Endangered and Threatened Wildlife and Plants; Listing Foreign Bird Species in Peru and Bolivia as Endangered Throughout Their Range, 606-649 [E9-31102]
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Federal Register / Vol. 75, No. 2 / Tuesday, January 5, 2010 / Proposed Rules
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R9-IA-2009-0059]
[96100-1671-0000-B6]
[RIN 1018-AV77]
Endangered and Threatened Wildlife
and Plants; Listing Foreign Bird
Species in Peru and Bolivia as
Endangered Throughout Their Range
AGENCY:
Fish and Wildlife Service,
srobinson on DSKHWCL6B1PROD with PROPOSALS2
Interior.
ACTION: Proposed rule.
SUMMARY: We, the U.S. Fish and
Wildlife Service (Service), propose to
list the following six South American
bird species (collectively referred to as
‘‘species’’ for purposes of this proposed
rule) as endangered under the
Endangered Species Act of 1973, as
amended (Act) (16 U.S.C. 1531 et seq.):
ash-breasted tit-tyrant (Anairetes
´
alpinus), Junın grebe (Podiceps
´
taczanowskii), Junın rail (Laterallus
tuerosi), Peruvian plantcutter
(Phytotoma raimondii), royal cinclodes
(Cinclodes aricomae), and white-browed
tit-spinetail (Leptasthenura
xenothorax)—all native to Peru. The
ash-breasted tit-tyrant and royal
cinclodes are also native to Bolivia. 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
March 8, 2010. We must receive
requests for public hearings, in writing,
at the address shown in the FOR FURTHER
INFORMATION CONTACT section by
February 19, 2010.
ADDRESSES: You may submit comments
by one of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting
comments on Docket No. FWS-R9IA-2009-0059.
• U.S. mail or hand-delivery: Public
Comments Processing, Attn: FWSR9-IA-2009-0059; Division of Policy
and Directives Management; U.S.
Fish and Wildlife Service; 4401 N.
Fairfax Drive, Suite 222; Arlington,
VA 22203.
We will not accept comments by email or fax. 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).
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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), 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
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) Additional 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 such 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 at
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,
PO 00000
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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 a species to, remove a species from,
or reclassify a species on the Federal
Lists of Endangered and Threatened
Wildlife and Plants has presented
substantial information indicating that
the requested action may be warranted.
To the maximum extent practicable, we
make the finding within 90 days
following receipt of the petition and
publish our finding 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
(‘‘12–month finding’’) on whether the
requested action is warranted, not
warranted, or warranted but precluded
by higher priority listing actions.
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 review (ANOR) of
findings on resubmitted petitions for all
foreign species for which listings were
previously found to be warranted but
precluded.
Previous Federal Actions
On May 6, 1991, we received a
petition (the 1991 petition) from the
International Council for Bird
Preservation (ICBP) to add 53 foreign
bird species to the List of Endangered
and Threatened Wildlife, including the
six Peruvian bird species that are the
subject of this proposed rule. In
response to the 1991 petition, we
published a substantial 90–day finding
on December 16, 1991 (56 FR 65207), for
all 53 species and initiated 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 (which included 15
species from the 1991 petition). In that
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document, we announced our finding
that listing the remaining 38 species
from the 1991 petition, including the six
Peruvian bird species that are the
subject of this proposed rule, was
warranted but precluded by higher
priority listing actions. We made a
subsequent warranted–but-precluded
finding for all outstanding foreign
species from the 1991 petition,
including the six Peruvian bird species
that are the subject of this proposed
rule, as published in our ANOR on May
21, 2004 (69 FR 29354).
Per the Service’s listing priority
guidelines (September 21, 1983; 48 FR
43098), our 2007 ANOR identified the
listing priority numbers (LPNs) (ranging
from 1 to 12) for all outstanding foreign
species. The six Peruvian bird species
that are the subject of 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
actions. A listing priority of 2 indicates
that the subject species face imminent
threats of high magnitude. With the
exception of the listing priority ranking
of 1, which addresses monotypic genera
that face imminent threats of high
magnitude, categories 2 and 3 represent
the Service’s highest priorities.
On July 29, 2008 (73 FR 44062), we
published in the Federal Register a
notice announcing our annual petition
findings for foreign species. In that
notice, we announced listing to be
warranted for 30 foreign bird species,
including the six Peruvian bird species
which are the subject of this proposed
rule, and stated that we would
‘‘promptly publish proposals to list
these 30 taxa.’’ In selecting these six
species from the list of warranted-butprecluded species, we took into
consideration the magnitude and
immediacy of the threats to the species,
consistent with the Service’s listing
priority guidelines.
On September 8, 2008, the Service
received a 60–day notice of intent to sue
from the Center for Biological Diversity
(CBD) and Peter Galvin over violations
of section 4 of the Act for the Service’s
failure to promptly publish listing
proposals for the 30 ‘‘warranted’’
species identified in our 2008 ANOR.
Under a settlement agreement approved
by the U.S. District Court for the
Northern District of California on June
15, 2009, (CBD, et al. v. Salazar, 09-cv02578-CRB), the Service must submit to
the Federal Register proposed listing
rules for the ash-breasted tit-tyrant,
´
´
Junın grebe, Junın rail, Peruvian
plantcutter, royal cinclodes, and whitebrowed tit-spinetail by December 29,
2009.
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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. Listing actions may be
warranted based on any of the above
threat factors, singly or in combination.
Below is a species-by-species analysis
of the five factors. The species are
considered in alphabetical order,
beginning with the ash-breasted tit´
tyrant, followed by the Junın grebe,
´
Junın rail, Peruvian plantcutter, royal
cinclodes, and the white-browed titspinetail.
I. Ash-breasted tit-tyrant (Anairetes
alpinus)
Species Description
The ash-breasted tit-tyrant, locally
known as ‘‘torito pechicenizo,’’ is a
small New World tyrant flycatcher in
the Tyrannidae family that is native to
high-altitude woodlands of the Bolivian
and Peruvian Andes (BirdLife
International (BLI) 2000, p. 392; Collar
et al. 1992, p. 753; del Hoyo et al. 2004,
˚
pp. 170, 281; Fjeldsa and Krabbe 1990,
pp. 468-469; InfoNatura 2007, p. 1;
Supreme Decree No. 034-2004-AG 2004,
p. 276854). The sexes are similar, with
adults approximately 5 inches (in) (13
centimeters (cm)) in length, with dark
gray, inconspicuously black-streaked
upperparts (BLI 2009o, p. 1; del Hoyo et
al. 2004, p. 281). Two subspecies (see
Taxonomy) are distinguished by their
underbelly color, which is yellowishwhite in the nominate subspecies and
white in the other (BLI 2009o, p. 1) (see
Taxonomy). Juvenile plumage is duller
in appearance, but otherwise similar to
the adult coloration (del Hoyo et al.
2004, p. 281).
Taxonomy
When the species was first
taxonomically described by Carriker
(1933, pp. 27-29), it was placed in its
own genus, Yanacea; this decision was
soon questioned by Zimmer (1940, p.
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607
10). It was not until the 1960s that
Yanacea was merged into Anairetes (a
genus long-known as Spizitornis) by
Meyer de Schauensee (1966, p. 376).
Some contemporary researchers have
suggested retaining the species within
˚
Yanacea (Fjeldsa and Krabbe 1990, p.
468). Smith (1971, pp. 269, 275) and
Roy et al. (1999, p. 74) confirmed that
the ash-breasted tit tyrant is a valid
species based on its phylogenetic
placement and degree of genetic
divergence from other species of
Anairetes, and recent texts continue to
place it in Anairetes (e.g., del Hoyo et
al. 2004, p. 281). Therefore, we accept
the species as Anairetes alpinus, which
also follows the Integrated Taxonomic
Information System (ITIS 2009, p. 1).
Two subspecies are recognized,
including, A. alpinus alpinus (the
nominate subspecies) and A. alpinus
bolivianus. These subspecies occur in
two disjunct (widely separated) areas
(see Current Range) (BLI 2000, p. 392;
del Hoyo et al. 2004, p. 281; ITIS 2009,
p. 1) and are distinguished by the color
of their underbellies (see Taxonomy)
(BLI 2009o, p. 1).
Habitat and Life History
The ash-breasted tit-tyrant is
restricted to semihumid Polylepis or
Polylepis - Gynoxys woodlands, where
the species is found at elevations
between 12,139 and 15,092 feet (ft)
(3,700 and 4,600 meters (m)) above sea
level (BLI 2000, p. 392; Collar et al.
1992, p. 753; del Hoyo et al. 2004, p.
˚
281; Fjeldsa and Krabbe 1990, pp. 468469; InfoNatura 2007, p. 1). The genus
Polylepis (no English common name;
˜
locally referred to as ‘‘queuna’’) (Aucca
and Ramsay 2005, p. 1), in the Rosaceae
family, comprises approximately 20
species of evergreen bushes and trees
(De la Via 2004, p. 10; Kessler 1998, p.
1; Kessler and Schmidt-Lebuhn 2006,
pp. 1-2), 19 of which occur in Peru
(Chutas et al. 2008, p. 3). In Bolivia, the
ash-breasted tit-tyrant is associated only
with P. pepei forests, but the bird is
found among a greater variety of
Polylepis species in Peru (Chutas et al.
´
2008, p. 16; I. Gomez, National Museum
of National History-Ornithology
Section-Bolivian Fauna Collection, La
Paz, Bolivia, e-mail to Division of
Scientific Authority, in litt. December 4,
2007, p. 1). On average, Polylepis
species are 10-33 ft (3-10 m) tall, but
may grow to a height of 118 ft (36 m)
(Purcell et al. 2004, p. 455).
Polylepis woodlands occur as dense
forests, as open-canopied stands with
more arid understories, or as shrubland
with scattered trees (De la Via 2004, pp.
˚
10-11; Fjeldsa and Kessler 1996, as cited
˚
in Fjeldsa 2002a, p. 113; Lloyd and
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Marsden in press, as cited in Lloyd
2008, p. 532). Ash-breasted tit-tyrants
˚
prefer dense Polylepis forests (Fjeldsa
2002a, p. 114; Smith 1971, p. 269),
which often include a mixture of
Gynoxys trees (no common name), in
the Asteraceae family (De la Via 2004,
pp. 10; International Plant Names Index
(IPNI) 2009, p. 1). Dense Polylepis
woodlands are characterized by mossor vine-laden vegetation, with a shaded
understory and a rich diversity of
insects, making good feeding grounds
for insectivorous birds (De la Via 2004,
p. 10), such as the ash-breasted tit-tyrant
(BLI 2009o, p. 1; Lloyd 2008, p. 535).
There is little information about the
ecology and breeding behavior of the
ash-breasted tit-tyrant. The species’
territory ranges from 2.5–5 acres (ac) (1–
2 hectares (ha)) (BLI 2009o, p. 1). The
breeding season appears to occur during
late dry season (Collar et al. 1992, p.
754)—November and December (BLI
2009o, p. 1). Juveniles have been
observed in March and July (Collar et al.
1992, p. 754; del Hoyo et al. 2004, p.
281). Although species-specific
information is not available, tit-tyrant
nests are generally finely woven, open
˚
cups, built in a bush (Fjeldsa and
Krabbe 1990, p. 468). The species may
share in rearing responsibilities, as pairs
of ash-breasted tit-tyrants have been
observed feeding young (BLI 2009o, p.
1; Collar et al. 1992, p. 754).
The ash-breasted tit-tyrant forages
alone, in family groups, and sometimes
in mixed-species flocks. The bird takes
short flights, either hovering or perching
to consume invertebrates near the tops
and outer edges of Polylepis shrubs and
trees (BLI 2009o, p. 1; del Hoyo et al.
2004, p. 281; Engblom et al. 2002, p. 58;
˚
Fjeldsa and Krabbe 1990, p. 468; Lloyd
2008, p. 535). In winter, when
invertebrate populations diminish, tit˚
tyrants may also forage on seeds (Fjeldsa
and Krabbe 1990, p. 468).
burning and grazing, which have
prevented regeneration of the
woodlands and resulted in the
fragmented habitat distribution seen
˚
today (Fjeldsa and Kessler 1996, Kessler
1995a, Kessler 1995b, and L#gaard
˚
1992, as cited in Fjeldsa 2002a, p. 112;
Herzog et al. 2002, p. 94; Kessler 2002,
pp. 97-101; Kessler and Herzog 1998,
˚
pp. 50-51). Modeling studies by Fjeldsa
(2002a, p. 116) indicate that this habitat
reduction was accompanied by a loss in
species richness. It is estimated that
only 2-3 and 10 percent of the original
forest cover still remain in Peru and
˚
Bolivia, respectively (Fjeldsa and
˚
Kessler 1996, as cited in Fjeldsa 2002a,
p. 113). Of this amount, only 1 percent
of the remaining Polylepis woodlands
are found in humid areas, where denser
˚
stands occur (Fjeldsa and Kessler 1996,
˚
as cited in Fjeldsa 2002a, p. 113) and
which are preferred by the ash-breasted
˚
tit-tyrant (BLI 2009o, p. 1; Fjeldsa
2002a, p. 114; Lloyd 2008, p. 535; Smith
1971, p. 269) (see Factor A).
Current Range and Distribution
The current range of the ash-breasted
tit-tyrant is estimated to be 4,595 square
miles (mi2) (11,900 square kilometers
(km2)) (BLI 2009o, p. 1). However,
BirdLife International (2000, pp. 22, 27)
defines a species’ ‘‘Range’’ as the
‘‘Extent of Occurrence,’’ which is ‘‘the
area contained within the shortest
continuous imaginary boundary which
can be drawn to encompass all the
known, inferred, or projected sites of
present occurrence of a species,
excluding cases of vagrancy.’’ Given that
the species is known to occur in two
disjunct locations, this range estimate,
therefore, includes a large area of habitat
where the species is not known to
occur.
The species is restricted to patches of
high-elevation semihumid Polylepis or
Polylepis - Gynoxys woodlands of Peru
and Bolivia, where ash-breasted titHistorical Range and Distribution
tyrant is found only at 12,139–15,092 ft
The ash-breasted tit-tyrant may once
(3,700–4,600 m) (BLI 2000, p. 392;
have been well-distributed throughout
Collar et al. 1992, p. 753; del Hoyo et
previously dense and contiguous
˚
al. 2004, pp. 170, 281; Fjeldsa and
Polylepis high-Andes woodlands of Peru Krabbe 1990, pp. 468-469; InfoNatura
and Bolivia. Researchers believe that
2007, p. 1). The ash-breasted tit-tyrant is
these woodlands were historically
known only in two disjunct areas: one
contiguous with lower-elevation
location in west-central Peru and
cloudforests and widespread above
another ranging from southern Peru into
9,843 ft (3,000 m) (Collar et al. 1992, p.
northern Bolivia (BLI 2000, p. 392; del
˚
753; Fjeldsa 2002a, pp. 111-112, 115;
Hoyo et al. 2004, p. 281; ITIS 2009, p.
Herzog et al. 2002, p. 94; Kessler 2002,
1).
In west-central Peru, the northern
pp. 97-101). Today, Polylepis
subspecies (A. alpinus alpinus) occurs
woodlands are found only at elevations
of 11,483 to 16,404 ft (3,500 to 5,000 m) in the Cordilleras Central and
˚
(Fjeldsa 1992, p. 10). Researchers
Occidental (in the Peruvian
consider the reduction in Polylepis
Administrative Regions of Ancash,
´
forest habitat to be the result of
Huanuco, La Libertad, and Lima) (BLI
historical human activities, including
2007, p. 1; BLI 2009g, p. 1; BLI 2009i,
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p. 1; BLI 2009l, p. 1; BLI 2009o, p. 1;
Collar et al. 1992, p. 753; del Hoyo et
al. 2004, p. 281). Until 1992, the taxon
in this locality was highly localized and
known only in Ancash Region (Collar et
al. 1992, p. 753). The species was
´
subsequently reported in Huanuco
Region, in 2003 (BLI 2007, p. 5; BLI
2009i, p. 1); La Libertad Region, in 2004
(del Hoyo et al. 2004, p. 281); and Lima
´
Region and again in Huanuco Region, in
2007 (BLI 2007, pp. 1, 5). Also in 2007,
the ash-breasted tit-tyrant was also
observed in a new locality in Ancash
Region, Corredor Conchucos (Chutas
2007, pp. 4, 8), where a Polylepis
reforestation project is under way to
connect two protected areas where ashbreasted tit-tyrants were already known
´
to occur, Parque Nacional Huascaran
and Zona Reservada de la Cordillera
Huayhuash (Antamina Mine 2006, p. 5;
MacLennan 2009, p. 1) (see Factor A).
The second location spans the
Peruvian-Bolivian border—in the
Peruvian Administrative Regions of
´
Apurımac, Cusco, Puno, and Arequipa
(from north to south) and in the
Bolivian Department of La Paz. Here,
the southern subspecies (A. alpinus
bolivianus) occurs in Cordillera Oriental
´
(Apurımac and Cusco), Cordilleras
Vilcanota and Vilcabamba (Cusco), and
Cordillera de Carabaya (Puno)—in
Peru—and ranges into Bolivia, where it
is found in the Cordillera Real and the
Cordillera Apolobamba (La Paz) (BLI
2000, p. 392; BLI 2009a, p. 1; BLI 2009b,
p. 1; BLI 2009c, p. 1; BLI 2009d, p. 1;
BLI 2009e, p. 1; BLI 2009f, p. 1; BLI
2009k, p. 1; BLI 2009m, p. 1; BLI 2009n,
p. 1; BLI 2009o, p. 5; Chutas 2007, p. 8;
Collar et al. 1992, p. 753; del Hoyo et
˚
al. 2004, p. 281; Fjeldsa and Krabbe
1990, pp. 468-469; InfoNatura 2007, p.
1). The ash-breasted tit-tyrant was only
recently (in 2008) reported in Arequipa
Region, Peru (BLI 2009j, p. 1).
The ash-breasted tit-tyrant is highly
localized (Collar et al. 1992, p. 753) and
has been described as ‘‘very rare and
local, with usually only 1–2 pairs per
˚
occupied woodland’’ (Fjeldsa and
Krabbe 1990, p. 469). It exists at such
low densities in some places that it goes
undetected (Collar et al. 1992, p. 753).
The species appears to be unable to
persist in forest remnants smaller than
2.5 ac (1 ha) (BLI 2009o, p. 1).
Population Estimates
Population information is presented
first on the range country level and then
in terms of a global population estimate.
The range country estimates begin with
Peru, where the majority of the
population resides.
Local population estimate, Peru:
Chutas (2007, p. 8) surveyed five
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disjunct Polylepis forest patches in Peru
and estimated that 461 ash-breasted tittyrants were located there. This
included 30 birds in Corredor
Conchucos (Ancash Region); 181 birds
and 33 birds in Cordilleras Vilcanota
and Vilcabamba, respectively (Cusco
Region); 22 birds in Cordillera de
Carabaya (Puno Region); and 195 birds
in a study site called ‘‘Cordillera del
´
´
Apurımac’’ (Apurımac Region) (Chutas
2007, pp. 4, 8), referring to an area
within the Runtacocha highlands. Other
research in the Runtacocha highlands
has indicated that the ash-breasted tittyrant is ‘‘relatively common’’ there (BLI
2007, p. 1; BLI 2009o, p. 1), with an
estimated 100 pairs of birds found in
˚
approximately 40 forest patches (Fjeldsa
in litt. 1990, as cited in Collar et al.
1992, p. 753). ‘‘Small numbers’’ of birds
are reported in La Libertad Region (del
Hoyo et al. 2004, p. 281). There are no
population estimates within Arequipa,
´
Huanuco, or Lima Regions, where the
ash-breasted tit-tyrant is also reported to
occur (BLI 2009g, p. 1; BLI 2009i, p. 1;
BLI 2009j, p. 1; BLI 2009o, p. 1).
Local population estimate, Bolivia:
Although BirdLife International reports
an estimated population size of 150–300
ash-breasted tit-tyrants in Bolivia
´
(Gomez in litt., 2003 and 2007, as cited
in BLI 2009o, p. 1), recent surveys
indicate that the estimate is smaller.
´
Over a six-year period, Gomez (in litt.
2007, p. 1) conducted intensive searches
throughout 80 percent of the suitable
habitat in Bolivia in the Cordillera Real
and the Cordillera Apolobamba (La Paz
Department), using song playback and
point census, to detect the presence of
the ash-breasted tit-tyrant. From this
work, researchers inferred or observed
the presence of 2–10 individuals in each
of four forest patches and estimated that
approximately 180 ash-breasted tittyrants occur in Bolivia.
Global population estimate: BirdLife
International, a global organization that
consults with and assimilates
information from species experts,
categorizes the ash-breasted tit-tyrant as
having a population size between 250
and 999 individuals, with an estimated
actual population size to be in the midto upper-hundreds (BLI 2000, p. 392;
BLI 2007, p. 1; BLI 2009o, p. 1).
Combining the estimated number of ashbreasted tit-tyrants in Peru and Bolivia,
the total population consists of at least
641 individuals (Chutas 2007, pp. 4, 8;
´
Gomez in litt. 2007, p. 1), consistent
with the BirdLife International category
of 250–999 individuals.
However, the total population size,
which includes immature individuals,
is not an accurate reflection of the
species’ effective population size (the
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number of breeding individuals that
contribute to the next generation)
´
(Shaffer 1981, pp. 132-133; Soule 1980,
pp. 160-162). Because the ash-breasted
tit-tyrant exists as two subspecies (BLI
2000, p. 392; BLI 2009a, p. 1; BLI 2009b,
p. 1; BLI 2009c, p. 1; BLI 2009d, p. 1;
BLI 2009e, p. 1; BLI 2009f, p. 1; BLI
2009k, p. 1; BLI 2009m, p. 1; BLI 2009n,
p. 1; BLI 2009o, p. 5; Chutas 2007, p. 8;
Collar et al. 1992, p. 753; del Hoyo et
˚
al. 2004, p. 281; Fjeldsa and Krabbe
1990, pp. 468-469; InfoNatura 2007, p.
1; ITIS 2009, p. 1), it is reasonable to
conclude that there is little or no gene
flow between the two subspecies and
that the species does not breed as a
single population. Therefore, even if all
641 individuals were mature, they
would not breed as a single population,
such that the species’ effective
population size is less than 641.
There are also constraints to
determining the effective population
size on a subspecies level. According to
International Union for Conservation of
Nature (IUCN) criteria, it is estimated
that there are no more than 250 mature
individuals in any single subpopulation
of the ash-breasted tit-tyrant (IUCN
2001, pp. 8-12). However, the
parameters of a subpopulation are not
provided in existing research. For
instance, while ash-breasted tit-tyrants
occupy territories of 2.5–5 ac (1–2 ha)
(BLI 2009o, p. 1), there is no
information as to the taxon’s ability or
tendency to travel between territories or
forest patches. Research on Bolivian
localities indicates that gene flow occurs
between some subpopulations, but not
´
all (Gomez 2005, p. 86). In Bolivia,
where only 1 subspecies occurs, the
birds are distributed in 2
metapopulations, with at least 5
subpopulations in one location and 14
´
subpopulations in the other (Gomez
2005, p. 86). Peruvian population
estimates are incomplete, with no
estimates for the ash-breasted tit-tyrants
´
occurring in Arequipa, Huanuco, La
Libertad or Lima (BLI 2009g, p. 1; BLI
2009i, p. 1; BLI 2009j, p. 1; BLI 2009o,
p. 1; del Hoyo et al. 2004, p. 281).
Therefore, we can conclude that gene
flow occurs at the subspecies level, but
there is not sufficient information to
determine the extent to which
subpopulations interbreed.
The species has experienced a
population decline of between 10 and
19 percent in the past 10 years, and this
rate of decline is predicted to continue
(BLI 2009o, pp. 1, 4). The population is
considered to be declining in close
association with continued habitat loss
and degradation (see Factors A and E)
(BLI 2007, pp. 1, 4; BLI 2009o, p. 5).
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609
Conservation Status
The ash-breasted tit-tyrant is
considered ‘‘endangered’’ by the
Peruvian Government under Supreme
Decree No. 034-2004-AG (2004, p.
276855). The IUCN considers the ashbreasted tit-tyrant to be ‘‘Endangered’’
because it has a very small population
that is undergoing continued decline in
the number of mature individuals and is
confined to a habitat that is severely
fragmented and is also undergoing a
continuing decline in extent, area, and
quality (BLI 2008, p. 1; BLI 2009o, p. 4;
IUCN 2001, pp. 8-12). The ash-breasted
tit-tyrant occurs within the following
Peruvian protected areas: Parque
´
Nacional Huascaran, in Ancash, and
´
Santuario Historico Machu Picchu, in
Cusco, and Zona Reservada de la
Cordillera Huayhuash, spanning
´
Ancash, Huanuco, and Lima (BLI 2009i,
p. 1; BLI 2009l, p. 1; BLI 2009n, p. 1;
Chutas et al. 2008, p. 16). In La Paz
Department, Bolivia, the species is
´
found in Parque Nacional y area Natural
de Manejo Integrado Madidi, Parque
´
Nacional y area Natural de Manejo
Integrado Cotapata, and the co-located
protected areas of Reserva Nacional de
´
Fauna de Apolobamba, area Natural de
Manejo Integrado de Apolobamba, and
Reserva de la Biosfera de Apolobamba
(Auza and Hennessey 2005, p. 81; BLI
2009a, p. 1; BLI 2009b, p. 1; BLI 2009c,
p. 1; BLI 2009e, p. 1; BLI 2009i, p. 1;
Chutas et al. 2008, p. 16).
Summary of Factors Affecting the Ashbreasted Tit-tyrant
A. The Present or Threatened
Destruction, Modification, or
Curtailment of the Species’ Habitat or
Range
The ash-breasted tit-tyrant is
dependent upon high-elevation
semihumid Polylepis or Polylepis Gynoxys woodlands (BLI 2000, p. 392;
Collar et al. 1992, p. 753; del Hoyo et
˚
al. 2004, pp. 281; Fjeldsa and Krabbe
1990, pp. 468-469; InfoNatura 2007, p.
1). Researchers believe that this habitat
was historically contiguous with lowerelevation cloudforests and widespread
above 9,843 ft (3,000 m) (Collar et al.
˚
1992, p. 753; Fjeldsa 2002a, pp. 111,
115), but Polylepis woodlands occur
today only between 11,483–16,404 ft
˚
(3,500–5,000 m) (Fjeldsa 1992, p. 10).
As described above (see Habitat and Life
History), the species prefers dense
˚
woodlands (Fjeldsa 2002a, p. 114; Smith
1971, p. 269), where the best foraging
habitat occurs (De la Via 2004, p. 10),
and ash-breasted tit-tyrant occurs at
altitudes of 12,139–15,092 ft (3,700–
4,600 m) (BLI 2000, p. 392; Collar et al.
1992, p. 753; del Hoyo et al. 2004, pp.
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˚
170, 281; Fjeldsa and Krabbe 1990, pp.
468-469; InfoNatura 2007, p. 1).
High-Andean Polylepis woodlands are
considered by experts to be the most
threatened habitat in Peru and Bolivia
(Purcell et al. 2004, p. 457), throughout
the Andean region (BLI 2009a, p. 2), and
one of the most threatened woodland
ecosystems in the world (Renison et al.
2005, as cited in Lloyd 2009, p. 10). The
IUCN has listed several Polylepis
species as ‘‘Vulnerable,’’ including two
species that occur within the ashbreasted tit-tyrant’s range, Polylepis
incana and P. pepei (WCMC 1998a, p.
1; WCMC 1998b, p. 1). Peruvian and
Bolivian Polylepis woodlands today are
highly fragmented. In the late 1990s,
˚
Fjeldsa and Kessler (1996, as cited in
˚
Fjeldsa 2002a, p. 113) conducted
comprehensive ground surveys and
analyzed maps and satellite images of
the area. They estimated that the current
range of Polylepis woodlands had been
reduced from historical levels by 97–
98% in Peru and 90 percent in Bolivia.
Contemporary Polylepis woodlands are
dispersed and sparse, covering an
estimated area of 386 mi2 (1,000 km2)
and 1,931 mi2 (5,000 km2) in Peru and
˚
Bolivia, respectively (Fjeldsa and
˚
Kessler 1996, as cited in Fjeldsa 2002a,
p. 113). Of the remaining Polylepis
woodlands, only 1 percent are found in
humid areas, where denser Polylepis
˚
forests tend to occur (Fjeldsa and
˚
Kessler 1996, as cited in Fjeldsa 2002a,
p. 113). Dense habitat is preferred by the
ash-breasted tit-tyrant (BLI 2009o, p. 1;
˚
Fjeldsa 2002a, p. 114; Lloyd 2008, p.
535; Smith 1971, p. 269).
Habitat loss, conversion, and
degradation throughout the ash-breasted
tit-tyrant’s range have been and
continue to occur as a result of ongoing
human activity, including (1)
Clearcutting and burning; (2) extractive
activities; (3) human encroachment; and
(4) unpredictable climate fluctuations
that exacerbate the effects of habitat
fragmentation. Clearcutting and burning
are among the most destructive
activities, and are a leading cause for
Polylepis habitat loss (WCMC 1998a, p.
1; WCMC 1998b, p. 1). Forested areas
are cleared for agriculture and to create
pastureland for cattle, sheep, and
camels (BLI 2009a, p. 2; BLI 2009c, pp.
1-2; BLI 2009d, pp. 1-2; BLI 2009e, pp.
1, 5; BLI 2009h, p. 1; BLI 2009m, p. 1;
BLI 2009n, p. 4). Grazing lands situated
amongst remaining forest patches are
regularly burned in order to maintain
the grassland vegetation (locally known
as, ‘‘chaqueo’’). Regular burning
prevents regeneration of native forests
and is considered the key factor limiting
the distribution of Polylepis forests (BLI
˚
2009f, p. 1; BLI 2009n, p. 4; Fjeldsa
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2002b, p. 8; WCMC 1998a, p. 1; WCMC
1998b, p. 1). In some areas, the burns
escape control, causing further habitat
destruction (BLI 2009a, p. 2; BLI 2009e,
pp. 1, 5). Burning and clearcutting occur
throughout the ash-breasted tit-tyrant’s
range, including in Ancash (BLI 2009h,
´
p. 1), Apurımac (BLI 2009m, p. 1), and
Cusco (BLI 2009n, p. 4), in Peru; and La
Paz, Bolivia (BLI 2009a, p. 2; BLI 2009c,
pp. 1-2; BLI 2009d, pp. 1-2; BLI 2009e,
pp. 1, 5). These activities are also
ongoing within protected areas,
´
including Parque Nacional Huascaran,
´
Santuario Historico Machu Picchu, and
Zona Reservada de la Cordillera
Huayhuash (Barrio 2005, p. 564; BLI
2009l, p. 4; BLI 2009n, p. 2) (see Factor
D).
As a result of the intensity of burning
and grazing, Polylepis species are
restricted to areas where fires cannot
spread, and where cattle and sheep do
not normally roam—in stream ravines
and on boulders, rock ledges, and sandy
˚
˚
ridges (Fjeldsa 2002a, p. 112; Fjeldsa
2002b, p. 8). Grazing and trampling by
domesticated animals further limit
˚
forest regeneration (Fjeldsa 2002a, p.
120) and contribute to the degradation
of remaining forest patches. Sheep and
cattle have solid, sharp hooves that
churn up the earth, damaging vegetation
and triggering erosion (Engblom et al.
2002, p. 56; Purcell et al. 2004, p. 458).
The loss of nutrient-rich soils leads to
habitat degradation, which reduces the
ability of the habitat to support dense
˚
stands of Polylepis woodlands (Fjeldsa
2002b, p. 8; Jameson and Ramsay 2007,
p. 42; Purcell et al. 2004, p. 458).
Ash-breasted tit-tyrant habitat is also
subject to conversion, degradation, or
destruction caused by extractive
activities, such as firewood collection,
timber harvest, and mining. Cutting
wood for fuel has a consistent and
ongoing impact throughout the species’
range (BLI 2009a, p. 2; BLI 2009b, pp.
1-2; BLI 2009c, pp. 1-2; BLI 2009d, pp.
1-2; BLI 2009f, p. 1; BLI 2009l, p. 1;
WCMC 1998a, p. 1). The high-altitude
zones where Polylepis occurs have long
been inhabited by subsistence farmers,
who rely on Polylepis wood for
firewood and charcoal production
(Aucca and Ramsay 2005, p. 287). Many
locals manage woodlands for firewood
extraction (Engblom et al. 2002, p. 56),
and community-based Polylepis
conservation programs fostered by the
Peruvian nongovernmental organization
´
Asociacion Ecosistemas Andinos
(ECOAN) have been under way in Peru
and Bolivia since 2004, encompassing
Cordilleras Vilcanota and Vilcabamba
(Cusco Region), highlands of the
´
Apurımac Region (Aucca and Ramsey
2005, p. 287; ECOAN no date (n.d.), p.
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1; Lloyd 2009, p. 10), and in the Ancash
Region (MacLennan 2009, p. 2). Known
as the ‘‘Vilcanota Project’’ or ECOAN
Projects (Aucca and Ramsey 2005, p.
287; ECOAN n.d., p. 1), local
communities enter into and enforce
management agreements aimed at the
primary causes for Polylepis
deforestation: burning, grazing, and
wood-cutting. These projects foster
local, sustainable use of resources
(Aucca and Ramsay 2005, p. 287;
ECOAN n.d., p. 1; Engblom et al. 2002,
p. 56), such as the use of more fuelefficient wood-burning stoves that
require half the amount of wood fuel
(MacLennan 2009, p. 2) (see the Factor
A analyses for royal cinclodes and
white-browed tit-spinetail for additional
examples).
Polylepis wood is also harvested for
local commercial use, including within
protected areas (BLI 2009a, p. 2; WCMC
1998a, p. 1) (Factor D). At one site, near
´
Abra Malaga (Cusco Region), wood is
harvested for sale to local hotels in the
towns of Urubamba and Ollantaytambo
to support tourism activity (Engblom
2000, p. 1). Engblom (2000, p. 1)
documented felling for firewood at this
site in Cusco over a 2–day period that
significantly reduced the size and
quality of the forest patch. Purcell et al.
(2004, p. 458) noted a positive
correlation between habitat destruction
and increased demand for (and the
concomitant rise in the price of) fuel.
Polylepis is also harvested for
construction, fencing, and tool-making
(Aucca and Ramsey 2005, p. 287; BLI
2009a, p. 2). Commercial-scale
activities, such as clearcutting, logging,
tourism, and infrastructure
development, are ongoing throughout
this species’ range, and alter otherwise
sustainable resource use practices
(Aucca and Ramsay 2005, p. 287;
Engblom 2000, p. 2; Engblom et al.
2002, p. 56; MacLennan 2009, p. 2;
Purcell and Brelsford 2004, pp. 156-157;
Purcell et al. 2004, pp. 458-459; WCMC
1998a, p. 1). Commercial-scale resource
use is exacerbated by ongoing human
encroachment, discussed below.
Mining in Polylepis habitat occurs in
the Peruvian Regions of Ancash and
´
Huanaco and in the Bolivian
Department of La Paz (BLI 2009b, p. 1;
BLI 2009d, p. 1; BLI 2009g, p. 1).
Ancash (Peru) is home to the largest
zinc and copper mine ‘‘in the world,’’
with a monthly average production rate
of 231,485 pounds (105,000 metric tons)
of minerals per day and a 186-mile (mi)
(300 kilometer (km)) pipeline that
stretches from the mine to the port of
Punta Lobitos along the coast (Antamina
Mine 2006, pp. 4, 9;
www.antamina.com/02_operacion/
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En_puerto.html). Mining occurs in ashbreast tit-tyrant habitat in La Paz,
Bolivia, where there are active gold, tin,
silver, and tungsten mines, in addition
to gravel excavation for cement
production (USGS Minerals Yearbook
2005, pp. 4-7). Antamina Mine has
undertaken habitat conservation
programs within the areas affected by
mineral extraction, similar to the
ECOAN Polylepis conservation
programs, investing millions of dollars
in programs ranging from education and
tourism, to organic agriculture and
sustainable development. However,
tourism has had negative effects in other
areas where the ash-breasted tit-tyrant
´
occurs, including Ancash, Huanuco,
and Lima, Peru, and La Paz, Bolivia
(Barrio 2005, p. 564; BLI 2009e, p. 5)
(see below). The Antamina Mining
Company conservation program also
supports the planned reforestation of
123,552 ac (50,000 ha) of Polylepis
forest that will connect two protected
´
areas, Parque Nacional Huascaran and
Zona Reservada de la Cordillera
Huayhuash (Antamina Mine 2006, p. 5).
To date, the project has succeeded in
restoring 371 ac (150 ha) of forest, with
a 95 percent survival rate (MacLennan
2009, p. 1). Known as Corredor
Conchucos, at least 30 ash-breasted tittyrants have recently been observed
there (Chutas 2007, p. 8).
Human encroachment and
concomitant increasing human
population pressures exacerbate the
destructive effects of ongoing human
activities throughout the ash-breasted
tit-tyrant’s habitat. Mining and
hydroelectric projects open new areas to
exploitation and attract people seeking
employment (Purcell et al. 2004, p.
458). Increased urbanization and mining
have led to increased infrastructure
development. Road building and mining
projects further facilitate human access
to remaining Polylepis forest fragments,
throughout the ash-breasted tit-tyrant’s
range (Purcell et al. 2004, pp. 458-459;
Purcell and Brelsford, 2004, pp. 156157), including protected areas. In the
Bolivian Department of La Paz, one of
the most transited highways in the
country is located a short distance from
´
the Parque Nacional y area Natural de
Manejo Integrado Cotapata (BLI 2009b,
p. 2) (see Factor D). Road building,
mining, and other large-scale resource
exploitations are considered to have
major impacts on the habitat, as
compared to exploitation by local
communities (Purcell and Brelsford
2004, p. 157).
Ecotourism within protected areas
where the ash-breasted tit-tyrant occurs
(such as in the Zona Reservada de la
Cordillera Huayhuash in Peru, and in
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the Apolobamba protected areas in
Bolivia) is considered a growing
problem (Barrio 2005, p. 564; BLI 2009e,
p. 5) (see Factor D). In the Department
of La Paz, Bolivia, which encompasses
Bolivia’s largest urban area, most of the
Polylepis forest had been eliminated
prior to the late 1990s (Purcell and
Brelsford 2004, p. 157). Recently, an
accelerated rate of Polylepis forest
destruction has been attributed to
clearcutting for road building and
industrialization projects, such as
mining and construction of
hydroelectric power stations (Purcell
and Brelsford 2004, pp. 156-157).
Between 1991 and 2003, approximately
494 ac (200 ha) of Polylepis habitat was
destroyed. Thus, nearly two-thirds of
the forest cover that existed in the 1990s
no longer existed in 2003 (Purcell and
Brelsford 2004, p. 155). With this
research, it was estimated that only
1,285 ac (520 ha) of Polylepis forest
remain in the Bolivian Department of La
Paz, representing approximately a 40
percent rate of habitat loss in just over
one decade. The researchers inferred
that thisrate of destruction could result
in extirpation of the remaining Polylepis
forest in La Paz within the next 30 years
(Purcell and Brelsford 2004, pp. 157).
Larger concentrations of people put
greater demand on the natural resources
in the area. Increasing demand for
firewood upsets informal and otherwise
sustainable community-based forest
management traditions (Purcell and
Brelsford, 2004, p. 157). Increasing
human populations in the high-Andes
of Bolivia and Peru have also resulted
in a scarcity of arable land. This has led
many farmers to burn down additional
patches of Polylepis forests to plant
crops, even on steep hillsides not
suitable for cultivation (BLI 2009b, p. 2;
BLI 2009h, p. 1; Hensen 2002, p. 199).
These ongoing farming practices result
in the rapid loss of Polylepis forests
from Bolivia to Peru.
Habitat destruction is often caused by
a combination of human activities that
promote habitat degradation. In the
Cordillera de Vilcanota (Cusco, Peru),
where an estimated 181 birds are found
(Chutas 2007, pp. 4, 8), the rate of
habitat loss was studied by comparing
forest cover between 1956 and 2005.
This study revealed a rate of habitat loss
averaging only 1 percent. However,
remaining patches of Polylepis
woodland were small, with a mean
patch size of 7.4 ac (3 ha); four forest
patches had disappeared completely;
and no new patches were located within
the study area (Jameson and Ramsay
2007, p. 42). Lloyd (2008, p. 532)
studied bird foraging habits at three
Polylepis woodland sites in the
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611
Cordillera Vilcanota during 2003–2005.
The sites were described as highly
fragmented, consisting of many small
remnant patches (less than 2.5 ac (1 ha))
and scattered trees, separated from
larger woodland tracts (greater than 25
ac (10 ha)) by distances of 98–4,921 ft
(30–1,500 m) (Lloyd and Marsden in
press, as cited in Lloyd 2008, p. 532).
Given that the species territory ranges
from 2.5–5 ac (1–2 ha) and that the ashbreasted tit-tyrant appears to be unable
to persist in forest remnants smaller
than 2.5 ac (1 ha) (BLI 2009o, p. 1),
these patch sizes have met or are
approaching the lower threshold of the
species’ ecological requirements.
Moreover, 10 percent of the remaining
forest patches showed a decline in forest
density over this time-period.
Thus, habitat degradation also has
serious impacts in Polylepis woodlands
(Jameson and Ramsay 2007, p. 42),
especially given the species’ preference
˚
for dense woodlands (Fjeldsa 2002a, p.
114; Smith 1971, p. 269). The fact that
no new Polylepis forest patches had
become established between 1956 and
2005 underscores the long-term
ramifications of ongoing burning,
clearing, grazing, and other habitataltering human activities that are
pervasive throughout the ash-breasted
tit-tyrant’s range (BLI 2009f, p. 1; BLI
˚
2009n, p. 4; Fjeldsa 2002b, p. 8; WCMC
1998a, p. 1; WCMC 1998b, p. 1). These
activities are considered to be key
factors both in preventing regeneration
˚
of Polylepis woodlands (Fjeldsa 2002a,
˚
p. 112, 120; Fjeldsa 2002b, p. 8) and in
the historical decline of Polylepis
-dependent bird species, including the
˚
ash-breasted tit-tyrant (Fjeldsa 2002a, p.
116). Researchers consider the species’
population to be declining in close
association with the continued habitat
loss and degradation (BLI 2007, pp. 1,
4; BLI 2008, p. 1; BLI 2009o, p. 1).
Therefore, further habitat loss will
continue to impact the species’ already
small population size (see Factor E).
Peru is subject to unpredictable
climate fluctuations that exacerbate the
effects of habitat fragmentation, such as
˜
those that are related to the El Nino
Southern Oscillation (ENSO). According
to the U.S. Dept. of Commerce–National
Oceanic and Atmospheric
Administration (NOAA), the term ENSO
refers to a range of variability associated
with the southern trade winds in the
eastern and central equatorial Pacific
˜
Ocean. El Nino events are characterized
by unusual warming of the ocean, while
˜
La Nina events bring cooler ocean
temperatures (Tropical Atmosphere
Ocean (TAO) Project no date (n.d.), p.
1). Generally speaking, extreme ENSO
events alter weather patterns, so that
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precipitation increases in normally dry
areas, and decreases in normally wet
˜
areas. During an El Nino event, rainfall
dramatically increases, whereas a La
˜
Nina event brings near-drought
conditions (Holmgren et al. 2001, p. 89).
If we consider that wildlife habitat is
not only defined by substrates
(vegetation, soil, water), but also
atmospheric conditions, then changes in
air temperature and moisture can
effectively change a species’ habitat.
Climate change is characterized by
variations in the earth’s temperature and
precipitation, causing changes in
atmospheric, oceanic, and terrestrial
conditions (Parmesan and Mathews
2005, p. 334). Global climate change and
other periodic climatic patterns (e.g., El
˜
˜
Nino and La Nina) can cause or
exacerbate such negative impacts on a
broad range of terrestrial ecosystems
and Neotropical bird populations
(England 2000, p. 86; Holmgren et al.
2001, p. 89; Plumart 2007, pp. 1-2;
Timmermann 1999, p. 694).
Unpredictable climate fluctuations
negatively impact populations
undergoing habitat fragmentation. In the
face of an unpredictable climate, the
risk of population decline due to habitat
fragmentation is heightened. Mora et al.
(2007, p. 1027) found that the combined
effects of habitat fragmentation and
climate change (in this case, warming)
had a synergistic effect, rather than
additive. In other words, the interactive
effects of both climate fluctuation and
habitat fragmentation led to a greater
population decline than if either climate
change or habitat fragmentation were
acting alone on populations. Jetz et al.
(2007, p. 1211) investigated the effects
of climate change on 8,750 land bird
species, including the ash-breasted tittyrant, that are exposed to ongoing
manmade land cover changes (i.e.,
habitat loss). They determined that a
narrow endemic, such as the ashbreasted tit-tyrant, is likely to suffer
greater impacts from climate change,
especially where projected range
contractions are driven by manmade
land conversion activities (Jetz et al.
2007, p. 1213). This is due to the
species’ already small population size,
specialized habitat requirements, and
heightened risk of extinction from
stochastic demographic processes (see
also Factor E). According to this study,
by 2050, up to 18 percent of the ashbreasted tit-tyrant’s current remaining
range is likely to be unsuitable for this
species due to climate change; and, by
2100, it is predicted that about 18 to 42
percent of the species’ range is likely to
be lost as a direct result of global
climate change (Jetz et al. 2007,
Supplementary Table 2, p. 73).
