Endangered and Threatened Wildlife and Plants; Four Foreign Parrot Species, 49202-49236 [2011-19532]
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Federal Register / Vol. 76, No. 153 / Tuesday, August 9, 2011 / Proposed Rules
FOR FURTHER INFORMATION CONTACT:
DEPARTMENT OF THE INTERIOR
Janine Van Norman, Chief, Branch of
Foreign Species, Endangered Species
Program, U.S. Fish and Wildlife Service,
4401 North Fairfax Drive, Room 420,
Arlington, VA 22203; telephone 703–
358–2171. If you use a
telecommunications device for the deaf
(TDD), call the Federal Information
Relay Service (FIRS) at 800–877–8339.
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS–R9–ES–2010–0099; MO
92210–0–0010 B6]
RIN 1018–AX50
Endangered and Threatened Wildlife
and Plants; Four Foreign Parrot
Species
AGENCY:
SUPPLEMENTARY INFORMATION
Fish and Wildlife Service,
Interior.
Proposed rule; 12-month
finding.
ACTION:
We, the U.S. Fish and
Wildlife Service (Service), propose to
list as endangered the Philippine
cockatoo (Cacatua haematuropygia) and
the yellow-crested cockatoo (C.
sulphurea), and to list as threatened the
white cockatoo (C. alba), under the
Endangered Species Act of 1973, as
amended (ESA). We are taking this
action in response to a petition to list
the following four parrot species:
Crimson shining parrot (Prosopeia
splendens), Philippine cockatoo
(Cacatua haematuropygia), white
cockatoo (C. alba), and yellow-crested
cockatoo (C. sulphurea) as endangered
or threatened under the ESA. This
document, which also serves as the
completion of the status review and as
the 12-month finding on the petition,
announces our finding that listing is not
warranted for the crimson shining
parrot. We also propose a special rule
for the white cockatoo in conjunction
with our proposed listing as threatened
for this species. We seek information
from the public on the proposed listing,
proposed special rule, and status review
for these species.
DATES: We will consider comments and
information received or postmarked on
or before October 11, 2011.
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–ES–2010–0099.
• U.S. mail or hand-delivery: Public
Comments Processing, Attn: FWS–R9–
ES–2010–0099, Division of Policy and
Directives Management; U.S. Fish and
Wildlife Service; 4401 N. Fairfax Drive,
MS 2042–PDM; 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 Information Requested section
below for more information).
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SUMMARY:
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Background
Section 4(b)(3)(B) of the ESA (16
U.S.C. 1531 et seq.) requires that, for
any petition to revise the Federal Lists
of Endangered and Threatened Wildlife
and Plants that contains substantial
scientific or commercial information
that listing the species may be
warranted, we make a finding within 12
months of the date of receipt of the
petition (‘‘12-month finding’’). In this
finding, we determine whether the
petitioned action is: (a) Not warranted,
(b) warranted, or (c) warranted, but
immediate proposal of a regulation
implementing the petitioned action is
precluded by other pending proposals to
determine whether species are
endangered or threatened, and
expeditious progress is being made to
add or remove qualified species from
the Federal Lists of Endangered and
Threatened Wildlife and Plants. Section
4(b)(3)(C) of the ESA requires that we
treat a petition for which the requested
action is found to be warranted but
precluded as though resubmitted on the
date of such finding, that is, requiring a
subsequent finding to be made within
12 months. We must publish these 12month findings in the Federal Register.
If the listing of a species is found to
be warranted but precluded by higherpriority listing actions, then the petition
to list that species is treated as if it is
a petition that is resubmitted on the date
of the finding and is, therefore, subject
to a new 12-month finding within one
year. The Service publishes an annual
notice of resubmitted petition findings
(annual notice) for all foreign species for
which listings were previously found to
be warranted but precluded.
In this document, we announce that
listing Philippine cockatoo and yellowcrested cockatoo as endangered is
warranted, and we are issuing a
proposed rule to add those species as
endangered under the Federal Lists of
Endangered and Threatened Wildlife
and Plants. We find that listing the
crimson shining parrot as endangered or
threatened is not warranted. We further
find that listing white cockatoo as
threatened is warranted, and we are
issuing a proposed rule to add that
species as threatened under the Federal
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Lists of Endangered and Threatened
Wildlife and Plants.
Prior to issuing a final rule on this
proposed action, we will take into
consideration all comments and any
additional information we receive. Such
information may lead to a final rule that
differs from this proposal. All comments
and recommendations, including names
and addresses of commenters, will
become part of the administrative
record.
Previous Federal Actions
Petition History
On January 31, 2008, the Service
received a petition dated January 29,
2008, from Friends of Animals, as
represented by the Environmental Law
Clinic, University of Denver, Sturm
College of Law, requesting we list 14
parrot species under the ESA. The
petition clearly identified itself as a
petition and included the requisite
information required in the Code of
Federal Regulations (50 CFR 424.14(a)).
On July 14, 2009 (74 FR 33957), we
published a 90-day finding in which we
determined that the petition presented
substantial scientific and commercial
information to indicate that listing may
be warranted for 12 of the 14 parrot
species. In our 90-day finding on this
petition, we announced the initiation of
a status review to list as endangered or
threatened under the ESA the following
12 parrot species: Blue-headed macaw
(Primolius couloni), crimson shining
parrot (Prosopeia splendens), great
green macaw (Ara ambiguus), greycheeked parakeet (Brotogeris
pyrrhoptera), hyacinth macaw
(Anodorhynchus hyacinthinus), military
macaw (Ara militaris), Philippine
cockatoo (Cacatua haematuropygia),
red-crowned parrot (Amazona
viridigenalis), scarlet macaw (Ara
macao), white cockatoo (Cacatua alba),
yellow-billed parrot (Amazona collaria),
and yellow-crested cockatoo (Cacatua
sulphurea). We initiated the status
review to determine if listing each of the
12 species is warranted, and initiated a
60-day public comment period to allow
all interested parties an opportunity to
provide information on the status of
these 12 species of parrots. The public
comment period closed on September
14, 2009.
On July 21, 2010, a settlement
agreement was approved by the Court
(CV–10–357, D. D.C.), in which the
Service agreed to (in part) submit to the
Federal Register by July 29, 2011, a
determination whether the petitioned
action is warranted, not warranted, or
warranted but precluded by other listing
actions for no less than four of the
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petitioned species. This Federal
Register document complies with the
first deadline in that court-ordered
settlement agreement. We will
announce the 12-month findings for the
remaining parrot species for which a 90day finding was made on July 14, 2009
(74 FR 33957) in subsequent Federal
Register notices.
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Information Requested
We intend that any final actions
resulting from this proposed rule will be
based on the best scientific and
commercial data available. Therefore,
we request comments or information
from other concerned governmental
agencies, the scientific community, or
any other interested parties concerning
this proposed rule. We particularly seek
clarifying information concerning:
(1) Information on taxonomy,
distribution, habitat selection and
trends (especially breeding and foraging
habitats), diet, and population
abundance and trends (especially
current recruitment data) of these
species.
(2) Information on the effects of
habitat loss and changing land uses on
the distribution and abundance of these
species (particularly the conversion of
habitat to biofuel production on
Halmahera Island and any data on
Bacan Island related to the white
cockatoo).
(3) Information on the effects of other
potential threat factors, including live
capture and hunting, domestic and
international trade, predation by other
animals, and any diseases that are
known to affect these species or their
principal food sources.
(4) Information on management
programs for parrot conservation,
including mitigation measures related to
conservation programs, and any other
private, nongovernmental, or
governmental conservation programs
that benefit these species.
(5) The potential effects of climate
change on these species and their
habitats.
Please include sufficient information
with your submission (such as full
references) to allow us to verify any
scientific or commercial information
you include. Submissions merely stating
support for or opposition to the action
under consideration without providing
supporting information, although noted,
will not be considered in making a
determination. Section 4(b)(1)(A) of the
ESA directs that determinations as to
whether any species is an endangered or
threatened species must be made
‘‘solely on the basis of the best scientific
and commercial data available.’’
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Public Hearing
At this time, we do not have a public
hearing scheduled for this proposed
rule. The main purpose of most public
hearings is to obtain public testimony or
comment. In most cases, it is sufficient
to submit comments through the Federal
eRulemaking Portal, described above in
the ADDRESSES section. If you would like
to request a public hearing for this
proposed rule, you must submit your
request, in writing, to the person listed
in the FOR FURTHER INFORMATION
CONTACT section by September 23, 2011.
Factors Affecting the Species
Section 4 of the ESA (16 U.S.C. 1533)
and implementing regulations (50 CFR
424) set forth procedures for adding
species to the Federal Lists of
Endangered and Threatened Wildlife
and Plants. Under section 4(a)(1) of the
ESA, a species may be determined to be
endangered or threatened based on any
one or a combination of the following
five factors:
(A) The present or threatened
destruction, modification, or
curtailment of its habitat or range;
(B) Overutilization for commercial,
recreational, scientific, or educational
purposes;
(C) Disease or predation;
(D) The inadequacy of existing
regulatory mechanisms; or
(E) Other natural or manmade factors
affecting its continued existence.
In considering what factors might
constitute threats, we look beyond the
actual or perceived exposure of the
species to the factor to determine how
the species responds to the factor and
whether the factor causes actual impacts
to the species. If there is exposure to a
factor, but no response, or only a
positive response, that factor is not a
threat. If there is exposure and the
species responds negatively, the factor
may be a threat and we then attempt to
determine how significant a factor it is.
If the factor is significant, it may drive
or contribute to the risk of extinction of
the species such that it is considered to
be a threat. In some cases, there is little
information available regarding the
status of the species, in part due to their
remoteness.
This finding addresses the following
four species of parrots: crimson shining
parrot, Philippine cockatoo, white
cockatoo, and yellow-crested cockatoo.
For each of these parrots, we evaluate
the five factors under ESA Section
4(a)(1) on the species. In some cases, we
found under a factor that a threat was
contributing to the extinction risk for
multiple species, while some factors
constituted a threat for some of the
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species but not others. In some cases,
the factors affecting species are the same
or very similar and in other cases the
factors are unique. In each evaluation,
we clearly identify what species is being
addressed, and if the threat applies to
more than one species.
Species Information
A. Crimson Shining Parrot (Prosopeia
splendens)
Taxonomy and Species Description
The crimson shining parrot
(Prosopeia splendens, Peale, 1848) is
endemic to Fiji, where it is found in
forests, on agricultural lands, and
around human habitation (International
Union for Conservation of Nature
(IUCN) 2008). Its most closely related
species are P. personata (G. R. Gray,
1848), masked shining parrot, which
occurs on Viti Levu; and P. tabuensis
(Gmelin, 1788), maroon (red) shining
parrot, which occurs on Vanua Levu
and Taveuni. P. splendens and these
two other species are recognized by the
Integrated Taxonomic Information
System (ITIS) (ITIS 2011, https://
www.itis.gov) as valid species. Absent
peer-reviewed information to the
contrary and based on the best available
information, we consider P. splendens
to be a valid species.
The crimson shining parrot’s head,
neck, and underparts are a bright red. It
is a medium-sized parrot, with a length
of 45 centimeters (cm) (18 inches (in)).
It has been observed in flocks of up to
40 birds in the past, but more recently
in flocks of up to 12 birds. During the
day, this species is generally quiet and
becomes vocal towards dusk, at which
time it becomes more active. A blue
collar extends across the back of its
neck; its back and rump are bright
green. Its flight feathers and tail are
green, strongly covered with blue. Its
bill and feet are black, and its irises are
orange. Males and females are similar
morphologically; however, the bill of
males is larger, and the head of males
is more square-shaped than females. It
differs from the maroon shining parrot
in its size and coloration; crimson
shining parrots are generally smaller
than maroon shining parrots. Rump
feathers on the crimson shining parrot
do not have the red edges that can be
seen on the maroon shining parrot. The
main visible features that distinguish
the crimson shining parrot from the
masked shining parrot and the maroon
shining parrot are the scarlet rather than
maroon underparts and the blue collar
at the back of the neck.
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Distribution, Habitat, Biology
There is little to no information
available regarding this species. The
crimson shining parrot, also known as
the Kadavu musk parrot, is endemic to
the islands of Kadavu and Ono in Fiji.
These two islands are separated by a
narrow channel, often navigated by
kayaks and other small boats. This
species has also been reported on the
island of Viti Levu in the Upper Navua
Conservation Area (Tokaduadu 2008,
pp. 5, 7), where they are thought to be
escaped pet birds. There are no known
records of this species successfully
breeding other than on the islands of
Kadavu and Ono (https://
www.NatureFiji.org, accessed January 4,
2011). The island of Kadavu is
remarkable in that it has the highest
number of endemic birds per land area
in the world. It hosts two areas
designated by Birdlife International
(BLI) as Important Bird Areas (IBAs),
including Mount Nabukelevu which is
located on the southwestern end of
Kadavu Island. Mt. Nabukelevu, has the
largest area of montane forest on the
island. These IBAs are a way to identify
conservation priorities (BLI 2008j, pp.
1–2) and are considered to be globally
important areas for the conservation of
bird populations. A site is recognized as
an IBA based on the occurrence of key
bird species that are vulnerable to global
extinction or whose populations are
otherwise irreplaceable. These key sites
for conservation are small enough to be
conserved in their entirety and large
enough to support self-sustaining
populations of the key bird species.
Mount Nabukelevu’s montane forest is
critical for five globally threatened bird
species, including the crimson shining
parrot (BLI 2011d, p. 1; BLI 2010c, p. 1).
Very little is known about the ecology
of this species in the wild (NatureFiji
2011, pp. 1–2). Although in captivity
this species has been known to exhibit
aggression in males, it is a social species
in the wild (Lin and Lee 2006, p. 188).
It has been observed in flocks of up to
approximately 40 birds (Tabaranza 1992
as cited in BLI 2001, p. 1679) but more
recently it has been observed in flocks
of up to 12 individuals. Flocking is
thought to serve several purposes
including mate selection, and learning
food sources and eating techniques
(Cameron 2007, pp. 115, 144)
In 2004, the population estimate was
6,000 mature birds, with a declining
population (Jackson and Jit 2004 in BLI
2010a, p. 1). However, the species’
population estimate was inferred from
population surveys conducted on
another species, the Masked ShiningParrot (Prosopeia personata) (BLI 2010a,
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pp. 1–2). Surveys found that the
crimson shining parrot occurred at
similar population densities as that of
the masked shining parrot. In two
BirdLife International surveys, 86
crimson shining parrots were recorded
in 38 standardized observer-hours,
similar to the mean of 1.9 masked
shining parrots per hour recorded at 18
sites across Viti Levu (BLI 2010a, pp. 1–
2). Masked shining parrots were
estimated to occur at approximately 29
birds per km2 in lowland native forest.
The 2004 crimson shining parrot
population was estimated using the
density of masked shining parrots and
the estimated 225 km2 (87 mi2) area of
dense and medium-dense forest on
Kadavu (Jackson and Jit 2004 in BLI
2010a, p. 1). However, we do not have
detailed information about how the
surveys on Kadavu were conducted;
they may have occurred at a time when
the species is not active or visible. There
is no evidence that the survey protocol
used is appropriate to infer the
population density of this species. Nor
is there evidence suggesting the two
species have the same ecological
characteristics, levels of disturbance,
and habitat requirements. For example,
Viti Levu has a more dense human
population than that on the islands of
Kadavu and Ono, and human
population density often directly
influences species population density.
Additionally, we do not know the
historical population of the crimson
shining parrot; this species may never
have had a large population, as it is only
known to be endemic to Kadavu and
Ono Islands, so we do not know if this
species has experienced a decrease in
population size or if its population has
been fairly consistent. Furthermore,
species that are endemic to islands tend
to have smaller population sizes due to
a smaller carrying capacity of the island.
This species is described as being
‘‘widespread and common’’ on Kadavu
and population information on the East
Kadavu IBA also lists this species as
common (BLI 2011a, p. 1; BLI 2011f,
unpaginated). Additionally, notes from
a 2006 birding trip report indicate that
the crimson shining parrot would be
‘‘hard to miss’’ on Kadavu (Skevington
and Mathieson 2006, unpaginated).
Although the best scientific information
available indicates the population of
crimson shining parrots number 6,000
individuals, there is no historical
population data to indicate this species
has declined or is currently declining.
Given the reports from BirdLife
International (BLI 2011a, p. 1; BLI
2011f, unpaginated) and the lack of
support for a declining population, we
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consider the crimson shining parrot to
be common on Kadavu.
Its range is estimated to be 460 km2
(178 mi2). However, BLI (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.’’
Kadavu is the fourth largest of Fiji’s
islands, at 410 km2 (158 mi2). Kadavu
has a human population of 8,700 people
and is a mountainous, rugged island
with high peaks and precipitous cliffs
(Fiji Guide 2011). There are few roads
and is therefore mainly accessible by
boat. The Kadavu Island group is 83 km
(45 nautical miles) south of Viti-Levu,
Fiji’s main island. Kadavu is rugged and
mountainous with few roads. The
Kadavu Island group also includes
nearby Ono Island, off the eastern tip of
Kadavu, as well as a number of smaller
islands. Ono is 30 km2 (12 mi2) in size
(Planetary Coral Reef Foundation
(PCRF) 2010). This island group has
12,000 Fijians living in 72 traditional
village communities (PCRF 2010), and
there is one airstrip. The primary means
of income is subsistence agriculture and
fishing.
Conservation Status for the Crimson
Shining Parrot
Fiji is actively involved in forest
protection efforts; a new Forest Policy
was adopted in 2007 (Fiji Ministry of
Fisheries and Forestry 2009, p. 1).
Crimson shining parrot is also protected
by Fiji’s Endangered and Protected
Species (EPS) Act of 2002. Additionally,
Fiji’s first national nongovernmental
organization (NGO), Nature Fiji, was
established recently, and its goal is
conservation of its wildlife. Nature Fiji
is working closely with BLI to develop
a conservation program to protect
endangered wildlife in Fiji such as the
crimson shining parrot.
In 1981, the crimson shining parrot
was listed in Appendix II of the
Convention on International Trade in
Endangered Species of Wild Fauna and
Flora (CITES). At that time, almost all
Psittaciformes species (i.e., parrots)
were included in Appendix II. CITES is
an international agreement where
member countries work together to
ensure that international trade in CITESlisted animals and plants is not
detrimental to the survival of wild
populations. This is achieved by
regulating import, export, and re-export
of CITES-listed animal and plant species
and their parts and products through the
use of a permitting system (https://
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www.cites.org). CITES entered into force
in 1975, and is an international treaty
among 175 nations, including Fiji and
the United States. In the United States,
CITES is implemented through the U.S.
Endangered Species Act of 1973, as
amended (ESA; 16 U.S.C. 1531 et seq.).
Appendix II includes species that are
not necessarily threatened with
extinction, but may become so unless
trade is subject to strict regulation to
avoid utilization incompatible with the
species’ survival. International trade in
specimens (dead or live) of Appendix II
species is authorized through permits or
certificates. International trade in
specimens of Appendix II species is
authorized when: (1) The CITES
Scientific Authority of the country of
export has determined that the export
will not be detrimental to the survival
of the species in the wild; and (2) the
CITES Management Authority of the
country of export has determined that
the specimens to be exported were
legally acquired (UNEP–WCMC 2008a,
p. 1).
In 1988, the crimson shining parrot
was described by the IUCN as lower
risk/least concern, and the status
changed to vulnerable in 2000 (IUCN
2008; BLI 2010a), which is its current
IUCN classification. The authority for
compilation of information and
determining the appropriate risk
extinction category for bird species on
the IUCN Red List is Birdlife
International, and is cited frequently
throughout this document. However,
IUCN rankings do not confer any actual
protection or management.
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Evaluation of Factors Affecting the
Crimson Shining Parrot
This section contains an assessment
in which we evaluate the effects of any
of the five factors listed in section
4(a)(1) of the ESA on the species. Listing
actions may be warranted based on
whether any of the five factors under
section 4(a)(1), singly or in combination,
places the species in danger of
extinction now or in the foreseeable
future. Each evaluation is specific to
this species identified unless we specify
that the evaluation is for more than one
species.
Factor A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
There is little to no evidence of
destruction, modification, or
curtailment of this species’ habitat, in
fact, there is recent evidence of
reforestation efforts and conservation of
the species’ habitat taking place (BLI
2011a, p. 1; Fiji Daily Post 2007, 2009,
unpaginated). It was suggested that this
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species is roughly estimated to be
declining at the rate of forest loss, which
had been estimated to be 0.5 to 0.8
percent per year across Fiji (Claasen
1991 in BLI 2011a, p. 1), and that forest
loss may be higher on Kadavu due to
fires in recent years (BLI 2011a, p. 1).
However, there is no information on the
extent of past or current forest loss. Not
only does the United Nations describe
deforestation in Fiji as modest when
compared with the rest of Melanesia
(UN 2011, p. 1), but also local
communities on Kadavu are
implementing reforestation efforts and
conservation of this species’ habitat as
described above (Fiji Daily News 2007,
unpaginated). Although the eastern part
of the island is experiencing pressures
from agricultural encroachment, there is
no evidence that agricultural
encroachment or forest loss due to fires
currently threatens the crimson shining
parrot (NatureFiji 2011, pp. 1–2).
Forests on Kadavu were heavily
logged in the late 1960s and early 1970s,
and habitat loss and degradation of
habitat for agricultural purposes
continues. However, approximately 75
percent of the island remains forested;
East Kadavu IBA is reported to have the
largest area of old-growth forest in
Kadavu, including extensive areas of
lowland rainforest. Furthermore, the
crimson shining parrot is reported to
use degraded habitats extensively (BLI
2011a, p. 1; BLI 2011f, unpaginated).
Most river estuaries and bays still hold
large areas of mangroves, which are
used by the crimson shining parrot for
feeding (and possibly breeding), and
pressure on mangrove forest here is not
currently significant (BLI 2011a, p. 1).
BLI and Nature Fiji are working with
landowners on Kadavu to conserve
these forested natural areas and to
increase awareness of the value of
maintaining these areas in a littledisturbed state (BLI 2011e, p. 1). NGOs
are working with the landowners in the
Mount Nabukelevu area to create
awareness about the value of their
forests and the benefits of establishing
‘‘Permanent Forest Estates’’ (PFEs)
(described below) on their lands. These
NGOs are also working to help build the
capacity of indigenous communities to
continue forest conservation on their
own (BLI 2011e, p. 3). BLI, through the
Darwin Initiative, has worked with the
Kadavu’s Department of Forestry and
local communities on Kadavu to protect
this species’ habitat. The Darwin
Initiative, implemented by the United
Kingdom, assists countries that are rich
in biodiversity but poor in financial
resources to meet their objectives under
one or more of the three major
biodiversity conventions. BLI conducted
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a workshop on Kadavu to teach
sustainable agricultural practices and
ways to reduce soil erosion which
subsequently supports community
livelihoods. Later, the villages of
Lomati, Nabukelevuira, Qalira, and
Daviqele committed to protect 1,500
hectares (3,707 ac) of their forest that
had been designated as an Important
Bird Area (IBA) on Mount Nabukelevu
in Kadavu (Fiji Daily News 2007).
On Kadavu, particularly in the area of
Mount Nabukelevu, many forest-owning
mataqalis (clan or landowning units) are
under pressure to convert their forests
into agricultural land (BLI 2011e, p. 1).
In 2010, 10 mataqalis signed an
agreement with an NGO to protect the
forests of Mount Nabukelevu for the
next 20 years (BLI 2011f; NatureFiji
2011). The community-declared
protected area now includes 10 mataqali
(clan) lands plus a native reserve.
Additionally, the Government of Fiji
recognizes that maintaining forests is
critically important for Fiji’s people and
biodiversity and has taken steps to
preserve its country’s resources. In
2007, Fiji introduced the Fiji Forest
Policy, which promotes sustainable
forest management. One of the
foundations of the new Forest Policy is
the concept of ‘‘Permanent Forest
Estates’’ (PFEs). The policy promotes
sustainable management of healthy
forests by providing sustainable
development incentives for landowners.
In addition, the government of Fiji
initiated a campaign to plant one
million trees in 2010 to halt or slow
ecological degradation associated with
the depletion of the world’s forests. Fiji
launched its One Million Trees
Campaign in support of the 2010
International Year of Biodiversity, and
in 2011 as the International Year of
Forests. Fiji indicated that they had
surpassed their goal, and participants
had succeeded in planting over one
million trees (Fiji Ministry of
Information 2011).
Although forest loss may be occurring
within the range of the crimson shining
parrot, we have no information on the
extent of forest loss or evidence to
suggest that this loss has impacted or is
currently affecting this species. The
crimson shining parrot is found in
forests, agriculture lands, around human
habitation, and is known to use
degraded habitats extensively.
Furthermore, there is no information
indicating this species is declining.
Additionally, we have no information to
suggest that habitat loss may become a
threat to this species in the future such
that it may contribute to the risk of
extinction of this species. Fiji has
implemented proactive policies and
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protections with respect to its forests.
Local conservation activities are
occurring on Kadavu; indigenous
communities are interested in
preserving this species and its habitat.
Therefore, we do not find that the
present or threatened destruction,
modification, or curtailment of its
habitat or range is a threat to the
crimson shining parrot now or in the
foreseeable future.
Factor B. Overutilization for
Commercial, Recreational, Scientific, or
Educational Purposes
Conservation projects on Kadavu are
believed to have reduced the numbers of
parrots trapped for trading, but this
species is still thought to be captured in
small numbers for domestic and
international trade (BLI 2010a, p. 1). As
indicated above, this species has been
listed in Appendix II of CITES since
1981. The United Nations Environment
Programme—World Conservation
Monitoring Centre (UNEP–WCMC)
manages a CITES Trade Database on
behalf of the CITES Secretariat. We
queried the UNEP–WCMC CITES Trade
Database for gross data on export and
import of this species since 2000, and
found no record of trade in this species
(UNEP–WCMC 2011, accessed January
4, 2011.)
Each Party to CITES is responsible for
compiling and submitting annual
reports to the CITES Secretariat
regarding their country’s trade in
species listed in the CITES Appendices.
The data from submitted annual reports
is compiled into the database, and it
provides a mechanism by which CITES
trade can be assessed. Due to the time
needed to compile the data, the most
recent year for which comprehensive
trade statistics are available is normally
2 years prior to the current year. UNEP–
WCMC acknowledges that the data are
not always accurate (UNEP–WCMC
2011, p. 5). They indicate that it is not
uncommon for the quantity of
specimens traded to be considerably
less than the amount specified on the
permits and that the quantity specified
on the permits is frequently the quantity
that is reported in annual reports. They
further clarify that trade transactions
that may have been authorized by the
issuance of permits but never have
taken place, as well as inaccurately
reported volumes of trade, will exist in
the UNEP–WCMC CITES database.
UNEP–WCMC also acknowledges that
gross and net outputs from the CITES
database are often overestimates of the
quantities traded because in cases where
different quantities are reported by the
importing and exporting countries, the
CITES database program selects the
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larger quantity. Errors do occur in the
database, and the numbers may not be
entirely accurate, but they do provide an
approximate representation of
international trade that is occurring
through CITES. However, we consider
the UNEP–WCMC CITES trade data to
be the best available information
pertaining to international trade in
CITES-listed species.
Although it has been reported that
birds are taken as gifts and there is some
illegal trade overseas, it is thought to
occur in small numbers (BLI 2010a, p.
1). Conservation projects described
under Factor A have reduced the
numbers of birds trapped for the pet
bird trade (BLI 2011a, p. 1). BLI reports
that four communities have set up
village protected areas on Kadavu, and
they conduct regular bird surveys under
their own initiative. Additionally, it is
protected by law against trading and
transfers out of Kadavua and Ono
(NatureFiji 2011, p. 2). There appears to
be substantial protection, awareness,
and local conservation of this species
occurring. Because there is no evidence
of poaching (i.e., hunting by people to
gain at least a temporary living from the
activity) or illegal trade of this species
occurring at levels such that it may
contribute to the risk of extinction of the
crimson shining parrot, or information
indicating poaching or trade may
increase in the future and rise to the
level of a threat, we believe that
overutilization for commercial,
recreation, scientific, or educational
purposes is not a threat to the species.
We are unaware of any other
information currently available that
addresses overutilization for
commercial, recreation, scientific, or
education purposes that may be
affecting the crimson shining parrot. We
found no evidence of overutilization
due to historic or cultural use of this
species by local populations. Based on
the best available scientific and
commercial information, we find that
overutilization for commercial,
recreational, scientific, or educational
purposes is not a threat to the crimson
shining parrot now or in the foreseeable
future.
Factor C. Disease or Predation
Predation by introduced mammals
such as feral cats (Felis catus) and rats
(Rattus spp.) were identified as possible
factors affecting this species. There was
little to no information found regarding
the occurrence of predation or disease
in Fiji, particularly with respect to the
crimson shining parrot. As is the case
on many remote islands, Fiji has no
native terrestrial mammals. Introduced
mammals such as rats, mongoose
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(Herpestes javanicus), cats and dogs
prey heavily on Fiji’s native wildlife
(Morley 2004 in Olson et al. 2009, p. 1).
However, the mongoose is not present
on Kadavu Island and the only current
predator definitely known to occur on
Kadavu is cats. Cats on Kadavu are
known to threaten ground-nesting birds,
particularly on the coasts, but they are
not known to threaten the crimson
shining parrot. There are no known
predators on Ono Island to our
knowledge. Studies have found that
predation rates by introduced predators
are lowest in natural forests more than
4.5 km (2 mi) from forest edges or roads
(Olson et al. 2006). Kadavu’s terrain
consists of volcanic, mountainous,
dense rainforest; sandy beaches; rocky
coastline; and mangrove swamps. The
island has a significant portion of
relatively undisturbed forested areas.
The islands’ forested areas may act as
refugia from predation by alien
predators, such as the feral cat, for
native species such as the crimson
shining parrot.
Researchers suggest that maintaining
minimally-disturbed forests is one of the
most cost-effective strategies for
protecting species (Olson et al. 2009, p.
1). Because this species resides in dense
forests far from edges and roads, this
species is not likely to be significantly
affected by nonnative predators. The
crimson shining parrot likely has
natural predators, but we were unable to
find information that any natural
predators are having an impact on this
species. Although predation occurs in
Fiji, particularly by nonnative species,
the best available information does not
indicate that predation is a threat to the
crimson shining parrot on Kadavu or
Ono now, or may become a threat in the
future.
We are not aware of any occurrence
of disease that may be affecting the
crimson shining parrot. In conclusion,
we find that neither disease nor
predation is a threat to the crimson
shining parrot in any portion of its range
now or in the foreseeable future.
Factor D. The Inadequacy of Existing
Regulatory Mechanisms
Various regulatory mechanisms are in
place to protect the crimson shining
parrot. This species is listed on Fiji’s
Endangered and Protected Species (EPS)
Act of 2002 which is the legislation that
implements CITES. As discussed under
Factor B, the government of Fiji is
adequately controlling international
trade. According to a review conducted
for CITES with respect to national
legislation to determine each country’s
ability to implement CITES effectively,
Fiji meets the requirements for
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implementing CITES (CITES 2011a;
https://www.cites.org, SC59 Document
11, Annex p. 1). In addition to the
absence of legal trade, there is no
indication that this species is traded
illegally at levels such that it may
contribute to the risk of extinction of the
crimson shining parrot. Based on the
lack of trade, and as discussed under
Factor B, we do not consider
international trade to be a threat to the
crimson shining parrot. Therefore,
protection under CITES is an adequate
regulatory mechanism.
Wild Bird Conservation Act
The import into the United States of
all of these species: the crimson shining
parrot, Philippine cockatoo, white
cockatoo, and yellow-crested cockatoo,
is regulated by the Wild Bird
Conservation Act (WBCA) (16 U.S.C.
4901 et seq.), which was enacted on
October 23, 1992. The WBCA is
implemented under 50 CFR part 15 and
has limited or prohibited imports of
exotic bird species into the United
States since 1992. The purpose of the
WBCA is to promote the conservation of
exotic birds by ensuring that all trade
involving the United States is
sustainable and is not detrimental to the
species. The WBCA is a stricter
conservation measure than CITES, and
import of these parrot species into the
United States requires issuance of a
WBCA import permit. WBCA permits
may be issued to allow import of listed
birds for various purposes, such as
scientific research, zoological breeding
or display, or personal pets, when
certain criteria are met. The Service may
approve cooperative breeding programs
and subsequently issue import permits
under such programs. Under the
cooperative breeding program, wildcaught birds may be imported into the
United States if they are a part of
Service-approved management plans for
sustainable use. At this time, none of
the four parrot species discussed in this
document is part of a Service-approved
cooperative breeding program, and there
are no approved management plans for
wild-caught birds of these species.
Under the provisions of WBCA, any
individual importing their pet bird to
the United States for the first time must
reside outside of the United States for at
least 12 continuous months. In addition,
in order to control diseases, the U.S.
Department of Agriculture’s Animal and
Plant Health Inspection Service requires
veterinary health certificates and health
inspections for pet birds, and
implements quarantine procedures for
birds imported into the United States. A
report published in 2006 showed that
imports of parrot species to the United
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States declined from the mid-1980s to
1991 (Pain et al. 2006, pp. 322–324).
Parrot imports to the United States were
already declining before the enactment
of the WBCA, but the WBCA largely
curtailed the import of wild parrots; we
find it is an adequate regulatory
mechanism for all four of these parrot
species.
As discussed under Factor B, local
protections are in place on the islands
where this species exists. The
governmental institutions responsible
for oversight of the conservation of this
species have a good legal framework to
manage wildlife and their habitats. Not
only are local NGOs involved in
conservation activities for this species,
but there also appears to be adequate
capacity at various levels to protect this
species and its habitat. The forestry
regulations appear to be effective; there
are no reports of illegal logging on the
islands of Kadavu and Ono. Most of
Fiji’s forests are managed or owned by
local communities, which have
incentive to protect the native habitat.
Ownership of native lands is not
transferable through land sales, but user
rights can be transferred via land leases
(Leslie and Tuinivanua 2010, p. 10).
