve is covered by primary forest
interspersed with scrub forest and
streams. As of 2003, the Cauca guan has
been reported but not confirmed within
this Reserve. The western border of this
´
Reserve abuts the Otun-Quimbaya Flora
and Fauna Sanctuary (BLI 2007h, p. 12),
where the population is estimated to be
between 144 and 264 individuals
(Kattan et al. 2006, p. 304).
´
(4) Reserva Natural Cajibıo (Cauca):
This 0.52-km2 (0.2-mi2) reserve is
located on the slopes of the West Andes.
It ranges in altitude between 1,100 and
1,250 m (3,609 and 4,101 ft). The habitat
is mainly secondary forest, interspersed
with agricultural fields (sugarcane
(Saccharum officinarum), coffee,
bananas, and corn (Zea mays)) and
cattle ranching. This Reserve has been
altered by human encroachment and
indiscriminate logging. The Cauca guan
was not confirmed in this location in a
2003 survey (BLI 2007h, p. 15).
These refugia are limited in size,
isolated from each other, and
undergoing varying levels of human
encroachment and deforestation (Brooks
and Strahl 2000, pp. 13-14; Collar et al.
1994, pp. 61-62; del Hoyo 1994, pp. 337,
349; Kattan et al. 2006, p. 301; Renjifo
2002, p. 128). In addition, regulatory
mechanisms within these areas are
inadequate to protect the species from
ongoing habitat destruction (Factor D).
Summary of Factor A
The habitat preferred by the Cauca
guan—humid forests or secondary
forests, forest edges, and plantations in
proximity to humid forests—has been
largely destroyed by cultivation,
grazing, human settlements, road
building, and other human activities.
The species’ range has been reduced
from 24,900 km2 (9,614 mi2) to
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15:11 Jul 06, 2009
Jkt 217001
approximately 560 km2 (216 mi2), much
of this within the past 30 years. Habitat
fragmentation has isolated remaining
populations, relegated the species to the
edges of its former range, and led to a
shift in the species’ altitudinal range.
Habitat destruction, alteration,
conversion, and fragmentation have
been factors in the Cauca guan’s
historical decline (which commenced in
the second half of the 20th Century) and
continue to be factors in the species’
decline, even in areas designated as
protected (see also Factor E). Therefore,
we find that the present destruction,
modification, and curtailment of habitat
are a threat to the Cauca guan
throughout all of its range.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
Cracids are considered particularly
vulnerable to hunting pressures and are
among those species most rapidly
depleted by hunting (Redford 1992, p.
419). Several factors contribute to the
sensitivity of Cauca guans to hunting,
including: their large size, ease of
locating them during their breeding
season, their trusting nature, their low
productivity (1-2 eggs) relative to other
Galliformes, their long generation time,
their dependence upon specific habitat,
and their poor dispersal qualities
(Brooks 1999, p. 43; del Hoyo 1994, p.
336; Silva and Strahl 1991, p. 38). This
species, as with other guans, tends to
aggregate within its habitat, generally
based on resource availability. For
instance, Cauca guans tend to
congregate around fruit trees at certain
times of year (Kattan et al. 2006, p. 305).
This aggregation of individuals may
facilitate hunters in catching larger
numbers of the species. Cracids are also
slow to reproduce, with a replacement
rate of at least 6 years (Silva and Strahl
1991, p. 50).
The Cauca guan, as well as other
cracids (e.g., chachalacas (Ortalis sp.),
serve as a major source of protein for
indigenous people (Brooks and Strahl
2000, p. 8). The Cauca guan is hunted
by local residents for sustenance,
although this activity is illegal (del
˜
Hoyo 1994, p. 337; Munoz et al. 2006,
p. 50; Renjifo 2002, p. 128; Rios et al.
2006, pp. 22-23) (Factor D). The species
is sought after by hunters because it is
the largest bird in its area of distribution
(Renjifo 2002, p. 128). Rios et al. (2006,
pp. 22-23) interviewed local settlers
´
near the Otun-Quimbaya Flora and
Fauna Sanctuary (in Risaralda), where
the population is estimated to be
between 144 and 264 individuals
(Kattan et al. 2006, p. 304), who
admitted to hunting the Cauca guan
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Fmt 4701
Sfmt 4702
within the Sanctuary, claiming to take
between two and four birds per month.
This equates to approximately 100
Cauca guans per year (Rios et al. 2006,
p. 23).
Subsistence hunting may play a role
in the decline or possible local
extirpation of the species from at least
two locations. In the late 1990s,
subsistence hunting was widespread in
´
the Ucumarı Regional Park and
Munchique National Natural Park
(Collar et al. 1992, p. 60; del Hoyo 1994,
p. 349; Strahl et al. 1995, p. 81). The
Cauca guan may have been locally
extirpated from the Munchique National
Natural Park (Cauca) (BLI 2007h, p. 2:
Renjifo 2002, p. 124), where the species
was last observed in 1987 (Renjifo 2002,
p. 124). Despite subsequent searches of
the area (Wege and Long 1995, p. 149),
there have been no recent confirmations
at this locality (Kattan et al. 2006, p.
˜
305; Munoz et al. 2006, p. 54; Salaman
in litt. 1999, 2000, as cited in BLI 2007h,
´
p. 2). Ucumarı Regional Park is
considered the stronghold of the Cauca
guan (BLI 2007h, p. 1). Although Renjifo
(2002, p. 128) notes that the species has
recuperated within this Park, there have
only been scant reports of Cauca guan
sightings there between 1994 and 2004
(Renjifo 2002, p. 125; Scanlon 2004, pp.
1-3; Wege and Long 1995, p. 141), and
no population surveys have been
undertaken there (see Population
Estimates, above).
Habitat fragmentation and
concomitant human encroachment
(Factor A) have made the species’
habitat more accessible and the species
more vulnerable to hunting. A study
conducted in French Guiana provided a
quantitative estimate of the effect of
hunting on a related cracid species, the
black curassow (Crax alector) (del Hoyo
1994, p. 336). The black curassow has
similar habitat requirements
(undisturbed primary tropical to
subtropical humid forest at 0-1,400 m
(0-4,600 ft) elevation) as the Cauca guan
(BLI 2007e). The estimated population
density of black curassows in nonhunted areas was between 7 and 9 birds
per 1 km2 (0.4 mi2); in areas with
intermittent hunting, the numbers fell to
between 0.5 and 2.25 birds; and in areas
where hunting was regular, numbers fell
to between 0.5 and 0.73 birds (del Hoyo
1994, p. 336). We believe that the effects
of hunting on the Cauca guan would
result in similar population declines
based on similarities of habitat and
species characteristics.
Summary of Factor B
Cracids serve as a major food source
in Colombia, and the Cauca guan, as the
largest cracid living within its area of
E:\FR\FM\07JYP3.SGM
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distribution, is sought after by locals.
Hunting results in the direct removal of
eggs, juveniles, and adults from the
population. Cauca guans are slow to
reproduce, produce a low clutch size,
require a long fledging period, and
exhibit a poor replacement rate (see
Habitat and Life History, above).
Hunting can destroy pair bonds and
remove potentially reproductive adults
from the breeding pool. Hunting is
facilitated by habitat fragmentation
(Factor A), which increases access to the
forest by hunters. The Cauca guan is
hunted throughout its current range,
including within protected areas, and
hunting may be responsible for a
decline or local extirpation of the
species from at least two of these
´
protected areas (Ucumarı Regional Park
and Munchique National Natural Park).
Therefore, we find that subsistence
hunting for domestic consumption is a
threat to the Cauca guan throughout its
range.
reproduce, produce a low clutch size,
require a long fledging period, and
exhibit a poor replacement rate (see
Habitat and Life History, above).
Predation can destroy pair bonds and
remove potentially reproductive adults
from the breeding pool. Cauca guan
habitat is fragmented and small (Factor
A), and studies on similar species in
similar Andean habitats indicate that
vulnerability to predation by generalist
predators increases with increased
habitat fragmentation and smaller patch
sizes. Predation exacerbates the genetic
complications associated with the
species’ small population size (Factor
E). Because of the species’ small
population size and inability to
recolonize isolated habitat fragments
(Factor E), predation renders the species
vulnerable to local extirpation.
Therefore, we find that predation,
exacerbated by ongoing habitat
destruction (Factor A) and hunting
(Factor B), is a threat to the Cauca guan.
C. Disease or Predation
Disease: We are unaware of any
information regarding disease or the
potential for significant disease
outbreaks in the Cauca guan
populations. As a result, we do not
consider disease to be a threat to the
species.
Predation: Predators of cracids
include snakes, foxes, feral cats, feral
dogs, and raptors (Delacour and
Amadon 1973). Cauca guans are also
slow to reproduce, with a long fledging
period (up to 1 year) and a replacement
rate of at least 6 years (Rios et al. 2006,
p. 17; Silva and Strahl 1991, p. 50).
Cauca guans require large territories for
foraging (Kattan 2004, p. 11), but today
are relegated mostly to small forest
fragments (Kattan et al. 2006, p. 301). As
discussed in detail above for the bluebilled curassow (Factor C, Predation),
studies have shown that habitat
fragmentation increases the potential
predation pressure within habitat
fragments by facilitating the predators’
access throughout the fragment and
because smaller fragments support
smaller predators, which tend to
depredate on the more vulnerable lifehistory stages of the Cauca guan, eggs
´
and juveniles (Arango-Velez and Kattan
1997, pp. 137-143; Gibbs 1991, p. 157;
Hoover et al. 1995, p. 151; Keyser et al.
1998, p. 991; 2002, p. 186; Renjifo 1999,
p. 1133; Wilcove 1985, p. 1214).
D. The Inadequacy of Existing
Regulatory Mechanisms
Regulatory mechanisms may provide
species-specific or habitat-specific
protections. An evaluation of the
adequacy of regulatory mechanisms
within Colombia to mitigate or remove
the threats to the Cauca guan is
provided below, beginning with speciesspecific and followed by habitat-specific
protection mechanisms.
Colombia has enacted numerous laws
to protect species and their habitats
(Matallana-T. 2005, p. 121). The Cauca
guan is listed as an endangered species
under Colombian Law 99 of 1993
(EcoLex 1993, p. 2) and Resolution No.
584 of 2002 (EcoLex 2002, pp. 10, 12).
A full description of these laws and the
categorization of threatened species in
Colombia were provided above, as part
of the Factor D analysis for the bluebilled curassow. This threat status
confers protections upon the species,
including protection from commercial
take under Resolution No. 849 of 1973
and Resolution No. 787 of 1977 (EcoLex
1973, p.1; EcoLex 1977, p. 3). Neither
Resolution prohibits subsistence
hunting. As discussed under Factor B,
commercial and sport hunting are not
threats to this species, but subsistence
hunting continues to threaten the
species throughout its range, including
within protected areas. Hunting may
play a role in the decline or possible
local extirpation of the species from two
protected areas, Munchique National
´
Natural Park and Ucumarı Regional
Park, where subsistence hunting was
widespread in the 1990s (Collar et al.
1992, p. 60; del Hoyo 1994, p. 349;
Strahl et al. 1995, p. 81) (Factor B).
Summary of Factor C
Snakes, foxes, feral cats, feral dogs,
and raptors are all predators of cracids.
Predation results in the direct removal
of eggs, juveniles, and adults from the
population. Cauca guans are slow to
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32331
Cauca guans have not been observed in
Munchique National Natural Park since
1987 (BLI 2007h, p. 2: Renjifo 2002, p.
124), despite subsequent searches of the
area (Wege and Long 1995, p. 149).
Similarly, since 1994, there have been
only scant sightings of Cauca guans in
´
the Ucumarı Regional Park (Renjifo
2002, p. 125; Scanlon 2004, pp. 1-3;
Wege and Long 1995, p. 141) (see
Population Estimates, above).
Researchers have indicated that local
residents continue to hunt the Cauca
guan despite the illegality of this
˜
activity (del Hoyo 1994, p. 337; Munoz
et al. 2006, p. 50; Renjifo 2002, p. 128;
Rios et al. 2006, pp. 22-23), even within
areas designated as ‘‘protected’’ under
Colombian law (see also next
paragraph). For instance, settlers in the
´
Otun-Quimbaya Flora and Fauna
Sanctuary admit to taking between 24
and 48 Cauca guans a year (Rios et al.
2006, pp. 22-23) (Factor B). Thus, these
Resolutions are ineffective at reducing
the existing threat of subsistence
hunting to the Cauca guan.
Colombia has enacted numerous
forestry laws and forestry management
practices (Law No. 2 (EcoLex 1959);
Decree No. 2,811 (Faolex 1974); Decree
No. 1,791 (Faolex 1996); Law No. 1,021
(EcoLex 2006)). Weaknesses in the
implementation of these laws and the
decentralized nature of Colombian
resource management are described in
detail above for the blue-billed curassow
(Factor D) (ITTO 2006, pp. 218-9, 222;
Matallana-T. 2005, pp. 121-122). Experts
consider these decentralized
management mechanisms to be
ineffective at protecting the Cauca guan
from habitat destruction (Factor A) or
˜
hunting (Factor B) (Munoz et al. 2006,
p. 50). Habitat destruction and hunting
are ongoing throughout the species’
range, indicating that forestry
regulations are ineffective at mitigating
the threats to the Cauca guan from
habitat destruction (Factor A) or hunting
(Factor B).
Colombia has several categories of
national habitat protection (Matallana-T.
2005, p. 121-122), which were described
above, as part of the Factor D analysis
for the blue-billed curassow (MatallanaT. 2005, p. 121-122). The Cauca guan
occurs within national parks (including
´
the Ucumarı Regional Park, last
confirmed Cauca guan sighting in 2004
(Scanlon 2004, pp. 1-3), and Munchique
National Natural Park, confirmed in
˜
1987 (Kattan et al. 2006, p. 305; Munoz
et al. 2006, p. 54; Salaman in litt. 1999,
2000, as cited in BLI 2007h, p. 2));
reserves (Reserva Forestal de Bremen,
confirmed in 1997 (Renjifo 2002, pp.
124-125), Reserva Forestal de Yotoco,
confirmed in 2000-2001 (Renjifo 2002,
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pp. 124-125), and Reserva La Sirena,
confirmed in 2000-2001 (Kattan et al.
´
2006, p. 302)); and sanctuaries (OtunQuimbaya Flora and Fauna Sanctuary,
confirmed in 2000-2001 (Kattan et al.
2006, p. 302)). Within the last 20 years,
the Cauca guan population may have
declined or been extirpated from at least
two Parks, the Munchique National
´
Natural Park and the Ucumarı Regional
Park, where the species has not been
observed since 1987 (Renjifo 2002, pp.
124-125) and 2004 (Scanlon 2004, pp. 13), respectively. These Parks were
subject to subsistence hunting in the
late 1990s (Collar et al. 1992, p. 60; del
Hoyo 1994, p. 349; Strahl et al. 1995, p.
81), and subsistence hunting of Cauca
guan continues in these and other
´
protected areas, such as Otun-Quimbaya
Flora and Fauna Sanctuary (Rios et al.
2006, pp. 22-23) (Factor B). In addition,
logging, population pressure and
agriculture are ongoing within these
´
Parks. Ucumarı Regional Park,
considered the stronghold for the
species (BLI 2007h, p. 2), continues to
be managed for multiple uses (including
pasture land and other commercial
ventures) (Factor A). In light of the
multiple land uses allowed within the
Park, and the ongoing human-induced
habitat destruction, the Park provides
little or no protection to the species
from the threat of habitat destruction
(Factor A).
The Cauca guan ranges in multiple
Departments (currently known in Cauca,
´
Quindıo, Risaralda, Valle de Cauca),
each of which administers their own
natural resources under different
´
autonomous Corporaciones (ITTO 2006,
p. 219; Law 99 of 1993). We are unaware
of any coordinated species management
plan. Therefore, in view of the
decentralized resource management
structure, the absence of a conservation
strategy for the species, the threats to
the Cauca guan from habitat destruction
(Factor A) and hunting (Factor B) are
not mitigated.
Summary of Factor D
Colombia has numerous laws and
regulatory mechanisms to administer
and manage wildlife and their habitats.
The Cauca guan is listed as endangered
under Colombian law and occurs within
several protected areas. However, onthe-ground enforcement of existing
wildlife protection and forestry laws
and oversight of the local jurisdictions
implementing and regulating activities
are ineffective at mitigating the primary
threats to the Cauca guan. As discussed
for Factor A, habitat destruction,
degradation, and fragmentation
continue throughout the existing range
of the Cauca guan. As discussed for
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Factor B, uncontrolled subsistence
hunting of the Cauca guan is ongoing
and continues to negatively affect the
continued existence of the species.
Moreover, the lack of a species
conservation strategy and the
decentralized management of natural
resources in Colombia provide no
overall coordination in the conservation
of species such as Cauca guans, which
range in multiple jurisdictions.
Therefore, we find that the existing
regulatory mechanisms currently in
place are inadequate to mitigate the
primary threats to the Cauca guan.
E. Other Natural or Manmade Factors
Affecting the Continued Existence of the
Species
Two additional factors affect the
Cauca guan: Its minimal likelihood for
dispersal and the species’ small
population size.
Likelihood to Disperse: The Cauca
guan exhibits characteristics indicative
of an inability to disperse into isolated
habitat fragments and recolonize
patches of suitable habitat that have
undergone a localized extirpation. The
Cauca guan prefers habitat of mature
humid forests (Collar et al. 1994, p.
136), has generally been found only in
secondary habitats that are situated
within 1 km (0.62 mi) of primary forest
(Renjifo 2002, p. 127), and is reported as
timid in the presence of humans (Rios
et al. 2006, p. 21). The remaining
suitable habitat available to the Cauca
guan is limited to a few disjunct and
isolated forest fragments only a few
hundred hectares (100 hectares = 1 km2
= 0.39 mi2) in size (Kattan 2004, p. 6;
Kattan et al. 2006, p. 301; Renjifo 2002,
p. 128).
Existing habitat for the Cauca guan is
fragmented, with large distances
between the remaining primary forest
fragments (Cuervo and Salaman 1999, p.
7; Hanski 1998, pp. 45-46) and an evergrowing human presence in and around
the species’ existing habitat (BLI 2004c,
p. 2; Cuervo 2002, p. 327; Cuervo and
Salaman 1999, p. 8; Renjifo 2002, pp.
124-128; Stattersfield et al. 1998, p.
205). Without human intervention, the
Cauca guan is unlikely to repopulate an
isolated patch of suitable habitat
following decline or local extirpation.
Evidence for the Cauca guan’s inability
to disperse across fragmented habitat
patches is provided by the fact that
there are several areas of suitable
habitat, located near previously reported
localities for the species, in which the
Cauca guan has not been observed (see
Factor A, Refugia).
Small Population Size: Habitat
destruction (Factor A) and hunting
(Factor B) have affected the current
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population size and distributional range
of the Cauca guan (Collar et al. 1992, pp.
126-127; Collar et al. 1994, p. 60). By the
1980s, the species was believed extinct
or on the verge of extinction (Brooks
and Strahl 2000, p. 14; del Hoyo 1994,
pp. 337, 349; Hilty 1985, p. 1004; Hilty
and Brown 1986, p. 125). The Cauca
guan is now confirmed only in several
isolated locations. Overall, the
population is considered to be in
decline, with the current isolated
populations ranging from tens of
individuals to a few hundred
individuals at best (BLI 2007h, p. 2;
Kattan 2004, p. 6; Renjifo 2002, p. 129),
but there have been few population
surveys of the Cauca guan. In 2006,
˜
Kattan (in litt., as cited in Munoz et al.
2006 p. 55) estimated the global
population to be between 196 and 342
individuals. Kattan et al. (2006, p. 302)
conducted the only two population
˜
surveys, in 2000 and 2001 (Munoz et al.
2006 p. 55). They estimated population
´
densities at two locations, OtunQuimbaya Flora and Fauna Sanctuary
(Risaralda) and Reserva Forestal de
Yotoco (Valle de Cauca), to be between
144 and 264 individuals, and 35 to 61
individuals, respectively (Kattan et al.
2006, p. 304).
Small population sizes render species
vulnerable to genetic risks that can have
individual or population-level
consequences on the genetic level and
can increase the species’ susceptibility
to demographic problems, as explained
in more detail above for the blue-billed
curassow (Factor E, Small Population
Size) (Charlesworth and Charlesworth
1987, p. 238; Shaffer 1981, p. 131). Once
a population is reduced below a certain
number of individuals, it tends to
rapidly decline towards extinction
(Franklin 1980, pp. 147-148; Gilpin and
´
Soule 1986, p. 25; Holsinger 2000, pp.
´
64-65; Soule 1987, p. 181).
In the absence of quantitative studies
specific to this species, a general
approximation of minimum viable
population size is the 50/500 rule, as
described above as part of the Factor E
analysis for the brown-banded antpitta
´
(Shaffer 1981, pp. 132-133; Soule 1980,
pp. 160-162). The total population size
of the Cauca guan is estimated to be
between 196 and 342 individuals. While
196 individuals is above the minimum
population size required to avoid shortterm genetic consequences, 342 falls
below the threshold minimum number
of 500 individuals required for longterm fitness of a population.
Moreover, because the Cauca guan
exists in isolated forest fragments and is
unlikely or incapable of dispersing to
disjunct patches, each disjunct locality
likely acts as a subpopulation.
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Therefore, the resiliency of each of these
subpopulations will be lower than that
of the global population. The largest
´
reported subpopulation, in OtunQuimbaya Flora and Fauna Sanctuary,
contains between 144 and 264
individuals (Kattan et al. 2006, p. 304).
The lower figure, 144 individuals, is
above the minimum effective
population size required to avoid
imminent risks from inbreeding (Ne =
50). The upper limit of the
subpopulation, 264 birds, represents the
maximum number of individuals in the
subpopulation, but does not take into
account that not all members of the
population will be reproductive. This
figure is well below the upper threshold
(Ne = 500 individuals) required for longterm fitness of a population to ensure
that the species will not lose its genetic
diversity over time and will maintain an
enhanced capacity to adapt to changing
conditions. The only other
subpopulation figures are for Reserva
Forestal de Yotoco, with an estimated
35 to 61 individuals (Kattan et al. 2006,
p. 304). Both of these figures are well
below the 50/500 threshold. Therefore,
we currently consider these
subpopulations (and the species as a
whole) to be at risk from genetic
complications due to the lack of shortand long-term viability.
The Cauca guan’s small population
size, combined with its restricted range
and inability to repopulate suitable
habitat following local extirpations
(Cuervo and Salaman 1999, p. 7; del
Hoyo 1994, p. 361; Renjifo 2002, p. 138),
makes the species particularly
vulnerable to the threat of adverse
natural (e.g., genetic, demographic, or
environmental) and manmade (e.g.,
hunting or deforestation) events that
destroy individuals and their habitat
(BLI 2007, pp. 1-2; Holsinger 2000, pp.
64-65; Renjifo 2002, p. 140; Young and
Clarke 2000, pp. 361-366).
Summary of Factor E
The Cauca guan is now confirmed
only in several isolated locations. The
Cauca guan is unlikely or incapable of
dispersing into suitable habitat that is
isolated from extant populations, and
the species’ overall small population
size makes it vulnerable to genetic and
demographic risks that negatively
impact the species’ short- and long-term
viability. The Cauca guan’s small
population size, restricted range, and
inability to repopulate suitable habitat
following local extirpations expose the
species to threats associated with
adverse natural (e.g., genetic,
demographic, or environmental) and
manmade (e.g., hunting or deforestation)
events that destroy individuals and their
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habitat. Therefore, we believe that, in
combination with the risks to the
species from habitat destruction (Factor
A), hunting (Factor B), and predation
(Factor C), the Cauca guan is vulnerable
to localized extirpation or extinction
from which the species would be unable
to recover, due it its small population
size and apparent inability to repopulate
fragmented, isolated habitats such as
those currently present within this
species’ range.