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In 1999, Timmermann (1999, p. 694)
predicted that climate change events
would increase the periodicity and
severity of droughts and excessive
rainfalls, such as those caused by El
˜
˜
Nino and La Nina events. Evidence
suggests that this is the case in Peru
(Richter 2005, p. 24-25). Over the past
˜
decade, there have been four El Nino
events (1997–1998, 2002–2003, 2004–
˜
2005, and 2006–2007) and three La Nina
events (1998-2000, 2000-2001, and
2007-2008) (National Weather Service
(NWS) 2009, p. 2). In Peru, the Andean
highlands, and Polylepis species in
particular, are strongly influenced by
ENSO events (Christie et al. 2008, p. 1).
Christie et al. (2008, p. 1) found that tree
growth in P. tarapacana is highly
influenced by ENSO events because
ENSO cycles on the Peruvian Coast are
strongest during the growing season
(December–February). ENSO-related
droughts can increase tree mortality and
dramatically alter age structure within
tree populations, especially where
woodlands have undergone disturbance,
such as fire and grazing (Villalba and
Veblen 1997, pp. 121-123; Villalba and
Veblen 1998, pp. 2624, 2637).
With years of extremely high rainfall
followed by years of extremely dry
weather (Block and Richter 2007, p. 1),
fire hazard is increased from the
biomass accumulated during the wet
period that dries and adds to the fuel
load in the dry season (Block and
Richter 2007, p. 1; Power et al. 2007, p.
898). Evidence suggests that the fire
cycle in Peru has shortened, particularly
in coastal Peru and west of the Andes
(Power et al. 2007, pp. 897-898).
Changes in the fire-regime can have
broad ecological consequences (Block
and Richter 2007, p. 1; Power et al.
2007, p. 898). In the case of the ashbreasted tit-tyrant, burning is
considered to be a key factor preventing
˚
Polylepis regeneration (Fjeldsa 2002a, p.
˚
112, 120; Fjeldsa 2002b, p. 8). Research
in Ecuadorian Polylepis - Gynoxys
mixed woodlands indicated a strong
reduction in P. incana adult and
seedling survival following a single fire.
This indicates that the species does not
recover well from even a single fire
event (Cierjacks et al. 2007, p. 176). An
accelerated fire cycle would exacerbate
this situation.
Activities that destroy and alter
habitat are ongoing within protected
areas. This is further discussed under
Factor D.
breasted tit-tyrant’s range has been and
continues to be altered and destroyed as
a result of human activities, including
clearcutting and burning for agriculture,
grazing lands, tourism, and
industrialization; extractive activities,
including firewood, timber, and mineral
extraction; and human encroachment
and concomitant increased pressure on
natural resources. Researchers estimate
that 1 percent of the dense woodlands
preferred by the species remains, and
that all remaining habitat is fragmented
and degraded. The ash-breasted tittyrant currently occupies an area of
approximately 4,595 mi2 (11,900 km2)
and appears to be unable to persist in
forest remnants smaller than 2.5 ac (1
ha). Forest fragments in some portions
of the ash-breasted tit-tyrant’s range are
approaching the lower threshold of the
species’ ecological requirements. The
historical decline of habitat suitable for
this species is attributed to the same
human activities that are causing habitat
loss today. Ongoing and accelerated
habitat destruction of the remaining
Polylepis forest fragments in Peru and
Bolivia continues to reduce the
quantity, quality, distribution, and
regeneration of remaining patches.
Human activities that degrade, alter, and
destroy habitat are ongoing throughout
the species’ range, including within
protected areas (see also Factor D).
Current research indicates that climate
fluctuations exacerbate the risks to
species that are already undergoing
range reduction due to habitat
alteration. Climate models predict that
this species’ habitat will continue to
decline. Experts consider the species’
population decline to be commensurate
with the declining habitat (Factor E).
Therefore, we find that destruction and
modification of habitat are threats to the
continued existence of the ash-breasted
tit-tyrant throughout its range.
Summary of Factor A
The ash-breasted tit-tyrant is
dependent on Polylepis habitat, with a
preference for dense woodlands.
Polylepis habitat throughout the ash-
We are not aware of any scientific or
commercial information that indicate
disease or predation poses a threat to
this species. As a result, we are not
considering disease or predation to be a
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B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
We are not aware of any information
currently available that indicates that
overutilization of the species for
commercial, recreational, scientific, or
educational purposes has occurred or is
occurring at this time. As a result, we
are not considering overutilization to be
a threat to the continued existence of
the ash-breasted tit-tyrant.
C. Disease or Predation
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threat to the continued existence of the
ash-breasted tit-tyrant.
D. Inadequacy of Existing Regulatory
Mechanisms
This analysis of regulatory
mechanisms is discussed on a countryby-country basis, beginning with Peru.
Peru: The ash-breasted tit-tyrant is
considered ‘‘endangered’’ by the
Peruvian Government under Supreme
Decree No. 034-2004-AG (2004, p.
276855). This Decree prohibits hunting,
take, transport, and trade of protected
species, except as permitted by
regulation. As hunting, take, transport,
and trade are not currently threats to the
ash-breasted tit-tyrant (Factor B), this
regulation does not mitigate any current
threats to this species.
The Peruvian national protected area
system includes several categories of
habitat protection. Habitat may be
designated as any of the following: (1)
Parque Nacional (National Park, an area
managed mainly for ecosystem
conservation and recreation ); (2)
Santuario (Sanctuary, for the
preservation of sites of notable natural
or historical importance); (3) Reserva
Nacional (National Reserve, for
sustainable extraction of certain
biological resources); (4) Bosque de
´
Proteccion (Protection Forest, to
safeguard soils and forests, especially
for watershed conservation); (5) Zona
Reservada (Reserved Zone, for
temporary protection while further
study is under way to determine their
importance); (6) Bosque Nacional
(National Forest, to be managed for
utilization); (7) Reserva Comunal
(Communal Reserve, for local area use
and management, with national
oversight); and (8) Cotos de Caza
(Hunting Reserve, for local use and
management, with national oversight)
´
(BLI 2008, p. 1; Rodrıguez and Young
2000, p. 330). National reserves,
national forests, communal reserves,
and hunting reserves are managed for
the sustainable use of resources (IUCN
1994, p. 2). The designations of National
Parks, Sanctuaries, and Protection
Forests, are established by supreme
decree that supersedes all other legal
claim to the land and, thus, these areas
tend to provide more habitat protection.
All other protected areas are established
by supreme resolution, which is viewed
as a less powerful form of protection
´
(Rodrıguez and Young 2000, p. 330).
Protected areas have been established
through regulation in at least three sites
occupied by the ash-breasted tit-tyrant
´
in Peru: Parque Nacional Huascaran
´
(Ancash), and Santuario Historico
Machu Picchu (Cusco); and Zona
Reservada de la Cordillera Huayhuash
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´
(spanning Ancash, Huanuco, and Lima)
(Barrio 2005, p. 563; BLI 2009i, p. 1; BLI
2009l, p. 1; BLI 2009n, p. 1). Habitat
destruction and alteration, including
burning, cutting, and grazing are
ongoing within Parque Nacional
´
´
Huascaran and Santuario Historico
Machu Picchu (BLI 2009l, p. 4; BLI
2009n, p. 2; Engblom et al. 2002, p. 58),
where resources are supposed to be
´
managed for conservation (Rodrıguez
and Young 2000, p. 330). Reserved
zones are intended to be protected
´
pending further study (Rodrıguez and
Young 2000, p. 330). However, burning
for habitat conversion and maintenance
of pastures for grazing and increasing
ecotourism are ongoing within Zona
Reservada de la Cordillera Huayhuash
(Barrio 2005, p. 564). Therefore, the
occurrence of the ash-breasted tit-tyrant
within protected areas in Peru does not
protect the species, nor does it mitigate
the threats to the species from ongoing
habitat loss (Factor A) and concomitant
population decline (Factor E).
Recent studies by the Peruvian
Society for Environmental Law (SPDA)
have concluded that there are
approximately 5,000 laws and
regulations directly or indirectly related
to environmental protection and natural
resource conservation in Peru. However,
many of these are not effective because
of limited implementation and/or
enforcement capability (Muller 2001,
pp. 1-2).
Bolivia: The 1975 Law on Wildlife,
National Parks, Hunting and Fishing
(Decree Law No. 12,301 1975, pp. 1-34)
has the fundamental objective of
protecting the country’s natural
resources. This law governs the
protection, management, utilization,
transportation, and selling of wildlife
and their products; the protection of
endangered species; habitat
conservation of fauna and flora; and the
declaration of national parks, biological
reserves, refuges, and wildlife
sanctuaries, tending to the preservation,
promotion, and rational use of these
resources (Decree Law No. 12,301 1975,
pp. 1-34; eLAW 2003, p. 2). Although
this law designates national protection
for all wildlife, there is no information
as to the actual protections this confers
to ash-breasted tit-tyrants. Law No.
12,301 (1975, pp. 1-34) also placed into
public trust all national parks, reserves,
refuges, and wildlife sanctuaries.
However, there is no specific
information as to the governmental
protections afforded within the
protected areas to either the ashbreasted tit-tyrant or its habitat. Given
the ongoing habitat destruction
throughout the species’ range in Bolivia,
this law does not protect the species,
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613
nor does it mitigate the threats to the
species from ongoing habitat loss
(Factor A) and concomitant population
decline (Factor E).
Bolivia passed an overarching
environmental law in 1992 (Law No.
1,333 1992), with the intent of
protecting and conserving the
environment and natural resources.
However, there is no specific legislation
to implement these laws (eLAW 2003, p.
1). Therefore, we cannot determine that
this law protects the species or mitigates
the threats to the species from ongoing
habitat loss (Factor A) and concomitant
population decline (Factor E).
In Bolivia, habitat is protected either
on the national or departmental level
through the following designations: (1)
Parque (Park, for strict and permanent
protection of representative of
ecosystems and provincial habitats, as
well as plant and animal resources,
along with the geographical, scenic and
natural landscapes that contain them);
(2) Santuario (Sanctuary, for the strict
and permanent protection of sites that
house endemic plants and animals that
are threatened or in danger of
extinction); (3) Monumento Natural
(Natural Monument, to preserve areas
such as those with distinctive natural
landscapes or geologic formations, and
to conserve the biological diversity
contained therein); (4) Reserva de Vida
Silvestre (Wildlife Reserve, for
protection, management, sustainable use
and monitoring of wildlife); (5) Area
Natural de Manejo Integrado (Natural
Area of Integrated Management, where
conservation of biological diversity is
balanced with sustainable development
of the local population; and (6) Reserva
´
Natural de Inmovilizacion
(‘‘Immobilized’’ Natural Reserve, a
temporary (5–year) designation for an
area that requires further research before
any official designations can be made
and during which time no natural
resource concessions can be made
within the area) (Supreme Decree No.
24,781 1997, p. 3). Within parks,
sanctuaries and natural monuments,
extraction or consumption of all
resources are prohibited, except for
‘‘scientific research, eco-tourism,
environmental education, and activities
of subsistence of original towns,
properly described and authorized.’’
National protected areas are under the
management of the national
government, while departmental
protected areas are managed at the
department level (eLAW 2003, p. 3;
Supreme Decree No. 24,781 1997, p. 3).
The ash-breasted tit-tyrant occurs
within several protected areas in the
Department of La Paz, Bolivia: Parque
´
Nacional y area Natural de Manejo
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Integrado Madidi, Parque Nacional y
´
area Natural de Manejo Integrado
Cotapata, and the co-located protected
areas of Reserva Nacional de Fauna de
´
Apolobamba, area Natural de Manejo
Integrado de Apolobamba, and Reserva
de la Biosfera de Apolobamba (Auza
and Hennessey 2005, p. 81; BLI 2009a,
p. 1; BLI 2009b, p. 1; BLI 2009c, p. 1;
BLI 2009e, p. 1). Although national
parks are intended to be strictly
protected, the two parks in which the
´
species occurs (Parque Nacional y area
Natural de Manejo Integrado Madidi
´
and Parque Nacional y area Natural de
Manejo Integrado Cotapata) are also
designated as areas of integrated
management, which are managed for the
biological conservation balanced with
the sustainable development of the local
population (Supreme Decree No. 24,781
1997, p. 3). Grazing and firewood
extraction are ongoing within Parque
´
Nacional y area Natural de Manejo
Integrado Cotapata (BLI 2009b, p. 2; BLI
2009c, p. 2). Commercial logging has
´
occurred within Parque Nacional y area
Natural de Manejo Integrado Madidi
(BLI 2009a, p. 2; WCMC 1998a, p. 1).
Uncontrolled clearing, extensive
agriculture, grazing, and ‘‘irresponsible’’
tourism are ongoing within the
Apolobamba protected areas (Auza and
Hennessey 2005, p. 81; BLI 2009e, p. 5).
Habitat degradation and destruction
from grazing, forest fires, and timber
extraction are ongoing in other
protected areas, such as Tunari National
Park (Department of Cochabamba,
Bolivia), where suitable habitat exists
for this species (De la Vie 2004, p. 7).
Therefore, the occurrence of the ashbreasted tit-tyrant within protected
areas in Bolivia does not protect the
species, nor does it mitigate the threats
to the species from ongoing habitat loss
(Factor A) and concomitant population
decline (Factor E).
Summary of Factor D
Peru and Bolivia have enacted various
laws and regulatory mechanisms to
protect and manage wildlife and their
habitats. The ash-breasted tit-tyrant is
‘‘endangered’’ under Peruvian law and
occurs within several protected areas in
Peru and Bolivia. As discussed under
Factor A, the ash-breasted tit-tyrant
prefers dense woodlands, which have
been reduced by an estimated 99
percent in Peru and Bolivia, and the
remaining habitat is fragmented and
degraded. Habitat throughout the
species’ range has been and continues to
be altered as a result of human
activities, including clearcutting and
burning for agriculture, grazing lands,
and industrialization; extractive
activities, including, firewood, timber,
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and mineral extraction; and human
encroachment and concomitant
increased pressure on natural resources.
Despite the species’ ‘‘endangered’’
status in Peru and Bolivian laws
intended to protect all wildlife and
natural resources, these activities are
ongoing within protected areas,
indicating that the laws governing
wildlife and habitat protection in both
countries are either inadequate or
inadequately enforced to protect the
species or to mitigate ongoing habitat
loss (Factor A) and population declines
(Factor E). Therefore, we find that the
existing regulatory mechanisms are
inadequate to mitigate the current
threats to the continued existence of the
ash-breasted tit-tyrant throughout its
range.
E. Other Natural or Manmade Factors
Affecting the Continued Existence of the
Species
An additional factor that affects the
continued existence of the ash-breasted
tit-tyrant is the species’ small
population size. As discussed above (see
Population Estimates), the global
population estimate is not an accurate
reflection of the species’ effective
population size because gene flow does
not occur between the subspecies. At
the same time, there is insufficient
information on the subspecies or
subpopulation level (in terms of
numbers of individuals and breeding
structure) to estimate the effective
population size at the subspecies level.
However, with an estimated global
population size in the mid- to upperhundreds (BLI 2000, p. 392; BLI 2007,
p. 1; BLI 2009o, p. 1), and the most
recent estimate of 641 individuals
´
(Chutas 2007, pp. 4, 8; Gomez in litt.
2007, p. 1), the ash-breasted tit-tyrant is
considered to have a ‘‘very small
population’’ size (BLI 2000, p. 392; BLI
2008, p. 1; BLI 2009o, p. 1).
Small population size renders a
species vulnerable to any of several
risks, including inbreeding depression,
loss of genetic variation, and
accumulation of new mutations.
Inbreeding can have individual or
population-level consequences either by
increasing the phenotypic expression
(the outward appearance or observable
structure, function, or behavior of a
living organism) of recessive,
deleterious alleles (harmful gene
sequences) or by reducing the overall
fitness of individuals in the population
(Charlesworth and Charlesworth 1987,
p. 231; Shaffer 1981, p. 131). Small,
isolated wildlife populations are also
more susceptible to environmental
fluctuations and demographic shifts
(Pimm et al. 1988, pp. 757, 773-775;
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Shaffer 1981, p. 131), such as reduced
reproductive success of individuals and
chance disequilibrium of sex ratios.
Species tend to have a higher risk of
extinction if they occupy a small
geographic range and occur at low
density (Purvis et al. 2000, p. 1949).
The ash-breasted tit-tyrant population
declined at a rate between 10 and 19
percent in the past 10 years, and this
decline is expected to continue in close
association with continued habitat loss
and degradation (see Factor A) (BLI
2009o, p. 1). Extinction risk is
heightened in small, declining
populations by an increased
vulnerability to the loss of genetic
variation due to inbreeding depression
and genetic drift (changes in relative
frequency of gene sequences). This, in
turn, compromises a species’ ability to
adapt genetically to changing
environments (Frankham 1996, p. 1507)
and reduces fitness, thus increasing
extinction risk (Reed and Frankham
2003, pp. 233-234). 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).
Complications arising from the
species’ small population size are
exacerbated by the species’ fragmented
distribution. The ash-breasted tit-tyrant
is currently confined to restricted and
severely fragmented forest patches in
the high Andes of Peru and Bolivia (BLI
2000, p. 392; BLI 2007, pp. 1; BLI 2008,
p. 1; BLI 2009o, p. 1; Collar et al. 1992,
˚
p. 753; Fjeldsa and Kessler 1996, as
˚
cited in Fjeldsa 2002a, p. 113; del Hoyo
et al. 2004, p. 281; InfoNatura 2007, p.
1) , where it is estimated that only 1
percent of the dense woodlands
˚
preferred by the species remain (Fjeldsa
2002a, p. 114; Smith 1971, p. 269) (see
Habitat and Life History). Habitat
fragmentation can cause genetic
isolation and heighten the risks to the
species associated with short-term
genetic viability. Species with a small
population size, combined with a
restricted and severely fragmented
range, are exposed to increased
vulnerability to adverse natural events
and manmade activities that destroy
individuals and their habitat (Holsinger
2000, pp. 64-65; Primack 1998, pp. 279308; Young and Clarke 2000, pp. 361366).
Summary of Factor E
The ash-breasted tit-tyrant has a small
population size that renders it
vulnerable to genetic risks that
negatively impact the species’ viability.
The species occurs in two disjunct
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populations, where habitat is highly
fragmented and continues to be altered
by human activities (Factor A). The
restricted and fragmented range, as well
as its small population size, increases
the species’ vulnerability to extinction,
through demographic or environmental
fluctuations. Based on its small
population size and fragmented
distribution, we have determined that
the ash-breasted tit-tyrant is particularly
vulnerable to the threat of adverse
natural events (e.g., genetic,
demographic, or environmental) and
human activities (e.g., deforestation,
habitat alteration, and infrastructure
development) that destroy individuals
and their habitat. The genetic and
demographic risks associated with small
population sizes are exacerbated by
ongoing human activities that continue
to curtail the species’ habitat throughout
its range. The species’ population has
declined and is predicted to continue
declining commensurate with ongoing
habitat loss (Factor A). Therefore, we
find that the species’ small population
size, in concert with its fragmented
distribution and its heightened
vulnerability to adverse natural events
and manmade activities, are threats to
the continued existence of the ashbreasted tit-tyrant throughout its range.
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Status Determination for the AshBreasted Tit-Tyrant
The ash-breasted tit-tyrant, a small
New World tyrant flycatcher, exists in
two disjunct areas in Peru and Bolivia.
Preferring dense, semihumid Polylepis
or Polylepis -mixed woodlands, the ashbreasted tit-tyrant occupies a narrow
range of distribution, at elevations
between 12,139 and 15,092 ft (3,700 and
4,600 m). The species has a highly
restricted and severely fragmented range
(approximately 4,595 mi2 (11,900 km2)),
and is known only in two disjunct areas:
one location in west-central Peru (in the
Peruvian Administrative Regions of
´
Ancash, Huanuco, La Libertad, and
Lima) and another location ranging from
´
southern Peru (Apurımac, Cusco, Puno,
and Arequipa Regions) into northern
Bolivia (in the Department of La Paz).
The known population of the ashbreasted tit-tyrant is estimated to be 641
individuals.
We have carefully assessed the best
available scientific and commercial
information regarding the past, present,
and potential future threats faced by the
ash-breasted tit-tyrant and have
concluded that there are three primary
factors that threaten the continued
existence of the ash-breasted tit-tyrant:
(1) Habitat destruction, fragmentation,
and degradation; (2) limited size and
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isolation of remaining populations; and
(3) inadequate regulatory mechanisms.
Human activities that degrade, alter,
and destroy habitat are ongoing
throughout the ash-breasted tit-tyrant’s
range. Widespread deforestation and the
conversion of forests for grazing,
agriculture, and human settlement have
led to the fragmentation and
degradation of habitat throughout the
range of the ash-breasted tit-tyrant
(Factor A). Researchers estimate that
only 1 percent of the dense Polylepis
woodlands preferred by the species
remain extant. Limited by the
availability of suitable habitat, the
species occurs today only in some of
these fragmented and disjunct locations.
Ash-breasted tit-tyrant habitat continues
to be altered by human activities, such
as burning, grazing, extractive activities,
and human encroachment, which result
in the continued degradation,
conversion, and destruction of habitat
and reduce the quantity, quality,
distribution, and regeneration of
remaining forest patches.
The ash-breasted tit-tyrant population
is small, rendering the species
particularly vulnerable to the threat of
adverse natural events (e.g., genetic,
demographic, or environmental) and
human activities (e.g., deforestation and
habitat alteration) that destroy
individuals and their habitat. Ongoing
human activities that curtail the species’
habitat throughout its range exacerbate
the genetic and demographic risks
associated with small population sizes
(Factor E). The population has declined
10–19 percent in the past 10 years (see
Population Estimates), and is predicted
to continue declining commensurate
with ongoing habitat loss (Factor A).
Habitat loss was a factor in the ashbreasted tit-tyrant’s historical
population decline (see Historical Range
and Distribution), and the species is
considered to be declining today in
association with the continued
reduction in habitat (Factors A and E).
Moreover, current research indicates
that narrow endemics, such as the ashbreasted tit-tyrant, are especially
susceptible to climate fluctuations,
because of the synergistic effect these
fluctuations have on declining
populations that are also experiencing
range reductions due to human
activities (Factor A).
Despite the species’ ‘‘endangered’’
status in Peru and its occurrence within
several protected areas in Peru and
Bolivia (Factor D), human activities that
degrade, alter, and destroy habitat are
ongoing throughout the species’ range,
including within protected areas.
Therefore, regulatory mechanisms are
either inadequate or ineffective at
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615
curbing the threats to the ash-breasted
tit-tyrant of habitat loss (Factor A) and
corresponding population decline
(Factor E).
Section 3 of the Act defines an
‘‘endangered species’’ as ‘‘any species
which is in danger of extinction
throughout all or a significant portion of
its range’’ and a ‘‘threatened species’’ as
‘‘any species which is likely to become
an endangered species within the
foreseeable future throughout all or a
significant portion of its range.’’ Based
on the immediate and ongoing threats to
the ash-breasted tit-tyrant throughout its
entire range, as described above, we
determine that the ash-breasted tittyrant is in danger of extinction
throughout all of its range. Therefore, on
the basis of the best available scientific
and commercial information, we are
proposing to list the ash-breasted tittyrant as an endangered species
throughout all of its range.
´
II. Junın grebe (Podiceps
taczanowskii)
Species Description
´
The Junın grebe is a highly social,
flightless water bird in the
Podicipedidae family that is endemic to
´
a single location (Lake Junın) in Peru.
Other common names for the species (in
´
English) are: Junın flightless grebe, puna
grebe, and Taczanowski’s grebe. This
species is also known by two Spanish
´
´
names: ‘‘zampullın del Junın’’ or
´
‘‘zambullidor de Junın’’ (del Hoyo et al.
˚
1992, p. 195; Fjeldsa 2004, p. 199;
Instituto Nacional de Recursos
Naturales (INRENA) 1996, p. 3; Ramsen
et al. 2007, p. 18; Supreme Decree 0342004-AG 2004, p. 276854).
´
A slim, long-necked bird, the Junın
grebe is about 13.78 in (35 cm) in
length, and its weight ranges from 0.66
to 1.04 pounds (0.30 to 0.47 kilograms)
(BLI 2009b, p. 1; UNEP-WCMC 2009, p.
´
1). The Junın grebe has a pointed head,
with dark feathers on its back, a white
throat, and mottled, dusky-colored
underparts. This grebe is distinguished
by its slender gray bill, red iris, and dull
yellow-orange colored feet. Immature
birds are darker gray on the flanks than
mature birds (BLI 2009b, p. 1).
Taxonomy
´
The Junın grebe was taxonomically
described by Berlepsch and Stolzmann
in 1894 (ITIS 2009, p. 1). It is one of
nine species of grebes in the genus
Podiceps worldwide (Dickinson 2003,
p.80). The species’ taxonomic status as
Podiceps taczanowskii is valid (ITIS
2009, p. 1).
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Habitat and Life History
´
The Junın grebe is endemic to the
open waters and marshlands of Lake
´
Junın, located at 13,390 ft (4,080 m)
above sea level in the Peruvian
´
Administrative Region of Junın (BLI
2003, p. 1; BLI 2009b, p. 1). The 57-mi2
(147-km2) lake, also known as
´
‘‘Chinchaycocha’’ or ‘‘Lago de Junın,’’ is
large but fairly shallow (BLI 2003, p. 1;
BLI 2009a, p. 1; BLI 2009b, p. 1;
ParksWatch 2009, p. 1; Tello 2007, p. 1).
Situated within ‘‘puna’’ habitat, the
climate is seasonal and can be ‘‘bitterly
˚
cold’’ in the dry season (Fjeldsa 1981, p.
240). Local vegetation is characterized
by tall dense grasslands and scrubland
with open, rocky areas, all interspersed
with wetlands and woodlands (BLI
2003, p. 1; ParksWatch 2009, pp. 1, 4).
The dominant terrestrial plant species
surrounding the lake includes 43
species of grass (Poaceae family), 15
species of asters (Asteraceae family),
and 10 species of legumes (Fabaceae
family) (ParksWatch 2009, p. 1). Aquatic
vegetation includes Andean
watermilfoil (Myriophyllum quitense),
several species of pondweed (including
Elodea potamogeton, Potamogeton
ferrugineus, and P. filliformis), and
bladderwort (Utricularia spp.). Floating
plants, such as duckweed (Lemna
species (spp.)), large duckweed
(Spiodela spp.), and water fern (Azolla
filiculoides), also occur on the lake
(ParksWatch 2009, p. 2). The Lake is
surrounded by extensive marshland
along the lake shore (BLI 2009a, p. 1;
BLI 2009b, p. 1) that extends into the
lake up to 1–3 mi (2–5 km) from shore
˚
(O’Donnel and Fjeldsa 1997, p. 29). The
marshes are dominated by two robust
species of cattails, giant bulrush
(Schoenoplectus californicus var. totara)
and totorilla (Juncus articus var.
˚
andicola) (Fjeldsa 1981, pp. 244, 246).
Both cattail species can reach nearly 6.6
ft (2 m) in height. These plant
communities, or ‘‘tortoras,’’ grow so
densely that stands are often
impenetrable (ParksWatch 2009, p. 1).
In shallow water, during low lake levels,
‘‘tortora’’ communities can become
partially or completely dry (BLI 2009b,
p. 1; ParksWatch 2009, p. 2).
´
Lake Junın supports one of the richest
and most diverse arrays of bird species
of all Peruvian high Andean wetlands
(ParksWatch 2009, p. 3). These bird
species include migratory birds, birds
that nest at high altitude, aquatic birds,
and local endemic species, such as the
´
´
Junın grebe and the Junın rail
(Laterallus tuerosi; also the subject of
this proposed rule), the giant coot
(Fulica ardesiaca), and the Chilean
flamingo (Phoenicopterus chilensis)
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(BLI 2009a, pp. 2-3; ParksWatch 2009, p.
3; Tello 2007, p. 2). Mammals are
relatively scarce in the area, although
there are some predators (ParksWatch
2009, p. 4) (see Factor C).
Breeding season for this species
occurs annually from November to
˚
March (Fjeldsa 1981, pp. 44, 246;
˚
O’Donnel and Fjeldsa 1997, p. 29). The
´
Junın grebe nests in the protective cover
of the marshlands during the breeding
˚
season (Fjeldsa 1981, p. 247; Tello 2007,
p. 3), particularly in stands of giant
bulrush (ParksWatch 2009, p. 4). Under
natural conditions, winter rains increase
the lake water level during the breeding
season, allowing the grebes to venture
into local bays and canals, although
they are never found nesting on the
lake’s shore (Tello 2007, p. 3). The
species nests in the giant bulrush
marshlands (ParksWatch 2009, p. 4).
Well-hidden floating nests can contain
up to three eggs, with an average of two
eggs, laid during November and
˚
December (Fjeldsa 1981, p. 245). The
species is believed to have a deferred
˚
sexual maturation (Fjeldsa 2004, p. 201)
and exhibits low breeding potential,
perhaps as a reflection to adaptation to
a ‘‘highly predictable, stable
environment’’ (del Hoyo et al. 1992, p.
195), laying one clutch during the
breeding season (ParksWatch 2009, p.
´
4). Junın grebes occasionally produce a
replacement clutch if their original nest
˚
is disturbed (Fjeldsa 2004, pp. 199, 201).
After the eggs hatch, the male grebe
cares for the chicks, and does not leave
the nest to feed. The female grebe is
responsible for feeding the male and
chicks until the chicks can leave the
´
nest (Tello 2007, p. 3). The Junın grebe
˚
is likely a long-lived species (Fjeldsa
2004, p. 201), and its breeding success
and population size are highly
influenced by the climate (BLI 2008, pp.
1, 3-4; BLI 2009b, p. 2; Elton 2000, p.
˚
3; Fjeldsa 2004, p. 200; Hirshfeld 2007,
p. 107) (see Factor A).
´
The Junın grebe feeds in the open
waters of the lake and around the marsh
edges, moving into the open waters of
the lake to feed where it is easier to dive
˚
for food during the winter (Fjeldsa 1981,
pp. 247-248; Tello 2007, p. 3). Fish
(primarily pupfish (Orestias spp.))
account for over 90 percent of the
˚
grebe’s diet (Fjeldsa 1981, pp. 251-252).
Pupfish become scarce when the
marshlands dry during periods of
´
reduced water levels, and the Junın
grebe is then known to vary its diet with
midges (Order Diptera), corixid bugs
(Trichocorixa reticulata), amphipods
(Hyalella simplex), and shore fly
maggots and pupa (Ephydriid spp.).
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Historical Range and Distribution
´
The Junın grebe was historically
´
known to be endemic to Lake Junın, in
the Peruvian Administrative Region of
˚
˚
´
Junın (Fjeldsa 1981, p. 238; Fjeldsa
˚
2004, p. 200; Fjeldsa and Krabbe 1990,
p. 70; INRENA 1996, p. 1). Experts
believe that the species was previously
distributed throughout the entire 57-mi2
(147-km2) lake (BLI 2003, p. 1; BLI
˚
2009a, p. 1; Fjeldsa 1981, p. 254; F. Gill
and R.W. Storer, pers. comm. as cited in
˚
´
Fjeldsa 2004, p. 200). In 1938, the Junın
grebe was encountered throughout the
entire lake (Morrison 1939, p. 645). The
´
Junın grebe is now absent from the
´
northwest portion of Lake Junın due to
mine waste contamination and a severe
˚
decline in population (Fjeldsa 1981, p.
254; F. Gill and R.W. Storer, pers.
˚
comm. as cited in Fjeldsa 2004, p. 200).
Current Range and Distribution
´
The Junın grebe continues to be
endemic to the 57-mi2 (147-km2) Lake
´
Junın, located at 13,390 ft (4,080 m)
above sea level in the Peruvian High
Andes (BLI 2003, p. 1; BLI 2009a, p. 1;
BLI 2009b, p. 1). Although BirdLife
International (2009b, p. 1) reports the
current estimated range of the species as
55 mi2 (143 km2), their definition of a
species’ range is the total area within its
extent of occurrence (see Current Range
and Distribution of the ash-breasted tittyrant) (BLI 2000, pp. 22, 27). Noting
´
that Lake Junın is only a 57-mi2 (147km2) lake (BLI 2003, p. 1; BLI 2009a, p.
´
1) and that the Junın grebe is restricted
to the southern portion of the lake
˚
(Fjeldsa 1981, p. 254; F. Gill and R.W.
˚
Storer, pers. comm. as cited in Fjeldsa
2004, p. 200), its current range is
actually smaller than the figure reported
by BirdLife International. The entire
population of this species is located
´
within a protected area, the Junın
National Reserve (BLI 2008, p. 2; BLI
2009a, p. 1; BLI 2009b, p. 1; ParksWatch
2009, p. 4).
Population Estimates
´
The current population of the Junın
grebe is estimated to be 100–300
individuals (BLI 2009b, p. 3), having
undergone a severe population decline
in the latter half of the 20th century,
with extreme population fluctuations
˚
during this time (Fjeldsa 1981, p. 254).
Field studies in 1938 indicated that the
´
Junın grebe was ‘‘extremely abundant’’
´
throughout Lake Junın (Morrison 1939,
p. 645). Between 1961 and 1979 the
population fell from greater than 1,000
individuals to an estimated 250–300
birds (BLI 2009b, p. 2; Collar et al. 1992,
p. 43; Harris 1981, as cited in O’Donnell
˚
˚
and Fjeldsa 1997, p. 30; Fjeldsa 1981, p.
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254). Surveys during the mid-1980s
estimated a total of 250 individuals
inhabiting the southern portion of Lake
´
Junın (BLI 2009b, p. 2; Collar et al. 1992,
p. 43). In 1992, only 100 birds were
observed and, by 1993, the population
had declined to 50 birds, of which fewer
than half were breeding adults (BLI
2008, p. 3; BLI 2009b, p. 2). In 1995, an
´
estimated 205 Junın grebes were present
˚
´
on Lake Junın (O’Donnell and Fjeldsa
1997, p. 30). Breeding and fledging were
apparently unsuccessful from 1995 to
1997. However, there were two
successful broods fledged during the
1997 and 1998 breeding seasons (BLI
2008, p. 3; T. Valqui in litt., as cited in
BLI 2009b, p. 2). In 1998, more than 250
´
Junın grebes were counted in a 1.5-mi2
(4-km2) area in the southern portion of
´
Lake Junın, suggesting a total
population of 350 to 400 birds (T.
Valqui in litt., as cited in BLI 2009b, p.
2). In 2001, field surveys indicated that
there may have been a total population
of 300 birds, but that estimate has been
˚
considered overly optimistic (Fjeldsa in
litt. 2003, as cited in BLI 2009b, p. 2).
˚
Fjeldsa (in litt. 2003, as cited in BLI
2009b, p. 2) postulated that perhaps
only half that number would have been
mature individuals. These population
fluctuations are strongly linked to
precipitation (see Factor A).
The species has experienced a
population decline of 14 percent in the
past 10 years, and is expected to
continue to decline (BLI 2009b, pp. 1, 67). The species’ decline is associated
with continued habitat loss and
˚
degradation (Fjeldsa 1981, p. 254; F. Gill
and R.W. Storer, pers. comm. as cited in
˚
Fjeldsa 2004, p. 200) (See Factors, A, C,
and E).
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Conservation Status
´
The Junın grebe is considered
‘‘critically endangered’’ by the Peruvian
Government under Supreme Decree No.
034-2004-AG (2004, p. 276853). The
´
IUCN categorizes the Junın grebe as
‘‘Critically Endangered’’ because it is
endemic to one location and has
undergone ‘‘significant population
declines, such that an extremely small
number of adults remain’’ (BLI 2008, p.
1; BLI 2009b, pp. 1, 3). The single
´
known population of the Junın grebe
occurs wholly within one protected area
´
in Peru, the Junın National Reserve (BLI
2009b, pp. 1-2).
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´
Summary of Factors Affecting the Junın
Grebe
A. The Present or Threatened
Destruction, Modification, or
Curtailment of the Species’ Habitat or
Range
´
The Junın grebe is endemic to Lake
´
Junın, where it resides year-round. The
species is completely dependent on the
open waters and marshland margins of
the lake for feeding and on the
protective cover of the marshlands
during the breeding season (BLI 2008, p.
˚
1; BLI 2009a, p. 1; Fjeldsa 1981, p. 247;
Tello 2007, p. 3). The current estimated
range of the species is 55 mi2 (143 km2)
(BLI 2009b, p. 1). However, as described
under Current Range and Distribution,
its actual range is smaller, because the
species is restricted to the southern
portion of the lake (BLI 2009b, p. 1;
˚
Fjeldsa 1981, p. 254; F. Gill and R.W.
˚
Storer, pers. comm. as cited in Fjeldsa
2004, p. 200). Breeding season begins in
˚
November (Fjeldsa 1981, pp. 44, 246;
˚
´
O’Donnel and Fjeldsa 1997, p. 29). Junın
grebes build their nests (BLI 2008, p. 1;
˚
Fjeldsa 1981, p. 247; Tello 2007, p. 3)
and obtain their primary prey, pupfish,
in the expansive offshore flooded
marshlands that may extend into the
lake up to 1–3 mi (2–5 km) from shore
˚
(Fjeldsa 2004, p. 200; O’Donnel and
˚
Fjeldsa 1997, pp. 29-30).
´
The quality of Junın grebe habitat and
the species’ reproductive success is
highly influenced by water levels and
the water quality of the lake. Water
levels in the lake are affected by
manmade activities (such as
hydropower generation) that are
exacerbated by unpredictable climate
fluctuations (such as drought or
excessive rain). Water quality in Lake
´
Junın has been compromised by
contamination.
The Upamayo Dam, located at the
northwest end of the lake, has been in
operation since 1936, and lake water is
used to power the 54-megawatt Malpaso
hydroelectric plant (Martin et al. 2001,
p. 178; ParksWatch 2006, p. 5). Dam
operations have caused seasonal water
level fluctuations of as much as 6 ft (2
´
m) in Lake Junın (Martin and McNee
1999, p. 659). Under normal conditions,
water levels are lower in the dry season
and the marshlands can become
partially or completely dry (BLI 2009b,
p. 1; ParksWatch 2009, p. 2). The
floodgates of the dam are often opened
during the dry season (June to
November) (BLI 2009b, p. 1; ParksWatch
2009, p. 2), and water offtake for
hydropower generation further drains
the lake, such that by the end of the dry
season, in November, the marshlands
encircling the lake are more apt to
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617
˚
become completely desiccated (Fjeldsa
2004, p. 123).
Reduced water levels directly impact
´
the Junın grebe’s breeding success, by
reducing the amount of available
˚
nesting habitat (BLI 2008, p. 1; Fjeldsa
2004, p. 200). The giant bulrush
´
marshlands, upon which the Junın grebe
relies for nesting and foraging habitat,
have virtually disappeared from some
sections of the lake (O’Donnel and
˚
Fjeldsa 1997, p. 29). When the
marshlands are completely desiccated,
´
the Junın grebe does not breed at all
˚
(Fjeldsa 2004, p. 123).
Reduced water levels also impact the
´
species by reducing the Junın grebe’s
˚
primary prey, pupfish (Fjeldsa 2004, p.
200) (see Habitat and Life History). The
perimeter of the flooded marshlands
provides the primary recruitment
habitat for fish in the lake during
extremely dry years, including 1983–
˚
1987, 1991, and 1994–1997 (Fjeldsa
˚
2004, p. 200; O’Donnel and Fjeldsa
1997, p. 29). Submerged aquatic
vegetation, habitat for pupfish, has
become very patchy, further triggering
declines in the prey population. Few
marshlands are permanently inundated
now, due to the power generation
requirements of the Upamayo Dam, and
the giant bulrushes that previously grew
tall and provided extensive cover for
this species for breeding and feeding
have virtually disappeared, reducing
both nesting and foraging habitat for the
´
Junın grebe. The reduction in nesting
and foraging habitat are believed to
´
contribute to mass mortality of Junın
grebes during extreme drought years
˚
(O’Donnel and Fjeldsa 1997, p. 30).
´
Manipulation of the Lake Junın’s
water levels also results in competition
between the white-tufted grebe
´
(Rollandia rolland) and the Junın grebe
´
for food resources during the Junın
˚
grebe’s breeding season (Fjeldsa 2004, p.
200). Under normal conditions, the
expansive offshore marshlands may
extend into the lake up to 1–3 mi (2–5
˚
km) from shore (O’Donnel and Fjeldsa
1997, p. 29). In years when water levels
´
remain high, the Junın grebe and whitetufted grebe are spatially segregated
during the breeding season, with whitetufted grebes utilizing the interior of the
´
reed marsh and Junın grebes remaining
at the edges of the marshlands, closer to
˚
the center of the lake (Fjeldsa 1981, pp.
245, 255). Near the end of the dry
season, as early as October, when water
levels are lower in the lake and the
marshlands can partially or completely
dry out (BLI 2009b, p. 1; ParksWatch
2009, p. 2), thousands of white-tufted
grebes move from the interior of the
marshlands to the edges, where they
´
compete with the Junın grebe for food
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˚
(Fjeldsa 1984, pp. 413-414). As the
´
breeding season for the Junın grebe
˚
begins in November (Fjeldsa 1981, pp.
˚
44, 246; O’Donnel and Fjeldsa 1997, p.
´
29), Junın grebes build floating nests
and breed on the margins of marshlands
˚
(BLI 2008, p. 1; Fjeldsa 1981, p. 247;
Tello 2007, p. 3), and a plentiful supply
of fish becomes more important
˚
(O’Donnel and Fjeldsa 1997, p. 29).
Competition becomes more critical the
longer the water level remains low at
the end of the dry season, and activities
that further reduce low water levels
only accentuate this competition
˚
(Fjeldsa 1981, pp. 252-253).
Water quality affects the availability
´
of habitat for the endemic Junın grebe.
´
The water in Lake Junın has been
contaminated from mining waste,
agricultural runoff, and organic matter
from the land surrounding the lake.
There are several mining operations
(lead, copper, and zinc) north of Lake
´
Junın, and wastewater from the mines
´
flows untreated into the lake via the Rıo
˚
San Juan (Fjeldsa 1981, p. 255; Martin
and McNee 1999, pp. 660-661;
ParksWatch 2006, p. 2; Shoobridge
2006, p. 3). Agricultural insecticides
´
wash into Lake Junın from surrounding
fields and through drainage systems
from villages around the lake
(ParksWatch 2006, pp. 5, 19). Organic
matter originating from local
communities is piped untreated into the
lake, resulting in eutrophication (a
process whereby excess nutrients
facilitate excessive plant growth, which
ultimately reduces the amount of
dissolved oxygen in the water, harming
oxygen-dependent organisms)
(ParksWatch 2006, p. 5; Shoobridge
2006, p. 3).
´
Lake Junın is a sink for several
streams that transport mining wastes
and other pollution downstream and
into the lake (ParksWatch 2006, p. 19).
´
The Rıo San Juan is the primary source
´
of water for Lake Junın and feeds into
˚
the lake from the northern end (Fjeldsa
1981, p. 255; Martin and McNee 1999,
pp. 660-661; Shoobridge 2006, p. 3).
´
Tests indicate that the Rıo San Juan
contains trace metals, including copper,
lead, mercury, and zinc, in excess of
currently accepted aquatic life
thresholds (Martin and McNee 1999, pp.
660-661). Non-point source pollutants
from agricultural fertilizers, such as
ammonium and nitrate concentrations,
are also suspended in the water column
(Martin and McNee 1999, pp. 660-661).
Iron oxide contamination is visible near
´
the outflow of the Rıo San Juan because
iron oxide produces a reddish tinge to
the water and reed borders. Vegetation
near the river’s outflow is completely
˚
absent (Fjeldsa 2004, p. 124;
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ParksWatch 2006, pp. 20-21), and this
portion of the lake has been rendered
lifeless by the precipitation of iron
oxide from mining wastewaters (BLI
2008, p. 4). The giant bulrush
marshlands, which once existed in great
expanses around the entire perimeter of
´
the lake and upon which the Junın grebe
relies for nesting and foraging habitat,
have virtually disappeared and at least
one species of catfish (Pygidium oroyae)
may have been extirpated from the lake
˚
(O’Donnel and Fjeldsa 1997, p. 29).
Heavy metal contamination is not
limited to the northern end of the lake
(ParksWatch 2006, p. 20), but extends
throughout the southern end (Martin
and McNee 1999, p. 662), where the
´
Junın grebe is now restricted (BLI 2003,
˚
p. 1; BLI 2009b, p. 1; Fjeldsa 1981, p.
254; F. Gill and R.W. Storer, pers.
˚
comm. as cited in Fjeldsa 2004, p. 200).
Near the center of the lake, the bottom
has been described as ‘‘lifeless,’’ due to
˚
sedimentation of iron oxides (Fjeldsa
˚
1981, pp. 255-256; Fjeldsa 2004, p. 124).
Martin et al. (2001, p. 180) determined
that sediments at the lake’s center are
enriched with copper, zinc, and lead
and are anoxic (having low levels of
dissolved oxygen). High concentrations
of dissolved copper, lead, and zinc have
damaged an estimated one-third of the
lake, increasing turbidity of the lake,
and exceeding established aquatic life
thresholds (Martin and McNee 1999, pp.
660-661; ParksWatch 2006, pp. 2, 20;
Shoobridge 2006, p. 3). This has
severely affected animal and plant
populations in the area, contributing to
´
mortality of species, including the Junın
grebe, around the lake (ParksWatch
2006, pp. 3, 20) (see Factor C).
