Endangered and Threatened Wildlife and Plants; Listing Two Lion Subspecies, 79999-80056 [2015-31958]
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Vol. 80
Wednesday,
No. 246
December 23, 2015
Part II
Department of the Interior
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Fish and Wildlife Service
50 CFR Part 17
Endangered and Threatened Wildlife and Plants; Listing Two Lion
Subspecies; Final Rule
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Federal Register / Vol. 80, No. 246 / Wednesday, December 23, 2015 / Rules and Regulations
DEPARTMENT OF THE INTERIOR
II. Major Provision of the Regulatory
Action
Fish and Wildlife Service
This action revises the taxonomic
classification of the Asiatic lion
(currently classified as P. l. persica and
listed as an endangered species under
the Act) to P. l. leo based on a
taxonomic change. The P. l. leo
subspecies will be listed as an
endangered species and the P. l.
melanochaita subspecies will be listed
as a threatened species in the List of
Endangered and Threatened Wildlife in
title 50 of the Code of Federal
Regulations (CFR) at 50 CFR 17.11(h).
This action will also add a rule under
section 4(d) of the Act for P. l.
melanochaita which is set forth at 50
CFR 17.40(r).
50 CFR Part 17
[Docket No. FWS–R9–ES–2012–0025; 450
003 0115]
RIN 1018–BA29
Endangered and Threatened Wildlife
and Plants; Listing Two Lion
Subspecies
Fish and Wildlife Service,
Interior.
ACTION: Final rule.
AGENCY:
We, the U.S. Fish and
Wildlife Service (Service), determine
endangered status for the lion
subspecies Panthera leo leo and
threatened status for P. l. melanochaita
under the Endangered Species Act of
1973, as amended (Act). We are also
publishing a concurrent rule under
section 4(d) of the Act. This rule
provides for conservation measures for
P. l. melanochaita.
DATES: This rule is effective January 22,
2016.
ADDRESSES: This final rule is available
on the Internet at https://
www.regulations.gov and comments and
materials received, as well as supporting
documentation used in the preparation
of this rule, will be available for public
inspection, by appointment, during
normal business hours at: U.S. Fish and
Wildlife Service; 5275 Leesburg Pike;
Falls Church, VA 22041.
FOR FURTHER INFORMATION CONTACT:
Branch of Foreign Species, Ecological
Services, U.S. Fish and Wildlife Service,
MS: ES, 5275 Leesburg Pike, Falls
Church, VA 22041–3803; telephone,
703–358–2171; facsimile, 703–358–
1735. If you use a telecommunications
device for the deaf (TDD), call the
Federal Information Relay Service
(FIRS) at 800–877–8339.
SUPPLEMENTARY INFORMATION:
SUMMARY:
Executive Summary
asabaliauskas on DSK5VPTVN1PROD with RULES
I. Purpose of the Regulatory Action
We are listing two subspecies of lion,
Panthera leo leo and P. l. melanochaita,
under the Endangered Species Act of
1973, as amended (Act). We are listing
the P. l. leo subspecies as an endangered
species and the P. l. melanochaita
subspecies as a threatened species
under the Act. We are also finalizing a
rule under section 4(d) of the Act that
will provide for conservation measures
for P. l. melanochaita.
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Background
The Endangered Species Act of 1973,
as amended (Act) (16 U.S.C. 1531 et
seq.), is a law that was passed to prevent
extinction of species by providing
measures to help alleviate the loss of
species and their habitats. Before a plant
or animal species can receive the
protection provided by the Act, it must
first be added to the Federal List of
Endangered and Threatened Wildlife or
the Federal List of Endangered and
Threatened Plants in part 17 of title 50
of the Code of Federal Regulations
(CFR). Section 4 of the Act and its
implementing regulations at 50 CFR part
424 set forth the procedures for adding
species to these lists.
Previous Federal Actions
In a final rule published in the
Federal Register on June 2, 1970 (35 FR
8491), the Asiatic lion (currently listed
under the Act as Panthera leo persica)
was listed under the Act’s precursor, the
Endangered Species Conservation Act of
1969, as an endangered species and has
remained listed as an endangered
species under the Act.
On March 1, 2011, we received a
petition dated the same day from the
International Fund for Animal Welfare,
the Humane Society of the United
States, Humane Society International,
the Born Free Foundation/Born Free
USA, Defenders of Wildlife, and the
Fund for Animals requesting that the
African lion subspecies be listed as
endangered under the Act. The petition
identified itself as such and included
the information as required by 50 CFR
424.14(a). On November 27, 2012, we
published a ‘‘positive’’ 90-day finding
(77 FR 70727) indicating that we would
initiate a status review of the African
lion.
On October 29, 2014 (79 FR 64472)
we published in the Federal Register a
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finding that listing the African lion
subspecies (Panthera leo leo) as a
threatened species was warranted and
proposed to list the subspecies as a
threatened species under the Act. We
also proposed a rule under section 4(d)
of the Act to provide conservation
measures for the African lion.
Summary of Changes From the
Proposed Rule
We fully considered comments from
the public and the peer reviewers on the
proposed rule to determine our final
listing status of lion. This final rule
incorporates changes to our proposed
rule based on the comments we received
that are discussed under Summary of
Comments and Responses and newly
available scientific and commercial
information that became available after
the close of the comment period. We
accept the taxonomy as recommended
by the International Union for
Conservation of Nature (IUCN) Species
Survival Commission Cat Classification
Task Force: P. l. leo (Asia and western,
central, and northern Africa) and P. l.
melanochaita (southern and eastern
Africa). Here we evaluate the status of
the lion species (P. leo), which includes
the previously unreviewed population
of P. l. leo in India (formerly P. l.
persica). Additionally, we have
incorporated new population estimates
and population trends for the lion into
our Species Information section.
Based on comments by peer reviewers
and others, we revised the section on
trophy hunting, providing additional
information on the practices that experts
have identified as undermining the
sustainability of trophy hunting,
recommended best practices and
reforms, biological impacts of trophy
hunting on lion populations, and
corruption in range countries, and
expanded our assessment of the level of
threat that trophy hunting presents to
the species. Additionally, we have
incorporated information on infanticide,
corruption, traditional use of lion parts
and products, disease, and climate
change. Under the discussion of the 4(d)
rule in the preamble, we further clarify
factors we will consider when making
an enhancement finding for importation
of sport-hunted trophies of P. l.
melanochaita.
Based on the information we received
and our assessment of that information,
we have altered our finding. Some of the
information we received indicated
threats may be worse than previously
indicated. Due to significant differences
in the impacts of threats within the
species, we found that P. l. leo and P.
l. melanochaita qualify for different
statuses under the Act.
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Federal Register / Vol. 80, No. 246 / Wednesday, December 23, 2015 / Rules and Regulations
and, consequently, by several
international organizations and
Taxonomy
governing bodies. As a result, this is the
The lion (Panthera leo) was first
classification on which the conservation
described by Linnaeus (1758, in Haas et of the species is largely based. However,
al. 2005, p. 1), who gave it the name
results of recent genetic research call
Felis leo. It was later placed in the genus into question this classification.
Panthera (Pocock 1930, in Haas et al.
In recent years, several genetic studies
2005, p. 1). Although the classification
have provided evidence of an
of the modern lion as P. leo is accepted
evolutionary division within lions in
within the scientific community, there
Africa (see Barnett et al. 2014, p. 6;
was a lack of consensus regarding lion
Dubach et al. 2013, p. 746; Bertola et al.
intraspecific taxonomy (Mazak 2010, p.
2011 (entire); Antunes et al. 2008
194; Barnett et al. 2006b, p. 2120).
(entire); Barnett et al. 2006a, pp. 511–
Based on morphology, traditional
512). These studies include analysis of
classifications recognize anywhere from DNA samples from all major regions of
zero subspecies (classifying lions as one the species’ range, though some regions
monotypic species) up to nine
are sparsely represented. A major
subspecies (Mazak 2010, p. 194, citing
genetic subdivision among lions occurs
several sources). The most widely
in Africa, with lions in southern and
referenced of the morphology-based
eastern Africa being distinct from and
taxonomies is an eight-subspecies (six
more diverse than lions elsewhere
extant) classification provided by
(western and central Africa and Asia)
Hemmer (1974, in Nowell and Jackson
(Figure 1). Lions in western and central
1996, p. 312; Barnett et al. 2006a, p. 507; Africa (as well as now-extinct North
Barnett et al. 2006b, p. 2120), which is
African lions) are more closely related
recognized by the Integrated Taxonomic to lions in India than to lions in
Information System (ITIS) (ITIS 2013,
southern and eastern Africa (Barnett et
unpaginated). It divides the lion species al. 2014, pp. 4–8; Dubach et al. 2013,
into: Panthera leo persica (India); P. l.
pp. 741, 746–747, 750–751; Bertola et
leo, commonly referred to as the Barbary al. 2011, entire). According to Dubach et
lion (Morocco through Tunisia, extinct); al. (2013, p. 753), current range collapse
P. l. senegalensis (West Africa east to
and fragmentation is too recent a
the Central African Republic (CAR));
phenomenon to explain the reduced
P. l. azandica (northern Zaire); P. l.
genetic variability in these regions.
bleyenberghi (southern Zaire and
Rather, the low genetic diversity in and
presumably neighboring areas of Zambia between western and central African
and Angola); P. l. nubica (East Africa);
lion populations suggests they have a
P. l. krugeri (Kalahari region east to the
shorter evolutionary history than the
Transvaal and Natal regions of South
more genetically diverse lions in
Africa), and P. l. melanochaita, also
southern and eastern Africa (Bertola et
called the Cape lion (Cape region of
al. 2011, p. 1362). Several authors argue
South Africa, extinct) (Nowell and
that the origin of these genetically
Jackson 1996, p. 312).
distinct groups may be the result of
In 1987, O’Brien (1987a, entire;
regional extinctions and recolonizations
1987b, entire) reported the first results
during major climate (and consequently
of genetic studies conducted on lion
biome) fluctuations during the
samples from some, but not all, regions
Pleistocene Epoch (Barnett et al. 2014,
of the species’ range using early genetic
pp. 5–8; Bertola et al. 2011, pp. 1362–
techniques. Lions in India differed from 1364).
lions in Africa, supporting a twoThese findings on lion genetic
subspecies classification for extant
relationships are based primarily on
lions: P. l. leo and P. l. persica, the
analysis of mitochondrial DNA
African and Asiatic lion, respectively
(mtDNA), which is inherited only from
(O’Brien et al. 1987, Meester and Setzer the mother. Because lions display sex1971, Ellerman et al. 1953, in Dubach
biased dispersal, in which males leave
their natal range and females tend to
2005, p. 16). According to Dubach
remain in their natal range, one would
(2005, p. 16), most taxonomic
expect gene flow in females to be lower
authorities recognize this twothan in males, resulting in greater
subspecies taxonomy. This taxonomy
was also recognized by the International geographic differentiation in females
(Mazak 2010, p. 204). Consequently,
Union for Conservation of Nature
some authors state that results of
(IUCN) (Bauer et al. 2012, unpaginated)
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mtDNA analyses should be backed up
by studies on nuclear DNA (nDNA,
inherited from both parents) and
morphological traits before assigning
taxonomic importance to them (Barnett
et al. 2014, pp. 1, 8).
Recently, Mazak (2010, entire)
examined morphological characteristics
of 255 skulls of wild lions and found
considerable variation throughout the
species’ range, with variation being
greater within populations than between
them. However, according to Dubach et
al. (2013, p. 742), the genetic distinction
of lions in southern and eastern Africa
from those elsewhere in the species’
range is confirmed by results of studies
by Antunes et al. (2008, entire) which,
in addition to analysis of mtDNA, also
included analysis of nDNA sequence
and microsatellite variation.
The recent results of genetic research
renewed the debate on lion taxonomy
among the experts. For this reason, the
IUCN Species Survival Commission Cat
Specialist Group commissioned a Cat
Classification Task Force from among its
expert members to reach a consensus on
taxonomy for the group. As we
explained in our proposed rule, until
the results of the IUCN Cat
Classification Task Force became
available, we concluded that the
taxonomy of the species was
unresolved, but, as required by the Act,
we based our status review in our
proposed rule on the best available
scientific and commercial information,
which was the taxonomy that was most
widely recognized by taxonomic
experts: P. leo leo (African lion) and P.
leo persica (Asiatic lion) and reviewed
the status of the petitioned entity, the
African lion.
In June 2015, after the close of the
comment period on our proposed rule,
IUCN posted an updated Red List
Assessment for lion. In this assessment,
a new two-subspecies classification is
proposed based on the recommendation
of the IUCN Cat Classification Task
Force: P. l. leo of Asia (India) and
western, central, and northern Africa,
and P. l. melanochaita for southern and
eastern Africa (Bauer et al. 2015a,
unpaginated) (Figure 1), which is
supported by Barnett et al. (2014, p. 6),
Dubach et al. (2013, p. 746), Bertola et
al. (2011, entire), Antunes et al. (2008,
entire), and Barnett et al. (2006a, pp.
511–512).
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As required by the Act, and as
explained in our proposed rule, we base
our listing determinations on the best
available scientific and commercial
information. We accept the taxonomy as
recommended by the IUCN Cat
Classification Task Force, which is
supported by mtDNA analysis, as well
as analysis of nDNA sequence and
microsatellite variation: P. l. leo (Asia
and western, central, and northern
Africa) and P. l. melanochaita (southern
and eastern Africa) (Figure 1) as the best
available scientific and commercial
information. Because this new
classification for lion includes
subspecies whose ranges span two
continents, we assessed the status of the
entire lion species (P. leo).
Currently, the Asiatic lion (P. l.
persica) is listed as an endangered
species under the Act. Based on the new
taxonomic classification for lions, we
are revising the List of Endangered and
Threatened Wildlife at 50 CFR 17.11(h).
In the Regulation Promulgation section
of this document, we implement a
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taxonomic change by removing the
invalid subspecies P. l. persica. This
entity is now included in the
assessment of the lion species (P. leo).
Species Description
The lion is the second-largest extant
cat species (second in size only to the
tiger) and the largest carnivore in Africa
(Ray et al. 2005, p. 67). As with other
widely distributed large cats, there is
considerable morphological variation
within the species as a result of sexual
selection, regional environmental
adaptations, and gene flow (Mazak
2010, p. 194). These include, among
others, variation in size, coat color and
thickness, mane color and form, and
skull characteristics (Mazak 2010, p.
194, citing several sources; Hollister
1917, in Dubach 2005, p. 15). They are
described in the Convention on
International Trade in Endangered
Species of Wild Fauna and Flora
(CITES) Periodic Review of the Status of
African Lion Across Its Range (CITES
2014, p. 3) as follows:
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Characteristics include sharp, retractile
claws, a short neck, a broad face with
prominent whiskers, rounded ears and a
muscular body. Lions are typically a tawny
color with black on the backs of the ears and
white on the abdomen and inner legs. Males
usually have a mane around the head, neck
and chest. Lions are sexually dimorphic,
with males weighing about 20–27 percent
more than females. Adult males, on average,
weigh about 188 kilograms (kg) (414 pounds
(lbs)) with the heaviest male on record
weighing 272 kg (600 lbs). Females are
smaller, weighing, on average, 126 kg (278
lbs). The male body length, not including the
tail, ranges from 1.7 meters (m) to 2.5 m (5.6
feet (ft to 8.2 ft) with a tail from 0.9 m to 1
m (3 ft to 3.2 ft) (Nowell and Jackson, 1996).
Lions in India tend to be smaller than
those in Africa. Adult males weigh
between 160–190 kg (353–419 lb), while
females weigh between 110–120 kg
(243–265 lb) (Chellam in litt. in Nowell
and Jackson 1996, p. 37). The record
total length for a male lion in India,
including the tail, is 2.92 m (9.6 ft)
(Sinha 1987 in Nowell and Jackson
1996, p. 37). One characteristic unique
to lions in India is a longitudinal fold
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of skin that runs along the belly
(O’Brien et al. 1987, p. 100).
Additionally, male lions in India do not
have as large and full a mane as those
in Africa, allowing their ears to always
be visible, whereas the manes of male
lions in Africa completely hide the ears
(Nowell and Jackson 1996, p. 37;
O’Brien et al. 1987, p. 100).
and death can also occur during hunting
attempts on some of their larger prey.
Haas et al. (2005, entire) provide a
summary of information on lion,
including the following:
Lions are well studied. Much
information exists on habits, behavior,
and ecology of lions in Africa. CITES
(2014, p. 3) provides a general overview
as follows:
Prides vary in size and structure, but
typically contain 5–9 adult females (range, 1–
18), their dependent offspring, and a
coalition of 2–6 immigrant males (Heinsohn
and Packer 1995; Packer et al. 1991). . . .
Pride sizes are smallest in arid environments
with limited prey species (Elliott and Cowan
1977; Hanby and Bygott 1979; Ruggiero 1991;
Schaller 1972; Stander 1992b; Wright
1960). . . . Males reside in a pride for
[approximately] 2 years before being replaced
by another group of males (Packer et al.
1988). . . . In the absence of a pride
takeover, males generally leave their natal
pride when 2–4 years old (Bertram 1975b;
Pusey and Packer 1987). Most females are
incorporated into their natal prides (Pusey
and Packer 1987; Van Orsdol et al.
1985). . . . A small proportion of lions is
nomadic, including young and adult males
without a pride. Nomadic lions follow the
migrations of prey and hunt and scavenge
cooperatively (Bertram 1975a; Bygott et al.
1979; Schaller 1968, 1969; Van Orsdol et al.
1985).
. . . Lion productivity (measured as
number of surviving cubs) is limited by food.
. . . Cub mortality is high in lions and is
linked to periods of prey scarcity and
infanticide by male lions during pride
takeovers (Packer and Pusey 1983b; Schaller
1972; Van Orsdol et al. 1985; Whitman and
Packer 1997).
. . . Lions are mainly active at night. . . .
[They] usually hunt in groups; males hunt
less frequently than do females, but males are
stronger and can gain access to kills made by
females (Bertram 1975a; Scheel and Packer
1991). Prey selection is related to seasonal
weather patterns and the migration of large
herbivores in some parts of Africa (Hanby et
al. 1995). . . . Lions exhibit individual
preferences in prey selection within and
between prides in the same area (Rudnai
1973b; Van Orsdol 1984).
Lions are generalist, cooperative hunters,
with foraging preferences changing with
season and with lion group size. Lions live
in groups called ‘‘prides,’’ which are ‘‘fissionfusion’’ social units with a stable
membership that sometimes divide into
small groups throughout the range. Lions
have no fixed breeding season. Females give
birth every 20 months if they raise their cubs
to maturity, but the interval can be as short
as 4–6 months if their litter is lost. Gestation
lasts 110 days, litter size ranges 1–4 cubs,
and sex ratio at birth is 1:1. At about 4 years
of age, females will have their first litter and
males will become resident in a pride. Pride
takeovers by male lions and subsequent
infanticide of cubs sired by the ousted male
lions greatly influences reproductive success.
Lionesses defending their cubs from the
victorious males are sometimes killed during
the takeover. Infanticide accounts for 27
percent of cub mortality. Adult mortality is
typically caused by humans, starvation,
disease, or attacks from other lions. Injury
Lion prides in India tend to be smaller
than those in Africa; most prides in
India contain an average of two females,
with the largest having five. Coalitions
of males will defend home ranges that
contain one or more groups of females,
but unlike lions in Africa, in India male
lions only associate with pride females
when mating or on a large kill (Meena
2009, p. 7; Nowell and Jackson 1996, p.
37). Females are approximately 4 years
old at first reproduction, males 5–8
years (Banerjee and Jhala 2012, p. 1424;
Nowell and Jackson 1996, p. 37).
Banerjee and Jhala (2012, p. 1424) found
that mating occurred throughout the
year, but mostly in winter. Gestation
lasts 110 days; births peaked in the
summer (April–May). Average litter size
is 2.5 cubs, but as many as 5 have been
observed (Banerjee and Jhala 2012, pp.
1424, 1427; Nowell and Jackson 1996, p.
Habitat
Historically, the species occurred in
all habitats in Africa, except rainforest
and the hyper-arid interior of the Sahara
(Ray et al. 2005, p. 66). Today they are
found primarily in savannas, although
there are some remnant populations in
other habitat types (Riggio et al. 2013, p.
19). According to Nowell and Jackson
(1996, p. 19), optimal habitat appears to
be open woodlands and thick bush,
scrub, and grass complexes, where
sufficient cover is provided for hunting
and denning. The highest lion densities
are reached in savanna woodlands
plains mosaics of southern and eastern
Africa (Ray et al. 2005, p. 66). The
species is intolerant of anthropogenic
(human-caused) habitat conversion,
such as farming or overgrazing by
livestock (Ray et al. 2005, p. 66). In
India, the lion occurs in dry deciduous
forests (Meena et al. 2014, p. 121). Moist
mixed and mixed forest habitats are
critical to lions as they seek moist shady
habitats that provide shelter from the
heat and cover to hide during peak
times of human activities (Jhala et al.
2009, p. 3391).
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37). Lion reproduction in India appears
to coincide with the fawning peak of
chital deer (Axis axis) between
December and January or with the
rutting season of chital and peak
fawning for sambar deer (Cervus
unicolor) between May and June.
Breeding lionesses may cue into these
times of increased availability of food
sources to time births for maximum
survival of cubs (Banerjee and Jhala
2012, p. 1427). Average interbirth
interval is estimated to be 1.37 years;
however, if cubs of the previous litter
survived to independence, it could be
higher. After territorial takeovers and
infanticides, females mated within an
average 4.8 months (Banerjee and Jhala
2012, p. 1424). Banjeree and Jhala (2012,
p. 1424) found that the major cause of
cub mortality is infanticide due to
territorial takeovers by adult males.