These landowning groups are deeply
attached to their lands and Fiji’s forestry
policy supports the local ownership of
its lands. Within this species’ habitat,
the forested areas are being adequately
managed and protected by these
mataqalis.
Environmental education,
conservation initiatives, and restoration
efforts are occurring on Kadavu.
Another NGO working on Kadavu to
protect this species is the Matava
Foundation (https://
foundation.matava.com/2011-projects)
which is a local NGO associated with a
resort on the island. In addition to the
conservation efforts in place, the
remoteness of these islands likely serves
as an additional protection for this
species. The crimson shining parrot
occurs on two islands, and both islands
are extremely remote and fairly
undeveloped. These factors all likely
serve as additional protections for this
species.
In summary, the existing regulatory
mechanisms appear to be adequate.
There are no current records of this
species in international trade, and the
government of Fiji is actively
conducting environmental stewardship
projects. There is nothing to suggest that
this factor is a threat to the species.
Local conservation activities involving
indigenous communities are occurring
on Kadavu and this species and its
habitat appear to be well protected. Fiji
has enacted various laws and regulatory
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mechanisms to protect and manage
wildlife and their habitats. As described
above in our review, we found that the
government of Fiji and NGOs are
implementing many projects and
mechanisms that will likely have a
positive impact on this species and its
habitat. Reforestation and conservation
efforts are occurring. The best scientific
and commercial information available
indicates that the crimson shining
parrot is not in danger of extinction or
likely to become so within the
foreseeable future due to inadequate
regulatory mechanisms.
Factor E. Other Natural or Manmade
Factors Affecting the Continued
Existence of the Species
In this section, we examined whether
invasive species are threats to the
crimson shining parrot. The eastern part
of Kadavu supports several bird species
that are endemic to Kadavu. BLI
indicated that logging and roads (see
Factor A) may be facilitating the
movement of invasive species. Logging
enables alien invasive species such as
rats and cats, and in some cases, Indian
or common mynahs (Acridotheres
tristis), jungle mynahs (Acridotheres
fuscus), and Spathodea campanulata
(African tulip trees), to invade the
forests along logging roads and
clearings. The island of Kadavu may be
experiencing invasive species, but there
is no evidence that invasive species are
occurring to an extent that they are
threats to the crimson shining parrot.
Nor is there evidence that invasive
species are a threat on Ono Island,
where the crimson shining parrot is also
known to occur. BLI is creating
community-based conservation groups
at Fiji’s key conservation sites such as
Kadavu Island, and is working with
communities to address issues such as
effectively dealing with invasive species
(BLI 2011g, p. 3). We found no other
natural or manmade factors that might
affect the continued existence of the
crimson shining parrot now or in the
future. Based on the best available
information, we find that there are no
other natural or manmade threats to the
continued existence of the crimson
shining parrot throughout its range now
or in the foreseeable future.
Significant Portion of the Range
Having determined that the crimson
shining parrot is not in danger of
extinction or likely to become so within
the foreseeable future throughout all of
its range, we must next consider
whether there are any significant
portions of the range where the crimson
shining parrot is in danger of extinction
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or is likely to become endangered in the
foreseeable future.
The Act defines an endangered
species as one ‘‘in danger of extinction
throughout all or a significant portion of
its range,’’ and a threatened species as
one ‘‘likely to become an endangered
species within the foreseeable future
throughout all or a significant portion of
its range.’’ The term ‘‘significant portion
of its range’’ is not defined by the
statute. For the purposes of this finding,
a portion of a species’ range is
‘‘significant’’ if it is part of the current
range of the species, and it provides a
crucial contribution to the
representation, resiliency, or
redundancy of the species. For the
contribution to be crucial it must be at
a level such that, without that portion,
the species would be in danger of
extinction.
In determining whether a species is
threatened or endangered in a
significant portion of its range, we first
identify any portions of the range of the
species that warrant further
consideration. The range of a species
can theoretically be divided into
portions in an infinite number of ways.
However, there is no purpose to
analyzing portions of the range that are
not reasonably likely to be significant
and threatened or endangered. To
identify only those portions that warrant
further consideration, we determine
whether there is substantial information
indicating that: (1) The portions may be
significant, and (2) the species may be
in danger of extinction there or likely to
become so within the foreseeable future.
In practice, a key part of this analysis is
whether the threats are geographically
concentrated in some way. If the threats
to the species are essentially uniform
throughout its range, no portion is likely
to warrant further consideration.
Moreover, if any concentration of
threats applies only to portions of the
species’ range that clearly would not
meet the biologically based definition of
‘‘significant’’ (i.e., the loss of that
portion clearly would not reasonably be
expected to increase the vulnerability to
extinction of the entire species to the
point that the species would then be in
danger of extinction), such portions will
not warrant further consideration.
If we identify portions that warrant
further consideration, we then
determine their status (i.e., whether in
fact the species is endangered or
threatened in a significant portion of its
range). Depending on the biology of the
species, its range, and the threats it
faces, it might be more efficient for us
to address either the ‘‘significant’’
question first, or the status question
first. Thus, if we determine that a
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portion of the range is not ‘‘significant,’’
we do not need to determine whether
the species is endangered or threatened
there; if we determine that the species
is not endangered or threatened in a
portion of its range, we do not need to
determine if that portion is
‘‘significant.’’
Applying the process described above
for determining whether a species is
threatened in a significant portion of its
range, we considered status first to
determine if any threats or potential
threats acting individually or
collectively threaten or endanger the
species in a portion of its range. We
have analyzed the potential threats and
determined they are essentially uniform
throughout the species’ range.
Finding for the Crimson Shining Parrot
Section 3 of the ESA 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.’’ In this
finding, we determine whether the
petitioned action is: (a) Not warranted,
(b) warranted, or (c) warranted but
precluded (see Background, above).
As required by the ESA, we
considered the five factors separately
and in combination in assessing
whether the crimson shining parrot is
endangered or threatened throughout all
or a significant portion of its range. We
examined the best scientific and
commercial information available
regarding the past, present, and future
threats faced by the crimson shining
parrot. We reviewed the petition,
information available in our files, and
available published and unpublished
information regarding this species and
its habitat.
We do not have long-term population
trend data for the crimson shining
parrot. This species has always been an
island endemic and may have always
had a small population; island endemics
tend to have smaller population sizes.
Without historical population
information, we do not know if this
species has experienced a decrease in
population size or if its population has
been fairly consistent. Furthermore, this
species is reported as common and
widespread. During our review of the
status of the species, we evaluated the
potential threats to the crimson shining
parrot including: habitat loss and
habitat degradation, take for the pet
trade, disease and predation, the
inadequacy of regulatory mechanisms,
and other natural or manmade factors
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such as invasive species. We found no
information that habitat loss is a threat
to the crimson shining parrot. We
conclude that the present or threatened
destruction, modification, or
curtailment of its habitat or range is not
a threat to the crimson shining parrot.
We found no information that poaching
for the pet trade is a threat to the
species. This species is not in
international trade according to the
UNEP–WCMC trade database.
Additionally, education and public
awareness campaigns are occurring in
Kadavu. Fiji is actively involved in
forest protection efforts; a new Forest
Policy was adopted in 2007 (Fiji
Ministry of Fisheries and Forestry 2009,
p. 1). We found no evidence that disease
or predation affects the wild crimson
shining parrot population. In addition,
this species is protected by laws against
trading and transfers out of Kadavu and
Ono. We also concluded that there are
no other natural or manmade factors
that are threats to the species (Factor E).
The best available information
indicates that there is little disturbance
on the islands where the crimson
shining parrot naturally occurs. Habitat
loss is often a threat to wildlife,
however, in this case, there is no
evidence that habitat loss is affecting the
crimson shining parrot. On the contrary,
this species is said to occupy altered
habitat extensively. Conservation efforts
for this species have been underway
within the past few years to ensure longterm conservation of habitat where this
species exists; local groups on Kadavu
are implementing reforestation and
conservation programs. Based on the
lack of threats acting on this species
throughout its range as described above,
and the lack of information indicating
the species population is in decline, we
determine that this species is not in
danger of extinction now, nor is it likely
to become endangered within the
foreseeable future, throughout all or a
significant portion of its range.
Therefore, we find that listing the
crimson shining parrot as a threatened
or endangered species is not warranted.
Species Information
B. Philippine Cockatoo (Cacatua
haematuropygia)
Taxonomy and Species Description
The species was first taxonomically
¨
described by Muller in 1776 (BLI
2011b). We accept the species as C.
haematuropygia, which follows the
Integrated Taxonomic Information
System (ITIS 2011).
Cockatoos are only found in
Australasia—a few archipelagos in
Southeast Asia (Philippines, Indonesia,
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East Timor, Tanimbar, Bismarck, and
Solomon), New Guinea, and Australia—
suggesting that the modern species arose
after the breakup of Gondwanaland, the
southern supercontinent that existed
200 to 500 million years ago. The 19th
century naturalist Alfred Russell
Wallace was among the first to note the
break in Australasian and Asian fauna.
Wallace’s line runs between the islands
of Bali and Lombok, Borneo and
Sulawesi, and south of the Philippines.
Cockatoos are present on Lombok and
Sulawesi, but not on Bali and Borneo.
The line represents the western edge of
a zone of overlap between Australasian
and Asian fauna (known as Wallacea),
with the eastern edge defined by the
Australian continental shelf (Lydekker’s
Line) (White and Bruce 1986, p. 32;
Cameron 2007, pp. 1–3). These oceanic
islands of Wallacea have high levels of
endemism, meaning the species that
occur there are unique to those islands.
The Philippine cockatoo, or redvented cockatoo, is locally known as the
‘‘katala’’ and ‘‘kalangay,’’ and has a
helmet crest and a red undertail
(Rowley 1997). Cockatoos are a distinct
group of parrots (order Psittaciformes),
distinguished by the presence of an
erectile crest (Collar 1989, p. 5; Cameron
2007, p. 1) and the lack of dyck texture
in their feathers. Dyck texturing is a
microscopic texturing that produces
blue and green coloration and is present
in the plumage of other parrots (Brown
and Toft 1999, p. 141).
Biology, Distribution, and Habitat
This species is endemic to the
Philippines, an archipelago of
approximately 7,000 islands. The total
area of the Philippines is 30,000,000 ha
(74,131,614 ac) (Kummer 1991, p. 44).
The Philippine cockatoo requires
lowland primary or secondary forests
with suitable nesting tree cavities and
food sources, within or adjacent to
riparian or coastal areas with mangroves
(IUCN 2008i). The species is reported to
use regenerating forest and even heavily
degraded forest, as long as emergent
nest trees survive. However, its nest
sites are restricted to lowlands
(Widmann and Widmann 2010, pers.
comm.).
The Philippine cockatoo is a food
generalist; its diet varies based on the
seasons. It consumes seeds, legumes,
fruit, flowers, buds, and nectar. It will
also eat agricultural crops such as corn
and rice, and has been observed feeding
on Moringa oleifera (commonly known
as malunggay or horseradish tree).
Interestingly, the government of the
Philippines introduced a bill in 2010, in
the Fifteenth Congress of the Republic
of the Philippines, First Regular
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Session, to encourage planting Moringa
oleifera due to economic benefits
(Senate Bill 1349 2010, pp. 1–7). The
Philippine cockatoo has also been
observed feeding on the fruits of
Sonneratia, a mangrove species
(Tabaranza 1992; Lambert 1994b in BLI
2001, p. 1683).
This species nests in tree cavities, and
produces two to three eggs per season
(Cameron 2007, p. 140). Breeding
generally occurs March through June
(BLI 2001, p. 1684), and both sexes
participate in nest building (Widmann
et al. 2001, p. 135). The period between
incubation and fledging is generally
about 95 days (Cameron 2007, p. 140).
The species prefers nests high in the
tree canopy, generally around 30 m (98
ft) (BLI 2001, p. 1683), but nest heights
between 12 and 35 m (39 to 114 ft) have
also been observed (Widmann et al.
2001, p. 135). The diameter of the cavity
openings observed has been between 10
and 25 cm (4 and 10 in) (Widmann et
al. 2001, p. 135). Some artificial nest
boxes have been installed to increase
nesting habitat; the species exhibits a
preference for horizontal rather than
vertical nest boxes (Low 2001, p. 3).
Some of the tree species they use for
roosting include Dipterocarpus
grandiflorus (common names: apitong,
tempudau, tunden, lagan bras aput) and
Intsia bijuga (common names: Borneoteak, Moluccan ironwood, and merbau
asam), as well as coconut trees (Lambert
1994b in BLI 2001, p. 1686). They also
use Garuga floribunda (no common
name [ncn]) and Sonneratia alba (ncn)
(Cameron 2007, p. 35).
Population Estimates
Based on recent reports, it is likely
that between 450 and 1,245 individuals
remain in the wild. Surveys indicated
that until around the 1980s, the
Philippine cockatoo was fairly common
within the Philippine archipelago
(Collar et al. 1998; Boussekey 2000, p.
138, BLI 2010, p. 1). Historically, it was
known to exist on 52 islands in the
Philippines; now, it is believed to exist
on eight islands (BLI 2011a, p. 1).
The species’ current range is
significantly reduced from its historic
range. In the past, the species was
reported to have been commonly found
throughout the Philippines except for
northern and central Luzon (Delacour
and Mayr 1946; DuPont 1971 in
Boussekey 2000, p. 138; Collar et al.
1999 in Widmann and Widmann 2008,
p. 23). It was common throughout the
Philippines as recently as the 1950s.
Between 1980 and 2000, there was a 60
to 90 percent population decline
throughout its range (Boussekey 2000, p.
138). In the early 1990s, the population
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was estimated to be between 1,000 and
4,000 (Tabaranza 1992 and Lambert
1994b in BLI 2001, p. 1681).
Snyder et al. (2000) reported the
following population surveys. A 1991
survey estimated between 800 and 3,000
birds exist on Palawan (Pandanas,
Bugsok, and Bancalan Islands were
thought to support 100 to 300
individuals and Dumaran 150 to 250
individuals), and possibly a few
hundred were thought to exist in the
Tawi-Tawi region (Lambert 1993b,
1994b). A single pair was found on
Siquijor in 1991 (Evans et al. 1993). A
few were found at Mount Isarog, Luzon
in 1988 (Goodman and Gonzales 1990),
and a few pairs were found in Mindoro
at Malpalon (Dutson et al. 1992). On
Masbate, birds were observed in 1993
(Curio 1994), and the species has been
recorded a few times in singles or small
numbers in Rajah Sikatuna National
Park, Bohol since 1989 (Brooks et al.
1995b). In 1994, two pairs (Dutson in
litt. 1997) were seen on Tawi-Tawi, and
the species was considered widespread
there in 1995–1996, although apparently
more often seen in captivity than in the
wild (two singles were observed in
Batu-Batu and a single and a pair in
Buan) (Allen in litt. 1997). Three birds
were observed on Simunul, Tawi-Tawi
in 1996 (Allen in litt. 1997; Dutson et al.
1996). The species is considered extinct
on Cebu (Brooks et al. 1995a) and
Negros (Brooks et al. 1992). Recent
population counts and estimates are
below; however, this information is not
a complete representation of the
population, but is the best available
information. Some islands may not hold
viable populations and may be
functionally extinct.
Between 2004 and 2010, the
population estimate decreased from
1,000 to 4,000 individuals to 450 to
1,245 individual birds in the wild
(Widmann and Widmann 2008, p. 23;
BLI 2010b; Widmann and Widmann
2010, pers. comm.). This species
currently is found in the Culasian
Managed Resource Protected Area
(CMRPA), Palawan, Dumaran Island
(negligible population), Pandanan and
Bugsok Islands, Polillo Island Group,
Rasa Island, Tawi-Tawi, and possibly on
Samar Island. An estimated additional
400 individuals may survive in the Sulu
archipelago; however, only sparse
information is available for this area
(Widmann et al. 2007; Widmann et al.
2009a; Widmann et al. 2010a).
Subpopulations away from Palawan and
the Sulus are thought to be very small,
and do not likely have viable
populations (Widmann 2010, pers.
comm.) The extent these populations
are interbreeding is unclear at this time.
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Detailed discussion of each of these
areas follows.
TABLE 1—POPULATION COUNTS AND
ESTIMATES
OF
PHILIPPINE
COCKATOO BETWEEN 2007 AND
2010 ON ISLANDS IN THE PHILIPPINES
Number of individuals based on recent observation,
population count, or
estimate
60 ..........................
20 ..........................
3 ............................
23 ..........................
80 ..........................
2 ............................
280 ........................
4 ............................
200 ........................
672 ........................
Location
Bugsok Island (40 to 80
estimated).
Burdeos, Polillo Islands.
CMRPA, Palawan Island.
Dumaran, Lagan.
Pandanan Island.
Patnanungan, Polillo Islands.
Rasa Island.
Samar.
Tawi-Tawi (100 to 400
estimated).
TOTAL*
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* Note: This is not a full population survey; it
documents birds actually counted, observed,
or estimated (Widmann 2010, pers. comm.).
Culasian Managed Resource Protected
Area
This area is in the south of Palawan
Island and is 1,954 hectares (ha) (4,828
acres (ac)). The total land area of
Palawan is approximately 1.5 million ha
(3.7 million ac), including the 1,767
islands and islets surrounding the main
island. This species exists both within
the actual designated protected area
(CMRPA) and in the areas surrounding
the protected area on Palawan Island.
Philippine cockatoos are thought to
travel between Palawan Island and
nearby Rasa Island. This species has
been known to fly from the mainland to
offshore islands as far as 8 km (5 mi)
away from the mainland to roost and
breed. No roosting sites are known in
the CMRPA and surrounding areas
(Widmann et al. 2010a, p. 23); however,
there have been recent sightings there:
four were observed in September 2009,
and three were observed in December
2009 (Widmann et al. 2010a, p. 37). At
least two Philippine cockatoos persist
inside the protected area, but they have
not bred in the last 4 years.
CMRPA has been described as
exhibiting the ‘‘empty forest syndrome.’’
Although its forest is largely intact, little
wildlife remains due to hunting
pressure and poaching. In the small
population that was protected only
recently here, there are no indications
that the species’ status is improving.
Only one breeding pair exists outside of
the reserve. Cockatoo poaching occurred
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in this area within the past 3 years, and
breeding in the 2009–2010 season
failed. Because all nests have been
systematically poached over many
years, extinction of this population is
likely to occur suddenly due to lack of
recruitment (Widmann and Widmann
2010, pers. comm.).
Dumaran Island
On Dumaran Island, which is off the
northeastern coast of Palawan, three
areas are managed by the Katala
Foundation’s Philippine Cockatoo
Conservation Programme (PCCP). Two
of those are protected areas: the Omoi
Cockatoo Reserve and the Manambaling
Cockatoo Reserve (Widmann et al.
2009b, p. 7). The third area is Lagan,
which is also monitored and managed
by the PCCP. On Dumaran Island, the
protected suitable forest patches are
each very small: 1.5 and 0.6 km2 (0.6
and 0.2 mi2), respectively (Widmann
and Widmann 2008, p. 24). On this
island in 2008, although 10 eggs were
counted, only two birds fledged
(Widmann et al. 2009b, p. 6). Recovery
is slow; they started with fewer than 20
birds before protection started
(Widmann and Widmann 2010, pers.
comm.).
Pandanan and Bugsok Islands
Pandanan and Bugsok (119 km2) (46
mi2) are small islands south of Palawan,
within the Balabac Island Region. It is
likely that Pandanan holds possibly the
second-most important population of
Philippine cockatoos, containing at least
80 individuals (Widmann and Widmann
2010, pers. comm.). Approximately 40
birds were observed in a coconut
plantation in 2009 on Malinsuno Island,
a 10-hectare (24-acre) nearby island that
is part of the Pandanan Barangay
(equivalent to county or province)
(Widmann et al. 2010c, p. 5; Widmann
and Widmann 2010, pers. comm.). On
Bugsok Island, Balabac, also in the
Pandanan Barangay, approximately 40
cockatoos were also recently observed
roosting (Widmann et al. 2010c, p. 5). A
large part of Pandanan Island itself is
not easily accessible, and because it is
privately managed, it is protected for the
most part. PCCP is working on building
a relationship with organizations to
monitor and formally protect this
island, and wardens are being hired as
of 2010 (Widmann et al. 2010, pp. 26,
56).
Polillo Islands Group
This group of islands is
approximately 110 km (68 mi) east of
Manila, in Quezon Province in the
northern Philippines. Patnanungan
Island is part of the Polillo Island Group
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and is not yet very developed. Polillo
Island itself is 1,000 km2 (386 mi2). As
of 2009, within the Polillo group of
islands, Patnanungan Island was known
to contain a population of the
Philippine cockatoo (Widmann et al.
2010, p. 15). However, no roosting sites
have been identified on this island
(Widmann et al. 2010, p. 23).
Patnanungan Island is mainly covered
with secondary vegetation and coconut
plantations (Widmann et al. 2010, p.
22). Seven nest trees are being
monitored in this area (Widmann et al.
2009b, p. 7). To the best of our
knowledge, there is not a viable
population on Polillo Island, although
the species has been observed there. In
2009, in Burdeos, six Philippine
cockatoos were spotted in Duyan-Duyan
Forest in the Anibawan Barangay, where
it is regularly heard (Widmann et al.
2009a, p. 41; Widmann et al. 2010, p.
38). In part, because there were fewer
than 20 birds prior to their protection,
recovery is slow (Widmann and
Widmann 2010, pers. comm.).
Rasa Island
Rasa Island is a protected 8 km2 (3
mi2) island off the east coast of Narra,
Palawan. This island was declared a
wildlife sanctuary in 2006 (Widmann et
al. 2010, p. 15). As of 2007, 1.75 km2
(0.6 mi2) of the island was coastal and
mangrove forest. In 2008, 32 nest trees
were found to be occupied, 21 pairs had
successful fledglings, and the
population was estimated to be 205
individuals (Widmann et al. 2008, p. 14;
Widmann and Widmann 2008, p. 27;
Widmann et al. 2009b, p. 5–6). Breeding
success was 63 percent; 49 fledglings
were banded (Widmann and Widmann
2008, p. 24). Population recruitment in
years that experienced sufficient
precipitation in Rasa has been good. As
of 2009, Rasa Island had 64 nest trees,
and its cockatoo population was
approximately 280 individuals, making
it the area with the highest natural
density of Philippine cockatoos
(Widmann 2010b). PCCP estimates that
Rasa Island contains about 20 percent of
the total Philippine cockatoo population
(Widmann et al. 2010c, p. 19). The
success of cockatoos on this island is
likely due to the lack of potable water,
which makes it unattractive to human
settlement (BLI 2001, p. 1687). The
Philippine cockatoo population on this
island has grown due to intense
management; in 1997, there were only
about 50 birds on Rasa Island (Widmann
and Widmann 2008, p. 24).
Other Islands
Little current data exists regarding the
status of the Philippine cockatoo on
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other islands, such as Samar and TawiTawi, in part because these areas are
extremely remote. The Katala
Foundation Inc. (KFI) surveyed Samar
in 2002, at which time only two
individual Philippine cockatoos were
verified. Sightings were reported
recently in Busuanga Island (Coron) and
on Bellatan Island in the Tawi-Tawi
region. KFI recently received a report
from a member of the Wild Bird Club,
Philippines, that approximately 30 to 40
individuals were sighted on Bellatan
Island (Widmann and Widmann 2010,
pers. comm.). Sightings of this species
on Dinagat, Surigao del Norte, and
Samal Islands, Davao, have been
reported, but they remain unverified
(Widmann and Widmann 2010, pers.
comm.).
An older survey indicated that
possibly 100 to 200 Philippine
cockatoos existed in the Tawi-Tawi
region; however, those data are from
over 20 years ago, and, therefore, no
longer likely to be an accurate
population estimate (Lambert 1993,
Dutson 1997, and Allen 1997 in Snyder
2000, p. 84; BLI 2010b, p. 1). Tawi-Tawi
is in the southwestern part of the
Philippines in the Sulu Archipelago.
Tawi-Tawi consists of 107 islands and
islets and is approximately 1,197 km2
(462 mi2) in area. The island of TawiTawi itself is 484 km2 (187 mi2) (Dutson
et al. 1996, p. 32) and is part of the
Autonomous Region in Muslim
Mindanao (ARMM). This area has
experienced problems with logging,
military activity, and insurgency but is
now encouraging ecotourism
(Philippines Department of Natural
Resources (DENR) 2005; IUCN 2010b;
Manila Bulletin 2010), which may have
positive effects on the Philippine
cockatoo.
Samar is the third largest island in the
Philippines archipelago. It experienced
threats from logging and mining in the
past, but in 1989, an unexpected natural
disaster resulted in initiation of
conservation actions (Samar Island
Natural Park 2010, p. 1). Due to the
intense landslides that occurred as a
result of logging activities, a logging
moratorium was put into place that
year. Samar Island Natural Park was
subsequently established on the island,
which may have positive results for the
Philippine cockatoo. Samar has been
reported to contain one of the
Philippines’ largest unfragmented tracts
of lowland rainforest. There have been
several reports of Philippine cockatoo
sightings on Samar, but there is no
current estimate of how many exist
there other than the reported sightings
(Widmann et al. 2006, p. 13; BLI 2010
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p. 1; Widmann and Widmann 2010,
pers. comm.).
Conservation Status for the Philippine
Cockatoo
Protections exist through various
national, local, and international
mechanisms. This species was
transferred from Appendix II to
Appendix I of CITES in 1992 (refer to
the discussions under Factors B and D
for the crimson shining parrot above for
more information about CITES).
Inclusion in Appendix I means that
international commercial trade is
generally prohibited (https://
www.cites.org). From 1981 to 1992, the
Philippine cockatoo was listed in
Appendix II of CITES. The species is
protected under the Philippines
Republic Act 9147, otherwise known as
the Wildlife Resources Conservation
and Protection Act of 2001 or the
‘‘Wildlife Act of 2001.’’ It is classified as
‘‘Critically Endangered’’ by the
government of the Philippines under
this Act (DENR 2010b, p. 2). It is on the
Philippines list of protected species
(DENR 2010b, p. 2), under the Republic
Act No. 9147. The Republic No.
provides for the conservation and
protection of wildlife resources and
their habitats. It prohibits certain
activities such as capture and trade of
live wildlife, including the Philippine
cockatoo. It is also protected in the U.S.
by the WBCA (refer to discussion under
the Crimson Shining Parrot, factor D).
The Philippine cockatoo is also listed
as Critically Endangered in the 2010
IUCN Red List. Critically endangered is
IUCN’s most severe category of
extinction assessment, which equates to
an extremely high risk of extinction in
the wild. IUCN criteria include rate of
decline, population size, area of
geographic distribution, and degree of
population and distribution
fragmentation; however, IUCN rankings
do not confer any actual protection or
management.
Evaluation of Factors Affecting the
Philippine Cockatoo
Factor A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
Widespread deforestation and
destruction of native mangroves have
affected the habitat of the Philippine
cockatoo. The loss of this species’
habitat through deforestation largely
occurred prior to the 1980s (Kummer
1991, p. 46; Galang 2004, p. 13). Forest
cover decreased in Palawan from 10,703
km2 (4,132 mi2) in 1950, to 6,605 km2
(2,550 mi2) in 1987 (Kummer 1991, p.
57). In the 1990s, commercial logging on
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Palawan, the primary location of the
Philippine cockatoo, was suspended by
presidential decree; however, nearly all
of the island’s forests were already
leased to logging operations (Lambert
1994b in BLI 2001, p. 1686; Galang
2004, p. 14). Many of Palawan’s
mangroves, which covered 46,000 ha
(13,668 ac) in 1988, were also cleared
for fishpond construction (Quinnell and
Balmford 1988 in BLI 2001, p. 1686). As
a result of the pressures for resources,
much of the forest is now either
secondary forest or has been converted
to plantations or agriculture (Heaney et
al. 1998, 88 pp.; Galang 2004, pp. 13–
14). In most areas within the range of
the Philippine cockatoo, there is a
severe shortage of timber and firewood;
consequently, illegal logging is
widespread. In addition to mangrove
logging, slash-and-burn farming
(referred to as ‘‘kaingin’’ in the
Philippines) is a problem in many areas,
particularly in the Polillo Island Group.
Soil erosion is a secondary impact
that further degrades suitable habitat
(Kummer 1991, p. 41), as demonstrated
on Samar Island. In addition to habitat
degradation and destruction through
road construction, digging, removal of
trees, and mining are causing secondary
habitat degradation through severe
erosion. During the rainy season, water
creates deep clefts along the roads that
are created for mining operations,
causing road collapse. No mitigation
measures have been put into place to
reduce erosion (IUCNb 2010, pp. 1–2).
Virtually all chainsaw operations in
Patnanungan and Burdeos are not
registered with the appropriate
authority (Widmann et al. 2010).
Cockatoos are highly impacted by
selective logging of primary forests
because they are large birds and
subsequently require large nests.
Selective logging, which targets mature
trees, has a negative impact on treecavity nesters such as the Philippine
cockatoo. Research has found that the
abundance of cockatoos is positively
related to the density of its favored nest
tree and strangling figs (Ficus spp.)
(Kinnaird et al. 2003, p. 227). These are
trees that would be impacted by logging,
especially since reduced-impact logging
techniques are seldom applied. Once
the primary forest is logged, the
secondary forest is generally converted
to other uses or logged again rather than
being allowed to return to primary
forest. Therefore, although cockatoos
may continue to inhabit secondary
forests, the population is usually at a
substantially lower number due to a
decrease in suitable nesting sites.
It is well documented that habitat loss
is one of the most significant effects
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humans have on wild species (Fahrig
1997, p. 603; Vitousek et al. 1997). In
some cases, corridors are established to
promote connectivity between
populations of species to reduce the
effects of habitat fragmentation, and this
has been shown to be effective (Haddad
et al. 2003, pp. 609–615; Cameron 2007,
pp. 110–112). In the case of the
Philippine cockatoo, a ‘‘virtual’’
corridor is being created by artificially
transplanting captive-reared cockatoos
into suitable, relatively protected
habitat; however, it is unclear how
much this species naturally moves from
one island habitat to another. This
species in the past has been known to
fly from the mainland to nearby islands
at distances of 8 km (5 mi). Researchers
point out that at the metapopulation
scale, habitat fragmentation causes
habitat patches to be reduced in size
and to be isolated from one another, and
gene flow between patches is decreased
(Blanchet et al. 2010, p. 291). Because
this species’ population reduction and
fragmentation has occurred so recently
and rapidly, it is unlikely that there are
significant genetic differences between
the existing populations. However,
habitat loss and fragmentation are
affecting this species.
The Palawan Islands Region is
essentially the last area where
Philippine cockatoos have a viable
population. Although Palawan has been
seen as a center for environmental
preservation (McNally 2002, p. 9), it still
faces many threats, in part due to a
burgeoning human population (IUCN
2010b, p. 1; Laurance et al. 2010, p.
377). The human population of the
Philippines in 2009 was estimated at
91,983,000 (United Nations (UN) 2009,
p. 41) and is experiencing a growth rate
of 1.7 percent annually (UN 2009, p.
51). Palawan, in particular, has
experienced rapid human population
growth (McNally 2002, pp. 8–9). As of
2002, ‘‘Palawan remains a highly
attractive place of destination for
migrants from other areas within the
Philippines’’ (McNally 2002, p. 11).
While the burgeoning human
population on Palawan may not directly
affect the Philippine cockatoo, it does
indirectly affect the species by
contributing to the habitat losses and
pressures described within this section.
Despite the protection measures that
are in place to prohibit mining and
other activities that degrade habitat,
mining operations and oil palm
plantations are being developed on
Palawan Island (IUCN 2010c, pp. 1–3;
Novellino 2010, pp. 2–48). The
Philippine cockatoo has not been
recorded in areas in southern Palawan
where mining and oil palm plantations
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exist (Widmann and Widmann 2010,
pers. comm.). Although mining does not
occur directly within Philippine
cockatoo habitat, it indirectly adds to
habitat loss and degradation on the
island (Novellino et al. 2010, pp. 1–48).
These threats to the ecosystem still exist
despite legislative protections in
Palawan (refer to Factor D).
Rasa Island contains a large
percentage of the Philippine cockatoo
population, although small in actual
numbers. In addition to the formal
protection measures in place on Rasa
Island, this population is actively
monitored and protected by PCCP staff
(Widmann et al. 2010a, b, c). While this
population is reasonably protected, in
part due to island’s undesirable
characteristics for human settlement
such as the lack of potable water, any
deforestation and habitat loss here are
significant factors affecting the species.
This is because so little of the species’
habitat remains and because they are
experiencing other pressures as well,
such as poaching, described under
Factor B, below.
On Dumaran Island, the pending
implementation of a Jatropha plantation
is occurring within the few remaining
forest patches left (Widmann et al.
2010a, pp. 6, 32, 46). Jatropha curcas
trees produce a fruit with an inedible oil
that contains a high energy content and
is being explored as an alternative fuel
(Mendoza et al. 2007, p. 1). A hectare of
Jatropha has been claimed to produce
1,892 liters (500 gallons) of fuel. Many
industries such as the air transportation
industry are considering this as a
biofuel source, and it is also being
touted as a mechanism for carbon
credits. However, because this species
occurs in areas that are managed and
protected by the PCCP, the Omoi
Cockatoo Reserve and the Manambaling
Cockatoo Reserve (Widmann et al.
2009b, p. 7), we do not find that
pending implementation of a Jatropha
plantation is a threat to the species on
Dumaran Island.
PCCP currently manages three areas
on Dumaran Island, including a newly
acquired buffer area in Omoi (Widmann
et al. 2010, p. 32). Dumaran Island also
experiences widespread slash-and-burn
agriculture, which has begun to affect
more forested areas on steeper slopes
here (Widmann 2008a, p. 19). Larger
forested parts of the island are now
replaced with grass and shrubland, and
dense stands of bamboo, as a
consequence of this practice. Due to
lack of water, irrigation systems, and
level areas, lowland rice cultivation is
very restricted. However, permanent
forms of cultivation are coconut and
cashew plantations. Forest and grass
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fires are common, particularly during
the dry season. Fire is not only used to
clear areas for cultivation, but also to
further growth of fresh grass for
pastures.