In 2009, conservation organizations
and civil society groups demanded
action to reverse the deterioration of
´
Lake Junın and requested an
independent environmental audit and
continuous monitoring of the lake (BLI
2009b p. 4; BLI 2009c, p. 1). The
conservation groups BLI, American Bird
´
Conservancy (ABC), Asociacion
Ecosistemas Andinos (ECOAN), and
´
INRENA adopted the Junın grebe as the
symbol of wetland conservation for the
high Andes (BLI 2009c, p. 1). Although
translocation has been a consideration
´
for the conservation of the Junın grebe
since the mid-1990s, no suitable habitat
for the species has been located
˚
(O’Donnel and Fjeldsa 1997, pp. 30, 35;
BLI 2008, p. 5; BLI 2009b, p. 2). None
of these conservation organization’s
activities have been effective at curbing
the ongoing habitat degradation (see
also Factor D).
The effects of habitat alteration and
destruction (such as those caused by
artificially reduced water levels and
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water contamination) are accentuated by
unpredictable climate fluctuations (such
as droughts or excessive rains) (Jetz et
al. 2007, pp. 1211, 1213; Mora et al.
2007, p. 1027). Peru is subject to
unpredictable climate fluctuations, such
˜
as those that are related to the El Nino
Southern Oscillation (ENSO). Changes
in weather patterns, such as ENSO
˜
˜
cycles (El Nino and La Nina events),
tend to increase precipitation in
normally dry areas, and decrease
precipitation in normally wet areas
(Holmgren et al. 2001, p. 89; TAO
Project n.d., p. 1); thereby exacerbating
the effects of habitat reduction and
alteration on the decline of a species
(England 2000, p. 86; Holmgren et al.
2001, p. 89; Jetz et al. 2007, pp. 1211,
1213; Mora et al. 2007, p. 1027;
Parmesan and Mathews 2005, p. 334;
Plumart 2007, pp. 1-2; Timmermann
1999, p. 694), especially for narrow
endemics (Jetz et al. 2007, p. 1213) such
´
as the Junın grebe (see also Factor E).
´
Moreover, the Junın grebe’s low
breeding potential is considered to be a
reflection of its adaptation to being in a
‘‘highly predictable, stable
environment’’ (del Hoyo et al. 1992, p.
195).
´
The Junın grebe’s breeding success
and population size are highly
influenced by the climate, with
population declines occurring during
dry years, population increases during
rainy years, and mortality during
extreme cold weather events. Several
times during the last two decades (e.g.,
1983–1987, 1991–1992, 1994–1997), the
population has declined to 100 birds or
less following particularly dry years
(BLI 2008, pp. 1, 3-4; BLI 2009b, p. 2;
˚
Elton 2000, p. 3; Fjeldsa 2004, p. 200).
There have been short-term population
increases of 200 to 300 birds in years
with higher rainfall amounts following
˜
El Nino events (such as the 1997–1998
and 2001–2002 breeding seasons)
˚
(PROFONANPE 2002, as cited in Fjeldsa
2004, p. 133; T. Valqui pers. comm., as
cited in BLI 2009b, p. 2). However,
excessive rains also increase
´
contamination in Lake Junın, which
decreases the amount of suitable habitat
for the species (as described above) and
has adverse effects on the species’
´
health (see Factor C). Many Junın grebes
died during extremely cold conditions
in 1982 (BLI 2008, p. 4). In 2007, the
population declined again following
another cold weather event (Hirshfeld
2007, p. 107). ENSO cycles are ongoing,
having occurred several times within
the last decade (NWS 2009, p. 2), and
evidence suggests that ENSO cycles
have already increased in periodicity
and severity (Richter 2005, pp. 24-25;
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Timmermann 1999, p. 694), which will
exacerbate the negative impacts of
habitat destruction on a species.
Habitat degradation and alteration
caused by fluctuating water levels and
environmental contamination are
considered key factors in the species’
˚
historical decline (Fjeldsa 1981, p. 254;
F. Gill and R.W. Storer, pers. comm. as
˚
cited in Fjeldsa 2004, p. 200). The
species has experienced a population
decline of 14 percent in the past 10
years, and is expected to continue to
decline as a result of deteriorating
habitat and water quality (BLI 2009b,
pp. 1, 6-7). Therefore, further habitat
degradation is expected to continue
impacting this species’ already small
population size (see Factor E).
mortality of the species (see Factor C).
Severe water contamination has
rendered the northwest portion of the
lake lifeless, devoid of aquatic and
terrestrial species. Experts believe that
´
the Junın grebe once inhabited the
entire Lake, but the species is now
confined to the southern portion of the
lake due to water contamination
(Historical Range and Distribution).
Elevated levels of heavy metals may
reduce the fitness and overall viability
´
of the Junın grebe (Factor C), which
would heighten risks associated with
short- and long-term genetic viability
(Factor E). Therefore, we find that
destruction and modification of habitat
are threats to the continued existence of
´
the Junın grebe throughout its range.
Summary of Factor A
´
The habitat in and around Lake Junın,
´
where the Junın grebe is endemic, has
been and continues to be altered and
degraded as a result of human activities,
including artificial water level
fluctuations to generate hydropower and
water contamination caused by mining
waste, agricultural and organic runoff
from surrounding lands, and wastewater
´
from local communities. The Junın
grebe is dependent on the quantity and
quality of lake water for breeding and
´
feeding. Water levels in Lake Junın are
manipulated to generate electricity,
which leads to dramatic fluctuations in
water levels of up to 6 ft (1.8 m). The
´
Junın grebe relies on the protective
cover of flooded marshlands for nesting.
As water drawdown occurs near the end
of the dry season and the inception of
´
the Junın grebe’s mating season,
portions of the marshlands may dry out
completely. Reductions in water levels
decrease the availability of suitable
breeding and foraging habitat, and
´
decrease the availability of the Junın
grebe’s primary prey, forcing
competition with the white-tufted grebe
for food. Drought years have a negative
´
impact on the Junın grebe, resulting in
severe population fluctuations due to
poor breeding success and limited
recruitment of juveniles into the adult
population. Severed dry conditions can
cause total breeding failure (see also
Factor E).
Although the population appears to
rebound during wetter years (i.e.,
˜
following El Nino events) (see Habitat
and Life History and Population
Estimate), excessive rain decreases the
suitable habitat for the species, as
pollution washes into the water from
around the lake and the upstream rivers
that feed the lake, increasing
´
contamination levels in Lake Junın. This
increased contamination also affects the
´
Junın grebe’s health and has resulted in
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
We are not aware of any information
currently available that indicates that
´
overutilization of Junın grebe for
commercial, recreation, scientific, or
education purposes has occurred or is
˚
occurring at this time. Fjeldsa (1981, pp.
254-255) notes that local hunters are not
interested in grebes as food because they
have ‘‘too little meat.’’ As a result, we
are not considering overutilization to be
a threat to the continued existence of
´
the Junın grebe.
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C. Disease or Predation
Disease: Although no specific disease
´
threat has been identified for the Junın
´
grebe, contamination of Lake Junın has
contributed directly and indirectly to
´
Junın grebe mortality and has
potentially reduced the overall fitness
and health of the species. As discussed
under Factor A, lead, copper, and zinc
˚
mining residues (Fjeldsa 1981, p. 255;
Martin and McNee 1999, pp. 660-661;
Shoobridge 2006, p. 3), agricultural
runoff, organic matter, and wastewater
´
are discharged directly into Lake Junın
(ParksWatch 2006, pp. 5, 19; Shoobridge
2006, p. 3). High concentrations of
environmental contaminants (including
ammonium, copper, iron oxide, lead,
mercury, nitrate, and zinc) have been
˚
detected throughout the lake (Fjeldsa
˚
1981, pp. 255-256; Fjeldsa 2004, p. 124;
Martin and McNee 1999, pp. 660-662;
ParksWatch 2006, pp. 20-21) and exceed
established thresholds for aquatic life
(Martin and McNee 1999, pp. 660-661;
ParksWatch 2006, p. 20). Chemical
waste has rendered the northern portion
of the lake lifeless due to eutrophication
(BLI 2008, p. 4; Shoobridge 2006, p. 3)
and the sediments in the center of the
lake anoxic (containing no dissolved
oxygen) (Martin et al. 2001, p. 180).
High concentrations of suspended
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619
particulate matter increases the
turbidity of the water, making it less
penetrable to sunlight and resulting in
die-off of aquatic plants and algae
(ParksWatch 2006, p. 20). Chemical
waste has damaged at least one third of
the lake and has severely affected
animal and plant populations in the
˚
area (O’Donnel and Fjeldsa 1997, p. 29;
ParksWatch 2006, pp. 3, 20; Shoobridge
2006, p. 3). The northern portion of the
lake is completely devoid of vegetation
˚
(Fjeldsa 2004, p. 124; ParksWatch 2006,
pp. 20-21), and the giant bulrush
marshlands, which once existed in great
expanses around the entire perimeter of
´
the lake and upon which the Junın grebe
relies for nesting and foraging habitat,
have virtually disappeared. At least one
species of catfish (Pygidium oroyae)
may have been extirpated from the lake
˚
(O’Donnel and Fjeldsa 1997, p. 29).
During years of heavy rainfall, the lake
is filled, and the lakeshore becomes
polluted with ‘‘toxic acid gray
sediment’’ that has caused large-scale
mortality of cattle (approximately 2,000
in 1994) and birds, apparently due to
˚
lead poisoning (O’Donnel and Fjeldsa
1997, p. 30). Lead poisoning from the
presence of mine wastes is a common
cause of mortality in waterbirds, and is
medically described as an intoxication
resulting from absorption of hazardous
levels of lead into body tissues (Friend
and Franson 1999, p. 317).
Water contamination has directly
´
affected the health of the Junın grebe
population. As predators of aquatic
´
organisms, the Junın grebe occupies a
mid-tertiary level position in the food
chain and is prone to bioaccumulation
of pesticides, heavy metals, and other
contaminants that are absorbed or
˚
ingested by its prey (Fjeldsa 1981, pp.
˚
255-256; Fjeldsa 2004, p. 123). Green
plants form the first trophic, or feeding,
level; they are the primary producers.
Herbivores form the second trophic
level, while carnivores form the third
and even fourth trophic levels (The
University of the Western Cape 2009, p.
´
1). Moreover, species such as the Junın
grebe, which inhabit high trophic levels,
are strictly dependent upon the
functioning of a multitude of ecosystem
processes. The loss or absence of species
at lower trophic levels can result in
cascading ecosystem effects, causing
imbalances in the food web at all higher
trophic levels (The University of the
Western Cape 2009, p. 1). In parts of the
lake, increased turbidity has caused dieoff of aquatic plants and algae,
disrupting the food chain (ParksWatch
2006, p. 20). Studies indicate that lead
mining effluents severely reduce or
eliminate primary prey populations of
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fish and aquatic invertebrates, either
directly through lethal toxicity, or
indirectly through toxicity to their prey
species (Demayo et al. 1982, as cited in
Eisler 1988, p. 5). Analysis of feathers
´
and bone tissue of Junın grebes and of
pupfish, the species’ primary prey,
indicate that both the grebe and its prey
˚
contain elevated lead levels (Fjeldsa
1981, pp. 255-256).
Drought conditions exacerbate the
effects of water contamination and
bioaccumulation of contaminants in
aquatic species. From 1989 to 1992, an
extensive drought occurred in the Lake
´
Junın area. During that time, many dead
´
Junın grebes and other waterbirds were
found along the edges of the lakeshore
(T. Valqui and J. Barrio in litt. 1992, as
cited in Collar et al. 1992, p. 45, 190).
In 1992, one of the driest years in
decades, up to 10 dead grebes per
month were reported around the lake.
´
Three Junın grebe carcasses were found
along 1.2 mi (2 km) of shoreline in one
month alone (T. Valqui and J. Barrio in
litt. 1992, as cited in Collar et al. 1992,
p. 45). Experts consider the cause of
death to have been either heavy metal
contamination, which increased in
concentration as water levels decreased
(T. Valqui and J. Barrio in litt. 1992, as
cited in Collar et al. 1992, p. 45), or
˚
reduced prey availability (Fjeldsa 2004,
p. 124). Reduced prey availability is
exacerbated by manmade activities that
are reducing the water levels of the lake,
increasing competition among
sympatric grebe species (different
species that occupy the same range) and
decreasing the marshlands that provide
primary spawning habitat for the
pupfish, the grebe’s primary prey
species (Factor A).
Persistent exposure to contaminants
can contribute to a decline in fitness for
long-lived, mid-trophic level species,
which is inherited by offspring and can
impact embryonic development,
juvenile health, or viability (Rose 2008,
p. 624). The excessive contaminant load
´
in Lake Junın could also allow
opportunistic bacterial and viral
infections to overcome individuals.
˚
According to Fjeldsa (1981, p. 254), the
´
Junın grebe bears a heavy infestation of
stomach nematodes (parasitic
roundworms), especially as compared to
other grebe species. Stomach contents of
´
Junın grebes that have been examined
had an average of 16.7 nematodes,
compared with no nematodes in silver
grebes and 1.6 nematodes in white˚
tufted grebes. Fjeldsa (1981, p. 254)
postulates that the higher nematode
´
infestation in Junın grebes may be an
indicator of poor health.
Predation: Predators around Lake
´
Junın include the Andean fox
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(Pseudalopex culpaues), the long-tailed
weasel (Mustela frenata), Pampas cat
(Onicifelis colocolo), and hog-nosed
skunk (Conepatus chinga) (ParksWatch
2009, p. 4). However, nest sites of the
´
Junın grebe are generally inaccessible to
˚
mammalian predators (Fjeldsa 1981, p.
254). The only raptor likely to take a
´
grebe on Lake Junın is the Cinereus
harrier (Circus cinereus), which
primarily feeds in white-tufted grebe
habitats. Moorhens (Gallinula
chloropus), which also inhabit the lake
(ParksWatch 2009, p. 3; Tello 2007, p.
´
2), are egg stealers and may steal Junın
˚
grebe eggs for food (Fjeldsa 1981, p.
254). However, there is no direct
´
evidence of predation upon the Junın
grebe.
Summary of Factor C
Environmental contamination poses
´
direct and indirect threats to the Junın
grebe’s overall health and survival. The
species’ trophic level also exposes it to
bioaccumulation of toxins accumulated
in the tissue of prey species. Research
indicates that the species has elevated
lead levels and carries a high load of
nematodes, a possible indicator of
´
overall poor health. Junın grebes have
died as a direct result of contaminant
poisoning or reduction in the pupfish,
which has also been found to carry
elevated lead levels. Therefore, we find
that disease is a threat to the continued
´
existence of the Junın grebe. However,
there is no available evidence to
indicate that predation is causing
´
declines in Junın grebe populations or
otherwise contributing to the species’
risk of extinction. Therefore, we find
that predation is not a threat to the
´
Junın grebe.
D. Inadequacy of Existing Regulatory
Mechanisms
´
The Junın grebe is listed as ‘‘critically
endangered’’ by the Peruvian
Government under Supreme Decree No.
034-2004-AG (2004, p. 276853). This
Decree prohibits hunting, take,
transport, and trade of protected
species, except as permitted by
regulation. As hunting, take, transport,
and trade do not currently threaten the
´
Junın grebe, this regulation does not
mitigate any current threats to this
species.
Peru has several categories of national
habitat protection, which were
described above as part of the Factor D
analysis for the ash-breasted tit-tyrant
(BLI 2008, p. 1; IUCN 1994, p. 2;
´
Rodrıguez and Young 2000, p. 330). The
´
Junın grebe population occurs wholly
´
within one protected area: the Junın
´
National Reserve (Junın, Peru) (BLI
´
2009b, pp. 1-2). The Junın National
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Fmt 4701
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Reserve has an area of 133,437 ac
´
(53,000 ha), bordering Lake Junın and
its adjacent territories (Wege and Long
1995, p. 264). In Peru, National Reserves
are also created for the sustainable
extraction of certain biological resources
´
(BLI 2008, p. 1; Rodrıguez and Young
2000, p. 330). Established in 1974,
through Supreme Decree No. 0750-74´
AG, the stated objectives of the Junın
National Reserve include: integrated
conservation of the local ecosystem, its
associated flora and wildlife;
preservation of the scenic beauty of the
lake; and support of socioeconomic
development in the area through the
sustainable use of its renewable natural
resources (BLI 2009a, p. 2; Hirshfeld
2007, p. 107). Most of the lakeshore is
designated a ‘‘Direct Use Zone,’’ which
allows fishing, grazing, and other
educational, research, and recreational
activities (ParksWatch 2006, p. 12).
Although designation of this reserve has
heightened awareness of the ecological
´
problems at Lake Junın (BLI 2009c, p.
1), it has not reduced or eliminated the
´
primary threats to the Junın grebe: water
fluctuations and contamination (Factor
A), contamination resulting in poor
health (Factor C), and small population
size (Factor E). Therefore, the existence
of this species within a protected area
has not reduced or mitigated the threats
to the species.
´
The Junın National Reserve was
designated a Ramsar site under the
Convention on Wetlands of
International Importance (Ramsar
Convention) in 1997 (BLI 2009a, p. 2;
Hirshfeld 2007, p. 107; INRENA 1996,
pp. 1-14). The Ramsar Convention,
signed in Ramsar, Iran, in 1971, is an
intergovernmental treaty which
provides the framework for national
action and international cooperation for
the conservation and wise use of
wetlands and their resources. There are
presently 159 Contracting Parties to the
´
Convention (including Lake Junın), with
1,874 wetland sites, totaling more than
457 million ac (185 million ha),
designated for inclusion in the Ramsar
List of Wetlands of International
Importance (Ramsar 2009, p. 1). Peru
acceded to Ramsar in 1992. It has 13
sites on the Ramsar list, comprising 16.8
million ac (6.8 million ha) (Ramsar
2009, p. 5). In an examination of 5
Ramsar sites, experts noted that Ramsar
designation may provide nominal
protection (protection in name only) by
increasing both international awareness
of a site’s ecological value and
stakeholder involvement in
conservation (Jellison et al. 2004, pp. 1,
4, 19). However, activities that
´
negatively impact the Junın grebe are
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ongoing within this Ramsar wetland,
including water fluctuations and
contamination (Factor A),
contamination resulting in poor health
(Factor C), and small population size
(Factor E). Therefore, the Ramsar
designation has not mitigated the
´
impact of threats on the Junın grebe.
In 2002, the Peruvian Government
passed an emergency law to protect
´
Lake Junın. This law makes provisions
´
for the cleanup of Lake Junın, and
places greater restrictions on extraction
of water for hydropower and mining
˚
activities (J. Fjeldsa in litt. 2003, as cited
in BLI 2007, p. 3). However, this law has
not been effectively implemented, and
conditions around the lake may even
have worsened after passage of this law
(BLI 2009c, p. 1). The Ministry of
Energy and Mining has implemented a
series of Environmental Mitigation
Programs (PAMA) to combat mine waste
´
pollution in the Junın National Reserve
(ParksWatch 2006, p. 21; ParksWatch
2009 p. 3). The PAMAs were scheduled
to have been completed by 2002, but
extensions have been granted,
indicating that many of the mines
currently in operation are still
functioning without a valid PAMA.
Reductions in pollution are reported
because some mine companies have
begun to utilize drainage fields and
recycle residual water. However,
analysis of existing PAMAs indicate that
they do not address specific
responsibilities for mining waste
´
discharged into the Rıo San Juan and
delta, nor do they address deposition of
heavy metal-laced sediments in Lake
´
Junın (ParksWatch 2006, p. 21;
ParksWatch 2009, p. 3). Recent
information indicates that mining waste
contamination in the lake continues to
be a source of pollution (ParksWatch
˚
2006, pp. 20-21; Fjeldsa 2004, p. 124;
BLI 2009b, p. 1). Therefore, this law is
not effective at mitigating the threat of
habitat degradation (Factor A), health
issues associated with contamination
(Factor C) and small population size of
the species (Factor E).
There are approximately 5,000 laws
and regulations directly or indirectly
related to environmental protection and
natural resource conservation in Peru.
Recent studies by the Peruvian Society
for Environmental Law (SPDA) have
concluded that many of these are not
effective because of limited
implementation and/or enforcement
capability (Muller 2001, pp. 1-2).
Summary of Factor D
Peru has enacted various laws and
regulatory mechanisms for the
protection and management of wildlife
´
and their habitats. The Junın grebe is
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‘‘critically endangered’’ under Peruvian
law, and its entire population occurs
within one protected area. As discussed
´
under Factor A, the Junın grebe’s
distribution, breeding success and
recruitment, and food availability on
´
Lake Junın has been curtailed, and are
negatively impacted due to habitat
destruction that is caused by artificial
water fluctuations and water
contamination from human activities.
These habitat-altering activities are
ongoing throughout the species’ range,
which is wholly encompassed within
one protected area. Thus, despite the
species’ critically endangered status and
presence within a designated protected
area, laws governing wildlife and
habitat protection in Peru are
inadequately enforced or ineffective at
protecting the species or mitigating
ongoing habitat degradation (Factor A),
impacts from contaminants, and
concomitant population declines (Factor
E). Therefore, we find that the existing
regulatory mechanisms are inadequate
to mitigate the threats to the continued
´
existence of the Junın grebe throughout
its range.
E. Other Natural or Manmade Factors
Affecting the Continued Existence of the
Species
An additional factor that affects the
´
continued existence of the Junın grebe
is the species’ small population size.
´
The current population of the Junın
grebe is estimated to be 100–300
individuals, however, only an
‘‘extremely small number of adults
remain’’ (BLI 2008, p. 1; BLI 2009b, pp.
1, 3). The number of adults in a
population are important because these
individuals contribute to the next
generation (Shaffer 1981, pp. 132-133;
´
´
Soule 1980, pp. 160-162). The Junın
grebe underwent a severe population
decline in the latter half of the 20th
century, with extreme population
˚
fluctuations (Fjeldsa 1981, p. 254) (see
Population Estimates). For example, in
1993, the population size declined to
below 50 individuals, of which fewer
than half were breeding adults (BLI
2008, p. 3; BLI 2009b, p. 2). Even if the
estimate of 100–300 individuals is
correct, the number of mature
individuals is likely to be far smaller,
˚
perhaps only half (Fjeldsa in litt. 2003,
as cited in BLI 2009b, p. 2). Therefore,
100–300 individuals overestimates the
species’ effective population size (the
number of breeding individuals that
contribute to the next generation)
´
(Shaffer 1981, pp. 132-133; Soule 1980,
pp. 160-162).
Small population size renders species
vulnerable to genetic risks that can have
individual or population-level genetic
PO 00000
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621
consequences, such as inbreeding
depression, loss of genetic variation,
and accumulation of new mutations,
and may affect the species’ viability by
increasing its susceptibility to
demographic shifts or environmental
fluctuations, as explained in more detail
above in the Factor E analysis for the
ash-breasted tit-tyrant (Charlesworth
and Charlesworth 1987, p. 238; Pimm et
al. 1988, pp. 757, 773-775; Shaffer 1981,
p. 131). Small population size also leads
to a higher risk of extinction and, once
a population is reduced below a certain
number of individuals, it tends to
rapidly decline towards extinction
(Frankham 1996, p. 1507; Franklin
´
1980, pp. 147-148; Gilpin and Soule
1986, p. 25; Holsinger 2000, pp. 64-65;
Purvis et al. 2000, p. 1949; Reed and
´
Frankham 2003, pp. 233-234; Soule
1987, p. 181). In addition, species that
inhabit a small geographic range, occur
at low density, occupy a high trophic
level, and exhibit low reproductive rates
tend to have a higher risk of extinction
than species that are not limited by the
same risk factors (Purvis et al. 2000, p.
1949).
Complications arising from the
species’ small population size are
exacerbated by the species’ restricted
range and threat of disease (Factor C).
´
The Junın grebe is known only from a
´
single Andean lake, Lake Junın, in
central Peru (BLI 2000, p. 45; BLI 2009b,
p. 1; Collar et al. 1992, p. 43). Although
the species was believed to have been
previously distributed throughout the
˚
entire 57-mi2 (147-km2) lake (Fjeldsa
1981, p. 254; F. Gill and R.W. Storer,
˚
pers. comm. as cited in Fjeldsa 2004, p.
200; Morrison 1939, p. 645), it is now
restricted to the southern portion of
˚
´
Lake Junın (BLI 2009b, p. 1; Fjeldsa
1981, p. 254; F. Gill and R.W. Storer,
˚
pers. comm. as cited in Fjeldsa 2004, p.
200). The population has declined by at
least 14 percent in the last 10 years and
is expected to continue to decline, as a
result of declining water quality and
extreme water level fluctuations (BLI
2009b, pp. 1, 4, 6-7) (Factor A). We
consider that the risks associated with
small population size will continue to
impact this species and may accelerate,
if habitat destruction continues
unabated. Environmental contamination
poses direct and indirect threats to the
´
Junın grebe’s overall health and
survival, including the presence of
´
toxins in both the Junın grebe and its
primary prey species and mass die-offs
that are linked to contamination or
reduction in prey species (Factor C). A
species’ small population size,
combined with its restricted range and
threat of disease, increases the species’
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vulnerability to adverse natural events
and manmade activities that destroy
individuals and their habitat (Holsinger
2000, pp. 64-65; Primack 1998, pp. 279308; Young and Clarke 2000, pp. 361366).
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Summary of Factor E
´
The Junın grebe has a small
population size that renders it
vulnerable to genetic risks that
negatively impact the species’ long-term
viability and, possibly, its short-term
viability. The species has a restricted
range and occurs in habitat that
continues to undergo degradation and
curtailment due to human activities
(Factor A). Environmental contaminants
have caused die-offs of the species and
have likely reduced the overall general
´
health of the Junın grebe population
(Factor C). The small population size, as
well as its restricted range and health
issues associated with contamination,
increases the species’ vulnerability to
extinction, through demographic or
environmental fluctuations. Based on its
small population size, restricted range,
and threat of disease, we have
´
determined that the Junın grebe is
particularly vulnerable to the threat of
adverse natural events (e.g., genetic,
demographic, or environmental) and
human activities (e.g., water level
manipulation) that destroy individuals
and their habitat. The genetic and
demographic risks associated with small
population sizes are exacerbated by
ongoing human activities that continue
to curtail the species’ habitat throughout
its range. The species’ population has
declined and is predicted to continue
declining due to an ongoing reduction
in water quality and extreme water level
fluctuations (Factor A). Therefore, we
find that the species’ small population
size, in concert with its restricted range,
threat of disease, and its heightened
vulnerability to adverse natural events
and manmade activities, are threats to
´
the continued existence of the Junın
grebe throughout its range.
´
Status Determination for the Junın
Grebe
´
The Junın grebe, a flightless grebe, is
´
endemic to Lake Junın, found at 13,390
ft (4,080 m) above sea level in Peru,
where it resides year-round. The species
relies on the open waters and marshland
margins of the lake for feeding and on
the protective cover of the marshland
margins for nesting during the breeding
season. The species has a highly
restricted range (approximately 55 mi2
(143 km2)) and is currently known only
in one location in central Peru. The
species’ population size is estimated as
100–300 individuals, although the
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number of mature individuals may be
limited to half this amount.
We have carefully assessed the best
available scientific and commercial
information regarding the past, present,
and potential future threats faced by the
´
Junın grebe and have concluded that
there are four primary factors that
threaten the continued existence of the
´
Junın grebe: (1) Habitat destruction,
fragmentation, and degradation; (2)
disease; (3) limited size and isolation of
remaining populations; and (4)
inadequate regulatory mechanisms.
Human activities that degrade, alter,
and destroy habitat are ongoing
´
throughout the Junın grebe’s range. Lake
waters are artificially manipulated to
produce hydropower, resulting in
reductions in water levels that impact
the species’ nesting and foraging sites.
Manipulation of water levels for
hydropower production reduces prey
populations, causes increased food
competition with white-tufted grebes,
and results in the abandonment of
breeding in drought years. Reduced
water levels have permanently
destroyed segments of giant bulrush
communities, compromising the amount
of suitable flooded marshland available
for nesting (Factor A). Mining,
agricultural, and organic materials have
contaminated the water, causing
eutrophication and anoxia in portions of
the lake and the accumulation of trace
minerals in lake bottom sediments. This
´
has had direct effects on the Junın grebe,
destroying habitat in the northwest
portion of the lake so that the species’
range is restricted to only the southern
´
´
portion of Lake Junın and causing Junın
grebe mortality during times of drought
(Factors A and C). Contaminants have
also reduced or eliminated submerged
and emergent vegetation throughout the
lake, decreasing pupfish spawning
habitat and reducing prey availability
(Factor A).
´
Junın grebe habitat continues to be
altered by human activities, conversion,
and destruction of habitat, which reduce
the quantity, quality, distribution, and
regeneration of habitat available for the
´
´
Junın grebe on Lake Junın. Habitat loss
´
was a factor in the Junın grebe’s
historical population decline (see
Historical Range and Distribution).
Population declines have been
correlated with water availability, and
droughts have caused severe population
fluctuations that have likely
compromised the species’ long-term
´
viability. The Junın grebe population is
small, rendering the species vulnerable
to the threat of adverse natural (e.g.,
genetic, demographic) and human
activity (e.g., water extraction and
contaminants from mining) events that
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Sfmt 4702
destroy individuals and their habitat.
´
(Factor E). The Junın grebe’s
reproductive success and life cycle
relies on the availability of sufficient
´
water in Lake Junın. During drought
years, nesting and reproduction decline.
Although the population appears to
rebound during wetter years (such as
˜
following excessive rains from El Nino
events (see Population Estimate and
Factor A), excessive rains also bring
additional contaminants into the lake as
runoff from lands surrounding the lake
and upstream rivers. Research indicates
´
that both the Junın grebe and its primary
prey species, the pupfish, have
accumulated toxins resulting in elevated
lead levels. Environmental
contaminants have caused die-offs of
the species and have likely reduced the
´
general health of the Junın grebe
population (Factor C). The population
has declined 14 percent in the past 10
years (see Population Estimates), and
this decline is predicted to continue
commensurate with ongoing threats
from habitat destruction and water
contamination (Factor A).
Despite the species’ ‘‘critically
endangered’’ status in Peru and its
occurrence entirely within a protected
area, the lake continues to be destroyed
and degraded as a result of human
activities that alter the lake’s water
levels and compromise water quality
(Factors A and C). Therefore, regulatory
mechanisms are either inadequate or
ineffective at mitigating the existing
´
threats to the Junın grebe and its habitat
(Factor D).
Section 3 of the Act defines an
‘‘endangered species’’ as ‘‘any species
which is in danger of extinction
throughout all or a significant portion of
its range’’ and a ‘‘threatened species’’ as
‘‘any species which is likely to become
an endangered species within the
foreseeable future throughout all or a
significant portion of its range.’’ Based
on the immediate and ongoing threats to
´
the Junın grebe throughout its entire
range, as described above, we determine
´
that the Junın grebe is in danger of
extinction throughout all of its range.
Therefore, on the basis of the best
available scientific and commercial
information, we are proposing to list the
´
Junın grebe as an endangered species
throughout all of its range.
´
III. Junın rail (Laterallus tuerosi)
Species Description
´
The Junın rail is a secretive bird of the
Rallidae family that is endemic to a
´
single lake (Lake Junın) in Peru. The
´
species is also referred to as the Junın
˚
black rail (Fjeldsa 1983, p. 281) and is
´
locally known as ‘‘gallinetita de Junın’’
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(Supreme Decree 034-2004-AG 2004, p.
27684). This rail measures 4.7–5.1 in
(12–13 cm) in length, and has a dark
slate-colored head, throat and
underparts. Its belly and vent (anal
aperture) are black, with heavily-barred
white primary feathers along the back
and side. The under-tail coverts
(feathers on the underside of the base of
the tail) are buff in color, with a dull
rufous-brown back. The remaining
underparts are dark brown and boldly
barred in white, and the legs are
greenish-yellow (BLI 2009b, p. 1).
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Taxonomy
´
The Junın rail was first taxonomically
described as Laterallus spilonotus after
Gould’s 1841 description of the
˚
Galapagos crake (Fjeldsa 1983, p. 281;
˚
ITIS 2009b, p. 1). Fjeldsa (1983) later
described it as a subspecies of the black
rail (Laterallus jamaicensis tuerosi)
˚
˚
(Fjeldsa 1983, pp. 277-282; Fjeldsa and
Krabbe 1990, p. 146; ITIS 2009a, p. 1),
noting that the bird’s morphology may
suggest that it is a distinct species
˚
(Fjeldsa 1983, p. 281). Laterallus
jamaicensis has since been split into L.
jamaicensis and L. tuerosi (BLI 2009b, p.
1). ITIS continues to list the species as
the subspecies L. j. tuerosi based on
˚
Fjeldsa’s work in 1983 (ITIS 2009a, p.
1). BirdLife International considers this
rail a full species based on
morphological differences (BLI 2009b p.
1). Furthermore, the black rail,
Laterallus jamaicensis occurs at much
lower elevations (i.e., 0 to 4,429 ft (0 to
1,350 m) above sea level) (Collar et al.
1992, p. 190; BLI 2000, p. 170; BLI 2007,
p. 1). Based on the morphological
differences and the species’ distinct and
´
disjunct ranges, we consider the Junın
rail to be a discrete species and
recognize it as L. tuerosi.
It should be noted that it appears that
´
only 2 specimens of the Junın rail have
ever been collected (near Ondores)
˚
(Fjeldsa 1983, pp. 278-279) and that all
expert accounts of this species rely
solely on that collection and a
subsequent observation of the species in
˚
Pari (Fjeldsa in litt., 1992, as cited in
Collar et al. 1992, p. 190).
Habitat and Life History
´
´
The Junın rail inhabits Lake Junın at
13,390 ft (4,080 m) above sea level in
´
the Andean highlands of Peru (Junın
´
Region). The Junın rail occurs in the
dense, interior marshlands where rushes
(Juncus spp.) predominate or in more
open mosaics of rushes, mosses
(division Bryophyta), and low herbs
˚
´
(Fjeldsa 1983, p. 281). Lake Junın, home
´
to the Junın grebe that is also the subject
of this proposed rule, is located in the
seasonally climatic ‘‘puna’’ habitat, with
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a variety of species of grasses, asters,
and trees of the bean family forming tall,
dense grasslands and open scrubland,
interspersed with wetlands and
woodlands (ParksWatch 2006, p. 2;
ParksWatch 2009, pp. 1, 4). Giant
bulrushes and totorilla dominate the
extensive marshlands surrounding the
˚
lake (BLI 2009b, p. 1; Fjeldsa 1983, p.
281; ParksWatch 2009, p. 1). In shallow
water, during low lake levels, ‘‘tortora’’
communities can become partially or
completely dry (ParksWatch 2009, p. 2).
The lake supports a wide variety of bird
species and aquatic vegetation (BLI
2003, p. 1; BLI 2009a, pp. 2-3;
ParksWatch 2009, p. 3; Tello 2007, p. 2).
Mammals are relatively scarce in the
area, although there are some predators
(ParksWatch 2009, p. 4) (see Factor C).
A more detailed discussion of the flora
and fauna of the lake are provided above
as part of the analysis of the Habitat and
´
Life History of the Junın grebe.
There is little information regarding
´
the ecology of the Junın rail. The species
appears to be completely dependent on
the wide marshlands located around the
southeast shoreline of the lake for
nesting, foraging, and year-round
residence (BLI 2009b, p. 2; Collar et al.
˚
1992, p. 190; Fjeldsa 1983, p. 281) (see
also Current Range and Distribution).
´
Similar to all rails, the Junın rail is
furtive and remains well-hidden in the
marshes surrounding the lake (BLI
´
2009b, p.2). The Junın rail reportedly
nests at the end of the dry season, in
September and October. Nests are built
on the ground within dense vegetative
cover, and the species’ clutch size is two
eggs (BLI 2009b, p. 2; Collar et al. 1992,
´
p. 190). The diet of the Junın rail has not
been studied specifically, but other
black rail species feed primarily on
small aquatic and terrestrial
invertebrates and seeds (Eddleman et al.
1994, p. 1).
Historical Range and Distribution
´
The Junın rail is endemic to Lake
˚
´
Junın (Fjeldsa 1983, p. 278; BLI 2009b,
p. 2). The species may have been
historically common in the rushdominated marshlands surrounding the
˚
entire lake (Fjeldsa 1983, p. 281). In
addition to the species’ specific habitat
preferences (see Current Range and
Distribution), it is believed that the
´
Junın rail is now restricted to the
marshes at the southwest corner of the
lake because of the high level of water
contamination that flows into the
northwest margins of the lake via the
´
Rıo San Juan (Martin and McNee 1999,
p. 662).
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623
Current Range and Distribution
´
The Junın rail is restricted to the
southwest shore of the lake, and is
currently known in only two localities
(near the towns of Ondores and Pari)
(BLI 2009b, p. 2; Collar et al. 1992, p.
˚
190; Fjeldsa 1983, p. 281). The current
estimated range of the species is 62 mi2
(160 km2) (BLI 2009b, p. 1). However,
this is likely an overestimate of the
species’ actual range for several reasons.
First, BirdLife International’s definition
of a species’ range results in an
overestimate of the actual range (see
Current Range and Distribution of the
ash-breasted tit-tyrant) (BLI 2000, pp.
22, 27). Second, the species’ range was
calculated based on the availability of
´
presumed suitable habitat for the Junın
rail. It has long been assumed that the
rail potentially occupies the entire
´
marshland area surrounding Lake Junın
˚
(Fjeldsa 1983, p. 281). The total
marshland area has been estimated by
BirdLife International to be 58 mi2 (150
km2) (BLI 2000, p. 170; BLI 2007, p. 1;
BLI 2008, p. 3; BLI 2009b, p. 1).
However, the species has never been
confirmed outside the two known
localities on the southwest shore of the
lake. Moreover, a better understanding
of the ‘‘puna’’ habitat, as well as the
habitat specificity (the specific habitat
needs) of other rail species, indicates
that these may be the only two localities
for this species.
Despite the apparently uniform
appearance of the ‘‘puna,’’ the habitat
provides a complex mosaic of niches
that leads to the patchy distribution of
many bird species throughout the
region, indicating that the species have
specialized habitat requirements that are
˚
only satisfied locally (Fjeldsa and
Krabbe 1990, p. 32). The species’
distribution is highly localized around
´
the lake. The Junın rail apparently
prefers the dense, interior marshlands
comprised primarily of rushes (Juncus
spp.) and mosaics of rushes, mosses
(division Bryophyta), and low herbs in
˚
more open marsh areas (Fjeldsa 1983, p.
281). High habitat specificity is
consistent with related rail species.
Studies of the closely related California
black rail (Laterallus jamaicensis
coturniculus) indicate that this species
is a habitat specialist, whereby the
emergent vegetation used for cover,
water depth, and access to upland
vegetation, are all important factors in
the black rail’s habitat use (Flores and
Eddleman 1995, p. 362). Therefore, the
´
Junın rail’s actual range is clearly
smaller than the figure that continues to
be reported by BirdLife International
since 2000 (BLI 2000, p. 170; BLI 2007,
p. 1; BLI 2008, p. 3; BLI 2009b, p. 1).
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Population Estimates
Rigorous population estimates have
˚
not been made (Fjeldsa 1983, p. 281),
and the species’ elusiveness makes it
difficult to locate (BLI 2009b, p. 2). In
´
1983, the Junın rail was characterized as
possibly common, based on local
fishers’ sightings of groups of up to a
˚
dozen birds at a time (Fjeldsa 1983, p.
281). The species continues to be
reported as ‘‘fairly common,’’ assuming
that it occurs throughout the marshland
surrounding the lake (BLI 2007, p. 1;
BLI 2009b, p. 1). The BirdLife
International estimate that this species’
population size falls within the
population range category of 1,000–
2,499 (BLI 2000, p. 170; BLI 2007, p. 1;
BLI 2009b, p. 1). This estimate is an
extrapolation that continues to be based
on the assumption that the species ‘‘may
be fairly common in the entire c. 58 mi2
(150 km2) of available marshland’’
´
around Lake Junın (BLI 2000, p. 170;
BLI 2007, p. 1; BLI 2008, p. 3; BLI
2009b, p. 1). As indicated in the
analysis of this species’ Current Range
and Distribution, the species has never
been confirmed outside its two known
localities and, therefore, it is possible
that the species is locally common, but
´
not widely distributed. If the Junın rail
´
is not common throughout Lake Junın’s
marshland, the actual population size
may be much lower.
The species has experienced a
population decline of between 10 and
19 percent in the past 10 years (BLI
2009b, p. 2). The population is
considered to be declining in close
association with continued habitat loss
and degradation (see Factors A, C, and
E) (BLI 2008, p. 1).
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Conservation Status
´
The Junın rail is considered
‘‘endangered’’ by the Peruvian
Government under Supreme Decree No.
034-2004-AG (2004, p. 276855). The
´
IUCN categorizes the Junın rail as
‘‘Endangered’’ because it is known only
from a small area of marshland (i.e.,
near Ondores and Pari) around a single
lake, where habitat quality is declining
(BLI 2008, p. 3). The single known
´
population of the Junın rail occurs
wholly within one protected area in
´
Peru, the Junın National Reserve (BLI
2008, p. 1; BLI 2009b, pp. 1-2).
´
Summary of Factors Affecting the Junın
Rail
A. The Present or Threatened
Destruction, Modification, or
Curtailment of the Species’ Habitat or
Range
´
The Junın rail is endemic to Lake
´
Junın, where it resides year-round and
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is restricted to two localities within the
shallow marshlands encircling Lake
´
Junın (BLI 2008, p. 3; BLI 2009b, p. 2;
˚
Fjeldsa 1983, p. 278). The current
estimated range of the species, 62 mi2
(160 km2) (BLI 2009b, p. 1), is an
overestimate of this species’ range for
the reasons outlined above as part of the
analysis of this species’ Current Range
and Distribution. The species is known
only from two discrete locations, near
Ondores and Pari, on the southwest
shore of the lake. Breeding occurs near
the end of the dry season, in September
and October, and the birds build their
nests on the ground within the dense
vegetative cover of the rushes that make
up the marshland perimeter of the lake
(BLI 2000, p. 170; BLI 2007, p. 1; BLI
2009b, p. 2).
´
The habitat in and around Lake Junın
is subjected to manmade activities that
have altered, destroyed, and degraded
the quantity and quality of habitat
´
available to the Junın rail. These
activities include: (1) artificial
manipulation of water levels; (2) water
contamination; and (3) plant harvesting
in the species’ breeding grounds. The
negative impacts of these activities are
accentuated by unpredictable climate
fluctuations (such as droughts or
excessive rains) (Jetz et al. 2007, pp.
1211, 1213; Mora et al. 2007, p. 1027).
The Upamayo Dam went into operation
´
at the northwest end of Lake Junın in
1936 to generate electricity using
hydropower (Martin et al. 2001, p. 178;
ParksWatch 2006, p. 5). Under normal
conditions, water levels are lower
during the dry season, and the
marshlands can become partially or
completely desiccated (BLI 2009b, p. 1;
ParksWatch 2009, p. 2). The dam is
often opened during the dry season, to
generate power (June to November) (BLI
2009b, p. 1; ParksWatch 2009, p. 2),
leading to further drawdown of the lake.
Lake drawdown has been known to
cause water levels to fluctuate
seasonally up to 6 ft (2 m) (Martin and
McNee 1999, p. 659) and has at times
caused complete desiccation of the
marshlands by the end of the dry season
˚
(Fjeldsa 2004, p. 123). The ground
´
nesting Junın rail breeds near the end of
the dry season, in September and
October, and the species’ relies on the
dense vegetative cover of the rushes on
the lake perimeter in which to build
their nests (BLI 2009b, p. 2). A similar
species, the California black rail, may
tolerate decreases in water depth, but
only if the substrate remains moist
enough to support sufficient wetland
vegetation (Flores and Eddleman 1995,
p. 362). Eddleman et al. (1988, p. 463)
noted that water drawdown before
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Sfmt 4702
nesting season disrupts nest initiation
by rails. Therefore, water drawdown
near the end of the dry season that
results in complete desiccation of the
shallow marshlands (BLI 2009b, p. 1;
ParksWatch 2009, p. 2) is likely to
´
disrupt Junın rail nest initiation.
´
Experts believe that the Junın rail is
restricted to the marshes at the
southwest corner of the lake because of
the high level of contamination at the
northwest margins of the lake (Martin
and McNee 1999, p. 662). Experts also
believe that pollution and artificial
water level fluctuations will continue to
have adverse consequences for the
vegetation surrounding the lake and,
´
therefore, the Junın rail (BLI 2000, p.
˚
170; BLI 2007, p. 1; J. Fjeldsa in litt.,
1987, as cited in Collar et al. 1992, p.
190). Indeed, in some places, the tall
marshlands, which rely on inundated
soils to thrive, have virtually
disappeared because the reed-beds are
no longer permanently inundated
˚
(O’Donnel and Fjeldsa 1997, p. 30).
Moreover, as the marshes dry, livestock
(primarily sheep (Ovis aries), but also
cattle (Bos taurus), and some llamas
(Llama glama) and alpacas (Llama
pacos)) move into the desiccated
wetlands surrounding the lake to graze.
Overgrazing is a year-round problem
´
around Lake Junın because the entire
lakeshore is zoned for grazing by a large
number of livestock (approximately
60,000–70,000 head) (ParksWatch 2006,
pp. 12, 19). During the dry season, the
hoofed stock moves into the marshlands
to graze, compacting the soil and
trampling the vegetation (ParksWatch
2006, p. 31). Increased access to the
wetlands during the end of the dry
season, which coincides with the
´
inception of the Junın rail’s nesting
season, likely disrupts the rail’s nesting
activities or leads to nest trampling.
Therefore, activities that increase
lakeshore access, such as water
drawdown, decrease the amount of
´
available habitat for the Junın rail (for
nesting and feeding) and are likely to
´
negatively impact the Junın rail’s
reproduction (through trampling) and
mating habits (through disturbance) (BLI
2009b, p. 1).