Most observed adult mortalities (54.5
percent) were due to natural causes and
43 percent were due to human causes;
remaining mortalities were due to
unknown causes.
Diet and Prey
Lions are opportunistic hunters and
scavengers. As scavengers, lions are
dominant and can usually readily
displace other predators from their kills
(Packer 1986, Schaller 1972, in Haas et
al. 2005, pp. 4–5). As hunters, they are
known to take a variety of prey.
However, they are also the largest
carnivore in Africa and, as a result,
require large prey to survive. Ray et al.
(2005, pp. 66–67) summarizes lion prey
in Africa as follows:
Lions are generalists and have been
recorded to consume virtually every mammal
species larger than 1 kg in their range, as well
as a wide variety of larger reptiles and birds
(Nowell & Jackson 1996; Sunquist & Sunquist
2002). The constraints of large physical size
and extended social groups, however, bind
them to large-bodied prey, and their diet is
dominated by medium-large ungulates. In
fact, only a few species of large ungulates
comprise a majority of their diet wherever
they occur (Schaller 1972; Stander 1992;
Packer et al. 1995), and they are unable to
persist in areas without large-bodied prey.
The threshold of this requirement is perhaps
represented at Etosha National Park,
Namibia, where Stander (1992) showed that
lions hunting in pairs met their minimum
requirements hunting springboks which, at
< 50 kg, are the smallest preferred prey
species recorded.
In India, the lion’s diet is comprised
of both small and medium prey, as well
as vulnerable livestock (Meena et al.
2011, p. 61; Singh and Gibson 2011, p.
1753; Meena 2009, p. 8). The most
commonly taken species is chital, which
weighs approximately 50 kg (110 lb),
and a larger species, the sambar deer
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(Meena et al. 2011, p. 63; Nowell and
Jackson 1996, p. 37). The smaller size of
the prey available in India may be
responsible for the smaller lion group
sizes and less interaction between male
and female groups (Meena 2009, p. 8;
Nowell and Jackson 1996, p. 37).
Historically, domestic cattle also
constituted a major portion of the lion’s
diet (Nowell and Jackson 1996, p. 37)
and remains a significant portion today
(Meena et al. 2011, pp. 63, 64; Singh
and Gibson 2011, pp. 1753–1754). The
proportion of wild prey and domestic
livestock in a lion’s diet may vary by
season and between protected areas and
peripheral areas (Meena et al. 2011, pp.
64, 65).
Prey availability affects the
reproduction, recruitment, and foraging
behavior of lions and, as a result,
strongly influences lion movements,
abundance, and population viability
(Winterbach et al. 2012, p. 7, citing
several sources). Lion densities are
directly dependent on prey biomass
(Van Orsdol et al. 1985, in Packer et al.
2013, p. 636; Hayward et al. 2007,
entire). In Africa, lion densities range
from 8–13 lions per 100 square
kilometers (km2) in Selous Game
Reserve and up to 18 per 100 km2 in
protected areas of eastern Africa and
South Africa (Creel and Creel 1997,
Nowell and Jackson 1996, in Haas et al.
2005, p. 4). In India, densities are
estimated to be 15 lions per 100 km2 in
Gir Protected Area, 6 per 100 km2 in
Girnar Wildlife Sanctuary, and 2 per
100 km2 in the surrounding agropastoral land (Banerjee and Jhala 2012,
p. 1421; Banerjee et al. 2010, p. 249).
Aside from human-related mortality,
prey availability is likely the primary
determinant of lion density in Africa
(Fuller and Sievert 2001, in Winterbach
et al. 2012, p. 7). In areas of low natural
prey density, or high human contact,
lions may prey on livestock (see
Human-Lion Conflict).
Movements/Home Range
Availability of prey is perhaps the
primary factor that determines the
ranging behavior of large carnivores
(Gittleman & Harvey 1982, Van Orsdol
et al. 1985, Grant et al. 2005, Hayward
et al. 2009, in Winterbach et al. 2012,
p. 4). Home-range sizes of lion prides
correlate with lean-season prey biomass
(Van Orsdol et al. 1985, in Haas et al.
2005, p. 4) and, therefore, vary widely
among habitats. Average range sizes of
lion prides in Africa are 26–226 km2,
but can be considerably larger (Stander
1992b; Van Orsdol et al. 1985; Viljoen
1993, in Haas et al. 2005, p. 4). In areas
of low or variable prey biomass, annual
range requirements for a single lion
pride can exceed 1,000 km2 (Packer et
al. 2013, p. 636). Funston (2011, p. 5)
found the home ranges of lion prides in
the dune-savanna habitat of Kgalagadi
Transfrontier Park to range from 1,762
to 4,532 km2. In India, however, Jhala et
al. (2009, p. 3391) found the average
home range of a breeding group of
lionesses to be 33 km2. Similarly, Meena
(2009, pp. 7–8) found home ranges of
females and males to be 35 km2 and 85
km2, respectively.
Range
The historical range of the lion
included most current continental
African countries (Chardonnet 2002, pp.
25–28) and extended from Greece
through eastern Europe, southwest Asia
(the Middle East), and India (Bauer et al.
2015a, unpaginated; Nowell and Jackson
1996, p. 38). Lions have undergone
dramatic range retraction from this
historical distribution (Ray et al. 2005,
p. 67). Extirpation of lions in Europe
occurred almost 2,000 years ago. The
species was extirpated from southwest
Asia within the last 150 years and
northern Africa in the 1940s (Bauer et
al. 2015a, unpaginated; Black et al.
2013, p. 1; Nowell and Jackson 1996, p.
38). Today, lions occur only in Asia and
sub-Saharan Africa (Table 1). In Asia,
P. l. leo only remains in the Gir Forests
of India. Within sub-Saharan Africa, P.
l. leo and P. l. melanochaita remain in
34 range countries (35 with South
Sudan, which gained its independence
as a country in July 2011) and have been
recently extirpated from 12 African
range countries and potentially
extirpated from another 4 (Bauer et al.
2015a, unpaginated) (Table 1).
TABLE 1—RANGE COUNTRIES OF P. l. leo AND P. l. melanochaita
[Information derived from Bauer et al. 2015a, unpaginated, IUCN 2006a, IUCN 2006b, and Chardonnet 2002]
Subspecies
Countries
Panthera leo leo ..............................
ˆ
Algeria 1, Benin, Burkina Faso, Cameroon, CAR, Chad, Congo 2, Cote d’Ivoire 2, DRC, Egypt 1, Gabon 2,
Gambia 2, Ghana 3, Guinea 3, Guinea-Bissau 2, India, Liberia, Libya 1, Mali 2, Mauritania 2, Morocco 1,
Niger, Nigeria, Senegal, Sierra Leone 2, Togo 3, Tunisia 1.
Angola, Botswana, Burundi 2, Djibouti 2, Eritrea 2, Ethiopia, Kenya, Lesotho 2, Malawi, Mozambique, Namibia, Rwanda 3, Somalia, South Africa, Sudan/South Sudan, Swaziland, Tanzania, Uganda, Zambia,
Zimbabwe.
Panthera leo melanochaita .............
1 Lions
2 Lions
asabaliauskas on DSK5VPTVN1PROD with RULES
3 Lions
extirpated.
considered recently extirpated (Bauer et al. 2015a).
considered possibly extirpated (Bauer et al. 2015a).
The confirmed lion range in western
Africa (the total size of protected areas
where lions were confirmed) is
estimated at 49,000 km2, or 1.1 percent
of the historic range (Henschel et al.
2014, p. 5). The most recent estimate of
the lion’s range throughout Africa
comes from Bauer et al. (2015a,
unpaginated) who estimate the extant
lion range (areas reasonably confident
that lions persist based on recent
records) to be approximately 1.6 million
km2 (617,763 mi2), or 8 percent of the
historical range in Africa. The areas
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classified by Bauer et al. (2015,
unpaginted) as possibly extinct total
approximately 1.8 million km2 (694,984
mi2), which is over half (52 percent) of
the range classified as extant by the
previous estimate conducted by Riggio
et al. (2013, p. 26), which was based on
estimates of savanna habitat. The lion’s
range in Asia is estimated to be
approximately 10,500 km2 (4,054 mi2),
which occurs within the Gir National
Park and Wildlife Sanctuary (Gir
Protected Area), Girnar Wildlife
Sanctuary, and surrounding agro-
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pastoral land (Bauer et al. 2015a,
unpaginated; Banerjee and Jhala 2012,
p. 1421; Jhala et al. 2009, pp. 3384,
3385; Nowell and Jackson 1996, p. 38).
Distribution and Abundance
The general distribution of lions in
Africa is summarized by Ray et al.
(2005, p. 67) as follows:
Currently, lions are restricted mainly to
protected areas and surrounding
conservancies or ‘game management areas,’
with the largest populations in East and
southern Africa. Where protection is poor,
particularly outside protected areas, range
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loss or population decreases can be
significant. Declines have been most severe
in West and Central Africa, with only small,
isolated populations scattered chiefly
through the Sahel. Lions in the region are
declining in some protected areas and, with
the exception of southern Chad and northern
Central African Republic, are virtually absent
from unprotected areas (Bauer 2003).
There have been few efforts in the past to
estimate the number of lions in Africa. Myers
(1975) wrote, ‘‘Since 1950, their [lion]
numbers may well have been cut in half,
perhaps to as low as 200,000 in all or even
less.’’ Later, Myers (1986) wrote, ‘‘In light of
evidence from all the main countries of its
range, the lion has been undergoing decline
in both range and numbers, often an
accelerating decline, during the past two
decades.’’ In the early 1990s, IUCN SSC Cat
Specialist Group members made educated
‘‘guesstimates’’ of 30,000 to 100,000 for the
African Lion population (Nowell and Jackson
1996).
Estimates of lion abundance on a large
geographical scale are few in number.
For a variety of reasons—including low
densities, large ranges, cryptic
coloration, nocturnal and wary habits—
lions are difficult to count (Riggio et al.
2013, p. 31; Bauer et al. 2005, p. 6).
There are large areas of the species’
range in which no data are available on
lion occurrence or abundance (IUCN
2006b, pp. 12–13). Species experts
recognize that estimating the size of the
lion population in Africa is an
ambitious task, involving many
uncertainties (Bauer et al. 2012,
unpaginated). Estimates, particularly
throughout Africa or broad region-wide
estimates tend to rely to a considerable
extent on expert opinion or inference
(Riggio et al. 2013, p. 21; Chardonnet
2002, p. 19). Consequently, there is a
large degree of uncertainty in these
estimates. In addition, to date all efforts
to estimate the number of lions in Africa
have used different methods; therefore,
the results of earlier estimates cannot be
directly compared to those of later
estimates to determine population
trend.
The earliest estimates of lion
abundance in Africa were educated
guesses made during the latter half of
the 20th Century. Bauer et al. (2008,
unpaginated) summarize the
information as follows:
Ferreras and Cousins (1996, entire)
provided the first quantitatively derived
estimate of lion abundance in Africa
using a GIS-based model calibrated with
information obtained from lion experts.
Ferreras and Cousins predicted lion
abundance in Africa in 1980 to be
75,800. Later, four additional efforts—
Chardonnet (2002), Bauer and Van Der
Merwe (2004), IUCN (2006a, 2006b),
and Riggio et al. (2013)—estimated lion
population sizes ranging from 23,000 to
40,000 (Table 2).
Between 2006 and 2012, Henschel et
al. (2014, p. 2) conducted field surveys
in protected areas within designated
Lion Conservation Units (LCUs) of
western Africa to confirm lion presence
where evidence of occurrence was
lacking and to establish population
estimates where lions occurred. Lions
were absent from protected areas in 5 of
the 10 countries in western Africa
where lions were considered to be
present (Henschel et al. 2014, p. 4).
Henschel et al. (2014, p. 5) estimated
only 400 lions remain in the entire
western region, with most (about 350, or
80005
88 percent) concentrated in a single
population.
Bauer et al. (2015a, unpaginated)
attempted to correct for outdated
sources in Riggio et al. (2013) by
applying regional trends (discussed
below) to 2002 population estimates for
central, eastern, and southern Africa
from Bauer and Van Der Merwe (2004)
and Chardonnet (2002); estimates for
western Africa were taken from
Henschel et al. (2014) because of the
greater precision of their estimate.
Applying regional trends to Bauer and
Van Der Merwe (2004) lion populations
estimates, Bauer et al. (2015a,
unpaginated; supporting information,
Table 7) estimated lions in central
Africa to be 590, eastern Africa to be
7,345, and southern Africa to be 10,385
(Table 2). When regional trends were
applied to Chardonnet (2002) lion
estimates, Bauer et al. (2015,
unpaginated; supporting information,
Table 7) estimated lions in central
Africa to be 1,748, eastern Africa to be
13,316, and in southern Africa to be
15,925 (Table 2). In total, Bauer et al.
(2015, unpaginated) estimate the lion
population in Africa to be between
18,841 and 31,394. However, the
authors found that the study by Bauer
and Van Der Merwe (2004) was more
conservative and stricter on data
quality; therefore they have a greater
confidence in an estimate closer to
20,000 lions in Africa. Additionally, the
lion population in India was estimated
to be 445 by Bauer et al. (2015a,
unpaginated). In 2015, the Government
of Gujarat completed its latest census,
estimating 523 lions in India (BBC 2015,
unpaginated) (Table 2).
TABLE 2—ESTIMATES OF LION ABUNDANCE
[Rows may not tally due to rounding]
Source
Ferreras & Cousins 1996 (estimate for lion abundance in
1980).
Chardonnet 2002 ....................
asabaliauskas on DSK5VPTVN1PROD with RULES
Bauer & Van Der Merwe 2004
IUCN 2006 1 (as calculated by
Riggio et al. 2013).
Riggio 2013 (based on estimates of savanna habitat).
Henschel et al. 2014 ..............
Bauer et al. 2015a (trends applied to Bauer and Van Der
Merwe 2004).
Bauer et al. 2015a (trends applied to Chardonnet 2002).
Bauer et al. 2015a ..................
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Western Africa
(percent of
total)
Central Africa
(percent of
total)
Eastern Africa
(percent of
total)
Southern
Africa (percent
of total)
India
.......................
.......................
.......................
.......................
....................
75,800 (18,600 in protected
areas).
1,163 (3 percent).
850 (4 percent).
1,640 (5 percent).
480 (1 percent).
406 (n/a) ........
.......................
2,815 (7 percent).
950 (4 percent).
2,410 (7 percent).
2,419 (7 percent).
.......................
590 (3 percent).
15,744 (40
percent).
11,000 (48
percent).
17,290 (52
percent).
19,972 (57
percent).
.......................
7,345 (39 percent).
19,651 (50
percent).
10,000 (44
percent).
11,820 (37
percent).
12,036 (34
percent).
.......................
10,385 (55
percent).
....................
39,373
....................
23,000
....................
33,160
....................
34,907
....................
....................
18,726 *
.......................
1,748 (6 percent).
.......................
13,316 (42
percent).
.......................
15,925 (51
percent).
.......................
....................
31,394 *
.......................
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Total
445
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TABLE 2—ESTIMATES OF LION ABUNDANCE—Continued
[Rows may not tally due to rounding]
Western Africa
(percent of
total)
Source
Government of Gujarat
2015 **.
Central Africa
(percent of
total)
Eastern Africa
(percent of
total)
Southern
Africa (percent
of total)
.......................
.......................
.......................
.......................
India
Total
523
1 Estimates were made for individual Lion Conservation Units (defined management units), and were given as population size classes rather
than specific figures. As calculated by Riggio et al.
* Total includes estimate for western Africa taken from Henschel et al. (2014).
** As reported in BBC 2015, unpaginated.
As previously stated, extant lion
populations are limited to protected
areas. These populations are largely
isolated and many are small. P. l. leo
(totaling approximately 1,500 lions), is
divided into 15 populations in and
around protected areas; of these, 14 are
remaining populations from a total of 38
historical occurrences in western and
central Africa, while one occurs in India
(Bauer et al. 2015a, unpaginated;
Henschel et al. 2015b, unpaginated;
´
Brugiere et al. 2015, p. 515; Henschel et
al. 2014, pp. 4–5; Jhala et al. 2009, p.
3384). Nearly 90 percent of the lions in
western Africa persist in a single
population, the W-Arly-Pendjari (WAP)
Complex (Henschel et al. 2014, p. 5).
Based on Bauer et al. (2015a,
unpaginated; Supporting Information,
Table 3) and Bauer and Van Der Merwe
(2004, pp. 28–30), most P. l.
melanochaita occur in approximately 68
protected areas throughout southern and
eastern Africa, with larger populations
occurring in Botswana, Kenya, Namibia,
South Africa, Tanzania, Zambia, and
Zimbabwe.
Population Trends
Based on the best available
information, lion range and numbers
have clearly declined over the past
several decades. However, not all lion
populations have declined—some have
increased or remained stable, and some
have been restored to areas from which
they were previously extirpated (Bauer
et al. 2015a, unpaginated; Packer et al.
2013, p. 636; Funston 2011, p. 3;
Ferreira and Funston 2010, pp. 201,
203).
Bauer et al. (2015a, unpaginated),
using a time trend analysis of census
data, determined the trend of lion
populations from 1993 to 2014. Overall,
these lion populations decreased by 43
percent in 21 years (Table 3). However,
the authors found significant regional
differences. In Asia, the single
population increased by 55 percent
(Bauer et al. 2015a, unpaginated). The
population inside the protected area has
stabilized and expanded into
surrounding agro-pastoral land (Bauer et
al. 2015b, p. 2; Breitenmoser et al. 2008,
unpaginated). Additionally, the 2015
census of Gir Sanctuary and
surrounding forest areas showed a 27
percent increase from the 2010 census
(The Guardian 2015, unpaginated). In
southern Africa, the sample populations
overall increased by 8 percent (Bauer et
al. 2015a, unpaginated). However, one
of the largest populations, Okavango,
and populations of 6 unfenced reserves
are declining (Bauer et al. 2015a,
unpaginated, supporting information
Table 3; Bauer et al. 2015b, p. 1). Fifteen
of the 23 sample populations in
southern Africa were fenced; none
experienced sharp declines and many
small fenced populations are increasing
(Bauer et al. 2015a, unpaginated,
supporting information Table 3; Bauer
et al. 2015b, p. 1). South Africa was the
only African country with growth in
every population. However, these were
all fenced populations, and most were
reestablished in the past 20 years and
quickly reached capacity (Bauer et al.
2015b, pp. 1–2). Populations in eastern
Africa decreased overall by 59 percent
(Bauer et al. 2015a, unpaginated). The
Serengeti population was the only large
population surveyed that did not
decrease. Katavi National Park
experienced complete loss of lions from
an estimated 1,118 in 1993 to zero in
2014 (Bauer et al. 2015a, unpaginated,
supporting information Table 3; Bauer
et al. 2015b, p. 1). Western and central
Africa (combined) experienced the
largest decline at 66 percent (Table 3).
All populations are declining, except
the population in Pendjari; populations
´
in Comoe and Mole are now likely
extinct (Bauer et al. 2015a, unpaginated,
supporting information Table 3; Bauer
et al. 2015b, p. 1). Furthermore, almost
all lion populations in Africa that
historically exceeded 500 individuals,
the minimum number estimated to
constitute a viable population
(according to Riggio et al. 2013, p. 32
¨
and Bjorklund in Riggio et al. 2013, p.
32), are declining (Bauer et al. 2015b, p.
1).
Although these trends are based on 47
sample populations, they comprise a
substantial portion of the total
remaining lion populations; therefore,
the authors are confident in applying
the observed trends to regions and the
species as a whole (Bauer et al. 2015a,
unpaginated).
TABLE 3—REGIONAL TRENDS FOR 47 MONITORED LION POPULATIONS FROM 1993–2014
[Bauer et al. 2015a, unpaginated; supporting information Table 7].
Estimated lions in sample
populations
asabaliauskas on DSK5VPTVN1PROD with RULES
Region
1993
Percent
change
2014
Asia ..............................................................................................................................................
Southern Africa ............................................................................................................................
Eastern Africa ..............................................................................................................................
Western and Central Africa .........................................................................................................
312
4,887
3,112
1,304
485
5,265
1,266
439
+55
+8
-59
¥66
Total ......................................................................................................................................
9,615
7,455
¥22%
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asabaliauskas on DSK5VPTVN1PROD with RULES
Using these rates of change, the
authors calculated that the population
in 5 countries (Botswana, India,
Namibia, South Africa, and Zimbabwe),
or 25 percent of the lion’s range,
increased by 12 percent, while the
population in the remaining 75 percent
of the range decreased by 60 percent
(Bauer et al. 2015a, unpaginated),
resulting in a 43 percent population
decrease of the entire lion species
between 1993 and 2014.
The growth rate estimates discussed
above are the best available information
on global trends for lion populations,
although Bauer et al. (2015b, p. 2)
caution that these numbers are rough
estimates. However, it is unlikely that
regional declines are a product of
differences in methodological
shortcomings. Sample populations are
all monitored with at least partial
protection. Research sites are known to
be generally avoided by poachers and
encroachers. Therefore, the estimated
growth rates may be less optimistic. It
is likely that unmonitored, unfenced
populations will have suffered greater
rates of decline than reported since lack
of management generally means a lack
of conservation effort (Bauer et al.
2015b, p. 3).
The work of Packer et al. (2013a, pp.
639–640) predicts future declines
within a number of protected areas.