In the other areas where this species
exists, the current extent of the present
and threatened destruction,
modification, or curtailment of the
species’ habitat is unclear; however, it is
likely that the pressures on the species
are similar, if not worse (BLI 2010b;
Widmann et al. 2010, p. 15). Human
encroachment and concomitant
increasing human population pressures
exacerbate the destructive effects of
ongoing human activities throughout
the Philippine cockatoo’s habitat.
Increased urbanization and mining lead
to increased infrastructure development.
Road building and mining projects
further facilitate human access to
remaining forest fragments, throughout
the species’ range, including protected
areas. Mining projects, such as those
proposed or occurring on Palawan, open
new areas to exploitation and attract
people seeking employment; these
pressures from human development will
likely spill over into nearby Philippine
cockatoo habitat.
Summary of Factor A
We have identified a number of
threats to the habitat of the Philippine
cockatoo that have operated in the past,
are impacting the species now, and will
continue to impact the species. Habitat
loss and degradation from past events,
such as selective and commercial
logging, conversion to plantations or
agriculture, and mining, have decreased
this species’ suitable habitat; and these
activities are still occurring. Illegal
logging (discussed under Factor D) is
widespread in the Philippines (Kummer
1991, pp. 70–75; Galang 2004, pp. 12,
17, 22; Laurence 2007, p. 1544), which
adds to any pressures of legal
deforestation. Based on the best
available scientific and commercial data
available, we find that the present and
threatened destruction, modification, or
curtailment of the species’ habitats,
particularly in the Palawan area, is a
threat to the Philippine cockatoo
throughout all of its range.
Factor B. Overutilization for
Commercial, Recreational, Scientific, or
Educational Purposes
Illegal Pet Trade
The Philippine cockatoo, like all
cockatoos, is a desirable pet (Cameron
2007, p. vii). In the Philippines,
cockatoos are reported to be popular
pets due to their ability to mimic human
voices (Catigob-Sinha 1993 in
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Boussekey 2000, p. 138). On Palawan,
Pandanan, and Samar Islands, trapping
is a particularly serious threat
(Widmann et al. 2010a, pp. 21–22;
Widmann et al. 2010c, p. 16) and is still
considered to be one of the most
significant threats to the species.
Awareness campaigns have been
initiated since the late 1990s to increase
understanding of why these birds
should not be removed from the wild for
pets, and these campaigns are somewhat
effective (Widmann et al. 2010). Due to
the high value of these birds (valued at
$160 U.S. dollars (USD) in Manila in
1997, and $300 USD in 2006 (BLI 2010,
p. 1)), chicks are taken from virtually
every accessible nest on these islands
(Widmann et al. 2010a, pp. 21–22). A
researcher observed that in the 1980s,
up to 10 Philippine cockatoos were
trapped per day (Tabaranza 1992 in BLI
2001, p. 1685).
In recent years, several programs to
combat the poaching problem, such as
public awareness programs and the
rehabilitation and release of confiscated
parrots were established by the PCCP to
support the conservation of the
Philippine cockatoo. PCCP started these
awareness programs to educate adults
and children in villages near areas
where the birds are concentrated. The
programs use the Philippine cockatoo as
a flagship species for conservation,
especially with children, because the
image of the endemic Philippine
cockatoo is unique (Widmann et al.
2010, pp. 21–22). PCCP focuses in areas
where this species is found in the wild,
such as the CMRPA, to educate the local
communities in an attempt to reduce
poaching. In 2005, on Palawan Island,
PCCP began an initiative specifically
targeted towards anti-poaching in the
CMRPA. Former poachers were
identified and converted into wildlife
wardens. This ‘‘conversion’’ practice is
common in developing countries that
have human populations that rely
heavily on forests and wildlife for their
survival (Cribb 2006, p. 3). These
converted poachers-now-wardens
safeguard the nesting trees, and patrol
and monitor inside CMRPA in the
southwest region of Palawan (Widmann
et al. 2010).
Because illegal trade is difficult to
monitor and quantify, it is unclear to
what extent poaching for the pet trade
is affecting this species. Considering
that in the early 1990s, the population
was estimated to be only between 1,000
and 4,000 birds (Tabaranza 1992 and
Lambert 1994b in BLI 2001, p. 1681),
relatively high numbers were legally
traded internationally in the 1980s (e.g.,
422 reported in 1983; BLI 2010, p. 1).
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This species is still is being poached in
the wild (Widmann et al. 2010).
Although we are unsure of the
magnitude of the pet trade and its effect
on the survival of this species, several
reports describe how poaching is still a
problem for parrot species, particularly
in poorer countries (Dickson 2005, p.
548; https://www.philippinecockatoo.org,
accessed February 14, 2011). In areas
with extreme poverty, poaching can be
a lucrative and relatively risk-free
source of income (Dickson 2005; Cribb
2007; Widmann et al. 2010c, p. 22). In
many cases, poachers have limited
income prospects (Widmann et al.
2010a, p. 37). A common conservation
practice is to provide poachers with
alternative sources of income. After the
benefits of species and habitat
conservation are explained to them,
they are generally receptive to resource
conservation and ultimately gain a sense
of stewardship of the resources. This
technique has been effective in the past,
but it is resource-intensive and has only
a localized effect.
PCCP also broadcasts local radio
programs raising conservation
awareness. For example, in August
2010, they broadcast an interview
regarding wildlife trade and a recent
confiscation in Palawan (Widmann et
al. 2010c, p. 73). Conservation-focused
radio programs have occurred here since
1996 (Boussekey 2000, p. 140).
However, even with these education
and conservation measures in place,
poaching still occurs in the Philippines
(Widmann et al. 2010c). Based on the
available information, and the relatively
small number of Philippine cockatoos
remaining in the wild, we find that
poaching for the pet trade in the
Philippines is a threat to the Philippine
cockatoo throughout all of its range.
International Trade and CITES
The Philippine cockatoo was
transferred to CITES’ Appendix I in June
1992 because populations were
declining rapidly due to uncontrolled
trapping for the pet bird trade. Refer to
the Factor B discussion above under the
crimson shining parrot for additional
information about CITES. An AppendixI listing includes species threatened
with extinction whose trade is
permitted only under exceptional
circumstances, which generally
precludes commercial trade. The import
of an Appendix-I species requires the
issuance of both an import and export
permit. Import permits are issued only
if findings are made that the import
would be for purposes that are not
detrimental to the survival of the
species in the wild and that the
specimen will not be used for primarily
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commercial purposes (CITES Article
III(3)). Export permits are issued only if
findings are made that the specimen
was legally acquired and trade is not
detrimental to the survival of the
species. (CITES Appendix III(2)). These
two findings made prior to issuance of
a CITES permit are designed to ensure
that international trade in a CITES-listed
species is not detrimental to that
species.
An exception to permitting
requirements for international trade of
Appendix I species exists specimens
originating from a CITES-registered
captive-breeding operation. Under the
exception in the CITES Treaty and
Resolution Conf. 12.10 (Rev. CoP15),
specimens of Appendix-I species
originating from CITES-registered
captive-breeding operations can be
traded for commercial purposes, and
shipments only need to be accompanied
by an export permit issued by the
exporting country. An import permit is
not required because these specimens
are treated as CITES’ Appendix-II
species. There is one CITES-registered
captive-breeding operation in the
Philippines that is authorized to export
captive bred specimens of this species
(https://www.cites.org/common/reg/
e_cb.html, accessed December 12, 2010).
Countries operating CITES-registered
operations must ensure that the
operation ‘‘will make a continuing
meaningful contribution according to
the conservation needs of the species’’
(CITES 2007b, pp. 1–2). Countries that
are parties to CITES are advised to
restrict their imports of Appendix-I
captive-bred specimens to those coming
only from CITES-registered operations.
Additional information on CITESregistered operations can be found on
the CITES Web site at https://
www.cites.org/eng/resources/
registers.shtml.
We queried the UNEP–WCMC CITES
Trade Database for data on exports and
imports of this species from 2000 to
2009, and there were very few exports
from the Philippines reported as ‘‘wild’’
origin. Between 2000 and 2009, CITES
Party countries reported to UNEP–
WCMC that a total of 91 live Philippine
cockatoos were imported (https://
www.unep-wcmc-apps.org/citestrade)
into their countries, at an average of 10
birds per year. The majority of these (78)
originated from the Philippines; 77 of
these live shipments were reported to be
of captive-origin, and only one was
indicated to be of wild origin.
Additionally, in 2009, the UNEP–
WCMC CITES Trade Database indicated
that only two live birds were exported
from the Philippines. As the Philippine
cockatoo is listed as an Appendix-I
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species under CITES, legal commercial
international trade is very limited.
Based on the low numbers of live, wild
Philippine cockatoos in international
trade since 2000, and because the trade
was in parts and products from wild
specimens, rather than live birds, we
believe that international trade
controlled via valid CITES permits is
not a threat to the species.
Summary of Factor B
In summary, cockatoos are popular
pets, and poaching for the pet trade still
occurs, particularly on Pandanan Island
(Widmann et al. 2010c, p. 13). Although
we do not find that international trade
controlled via valid CITES permits is a
threat to the species, we do find that
poaching for the pet trade in the
Philippines continues to be a threat to
the Philippine cockatoo.
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Factor C. Disease or Predation
In the information provided and the
literature reviewed, there were
suggestions that diseases, particularly a
fungal disease, in the wild may be a
threat to this species. It was suggested
that Viscertropic Velogenic Newcastle
Disease, Psittacine Beak and Feather
Disease (PBFD), or the psittacid herpes
virus (PsHV–1 or PsHV–2) were
indicated as possible threats and may
have been introduced into the wild
population, possibly by the release of
captive birds (Lambert 1994 in BLI
2001, p. 1686; BLI 2010b, p. 1).
Cockatoo species are widely distributed
throughout Australasia, and some avian
species have developed resistance to
some diseases (Commonwealth of
Australia 2006, p. 1). These diseases
affect each cockatoo species differently.
Psittacine Beak and Feather Disease
Psittacine Beak and Feather Disease
(PBFD) is a viral disease that originated
in Australia and affects both wild and
captive birds, causing chronic infections
resulting in either feather loss or
deformities of beak and feathers
(Cameron 2007, p. 82). PBFD causes
immunodeficiency and affects organs
such as the feathers, liver, and brain.
Suppression of the immune system can
result in secondary infections due to
other viruses, bacteria, or fungi. The
disease can occur without obvious signs
(de Kloet and de Kloet 2004, p. 2394).
Birds usually become infected in the
nest by ingesting or inhaling viral
particles. Infected birds develop
immunity, die within a couple of weeks,
or become chronically infected. No
vaccine exists to immunize populations
(Cameron 2007, p. 82). While some
cockatoo species are susceptible to this
virus, there is no indication that PBFD
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adversely affects the Philippine
cockatoo at the population level in the
wild.
Proventricular Dilatation Disease
Another serious disease that has been
reported to infect some cockatoos is
Proventricular Dilatation Disease (PDD).
PDD is a fatal disease that may pose a
serious threat to domesticated and wild
parrots worldwide, particularly those
with very small populations (Waugh
1996, p. 112; Kistler et al. 2008, p. 1).
This contagious disease causes damage
to the nerves of the upper digestive
tract, so that food digestion and
absorption are negatively affected. The
disease has a 100 percent mortality rate
in affected birds, although the exact
manner of transmission between birds is
unclear. Although this is a particularly
virulent virus that affects cockatoos in
general, we are unaware of any reports
that this disease occurs in Philippine
cockatoos in the wild.
Avian Influenza
Wild birds, especially waterfowl and
shorebirds, are natural reservoirs of
avian influenza (also known as ‘‘bird
flu’’). Most strains of the avian influenza
virus have low pathogenicity and cause
few clinical signs in infected birds.
Pathogenicity is the ability of a
pathogen to produce an infectious
disease in an organism. However,
strains can mutate into highly
pathogenic forms, which is what
happened in 1997, when the highly
pathogenic avian influenza virus (called
H5N1) first appeared in Hong Kong
(USDA et al. 2006, pp. 1–2). H5N1 is
mainly propagated by commercial
poultry living in close quarters with
humans. The effect on migratory birds is
less clear (Metz 2006a, p. 24). Scientists
increasingly believe that at least some
migratory waterfowl carry H5N1,
sometimes over long distances, and
introduce the virus to poultry flocks
(World Health Organization 2006, p. 2).
H5N1 has infected and caused death in
domestic poultry, people, and some
wild birds in Asia, Europe, and Africa.
About half of humans infected die from
the disease (Service 2006, p. 1). A parrot
held in quarantine in the United
Kingdom was incorrectly diagnosed
with H5N1 is 2005. The original
identification of H5N1 was made from
a pool of tissues derived from a Pionus
parrot (from Surinam) and another avian
species called a mesia (Leiothrix spp.)
from Taiwan. The Department for
Environment, Food and Rural Affairs,
United Kingdom (DEFRA) stated that it
was not possible to say whether the
virus isolated came from the parrot
tissue or the mesia tissue or both
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(DEFRA 2005, p. 34). However, they
concluded that the source was more
likely the sample from the mesia
(DEFRA 2005, p. 34). Later, it was
determined that the samples had been
mixed, and the parrot did not have the
disease (Gauthier-Clerk et al. 2007, p.
208). Although in the Philippines, 339
smuggled parrots were euthanized
following confiscation even though
none were confirmed to have the virus
(Metz 2006a, pp. 24–25), we are
unaware of any reports that this disease
occurs in Philippine cockatoos in the
wild.
Aspergillosis
Aspergillosis is an infection or
allergic response to the Aspergillus
fungus. A literature review found that
cases of Aspergillosis were being
reported in captive-held, wild-origin
Philippine cockatoos in the Philippines
at the U.S. Air Force Base, Clark Field,
Angeles City (Burr 1981, p. 21). In all
known cases according to the report,
stress, such as enclosure in a small bird
cage, was indicated to be a factor prior
to death. Observations indicated that
free-flying birds in aviaries showed no
signs of stress, and there were no deaths
recorded in these birds. Natural
incidence of Aspergillosis in the wild
occurs in the Philippine cockatoo;
however, it appears to be more
prevalent in captive birds. During one
survey, Aspergillus spores were found
below nest holes in Palawan (Tabaranza
1992; Lambert 1994 in BLI 2001, p.
1686). The Philippine cockatoo is likely
a latent carrier of Aspergillus (Burr
1981, p. 23); however, based on a review
of the best available information, there
is no recent information indicating that
this disease negatively affects this
species at the population level in the
wild (Widmann et al. 2010c, p. 45).
Lice and Mites
Ectoparasitism by lice and mites was
documented as the possible cause of
death in some chick mortalities on Rasa
Island (Widmann et al. 2001, p. 146;
Widmann et al. 2010a, pp. 6, 38). Mites,
a form of arachnid, were found in some
monitored nests where chicks had died.
Although nests are being routinely
monitored on Rasa Island, mites are not
commonly found in these nests. Mites
have evolved in a symbiotic relationship
with avian species. Not all bird-mite
relationships are parasitic; some might
be benign or beneficial (Proctor and
Owens 2000, pp. 358, 362). Many mites
are nonparasitic scavengers and use the
nest or bird feathers as habitat. Despite
the presence of mites found in nests
where chick mortalities were observed,
there is no evidence that mites
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1987, the Government of the Philippines
established the Protected Areas and
Wildlife Bureau (PAWB) through the
DENR, under Executive Order 192. Its
responsibilities are in part to manage
and protect the country’s protected
areas. In 1992, the National Integrated
Protected Areas System Act (NIPAS Act
of 1992) was adopted in order to protect
and maintain the Philippines’ biological
diversity. In 1994, the PAWB signed a
memorandum of agreement (MOA)
regarding the conservation of this
species (Boussekey 2000, p. 138,
Philippines DENR 2009, pp. 1–2). This
MOA has been implemented by a
Summary of Factor C
nongovernmental organization, the
When conducting a status review, we
Katala Foundation, since 2006 through
evaluate the magnitude of each factor
the PCCP. Under this MOA, an intensive
that may be affecting a species, and, in
species conservation program has been
this case, we did not find evidence that
underway to conserve this species and
any disease or predator rises to the level its habitat. The PCCP accomplishes its
of a threat that is affecting this species
mission through intense local
in the wild. After conducting a literature management of the species. Some
search (Johnson et al. 1986, pp. 813–
aspects of the conservation program are
815; Latimer et al. 1992, pp. 165–168; de to educate local communities about the
Kloet 2004, pp. 2393–2412;
benefits of conserving endemic wildlife,
Tomaszewski et al. 2006, pp. 536–544),
protect and restore nesting sites and
we found no indication that disease or
habitat, conduct research, and
predation is a threat to the Philippine
reintroduce the species into the wild
cockatoo in the wild. Although
(Widmann et al. 2010, p. 22).
individual Philippine cockatoos may be
As a protected species (DENR 2010b,
subject to occasional infections or
p. 2), under the Republic Act No. 9147,
certain activities such as capture and
predation, there is no evidence that
either of these is occurring at a level that trade of live wildlife are prohibited.
Republic Act No. 9147 provides for
may affect the status of the species as a
whole to the extent that it is considered fines and penalties for prohibited acts.
However, within the Philippines, the
a threat to the species. Therefore, we
laws are generally ignored and only
find that the Philippine cockatoo is not
poorly enforced (Galang 2004, pp. 12–
threatened due to disease or predation.
17; Laurance 2007, p. 1544; Rose 2008,
Factor D. The Inadequacy of Existing
p. 232).
Regulatory Mechanisms
Additional protections exist under the
Several regulatory mechanisms are in Philippines’ Executive Order No. 247,
place at the national and local levels
which protects the rights of local people
that serve to conserve this species and
with respect to the use of natural
resources (https://www.elaw.gov,
the habitat on which it depends;
accessed January 4, 2011). This
however, the mechanisms are
Executive Order mandates that
ineffective at adequately protecting the
Philippine cockatoo. We find that CITES prospecting of biological and genetic
resources shall be allowed within the
effectively protects the species from
ancestral lands and domains of
unsustainable legal international trade.
indigenous cultural communities only
Factors hampering the regulatory
with the prior informed consent of such
mechanisms in place include
communities. Involving local tribal
remoteness of protected areas, poverty
communities adds an additional
that causes locals to unsustainably use
this species’ habitat or to poach, and the conservation measure. For example, the
Batak tribe (Boussekey 2000, p. 144) in
lack of resources to adequately enforce
northern Palawan has shown interest in
laws and regulations (Galang 2004, p.
participating in wildlife conservation.
17; Laurance 2007, p. 1544; Palawan
The protection of endemic natural
Council for Sustainable Development
resources has been demonstrated to
(PCSD) 2007, p. 1–3). These are
benefit native tribes and local
discussed below.
communities near sites that have unique
Domestic Regulatory Mechanisms
features (Widmann et al. 2010b, p. 36).
In the late 1980s and early 1990s,
Locals may be recruited as wardens, or
efforts were already underway to protect these areas can be developed for
ecotourism. However, in this case, it is
the Philippine cockatoo (Boussekey
likely that only around 300 to 400
2000, p. 140; Galang 2004, p. 17). In
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significantly contribute to chick
mortalities. We conducted a search of
available information, and there is no
other information indicating that lice
and mites significantly affect the
species, although mites may occur more
frequently during dryer seasons
(Widmann et al. 2010a, p. 38; Widmann
et al. 2010c, pp. 39, 45). It was suggested
that unusually high temperature, rather
than mites, may have contributed to the
lack of nest success in 2001 (Widmann
et al. 2010c, p. 45); however, the actual
reasons for nest failures (mortalities) are
unclear.
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members of the Batak tribe survive
today, so the effectiveness in the long
term is unclear (Cultural Survival 2010
and Survival International 2010, both
accessed November 18, 2010). These
regulatory mechanisms could have a
positive effect on the species, but
currently it is unclear whether
Executive Order No. 247 is benign or
actually constructive.
As discussed under Factor B, the
Philippine cockatoo is monitored and
managed in some, but not all, areas
where it exists. Some areas are
designated as protected specifically for
the Philippine cockatoo and wardens
are employed (Widmann et al. 2010a,
pp. 18–22; and refer to Conservation
Status for the Philippine Cockatoo
section above). An increase in the
population is occurring in some areas
where it is protected, such as on Rasa
Island, but in other areas where
protections are not robust, the
population is declining (Widmann et al.
2010a, p. 32). Although there are five
areas designated as being ‘‘protected,’’
under Philippine law, the levels of
protection vary. In 2006, Rasa Island,
the area containing the densest
population of the Philippine cockatoo,
was declared a wildlife sanctuary by
President Arroyo (Widmann 2006, p. 1).
The protected area consists of 1,983 ha
(4,900 ac). While this area is fairly well
protected and monitored, effective
reserve management here is hampered
by a shortage of staff, technical
expertise, and financial support
(Widmann 2010, pers. comm.). In
addition, the remoteness of protected
areas makes enforcement of activities
such as poaching and illegal logging
difficult. Overall, the management of
protected areas is insufficient. For
example, in 2010, despite management
of the species, 15 hatchlings died and 17
eggs did not hatch on Rasa Island during
an extreme weather event (refer to
Factor E discussion) (Widmann et al.
2010a, p. 38). Even in areas such as
Narra that are monitored by wardens,
poaching occurs (Widmann et al. 2010a,
p. 6). The protections in place for this
species are ultimately ineffective at
reducing the threats to this species. This
species resides in other areas that are
not protected; and habitat destruction
(see Factor A discussion above) and
poaching for the pet trade (see Factor B
discussion above) still occur even in
protected zones.
The Philippine cockatoo is carefully
monitored and managed in some, but
not all, areas where it exists. The
species exists in five protected areas: (1)
Rasa Island Wildlife Sanctuary (Narra,
Palawan), (2) Puerto Princesa
Subterranean River National Park
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(Palawan), (3) Omoi and Manambaling
Cockatoo Reserves in Dumaran
(Dumaran, Palawan), (4) Mt.
Mantalingahan Protected Landscape
(CMRPA) in Rizal, Palawan, and (5)
Samar Island Natural Park. Each
protected area in Palawan has its own
unique protections in place and
legislation to protect the species and its
habitat (Widmann and Widmann 2010,
pers. comm.).
Although there are five areas
designated as being ‘‘protected,’’ the
levels of protection vary. An increase in
the population is occurring in some
areas, but in other areas where
protections are not as robust, the
population is declining, in part due to
poaching. The PCCP, the Philippine
government, and individuals concerned
with the conservation of this species
have actively worked to protect the
Philippine cockatoo since 1998. The
PCCP is a nonprofit organization
dedicated to the conservation of wild
Philippine cockatoos. Its goals are to
teach the principles and value of
conservation, work to rehabilitate
Philippine cockatoos back into the wild,
and conduct scientific research. As of
2000, the local communities that live
within the range of this species have
been aware that it is illegal to capture
or trade this species (Boussekey 2000, p.
143).
At most sites where a viable
population appears to exist, PCCP is
actively managing this species to try to
increase the populations. For example,
artificial nest boxes for the Philippine
cockatoo were installed on Rasa Island
and the mainland (Palawan) (Widmann
and Widmann 2008, p. 27). Recovery of
the Philippine cockatoo on Rasa Island
has been fairly effective, where nestguarding by local people has virtually
stopped poaching (Boussekey, pers.
comm. in Cahill et al. 2006, p. 166).
Breeding success on Rasa Island has
been high (averaging 2.6 hatchlings per
nest in 2002, for example). On this
island, a population of approximately
20 birds increased four-fold between
1998 and 2003 (Boussekey, pers. comm.
in Cahill et al. 2006, p. 166; Widmann
et al. 2010). In Patnanungan, Polillo
Islands, the first artificial nest box for
the Philippine cockatoo was installed in
November 2009 (Widmann et al. 2010,
p. 13), and reforestation efforts are
occurring. These activities are
somewhat effective but slow because the
protection efforts are not able to
completely combat the negative factors
such as poaching and selective logging
that affect this species in many cases.
Recent efforts are being focused on
Pandanan Island (south of Palawan
Island), which has excellent habitat for
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this species, and has recently been
targeted by PCCP for protection of the
Philippine cockatoo. A grant under the
U.S. Fish and Wildlife Service’s
Wildlife Without Borders, Critically
Endangered Species Conservation Fund,
for the Pandanan project was approved
in September 2009 (Widmann et al.
2010, p. 5). This island has the potential
for the species to make a good recovery
because there is excellent forest cover
due in part to the protections provided
by the Jewelmer Corporation. This
company holds a marine mining
concession in the area of Pandanan. Due
to this concession, no human
inhabitants are legally allowed on
Pandanan Island. In January 2010, PCCP
obtained formal permission from the
Palawan Council for Sustainable
Development (PCSD) to conduct
conservation efforts on the island
(Widmann et al. 2010b, p. 5). Poaching
still needs to be abated, but PCCP has
been working to establish a local
warden program (Widmann et al. 2010a,
p. 50) on the island to address this
issue. Security has recently improved in
the area where a viable cockatoo
population has been confirmed, but the
species is still threatened by poaching
(Widmann et al. 2010a, p. 15). The
PCCP indicates that it is likely that with
the warden program in place, they can
eliminate or reduce poaching.
As resources allow, other protections
and conservation actions are in place for
this species. On Dumaran, Rizal, and
Patnanungan Islands, Philippine
cockatoo activity is observed through
wardens monitoring, and patrols occur
at protected areas and roost sites.
Monitoring of the population trend on
Rasa and Dumaran Islands is done
through counting individuals at
traditional roost sites. Due to both a lack
of funding and logistics, not all
Philippine cockatoo sites are actively
monitored and managed. This is
primarily because it is more efficient to
focus resources in the Palawan Islands
Region where the Philippine cockatoo
has a viable population.
In summary, while laws to protect
this species are in place, enforcement
often is severely lacking or difficult,
given the many islands that make up the
Philippines and considering that illegal
activities in many cases remain socially
acceptable at the local level. Illegal
logging is considered a leading cause of
forest degradation in the Philippines
(Galang 2004, pp. 12–17; Laurance 2007,
p. 1544; Rose 2008, p. 232). Laws and
regulations are frequently ignored,
which further reduces the effectiveness
of regulatory mechanisms (Galang 2004,
pp. 12–17), and this species continues
to suffer a decline in population
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numbers. Therefore, we find that,
although the Philippines has a good
legal framework to manage wildlife and
their habitats, actual implementation of
its laws and regulatory mechanisms is
inadequate to reduce the threats to the
Philippine cockatoo.
CITES
The evaluation of the effectiveness of
CITES as a regulatory mechanism is
cross-referenced under Factor B, as
CITES regulates international trade of
wildlife. The Treaty requires CITES
Parties to have in place adequate
legislation for its implementation.
Through Resolution Conf. 8.4 (Rev.
CoP15), the Parties to CITES adopted a
process, termed the National Legislation
Project, to evaluate whether Parties have
adequate domestic legislation to
successfully implement the Treaty. In
reviewing a country’s national
legislation, the CITES Secretariat
evaluates factors such as whether a
Party’s domestic laws designate the
responsible Scientific and Management
Authorities, prohibit trade contrary to
the requirements of the Convention,
have penalty provisions in place for
illegal trade, and provide for seizure of
specimens that are illegally traded or
possessed. The Philippines has enacted
domestic legislation to implement
CITES. That legislation is currently
being reviewed by the Secretariat to
determine if it meets all the necessary
criteria (CITES 2011a).
With respect to international trade,
we found CITES to be an adequate
existing regulatory mechanism for this
species (see our analysis under Factor B
for legal trade). See our analysis for the
crimson shining parrot for additional
discussion on how we made this
determination. As discussed under
Factor B, very few Philippine cockatoos
have been legally exported from the
Philippines since 2000. One operation
in the Philippines is registered to export
captive-bred specimens of this species
for commercial purposes and appears to
be adequately monitored and regulated.
Based on the information available,
CITES and the Government of the
Philippines have effectively controlled
legal international trade of this species.
Summary of Factor D
In summary, we find that the
Government of the Philippines appears
to have controlled legal international
trade through CITES (see discussion
under Factor B above). With respect to
trade, the existing domestic regulatory
mechanisms within the Philippines, as
implemented, are inadequate to reduce
or remove the current threats to the
Philippine cockatoo in the wild based
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on reports of poaching. As discussed
under Factor B above, uncontrolled
illegal domestic trade continues to
adversely impact the Philippine
cockatoo. Measures in place via the
MOA and the PCCP provide some
protection to the Philippine cockatoo.
Through the MOA, this species is
carefully monitored and managed in key
areas where the species has a good
chance of recovery, particularly in the
Rasa Island Wildlife Sanctuary (Narra,
Palawan). Despite efforts, management
of protected areas encompassing this
species’ habitat is hindered due to the
remoteness of protected areas, staff
shortages, lack of technical expertise,
and lack of funding; this is
acknowledged by the local NGO
(Widmann et al. 2010a).
Even with government controls,
poaching of cockatoos is relatively
common in areas that are not protected.
In addition, laws and regulations are
frequently ignored, in part due to the
difficulty in monitoring and
enforcement throughout the multitude
of islands in the Philippines. As
discussed under Factors A and B above,
we found that poaching, logging, and
conversion of forests to agriculture and
plantations are threats to the Philippine
cockatoo. Despite regulatory
mechanisms in place, illegal logging
continues to be a leading cause of forest
degradation in the Philippines
(Laurance 2007, pp. 1544–1555; Rose
2008, p. 231). There is no information
available to suggest these threats will
change in the foreseeable future;
therefore, we find that the existing
regulatory mechanisms, as
implemented, are inadequate to reduce
or remove the current threats to the
Philippine cockatoo.
Factor E. Other Natural or Manmade
Factors Affecting the Continued
Existence of the Species
Various other factors have been cited
as being potential threats to this species.
In addition to poaching, trapping, and
deforestation (Boussekey 2000, p. 138)
(refer to the discussions under Factors A
and B, above), hunting (to protect
crops), harassment by bees, and nest
flooding have been observed to affect
this species (Widmann et al. 2001, pp.
139–140; Widmann et al. 2007a, pp. 76–
77, 79). Because this species has been
viewed as an agricultural pest, it was
often killed if it was thought to be
consuming crops (Widmann and
Widmann 2008, p. 23). However, there
is no indication that this practice still
occurs. Nest flooding during a
thunderstorm was observed to affect
clutch survival during the 2000–2001
breeding season on Rasa Island
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(Widmann et al. 2001, pp. 139–140).
Although nest flooding may occur
occasionally, the PCCP indicates that it
is not a common occurrence, and we do
not consider this to be a threat to the
species.
Bees have been observed to attack
cockatoos. In 2005, on Patnanungan
Island, bees were documented attacking
Philippine cockatoos (Widmann et al.
2007a, pp. 76–77, 79). These cockatoos
were unable to nest due to the close
proximity of a beehive. The extent of
competition with bees for nesting sites
is not clear. Philippine cockatoos have
been monitored for many years, and this
is the only known report of nest site
competition with bees. Therefore, it
does not appear to be a significant factor
affecting this species.
Other factors affecting the species
include food shortages due to drought
and the lack of suitable nesting cavities
(Widmann and Widmann 2008, p. 25).
The lack of suitable nesting sites in
general is addressed under Factor A. In
2005, this species suffered from
starvation on Rasa Island due to a food
˜
shortage during an El Nino drought
year. However, several fledglings were
rescued. Of these, 10 developed
normally and were subsequently
released (Widmann and Widmann 2008,
p. 25). Additional factors affecting the
species include the lack of suitable
nesting cavities (in large, decayed trees)
and possibly the lack of adequate food
sources (Widmann et al. 2010a, p. 6).
Because this species has specific
nutrition and habitat requirements, it
was suggested that Rasa Island may be
at carrying capacity due to limited
habitat and food availability (Widmann
and Widmann 2008, p. 25). Because
Rasa Island is very small, with only 1.75
km2 (0.6 mi2) of the island being coastal
and mangrove forest, its suitable habitat
is limited. As of 2009, Rasa Island had
64 nest trees, and as of 2010, there were
280 individual Philippine cockatoos on
this island. There was a second
starvation event in 2010 (Widmann et
al. 2010a, p. 6). At this time, we are
unable to determine if limited food
availability on this island and starvation
due to drought are threats; however, the
Rasa Island population is carefully
monitored by the PCCP, and they
intervene and manage the species if
needed. Although in some years limited
food availability may be a concern, we
do not find that this factor rises to the
level of a threat to the species. Further,
the lack of suitable nesting cavities is
being monitored and addressed by the
PCCP. At this time, there is no evidence
that bees or nest flooding are threats to
the species.
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Small and Declining Population
The Philippine cockatoo has a
contracted geographic range and a
small, rapidly declining population,
primarily due to poaching. There are
between 450 and 1,245 individuals left
remaining in the wild, distributed on
eight islands (BLI 2011, p. 1). In many
cases, the Philippine cockatoo is now
geographically isolated from other
populations. Additionally, because it is
an island species that generally mates
for life and is long-lived, it is extremely
vulnerable to localized extinctions.
Species with small populations are
significantly influenced by individual
´
birth and death rates (Gilpin and Soule
1986, p. 27), immigration and
emigration rates, and changes in
population sex ratios. Natural variation
in survival and reproductive success of
individuals and chance disequilibrium
of sex ratios may act in concert to
negatively affect reproduction (Gilpin
´
and Soule 1986, p. 27).
Prior to the 1980s, the Philippine
cockatoo was common throughout the
Philippines (Boussekey 2000, p. 138;
Cameron 2007, p. 34). Its existing
populations are extremely localized due
to habitat loss and its preference for
lowland primary and secondary forest,
which is also preferred human habitat.
PCCP suggests that a rapid population
reduction may occur in the future based
on low recruitment in recent years,
especially for unprotected populations
(Widmann 2011a, pers. comm.). In the
Rizal (South Palawan) area, which was
protected only recently, there are no
indications of recovery. Only one
breeding pair exists outside of this
cockatoo reserve, and this area was
poached within the past 2 years.