Water quality is another factor
influencing the quality of habitat
´
available to the Junın rail. The degraded
´
water quality in Lake Junın was fully
discussed as part of the Factor A
´
analysis for the Junın grebe and is
summarized here. The water in Lake
´
Junın has been contaminated from
mining (Martin and McNee 1999, pp.
660-661; ParksWatch 2006, p. 2;
Shoobridge 2006, p. 3), agricultural
activities (Martin and McNee 1999, pp.
660-661; ParksWatch 2006, p. 2;
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Shoobridge 2006, p. 3), and from
organic matter and wastewater runoff
from local communities around the lake
(ParksWatch 2006, pp. 5, 19; Shoobridge
2006, p. 3). Water pollution has resulted
in heavy metal contamination
throughout the lake, exceeding
established thresholds for aquatic life
throughout at least one-third of the lake
(Martin and McNee 1999, pp. 660-661;
˚
O’Donnel and Fjeldsa 1997, p. 29;
ParksWatch 2006, pp. 3, 20; Shoobridge
2006, p. 3), and rendering the northern
portion of the lake lifeless (BLI 2008, p.
˚
4; Shoobridge 2006, p. 3; Fjeldsa 2004,
p. 124; Martin and McNee 1999, pp.
660-662; ParksWatch 2006, pp. 20-21).
At the lake’s center, lake bottom
sediments are lifeless and anoxic due to
˚
contaminants (Fjeldsa 2004, p. 124;
Martin et al. 2001, p. 180), and the
lakeshore has become polluted with
‘‘toxic acid gray sediment’’ (O’Donnel
˚
and Fjeldsa 1997, p. 30). There is no
vegetation at the northern end of the
˚
lake (Fjeldsa 2004, p. 124; ParksWatch
2006, pp. 20-21), and ongoing
contamination has the potential to
reduce vegetative cover in other areas of
the lake, including the marshlands
´
where the Junın rail occurs. In addition,
these pollutants have severely affected
animal and plant populations in the
area, contributing to mortality of species
around the lake (ParksWatch 2006, pp.
3, 20) and have the potential to reduce
´
the health and fitness of the Junın rail
(see Factor C).
Local residents also harvest and burn
cattails from the marshland habitat,
´
which the Junın rail depends upon.
Cattails are harvested for use in
construction (i.e., to assemble rafts,
baskets, and mats) and as forage for
livestock (ParksWatch 2006, p. 23).
Cattails are also burned to encourage
shoot renewal (ParksWatch 2006, p. 23)
and for hunting the montane guinea pig
(Cavia tschudii), which seeks cover in
the cattail marshes and is part of the
local diet. Burning cattail communities
has a negative and long-lasting impact
on species that use the cattails as
permanent habitat (INRENA 2000, as
cited in ParksWatch 2006, p. 22;
Eddleman et al. 1988, p. 464), including
´
the Junın rail, which relies on the dense
vegetative cover of the marshlands for
year-round residence and nesting (BLI
2000, p. 170; BLI 2007, p. 1; BLI 2009b,
p. 2).
The negative impacts of habitat
alteration and destruction (such as
artificially reduced water levels, water
contamination, and cattail harvesting
and burning) are accentuated by
unpredictable climate fluctuations (such
as droughts or excessive rains) (Jetz et
al. 2007, pp. 1211, 1213; Mora et al.
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Jkt 220001
2007, p. 1027). Peru is subject to
unpredictable climate fluctuations, such
˜
as those that are related to the El Nino
Southern Oscillation (ENSO). Changes
in weather patterns, such as ENSO
˜
˜
cycles (El Nino and La Nina events),
tend to increase precipitation in
normally dry areas, and decrease
precipitation in normally wet areas
(Holmgren et al. 2001, p. 89; TAO
Project n.d., p. 1). ENSO events
exacerbate the effects of habitat
reduction and alteration on the decline
of a species (England 2000, p. 86;
Holmgren et al. 2001, p. 89; Jetz et al.
2007, pp. 1211, 1213; Mora et al. 2007,
p. 1027; Parmesan and Mathews 2005,
p. 334; Plumart 2007, pp. 1-2;
Timmermann 1999, p. 694), particularly
for narrow endemics (Jetz et al. 2007, p.
´
1213) such as the Junın rail (see also
Factor E). As discussed above, droughts
increase access to the wetlands where
´
Junın rails live and breed. Excessive
rain increases contamination in the
water and causes soil toxicity (see
Factor C). ENSO cycles are ongoing,
having occurred several times within
the last decade (NWS 2009, p. 2).
Evidence suggests that ENSO cycles
have already increased in periodicity
and severity (Richter 2005, pp. 24-25;
Timmermann 1999, p. 694), which will,
thus, exacerbate the negative impacts on
a species.
Summary of Factor A
´
The habitat in and around Lake Junın,
´
where the Junın rail is endemic, has
been and continues to be altered and
degraded as a result of human activities,
including artificial water level
fluctuations to generate hydropower,
water contamination caused by mining
waste, agricultural and organic runoff
from surrounding lands, and wastewater
´
from local area communities. The Junın
rail is dependent on the marshland
habitat surrounding the lake for
breeding and feeding. Water levels in
´
Lake Junın are manipulated to generate
electricity, which leads to dramatic
fluctuations in water levels of up to 6 ft
´
(1.8 m). The Junın rail nests on the
ground, within the protective cover of
the marshlands. As water drawdown
occurs near the end of the dry season
´
and during the inception of the Junın
rail’s mating season, portions of the
marshlands may dry out completely,
affecting the availability of suitable
breeding and foraging habitat. This
species’ population decline has been
linked to deteriorating habitat quality
(see also Factor E). Overgrazing, cattail
harvest, and burning are ongoing around
the lakeshore, and water drawdown
increases access to the marshlands.
Severe water contamination in the
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Sfmt 4702
625
northwest portion of the lake has
rendered it lifeless, and experts believe
that water contamination limits the
´
Junın rail’s foraging and breeding
activities to the southern portion of the
lake. The effects of artificially reduced
water levels and water contamination
are accentuated by droughts or
˜
excessive rains caused by El Nino
events. Reduced water levels near the
´
end of the dry season (during Junın rail
nesting season) expose the species to
greater vulnerability to predation (see
Factor C), which also heightens the risks
to the species that are associated with
short- and long-term genetic viability
(Factor E). Therefore, we find that
destruction and modification of habitat
are threats to the continued existence of
´
the Junın rail throughout its range.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
We are not aware of any information
currently available that indicates that
´
overutilization of Junın rail for
commercial, recreation, scientific, or
education purposes has occurred or is
occurring at this time. As a result, we
are not considering overutilization to be
a threat to the continued existence of
´
the Junın rail.
C. Disease or Predation
Disease: Although no specific disease
´
threat has been identified for the Junın
´
rail, contamination of Lake Junın
´
exposes the Junın rail to mortality and
a reduction the overall fitness and
health of the species. The effects of
water contamination on the health of
´
species inhabiting Lake Junın were
discussed as part of the analysis of
´
Factor C for the Junın grebe and are
´
summarized here. In Lake Junın, mining
activities (Martin and McNee 1999, pp.
660-661; Shoobridge 2006, p. 3), and
agricultural runoff, organic matter, and
wastewater (ParksWatch 2006, pp. 5, 19;
Shoobridge 2006, p. 3) have
contaminated the entire lake with high
concentrations of dissolved chemicals
˚
(Fjeldsa 2004, p. 124; Martin and McNee
1999, pp. 660-662; ParksWatch 2006,
pp. 20-21). Environmental contaminants
exceed current established thresholds
for aquatic life (Martin and McNee 1999,
pp. 660-661; ParksWatch 2006, p. 20)
and have rendered the northern portion
of the lake lifeless from eutrophication
(BLI 2008, p. 4; Shoobridge 2006, p. 3).
Due to severe contamination, the
sediments in the center of the lake are
anoxic (Martin et al. 2001, p. 180), and
the lake’s turbidity has increased
(ParksWatch 2006, p. 20). Chemical
waste has damaged at least one third of
the lake, severely affecting animal and
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plant populations in the area (O’Donnel
˚
and Fjeldsa 1997, p. 29; ParksWatch
2006, pp. 3, 20; Shoobridge 2006, p. 3)
and completely eliminating vegetation
from the northern portion of the lake
˚
(Fjeldsa 2004, p. 124; ParksWatch 2006,
pp. 20-21). It is also believed that
contamination may, in fact, be
responsible forthe possible extirpation
of at least one fish species (a catfish)
˚
(O’Donnel and Fjeldsa 1997, p. 29).
Contamination from mining waste
may have direct and indirect impacts on
´
the fitness and health of the Junın rail.
As described above as part of the Factor
´
C analysis for the Junın grebe, a
waterbird that is sympatric with the
´
Junın rail, mine waste contamination
may have caused heavy metal poisoning
(T. Valqui and J. Barrio in litt. 1992, as
cited in Collar et al. 1992, pp. 45, 190)
˚
or reduced prey availability (Fjeldsa
´
2004, p. 124), leading to Junın grebe
mortality during an extensive drought
from 1989 to 1992. Large-scale bird
mortality has occurred on the lake,
apparently due to lead poisoning from
mining effluents—a common cause of
mortality in waterbirds (Friend and
Franson 1999, p. 317; O’Donnel and
˚
Fjeldsa 1997, p. 30). Heavy metals in the
water column and the lake’s sediments,
where this species feeds, would have
negative health consequences for the
´
´
Junın rail, as in the case for the Junın
grebe and other waterbirds that inhabit
the lake. Excessive contaminant load
can contribute to a decline in fitness
and vigor for long-lived, mid-trophic
level species (Rowe 2008, p. 624), such
´
as the Junın rail. Increased turbidity of
the water has resulted in die-offs of
aquatic plants and algae, which disrupts
the food chain (ParksWatch 2006, p. 20).
Higher trophic level species (discussed
in more detail as part of the Factor C
´
analysis for the Junın grebe), such as the
´
Junın rail, are more susceptible to
disruptions in the food chain at lower
˚
trophic levels (Fjeldsa 2004, p. 123; The
University of the Western Cape 2009, p.
1) and prone to bioaccumulation
because they ingest pesticides, heavy
metals, and other contaminants that are
present in their prey (Demayo et al.
1982, as cited in Eisler 1988, p. 5;
˚
Fjeldsa 2004, p. 123). Drought
conditions exacerbate the effects of
water contamination and
bioaccumulation for species at higher
trophic levels (Demayo et al. 1982, as
˚
cited in Eisler 1988, p. 5; Fjeldsa 2004,
p. 123).
Predation: Predators around Lake
´
Junın include the Andean fox
(Pseudalopex culpaues), the long-tailed
weasel (Mustela frenata), Pampas cat
(Onicifelis colocolo), and hog-nosed
skunk (Conepatus chinga) (ParksWatch
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´
2009, p. 4). Junın rails are preyed upon
by pampas cats (BLI 2008, p. 4; BLI
2009b, p 2). Under normal conditions,
water levels are lower in the dry season
and the marshlands can become
partially or completely dry (BLI 2009b,
p. 1; ParksWatch 2009, p. 2) reducing
protective cover and allowing predators
to more easily locate the rail. When the
floodgates of the Upumayo Dam are
opened during the dry season (June to
November) (BLI 2009b, p. 1; ParksWatch
2009, p. 2), drawdown has led to
complete desiccation of the marshlands
˚
by the end of the dry season (Fjeldsa
´
2004, p. 123). The ground nesting Junın
rail breeds near the end of the dry
season, in September and October, and
builds their nests in the dense
vegetative cover of the rushes on the
lake perimeter (BLI 2009b, p. 2). Water
drawdown and periods of drought
increases the bird’s vulnerability to
predation because nesting grounds
become exposed and larger areas of the
marsh are accessible to predators
(ParksWatch 2006, p. 23). Predation
increases the risk of extirpation due to
the species’ already small population
size. In addition, species that inhabit a
small geographic range, occur at low
density, occupy a high trophic level,
and exhibit low reproductive rates tend
to have a higher risk of extinction than
species that are not limited by the same
risk factors (Purvis et al. 2000, p. 1949)
(Factor E).
Summary of Factor C
Environmental contaminants (Factor
´
A) in Lake Junın may have negative
´
consequences on the health of the Junın
rail, given that extensive environmental
´
contamination in Lake Junın has
resulted in mortality of flora and fauna
that inhabit the lake and its margins.
The species’ trophic level also exposes
it to bioaccumulation of toxins
accumulated in the tissue of prey
species. There is documented evidence
that other waterbirds occupying the
same habitat have died as a direct result
of contaminant poisoning or reduction
of the availability of prey species.
Therefore, we find that disease is a
threat to the continued existence of the
´
Junın rail.
Predation by the pampas cat results in
the direct removal of individuals from
the population and can remove
potentially reproductive adults from the
breeding pool. Ongoing habitat
destruction (through reduced water
levels and contamination) continues to
degrade the quality of habitat available
´
to the Junın rail (Factor A) and the
species’ habitat becomes more
accessible to predators during droughts
and water drawdowns. Predation
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renders the species particularly
vulnerable to local extirpation due to its
small population size (Factor E).
Therefore, we find that predation,
exacerbated by ongoing habitat
destruction (Factor A), are threats to the
´
continued existence of the Junın rail
throughout its range.
D. Inadequacy of Existing Regulatory
Mechanisms
´
The Junın rail is listed as
‘‘endangered’’ by the Peruvian
Government under Supreme Decree No.
034-2004-AG (2004, p. 276855). This
Decree prohibits hunting, take,
transport, and trade of protected
species, except as permitted by
regulation. As hunting, take, transport,
and trade do not currently threaten the
´
Junın rail, this regulation does not
mitigate any current threats to this
species.
Peru has several categories of national
habitat protection, which were
described above as part of the Factor D
analysis for the ash-breasted tit-tyrant
(BLI 2008, p. 1; IUCN 1994, p. 2;
´
Rodrıguez and Young 2000, p. 330). The
´
single Junın rail population occurs
´
wholly within the Junın National
´
Reserve (Junın, Peru) (BLI 2009b, pp. 12), which encompasses the lake and
surrounding land and was established
in 1974 by Supreme Decree 0750- 74-AG
(BLI 2009a, p. 2; Wege and Long, p.
264). Peruvian National Reserves are
created for the sustainable extraction of
certain biological resources (BLI 2008,
´
p. 1; Rodrıguez and Young 2000, p.
330), and most of the lakeshore is
designated a ‘‘Direct Use Zone,’’
allowing fishing, grazing, and other
educational, research, and recreational
activities (ParksWatch 2006, p. 12).
Habitat destruction and alteration
(through artificial water level
fluctuations, contamination (BLI 2009b,
˚
p. 1; Fjeldsa 2004, p. 124; ParksWatch
2006, pp. 20-21; Wege and Long 1995,
p. 264)), overgrazing, and cattail harvest
and burning (ParksWatch 2006, pp. 2223) are ongoing throughout the Reserve
(Factor A), increasing the species’
susceptibility to predation (ParksWatch
2006, p. 23) (Factor C), and jeopardizing
the continued existence of the species,
given its already small population size
(Factor E). Therefore, the existence of
this species within a protected area has
not reduced or mitigated the threats to
´
the Junın rail.
´
The Junın National Reserve was
designated a Ramsar site in 1997 (BLI
2009a, p. 2; INRENA 1996, pp. 1-14;
Ramsar 2009, p. 2). As more fully
´
described for the Junın grebe, this
designation provides only nominal
protection of wetland habitat (Jellison et
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al. 2004, p. 19). Activities that
´
negatively impact the Junın rail are
ongoing throughout this wetland,
including water fluctuations and
contamination (Factor A), water
fluctuations that increase the species’
risk of predation (Factor C), and small
population size (Factor E). Therefore,
the Ramsar designation has not
mitigated the impact of threats on the
´
Junın rail.
There are approximately 5,000 laws
and regulations directly or indirectly
related to environmental protection and
natural resource conservation in Peru.
Recent studies by the Peruvian Society
for Environmental Law (SPDA) have
concluded that many of these are not
effective because of limited
implementation or enforcement
capability (Muller 2001, pp. 1-2).
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Summary of Factor D
Peru has enacted various laws and
regulatory mechanisms for the
protection and management of wildlife
´
and their habitats. The Junın rail is
‘‘endangered’’ under Peruvian law, and
its entire population occurs within a
protected area. As discussed under
Factor A, habitat destruction and
alteration have curtailed the species’
range and threaten the continued
existence of the species. Ongoing habitat
destruction (including water level
manipulation, contamination,
overgrazing, and cattail harvest and
burning (Factor A)), predation (Factor
C), and predators’ increased access due
to habitat destruction intensify the risks
to the species from its already small
population size (Factor E). These
activities are ongoing throughout the
species’ range, which is entirely
encompassed within a protected area.
Thus, despite its endangered status and
its presence within a designated
protected area, laws governing wildlife
and habitat protection in Peru are
inadequately enforced or ineffective at
protecting the species or mitigating
ongoing habitat degradation (Factor A)
and concomitant population declines
(Factor E). Therefore, we find that the
existing regulatory mechanisms are
inadequate to mitigate the threats to the
´
continued existence of the Junın rail
throughout its range.
E. Other Natural or Manmade Factors
Affecting the Continued Existence of the
Species
An additional factor that affects the
´
continued existence of the Junın rail is
the species’ small population size. As
discussed above (see Population
Estimates), BirdLife International has
´
placed the Junın rail in the population
category of between 1,000 and 2,499
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individuals (BLI 2009b, p. 2), and
considers the population to be likely
‘‘very small and presumably declining’’
(BLI 2000, p. 170; BLI 2009b, p. 1).
Small population size renders species
vulnerable to genetic risks that can have
individual or population-level genetic
consequences, such as inbreeding
depression, loss of genetic variation,
and accumulation of new mutations,
and may affect the species’ viability by
increasing its susceptibility to
demographic shifts or environmental
fluctuations, as explained in more detail
above in the Factor E analysis for the
ash-breasted tit-tyrant (Charlesworth
and Charlesworth 1987, p. 238; Pimm et
al. 1988, pp. 757, 773-775; Shaffer 1981,
p. 131). Small population size leads to
a higher risk of extinction and, once a
population is reduced below a certain
number of individuals, it tends to
rapidly decline towards extinction
(Frankham 1996, p. 1507; Franklin
´
1980, pp. 147-148; Gilpin and Soule
1986, p. 25; Holsinger 2000, pp. 64-65;
Purvis et al. 2000, p. 1949; Reed and
´
Frankham 2003, pp. 233-234; Soule
1987, p. 181). In addition, species that
inhabit a small geographic range, occur
at low density, occupy a high trophic
level, and exhibit low reproductive rates
tend to have a higher risk of extinction
than species that are not limited by the
same risk factors (Purvis et al. 2000, p.
1949). We consider that the risks
associated with small population size
will continue to impact this species and
may accelerate, if habitat destruction
continues unabated.
Complications arising from the
species’ small population size are
exacerbated by its restricted range and
the threat of predation (Factor C). The
´
Junın rail is known from two localities
(Ondores and Pari) on the southwest
shore of a single Andean lake, Lake
´
Junın, in central Peru (BLI 2000, p. 170;
˚
BLI 2009b, pp. 1-2; Fjeldsa 1983, p. 281;
˚
Fjeldsa in litt. 1992, as cited in Collar
et al. 1992, p. 190) (see Current Range
and Distribution). The population has
declined at a rate between 10 and 19
percent in the past 10 years, and this
decline is expected to continue, as a
result of the declining quality of habitat
within its small, restricted range (BLI
2009b, pp. 4-5) (Factor A). The pampas
´
cat is a known predator of Junın rails
(BLI 2008, p. 4; BLI 2009b, p 2). The
´
ground nesting Junın rail is particularly
vulnerable to predation near the end of
the dry season, when nesting begins and
the vegetative cover of the marshlands
within which they build their nests (BLI
2009b, p. 2) is more exposed and
accessible to predators (ParksWatch
´
2006, p. 23). The Junın rail’s small
population size, combined with its
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627
restricted range and threat of predation,
increases the species’ vulnerability to
adverse natural events and manmade
activities that destroy individuals and
their habitat (Holsinger 2000, pp. 64-65;
Primack 1998, pp. 279-308; Young and
Clarke 2000, pp. 361-366).
Summary of Factor E
´
The Junın rail has a small population
size that renders it vulnerable to genetic
risks that negatively impact the species’
viability. The species occupies a
restricted range and occurs in habitat
that continues to be altered and
destroyed due to human activities
(Factor A). Predation jeopardizes the
species’ already small population size
because it results in the direct removal
´
of Junın rail individuals from the
population, can remove potentially
reproductive adults from the breeding
pool, and could lead to extirpation
(Factor C). The small population size, as
well as its restricted range and threat of
predation, increases the species’
vulnerability to extinction through
demographic or environmental
fluctuations. Based on the species’ small
population size, restricted range, and
threat of predation, we have determined
´
that the Junın rail is particularly
vulnerable to the threat of adverse
natural events (e.g., genetic,
demographic, or environmental) and
human activities (e.g., water level
manipulation, contamination, cattail
harvest, and overgrazing) that destroy
individuals and their habitat. The
genetic and demographic risks
associated with small population sizes
are exacerbated by ongoing human
activities that continue to curtail the
species’ habitat throughout its range.
The species’ population has declined
and is predicted to continue declining
due to an ongoing reduction in the
quality of its habitat (Factor A).
Therefore, we find that the species’
small population size, in concert with
its restricted range, threat of predation,
and its heightened vulnerability to
adverse natural events and manmade
activities, are threats to the continued
´
existence of the Junın rail throughout its
range.
´
Status Determination for the Junın Rail
´
The Junın rail is a ground nesting bird
´
endemic to Lake Junın, found at 13,390
ft (4,080 m) above sea level in Peru,
where it resides year-round. The species
has high habitat specificity and occurs
only in two localities within the
marshland mosaic habitat that
surrounds the lake. The current
estimated range of the species is 62 mi2
(160 km2), and its population size is
estimated to be 1,000–2,499. However,
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both of these figures are likely to be
overestimates; despite suggestions that
the species inhabits the entire area of
marshland surrounding the lake, the
species has only been confirmed in two
localities.
We have carefully assessed the best
available scientific and commercial
information regarding the past, present,
and potential future threats faced by the
´
Junın rail and have concluded that there
are four primary factors that threaten the
continued existence of the rail: (1)
Habitat destruction, fragmentation, and
degradation; (2) disease and predation;
(3) limited size and isolation of
remaining populations; and (4)
inadequate regulatory mechanisms.
Human activities that degrade, alter,
and destroy habitat are ongoing
´
throughout the Junın rail’s range. Lake
waters are artificially manipulated to
produce hydropower, resulting in
reductions in water levels that impact
the species’ nesting and foraging sites,
especially near the end of the dry season
when this ground nesting bird begins
breeding. Reduced water levels and
aquatic contaminants have permanently
destroyed segments of cattail
communities, compromising the amount
of suitable flooded marshland available
for nesting. Climate fluctuations
exacerbate the effects of habitat
alteration, as droughts further decrease
available nesting grounds and excessive
rains increase contaminant runoff into
the lake (Factor A). Environmental
contaminants have caused mortality in
other waterbirds and have likely
reduced the overall general health of the
´
Junın rail population (Factor C).
Overgrazing and cattail harvest and
burning further alter and destroy the
marshland upon which the rails depend
(Factor A). Water drawdown exposes
the birds and their marshland nesting
areas to greater access by grazing
animals, cattail harvesters, and
predators (Factors A and C).
´
Junın rail habitat continues to be
altered by human activities, which
results in the continued degradation and
destruction of habitat and reduces the
quality and distribution of remaining
suitable habitat. Habitat loss was a
´
factor in the Junın rail’s historical
decline (see Historical Range and
Distribution), and the species is
considered to be declining today due to
continued reduction of available habitat
´
(Factors A and E). The Junın rail
population is small, increasing the
species’ vulnerability to the threat of
adverse natural events (e.g., genetic,
demographic, or environmental) and
human activities (e.g., water
contamination, water level
manipulation, cattail harvest, and
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Jkt 220001
overgrazing) that destroy individuals
and their habitat. Human activities that
continue to curtail the species’ habitat
throughout its range exacerbate the
genetic and demographic risks
associated with small population sizes
(Factor E). Predation jeopardizes the
species’ already small population size
because it results in the direct removal
´
of Junın rail individuals from the
population, can remove potentially
reproductive adults from the breeding
pool, and could lead to extirpation
´
(Factor C). The Junın rail population has
declined at a rate between 10 and 19
percent during the past 10 years (see
Population Estimates), and this decline
is predicted to continue commensurate
with ongoing threats from habitat
destruction, water contamination,
overgrazing, and cattail harvest and
burning (Factor A).
Despite the species’ endangered status
in Peru and its occurrence entirely
within one protected area (Factor D),
habitat destruction and degradation
continue as a result of human activities
that alter lake levels and compromise
water quality and increase the species’
susceptibility to overgrazing and
predation (Factors A and C). Therefore,
regulatory mechanisms are either
inadequate or ineffective at mitigating
the existing threats to the species and its
habitat (Factor D).
Section 3 of the Act defines an
‘‘endangered species’’ as ‘‘any species
which is in danger of extinction
throughout all or a significant portion of
its range’’ and a ‘‘threatened species’’ as
‘‘any species which is likely to become
an endangered species within the
foreseeable future throughout all or a
significant portion of its range.’’ Based
on the immediate and ongoing threats to
´
the Junın rail throughout its entire
range, as described above, we determine
´
that the Junın rail is in danger of
extinction throughout all of its range.
Therefore, on the basis of the best
available scientific and commercial
information, we are proposing to list the
´
Junın rail as an endangered species
throughout all of its range.
IV. Peruvian plantcutter (Phytotoma
raimondii)
Species Description
The Peruvian plantcutter, locally
known as ‘‘cortarrama Peruana,’’ is a
small finch-like bird endemic to the dry
forests of coastal northwest Peru (Collar
et al. 1992, p. 805; Goodall 1965, p. 636;
Ridgely and Tudor 1994, p. 733; Sibley
and Monroe 1990, p. 371; Schulenberg
et al. 2007, p. 488; Walther 2004, p. 73).
The Peruvian plantcutter is an herbivore
with a predominantly leaf-eating diet
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(Bucher et al. 2003, p. 211; Schulenberg
et al. 2007, p. 488; Walther 2004, p. 73).
Plantcutters have bright yellow eyes,
short wings and rather long tails, and
their crown feathers form a slight crest
(Goodall 1965, p. 635; Ridgely and
Tudor 1994, p. 732). Adult birds are
7.28 to 7.48 in (18.5 to 9 cm) in length
and weigh approximately 1.26 to 1.55
ounces (oz) (36 to 44 grams (g))
(Schulenberg et al. 2007, p. 488;
Walther 2004, p. 73). Males are pale
ashy gray, except a broad cinnamonrufous color band on the belly and
above the bill, and white colored bands
on their wings (BLI 2000, p. 401; BLI
2009a, p. 1; Goodall 1965, p. 636;
Ridgely and Tudor 1994, p. 733).
Females are buff-brown with broad,
dark brown stripes above, and white
with heavy black-striped underparts
(BLI 2009a, p. 1; Collar et al. 1992, p.
805). Juvenile birds have not been
described (Walther 2004, p. 73). The
Peruvian plantcutter’s bill is stout,
short, conical, and finely serrated with
sharp tooth-like projections that run the
length of the beak on both sides, and
which are well suited for plucking buds,
leaves, shoots, and fruits (Goodall 1965,
p. 635; Ridgely and Tudor 1994, p. 732;
Schulenberg et al. 2007, p. 488) (see
Habitat and Life History).
Taxonomy
The Peruvian plantcutter was first
taxonomically described as Phytotoma
raimondii by Taczanowski in 1883 (ITIS
2009, p. 1; Sibley and Monroe 1990, p.
371). The type-specimen of the Peruvian
plantcutter (the specimen that was
described by Taczanowski) was
collected by the ornithologist Konstanty
Jelski, who recorded the specimen as
being collected in the Tumbes
Department of Peru (Flanagan et al. in
litt. 2009, p. 2). However, the reported
collection location may have been
inaccurate (see Historical range and
Distribution, below).
The genus Phytotoma contains three
species of plantcutters, all endemic to
South America (Dickinson 2003, p. 346;
Goodall 1965, p. 635; Sibley and
Monroe 1990, p. 371; Walther 2004, p.
73). Ornithologists have long debated to
which family this genus belongs. Some
ornithologists have recommended that
the genus be placed in its own family,
Phytotomidae (Lanyon and Lanyon
1989, p. 422), while others placed the
genus within the Tyrannidae family
(Sibley and Monroe 1990, p. 371).
Molecular research using DNA
sequencing supports the inclusion of
Phytotoma in the Cotingidae family
(Irestedt et al. 2001, p. 23; Johansson et
al. 2002, p. 993; Ohlson et al. 2006, p.
10). The Cotingidae family includes a
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wide diversity of species that are found
in Central America and tropical South
America (Snow 2004, p. 32). Therefore,
based on the information currently
available to us, we accept that the
Peruvian plantcutter belongs to the
Cotingidae family, which also follows
the Integrated Taxonomic Information
System (ITIS 2009, p. 1).
Habitat and Life History
The Peruvian plantcutter is reportedly
selective in its habitat preference and
requires a variety of arid tree and shrub
species with dense low-hanging
branches to the ground (Collar et al.
1992, p. 805; Flanagan and More 2003,
p. 5; Flanagan et al. in litt. 2009, p. 7;
Williams 2005, p. 2). The primary
habitat for the Peruvian plantcutter is
seasonally dry tropical forest, which is
also referred to equatorial dry tropical
forest, and which occurs in the semiarid
lowlands of northwest Peru (LinaresPalomino 2006, pp. 260, 263-266;
Schulenberg et al. 2007, p. 21; Walther
2004, p. 73). The Peruvian plantcutter
also uses arid lowland scrub (dense and
open) and dense riparian shrub
communities (BLI 2009a. p. 2; Collar et
al. 1992, p. 805; Schulenberg et al. 2007,
pp. 21, 488; Stotz et al. 1996, p. 19;
Walther 2004, p. 73). Stotz et al. (1996,
pp. 19, 428) identified the Peruvian
plantcutter as a key indicator species for
Equatorial Pacific Coast arid lowland
scrub. The lowland dry tropical forest
and scrub are characterized as small and
heavily fragmented patches of plant
species adapted to the arid conditions of
the prolonged dry season of northwest
Peru (Best and Kessler 1995, p. 40;
Bridgewater et al. 2003, pp. 132, 140;
Ridgely and Tudor 1994, p. 734).
The lowland dry forest or woodlands
in northwest Peru are open canopied,
with trees occurring in scattered clumps
or individually (Flanagan and More
2003, p. 4). The dominant tree species
of the lowland dry forest is Prosopis
pallida (common name ‘‘kiawe;’’ also
locally referred to as ‘‘algarrobo’’) in the
Fabaceae family (legume family) (Lopez
et al. 2005, p. 542; More 2002, p. 39).
Prosopis pallida is a wide-spreading
tree or large shrub, 26–65 ft (8–20 m)
tall, with dense branches; spines can be
present or absent (Pasiecznik et al. 2001,
p. 36). This deep-rooted droughttolerant species, related to mesquite
species of southwest United States and
Mexico, provides an important
ecological function by improving and
stabilizing soil conditions (Brewbaker
1987, p. 1; Pasiecznik et al. 2001, pp.
101-102). Typical of legumes, P. pallida
is able to ‘‘fix’’ atmospheric nitrogen for
plant utilization and growth (Brewbaker
1987, p. 1; Pasiecznik et al. 2001, p. 3).
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Three of the most common tree
species associated with P. pallida dry
forest habitat used by the Peruvian
plantcutter are Capparis scabrida (no
common name, but locally known as
‘‘sapote’’), in the Capparaceae (caper)
family, and Acacia macracantha (longspine acacia, locally known as ‘‘faique’’)
and Parkinsonia aculeata (Jerusalem
thorn, locally known as ‘‘palo verde’’),
both in the Fabaceae (legume) family
(More 2002, pp. 17-23). Associated
flowering shrubs in dry forest habitat
include Capparis avicennifolia (no
common name, but locally known as
‘‘bichayo’’) and C. crotonoides (no
common name, but locally known as
‘‘guayabito de gentil’’), both in the
Capparaceae (caper) family; Cordia lutea
(no common name, but locally known as
‘‘overall’’) in the Boraginaceae (borage)
family; and Maytenus octogona (no
common name, but locally known as
‘‘realengo’’) in the Celastraceae
(bittersweet) family. Other commonly
occurring dry forest vegetation includes
vines (e.g., Convolvulaceae (morningglory) and Cucurbitaceae (gourd)
families), Psittacanthus chanduyensis
(tropical mistletoe; locally known as
‘‘suelda con suelda’’) in the
Loranthaceae (mistletoe) family,
scattered herbaceous species (e.g.,
Asteraceae (sunflower),
Scrophulariaceae (figwort), and
Solanaceae (nightshade) families), and
grasses (e.g., Poaceae (grass) family)
(Elton 2004, p. 2; Ferreyera 1983, pp.
248-250; More 2002, pp. 14-17; Walther
2004, p. 73). Riparian vegetation
includes dense shrub and small trees of
P. pallida, A. macracantha, Capparis
spp., and Salix spp. (willow spp.)
(Lanyon 1975, p. 443).
The arid climate of northwest Peru is
due to the influence of the cold
Humboldt Current that flows north,
parallel to the Peruvian Coast (UNEP
2006, p. 16; Linares-Palomino 2006, p.
260; Rodriguez et al 2005, p. 2). The
Humboldt Current has a cooling
influence on the climate of coastal Peru,
as the marine air is cooled by the cold
current and, thus, is not conducive to
generating rain. To the east, the Andean
Mountains prevent humid air from the
Amazon from reaching the western
lowlands (Lanyon 1975, p. 443; LinaresPalomino 2006, p. 260).
Coastal northwest Peru experiences a
short rainy season during the summer
months (January–April) (LinaresPalomino 2006, p. 260), which can also
include precipitation in the form of mist
or fine drizzle along the coast (Lanyon
1975, p. 443). The mean annual
precipitation across the range of the
Peruvian plantcutter is 0.196 to 3.80 in
(5.0 to 99 mm) (hyper-arid to arid)
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(Galan de Mera et al. 1997, p. 351). The
climate is warm and dry with the
annual temperature range of 74° to 77°
F (23° to 25° C) at elevations below
1,968 ft (600 m) (Linares-Palomino
2006, p. 260). Northwest Peru is
˜
strongly influenced by the El Nino
Southern Oscillation (ENSO) cycle
(Rodriguez et al 2005, p. 1), which can
have particularly profound and longlasting effects on arid terrestrial
ecosystems (Holmgren et al. 2006a, p.
87; Mooers et al. 2007, p. 2) (see Factor
A).
Knowledge of the breeding of most
species within the Cotingidae family,
including the Peruvian plantcutter, is
not well known (Walther 2004, p. 73).
The Peruvian plantcutter is considered
a resident species in Peru, which
indicates that it breeds there (Snow
2004, p. 61; Walther 2004, p. 73).
Nesting activity of plantcutters appears
to occur from March to April (Collar et
al. 1992, p. 805; Walther 2004, p. 73).
Plantcutters build shallow, cup-shaped
nests that are made of thin dry twigs
and lined with root fibers and other
softer material (Snow 2004, p. 55). Nests
range from 2.4 to 3.5 in (6 to 9 cm) in
height and 3.9 to 7.0 in (10 to 18 cm)
in diameter, and can be placed 3.3 to 9.8
ft (1 to 3 m) above the ground inside a
thick thorny shrub or higher in the fork
of a tree (Elton 2004, p. 2; Flanagan and
More 2003, p. 3; Snow 2004, p. 55).
Each female lays two to four eggs, and
the incubation period lasts about 2
weeks (Snow 2004, p. 56; Goodall 1965,
p. 636; Walther 2004, p. 73). The eggs
have been described as short oval to
sub-elliptical in shape and grayish olive
in color with dark brownish olive spots
at the larger end (Flanagan and Millen
2008, p. 1). Males assist rearing the
chicks, which fledge after 17 days or so
(Snow 2004, p. 56).
Plantcutters are herbivores with a
predominantly leaf-eating diet (Bucher
et al. 2003, p. 211; Snow 2004, p. 46).
As an herbivore, the Peruvian
plantcutter is dependent on year-round
availability of high-quality food,
particularly during the dry season when
plant growth is very limited (Bucher et
al. 2003, p. 216). Peruvian plantcutters
eat buds, leaves, and shoots of P. pallida
and various other trees and shrubs, as
well as some fruits (e.g., mistletoe)
(Goodall 1965, p. 635; Schulenberg et al.
2007, p. 488; Walther 2004, p. 73). The
seeds, green seed pods, leaves, and
flowers of P. pallida provide a proteinrich food source for animals (Lewis et
al. 2006, p. 282). Research studies on
the two related plantcutter species, the
rufous-tailed plantcutter (P. rara) and
the white-tipped plantcutter (P. rutila),
showed that the herbivore diet of these
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two species did not affect the energy
levels of observed birds (Lopez-Calleja
and Bozinovic 1999, p. 709; Meynard et
al. 1999, p. 906; Rezende et al. 2001, p.
783). The Peruvian plantcutter appears
to prefer to feed while perched in
shrubs and trees, although individuals
also have been observed foraging on the
ground (Snow 2004, p. 50). Birds have
been observed in pairs and small groups
(Collar et al. 1992, p. 804; Flanagan and
More 2003, p. 3; Schulenberg et al.
2007, p. 488; Walther 2004, p. 73).
Historical Range and Distribution
The Peruvian plantcutter is a
restricted-range species that is confined
to the mostly flat, narrow desert zone,
which is less than 31 mi (50 km) in
width (Lanyon 1975, p. 443) and runs
along the coast of northwest Peru
(Ridgely and Tudor 1994, p. 734;
Stattersfield et al. 1998, p. 213; Walther
2004, p. 73). The historical range of the
Peruvian plantcutter reportedly
extended from the town of Tumbes,
located in extreme northwest corner of
Peru and approximately south to north
of Lima within the Regions of Tumbes,
Piura, Lambayeque, La Libertad,
Ancash, and Lima (from north to south)
(Collar et al. 1992, pp. 804-805).
The historical distribution of the
Peruvian plantcutter was most likely
throughout the contiguous lowland P.
pallida dry forest and riparian
vegetation, below 1,804 ft (550 m)
(Collar et al. 1992; Williams 2005, p. 1).
According to Collar et al. (1992, pp.
804-805), the Peruvian plantcutter is
known from 14 historical sites.
The type-specimen of the Peruvian
plantcutter, which was collected and
labeled by Konstanty Jelski as being
found in Tumbes in the late 1870s, was
most likely collected south of the town
of Tumbes (Flanagan et al. in litt. 2009,
pp. 2, 15). It is unknown whether the
type specimen was lost or destroyed, or
if it was ever returned to Peru (Flanagan
et al. in litt. 2009, p. 2). Today, there is
good indication that the type-specimen
was mislabeled as being collected in
Tumbes (Flanagan et al. in litt. 2009, pp.
2). Although the Tumbes Region has
been extensively surveyed for the
Peruvian plantcutter, including the
North-West Biosphere Reserve, there
have never been other collections in or
near the vicinity of Tumbes or other
evidence to suggest that the Peruvian
plantcutter ever occurred in the area
(Flanagan et al. in litt. 2009, p. 2). Thus,
it appears that the Peruvian plantcutter
never occurred in the Tumbes Region.
Researchers consider the reduction in
dry forest habitat to be the result of
historical human activities, including
extensive land clearing for agriculture,
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timber and firewood extraction,
charcoal production, and overgrazing.
These activities have led to the
reduction and severe fragmentation of
dry forest habitat today (BLI 2009a, pp.
2-3; Bridgewater et al. 2003, p. 132;
Flanagan et al. in litt. 2009, pp. 1-9;
Lanyon 1975, p. 443; Lopez et al. 2006,
p. 898; Pasiecznik et al. 2001, pp. 10, 75,
78, 95; Ridgely and Tudor 1994. p. 734;
Schulenberg et al. 2007, p. 488; Stotz et
al. 1998, p. 52) (see Factor A).
Current Range and Distribution
The current range of the Peruvian
plantcutter is approximately 1,892 mi2
(4,900 km2) (BLI 2009a, p. 1), which is
between 33 and 1, 804 ft (10 and 550 m)
above sea level and within the Peruvian
Regions of Piura, Lambayeque,
Cajamarca, La Libertad, and Ancash
(from north to south) (Flanagan et al. in
litt. 2009, pp. 14-15). The species’
reported range is an overestimate
because BirdLife International defines a
species’ range as the total area within its
extent of occurrence (see Current Range
and Distribution of the ash-breasted tittyrant) (BLI 2000, pp. 22, 27). The
Peruvian plantcutter’s current
distribution is severely fragmented and
distributed amongst small, widely
separated remnant patches of P. pallida
dry forest (BLI 2009a, pp. 2-3; Flanagan
et al. in litt. 2009, pp. 1-9; Ridgely and
Tudor 1994. p. 18), which are usually
heavily disturbed fragments of forest
(Bridgewater et al. 2003, p. 132).
Therefore, the species’ actual range is
smaller than this figure.
The Peruvian plantcutter is extirpated
from 11 of its 14 historical sites due to
loss of habitat or degradation of habitat
(Elton 2004, p. 1; Flanagan and More
2003, p. 5; Hinze 2004, p. 1). Depending
on habitat quality, it is estimated that
the Peruvian plantcutter requires
approximately 2.5 ac (1 ha) of habitat for
suitable food and nesting sites (Flanagan
and More 2003, p. 3; Flanagan et al. in
litt. 2009, p. 7). Although the Peruvian
plantcutter has been found in patches of
P. pallida dry forest habitat that are in
close proximity to agricultural lands,
tracks or roads, and human settlement
(Flanagan et al. in litt. 2009, pp. 2-7),
much of the available P. pallida dry
forest habitat is unoccupied (BLI 2000,
p. 401; Schulenberg et al. 2007, p. 488;
Snow 2004, p. 69; Walther 2004, p. 73).
Flanagan et al. (in litt. 2009, pp. 1-15)
recently completed a comprehensive
review of 53 locations where there have
been documented sightings of the
Peruvian plantcutter, of which the
authors determined 29 sites were extant.
Flanagan et al. (in litt. 2009, pp. 2-4, 14)
reported that 17 of the 22 documented
sites of the Peruvian plantcutter in the
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Piura Region are extant. In this region,
Talara Province contains the largest
concentration of intact P. pallida dry
forest habitat in northwest Peru and the
largest subpopulation of the Peruvian
plantcutter (BLI 2009a, p. 2; Flanagan et
al. in litt. 2009, p. 3; Flanagan and More
2003, p. 5; Walther 2004, p. 73).
Additionally, there are several other
documented sites of the Peruvian
plantcutter in the Piura Region (e.g.,
Manglares de San Pedro, Illescas
Peninsula, and Cerro Illescas) (BLI
2009c, p. 1; Flanagan et. al. in litt. 2009,
pp. 4, 14).
Flanagan et al. (in litt. 2009, pp. 4-5,
14) reported a total of 13 locations of the
Peruvian plantcutter in the Lambayeque
Region, of which 5 are considered
extant. Within the Region, there are four
important areas for the Peruvian
plantcutter:
´
(1) The Pomac Forest Historical
´
Sanctuary (Santuario Historico de
´
Bosque de Pomac), designated as a
protected archeological site in 2001, is
comprised of 14,547 ac (5,887 ha) of P.
pallida dry forest (BLI 2009e, p. 1;
Flanagan et al. in litt. 2009, p. 4). The
Sanctuary includes the archeological
site Batan Grande, an area comprised of
1,235 ac (500 ha) of P. pallida dry forest
(BLI 2009e, p. 1; Flanagan et al. in litt.
2009, p. 4).
(2) Near the small town of Rafan are
remnant patches of P. pallida dry forest,
encompassing approximately 3,706 ac
(1,500 ha) (BLI 2009f, p. 1). The Rafan
area has become a popular birding site
for the Peruvian plantcutter (BLI 2009f,
p. 1; Engblom 1998, p. 1).
(3) Murales Forest (Bosque de
Murales), comprised of P. pallida dry
forest, is a designated Archeological
Reserved Zone (BLI 2009a, p. 3;
Stattersfield et al. 2000, p. 402).
(4) Chaparri Ecological Reserve,
comprised of 85,033 ac (34,412 ha) with
P. pallida dry forest, is a communityowned and managed protected area
(Walther 2004, p. 73). The remaining
sites in the Lambayeque Region are
small remnant patches of P. pallida dry
forest and comprised of a few acres
(Flanagan et al. in litt. 2009, pp. 4-5;
Walther 2004, p. 73). The protected
areas are further discussed under
Factors A and D.
Flanagan et al. (in litt. 2009, pp. 5, 14)
reported one occupied site of the
Peruvian plantcutter in the Cajamarca
Region, consisting of approximately
14.8 ac (6 ha) of remnant P. pallida dry
´
forest in the Rıo Chicama Valley. Six of
the 12 known sites of the Peruvian
plantcutter in the La Libertad Region are
considered extant (Flanagan et al. in litt.
2009, pp. 5-6, 14). Each of these sites
consists of small patches of remnant P.
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pallida dry forest habitat (Walther 2004,
p. 73; Flanagan et al. in litt. 2009, pp.
5-6). Of the three known sites of the
Peruvian plantcutter in the Ancash
Region, only one is reported to be extant
(Flanagan et al. in litt. 2009, pp. 6, 14).
Additionally, the authors reported that
the two historical sites in the Lima
Region were also unoccupied in the
most recent survey (Flanagan et al. in
litt. 2009, pp. 7, 15).