Bauer et al. (2015b, p. 2) found that if
regional trends remain unchanged in the
future, lions in western and central
Africa would likely lose a third of their
population in 5 years and half of their
population in 10 years. The population
in eastern Africa is likely to decline by
a third in 20 years and half in 30 years.
The Okavago population, Botswana,
will also likely decline by a third in 20
years (Bauer et al. 2015b, p. 2). Many
lion populations are expected to
disappear within the next few decades
such that the intensely managed
populations in southern Africa will
replace savanna landscapes as sites for
the most successful conservation of
lions.
protected areas where lions occur will
be under increased pressure as more
land is needed to satisfy the agricultural
needs of the human population.
Inadequate management and law
enforcement has led to poaching of the
lion’s prey base in Africa for bushmeat,
which has been critically depleted.
Additionally, human population growth
in Africa has led to human-lion conflict,
particularly on the edge of protected
areas, when pastoralists invade
protected areas to allow their herds to
graze or when lions move out of
protected areas in search of prey, often
preying on domestic livestock. Humanlion conflict leads to indiscriminate
killing of lions, primarily as a result of
retaliatory or preemptive actions to
protect livestock and human lives. The
close proximity of lions to humans and
domestic livestock throughout their
range exposes them to diseases, mainly
transmitted through livestock and
domestic dogs, which can impact
general fitness, reproduction, and
lifespan. These are in addition to
diseases that naturally occur in lion
populations in Africa. Furthermore, in
some areas of Africa improper
management has resulted in reduced
lion numbers due to excessive lion
harvests from trophy hunting.
Subsequently, some lion populations
are negatively impacted by infanticide
following pride takeovers by new males.
Because habitat loss has resulted in
small, isolated populations across its
range, lions face threats from stochastic
events, such as a disease epidemic and
inbreeding depression. An emerging
threat to lions is trade in bones and
other body parts for traditional
medicine. These causes of lion
population declines are widespread and
likely to continue. The impacts of these
threats are likely to be exacerbated by
climate change. Projected changes
indicate negative impacts to available
habitat and, therefore, the range of the
lion, prey availability, and the number
of disease outbreaks as well as
susceptibility to those diseases.
Summary of Threats
Today, lions are mainly restricted to
protected areas; however, they still face
serious threats that stem from
inadequate management of those areas
and increasing pressure on natural
resources to meet the needs of a growing
human population. Habitat loss has
been extensive throughout the range of
the lion, resulting in local and regional
lion population extirpations and a
dramatically reduced range with
isolated lion populations that are
increasingly limited to protected areas.
As the human population increases, the
Habitat Loss
Habitat destruction and degradation
have been extensive throughout the
range of the lion, resulting in local and
regional lion population extirpations,
reduced lion densities, a dramatically
reduced range (see Range), and small,
fragmented, and isolated lion
populations that are increasingly
limited to protected areas (see
Distribution and Abundance) (Singh
2007, in Jhala et al. 2009, p. 3384; Ray
et al. 2005, p. 69; Bauer and Van der
Merwe 2004, pp. 29–30; Nowell and
Jackson 1996, pp. 20–21). In India,
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habitat loss is partly responsible for the
decline of lions to a single population
in a protected area. However, due to
good protection and management, lions
have dispersed to forested areas outside
the protected area, extending their range
from an initial 1,883 km2 to 10,500 km2
(Johningh et al. 2007, Singh 2007, and
Divyabhanusinh 2005, in Banerjee et al.
2010, p. 248; Singh 2007, in Jhala et al.
2009, p. 3384). Farming has been
encouraged in the area and has
flourished. Cultivated areas have
created refuge areas and corridors for
lion movement (Vijayan and Pati 2001
in Meena et al. 2014, p. 124). At this
time, no information indicates habitat
loss is currently threatening the lion
population in India. In Africa, however,
despite lions being mainly found in
protected areas, habitat loss and
degradation continue to be among the
main threats to lions (IUCN 2006a, p.
18; Ray et al. 2005, pp. 68–69).
The main cause of lion habitat loss
and degradation is expansion of human
settlements and activities, particularly
due to agriculture and intensive
livestock grazing (IUCN 2006a, p. 18;
IUCN 2006b, p. 23; Ray et al. 2005, pp.
68–69; Chardonnet 2002, pp. 103–106).
From 1970 to 2000, the human
population in sub-Saharan Africa
increased by 126 percent (from 282
million to 639 million) (United Nations
(UN) 2013, p. 9), while at about the
same time (1975 to 2000), agriculture
area increased by 57 percent (from just
over 200 million ha to almost 340
million ha) and natural vegetation in the
region decreased by 21 percent (Brink
and Eva 2009, p. 507). In 2009,
approximately 1.2 billion ha, or 40
percent, of Africa’s land area was in
permanent pasture or crops, with the
vast majority (31 percent) in pasture
(UNEP 2012b, p. 68). Riggio et al. (2013,
p. 29) estimate the original extent of
savanna habitat in Africa to be
approximately 13.5 million km2. Based
on an analysis of land-use conversion
and human population densities, Riggio
et al. (2013, p. 29) found current
savanna habitat that is suitable for lions
to be fragmented and to total about 3.4
million km2 (or 25 percent of African
savanna habitat). This indicates a
substantial decrease in lion habitat over
the past 50 years and explains, in part,
why lions are limited to protected areas.
Based on a comparison of land-use
and human population data, Riggio et
al. (2013, p. 23) determined that a
density of 25 or more people per km2
served as a proxy for the extent of landuse conversion that would render
habitat unsuitable for lions. Woodroffe
(2000, p. 167) analyzed the impact of
people on predators by relating local
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carnivore extinctions to past and
projected human population densities
and estimated 26 people per km2 as the
mean human density at which lions
went locally or regionally extinct. In
1960, 11.9 million km2 of the original
13.5 million km2 of savanna habitat had
fewer than 25 people per km2; however,
in 2000 that number decreased to 9.7
million km2 (Riggio et al. 2013, p. 29).
Expansion of human settlements,
agriculture, and/or livestock grazing are
reported as occurring in or on the
periphery of several areas identified by
Riggio et al. (2013, suppl. 1) as lion
strongholds (viable populations) and
potential strongholds (IUCN 2006a, p.
16; IUCN 2006b, pp. 20–22), and are
particularly a threat in western, central,
and eastern Africa and some parts of
southern Africa. Expansion of
agriculture and livestock grazing are
reported in or around two of the larger
populations of P. l. leo in Africa, WAP
Complex and a Chad-CAR population
(Heschel et al. 2014, pp. 5–6; Houessou
et al. 2013, entire; Chardonnet et al.
2010, pp. 24–26; IUCN 2008, pp. 8, 28–
29); management in portions of both is
reported as weak (Heschel et al. 2014,
pp. 5–6; IUCN 2008, p. 8). Eastern
Africa contains approximately 40
percent of all the lions in Africa (Table
2). Seven of the seventeen major P. l.
melanochaita populations identified by
Riggio et al. occur in eastern Africa; six
of which occur in Tanzania and Kenya.
Between 1990 and 2010, Kenya’s human
population grew from 23 million (40/
km2) to 41 million (70/km2), whereas
Tanzania’s grew from 25 million (27/
km2) to 45 million (48/km2) (UN 2013,
pp. 421, 798). Not unexpectedly,
expansion of agriculture and livestock
grazing is occurring in these countries
(Brink et al. 2014, entire; UNEP 2009, p.
91; Mesochina et al. 2010a, p. 74),
including in or around these major
populations (Ogutu et al. 2011, entire;
Mesochina et al. 2010a, pp. 71–74, 76;
Packer et al. 2010, pp. 8–9; UNEP 2009,
pp. 98–99; Newmark 2008, pp. 322–324;
IUCN 2006b, pp. 20–22; Ogutu et al.
2005, entire). Mesochina et al. (2010a, p.
74) state that widespread destruction of
wildlife habitat and human
encroachment in wildlife corridors are
major threats to lion conservation in
Tanzania and consider loss of suitable
habitat as a top threat to lion survival in
the country. The Kenya Wildlife Service
indicates that habitat loss due to landuse changes and human encroachment
into previously wild areas is having a
major impact on lion range size in
Kenya (Kenya’s National Large
Carnivore Task Force 2010, p. 21).
In southern Africa, the extent of
current habitat destruction and
degradation appears to vary widely. For
example, according to the Zambia
Wildlife Authority (2009 pp. 4–5),
unplanned human settlement and other
land-use activities in game management
areas are a major threat to the long-term
survival of the lion in Zambia. They
note that conversion of natural habitat
in game management areas for cropping
and grazing of livestock has led to
habitat destruction and indicate that
elimination of tsetse flies and
subsequent increase in pastoralist
activities in game management areas
places the lion under renewed direct
conflict with humans. On the other
hand, according to Funston (2008, pp.
123–126), in several areas of southern
Africa where lions were recently
extirpated, lions are reestablishing as a
result of, among other factors, adequate
protection of habitat and prey.
Projections of future growth in human
populations, areas converted to
agriculture, and livestock numbers
suggest suitable lion habitat will
continue to decrease across its range
into the foreseeable future. Between
2015 and 2050, half of the world’s
population growth is expected to occur
in 9 countries, 6 of which are within the
lion’s range (India, Nigeria, Democratic
Republic of the Congo (DRC), Ethiopia,
Tanzania, and Uganda (UN 2015, p. 4).
Africa has the fastest population growth
rate in the world (UN 2015, pp. 3, 9;
UNEP 2012a, p. 2), and future
population growth in sub-Saharan
Africa is projected to be large and rapid
(UN 2013, p. 9). By 2100, Angola,
Burundi, DRC, Malawi, Mali, Niger,
Somalia, Uganda, Tanzania and Zambia
are projected to increase by at least fivefold (UN 2015, p. 9).
By 2050, the UN projects the human
population of Tanzania to almost triple
its 2010 population, reaching a density
of 137 people per km2, whereas Kenya’s
population is projected to more than
double, reaching a density of 167 people
per km2 (Table 4). Human population
growth, and resulting pressures exerted
on habitat, are also expected to vary
widely in the southern region.
Population increases from 2010 to 2050
are projected to range from about 23
percent (South Africa) to well over 200
percent (Zambia), with 2050 densities in
the region ranging from 5 people per
km2 (Botswana and Namibia) to 432
people per km2 (Uganda) (Table 4). The
human populations of most other
current and recent lion range countries
are also expected to have very high
growth rates (Table 4). The countrywide human population densities
provided here (and in Table 4) are not
directly comparable to the density
thresholds determined by Riggio et al.
(discussed above) due to the differences
in scale at which they were made.
However, country-wide population
densities relate the number of humans
to land area and, consequently, are
indicative of the level of pressure that
will exist to convert land to uses that
will meet the needs of the human
population. This situation is
particularly the case given that much of
sub-Saharan Africa is rural and locals
depend on agriculture for their
livelihood.
TABLE 4—HUMAN POPULATION PROJECTIONS IN COUNTRIES CONTAINING THE 47 SAMPLE LION POPULATIONS USED BY
ˆ
BAUER ET AL. (2015), EXCEPT COTE D’IVOIRE AND GHANA WHERE LIONS ARE CONSIDERED EXTIRPATED
[Population data is from UN 2013]
Subspecies
UN Population estimate, in thousands
(people/km2)
Country
asabaliauskas on DSK5VPTVN1PROD with RULES
1950
P. l. leo ......................
India .........................................................................
Benin ........................................................................
Burkino Faso ...........................................................
Cameroon ................................................................
Nigeria .....................................................................
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376,325
(114)
2,255
(20)
4,284
(16)
4,467
(9)
37,860
2010
2050
2100
1,205,625
(367)
9,510
(84)
15,540
(57)
20,624
(43)
159,708
1,620,051
(493)
22,137
(197)
40,932
(149)
48,599
(102)
440,355
1,546,833
(471)
32,944
(293)
75,274
(275)
82,393
(173)
913,834
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80009
TABLE 4—HUMAN POPULATION PROJECTIONS IN COUNTRIES CONTAINING THE 47 SAMPLE LION POPULATIONS USED BY
ˆ
BAUER ET AL. (2015), EXCEPT COTE D’IVOIRE AND GHANA WHERE LIONS ARE CONSIDERED EXTIRPATED—Continued
[Population data is from UN 2013]
Subspecies
UN Population estimate, in thousands
(people/km2)
Country
1950
Senegal ....................................................................
P. l. melanochaita ......
Kenya .......................................................................
Tanzania ..................................................................
Botswana .................................................................
Mozambique ............................................................
Namibia ....................................................................
South Africa .............................................................
Uganda ....................................................................
Zambia .....................................................................
asabaliauskas on DSK5VPTVN1PROD with RULES
Zimbabwe ................................................................
Although urbanization is increasing
in sub-Saharan Africa, the majority of
the population is rural (UN 2014, p. 20).
About 60–70 percent of the sub-Saharan
population relies on agriculture and
livestock for their livelihood (UNEP
2006, pp. 82, 100, 106; IAASTD 2009, p.
2). Much of the agriculture and
livestock-raising is at subsistence level
(IAASTD 2009, pp. 8, 28). As a result,
a large portion of the growing
population will depend directly on
expansion of agriculture and livestock
grazing to survive. Between 2010 and
2050, the population of sub-Saharan
Africa is projected to more than double
to more than 2 billion (from 831 million
to 2.1 billion) (UN 2013, p. 9). During
about this same time period (2005 to
2050), the area of cultivated land is
projected to increase by 51 million ha
(approximately 21 percent)
(Alexandratos and Bruinsma 2012, p.
107). However, this figure does not
include range land, and the majority of
agricultural land in Africa is devoted to
grazing (UNEP 2012b, p. 68). The
number of livestock (cattle, sheep, and
goats) in sub-Saharan Africa is projected
to increase about 73 percent, from 688
million to 1.2 billion, by 2050
(Alexandratos and Bruinsma 2012, p.
133).
Expansion of human settlements and
activities into lion habitat renders the
habitat unsuitable for lions primarily
because it results in reduced availability
of the wild prey that lions depend on for
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(41)
2,477
(13)
6,077
(10)
7,650
(8)
413
(1)
6,442
(8)
485
(1)
13,683
(11)
5,158
(21)
2,372
(3)
2,747
(7)
survival (see Loss of Prey Base) and
increased human-lion conflict resulting
in lion mortality (see Human-Lion
Conflict)—two of the main factors that
influence the distribution and
population viability of large carnivores
such as lions (Winterbach et al. 2014, p.
1; Riggio et al. 2013, p. 18). Ray et al.
(2005, p. 69) note that, although lions
have a wide tolerance for habitats, they
are generally incompatible with humans
and human-caused habitat alteration
and loss; they are the least successful
large African carnivore outside
conservation areas (Woodroffe 2001, in
Winterbach et al. 2012, p. 6). Further
fragmentation and isolation of lion
habitat and populations can also impact
dispersal and genetic viability (see
Deleterious Effects Due to Small
Population Sizes).
Large carnivores with low potential
for cohabitation with humans have a
high risk of local extinction. In order to
survive, they require larger contiguous
habitats with fewer negative human
impacts than do more resilient species
(Winterbach et al. 2012, p. 5). As human
populations continue to rise in subSaharan Africa, the amount of land
required to meet the needs of those
populations is constantly increasing
(Brink et al. 2014, entire; Brink and Eva
2009, entire; Eva et al. 2006, p. 4), a
problem accentuated by slow rates of
technological progress in food
production and land degradation from
both overuse and natural causes (United
PO 00000
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Fmt 4701
Sfmt 4700
2010
2050
(173)
12,951
(66)
40,909
(70)
44,973
(48)
1,969
(3)
23,967
(30)
2,179
(3)
51,452
(42)
33,987
(141)
13,217
(18)
13,077
(33)
(477)
32,933
(167)
97,173
(167)
129,417
(137)
2,780
(5)
59,929
(75)
3,744
(5)
63,405
(52)
104,078
(432)
44,206
(59)
26,254
(67)
2100
(989)
58,180
(296)
160,423
(276)
275,624
(292)
3,025
(5)
112,018
(140)
4,263
(5)
64,135
(53)
204,596
(849)
124,302
(165)
32,608
(83)
Nations Environment Programme
(UNEP) 2012a, p. 3; Chardonnet et al.
2010a, p. 19; International Assessment
of Agricultural Knowledge, Science and
Technology for Development (IAASTD)
2009, pp. 3–4, 8; United Nations
Economic Commission for Africa 2008,
pp. 3–5). The result of this process is
accelerated transformation of natural
landscapes at the expense of wilderness
that sustains species such as lions and
their prey (Chardonnet et al. 2010a, p.
19).
Urbanization is also increasing in
India, but like sub-Saharan Africa, the
majority of the population is rural (UN
2014, p. 22; Swain et al. 2012, p. 1). In
the State of Gujarat, 70 percent of all
workers are rural based, with almost 52
percent being cultivators and
agricultural laborers (Swain et al. 2012,
p. 1). Suitable lion habitat within the
Gir Protected Area appears to be secure;
however, habitat outside this area that is
vital for dispersal may experience
increasing pressure in the future.
Dispersal corridors and resource-rich
habitats outside the protected area are
important to avoid inbreeding
depression and extirpation of the lion
population from stochastic events. Due
to the population growth of lions in
India, there is increased movement,
dispersal, and establishment of lion in
natural habitats outside the protected
area. Twenty-five percent of the lion
population is found in Girnar Wildlife
Sanctuary, coastal areas, and natural
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habitats along the Shetrunji River
northeast of Gir (Meena 2014, p. 27).
Additionally, the size of the Gir
Protected Area implies that dispersing
lions will inevitably cross the protected
area boundaries (Meena 2010, p. 212).
When lions move, they must cross
heavily populated human settlements
and agricultural fields (Meena 2010, p.
209). Traditional land uses are quickly
changing in the region due to limestone
mine and infrastructure development
(Banerjee et al. 2010, p. 250).
Additionally, tourist activities (safaris to
see the lions and religious pilgrimages
to visit temples located within and on
the border of protected areas) can have
detrimental impacts to wildlife if not
carefully planned. For example,
construction of a road has been
proposed to circle the outside of the
whole Gir Protected Area System
(Meena 2014, p. 28). Altering this
habitat would result in land-use
changes, promoting rapid development
and urbanization and thereby
disconnecting corridors for lion
movement (Meena 2014, p. 28; Banerjee
et al. 2010, p. 250). Furthermore,
crossing these areas renders lions more
vulnerable to disease transmission (See
Disease below) and conflict with
humans (see Human-Lion Conflict
below). Because lions are social and
territorial, they need adequate space to
survive. Lack of adequate habitat will
have a bearing on the lion’s ecology,
behavior, and population structure
(Meena 2014, p. 28).
Growing human populations have
been associated with declines in large
carnivore populations all over the
world, and high human density is
strongly associated with local
extirpation of large carnivores (Linnell
et al. 2001, Woodroffe 2001, in
Woodroffe and Frank 2005, p. 91;
Woodroffe 2000, entire). Chardonnet et
al. (2002, p.103) indicate that the
distribution maps of lion
subpopulations tend to confirm a direct
inverse correlation of lion density and
numbers with human activity and
presence. Further, Packer et al. (2013a,
entire) found that lions in unfenced
reserves are highly sensitive to human
population densities in surrounding
communities.
Loss of Prey Base
One of the most important
requirements for carnivore survival,
including lion, is prey availability, as it
affects reproduction, recruitment, and
foraging behavior and, therefore, also
impacts lion movement, abundance, and
population viability (Winterbach et al.
2012, p. 7, citing several sources). In
India, prey abundance does not appear
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to be a concern for the lion population
as conservation initiatives have ensured
availability of ample prey (Banerjee et
al. 2010, p. 249; Khan et al. 1996 and
Singh and Kamboj 1996 in Meena 2010,
p. 209; Jhala et al. 2009, p. 3384). The
semi-nomadic pastoral communities
that inhabit the Gir Forests are primarily
vegetarian (Banerjee et al. 2013, p. 2);
therefore, there is no great demand for
bushmeat. However, in most African
countries, large carnivores such as lions
are under serious threat through
decreased prey abundance (Bauer et al.
2014, p. 97) due to unsustainable and
increasingly commercialized bushmeat
hunting in and around protected areas
(Bauer et al. 2015a, unpaginated;
Henschel et al. 2015, unpaginated;
Henschel et al. 2014, p. 5; Lindsey et al.
2013b, p. 84; Lindsey and Bento 2012,
´
pp. 1–2, 61; Scholte 2011, p. 7; Bouche
et al. 2010, pp. 1000, 1001; Cragie et al.
2010, p. 2227; Brashares et al. 2004, p.
1181; Fischer and Linsenmair 2001, pp.
132, 133).
Humans in Africa rely on protein
obtained from bushmeat, resulting in
direct competition for prey between
humans and lions, and commercial
poaching of wildlife is becoming a
significant threat to many species,
including those that lions rely upon for
food. Subsistence hunting was
traditionally carried out with the use of
spears, which had minimal impact to
wildlife populations. Spears have since
been replaced by automatic weaponry
(Chardonnet et al. 2010, p. 27) and
snares, which are most commonly used
(Lindsey et al. 2013b, p. 83). These
methods allow for poaching of large
numbers of animals for the bushmeat
trade, particularly snares, which are
cheap, difficult to detect, and
unselective as they can kill nontarget
animals ranging from rodents to
elephants (Lindsey et al. 2013b, p. 83).
The human population in a majority
of African countries within the range of
the lion has quadrupled since the 1960s
(Riggio et al. 2013, p. 29; IUCN 2009, p.