Breeding here did not occur in the
2009–2010 season. Since all nests have
been systematically poached in this area
over many years, extinction of this
population might occur suddenly due to
lack of reproduction success. This is
partly a consequence of mating
characteristics of this species: It is longlived and generally mates for life. At
least two birds persist inside the
protected area, but they have not bred
in the past 4 years (Widmann 2011a,
pers. comm.).
Small, isolated populations of wildlife
species such as the Philippine cockatoo
that have gone through a reduction in
population numbers can be susceptible
to demographic and genetic problems
(Shaffer 1981, pp. 130–134). Factors that
could affect their susceptibility include:
Natural variation in survival and
reproductive success of individuals;
changes in gene frequencies due to
genetic drift; diminished genetic
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diversity and associated effects due to
inbreeding (i.e., inbreeding depression);
dispersal of just a few individuals; a few
clutch failures; a skewed sex ratio in
recruited offspring over just 1 or a few
years; and chance mortality of just a few
reproductive-age individuals. These
small, rapidly declining populations are
also susceptible to natural levels of
environmental variability and related
‘‘catastrophic’’ events (e.g., severe
storms, extreme cold spells, wildfire),
which we refer to as environmental
stochasticity (Dunham et al. 1999, p. 9;
Mangel and Tier 1994, p. 612; Young
1994, pp. 410–412).
Threats to species typically operate
synergistically. Initial effects of one
threat factor can later exacerbate the
effects of other threat factors (Gilpin and
´
Soule 1986, pp. 25–26). Any further
fragmentation of populations may likely
result in the further removal or dispersal
of individuals. The lack of a sufficient
number of individuals in a local area or
a decline in their individual or
collective fitness may also cause a
decline in the population size, despite
the presence of suitable habitat patches.
The combined effects of habitat loss
and fragmentation (Factor A) and threats
associated with small, declining, and
isolated populations (Factor E) on a
species’ population are referred to as
patch dynamics. Patch dynamics can
have profound effects on fragmented
populations and can potentially reduce
a species’ effective population by orders
´
of magnitude (Gilpin and Soule 1986, p.
31). For example, an increase in habitat
fragmentation can separate populations
to the point where individuals can no
longer disperse and breed among habitat
patches, causing a shift in the
demographic characteristics of a
population and a reduction in genetic
´
fitness (Gilpin and Soule 1986, p. 31).
Furthermore, as a species’ status
continues to decline, often as a result of
deterministic forces such as habitat loss
or overutilization, it becomes
increasingly vulnerable to a broad array
of other forces. Despite the mitigation
and conservation measures in place, if
this trend continues, its ultimate
extinction due to one or more stochastic
events becomes more likely. Given the
species’ dispersed nature, the fact that it
is a long-lived species that generally
mates for life, and that the largest
population is approximately 280
individuals, we find that this factor
threatens the continued existence of this
species. Based on the best scientific and
commercial information available, we
conclude that based on its small, rapidly
declining population, the Philippine
cockatoo is at risk of extinction,
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resources, its remote island habitat, and
by the nature of this species’ life-history
characteristics (such as the tendency to
Summary of Factor E
mate for life and they do not reproduce
Several other factors were identified
until a late age). Efforts to improve the
as affecting the success of this species
habitat of this species (e.g.,
such as harassment by bees, nest
reforestation, building of nest boxes) are
flooding, and starvation. These factors
continuing and may improve its habitat
are a normal occurrence in the ecology
and population numbers. In Polillo,
of this species, and we do not find that
Dumaran, and Rasa, the species may
these factors significantly affect this
slowly increase in population numbers,
species such that they rise to the level
but in other areas, the species’
of a threat. However, we find that its
population continues to decline. The
small, rapidly declining population,
best population estimates of this species
when combined with the other threats
were compiled in the early 1990s, at
of habitat loss and poaching, is a threat
which time the population was
to the species throughout its range.
estimated to be between 1,000 and 4,000
individuals (Snyder et al. 2000). Experts
Finding for the Philippine Cockatoo
believe the population is now between
We considered the five factors in
450 and 1,245 individuals, and most
assessing whether the Philippine
populations are fairly well monitored
cockatoo is endangered or threatened
(Widmann et al. 2010); however,
throughout all of its range. We
poaching for the domestic pet trade
examined the best scientific and
continues to be a threat to the species.
commercial information available
It is unlikely that this species’ rapidly
regarding the past, present, and future
declining and small population can
threats faced by the Philippine
withstand this level of poaching.
cockatoo. We reviewed the petition,
Therefore, we find overutilization for
information available in our files, and
commercial, recreational, scientific, or
other available published and
educational purposes (Factor B) is a
unpublished information, and we
threat to the Philippine cockatoo.
consulted with recognized Philippine
We found no evidence that diseases
cockatoo experts and local and
significantly affect the wild Philippine
international NGOs.
cockatoo population. Other avian
The primary factors affecting the
species, particularly cockatoo species,
Philippine cockatoo include habitat loss are susceptible to avian diseases, but
and habitat degradation and poaching
there was no evidence that disease
for the pet trade. Habitat loss associated occurs in the wild to an extent that it
with logging, an expanding human
is a threat to this species. Predation was
population and associated development, not found to affect Philippine cockatoo
conversion of lowland forests to
populations. Based on the best available
agriculture are the some of the greatest
information, we conclude that disease
threats to the continued survival of this
and predation (Factor C) are not threats
species (BLI 2001, p. 1685; Galang 2004, to the species.
pp. 5–22; Posa et al. 2008, pp. 231–236;
The Philippine cockatoo is classified
Widmann and Widmann 2008, p. 23;
as a protected species by the Philippine
Widmann et al. 2010, p. 14). Habitat loss government. The current range of the
due to the above activities continues to
Philippine cockatoo is much smaller
occur; this species’ population is
than its historical range (BLI 2010b).
declining range wide as a result.
However, as a result of conservation
Based on the best available
efforts by the various entities working to
information, poaching is still occurring, ensure long-term conservation of the
despite education and public awareness Philippine cockatoo, its range may
campaigns and protections in place at
slowly increase, but current efforts are
the national level (Widmann et al.
indicating mixed levels of success.
2010c., p. 13). Awareness campaigns
Despite conservation efforts of various
have been conducted on Mindanao,
entities, we have determined that
Palawan, and Polillo Islands (Widmann existing regulatory mechanisms
2010, pers. comm.). On Dumaran Island, continue to be inadequate because
the Katala Pride Campaign has focused
habitat loss and poaching are still
on raising awareness among students
occurring (Factor D). In summary, we
and farmers. Trilingual conservation
conclude that inadequate regulatory
posters have been distributed
mechanisms are a threat to the
throughout the Philippines, and in
Philippine cockatoo.
This species has a small and rapidly
1992, a captive-breeding program was
initiated. This species is being intensely declining population. This species no
longer exists in many of the areas where
managed in some areas, but the
it occurred historically. This species is
management and protection of the
in competition with humans for habitat;
species is hampered by the lack of
particularly when combined with the
other threats.
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development and related infrastructure
take the place of its habitat. Within its
current range, where there are few
viable populations remaining, the PCCP
is managing the species to the best of its
ability; however, the PCCP
acknowledges that this species still
faces a rapid population reduction in
the future based on low recruitment in
recent years, especially for unprotected
populations. When combined with other
threats, and when considering its
fragmented population, we conclude
that its small, rapidly declining
population is a threat to the species
(Factor E). Due to this species’
extremely small, declining, and
fragmented population and due to the
existing threats (Factors A, B, D, and E),
it is currently in danger of extinction.
Despite the conservation measures in
place, this species faces severe threats,
and the population trend for this species
continues to decline. Based on our
review of the best available scientific
and commercial information pertaining
to the five factors, we find that the
Philippine cockatoo is in danger of
extinction (endangered) throughout all
of its range. We do not find that the
effects of current threats acting on the
species are likely to be sufficiently
ameliorated in the foreseeable future.
These threats are consistent throughout
its range. Therefore, we find that listing
the Philippine cockatoo as endangered
is warranted throughout its range, and
we propose to list the Philippine
cockatoo as endangered under the ESA.
Species Information
C. White cockatoo (Cacatua alba)
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Taxonomy and Species Description
The white cockatoo is also known as
the umbrella cockatoo. ITIS, CITES, and
BirdLife International recognize the
species as Cacatua alba (BLI 2010).
Therefore, we accept the species as C.
alba. The white cockatoo is completely
white except for the underside of its
wings and tail, which are pale yellow.
It has a long, backward-curving white
crest on its head. Its bill is grey-black,
and it has a white bare eye-ring. The
bird has either yellowish-white or
slightly grey-blue legs.
Population Estimates
Population estimates for the white
cockatoo vary, in part due to the
remoteness of the islands where this
species exists. Population estimates
prior to 2000 indicated that the Lalobata
protected area on Halmahera Island
contained between 28,500 and 42,900
white cockatoos (MacKinnon et al.
1995; Snyder et al. 2000, p. 67),
although they did not survey lowland
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forest, which they thought may contain
more white cockatoos. The white
cockatoo was described as being
common in the early 1990s. Survey
work carried out in 1991 and 1992
suggested a population estimate of
between 49,765 and 212,430 birds
(Lambert 1993a; Snyder et al. 2000, p.
671; BLI 2010c, p. 1). BLI reported that
the total population is between 43,000
and 183,000 mature individuals;
however, this population estimate is
based on 1993 data (Lambert 1993 in
BLI 2010). Burung Indonesia estimated
that based on surveys conducted in
2008 and 2009, there are between 8,629
and 48,393 white cockatoos remaining
in the wild (Burung Indonesia 2010,
pers. comm.) on Halmahera Island.
Distribution, Habitat, Biology
While the exact life span is unknown,
reports of the white cockatoo’s lifespan
vary between 20 and 50 years in
captivity (Lambert 1993, p. 147; Jordan
2010, pers. comm.). Wild-caught birds
have been reported not to breed until
they are 6 years old. The highest
productive period for the white
cockatoo is between 6 and 20 years
(Jordan 2010, pers. comm.). However,
some pairs have been recorded to breed
well into their thirties, and a few
exceptions have been reported with
pairs or individuals that have
reproduced into their forties or fifties
(Lambert 1993, p. 147). Clutch-size of
white cockatoos in captivity is reported
to be 2 to 3 eggs per season, and
incubation takes 25 to 28 days; nestlings
reside in the nest approximately 90 days
before fledging (Cameron 2007, p. 140).
Both parents share responsibility for
raising chicks, and the species is
thought to be monogamous for life.
The white cockatoo is endemic to a
few islands in North Maluku, Indonesia,
and it inhabits primary, logged, and
secondary forests possibly up to 900 m
(2,953 ft) (IUCN 2008h). It is not thought
to inhabit forests on ultra basic rock
(BLI 2001, p. 1674). This species is
believed to occur in three protected
areas: Gunung Sibela Strict Nature
Reserve on Bacan Island (although this
site is threatened by agricultural
encroachment and gold prospecting),
and Aketajawe Nature Reserve and the
Lalobata Protected Forest (ALNP), both
on Halmahera Island (BLI 2010).
Historically, its range has been the
islands of Halmahera, Bacan, Ternate,
Tidore, Kasiruta and Mandiole in North
Maluku (Snyder et al. 2000, p. 67; BLI
2010c). ALNP consists of approximately
167,300 hectares (413,407 acres) of
primary and secondary forest. This total
area represents 7.5 percent of
Halmahera Island (Burung International
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2010, pers. comm). Now the white
cockatoo is thought to only inhabit
Halmahera and Bacan Islands (Wildlife
Conservation Society (WCS) 2010, pers.
comm.). The Bacan Island group, also
known as Palau Batjan, is about 16 km
(10 mi) southwest of Halmahera Island.
Little is known about the status of the
species other than on Halmahera Island.
Due to the lack of information, this
status review only addresses its status
on Halmahera Island unless otherwise
specified.
The Maluku Islands are also known as
the Moluccas or the Spice Islands, and
they are between Sulawesi and New
Guinea, below the Philippines. The
white cockatoo, like most cockatoos, is
a resident (nonmigratory) species, but
cockatoos are strong fliers, and they will
likely travel to nearby islands in search
of habitat or food, if it is not readily
available. The highest densities of this
species occur in primary (old-growth)
forest (BLI 2009; Burung International
2011), but the species seems to tolerate
some habitat modification. White
cockatoos inhabit mangroves,
plantations (including coconut), and
agricultural land (BLI 2010c). This
species requires large trees for nesting
and roosting, is often observed feeding
in large flocks, and eats seeds, fruit, and
insects. Their preferred nesting holes
were observed to be situated at points
where large branches had broken off the
main trunk (Lambert 1993, p. 146).
Halmahera (also known as Jilolo or
Gilolo Island) is the largest island in the
North Maluku province, and is 17,780
km2 (6,865 mi2) in size. Its annual
precipitation is 2,000 to 3,000 mm (79
to 118 in). Halmahera, a four-pronged
island, is considered to be a biodiversity
hotspot (Myers et al. 2000 in Setiadi et
al. 2010, p. 560). North Maluku
province consists of eight provincial
districts: North Halmahera, West
Halmahera, East Halmahera, Central
Halmahera, South Halmahera, Ternate
Municipality, Tidore City and Islands,
and Sula Islands. In North Halmahera,
the number of districts on the island has
recently increased to 22, and the
number of villages has increased from
174 to 260. The human population in
Maluku Province in 2010 was estimated
to be 1,531,402 (Badan Pusat Statistik
Provinsi Maluku 2010). AketajaweLolobata National Park, established in
2004, was the first national park
established in North Maluku
(Keputusan Menteri Kehutanan No.
SK.397/MenHut-II/2004), and is
described as being one of the most
pristine and unvisited areas in all of
Indonesia.
Bacan, a smaller island to the
southwest of Halmahera, is also
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inhabited by the white cockatoo,
although very little is known about the
status of the species here. This remote,
sparsely populated island is not well
known. It is 1,900 km2 (733 mi2) in area
and still contains relatively undisturbed
forests. A recent human population
estimate is between 13,000 and 59,000
individuals, and the majority resides on
the west side of the island, in the capital
(Labuha) and nearby villages. The
current number of white cockatoos on
the island is unknown. Reports from
locals indicated that the species had
declined on Bacan due to trapping
between the 1970s and 1980s (Lambert
1993, p. 146). Surveys conducted here
in 1985 found only 76 white cockatoos.
In 1991, the population on Bacan and its
satellite islands was estimated to be
7,220 to 29,300 white cockatoos
(Lambert 1993a, b), but this may be an
overestimate of the population size
based on the survey methods used
(Gilardi 2011, pers. comm.).
Accuracy of survey methodologies
varies (Thomas 1996, pp. 49–58; Pollack
2006, p. 882; Thomas et al. 2009, pp. 5–
14), and there are limits to how much
confidence we can place in various
population surveys (Royle and Nichols
2003). One researcher pointed out that
differing methodologies can result in
differences in at least an order of
magnitude. In situations where species
are rare or have small populations, the
number of observations made per survey
may be very small and the number of
sites limited, and, therefore, estimates
and projections may not be accurate
(Marsden 1999, pp. 377–390; Pollack
2006, p. 891). In some areas, suitable
habitat may have been recently
disturbed due to habitat modification
and infrastructure development. As a
result, species’ breeding, nesting, and
forage habitat have subsequently been
destroyed, and the birds are dispersing.
It may appear as though the population
is larger than it actually is due to
sightings in new locations or the
perception that the species is more
common because it has been displaced
from its original habitat.
In the case of white cockatoos, the
population estimate may not be accurate
based on the survey methodology used
and the inferences made. A recent
survey indicated that the population
density estimation for this species in the
Aketajawe block was between 1.6 and
8.9 individuals per km2 (Burung 2011,
pp. 1–5). From this survey, a projection
was made to the surrounding area of
5,462 km2 (2,109 mi2) of the remaining
natural forest area in the vicinity of the
national park. Based on this projection,
Burung estimated the population in the
western Halmahera natural forests was
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8,630 to 48,393 individuals. This
estimate may be optimistic based, in
part, on the studies described above
(Marsden 1999, pp. 377–390; Royle and
Nichols 2003, p. 777; Pollock 2006, p.
882). In addition, because the survey
extrapolated the population density for
the surrounding area outside of the
Aketajawe block (which contains less
suitable habitat for the species and is
more accessible to poachers) from the
estimated density within the Aketajawe
Nature Reserve (which contains the
preferred habitat for the species and is
less accessible to poachers), the density
levels outside of the Aketajawe Nature
Reserve may be an overestimate.
Assuming that there were anywhere
between 8,629 and 48,393 individuals
on Halmahera in 2009 and there was an
estimated 49,765 to 212,430 individuals
in 1992, this trend in population
estimates indicates a decrease in the
population. This decrease is extremely
likely based on the negative effects of
habitat loss and poaching that are
commonly known to occur on this
island.
Recent local anecdotal accounts of
this species’ population also vary. One
recent observation was that the
population of white cockatoos was
thought to be ‘‘very sparse’’ (WCS 2010,
pers. comm.) and rapidly declining (BLI
2010c, p. 1). Populations were
conversely described as still being
relatively widespread across Halmahera
Island, and birds were occasionally
observed in flocks (WCS 2010, pers.
comm.). In November 2010, this species
was observed daily, with flocks up to 23
birds observed during a recent 5-day
trip to Halmahera (WCS 2010, pers.
comm.). However, local people consider
them to have declined from former
population levels.
We have no recent estimate of the
population on Bacan Island. Although
the last estimate, in 1993, was between
7,220 to 29,300 individuals on Bacan
Island, a 1985 survey only found 76
cockatoos. We are unsure of the
population trend. Further, in 1993, there
were reported to be over 100 people
who regularly trapped parrots on Bacan,
and this practice was a major source of
income (Lambert 1993, p. 155).
Poaching is a common practice in
Indonesia, and it likely still occurs with
regularity on Bacan Island.
Conservation Status for the White
Cockatoo
The white cockatoo has been listed in
Appendix II of CITES since 1981. It is
listed on the 2010 IUCN Red list as
vulnerable. It is also protected in the
U.S. by the WBCA (refer to discussion
under the Crimson Shining Parrot,
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factor D). The purpose of the WBCA is
to promote the conservation of exotic
birds and to ensure that international
trade involving the United States does
not harm exotic birds. Although there is
a national ban against harvest for the
white cockatoo, the quota is not
effective at eliminating poaching in the
wild. Cockatoos are still poached and
smuggled into local markets illegally
(ProFauna Indonesia 2008, pp. 1–9;
ProFauna 2010). The white cockatoo is
not listed as a protected species by the
Indonesian Republic Forestry Ministry
(WCS 2010, pers. comm.).
Information available suggests that a
few local protections are in fairly
preliminary stages but occurring.
Existence of the Aketajawe-Lolobata
National Park on Halmahera may serve
to reduce hunting pressure and habitat
loss if game wardens are monitoring the
park. Also on Halmahera, some of the
foreign-owned mining operations are
considering their environmental impact
(see Factor A discussion on mining).
Very few private or nongovernmental
organizations (NGOs) operate in the
area, in part due to the lack of funding
available. Burung Indonesia (https://
www.burung.org) does some work in
this area, mostly in relation to the
national park, and there is another local
NGO, Konservasi Alam Maluku Utara
(KAMU), that is working to try to
protect this species (Wildlife
Conservation Society (WCS) 2010, pers.
comm.). There may be carbon-funded
forest protection projects starting in the
area that also may convey protection
measures, but none is operating yet.
Evaluation of Factors Affecting the
White Cockatoo
Factor A. The Present or Threatened
Destruction, Modification, or
Curtailment of the Species’ Habitat or
Range
It is commonly accepted that
deforestation and habitat loss is a
significant problem in Indonesia
(Galang 2004, p. 14; Laurance 2007, p.
1544; BLI 2010k, p. 1). Indonesia
consists of 17,508 islands and 33
provinces. It is a rapidly developing
country, with a population of 230
million (United Nations 2009, p. 11). It
is the world’s fourth most populous
country (United Nations 2009, p. 11).
Countries with the highest human
population growth rates tend to have the
highest rates of deforestation as well
(Laurance 2007, p. 1545). As available
land becomes more scarce, companies
and humans move towards more remote
areas in search of resources (BLI 2008,
p. 100). Human settlements and
plantations are typically located in
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lowland coastal areas, which is the
white cockatoo’s preferred habitat
(Smiet 1985, pp. 181, 183). The habitat
required by the white cockatoo has been
impacted by activities such as
conversion of its habitat to uses such as
development of towns, mining, and
logging (particularly illegal logging,
which generally fails to use sustainable
logging practices) (Lambert 1993, p.
146). Pressure on the islands’ resources
is increasing (https://www.indonesiatourism.com/north-maluku/
halmahera_history.html), in part from
the increase in human population on
the island, a demand for more resources
such as biofuel and agriculture, and to
a lesser extent, an increase in
ecotourism. Historically, 75 percent of
the population on Halmahera has
depended on farming or fishing for their
livelihood, but this is changing as
investors and human development
move to the island.
Part of the Indonesian government’s
long-term planning strategy is to
develop more efficient agriculture to
help alleviate poverty. For example, the
government of Indonesia has sold land
to a company called the Sustainable
Pacific Corporation (SPC), which
purchased 300,000 ha (750,000 ac) of
land to be used for organic agriculture
and livestock breeding, agricultural
packing houses, warehouses, tourism,
and a sea port (https://www.associated
content.com/article/2412420/
halmahera_a_world_sustainable_
development.html?cat=3 and https://
worldteakplantation.itrademarket.com/
profile/sustainable-pacific-corp.htm,
accessed February 23, 2011). An
essential part of this process is
infrastructure development, primarily
the improvement of roads, which can
lead to further illegal logging and land
clearance, and also facilitates bird
trapping (poaching). This initiative will
likely convert land that is currently
suitable white cockatoo habitat into
land for other uses that are no longer
suitable for this species, such as
Jatropha curcas plantations, which are
discussed below.
Logging
Illegal logging is considered to be a
leading cause of forest degradation in
Indonesia (Rhee et al. 2004, chap. 6, p.
7). Between 2000 and 2005, Indonesia’s
forest cover declined by more than
90,000 km2 (34,740 mi2). Unsustainable
logging practices that destroy the forest
canopy also reduce habitat available to
the white cockatoo (Lusli 2008, p. 22).
Logging creates a network of roads,
which can lead to secondary problems
(BLI 2008k, p. 6), such as providing
access for poachers. The Center for
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International Forestry Research
estimated that between 55 and 75
percent of logging in Indonesia is illegal
(https://www.cifor.cgiar.org, accessed
December 10, 2010). Jepson and Ladle
(2005, pp. 442–448) concluded that
illegal logging was becoming semi-legal
and the de facto arrangement for
governing Indonesia’s forests. Illegal
logging is pervasive, and the Indonesian
government has been unable to enforce
protected forest boundaries (Barr 2001,
p. 40; Laurance 2007, pp. 1544–1547).
Illegal logging activities include:
Overharvesting beyond legal and
sustainable quotas, harvesting trees from
steep slopes and riparian habitat, illegal
timber harvest and land encroachment
in conservation areas and protected
forests, and falsification of documents.
Overexploitation of the forests and
illegal logging are driven by the woodprocessing industry, which is reported
to consume at least six times the
officially allowed harvest (Rhee et al.
2004, p. xvii, chap. 6, p. 8). Illegal
logging in national parks is reported
with regularity, and the people involved
have in the past been armed and
described as being ruthless (Whitten et
al. 2001, p. 2).
Selective logging is the primary legal
method used for the extraction of timber
in Indonesia (BLI 2008k, p. 6). In
selective logging, the most valuable
trees from a forest are commercially
extracted (Johns 1988, p. 31), and the
forest is left to regenerate naturally or
with some management until being
subsequently logged again. Johns (1988,
p. 31), studying a West Malaysian
dipterocarp forest, found that
mechanized selective logging in tropical
rain forests, which usually removes a
small percentage of timber trees, caused
severe incidental damage. The
extraction of 3 percent of trees
destroyed 51 percent of the forest. He
concluded that this type of logging
reduced the availability of food sources
for frugivores (fruit-eaters). Loggers
occasionally find parrots, including
Cacatua alba, in commercially valuable
trees that they fell, such as Anisoptera
(locally known as mersawa) in the
Dipterocarpaceae family. The white
cockatoo has been observed in
commercially valuable trees such as
Anisoptera and Canarium species
(kenari or kiharpan) (Lambert 1993, p.
146). The most recent BLI assessment
stated that much of the habitat for the
species was still intact, and even where
degraded, the species used degraded
areas. This was confirmed by WCS,
which indicated that the islands of
Halmahera and Bacan still have
extensive forest cover; however, as
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selective logging targets mature trees, it
can have a disproportionate impact on
hole-nesters, such as cockatoos, because
fewer nest sites remain (BLI 2008k, p.
6).
Although almost 80 percent of its
original forest is still intact, the
Halmahera Rain Forests ecoregion
(including Bacan Island) still faces
habitat deforestation threats. As the
forests are lost on other Indonesian
islands, there is an increasing potential
for forestry operations to move to
Halmahera and other islands with large,
desirable trees. Despite Presidential
Instruction No. 4/2005 to eradicate
illegal logging in forest areas and
distribution of illegally cut timber
throughout Indonesia (FAOLEX 2009, p.
1), illegal logging continues (refer to
Factor D discussion). Contributing
factors include poor forest management
practices, rapid decentralization of
government, abuse of local political
powers, complicity of the military and
police in some areas of the country,
inconsistent law enforcement, and
dwindling power of the central
government (USAID 2004, pp. 3, 9;
Laurence 2007, p. 1544).
Although illegal logging still occurs,
the Indonesian government is actively
working to conserve its resources. The
year 2011 was declared the International
Year of Forests. Many countries,
including Indonesia, are working
towards reducing emissions from
deforestation and forest degradation
(termed REDD) (Ministry of Forestry of
the Republic of Indonesia 2008, 185
pp.). Despite these efforts, illegal logging
still occurs within this species’ range.
Mining
Mining and its associated impacts is
a fairly new factor affecting this species.
Several companies have mining rights
in the Maluku area, particularly on
Halmahera (WCS 2010, pers. comm.).
PT Antam, the largest mining company
in Indonesia, currently operates three
nickel mines on the northeast prong of
Halmahera (PT Antam 2009). Another
mining company, PT Nusa Halmahera
Mineral (NHM), is a joint venture
company between Newcrest Mining of
Australia and PT Antam Tbk, an
Indonesian-owned company. They have
an exploration license for Bacan and
nearby islands to look for gold and other
minerals. A third mining company has
a license to mine nickel near Ake Tajawi
on Halmahera (WWF 2010a).
Two gold mines have been in
operation on Halmahera (Newcrest
Mining 2010, p. 1). The Gosowong mine
was an open-pit, cyanide-leach mine
that operated from 1999 to 2002, and is
now closed. The Toguraci mine began
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operation in 2004. Toguraci is located 2
km (1.2 mi) southwest of the original
Gosowong pit mine. This mining
operation is operated by a joint venture
company, Pt Nusa Halmahera Minerals
(PTNHM) and PT Aneka Tambang.
Development of this mine began in July
2003, after approval of a feasibility
study and environmental impact
statement by the Indonesian Minister of
Mines. Actual mining of ore and the
first gold production began in February
2004. This mine has been the subject of
conflict between local residents and the
mining company. Between October and
December 2003, several illegal miners
occupied the Toguraci mine site.
Additionally, the mine is located in a
forested area that, according to local
residents, is protected under Indonesian
law, and, therefore, mining operations
should not be allowed. The current
operating status of the Toguraci mine is
unclear; however, local NGOs indicate
that mining on Halmahera does affect
the white cockatoo (Vetter 2009, pp. 2,
14, 15; WCS 2010, pers. comm.). Mining
activities can affect the white cockatoo’s
habitat either directly or indirectly,
through pressures such as illegal
poaching or human encroachment and
habitat disturbance.
Yet another mining company, PT
Weda Bay Nickel, proposed a nickel and
cobalt mining project in 2009 on the
island and has submitted an
environmental monitoring plan (PT
Weda Bay Nickel 2009, 204 pp.; Cardiff
2010, pp. 1–14). The footprint of the
mining operation appears to be within
the boundaries of Aketajawe-Lolobata
National Park (Vetter 2009, p. 19;
Cardiff 2010, p. 1), which could have
significant detrimental effects on
Halmahera’s wildlife, including the
white cockatoo. A review of the
proposed mining project indicated that
it would likely destroy between 4,000
and 11,000 hectares (9,884 and 27,182
acres) of tropical forest, and between
2,000 and 6,000 ha (4,942 and 14,826
ac) of protected forested area (Cardiff
2010, pp. 6, 9, 12). The review indicated
that mining activities are extremely
destructive to this habitat. Based on
deforestation projections, the
population of the white cockatoo is
projected to decline more than 65
percent over three generations due to
deforestation (Vetter 2009, pp. 25, 26,
51). It is unclear whether this mining
operation will be approved, or if there
will be mitigation measures required;
however, it is clear that the extractable
resources on Halmahera are desirable,
and mining will very likely have a
significant negative impact on this
species and its habitat.
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Biofuel Production
Indonesia is investing in the planting
of Jatropha curcas trees and palm oil
(Elaeis guineesis) (Department for
Environment, Food and Rural Affairs,
United Kingdom 2008, pp. xvii, 47, 64,
65). Rapid expansion of biofuel
plantations has led to intense
international concern about wide-scale
environmental impacts. On Halmahera,
at least 500 hectares (3,750 acres) have
been allotted for cultivating the Jatropha
tree (Consulate General of the Republic
of Indonesia 2006, pp. 5–6). Many
industries, such as the air transportation
industry, are considering the use of fuel
from Jatropha as a biofuel source, and it
is also being encouraged as a
mechanism for carbon credits (https://
www.jatrophabiodiesel.org, https://
www.jatrophaworld.org, https://
www.jatropha-alliance.org). This oil has
been reported to produce energy similar
to diesel fuel. Although this species may
yield 4 times as much fuel per hectare
as soybeans, and possibly 10 times that
of corn, it requires 5 times more water
to produce than corn. It is also reported
to be desirable to developing countries
because its carbon emissions footprint is
thought to be relatively small when
burned.
Conversion of land to monocultures
destroys white cockatoo habitat.
Monocultures are generally not suitable
habitat for wildlife. White cockatoos
require large trees, which provide large
enough nesting cavity sites, and
Jatropha curcas trees require many
years to reach a size that would be
suitable for nesting. This will likely also
have a negative impact on this species’
suitable habitat due to road building,
infrastructure development, other
construction (Vetter 2009, pp. 1–10).
Additionally, because there is currently
no effective enforcement body to
monitor sustainable land development
(also refer to Factor D discussion) on
Halmahera, these activities threaten
white cockatoo habitat. Therefore, we
find that conversion of forests to
monocultures for biofuel, particularly
Jatropha, is a threat to the white
cockatoo.
Summary of Factor A
Deforestation affects endemic bird
species restricted to single islands more
severely than it affects other species
(Brooks et al. 1997, p. 392).
Monocultures such as exotic tree
plantations, agriculture, conversion to
human habitat, resource extraction,
agriculture, and logging are forms of
deforestation and habitat loss affecting
endemic island species such as the
white cockatoo in Indonesia (Laurance
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2007, p. 1544). Lowland areas that offer
vital habitat for Indonesia’s cockatoos
have been the most severely impacted
(Cameron 2007, p. 177; Vetter 2009, p.
4). As islands become more inhabited
and deforested, humans move to other
islands that contain available resources
(Laurance 2007, p. 1544).
Cockatoos are highly impacted by
selective logging of primary forests.
Selective logging, which targets mature
trees, has a negative impact on cavitynesters such as the white cockatoo.
Research found that the abundance of
cockatoos is positively related to the
density of its favored nesting trees (large
trees that would be impacted by
logging), especially since reducedimpact logging techniques are rarely
applied. Once the primary forest is
logged, experience on other nearby
Indonesian islands shows that the
secondary forest is generally converted
to other uses or logged again rather than
being allowed to return to primary
forest. Although cockatoos may
continue to inhabit secondary forests,
the population will be at a substantially
lower number. Additionally, species are
often found in secondary forest or
recently altered forest habitat; however,
this habitat tends to be marginal, and
the effects on the species’ population
may not be evident. The trend of high
loss of primary forests and degradation
of secondary forests is a concern, in part
because little is known about the
reproductive ecology of white cockatoos
in the wild, including breeding success
in mature forests versus secondary
forests, and whether this species of
cockatoo will survive in degraded
forests in the long term.
In summary, habitat modification and
deforestation activities, such as
conversion of primary or secondary
forests to exotic tree plantations for
biofuel production, agriculture, and
human habitat, combined with selective
logging and resource extraction
(mining), are likely to destroy much of
the white cockatoo’s habitat (the
lowland rain forests of Halmahera) in
the near future. While this species may
be tolerant of secondary-growth forests
or other disturbed sites, these areas do
not represent optimal conditions for the
species. Based on these factors, we find
that the present and threatened
destruction, modification, or
curtailment of its habitat is a threat to
the continued existence of the white
cockatoo throughout all of its range.
Factor B. Overutilization for
Commercial, Recreational, Scientific, or
Educational Purposes
The primary threat to white cockatoos
is poaching from the wild to meet the
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demand for the pet trade (Jepson and
Ladle 2005, p. 442; Defenders 2007, p.
7; ProFauna 2008; BLI 2010c). It is well
established that illegal collection for the
pet trade is a major problem for wild
birds in Indonesia and is the primary
threat to this species (BLI 2003, pp. 1–
2; ProFauna 2008, pp. 1–9; ProFauna
Indonesia 2010, pers. comm.). Birdkeeping is a popular pastime in
Indonesia, with deep cultural roots
(Jepson and Ladle 2005, p. 442). Parrots
have been traded for hundreds of years
by people living in the Moluccas. One
report indicated that 17 percent of the
global population was captured for trade
in 1991 alone (Lambert 1993, p. 160). As
of 1999, there appeared to be no
enforcement of the zero export quota;
cockatoos were widely available in local
markets.