Status Determination for the Cauca
Guan
The five primary factors that threaten
the survival of the Cauca guan are: (1)
habitat destruction, fragmentation, and
degradation; (2) overexploitation due to
hunting; (3) predation (Factor C); (4)
inadequacy of regulatory mechanisms to
reduce the threats to the species (Factor
D); and (5) small population size and
isolation of remaining populations
(Factor E). The Cauca guan, a large,
primarily terrestrial bird, prefers humid
forests or secondary forests, forest edges
and plantations that are in close
proximity (within 1 km (0.62 mi)) to
humid forests.
Habitat destruction, alteration,
conversion, and fragmentation were
factors in the Cauca guan’s historical
decline. The species has experienced a
95 percent range reduction since the
1950s, such that the estimated suitable
habitat available to the species is
approximately 560 km2 (216 mi2).
Experts estimate that more than 30
percent of this loss of habitat has
occurred within the last three
generations, or 30 years. Fifty years ago,
the species’ historic range was estimated
to have been an approximately 24,900km2 (9,614-mi2) area, encompassing
humid forests on the eastern slopes of
the West Andes and the dry forests of
´
the Cauca, Patıa, and Dagua Valleys, in
´
the Departments of Cauca, Quindıo,
Risaralda, and Valle de Cauca. Today,
the species has been locally extirpated
from the Cauca and Dagua Valleys. The
Cauca guan inhabits the western slopes
of the central and western Andes in the
few remaining upper-elevation forest
remnants at altitudes exceeding those
reported in the first half of the 20th
Century. These shifts to the extremes of
its range and shifts in elevational
distribution have resulted from
extensive habitat destruction throughout
the species’ range. The dry forests of the
´
Cauca, Dauga, and Patıa Valleys and the
humid forests on the slopes of these
valleys up to 2,000 m have been largely
destroyed for cultivation, grazing,
human settlements, road building, and
other human-induced habitat
alterations. Cultivation of illegal drug
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32333
crops, such as cocaine, has led to further
deforestation and altered soil
compositions, hindering regeneration of
abandoned fields. In addition, drug
eradication programs involving the
aerial spraying of non-specific
herbicides have led to further
environmental degradation and habitat
destruction (Factor A).
Although the Cauca guan, which is
listed in Colombia as endangered,
occurs on lands designated by the
Colombian government as ‘‘protected
areas,’’ and it is illegal to commercially
hunt the species, the existing laws and
their enforcement are inadequate (Factor
D) to mitigate the effects of ongoing
habitat destruction (Factor A) and
subsistence hunting (Factor B).
Moreover, natural resource management
within Colombia is highly
decentralized, each district managing
their resources autonomously. Thus,
there is no overall coordination for the
conservation and recovery of the Cauca
guan, which ranges in several
autonomous districts.
Widespread deforestation and
conversion of primary forests has led to
the fragmentation of habitat throughout
the Cauca guan’s range. The remaining
suitable habitat is limited to a few
disjunct and isolated forest fragments,
only a few hundred hectares (100
hectares = 1 km2 = 0.39 mi2) in size.
Habitat fragmentation affects resource
availability for the Cauca guan, which
requires large territories for foraging on
its preferred food source: seasonally
available fruits. Experts believe that
´
remaining refugia, such as the OtunQuimbaya Sanctuary, may not be large
enough to support viable populations,
lacking sufficient space and resources
needed for this large, terrestrial bird.
Habitat fragmentation also increases
the species’ susceptibility to hunting
(Factor B). The Cauca guan is hunted
throughout its current range. As the
largest cracid living within its area of
distribution, the Cauca guan is sought
after by locals as a major food source.
Despite being illegal (Factor D),
subsistence hunting of Cauca guans
continues throughout its range,
including within protected areas.
Hunting may be responsible for the
species’ local extirpation from the
´
Ucumarı Regional Park, considered the
stronghold for the species in the 1990s,
and the Munchique National Natural
Park.
Habitat fragmentation exposes the
species to greater risk of extinction
caused by adverse natural (e.g., genetic,
demographic, or environmental) and
manmade (e.g., hunting or deforestation)
events (Factor E). At the beginning of
the 20th Century through the 1950s, the
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species was considered common.
Habitat fragmentation has led to the
isolation of remaining subpopulations,
which are estimated to range from tens
of individuals or a few hundred
individuals at most, thus affecting the
species’ resiliency. The total population
estimate of 196-342 individuals falls
below the threshold minimum number
of 500 individuals required for longterm fitness of a population. It is
estimated that the species has lost up to
9 percent of its population in the last 10
years. Given that the Cauca guan is
likely to act as subpopulations and its
inability to disperse between
fragmented habitat patches, the species’
effective population size is actually
much less than the global population
estimate would imply. The fitness of the
subpopulations is vital to understanding
the viability of the species. The largest
subpopulation, estimated to contain
between 144 and 264 individuals, falls
below the threshold for long-term
viability. The other subpopulation for
which there is an estimate contains
between 35 and 61 individuals, which
figures are below the thresholds for both
short-term and long-term viability.
Thus, the Cauca guan is at risk from
both near-term genetic complications
(such as inbreeding and demographic
shifts) and the lack of long-term fitness
(such as the ability to adapt to changing
conditions). Because the species exists
in isolated subpopulations, the risk from
near-term genetic consequences, such as
inbreeding and demographic shifts, is
further magnified. These potential
genetic problems are exacerbated by
ongoing human-induced threats, such as
habitat destruction (Factor A) and
hunting (Factor B), factors which are not
being mitigated by existing regulations
(Factor D), and are further magnified by
the species’ inability to repopulate
isolated, fragmented patches of suitable
habitat, where Cauca guan populations
have undergone decline or local
extirpation (Factor E).
We have carefully assessed the best
available scientific and commercial
information regarding the past, present,
and potential future threats faced by the
Cauca guan. We consider the ongoing
threats to the Cauca guan, habitat
destruction (Factor A), hunting (Factor
B), and predation (Factor C),
exacerbated by the species’ small
population size and limited dispersal
ability (Factor E), and compounded by
inadequate regulatory mechanisms to
mitigate these threats (Factor D), to be
equally present and of the same
magnitude throughout the species’
entire current range. Based on this
information, we determine that the
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Habitat and Life History
despite the availability of suitable
habitat adjacent to the species’ current
locations, these areas are above the
elevational range of the species and are
not used. Moreover, in the most recent
´
population surveys in the Yarguıes
´
´
Mountains (Serranıa de los Yarguıes),
which range up to 3,200 m (10,498 ft),
researchers heard the species vocalizing
primarily at elevations between 1,800
and 1,900m (5,905 and 6,234 ft), and
none were heard above 1,950-2,000 m
(6,398-6,562 ft) (Donegan and Huertas
2005, p. 29; Donegan et al. 2003, p. 29;
Donegan et al. 2004, p. 19). There are no
recorded observations of this species at
ranges above 2,050 m (6,726 ft) (BLI
2007g, p. 2; Donegan and Huertas 2005,
p. 29; Donegan et al. 2003, p. 27; Sarria
´
and Alvarez 2002, p. 160; Turner 2006,
p. 22; Wege and Long 1995, pp. 143144). Therefore, we conclude that the
species’ preferred range remains at
elevations between 1,750 and 2,050 m
(5,741 and 6,726 ft).
The gorgeted wood-quail is primarily
terrestrial (Fuller et al. 2000, p. 2), living
on the forest floor and feeding on fruit,
seeds, and arthropods (Collar et al.
1992, pp. 171-172; del Hoyo 1994, p.
431; Fuller et al. 2000, pp. 27-28). There
appear to be two breeding seasons per
year, coinciding with the rainy seasons
from March through May and
September through November (BLI
2007g, p. 3). Gorgeted wood-quails are
ground-nesting birds, laying their eggs
in a small depression lined with
vegetation and almost always covered
with brush from the understory (Sarria
´
and Alvarez 2002, p. 159). Similar to
other wood-quails, gorgeted woodquails associate in small groups and call
to other groups by chorusing—singing
together (Donegan et al. 2003, p. 29).
Researchers consider this species to be
dependent on primary forest for at least
part of its life cycle (BLI 2007g, p. 3;
´
Sarria and Alvarez 2002, p. 159).
The gorgeted wood-quail prefers
montane temperate and humid
subtropical forests dominated by roble,
Tabebuia rosea, and secondary-growth
forests in proximity to mature forests
´
(Sarria and Alvarez 2002, p. 159),
especially those dominated by oak
(Quercus humboldtii). The species is
most often found at elevations between
1,750 and 2,050 m (5,741 and 6,726 ft)
(BLI 2007g, p. 2; Donegan and Huertas
2005, p. 29; Donegan et al. 2003, p. 27;
´
Sarria and Alvarez 2002, pp. 158-159;
Turner 2006, p. 22; Wege and Long
1995, pp. 143-144). Fuller et al. (2000,
pp. 27-28) suggested that the species’
range may be up to 2,500 m (8,202 ft)
in elevation. However, Sarria and
´
Alvarez (2002, p. 160) noted that,
Historical Range and Distribution
The gorgeted wood-quail historically
occurred on the western slope of the
East Andes, in the Departments of
Santander and Cundinamarca in
Colombia (del Hoyo 1994, p. 431;
¨
Fjeldsa and Krabbe 1990, p. 141; Hilty
and Brown 1986, p. 133). Since the 17th
Century, extensive logging and land
conversion in Cundimarca to
agricultural uses nearly denuded all the
forests of this area below 2,500m (8,202
ft) (BLI 2007g, p. 3; Hilty and Brown
1986, p. 133). Habitat destruction is
considered the primary factor that led to
the historical decline and extirpation of
this species from Cundinamarca (Fuller
et al. 2000, pp. 4-5; Wege and Long
1995, p. 146).
Cauca guan is in danger of extinction
throughout all of its range. Therefore,
we are proposing to list the Cauca guan
as an endangered species.
IV. Gorgeted Wood-Quail
(Odontophorus strophium)
Species Description
The gorgeted wood-quail, endemic to
Colombia and a member of the New
World Quail Family (Odontophoridae),
is approximately 25 cm (10 in) long (del
¨
Hoyo 1994, p. 431; Fjeldsa and Krabbe
1990, p. 141; Hilty and Brown 1986, p.
133). The species is locally known as
‘‘perdiz Santandereana’’ or ‘‘perdiz de
´
monte’’ (Sarria and Alvarez 2002, p.
158), and may be referred to by the more
general term ‘‘forest partridge’’ in
English (BLI 2007g, p. 1). Mainly dark
brown with black spots on upper parts,
the male has a speckled black and white
face, and a white collar on his throat
surrounded on the upper and lower side
by a band of black. Underparts are
rufous-chestnut colored with white
spotting. The female appears similar to
the male; however, the female has a
black collar surrounded by white bands
on her throat (BLI 2007g, p. 1).
Taxonomy
The gorgeted wood-quail was first
taxonomically described in 1844 by
Gould, who placed the species in the
Odontophoridae family, also known as
the New World Quails (BLI 2007g, p. 1).
The type specimen (the actual specimen
that was first described by Gould) was
obtained in the Colombian Department
of Cundinamarca (Hilty and Brown
1986, p. 133), although details on the
location were not provided with the
description (Warren 1966, p. 318).
Therefore, we will refer to the
Department of Cundinamarca as the
‘‘type locality.’’
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For many years, the species was
known only from two specimens
collected in 1915 from its type locality
in Cundinamarca (Hilty and Brown
1986, p. 133). Although the species was
reported at this site again in 1923 and
1954, it has not been seen there since
that time (Wege and Long 1995, p. 146).
The species was believed extinct until a
record of a male bird and chicks was
reported in 1970 in Santander
Department in the Cuchilla del Ramo
forest (Collar et al. 1992, p. 171; Fuller
et al. 2000, p. 27).
Current Range and Distribution
The gorgeted wood-quail is endemic
to the west slope of the East Andes, in
the Magdalena Valley (Donegan and
Huertas 2005, p. 29), and is known only
in the central Colombian Department of
Santander (del Hoyo 1994, p. 431;
¨
Fjeldsa and Krabbe 1990, p. 141; Hilty
and Brown 1986, p. 133). The current
range of this species is between 10 km2
´
(4 mi2) (Sarria and Alvarez 2002, p. 160)
and 27 km2 (10.42 mi2) (BLI 2007g, pp.
2, 5).
Since 1970, the species has only been
reported in the central Colombian
Department of Santandar, with fewer
than 10 sightings. Visual observations of
this species have been scant; most
reports have been inferred from auditory
´
detections (Sarria and Alvarez 2002, pp.
158-159). In 1970, the species was
observed in Cuchilla del Ramo forest
(Wege and Long 1995, p. 143), but has
not been confirmed there since that time
(BLI 2007g, p. 2) (see also Factor A). The
species has been observed and most
recently confirmed in three locations:
´
(1) Guanenta-Alto Rio Fonce Flora and
´
Fauna Sanctuary, (2) Cachalu Biological
´
Reserve, and (3) Serranıa de los
´
Yarguıes. These confirmed sightings are
briefly described below.
´
(1) Guanenta-Alto Rio Fonce Flora
and Fauna Sanctuary (Santander
Department): The gorgeted wood-quail
was confirmed at this location in 1979
(BLI 2007g, p. 2) and again in 1988
´
(Sarria and Alvarez 2002, p. 160; Wege
and Long 1995, p. 144). In 2004, the
species was reported in the oak forests
´
within the Province of Guanenta (BLI
2007g, p. 2), but it is unclear whether
these observations occurred within the
Sanctuary.
´
(2) Cachalu Biological Reserve
(Santander Department): The gorgeted
wood-quail was confirmed in this
Reserve in 1999, 2000, and 2001 (BLI
2007g, p. 2; Fuller et al. 2000, p. 27;
´
Sarria and Alvarez 2002, pp. 158-159).
´
´
(3) Serranıa de los Yarguıes
(Santander Department): The species
has also been confirmed at this location
in 2003 and 2004 (BLI 2007g, p. 2;
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Donegan and Huertas 2005, p. 29;
Donegan et al. 2003, p. 27; Turner 2006,
´
´
p. 22). The Serranıa de los Yarguıes
locale reportedly harbors the largest
known population and is the stronghold
for the species (Donegan and Huertas
2005, p. 29; Turner 2006, p. 22) (see
Population Estimates, below).
Generally speaking, these localities
are in two disjunct locations within the
´
Department of Santander. Serranıa de
´
los Yarguıes is in northern Santander
and the other two localities are adjacent
to each other in southern Santander
(Donegan and Huertas 2005, p. 30;
Rainforest Alliance 2008, p. 2). These
habitats are described more fully under
Factor A (Refugia).
Population Estimates
To the best of our knowledge, there
have been no quantitative studies to
determine the species’ population size.
The population estimates for the
gorgeted wood-quail are based on
qualitative surveys and extrapolations
using suitable habitat estimates (BLI
2007g, p. 2; Donegan and Huertas 2005,
p. 29; Donegan et al. 2003, p. 27; Fuller
´
et al. 2000, p. 27; Sarria and Alvarez
2002, pp. 158-159; Turner 2006, p. 22).
As noted above (see Current Range), a
total of 3 adults and 2 chicks were
observed between 1923 and 1970 (Sarria
´
and Alvarez 2002, p. 158; Wege and
Long 1995, p. 143). The largest number
of visual confirmations of individual
birds has been reported in the Reserva
´
´
Biologico Cachalu. In 1999, two groups
of 7-9 individuals were observed.
Between 2001 and 2002, six groups of
5-11 individuals were observed (Sarria
´
in litt., as cited in Sarria and Alvarez
2002, p. 159). Based on these direct
observations, the population in the
´
´
Reserva Biologico Cachalu may consist
of between 30 and 66 individuals.
All other population estimates have
been inferred from auditory calls or
suitable habitat extrapolations. It is not
unusual to infer population estimates
for elusive, ground-dwelling species,
such as the gorgeted wood-quail, for
which direct observation is difficult.
However, extrapolating population
estimates based on suitable habitat can
lead to overestimations of population
sizes, especially for narrow-ranging
species, such as the gorgeted woodquail. The potential for overestimation
was discussed above, in the analysis of
the brown-banded antpitta (Factor E,
Small Population Size). For instance,
researchers recently estimated that the
´
´
Serranıa de los Yarguıes population may
hold a significantly greater number of
birds than ever known. Given the
inferred density of the species (based on
auditory observation) and the extent of
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32335
´
forest cover in the Serranıa de los
´
Yarguıes, researchers predicted that an
excess of 250 individuals was present at
the site (Donegan and Huertas 2005, p.
30; Donegan et al. 2004, p. 19). Turner
(2006, p. 22) extrapolated the
population size, based on satellite
images of the area, which indicated that
30,000 ha (74,131 ac) of forest at
elevations between 1,500 and 2,200 m
(4,921 and 7,218 ft) on the western slope
and 2,700 and 2,900 m (8,858 and 9,514
ft) on the eastern slope were available to
the species. This yielded a predicted
population size of between 1,800 and
3,300 individuals. However, we believe
that this population estimate, based on
the availability of suitable habitat, may
be an overestimate for this species for
two reasons: (1) the population may not
be randomly distributed throughout the
suitable habitat, as assumed by these
researchers, and (2) the extrapolation
does not take into account humaninduced threats, such as hunting (Sarria
´
and Alavarez 2002, pp. 160-161) (Factor
B). Therefore, until Turner’s (2006, p.
22) predictions have been groundtruthed, we are unable to consider the
predicted population estimate of
between 1,800 and 3,300 individuals to
be a reliable reflection of the current
population size. Consequently, we
consider the population estimate of
between 189 to 486 individuals (BLI
2007g, p. 1) to be the best available
estimate of the gorgeted wood-quail.
Conservation Status
The gorgeted wood-quail is identified
as a critically endangered species under
Colombian law (EcoLex 2002, p. 12).
The species is classified as ‘Critically
Endangered’ on the IUCN Red List, due
to its small and highly fragmented
range, with recent population records
from only two areas (BLI 2004d; BLI
2007g, pp. 1, 5).
Summary of Factors Affecting the
Gorgeted Wood-Quail
A. The Present or Threatened
Destruction, Modification, or
Curtailment of the Habitat or Range
In the early part of the 20th Century,
the gorgeted wood-quail was known
only in the oak forests in the
Department of Cundinamarca. However,
extensive deforestation and habitat
conversion for agricultural use nearly
denuded all the oak forests in
Cundinamarca below 2,500 m (8,202 ft)
(BLI 2007g, p. 3; Hilty and Brown 1986,
p. 133). Deforestation left little
remaining suitable habitat for the
gorgeted wood-quail, which prefers
primary forests and tolerates secondarygrowth forests near primary forests (BLI
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´
2007g, p. 3; Sarria and Alvarez 2002, p.
159) at altitudes from 1,500 to 2,500 m
(4,921 to 8,202 ft) (del Hoyo 1994, p.
431; Fuller et al. 2000, pp. 27-28; Hilty
and Brown 1986, p. 133). Subsequent
surveys have not located the species in
the Department of Cundinamarca since
1954 (Collar et al. 1992, p. 171; Fuller
´
et al. 2000, p. 27; Sarria and Alvarez
2002, p. 158), and researchers consider
the gorgeted wood-quail to be locally
extirpated from Cundinamarca (BLI
2007g, p. 3; Fuller et al. 2000, pp. 4-5;
´
Sarria and Alvarez 2002, p. 160-161;
Wege and Long 1995, p. 146).
Deforestation, in combination with
hunting (Factor B), may have led to the
local extirpation of the gorgeted woodquail from another location. After no
confirmed reports of the species in
´
nearly 20 years (Sarria and Alvarez
2002, pp. 158-159), the species was
rediscovered in Cuchilla del Ramo
forest (in the Department of Santander)
´
in 1970 (Sarria and Alvarez 2002, pp.
158-159; Wege and Long 1995, p. 143)
and last confirmed there in 1988 (Collar
et al. 1992, p. 172). However the species
has not been confirmed at that location
since that time (BLI 2007g, p. 2; Sarria
´
and Alvarez 2002, pp. 158-159).
According to Wege and Long (1995, p.
143), Cuchilla del Ramo, an unprotected
area on the western slopes of the East
Andes, has been largely cleared of its
forest such that only fragments remain.
Thus, it is possible that deforestation
within the past 30 years has led to the
extirpation of the gorgeted wood-quail
from this location.
Today, the gorgeted wood-quail is
endemic to the western slopes of the
East Andes in the Department of
Santander, Colombia (Collar et al. 1994,
¨
p. 70; del Hoyo 1994, p. 431; Fjeldsa
and Krabbe 1990, p. 141; Hilty and
Brown 1986, p. 133). The gorgeted
wood-quail is currently confirmed in
three locations (see Refugia, below), and
its current range is between 10 km2 (4
´
mi2) (Sarria and Alvarez 2002, p. 160)
and 27 km2 (10.42 mi2) (BLI 2007g, pp.
2, 5). The species has lost 92 percent of
´
its former habitat (Sarria and Alvarez
2002, p. 160), and habitat loss continues
throughout its range (BLI 2007g, p. 2;
Collar et al. 1992, p. 172; Collar et al.
1994, p. 70; Donegan et al. 2003, p. 26;
Hilty and Brown 1986, p. 133; Sarria
´
and Alvarez 2002, pp. 159-160).
Deforestation rates and patterns:
Colombian forests have undergone
extensive alteration during the 20th
Century to establish human settlements,
build roads, extract timber, and pursue
agriculture. Between 1973 and 1996,
these activities reduced the amount of
primary forest cover in Colombia by
approximately 3,605 ha (8,908 ac)
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annually, representing a nearly onethird total loss of primary forest habitat
˜
(Vina et al. 2004, pp. 123-124). Habitat
loss accelerated dramatically in the
1980s as an influx of people settled in
formerly pristine forests (Perz et al.
˜
2005, pp. 26-28; Vina et al. 2004, p.
124). Recent studies indicate that the
rate of habitat destruction is
accelerating. Between the years 1990
and 2005, Colombia lost approximately
52,800 ha (130,471 ac) of primary forest
annually (Butler 2006a, pp. 1-3; FAO
2003a, p. 1). These studies and activities
were described in greater detail above,
as part of the Factor A analysis for the
blue-billed curassow (under
Deforestation Rates and Patterns).
Logging is especially common in the flat
lower-elevation areas and areas below
2,500 m (8,202 ft), where deforestation
is nearly complete. Logging continues in
steeper-sloped areas, where
commercially valuable trees are still
being extracted, and forested areas are
being cleared for agricultural purposes
(Fuller et al. 2000, p. 4; Stattersfield et
al. 1998, p. 192).
Human-induced deforestation and
environmental degradation have caused
the gorgeted wood-quail to shift its
range from the Department of
Cundinamarca to the Department of
Santander. The species was first
observed in Santander within Cuchilla
del Ramo forest in 1970 (Wege and Long
1995, p. 143), but has not been
confirmed there since then (BLI 2007g,
p. 2). The presence of the species has
been documented only about 10 times,
and most documentations have been
auditory. The species has been most
recently confirmed in the following
´
three locations: (1) Guanenta-Alto Rio
Fonce Flora and Fauna Sanctuary (BLI
´
2007g, p. 2; Sarria and Alvarez 2002, p.
160; Wege and Long 1995, p. 144), (2)
´
Cachalu Biological Reserve (BLI 2007g,
p. 2; Fuller et al. 2000, p. 27; Sarria and
´
Alvarez 2002, pp. 158-159), and (3) the
´
´
Serranıa de los Yarguıes (BLI 2007g, p.
2; Donegan and Huertas 2005, p. 29;
Donegan et al. 2003, p. 27; Turner 2006,
p. 22).