In summary, the extant population of
the Peruvian plantcutter is comprised of
two disjunct subpopulations (BLI 2009g,
pp. 1-2; Walther 2004, p. 73), with
several smaller sites (Flanagan and More
2003, pp. 5-9; Flanagan et al. in litt.
2009, pp. 2-7; Walther 2004, p. 73;
Williams 2005, p. 1). Additional surveys
are needed to determine if available P.
pallida dry forest habitat is occupied by
the Peruvian plantcutter (Flanagan et al.
in litt. 2009, p. 7).
Population Estimates
There have been no rigorous
quantitative assessments of the Peruvian
plantcutter’s population size (Williams
2005, p. 1). The estimated extant
population size is between 500 and
1,000 individuals, and is comprised of
2 disjunct subpopulations (BLI 2009g,
pp. 1-2; Walther 2004, p. 73) and several
smaller sites (Flanagan and More 2003,
pp. 5-9; Flanagan et al. in litt. 2009, pp.
2-7; Walther 2004, p. 73; Williams 2005,
p. 1).
The northern subpopulation, located
in the Talara Province in Piura Region,
reportedly has between 400 and 600
individuals, or approximately 60 to 80
percent of the total population of the
Peruvian plantcutter (BLI 2009a, p. 2;
Snow 2004, p. 69; Walther 2004, p. 73;
Williams 2005, p. 1). The second
´
subpopulation, located at Pomac Forest
Historical Sanctuary (Lambayeque
Region), reportedly has 20 to 60
individuals (BLI 2009a, p. 2; BLI 2009e
2009, p. 1; Walther 2004, p. 73). The
smaller sites are estimated to consist of
a few individuals, up to 40 individuals
(Flanagan and More 2003, pp. 5-9;
Flanagan et al. in litt. 2009, pp. 2-7;
Walther 2004, p. 73; Williams 2005, p.
1).
The population estimate for the
Peruvian plantcutter—that is, the total
number of mature individuals—is not
the same as the effective population size
(i.e., the number of individuals that
actually contribute to the next
generation). Further, the subpopulation
structure and the extent of interbreeding
among the occurrences of the Peruvian
plantcutter are unknown. Although the
two large subpopulations and many of
the smaller occurrences of the Peruvian
plantcutter are widely separated (BLI
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2009a, pp. 2-3; Flanagan et al. in litt.
2009, pp. 1-9; Ridgely and Tudor 1994.
p. 18), there is insufficient information
to determine whether these occurrences
function as genetically isolated
subpopulations.
The Peruvian plantcutter has
experienced a population decline of
between 1 and 9 percent in the past 10
years, and this rate of decline is
predicted to continue (BLI 2009g, p. 1).
The population is considered to be
declining in close association with
continued habitat loss and degradation
of habitat (see Factors A and E) (BLI
2009a, pp. 1-3; BLI 2009g, pp. 1-3;
Ridgely and Tudor 1994, p. 18; Snow
2004, p. 69).
Conservation Status
The Peruvian plantcutter is
considered ‘‘endangered’’ by the
Peruvian Government under Supreme
Decree No. 034-2004-AG (2004, p.
276855). The IUCN considers the
Peruvian plantcutter to be
‘‘Endangered’’ because of ongoing
habitat destruction and degradation of
its small and severely fragmented range
(BLI 2000, p. 402; BLI 2009a, pp. 2-3;
BLI 2009g 2009, pp. 1-2). From 1996 to
2000, the IUCN considered the Peruvian
plantcutter to be ‘‘Critically
Endangered’’ (BLI 2009g, p. 1),
following changes to the IUCN listing
criteria in 2001. Experts have suggested
returning the the species to its previous
classification of ‘‘Critically
Endangered,’’ due to the numerous and
immediate threats to the species (Jeremy
N. M. Flanagan, Conservation Biologist,
Sullana, Peru, in litt. 2009 e-mail to
DSA, p. 1; Snow 2004, p. 69; Walther
2004, p. 74).
The Peruvian plantcutter occurs
within two protected areas in Peru. It
has been documented in the P. pallida
dry forest within the protected
´
archeological sites of the Pomac Forest
Historical Sanctuary (BLI 2009e, p. 1)
and Murales Forest (Walther 2004, p.
73).
Summary of Factors Affecting the
Peruvian plantcutter
A. The Present or Threatened
Destruction, Modification, or
Curtailment of the Species’ Habitat or
Range
The Peruvian plantcutter is
dependent upon undisturbed Prosopis
pallida dry forest with good floristic
diversity (Collar et al. 1992, p. 805;
Engblom 1998, p. 1; Flanagan and More
2003, p. 4). In northwest Peru, P. pallida
dry forest was historically contiguous,
covering approximately 2,703 m2 (7,000
km2) of the coastal lowland of northwest
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Peru (Ferreyera 1983, p. 248). There
were also extensive wooded stands of
small to medium trees of P. pallida,
Acacia spp., Capparis spp., and willows
(Salix spp.) along permanent lowland
rivers, which have since been cleared
for agricultural purposes (Lanyon 1975,
p. 443).
Today, with the exception of three
relatively large intact dry forests (i.e.,
Talara Province, Murales Forest, and
´
Pomac Forest Historical Sanctuary), the
vast majority of P. pallida dry forest,
arid lowland scrub, and riparian
vegetation has been reduced due to
human activities. Seasonally dry
tropical forests are considered the most
threatened of all major tropical forest
types (Janzen 1988, p. 130), with higher
threat levels than any other Neotropical
habitat (Stotz et al. 1996, p. 51). The
Peruvian plantcutter has been extirpated
from most of its historical sites due to
loss or degradation of habitat (Elton
2004, p. 1; Flanagan et. al. in litt. 2009,
pp. 1-15; Flanagan and More 2003, pp.
5-9; Snow 2004, p. 69). Current
information indicates that the vast
majority of occupied sites of the
Peruvian plantcutter are small, remnant,
disjunct patches of P. pallida dry forest
with each a few acres in size (BLI 2000,
p. 402; Flanagan et. al. in litt. 2009, pp.
2-7; Snow 2004, p. 69; Walther 2004, p.
73).
Habitat loss, conversion, and
degradation throughout the Peruvian
plantcutter’s range have been and
continue to occur as a result of human
activities (BLI 2000, p. 402; BLI 2009a,
p. 2; BLI 2009b, p. 1; BLI 2009e, p. 1;
BLI 2009f, p. 1; Bridgewater et al. 2003,
p. 132; Flanagan et al. in litt. 2009, p.
15; Lanyon 1975, p. 443; Schulenberg et
al. 2007, p. 488; Snow 2004, p. 69;
Walther 2004, p. 73), including:
(1) Clearcutting and burning of dry
forest for agriculture and other purposes
(BLI 2000, p. 402; BLI 2009a, p. 2; BLI
2009d, pp. 1-2; BLI 2009f, p. 1; BLI
2009g, p. 2; Bridgewater et al. 2003, p.
132; Collar et al. 1992, p. 806; Engblom
1998, p. 1; Flanagan et al. 2005, p. 244;
Ridgely and Tudor 1994, p. 734; Snow
2004, p. 69; Walther 2004, p. 73;
Williams 2005, p. 2);
(2) Extraction activities, including
cutting for timber, firewood, and
charcoal production (Best and Kessler
1995, p. 196; BLI 2000, p. 402; BLI
2009d, pp. 1-2; BLI 2009g, p. 2; Ridgely
and Tudor 1994, p. 734; Rodriguez et al.
2007, p. 269; Snow 2004, p. 69;
Williams 2005, p. 1);
(3) Grazing by goats of P. pallida dry
forests, and arid scrub and riparian
vegetation (Capra species) (BLI 2000, p.
402; BLI 2009a, p. 2; BLI 2009b, p. 1;
BLI 2009d, pp. 1-2; Best and Kessler
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1995, p. 196; More 2002, p. 37; Snow
2004, p. 69);
(4) Human encroachment (FernandezBaca et al. 2007, p. 45); and
(5) Unpredictable climate fluctuations
that exacerbate human activities and
encourage further habitat destruction
(Block and Richter 2007, p. 1; Jetz et al.
2007, p. 1211; Richter 2005, p. 26).
The vast majority of P. pallida dry
forest habitat has been converted to
commercial agricultural production,
which is the primary factor in the
historical decline of the Peruvian
plantcutter (BLI 2000, p. 402; BLI 2009a,
p. 2; BLI 2009d, pp. 1-2; BLI 2009f, p.
1; Collar et al. 1992, p. 806; Engblom
1998, p. 1; Ridgely and Tudor 1994, p.
734; Snow 2004, p. 69; Walther 2004, p.
73; Williams 2005, p. 2). Agriculture in
the coastal lowlands of northwest Peru
consists of modern large, privately
owned farms and large cooperatives that
primarily produce crops (e.g.,
sugarcane, cotton, rice) for export
(Lanyon 1975, p. 443; Roethke 2003, pp.
58-59).
Continual habitat destruction and
degradation of the dry forest is mostly
due to firewood cutting and charcoal
production. Prosopis pallida is the
dominant tree of the dry forest habitat,
and is highly sought after because the
wood provides an important source of
high-quality cooking fuel (Brewbaker
1987, p. 1; Pasiecznik et al. 2001, p. 75).
Throughout the Peruvian plantcutter’s
range, whole trees, branches, and roots
of P. pallida are cut for firewood and
production of charcoal, which is used
for cooking fuel in homes, restaurants,
and businesses that use brick kilns, both
locally and in urban centers (Flanagan
et al. in litt. 2009, p. 7). Wood of P.
pallida is also used for construction and
fence posts (Pasiecznik et al. 2001, p.
78). Additionally, roots of older P.
pallida trees are used in wooden art
crafts (BLI 2009a, p. 2).
Talara Province (in Piura Region)
contains the largest remaining intact P.
pallida dry forest in northwest Peru,
encompassing approximately 123,553 ac
(50,000 ha) (Flanagan et al. in litt. 2009,
pp. 2-3; Flanagan and More 2003, p. 5;
Walther 2004, p. 73). The Province also
has the largest subpopulation of the
Peruvian plantcutter, reportedly
between 400 and 600 individuals or
approximately 60 to 80 percent of the
total population (BLI 2009a, p. 2; Elton
2004, pp. 3-4; Snow 2004, p. 69;
Walther 2004, p. 73; Williams 2005, p.
1). Until recently, a large portion of the
Province, including P. pallida dry forest
habitat, was owned by the State-owned
petroleum company PetroPeru, which
prohibited access to approximately
90,000 ac (36,422 ha). Under the
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management of PetroPeru, the P. pallida
dry forest was not subject to the same
habitat destruction and degradation
activities (e.g., clearing of trees,
firewood cutting and charcoal
production) as other dry forest habitat
areas (Elton 2004, pp. 3-4; Hinze 2004,
p. 1). Recently, the land was reverted to
the Peruvian Government, and it is
unclear whether the government plans
to issue private concessions as in other
areas of the Province (Elton 2004, p. 4).
Consequently there have been recent
efforts, including a formal petition to
the Peruvian Government, to create a
12,000 to 24,710-ac (4,856- to 10,000-ha)
protected reserve for the northern
subpopulation of the Peruvian
plantcutter (Elton 2004, p. 4; Walther
2004, p. 73). However, the government
has not designated such a reserve for the
species (Elton 2004, p. 4; Williams 2005,
p. 3).
Habitat destruction and degradation
of P. pallida dry forest, including
firewood cutting and charcoal
production, is ongoing in the Talara
Province, including on the land
previously owned by PetroPeru and an
area identified as the Talara Important
Birding Area by BirdLife International
(Flanagan in litt. 2009, p. 1). Since 2005,
there has been extensive cutting and
clearing of P. pallida trees for fuel to
cook and dry Humboldt giant squid
(Dosidicus gigas) carcasses (Flanagan et
al. in litt. 2009, p. 8). The most
important commercial fishery of the
Humboldt giant squid occurs along the
coast of Peru (UNEP 2006, p. 33;
Zeidberg and Robison, 2007, p. 12, 948).
Harvested carcasses are transported by
truck from the Talara port to recently
cleared areas in the dry forest, where
they are boiled and dried (Flanagan et
al. in litt. 2009, p. 8). Therefore, this
fishery not only adds to the collection
pressure on Prosopis species for use as
fuel, but also adds to forest clearing in
the area. Another relatively new
demand for P. pallida firewood is
associated with the illegal extraction of
crude oil from above-ground pipes in
the Talara Province. The stolen oil is
distilled by heating it with firewood
(Flanagan et al. in litt. 2009, p. 8).
Capparis scabrida (no common name,
but locally known as ‘‘sapote’’) is a tree
that occurs with P. pallida and is also
a food source for the Peruvian
plantcutter. Although the tree is listed
as ‘‘Critically Endangered’’ by the
Peruvian Government, the highly sought
after wood is cut to produce handicrafts
for the local, national, and international
market, as well as for firewood and
charcoal production (Rodriguez et al.
2007, p. 269).
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Habitat alteration is also caused by
grazing goats, which remove or heavily
degrade the shrubs and trees (BLI 2000,
p. 402; BLI 2009a, p. 2; Elton 2004, pp.
3-4; Snow 2004, p. 69; Williams 2005,
p 2). The seed pods and leaves of P.
pallida provide highly nutritious fodder
for goats (Brewbaker 1987, pp. 1-2;
Pasiecznik et al. 2001, p. 95). Goats
roam freely and graze on trees and
shrubs, particularly lower branches
close to ground which are preferred by
the Peruvian plantcutter for foraging
and nesting (Elton 2004, pp. 3-4; Snow
2004, p. 50; Williams 2005, p 2).
Human encroachment and
concomitant increasing human
population pressures exacerbate the
destructive effects of ongoing human
activities (e.g., clearing of P. pallida dry
forest, firewood cutting, and charcoal
production) throughout the Peruvian
plantcutter’s range. Although the coastal
lowlands represent only about 10
percent of country’s total territory, more
urban centers are located on the coast,
which represent approximately 52
percent of the total population of Peru
(Fernandez-Baca et al. 2007, p. 45).
Larger concentrations of people put
greater demand on the natural resources
in the area, which spurs additional
habitat destruction and increases
infrastructure development that further
facilitates encroachment.
Peruvian plantcutters are also
impacted by unpredictable climate
fluctuations that exacerbate the effects
of habitat fragmentation. Unpredictable
climate fluctuations are more fully
described under the Factor A analysis of
the ash-breasted tit-tyrant and are
summarized here. Changes in weather
˜
patterns, such as ENSO cycles (El Nino
˜
and La Nina events), tend to increase
precipitation in normally dry areas, and
decrease precipitation in normally wet
areas (Holmgren et al. 2001, p. 89; TAO
Project n.d., p. 1) while intensifying the
effects of habitat fragmentation on the
decline of a species (England 2000, p.
86; Holmgren et al. 2001, p. 89; Jetz et
al. 2007, pp. 1211, 1213; Mora et al.
2007, p. 1027; Parmesan and Mathews
2005, p. 334; Plumart 2007, pp. 1-2;
Timmermann 1999, p. 694), especially
for narrow endemics (Jetz et al. 2007, p.
1213) such as the Peruvian plantcutter.
The arid terrestrial ecosystem of
Northwest Peru, where the Peruvian
plantcutter occurs, is strongly
influenced by the ENSO cycle
(Rodriguez et al 2005, p. 1), which can
have profound and long-lasting effects
(Holmgren et al. 2006a, p. 87; Mooers et
al. 2007, p. 2). The amount of rainfall
˜
during an El Nino year can be more than
25 times greater than during normal
years in northern Peru (Holmgren et al.
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2006a, p. 90; Rodriguez et al 2005, p. 2).
˜
El Nino events are important triggers for
regeneration of plants in semiarid
ecosystems, particularly the dry forest of
northwest Peru (Holmgren et al. 2006a,
p. 88; Lopez et al. 2006, p. 903;
´
Rodrıguez et al. 2005, pp. 2-3). During
˜
El Nino events, plant communities and
barren lands are transformed into lush
vegetation, as seeds germinate and grow
more quickly in response to increased
rainfall (Holmgren et al. 2006a, p. 88;
Holmgren et al. 2006b, pp. 2-8;
´
Rodrıguez et al. 2005, pp. 1-6). Over the
last 20 years, recruitment of P. pallida
in northwest Peru doubled during El
˜
Nino years, when compared to non-El
˜
Nino years (Holmgren et al. 2006b, p. 7).
However, the abundant supply of
vegetation encourages locals to expand
goat breeding operations, which results
in overgrazing by goats and further land
degradation (Richter 2005, p. 26).
ENSO cycles increase the risk of fire
˜
because El Nino events are often
followed by years of extremely dry
weather (Block and Richter 2007, p. 1),
and accumulated biomass dries and
adds to the fuel load in the dry season
(Block and Richter 2007, p. 1; Power et
al. 2007, p. 898). Evidence suggests that
the fire cycle in Peru has shortened,
particularly coastal Peru and west of the
Andes (Power et al. 2007, pp. 897-898),
which can have broad ecological
consequences (Block and Richter 2007,
p. 1; Power et al. 2007, p. 898).
According to Block and Richter (2007,
p. 1), P. pallida dry forest and Capparis
spp. scrublands in northwest Peru
would likely experience a long-term
change in plant species composition
that favor aggressive, annual, non-native
weedy plant species (Richter 2005, p.
26). An accelerated fire cycle would
further exacerbate changes in species
composition that hinder long-lived
perennial, native plant species, such as
Prosopis species, upon which the
Peruvian plantcutter relies.
ENSO cycles are ongoing, having
occurred several times within the last
decade (NWS 2009, p. 2), and evidence
suggests that ENSO cycles have already
increased in periodicity and severity
(Richter 2005, pp. 24-25; Timmermann
1999, p. 694), which will exacerbate the
negative impacts of habitat destruction
on a species. It is predicted that, by
2050, approximately 11 to 16 percent of
existing land is likely to be unsuitable
for this species due to climate change;
and, by 2100, it is predicted that about
24 to 35 percent of the species’ range is
likely to be lost as a direct result of
global climate change (Jetz et al. 2007,
p. 81).
Habitat destruction is often caused by
a combination of human activities that
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promote habitat degradation. In
Lambayeque Region, a 3,706-ac (1,500ha) section of remnant P. pallida dry
forest is under continual threat from
human activities, including conversion
to agriculture, firewood cutting and
charcoal production, and grazing by
goats. This area may support between 20
and 40 Peruvian plantcutters (BLI 2009f,
p. 1; Walther 2004, p. 73). In the 1990s,
a significant portion of this dry forest
was converted to sugarcane fields
(Engblom in litt. 1998, p. 1; Snow 2004,
p. 69; Walther 2004, p. 73; Williams
2005, p. 2). Within Piura and
Lambayeque Regions, threats to the dry
forest habitat include conversion to
agriculture, firewood and timber
cutting, and grazing by goats (BLI
2009d, pp. 1-2). Habitat destruction and
alteration also occurs within two
protected areas where the Peruvian
plantcutter occurs (in Lambayeque
´
Region), Pomac Forest Historical
Sanctuary (Andean Air Mail and
Peruvian Times 2009, p. 1; Flanagan et
al. in litt. 2009, pp. 7-8; Williams 2005,
p. 1), and the Murales Forest (BLI 2000,
p. 402; BLI 2009a, p. 3; Stattersfield et
al. 2000, p. 402; Walther 2004, p. 73).
Habitat destruction and alteration
activities within these protected areas
are discussed under Factor D.
Experts consider the population of
this range-restricted endemic species to
be declining in close association with
the continued habitat loss and
degradation (BLI 2000, p. 401; BLI
2009a, pp. 1-2; BLI 2009g, pp. 1-3), and
that the effects are higher in dry forest
habitat than in any other Neotropical
habitat (Stotz et al. 1998, p. 51).
Summary of Factor A
The Peruvian plantcutter is
dependent upon intact P. pallida dry
forest with low-hanging branches and
high floristic diversity, and associated
arid lowland scrub and riparian
vegetation. Prosopis pallida dry forest
habitat, as well as arid lowland scrub
and riparian shrub habitats, throughout
Peruvian plantcutter’s range have been
and continue to be altered and
destroyed as a result of human
activities, including conversion to
agriculture; timber and firewood cutting
and charcoal production; grazing of
goats; and human encroachment. Extant
P. pallida dry forest today consists of
remnant, disjunct patches of woodlands,
which are heavily disturbed and under
continued threat of degradation by
human activities. Although observations
suggest that this dry forest–dependent
species is able to occupy very small
remnant patches of dry forest with lowhanging branches and floristic diversity,
and is able to persist to some degree
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633
near developed lands, many of these
sites are approaching the lower
threshold of the species’ ecological
requirements. This species has been
extirpated from most of its historical
sites due to loss or degradation of
habitat. Additionally, many of the
extant occupied sites are separated by
great distances, which may lead to
genetic isolation of the species (See
Factor E). The same activities that
caused the historical decline in this
species are ongoing today. These
habitat-altering activities are
compounded by unexpected climate
fluctuations, especially for narrow
endemics, such as the Peruvian
plantcutter. Excessive rains that are
˜
accompanied by El Nino events induce
further habitat destruction, as people
take advantage of better grazing and
growing climate conditions. Climate
models predict that this species’ habitat
will continue to decline. Destruction of
the remaining P. pallida dry forest
fragments in Peru continues to reduce
the quantity, quality, distribution, and
regeneration of remaining patches of dry
forest. Human activities that degrade,
alter, and destroy habitat are ongoing
throughout the species’ range, including
within the one protected area (Factor D).
Therefore, we find that destruction and
modification of habitat are threats to the
continued existence of Peruvian
plantcutter throughout its range.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
We are not aware of any information
currently available that indicates that
overutilization of Peruvian plantcutter
for commercial, recreation, scientific, or
education purposes has occurred or is
occurring at this time. As a result, we
are not considering overutilization to be
a threat to the continued existence of
the Peruvian plantcutter.
C. Disease or Predation
We are not aware of any scientific or
commercial information that indicates
disease or predation poses a threat to
the Peruvian plantcutter. As a result, we
do not consider disease or predation to
be a threat to the continued existence of
the Peruvian plantcutter.
D. The Inadequacy of Existing
Regulatory Mechanisms
The Peruvian plantcutter is
considered ‘‘endangered’’ by the
Peruvian Government under Supreme
Decree No. 034-2004-AG (2004, p.
276854). This Decree prohibits hunting,
take, transport, and trade of protected
species, except as permitted by
regulation. As hunting, taking, or trade
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do not currently threaten the Peruvian
plantcutter (Factor B), this regulation
does not mitigate any current threats to
the species.
Peru has several categories of national
habitat protection, which were
described above as part of Factor D for
the ash-breasted tit-tyrant (BLI 2008, p.
´
1; IUCN 1994, p. 2; Rodrıguez and
Young 2000, p. 330). The Peruvian
plantcutter is known to occur within
two Peruvian nationally protected areas,
´
the Pomac Forest Historical Sanctuary
and the Murales Forest (both
´
Lambayeque Region). The Pomac Forest
Historical Sanctuary supports an
estimated 20 to 60 Peruvian plantcutters
(BLI 2009a, p. 2; BLI 2009e, p. 1;
Walther 2004, p. 73). Resources within
´
the Pomac Forest Historical Sanctuary
are managed for the preservation of the
archeological site, P. pallida dry forest,
and wildlife species. However, habitat
destruction and alteration, including
illegal forest clearing for farming, timber
and firewood cutting, and grazing,
continually threaten the Sanctuary
(Williams 2005, p. 1). For 8 years, more
than 250 families illegally occupied and
farmed land in the Sanctuary. During
the illegal occupancy, the inhabitants
logged 4,942 ac (2,000 ha) of P. pallida
trees for firewood and burned many
other trees for charcoal production
(Andean Air Mail and Peruvian Times
2009, p. 1). The logged forest was
subsequently converted to agricultural
crops, while remaining forest habitat
was continually degraded by firewood
cutting, charcoal production, and
grazing of goats (Flanagan et al. in litt.
2009, p. 8.). In January 2009, the
government forcibly removed the
inhabitants, but it is too soon to
determine the effect that habitat
destruction has had on the suitability of
the habitat for the Peruvian plantcutter.
There is insufficient information to
conclude that recent efforts to stop the
illegal human occupancy of the area
will have a positive impact on the
species or remaining habitat within the
protected area. Therefore, any
protections afforded by this Sanctuary
has not mitigated the threats to the
species from ongoing habitat loss and
associated population decline (Factor
A).
The Murales Forest is a designated
Archeological Reserved Zone (BLI 2000,
p. 401; BLI 2009a, p. 3; Stattersfield et
al. 2000, p. 402), and supports a
declining population of Peruvian
plantcutters. According to Peruvian law,
designation as a Reserved Zone allows
for temporary protection while further
study is under way to determine the
area’s importance (BLI 2008, p. 1;
´
Rodrıguez and Young 2000, p. 330).
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Although strict monitoring has
protected some habitat (BLI 2009a, p. 3),
the actual dry forest is not protected. In
1999, land rights to sections of the forest
were sold for agricultural conversion,
and government intervention has been
necessary to prevent further sales of
land for conversion to agriculture (BLI
2009a, p. 3). In 1999, Murales Forest
and adjacent areas contained
approximately 1,221 ac (494 ha) of
habitat, and reportedly supported 140
Peruvian plantcutters (BLI 2000, p. 402).
In 2004, the population was estimated
to be 20 to 40 individuals (Walther
2004, p. 73). Therefore, the presence of
the Peruvian plantcutter within this
protected area has not mitigated the
threats to the species from ongoing
habitat loss and associated population
decline (Factor A).
Incidences of illegal activity that
occur throughout the species’ range also
impact the Peruvian plantcutter.
Ongoing firewood cutting and charcoal
production degrades the small amount
of remaining dry forest habitat
throughout the species’ range (BLI
2009d, pp. 1-2; BLI 2009g, p. 2; Ridgely
and Tudor 1994, p. 734; Rodriguez et al.
2007, p. 269; Snow 2004, p. 69;
Williams 2005, p. 1). In Talara Province
(Piura Region), a recent increase in the
illegal extraction of crude oil has
generated further demand for P. pallida
firewood, which is used as fuel to heatdistill the oil. According to Flanagan et
al. (in litt. 2009, p. 8), enforcement to
combat this illegal activity is difficult.
Therefore, existing laws are ineffective
at mitigating the ongoing threat of
habitat destruction (Factor A).
Summary of Factor D
Peru has enacted various laws and
regulatory mechanisms to protect and
manage wildlife and their habitats. The
Peruvian plantcutter is ‘‘endangered’’
under Peruvian law and occurs within
two protected areas in Peru. As
discussed under Factor A, the Peruvian
plantcutter prefers P. pallida dry forest.
This habitat has been drastically
reduced and remaining habitat is
comprised of small remnant patches of
dry forest that are separated by great
distances. Habitat throughout the
species’ range has been and continues to
be destroyed and altered as a result of
human activities, primarily conversion
to agriculture, and continual
degradation by timber and firewood
harvest and charcoal production, and
grazing by goats. These activities are
ongoing, including within protected
areas and despite the species’
‘‘endangered’’ status, indicating that the
laws governing wildlife and habitat
protection in Peru are either inadequate
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or inadequately enforced to protect the
species or to mitigate ongoing habitat
loss (Factor A) and population declines
(Factor E). Therefore, we find that the
existing regulatory mechanisms are
inadequate to mitigate the current
threats to the continued existence of the
Peruvian plantcutter throughout its
range.
E. Other Natural or Manmade Factors
Affecting the Continued Existence of the
Species
An additional factor that affects the
continued existence of the Peruvian
plantcutter is the species’ small
population size. BirdLife International
has placed the Peruvian plantcutter in
the population category of between 500
and 1,000 individuals (BLI 2009g, p. 1).
The species’ population size is not
characterized as ‘‘small’’ in published
literature and there is insufficient
information on similar species (i.e., the
other South American plantcutters) to
understand whether the Peruvian
plancutter’s population size is small
relative to other plantcutters. However,
there are several indications that this
number of individuals represents a
small population.
First, the Peruvian plantcutter’s
population size—which is defined by
BirdLife International as the total
number of mature individuals—is not
the same as the effective population
size—the number of individuals that
actually contribute to the next
generation (Shaffer 1981, pp. 132-133;
´
Soule 1980, pp. 160-162). Not all
individuals in a population will
contribute to reproduction each year.
Therefore, the estimated population size
for the Peruvian plantcutter is an
overestimate of the species’ effective
population size. Moreover, the
subpopulation structure and the extent
of interbreeding among the occurrences
of the Peruvian plantcutter are unknown
(see Population Estimates). If further
research indicates that species does not
breed as a single population, its
effective population size would be
further reduced.
Second, the extant Peruvian
plantcutter population occurs primarily
in 2 disjunct subpopulations—Talara
´
and Pomac Forest Historical Sanctuary
(BLI 2009g, pp. 1-2; Walther 2004, p.
73)—and in several smaller sites
(Flanagan and More 2003, pp. 5-9;
Flanagan et al. in litt. 2009, pp. 2-7;
Walther 2004, p. 73; Williams 2005, p.
´
1). Talara and Pomac Forest Historical
Sanctuary are approximately 160 mi
(257 km) apart (FCC (Federal
Communications Commission)-Audio
Division 2009). The Peruvian
plantcutter is dependent upon
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undisturbed Prosopis pallida dry forest
with good floristic diversity (Collar et al.
1992, p. 805; Engblom 1998, p. 1;
Flanagan and More 2003, p. 4). Its
habitat is heavily degraded and
localities are small, severely fragmented,
and widely separated (BLI 2009a, pp. 23; Bridgewater et al. 2003, p. 132;
Flanagan et al. in litt. 2009, pp. 1-9;
Ridgely and Tudor 1994. p. 18) (see
Factor A). It is possible that the distance
between patches of suitable habitat is
too great to support interbreeding
between localities, so that the extant
occurrences of this species would
function as genetically isolated
subpopulations.
For these reasons, we consider the
Peruvian plantcutter’s current estimated
population to be small and, as such, this
species is subject to the risks associated
with small population sizes. Small
population size renders a species
vulnerable to any of several risks,
including inbreeding depression, loss of
genetic variation, and accumulation of
new mutations. Inbreeding can have
individual or population-level
consequences either by increasing the
phenotypic expression (the outward
appearance or observable structure,
function, or behavior of a living
organism) of recessive, deleterious
alleles or by reducing the overall fitness
of individuals in the population
(Charlesworth and Charlesworth 1987,
p. 231; Shaffer 1981, p. 131). Small,
isolated wildlife populations are also
more susceptible to environmental
fluctuations and demographic shifts
(Pimm et al. 1988, pp. 757, 773-775;
Shaffer 1981, p. 131), such as reduced
reproductive success of individuals and
chance disequilibrium of sex ratios.
Species tend to have a higher risk of
extinction if they occupy a small
geographic range and occur at low
density (Purvis et al. 2000, p. 1949).
The Peruvian plantcutter has
experienced a population decline of
between 1 and 9 percent in the past 10
years due to habitat loss and this
decline is expected to continue in close
association with continued habitat loss
and degradation (see Factor A) (BLI
2009a, pp. 1-3; BLI 2009g, pp. 1-3;
Ridgely and Tudor 1994, p. 18; Snow
2004, p. 69). Extinction risk is
heightened in small, declining
populations by an increased
vulnerability to the loss of genetic
variation due to inbreeding depression
and genetic drift. This, in turn,
compromises a species’ ability to adapt
genetically to changing environments
(Frankham 1996, p. 1507) and reduces
fitness, thus increasing extinction risk
(Reed and Frankham 2003, pp. 233-234).
Once a population is reduced below a
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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).
Complications arising from the
species’ small population size are
exacerbated by its fragmented
distribution. Because remaining habitat
patches are small, heavily degraded, and
widely separated, the Peruvian
plantcutter’s current distribution is
highly restricted and severely
fragmented (BLI 2009a, pp. 2-3;
Bridgewater et al. 2003, p. 132;
Flanagan et al. in litt. 2009, pp. 1-9;
Ridgely and Tudor 1994. p. 18). Habitat
fragmentation can cause genetic
isolation and heighten the risks to the
species associated with short-term
genetic viability. A species’ small
population size, combined with a
restricted and fragmented distribution,
exacerbates a species’ vulnerability to
adverse natural events (e.g., genetic,
demographic, or environmental) and
manmade activities (e.g., land clearing,
timber and firewood cutting, and
grazing by goats) (Holsinger 2000, pp.
64-65; Primack 1998, pp. 279-308;
Young and Clarke 2000, pp. 361-366).
Summary of Factor E
The Peruvian plantcutter has a small
population size that renders it
vulnerable to genetic risks that
negatively impact the species’ viability.
The species occurs primarily in two
disjunct subpopulations, and remaining
habitat is highly fragmented and
continues to be altered by human
activities (Factor A). Its small
population size, combined with its
restricted and fragmented range,
increases the Peruvian plantcutter’s
vulnerability to extinction, through
demographic or environmental
fluctuations. Based on its small
population size and fragmented
distribution, we have determined that
the Peruvian plantcutter is particularly
vulnerable to the threat of adverse
natural events (e.g., genetic,
demographic, or environmental) and
human activities (e.g., deforestation,
habitat alteration, and infrastructure
development) that destroy individuals
and their habitat. The genetic and
demographic risks associated with small
population sizes are exacerbated by
ongoing human activities that continue
to curtail the species’ habitat throughout
its range. The species’ population has
declined and is predicted to continue
declining commensurate with ongoing
habitat loss (Factor A) and we consider
that the risks associated with small
population size will continue to impact
this species and may accelerate, if
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635
habitat destruction continues unabated.
Therefore, we find that the species’
small population size, in concert with
its fragmented distribution and its
heightened vulnerability to adverse
natural events and manmade activities,
are threats to the continued existence of
the Peruvian plantcutter throughout its
range.
Status Determination for the Peruvian
Plantcutter
The Peruvian plantcutter, a small,
herbivorous bird, is endemic to semiarid
lowland dry forests of coastal northwest
Peru. The species’ primary habitat is
Prosopis pallida dry forest between 33
and 1, 804 ft (10 and 550 m) above sea
level. The species is dependent on yearround availability of high-quality food
and is known primarily in two disjunct
subpopulations, with several smaller,
widely separated sites in the Regions of
Piura, Lambayeque, Cajamarca, La
Libertad, and Ancash (from north to
south). The actual range of the Peruvian
plantcutter is smaller than the reported
range of 1,892 mi2 (4,900 km2), given
the severely fragmented distribution of
the species. The species’ population size
is estimated to be 500-1,000 individuals.
We have carefully assessed the best
available scientific and commercial
information regarding the past, present,
and potential future threats faced by the
Peruvian plantcutter and have
concluded that there are three primary
factors that threaten the continued
existence of the Peruvian plantcutter: (1)
Habitat destruction, fragmentation, and
degradation; (2) limited size and
isolation of remaining populations; and
(3) inadequate regulatory mechanisms.
Human activities that degrade, alter,
and destroy habitat are ongoing
throughout the Peruvian plantcutter’s
range. Widespread land conversion to
agriculture has removed the vast
majority of P. pallida dry forest habitat
throughout the range of the Peruvian
plantcutter. Peruvian plantcutter habitat
continues to be altered by human
activities, such as timber and firewood
cutting, burning, and grazing, which
result in the continued degradation,
conversion, and destruction of habitat
and reduce the quantity, quality,
distribution, and regeneration of
remaining dry forest habitat. Current
research indicates that narrow
endemics, such as the Peruvian
plantcutter, are especially susceptible to
climate fluctuations, because of the
synergistic effect these fluctuations have
on declining populations that are also
experiencing range reductions due to
human activities. Remaining habitat is
highly fragmented and disjunct,
separated by large areas of converted
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land (e.g., agriculture, urban areas) and
sparse vegetation (e.g., Sechura Desert),
and excessive rains induce further
habitat destruction and prevent
regeneration, as people take advantage
of better grazing and growing climate
conditions.
The Peruvian plantcutter’s population
is small, rendering the species
particularly vulnerable to the threat of
adverse natural events (e.g., genetic,
demographic, or environmental) and
human activities (e.g., deforestation and
firewood extraction) that destroy
individuals and their habitat. Ongoing
human activities that cause habitat loss
throughout the species’ range exacerbate
the genetic and demographic risks
associated with small population sizes
(Factor E). The population has declined
1–9 percent in the past 10 years (see
Population Estimates), in association
with continued habitat loss (Factor A).
Habitat loss was a factor in this species’
historical decline (see Historical Range
and Distribution)—the Peruvian
plantcutter has been extirpated from 11
of its 14 historical sites (see Current
Range and Distribution)—and the
species is considered to be declining
today in association with the continued
reduction in habitat (Factors A and E).
Moreover, current research indicates
that narrow endemics, such as the
Peruvian plantcutter, are especially
susceptible to climate fluctuations
because of the synergistic effect these
fluctuations have on declining
populations that are also experiencing
range reductions due to human
activities (Factor A).
Despite the species’ endangered status
in Peru and its occurrence within two
protected areas (Factor D), habitat loss
and degradation continue throughout
the Peruvian plantcutter’s habitat
(Factor A). Therefore, regulatory
mechanisms are either inadequate or
ineffective at mitigating the existing
threats to the Peruvian plantcutter and
its habitat (Factor D).
Section 3 of the Act defines an
‘‘endangered species’’ as ‘‘any species
which is in danger of extinction
throughout all or a significant portion of
its range’’ and a ‘‘threatened species’’ as
‘‘any species which is likely to become
an endangered species within the
foreseeable future throughout all or a
significant portion of its range.’’ Based
on the immediate and ongoing
significant threats to the Peruvian
plantcutter throughout its entire range,
as described above, we determine that
the Peruvian plantcutter is in danger of
extinction throughout all of its range.
Therefore, on the basis of the best
available scientific and commercial
information, we are proposing to list the
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Peruvian plantcutter as an endangered
species throughout all of its range.
V. Royal cinclodes (Cinclodes
aricomae)
Species Description
The royal cinclodes, also known as
‘‘churrete real’’ and ‘‘remolinera real,’’
is a large-billed ovenbird in the
Furnaridae family that is native to highaltitude woodlands of the Bolivian and
Peruvian Andes (BLI 2009i, pp. 1-2; del
Hoyo et al. 2003, p. 253; InfoNatura
2007, p. 1; Supreme Decree No. 0342004-AG 2004, p. 27685; Valqui 2000, p.
104). The adult is nearly 8 in (20 cm)
in length, with dark chocolate-brown
plumage on the upperparts, with a
darker crown and a buff-colored area
above the eyes. The throat is buffcolored, and the remaining underparts
are gray-brown to buff-white. The wings
are dark with prominent edging that
forms a distinctive wing-bar in flight.
The large, dark bill is slightly curved at
the tip (BLI 2009i, p. 1).
Taxonomy
When the species was first
taxonomically described, the royal
cinclodes was placed in the genus
Upucerthia (Carriker 1932, pp. 1-2) and
was then transferred to Geositta as a
subspecies (Geositta excelsior aricomae)
(Vaurie 1980, p. 14). Later, it was
transferred to the genus Cinclodes,
where it was considered a race or
subspecies of the stout-billed cinclodes
(Cinclodes excelsior) until recently (BLI
˚
2009i, p. 1; Fjeldsa and Krabbe 1990,
pp. 337-338; Vaurie 1980, p. 15). The
royal cinclodes is now considered a
distinct species (C. aricomae) based on
differences in its habitat, morphology,
and genetic distance (Chesser 2004, p.
763; del Hoyo et al. 2003, p. 253).
Therefore, we accept the species as
Cinclodes aricomae, which also follows
ITIS (2009, p. 1).
Habitat and Life History
The royal cinclodes is restricted to
moist and mossy habitat amidst the
steep, rocky slopes of semihumid
Polylepis or Polylepis - Gynoxys
woodlands, where the species is found
at elevations between 11,483 and 12,092
ft (3,500 and 4,600 m) (BLI 2000, p. 345;
BLI 2009i, p. 2; Collar et al. 1992, p.
588; del Hoyo et al. 2003, p. 253). The
characteristics of Polylepis habitat were
described above as part of the Habitat
and Life History of the ash-breasted tittyrant (Aucca and Ramsay 2005, p. 1;
Chutas et al. 2008, p. 3; De la Via 2004,
p. 10; IPNI 2009, p. 1; Kessler 1998, p.
1; Kessler and Schmidt-Lebuhn 2006,
pp. 1-2; Purcell et al. 2004, p. 455). The
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royal cinclodes prefers dense
woodlands (BLI 2000, p. 345; BLI 2009i,
p. 2; Collar et al. 1992, p. 588; del Hoyo
et al. 2003, p. 253), with more closed
canopies that provide habitat for more
lush moss growth (Engblom et al. 2002,
p. 57). The moss-laden vegetation and
shaded understory harbor a rich
diversity of insects, making good
feeding grounds for insectivorous birds
(De la Via 2004, p. 10) such as the royal
cinclodes (del Hoyo et al. 2003, p. 253;
Engblom et al. 2002, p. 57). In Bolivia,
the royal cinclodes has been observed
only in P. pepei forests, but it is found
amongst a greater variety of Polylepis
species in Peru (Chutas et al. 2008, p.
´
16; I. Gomez, National Museum of
National History-Ornithology SectionBolivian Fauna Collection, La Paz,
Bolivia, e-mail to Division of Scientific
Authority, in litt. December 4, 2007, p.
1).
Information on the ecology and
breeding behavior of royal cinclodes is
limited. The species’ feeding territory
ranges from 7 to 10 ac (3 to 4 ha) (del
Hoyo et al. 2003, p. 253; Engblom et al.
2002, p. 57). Breeding pairs may occupy
smaller, 2.5-ac (2-ha) territories (Chutas
2007, p. 7). The royal cinclodes is
described as ‘‘nervous’’ and is easily
disturbed by humans (Engblom et al.
2002, p. 57). The breeding season
probably begins in December, but
territorialism among pairs can be seen
in austral winter (June-August) (BLI
2000, p. 345; del Hoyo et al. 2003, p.
253). Cinclodes species construct
burrows or use natural cavities,
crevices, or rodent burrows for nesting
˚
(Fjeldsa and Krabbe 1990, p. 337; Vaurie
1980, pp. 30, 34). The royal cinclodes’
clutch size may be similar to that of the
closely-related stout-billed cinclodes (C.
excelsior), which, according to Graves
and Arango (1988, p. 252), is two eggs
per clutch.
Its diet consists primarily of
invertebrates, sometimes seeds, and
occasionally small vertebrates (small
frogs) (del Hoyo et al. 2003, p. 253). The
royal cinclodes forages, solitary or in
pairs, by probing through moss and
debris on the forest floor (BLI 2000, p.
345; Collar et al. 1992, p. 589; del Hoyo
˚
et al. 2003, p. 253; Fjeldsa 2002b, p. 9).
This ground-feeding strategy generally
requires a relatively large territory and
may also facilitate interbreeding
amongst groups located on adjoining
mountain peaks when the species likely
descends the mountains during periods
of snow cover (Engblom et al. 2002, p.
57).
Historical Range and Distribution
The royal cinclodes may once have
been locally common and distributed
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across most of central to southern Peru
and into the Bolivian highlands, in
once-contiguous expanses of Polylepis
forests above 9,843 ft (3,000 m) (BLI
˚
2000, p. 345; BLI 2009i, p. 1; Fjeldsa
2002a, pp. 111-112, 115; Herzog et al.
2002, p. 94; Kessler 2002, pp. 97-101).
Polylepis woodlands are now restricted
to elevations of 11,483 to 16,404 ft
˚
(3,500 to 5,000 m) (Fjeldsa 1992, p. 10).
As discussed above for the Historical
Range and Distribution of the ashbreasted tit-tyrant, researchers consider
human activity to be the primary cause
for historical habitat decline and
resultant decrease in species richness
˚
(Fjeldsa and Kessler 1996, Kessler
1995a, b, and L#gaard 1992, as cited in
˚
˚
Fjeldsa 2002a, p. 112; Fjeldsa 2002a, p.
116; Herzog et al. 2002, p. 94; Kessler
2002, pp. 97-101; Kessler and Herzog
1998, pp. 50-51). The royal cinclodes
may have been extirpated from its type
locality (Aricoma Pass, Puno), and
possibly throughout the entire Puno
Region, where Polylepis forest no longer
occurs exists (Collar et al. 1992, p. 589;
Engblom et al. 2002, p. 57) (see
Population Estimates). It is estimated
that between 2-3 percent and 10 percent
of the original forest cover still remains
in Peru and Bolivia, respectively (BLI
˚
2009i, p. 1; Fjeldsa and Kessler 1996, as
˚
cited in Fjeldsa 2002a, p. 113) (see
Factor A). Of this amount, less than 1
percent of the remaining woodlands
occur in humid areas, where Polylepis
˚
denser stands occur (Fjeldsa and Kessler
˚
1996, as cited in Fjeldsa 2002a, p. 113)
and which are preferred by the royal
cinclodes (del Hoyo et al. 2003, p. 253;
Engblom et al. 2002, p. 57). The royal
cinclodes was initially discovered in
Bolivia in 1876, but was not observed
there again until recently (BLI 2009i, p.
2; Hirshfeld 2007, p. 198) (see Current
Range and Distribution).
Current Range and Distribution
The royal cinclodes is restricted to
moist and mossy habitat amidst the
steep rocky slopes of semihumid
Polylepis or Polylepis - Gynoxys
woodlands, where the species is found
at elevations between 11,483 and 12,092
ft (3,500 and 4,600 m) (BLI 2000, p. 345;
BLI 2009i, p. 2; Collar et al. 1992, p.