In 2002, an investigation found 500
white cockatoos were caught to supply
the pet trade (ProFauna Indonesia 2010,
pers. comm.). In addition, parrots are an
important part of the Indonesian
culture, which creates significant
demand for parrots domestically (BLI
2008k, p. 10). In a survey on birdkeeping among households in five major
Indonesian cities, Jepson and Ladle
(2005, pp. 442–448) found that as many
as 2.5 million birds are kept in the five
cities. Of these, 60,230 wild-caught,
native parrots were kept by 51,000
households, and 50,590 wild-caught,
native parrots were acquired each year
(changed hands, not an indication of
birds taken from the wild each year).
The study recommended a conservation
intervention based on the level of birdkeeping among urban Indonesians. As of
2006, an average of 100 white cockatoos
were found for sale in bird markets in
Java annually (ProFauna Indonesia
2010, pers. comm.). The sale of live
parrots can be a significant source of
income. Parrots can sell for 75,000 to
500,000 Indonesian Ruphiahs (IDR or
Rp) each, which equates to between
$7.50 and $50 U.S. dollars. A young
cockatoo can sell for $20 to $25 USD
(ProFauna 2008, p. 3; Sasaoka 2009,
pers. comm., pp. 1–2; ProFauna
Indonesia 2010, pers. comm.). In 1993,
cockatoos were described as generally
rare in the Java and Bali markets; only
two white cockatoos, or 1.2 percent of
parrots for sale, were seen in these
markets visited (Lambert 1993, p. 158).
However, of 381 parrots of 19 species
observed at markets in Indonesia, white
cockatoo was represented by 11 pets
(9.7 percent) and 44 individuals (11.5
percent) in the market sample.
Between 1993 and 2002, although
Indonesia had reported the export of
712 wild-caught birds, import records
from other CITES countries recorded
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1,646 (Cahill et al. 2006, p. 162; UNEP–
WCMC 2010). Discrepancies in the
UNEP–WCMC Trade Database are
common. For example, the Service
found a report in 2009 of one shipment
of white cockatoo to the United Arab
Emirates (UAE) from South Africa that
was reported as 965 by the UAE;
however, there was no corresponding
export entry from South Africa (UNEP–
WCMC 2010). The largest shipment
from South Africa in 2009 to the UAE
was 614, so we believe it to be a
reporting error.
Even with government controls, the
commercial hunting of cockatoos (i.e.,
hunting by people to gain at least a
temporary living from the activity) is
relatively common. There is still a
demand for this species as pets, and
wild-origin birds are less expensive to
obtain than captive-bred birds
(Reynolds 2010, pers. comm.; Horsfield
2010, pers. comm.). Field research
conducted in 2003 through 2005 in a
small village (320 people, 60
households) located in the Manusela
Valley, Seram, led to the conclusion that
collecting wild parrots, including
cockatoos, is a way for villagers to
supplement their income during times
of hardship (Sasaoka 2009, pers. comm.,
p. 1; Sasaoka 2008, p. 158). In 2003, 21
cockatoos were trapped in the research
site by 3 households; in 2004, 25
cockatoos by 5 households; and in 2005,
26 cockatoos by 10 households. These
researchers found that villagers
sometimes kept the cockatoos for
several months while waiting for the
best price, but normally did not keep
them as pets.
Exploitation for commercial purposes
prior to 1992 is widely accepted as the
primary cause of drastic, rangewide
population decline of many parrot
species. The commercial market for pet
´
cockatoos is highly lucrative (Cantu´
Guzman et al. 2007, 121 pp.). Prior to
1992, when the U.S. Wild Bird
Conservation Act was enacted, critical
scientific studies to address issues of
detriment to populations, appropriate
management of species, and sustainable
levels of trade had not been undertaken
for most CITES Appendix-II bird species
in trade. Even in 1992, there was serious
concern that the international
commercial trade in wild-caught birds
was contributing to the decline in the
wild of some species of birds listed in
CITES Appendix II.
Poaching poses a serious threat to the
species. The scope of the illegal trade in
white cockatoos is unknown.
ProFauna’s investigation in 2008 found
that this species is regularly poached
from the wild and shipped to the
Philippines. (After reaching the
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Philippines, it is unclear what occurs to
the birds.) Based on ProFauna’s
investigation, it appears that many of
the birds being poached from the wild
may be, ‘‘laundered with wild cockatoos
possibly being described as being of
captive-origin.’’ In general, it is difficult,
if not impossible, to determine the
source of cockatoos (BLI 2003, p. 1).
ProFauna found that around 9,800
individual parrots, including white
cockatoos, are poached every year
(ProFauna 2008, p. 3). An investigation
completed in 2008 found that the white
cockatoo is poached from Maluku and
smuggled into the Philippines
(ProFauna 2008; ProFauna Indonesia
2010, pers. comm.). Parrot poaching
took place most frequently in the central
part of Halmahera, as well as Bacan,
Obi, and Mandioli (2008, p. 7). The
investigation indicated that
approximately 10 percent of the 4,000
parrots smuggled annually were white
cockatoos. In their investigation, they
found bird poachers in Togawa, for
example, were able to catch 15
individuals of white cockatoo in a week
(ProFauna 2008, p. 3).
During the illegal trade process, many
birds die prior to being exported
(Lambert 1993, p. 157; Cameron 2007, p.
´
´
163; Cantu-Guzman et al. 2007, p. 60).
Methods used for poaching lead to
significant mortality. In some cases,
white cockatoos in the past have been
caught with gum or glue, which would
stick to their feathers (Lambert 1993, p.
155; ProFauna 2008, p. 2). Some
trappers reported mortality rates
between 77 and 80 percent before
parrots reach customers, and nestlings
experience a higher mortality rate
´
´
(Cantu-Guzman et al. 2007, p. 60).
ProFauna Indonesia estimated that
parrot smuggling in North Maluku,
Indonesia, results in approximately 40
percent mortality (5 percent during glue
trapping, 10 percent during
transportation, and 25 percent during
holding to sell in bird markets (due to
malnutrition, disease, and stress) (2008,
p. 5)). The estimates do not always
include deaths of birds before export,
smuggled birds, and birds domestically
traded. Others estimate that as few as
one-fourth of those poached survive the
process of removal from their native,
wild habitat to captivity.
Undocumented illegal trade
(international and domestic) is difficult
to quantify (Thomsen et al. 1992, p. 3;
Pain et al. 2006, p. 322), and a listing
in Appendix I of CITES does not
completely stop illegal trade (Pain et al.
2006, p. 328). Seizures reported to the
CITES Secretariat since 1990, however,
are small—1 live bird seized in Austria
in 1997; 25 live birds seized in the
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United Arab Emirates in 1998; and 4
live birds seized in Indonesia in 1999
(Sellar 2009, pers. comm., p. 2). Since
2000, the United States refused import
clearance for three birds reported as
Cacatua species. One bird was
described as C. alba in 2010; the other
two birds were unknown Cacatua
species. All three birds were reexported.
Illegal trade of parrot species occurs
quite frequently; in fact, an investigative
report recently conducted of the illegal
parrot trade in Mexico demonstrates this
´
´
(Cantu-Guzman et al. 2007, 121 pp.).
The investigation found that documents
are frequently forged to smuggle
desirable and increasingly rare parrot
species (p. 38). The organization that
seizes parrots in Mexico, the Federal
Attorney for the Protection of the
Environment (PROFEPA), indicated that
their most serious problem is combating
the illegal bird trade (p. 45). Although
this investigation was done in Mexico,
it reflects a problem that occurs within
many countries with endemic parrots.
Locally, a high level of parrot
poaching in north Halmahera is due in
part to the lack of supervision by
Natural Resources Conservation (KSDA)
officers in the Forestry Department
(ProFauna 2008, p. 3). There is no
regular enforcement or patrol by the
KSDA officers. An NGO working with
this species indicated that they had
recently received several white
cockatoos from Indonesian authorities
who had confiscated them from
poachers (Metz 2010, pers. comm.).
Most of the Indonesian parrots come
from Halmahera Island and are shipped
to the Philippines. According to a recent
investigation, 40 percent of parrots were
smuggled to the Philippines from the
port in Pelita Village, Galela District in
northern Halmahera (ProFauna 2008, p.
5). The birds are apparently smuggled to
Balut Island or to General Santos in the
Philippines. The journey to smuggle
parrots from Halmahera, Indonesia, to
General Santos, the Philippines, takes
over 9 hours, not including the time it
takes to transport birds from the forest,
to villages, and then to the port. The
transactions are done offshore or in the
sea, where the Philippine dealers collect
the parrots from Indonesian ships. Upon
arrival at General Santos, the birds are
sent to Cartimar market in Manila, the
capital of the Philippines (ProFauna
2008, p. 4). Since there is little
disincentive for locals, it is a low-risk
and lucrative source of income. Despite
the existence of legislation, this illegal
trade of protected parrots continues.
Law No. 5, 1990, governing the
conservation of biological resources and
their ecosystems, was enacted to protect
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natural resources and the ecosystems
(Yeager 2008, pp. 3–4); however,
poaching and illegal trade continue to
occur (also see discussion under Factor
D).
The presence of recent and upcoming
mining projects in Halmahera is also
likely to increase demand locally for
birds (see to Factor A discussion above).
Temporary workers are known to buy
these birds as gifts. It is apparently a
problem even among police and military
personnel posted to the area (WCS 2010,
pers. comm.). ProFauna has encouraged
the Navy of Indonesian Armed Force
(TNI) and the Indonesian Marine Police
to improve the patrol of marine
boundaries between Indonesia and the
Philippines in order to decrease this
illegal trade. NGOs are encouraging both
Indonesian and the Philippines
governments to implement and enforce
their wildlife laws and encouraging
Indonesia to list Cacatua alba as a
protected species (ProFauna 2008, pp.
8–9); however, poaching continues.
Stopping illegal trade is further
complicated by the vast size of
Indonesia’s coastline, and government
officials have limited resources and
knowledge to deal with the illegal pet
trade (Metz 2007c, p. 2; Laurence 2007,
p. 1544). To combat illegal wildlife
trade, Southeast Asian countries,
including Indonesia, formed the
Association of South East Asian
Nations–Wildlife Enforcement Network
(ASEAN–WEN) in 2005 to protect the
region’s biodiversity (https://
www.asean.org, accessed March 3,
2011). ASEAN–WEN uses a cooperative
approach to law enforcement (Cameron
2007, p. 164). It focuses on the gathering
and sharing of intelligence, capacity
building, and better cooperation in antismuggling and Customs controls across
Southeast Asia (Lin 2005, p. 192). For
example in 2008, Indonesian police
officers and forestry and Customs
officers participated in an intensive
Wildlife Crime Investigation Course
presented by the U.S. Fish and Wildlife
Service to help the government tackle
poaching and smuggling (Wildlife
Alliance 2008, p. 2). Despite these
efforts, illegal trade of white cockatoo
still occurs within Indonesia.
Summary of Factor B
In summary, overutilization of the
white cockatoo for the pet trade is a
significant threat to the species, and this
species is undergoing a rapid
population decline. Poaching and illegal
trade is difficult to control, in part
because Indonesia has a vast coastline,
and because income derived from
poaching can be a significant source of
income. Birds are clearly being poached
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and shipped to the Philippines, and
there is strong demand for this species
within Indonesia. Additionally, having
a parrot as a household pet is a common
part of Indonesian culture. Government
officials have limited resources to deal
with the illegal pet trade. Indonesia is
a founding member of ASEAN–WEN
and has made an effort to train its
police, forestry, and Customs officers in
methods to tackle poaching and
smuggling. However, the wildlife
protection laws are not vigorously
enforced at local levels for this species.
Despite ProFauna Indonesia and the
Indonesian Institute of Sciences having
requested that the Forestry Department
of Indonesia list white cockatoo as a
protected species, and the Sultan of
Ternate Palace having forbidden the
poaching of this species (ProFauna
Indonesia 2010, pers. comm.), poaching
and illegal cross-border trade still occur.
The ProFauna investigation in 2008
found that enforcement in both
Indonesia and the Philippines is
lacking. In part because this species
does not begin to reproduce until
approximately 6 years of age, and
because this species is thought to be
monogamous and usually mates for life,
this level of poaching for the pet trade
is a considerable threat to the species in
its ability to maintain its population.
Based on the best available information,
we find that overutilization is a threat
to the continued existence of this
species.
Factor C. Disease or Predation
There is no evidence that either
disease or predation is a threat to the
white cockatoo in the wild. We are
unaware of any reports of diseases
negatively affecting white cockatoos in
the wild. Since disease and predation
associated with this species in the wild
are not well documented, we
extrapolate from what is known about
cockatoos in general (see analysis under
Factor C for the Philippine cockatoo).
Although some serious diseases such as
beak and feather disease and PDD occur
in cockatoos in the wild, we found no
information that these diseases occur in
cockatoos in the wild in Indonesia.
Cases of avian influenza (H5N1) do
occur in Indonesia, but parrots,
particularly cockatoos, are not
considered to be natural reservoirs of
this disease (IPP 2006). With respect to
predation, the white cockatoo has
natural predators, but we were unable to
find information that these natural
predators are having a negative impact
on the productivity of this species.
Therefore, we find that the white
cockatoo is not threatened due to
disease or predation.
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Factor D. The Inadequacy of Existing
Regulatory Mechanisms
Domestic Regulatory Mechanisms
Indonesia has laws and regulations in
place to conserve biodiversity, manage
forests, regulate trade, provide species
protection, and develop and manage
protected areas. However, these laws
and regulations are frequently ignored
(BLI 2008k, p. 7; Laurance 2007, p.
1544), and the country is unable to
monitor its vast area, which consists of
17,508 islands. The Indonesian
economic crisis that led to the downfall
of the Suharto regime resulted in the
government instituting a
decentralization that gave local
governments greater autonomy (Vetter
2009, p. 15). However, this
decentralization resulted in confusion of
roles and responsibilities, and
implementation of decentralization has
been slow and uncertain. Conflicting
interpretation of policies and priorities
and the lack of capacity or experience
of local governments have occurred
(Rhee et al. 2004, chap. 2, p. 20).
According to ProFauna, the high level
of parrot poaching in north Halmahera
is in part due to the lack of monitoring
by Natural Resources Conservation
(KSDA) officers in the Forestry
Department (ProFauna 2008, p. 3).
There is no regular enforcement or
patrol by the KSDA officers (ProFauna
2008, p. 3). The North Maluku
government and ProFauna Indonesia
have proposed to the Forestry Ministry
that the species be classified as a
protected species (BLI 2010c; ProFauna
2010, pers. comm.).
In general, the export of wild-caught
parrots is subject to harvest and export
quotas in Indonesia. However, because
the white cockatoo is not on the
Indonesian Government’s list of
protected species (Law No. 5 1990, pp.
1–44; Rhee et al. 2004, chap. 5, p. 2,
App. VIII; ProFauna 2010a, pers.
comm.), Indonesia has no legal export
quota for wild-caught specimens of this
species (IPP 2010). In 1988, the
Indonesian government began issuing
quotas on trapping for the white
cockatoo; however, these trapping
quotas were poorly enforced. In 1999,
no quota was issued, and all capture
was reported to be illegal since 1999
(BLI 2010c). However, an NGO reported
that there was a catch quota of the white
cockatoo for 2007. It was issued by the
General Director of Perlindungan Hutan
dan Konservasi Alam (PHKA), which
translates to the Forest Protection and
Nature Conservation under the
Indonesian Ministry of Forestry, and the
catch quota was for 10 pairs that were
to be used only for breeding (ProFauna
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2008, p. 3). However, that quota was
exceeded (ProFauna 2010, pers. comm.).
Recent information indicates that there
is no longer a catch quota (ProFauna
2010, pers. comm.), but that restriction
may apply to commercial purposes,
rather than breeding. According to WCS
(2010, pers. comm.), this species is
trapped and sold, and this can include
trapping on a ‘‘commercial’’ scale by
professionals, or farmers trapping
occasional birds and then selling them
to wholesalers. In 2007, at least 200
white cockatoos were caught from the
wild in North Halmahera, which far
exceeded the quota of 10 pairs
(ProFauna 2008, p. 3; https://
www.thegabrielfoundation.org/
indonesianparrots.html).
Additionally, in 2010, the Sultan of
Ternate Palace issued a fatwa (order)
forbidding the poaching of cockatoos in
the wild. However, as stated before,
enforcement often is severely lacking
(Shepherd et al. 2004, p. 4) or difficult,
and illegal activities remain socially
acceptable at the local level. Illegal trade
has been reported to the Natural
Resource Conservation Agency, which
is responsible for enforcing the law, but
to date enforcement efforts remain
ineffective (ProFauna Indonesia 2004, p.
8). To further complicate enforcement
efforts, some bird dealers claim that
members of the Department of Forest
Protection and Nature Conservation are
involved in the illegal trade of this
species (Shepherd et al. 2004, p. 4).
Existing regulatory mechanisms
within Indonesia, as implemented, are
inadequate to reduce or remove the
current threats to the white cockatoo.
Even with government controls,
poaching of cockatoos is relatively
common (WCS 2010, pers. comm.). As
discussed under Factor B, we found that
poaching is the primary threat to the
white cockatoo. There is some evidence
that the actions of Indonesian
government agencies and the military
are changing; however, if penalties are
not enforced for illegal trade, trapping
from the wild will continue (ProFauna
Indonesia 2004, pp. 9–11). In
conclusion, we find that the existing
regulatory mechanisms are inadequate
to reduce or remove the current threats
to the white cockatoo. There is no
information available to suggest that
these regulatory mechanisms will
improve in the foreseeable future.
CITES
Indonesia has been a member of
CITES since December 28, 1978. It has
designated Management, Scientific, and
Enforcement authorities to implement
the Treaty (CITES 2008b, p. 1) and has
played an active role in CITES meetings.
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Because this species is not listed in
Appendix I, which would mean that
commercial trade would be prohibited
except under certain circumstances,
legal international trade is still
occurring for this species.
Since 2000, there has generally been
a downward trend in exports of the
white cockatoo (UNEP–WCMC CITES
Trade Database, accessed January 4,
2011). According to the CITES UNEP–
WCMC Trade Database, there were 653
live exports of the white cockatoo in
2000, 269 in 2008, and 1,104 in 2009
(2009 may have been an anomaly).
Between 2000 and 2009, 8,505
specimens of live white cockatoos were
reported to have been exported. The
bulk of these exports was exported from
South Africa and was reported as
captive-origin. Between 2000 and 2009,
of the live shipments, there were 28
white cockatoos reported as wild origin.
None of these live specimens reported
as wild origin was exported directly
from Indonesia. Of the live shipments,
8,435 specimens were described as
captive origin, 19 were described as
‘‘unknown’’ origin, and 20 were
described as pre-Convention, seized, or
confiscated. Of the countries that
reported the most exports of live white
cockatoos, 273 specimens were exported
from Indonesia, 4,444 specimens were
exported from South Africa, and 384
specimens were exported from the
Philippines. Note that countries that are
not Parties to CITES do not submit
annual report trade data to UNEP–
WCMC (also refer to the CITES
discussion for the crimson shining
parrot). However, Parties, in their
annual reports, do include data on their
trade with non-parties, and these data
are recorded in the UNEP–WCMC Trade
Database. Also, while the Database does
not include CITES annual report trade
data from CITES Parties that did not
submit annual reports, it does include
CITES trade data from Parties that
submitted their annual reports and
engaged in CITES trade with those nonsubmitting Parties.
The purpose of CITES is to ensure
that international trade in animal and
plant species is not detrimental to the
survival of wild populations by
regulating the import, export, and reexport of CITES-listed animal and plant
species. The best available data indicate
that the current threat to this species of
cockatoo stems from illegal trade in the
domestic markets of Indonesia and
international surrounding countries. As
discussed under Factor B above,
uncontrolled illegal poaching for the pet
trade continues to adversely impact
white cockatoos. Despite illegal trade,
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international trade.
Summary of Factor D
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In summary, we find that the existing
regulatory mechanisms within
Indonesia, as implemented, are
inadequate to reduce or remove the
current threats to white cockatoos. Local
protections in place provide some
protection to white cockatoos. While
Indonesia has a good legal framework to
manage wildlife and their habitats,
implementation of its laws and
regulatory mechanisms has been
inadequate to reduce the threats to
white cockatoos. The national parks on
Halmahera may provide some
protection to white cockatoos; however,
management of protected areas is
hampered by staff shortages and lack of
expertise and money. As discussed
under Factors A and B above, we found
that habitat destruction and poaching
are threats to white cockatoos.
Deforestation and illegal activities are
still rampant in Indonesia (Laurance
2007, pp. 1–7). The national and local
regulations and management of this
species’ habitat are ineffective at
reducing the threats of habitat
destruction (see Factor A) and poaching
for the pet trade (see Factor B). The
white cockatoo is listed in Appendix II
of CITES (see discussion under
Conservation Status for the White
Cockatoo above), and CITES appears to
be an adequate regulatory mechanism to
address legal international trade.
Even with government restrictions,
poaching of cockatoos (i.e., hunting by
people to gain at least a temporary
living from the activity) is still relatively
common in Indonesia. Nestlings are
more desirable as pets, yet their
mortality rate when taken from the wild
is greater than that of adults (ProFauna
2008). Laws and regulations are
frequently ignored, and this adds to the
inability to enforce them due to the
remoteness of the areas where this
species is located. There is no
information available to suggest
regulatory mechanisms within
Indonesia will be adequate to protect
this species in the foreseeable future;
therefore, we find that the inadequacy of
regulatory mechanisms is a threat to the
white cockatoo throughout its range.
Factor E. Other Natural or Manmade
Factors Affecting the Continued
Existence of the Species
Ecotourism
The Halmahera region is an emerging
diving destination (WWF 2010a, p. 2).
An Internet search found several Web
sites offered diving trips that are in the
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Halmahera region, and there was even a
video available online (https://
www.youtube.com/watch?v=PEmEBZj_L4), entitled ‘‘Diving travel: The
North Halmahera Experience.’’
Although the Halmahera region is
remote and few diving operations exist,
there is the potential for the diving
industry to expand and exert more of an
effect on the islands in this area.
However, at this time, the best available
information does not indicate that
diving-related activities on or near
Halmahera negatively affect the white
cockatoo. We are not aware of any
tourist activities occurring on Bacan
Island. We found no other natural or
manmade factors affecting the
continued existence of the white
cockatoo. Therefore, we find there are
no threats to this species under this
factor.
Finding for the White Cockatoo
As required by the ESA, we
considered the five factors in assessing
whether the white cockatoo is
endangered or threatened throughout all
or a significant portion of its range. We
analyzed the potential threats to the
white cockatoo including: Habitat loss
and degradation, poaching for the pet
trade, disease and predation, the
inadequacy of regulatory controls, and
other natural or manmade factors, such
as the conversion of habitat to
monocultures for biofuel, and
ecotourism activities such as diving. We
found that habitat loss, particularly due
to selective logging, and conversion of
forests to agriculture, mining, or
biofuels, is a threat to the white
cockatoo; the population is declining
rangewide (see Factor A discussion).
Halmahera is becoming increasingly
more desirable to developers and
investors as natural resources become
more scarce.
We found that poaching for the pet
trade is the most significant threat to the
species, despite local public awareness
campaigns. It is estimated that there are
between 8,629 and 48,393 individuals of
this species remaining in the wild on
Halmahera; the number of white
cockatoos remaining on Bacan Island is
unknown, though poaching of wild
birds on this island is believed to be
occurring. Pet birds are an important
part of not only Indonesian culture, but
also Asian culture, with large numbers
of wild-caught parrots traded
domestically and internationally (Baula
et al. 2003, pp. 1–12; BLI 2004, pp. 1–
2, ProFauna 2008, pp. 3–4). Trappers
reportedly remain quite active. Wildcaught birds are openly sold in Asian
markets, particularly in the nearby
Philippines (ProFauna 2008, pp. 3–4;
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BLI 2003, pp. 1–2). An investigation
conducted by NGOs in Indonesia in
2002 and 2003 found evidence of wild
birds in local markets, and sellers
reported that they were destined to go
to countries such as Europe (BLI 2004,
pp. 1–2). Ending illegal trade is
hampered by Indonesia’s large coastline
and officials with limited resources and
knowledge.
Unsustainable poaching is
particularly detrimental to the white
cockatoo because of its estimated small
and rapidly declining population.
Excessive removal of individuals from
the wild for illegal trade is particularly
harmful to species such as the white
cockatoo, which are monogamous, longlived species that do not begin breeding
until they are 6 years of age.
Additionally, because this species has a
high monetary value (Basile personal
communication 2010, pp. 6–7) and there
is little risk in poaching, poaching is
financially lucrative. The Act describes
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.’’ The
best available information indicates that
poaching and trade are not at a level to
consider the species to be in danger of
extinction at this time. However, based
on the analysis of the five factors
discussed above, we determine that the
white cockatoo is likely to become an
endangered species within the
foreseeable future. Therefore, we find
overutilization for commercial,
recreational, scientific, or educational
purposes (Factor B), specifically
poaching for the pet trade, is a threat to
the white cockatoo throughout its range.
We found no evidence that disease or
predation significantly affect the wild
white cockatoo population throughout
its range.
The white cockatoo is not currently
classified as a protected species by the
Indonesian government. Although
Indonesia has a good legal framework to
manage wildlife and their habitats,
implementation of its laws and
regulatory mechanisms has been
inadequate to address the threats to the
white cockatoo, in part due to the
remoteness of the white cockatoo’s
habitat. Logging laws and policies are
frequently ignored and rarely enforced,
and illegal logging is rampant, even
occurring in national parks and nature
reserves. Current concession policies
and logging practices hamper
sustainable forestry. Threats to the
species have not decreased; local NGOs
indicate the population trend is
declining.
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Although diving activities are
increasing near islands containing white
cockatoo habitat, there is no evidence
that ecotourism is a threat to this
species now or in the foreseeable future.
Therefore, we conclude that there are no
other natural or manmade factors that
are threats to the species throughout its
range (Factor E).
Under the ESA, an ‘‘endangered
species’’ is defined as ‘‘any species
which is in danger of extinction
throughout all or a significant portion of
its range.’’ The ESA defines 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 our review of the best available
scientific and commercial information
pertaining to the above five factors, we
find that the white cockatoo meets the
definition of a ‘‘threatened species’’
under the ESA, and we are proposing to
list the white cockatoo as a threatened
species throughout its range. Although
the species is not currently in danger of
extinction and, thus, does not qualify as
an ‘‘endangered species’’ under the
ESA, we conclude that the species
qualifies as a threatened species. The
current distribution of white cockatoos
within its range and its disbursed
distribution on two islands provides
resiliency to the population against the
threats such that the species is not
currently in danger of extinction, but
may become so in the foreseeable future.
Significant Portion of the Range
Having determined that the white
cockatoo meets the definition of
threatened throughout its range, we
must next consider whether there are
any significant portions of its range that
meet the definition of endangered. See
our discussion under the crimson
shining parrot for how we make this
determination. For the purpose of this
analysis, we consider a portion of the
white cockatoo’s range to be significant
if it is important to the conservation of
its range because it contributes
meaningfully to the representation,
resiliency, or redundancy of its range
(see Redford et al. 2011). The best
available information indicates that
threats to the species occur throughout
its range. Although declines on
Halmahera have been quantified to
some extent, the lack of any
information, including quantitative
population trend information for Bacan
Island, precludes a comparison of the
declines in these two portions of its
range. Further, we found no information
indicating that the threats are of greater
magnitude or extent in any portion of its
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range on Halmahera Island. The limited
information available for the white
cockatoo does not allow us to determine
what portion of the range if any, would
be impacted to a significant degree more
than any other. Therefore, we conclude
that the threats to the species are
uniform throughout its range, and no
portion of its range is currently in
danger of extinction.
Species Information
D. Yellow-Crested Cockatoo (Cacatua
sulphurea)
Taxonomy and Description
There are four recognized subspecies
of the yellow-crested cockatoo: Cacatua
sulphurea abbotti (Oberholser, 1917), C.
s. citrinocristata (Fraser, 1844), C. s.
sulphurea (Bonaparte, 1850), and C. s.
parvula (Gmelin, 1788). IUCN and BLI
recognize C. sulphurea at the species
level only. All four subspecies are
recognized by ITIS (https://www.itis.gov).
These four subspecies are endemic to
Timor-Leste (an independent state
which is adjacent to West Timor, a part
of Indonesia) and Indonesia. The
yellow-crested cockatoo inhabits forest,
forest edge, scrub, and agricultural land
(IUCN 2008j; BLI 2010d, p. 1), but
prefers primary lowland forest.
Historically, it was found throughout
the Lesser Sundas, on Sulawesi and its
satellite islands, on Nusa Penida (off
Bali), and the Masalembu Islands (in the
Java Sea). These subspecies (hereafter
collectively referred to as the species)
are found in forested habitat in the
lowlands up to 500 m (1,640 ft) on
Sulawesi and up to 800 m (2,625 ft), and
sometimes 1,200 m (ft), in the Lesser
Sundas (Collar 1994; Jones et al. 1995;
Snyder 2000, p. 69). They prefer large,
mature trees with nesting areas higher
in the canopy, and they prefer internal
forested areas to forest edges (Jones et al.
1995, pp. 27–28, 39).
There is substantial discussion in
scientific literature that debates the
classification of island species and
whether they deserve species status
rather than subspecies status
(Phillimore 2010, pp. 42–53; James
2010, pp. 1–5; Pratt 2010 pp. 79–89).
This is sometimes significant with
respect to conservation measures,
particularly when considering the
criteria used by organizations such as
the IUCN. Assessments of subspecies
are only accepted by IUCN provided
there is a global assessment of the
species as a whole. These four
subspecies may all be in fact species,
but for the purpose of this proposed rule
and 12-month finding, these four
subspecies essentially face the same
threats, are all generally in the same
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region of Indonesia, and all have quite
small populations. Absent peerreviewed information to the contrary
and based on the best available
information, we recognize all four
subspecies as being valid. For the
purpose of this rule, it is prudent to
propose listing C. sulphurea, which
includes all subspecies.
Use of Scientific Names in This Section
It is generally our practice to use the
scientific name of the species in the
beginning of the document for avian
species, and, subsequently, refer to each
species by their common name;
however, in this section, we will
generally refer to the species by their
scientific names. There are many similar
cockatoo species, some of which have
similar sounding common names and
may be confused. For example, the
yellow-crested cockatoo is also referred
to as the lesser sulphur-crested
cockatoo, which is Cacatua sulphurea,
but there is also the sulphur-crested
cockatoo, which is C. galerita.
Additionally, because there are four
recognized subspecies of C. sulphurea,
using their scientific names is more
precise and clear. Finally, because there
are various local common names, it is
more effective to refer to these species
by their scientific names.
General Biology
Nest holes have been observed to be
6 to 18 m (20 to 60 ft) above ground
(Setiawan 1996 in Prijono 2008, p. 3).
Two tree species used by Cacatua
sulphurea for nesting include Sterculia
foetida (wild almond tree) and
Tetrameles nudiflora (Binong) (Widodo
2009, p. 85). There does not appear to
be a set or restricted breeding season
(Prijono 2008, p. 3); the breeding season
may coincide with the availability of
nutrients in food sources. Incubation is
shared by both parents. Incubation lasts
28 days, and the nestling period is 65
days until fledging (Cameron 2007, p.
140).
Their diet includes Mangifera indica
(mango); Carica papaya (papaya); Ficus
spp. (fig); Psidium guajava (guava);
Eugenia malaccensis (jambu bol);
Opuntia elation (prickly pear); Annona
squamosa (srikaya); flowers of Cocos
nucifer (coconut); Tamarindus indica
(tamarind); flowers and fruit of
Avicennia (mangrove); fruit of Dehaasia
(marangtaipa) and young leaves of
Sonneratia (mangrove); and ninifo,
thought to be within the Canarium
genus (Nandika 2006, p. 10).
Feral Populations
Feral populations of released or
escaped captive-held yellow-crested
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cockatoos have established themselves
outside of their native range; however,
they exist in low numbers (Ling and Lee
2006, p. 188). Between 1986 and 2000,
11 feral yellow-crested cockatoos were
observed in Taiwan (Ling and Lee 2006,
p. 190). Cacatua sulphurea has also
become feral in places such as
Singapore, Hong Kong, New Zealand,
and Western Australia. In 1998, the
species was described as being locally
common in south and east Singapore,
including the islets of St. John’s and
Sentosa, and reportedly breeding in
gardens and parks, with possibly
between 30 and 50 birds existing there
(PHPA/LIPI/BirdLife International-IP
1998 in BLI 2001, p. 1652).
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Population Estimates
This species was formerly locally
common throughout much of its range.
There is evidence of substantial
population declines on Sulawesi, where
it may already be beyond recovery
(Andrew and Holmes 1990; Cahyadin
and Arif 1994; Gilardi 2011, pers.
comm.), and the Lesser Sundas, where
it is believed to be close to extinction on
Sumbawa and Flores. It is still fairly
common in the Komodo National Park
(Butchart et al. 1993; Holmes in litt.
1994; Prijono et al. 2008, p. 7). As of
2001, Cacatua sulphurea sulphurea
only existed in tiny remnant numbers,
except perhaps for a small population in
Rawa Aopa Watumohai National Park
(BLI 2001, p. 1648). C. sulphurea is
extinct on Lombok (BirdLife-IP in litt.
1997). C. s. abbotti is at a critically +low
population level; C. s. parvula is doing
fairly well on Komodo in Komodo
National Park; and C. s. citrinocristata
persists but was steadily declining on
Sumba (BLI 2001, p. 1648). On Nusa
Penida, this subspecies was last
recorded in 1986 (van Helvoort in van
Balen 1994).