15), increasing the demand for
bushmeat. Bushmeat contributes
significantly to food security, and is
often the most important source of
protein in rural areas (Nasi et al. 2008
in Lindsey et al. 2013b, p. 82). It
comprises between 6 percent (southern
Africa) and 55 percent (CAR) of a
human’s diet within the lion’s range in
Africa (Chardonnet et al. 2005, p. 9;
IUCN 2006b, p. 19). In western Africa,
bushmeat is a secondary source of
protein, with fish being the primary
source. However, when widespread loss
of jobs and income occurs due to poor
fish harvests, bushmeat becomes an
important source of income and
PO 00000
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sustenance, leading to increased
presence of hunters in protected areas
and higher than average declines in
wildlife (Brashares et al. 2004, pp.
1180–1181).
The sale of bushmeat is an important
livelihood in Africa (Chardonnet et al.
2010, p. 27; Mesochina et al. 2010a, p.
38; Abwe and Morgan 2008, p. 26;
Bennett et al. 2007, p. 885; Fa et al.
2006, p. 507). The little meat produced
from domestic livestock is unaffordable
´
for common people (Bouche et al. 2010,
p. 1001). Bushmeat hunting is rarely
practiced solely for subsistence. It
supplies meat for local consumption
and trade, urban markets, and even
international markets (Lindsey et al.
2013b, pp. 86–87). Outlets for the sale
of bushmeat have arisen in some areas,
and full-time commercial bushmeat
traders occur in most southern and
eastern African countries (Lindsey et al.
2013b, p. 86). Significant distribution of
bushmeat to Europe and the United
States, where it is sold at elevated
prices, drives increasing
commercialization of trade, a greater
number of hunters, adoption of more
efficient hunting methods, and an
unprecedented pressure on wildlife
populations (Stiles 2011 and Barnett
2000 in Lindsey et al. 2013b, p. 88).
Many illegal hunters are poor (Barnett
2000 in Lindsey et al. 2013b, p. 88;
Lindsey and Bento 2012, p. 37; Scholte
2011, p. 7). Bushmeat trade can provide
a quick income to purchase other food
and essentials (Lindsey et al. 2013b, p.
82; Lindsey and Bento 2012, p. 62).
Hunters are wealthier than non-hunters
(Knapp 2007 in Lindsey et al. 2013b, p.
86) and enjoy elevated social status.
This growing demand and the
availability of modern weapons have led
to many African wildlife species being
hunted at unsustainable levels and the
lion prey base becoming depleted in
many areas (Hoppe-Dominik et al. 2011,
p. 452; Chardonnet et al. 2010, pp. 6,
13–14, 27; Packer et al. 2010, p. 8; Frank
et al. 2006, p. 12). Because wildlife has
been depleted in non-protected areas,
illegal bushmeat hunters are
increasingly focusing efforts on
protected areas (Lindsey et al. 2013b, p.
84). Weak management effectiveness
and inadequate law enforcement have
facilitated poaching for bushmeat in
protected areas and resulted in a
widespread decrease in large mammal
populations, including lion prey, in
these areas (Henschel et al. 2015b,
unpaginated; Henschel et al. 2014, pp.
5, 7; Lindsey et al. 2013b, pp. 84, 88;
Lindsey and Bento 2012, p. 61; Scholte
´
2011, p. 7; Bouche et al. 2010, pp. 99,
1001; Brashares et al. 2004 in Craigie et
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al. 2010, p. 2227; Fischer and
Linsenmair 2001, p. 134).
Significant decreases in prey
abundance have occurred in protected
areas throughout Africa (Lindsey et al.
2013b, pp. 84, 85; Scholte 2011, pp. 2,
8; Craigie et al. 2010, p. 2225); Botswana
(Bauer et al. 2014, pp. 101, 103); CAR
´
(Bouche et al. 2010, pp. 99, 1000; Roulet
´
2004 in Bouche et al. 2010, p. 1002);
´
Chad (Potgieter et al. 2009 in Bouche et
ˆ
al. 2010, p. 1002); Cote d’Ivoire (Fischer
and Linsenmair 2001, p. 134); DRC
(Martin and Hillman-Smith 1999 in
´
Bouche et al. 2010, pp. 1001–1002);
Ghana (Brashares et al. 2004, p. 1182);
Kenya (Western et al. 2009, pp. 2, 3, 4);
Mozambique (Lindsey and Bento 2012,
´
p. 63); Sudan (UNEP 2006 in Bouche et
al. 2010, p. 1001); Zambia (Simasiku et
al. 2008 in Lindsey et al. 2013b, p. 84);
and Zimbabwe (Zimbabwe Parks and
Wildlife Management Authority 2015, p.
´
9). Bouche et al. (2010, p. 1001) found
that large wilderness areas spanning the
boundaries of Chad, CAR, DRC, and
Sudan suffered depleted wildlife
abundance. Lindsey et al. (2013b, p. 84)
concluded that the case studies
represented only a tiny fraction of the
areas in savannas that are severely
impacted by bushmeat hunting. Craigie
et al. (2010, p. 2226) stated their study
might underestimate the extent of
decline that has occurred in Africa’s
protected areas because data came from
sites with resources to carry out longterm monitoring programs and
increased management may be
associated with greater capacity to
address threats.
Low lion population densities have
been found to correspond with low prey
densities (Van Orsdol et al. 1985,
Hayward et al. 2007 in Bauer et al.
2015a, unpaginated; Bauer et al. 2014,
p. 103; Bauer et al. 2010, p. 363).
Regional trends in lion populations, as
discussed above, mirror regional trends
in herbivore populations in western,
eastern, and southern Africa between
1970 and 2005 (Bauer et al. 2015a,
unpaginated; Henschel et al. 2015,
unpaginated). Overall, Craigie et al.
(2010, p. 2225) found a 59 percent
decline in large mammal populations.
Regional differences in herbivore
population abundance were also
detected. While population sizes in
southern Africa increased by 24 percent,
they declined by 52 percent and 85
percent in eastern and western Africa,
respectively (Craigie et al. 2010, p.
2225).
Continent-wide decreases in prey
abundance in African protected areas
are driven by human population growth
(Craigie et al. 2010, p. 2225), especially
along the boundaries of protected areas
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where human population growth rates
are high, encroachment and habitat loss
occurs, and people are dependent on
bushmeat. Protected areas in Ethiopia,
Mozambique, Tanzania, and Zambia are
increasingly settled (Lindsey et al.
2013b, pp. 87, 88; Lindsey and Bento
2012, p. 64; Scholte 2011, p. 7). Hunting
is more prevalent close to borders and
near human settlements as the longer
the distance, the more time, effort, and
cost is needed to find and transport
meat; the chances of detection are also
increased with distance (Lindsey et al.
2013b, pp. 84, 88; Brashares et al. 2001,
p. 2475). Additionally, communities
often retain livestock as assets and rely
on bushmeat for daily protein needs
(Barnett 2000 in Lindsey et al. 2013b, p.
88). Furthermore, many communities
lack the rights over land and in most
cases in Botswana, Tanzania, Zambia,
and Zimbabwe, the government retains
a significant portion of revenue from
wildlife; therefore, those that bear the
costs of wildlife do not receive benefits,
and bushmeat hunting is the only way
to benefit from wildlife (Lindsey et al.
2013b, p. 88).
Throughout the African range
countries, hunting of wildlife is
regulated by various laws and
regulations and harvests are controlled
through permitting systems and quotas
(Lindsey et al. 2013b, pp. 82–83). In
many countries, the use of snares,
poison, and automatic weapons, among
other methods, is prohibited. Singleshot firearms, muzzle-loading firearms,
shot guns, and bows and arrows are
legal under certain circumstances when
permitted, and in some cases specific
calibers and bow strengths are given
depending on the species being hunted
(Lindsey et al. 2013b, p. 82). Hunting
laws also specify hunting seasons and
prohibit hunting in certain protected
areas, hunting certain species, and
hunting young or pregnant animals.
Therefore, bushmeat hunting is illegal
in most situations due to violations of
one or more of these restrictions
(Lindsey et al. 2013b, p. 83). However,
penalties for violations are inadequate
and do not inhibit illegal bushmeat
hunting. Penalties typically comprise
warnings, community service, or fines
that are often lower than the value of the
meat, or the hunter is not penalized at
all. Many governments lack the will and
most state wildlife agencies lack the
resources or expertise to effectively
enforce laws (Lindsey et al. 2013b,
p.88). Some government officials and
police are known to purchase bushmeat,
despite it coming from an illegal source,
which further contributes to ineffective
regulation of illegal hunting (Lindsey
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80011
and Bento 2012, p. 63). Given the
widespread and significant decrease in
lion prey throughout its range in Africa,
it is apparent that enforcement of laws
and regulations is not adequate.
Additionally, weak management of
protected areas has caused declining
prey populations (Henschel et al. 2015,
unpaginated; Henschel et al. 2014, pp.
5–6; Craigie et al. 2010, entire).
The human population in the
developing world is projected to
increase rapidly, suggesting human
pressure on protected areas will also
increase (Lindsey et al. 2013b, p. 84;
Brashares et al. 2001, p. 2475). Without
intervention, wildlife resources will be
lost in many areas with severe
ecological impacts (Lindsey et al. 2013b,
p. 84). Because lion densities closely
mirror prey densities, we can expect
that lion populations will also be lost in
Africa.
Human-Lion Conflict
The lion population in and around
the Gir Protected Area, India, lives
among and is surrounded by many
pastoral and forest settlements (Banerjee
and Jhala 2012, p. 1421; Singh and
Gibson 2011 in Banerjee and Jhala 2012,
p. 1421; Banerjee et al. 2010, p. 249;
Singh 2007 in Jhala et al. 2009, p. 3385).
The lion population of Gir has increased
and dispersed into the large agropastoral area adjacent to the protected
area. Only 10 percent of lions in India
occur in the human-free portion of Gir
National Park (Banerjee et al. 2013, p.
8). Conflict there, like in Africa, arises
from predation of livestock and
associated threats to security of pastoral
livelihoods (Karanth and Chellam in
Banerjee et al. 2013, p. 1). The lion’s
diet there includes livestock (Banerjee et
al. 2013, p. 6; Meena et al. 2011, pp. 63–
65). Between 2001 and 2010 the number
of villages reporting depredation of
livestock increased (Meena et al. 2014,
pp. 122–123). Additionally, Meena
(2012, p. 36) found that in all Forest
Divisions, except Gir West, annual
livestock predation increased more than
100 percent in 5 years. However, despite
the lion’s close occupation with human
settlements and increased predation on
livestock, human-lion conflict and
associated retaliatory killing was not
found to be a major source of lion
mortality (Pathak et al. 2002 in Banerjee
and Jhala 2012, p. 1427), mainly due to
low economic losses via certain
husbandry practices and a
compensation scheme (Meena et al.
2014, pp. 123, 124; Banerjee et al. 2013,
pp. 6–7, 8), cultural ethics (Raval 1991
in Banerjee et al. 2013, p. 2; Banerjee et
al. 2013, p. 8), and strict legal
enforcement (Banerjee et al. 2013, p. 8).
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Although some lions have been killed
(Meena 2008 and Meena et al. 2007 in
Meena 2010, p. 211), the lion
population remained stable between
2001 and 2010 (Meena et al. 2014, p.
123).
Although human-lion conflict is not
currently considered a threat to the lion
population in India due to tolerance of
lion presence by the pastoralist
community (Banerjee et al. 2013, pp. 1–
2, 8; Pathak et al. 2002 in Banerjee and
Jhala 2012, p. 1427), human-caused
mortality is likely to increase in the
future due to increased human-lion
conflict and will be a major threat to the
persistence of the lion population
(Banerjee and Jhala 2012, p. 1428).
Similar to the observed transition in the
Maasai community in eastern Africa,
traditional value systems of pastoralists
in India are rapidly changing under the
influence of globalization and free
markets. The younger generation is
becoming less tolerant to even small
monetary losses. These changes in
attitudes will likely result in less
tolerance of livestock loss to lions
(Banerjee et al. 2013, p. 8). An indefinite
increase in humans and livestock within
Gir Forests would upset the current
balance by altering forest composition
or population dynamics of prey species
and would be detrimental to
conservation (Banerjee et al. 2013, p. 8).
Furthermore, with an expanding lion
population that disperses and uses
habitat in agro-pastoral areas densely
populated with human villages, there is
an increased potential for human-lion
conflict (Meena 2010 and Singh 2007 in
Meena et al. 2014, pp. 120, 121). Due to
high human density and demand for
land, most human-free protected areas
in India, and elsewhere, are too small to
hold viable populations of large
carnivores for the long term (Narain et
al. 2005 and Karanth 2003 in Banerjee
et al. 2013, p. 8).
Human-lion conflict and associated
retaliatory killing of lions has played a
major role in the reduction of lion
populations throughout Africa (Lion
Guardians 2013, p. 1; Lion Guardians
2011, p. 2; Hazzah and Dolrenry 2007,
p. 21; Frank et al. 2006, p. 1; Patterson
et al. 2004, p. 508) and is a threat to
remaining lion populations (Bauer et al.
2010, p. 363; Hazzah et al. 2009, p.
2428; Moghari 2009, p. 31; Kissui 2008,
p. 422; Frank et al. 2006, pp. 1, 3, 10;
Ray et al. 2005 in Hazzah 2006, p. 2;
IUCN 2006b, p. 18). Conflict between
humans and wildlife has been linked to
population declines, reduction in range,
impacts to small population
demographics, and even species
extinctions (Dickman 2013, p. 377;
Sogbohossou et al. 2011, p. 61; Begg and
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Begg 2010, p. 2; Hazzah et al. 2009, p.
2428; Moghari 2009, p. 36; Kissui 2008,
p. 422; Hazzah 2006, pp. 15, 23, 25).
Human-lion conflict stems from
human population growth and the
resulting overlap of humans and
wildlife habitat, with associated
livestock encroachment and decreasing
availability of prey (Hoppe-Dominik et
al. 2011, p. 452; Chardonnet et al. 2010,
pp. 6, 13–14; Frank et al. 2006, p. 12;
Hazzah 2006, pp. 14, 15). Lion
populations are increasingly restricted
to protected areas due to human
expansion and associated expansion of
livestock husbandry and agricultural
activities. Despite being within
protected areas, lions, due to their large
home range, often range beyond
protected area borders where they are
exposed to and impacted by people
living on adjacent land. Therefore, most
conflict occurs at protected area
boundaries (Henschel 2015, pers.
comm.; Woodroffe and Ginsberg 1998,
p. 2126). It is along these borders that
villages are often established and
human encroachment occurs due to
conversion of natural habitats for
agriculture and grazing livestock, which
increases the chance of human-lion
encounters (Sogbohossou et al. 2011,
pp. 51, 62; Chardonnet et al. 2010, p. 23;
Mesochina et al. 2010a, p. 39;
Mesochina et al. 2010b, p. 33; Moghari
2009, p. 14). Furthermore, cattle herders
enter the protected areas, and lions
move beyond the borders of protected
areas in search of food, increasing
interactions between humans and lions
and the risk of human-lion conflict
(Burkina Faso 2014, pp. 19–20, 21;
Hazzah et al. 2013, p. 1; Republic of
Namibia 2013, p. 13; Bauer et al. 2010,
p. 365; Chardonnet et al. 2010, pp. 11–
12; Mesochina et al. 2010a, p. 39;
Mesochina et al. 2010b, p. 33; Packer et
al. 2010, pp. 2, 6; Gebresenbet et al.
2009, p. 9; Moghari 2009, pp. 1, 14, 25,
26, 78; Kissui 2008, p. 422; Hazzah
2006, p. 2). Hunting zones are thought
to serve as buffers; however, these areas
are not adequate as a low density of
competitors in these areas may attract
wildlife, including lions, which further
disperse into villages, causing conflicts
(Sogbohossou et al. 2011, p. 51). Lion
attacks can have various impacts on
those communities that coexist with
conflict-causing animals, generating
resentment towards them. When lions
in Africa cause or are perceived to cause
damage to livestock, property, or
people, the response is generally to kill
them (Dickman 2013, pp. 378–379;
Moghari 2009, p. 25; Frank et al. 2006,
p. 1).
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Attacks on Livestock in Africa
The most significant cause of humanlion conflict is livestock depredation. In
addition to bushmeat trade, the demand
for food to meet increasing needs of a
growing population has been met by
intensified agriculture and livestock
practices (Chardonnet et al. 2010, p. 19).
As natural habitats are converted to
agricultural or pastoral land, the lion’s
natural prey base is further reduced
(Chardonnet et al. 2010, p. 27;
Gebresenbet et al. 2009, p. 9). As a result
of prey species becoming depleted in
many areas, lions seek out livestock
(and in some cases, humans) for food
(Zimbabwe Parks and Wildlife
Management Authority 2015, p. 9;
Burkina Faso 2014, p. 20; HoppeDominik et al. 2011, p. 452; Chardonnet
et al. 2010, pp. 6, 13–14, 27;
Gebresenbet et al. 2009, p. 9; Moghari
2009, pp. 78, 83; Frank et al. 2006, p.
12; Hazzah 2006, pp. 17–18; Patterson et
al. 2004, pp. 507, 514). Therefore, lion
attacks occur at the highest frequency in
areas where natural prey abundance is
lowest (Packer et al. 2010, p. 9; Frank
et al. 2006, pp. 9, 12; Patterson et al.
2004, p. 507).
Pastoralists allow increasing numbers
of livestock to graze in and adjacent to
protected areas, and villagers farm up to
the boundaries of protected areas,
subjecting livestock and humans to
lions and increasing the risk of
predation and the number of livestock
´
lost to predation (Brugiere et al. 2015, p.
514; Bauer et al. 2014, p. 98; Burkina
Faso 2014, pp. 19–22; Hazzah 2013, p.
1; Chardonnet et al. 2010, pp. 11–12;
Uganda Wildlife Authority 2010, p. 27;
Moghari 2009, pp. 1, 90). Additionally,
poor husbandry practices and grazing of
livestock within or adjacent to protected
areas increase exposure of livestock to
lions and increase livestock loss
(Uganda Wildlife Authority 2010, p. 27;
Woodroffe and Frank 2005 in Moghari
2009, p. 35; Hazzah and Dolrenry 2007,
pp. 22–23). Furthermore, conversion of
rangeland to agricultural use has
blocked several migratory routes for
Tanzania’s wildebeest and zebra
populations, which likely forces lions to
rely more on livestock (Packer et al.
2010, p. 9). Because most protected
areas are too small to support a lion’s
large home range, adjacent dispersal
areas are often used for supplementary
food, putting them in greater contact
with livestock and humans (Kissui
2009, p. 422; Moghari 2009, p. 27).
Conditions worsen as livestock numbers
and area under cultivation increase,
leading to overgrazing, further habitat
destruction, and greater depredation
rates (Gebresenbet et al. 2009, p. 9;
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Hazzah 2006, p. 61; Frank et al. 2005,
Ntiati 2002, Mishra 1997, Meriggi and
Lovari 1996, Rao 1996, Mech et al. 1988
in Hazzah 2006, p. 18).
The use of fences to subdivide
rangeland interferes with traditional wet
and dry season grazing schedules for
livestock and wildlife (Hazzah 2006, pp.
58–59). Restricting wildlife movement
reduces wild prey and, when combined
with an increase in livestock numbers,
increases the rate of human-lion conflict
(Hazzah 2006, pp. 59, 61). Although
well-built bomas (a livestock enclosure)
can effectively constrain cattle and keep
predators out (Frank et al. 2006, p. 8),
they are traditionally built to keep
livestock confined, but do not offer
effective protection from predators
(Moghari 2009, p. 35). In the absence of
reliable methods for protecting
livestock, some amount of depredation
can be expected, and some lions can
become habitual livestock killers (Frank
et al. 2006, p. 9).
Rates of livestock depredation vary
with regional rainfall that correlate with
prey availability, including changes in
herding strategies, movement of prey,
and movement of lions (Lion Guardians
2011, p. 6; Moghari 2009, p. 32; Hazzah
2006, pp. 17, 18; Patterson et al. 2004,
p. 514). For example, in some parts of
Zimbabwe, Kenya, and Tanzania,
livestock losses occur during the dry
season. During this time, herders travel
farther for forage and water, they use
temporary bomas that are typically
weak, they are unfamiliar with
carnivore movements in these new
areas, and livestock are weak due to
disease, which makes them more
vulnerable to predator attacks by lions
(Hazzah 2006, p. 17). Additionally,
herders are dependent on resources
within protected areas, and livestock
may be left to wander for days or weeks
during a prolonged drought to find
forage, increasing opportunities for
attacks on livestock by lions
(Sogbohossou et al. 2011, p. 44;
Chardonnet et al. 2010, p. 24; Frank et
al. 2006, p. 6). In Benin, other parts of
Kenya, the Maasai Steppe region of
Tanzania, and Queen Elizabeth National
Park, Uganda, livestock losses were
greater during or following the rainy
season (Sogbohossou et al. 2011, p. 49;
Moghari 2009, p. 88; Kissui 2008, pp.
427, 428; Frank et al. 2006, p. 6;
Patterson et al. 2004, pp. 510, 514).
Weakened prey and readily available
carcasses provide easy meals during
times of drought, and wild herbivores
tend to concentrate near available water
sources, making them easier to prey on
and leading to fewer livestock attacks.
However, when rains return, the
abundant grass makes wild prey harder
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to catch, and lions may turn to
livestock. Migratory prey species such
as zebra and wildebeest will move to
other areas for forage and replenished
water sources, leaving lions to turn to
livestock as an alternate food source.
Migratory prey may also move outside
of protected areas. Opportunities for
livestock predation on communal land
increase when lions follow migratory
prey out of protected areas
(Sogbohossou et al. 2011, p. 50; Packer
et al. 2010, p. 9; Kissui 2008, p. 427;
Patterson et al. 2004, p. 514; Frank et al.