Illegal drugs and their eradication:
Cocaine and opium has been cultivated
throughout the gorgeted wood-quail’s
range. The cultivation of illegal crops
(including coca and opium) in Colombia
destroys montane forests (Balslev 1993,
p. 3). Coca crops also destroy the soil
quality by causing the soil to become
more acidic, which depletes the soil
nutrients and ultimately impedes the
regrowth of secondary forests in
abandoned fields (Van Schoik and
Schulberg 1993, p. 21). As of 2004, an
estimated 80,000 ha (197,683 ac) were
under cocaine cultivation and 4,000 ha
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(9,884 ac) were under opium cultivation
(UNODC et al. 2007, pp. 7-8). These
figures include habitat within the
gorgeted wood-quail’s range. Between
2003 and 2004, cocaine cultivation areas
increased 25 percent in Cundinamarca,
from 57 to 71 ha (140 to 175 ac), and
by 78 percent in Santander, from 632 to
1,124 ha (1562 to 2777 ac) (UNODC and
GOC 2005, p. 15).
Colombia continues to be the leading
coca bush producer (UNODC et al. 2007,
p. 7). However, since 2003, cocaine
cultivation has remained stable, with
about 800 km2 (309 mi2) of land under
cultivation (UNODC et al. 2007, p. 8).
This stabilization of production is, in
part, attributed to alternative
development projects implemented
between 1999 and 2004, to encourage
pursuits other than illegal crop
cultivation (UNODC et al. 2007, p. 77).
This stabilization of production area is
also attributed to heightened eradication
efforts. Between 2002 and 2004, aerial
spraying occurred over more than 1,300
km2 (502 mi2) of land annually, peaking
in 2004, when 1,360 km2 (525 mi2) of
illicit crops were sprayed (UNODC and
GOC 2005, p. 11). In 2006, eradication
efforts were undertaken on over 2,130
km2 (822 mi2) of land, consisting of
1,720 km2 (664 mi2) of land being
sprayed and manual eradication being
used on the remaining land. Eradication
efforts undertaken in 2006 occurred
over an area representing 2.7 times more
land than the net cultivation area
(UNODC et al. 2007, p. 8). In Santander
alone, 1,855 ha (4,583 ac) of coca fields
were sprayed or manually eradicated in
2004 (UNODC 2005, p. 66). Drug
eradication efforts in Colombia have
further degraded and destroyed primary
forest habitat by using nonspecific aerial
herbicides to destroy illegal crops
´
(Alvarez 2005, p. 2042; BLI 2007d, p. 3;
´
´
Cardenas and Rodrıguez Becerra 2004,
p. 355; Oldham and Massey 2002, pp. 912). Herbicide spraying has introduced
harmful chemicals into gorgeted woodquail habitat and has led to further
destruction of the habitat by forcing
illicit growers to move to new,
previously untouched forested areas
´
´
(Alvarez 2002, pp. 1088-1093; Alvarez
´
2005, p. 2042; Alvarez 2007, pp. 133´
143; BLI 2007d, p. 3; Cardenas and
´
Rodrıguez Becerra 2004, p. 355; Oldham
and Massey 2002, pp. 9-12). Between
1998 and 2002, cultivation of illicit
crops increased by 21 percent each year,
with a concomitant increase in
deforestation of formerly pristine areas
´
of approximately 60 percent (Alvarez
2002, pp. 1088-1093).
Effects of habitat fragmentation: An
analysis of the effects of habitat
fragmentation on Andean birds within
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western Colombia determined that 31
percent of the historical bird
populations have become extinct or
were locally extirpated by 1990, largely
as a result of habitat fragmentation from
deforestation and human encroachment
´
(Kattan and Alvarez-Lopez 1996, p. 5;
Kattan et al. 1994, p. 141). The gorgeted
wood-quail, which depends on primary
forest for at least part of its life cycle
´
(BLI 2007g, p. 3; Sarria and Alvarez
2002, p. 159), has been extirpated from
its type locality in Cundinaramaca
(Fuller et al. 2000, pp. 4-5; Wege and
Long 1995, p. 146). The study also noted
that species at the upper or lower limit
of their altitudinal distribution are more
susceptible to local extirpation and
´
extinction (Kattan and Alvarez-Lopez
1996, pp. 5-6). This is the case for the
gorgeted wood-quail; the species prefers
habitat at 1,750-2,050 m (5,741-6,726 ft),
most of which has been destroyed (BLI
2007g, p. 2; Donegan and Huertas 2005,
p. 29; Donegan et al. 2003, p. 27; Sarria
´
and Alvarez 2002, pp. 158-159; Turner
2006, p. 22; Wege and Long 1995, pp.
143-144), and it has not been
documented at higher elevations,
despite the availability of suitable
habitat (BLI 2007g, p. 2; Donegan and
Huertas 2005, p. 29; Donegan et al.
´
2003, p. 27; Sarria and Alvarez 2002,
pp. 158-160; Turner 2006, p. 22; Wege
and Long 1995, pp. 143-144). Another
study on the effects of habitat
fragmentation in Colombia found that
habitat fragmentation facilitates
predation and hunting pressure
´
(Arango-Velez and Kattan 1997, pp. 140142) (Factors B and C).
Refugia: The gorgeted wood-quail has
been observed, and most recently
confirmed, in the following three
´
locations: (1) Guanenta-Alto Rio Fonce
´
Flora and Fauna Sanctuary, (2) Cachalu
´
Biological Reserve, and (3) the Serranıa
´
de los Yarguıes.
´
(1) Guanenta-Alto Rio Fonce Flora
and Fauna Sanctuary (Santander
Department): This 10,420-ha (25,748-ac)
humid subtropical and temperate oak
forest on the western slope of the East
Andes was declared a protected natural
area in 1993 (Andrade and Repizzo
1994, p. 43; Rainforest Alliance, p. 2;
The Nature Conservancy (TNC) 2008, p.
1). This area has long been considered
the largest remaining sizeable oak forest
tract remaining in the northern area of
the East Andes, even as recently as the
year 2005 (Donegan and Huertas 2005,
´
p. 11; Sarria and Alvarez 2002, p. 160;
Stattersfield et al. 1998, p. 193; Wege
and Long 1995, p. 144). The gorgeted
wood-quail was first observed in the
Sanctuary in 1979 (BLI 2007g, p. 2) and
´
again 1988 (Sarria and Alvarez 2002, p.
160; Wege and Long 1995, p. 144). In
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2004, the species was reported in the
oak forests within the Province of
´
Guanenta (BLI 2007g, p. 2), but it is
unclear whether these observations
occurred within the Sanctuary.
Beginning in the 1960s, habitat
conversion accelerated in the East
Andes (Stattersfield et al. 1998, p. 192).
The forests of the Colombian East Andes
have been extensively degraded (Collar
¨
et al., 1992, p. 172; Fjeldsa and Krabbe
1990; Hilty and Brown 1986, p. 133;
Stattersfield et al. 1998, p. 192). The
western slopes have been largely
converted to agricultural use and to
pastureland for cattle (Stattersfield et al.
1998, p. 192), and deforestation
continues on the lower slopes of the
East Andes (Wege and Long 1995, p.
143). Selective logging affects birds in
´
the lower part of the Guanenta Alto Rio
Fonce (Fuller et al. 2000, p. 28; Sarria
´
and Alvarez 2002, p. 160), including the
gorgeted wood-quail. Stattersfield et al.
(1998, p. 192) reported that forest loss
below 2,500 m (8,202 ft) has been
almost complete, although Fuller et al.
(2000, p. 28) noted that the forest was
‘‘largely intact’’ above 1,950–2,200 m
(6,398-7,218 ft). However, elevations
above this altitude would not serve the
needs of the gorgeted wood-quail,
because this species is found most often
at 1,750-2,050 m (5,741-6,726 ft) in
altitude (BLI 2007g, p. 2; Donegan and
Huertas 2005, p. 29; Donegan et al.
´
2003, p. 27; Sarria and Alvarez 2002,
pp. 158-159; Turner 2006, p. 22; Wege
and Long 1995, pp. 143-144) (see
discussion under Habitat and Life
History for the gorgeted wood-quail).
´
(2) Cachalu Biological Reserve: This
1,300-ha (3,212-ac) Reserve (TNC 2008,
p. 1) was established in 1997 adjacent
´
to Guanenta Alto Rio Fonce Flora and
Fauna Sanctuary (Rainforest Alliance
2008, p. 2). It encompasses primarily
mature oak forests and secondary areas
(regenerating pastureland) at altitudes
between 1,850 and 2,750 m (6,070 and
9,022 ft). Most of the secondary areas
within the Reserve have been
regenerating for 20 years. About 4
percent of land formerly used for
pastureland and slash-and-burn
agriculture has been left to regenerate
within the last 8 years (BLI 2007g, p.
10). The species was first observed at
this location in 1999 and again in 2000
and 2001 (BLI 2007g, p. 2; Fuller et al.
´
2000, p. 27; Sarria and Alvarez 2002,
pp. 158-159).
While human population pressures in
northern Santander have not been as
great as in other parts of the Andes, 70
percent of the subsistence population
living locally has had a major influence
on the upper montane forest system.
Slash-and-burn agriculture (clearing
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small plots of land for agriculture and
settlement) and subsistence extractive
activities (such as harvesting wood,
plant fibers, and animals) have turned
the upper montane forests into
extraction forests (Rainforest Alliance
2008, p. 2). Ongoing slashing and
burning on the outskirts of the Reserve
could further degrade the integrity of
the habitat within the Reserve (BLI
2007g, p. 11).
´
´
´
(3) Serranıa de los Yarguıes (Yarguıes
Mountains): This 175,000-ha (432,425ac) forest is located in southern
Santander and ranges in altitude
between 200 and 3200 m (656 and
10,499 ft) (BLI 2007g, p. 12; Donegan
and Huertas 2005, p. 30). This area was
previously unsurveyed for birds, due to
political instability and occupation by
revolutionary armed forces (Donegan
and Huertas 2005, pp. 11, 29-30;
Donegan et al. 2004, p. 19; Sarria and
´
Alvarez 2002, p. 160). The gorgeted
wood-quail was first observed in
´
Yarguıes in 2003 and again in 2004 (BLI
2007g, p. 2; Donegan and Huertas 2005,
p. 29; Donegan et al. 2003, p. 27; Turner
2006, p. 22). This site is now considered
to be the stronghold for the species
(Donegan and Huertas 2005, p. 29;
Donegan et al. 2004, p. 19; Turner 2006,
p. 22) (see Population Estimates, above).
This forest does not have protected
status (BLI 2007g, p. 13) and land
clearing for slash-and-burn agriculture
continues to be a problem within the
´
´
Serranıa de los Yarguıes (BLI 2007g, p.
13; Donegan and Huertas 2005, p. 29;
Turner 2006, p. 22).
Summary of Factor A
Habitat destruction, alteration,
conversion, and fragmentation were
factors in the species’ historical decline
and continue to be factors affecting the
gorgeted wood-quail. The direct loss of
habitat through widespread
deforestation and conversion of primary
forests for agricultural uses has led to a
95 percent range reduction for the
species, leading to extirpation of the
species in its type locality (in
Cundinamarca) and an apparent shift in
the species’ range (to Santander). The
species is known only in three
locations, where habitat conversion and
poaching of the gorgeted wood-quail are
ongoing. Deforestation, habitat
conversion, and drug eradication efforts
have reduced the amount of suitable
habitat at elevations preferred by the
species, such that its current range is
between 10 and 27 km2 (4 and 10 mi2).
The destruction and fragmentation of
the remaining primary forested habitat
are ongoing throughout the species’
range and are expected to continue.
Therefore, we find that the present
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destruction, modification, and
curtailment of habitat are threats to the
gorgeted wood-quail throughout all of
its range.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
Galliformes such as the gorgeted
wood-quail are chiefly terrestrial birds
that are easily hunted or trapped, and
they have been closely associated with
humans throughout history as a source
for food, ornamental collection,
commercial trade, and recreational
hunting (Fuller et al. 2000, p. 2).
Hunting the gorgeted wood-quail is
illegal in Colombia (Factor D) and is
considered poaching. Poaching for
subsistence use and for local food trade
is ongoing throughout the species’ range
(BLI 2007g, pp. 7, 11-13; Donegan and
Huertas 2005, p. 29; Turner 2006, p. 22)
(BLI 2007g, p. 7). Hunting affects birds
´
in the lower part of the Guanenta-Alto
Rio Fonce Flora and Fauna Sanctuary
(Fuller et al. 2000, p. 28; Sarria and
´
Alvarez 2002, p. 160), including the
gorgeted wood-quail. Illegal hunting is
an ongoing problem on the outskirts of
´
the Cachalu Biological Reserve, where
the species has been observed within
the past decade (BLI 2007g, p. 10; Sarria
´
and Alvarez 2002, p. 158). Poaching of
the gorgeted wood-quail continues to be
´
a problem within the Serranıa de los
´
Yarguıes, considered the stronghold for
the species (BLI 2007g, p. 13; Donegan
and Huertas 2005, p. 29; Turner 2006,
p. 22). The IUCN Partridge, Quail, and
Francolin Specialist Group (PQF
Specialist Group) considers unregulated
hunting to be a factor affecting gorgeted
wood-quail populations throughout the
species’ range (Fuller et al. 2000, p. 28).
Hunting, in combination with
deforestation, may have led to the local
extirpation of this species from Cuchilla
del Ramo (Department of Santander),
where the species was first observed in
´
1970 (Sarria and Alvarez 2002, pp. 158159; Wege and Long 1995, p. 143) and
last confirmed in 1988 (Collar et al.
1992, p. 172). The gorgeted wood-quail
has not been confirmed at this location
again (BLI 2007g, p. 2; Sarria and
´
Alvarez 2002, pp. 158-159), which may
be due to a combination of habitat
destruction and hunting pressures. This
unprotected area on the western slopes
of the East Andes is severely fragmented
due to deforestation (Factor A). In
addition, active hunting was reported in
this location in the late 1980s. Collar et
al. (1992, p. 172) interpreted this level
of hunting to imply that the species was
capable of withstanding some hunting
pressure. Andrade (in litt., Collar et al.
1992, p. 172) noted that this would be
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Jkt 217001
the case only where the species is
capable of retreating into suitable
adjacent habitat. However, little suitable
habitat is located in this area. Thus,
hunting, in combination with
deforestation, may have led to the
extirpation of the gorgeted wood-quail
from Cuchilla del Ramo.
´
In addition, Arango-Velez and Kattan
(1997, pp. 140-142) conducted a study
on the effect of habitat fragmentation on
birds in Colombia and found that
habitat fragmentation facilitates hunting
because smaller habitat patches allow
hunters to more easily penetrate the
´
entire plot (Arango-Velez and Kattan
1997, pp. 140-142).
Summary of Factor B
The gorgeted wood-quail is hunted
(poached) throughout its current range
for local consumption or local food
trade. Hunting results in the direct
removal of individuals from the
population and can remove potentially
reproductive adults from the breeding
pool. This primarily terrestrial species is
particularly vulnerable to hunting
pressures due to its small population
size (Factor E) and fragmented
distribution (Factor A). Researchers
believe that the gorgeted wood-quail is
only capable of escaping hunting
pressures when adjacent suitable habitat
exists. There are continued reports of
hunting pressures on the species; these
pressures have been and continue to be
exacerbated by ongoing human
encroachment into previously
undisturbed forests (Factor A). Hunting,
combined with habitat fragmentation
(Factor A), increases the possibility of
local extirpation since the gorgeted
wood-quail is unlikely to re-occupy an
area that has been depleted through
hunting (Factor E, Likelihood to
Disperse). Hunting may have led to the
local extirpation of the species in a
portion of its range. Hunting pressures
are ongoing and affect the entire
population of gorgeted wood-quail.
Therefore, we find that hunting is a
threat to the gorgeted wood-quail
throughout its range.
C. Disease or Predation
Disease: We are not aware of any
information regarding disease or the
potential for significant disease
outbreaks in gorgeted wood-quail
populations. As a result, we do not
consider disease to be a threat to the
species.
Predation: Potential quail predators
include feral dogs, tayras, dwarf
squirrels (Microsciurus sp.), tree
squirrels (Sciurus granatensis), common
opossums (Didelphis marsupialis),
kinkajous (Potos flavus), Central
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American agoutis (Dasyprocta
punctata), and South American coatis
´
(Nasua nasua) (Arango-Velez and
Kattan 1997, p. 141). A predation study
conducted in the Colombian Andes
demonstrated that habitat fragmentation
increased predation pressure on the eggs
of the common quail (Coturnix coturnix)
when situated within smaller, isolated
´
habitat fragments (Arango-Velez and
Kattan 1997, pp. 137-143). Similar
studies have found that nest predation
is more prevalent in smaller, isolated
forest patches because the small size of
the patch facilitated predators’ access to
prey throughout the entire plot (Gibbs
1991, p. 157; Hoover et al. 1995, p. 151;
Keyser et al. 1998, p. 991; 2002, p. 186;
Renjifo 1999, p. 1133; Wilcove 1985, p.
´
1214). Arango-Velez and Kattan (1997,
pp. 140-142) also found that smaller
fragments support smaller predators,
which tend to depredate on eggs and
juveniles, rendering understory nesting
birds, such as the gorgeted wood-quail,
particularly vulnerable to predation
during these life-history stages (Arango´
Velez and Kattan 1997, pp. 140-142).
These studies were described in more
detail above, as part of the Factor C
analysis for the blue-billed curassow.
Summary of Factor C
Feral dogs, tayras, dwarf squirrels,
tree squirrels, common opossums,
kinkajous, Central American agoutis,
and South American coatis are potential
gorgeted wood-quail predators.
Predation results in the direct removal
of individuals from the population and
can remove potentially reproductive
adults from the breeding pool. This
primarily terrestrial species is
particularly vulnerable to predation
pressures due to its small population
size (Factor E) and fragmented
distribution (Factor A). Habitat
fragmentation has occurred and is
ongoing throughout the species’ range.
Studies on similar species in similar
Andean habitats indicate that
vulnerability to predation increases
with increased habitat fragmentation
and smaller patch sizes. Predation
exacerbates the genetic complications
associated with the species’ small
population size (Factor E). Because of
the species’ small population size and
inability to recolonize isolated habitat
fragments (Factor E), predation renders
the species vulnerable to local
extirpation. Therefore, we find that
predation, exacerbated by ongoing
habitat destruction (Factor A) and
hunting (Factor B), is a threat to the
gorgeted wood-quail.
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D. The Inadequacy of Existing
Regulatory Mechanisms
Regulatory mechanisms may provide
species-specific or habitat-specific
protections. An evaluation of the
adequacy of regulatory mechanisms
within Colombia to mitigate or remove
the threats to the gorgeted wood-quail is
provided below, beginning with speciesspecific and followed by habitat-specific
protection mechanisms.
Colombia has enacted numerous laws
to protect species and their habitats
(Matallana-T. 2005, p. 121). The
gorgeted wood-quail is listed as a
critically endangered species under
Colombian Law 99 of 1993 (EcoLex
1993, p. 2) and Resolution No. 584 of
2002 (EcoLex 2002, pp. 10, 12). A full
description of these laws and the
categorization of threatened species in
Colombia were provided above, as part
of the Factor D analysis for the bluebilled curassow. Because of its status as
a critically endangered species, the
Ministry of the Environment does not
permit the gorgeted wood-quail to be
hunted commercially or for sport under
Resolution No. 849 of 1973 and
Resolution No. 787 of 1977 (EcoLex
1973, p.1; EcoLex 1977, p. 3). Neither
Resolution prohibits subsistence
hunting, which is a threat to the species
throughout its range (Factor B).
Gorgeted wood-quail is hunted within
´
´
the Serranıa de los Yarguıes, which has
no protected status (BLI 2007g, p. 13)
despite being considered the stronghold
for the species (Donegan and Huertas
2005, p. 29; Turner 2006, p. 22). Thus,
these Resolutions are ineffective at
reducing the existing threat of
subsistence hunting to the gorgeted
wood-quail (Factor B).
Colombia has enacted numerous
forestry laws and forestry management
practices (Law No. 2 (EcoLex 1959);
Decree No. 2,811 (Faolex 1974); Decree
No. 1,791 (Faolex 1996); Law No. 1,021
(EcoLex 2006)). Weaknesses in the
implementation of these laws and the
decentralized nature of Colombian
resource management are described in
detail above for the blue-billed curassow
(Factor D) (ITTO 2006, pp. 218-9, 222;
Matallana-T. 2005, pp. 121-122). These
regulatory mechanisms are ineffective at
protecting the gorgeted wood-quail (BLI
2007g, p. 13; ITTO 2006, p. 222). Habitat
destruction continues to be a problem
within the unprotected forests of
´
´
Serranıa de los Yarguıes (BLI 2007g, p.
13), considered the stronghold of the
species (Donegan and Huertas 2005, p.
29; Turner 2006, p. 22), and on the
´
outskirts of the Reserva Biologica
´
Cachalu, where the species has also
been observed (BLI 2007g, p. 10).
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Therefore, we determine that forestry
regulations are not effective in
mitigating the threats to the gorgeted
wood-quail from habitat destruction
(Factor A).
Colombia has several categories of
national habitat protection (Matallana-T.
2005, p. 121-122), which were more
fully described above, as part of the
Factor D analysis for the blue-billed
curassow (Matallana-T. 2005, p. 121122). The gorgeted wood-quail occurs
within two protected areas: the
´
Guanenta-Alto Rio Fonce Flora and
Fauna Sanctuary (Fuller et al. 2000, p.
´
28; Sarria and Alvarez 2002, p. 160) and
´
the Cachalu Biological Reserve (BLI
´
2007g, p. 10; Sarria and Alvarez 2002,
p. 158). Habitat destruction and
subsistence hunting (poaching) are
ongoing within these protected areas,
despite being illegal (BLI 2007g, p. 10).
Therefore, these sanctuaries and
reserves provide little or no protection
to the species from the threats of habitat
destruction (Factor A) or poaching
(Factor B).
Summary of Factor D
Colombia has adopted numerous laws
and regulatory mechanisms to
administer and manage wildlife and
their habitats. The gorgeted wood-quail
is considered critically endangered
under Colombian law and lives within
two protected areas. However, on-theground enforcement of existing wildlife
protection and forestry laws and
oversight of the local jurisdictions
implementing and regulating activities
are ineffective at mitigating the primary
threats to the gorgeted wood-quail. As
discussed for Factor A, habitat
destruction, degradation, and
fragmentation continue throughout the
existing range of the gorgeted woodquail. As discussed for Factor B,
uncontrolled hunting of the gorgeted
wood-quail is ongoing and negatively
affects the continued existence of the
species. Therefore, we find that the
existing regulatory mechanisms
currently in place are inadequate to
mitigate the primary threats of habitat
destruction (Factor A) and hunting
(Factor B) to the gorgeted wood-quail.
E. Other Natural or Manmade Factors
Affecting the Continued Existence of the
Species
Two additional factors affect the
gorgeted wood-quail: its minimal
likelihood for dispersal and the species’
small population size.
Likelihood to Disperse: The gorgeted
wood-quail is currently known in three
localities in two disjunct locations
within the Department of Santander:
´
´
Serranıa de los Yarguıes, in northern
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32339
´
Santander, and Cachalu Biological
´
Reserve and Guanenta-Alto Rio Fonce
Flora and Fauna Sanctuary, in southern
Santander (Donegan and Huertas 2005,
p. 30; Rainforest Alliance 2008, p. 2;
TNC 2008, p. 1). Although there is little
information on the species’ dispersal
capabilities, the isolated, fragmented
nature of the remaining suitable habitat
is considered by researchers to be a
hindrance to its ability to disperse
because: (1) gorgeted wood-quail is
primarily a terrestrial species that is
found at mid-to-upper-elevation forests
(1,750-2,050 m (5,741-6,726 ft)) on the
western slopes of the East Andes (BLI
2007g, p. 2; Donegan and Huertas 2005,
p. 29; Donegan et al. 2003, p. 27; Collar
et al. 1992, pp. 171-172; del Hoyo 1994,
p. 431; Fuller et al. 2000, pp. 2, 27-28;
´
Sarria and Alvarez 2002, pp. 158-159;
Turner 2006, p. 22; Wege and Long
1995, p. 143-144); (2) the species is
dependent on mature forest for at least
part of its life cycle and is not found in
secondary habitats that are not adjacent
to primary forests (BLI 2007g, p. 3;
´
Sarria and Alvarez 2002, p. 159); (3)
researchers believe that the species is
capable of escaping hunting pressures
only when adjacent to suitable habitat
(Andrade in litt., as cited in Collar et al.