Population estimates for each
subspecies vary in part due to the
remoteness of the islands where they
exist. The BLI 2010 Web site reported
that there are between 2,500 and 9,999
mature individuals collectively
remaining in the wild; however, these
data have not been updated based on
recent information reported from a local
organization in Indonesia. Population
estimates for each subspecies are as
follows: Cacatua sulphurea abbotti, 40;
C. s. citrinocristata, 100 to 2,000; C. s.
parvula, 800 to 1500; C. s. sulphurea,
100 to 150. The population estimates
and a discussion of the subspecies’
status are presented in more detail
below.
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Cacatua sulphurea abbotti
Abbott’s cockatoo, the largest of the
yellow-crested cockatoos, is only known
from a single island, Solombo kecil (or
Masalembu kecil pulau), which is 500
ha (1,235 ac) and in the Masalembu
Archipelago in the Sulawesi Strait. This
island is in the Java Sea, north of the
cities of Surabaya and Bali, and east of
southern Sumatra. The subspecies is
considered to be extirpated from
Masalembu Island (also known as
Salembo Besar) (Indonesian Parrot
Project 2010). C. s. abbotti has a mostly
white body with a brilliant yellow,
forward-curving crest, and slight yellow
on its ear covert feathers. The species
prefers very large trees within the
Datiscaceae family for nesting (Snyder
2000, p. 69). When Abbott first found
the endemic form abbotti in 1907, he
‘‘reported it in hundreds’’ on
Masalembu (Oberholser 1917 in BLI
2001, p. 1651). Only between 8 and 10
individuals of the subspecies abbotti
were located in 1993 on the Masalembu
Islands (Jones et al. in prep. in Cahyadin
and Arif 1994), and 6 to 8 birds were
found in 1998. In 2008, a few
individuals were found on Solombo
kecil Island. In IPP’s last population
survey, they found that on Solombo
kecil, only about 30 individuals remain
(Metz 2010, pers. comm.). The
population of this subspecies as a whole
has declined over 80 percent within
three generations (45 years). Although
the Indonesian Parrot Project has started
a conservation program for this
subspecies, it is too early to report on
progress of the conservation program.
Cacatua sulphurea citrinocristata
The subspecies citrinocristata is
found on Sumba, where the 2002
estimate of the population was between
565 and 2,054 individuals (Cahill et al.
2006, p. 265; Persulessy et al. 2003 in
Prijono 2008, p. 5). Another 2002 survey
by WCS found a density of 4.3 birds per
km2 within the two national parks,
Manupeu-Tanadaru and LaiwangiWanggameti (Kinnaird 2003 in Prijono
2008, p. 5). On Sumba. C. s.
citrinocristata’s population in 1995 was
estimated to be just over 3,000 (Jones et
al. 1995, p. 39). Earlier surveys in 1989
and 1992 (Marsden 1995 in Prijono
2008, p. 5) estimated the total
population of C. s. citrinocristata was
between 1,150 and 2,644 birds. On
Sumba, C. s. citrinocristata populations
increased between 1992 and 2002, likely
due to moratoria on international trade
and local protections (Cahill et al. 2006,
p. 162). The most recent survey is not
publicly available, but the population
on Sumba is now thought to be roughly
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100 birds (Gilardi 2011a, pers. comm.).
The earlier population estimates may
have been overly optimistic based on
surveying techniques, or the population
has rapidly declined.
Sumba Island is located in the Lesser
Sundas in southeastern Indonesia. The
island is 12,000 km2 (4,633 mi2), 210 km
(130 mi) in length, and 50 km (31 mi)
south of Flores Island. Its highest point
is Gunung Wanggameti at 1,225 m
(4,019 ft). Precipitation is between 500
and 2,000 mm annually (20 to 79
inches). As of 1995, forest covered less
than 11 percent of the island (McKnight
et al. in prep in Jones et al. 1995, p. 22)
and was confined to relatively small and
fragmented pockets.
The two national parks, covering
1,350 km2 (521 mi2), were established
on Sumba through Ministerial Decree
No. 576/Kpts-II in 1998. ManupeuTanadaru (280 km2 or 108 mi2) seems to
have the healthiest population of
cockatoos. It had the highest density of
cockatoos when surveyed both in 1992
and 2002 (Cahill et al. 2006, p. 164).
However, of 33 forest patches surveyed,
cockatoos were recorded in only 17
(O’Brien et al. 1997 in Cahill et al. 2006,
p. 166).
Cacatua sulphurea parvula
Historically, C. s. parvula was found
on most of the Lesser Sunda Islands
(also known as Nusa Tenggara)
including Penida, Lombok, Sumbawa,
Moyo, Komodo, Flores, Pantar, Alor,
Timor, and Semau Islands. Now this
subspecies is found on Alor, Pantar,
Komodo, and Sumbawa Islands. In the
past 10 years, populations of more than
10 cockatoos have been found at only
two locations (Setiawan et al. 2000;
Prijono 2008, p. 6). In 1994, on
Sumbawa, this subspecies was observed
at three sites and reported by islanders
to occur at 14 more, although in very
low numbers (Setiawan et al. 2000;
Widodo 2009, p. 84). In 2000, 80
individuals were observed on Alor
Island; the population estimate was 678
to 784 individuals.
As of 2001, it was thought that West
Timor and other small islands in the
Lesser Sundas could only support a few
individuals (PHKA/LIPI/BirdLife
International-IP 1998; Setiawan et al.
2000; Agista & Rubyanto 2001). The
most recent population estimate on
Timor-Leste (East Timor) is between 500
and 1,000 individuals (Trainor et al. in
litt. 2004). On Timor-Leste, C. s. parvula
was recorded in six locations (Tilomar,
Fatumasin, Sungai Clere, Lore, Monte
Paitchau–Iralalora, Mount Diatuto)
(Trainor 2002, pp. 93–99). Below is a
summary of recent observations and
population estimates for this subspecies.
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• Alor Island: 80 individuals
observed; population estimate was 678
to 784 individuals (Setiawan et al. 2000
in Widodo 2009, p. 84).
• Flores Island: 14 individuals
observed (Ria; Watubuku forest, part of
Lewotobi area, see Butchart et al. 1996
in Widodo 2009, p. 84).
• Komodo Island: 137 individuals
observed; population estimate was 150
(Imansyah et al. 2005).
• Moyo Island: 10 individuals
observed (Setiawan et al. 2000).
• Pantar Island: 29 individuals
observed; population estimate was 444
to 534 individuals (Setiawan et al.
2000).
• Sumbawa Island: 14 individuals
observed in 1996; subspecies observed
at three sites and reported by islanders
to occur at 14 more, although in very
low numbers (Setiawan et al. 2000).
• East Timor (Timor-Leste):
Population estimate was 500 to 1,000
individuals in 2004 (Trainor et al. 2005,
pp. 121–130).
• West Timor: 8 individuals observed
(Setiawan et al. 2000).
The largest known population, which
is on Komodo Island (311 km2 (120 mi2)
in size) in Komodo National Park, was
previously thought to be doing well, but
the subspecies’ population is declining
even here although the exact reasons are
unclear (Imansyah et al. 2005, 2 pp.).
Cockatoo poaching is believed to be
effectively eliminated due to
surveillance and enforcement, and there
is negligible loss of mature trees or
forest loss due to illegal logging (Ciofi &
de Boer 2004 in Prijono 2008, p. 8).
Flocks of 20 to 30 birds were seen
during observations between 1989 and
1995, and, in 1999, an estimated 100
birds were observed (Agista & Rubyanto
2001 and BirdLife 2001 in Prijono 2008,
p. 8). In Komodo National Park, C. s.
parvula was still relatively common
prior to 2001, and was most frequently
recorded in dry tropical forest (from sea
level to 350 m (1,148 ft)) dominated by
T. indicus (common name: date or
tamarind) and Sterculia foetida (Javaolive, poon tree, or skunk tree) (Agista
& Rubyanto 2001). The total population
size in Komodo National Park, which
spans several islands, is estimated to be
approximately 150 individuals on
Komodo Island (Imansyah et al. 2005, p.
2) and about 100 individuals on Rinca
Island (BLI 2010f).
Cacatua sulphurea sulphurea
The most recent information from
local NGOs suggests that only about 100
to 150 individuals of this subspecies
remain in the wild, and they are likely
only on Sulawesi Island. C. s. sulphurea
was formerly widely distributed in
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Sulawesi (formerly called Celebes);
however, since the early 1980s, this
subspecies has become very rare
(Prijono 2008, pp. 2–3). This was due to
high rates of poaching (CITES 2004a, p.
2). In 2001, between 7 and 15
individuals were observed on Pasoso
Island; however, the south and central
parts of the island have limited suitable
habitat consisting of mixed secondary
forest, scrub, and dryland agricultural
plots (Agista et al. 2001 in Prijono 2008,
p. 5).
Now, the subspecies is believed to
occur only in a small region of Sulawesi
(Metz 2010, pers. comm.).
Approximately 10 years ago, it was
documented in Rawa Aopa Watumohai
National Park (RAWNP) (Agista et al.
2001 in Prijono 2008, p. 5). Older
studies suggested that although some
small populations of this subspecies
may exist elsewhere, the remaining
cockatoos were likely confined to two
locations in southern Sulawesi: RAWNP
and Buton Island and in central
Sulawesi on Pasoso Island. Of these,
RAWNP is clearly the most significant
site. RAWNP is unique because it has
seven ecosystem types: tidal mudflats,
mangrove forest, wooded savannas, hill
forest, swamp forest, peat swamp, and
cultivation. Therefore this is a
significant site to concentrate
conservation efforts. However, it is
unlikely that this species occurs here
currently, although a separate species,
C. galerita, is believed to occur in this
park.
Conservation Status for the YellowCrested Cockatoo
In 1981, Cacatua sulphurea (and all of
its subspecies) was listed in CITES
Appendix II. In 2005, it was uplisted to
Appendix I, thus commercial trade is
generally prohibited (see above
discussion with respect to CITES for
additional information). C. sulphurea is
listed on the IUCN Redlist as Critically
Endangered. It is also protected in the
U.S. by the WBCA (refer to discussion
under the Crimson Shining Parrot,
factor D).
It is against Indonesian law to capture
Cacatua sulphurea for the export trade.
C. sulphurea is protected by the Act on
the Conservation of Biological
Resources and their Ecosystems (Act
No. 5 of 1990), and there has been no
catch quota for this species since 1994.
Violation of this law by capture,
possession, or trade in this species
could result in up to 5 years in prison
and a fine of up to 200 million rupiahs
($22,870 USD; Prijono 2008, p. 13). In
1997, C. sulphurea was protected within
Indonesia by Forestry Ministerial
Decrees No. 350/Kpts-II/1997 and No.
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49229
522/Kpts-II/1997. Although a
cooperative recovery plan has been
developed and put into place for C.
sulphurea, it is unclear how effective it
is; there are no clear indications that the
species’ situation is improving.
Protections exist in several areas such as
the Rawa Aopa Watumohai and
Caraente National Parks (on Sulawesi),
which may support approximately 100
individuals (Nandika 2006, pp. 10–11);
Suaka Margasatwa Nature Reserve on
Pulau Moyo; Komodo National Park;
and two national parks on Sumba,
Manupeu-Tanahdaru and LaiwangiWanggameti. The Nini Konis Santana
National Park in Timor also may have
a population of approximately 100 birds
(Trainor 2002 in Prijono 2008, p. 9). In
Timor-Leste, BirdLife International
identified 16 Important Bird Areas
(IBAs). Although this designation does
not confer any measure of protection,
some of these IBAs may be vital to this
species, particularly since the majority
of the IBAs are located in coastal areas
(BirdLife International 2007).
For Cacatua sulphurea abbotti, the
Indonesian Parrot Project (IPP) initiated
an intensive conservation program on
Solombo kecil Island. Visits were made
to junior and senior high schools to
teach students about the principles of
conservation, increase their awareness
of the plight of this species, and foster
pride in this species, emphasizing that
it is their rare and unique bird. Laws to
protect these birds have been passed but
only in the distant ‘‘kabupatan’’
(district) of Madura. These decrees are
out of date, but there are plans to update
them and extend them locally to the
islands of the Masalembu Archipelago
themselves, where they are more likely
to be enacted. Officers from the local
armed forces and police were taught
about the protections already in place
nationally and internationally, and were
encouraged to conserve the birds (IPP
2008, pp. 3–4). Nest boxes and use of
wardens are other conservation methods
used. Konservasi Kakatua Indonesia
(KKI, also known as Cockatoo
Conservation Indonesia) is another NGO
working to protect this species.
There are only about 100 to 150
Cacatua sulphurea sulphurea left in the
wild, solely on Sulawesi Island. IPP
recently instituted a conservation
program for this subspecies; however, it
is still in its preliminary stages.
Evaluation of Factors Affecting the
Yellow-Crested Cockatoo
We examine the effects on the species
based on each of the 5 factors listed
under the section 4(a)(1) of the ESA.
Under the ESA and our implementing
regulations, a species may warrant
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listing if it is endangered or threatened
throughout all or a significant portion of
its range. The yellow-crested cockatoo is
highly restricted in its range and the
threats to it occur throughout its range.
Therefore, we assessed the status of the
species throughout its entire range. The
threats to the survival of this species
occur throughout the species’ range and
are not restricted to any particular
portion of its range. Accordingly, our
assessment and proposed determination
applies to the species throughout its
entire range. Unless our status review
finds that there is a unique threat to a
particular subspecies, we will consider
all of the subspecies to be facing
equivalent threats, as their habitats are
very similar and they are all island
endemics in the same region. Like the
white cockatoo, the greatest threats to
cockatoos in Indonesia and other range
countries is poaching from the wild for
the illegal pet trade (usually nestlings
are taken), logging, and other forms of
deforestation and habitat destruction. In
order to be efficient, if the threats are
the same threats affecting a species
discussed above, we will summarize
these threats and refer to a discussion in
the document above if it is not unique
to this species or subspecies.
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Factor A. The Present or Threatened
Destruction, Modification, or
Curtailment of the Species’ Habitat or
Range
Habitat destruction such as that
described above for white cockatoos
also threatens Cacatua sulphurea.
Deforestation is pervasive throughout
Indonesia and Timor-Leste (Costin and
Powell 2006, p. 2; Laurance 2007, p.
1,544). For example, on Solombo kecil
Island, trees that have suitable habitat to
provide food and nest holes for C. s.
abbotti are logged. Their habitat on this
island has been essentially destroyed
and replaced with coconut palms.
Almost total destruction of habitat flora,
such as kapuk trees (Ceiba pentandra)
and mangrove (Avicennia apiculata)
which are preferred by the species, has
occurred (IPP 2008, p. 3). Cockatoos
consume fruit of tall timber trees such
as ‘‘kayu besi’’ (Intsia bijuga), the source
of ‘‘ironwood’’ for building, and
tangkalase (scientific name unknown), a
deciduous hardwood tree (Nandika
2006, p. 10). These trees are
disappearing or gone from the island. In
the past, cockatoo nests seemed to be
safe from trappers if they were
sufficiently high. The decrease in such
trees likely played a vital role in the
species’ decline (Marsden and Jones
1997 in Snyder 2000, p. 70) in two
ways: by decreasing suitable trees for
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nesting sites and by forcing cockatoos to
locate nesting sites lower in the canopy.
This type of habitat loss affects all
four subspecies. In the case of Cacatua
sulphurea abbotti, coconut palms have
been planted, displacing their favored
habitat flora such as kapuk trees and
mangrove. The main cause of forest loss
for C. s. citrinocristata has been the
clearing and repeated burning of
vegetation to provide land for grazing
and cultivation, although between 1992
and 2002, there was no evidence of
additional forest loss (Cahill et al. 2006,
p. 165). Removal of trees for local use
occurs, but there is no commercial
logging on Sumba. In many areas, as a
result of the shifting cultivation and
annual burning for cattle grazing, the
original vegetation has been replaced by
fire-resistant trees, shrubs, and grasses.
Where grazing and burning have been
particularly intensive, the grasslands
have become degraded and soil erosion
is evident. A study found that on Sumba
Island, birds were absent or rare in
forest areas of less than 10 km2
(Kinnaird et al. 2003 in Prijono 2008, p.
4). Jones et al. indicated that in order to
protect the few remaining C. s.
citrinocristata, the areas of remaining
forest on Sumba Island must be
preserved (1995, p. 49).
For Cacatua sulphurea parvula, the
largest population is thought to be on
Komodo Island in Komodo National
Park. This park includes three major
islands: Komodo, Rinca and Padar, in
addition to several smaller islands
(https://www.komodonationalpark.org,
accessed March 3, 2011). Its total marine
and land surface area is 1,817 km2 (701
mi2). Due to the dryer climate, wildfires
are a problem (Imansyah, unpublished,
in Imansyah et al. 2005, p. 2).
Researchers believe that the species’
decline may be due to the lack of
nesting sites.
The yellow-crested cockatoo resides
in lowland forests predominately
between 100 to 600 m (328 to 1,968 ft)
throughout these islands, with the
highest densities of birds occurring in
little-disturbed forests. The locations
where the subspecies is thought to exist
currently, as well as the most recent
population estimates, may be found
below under the Factor B discussion.
Both legal and illegal logging have been
the primary threats to the habitat of this
species, with the threats occurring
throughout the islands in lowland
forests, decreasing available habitat
(Prijono 2008, p. 1; Widodo 2009, p. 81).
For example, research found that for
every 100 km2 (38.6 mi2) of Seram’s
primary forests that were selectively
logged in the last 6 years, 700 birds were
likely lost from the cockatoo population
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(Marsden 1992, p. 12). Similarly, for
every 100 km2 of locally disturbed
secondary forest that were converted to
plantations, 600 birds were likely lost
from the cockatoo population. Even
when habitat is protected, there is
generally little undisturbed habitat
available, and it is of less suitable
quality.
Cockatoos are highly impacted by
selective logging of primary forests,
especially since reduced-impact logging
techniques are seldom applied.
Selective logging, which targets mature
trees, has a substantial negative impact
on tree-cavity nesters such as Cacatua
sulphurea. The abundance of cockatoos
is positively related to the density of its
preferred nest trees (large trees that
would be impacted by logging).
Once the primary forest is logged,
land use on other Indonesian islands
shows that the secondary forest is
generally converted to other uses or
logged again rather than being allowed
to return to primary forest. Therefore,
although cockatoos may continue to
inhabit secondary or degraded forests on
their respective islands, their
populations will be at substantially
lower numbers. The trend of high loss
of primary forests and degradation of
secondary forests is of concern because
little is known about the reproductive
ecology of Cacatua sulphurea in the
wild, including breeding success in
mature forests versus secondary forests,
and whether these cockatoos will
survive in degraded forests in the long
term. However, surveys indicate that the
species is declining in the wild.
In summary, extensive logging, both
legal and illegal, has damaged Cacatua
sulphurea habitat. In some areas,
deforestation and habitat degradation
are still occurring. The populations have
decreased on all islands, and there is no
sign of improvement. Therefore, we find
that the present and threatened
destruction, modification, or
curtailment of its habitat is a threat to
the continued existence of this species
throughout all of its range.
Factor B. Overutilization for
Commercial, Recreational, Scientific, or
Educational Purposes
Poaching for the pet trade is a factor
that also affects Cacatua sulphurea. Not
only are cockatoos desirable pets, but
this species is also very vocal and
conspicuous, making it an easy target
for poaching (Jepson and Ladle 2005,
pp. 442, 447; Prijono 2008, pp. 4–5).
Extremely heavy trade during the 1970s
and 1980s was indicated as the main
cause of the decline of this species
(BirdLife International-IP, 1998; BLI
2004 in Cahill et al. 2006, p. 161).
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Between 1981 and 1992, 96,785 C.
sulphurea were reported to have been
exported from Indonesia (UNEP–
WCMC, in Cahill 2006, p. 162). In 1992,
cockatoos were worth approximately
$55 USD to the wholesalers who export
birds to Java (Marsden 1995 in Cahill et
al. 2006, p. 165).
From the data collected by ProFauna
about animal markets in Java and Bali,
the domestic trade in parrots is still at
a high level (ProFauna 2008, pp. 2–8).
Many investigations indicate that these
cockatoos could fairly easily be
exported and at some point their origin
would be unknown, yet indicated as
captive-origin (BLI 2003, p. 2).
TABLE 2—LIVE EXPORTS OF Cacatua
sulphurea BETWEEN 2000 AND
2009 (UNEP–WCMC 2010)
Total number of specimens exported .......
Total number of specimens exported as
captive ...................................................
Total number of specimens exported as
wild .........................................................
Total other or unknown .............................
No source code reported ..........................
Top 3 exporters:
Number of specimens exported from
South Africa ....................................
Number of specimens exported from
Indonesia ........................................
Number of specimens exported from
the Philippines ................................
4,806
4,719
50
23
9
1,799
508
481
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Note: This number does not report specimens exported as Cacatua sulphurea citrinocristata. There
was data reported in the UNEP–WCMC database
for this subspecies but not for the other C.
sulphurea
subspecies
(https://www.unepwcmc.org).
On Sumba Island, evidence of
cockatoo trapping was seen in 1996
(Kinnaird 1999), and shipments of
cockatoos were confiscated on Sumba in
1998 and again in 2002 (when 32 were
seized). In 2002, an investigation found
that one collector in Waikabubak
exported 52 yellow-crested cockatoos to
other islands (Persulessy et al. 2003 in
CITES 2004a, p. 6). In 2002, evidence
was found of cockatoo trapping at
Manupeu and Langgaliru, mainly in the
form of snaring. Many nests at
Poronumbu even had ladders attached
to them for nest raiding, suggesting that
trapping activity was relatively high at
this site even in 2002 (Cahill et al. 2006,
p. 166).
IPP, a local NGO which is actively
working to protect Cacatua sulphurea,
noted specific threats to the subspecies
on Solombo kecil Island. They found
that usually nestlings, rather than adult
birds, are taken. According to ProFauna,
nestlings are worth 2 to 3 times more
than adults (2008, p. 8). Historically,
cockatoos were trapped in large
numbers by outside visitors who took
them to Bali and Sumbawa Islands.
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Studies by social anthropologists of
locals in Seram and Halmahera showed
that parrot catching accounted for 25 to
30 percent of their cash income
(Badcock in litt. 1997, in Snyder et al.
2000, p. 60). Among the Halafara people
of the Manusela valley on Seram, locals
would catch and sell parrots to raise
their bride price (Badcock in litt. 1997,
in Snyder et al. 2000, p. 60). Now, with
the marked decline in their numbers,
the birds are even sought by government
officials, who keep them as pets due to
the prestige of owning such a rare bird
(IPP 2008, p. 3).
Due to high demand for cockatoos and
based on trade reports in 1993, the
CITES Standing Committee
recommended that countries suspend
imports from Indonesia, pending
surveys to assess the status of the
species after a significant trade review
(CITES 2001, AC17 Inf. 3 p. 4; CITES
Notification to the Parties No. 737).
Singapore continued to re-export wildcaught birds originating from Indonesia
after the export suspension of Indonesia
in 1994 (CITES 2001, AC17 Inf. 3 p. 4).
In total, 1,229 wild-caught birds were
reported to be re-exported from
Singapore between 1994 and 1999
(CITES 2001, AC17 Inf. 3 p. 4; WCMC
2001 in CITES 2004a, pp. 9–10).
Although trade was recognized to be a
problem, this species was not listed on
Appendix I of CITES until 2005.
Poaching for the pet trade, as with all
cockatoo species referenced in this rule,
is a significant threat to this species as
well.
Although some subspecies are
monitored and are on remote islands,
poaching still occurs. Poaching can be
extremely lucrative, and there is
relatively low risk involved in poaching.
None of these subspecies is fully
protected from the illegal pet trade.
Based on our review, we find that
overutilization, specifically poaching for
the pet trade, continues to be a threat to
Cacatua sulphurea throughout its range.
Factor C. Disease or Predation
There is no evidence that disease or
predation is a threat to Cacatua
sulphurea in the wild. Our review did
not find any indication that disease is a
threat to C. sulphurea. With respect to
predation, two predators, a spotted
kestrel (Falco moluccensis) and a white
bellied sea-eagle (Haliaeetus
leucogaster), have been observed
attacking cockatoos (Prijono 2008, pp.
4–5). Although C. sulphurea has natural
predators, to our knowledge, these
predators are not having a negative
impact on the species. After a review of
the best scientific and commercial
information, we conclude that neither
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disease nor predation are threats to C.
sulphurea.
Factor D. The Inadequacy of Existing
Regulatory Mechanisms
After surveys conducted in the late
1990s by the Directorate-General of
Forest Protection and Nature
Conservation (PHPA) and BirdLife
International-Indonesia, it was
determined that Cacatua sulphurea
populations had collapsed (Snyder et al.
2000, p. 59). Prior to 1993, at which
time legal trade was prohibited, there
was a reported average of 1,600 C. s.
citrinocristata individuals being
removed from Sumba annually, yet the
1992 population was only
approximately 3,200 (Cahill et al. 2006,
p. 161). This level of trade was quite
obviously unsustainable. The
population had increased, likely due to
the moratorium on international trade
and local protections (Cahill et al. 2006,
p. 164); however, the population is
declining now (BLI 2010d; Metz 2010,
pers. comm.). In 1992, the Regent of
West Sumba (Decree no. 147) banned
trapping and transport of cockatoos.
This was followed by a similar decree
in East Sumba (Decree no. 21), and in
1994, the government of Indonesia
imposed a zero export quota (Cahill et
al. 2006, p. 162). In 1997, this species
was provided additional protection by
the Forestry Ministerial Decrees No.
350/Kpts–II/1997 and No. 522/Kpts–II/
1997.
According to a CITES 2004 proposal
to uplist Cacatua sulphurea to
Appendix I, the Philippines, Singapore,
South Africa, and Indonesia were the
main countries exporting captive-bred
specimens of Cacatua sulphurea. In
Indonesia and Singapore, there has been
a ‘‘sudden turn up of captive bred
specimens since 1994, the time the legal
trade in wild specimens stopped’’
(CITES 2004, p. 5). In 2004, two captive
breeding operations of C. sulphurea
were identified in Indonesia: PT. Bali
Exotica Fauna and PT. Anak Burung
Tropikana. Both of these companies
were located in Bali Province (CITES
2004a, p. 5). Currently, however, there
are no CITES-registered operations for
breeding C. sulphurea for commercial
purposes (CITES 2010d, npn.).
When the proposal to transfer the
Cacatua sulphurea from Appendix II to
Appendix I (CITES CoP13, 2–14
October, Bangkok, Thailand) was being
considered in 2004, BLI noted in their
position paper that the difficulty in
distinguishing captive-bred birds from
wild ones is facilitating both illegal
capture from the wild and illegal
international trading of the captured
birds (BLI 2003). They pointed to
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examples of these birds found in
markets in Indonesia (BLI 2003 p. 2).
Between 2000 and 2009, the UNEP–
WCMC Trade Database indicated that
4,837 live specimens of Cacatua
sulphurea were exported (subspecies
are unknown). Between the same time
period, an additional 1,648 live
specimens of C. s. citrinocristata were
reported to be exported. In 2009 alone,
11 live specimens of C. s. citrinocristata
were exported from South Africa to the
United Arab Emirates, one of the
countries most frequently importing
cockatoos (https://www.unep-wcmc.org/
citestrade). Nearly all of these were
documented as captive-bred, but
wildlife laundering does still occur
´
´
(ProFauna 2008; 2010; Cantu-Guzman et
al. 2007, 121 pp.) and is quite lucrative.
A 2003 IUCN review found that
Cacatua sulphurea is readily available
in Indonesian bird markets (BLI 2003,
pp. 1–2). Poaching is relatively easy,
poverty is widespread, and there is little
incentive or awareness for local
communities to conserve their
resources. Although the species occurs
within a number of protected areas and
a recovery plan was initiated in 1998,
declines are still occurring. Birds are
still likely smuggled to and exported
from Singapore and the Philippines, at
a minimum (ProFauna 2008). Continued
trapping and large-scale logging that are
not sufficiently regulated or mitigated
by the Indonesian government remain
threats to the species. For some
subspecies, there are specific local
protections in place, but they are
inadequate to combat the threats facing
the species according to a local NGO
who works on the conservation of this
species. For example, a local law for the
protection of C. s. abbotti exists, which
IPP assisted in obtaining in 2010 (Metz
2010, pers. comm.).
With respect to the adequacy of
internal government controls within
Indonesia, we find that they are
inadequate (refer to discussion and
finding under Factor D for the white
cockatoo, which faces the same threats
with respect to this factor). Poaching
and illegal trade of this species continue
to occur. This species continues to
experience population declines, and the
protections in place are inadequate to
protect this species. CITES regulates
international trade of this species, and
we have no evidence to suggest that
CITES is inadequate in regulating legal
trade of this species. Therefore, we find
that the inadequacy of regulatory
mechanisms is a threat to Cacatua
sulphurea throughout its range.
Factor E. Other Natural or Manmade
Factors Affecting Its Continued
Existence
Interspecific Competition
The Komodo dragon (Varanus
komodoensis) preys upon eggs and uses
nests of Cacatua sulphurea during the
species’ arboreal phase. Observations
have been made of competition between
the dragon and cockatoo when using the
tree Sterculia foetida for nesting (Agista
& Rubyanto 2001 in Prijono 2008, p. 4).
Although individuals of C. sulphurea
may be subject to occasional
competition with Komodo dragons,
there is no evidence that this is
occurring at a level which may affect the
status of C. sulphurea on Komodo
Island as a whole.
Small and Declining Population
All four subspecies of Cacatua
sulphurea have very limited geographic
ranges and small, declining populations.
Their existing populations are extremely
localized, and sometimes geographically
isolated from one another, leaving them
vulnerable to localized extinctions from
habitat modification and destruction;
natural catastrophic changes to their
habitat (e.g., flood scour, drought); other
stochastic disturbances; and decreased
fitness from reduced genetic diversity. It
is likely that fewer than 1,000 to 2,000
individuals representing each
subspecies remain in the wild; in the
case of C. s. abbotti and C. s. sulphurea,
there are likely fewer than 100 of each
subspecies (Metz 2010, pers. comm.)
(see Table 3).
TABLE 3—YELLOW-CRESTED COCKATOO POPULATION ESTIMATES
Species
Where found and date of population estimate
Estimated number remaining in
the wild
Yellow-crested cockatoo (Cacatua sulphurea) ..........................
Subspecies:
C. s. abbotti ........................................................................
C. s. citrinocristata ..............................................................
C. s. parvula .......................................................................
Indonesia and Timor-Leste ......................................................
2,500 to 6,000*
Sulawesi Strait (2010) ..............................................................
Sulawesi Strait (2002) ..............................................................
Sulawesi Strait (2000, 2009) ....................................................
Timor (2000, 2004) ...................................................................
Sulawesi Strait (2010) ..............................................................
30
565 to 2,054
500 to 2,000
500
100 to 150
C. s. sulphurea ...................................................................
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* Number includes all four subspecies.
Species with limited geographic
ranges and small, declining populations
are extremely vulnerable. Demographic
stochasticity may affect this species as
well, and is defined as chance changes
in the population growth rate for a
´
species (Gilpin and Soule 1986, p. 27).
Population growth rates are influenced
by individual birth and death rates
´
(Gilpin and Soule 1986, p. 27),
immigration and emigration rates, and
changes in population sex ratios.
Natural variation in survival and
reproductive success of individuals and
chance disequilibrium of sex ratios may
act in concert to contribute to
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demographic stochasticity (Gilpin and
´
Soule 1986, p. 27).
Genetic stochasticity is caused by
changes in gene frequencies due to
genetic drift, diminished genetic
diversity, effects due to inbreeding (i.e.,
inbreeding depression), or a
combination of these factors (Lande
1995, p. 786). 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
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of individuals in the population
(Charlesworth and Charlesworth 1987,
p. 231; Shaffer 1981, p. 131).
Environmental stochasticity is defined
as the susceptibility of small, isolated
populations of wildlife species to
natural levels of environmental
variability and related ‘‘catastrophic’’
events (e.g., severe storms, extreme cold
spells, wildfire) (Dunham et al. 1999, p.
9; Mangel and Tier 1994, p. 612; Young
1994, pp. 410–412). Each risk will be
analyzed specifically for each species.
Small, isolated populations of wildlife
species that have gone through a
reduction in population numbers can be
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susceptible to demographic and genetic
problems (Shaffer 1981, pp. 130–134).
These threat factors, which may act in
concert, include: Natural variation in
survival and reproductive success of
individuals; chance disequilibrium of
sex ratios; changes in gene frequencies
due to genetic drift; diminished genetic
diversity and associated effects due to
inbreeding (i.e., inbreeding depression);
dispersal of just a few individuals; a few
clutch failures; a skewed sex ratio in
recruited offspring over just one or a few
years; and chance mortality of just a few
reproductive-age individuals. These
small populations are also susceptible to
natural levels of environmental
variability and related catastrophic
events, which we will refer to as
environmental stochasticity (Dunham et
al. 1999, p. 9; Mangel and Tier 1994, p.
612; Young 1994, pp. 410–412).
Based on the best scientific and
commercial information available, we
conclude that Cacatua sulphurea’s very
small and rapidly declining populations
are a threat to the species throughout its
range, particularly when combined with
other threats to this species.
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Finding for the Yellow-Crested
Cockatoo
As required by the ESA, we
considered the five factors in assessing
whether Cacatua sulphurea is
endangered or threatened throughout all
or a significant portion of its range. We
examined the best scientific and
commercial information available
regarding the past, present, and future
threats faced by C. sulphurea. We
reviewed the petition, information
available in our files, and other
available published and unpublished
information.
We analyzed the potential threats to
Cacatua sulphurea, including habitat
loss and habitat degradation, take for the
pet trade, disease and predation, and the
inadequacy of regulatory controls. We
found that habitat loss as a result of
deforestation is a threat to C. sulphurea,
and the subspecies are declining
rangewide. This species faces
immediate and significant threats,
primarily from the destruction and
modification of its habitats from logging
(Factor A). Efforts such as reforestation
and building of nest boxes may continue
to improve the habitat of this species,
which may subsequently increase their
numbers. However, no improvement has
been seen yet as a result of conservation
efforts (Metz 2010, pers. comm.). We
conclude that the present or threatened
destruction, modification, or
curtailment of its habitat or range is a
significant threat to C. sulphurea.