2006, p. 6).
Traditional livestock husbandry
practices are effective at reducing
depredation of livestock by lions
(Chardonnet et al. 2010, p. 35; Moghari
2009, p. 35; Frank et al. 2006, p. 2;
Hazzah 2006, p. 22). These practices
include livestock being closely herded
by men and dogs during the day and
being brought into bomas at night with
people living in huts around them
(Frank et al. 2006, p. 4). However,
traditional practices are being replaced
by less diligent husbandry practices,
which is increasing conflict (Woodroffe
and Frank 2005 in Moghari 2009, p. 35;
Frank et al. 2006, pp. 2, 10; Hazzah and
Dolrenry 2007, p. 23). In Botswana,
livestock are often left to wander
outside bomas at night (Frank et al.
2006, p. 5). In Kenya and Tanzania,
social changes are altering traditional
Maasai pastoral livelihoods, reducing
dependency on livestock, and reducing
traditional livestock care and
management, leaving livestock more
vulnerable to predation (Chardonnet et
al. 2010, p. 35; Hazzah and Dolrenry
2007, pp. 22–23). Young Maasai boys
traditionally guarded herds at night;
however, increased access to schools
has left herds unattended to wander into
predator areas at night (Chardonnet et
al. 2010, p. 35).
In the Pendjari area of Benin,
traditional enclosures are low with few
branches. These structures and the lack
of enclosures encourage livestock
predation (Butler 2000, Mazzolli et al.
2002, and Wang and Macdonald 2006 in
Sogbohossou et al. 2011, p. 51).
Surveillance of a main pasture area
south of Waza National Park in
Cameroon and improved enclosures
around Waza National Park and
Pendjari National Park, Benin, led to a
significant decrease in depredation
(Bauer et al. 2010, p. 365). However,
people do not invest much into
improving enclosures even though they
appear to be economically efficient,
ecologically effective, and culturally
acceptable. Even enclosures that were
built as part of a conservation project
were not used full time due to lack of
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labor and, in some cases, the herd being
too large for the enclosures (Bauer et al.
2010, p. 365).
Attacks on Humans in Africa
Although lions generally avoid
people, they will occasionally prey on
humans, causing serious injury or death
(Dickman 2013, pp. 380, 384;
Chardonnet et al. 2010, pp. 11, 12, 13;
Moghari 2009, pp. 14, 49, 26, 88; Bauer
et al. 2001 in Moghari 2009, pp. 31, 78,
84; Frank et al. 2006, p. 1; Hazzah 2006,
pp. 14, 17; Patterson et al. 2004, p. 507).
Attacks on humans appear to be more
frequent in southern and eastern Africa
and rare in western and central Africa
(Bauer et al. 2010, p. 363; Chardonnet et
al. 2010, pp. 12, 13; Mesochina et al.
2010a, pp. 29–30; Frank et al. 2006, pp.
1, 10), although attacks on humans have
been reported in Burkina Faso (Burkina
Faso 2014, pp. 19, 22). Environmental
factors such as vegetative cover, habitat,
climate, seasonality, and prey
availability may affect the rate of attacks
on humans. A certain amount of
vegetative cover is crucial for lion’s
hunting success; however, in some
cases, the vegetative cover may make it
more difficult to catch prey, leading to
more attacks on humans. Additionally,
dense cover near settlements allows
lions to hide or stalk humans at a close
distance (Mesochina et al. 2010a, p. 39;
Moghari 2009, p. 85; Frank et al. 2006,
p. 12).
Provoked attacks on humans are
usually associated with someone
approaching a lion too closely or trying
to injure or kill it and stealing a lion’s
prey for bushmeat (Chardonnet et al.
2010, p. 14; Uganda Wildlife Authority
2010, p. 27). Unprovoked attacks are
usually associated with old, sick, or
injured lions that turn to humans as
easy prey. Additionally, there are risks
of unprovoked attacks associated with
certain human activities. These
activities include walking alone at
night, sleeping outside, and surprising a
lion, particularly if it has cubs (Begg and
Begg 2010, pp. 3, 21; Chardonnet et al.
2010, pp. 14, 15; Mesochina et al.
2010a, pp. 38, 39; Mesochina et al.
2010b, p. 32; Uganda Wildlife Authority
2010, p. 27; Moghari 2009, p. 85; Frank
et al. 2006, pp. 11, 12). The most
common context for attacks on humans
occurs during harvest, due to prey
dispersal during the wet season, bush
pig attraction to crops, and because
humans are particularly vulnerable in
makeshift tents while protecting crops
(Frank et al. 2006, p. 12).
Retaliatory Killing of Lions in Africa
Livestock provide an economic value
to humans, particularly those in extreme
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poverty who rely solely on livestock for
their protein source and livelihood.
When lions have no economic value to
local communities and they kill or are
perceived to kill livestock, the economic
impact can be significant (Bauer et al.
2015a, unpaginated; Hazzah et al. 2014,
p. 852; Chardonnet et al. 2010, p. 12;
Mesochina et al. 2010a, p. 38;
Mesochina et al. 2010b, p. 33;
Gebresenbet et al. 2009, p. 9; Moghari
2009, pp. 4, 25, 49; Kissui 2008, pp. 423,
429; Hazzah 2006, p. 24; IUCN 2006a,
pp. 23, 24; IUCN 2006b. pp. 18–19;
Frank et al. 2006, p. 3). Subsequently,
those lions that reside on the edge and
outside of protected areas, where there
is an increased risk of exposure to
humans and livestock, are subject to
retaliatory killing across Africa.
Boundary transgression leads to lions
predating on livestock, and in turn, be
subject to pre-emptive or retaliatory
killing (Bauer et al. 2014, pp. 98, 103;
Funston 2011, pp. 1, 3, 5, 6–7);
however, this type of killing of lions
also occurs within protected areas
(Henschel et al. 2015, unpaginated;
Zimbabwe Parks and Wildlife
Management Authority 2015, p. 10;
Burkina Faso 2014, pp. 19, 21, 22;
Tumenta et al. 2009 and Henschel et al.
2010 in Sogbohossou et al. 2011, p. 100;
Moghari 2009, p. 49). Furthermore,
killing of lions outside of protected
areas may disrupt movement of lions to
other areas that could contribute to the
viability of larger resident populations
(White 2015, pers. comm.). This
occurrence greatly impacts alreadydwindling lion populations. Even if
mortality occurs outside of protected
areas, population dynamics inside
protected areas are negatively impacted.
When lions outside of protected areas
are removed, either through retaliatory
killings or trophy hunting, territorial
gaps that are left are filled by lions from
closer to the core of the protected area,
exposing more lions to human–lion
conflict along the borders of the
protected area and creating a population
´
sink (Brugiere et al. 2015, p. 514;
Sogbohossou 2014, p. 3; Loveridge et al.
2007, pp. 552, 555; Woodroffe and
Ginsberg 1998, p. 2162).
The availability of guns and poison
makes killing suspected predators
cheaper and easier than other control
methods, such as reinforcing bomas
(Hazzah et al. 2009, p. 2429; Moghari
2009, p. 35; Frank et al. 2006, p. 14;
Hazzah 2006, p. 3). Spearing, shooting,
trapping, and poisoning of lions, as
either a preventive measure or in
retaliation for livestock and human
´
attacks, occurs regularly (Brugiere et al.
2015, p. 519; Bauer et al. 2015a,
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unpaginated; Tanzania 2015, p. 13;
Republic of Namibia 2013, pp. 12, 13–
14; Begg and Begg 2010, p. 15;
Chardonnet et al. 2010, pp. 41–42;
Packer et al. 2010, pp. 9–10; Uganda
Wildlife Authority 2010, pp. 13, 42;
Gebrensenbet et al. 2009, p. 7; Hazzah
et al. 2009, p. 2429; Moghari 2009, pp.
52, 89, 91; Ikanda 2008, pp. 5–6; Hazzah
and Dolrenry 2007, p. 21; Frank et al.
2006, pp. 2–4, 7; Hazzah 2006, p. 52;
IUCN 2006b, p. 15). Retaliatory killings
have been reported as a significant
threat to lion populations in protected
areas of western and central Africa
(Tumenta et al. 2009 and Henschel et al.
2010 in Sogbohossou et al. 2011, p.
100), Botswana (Bauer et al. 2014, pp.
98, 103), Botswana and South Africa
(Kgaladi Transfrontier Park; Funston
2011, p. 1), Cameroon (Delongh et al.
2009 and Tumenta et al. 2010 in
Sogbohossou et al. 2011, p. 60), Kenya
(Patterson et al. 2004, Kolowski and
Holekamp 2006, and Hazzah et al. 2009
in Sogbohossou et al. 2011, p. 60),
Tanzania (Tanzania 2015, p. 13; Kissui
2008 in Sogbohossou et al. 2011, p. 60),
and Zimbabwe (Zimbabwe Parks and
Wildlife Management Authority 2015, p.
10).
In areas of high conflict, identifying
the responsible animal is often difficult,
and a token animal may be killed
instead (Hazzah 2006, p. 25), leaving the
problem lion to continue to attack and
the potential for additional retaliatory
killings. In Tanzania, game officers kill
numerous lions each year in retaliation
for attacks (Frank et al. 2006, p. 12).
Whereas shooting or spearing target
specific problem animals, poisoning is
indiscriminate and is known to remove
entire prides at once (Frank et al. 2006,
pp. 2, 10, Living with Lions no date,
unpaginated). In the absence of reliable
methods for protecting livestock, rural
people often turn to indiscriminant
methods, like poisoning, to control
livestock depredation. Poisoning is an
easy method for lethal control since it
is readily available, and reinforcing
bomas or more carefully tending
livestock requires time and effort. The
use of Furadan, a widely available and
cheap agricultural pesticide, is
particularly lethal to wildlife and is
increasingly being used to kill predators
in small pastoralist areas of Kenya and
Tanzania. Livestock carcasses are
doused with the poison, killing
predators and scavengers that feed on
them (Frank et al. 2006, pp. 2, 10, Living
with Lions no date, unpaginated).
Poisoning of bush pig carcasses to kill
lions is not uncommon after attacks on
humans. These practices have serious
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negative impacts on lion populations
(Frank et al. 2006, p. 9).
Studies have shown that lion
populations are declining in areas
where pastoralism persists and the
presence of mobile pastoralists are a
good indicator of lion extinction
´
(Brugiere et al. 2015, p. 519; Hazzah et
al. 2009, p. 2428). Within protected
areas, human–wildlife conflict is likely
under-reported because cattle herders
are within the protected areas illegally
and, therefore, unlikely to report it
(Chardonnet et al. 2010, p. 14;
Mesochina et al. 2010b, p. 34). For
example, Etosha National Park and
Caprivi Game Park have the highest
rates of lions killed per 100 km2, yet it
may be that just under half of the lions
that are killed are reported (Republic of
Namibia 2013, p. 14). Although we do
not have information on human–lion
conflict from all lion range countries, it
is reasonable to conclude that lions are
being killed as a result of conflict in all
major African range countries, due to
their depredation on livestock (Frank et
al. 2006, p. 4).
Factors That Drive Retaliation in Africa
Several anthropogenic factors drive
the level of resentment towards lions
and the extent of retaliatory killing
(Dickman 2013, pp. 379, 385), including
the extent of the loss caused by the lions
and the wealth and security of the
people affected (Dickman 2013, p. 381;
Mesochina et al. 2010b, p. 54; Moghari
2009, pp. 14, 25; Hazzah 2006, p. 81).
Depending on alternative assets or
incomes, the economic impact of lions
killing livestock can be significant.
Domestic livestock can provide manure,
milk, and meat, and are the basis of
many family incomes, savings, and
social standing; losses can amount to a
large proportion of a subsistence
herder’s annual income. These losses
are generally uncompensated,
reinforcing negative community
attitudes toward lions and causing
retaliation (Dickman 2013, pp. 380, 381;
Chardonnet et al. 2010, pp. 11, 12, 18,
29; Hazzah et al. 2009, p. 2428; Moghari
2009, pp. 14, 25, 27, 36; Kissui 2008, pp.
422–423). Furthermore, a common
perception among local communities is
that lions are conserved at the cost of
community safety and uncompensated
financial losses. When the people who
suffer significant costs from wildlife feel
that the wildlife’s needs are being put
before their own needs, their frustration
can lead to retaliatory killings (Dickman
2013, p. 382). Additionally, government
officials and local tour and hunting
operators experience economic gain
from lions, whereas the communities
bear the costs in livestock losses
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(Hazzah et al. 2014, p. 852). This
situation further contributes to negative
attitudes toward lion conservation
programs (Moghari 2009, p. 37).
Lions are particularly vulnerable to
retributive killing because they are often
driven by a perceived level of lion
predation on livestock rather than actual
levels of conflict. In some locations,
other predators (e.g., baboons (Papio
ursinus), spotted hyenas (Crocuta
crocuta), and leopards (Panthera
pardus)) as well as disease are
responsible for the majority of livestock
losses and human casualties, yet it is
lions that are sought and killed more
often. In the Pendjari Biosphere Reserve,
Sogbohossou et al. (2011, p. 74) found
that just one case of a nonlethal attack
on a human in a decade and mere
rumors of attacks in other regions was
enough to cause people to perceive lions
as a threat. Negative perceptions of lions
may be based on an over-estimated
number of lions in a community or
protected area and an over-estimated
number of human–lion conflicts
(Dickman 2013, p. 380; Begg and Begg
2010, p. 20; Chardonnet et al. 2010, pp.
12, 21–22; Hazzah et al. 2009, p. 2436;
Maclennan et al. 2009 in Hazzah et al.
2009, p. 2429; Moghari 2009, pp. 77–78,
107, 150; Holmern et al. 2007 in
Moghari 2009, p. 34; Butler 2001 in
Moghari 2009, p. 34; Kissui 2008, pp.
426, 428, 429; Hazzah 2006, pp. 18–19,
83–85, 96, 98, 107, 111; Patterson et al.
2004, pp. 514, 515). One cause for the
disproportionate blame put on lions is
that the lion is a highly visible species.
It is a large-bodied species that lives in
groups and has cultural significance.
Because of its physical presence, there
is often a hyper-awareness of the
potential risk for lion attacks and lions
may be blamed simply because they
have been seen in an area (Dickman
2013, pp. 380–381).
Cultural beliefs and traditions can
have a negative impact on lions.
Because cattle are of great cultural
significance to Maasai, their loss can
impose social or cultural costs and
incite greater resentment and higher
levels of retributive killing (Dickman
2013, p. 384; Kissui 2008, p. 429;
Hazzah 2006, p. 99). Cultural beliefs
still motivate ritual lion hunts for young
Maasai warriors. Despite being
outlawed, this practice persists due to
community secrecy. However, it is
easily disguised as retaliatory killings
for livestock predation. The prohibition
of ritual lion hunts provides a greater
incentive for participating in retaliatory
hunts (Hazzah et al. 2014, p. 852; Packer
et al. 2010, p. 10; Moghari 2009, pp. 13–
14, 28; Ikanda 2008, pp. 5, 6; Kissui
2008, p. 423; Frank et al. 2006, p. 10;
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Hazzah 2006, p. 99). In some areas of
Africa, locals believe in ‘‘spirit lions,’’ a
lion whose body is overtaken by evil to
kill rivals or their livestock (West 2001
in Dickman 2013, pp. 381–382). Because
people believe spirit lions are created by
their enemies, the number of perceived
spirit lions, and killing of these lions,
increases during times of social tension
(Dickman 2013, p. 382.)
Cultural beliefs can also have a
positive impact on lions. An association
with a totem is an important component
of certain cultures and could explain
why retaliatory killing is uncommon in
some areas despite negative perceptions.
However, the positive impact may not
continue as cultural beliefs dwindle due
to urbanization and modernization
(Sogbohossou et al. 2011, pp. 73, 75).
Social tensions within tribes and
between local communities and other
communities, the government, park
officials, or tourists can lead to conflict
and retributive killing of lions (Dickman
2013, p. 382; Hazzah 2006, p. 75).
Locals often report that wildlife
authorities do not react effectively when
chronic livestock raiders are reported
(Frank et al. 2006, p. 9). Significant
numbers of lions have been killed when
promised benefits were not received or
adequate compensation was not
provided for livestock and human losses
(Dickman 2013, p. 383; Hazzah 2006, p.
45).
Trophy Hunting
Lions are a key species in sport
hunting, or trophy hunting, as they are
considered one of the ‘‘big five’’ African
species (lion, leopard, elephant, rhino,
and cape buffalo) touted to be the most
challenging to hunt due to their
nimbleness, speed, and behavioral
unpredictability (Lindsey et al. 2012a,
p. 2). However, with the documented
decline in lion population numbers
throughout Africa, sport hunting of
lions for trophies has become a highly
complex issue.
Trophy hunting is carried out in a
number of range countries and is
considered an important management
tool for conserving land and providing
financial resources for lion
conservation. However, management
programs are not always sufficient to
deter unsustainable off takes (harvests),
which has occurred in many areas
(Lindsey et al. 2013a, pp. 8–9; Packer et
al. 2006 in Bauer et al. 2015a,
unpaginated). Documented declines in
lion populations of Africa are a result,
in part, of mismanaged trophy hunting
(Rosenblatt et al. 2014, entire;
Sogbohossou et al. 2014, entire; Becker
et al. 2013, entire; Lindsey et al. 2013a,
entire; Packer et al. 2013, p. 636; Croes
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et al. 2011, entire; Packer et al. 2011,
entire; Loveridge et al. 2007, entire).
Depending on how trophy hunting is
regulated and managed, trophy hunting
can be a tool for conservation, but may
also have negative impacts on lions
(Bauer et al. 2015a, unpaginated;
Lindsey et al. 2013a, p. 1; Whitman et
al. 2004, pp. 176–177; Loveridge et al.
2007, p. 548).
In response to growing international
recognition of reduced population
numbers, many countries began
implementing moratoriums banning the
sport hunting of lions. In this document
we use the terms moratorium and ban
interchangeably. A ban or moratorium
can be permanent, long term, or
temporary, and can occur in countries
that have hunting quotas in place (e.g.,
Botswana and Zambia). Having both a
moratorium and a quota in place at the
same time means that, although the
country may have a hunting quota, the
country has halted authorization of
trophy hunting pursuant to that quota
until some later date or until some
further action is taken, as prescribed by
that country.
Trophy hunting is currently banned
in 12 range countries: Angola,
Botswana, Congo, Gabon, Ghana, India,
Kenya, Malawi, Mauritania, Niger,
Nigeria, and Rwanda (CITES 2014, p.
14; Meena 2014, p. 26; Lindsey et al.
2013a, entire; Lindsey 2013, pers.
comm.; Jackson 2013, pp. 7–8). In 1977,
Kenya banned all sport hunting (Elliot
and Mwangi 1998, p. 3). Botswana
banned lion hunting between 2001 and
2004, and then again from 2008 to the
present (Davison et al. 2011, p. 114).
Benin imposed a 2-year moratorium,
and CAR a 3-year moratorium, in the
early 2000s (Lindsey et al. 2013a, p. 4).
In January of 2013, Zambia placed a
moratorium on sport hunting in 19 game
management areas. While a few other
game management areas and private
game ranches in Zambia remain open
for sport hunting for other species, the
nationwide moratorium on sport
hunting of cats remains in place (White
2015, pers. comm.; ABC News 2014,
unpaginated; Flocken 2013,
unpaginated). Trophy hunting is
restricted to problem or dangerous
animals in Ethiopia and Uganda
(Lindsey 2008, p. 42). In our proposed
rule, we had conflicting information
regarding whether Cameroon had or has
a lion hunting moratorium (CITES 2014,
p. 14; Lindsey 2013, pers. comm.;
Jackson 2013, p. 8). During the public
comment period, a peer reviewer
confirmed that Cameroon has not put a
moratorium in place for lions, either in
the past or present (Bauer 2015, pers.
comm.). Additionally, Zimbabwe has
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suspended trophy hunting in the
Gonarezhou area (Conservation Force
2015, pers. comm.).
As of May 2014, approximately 18
countries in Africa allowed legal
hunting of lions for trophies: Benin,
ˆ
Burkina Faso, CAR, DRC, Ethiopia, Cote
d’Ivoire, Mali, Mozambique, Namibia,
Senegal, Somalia, RSA, Sudan,
Tanzania, Togo, Uganda, Zambia
(nationwide moratorium on sport
hunting of cats is currently in place),
and Zimbabwe. However, in 2013 lion
trophy hunting was documented to
occur in only 8 countries, specifically
Benin, Burkina Faso, CAR,
Mozambique, Namibia, South Africa
(RSA), Tanzania, and Zimbabwe
(Lindsey 2013, pers. comm.). Four
countries, Burundi, Guinea Bissau,
Lesotho, and Swaziland, provide no
legal protection for lions (CITES 2014,
p. 14).
Where trophy hunting occurs, quotas
are set by the government for the
purpose of limiting the actual number of
lions killed (offtake) during a given
timeframe. A scientifically based quota
is the maximum number of a given
species that can be removed from a
specific population without damaging
the biological integrity and
sustainability of that population (World
Wildlife Fund (WWF) 1997, p. 9). Two
primary concerns have been raised by
the scientific and international
community with regard to current lion
quotas. These are that (1) existing quotas
are set above sustainable levels, and (2)
the data used for setting quotas is
inconsistent and not scientifically based
(Hunter et al. 2013, unpaginated;
Lindsey et al. 2006, p. 284) (see
Potential Impacts of Trophy Hunting).