1992, p. 172); (4) the species is currently
located in two disjunct areas, one in
northern Santander and the other in
southern Santander; and (5) most of the
habitat below 1,950-2,500 m (6,3988,202 ft) in the East Andes has been
destroyed, leaving only isolated,
fragmented habitat patches (Fuller et al.
2000, p. 28; Stattersfield et al. 1998, p.
192). Because the species has not
demonstrated an aptitude to disperse
into secondary-growth areas that are not
adjacent to primary forest, and given the
isolated, disjunct nature of remaining
forest fragments, the gorgeted woodquail as with other narrow-ranging
species found in fragmented habitat
(Hanski 1998, pp. 45-46), is unlikely or
incapable of dispersing to suitable
habitat that is not adjacent to existing
locales.
Small Population Size: Deforestation
(Factor A) and overutilization (Factor B)
have greatly affected the current
population size and distributional range
of the gorgeted wood-quail (Collar et al.
1992, pp. 126-127; Collar et al. 1994, p.
60). The species was thought to be
extinct or on the verge of extinction
until its rediscovery in 1970 (Collar et
al. 1992, p. 171; Fuller et al. 2000, pp.
4-5, 27; Wege and Long 1995, p. 146).
The gorgeted wood-quail is now
confirmed in three isolated areas: the
´
Sanctuary of Fauna and Flora GuanentaAlto Rio Fonce, the Natural Reserve
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´
´
Cachalu, and the Serranıa de los
´
Yariguıes (Donegan and Huertas 2005,
pp. 11, 29-30; Donegan et al. 2004, p. 19;
´
Sarria and Alvarez 2002, p. 160). The
population of the gorgeted wood-quail is
currently estimated to include 189 to
486 individuals, with a declining
population trend (BLI 2007g, pp. 1, 5).
The gorgeted wood-quail’s restricted
range, combined with its small
population size (Cuervo and Salaman
1999, p. 7; del Hoyo 1994, p. 361; Sarria
´
and Alvarez 2002, p. 138), makes the
species particularly vulnerable to the
threat of adverse natural (e.g., genetic,
demographic, or environmental) and
manmade (e.g., hunting or deforestation)
events that destroy individuals and their
habitat (Holsinger 2000, pp. 64-65;
Primack 1998, pp. 279-308; Young and
Clarke 2000, pp. 361-366). Small
population sizes render species
vulnerable to genetic risks that can have
individual or population-level
consequences on the genetic level and
can increase the species’ susceptibility
to demographic problems, as explained
in more detail above for the blue-billed
curassow (Factor E, Small Population
Size) (Charlesworth and Charlesworth
1987, p. 238; Shaffer 1981, p. 131). Once
a population is reduced below a certain
number of individuals, it tends to
rapidly decline towards extinction
(Franklin 1980, pp. 147-148; Gilpin and
´
Soule 1986, p. 25; Holsinger 2000, pp.
´
64-65; Soule 1987, p. 181).
In the absence of quantitative studies
specific to this species, a general
approximation of minimum viable
population size is the 50/500 rule, as
described above as part of the Factor E
analysis for the brown-banded antpitta
´
(Shaffer 1981, pp. 132-133; Soule 1980,
pp. 160-162). The total population size
of the gorgeted wood-quail is estimated
to be between 186 and 486 individuals.
While 186 individuals is above the
minimum population size required to
avoid short-term genetic consequences,
486 falls just below the threshold
minimum number of 500 individuals
required for long-term fitness of a
population and does not take into
account that not all members of the
population will be contributing to
population growth at any one time.
Because the gorgeted wood-quail
exists in two isolated, disjunct habitat
fragments, between which they are
unlikely to disperse, an examination of
the fitness of each subpopulation is
more appropriate. For the purposes of
this analysis, although we have
reservations about the precision of these
estimates (see Population Estimates
discussion above), we will use the
following two population estimates: 250
individuals in Northern Santander and
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30-66 individuals in southern
Santander. Upon examination of these
estimates, both populations are clearly
below the threshold required for longterm fitness in a population. The lower
limit of the population estimate for the
southern Santander population is below
the threshold required to avoid shortterm risks such as inbreeding and
demographic shifts, whereas the upper
limit is barely above the 50-individual
threshold. Therefore, we currently
consider these subpopulations (and the
species as a whole) to be at risk due to
the lack of short- and long-term
viability.
Summary of Factor E
The gorgeted wood-quail is unlikely
or incapable of dispersing into suitable
habitat that is isolated from extant
populations, and the species’ overall
small population size makes it
vulnerable to genetic and demographic
risks that negatively impact the species’
short- and long-term viability. Habitat
destruction through deforestation
(Factor A) and overutilization through
hunting (Factor B) have greatly affected
the species’ current population size.
Believed to be extinct or on the verge of
extinction within the past 30 years, the
species is now confirmed in 3 areas of
2 disjunct locations. The gorgeted woodquail’s small population size, combined
with its restricted range and inability to
repopulate disjunct suitable habitat
following local extirpations, makes the
species particularly vulnerable to the
threat of adverse natural (e.g., genetic,
demographic, or environmental) and
manmade (e.g., hunting or deforestation)
events that destroy individuals and their
habitat.
Status Determination for the Gorgeted
Wood-Quail
The five primary factors that threaten
the survival of the gorgeted wood-quail
are: (1) Habitat destruction,
fragmentation, and degradation (Factor
A); (2) overexploitation due to hunting
(Factor B); (3) predation (Factor C); (4)
inadequacy of regulatory mechanisms to
reduce the threats to the species (Factor
D); and (5) small population size and
isolation of remaining populations
(Factor E). The gorgeted wood-quail, a
small terrestrial bird, prefers primary
montane forests or adjacent secondary
forests at altitudes between 1,750 and
2,050 m (5,741 and 6,726 ft). The
species’ historic range has been reduced
by 92 percent, extirpating the species
from its type locality in the Department
of Cundinamarca and causing the
species to shift to the extremes of its
range and elevational distribution
(Factor A). The estimated suitable
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habitat available to the species is
approximately 10-27 km2 (4-10 mi2).
Within the past decade, the gorgeted
wood-quail has been confirmed in only
´
three locations: Serranıa de los
´
Yarguıes, in northern Santander, and
´
adjacent localities in the Guanenta-Alto
Rio Fonce Flora and Fauna Sanctuary
´
and Cachalu Biological Reserve, in
southern Santander. Much of the
primary forest, mid-elevation habitat
preferred by the species has been
destroyed by human activities, such as
slash-and-burn agriculture, grazing, and
extractive industries (Factor A). Illegal
crop production, which continues
throughout the species’ range, has
altered soil compositions, hindering
regeneration of abandoned fields. In
addition, drug eradication programs
involving the aerial spraying of nonspecific herbicides have further
degraded the environment and
destroyed primary forest habitat.
In combination, these threats
exacerbate the negative consequences to
the species. For example, habitat
fragmentation (Factor A) increases the
species’ vulnerability to hunting (Factor
B). Poaching, in combination with
habitat destruction, may have led to the
local extirpation of the gorgeted woodquail from Cuchilla del Ramo. This
population was only discovered in 1970
and, amidst ongoing habitat destruction
and hunting pressures, has not been
observed there since 1988. Thus,
deforestation and hunting within the
past 30 years may have led to the
extirpation of the gorgeted wood-quail
from this location.
Habitat fragmentation also exposes
the species to greater risk of extinction
caused by adverse natural (e.g., genetic,
demographic, or environmental) and
manmade (e.g., hunting or deforestation)
events (Factor E). The species’
population has decreased by up to 9
percent in the past 10 years and has
likely been extirpated from at least one
location (Cundinamarca) due to habitat
loss and from another locality (Cuchilla
del Ramo) due to a combination of
habitat loss and hunting. The global
population of the gorgeted wood-quail is
estimated to be between 187 and 486
individuals. Given that the gorgeted
wood-quail is likely to interact as
subpopulations and is unlikely to
disperse between patches of fragmented
habitat, the effective population size is
actually much smaller. This small
population size puts the gorgeted woodquail at risk from both near-term genetic
complications (such as inbreeding and
demographic shifts) and lack of longterm fitness (such as the ability to adapt
to changing conditions). These potential
genetic problems are exacerbated by
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ongoing human-induced threats, such as
habitat destruction (Factor A) and
hunting (Factor B), factors which are not
being mitigated by existing regulations
(Factor D) and are further magnified
because the species is unlikely to
repopulate isolated patches of suitable
habitat where the species has undergone
decline or local extirpation, increasing
the likelihood of local extirpations
(Factor E).
The gorgeted wood-quail is listed as
critically endangered, making it illegal
to hunt the species, and two of the three
known localities are within protected
areas. However, habitat destruction and
poaching are ongoing throughout the
species’ range (Factor D). Thus, the
regulations in place are ineffective in
protecting the gorgeted wood-quail and
its habitat.
We have carefully assessed the best
available scientific and commercial
information regarding the past, present,
and potential future threats faced by the
gorgeted wood-quail. We consider the
ongoing threats to the gorgeted woodquail, habitat destruction (Factor A),
hunting (Factor B), and predation
(Factor C), exacerbated by the species’
small population size and limited
dispersal ability (Factor E), and
compounded by inadequate regulatory
mechanisms to mitigate these threats
(Factor D), to be equally present and of
the same magnitude throughout the
species’ entire current range. Based on
this information, we conclude that the
gorgeted wood-quail is in danger of
extinction throughout its range.
Therefore, we are proposing to list the
gorgeted wood-quail as an endangered
species.
Ecuadorian Bird Species
V. Esmeraldas Woodstar (Chaetocercus
berlepschi)
Species Description
Esmeraldas woodstar, a member of the
hummingbird family (Trochilidae) and
endemic to Ecuador, is approximately
6.5 cm (2.5 in.) in length (del Hoyo et
al. 1999, p. 678; Ridgely and Greenfield
2001b, p. 295; Schuchmann 1999, p.
468; Williams and Tobias 1991, p. 39).
´
The species is locally known as ‘‘Colibrı
de Esmeraldas’’ or ‘‘Estrellita
˜
esmeraldena’’ (UNEP-WCMC 2008b).
Both sexes have striking violet, green,
and white plumage. The male has a
narrow band across its breast, whereas
the female has a full white underbody
(BLI 2007c, p. 1; Ridgely and Greenfield
2001b, plate 42).
Taxonomy
Esmeraldas woodstar was first
taxonomically described by Simon in
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1889 (BLI 2007e, p. 1). The type
specimen (the actual specimen that was
first described) of the Esmeraldas
woodstar was obtained from the moist
forest habitat near Esmeraldas City, in
the Department of Esmeraldas (Collar et
al. 1992, p. 533). Esmeraldas City is,
therefore, referred to as the ‘‘type
locality.’’
Simon placed the species in the
Trochilidae family, under the name
Chaetocercus berlepschi. The species is
also known by the synonym Acestrura
berlepschi. Both CITES and BirdLife
International recognize the species as
Chaetocercus berlepschi (BLI 2007e, p.
1; UNEP-WCMC 2008b, p. 1). Therefore,
we accept the species as Chaetocercus
berlepschi, which follows the Integrated
Taxonomic Information System (ITIS
2008).
Habitat and Life History
Esmeraldas woodstar is a rangerestricted, forest-dwelling species with
highly localized populations (BLI 2007f,
pp.1-3; Collar et al. 1992, p. 533;
Schuchmann 1999, p. 532). Esmeraldas
woodstar prefers primary forest and is
usually found in lowland semievergreen forests (cloud or fog forests)
and has occasionally been seen in
secondary-growth semi-humid (moist)
habitat during the breeding season (Best
and Kessler, p. 141; BLI 2004, p. 2; BLI
2007c, p. 3; Collar et al. 1992, p. 533;
del Hoyo et al. 1999, p. 678;
Hummingbird Monitoring Network
2006, p. 1; Ridgely and Greenfield
2001b, p. 295; Schuchmann 1999, p.
468; Stattersfield et al. 1998, p. 211;
Williams and Tobias 1991, p. 39).
Esmeraldas woodstar has not been seen
in secondary-growth forests at any other
time of year, and researchers are not
certain that the species can survive in
secondary forests year-round (BLI
2007c, p. 3). The species has mostly
been recorded at elevations between 50
and 150 m (164 and 492 ft) (Ridgely and
Greenfield 2001a, p. 390; Ridgely and
Greenfield 2001b, p. 295), but has
occasionally been observed above 500 m
(1,640 ft) (i.e., at Loma Alta; Factor A)
(Best and Kessler, p. 141; del Hoyo et al.
1999, p. 678; Ridgely and Greenfield
2001b, p. 295; Schuchmann 1999, p.
468; Stattersfield et al. 1998, p. 211;
Williams and Tobias 1991, p. 39).
Esmeraldas woodstar has been seen
most often along forest borders, with
females especially seen perching on
dead twigs (Ridgely and Greenfield
2001b, p. 295). The species forages
mainly in the canopy and has been
recorded ‘‘hawking’’ insects from the
air, as well as foraging nectar from
flowers of the strawberry tree
(Muntingia calabura), river koko (Inga
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32341
vera), and mango tree (Mangifera spp.)
(Becker et al. 2000, p. 55; del Hoyo et
al. 1999, p. 678; Ridgely and Greenfield
2001b, p. 295). As recently as 1999,
there were no known breeding sites for
the Esmeraldas woodstar (del Hoyo et
al. 1999, p. 678). Today, one breeding
site has been located in the cloud forests
of the Colonche Hills (Hummingbird
Monitoring Network 2006, p. 1), in the
Department of Guayas (Best and Kessler
1995, p. 54). The breeding season is
from December to March (BLI 2007c, p.
3). Little else is known of the
Esmeraldas woodstar’s breeding habits
or other activities during most of the
year (Ridgely and Greenfield 2001a, pp.
389-390). The species seems to
‘‘disappear’’ from known locations
during non-breeding months (BLI 2007c,
p. 2; Becker et al. 2000, p. 55). In
general, male hummingbirds breed with
several females in one breeding season
and the females take responsibility for
all remaining reproductive
responsibilities, including nest building,
incubation, and rearing. Hummingbirds
typically produce 2 eggs per clutch
(Schuchmann 1999, pp. 506, 509).
Historical Range and Distribution
The type locality for the Esmeraldas
woodstar (the location of its first
discovery) was in Esmeraldas, near
Esmeraldas City, and the last specimen
was observed there and in the
´
Department of Manabı in 1912 (Collar et
al. 1992, p. 533). The species’ historic
range has been reduced by 99 percent
(Dodson and Gentry 1991, p. 293). The
area around its type locality (Esmeraldas
City) has been replaced by pastureland
and is nearly devoid of all trees (Collar
et al. 1992, p. 533). After the species
went unobserved following the 1912
sightings, it was thought to be extinct,
until it was rediscovered in 1990
(Ridgely and Greenfield 2001a, pp. 389390; Williams and Tobias 1991, p. 39).
Current Range and Distribution
Today, Esmeraldas woodstar ranges in
northwestern Ecuador, in the
´
Departments of Esmeraldas, Manabı,
and Guayas, along the slopes of the
coastal cordillera up to 500 m (1,640 ft)
(del Hoyo et al. 1999, p. 678; Ridgely
and Greenfield 2001b, p. 295;
Schuchmann 1999, p. 468; Williams and
Tobias 1991, p. 39). The current extent
of the species’ range is approximately
1,155 km2 (446 mi2), in three disjunct
and isolated areas (BLI 2004, p. 2;
Dodson and Gentry 1991, p. 293).
The species was rediscovered on
´
ridges above the lower Rıo Ayampe (in
´
northwest Guayas/Manabı) in March
1990, near the Machalilla National Park
(Becker et al. 2000, p. 55; BLI 2007c, p.
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2; Williams and Tobias 1991, p. 39), and
again in January 1991 (Ridgely and
Greenfield 2001a, p. 389). Subsequent
´
attempts to relocate the species at Rıo
Ayampe (in August 1991 and July 1993)
were unsuccessful (Collar et al. 1992, p.
533; Ridgely and Greenfield 2001a, p.
389). Researchers subsequently
determined that the species occupies
this habitat only seasonally, frequenting
the Park from December through the
spring (March), but is absent from this
location during non-breeding months
(Becker et al. 2000, p. 55; BLI 2007c, p.
2; and Greenfield 2001a, p. 389).
Since then, the species has been
observed at the following locations:
´
Esmeraldas: Sua, in January 1993, and
Muisne, in 1994 (month unknown);
´
Manabı: Isla de La Plata (part of the
Machalilla National Park), DecemberJanuary 1998 (BLI 2007c, p. 2; Ridgely
and Greenfield 2001a, p. 389; Williams
and Tobias 1991, p. 39). The species
was not observed on Isla de La Plata
during a bird survey conducted in June
2000 (Cisneros-Heredia 2005, p. 24),
reconfirming their absence from this
habitat during non-breeding months.
Population Estimates
Esmeraldas woodstar is considered a
rare, range-restricted species with
highly localized populations in three
general areas (BLI 2007c, pp. 1-3;
Schuchmann 1999, p. 532). There have
been no population surveys of this
species. BirdLife International estimated
that the population currently includes
between 186 and 373 individuals, based
on estimates using similar species of
hummingbirds (BLI 2007c, p. 6).
Conservation Status
The Esmeraldas woodstar is identified
as an endangered species under
Ecuadorian law (EcoLex 2003b, p. 36, p.
36). This species is classified as
‘Endangered’ on the IUCN Red List, due
to severe fragmentation within the
woodstar’s restricted range (IUCN 2006).
Summary of Factors Affecting the
Esmeraldas Woodstar
A. The Present or Threatened
Destruction, Modification, or
Curtailment of the Habitat or Range
The Esmeraldas woodstar is restricted
to the semi-humid forests and
woodlands from sealevel to 500 m
(1,600 ft) along the Coastal Cordillera of
western Ecuador (del Hoyo et al. 1999,
p. 678; Ridgely and Greenfield 2001b, p.
295). The current extent of the species’
range is approximately 1,155 km2 (446
mi2), in three disjunct and isolated areas
(BLI 2004, p. 2).
Deforestation Rates and Patterns: The
semi-humid, semi-evergreen forest
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environment preferred by the
Esmeraldas woodstar is one of the most
threatened forest habitats in the
Neotropics (Collar et al. 1992, p. 533;
Schuchmann 1999, p. 532). This region
is also known as the Tumbesian region
(which encompasses the coast and
foothills beginning in southwestern
Ecuador and into the mid-coastal area of
northwestern Peru) (World Land Trust
U.S. 2008, p. 1). This habitat type has
been reduced by over 99 percent
(Dodson and Gentry 1991, p. 293),
making this region one of the most
vulnerable endemic bird areas in South
America (Stattersfield et al. 1998, p.
214). Deforestation, understory
degradation, and limited habitat size are
among the biggest impacts to resident
birds in the Tumbesian region
(Stattersfield et al. 1998, p. 214).
Forested habitat within western
Ecuador, including that within the
Esmeraldas woodstar’s range, has
diminished rapidly due to logging,
clearing for agriculture, and road
development (Dodson and Gentry 1991,
pp. 283-293). The primary moist forest
habitat at the species’ type locality
(Esmeraldas City) has been replaced
with pastures and scattered trees (Collar
et al. 1992, p. 533). Dodson and Gentry
(1991, p. 293) indicated that rapid
habitat loss is continuing and that
extant forests will be eliminated in the
near future if deforestation continues.
Recent reports indicate that forest
habitat loss continues in Ecuador.
Between the years 1990 and 2005,
Ecuador has lost a total of 2.96 million
ha (7.31 million ac) of primary forest,
which represents a 16.7 percent
deforestation rate and a total loss of 21.5
percent of forested habitat since 1990
(Butler 2006b, pp. 1-3; FAO 2003b, p. 1).
Very little suitable habitat remains for
the species and remaining habitat is
highly fragmented (BLI 2004a, p. 2).
Other Human Factors: Ongoing
deforestation has transformed forested
habitat within the region to a patchwork
of cropland, with fewer than 5 percent
of the forested areas remaining only on
steep slopes that cannot be cultivated
(Best and Kessler 1995, p. 35;
Stattersfield et al. 1998, p. 214).
Persistent grazing from goats and cattle
has decimated the understory vegetation
and any secondary forest growth (BLI
2004a, p. 2). Researchers have observed
that road building and other
infrastructure improvements in
previously remote forested areas have
increased accessibility and further
facilitated habitat destruction,
exploitation, and human settlement
´
´
(Alvarez 2005, p. 2042; Cardenas and
´
Rodrıguez Becerra 2004, pp. 125-130;
Etter et al. 2006, p. 1; Hunter 1996, p.
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˜
158-159; Vina et al. 2004, pp. 118-119).
Fragmented habitat also increases
predator access to the forest, exposing
the species to increased risk of
predation (Factor C).
Refugia: The species is currently
known in three localities: (1) Isla de la
Plata, (2) Machalilla National Park, and
(3) Loma Alta Communal Ecological
Reserve.
(1) Isla de la Plata: This 1,420-ha
(3,508-ac) island is approximately 27
km (17 mi) from the coast of the
´
Department of Manabı and is actually
part of the Machalilla National Park (see
below). The species was last observed
on the island in 1998 (Becker et al.
2000, p. 55; BLI 2007c, p. 2). The island
is mostly uninhabited, but tourism for
bird-watching occurs there year-round
(BLI 2007c, p. 9), which occasionally
disturbs the native birds. Non-native
domestic animals, including goats
(Capra hircus), were introduced to the
island many years ago (Curry 1993, p.
24). Non-native predators, which have
also been introduced to the island, are
discussed below under Factor C. The
grazing activity of the goats has
destroyed understory habitat on the
island. As of 2007, BirdLife
International reports that an eradication
program is underway to remove these
feral animals from the island (BLI
2007c, p. 10). Despite a report, in 1991,
that the goat population on the island
had reportedly been reduced from an
estimated 300 to 30 animals (Curry
1993, p. 24), the colony of goats
apparently remains extant to this day
(BLI 2007c, p. 10).
(2) Machalilla National Park: This
34,393-ha (84,985-ac) Park was
established in 1979 (BLI 2007c, pp. 11,
13) and is designated as a Ramsar
Wetland of International Importance
(BLI 2007c, p. 13) (see Factor D). In
addition to the male sighting on Isla de
La Plata, a female was also observed
within the Park in 1998 (Becker et al.
2000, p. 55). The Park encompasses a
variety of habitats, including highelevation humid and cloud forests and
lower-elevation slopes covered with
semi-deciduous and deciduous forests
(BLI 2007c, pp. 11).
This park is populated, and residents
subsist on farming and cattle-raising
(BLI 2007c, pp. 11, 13; Lasso 1997, p. 3).
Portions of land within the Park have
been converted to pastures or cropland
(Lasso 1997, p. 3). Some previously
deforested areas have been left to
regenerate (BLI 2007c, p. 13). However,
ongoing grazing is hindering understory
development in forest areas left to
regenerate (BLI 2007c, pp. 10, 13, 17).
Residents continue to selectively
harvest trees and non-timber products;
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this activity is not monitored and the
extent of the impact is unknown (BLI
2007c, p. 13). The Park is surrounded by
a matrix of altered habitat, dominated
by agricultural crops such as bananas,
corn, sugarcane, tomatoes (Lycopersicon
esculentum), yucca (Yucca spp.), and
pasturelands (BLI 2007c, p. 11; Lasso
1997, p. 3). A highway built around the
outskirts of the park provides greater
access to more areas within the Park
(BLI 2007c, p. 13). Other activities in the
area, including a fish meal processing
plant, petroleum waste discharges into
the sea, and accumulation of solid
waste, are potential sources of pollution
within the Park (Lasso 1997, p. 3).