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We found information that poaching
for the pet trade is also a significant
threat to the species. Illegal poaching of
the cockatoo for the pet trade is still
common, despite existing laws,
education, and public awareness
campaigns. Pet birds are an important
part of Indonesian culture, with large
numbers of wild-caught parrots traded
domestically and internationally.
Trappers remain active, and wild-caught
birds are openly sold in Asian markets
(Prijono 2008, p. 18). Efforts to curtail
illegal trade are hampered by
Indonesia’s large coastline and
enforcement officials with limited
resources and knowledge. The
continuing illegal trade of the cockatoo
is a threat to the survival of the species.
Therefore, we find overutilization for
commercial, recreational, scientific, or
educational purposes (Factor B) is a
threat to Cacatua sulphurea throughout
its range.
We found no evidence that diseases
significantly affect Cacatua sulphurea
in the wild. Other avian species may be
susceptible to certain diseases, but there
is no evidence that disease occurs to an
extent that it is a threat to this species.
Predation was not found to affect C.
sulphurea populations; however, we
will continue to monitor this factor.
Based on the best available information,
we conclude that neither disease nor
predation (Factor C) is a threat to the
species throughout its range.
Although Indonesia has a good legal
framework to manage wildlife and their
habitats, implementation of its laws and
regulatory mechanisms has been
inadequate to address the threats to
Cacatua sulphurea. Logging laws and
policies are frequently ignored and
rarely enforced, and illegal logging is
rampant, even occurring in national
parks and nature reserves (Prijono
2008). The illegal trade of this species
continues to occur. The current range of
C. sulphurea is much smaller than its
historical range. The population
estimates for each subspecies range from
30 to 2,054 individuals. Threats to C.
sulphurea continue, and based on the
best available information, the
population trends are declining. Thus,
we conclude that inadequate regulatory
mechanisms are a threat to C. sulphurea
throughout its range.
Finally, we conclude that small,
declining populations of Cacatua
sulphurea are a threat to the species,
particularly when combined with the
other threats to the species (Factor E).
Despite the conservation measures in
place, this species faces severe threats,
and the population trend for this species
continues to decline. Based on our
review of the best available scientific
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49233
and commercial information pertaining
to the five factors, we find that Cacatua
sulphurea is in danger of extinction
(endangered) throughout all of its range.
Therefore, we propose to list C.
sulphurea as endangered under the
ESA.
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.
The ESA and its implementing
regulations set forth a series of general
prohibitions and exceptions that apply
to all endangered and threatened
wildlife. These prohibitions, at 50 CFR
17.21 and 17.31, in part, make it illegal
for any person subject to the jurisdiction
of the United States to ‘‘take’’ (includes
harass, harm, pursue, hunt, shoot,
wound, kill, trap, capture, or to attempt
any of these) within the United States or
upon the high seas; import or export;
deliver, receive, carry, transport, or ship
in interstate commerce in the course of
commercial activity; or sell or offer for
sale in interstate or foreign commerce
any endangered wildlife species. It also
is illegal to possess, sell, deliver, carry,
transport, or ship any such wildlife that
has been taken in violation of the ESA.
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 for endangered species are
codified at 50 CFR 17.22. 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. For
threatened species, a permit may be
issued for the same activities, as well as
zoological exhibition, education, and
special purposes consistent with the
ESA.
Special Rule
Section 4(d) of the ESA states that the
Secretary of the Interior (Secretary) may,
by regulation, extend to threatened
species prohibitions provided for
endangered species under section 9 of
the ESA. Our implementing regulations
for threatened wildlife at 50 CFR 17.31
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incorporate the section 9 prohibitions
for endangered wildlife, except when a
special rule is promulgated. For
threatened species, section 4(d) of the
ESA gives the Secretary discretion to
specify the ESA prohibitions and any
exceptions to those prohibitions that are
appropriate for the species. A special
rule allows us to include provisions that
are tailored to the specific conservation
needs of the threatened species and
which may be more or less restrictive
than the general provisions at 50 CFR
17.31.
The proposed special rule for the
white cockatoo, in most instances,
adopts the existing conservation
regulatory requirements of CITES and
the WBCA as the appropriate regulatory
provisions for the import and export of
certain captive white cockatoos. It
would also allow interstate commerce.
However, import and export of birds
taken from the wild after the date this
species is listed under the ESA, take,
and foreign commerce would need to
meet the requirements of 50 CFR 17.31
and 17.32. ‘‘Take’’ under the ESA
includes both harm and harass. When
applied to captive wildlife, take does
not include generally accepted animal
husbandry practices, breeding
procedures, or provisions of veterinary
care for confining, tranquilizing, or
anesthetizing, when such practices,
procedures, or provisions are not likely
to result in injury to the wildlife. When
conducting an activity that could take or
incidentally take wildlife, a permit
under the ESA is required.
If adopted, the proposed special rule
would allow import and export of
certain white cockatoos and interstate
commerce of this species without a
permit under the ESA as explained
below.
Import and export. The proposed
special rule would apply to all
commercial and noncommercial
international shipments of live white
cockatoos and parts and products,
including the import and export of
personal pets and research samples. It
proposes to allow a person to import or
export a specimen that was held in
captivity prior to the date this species is
listed under the ESA or that was
captive-bred provided the import is
authorized under CITES and the WBCA
and export is authorized under CITES.
The terms ‘‘captive-bred’’ and
‘‘captivity’’ used in the proposed special
rule are defined in the regulations at 50
CFR 17.3 and refer to wildlife produced
in a controlled environment that is
intensively manipulated by man from
parents that mated or otherwise
transferred gametes in captivity. The
proposed special rule would apply to
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birds captive-bred in the United States
and abroad. Import and export of
specimen that have been held in
captivity prior to the date this species is
list under the ESA or that was captivebred would be allowed without a permit
under the ESA provided the provisions
of CITES and WBCA are met. With
respect to captive-bred specimens, the
CITES import and export permits would
need to indicate that the specimen was
not taken from the wild by using a
source code on the face of the permit
other than U (unknown) or W (taken
from the wild). If the specimen was
taken from the wild prior to the date
this species is listed under the ESA, the
importer or exporter would need to
demonstrate that the cockatoo was taken
from the wild prior to that date. Under
the special rule, a person would need to
provide records, receipts, or other
documents when applying for permits
under CITES and WBCA to show the
specimen was held in captivity prior to
the date this species is listed under the
ESA.
We assessed the conservation needs of
the white cockatoo in light of the broad
protections provided to the species
under the WBCA and CITES. The
purpose of the WBCA is to promote the
conservation of exotic birds and to
ensure that international trade involving
the United States does not harm exotic
birds. The white cockatoo is also
protected by CITES, a treaty which
contributes to the conservation of the
species by monitoring international
trade and ensuring that trade in
Appendix II species is not detrimental
to the survival of the species (see
Conservation Status for the white
cockatoo). The best available
commercial data indicate that the
current threat to the white cockatoo
stems from illegal trade in the domestic
and international markets of Indonesia
and surrounding countries. Thus, the
general prohibitions on import and
export contained in 50 CFR 17.31,
which only extend within the
jurisdiction of the United States, would
not regulate such activities. Accordingly
we find that the import and export
requirements of the proposed special
rule provide the necessary and
advisable conservation measures that
are needed for this species.
Interstate commerce. Under the
proposed special rule, a person may
deliver, receive, carry, transport, ship,
sell, offer to sell, purchase, or offer to
purchase a white cockatoos in interstate
commerce. Although we do not have
current data, we believe there are a large
number of white cockatoos in the
United States. Current ISIS
(International Species Information
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System) information shows 252 white
cockatoos are held in U.S. zoos (ISIS
2008, p. 4). This number is an
underestimate, as some zoos do not
enter data into the ISIS database. We
have no information to suggest that
interstate commerce activities are
associated with threats to the white
cockatoo or would negatively affect any
efforts aimed at the recovery of wild
populations of the species. At the same
time, the prohibitions on take under 50
CFR 17.31 would apply under this
special rule, and any interstate
commerce activities that could
incidentally take cockatoos would
require a permit under 50 CFR 17.32.
Pet Birds
A ‘‘Pre’’-ESA (or ‘‘Pre-Act’’) specimen
of a species is one that was made or
obtained prior to the species being listed
under the ESA and has not been
involved in a commercial transaction
since that time. Specimens of species
held in captivity or in a controlled
environment on (a) December 28, 1973,
or (b) the date of publication in the
Federal Register for a final species
listing, whichever is later, are exempt
from prohibitions of the ESA, provided
such holding or any subsequent holding
or use of the specimen was not in the
course of a commercial activity (any
activity that is intended for profit or
gain). An affidavit and supporting
material documenting pre-ESA status
must accompany the shipment of any
listed species. A pre-ESA exemption
does not apply to wildlife, including
parts and products, offered for sale. In
order to export a pet bird, an owner
would need to provide information that
the specimen was acquired or held in a
controlled environment on or before (a)
December 28, 1973, or the date when
the species was listed, and (b) has not
entered into commerce (e.g., been
bought, sold, or offered for sale by you
or anyone else) since December 28,
1973, or the date when listed. Any
specimens of an endangered or
threatened species born in captivity
from pre-ESA parents are fully protected
and are not considered pre-ESA. See
https://www.fws.gov/forms/3-200-23.pdf
for additional information.
Section 7(a) of the Act, as amended,
and as implemented by regulations at 50
CFR part 402, requires Federal agencies
to evaluate their actions within the
United States or on the high seas with
respect to any species that is proposed
or listed as endangered or threatened
and with respect to its critical habitat,
if any is being designated. However,
given that these species are not native
to the United States, we are not
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designating critical habitat for these
species under section 4 of the Act.
Peer Review
In accordance with our policy,
‘‘Notice of Interagency Cooperative
Policy for Peer Review in Endangered
Species Act Activities,’’ that was
published on July 1, 1994 (59 FR
34270), we will seek the expert opinion
of at least three appropriate
independent specialists regarding this
proposed rule. The purpose of such
review is to ensure listing decisions are
based on scientifically sound data,
assumptions, and analysis. We will send
copies of this proposed rule to the peer
reviewers immediately following
publication in the Federal Register. We
will invite these peer reviewers to
comment, during the public comment
period, on the specific assumptions and
the data that are the basis for our
conclusions regarding the proposal to
list as endangered the Philippine
cockatoo (Cacatua haematuropygia) and
the yellow-crested cockatoo (C.
sulphurea), and to list as threatened the
white cockatoo (C. alba), under the ESA.
We will consider all comments and
information we receive during the
comment period on this proposed rule
during preparation of a final
rulemaking. Accordingly, our final
decision may differ from this proposal.
(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 names 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.
Paperwork Reduction Act (44 U.S.C.
3501 et seq.)
This proposed rule does not contain
any new collections of information that
require approval by the Office of
Management and Budget (OMB) under
the Paperwork Reduction Act. This rule
will not impose new recordkeeping or
reporting requirements on State or local
governments, individuals, businesses, or
organizations. We may not conduct or
sponsor, and you are not required to
respond to, a collection of information
unless it displays a currently valid OMB
control number.
Required Determinations
National Environmental Policy Act (42
U.S.C. 4321 et seq.)
Clarity of Rule
We are required by Executive Orders
12866 and 12988 and by the
Presidential Memorandum of June 1,
1998, to write all rules in plain
language. This means that each rule we
publish must:
(a) Be logically organized;
(b) Use the active voice to address
readers directly;
We have determined that we do not
need to prepare an environmental
assessment, as defined under the
authority of the National Environmental
Policy Act of 1969, in connection with
regulations adopted under section 4(a)
of the Act. We published a notice
outlining our reasons for this
determination in the Federal Register
on October 25, 1983 (48 FR 49244).
Species
Vertebrate population where endangered or threatened
Historic range
Common name
*
BIRDS
*
mstockstill on DSK4VPTVN1PROD with PROPOSALS2
*
Cockatoo, Philippine
Cockatoo, white .......
Cockatoo, yellowcrested.
*
Scientific name
*
*
Cacatua
haematuropygia.
Cacatua alba ..........
Cacatua sulphurea
20:38 Aug 08, 2011
Author
The primary authors of this notice are
staff members of the Branch of Foreign
Species, Endangered Species Program,
U.S. Fish and Wildlife Service.
List of Subjects in 50 CFR Part 17
Endangered and threatened species,
Exports, Imports, Reporting and
recordkeeping requirements,
Transportation.
Proposed Regulation Promulgation
Accordingly, we propose to amend
part 17, subchapter B of chapter I, title
50 of the Code of Federal Regulations,
as set forth below:
PART 17—[AMENDED]
1. The authority citation for part 17
continues to read as follows:
Authority: 16 U.S.C. 1361–1407; 16 U.S.C.
1531–1544; 16 U.S.C. 4201–4245; Pub. L. 99–
625, 100 Stat. 3500; unless otherwise noted.
2. Amend § 17.11(h) by adding new
entries for ‘‘Cockatoo, Philippine,’’
‘‘Cockatoo, white,’’ and ‘‘Cockatoo,
yellow-crested’’ in alphabetical order
under BIRDS to the List of Endangered
and Threatened Wildlife, as follows:
§ 17.11 Endangered and threatened
wildlife.
*
Status
*
*
(h) * * *
*
When listed
*
*
Critical
habitat
*
Special
rules
*
*
Entire ......................
*
E
*
786
NA
NA
Indonesia ................
Indonesia and
Timor-Leste (East
Timor).
Entire ......................
Entire ......................
T
E
786
786
NA
NA
17.41(d)
NA
*
*
*
Jkt 223001
A list of all references cited in this
document is available at https://
www.regulations.gov, Docket No. FWS–
R9–ES–2010–0099, or upon request
from the U.S. Fish and Wildlife Service,
Endangered Species Program, Branch of
Foreign Species (see FOR FURTHER
INFORMATION CONTACT section).
*
Philippines ..............
*
3. Amend § 17.41 by adding
paragraph (d) to read as follows:
VerDate Mar<15>2010
*
References Cited
*
§ 17.41
*
Special rules—birds.
*
*
*
*
(d) White cockatoo (Cacatua alba).
PO 00000
Frm 00035
Fmt 4701
Sfmt 4702
*
*
(1) Except as noted in paragraphs
(d)(2) and (d)(3) of this section, all
prohibitions and provisions of §§ 17.31
E:\FR\FM\09AUP2.SGM
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Federal Register / Vol. 76, No. 153 / Tuesday, August 9, 2011 / Proposed Rules
mstockstill on DSK4VPTVN1PROD with PROPOSALS2
and 17.32 of this part apply to the white
cockatoo.
(2) Import and export. You may
import or export a specimen without a
permit issued under § 17.32 of this part
only when the provisions of parts 13,
14, 15, and 23 of this chapter have been
met and you meet the following
requirements:
(i) Captive-bred specimens: The
source code on the Convention on
International Trade in Endangered
Species of Wild Fauna and Flora
(CITES) document accompanying the
specimen must be ‘‘F’’ (captive-bred),
VerDate Mar<15>2010
20:38 Aug 08, 2011
Jkt 223001
‘‘C’’ (bred in captivity), or ‘‘D’’ (bred in
captivity for commercial purposes) (see
50 CFR 23.24); or
(ii) Specimens held in captivity prior
to the date this species was listed under
the Endangered Species Act of 1973, as
amended (16 U.S.C. 1531 et seq.): You
must provide documentation to
demonstrate that the specimen was held
in captivity prior to the date the species
is listed under the ESA. Such
documentation may include copies of
receipts, accession or veterinary records,
CITES documents, or wildlife
declaration forms, which must be dated
PO 00000
Frm 00036
Fmt 4701
Sfmt 9990
prior to the date this species was listed
under the Endangered Species Act of
1973, as amended.
(3) Interstate commerce. Except where
use after import is restricted under
§ 23.55 of this subchapter, you may
deliver, receive, carry, transport, ship,
sell, offer to sell, purchase, or offer to
purchase in interstate commerce a live
white cockatoo.
Dated: July 26, 2011.
James J. Slack,
Director, U.S. Fish and Wildlife Service.
[FR Doc. 2011–19532 Filed 8–8–11; 8:45 am]
BILLING CODE 4310–55–P
E:\FR\FM\09AUP2.SGM
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Agencies
[Federal Register Volume 76, Number 153 (Tuesday, August 9, 2011)]
[Proposed Rules]
[Pages 49202-49236]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-19532]
[[Page 49201]]
Vol. 76
Tuesday,
No. 153
August 9, 2011
Part III
Department Of The Interior
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Fish and Wildlife Service
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50 CFR Part 17
Endangered and Threatened Wildlife and Plants; Four Foreign Parrot
Species; Proposed Rule
Federal Register / Vol. 76, No. 153 / Tuesday, August 9, 2011 /
Proposed Rules
[[Page 49202]]
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DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R9-ES-2010-0099; MO 92210-0-0010 B6]
RIN 1018-AX50
Endangered and Threatened Wildlife and Plants; Four Foreign
Parrot Species
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Proposed rule; 12-month finding.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), propose to
list as endangered the Philippine cockatoo (Cacatua haematuropygia) and
the yellow-crested cockatoo (C. sulphurea), and to list as threatened
the white cockatoo (C. alba), under the Endangered Species Act of 1973,
as amended (ESA). We are taking this action in response to a petition
to list the following four parrot species: Crimson shining parrot
(Prosopeia splendens), Philippine cockatoo (Cacatua haematuropygia),
white cockatoo (C. alba), and yellow-crested cockatoo (C. sulphurea) as
endangered or threatened under the ESA. This document, which also
serves as the completion of the status review and as the 12-month
finding on the petition, announces our finding that listing is not
warranted for the crimson shining parrot. We also propose a special
rule for the white cockatoo in conjunction with our proposed listing as
threatened for this species. We seek information from the public on the
proposed listing, proposed special rule, and status review for these
species.
DATES: We will consider comments and information received or postmarked
on or before October 11, 2011.
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-
ES-2010-0099.
U.S. mail or hand-delivery: Public Comments Processing,
Attn: FWS-R9-ES-2010-0099, Division of Policy and Directives
Management; U.S. Fish and Wildlife Service; 4401 N. Fairfax Drive, MS
2042-PDM; 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 Information
Requested section below for more information).
FOR FURTHER INFORMATION CONTACT: Janine Van Norman, Chief, Branch of
Foreign Species, Endangered Species Program, U.S. Fish and Wildlife
Service, 4401 North Fairfax Drive, Room 420, Arlington, VA 22203;
telephone 703-358-2171. If you use a telecommunications device for the
deaf (TDD), call the Federal Information Relay Service (FIRS) at 800-
877-8339.
SUPPLEMENTARY INFORMATION
Background
Section 4(b)(3)(B) of the ESA (16 U.S.C. 1531 et seq.) requires
that, for any petition to revise the Federal Lists of Endangered and
Threatened Wildlife and Plants that contains substantial scientific or
commercial information that listing the species may be warranted, we
make a finding within 12 months of the date of receipt of the petition
(``12-month finding''). In this finding, we determine whether the
petitioned action is: (a) Not warranted, (b) warranted, or (c)
warranted, but immediate proposal of a regulation implementing the
petitioned action is precluded by other pending proposals to determine
whether species are endangered or threatened, and expeditious progress
is being made to add or remove qualified species from the Federal Lists
of Endangered and Threatened Wildlife and Plants. Section 4(b)(3)(C) of
the ESA requires that we treat a petition for which the requested
action is found to be warranted but precluded as though resubmitted on
the date of such finding, that is, requiring a subsequent finding to be
made within 12 months. We must publish these 12-month findings in the
Federal Register.
If the listing of a species is found to be warranted but precluded
by higher-priority listing actions, then the petition to list that
species is treated as if it is a petition that is resubmitted on the
date of the finding and is, therefore, subject to a new 12-month
finding within one year. The Service publishes an annual notice of
resubmitted petition findings (annual notice) for all foreign species
for which listings were previously found to be warranted but precluded.
In this document, we announce that listing Philippine cockatoo and
yellow-crested cockatoo as endangered is warranted, and we are issuing
a proposed rule to add those species as endangered under the Federal
Lists of Endangered and Threatened Wildlife and Plants. We find that
listing the crimson shining parrot as endangered or threatened is not
warranted. We further find that listing white cockatoo as threatened is
warranted, and we are issuing a proposed rule to add that species as
threatened under the Federal Lists of Endangered and Threatened
Wildlife and Plants.
Prior to issuing a final rule on this proposed action, we will take
into consideration all comments and any additional information we
receive. Such information may lead to a final rule that differs from
this proposal. All comments and recommendations, including names and
addresses of commenters, will become part of the administrative record.
Previous Federal Actions
Petition History
On January 31, 2008, the Service received a petition dated January
29, 2008, from Friends of Animals, as represented by the Environmental
Law Clinic, University of Denver, Sturm College of Law, requesting we
list 14 parrot species under the ESA. The petition clearly identified
itself as a petition and included the requisite information required in
the Code of Federal Regulations (50 CFR 424.14(a)). On July 14, 2009
(74 FR 33957), we published a 90-day finding in which we determined
that the petition presented substantial scientific and commercial
information to indicate that listing may be warranted for 12 of the 14
parrot species. In our 90-day finding on this petition, we announced
the initiation of a status review to list as endangered or threatened
under the ESA the following 12 parrot species: Blue-headed macaw
(Primolius couloni), crimson shining parrot (Prosopeia splendens),
great green macaw (Ara ambiguus), grey-cheeked parakeet (Brotogeris
pyrrhoptera), hyacinth macaw (Anodorhynchus hyacinthinus), military
macaw (Ara militaris), Philippine cockatoo (Cacatua haematuropygia),
red-crowned parrot (Amazona viridigenalis), scarlet macaw (Ara macao),
white cockatoo (Cacatua alba), yellow-billed parrot (Amazona collaria),
and yellow-crested cockatoo (Cacatua sulphurea). We initiated the
status review to determine if listing each of the 12 species is
warranted, and initiated a 60-day public comment period to allow all
interested parties an opportunity to provide information on the status
of these 12 species of parrots. The public comment period closed on
September 14, 2009.
On July 21, 2010, a settlement agreement was approved by the Court
(CV-10-357, D. D.C.), in which the Service agreed to (in part) submit
to the Federal Register by July 29, 2011, a determination whether the
petitioned action is warranted, not warranted, or warranted but
precluded by other listing actions for no less than four of the
[[Page 49203]]
petitioned species. This Federal Register document complies with the
first deadline in that court-ordered settlement agreement. We will
announce the 12-month findings for the remaining parrot species for
which a 90-day finding was made on July 14, 2009 (74 FR 33957) in
subsequent Federal Register notices.
Information Requested
We intend that any final actions resulting from this proposed rule
will be based on the best scientific and commercial data available.
Therefore, we request comments or information from other concerned
governmental agencies, the scientific community, or any other
interested parties concerning this proposed rule. We particularly seek
clarifying information concerning:
(1) Information on taxonomy, distribution, habitat selection and
trends (especially breeding and foraging habitats), diet, and
population abundance and trends (especially current recruitment data)
of these species.
(2) Information on the effects of habitat loss and changing land
uses on the distribution and abundance of these species (particularly
the conversion of habitat to biofuel production on Halmahera Island and
any data on Bacan Island related to the white cockatoo).
(3) Information on the effects of other potential threat factors,
including live capture and hunting, domestic and international trade,
predation by other animals, and any diseases that are known to affect
these species or their principal food sources.
(4) Information on management programs for parrot conservation,
including mitigation measures related to conservation programs, and any
other private, nongovernmental, or governmental conservation programs
that benefit these species.
(5) The potential effects of climate change on these species and
their habitats.
Please include sufficient information with your submission (such as
full references) to allow us to verify any scientific or commercial
information you include. Submissions merely stating support for or
opposition to the action under consideration without providing
supporting information, although noted, will not be considered in
making a determination. Section 4(b)(1)(A) of the ESA directs that
determinations as to whether any species is an endangered or threatened
species must be made ``solely on the basis of the best scientific and
commercial data available.''
Public Hearing
At this time, we do not have a public hearing scheduled for this
proposed rule. The main purpose of most public hearings is to obtain
public testimony or comment. In most cases, it is sufficient to submit
comments through the Federal eRulemaking Portal, described above in the
ADDRESSES section. If you would like to request a public hearing for
this proposed rule, you must submit your request, in writing, to the
person listed in the FOR FURTHER INFORMATION CONTACT section by
September 23, 2011.
Factors Affecting the Species
Section 4 of the ESA (16 U.S.C. 1533) and implementing regulations
(50 CFR 424) set forth procedures for adding species to the Federal
Lists of Endangered and Threatened Wildlife and Plants. Under section
4(a)(1) of the ESA, a species may be determined to be endangered or
threatened based on any one or a combination of the following five
factors:
(A) The present or threatened destruction, modification, or
curtailment of its habitat or range;
(B) Overutilization for commercial, recreational, scientific, or
educational purposes;
(C) Disease or predation;
(D) The inadequacy of existing regulatory mechanisms; or
(E) Other natural or manmade factors affecting its continued
existence.
In considering what factors might constitute threats, we look
beyond the actual or perceived exposure of the species to the factor to
determine how the species responds to the factor and whether the factor
causes actual impacts to the species. If there is exposure to a factor,
but no response, or only a positive response, that factor is not a
threat. If there is exposure and the species responds negatively, the
factor may be a threat and we then attempt to determine how significant
a factor it is. If the factor is significant, it may drive or
contribute to the risk of extinction of the species such that it is
considered to be a threat. In some cases, there is little information
available regarding the status of the species, in part due to their
remoteness.
This finding addresses the following four species of parrots:
crimson shining parrot, Philippine cockatoo, white cockatoo, and
yellow-crested cockatoo. For each of these parrots, we evaluate the
five factors under ESA Section 4(a)(1) on the species. In some cases,
we found under a factor that a threat was contributing to the
extinction risk for multiple species, while some factors constituted a
threat for some of the species but not others. In some cases, the
factors affecting species are the same or very similar and in other
cases the factors are unique. In each evaluation, we clearly identify
what species is being addressed, and if the threat applies to more than
one species.
Species Information
A. Crimson Shining Parrot (Prosopeia splendens)
Taxonomy and Species Description
The crimson shining parrot (Prosopeia splendens, Peale, 1848) is
endemic to Fiji, where it is found in forests, on agricultural lands,
and around human habitation (International Union for Conservation of
Nature (IUCN) 2008). Its most closely related species are P. personata
(G. R. Gray, 1848), masked shining parrot, which occurs on Viti Levu;
and P. tabuensis (Gmelin, 1788), maroon (red) shining parrot, which
occurs on Vanua Levu and Taveuni. P. splendens and these two other
species are recognized by the Integrated Taxonomic Information System
(ITIS) (ITIS 2011, https://www.itis.gov) as valid species. Absent peer-
reviewed information to the contrary and based on the best available
information, we consider P. splendens to be a valid species.
The crimson shining parrot's head, neck, and underparts are a
bright red. It is a medium-sized parrot, with a length of 45
centimeters (cm) (18 inches (in)). It has been observed in flocks of up
to 40 birds in the past, but more recently in flocks of up to 12 birds.
During the day, this species is generally quiet and becomes vocal
towards dusk, at which time it becomes more active. A blue collar
extends across the back of its neck; its back and rump are bright
green. Its flight feathers and tail are green, strongly covered with
blue. Its bill and feet are black, and its irises are orange. Males and
females are similar morphologically; however, the bill of males is
larger, and the head of males is more square-shaped than females. It
differs from the maroon shining parrot in its size and coloration;
crimson shining parrots are generally smaller than maroon shining
parrots. Rump feathers on the crimson shining parrot do not have the
red edges that can be seen on the maroon shining parrot. The main
visible features that distinguish the crimson shining parrot from the
masked shining parrot and the maroon shining parrot are the scarlet
rather than maroon underparts and the blue collar at the back of the
neck.
[[Page 49204]]
Distribution, Habitat, Biology
There is little to no information available regarding this species.
The crimson shining parrot, also known as the Kadavu musk parrot, is
endemic to the islands of Kadavu and Ono in Fiji. These two islands are
separated by a narrow channel, often navigated by kayaks and other
small boats. This species has also been reported on the island of Viti
Levu in the Upper Navua Conservation Area (Tokaduadu 2008, pp. 5, 7),
where they are thought to be escaped pet birds. There are no known
records of this species successfully breeding other than on the islands
of Kadavu and Ono (https://www.NatureFiji.org, accessed January 4,
2011). The island of Kadavu is remarkable in that it has the highest
number of endemic birds per land area in the world. It hosts two areas
designated by Birdlife International (BLI) as Important Bird Areas
(IBAs), including Mount Nabukelevu which is located on the southwestern
end of Kadavu Island. Mt. Nabukelevu, has the largest area of montane
forest on the island. These IBAs are a way to identify conservation
priorities (BLI 2008j, pp. 1-2) and are considered to be globally
important areas for the conservation of bird populations. A site is
recognized as an IBA based on the occurrence of key bird species that
are vulnerable to global extinction or whose populations are otherwise
irreplaceable. These key sites for conservation are small enough to be
conserved in their entirety and large enough to support self-sustaining
populations of the key bird species. Mount Nabukelevu's montane forest
is critical for five globally threatened bird species, including the
crimson shining parrot (BLI 2011d, p. 1; BLI 2010c, p. 1).
Very little is known about the ecology of this species in the wild
(NatureFiji 2011, pp. 1-2). Although in captivity this species has been
known to exhibit aggression in males, it is a social species in the
wild (Lin and Lee 2006, p. 188). It has been observed in flocks of up
to approximately 40 birds (Tabaranza 1992 as cited in BLI 2001, p.
1679) but more recently it has been observed in flocks of up to 12
individuals. Flocking is thought to serve several purposes including
mate selection, and learning food sources and eating techniques
(Cameron 2007, pp. 115, 144)
In 2004, the population estimate was 6,000 mature birds, with a
declining population (Jackson and Jit 2004 in BLI 2010a, p. 1).
However, the species' population estimate was inferred from population
surveys conducted on another species, the Masked Shining-Parrot
(Prosopeia personata) (BLI 2010a, pp. 1-2). Surveys found that the
crimson shining parrot occurred at similar population densities as that
of the masked shining parrot. In two BirdLife International surveys, 86
crimson shining parrots were recorded in 38 standardized observer-
hours, similar to the mean of 1.9 masked shining parrots per hour
recorded at 18 sites across Viti Levu (BLI 2010a, pp. 1-2). Masked
shining parrots were estimated to occur at approximately 29 birds per
km\2\ in lowland native forest. The 2004 crimson shining parrot
population was estimated using the density of masked shining parrots
and the estimated 225 km\2\ (87 mi\2\) area of dense and medium-dense
forest on Kadavu (Jackson and Jit 2004 in BLI 2010a, p. 1). However, we
do not have detailed information about how the surveys on Kadavu were
conducted; they may have occurred at a time when the species is not
active or visible. There is no evidence that the survey protocol used
is appropriate to infer the population density of this species. Nor is
there evidence suggesting the two species have the same ecological
characteristics, levels of disturbance, and habitat requirements. For
example, Viti Levu has a more dense human population than that on the
islands of Kadavu and Ono, and human population density often directly
influences species population density. Additionally, we do not know the
historical population of the crimson shining parrot; this species may
never have had a large population, as it is only known to be endemic to
Kadavu and Ono Islands, so we do not know if this species has
experienced a decrease in population size or if its population has been
fairly consistent. Furthermore, species that are endemic to islands
tend to have smaller population sizes due to a smaller carrying
capacity of the island. This species is described as being ``widespread
and common'' on Kadavu and population information on the East Kadavu
IBA also lists this species as common (BLI 2011a, p. 1; BLI 2011f,
unpaginated). Additionally, notes from a 2006 birding trip report
indicate that the crimson shining parrot would be ``hard to miss'' on
Kadavu (Skevington and Mathieson 2006, unpaginated). Although the best
scientific information available indicates the population of crimson
shining parrots number 6,000 individuals, there is no historical
population data to indicate this species has declined or is currently
declining. Given the reports from BirdLife International (BLI 2011a, p.
1; BLI 2011f, unpaginated) and the lack of support for a declining
population, we consider the crimson shining parrot to be common on
Kadavu.
Its range is estimated to be 460 km\2\ (178 mi\2\). However, BLI
(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.''
Kadavu is the fourth largest of Fiji's islands, at 410 km\2\ (158
mi\2\). Kadavu has a human population of 8,700 people and is a
mountainous, rugged island with high peaks and precipitous cliffs (Fiji
Guide 2011). There are few roads and is therefore mainly accessible by
boat. The Kadavu Island group is 83 km (45 nautical miles) south of
Viti-Levu, Fiji's main island. Kadavu is rugged and mountainous with
few roads. The Kadavu Island group also includes nearby Ono Island, off
the eastern tip of Kadavu, as well as a number of smaller islands. Ono
is 30 km\2\ (12 mi\2\) in size (Planetary Coral Reef Foundation (PCRF)
2010). This island group has 12,000 Fijians living in 72 traditional
village communities (PCRF 2010), and there is one airstrip. The primary
means of income is subsistence agriculture and fishing.
Conservation Status for the Crimson Shining Parrot
Fiji is actively involved in forest protection efforts; a new
Forest Policy was adopted in 2007 (Fiji Ministry of Fisheries and
Forestry 2009, p. 1). Crimson shining parrot is also protected by
Fiji's Endangered and Protected Species (EPS) Act of 2002.
Additionally, Fiji's first national nongovernmental organization (NGO),
Nature Fiji, was established recently, and its goal is conservation of
its wildlife. Nature Fiji is working closely with BLI to develop a
conservation program to protect endangered wildlife in Fiji such as the
crimson shining parrot.