588; del Hoyo et al. 2003, p. 253). The
current range of the species is
approximately 1,042 mi2 (2,700 km2)
(BLI 2009i, p. 1), which is an
overestimate of the actual range (as
discussed under the Current Range and
Distribution of the ash-breasted tittyrant) (BLI 2000, pp. 22, 27), given the
fragmented nature of the species’
remaining habitat (BLI 20091, p. 1;
˚
Fjeldsa and Kessler 1996, as cited in
˚
Fjeldsa 2002a, p. 113).
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The royal cinclodes was only
rediscovered in Bolivia within the last
decade, after more than 100 years of not
being observed there (BLI 2009i, p. 2;
Hirshfeld 2007, p. 198). Within the last
15 years, royal cinclodes has been
observed in Peru’s Runtacocha
´
highlands (Apurımac), Pariahuanca
´
Valley (Junın), and Cordillera Vilcanota
(Cusco), and in Bolivia’s Cordillera
Apolobamba and the Cordillera Real
(including Ilampu Valley, Sanja Pampa,
and Cordillera de La Paz), all in the
Bolivian Department of La Paz (BLI
2007, pp. 1-2; BLI 2009i, pp. 1-2; del
Hoyo et al. 2003, p. 253; Engblom et al.
2002, p. 57; Hirshfeld 2007, p. 198;
InfoNatura 2007, p. 1; Valqui 2000, p.
104).
Population Estimates
Population information is presented
first on the range-country level and then
in terms of a global population estimate.
The range country estimates begin with
Peru, where the majority of the
population resides.
Local population estimate, Peru: In
1990, the global population was
estimated to be 100-150 individuals
˚
(Fjeldsa and Krabbe 1990, p. 338). This
number represents the estimated
Peruvian population because the royal
cinclodes was only thought to be extant
in Peru at the time of this estimate (BLI
2009i, p. 2; Hirshfeld 2007, p. 198).
Chutas (2007, p. 8) reported an
estimated 189 birds located within four
disjunct Polylepis forest patches in Peru,
with a combined area of 1,554 ac (629
ha). This estimate included 116 birds
and 30 birds in Cordilleras Vilcanota
and Vilcabamba, respectively (Cusco); 2
birds in Cordillera de Carabaya (Puno);
and 41 birds in ‘‘Cordillera del
´
Apurımac’’ (Runtacocha highlands in
´
Apurımac) (Chutas 2007, pp. 4, 8).
Subpopulations at four locations in the
Cordillera Vilcanota contain as few as 14 individuals (BLI 2008, p. 2).
In the Puno Region of Peru, it is
unclear whether a viable population of
royal cinclodes remains. The royal
cinclodes was first observed in Puno in
˚
1930 (Fjeldsa and Krabbe 1990, p. 338)
and has continued to be reported there
in general terms (BLI 2007, pp. 1-2; BLI
2009i, pp. 1-2; Collar et al. 1992, p. 588;
del Hoyo 2003, p. 253). However, based
on habitat availability, InfoNatura (2007,
p. 1) predicted that the royal cinclodes
does not occur in Puno because the
habitat no longer exists there. Indeed,
only two royal cinclodes individuals
have been reported in the Puno Region
(Cordillera de Carabaya) in recent
decades (Chutas 2007, pp. 4, 8). There
are no other recent observations of the
royal cinclodes in Puno (BLI 2009i, p.
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637
2; del Hoyo 2003, p. 283; Engblom et al.
2002, p. 57). The species is believed to
be extirpated from its type locality
(Collar et al. 1992, p. 589; Engblom et
al. 2002, p. 57).
Local population estimate, Bolivia:
The species’ current range is more
widespread in Bolivia than previously
understood. The royal cinclodes had not
been observed in Bolivia for more than
one century, when it was rediscovered
there in 1997 (BLI 2009i, p. 2; Hirshfeld
2007, p. 198). Recent surveys in La Paz
Department found at least 13 localities
(8 in Cordillera Apolobamba and 5 in
Cordillera La Paz) (BLI 2009i, p. 1).
Although BirdLife International
reports an estimated population size of
´
50-70 royal cinclodes in Bolivia (Gomez,
in litt. 2003, 2008, as cited in BLI 2009i,
p. 2), recent surveys indicate that the
estimate may be smaller. As discussed
above for the local population estimate
of the ash-breasted tit-tyrant in Bolivia,
´
Gomez (in litt. 2007, p. 1) conducted
intensive studies in Bolivia. From this
research, the presence of 1-8 royal
cinclodes in each of 30 forest patches
was inferred or observed. Thus, they
estimated that the royal cinclodes
population in Bolivia totals
approximately 30 birds. Researchers add
that, because the royal cinclodes does
not always respond to tape-playbacks,
these numbers may underestimate the
´
actual population size (Gomez in litt.
2007, p. 1).
Global population estimate: In 1990,
the global population of the royal
cinclodes was estimated to be 100-150
˚
individuals (Fjeldsa and Krabbe 1990, p.
338). Since at least 2000, BirdLife
International has placed this species in
the population category of between 50
and 249 individuals (BLI 2000, p. 345).
In 2002, Engblom et al. (2002, p. 57)
estimated a total population size of up
to 250 pairs of birds. This amount far
exceeds any previous estimates and has
not been confirmed by BirdLife
International (BLI 2009i, p. 1). In 2003,
the global population was once again
reported to include only ‘‘a few hundred
individuals’’ (del Hoyo et al. 2003, p.
253). Based on recent observations in
both countries, there are approximately
189 birds in Peru and 50-70 in Bolivia,
totaling 239-259 individuals.
Recognizing that the royal cinclodes
does not always respond to tapeplaybacks, this could be an
underestimate of the population size
´
(Gomez in litt. 2007, p. 1). While the
species continues to be categorized by
BirdLife International as having an
estimated population between 50-249
individuals (BLI 2007, p. 1; BLI 2009i,
˚
p. 1; Fjeldsa 2002b, p. 9; Hirshfeld 2007,
p. 198), it is possible that the recent
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observations in Bolivia will lead to a
revision of the species’ population
estimate (BLI 2009i, p. 1).
It should be noted that the total
population size, which includes
immature individuals, is not an accurate
reflection of the species’ effective
population size (the number of breeding
individuals that contribute to the next
generation) (Shaffer 1981, pp. 132-133;
´
Soule 1980, pp. 160-162). The IUCN
estimated that the entire royal cinclodes
population contains fewer than 250
mature individuals and no more than 50
mature individuals in any
subpopulation (BLI 2008, p. 1; IUCN
2001, pp. 8-12). However, population
estimates are incomplete for several of
the known localities, and the
subpopulation structure and the extent
of interbreeding amongst the various
localities are unknown. The species’
territory ranges from 7 to 10 ac (3 to 4
ha), and its habitat is fragmented,
dispersed and sparse (del Hoyo et al.
2003, p. 253; Engblom et al. 2002, p. 57).
However, there is no information to
indicate the distance that this species is
capable of or likely to travel between
localities. Engblom et al. (2002, p. 57)
noted that gene flow between localities
likely occurs when the species descends
the mountains to forage in the valleys
during periods of snow cover at the
higher altitudes such that interbreeding
may occur at least among localities with
shared valleys. This suggests that the
species does not breed as a single
population. However, there is
insufficient information to determine
the extent to which this species
functions as genetically isolated
subpopulations.
The species has experienced a
population decline of between 30 and
49 percent in the past 10 years, and this
rate of decline is predicted to continue
(BLI 2009i, pp. 1, 5). The population is
considered to be declining in close
association with continued habitat loss
and degradation (BLI 2009i, p. 6) (see
Factors A and E).
Conservation Status
The royal cinclodes is considered
‘‘critically endangered’’ by the Peruvian
Government under Supreme Decree No.
034-2004-AG (2004, p. 276854). The
IUCN considers the royal cinclodes to
be ‘‘Critically Endangered’’ due to its
extremely small population, which
consists of ‘‘tiny’’ subpopulations that
are severely fragmented and dependent
upon a rapidly declining habitat (BLI
2007, p. 1; BLI 2009i, p. 1). The royal
cinclodes occurs within the Peruvian
´
protected area of Santuario Historico
Machu Picchu, in Cusco (BLI 2009h, p.
1; BLI 2009i, p. 6; Chutas et al. 2008, p.
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16). In La Paz Department, Bolivia, the
species is found in Parque Nacional y
´
area Natural de Manejo Integrado
´
Madidi, Parque Nacional y area Natural
de Manejo Integrado Cotapata, and the
co-located protected areas of Reserva
´
Nacional de Fauna de Apolobamba, area
Natural de Manejo Integrado de
Apolobamba, and Reserva de la Biosfera
de Apolobamba (BLI 2009a, p. 1; BLI
2009b, p. 1; BLI 2009c, p. 1; BLI 2009d,
p. 1; BLI 2009i, p. 6; Chutas et al. 2008,
p. 16).
(1) Clearcutting and uncontrolled
burning for agriculture and pastureland
for domesticated animals, all of which
contributes to loss of understory moss
cover, soil erosion, and degradation,
which prevent woodland regeneration
(BLI 2009a, p. 2; BLI 2009b, p. 2; BLI
2009c, p. 2; BLI 2009d, p. 2; BLI 2009e,
p. 3; BLI 2009f, p. 1; BLI 2009g, p. 1; BLI
2009h, p. 4; BLI 2009i, pp. 2, 6;
˚
Engblom et al. 2002, p. 56; Fjeldsa
˚
2002a, pp. 112, 120; Fjeldsa 2002b, p. 8;
Jameson and Ramsay 2007, p. 42;
Purcell et al. 2004, p. 458; WCMC
Summary of Factors Affecting the Royal 1998a, p. 1; WCMC 1998b, p. 1);
Cinclodes
(2) Extractive activities, such as wood
and timber, for local and commercialA. The Present or Threatened
scale uses, including firewood and
Destruction, Modification, or
construction (Aucca and Ramsay 2005,
Curtailment of the Species’ Habitat or
p. 287; BLI 2009a, p. 2; BLI 2009b, p.
Range
2; BLI 2009c, p. 2; BLI 2009d, p. 2; BLI
The royal cinclodes is restricted to
2009e, p. 3; BLI 2009g, p. 1; BLI 2009i,
high-elevation (11,483-12,092 ft (3,500p. 2; Engblom 2000, p. 1; p. 2; Engblom
4,600 m)), moist, moss-laden areas of
et al. 2002, p. 56; Purcell et al. 2004, p.
semihumid Polylepis or Polylepis 458; WCMC 1998a, p. 1);
Gynoxys woodlands (BLI 2000, p. 345;
(3) Human encroachment, including
BLI 2009i, p. 2; Collar et al. 1992, p.
tourism and industrialization projects,
588; del Hoyo et al. 2003, p. 253). As
which puts greater demand on natural
described more fully for the ashresources, spurs additional habitat
breasted tit-tyrant (Factor A), Polylepis
destruction as arable land becomes
habitat is characterized as a threatened
scarce, and increases infrastructure
woodland ecosystem on national,
development that further facilitates
regional, and global levels (BLI 2009a, p. encroachment (BLI 2009b, p. 2; BLI
2; Purcell et al. 2004, p. 457; Renison et 2009d, p. 2; Hensen 2002, p. 199;
al. 2005, as cited in Lloyd 2009, p. 10),
Purcell and Brelsford, 2004, pp. 156with several Polylepis species within
157; Purcell et al. 2004, pp. 458-459);
the royal cinclodes’ range considered to and
be ‘‘Vulnerable,’’ according to the IUCN
(4) Unpredictable climate fluctuations
(WCMC 1998a, p. 1; WCMC 1998b, p. 1). that exacerbate the effects of habitat
Polylepis woodlands are dispersed and
fragmentation (Jetz et al. 2007, pp. 1211,
sparse, with an estimated remaining
1213; Mora et al. 2007, p. 1027).
area of 386 mi2 (1,000 km2) in Peru and
These habitat-altering activities are
˚
1,931 mi2 (5,000 km2) in Bolivia (Fjeldsa ongoing throughout the royal cinclodes’
˚
´
and Kessler 1996, as cited in Fjeldsa
range, including the Apurımac (BLI
2002a, p. 113). Within the remaining
2009g, p. 1) and Cusco Regions (BLI
Polylepis woodlands, the royal
2009e, p. 1; BLI 2009f, p. 1; BLI 2009h,
cinclodes’ range is approximately 1,042 p. 1) in Peru and also in the Bolivian
mi2 (2,700 km2) (BLI 2009i, p. 1). Less
Department of La Paz (BLI 2009a, p. 1;
than 1 percent of the remaining
BLI 2009b, p. 1; BLI 2009c, pp. 1; BLI
woodlands occur in humid areas, where 2009d, p. 1; Hensen 2002, p. 199;
˚
denser stands occur (Fjeldsa and Kessler Purcell and Brelsford 2004, p. 157;
˚
1996, as cited in Fjeldsa 2002a, p. 113).
Purcell et al. 2004, pp. 458-459). A
The optimal habitat for the royal
combination of urbanization, road
cinclodes is dense woodlands, with a
building, and industrialization projects
closed canopy that supports the best
(such as construction of hydroelectric
foraging habitat (shady, moss-laden
power stations) in the Bolivian
vegetation) for this and other
Department of La Paz have resulted in
insectivorous birds (see Habitat and Life a nearly 40 percent loss of the forest
History) (De la Via 2004, p. 10; del Hoyo cover between 1991 and 2003 alone; at
et al. 2003, p. 253; Engblom et al. 2002,
this rate it is predicted that the
p. 57).
remaining Polylepis forest in La Paz will
Habitat loss, conversion, and
be extirpated within the next 30 years
degradation occur throughout the royal
(Purcell and Brelsford 2004, pp. 156cinclodes’ range and have been
157).
Community-based Polylepis
attributed to human activities (a full
conservation programs have been under
description of which is provided above
way in Peru and Bolivia since 2004
as part of the Factor A analysis for the
´
(Gomez in litt. 2003, 2008, as cited in
ash-breasted tit-tyrant). These activities
BLI 2009i, p. 2; MacLennan 2009, p. 2),
include:
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and have focused on known sites for the
royal cinclodes (BLI 2009i, p. 2),
including Cordilleras Vilcanota and
Vilcabamba, and highlands of the
´
Apurımac Region (Aucca and Ramsey
2005, p. 287; ECOAN n.d., p. 1; Lloyd
2009, p. 10). These programs confront
the main causes of Polylepis woodland
loss—burning, grazing, and woodcutting (Aucca and Ramsay 2005, pp.
187-288; BLI 2009i, p. 2; ECOAN n.d.,
´
p. 1; Engblom et al. 2002, p. 56; Gomez
in litt. 2003, 2008, as cited in BLI 2009i,
p. 2; Lloyd 2009, p. 10; MacLennan
2009, p. 2) —and are more fully
described above as part of the Factor A
analysis for the ash-breasted tit-tyrant
(Aucca and Ramsay 2005, p. 287;
Engblom et al. 2002, p. 56; MacLennan
2009, p. 2). While the Polylepis
conservation programs foster local,
sustainable use of resources (Aucca and
Ramsay 2005, p. 287; ECOAN n.d., p. 1;
Engblom et al. 2002, p. 56), commercialscale activities, such as clearcutting,
logging, tourism, and infrastructure
development, that are ongoing
throughout this species’ range, alter
otherwise sustainable resource use
practices (Aucca and Ramsay 2005, p.
287; Engblom 2000, p. 2; Engblom et al.
2002, p. 56; MacLennan 2009, p. 2;
Purcell and Brelsford 2004, pp. 156-157;
Purcell et al. 2004, pp. 458-459; WCMC
1998a, p. 1). Tourism and human
encroachment are particularly
problematic for the royal cinclodes,
which is described as a ‘‘nervous’’
species that is easily disturbed by
humans (Engblom et al. 2002, p. 57).
In the Cordillera de Vilcanota (Cusco,
Peru), where a large portion of the
known royal cinclodes population
occurs (116 birds were observed there,
out of 189 total birds observed in 4
study sites in Peru) (Chutas 2007, pp. 4,
8), Polylepis woodland habitat is highly
fragmented and degraded. As described
more fully for the ash-breasted tit-tyrant
(Factor A), recent research indicated:
(1) That four forest patches in the
Cordillera de Vilcanota disappeared
completely in the last half a century,
that the size of remaining Polylepis
remnants is small (with a mean patch
size of 7.4 ac (3 ha)) (Jameson and
Ramsay 2007, p. 42), and that many
patches are less than 2.5 ac (1 ha) (Lloyd
and Marsden in press, as cited in Lloyd
2008, p. 532);
(2) Ten percent of the remaining forest
patches showed a decline in forest
density (Jameson and Ramsay 2007, p.
42); and
(3) There were no indications of forest
regeneration within the study area.
Thus, forest patches in Cordillera
Vilcanota are at or below the minimum
area required for the royal cinclodes to
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obtain food, given that the groundfeeding strategy used by the royal
cinclodes generally requires a relatively
large territory, from 7 to 10 ac (3 to 4
ha) (del Hoyo et al. 2003, p. 253;
Engblom et al. 2002, p. 57). Because the
moist, moss-covered woodlands that
provide optimal foraging habitat for
insectivorous birds (De la Via 2004, p.
10), and which this ground-feeding
species prefers (del Hoyo et al. 2003, p.
253; Engblom et al. 2002, p. 57), require
a closed canopy, degradation of the
royal cinclodes habitat has serious
consequences for this species.
Reduction of forest density (or,
decreased canopy cover) increases
desiccation of the moist and mossy
ground cover, which, in turn, reduces
foraging microhabitats for the species
(Engblom et al. 2002, p. 57).
Lack of Polylepis forest regeneration
during nearly 50 years underscores the
ramifications of continued burning and
clearing to maintain pastures and
farmland, which are prevalent activities
throughout the royal cinclodes’ range
(BLI 2009a, p. 2; BLI 2009b, p. 2; BLI
2009c, p. 2; BLI 2009d, p. 2; BLI 2009e,
p. 3; BLI 2009f, p. 1; BLI 2009g, p. 1; BLI
2009h, p. 4; BLI 2009i, p. 2; Engblom et
˚
al. 2002, p. 56; Fjeldsa 2002a, pp. 112,
˚
120; Fjeldsa 2002b, p. 8; Purcell et al.
2004, p. 458; WCMC 1998a, p. 1; WCMC
1998b, p. 1). These habitat-altering
activities are considered to be key
factors preventing regeneration of
˚
Polylepis woodlands (Fjeldsa 2002a, p.
˚
112, 120; Fjeldsa 2002b, p. 8) and are
factors in the historical decline of
Polylepis -dependent bird species,
including the royal cinclodes (BLI
˚
2009i, p. 6; Fjeldsa and Kessler 1996,
Kessler 1995a, b, and L#gaard 1992, as
˚
˚
cited in Fjeldsa 2002a, p. 112; Fjeldsa
2002a, p. 116; Herzog et al. 2002, p. 94;
Kessler 2002, pp. 97-101; Kessler and
Herzog 1998, pp. 50-51).
The royal cinclodes may once have
been locally common and distributed
across most of central to southern Peru
and into the Bolivian highlands, in once
contiguous expanses of Polylepis forests
(BLI 2000, p. 345; BLI 2009i, p. 1;
˚
Fjeldsa 2002a, pp. 111-112, 115). The
royal cinclodes’ population size is
considered to be declining in close
association with continued habitat loss
and degradation (BLI 2007, p. 1; BLI
2008, p. 1; BLI 2009i, p. 6). The species
may have been extirpated from its type
locality (Aricoma Pass, Puno), where
Polylepis forest no longer occurs, and a
search for the species in 1987 resulted
in no observations of the royal cinclodes
(Collar et al. 1992, p. 589; Engblom
2002, p. 57). Based on habitat
availability, the royal cinclodes is not
predicted to occur in Puno because the
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639
habitat no longer exists there
(InfoNatura 2007, p. 1), and only two
birds have been observed there in recent
years (Chutas 2007, pp. 4, 8). Therefore,
further habitat loss will continue to
impact the species’ already small
population size (see Factor E).
Royal cinclodes are also impacted by
unpredictable climate fluctuations,
which are more fully described under
the Factor A analysis of the ash-breasted
tit-tyrant and are summarized here. Peru
is subject to unpredictable climate
fluctuations that exacerbate the effects
of habitat fragmentation, such as those
˜
that are related to the El Nino Southern
Oscillation (ENSO). Changes in weather
˜
patterns, such as ENSO cycles (El Nino
˜
and La Nina events), tend to increase
precipitation in normally dry areas, and
decrease precipitation in normally wet
areas (Holmgren et al. 2001, p. 89; TAO
Project n.d., p. 1), exacerbating the
effects of habitat fragmentation on the
decline of a species (England 2000, p.
86; Holmgren et al. 2001, p. 89; Jetz et
al. 2007, pp. 1211, 1213; Mora et al.
2007, p. 1027; Parmesan and Mathews
2005, p. 334; Plumart 2007, pp. 1-2;
Timmermann 1999, p. 694), especially
for narrow endemics (Jetz et al. 2007, p.
1213) such as the royal cinclodes (see
also Factor E). ENSO cycles strongly
influence the growth of Polylepis
species (Christie et al. 2008, p. 1) by
altering the Polylepis species’ age
structure and mortality, especially
where woodlands have undergone
disturbance, such as fire and grazing
(Villalba and Veblen 1997, pp. 121-123;
Villalba and Veblen 1998, pp. 2624,
2637).
ENSO cycles may have already
accelerated the fire cycle (Block and
Richter 2007, p. 1; Power et al. 2007, pp.
897-898), which is a key factor
preventing Polylepis regeneration
˚
˚
(Fjeldsa 2002a, p. 112, 120; Fjeldsa
2002b, p. 8) because Polylepis species
recover poorly following a fire
(Cierjacks et al. 2007, p. 176). ENSO
cycles are ongoing, having occurred
several times within the last decade
(NWS 2009, p. 2), and evidence suggests
that ENSO cycles have already
increased in periodicity and severity
(Richter 2005, pp. 24-25; Timmermann
1999, p. 694), which will exacerbate the
negative impacts of habitat destruction
on a species. It is predicted that, by
2050, approximately 3 to 15 percent of
the royal cinclodes’ current remaining
range is likely to be unsuitable for this
species due to climate change and, by
2100, it is predicted that about 8 to 18
percent of the species’ range is likely to
be lost as a direct result of global
climate change (Jetz et al. 2007,
Supplementary Table 2, p. 89).
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Human activities that alter the
species’ habitat are also ongoing within
protected areas, including Santuario
´
Historico Machu Picchu (in Peru) (BLI
´
2009h, p. 4), and Parque Nacional y area
Natural de Manejo Integrado Madidi,
´
Parque Nacional y area Natural de
Manejo Integrado Cotapata, and the colocated protected areas of Reserva
´
Nacional de Fauna de Apolobamba, area
Natural de Manejo Integrado de
Apolobamba, and Reserva de la Biosfera
de Apolobamba (in Bolivia) (BLI 2009a,
p. 2; BLI 2009b, p. 2; BLI 2009c, p. 2;
BLI 2009d, p. 5). Ongoing habitat
destruction and alteration within
protected areas, including clearing and
human encroachment, is further
discussed under Factor D.
Summary of Factor A
Polylepis habitat throughout the royal
cinclodes’ range has been and continues
to be altered and destroyed as a result
of human activities, including
clearcutting and burning for agriculture,
grazing lands, and industrialization;
extractive activities, including firewood
and timber extraction; and human
encroachment and concomitant
increased pressure on natural resources.
An estimated 1 percent of the onceextensive dense Polylepis woodlands
remains, and other remaining Polylepis
woodlands are fragmented and
degraded. The royal cinclodes occupies
an area of approximately 1,042 mi2
(2,700 km2), and is particularly
vulnerable to reduction in forest cover,
because the moist habitats that serve as
their feeding grounds quickly dry out as
the forest canopy diminishes.
Researchers estimate that the royal
cinclodes territories are 7-10 ac (3-4 ha).
In Cordillera Vilcanota (Cusco, Peru),
where a large concentration of the royal
cinclodes individuals were observed in
2007, the average size of forest
fragments just meets the lower threshold
of the species’ ecological requirements.
While the species’ range is more
widespread in Bolivia than previously
understood, ongoing and accelerated
habitat destruction of the remaining
Polylepis forest fragments in Peru and
Bolivia continues to reduce the
quantity, quality, distribution, and
regeneration of remaining patches. In
the Administrative Region of Puno,
Peru, habitat loss may have led to
extirpation of the species from its type
locality and the species may no longer
be viable in that Region due to habitat
loss. Current research indicates that
climate fluctuations exacerbate the
effects of habitat loss on species,
especially for narrow endemics such as
the royal cinclodes that are already
undergoing range reduction due to
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human activities. Historical decline in
habitat availability is attributed to the
same human activities that are causing
habitat loss today, and climate models
predict that this species’ habitat will
continue to decline. In addition, the
royal cinclodes is ‘‘nervous’’ around
humans, such that human
encroachment is a particular problem.
Human activities that degrade, alter, and
destroy habitat are ongoing throughout
the species’ range, including within
protected areas (see also Factor D).
Experts consider the species’ population
decline to be commensurate with the
declining habitat (Factor E). Therefore,
we find that destruction and
modification of habitat are threats to the
continued existence of the royal
cinclodes throughout its range.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
We are not aware of any information
currently available that indicates that
overutilization of the royal cinclodes for
commercial, recreational, scientific, or
educational purposes has occurred or is
occurring at this time. As a result, we
are not considering overutilization to be
a threat to the continued existence of
the royal cinclodes.
C. Disease or Predation
We are not aware of any scientific or
commercial information that indicate
disease or predation poses a threat to
this species. As a result, we are not
considering disease or predation to be a
threat to the continued existence of the
royal cinclodes.
D. Inadequacy of Existing Regulatory
Mechanisms
Existing regulatory mechanisms
within Peru and Bolivia that have the
potential to confer protection to the
royal cinclodes or its habitat are
analyzed on a country-by-country basis,
beginning with Peru.
Peru: The royal cinclodes is
considered ‘‘critically endangered’’ by
the Peruvian Government under
Supreme Decree No. 034-2004-AG
(2004, p. 276855). This Decree prohibits
hunting, take, transport, and trade of
protected species, except as permitted
by regulation. As hunting, take,
transport, and trade do not currently
threaten the royal cinclodes, this
regulation does not mitigate any current
threats to this species.
Peru has several categories of national
habitat protection, which were
described above as part of the Factor D
analysis for the ash-breasted tit-tyrant
(BLI 2008, p. 1; IUCN 1994, p. 2;
´
Rodrıguez and Young 2000, p. 330).
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Protected areas have been established
through regulation at one site occupied
by the royal cinclodes in Peru:
´
Santuario Historico Machu Picchu
(Cusco, Peru) (BLI 2009h, p. 4). Within
the sanctuary, resources are supposed to
´
be managed for conservation (Rodrıguez
and Young 2000, p. 330). However,
habitat destruction and alteration,
including burning to maintain pastures
for grazing, are ongoing within
´
Santuario Historico Machu Picchu,
preventing the regeneration of the
woodlands (BLI 2009h, p. 4; Engblom et
al. 2002, p. 58). Therefore, the
occurrence of the royal cinclodes within
protected areas in Peru does not protect
the species, nor does it mitigate the
threats to the species from ongoing
habitat loss (Factor A) and concomitant
population decline (Factor E).
Bolivia: The 1975 Law on Wildlife,
National Parks, Hunting, and Fishing
(Decree Law No. 12,301 1975, pp. 1-34;
eLAW 2003, p. 2), was described above
as part of the Factor D analysis for the
ash-breasted tit-tyrant. This law
designates national protection for all
wildlife. However, there is no
information as to the actual protections
this confers to the species itself or its
habitat, and ongoing habitat destruction
throughout the species’ range indicates
that this law does not protect the
species nor does it mitigate the threat to
the species from ongoing habitat loss
(Factor A) and concomitant population
decline within Bolivia (Factor E).
Environmental Law No. 1333 (eLAW
2003, p. 1; Law No. 1,333 1992, pp. 126), was signed in 1992 to protect and
conserve the environment. However, we
are not aware that any specific
legislation needed to implement these
laws has been passed (eLAW 2003, p. 1).
Therefore, this law does not protect the
species, nor does it mitigate the threats
to the species from ongoing habitat loss
(Factor A) and concomitant population
decline (Factor E).
Various levels of habitat protection in
Bolivia were described above as part of
the Factor D analysis for the ashbreasted tit-tyrant (eLAW 2003, p. 3;
Supreme Decree No. 24,781 1997, p. 3).
The royal cinclodes occurs within
several protected areas in the
Department of La Paz, Bolivia: Parque
´
Nacional y area Natural de Manejo
Integrado Madidi, Parque Nacional y
´
area Natural de Manejo Integrado
Cotapata, and the co-located protected
areas of Reserva Nacional de Fauna de
´
Apolobamba, area Natural de Manejo
Integrado de Apolobamba, and Reserva
de la Biosfera de Apolobamba (Auza
and Hennessey 2005, p. 81; BLI 2009a,
p. 1; BLI 2009b, p. 1; BLI 2009c, p. 1;
BLI 2009d, p. 1). Within Parque
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´
Nacional y area Natural de Manejo
Integrado Madidi, habitat destruction is
caused by timber harvest used for
construction, wood collection for
firewood, and burning that often goes
out of control to maintain pastures (BLI
2009a, p. 2; WCMC 1998a, p. 1). In
addition, one of the most transited
highways in the country is located a
short distance from the Parque Nacional
´
y area Natural de Manejo Integrado
Cotapata; firewood collection and
grazing also occur within the protected
area (BLI 2009b, p. 2; BLI 2009c, p. 2).
Within the Apolobamba protected areas,
uncontrolled clearing, extensive
agriculture, grazing, and tourism are
ongoing (Auza and Hennessey 2005, p.
81; BLI 2009d, p. 5). Therefore, the
occurrence of the royal cinclodes within
protected areas in Bolivia does not
protect the species, nor does it mitigate
the threats to the species from ongoing
habitat loss (Factor A) and concomitant
population decline (Factor E).
srobinson on DSKHWCL6B1PROD with PROPOSALS2
Summary of Factor D
Peru and Bolivia have enacted various
laws and regulatory mechanisms to
protect and manage wildlife and their
habitats. The royal cinclodes is
‘‘critically endangered’’ under Peruvian
law and occurs within several protected
areas in Peru and Bolivia. As discussed
under Factor A, the royal cinclodes
requires dense woodlands, which has
been reduced by an estimated 99
percent in Peru and Bolivia. The
remaining habitat for the royal cinclodes
is fragmented and degraded. Habitat
throughout the species’ range has been
and continues to be altered as a result
of human activities, including
clearcutting and burning for agriculture,
grazing lands, and industrialization;
extractive activities, including,
firewood, timber, and mineral
extraction; and human encroachment
and concomitant increased pressure on
natural resources. These activities are
ongoing within protected areas and
despite the species’ critically
endangered status in Peru, indicating
that the laws governing wildlife and
habitat protection in both countries are
either inadequate or inadequately
enforced to protect the species or to
mitigate ongoing habitat loss (Factor A)
and population declines (Factor E).
Therefore, we find that the existing
regulatory mechanisms are inadequate
to mitigate the current threats to the
continued existence of the royal
cinclodes throughout its range.
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E. Other Natural or Manmade Factors
Affecting the Continued Existence of the
Species
An additional factor that affects the
continued existence of the royal
cinclodes is the species’ small
population size. Based on recent
observations in Peru and Bolivia, the
total population is between 239 and 259
individuals (Chutas 2007, pp. 4, 8;
´
Gomez in litt. 2007, p. 1) (see
Population Estimates), and BirdLife
International characterizes the species
as having an ‘‘extremely small
population’’ size (BLI 2000, p. 345; BLI
2009i, p. 1). Although there is
insufficient information to fully
understand gene flow within this
species (see Population Estimates),
Engblom et al. (2002, p. 57) noted that
the royal cinclodes may descend the
mountains to forage in the valleys
during periods of snow cover at the
higher altitudes. Thus, interbreeding
may occur at least among localities with
shared valleys, but there is insufficient
information to determine that the
species breeds as a single population.
Moreover, the total population size,
which includes immature individuals,
is not an accurate reflection of the
species’ effective population size (the
number of breeding individuals that
contribute to the next generation)
´
(Shaffer 1981, pp. 132-133; Soule 1980,
pp. 160-162). Therefore, 239–259 is an
overestimate of the species’ effective
population size.
Small population size renders species
vulnerable to genetic risks that can have
individual or population-level genetic
consequences, such as inbreeding
depression, loss of genetic variation,
and accumulation of new mutations.
These genetic problems may affect the
species’ viability by increasing its
susceptibility to demographic shifts or
environmental fluctuations, as
described above in the Factor E analysis
for the ash-breasted tit-tyrant
(Charlesworth and Charlesworth 1987,
p. 238; Pimm et al. 1988, pp. 757, 773775; Shaffer 1981, p. 131).
Small population size leads to a
higher risk of extinction and, once a
population is reduced below a certain
number of individuals, it tends to
rapidly decline towards extinction
(Frankham 1996, p. 1507; Franklin
´
1980, pp. 147-148; Gilpin and Soule
1986, p. 25; Holsinger 2000, pp. 64-65;
Purvis et al. 2000, p. 1949; Reed and
´
Frankham 2003, pp. 233-234; Soule
1987, p. 181). If further research
indicates that interbreeding does not
between subpopulations, this would
heighten the risks to the species
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641
associated with short-term genetic
viability.
Complications arising from the
species’ small population size are
exacerbated by the species’ fragmented
distribution. The royal cinclodes is
currently restricted to high-elevation,
moist, moss-laden patches of
semihumid woodlands in Peru and
Bolivia (BLI 2009i, p. 6) (Factor A).
˚
Fjeldsa and Kessler (1996, as cited in
˚
Fjeldsa 2002a, p. 113). Remaining
Polylepis woodlands are highly
fragmented and degraded, and it is
estimated that only 1 percent of the
dense woodlands preferred by the
species remain (del Hoyo et al. 2003, p.
253; Engblom et al. 2002, p. 57) (see
Habitat and Life History and Historical
Distribution). Therefore, the species’
current range is restricted and severely
fragmented (BLI 2000, p. 345; BLI 2009i,
pp. 1-2; Collar et al. 1992, p. 588; del
Hoyo et al. 2003, p. 253). Habitat
fragmentation can cause genetic
isolation and heighten the risks to the
species associated with short-term
genetic viability. The royal cinclodes
has undergone a population decline
between 30 and 49 percent in the past
10 years, in close association with the
continued loss and degradation of the
Polylepis forest (BLI 2009i, p. 6) (Factor
A). The species’ small population size,
combined with its restricted and
severely fragmented range, increases the
species’ vulnerability to adverse natural
events and manmade activities that
destroy individuals and their habitat
(Holsinger 2000, pp. 64-65; Primack
1998, pp. 279-308; Young and Clarke
2000, pp. 361-366).
Summary of Factor E
The royal cinclodes has a small
population size that renders it
vulnerable to genetic risks that
negatively impact the species’ long-term
viability, and possibly its short-term
viability. The species has a restricted
range and occurs in highly fragmented
habitat that continues to undergo
degradation and curtailment due to
human activities (Factor A). The
restricted and fragmented range, as well
as the small population size, increases
the species’ vulnerability to extinction
through demographic or environmental
fluctuations. Based on its small
population size and fragmented
distribution, we have determined that
the royal cinclodes is particularly
vulnerable to the threat of adverse
natural events (e.g., genetic,
demographic, or environmental) and
human activities (e.g., deforestation,
habitat alteration, and infrastructure
development) that destroy individuals
and their habitat. The genetic and
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demographic risks associated with small
population sizes are exacerbated by
ongoing human activities that continue
to curtail the species’ habitat throughout
its range. The species’ population has
declined and is predicted to continue
declining commensurate with ongoing
habitat loss (Factor A). Therefore, we
find that the species’ small population
size, in concert with its fragmented
distribution and its heightened
vulnerability to adverse natural events
and manmade activities, are threats to
the continued existence of the royal
cinclodes throughout its range.
srobinson on DSKHWCL6B1PROD with PROPOSALS2
Status Determination for the Royal
Cinclodes
The royal cinclodes, a large-billed
ovenbird, is native to the high-altitude,
semihumid Polylepis or Polylepis Gynoxys woodlands of the Bolivian and
Peruvian Andes, where it occupies a
narrow range of distribution at
elevations between 11,483 and 12,092 ft
(3,500 and 4,600 m). Preferring dense
woodlands with more closed canopies,
the royal cinclodes is a ground-feeding
insectivore that probes the mossy forest
undergrowth for food. The species has
a highly restricted and severely
fragmented range (approximately 1,042
mi2 (2,700 km2)), and is found only in
the Peruvian Administrative Regions of
´
´
Apurımac, Cusco, Junin, and Puno, and
in the Bolivian Department of La Paz.
The known population of the royal
cinclodes is estimated to be 239–259
individuals.
We have carefully assessed the best
available scientific and commercial
information regarding the past, present,
and potential future threats faced by the
royal cinclodes and have concluded that
there are three primary factors
impacting the continued existence of
the royal cinclodes: (1) Habitat
destruction, fragmentation, and
degradation; (2) limited size and
isolation of remaining populations; and
(3) inadequate regulatory mechanisms.
Human activities that degrade, alter,
and destroy habitat are ongoing
throughout the royal cinclodes’ range.
Widespread deforestation and the
conversion of forests for grazing,
agriculture, and human settlement have
led to the fragmentation of habitat
throughout the range of the royal
cinclodes (Factor A). Researchers
estimate that only 1 percent of the dense
Polylepis woodlands preferred by the
species remain extant. Limited by the
availability of suitable habitat, the
species occurs today only in some of
these fragmented and disjunct locations.
Royal cinclodes habitat is particularly
vulnerable to the drying effects
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accompanied by diminished forest
cover.
Royal cinclodes habitat continues to
be altered by human activities, which
result in the continued degradation,
conversion, and destruction of habitat
and reduction of the quantity, quality,
distribution, and regeneration of
remaining patches. Habitat loss was a
factor in this species’ historical decline,
resulting in extirpation of the species
from its type locality and, possibly, the
loss of a viable population in the entire
Region of Puno, Peru (see Historical
Range and Distribution). Thespecies’
population is considered to be declining
in association with the reduction in
habitat (Factors A and E).
The royal cinclodes population is
small, rendering the species particularly
vulnerable to the threat of adverse
natural events (e.g., genetic,
demographic, or environmental) and
human activities (e.g., deforestation and
habitat alteration) that destroy
individuals and their habitat. Human
activities that continue to curtail the
species’ habitat throughout its range
exacerbate the genetic and demographic
risks associated with small population
sizes (Factor E). The population has
declined 30-49 percent in the past 10
years (see Population Estimates), and is
predicted to continue declining
commensurate with ongoing habitat loss
(Factor A). Current research indicates
that narrow endemics, such as the royal
cinclodes, are especially susceptible to
climate fluctuations because of the
synergistic effect these fluctuations have
on declining populations that are also
experiencing range reductions due to
human activities (Factor A).
Despite the species’ ‘‘critically
endangered’’ status in Peru and its
occurrence within several protected
areas in Peru and Bolivia (Factor D), the
species’ habitat continues to be
destroyed and degraded as a result of
human activities (Factor A), which
corresponds with population declines
(Factor E). Therefore, regulatory
mechanisms are either inadequate or
ineffective at mitigating the existing
threats to the royal cinclodes and its
habitat (Factor D).
Section 3 of the Act defines an
‘‘endangered species’’ as ‘‘any species
which is in danger of extinction
throughout all or a significant portion of
its range’’ and a ‘‘threatened species’’ as
‘‘any species which is likely to become
an endangered species within the
foreseeable future throughout all or a
significant portion of its range.’’ Based
on the immediate and ongoing threats to
the royal cinclodes throughout its entire
range, as described above, we determine
that the royal cinclodes is in danger of
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extinction throughout all of its range.
Therefore, on the basis of the best
available scientific and commercial
information, we are proposing to list the
royal cinclodes as an endangered
species throughout all of its range.
VI. White-browed tit-spinetail
(Leptasthenura xenothorax)
Species Description
The white-browed tit-spinetail, or
‘‘tijeral cejiblanco,’’ is a small dark
ovenbird in the Furnaridaii family that
is native to high-altitude woodlands of
the Peruvian Andes (BLI 2000, p. 347;
Chapman 1921, pp. 8-9; del Hoyo et al.
˚
2003, pp. 266-267; Fjeldsa and Krabbe
1990, p. 348; Parker and O’Neill 1980,
p. 169). The sexes are similar, with
individuals approximately 7 in (18 cm)
in length. The species is characterized
by its bright rufous crown and
prominent white supercilium (eyebrow)
(del Hoyo et al. 2003, p. 267; Lloyd
2009, p. 2), which gives the species its
name. The species is highly vocal,
‘‘often singing while acrobatically
foraging from the outermost branches of
Polylepis trees’’ (Lloyd 2009, p. 2).
Taxonomy
The white-browed tit-spinetail was
first described by Chapman in 1921 (del
Hoyo et al. 2003, p. 267). The species
has been synonymized with the
nominate subspecies of the rustycrowned tit-spinetail (Leptasthenura
pileata pileata) by Vaurie (1980, p. 66),
but examination of additional
specimens in combination with field
observations strongly suggests that L.
xenothorax is a valid species (Collar et
˚
al. 1992, p. 596; Fjeldsa and Krabbe
1990, p. 348; Parker and O’Neill 1980,
p. 169). Therefore, we accept the species
as Leptasthenura xenothorax, which
also follows the Integrated Taxonomic
Information System (ITIS 2009, p. 1).
Habitat and Life History
The white-browed tit-spinetail is
restricted to high-elevation, semihumid
Polylepis and Polylepis-Gynoxys
woodlands, where the species is found
between 12,139 and 14,928 ft (3,700 and
4,550 m) above sea level (BLI 2000, p.
347; Collar et al. 1992, p. 595; del Hoyo
˚
et al. 2003, p. 267; Fjeldsa and Krabbe
1990, p. 348; Lloyd 2009, pp. 5-6). The
characteristics of Polylepis habitat were
described above as part of the Habitat
and Life History of the ash-breasted tittyrant (Aucca and Ramsay 2005, p. 1;
Chutas et al. 2008, p. 3; De la Via 2004,
p. 10; IPNI 2009, p. 1; Kessler 1998, p.
1; Purcell et al. 2004, p. 455). The whitebrowed tit-spinetail prefers areas of
primary forest that have a high density
of tall, large trees and dense Polylepis
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stands and vegetation cover (Lloyd
2008a, as cited in Lloyd 2009, p. 6).
Dense stands of Polylepis woodlands
are characterized by moss-laden
vegetation and a shaded understory, and
provide for a rich diversity of insects,
making these areas good feeding
grounds for insectivorous birds (De la
Via 2004, p. 10), such as the whitebrowed tit-spinetail (BLI 2009d, p. 2).
According to Engblom et al. (2002, pp.
57-58), the species has been recorded in
patches of woodland as small as 0.6 ac
(0.25 ha) in Cordillera Vilcabamba.
Based on these observations, Engblom et
al. (2002, p. 58) suggest that the species
is able to persist in very small forest
fragments, especially if a number of
these patches are in close proximity.
The lower elevation of this species’
range changes to a mixed PolylepisEscallonia (no common name)
woodland, and the white-browed titspinetail has been observed there on
occasion, such as during a snowstorm
(Collar et al. 1992, p. 595; del Hoyo et
˚
al. 2003, p. 267; Fjeldsa and Krabbe
1990, p. 348).
There is limited information the
ecology and breeding behavior of the
white-browed tit-spinetail. Lloyd (2006,
as cited in Lloyd 2009, p. 8) reports that
the species breeds in October in
Cordillera Vilcanota in southern Peru.
In the same area, one adult was seen
attending a nesting hole in a Polylepis
tree in November 1997 (del Hoyo et al.
2003, p. 267; C. Bushell in litt. (1999),
as cited in BLI 2009d, p. 2). Only one
nest of the white-browed tit-spinetail
has ever been described. According to
Lloyd (2006, as cited in Lloyd 2009, p.
8), the nest was located within a natural
cavity of a Polylepis racemosa tree’s
main trunk, approximately 7 ft (2 m)
above the ground. To construct their
nest, the white-browed tit-spinetail pair
uses moss, lichen, and bark fibers they
stripped from Polylepis tree trunks,
large branches and large boulders while
foraging. The nest was cup-shaped and
contained two pale-colored eggs (Lloyd
2006, as cited in Lloyd 2009, p. 8).
The white-browed tit-spinetail is
insectivorous, with a diet consisting
primarily of arthropods (del Hoyo et al.
2003, p. 267; Lloyd 2009, p. 7). The
species forages in pairs or small family
groups of three to five, and often in
mixed-species flocks, gleaning insects
from bark crevices, moss, and lichens on
twigs, branches, and trunks (BLI 2009d,
pp. 2-3; Engblom et al. 2002, pp. 57-58;
Parker and O’Neill 1980, p. 169). The
white-browed tit-spinetail is highly
arboreal, typically foraging acrobatically
from the outer branches of Polylepis
trees while hanging upside-down (del
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Hoyo et al. 2003, p. 267; Lloyd 2008b,
as cited in Lloyd 2009, p. 7).
Historical Range and Distribution
In our 2008 Annual Notice of
Findings on Resubmitted Petitions for
Foreign Species (73 FR 44062; July 29,
2008), we stated that historically, the
white-browed tit-spinetail may have
occupied the Polylepis forests of the
high-Andes of Peru and Bolivia. We
included both countries in the historical
range of the species because the species’
primary habitat, the Polylepis forest,
was historically large and contiguous
throughout the high-Andes of both Peru
˚
and Bolivia (Fjeldsa 2002a, p. 115).