(3) Loma Alta Communal Ecological
Reserve: This 6,000-ha (14,826-ac) area
was declared a Reserve in 1996 (BLI
2007c, p. 17). The Reserve was created
to protect the watershed and to help
preserve the land of four groups of
indigenous inhabitants. The Reserve
encompasses a variety of habitats from
dry to cloud forests (BLI 2007c, p. 15).
About 500 ha (1,235 ac) of the Reserve
is dedicated to cultivation of the
Panama hat plant (Carludovica palmata,
locally known as ‘‘Paja Toquilla’’),
which is processed and sold by the
community. Cattle-raising has increased
in recent years and the regenerating
forests have again been decimated by
overgrazing. Logging, agriculture, and
slash-and-burn farming continue to
impact this Reserve (BLI 2007c, p. 17).
Summary of Factor A
Esmeraldas woodstars are rare, rangerestricted species with highly localized
populations in three disjunct locations
within an area of approximately 1,155
km2 (446 mi2) (BLI 2004, p. 2; Dodson
and Gentry 1991, p. 293). The evergreen
forests preferred by this species have
undergone extensive deforestation, and
remaining habitat is highly fragmented.
Habitat alteration and human activities,
such as slash-and-burn agriculture and
cattle and goat grazing, are occurring
throughout the species’ range, including
the protected areas in which the species
occurs (Machalilla National Park,
including Isla de la Plata, and Loma
Alta Communal Ecological Reserve).
Infrastructure development and
economic activities (such as fish meal
processing and non-timber forest
product extraction) occur throughout
the species’ known breeding range.
Logging, road development, and
pollution from industrial activities
occur within or near protected areas.
Habitat destruction, alteration, and
conversion have reduced the available
habitat for this species by 99 percent.
These activities are ongoing throughout
the species’ range, including within
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protected areas (Factor D), and are
expected to continue.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
Stattersfield et al. (1998, p. 214)
reported that birds in the Tumbesian
region are, in part, impacted by hunting
and trade (Stattersfield et al. 1998, p.
214). However, we have no current
information to suggest that hunting for
domestic or international consumption
or trade is impacting the Esmeraldas
woodstar (including, Best and Kessler,
pp. 124, 141; BLI 2007c, p. 3). Locally,
the communities in Loma Alta, where
this species occurs, are involved in
conservation activities, including
protecting native species in Loma Alta
Communal Ecological Reserve against
hunting, timber harvest and agricultural
expansion.
In 1987, the Esmeraldas woodstar was
listed in CITES Appendix II (UNEPWCMC 2008b, p. 1), which includes
species that are not necessarily
threatened with extinction, but which
require regulation of international trade
to ensure that trade of the species is
compatible with the species’ survival.
International trade in specimens of
Appendix-II species is authorized
through permits or certificates under
certain circumstances, including
verification that trade will not be
detrimental to the survival of the
species in the wild and that the
specimens were legally acquired (UNEPWCMC 2008a, p. 1). According to the
World Conservation Monitoring Centre
(WCMC), there has been one
international transaction permitted by
CITES since listing. In 1993, 100
‘‘bodies’’ were imported to Mexico
through the United States. According to
the trade data, the specimens were being
traded for commercial purposes and
were seized by inspectors (UNEPWCMC 2008d, p. 1). There has been no
further CITES-recorded trade in this
species since that time. Although we are
no longer able to determine the exact
details surrounding this seizure, we
consider the seizure and lack of ensuing
trade to be supportive that CITES has
been effective in controlling commercial
trade in this species. Therefore, we do
not consider international trade for
commercial purposes to be a threat to
the species.
Tourism occurs year-round at Isla de
la Plata and has been known to
occasionally disturb the native birds
(BLI 2007c, pp. 2, 9-10). There is no
information regarding whether
Esmeraldas woodstar is among the
native species that is adversely affected
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32343
by ecotourism or other human
disturbance.
We are unaware of any other
information currently available that
addresses the occurrence of
overutilization for commercial,
recreation, scientific, or education
purposes that may be affecting the
Esmeraldas woodstar population.
Consequently, we do not consider this
factor to be a threat to the species.
C. Disease or Predation
Disease: We are unaware of
information regarding disease or the
potential for significant disease
outbreaks in the Esmeraldas woodstar.
As a result, we do not consider disease
to be a threat to the species.
Predation: Hummingbird eggs and
chicks are most vulnerable to predation.
Known hummingbird predators that are
found in cloud forest habitat in Ecuador
include domestic cats (Felis catus), feral
cats, hawks (family Accipitridae), owls
(order Strigiformes), and snakes
(suborder Serpentes) (Borchardt 2004, p.
5; The Hummingbird Society no date
(n.d.), p 1; Rosso 2006, p. 35). Because
of their small size, many insect-eating
predators have been known to prey on
hummingbirds, including, praying
mantis (family Mantidae), spiders (class
Arachnida), bees and wasps (order
Hymenoptera), frogs (order Anura), and
largemouth bass (Micropterus
salmoides) (Borchardt 2004, p. 5; The
Hummingbird Society no date (n.d.), p
1; Rosso 2006, p. 35). According to the
FAO-Fisheries and Aquaculture
Department (2000, p. 1), largemouth
bass is a non-native invasive species
that was introduced to Ecuador
sometime prior to 1988. Many of these
potential Esmeraldas woodstar
predators are found within the
Machalilla National Park (Emmons and
Albuja 1992, pp. 120-121), both on the
mainland and on Isla de La Plata (see
Factor A).
On Isla de La Plata, non-native
predators, including cats and spiny rats
(Proechimys decumanus), were
introduced to the island many years ago
(BLI 2007c, p. 10; Curry 1993, p. 24).
Cats are opportunistic predators and
their diet is comprised of a variety of
animals, including birds (Rosero 2006,
p. 5). It was conjectured that the wild
cats on Isla de La Plata would keep the
rat population in check. However, Curry
(1993, p. 24) examined the stomach
contents of several cats on the Island
and found that they contained egg shell
fragments, not mammal hair, indicating
that the cats were preying upon bird
nests. Because Esmeraldas woodstar is
only observed on Isla de La Plata during
breeding season (BLI 2007c, p. 2; Becker
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et al. 2000, p. 55; Cisneros-Heredia
2005, p. 24), this renders the woodstar
especially vulnerable to egg predation
by cats. Cats are also considered among
the most common predators of nonnesting hummingbirds, especially
during torpor, a resting state induced in
hummingbirds when energy levels are
low (BLI 2008b, p. 1; The Hummingbird
Society n.d., p. 1; Schuchmann 1999, p.
485). During torpor, hummingbirds are
slow to react to external stimuli
(Schuchmann 1999, p. 485). Cats are
responsible for endangering other
island-dwelling hummingbirds,
including the critically endangered
´
Fernandez firecrown (Sephanoides
fernandensis) (native to the Juan
´
Fernandez Islands, Chile) (BLI 2008b, p.
1; The Hummingbird Society n.d., p. 1).
According to BirdLife International,
an eradication program is underway to
remove feral animals from the island
(BLI 2007c, p. 10). One project to
control the introduced cat population
on Isla De La Plata, being supported by
the World Conservation Foundation,
would trap the feral cats, neuter them,
and return them to the wild, with the
eventual goal of preventing further
reproduction of the feral population.
This project will also help to better
quantify the extent of the invasion on
the island (Rosero 2006, p. 5). However,
predation on the island continues to be
a threat to native bird species, including
the Esmeraladas woodstar, both on the
Island and in Machalilla National Park
(BLI 2007c, p. 10; Emmons and Albuja
1992, pp. 120-121; Rosero 2006, p. 5).
The Esmeraldas woodstar’s historic
range has been reduced by 99 percent
(Dodson and Gentry 1991, p. 293) and
remaining suitable habitat is highly
fragmented (Best and Kessler 1995, p.
35; BLI 2004a, p. 2; Stattersfield et al.
1998, p. 214). Studies have shown that
habitat fragmentation increases the
potential predation pressure within
habitat fragments by facilitating the
predators’ access throughout the
fragment and because smaller fragments
support smaller predators, which tend
to prey upon the more vulnerable lifehistory stages of the Esmeraldas
woodstar, eggs and juveniles (Arango´
Velez and Kattan 1997, pp. 137-143;
Gibbs 1991, p. 157; Hoover et al. 1995,
p. 151; Keyser et al. 1998, p. 991; 2002,
p. 186; Renjifo 1999, p. 1133; Wilcove
1985, p. 1214). These studies were
described in more detail above, as part
of the Factor C analysis for the bluebilled curassow.
Summary of Factor C
Domestic and feral cats, rats, hawks,
owls, snakes, praying mantis, spiders,
bees, wasps, frogs, and largemouth bass
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are all predators of hummingbirds that
are found in Esmeraldas woodstar
habitat. Predation results in the direct
removal of eggs, juveniles, and adults
from the population. Esmeraldas
woodstars produce a low clutch size
and are particularly vulnerable to egg
predation by cats on Isla de la Plata (see
Habitat and Life History). Esmeraldas
woodstar habitat is much reduced and
highly fragmented (Factor A), and
studies on similar species in similar
Andean habitats indicate that
vulnerability to predation by generalist
predators increases with increased
habitat fragmentation and smaller patch
sizes. Predation can remove potentially
reproductive adults from the breeding
pool and exacerbates the genetic
complications associated with the
species’ small population size (Factor
E), increasing the species’ vulnerability
to local extirpation. Therefore, we find
that predation, exacerbated by ongoing
habitat destruction (Factor A), is a threat
to the Esmeraldas woodstar.
D. The Inadequacy of Existing
Regulatory Mechanisms
Regulatory mechanisms may provide
species-specific or habitat-specific
protections. An evaluation of the
adequacy of regulatory mechanisms
within Ecuador to mitigate or remove
the threats to the Esmeraldas woodstar
is provided below, beginning with
species-specific and followed by
habitat-specific protection mechanisms.
The Esmeraldas woodstar is protected
under Ecuadorian law by Decree No.
3,516 of 2003 (Unified Text of the
Secondary Legislation of the Ministry of
Environment (EcoLex 2003b, pp. 1-2
and 36). Decree No. 3,516 summarizes
the laws governing environmental
policy in Ecuador and provides that the
country’s biodiversity be protected and
used primarily in a sustainable manner.
Appendix 1 of Decree No. 3,516 lists the
Ecuadorian fauna and flora that are
categorized as critically endangered (En
peligro critico), endangered (En peligro),
or vulnerable (Vulnerable) (EcoLex
2003b, p.17). Under this law,
Esmeraldas woodstar is categorized as
endangered, under the synonym
Acestrura berlepschi (EcoLex 2003b, p.
36). This threat status confers
protections upon the species, including
protection from hunting or commercial
take, under Resolution No. 105 of 2000
(Regulatory control of hunting seasons
and wildlife species in the country) and
Agreement No. 143 of 2003 (Standards
for the control of hunting seasons and
licenses for hunting of wildlife).
Resolution No. 105 and Agreement No.
143 regulate and prohibit commercial
and sport hunting of all wild bird
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species, except those specifically
identified by the Ministry of the
Environment or otherwise permitted
(EcoLex 2000, p.1; EcoLex 2003a, p. 1).
Under this law, the Ministry of the
Environment does not permit
commercial or sport hunting of the
Esmeraldas woodstar because of its
status as a critically endangered species
(EcoLex 2002b, p. 17). However, we do
not consider hunting (Factor B) to be a
current threat to the Esmeraldas
woodstar and these laws do not mitigate
threats to the species from habitat
destruction (Factor A), predation (Factor
C), or its small population size (Factor
E). Therefore, protection under these
laws does not reduce any existing
threats to the species.
Esmeraldas woodstar is listed in
Appendix II of CITES, to which Ecuador
became a Party in 1975 (UNEP-WCMC
2008a, p. 1; USFWS 2008, p. 1). CITES
was described in more detail above, as
part of the Factor E analysis for the bluebilled curassow. As discussed under
Factor B for the Esmeraldas woodstar,
we consider that this international
treaty has minimized the potential
threat to the species from international
trade and do not consider international
trade to be a threat impacting the
Esmeraldas woodstar. However, this
treaty does not mitigate threats to the
species from habitat destruction (Factor
A), predation (Factor C), or its small
population size (Factor E). Therefore,
protection under this Treaty does not
reduce any existing threats to the
species.
Ecuador has numerous laws and
regulations pertaining to forests and
forestry management, including: the
Forestry Act (comprised of Law No. 74
of 1981 — Forest Act and conservation
of natural areas and wildlife (Faolex
1981, pp. 1-54)—and Law No. 17 of
2004—Consolidation of the Forest Act
and conservation of natural areas and
wildlife (Faolex 2004, pp. 1-29); a
Forestry Action Plan (1991-1995); the
Ecuadorian Strategy for Forest
Sustainable Development of 2000
(Estrategia para el Desarrollo Forestal
Sostenible); and Decree 346, which
recognizes that natural forests are highly
vulnerable (ITTO 2006, p. 225).
However, the International Tropical
Timber Organization considers
ecosystem management and
conservation in Ecuador, including
effective implementation of mechanisms
that would protect the Esmeraldas
woodstar and its habitat, to be lacking
(ITTO 2006, p. 229). Habitat destruction
is ongoing (Butler 2006b, pp. 1-3; FAO
2003b, p. 1) and extensive (Best and
Kessler 1995, p. 35; BLI 2004a, p. 2;
Stattersfield et al. 1998, p. 214)
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throughout the species’ range (Factor A).
Thus, these laws are ineffective at
protecting Esmeraldas woodstar habitat.
Extractive harvest practices may pose
a threat to the Esmeraldas woodstar (BLI
2007c, p. 13) (Factor A). In 2004, Law
No. 17 (Faolex 2004, pp. 1-29) amended
the Forest Act of 1981 (Law No. 74)
(Faolex 1981, pp. 1-54) to include five
criteria for sustainable forest
management: (i) sustainable timber
production; (ii) the maintenance of
forest cover; (iii) the conservation of
biodiversity; (iv) co-responsibility in
management; and (v) the reduction of
negative social and environmental
impacts (Aguilar and Vlosky 2005, pp.
9-10; ITTO 2006, p. 225). In 2001, the
Ecuadorian government worked with
the private sector to develop a system of
monitoring and control of forest harvest
practices. However, in 2003, the
Supreme Court of Ecuador declared that
the control system was unconstitutional,
and new control systems are now being
developed (ITTO 2006, p. 225).
Approximately 70 percent of the forest
products harvested are harvested
illegally, are used as fuel wood, or are
discarded as waste (Aguilar and Vlosky
2005, p. 4; ITTO 2006, p. 226). Because
the extractive harvesting industry is not
monitored, the extent of the impact is
unknown (BLI 2007c, p. 13). However,
we find this law is currently inadequate
in monitoring the impacts of extractive
harvesting on the Esmeraldas woodstar
or to protect the species from potential
impacts of extractive harvesting (Factor
A).
The governmental institutions
responsible for natural resource
oversight in Ecuador appear to be
under-resourced, and there is a lack of
law enforcement on the ground. Despite
the creation of a national forest plan,
there appears to be a lack of capacity to
implement this plan due to insufficient
political support, unclear or unrealistic
forestry standards, inconsistencies in
application of regulations, discrepancies
between actual harvesting practices and
forestry regulations, the lack of
management plans for protected areas,
and high bureaucratic costs. These
inadequacies have facilitated logging
(Dodson and Gentry 1991, pp. 283-293);
cattle-raising and persistent grazing
from goats and cattle (BLI 2004a, p. 2;
BLI 2007c, pp. 11, 13, 17; Curry 1993,
p. 24; Lasso 1997, p. 3); clearing for
agriculture, subsistence farming, and
small local industries (BLI 2007c, pp.
11, 13, 17; Dodson and Gentry 1991, pp.
283-293; Lasso 1997, p. 3); selective
harvest of trees for fuelwood and nontimber products (Aguilar and Vlosky
2005; BLI 2007c, p. 13); road
development (BLI 2007c, p. 13; Dodson
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and Gentry 1991, pp. 283-293); and
pollution from industrial activities
occur within or near protected areas
(Lasso 1997, p. 3). In addition, most of
Ecuador’s forests are privately owned or
owned by communities (ITTO 2006, p.
224; Lasso 1997, pp. 2-3), and the
management and administration of
Ecuador’s forest resources and forest
harvest practices is insufficient and
unable to protect against unauthorized
forest harvesting, degradation, and
conversion (ITTO 2006, p. 229). Habitat
conversion and alteration are ongoing
throughout the range of the Esmeraldas
woodstar, including within protected
areas (BLI 2007c, pp. 10, 13, 17; Butler
2006b, pp. 1-3; FAO 2003b, p. 1).Thus,
Ecuadorian forestry regulations have not
mitigated the threat of habitat
destruction (Factor A).
The Ecuadorian government
recognizes 31 different legal categories
of protected lands (e.g., national parks,
biological reserves, geo-botanical
reserves, bird reserves, wildlife reserves,
etc.). Currently, the amount of protected
land (both forested and non-forested) in
Ecuador totals approximately 4.67
million ha (11.5 million ac) (ITTO 2006,
p. 228). However, only 38 percent of
these lands have appropriate
conservation measures in place to be
considered protected areas according to
international standards (i.e., areas that
are managed for scientific study or
wilderness protection, for ecosystem
protection and recreation, for
conservation of specific natural features,
or for conservation through management
intervention) (IUCN 1994, pp. 17-20).
Moreover, only 11 percent have
management plans, and fewer than 1
percent (13,000 ha (32,125 ac)) have
implemented those management plans
(ITTO 2006, p. 228).
The Esmeraldas woodstar has been
recorded in or near two protected areas:
(1) Machalilla National Park (Collar et
al. 1992, p. 533) and (2) Loma Alta
Communal Ecological Reserve. As
described under Factor A, both of these
protected areas are inhabited and,
among other activities, deforestation,
livestock grazing, and slash-and-burn
agriculture are ongoing within these
areas (BLI 2004, p. 2; Wege and Long
1995, p. 174). Thus, this protected area
status does not mitigate the threats from
habitat destruction (Factor A).
Esmeraldas woodstar occurs within
the Machalilla National Park, which was
included in the Ramsar List of Wetlands
of International Importance in 1990 (BLI
2007c, p. 13). The Ramsar Convention,
signed in Ramsar, Iran, in 1971, is an
intergovernmental treaty that provides
the framework for national action and
international cooperation for the
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conservation and wise use of wetlands
and their resources. There are presently
158 Contracting Parties to the
Convention (including Ecuador, where
the Esmeraldas woodstar occurs), with
1,828 wetland sites, totaling 169 million
ha (418 million ac), designated for
inclusion in the Ramsar List of
Wetlands of International Importance
(Ramsar Convention Secretariat 2008, p.
1). Experts consider Ramsar to provide
only nominal protection of wetlands,
noting that such a designation may
increase international awareness of the
site’s ecological value (Jellison et al.
2004, p. 19). However, habitat alteration
(Factor A) (BLI 2007c, pp. 10-11, 13;
Lasso 1997, p. 3) and predation by feral
animals (Factor C) (BLI 2007c, p. 10;
Curry 1993, p. 24; Rosero 2006, p. 5),
key threats to the Esmeraldas woodstar,
are ongoing within the Park and
predation has not been considered as
part of the most recent Ramsar site
review (Lasso 1997, pp. 1-4). Therefore,
this designation as a Ramsar Wetland of
International Importance does not
mitigate the threats from habitat
destruction (Factor A).
Summary of Factor D
Ecuador has adopted numerous laws
and regulatory mechanisms to
administer and manage wildlife and
their habitats. The Esmeraldas woodstar
is protected under CITES, which we
consider has been effective in mitigating
the potential threat to this species from
commercial trade (Factor B). Esmeraldas
woodstar is listed as endangered and
ranges within at least two protected
areas (Machalilla National Park and
Loma Alta Communal Ecological
Reserve). However, on-the-ground
enforcement of these laws and oversight
of the local jurisdictions implementing
and regulating activities is insufficient
for these measures to be effective in
conserving the Esmeraldas woodstar or
its habitat. As discussed for Factor A,
habitat destruction, degradation, and
fragmentation continue throughout the
species’ range, including lands within
protected areas. Therefore, we find that
the existing regulatory mechanisms, as
implemented, are inadequate to mitigate
the primary threats to the Esmeraldas
woodstar from habitat destruction
(Factor A), predation (Factor C), or its
small population size (Factor E).
E. Other Natural or Manmade Factors
Affecting the Continued Existence of the
Species
Two additional factors affect the
Esmeraldas woodstar: Its minimal
likelihood for dispersal and the species’
small population size.
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Likelihood to Disperse: The
Esmeraldas woodstar is confined to
locations within the Departments of
´
Esmeraldas, Manabı, and Guayas, in
lowland moist forest patches that are
disjunct and fragmented (BLI 2007f, pp.
1-3; del Hoyo et al. 1999, p. 678;
Williams and Tobias 1991, p. 39). The
distance between known occupied areas
is between 125 and 200 km (78 and 124
mi), with minimal habitat between
occupied sights (Best and Kessler 1995,
p. 141). In light of the species’ small
overall population size and the distance
between the remaining fragmented
primary forested habitats, it is unlikely
that the Esmeraldas woodstar would
repopulate an isolated patch of suitable
habitat following decline or extirpation
of that patch (Hanski 1998, pp. 45-46).
Small Population Size: The
Esmeraldas woodstar inhabits a very
small and severely fragmented range,
which is decreasing rapidly in size due
to habitat destruction and various other
human factors (Collar et al. 1992, p. 533;
Ridgely and Greenfield 2001a, pp. 389390). Ongoing declines in the bird’s
population are linked to persistent
habitat destruction (BLI 2007c, p. 2).
Before the species was rediscovered in
1991, it was thought to be extinct after
not being seen since 1912 (Ridgely and
Greenfield 2001a, pp. 389-390).
Subsequent surveys of previously
known occupied areas have not been
successful in locating the species on a
consistent basis, and little is known of
breeding habits or other activities
during most of the year (Ridgely and
Greenfield 2001a, pp. 389-390). Experts
estimate that the species has undergone
a 50-79 percent reduction in population
size within the past 10 years and predict
that this trend will continue (BLI 2007c,
p. 5). The current population estimate
for this species is between 186 to 373
birds, with a decreasing population
trend (BLI 2007, pp. 2, 6).
Small population sizes render species
vulnerable to genetic risks that can have
individual or population-level
consequences on the genetic level and
can increase the species’ susceptibility
to demographic problems, as explained
in more detail above for the blue-billed
curassow (Factor E, Small Population
Size) (Charlesworth and Charlesworth
1987, p. 238; Shaffer 1981, p. 131). Once
a population is reduced below a certain
number of individuals, it tends to
rapidly decline towards extinction
(Franklin 1980, pp. 147-148; Gilpin and
´
Soule 1986, p. 25; Holsinger 2000, pp.
´
64-65; Soule 1987, p. 181).
In the absence of quantitative studies
specific to this species, a general
approximation of minimum viable
population size is the 50/500 rule, as
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described above, as part of the Factor E
analysis for the brown-banded antpitta
´
(Shaffer 1981, pp. 132-133; Soule 1980,
pp. 160-162). The total population size
of the Esmeraldas woodstar is estimated
to be between 186 and 373 individuals.
The lower estimate of 186 individuals
meets the theoretical threshold for the
minimum effective population size
required to avoid risks from inbreeding
(Ne = 50 individuals). However, the
upper limit of the population, 373
individuals, is below the minimum
threshold (Ne = 500 individuals)
required for long-term fitness of a
population that will not lose its genetic
diversity over time and will maintain an
enhanced capacity to adapt to changing
conditions.