In 1981, the crimson shining parrot was listed in Appendix II of
the Convention on International Trade in Endangered Species of Wild
Fauna and Flora (CITES). At that time, almost all Psittaciformes
species (i.e., parrots) were included in Appendix II. CITES is an
international agreement where member countries work together to ensure
that international trade in CITES-listed animals and plants is not
detrimental to the survival of wild populations. This is achieved by
regulating import, export, and re-export of CITES-listed animal and
plant species and their parts and products through the use of a
permitting system (https://
[[Page 49205]]
www.cites.org). CITES entered into force in 1975, and is an
international treaty among 175 nations, including Fiji and the United
States. In the United States, CITES is implemented through the U.S.
Endangered Species Act of 1973, as amended (ESA; 16 U.S.C. 1531 et
seq.).
Appendix II includes species that are not necessarily threatened
with extinction, but may become so unless trade is subject to strict
regulation to avoid utilization incompatible with the species'
survival. International trade in specimens (dead or live) of Appendix
II species is authorized through permits or certificates. International
trade in specimens of Appendix II species is authorized when: (1) The
CITES Scientific Authority of the country of export has determined that
the export will not be detrimental to the survival of the species in
the wild; and (2) the CITES Management Authority of the country of
export has determined that the specimens to be exported were legally
acquired (UNEP-WCMC 2008a, p. 1).
In 1988, the crimson shining parrot was described by the IUCN as
lower risk/least concern, and the status changed to vulnerable in 2000
(IUCN 2008; BLI 2010a), which is its current IUCN classification. The
authority for compilation of information and determining the
appropriate risk extinction category for bird species on the IUCN Red
List is Birdlife International, and is cited frequently throughout this
document. However, IUCN rankings do not confer any actual protection or
management.
Evaluation of Factors Affecting the Crimson Shining Parrot
This section contains an assessment in which we evaluate the
effects of any of the five factors listed in section 4(a)(1) of the ESA
on the species. Listing actions may be warranted based on whether any
of the five factors under section 4(a)(1), singly or in combination,
places the species in danger of extinction now or in the foreseeable
future. Each evaluation is specific to this species identified unless
we specify that the evaluation is for more than one species.
Factor A. The Present or Threatened Destruction, Modification, or
Curtailment of Its Habitat or Range
There is little to no evidence of destruction, modification, or
curtailment of this species' habitat, in fact, there is recent evidence
of reforestation efforts and conservation of the species' habitat
taking place (BLI 2011a, p. 1; Fiji Daily Post 2007, 2009,
unpaginated). It was suggested that this species is roughly estimated
to be declining at the rate of forest loss, which had been estimated to
be 0.5 to 0.8 percent per year across Fiji (Claasen 1991 in BLI 2011a,
p. 1), and that forest loss may be higher on Kadavu due to fires in
recent years (BLI 2011a, p. 1). However, there is no information on the
extent of past or current forest loss. Not only does the United Nations
describe deforestation in Fiji as modest when compared with the rest of
Melanesia (UN 2011, p. 1), but also local communities on Kadavu are
implementing reforestation efforts and conservation of this species'
habitat as described above (Fiji Daily News 2007, unpaginated).
Although the eastern part of the island is experiencing pressures from
agricultural encroachment, there is no evidence that agricultural
encroachment or forest loss due to fires currently threatens the
crimson shining parrot (NatureFiji 2011, pp. 1-2).
Forests on Kadavu were heavily logged in the late 1960s and early
1970s, and habitat loss and degradation of habitat for agricultural
purposes continues. However, approximately 75 percent of the island
remains forested; East Kadavu IBA is reported to have the largest area
of old-growth forest in Kadavu, including extensive areas of lowland
rainforest. Furthermore, the crimson shining parrot is reported to use
degraded habitats extensively (BLI 2011a, p. 1; BLI 2011f,
unpaginated). Most river estuaries and bays still hold large areas of
mangroves, which are used by the crimson shining parrot for feeding
(and possibly breeding), and pressure on mangrove forest here is not
currently significant (BLI 2011a, p. 1).
BLI and Nature Fiji are working with landowners on Kadavu to
conserve these forested natural areas and to increase awareness of the
value of maintaining these areas in a little-disturbed state (BLI
2011e, p. 1). NGOs are working with the landowners in the Mount
Nabukelevu area to create awareness about the value of their forests
and the benefits of establishing ``Permanent Forest Estates'' (PFEs)
(described below) on their lands. These NGOs are also working to help
build the capacity of indigenous communities to continue forest
conservation on their own (BLI 2011e, p. 3). BLI, through the Darwin
Initiative, has worked with the Kadavu's Department of Forestry and
local communities on Kadavu to protect this species' habitat. The
Darwin Initiative, implemented by the United Kingdom, assists countries
that are rich in biodiversity but poor in financial resources to meet
their objectives under one or more of the three major biodiversity
conventions. BLI conducted a workshop on Kadavu to teach sustainable
agricultural practices and ways to reduce soil erosion which
subsequently supports community livelihoods. Later, the villages of
Lomati, Nabukelevuira, Qalira, and Daviqele committed to protect 1,500
hectares (3,707 ac) of their forest that had been designated as an
Important Bird Area (IBA) on Mount Nabukelevu in Kadavu (Fiji Daily
News 2007).
On Kadavu, particularly in the area of Mount Nabukelevu, many
forest-owning mataqalis (clan or landowning units) are under pressure
to convert their forests into agricultural land (BLI 2011e, p. 1). In
2010, 10 mataqalis signed an agreement with an NGO to protect the
forests of Mount Nabukelevu for the next 20 years (BLI 2011f;
NatureFiji 2011). The community-declared protected area now includes 10
mataqali (clan) lands plus a native reserve. Additionally, the
Government of Fiji recognizes that maintaining forests is critically
important for Fiji's people and biodiversity and has taken steps to
preserve its country's resources. In 2007, Fiji introduced the Fiji
Forest Policy, which promotes sustainable forest management. One of the
foundations of the new Forest Policy is the concept of ``Permanent
Forest Estates'' (PFEs). The policy promotes sustainable management of
healthy forests by providing sustainable development incentives for
landowners. In addition, the government of Fiji initiated a campaign to
plant one million trees in 2010 to halt or slow ecological degradation
associated with the depletion of the world's forests. Fiji launched its
One Million Trees Campaign in support of the 2010 International Year of
Biodiversity, and in 2011 as the International Year of Forests. Fiji
indicated that they had surpassed their goal, and participants had
succeeded in planting over one million trees (Fiji Ministry of
Information 2011).
Although forest loss may be occurring within the range of the
crimson shining parrot, we have no information on the extent of forest
loss or evidence to suggest that this loss has impacted or is currently
affecting this species. The crimson shining parrot is found in forests,
agriculture lands, around human habitation, and is known to use
degraded habitats extensively. Furthermore, there is no information
indicating this species is declining. Additionally, we have no
information to suggest that habitat loss may become a threat to this
species in the future such that it may contribute to the risk of
extinction of this species. Fiji has implemented proactive policies and
[[Page 49206]]
protections with respect to its forests. Local conservation activities
are occurring on Kadavu; indigenous communities are interested in
preserving this species and its habitat. Therefore, we do not find that
the present or threatened destruction, modification, or curtailment of
its habitat or range is a threat to the crimson shining parrot now or
in the foreseeable future.
Factor B. Overutilization for Commercial, Recreational, Scientific, or
Educational Purposes
Conservation projects on Kadavu are believed to have reduced the
numbers of parrots trapped for trading, but this species is still
thought to be captured in small numbers for domestic and international
trade (BLI 2010a, p. 1). As indicated above, this species has been
listed in Appendix II of CITES since 1981. The United Nations
Environment Programme--World Conservation Monitoring Centre (UNEP-WCMC)
manages a CITES Trade Database on behalf of the CITES Secretariat. We
queried the UNEP-WCMC CITES Trade Database for gross data on export and
import of this species since 2000, and found no record of trade in this
species (UNEP-WCMC 2011, accessed January 4, 2011.)
Each Party to CITES is responsible for compiling and submitting
annual reports to the CITES Secretariat regarding their country's trade
in species listed in the CITES Appendices. The data from submitted
annual reports is compiled into the database, and it provides a
mechanism by which CITES trade can be assessed. Due to the time needed
to compile the data, the most recent year for which comprehensive trade
statistics are available is normally 2 years prior to the current year.
UNEP-WCMC acknowledges that the data are not always accurate (UNEP-WCMC
2011, p. 5). They indicate that it is not uncommon for the quantity of
specimens traded to be considerably less than the amount specified on
the permits and that the quantity specified on the permits is
frequently the quantity that is reported in annual reports. They
further clarify that trade transactions that may have been authorized
by the issuance of permits but never have taken place, as well as
inaccurately reported volumes of trade, will exist in the UNEP-WCMC
CITES database. UNEP-WCMC also acknowledges that gross and net outputs
from the CITES database are often overestimates of the quantities
traded because in cases where different quantities are reported by the
importing and exporting countries, the CITES database program selects
the larger quantity. Errors do occur in the database, and the numbers
may not be entirely accurate, but they do provide an approximate
representation of international trade that is occurring through CITES.
However, we consider the UNEP-WCMC CITES trade data to be the best
available information pertaining to international trade in CITES-listed
species.
Although it has been reported that birds are taken as gifts and
there is some illegal trade overseas, it is thought to occur in small
numbers (BLI 2010a, p. 1). Conservation projects described under Factor
A have reduced the numbers of birds trapped for the pet bird trade (BLI
2011a, p. 1). BLI reports that four communities have set up village
protected areas on Kadavu, and they conduct regular bird surveys under
their own initiative. Additionally, it is protected by law against
trading and transfers out of Kadavua and Ono (NatureFiji 2011, p. 2).
There appears to be substantial protection, awareness, and local
conservation of this species occurring. Because there is no evidence of
poaching (i.e., hunting by people to gain at least a temporary living
from the activity) or illegal trade of this species occurring at levels
such that it may contribute to the risk of extinction of the crimson
shining parrot, or information indicating poaching or trade may
increase in the future and rise to the level of a threat, we believe
that overutilization for commercial, recreation, scientific, or
educational purposes is not a threat to the species.
We are unaware of any other information currently available that
addresses overutilization for commercial, recreation, scientific, or
education purposes that may be affecting the crimson shining parrot. We
found no evidence of overutilization due to historic or cultural use of
this species by local populations. Based on the best available
scientific and commercial information, we find that overutilization for
commercial, recreational, scientific, or educational purposes is not a
threat to the crimson shining parrot now or in the foreseeable future.
Factor C. Disease or Predation
Predation by introduced mammals such as feral cats (Felis catus)
and rats (Rattus spp.) were identified as possible factors affecting
this species. There was little to no information found regarding the
occurrence of predation or disease in Fiji, particularly with respect
to the crimson shining parrot. As is the case on many remote islands,
Fiji has no native terrestrial mammals. Introduced mammals such as
rats, mongoose (Herpestes javanicus), cats and dogs prey heavily on
Fiji's native wildlife (Morley 2004 in Olson et al. 2009, p. 1).
However, the mongoose is not present on Kadavu Island and the only
current predator definitely known to occur on Kadavu is cats. Cats on
Kadavu are known to threaten ground-nesting birds, particularly on the
coasts, but they are not known to threaten the crimson shining parrot.
There are no known predators on Ono Island to our knowledge. Studies
have found that predation rates by introduced predators are lowest in
natural forests more than 4.5 km (2 mi) from forest edges or roads
(Olson et al. 2006). Kadavu's terrain consists of volcanic,
mountainous, dense rainforest; sandy beaches; rocky coastline; and
mangrove swamps. The island has a significant portion of relatively
undisturbed forested areas. The islands' forested areas may act as
refugia from predation by alien predators, such as the feral cat, for
native species such as the crimson shining parrot.
Researchers suggest that maintaining minimally-disturbed forests is
one of the most cost-effective strategies for protecting species (Olson
et al. 2009, p. 1). Because this species resides in dense forests far
from edges and roads, this species is not likely to be significantly
affected by nonnative predators. The crimson shining parrot likely has
natural predators, but we were unable to find information that any
natural predators are having an impact on this species. Although
predation occurs in Fiji, particularly by nonnative species, the best
available information does not indicate that predation is a threat to
the crimson shining parrot on Kadavu or Ono now, or may become a threat
in the future.
We are not aware of any occurrence of disease that may be affecting
the crimson shining parrot. In conclusion, we find that neither disease
nor predation is a threat to the crimson shining parrot in any portion
of its range now or in the foreseeable future.
Factor D. The Inadequacy of Existing Regulatory Mechanisms
Various regulatory mechanisms are in place to protect the crimson
shining parrot. This species is listed on Fiji's Endangered and
Protected Species (EPS) Act of 2002 which is the legislation that
implements CITES. As discussed under Factor B, the government of Fiji
is adequately controlling international trade. According to a review
conducted for CITES with respect to national legislation to determine
each country's ability to implement CITES effectively, Fiji meets the
requirements for
[[Page 49207]]
implementing CITES (CITES 2011a; https://www.cites.org, SC59 Document
11, Annex p. 1). In addition to the absence of legal trade, there is no
indication that this species is traded illegally at levels such that it
may contribute to the risk of extinction of the crimson shining parrot.
Based on the lack of trade, and as discussed under Factor B, we do not
consider international trade to be a threat to the crimson shining
parrot. Therefore, protection under CITES is an adequate regulatory
mechanism.
Wild Bird Conservation Act
The import into the United States of all of these species: the
crimson shining parrot, Philippine cockatoo, white cockatoo, and
yellow-crested cockatoo, is regulated by the Wild Bird Conservation Act
(WBCA) (16 U.S.C. 4901 et seq.), which was enacted on October 23, 1992.
The WBCA is implemented under 50 CFR part 15 and has limited or
prohibited imports of exotic bird species into the United States since
1992. The purpose of the WBCA is to promote the conservation of exotic
birds by ensuring that all trade involving the United States is
sustainable and is not detrimental to the species. The WBCA is a
stricter conservation measure than CITES, and import of these parrot
species into the United States requires issuance of a WBCA import
permit. WBCA permits may be issued to allow import of listed birds for
various purposes, such as scientific research, zoological breeding or
display, or personal pets, when certain criteria are met. The Service
may approve cooperative breeding programs and subsequently issue import
permits under such programs. Under the cooperative breeding program,
wild-caught birds may be imported into the United States if they are a
part of Service-approved management plans for sustainable use. At this
time, none of the four parrot species discussed in this document is
part of a Service-approved cooperative breeding program, and there are
no approved management plans for wild-caught birds of these species.
Under the provisions of WBCA, any individual importing their pet
bird to the United States for the first time must reside outside of the
United States for at least 12 continuous months. In addition, in order
to control diseases, the U.S. Department of Agriculture's Animal and
Plant Health Inspection Service requires veterinary health certificates
and health inspections for pet birds, and implements quarantine
procedures for birds imported into the United States. A report
published in 2006 showed that imports of parrot species to the United
States declined from the mid-1980s to 1991 (Pain et al. 2006, pp. 322-
324). Parrot imports to the United States were already declining before
the enactment of the WBCA, but the WBCA largely curtailed the import of
wild parrots; we find it is an adequate regulatory mechanism for all
four of these parrot species.
As discussed under Factor B, local protections are in place on the
islands where this species exists. The governmental institutions
responsible for oversight of the conservation of this species have a
good legal framework to manage wildlife and their habitats. Not only
are local NGOs involved in conservation activities for this species,
but there also appears to be adequate capacity at various levels to
protect this species and its habitat. The forestry regulations appear
to be effective; there are no reports of illegal logging on the islands
of Kadavu and Ono. Most of Fiji's forests are managed or owned by local
communities, which have incentive to protect the native habitat.
Ownership of native lands is not transferable through land sales, but
user rights can be transferred via land leases (Leslie and Tuinivanua
2010, p. 10). These landowning groups are deeply attached to their
lands and Fiji's forestry policy supports the local ownership of its
lands. Within this species' habitat, the forested areas are being
adequately managed and protected by these mataqalis.
Environmental education, conservation initiatives, and restoration
efforts are occurring on Kadavu. Another NGO working on Kadavu to
protect this species is the Matava Foundation (https://foundation.matava.com/2011-projects) which is a local NGO associated
with a resort on the island. In addition to the conservation efforts in
place, the remoteness of these islands likely serves as an additional
protection for this species. The crimson shining parrot occurs on two
islands, and both islands are extremely remote and fairly undeveloped.
These factors all likely serve as additional protections for this
species.
In summary, the existing regulatory mechanisms appear to be
adequate. There are no current records of this species in international
trade, and the government of Fiji is actively conducting environmental
stewardship projects. There is nothing to suggest that this factor is a
threat to the species. Local conservation activities involving
indigenous communities are occurring on Kadavu and this species and its
habitat appear to be well protected. Fiji has enacted various laws and
regulatory mechanisms to protect and manage wildlife and their
habitats. As described above in our review, we found that the
government of Fiji and NGOs are implementing many projects and
mechanisms that will likely have a positive impact on this species and
its habitat. Reforestation and conservation efforts are occurring. The
best scientific and commercial information available indicates that the
crimson shining parrot is not in danger of extinction or likely to
become so within the foreseeable future due to inadequate regulatory
mechanisms.
Factor E. Other Natural or Manmade Factors Affecting the Continued
Existence of the Species
In this section, we examined whether invasive species are threats
to the crimson shining parrot. The eastern part of Kadavu supports
several bird species that are endemic to Kadavu. BLI indicated that
logging and roads (see Factor A) may be facilitating the movement of
invasive species. Logging enables alien invasive species such as rats
and cats, and in some cases, Indian or common mynahs (Acridotheres
tristis), jungle mynahs (Acridotheres fuscus), and Spathodea
campanulata (African tulip trees), to invade the forests along logging
roads and clearings. The island of Kadavu may be experiencing invasive
species, but there is no evidence that invasive species are occurring
to an extent that they are threats to the crimson shining parrot. Nor
is there evidence that invasive species are a threat on Ono Island,
where the crimson shining parrot is also known to occur. BLI is
creating community-based conservation groups at Fiji's key conservation
sites such as Kadavu Island, and is working with communities to address
issues such as effectively dealing with invasive species (BLI 2011g, p.
3). We found no other natural or manmade factors that might affect the
continued existence of the crimson shining parrot now or in the future.
Based on the best available information, we find that there are no
other natural or manmade threats to the continued existence of the
crimson shining parrot throughout its range now or in the foreseeable
future.
Significant Portion of the Range
Having determined that the crimson shining parrot is not in danger
of extinction or likely to become so within the foreseeable future
throughout all of its range, we must next consider whether there are
any significant portions of the range where the crimson shining parrot
is in danger of extinction
[[Page 49208]]
or is likely to become endangered in the foreseeable future.
The Act defines an endangered species as one ``in danger of
extinction throughout all or a significant portion of its range,'' and
a threatened species as one ``likely to become an endangered species
within the foreseeable future throughout all or a significant portion
of its range.'' The term ``significant portion of its range'' is not
defined by the statute. For the purposes of this finding, a portion of
a species' range is ``significant'' if it is part of the current range
of the species, and it provides a crucial contribution to the
representation, resiliency, or redundancy of the species. For the
contribution to be crucial it must be at a level such that, without
that portion, the species would be in danger of extinction.
In determining whether a species is threatened or endangered in a
significant portion of its range, we first identify any portions of the
range of the species that warrant further consideration. The range of a
species can theoretically be divided into portions in an infinite
number of ways. However, there is no purpose to analyzing portions of
the range that are not reasonably likely to be significant and
threatened or endangered. To identify only those portions that warrant
further consideration, we determine whether there is substantial
information indicating that: (1) The portions may be significant, and
(2) the species may be in danger of extinction there or likely to
become so within the foreseeable future. In practice, a key part of
this analysis is whether the threats are geographically concentrated in
some way. If the threats to the species are essentially uniform
throughout its range, no portion is likely to warrant further
consideration. Moreover, if any concentration of threats applies only
to portions of the species' range that clearly would not meet the
biologically based definition of ``significant'' (i.e., the loss of
that portion clearly would not reasonably be expected to increase the
vulnerability to extinction of the entire species to the point that the
species would then be in danger of extinction), such portions will not
warrant further consideration.
If we identify portions that warrant further consideration, we then
determine their status (i.e., whether in fact the species is endangered
or threatened in a significant portion of its range). Depending on the
biology of the species, its range, and the threats it faces, it might
be more efficient for us to address either the ``significant'' question
first, or the status question first. Thus, if we determine that a
portion of the range is not ``significant,'' we do not need to
determine whether the species is endangered or threatened there; if we
determine that the species is not endangered or threatened in a portion
of its range, we do not need to determine if that portion is
``significant.''
Applying the process described above for determining whether a
species is threatened in a significant portion of its range, we
considered status first to determine if any threats or potential
threats acting individually or collectively threaten or endanger the
species in a portion of its range. We have analyzed the potential
threats and determined they are essentially uniform throughout the
species' range.
Finding for the Crimson Shining Parrot
Section 3 of the ESA 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.'' In this finding, we determine whether the petitioned action
is: (a) Not warranted, (b) warranted, or (c) warranted but precluded
(see Background, above).
As required by the ESA, we considered the five factors separately
and in combination in assessing whether the crimson shining parrot is
endangered or threatened throughout all or a significant portion of its
range. We examined the best scientific and commercial information
available regarding the past, present, and future threats faced by the
crimson shining parrot. We reviewed the petition, information available
in our files, and available published and unpublished information
regarding this species and its habitat.
We do not have long-term population trend data for the crimson
shining parrot. This species has always been an island endemic and may
have always had a small population; island endemics tend to have
smaller population sizes. Without historical population information, we
do not know if this species has experienced a decrease in population
size or if its population has been fairly consistent. Furthermore, this
species is reported as common and widespread. During our review of the
status of the species, we evaluated the potential threats to the
crimson shining parrot including: habitat loss and habitat degradation,
take for the pet trade, disease and predation, the inadequacy of
regulatory mechanisms, and other natural or manmade factors such as
invasive species. We found no information that habitat loss is a threat
to the crimson shining parrot. We conclude that the present or
threatened destruction, modification, or curtailment of its habitat or
range is not a threat to the crimson shining parrot. We found no
information that poaching for the pet trade is a threat to the species.
This species is not in international trade according to the UNEP-WCMC
trade database. Additionally, education and public awareness campaigns
are occurring in Kadavu. Fiji is actively involved in forest protection
efforts; a new Forest Policy was adopted in 2007 (Fiji Ministry of
Fisheries and Forestry 2009, p. 1). We found no evidence that disease
or predation affects the wild crimson shining parrot population. In
addition, this species is protected by laws against trading and
transfers out of Kadavu and Ono. We also concluded that there are no
other natural or manmade factors that are threats to the species
(Factor E).
The best available information indicates that there is little
disturbance on the islands where the crimson shining parrot naturally
occurs. Habitat loss is often a threat to wildlife, however, in this
case, there is no evidence that habitat loss is affecting the crimson
shining parrot. On the contrary, this species is said to occupy altered
habitat extensively. Conservation efforts for this species have been
underway within the past few years to ensure long-term conservation of
habitat where this species exists; local groups on Kadavu are
implementing reforestation and conservation programs. Based on the lack
of threats acting on this species throughout its range as described
above, and the lack of information indicating the species population is
in decline, we determine that this species is not in danger of
extinction now, nor is it likely to become endangered within the
foreseeable future, throughout all or a significant portion of its
range. Therefore, we find that listing the crimson shining parrot as a
threatened or endangered species is not warranted.
Species Information
B. Philippine Cockatoo (Cacatua haematuropygia)
Taxonomy and Species Description
The species was first taxonomically described by M[uuml]ller in
1776 (BLI 2011b). We accept the species as C. haematuropygia, which
follows the Integrated Taxonomic Information System (ITIS 2011).
Cockatoos are only found in Australasia--a few archipelagos in
Southeast Asia (Philippines, Indonesia,
[[Page 49209]]
East Timor, Tanimbar, Bismarck, and Solomon), New Guinea, and
Australia--suggesting that the modern species arose after the breakup
of Gondwanaland, the southern supercontinent that existed 200 to 500
million years ago. The 19th century naturalist Alfred Russell Wallace
was among the first to note the break in Australasian and Asian fauna.
Wallace's line runs between the islands of Bali and Lombok, Borneo and
Sulawesi, and south of the Philippines. Cockatoos are present on Lombok
and Sulawesi, but not on Bali and Borneo. The line represents the
western edge of a zone of overlap between Australasian and Asian fauna
(known as Wallacea), with the eastern edge defined by the Australian
continental shelf (Lydekker's Line) (White and Bruce 1986, p. 32;
Cameron 2007, pp. 1-3). These oceanic islands of Wallacea have high
levels of endemism, meaning the species that occur there are unique to
those islands.
The Philippine cockatoo, or red-vented cockatoo, is locally known
as the ``katala'' and ``kalangay,'' and has a helmet crest and a red
undertail (Rowley 1997). Cockatoos are a distinct group of parrots
(order Psittaciformes), distinguished by the presence of an erectile
crest (Collar 1989, p. 5; Cameron 2007, p. 1) and the lack of dyck
texture in their feathers. Dyck texturing is a microscopic texturing
that produces blue and green coloration and is present in the plumage
of other parrots (Brown and Toft 1999, p. 141).
Biology, Distribution, and Habitat
This species is endemic to the Philippines, an archipelago of
approximately 7,000 islands. The total area of the Philippines is
30,000,000 ha (74,131,614 ac) (Kummer 1991, p. 44). The Philippine
cockatoo requires lowland primary or secondary forests with suitable
nesting tree cavities and food sources, within or adjacent to riparian
or coastal areas with mangroves (IUCN 2008i). The species is reported
to use regenerating forest and even heavily degraded forest, as long as
emergent nest trees survive. However, its nest sites are restricted to
lowlands (Widmann and Widmann 2010, pers. comm.).
The Philippine cockatoo is a food generalist; its diet varies based
on the seasons. It consumes seeds, legumes, fruit, flowers, buds, and
nectar. It will also eat agricultural crops such as corn and rice, and
has been observed feeding on Moringa oleifera (commonly known as
malunggay or horseradish tree). Interestingly, the government of the
Philippines introduced a bill in 2010, in the Fifteenth Congress of the
Republic of the Philippines, First Regular Session, to encourage
planting Moringa oleifera due to economic benefits (Senate Bill 1349
2010, pp. 1-7). The Philippine cockatoo has also been observed feeding
on the fruits of Sonneratia, a mangrove species (Tabaranza 1992;
Lambert 1994b in BLI 2001, p. 1683).
This species nests in tree cavities, and produces two to three eggs
per season (Cameron 2007, p. 140). Breeding generally occurs March
through June (BLI 2001, p. 1684), and both sexes participate in nest
building (Widmann et al. 2001, p. 135). The period between incubation
and fledging is generally about 95 days (Cameron 2007, p. 140). The
species prefers nests high in the tree canopy, generally around 30 m
(98 ft) (BLI 2001, p. 1683), but nest heights between 12 and 35 m (39
to 114 ft) have also been observed (Widmann et al. 2001, p. 135). The
diameter of the cavity openings observed has been between 10 and 25 cm
(4 and 10 in) (Widmann et al. 2001, p. 135). Some artificial nest boxes
have been installed to increase nesting habitat; the species exhibits a
preference for horizontal rather than vertical nest boxes (Low 2001, p.
3). Some of the tree species they use for roosting include
Dipterocarpus grandiflorus (common names: apitong, tempudau, tunden,
lagan bras aput) and Intsia bijuga (common names: Borneo-teak, Moluccan
ironwood, and merbau asam), as well as coconut trees (Lambert 1994b in
BLI 2001, p. 1686). They also use Garuga floribunda (no common name
[ncn]) and Sonneratia alba (ncn) (Cameron 2007, p. 35).
Population Estimates
Based on recent reports, it is likely that between 450 and 1,245
individuals remain in the wild. Surveys indicated that until around the
1980s, the Philippine cockatoo was fairly common within the Philippine
archipelago (Collar et al. 1998; Boussekey 2000, p. 138, BLI 2010, p.
1). Historically, it was known to exist on 52 islands in the
Philippines; now, it is believed to exist on eight islands (BLI 2011a,
p. 1).
The species' current range is significantly reduced from its
historic range. In the past, the species was reported to have been
commonly found throughout the Philippines except for northern and
central Luzon (Delacour and Mayr 1946; DuPont 1971 in Boussekey 2000,
p. 138; Collar et al. 1999 in Widmann and Widmann 2008, p. 23). It was
common throughout the Philippines as recently as the 1950s. Between
1980 and 2000, there was a 60 to 90 percent population decline
throughout its range (Boussekey 2000, p. 138). In the early 1990s, the
population was estimated to be between 1,000 and 4,000 (Tabaranza 1992
and Lambert 1994b in BLI 2001, p. 1681).
Snyder et al. (2000) reported the following population surveys. A
1991 survey estimated between 800 and 3,000 birds exist on Palawan
(Pandanas, Bugsok, and Bancalan Islands were thought to support 100 to
300 individuals and Dumaran 150 to 250 individuals), and possibly a few
hundred were thought to exist in the Tawi-Tawi region (Lambert 1993b,
1994b). A single pair was found on Siquijor in 1991 (Evans et al.
1993). A few were found at Mount Isarog, Luzon in 1988 (Goodman and
Gonzales 1990), and a few pairs were found in Mindoro at Malpalon
(Dutson et al. 1992). On Masbate, birds were observed in 1993 (Curio
1994), and the species has been recorded a few times in singles or
small numbers in Rajah Sikatuna National Park, Bohol since 1989 (Brooks
et al. 1995b). In 1994, two pairs (Dutson in litt. 1997) were seen on
Tawi-Tawi, and the species was considered widespread there in 1995-
1996, although apparently more often seen in captivity than in the wild
(two singles were observed in Batu-Batu and a single and a pair in
Buan) (Allen in litt. 1997). Three birds were observed on Simunul,
Tawi-Tawi in 1996 (Allen in litt. 1997; Dutson et al. 1996). The
species is considered extinct on Cebu (Brooks et al. 1995a) and Negros
(Brooks et al. 1992). Recent population counts and estimates are below;
however, this information is not a complete representation of the
population, but is the best available information. Some islands may not
hold viable populations and may be functionally extinct.
Between 2004 and 2010, the population estimate decreased from 1,000
to 4,000 individuals to 450 to 1,245 individual birds in the wild
(Widmann and Widmann 2008, p. 23; BLI 2010b; Widmann and Widmann 2010,
pers. comm.). This species currently is found in the Culasian Managed
Resource Protected Area (CMRPA), Palawan, Dumaran Island (negligible
population), Pandanan and Bugsok Islands, Polillo Island Group, Rasa
Island, Tawi-Tawi, and possibly on Samar Island. An estimated
additional 400 individuals may survive in the Sulu archipelago;
however, only sparse information is available for this area (Widmann et
al. 2007; Widmann et al. 2009a; Widmann et al. 2010a). Subpopulations
away from Palawan and the Sulus are thought to be very small, and do
not likely have viable populations (Widmann 2010, pers. comm.) The
extent these populations are interbreeding is unclear at this time.
[[Page 49210]]
Detailed discussion of each of these areas follows.
Table 1--Population Counts and Estimates of Philippine Cockatoo Between
2007 and 2010 on Islands in the Philippines
------------------------------------------------------------------------
Number of individuals based on recent
observation, population count, or Location
estimate
------------------------------------------------------------------------
60..................................... Bugsok Island (40 to 80
estimated).
20..................................... Burdeos, Polillo Islands.
3...................................... CMRPA, Palawan Island.
23..................................... Dumaran, Lagan.
80..................................... Pandanan Island.
2...................................... Patnanungan, Polillo Islands.
280.................................... Rasa Island.
4...................................... Samar.
200.................................... Tawi-Tawi (100 to 400
estimated).
672.................................... TOTAL*
------------------------------------------------------------------------
* Note: This is not a full population survey; it documents birds
actually counted, observed, or estimated (Widmann 2010, pers. comm.).
Culasian Managed Resource Protected Area
This area is in the south of Palawan Island and is 1,954 hectares
(ha) (4,828 acres (ac)). The total land area of Palawan is
approximately 1.5 million ha (3.7 million ac), including the 1,767
islands and islets surrounding the main island. This species exists
both within the actual designated protected area (CMRPA) and in the
areas surrounding the protected area on Palawan Island. Philippine
cockatoos are thought to travel between Palawan Island and nearby Rasa
Island. This species has been known to fly from the mainland to
offshore islands as far as 8 km (5 mi) away from the mainland to roost
and breed. No roosting sites are known in the CMRPA and surrounding
areas (Widmann et al. 2010a, p. 23); however, there have been recent
sightings there: four were observed in September 2009, and three were
observed in December 2009 (Widmann et al. 2010a, p. 37). At least two
Philippine cockatoos persist inside the protected area, but they have
not bred in the last 4 years.
CMRPA has been described as exhibiting the ``empty forest
syndrome.'' Although its forest is largely intact, little wildlife
remains due to hunting pressure and poaching. In the small population
that was protected only recently here, there are no indications that
the species' status is improving. Only one breeding pair exists outside
of the reserve. Cockatoo poaching occurred in this area within the past
3 years, and breeding in the 2009-2010 season failed. Because all nests
have been systematically poached over many years, extinction of this
population is likely to occur suddenly due to lack of recruitment
(Widmann and Widmann 2010, pers. comm.).
Dumaran Island
On Dumaran Island, which is off the northeastern coast of Palawan,
three areas are managed by the Katala Foundation's Philippine Cockatoo
Conservation Programme (PCCP). Two of those are protected areas: the
Omoi Cockatoo Reserve and the Manambaling Cockatoo Reserve (Widmann et
al. 2009b, p. 7). The third area is Lagan, which is also monitored and
managed by the PCCP. On Dumaran Island, the protected suitable forest
patches are each very small: 1.5 and 0.6 km\2\ (0.6 and 0.2 mi\2\),
respectively (Widmann and Widmann 2008, p. 24). On this island in 2008,
although 10 eggs were counted, only two birds fledged (Widmann et al.
2009b, p. 6). Recovery is slow; they started with fewer than 20 bi