However, based on further research, we
have determined that historically, the
species was only known from two
Regions in south-central Peru, Cusco
´
and Apurımac (Collar et al. 1992, p. 594;
del Hoyo et al. 2003, p. 267), and not
in Bolivia.
The white-browed tit-spinetail may
once have been distributed throughout
south-central Peru, in previously
contiguous Polylepis forests above 9,843
ft (3,000 m) (BLI 2000, p. 347; BLI
˚
2009d, pp. 1-2; Fjeldsa 2002a, pp. 111112, 115; Herzog et al. 2002, p. 94;
Kessler 2002, pp. 97-101). However,
Polylepis woodlands are now restricted
to elevations of 11,483 to 16,404 ft
˚
(3,500 to 5,000 m) (Fjeldsa 1992, p. 10).
As discussed above for the Historical
Range and Distribution of the ashbreasted tit-tyrant, researchers consider
human activity to be the primary cause
for historical habitat decline and
resultant decrease in species richness
˚
(Fjeldsa and Kessler 1996, Kessler
1995a, b, and L#gaard 1992, as cited in
˚
˚
Fjeldsa 2002a, p. 112; Fjeldsa 2002a, p.
116; Herzog et al. 2002, p. 94; Kessler
2002, pp. 97-101; Kessler and Herzog
1998, pp. 50-51). It is estimated that
only 2-3 percent of the original forest
˚
cover still remains in Peru (Fjeldsa
2002a, pp. 111, 113). Less than 1
percent of the remaining woodlands
occur in humid areas, where denser
˚
stands are found (Fjeldsa and Kessler
˚
1996, as cited in Fjeldsa 2002a, p. 113),
and which are preferred by the whitebrowed tit-spinetail (BLI 2009d, p. 2;
Lloyd 2008a, as cited in Lloyd 2009, p.
6).
Current Range and Distribution
Today, the white-browed tit-spinetail
is restricted to high-elevation,
semihumid patches of Polylepis and
Polylepis-Gynoxys woodlands in the
Andes mountains of south-central Peru,
where the species occurs between
12,139-14,928 ft (3,700-4,550 m) (BLI
2000, p. 347; Collar et al. 1992, p. 595;
˚
del Hoyo et al. 2003, p. 267; Fjeldsa and
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643
Krabbe 1990, p. 348; InfoNatura 2007, p.
1; Lloyd 2009, pp. 1, 5-6). The species
has a highly restricted and severely
fragmented range, and is currently
known from only a small number of
sites: The Runtacocha highlands (in
´
Apurımac Region) and the Nevado
Sacsarayoc massif, Cordillera
Vilcabamba (Chapman 1921, p. 8), and
Cordillera Vilcanota (in the Cusco
Region) (BLI 2000, p. 347; BLI 2009d, p.
2; Lloyd 2009, p. 5). The estimated
range of the species is approximately
965 mi2 (2,500 km2) (BLI 2000, p. 347;
BLI 2009d, pp. 1, 5).
Population Estimates
Population information is presented
first on the local level and then in terms
of a global population estimate.
Local population estimates: Between
1987 and 1989, populations of 35-70
individuals were estimated to occur at
3 sites in Cusco; since then, declines in
the populations at some of these sites
˚
have been observed (Fjeldsa and Kessler
1996, as cited in BLI 2000, p. 347). At
´
Abra Malaga (Cusco Region), it is
estimated that there are approximately
30-50 birds (del Hoyo et al. 2003, p. 267;
Engblom et al. 2002, p. 58). In the
´
Runtacocha highlands (Apurımac
Region), the population density of the
white-browed tit-spinetail is very low
˚
(Fjeldsa and Kessler 1996, as cited in
BLI 2000, p. 347). Chutas (2007, p. 8)
reported an estimated 305 birds located
within 3 disjunct Polylepis forest
patches in Peru. This included 205 birds
and 36 birds in Cordilleras Vilcanota
and Vilcabamba, respectively (Cusco),
and 64 birds in ‘‘Cordillera del
´
Apurımac’’ (Runtacocha highlands of
´
Apurımac) (Chutas 2007, p. 8).
Density estimates derived from
surveys conducted at 3 sites in
Cordillera Vilcanota range from 25.3 (±
15.1) individuals per km2, to 9.6 (± 21.7)
individuals per km2, and the species
may occur at even higher densities in
other areas of Polylepis forests (Lloyd
2008c, as cited in Lloyd 2009, p. 9).
According to Lloyd (2008c, as cited in
Lloyd 2009, p. 9), this quantitative data
from Cordillera Vilcanota shows that the
white-browed tit-spinetail is ‘‘one of the
most abundant Polylepis specialists in
southern Peru.’’
Global population estimate: BirdLife
International categorizes the whitebrowed tit-spinetail as having a
population size between 500 and 1,500
individuals (BLI 2009d, pp. 1, 5). The
category was determined from the
population estimates reported by
Engblom et al. 2002 (p. 58), who
estimated ‘‘the known population to be
around 500 individuals with a possible
total population of 1,500 individuals.’’
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˚
In 2002, Fjeldsa (2002b, p. 9) estimated
a total population size of between 250
and 1,000 pairs of birds, which
coincides with the BirdLife
International category of 500–1,500
individuals.
The species has experienced a
population decline of between 10 and
19 percent in the past 10 years, and this
rate of decline is predicted to continue
(BLI 2009d, p. 5). The population is
considered to be declining in close
association with continued habitat loss
and degradation (see Factors A and E)
(BLI 2009d, p. 6).
Conservation Status
The white-browed tit-spinetail is
considered ‘‘endangered’’ by the
Peruvian Government under Supreme
Decree No. 034-2004-AG (2004, p.
276854). The IUCN considers the whitebrowed tit-spinetail to be ‘‘Endangered’’
due to its very small and severely
fragmented range and population,
which continue to decline with ongoing
habitat loss and a lack of habitat
regeneration (BLI 2009d, p. 1). The
white-browed tit-spinetail occurs within
the Peruvian protected area of Santuario
´
Historico Machu Picchu in Cusco (BLI
2009c, pp. 1, 3; BLI 2009d, p. 6; del
Hoyo et al. 2003, p. 267).
Summary of Factors Affecting the
White-browed Tit-Spinetail
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A. The Present or Threatened
Destruction, Modification, or
Curtailment of the Species’ Habitat or
Range
The white-browed tit-spinetail is
restricted to high-elevation, semihumid
Polylepis and Polylepis-Gynoxys
woodlands, where it is found between
12,139 and 14,928 ft (3,700 and 4,550
m) above sea level (BLI 2000, p. 347;
Collar et al. 1992, p. 595; del Hoyo et
˚
al. 2003, p. 267; Fjeldsa and Krabbe
1990, p. 348; Lloyd 2009, pp. 1, 5-6).
High-Andean Polylepis habitat is
characterized as a threatened woodland
ecosystem on national, regional, and
global levels (Purcell et al. 2004, p. 457;
Renison et al. 2005, as cited in Lloyd
2009, p. 10), with several Polylepis
species within the white-browed titspinetail’s range considered to be
‘‘Vulnerable,’’ according to the IUCN
(WCMC 1998a, p. 1; WCMC 1998b, p. 1).
As described more fully for the ashbreasted tit-tyrant (Factor A), Polylepis
woodlands have been much reduced
from historical estimates, with an
estimated remaining area of 386 mi2
˚
(1,000 km2) in Peru (Fjeldsa and Kessler
˚
1996, as cited in Fjeldsa 2002a, p. 113).
The majority of these remaining forests
are much dispersed, and less than 1
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percent is located in the humid parts of
the highlands, where denser stands
˚
occur (Fjeldsa and Kessler 1996, as cited
˚
in Fjeldsa 2002a, p. 113). The whitebrowed tit-spinetail prefers areas of
dense Polylepis primary forest with
understory vegetation that provides
optimal foraging habitat (BLI 2009d, p.
2; De la Via 2004, p. 10; Lloyd 2008a,
as cited in Lloyd 2009, p. 6) (see Habitat
and Life History).
In the Cordillera de Vilcanota (Cusco,
Peru), where a large portion of the
known white-browed tit-spinetail
population occurs (205 birds were
observed there, out of 305 total birds
observed in 3 study sites in Peru)
(Chutas 2007, p. 8), Polylepis woodland
habitat is highly fragmented and
degraded. As described more fully for
the ash-breasted tit-tyrant (Factor A),
recent research indicated that:
(1) Four forest patches in the
Cordillera de Vilcanota disappeared
completely in the last half a century,
and the remaining Polylepis remnants
are small (with a mean patch size of 7.4
ac (3 ha) (Jameson and Ramsay 2007, p.
42) and commonly separated from the
larger patches by distances of 98–4,921
ft (30–1,500 m) (Lloyd and Marsden in
press, as cited in Lloyd 2008, p. 532);
(2) Ten percent of the remaining forest
patches showed a decline in forest
density (Jameson and Ramsay 2007, p.
42); and
(3) There were no indications of forest
regeneration within the study area.
These findings have consequences for
the white-browed tit-spinetail given the
species’ ecological requirements. As
Polylepis woodlands decline in number,
the distances between patches increase.
According to Engblom et al. (2002, pp.
57-58), the species has been recorded in
patches of woodland as small as 0.6 ac
(0.25 ha) in Cordillera Vilcabamba, but
the species’ persistence in small patches
appears to be dependent on the patches
being in close proximity to each other.
Habitat degradation impacts the whitebrowed tit-spinetail, given its preference
for dense Polylepis woodlands, where
optimal foraging habitat is found (BLI
2009d, p. 2; De la Via 2004, p. 10; Lloyd
2008a, as cited in Lloyd 2009, p. 6). The
lack of Polylepis forest regeneration in
the area over nearly 50 years
underscores the ramifications of
continued burning and clearing to
maintain pastures and farmland that are
prevalent throughout the white-browed
tit-spinetail’s range (BLI 2009a, p. 1;
˚
Engblom et al. 2002, p. 56; Fjeldsa
˚
2002a, pp. 112, 120; Fjeldsa 2002b, p. 8;
Purcell et al. 2004, p. 458; WCMC
1998a, p. 1; WCMC 1998b, p. 1).
Habitat loss, conversion, and
degradation throughout the white-
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browed tit-spinetail’s range are
attributed to human activities (a full
description of which is provided above
as part of the Factor A analysis for the
ash-breasted tit-tyrant). Ongoing
activities include:
(1) Clearcutting and uncontrolled
burning for agriculture and pastureland
for domesticated animals, all of which
contributes to soil erosion, and habitat
degradation, which prevent forest
regeneration and restrict Polylepis
woodlands to localized and highly
fragmented landscapes (BLI 2009a, p. 2;
BLI 2009b, p. 1; BLI 2009c, p. 3; BLI
2009d, p. 3; Engblom et al. 2002, p. 56;
˚
˚
Fjeldsa 2002a, pp. 112, 120; Fjeldsa
2002b, p. 8; Jameson and Ramsay 2007,
p. 42; Purcell et al. 2004, p. 458;
Renison et al. 2006, as cited in Lloyd
2009, p. 11; WCMC 1998a, p. 1; WCMC
1998b, p. 1);
(2) Extractive activities, such as
harvest for timber, firewood, and
charcoal, for use on local- and
commercial-scales as fuel, construction,
fencing and tool-making (Aucca and
Ramsay 2005, p. 287; BLI 2009a, p. 2;
BLI 2009b, p. 1; BLI 2009d, p. 3;
Engblom 2000, pp. 1-2; Engblom et al.
˚
2002, p. 56; Fjeldsa and Kessler 1996, as
cited in BLI 2009d, p. 3; Purcell et al.
2004, pp. 458-459; WCMC 1998a, p. 1);
and
(3) Unpredictable climate fluctuations
that exacerbate the effects of habitat
fragmentation (Jetz et al. 2007, pp. 1211,
1213; Mora et al. 2007, p. 1027). These
habitat-altering activities are ongoing
throughout the range of the whitebrowed tit-spinetail, including in
´
Apurımac (BLI 2009b, p. 1) and Cusco
(BLI 2009a, pp. 1-2; BLI 2009c, pp. 1-3)
of south-central Peru and within the one
protected area in which the species
´
occurs, Santuario Historico Machu
Picchu (BLI 2009c, p. 3).
Polylepis conservation programs have
been under way in Peru since 2004,
including in Cordilleras Vilcanota and
Vilcabamba and highlands of the
´
Apurımac Region, where white-browed
tit-spinetail also occurs (Aucca and
Ramsey 2005, p. 287; Chutas 2007, p. 8;
ECOAN n.d., p. 1; Lloyd 2009, p. 10).
These community-based programs,
which are more fully described above as
part of the Factor A analysis for the ashbreasted tit-tyrant, confront the primary
causes of Polylepis deforestation:
Burning, grazing, and wood-cutting.
One such program, called the
‘‘Vilcanota Project,’’ is under way at
three locations in the Cordillera de
´
Vilcanota (Abra Malaga, Hulloc, and
Cancha-Cancha) (Aucca and Ramsay
2005, p. 287; ECOAN n.d., p. 1; Lloyd
2009, p. 10). Since local populations
rely on Polylepis wood for firewood and
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charcoal production (Aucca and Ramsay
2005, p. 287; Engblom et al. 2002, p. 56),
the Vilcanota Project works to deliver
non- Polylepis firewood to families for
cooking, as well as supply them with
fuel-efficient cooking stoves (ECOAN
n.d., p. 1). A short-term aim of these
projects is to restore balance to local
sustainable resource use (Aucca and
Ramsay 2005, p. 288; ECOAN n.d., p. 1).
´
However, at Abra Malaga (one of the
Vilcanota Project’s sites), Polylepis
woodlands continue to be impacted by
extraction for firewood and burning for
agriculture and pastureland (BLI 2009a,
pp. 1-2). In addition, commercial-scale
activities, such as logging and fuel wood
collection, which are ongoing
throughout this species’ range, alter
otherwise sustainable resource use
practices (Aucca and Ramsay 2005, p.
287; Engblom 2000, p. 2; Engblom et al.
2002, p. 56; MacLennan 2009, p. 2;
Purcell et al. 2004, pp. 458-459; WCMC
1998a, p. 1).
Habitat destruction caused by burning
and grazing, which have prevented
regeneration of habitat, is a factor in the
historical decline of Polylepis
˚
-dependent bird species (Fjeldsa 2002a,
p. 116). The white-browed tit-spinetail’s
population size is considered to be
declining in close association with the
continued habitat loss and degradation
of Polylepis woodlands (BLI 2009d, p.
6). The species may once have been
distributed throughout south-central
Peru, in once contiguous Polylepis
forests (BLI 2000, p. 347; BLI 2009d, pp.
˚
1-2; Fjeldsa 2002a, pp. 111-112, 115;
Herzog et al. 2002, p. 94; Kessler 2002,
pp. 97-101). Today, the species has a
highly restricted and severely
fragmented range, and is currently
known from only a small number of
´
sites in the Regions of Apurımac and
Cusco in south-central Peru (BLI 2000,
p. 347; BLI 2009d, pp. 1-2; Lloyd 2009,
p. 5).
White-browed tit-spinetails are also
impacted by unpredictable climate
fluctuations, which are more fully
described under the Factor A analysis of
the ash-breasted tit-tyrant and are
summarized here. Peru is subject to
unpredictable climate fluctuations that
exacerbate the effects of habitat
fragmentation, such as those that are
˜
related to the El Nino Southern
Oscillation (ENSO). Changes in weather
˜
patterns, such as ENSO cycles (El Nino
˜
and La Nina events), tend to increase
precipitation in normally dry areas, and
decrease precipitation in normally wet
areas (Holmgren et al. 2001, p. 89; TAO
Project n.d., p. 1), exacerbating the
effects of habitat fragmentation on the
decline of a species (England 2000, p.
86; Holmgren et al. 2001, p. 89; Jetz et
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al. 2007, pp. 1211, 1213; Mora et al.
2007, p. 1027; Parmesan and Mathews
2005, p. 334; Plumart 2007, pp. 1-2;
Timmermann 1999, p. 694), especially
for narrow endemics (Jetz et al. 2007, p.
1213) such as the white-browed titspinetail (see also Factor E). ENSO
cycles strongly influence the growth of
Polylepis species (Christie et al. 2008, p.
1) by altering Polylepis species’ age
structure and mortality, especially
where woodlands have undergone
disturbance, such as fire and grazing
(Villalba and Veblen 1997, pp. 121-123;
Villalba and Veblen 1998, pp. 2624,
2637). These cycles may have already
accelerated the fire cycle (Block and
Richter 2007, p. 1; Power et al. 2007, pp.
897-898), which is a key factor
preventing Polylepis regeneration
˚
˚
(Fjeldsa 2002a, p. 112, 120; Fjeldsa
2002b, p. 8) because Polylepis species
recover poorly following a fire
(Cierjacks et al. 2007, p. 176). ENSO
cycles are ongoing, having occurred
several times within the last decade
(NWS 2009, p. 2), and evidence suggests
that ENSO cycles have already
increased in periodicity and severity
(Richter 2005, pp. 24-25; Timmermann
1999, p. 694), which will exacerbate the
negative impacts of habitat destruction
on a species. It is predicted that, by
2050, another 1 percent of the whitebrowed tit-spinetail’s current remaining
range is likely to be unsuitable for this
species due to climate change; and, by
2100, it is predicted that about 43
percent of the species’ range is likely to
be lost as a direct result of global
climate change (Jetz et al. 2007,
Supplementary Table 2, p. 89).
Summary of Factor A
Polylepis habitat throughout the range
of the white-browed tit-spinetail has
been and continues to be altered and
destroyed as a result of human
activities, including clearcutting and
burning for agriculture and grazing
lands and extractive activities,
including harvest for timber, firewood,
and charcoal. It is estimated that only 1
percent of the dense Polylepis
woodlands preferred by the species
remain, and the remaining woodlands
are highly fragmented and degraded.
Observations suggest that the whitebrowed tit-spinetail is able to persist in
very small forest fragments (e.g., areas as
small as 0.6 ac (0.25 ha) in Cordillera
Vilcabamba); however, this depends on
whether or not a number of patches are
in close proximity to one another. Since
the remaining Polylepis woodlands are
and continue to be severely fragmented,
the distance between some of the small
woodland patches may be too large for
the species to be able to persist. Today,
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645
the species is known from only a small
number of sites at four locations: The
´
Runtacocha highlands (in Apurımac
Region), and the Nevado Sacsarayoc
massif, Cordillera Vilcabamba, and
Cordillera Vilcanota (in Cusco Region).
Historical decline in habitat availability
is attributed to the same human
activities that are causing habitat loss
today. Ongoing and accelerated habitat
destruction of the remaining Polylepis
woodlands in Peru continues to reduce
the quantity, quality, distribution, and
potential regeneration of Polylepis
forests. Human activities that degrade,
alter, and destroy habitat are ongoing
throughout the species’ range, including
within protected areas (see also Factor
D). Experts consider the species’
population decline to be commensurate
with the declining habitat (Factor E).
Current research indicates that climate
fluctuations exacerbate the effects of
habitat loss to species, especially for
narrow endemics such as the whitebrowed tit-spinetail that are already
undergoing range reduction due to
human activities. Climate models
predict that this species’ habitat will
continue to decline. Therefore, we find
that destruction and modification of
habitat are threats to the continued
existence of the white-browed titspinetail throughout its range.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
We are not aware of any information
currently available that indicates that
overutilization of the species for
commercial, recreational, scientific, or
educational purposes has occurred or is
occurring at this time. As a result, we
are not considering overutilization to be
a threat to the continued existence of
the white-browed tit-spinetail.
C. Disease or Predation
We are not aware of any scientific or
commercial information that indicates
that disease or predation poses a threat
to the species. As a result, we are not
considering disease or predation to be a
threat to the continued existence of the
white-browed tit-spinetail.
D. Inadequacy of Existing Regulatory
Mechanisms
The white-browed tit-spinetail is
considered ‘‘endangered’’ by the
Peruvian Government under Supreme
Decree No. 034-2004-AG (2004, p.
276854). This Decree prohibits hunting,
take, transport, and trade of protected
species, except as permitted by
regulation. As hunting, taking, or trade
do not currently threaten the whitebrowed tit-spinetail, this regulation does
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not mitigate any current threats to the
species.
Peru has several categories of national
habitat protection, which were
described above as part of Factor D for
the ash-breasted tit-tyrant (IUCN 1994,
´
p. 2; Rodrıguez and Young 2000, p.
330). Protected areas have been
established through regulation at one
site occupied by the white-browed titspinetail in Peru: the Santuario
´
Historico Machu Picchu (Cusco, Peru);
(BLI 2009c, pp. 1, 3; BLI 2009d, p. 6).
´
Resources within Santuario Historico
Machu Picchu are supposed to be
´
managed for conservation (Rodrıguez
and Young 2000, p. 330). However,
habitat destruction and alteration,
including burning, cutting, and grazing
are ongoing within the sanctuary,
preventing regeneration of the
woodlands (BLI 2009c, p. 3; Engblom et
al. 2002, p. 58). Therefore, the
occurrence of the white-browed titspinetail within protected areas in Peru
does not protect the species, nor does it
mitigate the threats to the species from
ongoing habitat loss (Factor A) and
concomitant population decline (Factor
E).
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Summary of Factor D
Peru has enacted various laws and
regulatory mechanisms to protect and
manage wildlife and their habitats. The
white-browed tit-spinetail is
‘‘endangered’’ under Peruvian law and
occurs within one protected area in
Peru. As discussed under Factor A, the
white-browed tit-spinetail prefers dense
Polylepis woodlands, which have been
reduced by an estimated 98 percent in
Peru. The Polylepis habitat that does
remain is highly fragmented and
degraded. Habitat throughout the
species’ range has been and continues to
be altered as a result of human
activities, including clearcutting and
burning for agriculture and grazing
lands; and extractive activities such as
timber harvest, firewood collection, and
charcoal production. These activities are
ongoing within protected areas despite
the species’ endangered status,
indicating that the laws governing
wildlife and habitat protection in Peru
are either inadequate or inadequately
enforced to protect the species or to
mitigate ongoing habitat loss (Factor A)
and population declines (Factor E).
Therefore, we find that the existing
regulatory mechanisms are inadequate
to mitigate the current threats to the
continued existence of the whitebrowed tit-spinetail throughout its
range.
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E. Other Natural or Manmade Factors
Affecting the Continued Existence of the
Species
An additional factor that affects the
continued existence of the whitebrowed tit-spinetail is the species’ small
population size. As discussed above (see
Population Estimates), BirdLife
International has placed the whitebrowed tit-spinetail in the population
category of between 500 and 1,500
individuals (BLI 2009d, pp. 1, 5), and
characterizes the species as having a
‘‘very small population’’ size (BLI 2000,
p. 347; BLI 2009d, p. 1).
Small population size renders species
vulnerable to genetic risks that can have
individual or population-level genetic
consequences, such as inbreeding
depression, loss of genetic variation,
and accumulation of new mutations,
and may affect the species’ viability by
increasing its susceptibility to
demographic shifts or environmental
fluctuations, as explained in more detail
above in the Factor E analysis for the
ash-breasted tit-tyrant (Charlesworth
and Charlesworth 1987, p. 238; Pimm et
al. 1988, pp. 757, 773-775; Shaffer 1981,
p. 131). Small population size leads to
a higher risk of extinction and, once a
population is reduced below a certain
number of individuals, it tends to
rapidly decline towards extinction
(Frankham 1996, p. 1507; Franklin
´
1980, pp. 147-148; Gilpin and Soule
1986, p. 25; Holsinger 2000, pp. 64-65;
Purvis et al. 2000, p. 1949; Reed and
´
Frankham 2003, pp. 233-234; Soule
1987, p. 181).
Complications arising from the
species’ small population size are
exacerbated by the species’ fragmented
distribution. The white-browed titspinetail is currently confined to highelevation, semihumid patches of forest
in the Andes of Peru, and its population
has declined at a rate between 10 and
19 percent in the past 10 years, in close
association with the continued loss and
degradation of the Polylepis forest (BLI
˚
2009d, pp. 5-6) (Factor A). Fjeldsa and
˚
Kessler (1996, as cited in Fjeldsa 2002a,
p. 113) describe the remaining Polylepis
woodlands as highly fragmented and
degraded, and estimate that only 1
percent of the dense woodlands
preferred by the species remain (BLI
2009d, p. 2; De la Via 2004, p. 10; Lloyd
2008a, as cited in Lloyd 2009, p. 6) (see
Habitat and Life History). As a result,
experts say that the species’ current
range is highly restricted and severely
fragmented (BLI 2000, p. 347; BLI
2009d, p. 1; Collar et al. 1992, p. 595;
˚
del Hoyo et al. 2003, p. 267; Fjeldsa and
Krabbe 1990, p. 348; InfoNatura 2007, p.
1; Lloyd 2009, p. 5). The species’ small
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population size, combined with its
highly restricted and severely
fragmented range, increases the species’
vulnerability to adverse natural events
and manmade activities that destroy
individuals and their habitat (Holsinger
2000, pp. 64-65; Primack 1998, pp. 279308; Young and Clarke 2000, pp. 361366).
Summary of Factor E
The white-browed tit-spinetail has a
small population size that renders it
vulnerable to genetic risks that
negatively impact the species’ viability.
The species has a severely restricted
range and occurs in highly fragmented
habitat that continues to undergo
degradation and curtailment due to
human activities (Factor A). The
restricted and fragmented range, as well
as the small population size, increases
the species’ vulnerability to extinction
through demographic or environmental
fluctuations. Based on its small
population size and fragmented
distribution, we have determined that
the white-browed tit-spinetail is
particularly vulnerable to the threat of
adverse natural events (e.g., genetic,
demographic, or environmental) and
human activities (e.g., deforestation and
habitat alteration) that destroy
individuals and their habitat. The
genetic and demographic risks
associated with small population sizes
are exacerbated by ongoing human
activities that continue to curtail the
species’ habitat throughout its range.
The species’ population has declined
and is predicted to continue declining
commensurate with ongoing habitat loss
(Factor A). Therefore, we find that the
species’ small population size, in
concert with its fragmented distribution
and its heightened vulnerability to
adverse natural events and manmade
activities, are threats to the continued
existence of the white-browed titspinetail throughout its range.
Status Determination for the WhiteBrowed Tit-Spinetail
The white-browed tit-spinetail, a
small dark ovenbird, is restricted to
high-altitude woodlands of the Peruvian
Andes. Preferring dense, semihumid
Polylepis and Polylepis-Gynoxys
woodlands, the ash-breasted tit-tyrant
occupies a narrow range of distribution
at elevations between 12,139 and 14,928
ft (3,700 and 4,550 m) above sea level.
The species has a highly restricted and
severely fragmented range
(approximately 965 mi2 (2,500 km2)),
and is currently known from only a
´
small number of sites in the Apurımac
and Cusco Regions, in south-central
Peru. The known population of the
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white-browed tit-spinetail is estimated
to be approximately 500 to 1,500
individuals.
We have carefully assessed the best
available scientific and commercial
information regarding the past, present,
and potential future threats faced by the
white-browed tit-spinetail. There are
three primary factors impacting the
continued existence of the whitebrowed tit-spinetail: (1) Habitat
destruction, fragmentation, and
degradation; (2) limited size and
isolation of remaining populations; and
(3) inadequate regulatory mechanisms.
Human activities that degrade, alter,
and destroy habitat are ongoing
throughout the white-browed titspinetail. Widespread deforestation and
the conversion of forests for grazing and
agriculture have led to the
fragmentation of habitat throughout the
range of the white-browed tit-spinetail
(Factor A). Researchers estimate that
only 1 percent of the dense Polylepis
woodlands preferred by the species
remain. Limited by the availability of
suitable habitat, the species occurs
today only in a few fragmented and
disjunct locations.
White-browed tit-spinetail habitat
continues to be altered by human
activities, which result in the continued
degradation, conversion, and
destruction of habitat and reduction of
the quantity, quality, distribution, and
regeneration of remaining forest
patches. Habitat loss was a factor in this
species’ historical decline (see
Historical Range and Distribution), and
the species is considered to be declining
today in association with the continued
reduction in habitat (Factors A and E).
The species’ severely restricted range,
combined with its small population
size, renders it 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.
Human activities that continue to curtail
the species’ habitat throughout its range
exacerbate the genetic and demographic
risks associated with small population
sizes (Factor E). The species has
experienced a population decline of
between 10 and 19 percent in the past
10 years (see Population Estimates), and
is predicted to continue declining
commensurate with ongoing habitat loss
and degradation. Current research
indicates that narrow endemics, such as
the white-browed tit-spinetail, are
especially susceptible to climate
fluctuations because of the synergistic
effect these fluctuations have on
declining populations that are also
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experiencing range reductions due to
human activities (Factor A).
Despite the species’ endangered status
in Peru and its occurrence within one
protected area, human activities that
degrade, alter, and destroy habitat are
ongoing throughout the white-browed
tit-spinetail’s range, including within
protected areas. Therefore, regulatory
mechanisms are either inadequate or
ineffective at curbing the threats to the
white-browed tit-spinetail of habitat loss
(Factor A) and corresponding
population decline (Factor E).
Section 3 of the Act defines an
‘‘endangered species’’ as ‘‘any species
which is in danger of extinction
throughout all or a significant portion of
its range’’ and a ‘‘threatened species’’ as
‘‘any species which is likely to become
an endangered species within the
foreseeable future throughout all or a
significant portion of its range.’’ Based
on the immediate and ongoing threats to
the white-browed tit-spinetail
throughout its entire range, as described
above, we determine that the whitebrowed tit-spinetail is in danger of
extinction throughout all of its range.
Therefore, on the basis of the best
available scientific and commercial
information, we are proposing to list the
white-browed tit-spinetail as an
endangered species throughout all of its
range.
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 Federal and State
governments, private agencies and
interest 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 has been proposed or designated.
However, given that the ash-breasted tit´
´
tyrant, Junın grebe, Junın rail, Peruvian
plantcutter, the royal cinclodes, and the
white-browed tit-spinetail are not native
to the United States, we are not
proposing critical habitat for these
species under section 4 of the Act.
Section 8(a) of the Act authorizes the
provision of limited financial assistance
for the development and management of
programs that the Secretary of the
Interior determines to be necessary or
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647
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 and threatened
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. As such, these prohibitions
would be applicable to the ash-breasted
´
´
tit-tyrant, Junın grebe, Junın rail,
Peruvian plantcutter, the royal
cinclodes, and the white-browed titspinetail. 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 to harass,
harm, pursue, hunt, shoot, wound, kill,
trap, capture, or collect, or to attempt to
engage in any such conduct) any
endangered wildlife species within the
United States or upon the high seas; or
to import or export; deliver, receive,
carry, transport, or ship in interstate or
foreign commerce in the course of
commercial activity; or to sell or offer
for sale in interstate or foreign
commerce any endangered wildlife
species. It is also 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.
Permits may be issued 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. With regard to
endangered wildlife, a permit may 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 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
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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 ash-breasted tit´
´
tyrant, Junın grebe, Junın rail, Peruvian
plantcutter, royal cinclodes, and whitebrowed tit-spinetail.
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.
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
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
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.
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, the sections where you feel
lists or tables would be useful, etc.
Required Determinations
References Cited
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
A complete list of all references cited
in this proposed rule is 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
FURTHER INFORMATION CONTACT).
Species
Common name
*
Historic
range
Scientific name
*
Vertebrate
population
where
endangered
or
threatened
*
Status
*
Author(s)
The primary authors of this proposed
rule are Jesse D’Elia (of the Pacific
Regional Office) and Patricia De
Angelis, Patricia Ford, Monica Horton,
and Marie Maltese (all of the Division of
Scientific Authority), U.S. Fish and
Wildlife Service.
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. 99625, 100 Stat. 3500; unless otherwise noted.
2. Amend § 17.11(h) by adding new
entries for ‘‘Cinclodes, royal,’’ ‘‘Grebe,
´
Junın,’’ ‘‘Plantcutter, Peruvian,’’ ‘‘Rail,
´
Junın,’’ ‘‘Tit-spinetail, white-browed,’’
and ‘‘Tit-tyrant, ash-breasted’’ in
alphabetical order under BIRDS to the
List of Endangered and Threatened
Wildlife, as follows:
§17.11 Endangered and threatened
wildlife.
*
*
*
(h) * * *
When listed
*
*
Critical habitat
Special rules
*
*
*
*
*
*
BIRDS
*
*
Cinclodes, royal
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*
´
Grebe, Junın
*
Plantcutter,
Peruvian
*
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*
Cinclodes aricomae
*
Bolivia, Peru
Entire
*
Podiceps taczanowskii
*
*
Peru
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*
E
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*
05JAP2
NA
*
NA
*
NA
*
NA
*
*
Frm 00044
*
E
*
Peru
NA
*
Entire
*
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*
*
Phytotoma raimondii
17:14 Jan 04, 2010
*
NA
*
649
Federal Register / Vol. 75, No. 2 / Tuesday, January 5, 2010 / Proposed Rules
Species
Common name
´
Rail, Junın
Historic
range
Scientific name
Laterallus tuerosi
*
Peru
*
Vertebrate
population
where
endangered
or
threatened
Entire
*
Status
When listed
Critical habitat
Special rules
NA
NA
E
*
*
*
*
Tit-spinetail,
white-browed
Leptasthenura xenothorax
Peru
Entire
E
NA
NA
Tit-tyrant, ashbreasted
Anairetes alpinus
Bolivia, Peru
Entire
E
NA
NA
*
*
*
*
*
*
*
*
*
*
Dated: December 16, 2009
Sam D. Hamilton,
Director, U.S. Fish and Wildlife Service
[FR Doc. E9–31102 Filed 1–4–10; 8:45 am]
*
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Agencies
[Federal Register Volume 75, Number 2 (Tuesday, January 5, 2010)]
[Proposed Rules]
[Pages 606-649]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-31102]
[[Page 605]]
-----------------------------------------------------------------------
Part IV
Department of the Interior
-----------------------------------------------------------------------
Fish and Wildlife Service
-----------------------------------------------------------------------
50 CFR Part 17
Endangered and Threatened Wildlife and Plants; Listing Foreign Bird
Species in Peru and Bolivia as Endangered Throughout Their Range;
Proposed Rule
Federal Register / Vol. 75, No. 2 / Tuesday, January 5, 2010 /
Proposed Rules
[[Page 606]]
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R9-IA-2009-0059]
[96100-1671-0000-B6]
[RIN 1018-AV77]
Endangered and Threatened Wildlife and Plants; Listing Foreign
Bird Species in Peru and Bolivia as Endangered Throughout Their Range
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), propose to
list the following six South American bird species (collectively
referred to as ``species'' for purposes of this proposed rule) as
endangered under the Endangered Species Act of 1973, as amended (Act)
(16 U.S.C. 1531 et seq.): ash-breasted tit-tyrant (Anairetes alpinus),
Junin grebe (Podiceps taczanowskii), Junin rail (Laterallus tuerosi),
Peruvian plantcutter (Phytotoma raimondii), royal cinclodes (Cinclodes
aricomae), and white-browed tit-spinetail (Leptasthenura xenothorax)--
all native to Peru. The ash-breasted tit-tyrant and royal cinclodes are
also native to Bolivia. 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
March 8, 2010. We must receive requests for public hearings, in
writing, at the address shown in the FOR FURTHER INFORMATION CONTACT
section by February 19, 2010.
ADDRESSES: You may submit comments by one of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov. Follow
the instructions for submitting comments on Docket No. FWS-R9-IA-2009-
0059.
U.S. mail or hand-delivery: Public Comments Processing, Attn:
FWS-R9-IA-2009-0059; Division of Policy and Directives Management; U.S.
Fish and Wildlife Service; 4401 N. Fairfax Drive, Suite 222; Arlington,
VA 22203.
We will not accept comments by e-mail or fax. 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), 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 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) Additional 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 such 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 at 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 a species to,
remove a species from, or reclassify a species on the Federal Lists of
Endangered and Threatened Wildlife and Plants has presented substantial
information indicating that the requested action may be warranted. To
the maximum extent practicable, we make the finding within 90 days
following receipt of the petition and publish our finding 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 (``12-month
finding'') on whether the requested action is warranted, not warranted,
or warranted but precluded by higher priority listing actions. 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 review (ANOR) of findings on resubmitted petitions for all
foreign species for which listings were previously found to be
warranted but precluded.
Previous Federal Actions
On May 6, 1991, we received a petition (the 1991 petition) from the
International Council for Bird Preservation (ICBP) to add 53 foreign
bird species to the List of Endangered and Threatened Wildlife,
including the six Peruvian bird species that are the subject of this
proposed rule. In response to the 1991 petition, we published a
substantial 90-day finding on December 16, 1991 (56 FR 65207), for all
53 species and initiated 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 (which
included 15 species from the 1991 petition). In that
[[Page 607]]
document, we announced our finding that listing the remaining 38
species from the 1991 petition, including the six Peruvian bird species
that are the subject of this proposed rule, was warranted but precluded
by higher priority listing actions. We made a subsequent warranted-but-
precluded finding for all outstanding foreign species from the 1991
petition, including the six Peruvian bird species that are the subject
of this proposed rule, as published in our ANOR on May 21, 2004 (69 FR
29354).
Per the Service's listing priority guidelines (September 21, 1983;
48 FR 43098), our 2007 ANOR identified the listing priority numbers
(LPNs) (ranging from 1 to 12) for all outstanding foreign species. The
six Peruvian bird species that are the subject of 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 actions. A listing priority of 2 indicates that the subject
species face imminent threats of high magnitude. With the exception of
the listing priority ranking of 1, which addresses monotypic genera
that face imminent threats of high magnitude, categories 2 and 3
represent the Service's highest priorities.
On July 29, 2008 (73 FR 44062), we published in the Federal
Register a notice announcing our annual petition findings for foreign
species. In that notice, we announced listing to be warranted for 30
foreign bird species, including the six Peruvian bird species which are
the subject of this proposed rule, and stated that we would ``promptly
publish proposals to list these 30 taxa.'' In selecting these six
species from the list of warranted-but-precluded species, we took into
consideration the magnitude and immediacy of the threats to the
species, consistent with the Service's listing priority guidelines.
On September 8, 2008, the Service received a 60-day notice of
intent to sue from the Center for Biological Diversity (CBD) and Peter
Galvin over violations of section 4 of the Act for the Service's
failure to promptly publish listing proposals for the 30 ``warranted''
species identified in our 2008 ANOR. Under a settlement agreement
approved by the U.S. District Court for the Northern District of
California on June 15, 2009, (CBD, et al. v. Salazar, 09-cv-02578-CRB),
the Service must submit to the Federal Register proposed listing rules
for the ash-breasted tit-tyrant, Junin grebe, Junin rail, Peruvian
plantcutter, royal cinclodes, and white-browed tit-spinetail by
December 29, 2009.
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. Listing actions may be
warranted based on any of the above threat factors, singly or in
combination.
Below is a species-by-species analysis of the five factors. The
species are considered in alphabetical order, beginning with the ash-
breasted tit-tyrant, followed by the Junin grebe, Junin rail, Peruvian
plantcutter, royal cinclodes, and the white-browed tit-spinetail.
I. Ash-breasted tit-tyrant (Anairetes alpinus)
Species Description
The ash-breasted tit-tyrant, locally known as ``torito
pechicenizo,'' is a small New World tyrant flycatcher in the Tyrannidae
family that is native to high-altitude woodlands of the Bolivian and
Peruvian Andes (BirdLife International (BLI) 2000, p. 392; Collar et
al. 1992, p. 753; del Hoyo et al. 2004, pp. 170, 281; Fjeldsa and
Krabbe 1990, pp. 468-469; InfoNatura 2007, p. 1; Supreme Decree No.
034-2004-AG 2004, p. 276854). The sexes are similar, with adults
approximately 5 inches (in) (13 centimeters (cm)) in length, with dark
gray, inconspicuously black-streaked upperparts (BLI 2009o, p. 1; del
Hoyo et al. 2004, p. 281). Two subspecies (see Taxonomy) are
distinguished by their underbelly color, which is yellowish-white in
the nominate subspecies and white in the other (BLI 2009o, p. 1) (see
Taxonomy). Juvenile plumage is duller in appearance, but otherwise
similar to the adult coloration (del Hoyo et al. 2004, p. 281).
Taxonomy
When the species was first taxonomically described by Carriker
(1933, pp. 27-29), it was placed in its own genus, Yanacea; this
decision was soon questioned by Zimmer (1940, p. 10). It was not until
the 1960s that Yanacea was merged into Anairetes (a genus long-known as
Spizitornis) by Meyer de Schauensee (1966, p. 376). Some contemporary
researchers have suggested retaining the species within Yanacea
(Fjeldsa and Krabbe 1990, p. 468). Smith (1971, pp. 269, 275) and Roy
et al. (1999, p. 74) confirmed that the ash-breasted tit tyrant is a
valid species based on its phylogenetic placement and degree of genetic
divergence from other species of Anairetes, and recent texts continue
to place it in Anairetes (e.g., del Hoyo et al. 2004, p. 281).
Therefore, we accept the species as Anairetes alpinus, which also
follows the Integrated Taxonomic Information System (ITIS 2009, p. 1).
Two subspecies are recognized, including, A. alpinus alpinus (the
nominate subspecies) and A. alpinus bolivianus. These subspecies occur
in two disjunct (widely separated) areas (see Current Range) (BLI 2000,
p. 392; del Hoyo et al. 2004, p. 281; ITIS 2009, p. 1) and are
distinguished by the color of their underbellies (see Taxonomy) (BLI
2009o, p. 1).
Habitat and Life History
The ash-breasted tit-tyrant is restricted to semihumid Polylepis or
Polylepis - Gynoxys woodlands, where the species is found at elevations
between 12,139 and 15,092 feet (ft) (3,700 and 4,600 meters (m)) above
sea level (BLI 2000, p. 392; Collar et al. 1992, p. 753; del Hoyo et
al. 2004, p. 281; Fjeldsa and Krabbe 1990, pp. 468-469; InfoNatura
2007, p. 1). The genus Polylepis (no English common name; locally
referred to as ``queu[ntilde]a'') (Aucca and Ramsay 2005, p. 1), in the
Rosaceae family, comprises approximately 20 species of evergreen bushes
and trees (De la Via 2004, p. 10; Kessler 1998, p. 1; Kessler and
Schmidt-Lebuhn 2006, pp. 1-2), 19 of which occur in Peru (Chutas et al.
2008, p. 3). In Bolivia, the ash-breasted tit-tyrant is associated only
with P. pepei forests, but the bird is found among a greater variety of
Polylepis species in Peru (Chutas et al. 2008, p. 16; I. Gomez,
National Museum of National History-Ornithology Section-Bolivian Fauna
Collection, La Paz, Bolivia, e-mail to Division of Scientific
Authority, in litt. December 4, 2007, p. 1). On average, Polylepis
species are 10-33 ft (3-10 m) tall, but may grow to a height of 118 ft
(36 m) (Purcell et al. 2004, p. 455).
Polylepis woodlands occur as dense forests, as open-canopied stands
with more arid understories, or as shrubland with scattered trees (De
la Via 2004, pp. 10-11; Fjeldsa and Kessler 1996, as cited in Fjeldsa
2002a, p. 113; Lloyd and
[[Page 608]]
Marsden in press, as cited in Lloyd 2008, p. 532). Ash-breasted tit-
tyrants prefer dense Polylepis forests (Fjeldsa 2002a, p. 114; Smith
1971, p. 269), which often include a mixture of Gynoxys trees (no
common name), in the Asteraceae family (De la Via 2004, pp. 10;
International Plant Names Index (IPNI) 2009, p. 1). Dense Polylepis
woodlands are characterized by moss- or vine-laden vegetation, with a
shaded understory and a rich diversity of insects, making good feeding
grounds for insectivorous birds (De la Via 2004, p. 10), such as the
ash-breasted tit-tyrant (BLI 2009o, p. 1; Lloyd 2008, p. 535).
There is little information about the ecology and breeding behavior
of the ash-breasted tit-tyrant. The species' territory ranges from 2.5-
5 acres (ac) (1-2 hectares (ha)) (BLI 2009o, p. 1). The breeding season
appears to occur during late dry season (Collar et al. 1992, p. 754)--
November and December (BLI 2009o, p. 1). Juveniles have been observed
in March and July (Collar et al. 1992, p. 754; del Hoyo et al. 2004, p.
281). Although species-specific information is not available, tit-
tyrant nests are generally finely woven, open cups, built in a bush
(Fjeldsa and Krabbe 1990, p. 468). The species may share in rearing
responsibilities, as pairs of ash-breasted tit-tyrants have been
observed feeding young (BLI 2009o, p. 1; Collar et al. 1992, p. 754).
The ash-breasted tit-tyrant forages alone, in family groups, and
sometimes in mixed-species flocks. The bird takes short flights, either
hovering or perching to consume invertebrates near the tops and outer
edges of Polylepis shrubs and trees (BLI 2009o, p. 1; del Hoyo et al.
2004, p. 281; Engblom et al. 2002, p. 58; Fjeldsa and Krabbe 1990, p.
468; Lloyd 2008, p. 535). In winter, when invertebrate populations
diminish, tit-tyrants may also forage on seeds (Fjeldsa and Krabbe
1990, p. 468).
Historical Range and Distribution
The ash-breasted tit-tyrant may once have been well-distributed
throughout previously dense and contiguous Polylepis high-Andes
woodlands of Peru and Bolivia. Researchers believe that these woodlands
were historically contiguous with lower-elevation cloudforests and
widespread above 9,843 ft (3,000 m) (Collar et al. 1992, p. 753;
Fjeldsa 2002a, pp. 111-112, 115; Herzog et al. 2002, p. 94; Kessler
2002, pp. 97-101). Today, Polylepis woodlands are found only at
elevations of 11,483 to 16,404 ft (3,500 to 5,000 m) (Fjeldsa 1992, p.