The Esmeraldas woodstar’s restricted
range combined with its small
population size (Cuervo 2002, p. 138;
Cuervo and Salaman 1999, p. 7; del
Hoyo 1994, p. 361) makes the species
particularly vulnerable to the threat of
adverse natural (e.g., genetic,
demographic, or environmental) and
manmade (e.g., deforestation, habitat
alteration, wildfire) events that destroy
individuals and their habitat (Holsinger
2000, pp. 64-65; Primack 1998, pp. 279308; Young and Clarke 2000, pp. 361366). Therefore, we currently consider
the single Esmeraldas woodstar
population to be at risk due to the lack
of long-term viability.
Summary of Factor E
The Esmeraldas woodstar is currently
limited to a few small populations
within a limited habitat range, with a
small estimated population size that
leaves the species vulnerable to genetic
and demographic risks that negatively
impact its long-term viability. The
species’ population size is estimated to
have declined considerably within the
past 10 years (50-79 percent), and this
rate of decline is expected to continue.
Based on this information, we have
determined that the species is
particularly vulnerable to the threat of
adverse natural (e.g., genetic,
demographic, or predation) and
manmade (e.g., slash-and-burn
agriculture or infrastructural
development) events that destroy
individuals and their habitat, and that
these genetic and demographic risks are
exacerbated by ongoing habitat
destruction (Factor A) and predation
(Factor C).
Status Determination for the Esmeraldas
Woodstar
The four primary factors that threaten
the survival of the Esmeraldas woodstar
are: (1) habitat destruction,
fragmentation, and degradation (Factor
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A); (2) predation (Factor C); (3)
inadequate regulatory mechanisms
(Factor D); and (4) limited size and
isolation of remaining populations
(Factor E). The Esmeraldas woodstar is
a tiny hummingbird endemic to
Ecuador. Esmeraldas woodstars are a
rare, range-restricted species with
highly localized populations in three
disjunct locations – in the Ecuadorean
Departments of Esmeraldas, Guayas, and
´
Manabı. The species occurs in lowland
semi-humid or semi-evergreen forests
and woodlands, from sealevel to 500 m
(1,600 ft) along the Coastal Cordillera of
western Ecuador. Preferring primary
evergreen forests, the species is also
known to occupy low-altitude
secondary-growth areas during the
breeding season (December-March). The
current extent of the species’ range is
approximately 1,155 km2 (446 mi2).
The primary threat to this species is
habitat loss (Factor A), caused by
widespread deforestation and
conversion of primary forests for
numerous human activities. The
species’ range has been reduced by 99
percent. The semi-humid and semievergreen forests preferred by this
species have undergone extensive
deforestation. Habitat-altering activities
that have occurred include: logging;
cattle-raising and persistent grazing
from goats and cattle; forest clearing for
agriculture, subsistence farming, and
small local industries; selective harvest
of trees for fuelwood and non-timber
products; road development; and
pollution from industrial activities
(Factors A). These activities are ongoing
and occurring throughout the species’
range – including within protected areas
where the species occurs (Machalilla
National Park, Isla de La Plata, and
Loma Alta Communal Ecological
Reserve). Because regulatory
mechanisms are ineffective at reducing
these activities (Factor D), habitat
destruction and alteration are expected
to continue.
The species’ population is estimated
to have declined between 50 to 79
percent within the last 10 years, a
decline which is attributed to habitat
loss. The Esmeraldas woodstar has a
small estimated population size
(between 186 and 373 individuals),
which renders the species vulnerable to
the threat of adverse natural (e.g.,
genetic, demographic, or predation) and
manmade (e.g., slash-and-burn
agriculture or infrastructural
development) events that destroy
individuals and their habitat (Factor E).
In addition, the direct loss of habitat
through widespread deforestation and
conversion for human activities has led
to habitat fragmentation and isolation of
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Federal Register / Vol. 74, No. 128 / Tuesday, July 7, 2009 / Proposed Rules
the remaining populations of the
Esmeraldas woodstar. The Esmeraldas
woodstar currently occupies three
disjunct, isolated patches that are
separated by large distances (between
125 and 200 km (78 and 124 mi)), with
minimal suitable habitat between
occupied sites. Given the species’ small
population size and the distance
between the remaining fragmented
primary forested habitats, the species is
unlikely to repopulate an isolated patch
of suitable habitat following decline or
extirpation of the species within that
patch (Factor E). This renders the
species particularly vulnerable to local
extirpation from ongoing habitat
destruction (Factor A) and predation
(Factor C).
Esmeraldas woodstars are vulnerable
to predation by a variety of predators,
including domestic and feral cats, rats,
hawks, owls, snakes, praying mantis,
spiders, bees, wasps, frogs, and
largemouth bass (Factor C). Habitat
fragmentation (Factor A) contributes to
this vulnerability, because research
indicates that predation increases with
increased habitat fragmentation and
smaller patch sizes. Predation leads to
the direct removal of eggs, juveniles,
and adults from the population,
exacerbating risks associated with the
species’ small population size.
Esmeraldas woodstars are particularly
vulnerable to predation by wild cats
during the breeding season on Isla de La
Plata, where cats have been known to
prey particularly upon bird eggs.
Esmeraldas woodstars produce a low
clutch size (see Habitat and Life
History), and predation can remove
potentially reproductive adults from the
breeding pool.
The Esmeraldas woodstar is classified
as an endangered species under
Ecuadorian law, and part of the species’
range is included within two protected
areas. Despite numerous laws and
regulatory mechanisns to administer
and manage wildlife and their habitats,
existing laws are inadequate (Factor D)
to protect the species and its habitat
from ongoing habitat loss (Factor A) and
predation by non-native animals (Factor
C), even within the protected areas.
We have carefully assessed the best
available scientific and commercial
information regarding the past, present,
and potential future threats faced by the
Esmeraldas woodstar. We consider the
ongoing threats to the Esmeraldas
woodstar, habitat loss (Factor A) and
predation (Factor C), exacerbated by the
species’ small population size and
limited dispersal ability (Factor E), and
compounded by inadequate regulatory
mechanisms (Factor D), to be equally
present and of the same magnitude
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throughout the species’ entire current
range. Based on this information, we
conclude that the Esmeraldas woodstar
is endangered throughout its range.
Therefore, we are proposing to list the
Esmeraldas woodstar as an endangered
species.
Available Conservation Measures
Conservation measures provided to
species listed as endangered or
threatened under the Act include
recognition, requirements for Federal
protection, and prohibitions against
certain practices. Recognition through
listing results in public awareness, and
encourages and results in conservation
actions by national governments, private
agencies and groups, and individuals.
Section 7(a) of the Act, as amended,
and as implemented by regulations at 50
CFR part 402, requires Federal agencies
to evaluate their actions within the
United States or on the high seas with
respect to any species that is proposed
or listed as endangered or threatened,
and with respect to its critical habitat,
if any is being designated. However,
given that the blue-billed curassow, the
brown-banded antpitta, the Cauca guan,
the gorgeted wood-quail, and the
Esmeraldas woodstar are not native to
the United States, no critical habitat is
being proposed for designation with this
rule.
Section 8(a) of the Act authorizes
limited financial assistance for the
development and management of
programs that the Secretary of the
Interior determines to be necessary or
useful for the conservation of
endangered and threatened species in
foreign countries. Sections 8(b) and 8(c)
of the Act authorize the Secretary to
encourage conservation programs for
foreign endangered species and to
provide assistance for such programs in
the form of personnel and the training
of personnel.
The Act and its implementing
regulations set forth a series of general
prohibitions and exceptions that apply
to all endangered and threatened
wildlife. Consequently, these
prohibitions would be applicable to the
blue-billed curassow, the brown-banded
antpitta, the Cauca guan, the gorgeted
wood-quail, and the Esmeraldas
woodstar. These prohibitions, under 50
CFR 17.21, make it illegal for any person
subject to the jurisdiction of the United
States to ‘‘take’’ (take includes harass,
harm, pursue, hunt, shoot, wound, kill,
trap, capture, collect, or to attempt any
of these) within the United States or
upon the high seas, import or export,
deliver, receive, carry, transport, or ship
in interstate or foreign commerce in the
course of a commercial activity or to sell
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32347
or offer for sale in interstate or foreign
commerce, any endangered wildlife
species. It also is illegal to possess, sell,
deliver, carry, transport, or ship any
such wildlife that has been taken in
violation of the Act. Certain exceptions
apply to agents of the Service and State
conservation agencies.
We may issue permits to carry out
otherwise prohibited activities
involving endangered and threatened
wildlife species under certain
circumstances. Regulations governing
permits are codified at 50 CFR 17.22 for
endangered species, and at 17.32 for
threatened species. With regard to
endangered wildlife, a permit must be
issued for the following purposes: for
scientific purposes, to enhance the
propagation or survival of the species,
and for incidental take in connection
with otherwise lawful activities.
Peer Review
In accordance with our joint policy
with the National Marine Fisheries
Service, ‘‘Notice of Interagency
Cooperative Policy for Peer Review in
Endangered Species Act Activities,’’
published in the Federal Register on
July 1, 1994 (59 FR 34270), we will seek
the expert opinions of at least three
appropriate independent specialists
regarding this proposed rule. The
purpose of peer review is to ensure that
our final determination is based on
scientifically sound data, assumptions,
and analyses. We will send copies of
this proposed rule to the peer reviewers
immediately following publication in
the Federal Register. We will invite
these peer reviewers to comment during
the public comment period on our
specific assumptions and conclusions
regarding the proposal to list the bluebilled curassow, the Cauca guan, the
gorgeted wood-quail, the brown-banded
antpitta, and the Esmeraldas woodstar
as endangered.
We will consider all comments and
information we receive during the
comment period on this proposed rule
during our preparation of a final
determination. Accordingly, our final
decision may differ from this proposal.
Public Hearings
The Act provides for one or more
public hearings on this proposal, if we
receive any requests for hearings. We
must receive your request for a public
hearing within 45 days after the date of
this Federal Register publication (see
DATES). Such requests must be made in
writing and be addressed to the Chief of
the Branch of Listing at the address
shown in the FOR FURTHER INFORMATION
CONTACT section. We will schedule
public hearings on this proposal, if any
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Federal Register / Vol. 74, No. 128 / Tuesday, July 7, 2009 / Proposed Rules
are requested, and announce the dates,
times, and places of those hearings, as
well as how to obtain reasonable
accommodations, in the Federal
Register at least 15 days before the first
hearing.
Required Determinations
National Environmental Policy Act
(NEPA)
We have determined that
environmental assessments and
environmental impact statements, as
defined under the authority of the
National Environmental Policy Act of
1969 (42 U.S.C. 4321 et seq.), need not
be prepared in connection with
regulations adopted under section 4(a)
of the Act. We published a notice
outlining our reasons for this
determination in the Federal Register
on October 25, 1983 (48 FR 49244).
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:
(a) be logically organized;
(b) use the active voice to address
readers directly;
(c) use clear language rather than
jargon;
(d) be divided into short sections and
sentences; and
(e) 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 the ADDRESSES
section. 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, or the sections where you feel
lists or tables would be useful.
References Cited
The references cited in this proposed
rule are available on the Internet at
https://www.regulations.gov or upon
request from the Branch of Listing,
Endangered Species Program, U.S. Fish
and Wildlife Service (see FOR MORE
INFORMATION CONTACT).
Author(s)
The primary authors of this proposed
rule are Arnold Roessler of the
Endangered Species Program
(Sacramento, California) and Dr. Patricia
De Angelis of the Division of Scientific
Authority U.S. Fish and Wildlife
Service.
Species
Historic range
Common name
Scientific name
List of Subjects in 50 CFR Part 17
Endangered and threatened species,
Exports, Imports, Reporting and
recordkeeping requirements,
Transportation.
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—[AMENDED]
1. The authority citation for part 17
continues to read as follows:
Authority: 16 U.S.C. 1361-1407; 16
U.S.C. 1531-1544; 16 U.S.C. 4201-4245;
Pub. L. 99-625, 100 Stat. 3500; unless
otherwise noted.
2. Amend § 17.11(h), by adding new
entries for ‘‘Curassow, bluebilled,’’‘‘Guan, Cauca,’’‘‘Wood-quail,
Gorgeted,’’‘‘Antpitta, Brown-banded,’’
and ‘‘Woodstar, Esmeraldas’’ in
alphabetical order under BIRDS to the
List of Endangered and Threatened
Wildlife to read as follows:
§ 17.11 Endangered and threatened
wildlife.
*
*
*
*
*
(h) Birds.
*
*
*
*
*
Vertebrate
population
where
endangered
or threatened
Status
When
listed
Critical
habitat
Special
rules
*******
BIRDS
*******
Antpitta, brown-banded
Grallaria milleri
Columbia, South America
Entire
E
NA
NA
Crax alberti
Columbia, South America
Entire
E
NA
NA
Penelope perspicax
Columbia, South America
Entire
E
NA
NA
Odontophorus strophium
Columbia, South America
Entire
E
NA
NA
Chaetocercus berlepschi
Ecuador, South America
Entire
E
NA
NA
*******
Curassow, blue-billed
*******
Guan, cauca
*******
Wood-quail, gorgeted
*******
Woodstar, Esmeraldas
*******
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Federal Register / Vol. 74, No. 128 / Tuesday, July 7, 2009 / Proposed Rules
Dated: May 28, 2009
Rowan W. Gould
Acting Director, U.S. Fish and Wildlife Service
[FR Doc. E9–15826 Filed 7–6– 09; 8:45 am]
BILLING CODE 4310-55-S
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Agencies
[Federal Register Volume 74, Number 128 (Tuesday, July 7, 2009)]
[Proposed Rules]
[Pages 32308-32349]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-15826]
[[Page 32307]]
-----------------------------------------------------------------------
Part IV
Department of the Interior
-----------------------------------------------------------------------
Fish and Wildlife Service
-----------------------------------------------------------------------
50 CFR Part 17
Endangered and Threatened Wildlife and Plants; Proposed Rule to List
Five Foreign Bird Species in Colombia and Ecuador, South America, Under
the Endangered Species Act; Proposed Rule
Federal Register / Vol. 74, No. 128 / Tuesday, July 7, 2009 /
Proposed Rules
[[Page 32308]]
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[FWS-R9-IA-2009-12; 96100-1671-9FLS-B6]
RIN 1018-AV75
Endangered and Threatened Wildlife and Plants; Proposed Rule to
List Five Foreign Bird Species in Colombia and Ecuador, South America,
under the Endangered Species Act
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), propose to
list as endangered four species of birds from Colombia -- the blue-
billed curassow (Crax alberti), the brown-banded antpitta (Grallaria
milleri), the Cauca guan (Penelope perspicax), and the gorgeted wood-
quail (Odontophorus strophium) -- and one bird species from Ecuador --
the Esmeraldas woodstar (Chaetocercus berlepschi) -- as endangered
under the Endangered Species Act of 1973, as amended (Act) (16 U.S.C.
1531 et seq.). This proposal, if made final, would extend the Act's
protection to these species. The Service seeks data and comments from
the public on this proposed rule.
DATES: We will accept comments received or postmarked on or before
September 8, 2009. We must receive requests for public hearings, in
writing, at the address shown in the ADDRESSES section by August 21,
2009.
ADDRESSES: You may submit comments by one of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments.
U.S. mail or hand-delivery: Public Comments Processing,
Attn: RIN 1018-AV75; Division of Policy and Directives Management; U.S.
Fish and Wildlife Service; 4401 N. Fairfax Drive, Suite 222; Arlington,
VA 22203.
We will post all comments on https://www.regulations.gov . This
generally means that we will post any personal information you provide
us (see the Public Comments section below for more information).
FOR FURTHER INFORMATION CONTACT: Douglas Krofta, Chief, Branch of
Listing, Endangered Species Program, U.S. Fish and Wildlife Service,
4401 N. Fairfax Drive, Room 420, Arlington, VA 22203; telephone 703-
358-2105; facsimile 703-358-1735. If you use a telecommunications
device for the deaf (TDD), you may call the Federal Information Relay
Service (FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Public Comments
We intend that any final action resulting from this proposal will
be as accurate and as effective as possible. Therefore, we request
comments or suggestions on this proposed rule. We are particularly seek
comments concerning:
(1) Biological, commercial trade, or other relevant data concerning
any threats (or lack thereof) to these species and regulations that may
be addressing those threats.
(2) Additional information concerning the taxonomy, range,
distribution, and population size of these species, including the
locations of any additional populations of these species.
(3) Any information on the biological or ecological requirements of
these species.
(4) Current or planned activities in the areas occupied by these
species and possible impacts of these activities on these species.
(5) Any information concerning the effects of climate change on
these species or their habitats.
You may submit your comments and materials concerning this proposed
rule by one of the methods listed in the ADDRESSES section. We will not
consider comments sent by e-mail or fax or to an address not listed in
the ADDRESSES section.
If you submit a comment via https://www.regulations.gov, your entire
comment--including any personal identifying information--will be posted
on the website. If you submit a hardcopy comment 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 comments 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, Endangered Species Program, 4401 N. Fairfax Drive,
Room 420, Arlington, VA 22203; telephone 703-358-2171.
Background
Section 4(b)(3)(A) of the Act requires us to make a finding (known
as a ``90-day finding'') on whether a petition to add, remove, or
reclassify a species from the list of endangered or threatened species
has presented substantial information indicating that the requested
action may be warranted. To the maximum extent practicable, the finding
shall be made within 90 days following receipt of the petition and
published promptly in the Federal Register. If we find that the
petition has presented substantial information indicating that the
requested action may be warranted (a positive finding), section
4(b)(3)(A) of the Act requires us to commence a status review of the
species if one has not already been initiated under our internal
candidate assessment process. In addition, section 4(b)(3)(B) of the
Act requires us to make a finding within 12 months following receipt of
the petition on whether the requested action is warranted, not
warranted, or warranted but precluded by higher-priority listing
actions (this finding is referred to as the ``12-month finding'').
Section 4(b)(3)(C) of the Act requires that a finding of warranted but
precluded for petitioned species should be treated as having been
resubmitted on the date of the warranted-but-precluded finding, and is,
therefore, subject to a new finding within 1 year and subsequently
thereafter until we publish a proposal to list or a finding that the
petitioned action is not warranted. The Service publishes an annual
notice of resubmitted petition findings (annual notice) for all foreign
species for which listings were previously found to be warranted but
precluded.
Previous Federal Action
On November 24, 1980, we received a petition (1980 petition) from
Dr. Warren B. King, Chairman of the International Council for Bird
Preservation (ICBP), to add 60 foreign bird species to the list of
Threatened and Endangered Wildlife (50 CFR 17.11(h)), including two
species from Colombia (the Cauca guan and the gorgeted wood-quail) that
are the subject of this proposed rule. In response to the 1980
petition, we published a positive 90-day finding on May 12, 1981 (46 FR
26464), to initiate a status review for 58 foreign species, noting that
2 of the species identified in the petition were already listed under
the Act. On January 20, 1984 (49 FR 2485), we published a 12-month
finding within an annual review on pending petitions and description of
progress on all species petition findings addressed therein. In that
notice, we found that all 58 foreign bird species from the 1980
petition were warranted but precluded by higher-priority listing
actions. On May 10, 1985, we published the first annual
[[Page 32309]]
notice (50 FR 19761), in which we continued to find that listing all 58
foreign bird species from the 1980 petition was warranted but
precluded. In our next annual notice, published on January 9, 1986 (51
FR 996), we found that listing 54 species from the 1980 petition,
including the two Colombian species mentioned above, continued to be
warranted but precluded, whereas new information caused us to find that
listing four other species in the 1980 petition was no longer
warranted. We published additional annual notices on the remaining 54
species included in the 1980 petition on July 7, 1988 (53 FR 25511);
December 29, 1988 (53 FR 52746); and November 21, 1991 (56 FR 58664),
in which we indicated that the Cauca guan and the gorgeted wood-quail,
along with the remaining species in the 1980 petition, continued to be
warranted but precluded.
On May 6, 1991, we received a petition (1991 petition) from Alison
Stattersfield, of ICBP, to add 53 species of foreign birds to the list
of Endangered and Threatened Wildlife, including the blue-billed
curassow and the brown-banded antpitta, from Colombia, and Esmeraldas
woodstar, from Ecuador. In response to the 1991 petition, we published
a positive 90-day finding on December 16, 1991 (56 FR 65207), for all
53 species and announced the initiation of a status review. On March
28, 1994 (59 FR 14496), we published a 12-month finding on the 1991
petition, along with a proposed rule to list 30 African birds under the
Act (15 each from the 1980 petition and 1991 petition). In that
document, we announced our finding that listing the remaining 38
species from the 1991 petition, including the blue-billed curassow and
the brown-banded antpitta, from Colombia, and Esmeraldas woodstar, from
Ecuador, was warranted but precluded by higher-priority listing
actions. On January 12, 1995 (60 FR 2899), we reiterated the warranted-
but-precluded status of the remaining species from the 1991 petition.
We made subsequent warranted but precluded findings for all outstanding
foreign species from the 1980 and 1991 petitions, including all five of
the Colombian and Ecuadorian bird species that are the subject of this
proposed rule, as published in our annual notices of review (ANOR) on
May 21, 2004 (69 FR 29354), and April 23, 2007 (72 FR 20184).
Per the Service's listing priority guidelines (September 21, 1983;
48 FR 43098), we identified the listing priority numbers (LPNs)
(ranging from 1 to 12) for all outstanding foreign species in our 2007
ANOR (72 FR 20184), published on April 23, 2007. In that notice, the
five species included in this proposed rule were designated with an LPN
of 2, and it was determined that their listing continued to be
warranted but precluded because of other listing activity. A listing
priority of 2 indicates that the subject species face imminent threats
of high magnitude. With the exception of LPN 1, which addresses
monotypic genera that face imminent threats of high magnitude, category
2 represents the Service's highest priority.
On July 29, 2008 (73 FR 44062), we published in the Federal
Register a notice announcing our annual petition findings for foreign
species (2008 ANOR). In that notice, we announced that listing was
warranted for 30 foreign bird species, including the five species that
are the subject of this proposed rule. The five species were selected
from the list of warranted-but-precluded species because of their LPN,
their similarity of habitat, and the similarity of threats to these
species. Combining species that face similar threats within the same
general geographic area into one proposed rule allows us to maximize
our limited staff resources, thus increasing our ability to complete
the listing process for warranted-but-precluded species.
Species Information and Factors Affecting the Species
Section 4 of the Act (16 U.S.C. 1533), and its implementing
regulations at 50 CFR part 424, set forth the procedures for adding
species to the Federal Lists of Endangered and Threatened Wildlife and
Plants. A species may be determined to be an endangered or threatened
species due to one or more of the five factors described in section
4(a)(1) of the Act. The five factors are: (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; and (E) other natural or manmade
factors affecting its continued existence.
Under the Act, we may determine a species to be endangered or
threatened. An endangered species is defined as a species that is in
danger of extinction throughout all or a significant portion of its
range. A threatened species is defined as a species that is likely to
become an endangered species within the foreseeable future throughout
all or a significant portion of its range. Therefore, we evaluated the
best available scientific and commercial information on each species
under the five listing factors to determine whether they met the
definition of endangered or threatened.
Below is a species-by-species analysis of these five factors using
the best available scientific and commercial information to determine
whether the species meet the definition of endangered or threatened.
The species are considered in alphabetical order, beginning with the
Colombian species: blue-billed curassow, brown-banded antpitta, Cauca
guan, gorgeted wood-quail, and followed by the Ecuadorian species: the
Esmeraldas woodstar.
Colombian Bird Species
I. Blue-Billed Curassow (Crax alberti)
Species Description
The blue-billed curassow, endemic to Colombia, is a large (82-92
centimeters (cm) (32-36 inches (in)), tree-dwelling member of the
Cracid family (Cracidae) (Collar et al. 1992, p. 154; del Hoyo 1994, p.
361; Salaman et al. 2001, p. 183). The species is locally known as
``Pauj[iacute]l de pico azul'' or ``Pav[oacute]n Colombiano'' and is
also referred to in English as the blue-knobbed curassow (Cuervo 2002,
p. 138; United Nations Environment Programme - World Conservation
Monitoring Centre (UNEP-WCMC) 2008c, p. 1). In older literature, the
species is referred to as Prince Albert's curassow (Throp 1964, p.