For example, recent quotas do not
appear to address safeguards for
sustainability nor has a systematic
approach been established for setting
lion quotas (Hunter et al. 2013, p. 2;
Lindsey et al. 2013b, p. 8). Additionally,
it has been noted that previous quotas
in Namibia, Mozambique, and
Zimbabwe may have been influenced by
human–lion conflict, with higher quotas
being allocated to locations with
reportedly higher levels of human–lion
conflict (Lindsey et al. 2013b, p. 4).
Generally, the conservation principle
behind scientifically based quotas is to
limit total offtake of the species to either
equal or slightly lower than the growth
rate of the target specimens (e.g., males
vs. female), such that damage to the
integrity and sustainability of that
population is prevented. Scientifically
based quotas do not apply solely to
sport hunting, but set the limits for total
offtake for a particular timeframe; other
potential offtake includes problemanimal control (to reduce human–
wildlife conflict), translocation (to
expand conservation), culling (reducing
population pressures), and local hunting
(for protein/meat or employment) (WWF
1997, pp. 8–10). For quotas to be
sustainable, scientists and policy
makers must evaluate a multitude of
factors including the species’ biological
factors (i.e., reproductive rate, gender
ratios, age, and behavior), as well as
community and client objectives (WWF
1997, pp. 14–19).
Creel and Creel (1997, p. 83, executive
summary) suggest that, for a quota to be
considered sustainable for lions, it
should be limited to no more than 5
percent of the population. Distinct from
the quota, Packer et al. (2011, p. 151)
recommend actual lion offtake should
not exceed more than 1 lion per 2,000
km2 (Bauer 2015, pers. comm.; Henschel
2015, pers. comm.; Packer et al. 2015,
per comm.; Creel and Creel 1997, p. 83,
executive summary). However, most
range countries have their quotas set
well above these recommendations
(Bauer 2015, pers. comm.; Henschel
2015, pers. comm.; Packer 2015, pers.
comm.). Specifically, Lindsey et al.
(2013a, p. 8) found that of the nine
countries allowing trophy hunting of
lions in 2013 (including data from
Zambia prior to the moratorium in
2013), eight have quotas set higher than
current recommendations by Packer et
al. (2011, p. 151) and five have quotas
set to more than double Packer’s
recommendations. Mozambique is the
only country with a lion quota less than
the recommended 1 lion per 2,000 km2.
It should be noted that although quotas
are currently set higher than
recommended, the actual offtake for
each of the countries overall has been
consistently lower than the set quota
(Table 5). However, in Burkina Faso,
Zambia, Namibia, and Zimbabwe, the
actual harvests are greater than Packer’s
recommended offtake (Lindsey et al.
2013a, p. 8). For instance, five countries
maintain quotas to allow for 5–31 lion
trophies to be taken per year: Benin (5),
Burkina Faso (20), Cameroon (30), CAR
(31), and Namibia (15). Only
Mozambique currently has a quota
lower than the recommendation of
Packer et al. (2001, p. 1651). In 2013, the
quota was set at 42–60 lions, which
translates to 1 lion per 2,400km2 (or 0.8
lions per 2,000km2). Between 2011 and
2012, Tanzania maintained the highest
quota for lions at 315 (Lindsey et al.
2013a, p. 6).
Several countries have begun to
reduce their quotas as they have begun
implementing recommendations as
outlined by Lindsey et al. (2013a, pp. 8–
9), Hunter et al. (2013, unpaginated),
and Packer et al. (2011, p. 151) (Bauer
2015, pers. comm.; Henschel 2015, pers.
comm.; White 2015, pers. comm.;
Tanzania 2015, pers. comm. Zimbabwe
2015, pers. comm.). In 2011,
Zimbabwe’s quota was set at 101 lions;
in 2014, it was reduced to 50 lions
following the implementation of age
restrictions (Henschel 2015, pers.
comm.). Following pressure from the
European Union to ban lion trophies if
their quota remained higher than the 1
lion per 2,000 km2 recommendation,
Burkina Faso proposed to reduce the set
quota of 20 lions in the 2014/2015
season to 6 in the 2015/2016 season
(Henschel 2015, pers. comm.). South
Africa has not set a quota for the take
of wild lions since 99 percent of the
trophy-hunted lions are reportedly not
of wild origin but captive born (Hunter
et al. 2013, p. 2; RSA 2013, pp. 5, 7)
(Table 5).
TABLE 5—ANNUAL TROPHY QUOTAS AND OFFTAKE BY COUNTRY (APPROXIMATE) AS OF 2013*
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Country
Annual lion
trophy quotas
Year(s) of data
Annual
offtakes
Year(s) of data
Panthera leo leo
Benin ................................................................................................................
Burkina Faso ....................................................................................................
Cameroon ........................................................................................................
CAR .................................................................................................................
Panthera leo melanochaita
Mozambique ....................................................................................................
Namibia ............................................................................................................
Tanzania ..........................................................................................................
Zambia (moratorium) 1 .....................................................................................
5.0±0
20.0±0
29.2±2
31
........................
42–60
14.5
315
74(50 2)
2007–2009
2006–2009
2006–2010
2009
........................
2013
2010
2011–2012
2012
2.0±0.4
13.3±1.45
6.9±1.0
13.7±6.9
........................
19.2±7.3
14.0±3.2
85
47
2007–2009
2006–2009
2006–2010
2008–2011
........................
2008–2011
2008–2011
2011–2012
2012
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TABLE 5—ANNUAL TROPHY QUOTAS AND OFFTAKE BY COUNTRY (APPROXIMATE) AS OF 2013*—Continued
Annual lion
trophy quotas
Country
Year(s) of data
101(503)
2011
Zimbabwe ........................................................................................................
Annual
offtakes
42.5±7.5
Year(s) of data
2008–2011
* Source: Lindsey et al. 2013a. p.6.
1 Zambia enacted a moratorium on sport hunting in 19 game management units. Sport hunting remained open in other game management
units and on some private game ranches. Sport hunting of all cats is currently banned throughout Zambia (White 2015, pers. comm.).
2 Approximate average quota for Zambia in the few years prior to the moratorium placed on cat hunting in 2013. (White 2015, pers. comm.).
3 In 2014, Zimbabwe reduced its quota to 50 due to implementation of age restrictions (Henschel 2015, pers. comm., citing Lindsey pers.
comm.)
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Potential Benefits of Trophy Hunting
Proponents and most lion experts
support trophy hunting as a
conservation tool for the lion if it is
practiced in a sustainable and
scientifically based manner (Henschel
2015, pers. comm.; Hunter 2011, entire;
van der Merwe 2013, entire; Hunter et
al. 2013, entire) because it can provide:
(1) Incentives for the conservation of
large tracts of prime habitat, and (2)
funding for park and reserve
management, anti-poaching activities,
and security activities.
As habitat loss has been identified as
one of the primary threats to lion
populations, it is notable that the total
amount of land set aside for hunting
throughout Africa, although not
ameliorating threats to habitat loss,
exceeds the total area of the national
parks, accounting for approximately half
of the amount of viable habitat currently
available to lions (Chardonnet et al.
2010, p. 34; Packer et al. 2006, pp. 9–
10). For example, in Tanzania, 25–33
percent of the total area, covering over
247,000 km2 and encompassing 190
hunting units, has been set aside for
sport hunting purposes; this has
resulted in an area 5.1 times greater than
Tanzania’s fully protected and gazetted
parks (Jackson 2013, p. 6; Barnett and
Patterson 2005, p. 61). Tanzania also has
land set aside for sport hunting in the
form of safari areas, communal land,
and privately owned properties that
make up 23.9 percent of the total land
base (Barnett and Patterson 2005, pp.
76–77).
In Botswana, despite the current ban
on lion hunting, the country currently
has over 128,000 km2 of gazetted
wildlife management areas and
controlled hunting areas set aside for
hunting purposes, which equates to 22.1
percent of the country’s total area. This
amount is in addition to 111,000 km2
(or 19.1 percent of the country’s total
area) set aside as habitat in the form of
national parks, game reserves, and forest
reserves (Barnett and Patterson 2005, p.
7). In 2000, five countries in southern
Africa (Botswana, Namibia, South
Africa, Tanzania, and Zimbabwe) set
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aside a combined 420,000 km2 of
communal land, 188,000 km2 of
commercial land, and 420,089 km2 of
state land totaling over 1,028,000 km2
for sport hunting purposes (Barnett and
Patterson 2005, p. iii).
As a species with a considerable range
(up to 1,000 km2) (Packer et al. 2013, p.
636; Haas et al. 2005, p. 4), suitable
habitat is important to the survival of
the species, and the marked decline in
suitable habitat is a significant threat to
the species (see Habitat Loss). The land
currently designated in Africa for use in
sport hunting has helped to reduce, but
not eliminate, the impact of habitat loss
on the lion.
If trophy hunting is part of a
scientifically based management
program, it may provide direct
economic benefits to the local
communities and may potentially create
incentives for local communities to
conserve lions, reduce the pressure on
lion habitat, and reduce retaliatory
killing, primarily because lions are
viewed as having value. Conversely,
lack of incentives could cause declines
in lion populations because lions are
viewed as lacking value and they kill
livestock, which are of great value to
communities (see Human–lion Conflict).
Over the last few decades,
conservationists and range countries
have realized the integral role local
communities play in the conservation of
lions and their habitat; when
communities benefit from a species,
they have incentive to protect it.
Therefore, using wildlife as a source of
income for rural populations has
increasingly been employed throughout
the lion’s range countries in Africa.
Many of these countries are classified as
‘‘developing’’ nations; specifically,
seven of the ten countries (we include
Cameroon here) where trophy hunting is
permitted have 27–64 percent of their
human populations living in severe
poverty (United Nations Development
Programme’s (UNDP) 2014,
unpaginated; Barnett and Patterson
2005, p. iii). These countries often have
high population growth, high
unemployment, limited industry, and a
Gross Domestic Product (GDP) per
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capita lower than the poverty level
(Barnett and Patterson 2005, p. iii).
These combined challenges highlight
the need for innovative solutions.
Conservationists and range countries
recognize the value of the wildlife
sector; if managed sustainably, there is
potential to contribute to rural economic
development while simultaneously
protecting the unique ecological habitats
and species contained therein
(Chardonnet et al. 2010, p. 33; Kiss
1990, pp. 1, 5–15).
For species such as the lion to persist,
local communities must benefit from or
receive a percentage of funds generated
from tourism such as wildlife viewing,
photography, or trophy hunting (White
2013, p. 21; Martin 2012, p. 57; Kiss
[editor] 1990, pp. 1, 5–15). The
economic value of a species, such as
lion, can encourage range countries to
develop management and conservation
programs that involve local
communities and which would
ultimately discourage indiscriminate
killings by local communities (Groom
2013, pp. 3, 5; Hazzah et al. 2013, p. 1;
White 2013, p. 21; Martin 2012, p. 49).
If local communities see no benefit of
lions being present in their communal
areas, sustainable use of lions becomes
less competitive with other land-use
options, such as grazing and livestock
management, and local communities
become unwilling and unable to manage
their wildlife heritage (Barnett and
Patterson 2005, p. iii). When the value
of lions in areas outside national parks
is diminished, those areas are likely to
be converted to forms of land use less
suitable for lions, such as agriculture,
livestock pastures, or areas of resource
extraction, making lions even more
vulnerable to expanding human
settlement (Van der Merwe 2013, p. 2).
Community conservancies that benefit
from trophy hunting have specifically
been formed as a way to protect wildlife
and habitat. As an example, in Namibia,
160,000 km2 of community
conservancies were established in part
due to revenue from trophy hunting.
These conservancies benefit the local
communities, which in turn protect lion
´
habitat. In 2012, the Save Valley
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Conservancy (Zimbabwe) ‘‘provided
over $100,000 USD worth of support to
adjacent villages or farmers in the
resettled areas. Assistance included
drilling boreholes, maintaining
boreholes, dredging of dams, building
clinics and schools, assisting with
repairs, maintenance and materials for
schools, education initiatives, school
field trips, provision of computer
equipment in schools, and craft
programs’’ (Groom 2013, p. 5).
Connecting conservation to community
benefits can provide a value for wildlife,
including lions, where there was
previously resentment or indifference,
helping to instill a sense of importance
for lion conservation. Additionally an
estimated 125,000 kg of game meat is
provided annually to rural communities
by trophy hunters in Zambia at an
estimated value of $250,000 USD per
year, which is considerable for rural
locations where severe poverty and
malnutrition exists (White 2013, p. 21),
further providing a value for wildlife,
including lions. As stated above, local
communities can benefit from the
trophy hunting industry by additional
employment opportunities and revenue
generated for local microbusinesses.
Many range countries have recognized
the need to incorporate incentives and
local community benefits into their
trophy hunting regulations, land
management policies, and lion
conservation action plans (Lindsey et al.
2013a, pp. 2–3; Zambia Wildlife
Authority 2009, p. 10; Windhoek 2008,
p. 18; IUCN 2006a, pp. 22, 24; IUCN
2006b, pp. 23, 28; Zimbabwe Parks and
Wildlife Management Authority 2006,
unpaginated). Of the ten countries
where lion trophy hunting currently
occurs (we are including Cameroon and
South Africa here), seven have
developed National Poverty Reduction
Strategies in partnership with the
International Monetary Fund (for a
complete list, see https://www.imf.org/
external/np/prsp/prsp.aspx). Each of
these countries has incorporated
sustainable natural resource
development as a priority and discussed
benefit distribution and management to
rural communities (Benin 2000,
unpaginated; Burkina Faso 2000,
unpaginated; CAR 2000, p. 45; United
Republic of Tanzania 2000, pp. 13, 21;
Zambia 2000, unpaginated). Although
we acknowledge the steps many
countries have taken to address local
community incentives, most of the
countries are currently not transparent
about the benefits provided to local
communities, and due to the high
revenue potential, are subject to
corruption (Packer 2015, pers. comm.;
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see Potential Impacts of Trophy
Hunting).
Many range countries rely heavily on
tourism (predominantly ecotourism and
safari hunting) to provide funding for
wildlife management (IUCN 2006a, p.
24). Additionally, revenue generated
from these industries provides jobs,
such as game guards, cooks, drivers, and
security personnel and often brings in
revenue for local microbusinesses that
sell art, jewelry, and other crafts.
Revenue generated from scientifically
based management programs can be
used to build and maintain fences,
provide security personnel with
weapons and vehicles, provide
resources for anti-poaching activities,
and provides resources for habitat
acquisition and management
(Chardonnet et al. 2010, pp. 33–34;
Newmark 2008, p. 321). For example,
´
trophy hunting revenue in the Save
Valley Conservancy in Zimbabwe has
enabled $150,000–$250,000 USD to be
invested in anti-poaching activities,
including the removal of wire-snares
(Groom 2013, p. 5). Revenue from
trophy hunting can also increase the
ability of many African countries to
manage wildlife populations both
within and adjacent to reserves; many of
these hunting areas are geographically
linked to national parks and reserves,
providing wildlife corridors and buffer
zones (Chardonnet et al. 2010, p. 34;
Newmark 2008, p. 321).
Depending on the country in which a
hunter visits, there may be several
different fees associated with trophy
hunts, including game fees, observer
fees, conservation fees, permit fees,
trophy handling fees, and government
payments in terms of taxes, as well as
safari operator fees (Barnett and
Patterson 2005, p. 71). In the late 1990s,
Tanzania reported annual revenue of
$29.9 million USD from all trophy
hunting, South Africa $28.4 million
USD, Zimbabwe $23.9 million USD,
Botswana $12.6 million USD, and
Namibia $11.5 million USD; the revenue
generated solely from lion hunting was
not broken out (Barnett and Patterson
2005, p. iv). According to Groom (2013,
´
p. 4), a 21-day lion hunt in Save Valley
Conservancy, Zimbabwe, may be sold
for approximately $2,500 USD per day,
with an additional trophy fee of
approximately $10,000 USD. Between
´
2005 and 2011, lion hunting in Save
Valley Conservancy provided an
estimated net income (based on 26
lions) of approximately $1,365,000 USD
in per-night charges and roughly
$260,000 USD in trophy fees (Groom
2013, p. 4). In the past, government and
private landowners were the primary
beneficiaries of the revenue gained;
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currently, efforts are being made in
many range countries to incorporate
incentives at the local level (Barnett and
Patterson 2005, p. vi).
In summary, if part of a scientifically
based management program (including a
scientifically based quota), trophy
hunting of lions can provide direct
benefits to the species and its habitat,
both at the national and local levels.
Trophy hunting and the revenue
generated from trophy hunting are tools
that range countries can use to facilitate
maintaining habitat to sustain large
ungulates and other lion prey,
protecting habitat for lions, supporting
the management of lion habitat, and
protecting both lions and their prey base
through anti-poaching efforts. While
scientifically based trophy hunting
alone will not address all of the issues
that are contributing to the declined
status of the lion, it can provide benefits
to the species.
Potential Impacts of Trophy Hunting
An issue critical to the conservation
of lions is sustainable management of
trophy hunting by lion range countries.
Lion experts agree that, if trophy
hunting is well regulated and managed,
it can be a tool for conservation (Bauer
et al. 2015a, unpaginated; Lindsey et al.
2013a, p. 1; Whitman et al. 2004, pp.
176–177; Loveridge et al. 2007, p. 548).
However, problems with the current
management of lion hunting increase
the likelihood of negative impacts on
the species (note that because 99
percent of hunted lions in South Africa
are captive-bred, we exclude them from
this discussion) (Hunter et al. 2013, p.
2). Lindsey et al. (2013a, pp. 8–9) and
Hunter et al. (2013, p. 2) identified six
key practices undermining sustainable
management of lions:
• Arbitrary establishment of quotas and
excessive harvest
• lack of age-restriction implementation
• fixed quotas
• hunting of females
• lack of minimum hunt lengths in
some countries
• general problems associated with
management of trophy hunting
As discussed above, one of the
primary practices experts identify as
undermining sustainable trophy hunting
is the use of non-scientific information
underlying the development of quotas
(Lindsey et al. 2013a, p. 8). The best
available monitoring data should be
used to set quotas if they are to be
scientifically based and sustainable.
However, monitoring data are often
lacking (Barnett and Patterson 2005, p.
102). A limited number of independent,
scientific population counts of lions
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have occurred across their range,
especially in hunting concessions
(LionAid 2014a, pers. comm.; Packer
2015, pers. comm.; Packer et al. 2011, p.
143). While some existing quota
allocations have been derived from
information provided by hunting
concession operators, it has been noted
that many hunting concession operators
have not allowed independent
population studies to take place,
possibly as a result of illegal activity
and corruption (LionAid 2014a, pers.
comm.; Packer 2015, pers. comm.). Lion
experts also describe an over-reliance on
subjective opinions, including input
from concession operators, in the
process of developing quotas (Lindsey et
al. 2013a, p. 8). As a result, information
underlying current quotas in much of
the species’ range has been inconsistent,
biased, and/or lacking. It is difficult to
predict with accuracy what level of
offtake would be appropriate to ensure
a quota is sustainable for a given
population without accurate
information on the size of the resource
(LionAid 2014a, pers. comm.; Barnett
and Patterson 2005, p. 102). Therefore,
quotas not scientifically based are often
too high to maintain sustainability and
overharvest occurs.
Lions are particularly vulnerable to
excessive harvests due to impacts
associated with the removal of males
(Hunter et al. 2013, p. 2). As stated
before, except in Mozambique, quotas
are higher than the recommended
maximum harvest of 1 lion per 2,000
km2. Additionally, mean actual harvests
are higher than the recommended 1 lion
per 2,000 km2 offtake in Burkina Faso,
Zambia, Namibia, and Zimbabwe
(Lindsey et al. 2013, p. 8). Multiple
researchers have documented declines
in lion populations across the range of
the species as a result of mismanaged
trophy hunting. Specifically, negative
impacts to lions from excessive offtakes
have been documented in Benin
(Sogbohossou et al. 2014, entire),
Cameroon (Croes et al. 2011, entire),
Tanzania (Packer 2011, entire), Zambia
(Rosenblatt et al. 2014, p. entire; Becker
et al. 2013, entire), and Zimbabwe
(Groom et al. 2014, entire; Davidson et
al. 2011, entire; Loveridge et al. 2007,
entire). Additionally, the effects of overharvesting can extend into adjacent
national parks where hunting does not
occur (Packer et al. 2013, p. 636).
Most experts consider the
recommendation by Packer et al. (2011,
p. 151) to limit offtake to no more than
1 lion per 2,000 km2 throughout its
range (or 1 per 1,000 km2 in areas with
high density of lions) to be the best
available science and recommend each
country impose a quota cap at those
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levels to ensure sustainability while
other methods are being developed and
refined. According to Hunter et al.
(2013, p. 5), ‘‘such caps provide a shortterm means of reducing the risk of
negative population impacts while more
robust methods are being implemented.
Areas that are smaller than 1,000 km2
should be granted the equivalent
fraction of 0.5 lions per year: For
example, an area of 200 km2 would be
allocated 0.1 lions per year, or one tag
every ten years. Such a system would
reduce the extent to which hunting in
small concessions adjacent to protected
areas affects protected populations, as in
Zambia and Zimbabwe.’’
Species experts also recommend, as
part of reforming trophy hunting,
adoption by range countries of an
adaptive quota management system that
would allow for quotas to fluctuate
annually based on the population trends
of the species. An adaptive quota
management system would not only
prevent over-harvesting of lions, but
would also prevent excessively
conservative quotas (Hunter et al. 2013,
p. 5).