10). Researchers consider the reduction in Polylepis forest habitat to
be the result of historical human activities, including burning and
grazing, which have prevented regeneration of the woodlands and
resulted in the fragmented habitat distribution seen today (Fjeldsa and
Kessler 1996, Kessler 1995a, Kessler 1995b, and L[aelig]gaard 1992, as
cited in Fjeldsa 2002a, p. 112; Herzog et al. 2002, p. 94; Kessler
2002, pp. 97-101; Kessler and Herzog 1998, pp. 50-51). Modeling studies
by Fjeldsa (2002a, p. 116) indicate that this habitat reduction was
accompanied by a loss in species richness. It is estimated that only 2-
3 and 10 percent of the original forest cover still remain in Peru and
Bolivia, respectively (Fjeldsa and Kessler 1996, as cited in Fjeldsa
2002a, p. 113). Of this amount, only 1 percent of the remaining
Polylepis woodlands are found in humid areas, where denser stands occur
(Fjeldsa and Kessler 1996, as cited in Fjeldsa 2002a, p. 113) and which
are preferred by the ash-breasted tit-tyrant (BLI 2009o, p. 1; Fjeldsa
2002a, p. 114; Lloyd 2008, p. 535; Smith 1971, p. 269) (see Factor A).
Current Range and Distribution
The current range of the ash-breasted tit-tyrant is estimated to be
4,595 square miles (mi\2\) (11,900 square kilometers (km\2\)) (BLI
2009o, p. 1). However, BirdLife International (2000, pp. 22, 27)
defines a species' ``Range'' as the ``Extent of Occurrence,'' which is
``the area contained within the shortest continuous imaginary boundary
which can be drawn to encompass all the known, inferred, or projected
sites of present occurrence of a species, excluding cases of
vagrancy.'' Given that the species is known to occur in two disjunct
locations, this range estimate, therefore, includes a large area of
habitat where the species is not known to occur.
The species is restricted to patches of high-elevation semihumid
Polylepis or Polylepis - Gynoxys woodlands of Peru and Bolivia, where
ash-breasted tit-tyrant is found only at 12,139-15,092 ft (3,700-4,600
m) (BLI 2000, p. 392; Collar et al. 1992, p. 753; del Hoyo et al. 2004,
pp. 170, 281; Fjeldsa and Krabbe 1990, pp. 468-469; InfoNatura 2007, p.
1). The ash-breasted tit-tyrant is known only in two disjunct areas:
one location in west-central Peru and another ranging from southern
Peru into northern Bolivia (BLI 2000, p. 392; del Hoyo et al. 2004, p.
281; ITIS 2009, p. 1).
In west-central Peru, the northern subspecies (A. alpinus alpinus)
occurs in the Cordilleras Central and Occidental (in the Peruvian
Administrative Regions of Ancash, Huanuco, La Libertad, and Lima) (BLI
2007, p. 1; BLI 2009g, p. 1; BLI 2009i, p. 1; BLI 2009l, p. 1; BLI
2009o, p. 1; Collar et al. 1992, p. 753; del Hoyo et al. 2004, p. 281).
Until 1992, the taxon in this locality was highly localized and known
only in Ancash Region (Collar et al. 1992, p. 753). The species was
subsequently reported in Huanuco Region, in 2003 (BLI 2007, p. 5; BLI
2009i, p. 1); La Libertad Region, in 2004 (del Hoyo et al. 2004, p.
281); and Lima Region and again in Huanuco Region, in 2007 (BLI 2007,
pp. 1, 5). Also in 2007, the ash-breasted tit-tyrant was also observed
in a new locality in Ancash Region, Corredor Conchucos (Chutas 2007,
pp. 4, 8), where a Polylepis reforestation project is under way to
connect two protected areas where ash-breasted tit-tyrants were already
known to occur, Parque Nacional Huascaran and Zona Reservada de la
Cordillera Huayhuash (Antamina Mine 2006, p. 5; MacLennan 2009, p. 1)
(see Factor A).
The second location spans the Peruvian-Bolivian border--in the
Peruvian Administrative Regions of Apurimac, Cusco, Puno, and Arequipa
(from north to south) and in the Bolivian Department of La Paz. Here,
the southern subspecies (A. alpinus bolivianus) occurs in Cordillera
Oriental (Apurimac and Cusco), Cordilleras Vilcanota and Vilcabamba
(Cusco), and Cordillera de Carabaya (Puno)--in Peru--and ranges into
Bolivia, where it is found in the Cordillera Real and the Cordillera
Apolobamba (La Paz) (BLI 2000, p. 392; BLI 2009a, p. 1; BLI 2009b, p.
1; BLI 2009c, p. 1; BLI 2009d, p. 1; BLI 2009e, p. 1; BLI 2009f, p. 1;
BLI 2009k, p. 1; BLI 2009m, p. 1; BLI 2009n, p. 1; BLI 2009o, p. 5;
Chutas 2007, p. 8; Collar et al. 1992, p. 753; del Hoyo et al. 2004, p.
281; Fjeldsa and Krabbe 1990, pp. 468-469; InfoNatura 2007, p. 1). The
ash-breasted tit-tyrant was only recently (in 2008) reported in
Arequipa Region, Peru (BLI 2009j, p. 1).
The ash-breasted tit-tyrant is highly localized (Collar et al.
1992, p. 753) and has been described as ``very rare and local, with
usually only 1-2 pairs per occupied woodland'' (Fjeldsa and Krabbe
1990, p. 469). It exists at such low densities in some places that it
goes undetected (Collar et al. 1992, p. 753). The species appears to be
unable to persist in forest remnants smaller than 2.5 ac (1 ha) (BLI
2009o, p. 1).
Population Estimates
Population information is presented first on the range country
level and then in terms of a global population estimate. The range
country estimates begin with Peru, where the majority of the population
resides.
Local population estimate, Peru: Chutas (2007, p. 8) surveyed five
[[Page 609]]
disjunct Polylepis forest patches in Peru and estimated that 461 ash-
breasted tit-tyrants were located there. This included 30 birds in
Corredor Conchucos (Ancash Region); 181 birds and 33 birds in
Cordilleras Vilcanota and Vilcabamba, respectively (Cusco Region); 22
birds in Cordillera de Carabaya (Puno Region); and 195 birds in a study
site called ``Cordillera del Apurimac'' (Apurimac Region) (Chutas 2007,
pp. 4, 8), referring to an area within the Runtacocha highlands. Other
research in the Runtacocha highlands has indicated that the ash-
breasted tit-tyrant is ``relatively common'' there (BLI 2007, p. 1; BLI
2009o, p. 1), with an estimated 100 pairs of birds found in
approximately 40 forest patches (Fjeldsa in litt. 1990, as cited in
Collar et al. 1992, p. 753). ``Small numbers'' of birds are reported in
La Libertad Region (del Hoyo et al. 2004, p. 281). There are no
population estimates within Arequipa, Huanuco, or Lima Regions, where
the ash-breasted tit-tyrant is also reported to occur (BLI 2009g, p. 1;
BLI 2009i, p. 1; BLI 2009j, p. 1; BLI 2009o, p. 1).
Local population estimate, Bolivia: Although BirdLife International
reports an estimated population size of 150-300 ash-breasted tit-
tyrants in Bolivia (Gomez in litt., 2003 and 2007, as cited in BLI
2009o, p. 1), recent surveys indicate that the estimate is smaller.
Over a six-year period, Gomez (in litt. 2007, p. 1) conducted intensive
searches throughout 80 percent of the suitable habitat in Bolivia in
the Cordillera Real and the Cordillera Apolobamba (La Paz Department),
using song playback and point census, to detect the presence of the
ash-breasted tit-tyrant. From this work, researchers inferred or
observed the presence of 2-10 individuals in each of four forest
patches and estimated that approximately 180 ash-breasted tit-tyrants
occur in Bolivia.
Global population estimate: BirdLife International, a global
organization that consults with and assimilates information from
species experts, categorizes the ash-breasted tit-tyrant as having a
population size between 250 and 999 individuals, with an estimated
actual population size to be in the mid- to upper-hundreds (BLI 2000,
p. 392; BLI 2007, p. 1; BLI 2009o, p. 1). Combining the estimated
number of ash-breasted tit-tyrants in Peru and Bolivia, the total
population consists of at least 641 individuals (Chutas 2007, pp. 4, 8;
Gomez in litt. 2007, p. 1), consistent with the BirdLife International
category of 250-999 individuals.
However, the total population size, which includes immature
individuals, is not an accurate reflection of the species' effective
population size (the number of breeding individuals that contribute to
the next generation) (Shaffer 1981, pp. 132-133; Soule 1980, pp. 160-
162). Because the ash-breasted tit-tyrant exists as two subspecies (BLI
2000, p. 392; BLI 2009a, p. 1; BLI 2009b, p. 1; BLI 2009c, p. 1; BLI
2009d, p. 1; BLI 2009e, p. 1; BLI 2009f, p. 1; BLI 2009k, p. 1; BLI
2009m, p. 1; BLI 2009n, p. 1; BLI 2009o, p. 5; Chutas 2007, p. 8;
Collar et al. 1992, p. 753; del Hoyo et al. 2004, p. 281; Fjeldsa and
Krabbe 1990, pp. 468-469; InfoNatura 2007, p. 1; ITIS 2009, p. 1), it
is reasonable to conclude that there is little or no gene flow between
the two subspecies and that the species does not breed as a single
population. Therefore, even if all 641 individuals were mature, they
would not breed as a single population, such that the species'
effective population size is less than 641.
There are also constraints to determining the effective population
size on a subspecies level. According to International Union for
Conservation of Nature (IUCN) criteria, it is estimated that there are
no more than 250 mature individuals in any single subpopulation of the
ash-breasted tit-tyrant (IUCN 2001, pp. 8-12). However, the parameters
of a subpopulation are not provided in existing research. For instance,
while ash-breasted tit-tyrants occupy territories of 2.5-5 ac (1-2 ha)
(BLI 2009o, p. 1), there is no information as to the taxon's ability or
tendency to travel between territories or forest patches. Research on
Bolivian localities indicates that gene flow occurs between some
subpopulations, but not all (Gomez 2005, p. 86). In Bolivia, where only
1 subspecies occurs, the birds are distributed in 2 metapopulations,
with at least 5 subpopulations in one location and 14 subpopulations in
the other (Gomez 2005, p. 86). Peruvian population estimates are
incomplete, with no estimates for the ash-breasted tit-tyrants
occurring in Arequipa, Huanuco, La Libertad or Lima (BLI 2009g, p. 1;
BLI 2009i, p. 1; BLI 2009j, p. 1; BLI 2009o, p. 1; del Hoyo et al.
2004, p. 281). Therefore, we can conclude that gene flow occurs at the
subspecies level, but there is not sufficient information to determine
the extent to which subpopulations interbreed.
The species has experienced a population decline of between 10 and
19 percent in the past 10 years, and this rate of decline is predicted
to continue (BLI 2009o, pp. 1, 4). The population is considered to be
declining in close association with continued habitat loss and
degradation (see Factors A and E) (BLI 2007, pp. 1, 4; BLI 2009o, p.
5).
Conservation Status
The ash-breasted tit-tyrant is considered ``endangered'' by the
Peruvian Government under Supreme Decree No. 034-2004-AG (2004, p.
276855). The IUCN considers the ash-breasted tit-tyrant to be
``Endangered'' because it has a very small population that is
undergoing continued decline in the number of mature individuals and is
confined to a habitat that is severely fragmented and is also
undergoing a continuing decline in extent, area, and quality (BLI 2008,
p. 1; BLI 2009o, p. 4; IUCN 2001, pp. 8-12). The ash-breasted tit-
tyrant occurs within the following Peruvian protected areas: Parque
Nacional Huascaran, in Ancash, and Santuario Historico Machu Picchu, in
Cusco, and Zona Reservada de la Cordillera Huayhuash, spanning Ancash,
Huanuco, and Lima (BLI 2009i, p. 1; BLI 2009l, p. 1; BLI 2009n, p. 1;
Chutas et al. 2008, p. 16). In La Paz Department, Bolivia, the species
is found in Parque Nacional y area Natural de Manejo Integrado Madidi,
Parque Nacional y area Natural de Manejo Integrado Cotapata, and the
co-located protected areas of Reserva Nacional de Fauna de Apolobamba,
area Natural de Manejo Integrado de Apolobamba, and Reserva de la
Biosfera de Apolobamba (Auza and Hennessey 2005, p. 81; BLI 2009a, p.
1; BLI 2009b, p. 1; BLI 2009c, p. 1; BLI 2009e, p. 1; BLI 2009i, p. 1;
Chutas et al. 2008, p. 16).
Summary of Factors Affecting the Ash-breasted Tit-tyrant
A. The Present or Threatened Destruction, Modification, or Curtailment
of the Species' Habitat or Range
The ash-breasted tit-tyrant is dependent upon high-elevation
semihumid Polylepis or Polylepis - Gynoxys woodlands (BLI 2000, p. 392;
Collar et al. 1992, p. 753; del Hoyo et al. 2004, pp. 281; Fjeldsa and
Krabbe 1990, pp. 468-469; InfoNatura 2007, p. 1). Researchers believe
that this habitat was historically contiguous with lower-elevation
cloudforests and widespread above 9,843 ft (3,000 m) (Collar et al.
1992, p. 753; Fjeldsa 2002a, pp. 111, 115), but Polylepis woodlands
occur today only between 11,483-16,404 ft (3,500-5,000 m) (Fjeldsa
1992, p. 10). As described above (see Habitat and Life History), the
species prefers dense woodlands (Fjeldsa 2002a, p. 114; Smith 1971, p.
269), where the best foraging habitat occurs (De la Via 2004, p. 10),
and ash-breasted tit-tyrant occurs at altitudes of 12,139-15,092 ft
(3,700-4,600 m) (BLI 2000, p. 392; Collar et al. 1992, p. 753; del Hoyo
et al. 2004, pp.
[[Page 610]]
170, 281; Fjeldsa and Krabbe 1990, pp. 468-469; InfoNatura 2007, p. 1).
High-Andean Polylepis woodlands are considered by experts to be the
most threatened habitat in Peru and Bolivia (Purcell et al. 2004, p.
457), throughout the Andean region (BLI 2009a, p. 2), and one of the
most threatened woodland ecosystems in the world (Renison et al. 2005,
as cited in Lloyd 2009, p. 10). The IUCN has listed several Polylepis
species as ``Vulnerable,'' including two species that occur within the
ash-breasted tit-tyrant's range, Polylepis incana and P. pepei (WCMC
1998a, p. 1; WCMC 1998b, p. 1). Peruvian and Bolivian Polylepis
woodlands today are highly fragmented. In the late 1990s, Fjeldsa and
Kessler (1996, as cited in Fjeldsa 2002a, p. 113) conducted
comprehensive ground surveys and analyzed maps and satellite images of
the area. They estimated that the current range of Polylepis woodlands
had been reduced from historical levels by 97-98% in Peru and 90
percent in Bolivia. Contemporary Polylepis woodlands are dispersed and
sparse, covering an estimated area of 386 mi\2\ (1,000 km\2\) and 1,931
mi\2\ (5,000 km\2\) in Peru and Bolivia, respectively (Fjeldsa and
Kessler 1996, as cited in Fjeldsa 2002a, p. 113). Of the remaining
Polylepis woodlands, only 1 percent are found in humid areas, where
denser Polylepis forests tend to occur (Fjeldsa and Kessler 1996, as
cited in Fjeldsa 2002a, p. 113). Dense habitat is preferred by the ash-
breasted tit-tyrant (BLI 2009o, p. 1; Fjeldsa 2002a, p. 114; Lloyd
2008, p. 535; Smith 1971, p. 269).
Habitat loss, conversion, and degradation throughout the ash-
breasted tit-tyrant's range have been and continue to occur as a result
of ongoing human activity, including (1) Clearcutting and burning; (2)
extractive activities; (3) human encroachment; and (4) unpredictable
climate fluctuations that exacerbate the effects of habitat
fragmentation. Clearcutting and burning are among the most destructive
activities, and are a leading cause for Polylepis habitat loss (WCMC
1998a, p. 1; WCMC 1998b, p. 1). Forested areas are cleared for
agriculture and to create pastureland for cattle, sheep, and camels
(BLI 2009a, p. 2; BLI 2009c, pp. 1-2; BLI 2009d, pp. 1-2; BLI 2009e,
pp. 1, 5; BLI 2009h, p. 1; BLI 2009m, p. 1; BLI 2009n, p. 4). Grazing
lands situated amongst remaining forest patches are regularly burned in
order to maintain the grassland vegetation (locally known as,
``chaqueo''). Regular burning prevents regeneration of native forests
and is considered the key factor limiting the distribution of Polylepis
forests (BLI 2009f, p. 1; BLI 2009n, p. 4; Fjeldsa 2002b, p. 8; WCMC
1998a, p. 1; WCMC 1998b, p. 1). In some areas, the burns escape
control, causing further habitat destruction (BLI 2009a, p. 2; BLI
2009e, pp. 1, 5). Burning and clearcutting occur throughout the ash-
breasted tit-tyrant's range, including in Ancash (BLI 2009h, p. 1),
Apurimac (BLI 2009m, p. 1), and Cusco (BLI 2009n, p. 4), in Peru; and
La Paz, Bolivia (BLI 2009a, p. 2; BLI 2009c, pp. 1-2; BLI 2009d, pp. 1-
2; BLI 2009e, pp. 1, 5). These activities are also ongoing within
protected areas, including Parque Nacional Huascaran, Santuario
Historico Machu Picchu, and Zona Reservada de la Cordillera Huayhuash
(Barrio 2005, p. 564; BLI 2009l, p. 4; BLI 2009n, p. 2) (see Factor D).
As a result of the intensity of burning and grazing, Polylepis
species are restricted to areas where fires cannot spread, and where
cattle and sheep do not normally roam--in stream ravines and on
boulders, rock ledges, and sandy ridges (Fjeldsa 2002a, p. 112; Fjeldsa
2002b, p. 8). Grazing and trampling by domesticated animals further
limit forest regeneration (Fjeldsa 2002a, p. 120) and contribute to the
degradation of remaining forest patches. Sheep and cattle have solid,
sharp hooves that churn up the earth, damaging vegetation and
triggering erosion (Engblom et al. 2002, p. 56; Purcell et al. 2004, p.
458). The loss of nutrient-rich soils leads to habitat degradation,
which reduces the ability of the habitat to support dense stands of
Polylepis woodlands (Fjeldsa 2002b, p. 8; Jameson and Ramsay 2007, p.
42; Purcell et al. 2004, p. 458).
Ash-breasted tit-tyrant habitat is also subject to conversion,
degradation, or destruction caused by extractive activities, such as
firewood collection, timber harvest, and mining. Cutting wood for fuel
has a consistent and ongoing impact throughout the species' range (BLI
2009a, p. 2; BLI 2009b, pp. 1-2; BLI 2009c, pp. 1-2; BLI 2009d, pp. 1-
2; BLI 2009f, p. 1; BLI 2009l, p. 1; WCMC 1998a, p. 1). The high-
altitude zones where Polylepis occurs have long been inhabited by
subsistence farmers, who rely on Polylepis wood for firewood and
charcoal production (Aucca and Ramsay 2005, p. 287). Many locals manage
woodlands for firewood extraction (Engblom et al. 2002, p. 56), and
community-based Polylepis conservation programs fostered by the
Peruvian nongovernmental organization Asociacion Ecosistemas Andinos
(ECOAN) have been under way in Peru and Bolivia since 2004,
encompassing Cordilleras Vilcanota and Vilcabamba (Cusco Region),
highlands of the Apurimac Region (Aucca and Ramsey 2005, p. 287; ECOAN
no date (n.d.), p. 1; Lloyd 2009, p. 10), and in the Ancash Region
(MacLennan 2009, p. 2). Known as the ``Vilcanota Project'' or ECOAN
Projects (Aucca and Ramsey 2005, p. 287; ECOAN n.d., p. 1), local
communities enter into and enforce management agreements aimed at the
primary causes for Polylepis deforestation: burning, grazing, and wood-
cutting. These projects foster local, sustainable use of resources
(Aucca and Ramsay 2005, p. 287; ECOAN n.d., p. 1; Engblom et al. 2002,
p. 56), such as the use of more fuel-efficient wood-burning stoves that
require half the amount of wood fuel (MacLennan 2009, p. 2) (see the
Factor A analyses for royal cinclodes and white-browed tit-spinetail
for additional examples).
Polylepis wood is also harvested for local commercial use,
including within protected areas (BLI 2009a, p. 2; WCMC 1998a, p. 1)
(Factor D). At one site, near Abra Malaga (Cusco Region), wood is
harvested for sale to local hotels in the towns of Urubamba and
Ollantaytambo to support tourism activity (Engblom 2000, p. 1). Engblom
(2000, p. 1) documented felling for firewood at this site in Cusco over
a 2-day period that significantly reduced the size and quality of the
forest patch. Purcell et al. (2004, p. 458) noted a positive
correlation between habitat destruction and increased demand for (and
the concomitant rise in the price of) fuel. Polylepis is also harvested
for construction, fencing, and tool-making (Aucca and Ramsey 2005, p.
287; BLI 2009a, p. 2). Commercial-scale activities, such as
clearcutting, logging, tourism, and infrastructure development, are
ongoing throughout this species' range, and alter otherwise sustainable
resource use practices (Aucca and Ramsay 2005, p. 287; Engblom 2000, p.
2; Engblom et al. 2002, p. 56; MacLennan 2009, p. 2; Purcell and
Brelsford 2004, pp. 156-157; Purcell et al. 2004, pp. 458-459; WCMC
1998a, p. 1). Commercial-scale resource use is exacerbated by ongoing
human encroachment, discussed below.
Mining in Polylepis habitat occurs in the Peruvian Regions of
Ancash and Huanaco and in the Bolivian Department of La Paz (BLI 2009b,
p. 1; BLI 2009d, p. 1; BLI 2009g, p. 1). Ancash (Peru) is home to the
largest zinc and copper mine ``in the world,'' with a monthly average
production rate of 231,485 pounds (105,000 metric tons) of minerals per
day and a 186-mile (mi) (300 kilometer (km)) pipeline that stretches
from the mine to the port of Punta Lobitos along the coast (Antamina
Mine 2006, pp. 4, 9; www.antamina.com/02--operacion/
[[Page 611]]
En--puerto.html). Mining occurs in ash-breast tit-tyrant habitat in La
Paz, Bolivia, where there are active gold, tin, silver, and tungsten
mines, in addition to gravel excavation for cement production (USGS
Minerals Yearbook 2005, pp. 4-7). Antamina Mine has undertaken habitat
conservation programs within the areas affected by mineral extraction,
similar to the ECOAN Polylepis conservation programs, investing
millions of dollars in programs ranging from education and tourism, to
organic agriculture and sustainable development. However, tourism has
had negative effects in other areas where the ash-breasted tit-tyrant
occurs, including Ancash, Huanuco, and Lima, Peru, and La Paz, Bolivia
(Barrio 2005, p. 564; BLI 2009e, p. 5) (see below). The Antamina Mining
Company conservation program also supports the planned reforestation of
123,552 ac (50,000 ha) of Polylepis forest that will connect two
protected areas, Parque Nacional Huascaran and Zona Reservada de la
Cordillera Huayhuash (Antamina Mine 2006, p. 5). To date, the project
has succeeded in restoring 371 ac (150 ha) of forest, with a 95 percent
survival rate (MacLennan 2009, p. 1). Known as Corredor Conchucos, at
least 30 ash-breasted tit-tyrants have recently been observed there
(Chutas 2007, p. 8).
Human encroachment and concomitant increasing human population
pressures exacerbate the destructive effects of ongoing human
activities throughout the ash-breasted tit-tyrant's habitat. Mining and
hydroelectric projects open new areas to exploitation and attract
people seeking employment (Purcell et al. 2004, p. 458). Increased
urbanization and mining have led to increased infrastructure
development. Road building and mining projects further facilitate human
access to remaining Polylepis forest fragments, throughout the ash-
breasted tit-tyrant's range (Purcell et al. 2004, pp. 458-459; Purcell
and Brelsford, 2004, pp. 156-157), including protected areas. In the
Bolivian Department of La Paz, one of the most transited highways in
the country is located a short distance from the Parque Nacional y area
Natural de Manejo Integrado Cotapata (BLI 2009b, p. 2) (see Factor D).
Road building, mining, and other large-scale resource exploitations are
considered to have major impacts on the habitat, as compared to
exploitation by local communities (Purcell and Brelsford 2004, p. 157).
Ecotourism within protected areas where the ash-breasted tit-tyrant
occurs (such as in the Zona Reservada de la Cordillera Huayhuash in
Peru, and in the Apolobamba protected areas in Bolivia) is considered a
growing problem (Barrio 2005, p. 564; BLI 2009e, p. 5) (see Factor D).
In the Department of La Paz, Bolivia, which encompasses Bolivia's
largest urban area, most of the Polylepis forest had been eliminated
prior to the late 1990s (Purcell and Brelsford 2004, p. 157). Recently,
an accelerated rate of Polylepis forest destruction has been attributed
to clearcutting for road building and industrialization projects, such
as mining and construction of hydroelectric power stations (Purcell and
Brelsford 2004, pp. 156-157). Between 1991 and 2003, approximately 494
ac (200 ha) of Polylepis habitat was destroyed. Thus, nearly two-thirds
of the forest cover that existed in the 1990s no longer existed in 2003
(Purcell and Brelsford 2004, p. 155). With this research, it was
estimated that only 1,285 ac (520 ha) of Polylepis forest remain in the
Bolivian Department of La Paz, representing approximately a 40 percent
rate of habitat loss in just over one decade. The researchers inferred
that thisrate of destruction could result in extirpation of the
remaining Polylepis forest in La Paz within the next 30 years (Purcell
and Brelsford 2004, pp. 157).
Larger concentrations of people put greater demand on the natural
resources in the area. Increasing demand for firewood upsets informal
and otherwise sustainable community-based forest management traditions
(Purcell and Brelsford, 2004, p. 157). Increasing human populations in
the high-Andes of Bolivia and Peru have also resulted in a scarcity of
arable land. This has led many farmers to burn down additional patches
of Polylepis forests to plant crops, even on steep hillsides not
suitable for cultivation (BLI 2009b, p. 2; BLI 2009h, p. 1; Hensen
2002, p. 199). These ongoing farming practices result in the rapid loss
of Polylepis forests from Bolivia to Peru.
Habitat destruction is often caused by a combination of human
activities that promote habitat degradation. In the Cordillera de
Vilcanota (Cusco, Peru), where an estimated 181 birds are found (Chutas
2007, pp. 4, 8), the rate of habitat loss was studied by comparing
forest cover between 1956 and 2005. This study revealed a rate of
habitat loss averaging only 1 percent. However, remaining patches of
Polylepis woodland were small, with a mean patch size of 7.4 ac (3 ha);
four forest patches had disappeared completely; and no new patches were
located within the study area (Jameson and Ramsay 2007, p. 42). Lloyd
(2008, p. 532) studied bird foraging habits at three Polylepis woodland
sites in the Cordillera Vilcanota during 2003-2005. The sites were
described as highly fragmented, consisting of many small remnant
patches (less than 2.5 ac (1 ha)) and scattered trees, separated from
larger woodland tracts (greater than 25 ac (10 ha)) by distances of 98-
4,921 ft (30-1,500 m) (Lloyd and Marsden in press, as cited in Lloyd
2008, p. 532). Given that the species territory ranges from 2.5-5 ac
(1-2 ha) and that the ash-breasted tit-tyrant appears to be unable to
persist in forest remnants smaller than 2.5 ac (1 ha) (BLI 2009o, p.
1), these patch sizes have met or are approaching the lower threshold
of the species' ecological requirements. Moreover, 10 percent of the
remaining forest patches showed a decline in forest density over this
time-period.
Thus, habitat degradation also has serious impacts in Polylepis
woodlands (Jameson and Ramsay 2007, p. 42), especially given the
species' preference for dense woodlands (Fjeldsa 2002a, p. 114; Smith
1971, p. 269). The fact that no new Polylepis forest patches had become
established between 1956 and 2005 underscores the long-term
ramifications of ongoing burning, clearing, grazing, and other habitat-
altering human activities that are pervasive throughout the ash-
breasted tit-tyrant's range (BLI 2009f, p. 1; BLI 2009n, p. 4; Fjeldsa
2002b, p. 8; WCMC 1998a, p. 1; WCMC 1998b, p. 1). These activities are
considered to be key factors both in preventing regeneration of
Polylepis woodlands (Fjeldsa 2002a, p. 112, 120; Fjeldsa 2002b, p. 8)
and in the historical decline of Polylepis -dependent bird species,
including the ash-breasted tit-tyrant (Fjeldsa 2002a, p. 116).
Researchers consider the species' population to be declining in close
association with the continued habitat loss and degradation (BLI 2007,
pp. 1, 4; BLI 2008, p. 1; BLI 2009o, p. 1). Therefore, further habitat
loss will continue to impact the species' already small population size
(see Factor E).
Peru is subject to unpredictable climate fluctuations that
exacerbate the effects of habitat fragmentation, such as those that are
related to the El Ni[ntilde]o Southern Oscillation (ENSO). According to
the U.S. Dept. of Commerce-National Oceanic and Atmospheric
Administration (NOAA), the term ENSO refers to a range of variability
associated with the southern trade winds in the eastern and central
equatorial Pacific Ocean. El Ni[ntilde]o events are characterized by
unusual warming of the ocean, while La Ni[ntilde]a events bring cooler
ocean temperatures (Tropical Atmosphere Ocean (TAO) Project no date
(n.d.), p. 1). Generally speaking, extreme ENSO events alter weather
patterns, so that
[[Page 612]]
precipitation increases in normally dry areas, and decreases in
normally wet areas. During an El Ni[ntilde]o event, rainfall
dramatically increases, whereas a La Ni[ntilde]a event brings near-
drought conditions (Holmgren et al. 2001, p. 89).
If we consider that wildlife habitat is not only defined by
substrates (vegetation, soil, water), but also atmospheric conditions,
then changes in air temperature and moisture can effectively change a
species' habitat. Climate change is characterized by variations in the
earth's temperature and precipitation, causing changes in atmospheric,
oceanic, and terrestrial conditions (Parmesan and Mathews 2005, p.
334). Global climate change and other periodic climatic patterns (e.g.,
El Ni[ntilde]o and La Ni[ntilde]a) can cause or exacerbate such
negative impacts on a broad range of terrestrial ecosystems and
Neotropical bird populations (England 2000, p. 86; Holmgren et al.
2001, p. 89; Plumart 2007, pp. 1-2; Timmermann 1999, p. 694).
Unpredictable climate fluctuations negatively impact populations
undergoing habitat fragmentation. In the face of an unpredictable
climate, the risk of population decline due to habitat fragmentation is
heightened. Mora et al. (2007, p. 1027) found that the combined effects
of habitat fragmentation and climate change (in this case, warming) had
a synergistic effect, rather than additive. In other words, the
interactive effects of both climate fluctuation and habitat
fragmentation led to a greater population decline than if either
climate change or habitat fragmentation were acting alone on
populations. Jetz et al. (2007, p. 1211) investigated the effects of
climate change on 8,750 land bird species, including the ash-breasted
tit-tyrant, that are exposed to ongoing manmade land cover changes
(i.e., habitat loss). They determined that a narrow endemic, such as
the ash-breasted tit-tyrant, is likely to suffer greater impacts from
climate change, especially where projected range contractions are
driven by manmade land conversion activities (Jetz et al. 2007, p.
1213). This is due to the species' already small population size,
specialized habitat requirements, and heightened risk of extinction
from stochastic demographic processes (see also Factor E). According to
this study, by 2050, up to 18 percent of the ash-breasted tit-tyrant's
current remaining range is likely to be unsuitable for this species due
to climate change; and, by 2100, it is predicted that about 18 to 42
percent of the species' range is likely to be lost as a direct result
of global climate change (Jetz et al. 2007, Supplementary Table 2, p.
73).
In 1999, Timmermann (1999, p. 694) predicted that climate change
events would increase the periodicity and severity of droughts and
excessive rainfalls, such as those caused by El Ni[ntilde]o and La
Ni[ntilde]a events. Evidence suggests that this is the case in Peru
(Richter 2005, p. 24-25). Over the past decade, there have been four El
Ni[ntilde]o events (1997-1998, 2002-2003, 2004-2005, and 2006-2007) and
three La Ni[ntilde]a events (1998-2000, 2000-2001, and 2007-2008)
(National Weather Service (NWS) 2009, p. 2). In Peru, the Andean
highlands, and Polylepis species in particular, are strongly influenced
by ENSO events (Christie et al. 2008, p. 1). Christie et al. (2008, p.
1) found that tree growth in P. tarapacana is highly influenced by ENSO
events because ENSO cycles on the Peruvian Coast are strongest during
the growing season (December-February). ENSO-related droughts can
increase tree mortality and dramatically alter age structure within
tree populations, especially where woodlands have undergone
disturbance, such as fire and grazing (Villalba and Veblen 1997, pp.
121-123; Villalba and Veblen 1998, pp. 2624, 2637).
With years of extremely high rainfall followed by years of
extremely dry weather (Block and Richter 2007, p. 1), fire hazard is
increased from the biomass accumulated during the wet period that dries
and adds to the fuel load in the dry season (Block and Richter 2007, p.
1; Power et al. 2007, p. 898). Evidence suggests that the fire cycle in
Peru has shortened, particularly in coastal Peru and west of the Andes
(Power et al. 2007, pp. 897-898). Changes in the fire-regime can have
broad ecological consequences (Block and Richter 2007, p. 1; Power et
al. 2007, p. 898). In the case of the ash-breasted tit-tyrant, burning
is considered to be a key factor preventing Polylepis regeneration
(Fjeldsa 2002a, p. 112, 120; Fjeldsa 2002b, p. 8). Research in
Ecuadorian Polylepis - Gynoxys mixed woodlands indicated a strong
reduction in P. incana adult and seedling survival following a single
fire. This indicates that the species does not recover well from even a
single fire event (Cierjacks et al. 2007, p. 176). An accelerated fire
cycle would exacerbate this situation.
Activities that destroy and alter habitat are ongoing within
protected areas. This is further discussed under Factor D.
Summary of Factor A
The ash-breasted tit-tyrant is dependent on Polylepis habitat, with
a preference for dense woodlands. Polylepis habitat throughout the ash-
breasted tit-tyrant's range has been and continues to be altered and
destroyed as a result of human activities, including clearcutting and
burning for agriculture, grazing lands, tourism, and industrialization;
extractive activities, including firewood, timber, and mineral
extraction; and human encroachment and concomitant increased pressure
on natural resources. Researchers estimate that 1 percent of the dense
woodlands preferred by the species remains, and that all remaining
habitat is fragmented and degraded. The ash-breasted tit-tyrant
currently occupies an area of approximately 4,595 mi\2\ (11,900 km\2\)
and appears to be unable to persist in forest remnants smaller than 2.5
ac (1 ha). Forest fragments in some portions of the ash-breasted tit-
tyrant's range are approaching the lower threshold of the species'
ecological requirements. The historical decline of habitat suitable for
this species is attributed to the same human activities that are
causing habitat loss today. Ongoing and accelerated habitat destruction
of the remaining Polylepis forest fragments in Peru and Bolivia
continues to reduce the quantity, quality, distribution, and
regeneration of remaining patches. Human activities that degrade,
alter, and destroy habitat are ongoing throughout the species' range,
including within protected areas (see also Factor D). Current research
indicates that climate fluctuations exacerbate the risks to species
that are already undergoing range reduction due to habitat alteration.
Climate models predict that this species' habitat will continue to
decline. Experts consider the species' population decline to be
commensurate with the declining habitat (Factor E). Therefore, we find
that destruction and modification of habitat are threats to the
continued existence of the ash-breasted tit-tyrant throughout its
range.
B. Overutilization for Commercial, Recreational, Scientific, or
Educational Purposes
We are not aware of any information currently available that
indicates that overutilization of the species for commercial,
recreational, scientific, or educational purposes has occurred or is
occurring at this time. As a result, we are not considering
overutilization to be a threat to the continued existence of the ash-
breasted tit-tyrant.
C. Disease or Predation
We are not aware of any scientific or commercial information that
indicate disease or predation poses a threat to this species. As a
result, we are not considering disease or predation to be a
[[Page 613]]
threat to the continued existence of the ash-breasted tit-tyrant.
D. Inadequacy of Existing Regulatory Mechanisms
This analysis of regulatory mechanisms is discussed on a country-
by-country basis, beginning with Peru.
Peru: The ash-breasted tit-tyrant is considered ``endangered'' by
the Peruvian Government under Supreme Decree No. 034-2004-AG (2004, p.
276855). This Decree prohibits hunting, take, transport, and trade of
protected species, except as permitted by regulation. As hunting, take,
transport, and trade are not currently threats to the ash-breasted tit-
tyrant (Factor B), this regulation does not mitigate any current
threats to this species.
The Peruvian national protected area system includes several
categories of habitat protection. Habitat may be designated as any of
the following: (1) Parque Nacional (National Park, an area managed
mainly for ecosystem conservation and recreation ); (2) Santuario
(Sanctuary, for the preservation of sites of notable natural or
historical importance); (3) Reserva Nacional (National Reserve, for
sustainable extraction of certain biological resources); (4) Bosque de
Proteccion (Protection Forest, to safeguard soils and forests,
especially for watershed conservation); (5) Zona Reservada (Reserved
Zone, for temporary protection while further study is under way to
determine their importance); (6) Bosque Nacional (National Forest, to
be managed for utilization); (7) Reserva Comunal (Communal Reserve, for
local area use and management, with national oversight); and (8) Cotos
de Caza (Hunting Reserve, for local use and management, with national
oversight) (BLI 2008, p. 1; Rodriguez and Young 2000, p. 330). National
reserves, national forests, communal reserves, and hunting reserves are
managed for the sustainable use of resources (IUCN 1994, p. 2). The
designations of National Parks, Sanctuaries, and Protection Forests,
are established by supreme decree that supersedes all other legal claim
to the land and, thus, these areas tend to provide more habitat
protection. All other protected areas are established by supreme
resolution, which is viewed as a less powerful form of protection
(Rodriguez and Young 2000, p. 330).
Protected areas have been established through regulation in at
least three sites occupied by the ash-breasted tit-tyrant in Peru:
Parque Nacional Huascaran (Ancash), and Santuario Historico Machu
Picchu (Cusco); and Zona Reservada de la Cordillera Huayhuash (spanning
Ancash, Huanuco, and Lima) (Barrio 2005, p. 563; BLI 2009i, p. 1; BLI
2009l, p. 1; BLI 2009n, p. 1). Habitat destruction and alteration,
including burning, cutting, and grazing are ongoing within Parque
Nacional Huascaran and Santuario Historico Machu Picchu (BLI 2009l, p.
4; BLI 2009n, p. 2; Engblom et al. 2002, p. 58), where resources are
supposed to be managed for conservation (Rodriguez and Young 2000, p.
330). Reserved zones are intended to be protected pending further study
(Rodriguez and Young 2000, p. 330). However, burning for habitat
conversion and maintenance of pastures for grazing and increasing
ecotourism are ongoing within Zona Reservada de la Cordillera Huayhuash
(Barrio 2005, p. 564). Therefore, the occurrence of the ash-breasted
tit-tyrant within protected areas in Peru does not protect the species,
nor does it mitigate the threats to the species from ongoing habitat
loss (Factor A) and concomitant population decline (Factor E).
Recent studies by the Peruvian Society for Environmental Law (SPDA)
have concluded that there are approximately 5,000 laws and regulations
directly or indirectly related to environmental protection and natural
resource conservation in Peru. However, many of these are not effective
because of limited implementation and/or enforcement capability (Muller
2001, pp. 1-2).
Bolivia: The 1975 Law on Wildlife, National Parks, Hunting and
Fishing (Decree Law No. 12,301 1975, pp. 1-34) has the fundamental
objective of protecting the country's natural resources. This law
governs the protection, management, utilization, transportation, and
selling of wildlife and their products; the protection of endangered
species; habitat conservation of fauna and flora; and the declaration
of national parks, biological reserves, refuges, and wildlife
sanctuaries, tending to the preservation, promotion, and rational use
of these resources (Decree Law No. 12,301 1975, pp. 1-34; eLAW 2003, p.
2). Although this law designates national protection for all wildlife,
there is no information as to the actual protections this confers to
ash-breasted tit-tyrants. Law No. 12,301 (1975, pp. 1-34) also placed
into public trust all national parks, reserves, refuges, and wildlife
sanctuaries. However, there is no specific information as to the
governmental protections afforded within the protected areas to either
the ash-breasted tit-tyrant or its habitat. Given the ongoing habitat
destruction throughout the species' range in Bolivia, this law does not
protect the species, nor does it mitigate the threats to the species
from ongoing habitat loss (Factor A) and concomitant population decline
(Factor E).
Bolivia passed an overarching environmental law in 1992 (Law No.
1,333 1992), with the intent of protecting and conserving the
environment and natural resources. However, there is no specific
legislation to implement these laws (eLAW 2003, p. 1). Therefore, we
cannot determine that this law protects the species or mitigates the
threats to the species from ongoing habitat loss (Factor A) and
concomitant population decline (Factor E).
In Bolivia, habitat is protected either on the national or
departmental level through the following designations: (1) Parque
(Park, for strict and permanent protection of representative of
ecosystems and provincial habitats, as well as plant and animal
resources, along with the geographical, scenic and natural landscapes
that contain them); (2) Santuario (Sanctuary, for the strict and
permanent protection of sites that house endemic plants and animals
that are threatened or in danger of extinction); (3) Monumento Natural
(Natural Monument, to preserve areas such as those with distinctive
natural landscapes or geologic formations, and to conserve the
biological diversity contained therein); (4) Reserva de Vida Silvestre
(Wildlife Reserve, for protection, management, sustainable use and
monitoring of wildlife); (5) Area Natural de Manejo Integrado (Natural
Area of Integrated Management, where conservation of biological
diversity is balanced with sustainable development of the local
population; and (6) Reserva Natural de Inmovilizacion (``Immobilized''
Natural Reserve, a temporary (5-year) designation for an area that
requires further research before any official designations can be made
and during which time no natural resource concessions can be made
within the area) (Supreme Decree No. 24,781 1997, p. 3). Within parks,
sanctuaries and natural monuments, extraction or consumption of all
resources are prohibited, except for ``scientific research, eco-
tourism, environmental education, and activities of subsistence of
original towns, properly described and authorized.'' National protected
areas are under the management of the national government, while
departmental protected areas are managed at the department level (eLAW
2003, p. 3; Supreme Decree No. 24,781 1997, p. 3).
The ash-breasted tit-tyrant occurs within several protected areas
in the Department of La Paz, Bolivia: Parque Nacional y area Natural de
Manejo
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Integrado Madidi, Parque Nacional y area Natural de Manejo Integrado
Cotapata, and the co-located protected areas of Reserva Nacional de
Fauna de Apolobamba, area Natural de Manejo Integrado de Apolobamba,
and Reserva de la Biosfera de Apolobamba (Auza and Hennessey 2005, p.
81; BLI 2009a, p. 1; BLI 2009b, p. 1; BLI 2009c, p. 1; BLI 2009e, p.
1). Although national parks are intended to be strictly protected, the
two parks in which the species occurs (Parque Nacional y area Natural
de Manejo Integrado Madidi and Parque Nacional y area Natural de Manejo
Integrado Cotapata) are also designated as areas of integrated
management, which are managed for the biological conservation balanced
with the sustainable development of the local population (Supreme
Decree No. 24,781 1997, p. 3). Grazing and firewood extraction are
ongoing within Parque Nacional y area Natural de Manejo Integrado
Cotapata (BLI 2009b, p. 2; BLI 2009c, p. 2). Commercial logging has
occurred within Parque Nacional y area Natural de Manejo Integrado
Madidi (BLI 2009a, p. 2; WCMC 1998a, p. 1). Uncontrolled clearing,
extensive agriculture, grazing, and ``irresponsible'' tourism are
ongoing within the Apolobamba protected areas (Auza and Hennessey 2005,
p. 81; BLI 2009e, p. 5). Habitat degradation and destruction from
grazing, forest fires, and timber extraction are ongoing in other
protected areas, such as Tunari National Park (Department of
Cochabamba, Bolivia), where suitable habitat exists for this species
(De la Vie 2004, p. 7). Therefore, the occurrence of the ash-breasted
tit-tyrant within protected areas in Bolivia does not protect the
species, nor does it mitigate the threats to the species from ongoing
habitat loss (Factor A) and concomitant population decline (Factor E).
Summary of Factor D
Peru and Bolivia have enacted various laws and regulatory
mechanisms to protect and manage wildlife and their habitats. The ash-
breasted tit-tyrant is ``endangered'' under Peruvian law and occurs
within several protected areas in Peru and Bolivia. As discussed under
Factor A, the ash-breasted tit-tyrant prefers dense woodlands, which
have been reduced by an estimated 99 percent in Peru and Bolivia, and
the remaining habitat is fragmented and degraded. Habitat throughout
the species' range has been and continues to be altered as a result of
human activities, including clearcutting and burning for agriculture,
grazing lands, and industrialization; extractive activities, including,
firewood, timber, and mineral extraction; and human encroachment and
concomitant increased pressure on natural resources. Despite the
species' ``endangered'' status in Peru and Bolivian laws intended to
protect all wildlife and natural resources, these activities are
ongoing within protected areas, indicating that the laws governing
wildlife and habitat protection in both countries are either inadequate
or inadequately enforced to protect the species or to mitigate ongoing
habitat loss (Factor A) and population declines (Factor E). Therefore,
we find that the existing regulatory mecha