124). The blue-billed curassow is described as mainly black with blue
at the base of its bill. The male has a white-plumaged crissum (the
area under the tail), whereas the female has a black and white crest
and black and white barring on her wings (BirdLife International (BLI)
2007d, p. 1; Throp 1964, p. 124).
Taxonomy
The species was first taxonomically described by Fraser in 1852 and
placed in the family Cracidae.
Habitat and Life History
Blue-billed curassows prefer undisturbed, heterogeneous primary
forests in the humid lowlands of the Sierra Nevada de Santa Marta
Mountains at elevations up to 1,200 meters (m) (3,937 feet (ft))
(Collar et al. 1992, p. 154; del Hoyo 1994, p. 361; Salaman et al.
2001, p. 183). The blue-billed curassow requires a large home range of
primary tropical forest (Cuervo 2002, pp. 138-140). The species will
rarely cross narrow deforested corridors, such as those caused by roads
or oil pipelines, and will not cross large open areas between forest
fragments (Cuervo and Salaman 1999, p. 7). The species is described as
being trusting of humans (del Hoyo 1994, p. 336).
[[Page 32310]]
This terrestrial bird feeds mostly on fruit and leaves, and
sometimes feeds upon worms and carrion. It plays an important role in
dispersing seeds and regenerating tropical forests (BLI 2007d, p. 1;
Brooks 2006, p. 17; Brooks and Strahl 2000, pp. 5-8; Cuervo and Salaman
1999, p. 8).
Cracids are also slow to reproduce, with a replacement rate of at
least 6 years (Silva and Strahl 1991, p. 50). Curassows reach sexual
maturity in their second year (Throp 1964, p. 130). Blue-billed
curassows form monogamous pairs that share responsibilities for young
(Cuervo and Salaman 1999, p. 9; Todd et al. 2008). The breeding season
begins in December and goes through March (Cuervo and Salaman 1999, p.
8). During the mating season, the male blue-billed curassows makes
``booming'' calls that can be heard 500 m (0.31 mi) away (Ochoa-
Quintero et al. 2005, pp. 42, 44). Large nests made of sticks and
leaves are built in dense lianas (woody vines) (Cuervo and Salaman
1999, p. 8). The typical blue-billed curassow clutch size is 1-2 large
white eggs, which is a low clutch size relative to other Galliformes
(del Hoyo 1994, p. 336; Throp 1964, p. 130), and young are hatched in
July after an approximately 29-day incubation period (del Hoyo 1994, p.
361; Hilty and Brown 1986, p. 129; Throp 1964, p. 131). In captivity,
curassows are long-lived species (Todd et al. 2008, p.7). Throp (1964,
p. 132) recorded a blue-billed curassow still laying eggs at 20 years
of age. However, in the wild, one generation is considered to be 10
years (Cuervo 2002, p. 141).
Historical Range and Distribution
The blue-billed curassow historically occurred in northern
Colombia, from the base of the Sierra Nevada de Santa Marta (in the
northern Departments of Magdalena La Guijaira, and Cesar), west to the
Sin[uacute] valley (Department of C[oacute]rdoba), through the
R[iacute]o Magdalena (through the Departments (from south to north) of
Huila, Tolima, Caldas, Antioquia, Santander, Bolivar, Magdalena, and La
Guajira) (BLI 2007a, p. 1; Cuervo and Salaman 1999, p. 7; del Hoyo
1994, p. 361). The species' historic range encompassed an area of
approximately 106,700 square kilometers (km\2\) (41,197 square miles
(mi\2\)) (Cuervo 2002, p. 141). There were no confirmed observations of
blue-billed curassows between 1978 and 1997 (Brooks and Gonzalez-Garcia
2001, p. 183), and surveys conducted in 1998 failed to locate any males
(BLI 2007d, p. 3) (as detailed under Factor B, below), prompting
researchers to believe the species to be extinct in the wild (del Hoyo
1994, p. 361). However, a series of reported observations made in 1993
were confirmed in the year 2000 (Cuervo 2002, pp. 136-137).
Current Range and Distribution
The current range of the blue-billed curassow is estimated to be a
2,090-km\2\ (807-mi\2\) area (BLI 2007d, p. 2) of fragmented, disjunct,
and isolated tropical moist and humid lowlands and premontane forested
foothills in the R[iacute]o Magdalena and lower Cauca Valleys of the
Sierra Nevada de Santa Marta Mountains. The species may be found at
elevations up to 1,200 m (3,937 ft) (Collar et al. 1992, p. 154; Cuervo
and Salaman 1999, p. 7; del Hoyo 1994, p. 361; Donegan and Huertas
2005, p. 29; Salaman et al. 2001, p. 183), but it is more commonly
found below 600 m (del Hoyo 1994, p. 361). Little information is
available on the size of the forest fragments in which the species has
been observed. However, researchers conducting fieldwork in the
Department of Antioqu[iacute]a in 1999 and 2001 noted that the patch
sizes varied from 3 km\2\ (1.2 mi\2\) to 10 km\2\ (3.9 mi\2\) in size
(Ochoa-Quintero et al. 2005, p. 46).
In 1993, sightings were reported in the northern Departments of
C[oacute]rdoba (at La Terretera, near Alto Sin[uacute]) and
Bol[iacute]var (in the Serran[iacute]a de San Jacinto (San Jacinto
Mountains)) (Williams, in litt., as cited in BLI 2007d, p. 2).
Additional observations were made in the northernmost Department of La
Guajira in 2003 (in the Valle de San Salvador Valley) (Strewe and
Navarro 2003, p. 32). More recently, individuals have been observed in
the tropical forests of the central Departments of Antioqu[iacute]a (on
the slopes of the Serran[iacute]a de San Lucas and Bajo Cauca-
Nech[iacute] Regional Reserve area), the Departments of Santander and
Boyac[aacute] (on the slopes of the Serran[iacute]a de las Quinchas),
and in the southeastern Department of Cauca (in northeastern and lower
Cauca Valley) (BLI 2007d, p. 2; Cuervo 2002, pp. 135-138; Donegan and
Huertas 2005, p. 29; Ochoa-Quintero et al. 2005, p. 43-4; Urue[ntilde]a
et al. 2006, p. 42). Experts consider the most important refuges for
this species to be: (1) Serran[iacute]a de San Lucas
(Antioqu[iacute]a); (2) Paramillo National Park (Antioqu[iacute]a and
C[oacute]rdoba Departments); (3) Bajo Cauca-Nech[iacute] Regional
Reserve (Antioqu[iacute]a and C[oacute]rdoba Departments); and, (4)
Serran[iacute]a de las Quinchas Bird Reserve (Santander and
Boyac[aacute] Departments) (BLI 2007d, p. 3; Cuervo 2002, p. 139).
These refugia are discussed under Factor A, below.
Population Estimates
There is little information on population numbers for the various
reported locations of the species, and political instability within the
country makes it difficult to know the exact population size of this
species (Houston Zoo 2008). In 2002, Cuervo (2002, p. 141) considered
the Serran[iacute]a de las Quinchas and Serran[iacute]a de San Lucas
populations to be the stronghold of the species. However, surveys in
2003 led researchers to believe that Serran[iacute]a de las Quinchas
serves as the species' stronghold (BLI 2007d, pp. 2, 5-6). In 2003, the
population at Serran[iacute]a de las Quinchas (Boyac[aacute]
Department) location was estimated to be between 250 and 1,000 birds.
The only other information on the subpopulation level is a report from
Strewe and Navarro (2003, p. 32), based on field studies conducted
between 2000 and 2001, that hunting had nearly extirpated the blue-
billed curassow from a site in San Salvador (La Guijara) (Factor B).
Using the International Union for Conservation of Nature and
Natural Resources (IUCN) categories, the blue-billed curassow
population was estimated according to IUCN criteria to be more than
1,000 but fewer than 2,500 in 1994 (BLI 2007d, p. 2). In 2001, Brooks
and Gonzalez-Garcia (2001, p. 184) estimated the total population to be
much fewer than 2,000 individuals. In 2002, it was estimated that the
species had lost 88 percent of its habitat and half of its population
within the last three generations, or 30 years (Cuervo 2002, p. 141).
Local reports indicate an overall declining trend characterized by
recent rapid declines of all subpopulations (BLI 2007d, p. 1; Cuervo
2002, p. 138; Strahl et al. 1995, p.25). For further information on
population size, see Factor E, below.
Conservation Status
The blue-billed curassow is identified as a critically endangered
species under Colombian law (EcoLex 2002, p. 12). The species is
considered one of the most threatened cracids by the IUCN Cracid
Specialist Group. The species is categorized by the IUCN as `Critically
Endangered,' with habitat loss as a primary threat (BLI 2004b, p. 1;
Cuervo 2002, p. 141; del Hoyo 1994 p. 340; Strahl et al. 1995, pp. 4-5;
Urue[ntilde]a et al. 2006, pp. 41-2).
[[Page 32311]]
Summary of Factors Affecting the Blue-Billed Curassow
A. The Present or Threatened Destruction, Modification, or Curtailment
of the Habitat or Range
The blue-billed curassow prefers undisturbed, heterogeneous forests
and is rarely found in secondary or even slightly disturbed forests
(Cuervo and Salaman 1999, p. 7). The blue-billed curassow occur today
in several disjunct locations along a much-restricted part of its
historic distribution (Brooks and Gonzalez-Garcia 2001, p. 183; Collar
et al. 1992, pp. 61-62; Cuervo and Salaman 1999, p. 7). Researchers
note that the blue-billed curassow requires large territories, but
there is little information as to the actual size of the remaining
forest fragments (Cuervo and Salaman 1999, p. 7). In 1999 and 2001,
researchers conducting fieldwork in the Department of Antioqui[aacute]
noted that the patch sizes in which the species were observed or heard
varied from 3 km\2\ (1.2 mi\2\) to 10 km\2\ (3.9 mi\2\) in size (Ochoa-
Quintero et al. 2005, p. 46). Since the 1990s, the species has been
observed in the Departments of C[oacute]rdoba (at La Terretera, near
Alto Sin[uacute], 1993) and Bol[iacute]var (in the Serran[iacute]a de
San Jacinto, 1993) (Williams in litt., as cited in BLI 2007d, p. 2); La
Guajira (in the Valle de San Salvador Valley, 2003) (Strewe and Navarro
2003, p. 32); Antioqu[iacute]a (on the slopes of the Serran[iacute]a de
San Lucas and Bajo Cauca-Nech[iacute] Regional Reserve area, 1999 and
2001) (Ochoa-Quintero et al. 2005, p. 43-44); Santander and
Boyac[aacute] (on the slopes of the Serran[iacute]a de las Quinchas);
and Cauca (in northeastern and lower Cauca Valley) (BLI 2007d, p. 2;
Cuervo 2002, pp. 135-138; Donegan and Huertas 2005, p. 29;
Urue[ntilde]a et al. 2006, p. 42).
Deforestation rates and patterns: Primary forest habitats
throughout Colombia have undergone extensive deforestation. Vi[ntilde]a
et al. (2004, pp. 123-124) used satellite imagery to analyze
deforestation rates and patterns along the Colombian-Ecuadorian Border
(in the Departments of Putumayo and Sucumbios, respectively), finding
that, from 1973 to 1996, a total of 829 km\2\ (320 mi\2\) of tropical
forests within the study area were converted to other uses. This
corresponds to a nearly one-third total loss of primary forest habitat,
or a nearly 2 percent mean annual rate of deforestation within the
study area. During the study, the area within Colombia experienced a
three-times-larger annual rate of loss than that in Ecuador, due to
more intense pressures from human colonization and illegal crop
cultivation (Vi[ntilde]a et al. 2004, p. 124). The human population
within the area increased from approximately 50,000 to over 250,000
people during the 23-year period (Perz et al. 2005, pp. 26-28). A
similar phenomenon occurred in the R[iacute]o Magdalena Valley, which
coincides with the species' historic range as well as its disjunct and
restricted current range. The R[iacute]o Magdalena runs from south to
north approximately 1,540 km (950 mi) through western Colombia and
served as the main waterway connecting coffee (Coffea spp.) plantations
to the ports on the Western Colombian coast in the 1920s, when the
river was reportedly plagued by occasional droughts and erosion. In the
1930s, a railway was completed along much of the R[iacute]o Magdalena
Valley; this infrastructural improvement contributed to a growth in
several industries, including coffee (throughout the R[iacute]o
Magdalena valley), bananas (Musa spp.) (Magdalena Department), and oil
fields (Santander Department) (Ocampo and Botero 2000, pp. 76-78).
Deforestation and habitat loss throughout the lowland forests across
northern Colombia over the past 100 years contributed to the increasing
rarity of the species, and extirpated the species from a large portion
of its previous range by the 1980s (Brooks and Gonzalez-Garcia 2001, p.
183; Collar et al. 1992, pp. 61-62; Cuervo and Salaman 1999, p. 7).
In a similar study specific to the western Andean Amazon area of
Colombia (in the Departments of Arauca, Casemere, Meta, Vichada,
Amazonas, Caquet[aacute], Guainia, Guaviare, Putumayo, and
Vaup[eacute]s), deforestation between 1980 and 1990 totaled 52,320
km\2\ (20,201 mi\2\) (Perz et al. 2005, pp. 26-28). The most recent
reports indicate that habitat loss is ongoing and may be accelerating.
Between the years 1990 and 2005, Colombia lost a total of 7,920 km\2\
(3,058 mi\2\) of primary forest (Butler 2006a, pp. 1-3; Food and
Agriculture Organization of the United Nations (FAO) 2003a, p. 1).
Researchers have observed that road building and other infrastructure
improvements in previously remote forested areas have increased
accessibility and facilitated further habitat destruction,
exploitation, and human settlement ([Aacute]lvarez 2005, p. 2042;
C[aacute]rdenas and Rodr[iacute]guez Becerra 2004, pp. 125-130; Etter
et al. 2006, p. 1; Hunter 1996, p. 158-159; Vi[ntilde]a et al. 2004,
pp. 118-119). In Antioquia, cattle ranches are extensive in areas where
the blue-billed curassow occurs; cattle ranching is considered a less
labor-intensive land use, meaning that more people need to turn to
alternative sources of income generation, such as cultivation or
extractive industries (Melo and Ochoa 2004, as cited in Urue[ntilde]a
et al. 2006, p. 42). In Serran[iacute]a de las Quinchas, the economy is
based principally on timber extraction, agriculture, and cattle
ranching (Urue[ntilde]a and Quevedo unpubl. data 2004, as cited in
Urue[ntilde]a et al. 2006, p. 47). These activities contribute to
further habitat fragmentation and reduction. In terms of habitat
destruction, an influx of settlers displaced from the Departments of
Antioquia, Tolima, and Cundinamarca, due to violence and public
disorder in these Departments, are the principal threat to the
mountainous regions in these Departments (Urue[ntilde]a et al. 2006, p.
42).
The decline in blue-billed curassow population numbers (see
Population estimates, above) is inextricably linked to habitat loss.
The blue-billed curassow became increasingly rare during the 20th
Century, as much of the lower-elevation forests in their historic range
of the R[iacute]o Magdalena and R[iacute]o Cauca Valleys were
deforested, forcing the blue-billed curassow to move to higher
elevations (Cuervo and Salaman 1999, p. 8). By the 1980s, the species
had disappeared from a large portion of its previous range (Collar et
al. 1992, pp. 61-62), which historically encompassed approximately
106,700 km\2\ (41,197 mi\2\) (Cuervo 2002, p. 141). In 2002, it was
estimated that, within the three prior generations (30 years), the
species had lost 88 percent of its original habitat and that the
remaining suitable habitat had been reduced to 13,300 km\2\ (5135 m2)
(Cuervo 2002, p. 141). The current range of the blue-billed curassow is
estimated to be 2,090 km\2\ (807 mi\2\) (BLI 2007d, p.2) (see also
``Small Population Size,'' Factor E).
Deforestation and fragmentation caused by human encroachment are
ongoing throughout the blue-billed curassow's range, including:
Antioqu[iacute]a (on the slopes of the Serran[iacute]a de San Lucas and
Bajo Cauca-Nech[iacute] Regional Reserve area); Santander and
Boyac[aacute] Departments (on the slopes of the Serran[iacute]a de las
Quinchas); and in the southeastern Department of Cauca (in northeastern
and lower Cauca Valley), where timber extraction and mining continue
(Urue[ntilde]a et al. 2006, p. 42). Human activities that are
contributing to habitat loss include: forest clearing for subsistence
agriculture, cash crops (such as coffee), and grazing ([Aacute]lvarez
2005, p. 2042; BLI 2007d, p. 3; C[aacute]rdenas and Rodr[iacute]guez
Becerra 2004, p. 355; Oldham and Massey 2002, pp. 9-12; Urue[ntilde]a
et al. 2006, p. 42); habitat alteration, human population displacement,
and hunting as a result of armed conflict ([Aacute]lvarez 2001, p. 305;
[Aacute]lvarez 2003, pp. 51-52); habitat
[[Page 32312]]
destruction and alteration as a result of fire ([Aacute]lvarez 2005, p.
2041; Moreno et al. 2006, p. 1); habitat loss for dams and reservoir
development (Cuervo 2002, p. 139; Kreger 2005, pp.5-6); illicit crop
cultivation (such as the coca plant (Erythroxylum coca))
([Aacute]lvarez 2001, pp. 1086-1087; [Aacute]lvarez 2007, pp. 133-135;
C[aacute]rdenas and Rodr[iacute]guez Becerra 2004, p. 355; Oldham and
Massey 2002, pp. 9-12); gold mining activities (Cuervo 2002, p. 139);
habitat pollution due to oil development and distribution
([Aacute]lvarez 2005, p. 2041; C[aacute]rdenas and Rodr[iacute]guez
Becerra 2004, p. 355); and increased access and habitat destruction
resulting from road development (Cuervo 2002, pp. 139-140). Roads
create barriers to animal movements, expose animals to traffic hazards,
and increase human access into habitat, thus facilitating further
exploitation and habitat destruction (Hunter 1996, 158-159). Local
human populations have recently settled in forested areas that
previously provided habitat for blue-billed curassows. This human
settlement is accelerating habitat loss and fragmentation with only 5
percent of the species' restricted range now covered by forest (Brooks
and Gonzalez-Garcia 2001, pp. 183-184), and is leaving only fragmented,
disjunct, and isolated populations in the remaining four or five
patches of tropical humid and premontane forests ([Aacute]lvarez 2003,
p. 51; Brooks and Strahl 2000, pp. 14-15; Collar et al. 1994, pp. 61-
62; Cuervo and Salaman 1999, p. 7; Donegan and Huertas 2005, p. 29).
Illegal drugs and their eradication: The cultivation of illegal
crops (including coca) poses additional threats to the environment
beyond encouraging the destruction of montane forests (Balslev 1993, p.
3). Van Schoik and Schulberg (1993, p. 21) noted that coca crop
production destroys the soil quality by causing the soil to become more
acidic, which depletes the soil nutrients and ultimately impedes the
regrowth of secondary forests in abandoned fields. Although Colombia
continues to be the leading coca bush producer (United Nations Office
of Drugs and Crime (UNODC) et al. 2007, p. 7), since 2003, cocaine
cultivation has remained stable at about 800 km\2\ (309 mi\2\) of land
under cultivation (UNODC et al. 2007, p. 8). This stabilization of
production is partially attributed to alternative development projects
that were implemented between 1999 and 2004 to encourage pursuits other
than illegal crop cultivation (UNODC et al. 2007, p. 77). This is also
attributed to heightened eradication efforts. Between 2002 and 2004,
aerial spraying occurred over more than 1,300 km\2\ (502 mi\2\)
annually, peaking in 2004, when 1,360 km\2\ (525 mi\2\) of illicit
crops were sprayed (UNODC and the Government of Colombia (GOC) 2005, p.
11). In 2006, eradication efforts were undertaken on over 2,130 km\2\
(822 mi\2\) of land, which included sraying of 1,720 km\2\ (664 mi\2\)
and manual eradication on the remaining land. Eradication efforts
undertaken in 2006 occurred over an area 2.7 times greater than the net
cultivation area (UNODC et al. 2007, p. 8). Drug eradication efforts in
Colombia have further degraded and destroyed primary forest habitat by
using nonspecific aerial herbicides to destroy illegal crops
([Aacute]lvarez 2005, p. 2042; BLI 2007d, p. 3; C[aacute]rdenas and
Rodr[iacute]guez Becerra 2004, p. 355; Oldham and Massey 2002, pp. 9-
12). Herbicide spraying has introduced harmful chemicals into blue-
billed curassow habitat and has led to further destruction of the
habitat by forcing illicit growers to move to new, previously untouched
forested areas ([Aacute]lvarez 2002, pp. 1088-1093; [Aacute]lvarez
2005, p. 2042; [Aacute]lvarez 2007, pp. 133-143; BLI 2007d, p. 3;
C[aacute]rdenas and Rodr[iacute]guez Becerra 2004, p. 355; Oldham and
Massey 2002, pp. 9-12). Between 1998 and 2002, cultivation of illicit
crops increased by 21 percent each year, with a concomitant increase in
deforestation of formerly pristine areas of approximately 60 percent
([Aacute]lvarez 2002, pp. 1088-1093).
Effects of habitat fragmentation: A study conducted on the effects
of habitat fragmentation on Andean birds within western Colombia
determined two primary conditions that increased a species'
vulnerability to habitat fragmentation and susceptibility to local
extirpation and extinction: (1) species that were located at the upper
or lower limit of their altitudinal or geographical distribution (as is
the case for the blue-billed curassow, which formerly occupied the now-
cleared lower elevation forests and is relegated to isolated forest
fragments within its current range), and (2) species that were large
fruit-eating birds with limited distributions and narrow habitat
preferences (also traits of the blue-billed curassow) (Kattan and
[Aacute]lvarez-Lopez 1996, pp. 5-6). The study also determined that 31
percent of the historical bird populations in western Colombia had
become extinct or locally extirpated by 1990, largely as a result of
habitat fragmentation from deforestation and human encroachment (Kattan
and [Aacute]lvarez-Lopez 1996, p. 5; Kattan et al. 1994, p. 141). The
most direct physical consequence of habitat fragmentation is loss of
habitat heterogeneity; habitat heterogeneity is a characteristic
preferred by the blue-billed curassow (see Habitat and Life History,
above) (Kattan and [Aacute]lvarez-Lopez 1996, p. 6). Local reports
indicate an overall declining trend characterized by recent rapid
declines of all the populations of blue-billed curassows (BLI 2007d, p.
1; Cuervo 2002, p. 138; Strahl et al. 1995, p. 25). Moreover, the
ability of the blue-billed curassow to repopulate an isolated patch of
suitable habitat following decline or extirpation is highly unlikely
due to the species' small overall population size, its tendency to
avoid degraded habitats, and the large distances between the remaining
primary forest fragments in addition to the species' reticence to cross
large areas of open habitat (Cuervo and Salaman 1999, p. 7; Hanski
1998, pp. 45-46).
In addition to the direct detrimental effect of habitat loss, blue-
billed curassows and other cracids are susceptible to indirect effects
of habitat disturbance and fragmentation (Brooks and Strahl 2000, p.
10; Silva and Strahl 1991, p. 38). A study conducted in northwestern
Colombia suggests that habitat destruction and fragmentation may
increase a species' vulnerability to predation (Arango-V[eacute]lez and
Kattan 1997, pp. 140-142) (Factor C). Habitat fragmentation, in
combination with growing numbers of human settlements, has made the
species' habitat more accessible and more vulnerable to hunting (Factor
B) and predation (Factor C). Habitat loss also compounds the species'
decline in population numbers (estimated to be between 1,000 and 2,500
individuals) (BLI 2004b, p. 1) (see Factor E, Small population size).