Recognizing the inconsistencies in the
process of setting a quota and the
information on which they are based,
range countries and conservationists
have been working to establish a set of
best practices in order to create a more
consistent, scientifically based approach
to determining quotas. The
recommended best practices include: (1)
establishing processes and procedures
that are clearly outlined, transparent,
and accountable; (2) establishing
processes and procedures that are CITES
compliant; (3) demonstrating
management capacity; (4) standardizing
information sources; (5) establishing
monitoring systems for critical data; (6)
recording and analyzing trophy hunting
data; (7) conducting data collection and
analysis for each hunting block and
concession; and (8) establishing a
primary body who will approve quotas
(Burnett and Patterson 2005, p. 103).
Each country that allows trophy
hunting has some data collection system
in place; most countries have a central
wildlife authority that requires
operators to submit data collection
forms or questionnaires providing
details of each of their hunts. However,
according to the authors, these
guidelines have not been followed
throughout much of the range countries,
which has led to a variety of compliance
issues. Some systems have been overly
complex and cumbersome. ‘‘In 2000,
Zimbabwe, for example, had nine
different forms, which contain
essentially the same information, that
had to be completed by safari operators
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for each client and submitted to
different government departments’’
(Barnett and Patterson 2005, p. 100).
Additionally, governmental bodies have
sometimes failed to analyze data and
provide feedback to operators; experts
agree this failure undermines the
purpose of the system and encourages
noncompliance.
In the absence of reliable population
estimates, age restriction on trophy
harvests can ensure sustainability
(Lindsey et al. 2013a, p. 8; Packer et al.
2006, pp. 6–8). Whitman et al. (2004,
pp. 176–177) found that if offtake is
restricted to males older than 6 years of
age, trophy hunting will likely have
minimal impact on the pride’s social
structure and young. By removing only
males 6 years of age or older, younger
males remain in residence long enough
to rear a cohort of cubs (allowing their
genes to enter the gene pool; increasing
the overall genetic diversity);
recruitment of these cubs ensures lion
population growth and therefore,
sustainability. Simulations indicate that
populations with quotas of more than
two male lions of minimum eligible age
of 3–4 years were more likely to
experience extinction events than
populations with hunting restricted to a
minimum eligible age of 5–6-year-old
males (Whitman et al. 2004, p. 176).
Additionally, full implementation and
enforcement of this age-based strategy
could potentially cause the need for
quotas to become irrelevant or
eliminated entirely. Age restrictions will
naturally restrict offtake to a limited
number of individuals that meet the age
criteria (Loveridge et al. 2007, p. 549;
Whitman et al. 2004, p. 177).
Implementing this approach in the
field involves conducting an age
assessment of male lions using
identification techniques, such as mane
development, facial markings, nose
pigmentation, and tooth-aging to
establish the relative age of the target
lion. Tooth wear on incisors, yellowing
and chipping of teeth, coupled with
scars, head size, mane length and color,
and thinning hair on the face, as well as
other factors can be an indicator of
advanced age in lions (Whitman and
Packer 2006, entire).
Whitman et al. (2004, p. 176)
postulated that ‘‘the most reliable index
in the Serengeti/Ngorongoro lions is the
extent of dark pigmentation in the tip of
the nose, which becomes increasingly
freckled with age. Individual variation
in nose coloration is sufficiently low
that age can be estimated up to 8–9
years. The noses of 5-yr-old males are 50
[percent] black so the rule of thumb
would be to restrict all trophy hunting
to males with noses that are more than
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half black.’’ Although this varies
individually and regionally,
recommended best practices could be
regionally tailored. Packer et al. (2006,
p. 7) note that males in South Africa
require an additional 1–2 years to
become competitive with other males,
and suggest a 7-year minimum might be
judicious for some regions. Therefore,
there is concurrence by species experts
that national or regional guidelines
should be developed to accompany
those produced in Tanzania and Zambia
(Lindsey et al. 2013a, p. 8; Packer and
Whitman 2006, entire).
According to Lindsey et al. (2013a, p.
8), some operators were uncertain of
their ability to age lions; however, based
on research conducted in Niassa
National Reserve, Mozambique, hunters
can be taught to age lions effectively.
While experts agree it may be difficult
to determine the exact age of a lion,
broader categories based on age have
been developed to assist officials. For
example, Tanzania officials have ‘‘aging
sessions’’ wherein each concession
operator is required to bring in the
skulls of their trophies for examination.
Each skull is then classified as
‘‘acceptable’’ (6+ years old), ‘‘accepted
with penalties’’ (4–5 years old), and
‘‘not accepted with deterrent penalties’’
(<4 years) (Tanzania 2015, pp. 23–24).
Tanzania reports that this step is
required prior to any issuance of a
CITES export permit.
Species experts place high emphasis
on the requirement for both enforcement
and transparency in the strategy. A fully
transparent quota allocation system
would be one in which a quota
allocation system is based on scientific
data received from all hunting areas and
concession units annually, and would
require trophies to be independently
evaluated, data on the trophies (e.g. age,
sex, origin) be available nationally and
internationally, and quotas based upon
data obtained from the previous hunting
season (Henschel pers. comm. 2015).
Lion experts recommend age-based
strategies be incorporated into lion
management action plans (Hunter et al.
2013, pp. 4–5; Lindsey et al. 2013a, p.
8). Although the 6-year method has
potential to reduce the rate of
infanticide in lion populations used for
trophy hunting (Hunter et al. 2013, p. 4–
5; Lindsey et al. 2013a, p. 8), the issue
of incorporating this strategy into each
country’s conservation strategy and/or
action plan, and following up with
implementation, enforcement, and
transparency has yet to be observed in
many of the lion’s range countries
(Henschel 2015, pers. comm.). While
several countries, including Benin,
Burkina Faso, Mozambique (only in
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Niassa National Reserve), Tanzania, and
Zimbabwe have committed to
implementing the age-based strategy
(White 2013, p. 14; Davidson et al. 2011,
p. 114; Whitman et al. 2004, p. 176),
only two have fully implemented it
(Henschel 2015, pers. comm.). Thus far,
Mozambique and Zimbabwe have
implemented this strategy and shown a
reduction in total offtake (Henschel
2015, pers. comm.). They also appear to
be transparent in their implementation.
Tanzania has implemented age
restrictions and shown reductions in
offtake; however, there is concern
related to transparency (in terms of
trophy quality data) and the scientific
objectivity of the evaluating body has
been questioned. Benin and Burkina
Faso committed to implementing age
restrictions in 2014; their progress is
currently pending. Lastly, Mozambique,
excluding Niassa National Reserve and
Cameroon have not yet instituted or
committed to the strategy (Henschel
2015, pers. comm.). Lack of
implementation of age-based strategies
may undermine the successful use of
trophy hunting as a sustainable
conservation strategy.
Additionally, experts believe that
importing countries should have the
ability to ascertain that the imported
trophies originated from hunting
concessions that fully comply with best
practices. According to Lindsey et al.
(2007, p. 3; Lindsey et al. 2006, pp. 285,
288), there is a market in the United
States for conservation-based hunting.
‘‘In a survey of prospective clients 45–
99 percent were unwilling to hunt
under various scenarios if conservation
objectives would be compromised, and
86 percent were more willing to
purchase a hunt if local communities
would benefit’’ (Lindsey et al. 2007, p.
3). Experts agree that a fully transparent
system would allow hunters to choose
operators who have demonstrated a
commitment to conservation principles;
this system could provide incentives for
operators to comply with the
recommended best practices.
Harvesting of males that are too young
can have devastating impacts to the
population. If male lions are harvested
too young (even as old as 3 years of age),
combined with quotas that are too high,
the population will be driven to
extinction as female populations
collapse as they eventually are unable to
mate (Whitman et al. 2004, p. 176).
Additionally, excessive trophy hunting
and taking of males under a certain age
cause male replacements and increased
infanticide rates (when males kill young
lion cubs sired by other males)
(Whitman et al. 2004, p. 175). Packer
(2001, p. 829, citing Bertram 1975,
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Packer and Pusey 1984, and Pusey and
Packer 1994) demonstrated that cub
mortality increases when a new male
joins a pride. Infanticide is a common
practice among many species, including
lions (Hausfater et al. 1984, pp. 31, 145,
173, 487). Removing a younger male
lion allows another male of the pride to
take over and kill the former patriarch’s
cubs; offspring younger than 2 years of
age are generally unable to defend
themselves and may be killed or forced
to disperse from the pride prematurely,
which also often leads to death (Elliot
et al. 2014, p. 1054; Packer 2001, p. 829;
Pusey and Packer 1984, p. 279). This
behavior is believed to be advantageous
to the incoming male as it increases and
accelerates the opportunity for the new
male to sire a cohort of cubs. When
females give birth to cubs, the female
generally does not return to estrus until
the cubs are around 18–24 months old
(Pusey and Packer 1984, p. 281).
Following the loss of her cubs, however,
a female will return to estrus rather
quickly; females will resume mating
within days or weeks, thus increasing
the likelihood that the new male will
have the chance to sire the next cohort.
Pusey and Packer (1984, p. 279)
calculated that infant fatality during
male takeovers accounted for 27 percent
of all cub fatalities under the age of 12
months.
Further, when an adult male lion in
a pride is killed, surviving males who
form the pride’s coalition are vulnerable
to takeover by other male coalitions, and
this often results in injury or death of
the remaining males (Davidson et al.
2011, p. 115).
Recently, Elliot (2014, p. 1054)
postulated that the impacts of male
takeovers due to trophy hunting may be
more severe than previously recognized.
Specifically, when a pride male is
removed and a new male takes over,
subadults may be forced to disperse
from the pride. These males are then at
a disadvantage as they are often
inexperienced and physically smaller
which may prevent them from being
able to compete with older males for
territory. In the study, Elliot found 100
percent fatality for all males who
dispersed earlier than 31 months old.
The study concluded that dispersal of
subadults is highly related to the
presence of incoming males, resulting in
a type of delayed infanticide, as many
of the subadults do not survive the
dispersal. This effect may be amplified
in populations that have a high offtake
rate. Therefore, the author concluded
that age restriction and reducing offtake
could reduce takeover rates by new
males, allowing subadults a longer
period to mature prior to dispersal and
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thus, reducing the number of subadult
deaths (Elliot et al. 2014, p. 1055).
A lack of mature males dispersing
reduces the genetic viability of
populations and may contribute to local
population extinctions (See Deleterious
Effects Due to Small Population Sizes).
Selective offtake of large males may also
modify the genetic evolution of lions.
Allendorf and Hard (2009, p. 9987) and
Loveridge et al. (2007, p. 553) consider
the genetic and evolutionary role of
selective hunting on wildlife
populations. As individuals who
display certain characteristics (such as
largest size) are more likely to be
harvested, this type of selective removal
will bring about genetic change in future
generations. Specifically, removing the
males with the most desirable traits
from a population ultimately affects
upcoming generations as those
individuals are no longer contributing to
the gene pool. ‘‘For example, the
frequency of elephants (Loxodonta
africana) without tusks increased from
10 percent to 38 percent in South
Luangwa National Park, Zambia,
apparently brought about by poaching of
elephants for their ivory’’ (Jachmann et
al. 1995 in Allendorf and Hard 2009, p.
9987). This comparison relates to lion as
the removal of the largest males
consequentially results in females
breeding with less desirable males and
thus, perpetuating the production of less
desirable individuals. Selective offtake
based on gender also has the potential
to skew sex ratios and impact breeding
success, as has been the case for lions
(Allendorf and Hard 2009, p. 9991;
Loveridge et al. 2007, p. 553). The
authors state that in order to maintain
the highest yield and viability of the
most desirable males, one option is to be
less selective (Allendorf and Hard 2009,
p. 9991). Specifically as related to lions,
this would mean implementing age
restrictions so that the more desirable
males are not harvested prior to
successful reproduction.
Whitman et al. (2004, pp. 175–177)
found that if offtake is restricted to
males 6 years of age or older, the
impacts of trophy hunting are likely to
be minimal on the prides social
structure and reproduction. Therefore,
experts recommend that a 6-year age
restriction should be implemented for
all hunting concessions throughout the
lion’s range.
Species experts have suggested an
additional mechanism that could help
reduce infanticide. In concessions
where operators can distinguish
between resident and solitary
individuals, removal of the nomadic
males may reduce the likelihood of a
possible conflict and take-over (Packer
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et al. 2006, p. 7; Whitman 2004, p. 177).
If concession operators selectively
remove males in a manner that
promotes healthy population growth,
the lion population could yield more
males in the long term (Davidson et al.
2011, p. 114; Packer et al. 2006, p. 7;
Whitman et al. 2004, p. 176).
Hunter et al. (2013, pp. 2, 5) and
Lindsey et al. (2013a, p. 9) identified
hunting of female lions to be another
aspect of trophy hunting that is harmful
to lion populations. Specifically,
females are the most productive portion
of a population; if females are removed
from a pride, there is inherent risk that
dependent cubs will die and the overall
breeding success of the pride will be
reduced. Packer et al. (2001 in Packer et
al. 2006, pp. 5, 7) report that ‘‘large
prides out-compete smaller prides and
per capita reproduction is lowest in
prides of only 1–2 females.’’ Lindsey et
al. (2013a, pp. 2, 4, 9) indicate that a
loss of a female increases a pride’s
vulnerability to territory loss. As a
result, removing females has injurious
effects on the overall success of the
population and, ultimately, the number
of harvestable males.
Lindsey et al. (2013a, pp. 2, 4, 9)
indicate that quotas are currently
available for female lions in some
locations within Namibia, and between
1990 and 2011, in Zimbabwe (Packer et
al. 2006, p. 4). Between 1998 and 2004,
Zimbabwe maintained a mean quota of
0.3 ± 0.1/100 km2 for female lions;
during the same period, actual offtake
was lower at 0.08 ± 0.1/100 km2, or a
mean of 30.6 percent of the quota
actually harvested (Loveridge et al.
2007, p. 551). Zimbabwe discontinued
issuing quotas for females in 2011.
Female hunting is not allowed
elsewhere within the range of the
species (Lindsey et al. 2013a, p. 2).
Species experts recommend that the
trophy hunting of females be prohibited,
unless the management plan is
specifically to control the size of the
lion population (Hunter et al. 2013, p.
5; Lindsey et al. 2013a, p. 9).
Another deficiency in current trophy
hunting management is the use of fixed
quotas. There are two primary types of
quotas, ‘‘fixed’’ and ‘‘optional.’’ Trophy
fees for fixed quotas require the
payment of a portion (40–100 percent)
of the lion trophy fee, regardless of
whether the hunt is successful, whereas
optional quotas are paid by operators
only when the lion is shot. Until 1999,
male lions were typically on fixed
quotas, whereas female lions were
under optional quotas. According to
Lindsey et al. (2013a, pp. 2–3),
Mozambique, Benin, Burkino Faso, and
Cameroon all have optional quotas in
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place, thereby, hunters only pay for
animals hunted. Other range countries
continue to have fixed quotas in place
and charge a percentage of the quota
regardless of success (CAR charges 50
percent; Namibia 100 percent; Tanzania
40 percent; Zambia 60 percent;
Zimbabwe 30 percent). This approach
facilitates harvesting of trophies even if
a sufficiently old lion is not found
(Hunter et al. 2013, p. 6). Therefore,
harvested lions are often of lower
quality, younger, and less desirable
male lions, as operators and hunters,
who had already paid the trophy fee,
had no incentive to be selective.
Abolishing fixed-quota fees and only
allowing optional quotas will encourage
and reward operators who are selective
and follow age restrictions (Lindsey et
al. 2013a, p. 9; Packer et al. 2006, pp.
5, 9).
To ensure hunters have adequate time
to be selective in trophies harvested,
and to ensure the revenue earning
potential is maximized, experts
recommend that a minimum stipulated
hunt length be set at 21 days. However,
many countries either have no limits on
length of hunting safaris or have too
short a minimum length (Lindsey et al.
2013a, p. 9). Currently, there are no set
lengths for hunting safaris in
Mozambique, Namibia, Zambia, and
Zimbabwe. Burkino Faso has a
minimum requirement of 12 days, and
Benin and Cameroon require 12 to 14
days. Tanzania has a minimum length of
21 days while CAR varies from 12 to 21
days (Lindsey et al. 2013a, pp. 2–3).
Several other problems with current
management of lion trophy hunting are
likely to worsen negative impacts
associated with hunting of lions and
undermine conservation incentives.
Corruption, allocation of hunting
concessions, and lack of benefits and
recognition of the role communities
play in conservation have been
identified (Lindsey et al. 2013a, pp. 2–
3, 9).
Corruption is widespread within the
range of the lion (Transparency
International 2014, unpaginated). All
but one lion range country (Botswana)
scored below 50 (out of 100) on
Transparency International’s 2014
Corruption Perception Index (CPI),
which measures perceived levels of
public sector corruption based on expert
opinion and is based on a scale of 0
(highly corrupt) to 100 (very clean).
Approximately half of the current lion
range countries—including Tanzania
and Kenya, where more than half of all
wild lions occur—are among the most
corrupt countries in the world, ranking
in the lower 30 percent of 174 countries
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assessed (Transparency International
2014, unpaginated).
Corruption is particularly prevalent in
areas with extreme poverty
(Transparency International 2014,
unpaginated; Michler 2013, pp. 1–3;
Kimati 2012, p. 1; Garnett et al. 2011, p.
1; IUCN 2009, p. 89; Leader-Williams et
al. 2009, pp. 296–298; Kideghesho 2008,
pp. 16–17). Certain circumstances tend
to promote corruption, such as
opportunity for financial gain, weak rule
of law, abnormal concentrations of
power in one individual or institution,
no counter-balancing mechanisms in
place among different government
agencies, and reliance on discretionary
powers for allocation of permits,
licenses, or activities (Smith et al. 2015,
p. 953; Nelson 2009, unpaginated; Luo
2005 in Smith et al. 2015, p. 953).
Corruption manifests itself in several
ways, such as embezzling of public
funds, fraud, demanding or accepting
bribes to overlook illegal activities,
interference in decisions to implement
conservation measures, and offering
patronage, nepotism, and political
influence (Vargas-Hernandez 2013 in
Smith et al. 2015, p. 953; Garnett et al.
2011, p. 1; Leader-Williams et al. 2009,
p. 301; Kaufmann 1997 in LeaderWilliams et al. 2009, p. 297). With
respect to lion management, it may
include, for example: Infringement of
hunting regulations in the field;
acceptance of bribes to overlook illegal
activities such as poaching; interference
or mismanagement in monitoring and
setting of hunting quotas and in issuing
of licenses; misappropriation of hunting
fees; allocation of hunting blocks based
on patronage and nepotism or to
persons presumably considered to be of
financial or other strategic importance;
and allocation of hunting blocks at less
than competitive prices (see LeaderWilliams et al. 2009, pp. 301–305;
Nelson 2009, unpaginated).
Peh and Dori (2010, pp. 336–337)
show that global indices of corruption
and governance are highly correlated
with those of environmental
performance—countries with high
levels of corruption have lower levels of
environmental performance. Further,
Smith et al. (2003, entire) found strong
associations between changes (declines)
in elephant and rhinoceros numbers and
governance scores. Governance scores,
which were based largely on
Transparency International’s CPI,
explained observed changes in numbers
of elephants and rhinoceroses better
than per capita GDP, Human
Development Index scores, and human
population density. These results
suggest that political corruption may
play a significant role in determining
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the success of national strategies to
conserve these species (Smith et al.
2003, p. 69). Corruption can reduce the
effectiveness of conservation programs
by reducing the funding, law
enforcement, and political support
available for conservation, and also by
acting as an incentive for the
overexploitation of resources (Garnett et
al. 2011, p. 1, citing several sources;
Smith and Walpole 2005, p. 252). Given
the financial gains to be made from lion
trophy hunting, and the high level of
corruption in many lion range countries
(Packer 2015, pers. comm.;
Transparency International 2014,
unpaginated), it is reasonable to
conclude that corruption and the
inability to control it are having
negative impacts on decisions made
about lion management in many areas of
the species’ range and on lion
populations, and undermine steps to
reform hunting of lions. The impacts
highlight the importance of
transparency within the hunting
industry and independent verification
of processes such as quota setting,
trophy monitoring, and concession
allocation (Lindsey et al. 2013a, p. 9).
In recent years, leadership in several
African lion range countries has taken
steps to address corruption, or activities
that facilitate corruption, associated
with wildlife management. For example,
in 2013, the Tourism Minister of Zambia
banned hunting in 19 game management
areas for 1 year due to allegations of
corruption and malpractice among the
hunting companies and various
government departments. Some game
management areas and privately owned
game ranches were not included in the
ban, but lion hunting appears to be
prohibited throughout the country
(Michler 2013, pp. 1–3). Whether recent
reforms taken by various lion range
countries will reduce the effect of
corruption on lion management and,
therefore, lion populations is as yet
unknown.
Most concessions in the African range
of the lion use a closed-tender process
for land management. A closed-tender
system is the process of selling a
product by inviting a specific group of
potential buyers to provide a written
offer by a specified date. In the case of
a hunting concession, the owner of the
property thus sells a lease on a property
for a given length of time. Countries that
use this process for state-owned lands
include Benin (lease is for 5 years);
Burkina Faso (20 years); Cameroon (10
years, renewable); CAR (10 years
(renewable); Mozambique (10+ years);
Tanzania (5 years); and Zambia (10–15
years based on status of wildlife). In
Namibia, state concessions lease land by
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public auctions for 3-year periods, while
community conservancies lease for a 5year period via a closed-tender process.
Zimbabwe holds a public auction for
state safari areas, with the option to
extend 5 years based on performance.
Communal Areas Management
Programme for Indigenous Resources
(CAMPFIRE) areas are leased on 3–10
year-period using a closed-tender
process (Lindsey et al. 2013a, pp. 2–3).