Refugia: Several areas within the blue-billed curassow's current
range are designated as national parks or other types of preserves,
including Tayrona and Sierra Nevada de Santa Marta National Parks (both
in Antioqu[iacute]a Department) (Cuervo 2002, p. 140) and the Colorados
Sanctuary (Bol[iacute]var Department), which protects part of the
Serran[iacute]a de San Jacinto (BLI 2007d, pp. 2-3; Urue[ntilde]a et
al. 2006, p. 42). Experts consider the most important refuges for this
species, containing the largest remaining areas of suitable habitat, to
be in the following areas (arranged geographically, from north to
south): (1) Serran[iacute]a de San Lucas, (2) Paramillo National Park,
(3) Bajo Cauca-Nech[iacute] Regional Reserve, and (4) El Pauj[iacute]l
Bird Reserve (BLI 2007d, p. 3; Cuervo 2002, p. 139-140; Urue[ntilde]a
et al. 2006, p. 42), four of the five locations where the species has
been observed in the 21st Century (see Current Range, above). The
habitat within these refugia underserves
[[Page 32313]]
the needs of the species for various reasons (including past and
ongoing habitat destruction and incomplete habitat inclusion), as
enumerated below. In addition, inadequate regulatory mechanisms hamper
protection of the species and its habitat (Factor D).
(1) Serran[iacute]a de San Lucas (Antioqu[iacute]a) is not a
protected area, but is one of the largest remaining tracts of forest
that is the least disturbed (WWF 2001b, p. 1). Even so, only a few
isolated forest patches survive above 1,000 m (3,280 ft) in the
northern lowlands (Antioqui[aacute] Department) (Donegan and Salaman
1999, p. 4). Ongoing pressures on this habitat include human
encroachment for natural resources, colonization, ranching, logging,
and crop production, as well as pollution of the Magdelena and Cauca
Rivers (WWF 2001b, p. 3). In 1996, there was a gold rush that led to
deforestation for logging, settlements, conversion to agriculture, and
coca production (BLI 2007d, p 3). Using satellite imagery and
fieldwork, Cuervo (2002, p. 140) determined that deforestation on the
eastern slopes of the Serran[iacute]a de San Lucas was extensive
between 1995 and 1996. In 2005, highway construction was underway as
part of a national plan to connect the East Andes, the West Andes, and
the Pacific ports, including roadbuilding through the Serran[iacute]a
de San Lucas and adjacent lowlands ([Aacute]lvarez 2005, p. 2042).
Because the species prefers pristine habitat, this ongoing habitat
alteration negatively impacts the integrity of this location and the
survival of the species therein.
(2) The Paramillo National Park (Antioqu[iacute]a and
C[oacute]rdoba Departments), created in 1977, encompasses an area 4600
km\2\ (1776 mi\2\) in size and includes moist and cloud forest habitats
(Corantioquia 2008, p. 1). However, it only protects the upper
elevational limit of the habitat occupied by the species, where the
species is rarer (Cuervo 2002, p. 140). This Park is inhabited by an
indigenous community (Ember[aacute]), for whom the Park was created.
Farmers also inhabit the interior regions of the Park (BLI 2007a, p. 1-
2). The areas to the south of the Park have undergone intense habitat
disturbance from logging, drug crop production, and inundation from
flooding caused by the construction of the Urr[aacute] Dam (Cuervo
2002, p. 139). Deforestation has occurred throughout a large portion of
the Park's buffer zone as well as in the extreme southern reaches
within Park boundaries (Cuervo 2002, p. 140). Between 2003 and 2004,
cocaine cultivation within the Paramillo National Park went from
1.1km\2\ to 4.6 km\2\ (UNODC and GOC 2005, p. 45). The Urr[aacute] Dam
was constructed on the Sin[uacute] River between 1993 and 1998; the
Sin[uacute] River Valley was part of the blue-billed curassows'
historic range (BirdLife International (BLI) 2007a, p. 1; Cuervo and
Salaman 1999, p. 7; del Hoyo 1994, p. 361). The reservoir flooded the
area and led to displacement of human populations and other habitat
alterations, including fish kills caused by blocked spawning and
migratory routes (NGO Working Group on Export Development Canada 2003,
p.31).
(3) The Bajo Cauca-Nech[iacute] Regional Reserve (Antioqu[iacute]a
and C[oacute]rdoba Departments), created in 1999, is located within a
large tract (450 km\2\ (174 mi\2\)) of forested land at an elevation of
800 m (2,625 ft). Bajo Cauca is the second most populated region in the
Department of Antioquia. Logging is important in this region, and the
Reserve allows commercial exploitation of wood (Fundaci[oacute]n Viztaz
2007, p. 2). Surveys are scant in this area, which is believed to be
home to many species as yet unidentified by science (Cuervo 2002, p.
137; Donegan and Salaman 1999, p. 12). Although the Reserve provides
suitable habitat for the species, and the blue-billed curassow is
presumed to inhabit this area, it has not been confirmed within the
Reserve (BLI 2007d, p. 3).
(4) El Pauj[iacute]l Bird Reserve (Santander and Boyac[aacute]
Departments) is a private reserve established in Serran[iacute]a de las
Quinchas (WorldTwitch Colombia 2004, p.3). In the early 1990s, the
Serran[iacute]a de las Quinchas (Boyac[aacute] Department, central
Colombia) was considered one of the last remaining well-preserved cloud
forests and the largest tract of lowland wet forest in the region, with
up to 500 km\2\ (193 mi\2\) of forest remaining. Within a decade, the
forest had dwindled to 120 km\2\ (46 mi\2\) (WorldTwitch Colombia 2004,
p. 3). In 2002, the largest known subpopulation of blue-billed curassow
was located in the Serran[iacute]a de las Quinchas and became regarded
as the stronghold of the species (BLI 2007d, p. 2). El Pauj[iacute]l
Bird Reserve was created in 2004 specifically to protect the blue-
billed curassow and its habitat (BLI 2007b, p. 2). Comprising 10 km\2\
(3.9 mi\2\) of lowland tropical forest up to elevations of 700 m (2297
ft), the Reserve includes suitable habitat for the species. However,
collection of eggs and chicks are ongoing within the region (Cuervo
2002, p. 139; Urue[ntilde]a et al. 2006, p. 42) (Factor B), and there
are questions as to the effectiveness of this Reserve to protect the
species (Factor D).
Summary of Factor A
The blue-billed curassow prefers undisturbed habitat, and the
remaining small populations are limited to four or five small,
disjunct, and isolated areas in seven different Departments. Within the
past three generations, or 30 years, the species is estimated to have
lost 88 percent of its habitat and half of its population.
Deforestation and conversion of primary forests for human settlements
and agriculture has led to habitat fragmentation throughout the
species' range and to isolation of remaining populations. Habitat loss
and fragmentation were factors in the species' historical decline (over
the past 50 years) and caused localized extirpations, and continue to
be factors negatively affecting the blue-billed curassow in the wild.
Human encroachment into the species' preferred primary forest habitat
has resulted in habitat alteration and disturbance activities that have
caused declines in the blue-billed curassow population. Cultivation of
illegal drug crops, such as cocaine, leads to further deforestation and
alters soil compositions, hindering regeneration of abandoned fields.
In addition, drug eradication programs involving the aerial spraying of
non-specific herbicides lead to further environmental degradation and
destruction of primary forest habitat. Three of the four most important
refugia continue to undergo habitat destruction, and regulatory
mechanisms are inadequate to mitigate the primary threats to this
species (Factor D). A private refuge, the El Pauj[iacute]l Bird
Reserve, was formed to protect the blue-billed curassow and its
habitat, which includes a large amount of suitable habitat, but may be
lacking in its ability to adequately protect the species (Factors B and
D). Habitat fragmentation contributes to the species' vulnerability to
hunting (discussed under Factor B) and predation (discussed under
Factor C) by increasing human and predator access to the habitat. The
species' historic range, which encompassed approximately 106,700 km\2\
(41,197 mi\2\), has been reduced to 2,090 km\2\ (807 mi\2\). Experts
estimate that 88 percent of this habitat loss has occurred within the
last three generations, or 30 years. Habitat destruction and
fragmentation of the remaining primary forest habitat is expected to
continue, as human encroachment and associated activities continue
within the blue-billed curassow's range. Therefore, we find that the
present destruction, modification, and curtailment of habitat
[[Page 32314]]
are threats to the blue-billed curassow throughout all of its range.
B. Overutilization for Commercial, Recreational, Scientific, or
Educational Purposes
Blue-billed curassows are hunted by indigenous people and local
residents for subsistence, sport, trade, and entertainment (Brooks and
Gonzalez-Garcia 2001, p. 183; Brooks and Strahl 2000, p. 10; Cuervo and
Salaman 1999, p. 9; Throp 1964, p. 127; Urue[ntilde]a et al. 2006, p.
42). Cracids, including the blue-billed curassow, are considered
particularly vulnerable to hunting pressures and are among those
species most rapidly depleted by hunting (Redford 1992, p. 419).
Several factors contribute to the species' vulnerability to hunting and
collection: their large size, ease of location during the breeding
season, trusting nature, and low productivity (1-2 eggs) relative to
other Galliformes (del Hoyo 1994, p. 336). Cracids are also slow to
reproduce, with a replacement rate of at least 6 years (Silva and
Strahl 1991, p. 50), which makes it difficult for the species to
rebound from hunting pressures.
Hunting affects the blue-billed curassow in all life stages. In
1999, hunters in Antioqu[iacute]o (where the blue-billed curassow is
known on the slopes of the Serran[iacute]a de San Lucas and Bajo Cauca-
Nech[iacute] Regional Reserve area) reported killing as many as 20
blue-billed curassows within the prior 20 years (Donegan and Salaman
1999, p. 21). In 2004, it was reported that hunting had abated
somewhat, because productive hunting grounds had become too remote from
villages and because the communities have access to domestic meat (Melo
and Ochoa 2004, as cited in Urue[ntilde]a et al. 2006, p. 42). However,
both eggs and chicks continue to be collected in some areas (such as
Serran[iacute]a de las Quinchas, where El Pauj[iacute]l Reserve is
located) to be sold at local markets (Cuervo 2002, p. 139;
Urue[ntilde]a et al. 2006, p. 42), despite measures to protect the
species from collection (Factor D). In 1999, live trapped birds
(typically chicks) sold for up to US$100 (greater than the average
monthly income) (Donegan and Salaman 1999, p. 21). These birds are
either consumed or maintained as captive animals. The blue-billed
curassow, as well as other cracids (e.g., chachalacas (Ortalis spp.)
and guans (Penelope spp.)) serve as a major source of protein for
indigenous people and attract a great deal of ecotourism (Brooks and
Strahl 2000, p. 8). People colonizing forested areas capture juvenile
birds as pets and hold them in captivity in fenced yards or in cages
(Cuervo and Salaman 1999, p. 8; Donegan and Salaman 1999, p. 21).
Indigenous people also collect feathers and other body parts of
curassows for rituals, ornamentation, arrowheads, and for sale to
tourists (Silva and Strahl 1991, p. 38).
Most hunting occurs during the mating season, when males are more
easily located by their booming mating calls (Cuervo and Salaman 1999,
p. 9; del Hoyo 1994, p. 336), which can be heard from up to 500 m (0.31
mi) away (Ochoa-Quintero et al. 2005, pp. 42, 44). The direct take of
males leads to disequilibrium of sex ratios for this species, which
forms monogamous pairs (Cuervo and Salaman 1999, p. 9; Todd et al.
2008), and it also leads to the disruption of mating activities (Cuervo
and Salaman 1999, p. 9; del Hoyo 1994, p. 336). Researchers attribute
hunting pressure as the cause for the near extinction of the blue-
billed curassow population in the San Salvador Valley (Strewe and
Navarro 2003, p. 32). Researchers also attribute to hunting the absence
of blue-billed curassows from parts of its historical range where
suitable habitat (primary forest) still exists to hunting (Brooks and
Strahl 2000, p. 10). In 1998, for instance, no males were observed
during field surveys, prompting researchers to conclude that hunting
continued to be a serious risk to the species (BLI 2007d, p. 3).
Habitat fragmentation and concomitant human encroachment (Factor A)
have made the species' habitat more accessible and more vulnerable to
hunting. A study conducted in French Guiana provided a quantitative
estimate of the effect of hunting on a related cracid species, the
black curassow (Crax alector) (del Hoyo 1994, p. 336). The black
curassow has similar habitat requirements (undisturbed primary tropical
to subtropical humid forest at 0-1,400 m (0-4600 ft) elevation) as the
blue-billed curassow (BLI 2007e). The estimated population density of
black curassows in non-hunted areas was between 7 and 9 birds per 1
km\2\ (0.4 mi\2\); in areas with intermittent hunting, the numbers fell
to between 0.5 and 2.25 birds; and in areas where hunting was regular,
numbers fell to between 0.5 and 0.73 birds (del Hoyo 1994, p. 336). We
believe that the effects of hunting on the blue-billed curassow would
result in similar population reductions based on its similarity of
habitat requirements and life history traits.
In 1988, Colombia listed the blue-billed curassow in Appendix III
of the Convention on International Trade in Endangered Species of Wild
Fauna and Flora (CITES) (UNEP-WCMC 2008c). An Appendix-III listing
requires that: (1) the listing range country (in this case, Colombia)
must issue an export permit for all exports of the species; (2)
specimens for these exports must be legally obtained; (3) live
specimens must be transported such that risk of injury, damage, and
cruelty are minimized; (4) exports from any other range countries
require a certificate of origin; and (5) re-exports require a re-export
certificate issued by the country of re-export (UNEP-WCMC 2008a).
According to the World Conservation Monitoring Centre (WCMC), a total
of 12 live birds have been traded internationally since 1990 (UNEP-WCMC
2008e). This trade included imports of two individuals into the United
States and five birds into Mexico in the early 1990s. Therefore,
commercial international trade in wild specimens over the past 20 years
has not been extensive.
The remaining CITES-documented trade has consisted of exports of
captive-bred specimens from the United States to Colombia and Belgium.
The blue-billed curassow has been collected from the wild for use in
zoos and in captive-breeding programs, both domestically and abroad. A
small number of birds have been collected by the Cali Zoo and Santa Fe
de Medellin Zoo in Colombia (Cuervo 2002, p. 142), and small
collections are held in the United States, including the Houston Zoo
and San Diego Zoo, as well as in Japan and Mexico (Brooks and Strahl
2000, p. 15; Cuervo 2002, p. 142). The Cali and Houston Zoo collections
are being used for captive breeding, which we consider vital to
conserving and recovering this species (Factor E). International trade
for zoos and captive-breeding purposes does not contribute to the
endangerment of the species. We believe that this limited amount of
international trade, controlled via CITES, is not a threat to the
species.
Summary of Factor B
The blue-billed curassow is hunted and collected from the wild at
all life stages throughout its current range. Blue-billed curassow eggs
and chicks are collected for food and sale in local markets, or are
often captured and held in captivity as pets or as a future food
source. Hunting results in the direct removal of eggs, juveniles, and
adults from the population. Blue-billed curassows are slow to
reproduce, produce a low clutch size, and exhibit a poor replacement
rate (see Habitat and Life History). Hunting can destroy pair bonds and
remove potentially reproductive adults from the breeding
[[Page 32315]]
pool. The species is particularly vulnerable to hunting and collection
pressures due to the ease in locating this large bird during its
breeding season. The majority of hunting occurs during the mating
season, when males are heard calling for females, leading to
disproportionate hunting of males. Hunting disturbances during the
breeding season disrupt breeding activities, further compounding the
threats associated with hunting mortalities. There are continued
reports of hunting pressures on the species; these pressures have been
and continue to be compounded by ongoing human encroachment into
previously undisturbed forests (Factor A). Hunting and collection
negatively affect the global population of the blue-billed curassow,
due to its small population size and fragmented distribution. Hunting,
combined with habitat fragmentation (Factor A), increases the
possibility of local extirpation since the blue-billed curassow is
unlikely to re-occupy an area that has been depleted through hunting
because it avoids crossing large, open areas between habitat fragments
(see Factor E, Likelihood to Disperse). Therefore, we find that
hunting, collection, and associated disturbances are threats to the
blue-billed curassow.
C. Disease or Predation
Disease: We are unaware of information regarding disease or the
potential for significant disease outbreaks in the blue-billed
curassow. As a result, we do not consider disease to be a threat to the
species.
Predation: According to Delacour and Amadon (1973), predators of
cracids include snakes (suborder Serpentes), foxes (family Canidae),
wild cats (Felis silvestris), feral dogs (Canus lupus familiaris), and
raptors (order Falconiformes). Arango-V[eacute]lez and Kattan (1997,
pp. 137-143) studied nest predation rates on Andean birds within
fragmented forest habitats of northwestern Colombia. Although not
specific to the blue-billed curassow, the study focused on understory
nesting birds with similar nesting habits and in forest fragment sizes
similar to where the blue-billed curassow is currently found (Arango-
V[eacute]lez and Kattan 1997, p. 138). The study found that nest
predation by generalist predators is more prevalent in smaller,
isolated forest patches. However, in the study, increased predation in
smaller habitat fragments could not be solely attributed to the ``edge
effect,'' whereby smaller patch sizes facilitate predators' access and
ability to capture prey throughout the fragments. Rather, reduced
habitat patch sizes caused a shift from larger to smaller predators,
which tended to prey upon the eggs and juveniles of understory birds,
rendering ground-dwelling birds such as blue-billed curassows
particularly susceptible (Arango-V[eacute]lez and Kattan 1997, pp. 140-
142). Other studies concerning the effects of habitat fragmentation on
avian predation show similar results (Hoover et al. 1995, p. 151;
Keyser 2002, p. 186; Keyser et al. 1998, p. 991; Renjifo 1999, p. 1133;
Wilcove 1985, p. 1214). Gibbs (1991, p. 157) found that a larger
proportion of ground-nests and elevated nests were predated in patches
smaller than 1 km\2\ (0.39 mi\2\) and that ground-nesting birds were
predated more heavily than elevated-nesting birds. In addition to the
importance of patch size for influencing the level of predation, the
composition of the areas surrounding the patch is also important
(Arango-V[eacute]lez and Kattan 1997, p. 141). For instance, in lowland
Costa Rica, the edge effect (where predation is greater at the edge of
forest patches than in the interior of the patch) was greatest in
forest patches bordered by secondary growth than by pasture (Gibbs
1991, p. 157).
Summary of Factor C
Snakes, foxes, feral cats, feral dogs, and raptors are all
predators of cracids. Predation results in the direct removal of eggs,
juveniles, and adults from the population. Blue-billed curassows are
slow to reproduce, produce a low clutch size, and exhibit a poor
replacement rate (see Habitat and Life History). Predation can destroy
pair bonds and remove potentially reproductive adults from the breeding
pool. Studies on similar species in similar Andean habitats indicate
that vulnerability to predation by generalist predators increases with
increased habitat fragmentation and smaller patch sizes. Predation
exacerbates the genetic complications associated with the species'
small population size (Factor E). Because of the species' small
population size and inability to recolonize isolated habitat fragments
(Factor E), predation renders the species vulnerable to local
extirpation. Therefore, we find that predation, compounded by ongoing
habitat destruction (Factor A) and hunting (Factor B), is a threat to
the blue-billed curassow.
D. The Inadequacy of Existing Regulatory Mechanisms
Regulatory mechanisms may provide species-specific or habitat-
specific protections. An evaluation of the adequacy of regulatory
mechanisms within Colombia to mitigate or remove the threats to the
blue-billed curassow is provided below, beginning with species-specific
and followed by habitat-specific protection mechanisms.
The Colombian government has enacted and ratified numerous domestic
and international laws, decrees, and resolutions for managing and
conserving wildlife and flora (Matallana-T. 2005, p. 121). Colombian
Law No. 99 of 1993 (Creating the Ministry of the Environment and
Renewable Natural Resources and organizing the National Environmental
System (SINA)) sets out the principles governing environmental policy
in Colombia, and provides that the country's biodiversity be protected
and used primarily in a sustainable manner (EcoLex 1993, p. 2).
Resolution No. 584 of 2002 (Species that are endangered wildlife in the
national territory) provides a list of Colombian wildlife and flora
that are considered threatened. Threatened is defined as those species
whose natural populations are at risk of extinction, as their habitat,
range, or ecosystems that support them have been affected by either
natural causes or human actions. Threatened species are further
categorized as critically endangered, endangered, or vulnerable. A
critically endangered species (CR) is one that faces a very high
probability of extinction in the wild in the immediate future, based on
a drastic reduction of its natural populations and a severe
deterioration of its range; an endangered species (EN) is one that has
a high probability of extinction in the wild in the near future, based
on a declining trend of its natural populations and a deterioration of
its range; and a vulnerable species (VU) is one that is not in imminent
danger of extinction in the near future, but it could be if natural
population trends continue downward and deterioration of its range
continues (EcoLex 2002, p. 10).
The blue-billed curassow is considered a critically endangered
species under Colombian law pursuant to paragraph 23 of Article 5 of
Law No. 99, as outlined in Resolution No. 584 (EcoLex 2002, p. 12).
This status confers certain protections upon the species. Resolution
No. 849 of 1973 ([Laws governing] commercial hunting of sa[iacute]nos,
boas, anacondas and birds throughout the country) and Resolution No.
787of 1977 ([Laws governing] sport hunting of mammals, birds and
reptiles of wildlife), regulate and prohibit commercial and sport
hunting of all wild bird species, respectively, except those
specifically identified by the Ministry of the Environment or otherwise
permitted (EcoLex 1973, p.1; EcoLex 1977, p. 3). Because of its status
as a critically endangered species, the
[[Page 32316]]
Ministry of the Environment does not permit the blue-billed curassow to
be hunted commercially or for sport. Neither Resolution prohibits
subsistence hunting. As discussed under Factor B, commercial and sport
hunting are not threats to this species, but subsistence hunting
continues to threaten the species throughout its range, including
within protected areas. Thus, these Resolutions are ineffective at
reducing the existing threat of subsistence hunting to the blue-billed
curassow.
Additional efforts to protect the species from subsistence hunting
are inadequate. Within El Pauj[iacute]l Reserve, for instance, there
are penalties for shooting or trapping the species (BLI 2007d, p. 3).
However, as recently as 2006, it was reported that both chicks and eggs
continued to be collected in the Serran[iacute]a de las Quinchas
region, where the Reserve is located, for domestic use and for sale at
local markets (Cuervo 2002, p. 139; Urue[ntilde]a et al. 2006, p. 42)
(Factor B). Thus, private efforts to protect the species from hunting
appear to be inadequate within a region where national laws are
ineffective at protecting the species from such take.
The blue-billed curassow is listed in Appendix III of CITES (see
Factor B). CITES is an international treaty among 174 nations,
including Colombia (which became a Party in 1981) and the United States
(which became a Party in 1975) (UNEP-WCMC 2008a, p. 1). In the United
States, CITES is implemented through the U.S. Endangered Species Act
(Act). The Act designates the Secretary of the Interior as the
Scientific and Management Authorities to implement the treaty, with all
functions carried out by the Service. Under this treaty, countries work
together to ensure that international trade in animal and plant species
is not detrimental to the survival of wild populations, by regulating
the import, export, re-export, and introduction from the sea of CITES-
listed animal and plant species (USFWS 2008, p. 1). As discussed under
Factor B, we do not consider commercial international trade to be a
threat impacting the blue-billed curassow.
Colombia has numerous laws and regulations pertaining to forests
and forestry management, including: the Forestry Law of 1959 (Law 2 -
[On] forest economy [of the] nation and conservation [of] renewable
natural resources) (EcoLex 1959); the Forestry Code of 1974 (Decree
2,811 - National code of renewable natural resources and protection of
the environment) (Faolex 1974), and the forest plan of 1996 (Decree
1,791 - Forest Improvement Plan) (Faolex 1996). A new forest law was
developed and approved in 2006 (Law No. 1,021, General [Forestry] Law).
The new law seeks to: (1) further promote forest plantations and create