The chief complaint regarding this
system is that concession areas are
leased to operators without regard for
the operators’ track record in
conservation. Zimbabwe is the only
country that renews based on operator
performance (Lindsey et al. 2013a, pp.
2, 9). Lindsey et al. (2007, p. 2) found
that various countries have problems
with their allocation process, ‘‘with the
effect that they are sometimes sold too
cheaply, allocated for periods too short
to promote responsible custodianship,
and occasionally given to unlicensed
operators. . .. In several countries large
citizen quotas are provided to urban
residents at low prices, reducing
revenues from trophy hunting and
reducing incentives for communities to
conserve wildlife.’’ Experts believe that
basing the ability to renew a concession
lease on operators’ past performance
records could be an incentive for
operators to comply with best practices.
Thus, experts recommend concession
allocation should base concession lease
renewals on operator performance in
regard to best practices compliance.
As discussed under Human–lion
Conflict, the risk of retaliatory killing is
elevated in many cases due to the fact
that communities living in close
proximity to lion populations often bear
the cost of that proximity (e.g., loss of
valuable livestock due to lion
depredation), but receive little of the
benefits generated by the presence of
lion in the trophy hunting and
ecotourism industries (Lindsey et al.
2013a, p. 9). Trophy hunting can
generate millions of dollars in annual
revenue (see Potential Benefits of
Trophy Hunting).
In the past, government and private
land owners were the primary
beneficiaries of the revenue gained;
currently efforts are being made in many
range countries to incorporate
incentives at the local level (Barnett and
Patterson 2005, p. vi). Many range
countries are now recognizing the need
to incorporate incentives and local
community benefits into their trophy
hunting regulations, land management
policies, and lion conservation action
plans. Most countries that allow lion
trophy hunting have developed National
Poverty Reduction Strategies and
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discussed benefit distribution and
management to rural communities (see
Potential Benefits of Trophy Hunting).
Although positive steps are being taken
to address local community incentives,
most of the countries are currently not
transparent about the benefits provided
to local communities, and due to the
high revenue potential are subject to
corruption.
Captive Lions
In analyzing threats to a species, we
focus our analysis on threats acting
upon wild specimens within the native
range of the species, because the goal of
the Act is survival and recovery of the
species within its native ecosystem. We
do not separately analyze ‘‘threats’’ to
captive-held specimens because the
statutory five factors under section 4 (16
U.S.C. 1533) are not well-suited to
consideration of specimens in captivity,
and captive-held specimens are not
eligible for separate consideration for
listing. However, we do consider the
extent to which specimens held in
captivity create, contribute to, reduce, or
remove threats to the species.
In 2009, approximately 3,600 captiveheld lions were managed for trophy
hunting across 174 breeding facilities in
South Africa ((Lindsey et al. 2012, p. 18,
citing Taijaard 2009; Barnett et al.
2006a, p. 513). The captive-breeding
industry often publicizes captive
breeding and reintroduction of captiveborn species into the wild as a potential
solution to the decrease in wild lion
populations. However, lions raised in
captivity often develop a variety of
issues that make them unsuitable for
reintroduction. Captive lions in general
are not suitable for reintroduction due
to their uncertain genetic origins
(Barnett et al. 2006a, p. 513; Hunter et
al. 2012, p. 3), potential maladaptive
behaviors, and higher failure risk
compared to translocated individuals
(Hunter et al. 2012, pp. 2–3). Research
has indicated that restoration efforts
using wild-caught individuals have a
much higher rate of success than those
using captive-raised individuals for a
large variety of species (Hunter et al.
2012, p. 21). Currently, reintroduction
efforts of captive-raised lions have not
been shown to address the underlying
causes of populations’ declines
throughout the species range.
We note that while the captive-lion
industry may not be contributing to the
conservation of the species in the wild
via reintroduction, the captive-lion
industry in South Africa may reduce the
pressures of trophy hunting on the wild
populations in South Africa (Hargreaves
2010b in Lindsey et al. 2012, p. 12;
Lindsey et al. 2012, p. 19), which is
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evidenced by the fact that 99 percent of
lion trophies from South Africa are of
captive origin. Lindsey et al. (2012, p.
21) warn that future efforts to control
hunting of captive-bred lions could
potentially increase the demand for
wild lion trophies and result in
excessive harvests. However, we also
note that trade in bones of captive lions
could stimulate harvest of wild lions to
supply a growing bone trade (Lindsey et
al. 2012, p. 20). Hunting of captive lions
could also potentially undermine the
price of wild hunts and reduce
incentives for conservation of wild lions
in other African countries (Lindsey et al.
2012, p. 12).
Limited research has been conducted
on the use of captive-raised lions for
reintroduction purposes. Existing
research has generally found that
captive-raised lions are not as able to
successfully adapt to conditions out of
captivity and therefore, the success rate
is much reduced compared to the use of
wild-caught lions. Although some
potential exists that the captive-lion
industry in South Africa may benefit
some local wild populations, additional
research would be needed to verify this
claim. As a result, we do not believe
that the captive-lion industry currently
contributes to, reduces, or removes
threats to the species.
Summary of Trophy Hunting
If trophy hunting of lions is part of a
scientifically based management
program, it can provide considerable
benefits to the species by reducing or
removing incentives to kill lions in
retaliation for livestock losses, and by
reducing the conversion of lion habitat
to agriculture. Trophy hunting, if
managed well and with local
communities in mind, can bring in
needed revenue, jobs, and a muchneeded protein source to impoverished
local communities, demonstrating the
value of lions (Groom 2013, pp. 1–3;
Lindsey et al. 2006, pp. 283, 289). In
addition, the amount of habitat that has
been set aside by range countries
specifically for trophy hunting has
greatly increased the range and habitat
of lions and their prey base, which
contrasts the overall ongoing rate of
habitat destruction occurring in Africa.
The total amount of land set aside for
trophy hunting throughout Africa
exceeds the total area of the national
parks, providing half the amount of
viable lion habitat (Chardonnet et al.
2010, p. 34; Packer et al. 2006, pp. 9–
10).
The main problem with mismanaged
trophy hunting stems from excessive
harvests and impacts associated with
removal of males (Hunter et al. 2013, p.
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2). Researchers have documented
declines in populations across the range
of the species that were a direct result
of mismanaged trophy hunting
(Rosenblatt et al. 2014, p. entire;
Sogbohossou et al. 2014, entire; Becker
et al. 2013, entire; Lindsey et al. 2013,
entire; Croes et al. 2011, entire; Packer
2011, entire; Loveridge et al. 2007,
entire). Six management weaknesses
have been identified in the current
management of lion hunting. These
weaknesses include: (1) A lack of
scientifically based quota that results in
excessive harvests; (2) a lack of
enforcement in age restrictions, which
leads to unsustainable harvests,
increased rates of infanticide, and
population declines; (3) hunting of
female lions in Namibia, which
decreases reproduction success, thereby
decreasing males available for trophy
hunting; (4) the use of fixed quotas,
which encourages hunters to be
unselective in their take of a trophy (i.e.,
they will kill younger, less desirable
males); (5) a lack of minimum hunt
lengths or minimum lengths that are too
short to allow hunters the time needed
to be more selective in their take of
trophies; and (6) general problems
associated with management of trophy
hunting, including corruption,
allocation of concessions, and lack of
benefits to communities and recognition
of the important role they play in
conservation.
Most P. l. leo populations are
extremely small, isolated, and rapidly
declining. Of the 18 countries
documented to allow lion trophy
hunting, 8 are in the range of P. l. leo.
However, we note that due to the lack
of lions in some of these countries, it is
unlikely that all of these countries could
conduct lion trophy hunts. A study
found that quotas in Benin and Burkina
Faso are too high for sustainability,
although Burkina Faso has proposed to
reduce their quota in the 2015–2016
season (Henschel 2015, pers. comm.;
Lindsey et al. 2013a, p. 6). Actual
harvests in Burkina Faso were also
found to be higher than the level
recommended by Packer et al. (2011, p.
151). Additionally, Benin and Burkina
Faso have committed to implementing
an age-based strategy, but have yet to
implement it. As a result, species
experts agree that there is no level of
offtake that would be sustainable for P.
l. leo populations in their current
condition (Bauer 2015, pers. comm.;
Henschel et al. 2014, entire; Henschel et
al. 2010, entire).
Of the 18 countries documented to
allow lion trophy hunting, 10 are in the
range of P. l. melanochaita. However,
we note that, like the situation with P.
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l. leo, due to a lack of lion populations
in some of these countries, it is likely
that fewer countries could conduct lion
trophy hunts. A study found that
Namibia, Tanzania, Zambia, and
Zimbabwe all had quotas higher than
the recommended level for
sustainability; however, Zimbabwe has
reduced their quota. Mozambique
(Niassa National Reserve) is the only
location found to have a quota below
the recommended level. Age-based
strategies have been implemented and
shown to reduce offtakes in
Mozambique (only in Niassa National
Reserve, excludes the rest of the
country), Tanzania, and Zimbabwe.
Furthermore, Zimbabwe and Niassa
National Reserve are the only two
locations that have fully implemented
an age-based strategy with transparency,
an element experts say is critical to a
quota allocation system. Several other
countries have made commitments to
implement the age-restrictions strategy
but their progress is pending. In South
Africa, 99 percent of the lion trophies
are captive bred, and, therefore, were
not the result of removing lions from the
wild.
Unless reforms are made to the
current management of trophy hunting,
we expect the declines specifically
documented from excessive offtakes in
Benin, Cameroon, Tanzania, Zambia,
and Zimbabwe to continue.
Furthermore, we expect excessive
harvests to further contribute to declines
in the species across its African range.
Import/Export of Lion Trophies
The lion species (Panthera leo) is
listed in Appendix II of CITES;
however, the former Asiatic lion (P. l.
persica) is listed in Appendix I. CITES
is an international agreement through
which member countries work together
to protect against over-exploitation of
animal and plant species found in
international trade. Parties regulate and
monitor international trade in CITESlisted species—that is, their import,
export, and reexport, and introduction
from the sea—through a system of
permits and certificates. CITES lists
species in one of three appendices—
Appendix I, II, or III.
An Appendix-I listing includes
species threatened with extinction
whose trade is permitted only under
exceptional circumstances, which
generally precludes commercial trade.
The import of specimens (both live and
dead, as well as parts and products) of
an Appendix-I species generally
requires the issuance of both an import
and export permit under CITES. Import
permits are issued only if findings are
made that the import would be for
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purposes that are not detrimental to the
survival of the species in the wild and
that the specimen will not be used for
primarily commercial purposes. For live
specimens, a finding must also be made
that the recipient is suitably equipped to
house and care for the specimens
(CITES Article III(3)). Export permits are
issued only if findings are made that the
specimen was legally acquired and the
export is not detrimental to the survival
of the species in the wild, and that a
living specimen will be so prepared and
shipped as to minimize the risk of
injury, damage to health, or cruel
treatment, and that the CITES
Management Authority of the exporting
country is satisfied that an import
permit has been granted for the
specimen (CITES Article III(2)).
CITES Appendix II includes species
that are less vulnerable to extinction
than species listed in Appendix I, and
‘‘although not necessarily now
threatened with extinction, may become
so unless trade in specimens of such
species is subject to strict regulation in
order to avoid utilization incompatible
with their survival.’’ Species listed in
Appendix II of CITES may be
commercially traded, subject to several
restrictions.
Although each country has its own
method of regulating trophy hunting,
international trade of lion trophies must
adhere to CITES. International trade of
lion parts and products (including
trophies) are reported by both the
exporting and importing countries and
tracked by the United Nations
Environment Programme World
Conservation Monitoring Centre
(UNEP–WCMC).
According to the UNEP–WCMC
CITES Trade Database, between 2005
and 2012, exports of lion trophies
demonstrated a decreasing trend, if
exports of captive-born lions from South
Africa are excluded (UNEP–WCMC
2014, unpaginated). UNEP–WCMC
indicates that 521 lion trophies were
exported (excluding South Africa) in
2005 and 303 were reported (excluding
South Africa) in 2012.
It should be noted that there are
limitations to interpreting the above
reported information. The 2004 guide to
using the CITES Trade Database
indicates that the outputs produced by
the CITES Trade Database can be easily
misinterpreted if one is not familiar
with it (CITES 2004b, p. 5). The number
of ‘‘trophies’’ reported does not
necessarily equate to the number of
lions hunted. Additionally, the number
of trophies reported for a given year in
the trade report does not equate directly
to the number of animals hunted in that
given year (CITES export permits are
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generally valid for 6 months, and a
trophy could in theory be exported the
year after it was hunted). The second
limitation to interpreting this
information is that, although many
permits may indicate that an animal is
of wild origin (source code ‘‘W’’), these
permits may be incorrectly coded. This
is true for South Africa, where during
the period of 2000 to 2009, animals that
were captive born and released into
private reserve systems were assigned
an incorrect source code of ‘‘W.’’ South
Africa has since requested their
provincial authorities to use the correct
source code for ‘‘captive bred’’ in order
to correctly reflect the source of sporthunted lion trophies; however, some
provinces are not complying (RSA 2013,
pp. 8–9). Based on South African trade
data, the bulk of lion exports and their
parts and products (including trophies)
are from captive-born lions (RSA 2013,
p. 7).
Tanzania, with one of the largest lion
populations (Hamunyela et al. 2013, pp.
29, 283; Riggio et al. 2013, p. 32; Ikanda
2008, p. 4; Baldus 2004, pp. 5, 6), was
the largest exporter of wild-origin lion
trophies, but their exports have
decreased significantly since 2008. In
2008, approximately 138 trophies were
exported from Tanzania; in 2010, 128
were exported; in 2011, 55 were
exported; in 2012, 62 were exported (it
should be noted that in 2012 Tanzania
established an annual quota to limit
trophy hunting to no more than 50
animals (Jackson 2013, p. 7); and in
2013, 11 were exported (UNEP–WCMC
2014, unpaginated). Again, it should be
noted that there may be discrepancies
between the annual quota and the actual
number of trophies exported in a given
year (see https://www.cites.org/common/
resources/TradeDatabaseGuide.pdf for
additional information). Regardless, the
numbers of lion trophies exported by
Tanzania according to the UNEP–
WCMC CITES Trade Database suggest a
decreasing trend.
Additionally, some trophies are
exported from source countries under
the ‘‘skins’’ category. According to the
most recent data available, the United
States imported skins of wild origin
from four African countries in 2013; 9
from Mozambique, 5 from Tanzania, 2
from South Africa, and 22 from
Zimbabwe. The purpose code for these
imports was ‘‘Trophy Hunt,’’ except for
the two skins from South Africa which
were coded as ‘‘Commercial.’’
For 2013, the most recent year for
which complete CITES trade data are
available, U.S. CITES Annual Report
trade data indicate that the United
States allowed the direct import of lion
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trophies from seven African countries,
as follows:
Botswana = 1 trophy (originated from
Mozambique)
Burkino Faso = 3 trophies
Mozambique = 5 trophies
Namibia = 9 trophies
South Africa = 545 trophies (the
majority of which are reported to be
of captive-born origin; additionally 2
captive trophies originated in South
Africa, imported to Canada, and then
imported into the United States)
Tanzania = 3 trophies
Zambia = 17 trophies
Zimbabwe = 44 trophies
Based on CITES trade data, lion
trophy exports have decreased
throughout most of the lion’s range,
including Tanzania, which has one of
the largest lion populations. South
Africa is the only country where exports
have increased because most of these
trophies are of captive origin.
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Traditional Use of Lion Parts and
Products
Lion parts and products are used in
many African countries as medicine,
nutrition, talismans, and decorations,
and in traditional ceremonies and
rituals (CITES 2014, p. 7; Burton et al.
2010, p. 4). CITES (2014, p. 8) reports
that many African countries, including
Somalia, Nigeria, Burkina Faso, Kenya,
and Cameroon, maintain local markets
in lion products. Parts used include
skin, teeth, claws, fat, whiskers, bone,
bile, testicles, meat, and tails. In
addition, lion bone is also used in Asia
as a substitute for tiger bone in
traditional Asian medicine (Williams et
al. 2015, pp. 2, 62).
While quantitative data is lacking,
according to a peer reviewer (Bauer
2015, pers. comm.), trade in lion parts
and products is very common within
western and central Africa. Responses to
the CITES periodic review consultation
process support this claim: Trade in lion
skins and partial skins is described as
‘‘frequent’’ in street markets in Abidjan,
ˆ
Cote d’Ivoire; lion skins and canines are
described as ‘‘easily found’’ in the
markets of Dakar, Senegal; and the scale
of domestic trade in illegal lion
products is described as ‘‘massive’’ in
Nigeria (CITES 2014, pp. 5–6). Further,
in the central African country of
Cameroon, the estimated value of a
single lion carcass exceeds the trophy
fee, and at a lion conservation
conference the Government of
Cameroon identified trade in lion skins
as a major cause of the decline in lion
populations in western and central
Africa (LAGA pers. comm., in CITES
2014, p. 12). According to Henschel (in
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CITES 2014, p. 12), the trade in lion
skins is most likely one of the biggest
threats to lion survival in western Africa
due to the rarity of lions in the region,
the extent of the trade, and the high
price of lion skins.
In southern and eastern Africa, trade
in lion parts, particularly lion bone, to
Asia is generally considered a severe
potential threat to the species (Bauer
2015, pers. comm.). According to CITES
(2014, p. 14), there is ‘‘clear scope for
the international trade in lion body
parts for [traditional Chinese medicine
and traditional African medicine] to
grow uncontrollably, as it has done for
other big cats.’’
Lion bones are used as a substitute for
tiger (Panthera tigris) bone in traditional
Asian medicine and in Asian luxury
products (Williams et al. 2015, pp. 2–3,
5; Graham–Rowe 2011, pp. s101–s102).
Lion bones are difficult to distinguish
from tiger bones (Williams et al. 2015,
pp. 8, 102; Wildlife Protection Society
of India 2007, unpaginated), and are
sold into Asian markets as tiger bone
fakes (Williams et al. 2015, pp. 2–3, 62,
citing several sources). Tiger bone is
highly valued in Asia, primarily in
China and Vietnam, and there is
considerable demand for it (Williams et
al. 2015, p. 1; Gratwicke et al. 2008, pp.
2–5; Graham-Rowe 2011, pp. s101–
s102). Consequently, tiger bones are one
of the most lucrative products on the
illegal wildlife market (Haken 2011, in
Williams et al. 2015, p. 1)—the retail
price of raw tiger bone can reach
$1,250–3,750 USD per kilogram (Nowell
and Ling 2007, p. 23).
Tigers are categorized by IUCN as
endangered (Goodrich 2015, p. 2).
Globally, the tiger population has
declined from what is believed to have
been 100,000 at the turn of the 19th
century (Jackson 1993, in Nijman and
Shepherd 2015, p. 1) to an estimated
5,000–7,000 in 1998, to 3,159 tigers in
2014 (Goodrich 2015, p. 7; Seidensticker
et al. 1999, in Goodrich et al. 2015, p.
7). Poaching for the illegal trade in tiger
parts, especially bone has become a
major driver in the species’ decline
(Goodrich et al. 2015, p. 9; Williams et
al. 2015, p. 1; Nowell and Ling 2007, p.
v). While wild tiger populations are
declining, the demand for tiger parts in
Asia is increasing (Williams et al. 2015,
p. 5; United Nations Office on Drugs
and Crime 2013, p. 81; United Nations
Office on Drugs and Crime 2010, pp. 10,
17; Nowell and Ling 2007, p. 4). This
increasing demand for tiger parts has
led to the rise of tiger farms, where live
captive bred tigers appear to be utilized
to supply the bone trade within China
(Denyer 2015, unpaginated). With tigers
difficult to obtain, lion bone may be
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increasingly used as a replacement for
tiger bone. Thus, the lion bone trade
could potentially follow the same
course as the tiger bone trade: Become
lucrative, spur considerable demand
from suppliers of the black market,
result in extensive poaching of wild
individuals, and have significant
impacts to wild populations.
Certain aspects of the current lion
bone trade suggest that the potential for
the trade to impact wild lion
populations may be high. For example,
evidence suggests that demand from
Asia for lion bone is increasing rapidly.
Based on Williams (2015, pp. ix–x, 46),
during 1982–2000, only nine lion
skeletons were exported from
worldwide sources, destined primarily
to Europe. CITES permit records show
only three exported from South Africa
prior to 2008, destined for Denmark. In
2008, South Africa began issuing CITES
permits for the export of skeletons of
captive-bred lions to Asia. These
exports currently appear to come
primarily from South Africa’s captivebred lion hunting industry as a
byproduct of trophy hunting. The
number of lion skeletons for which
South Africa issued permits for export
to Asia (China, Viet Nam, Thailand and
Lao PDR) increased tenfold from 2008 to
2011, from about 50 to about 573
skeletons, respectively, representing a
total of 1,160 skeletons or about 10.8
metric tons (11.9 US tons) of lion bone
in 4 years (Williams 2015, pp. ix–x, 46).
Further, according to the Government of
Kenya (2015, p. 3), the declared exports
of bones, skulls, and skeletons derived
from wild lions also show an increasing
trend through the period 2003–2012,
with total declared specimens in 2012
more than ten times those in 2003. With
respect to meeting demand for lion
bone, Lindsey et al. (2012, p. 20) state
that there are likely to be large numbers
of lion bones available for export from
game farms, from lionesses and nontrophy males, and as byproducts from
animals shot as trophies. In addition,
Williams et al. (2015, p. 41) report that
there may be between 1,400 and 6,200
lion skeletons from past trophy hunts on
South African game farms that could
potentially be used to supply demand
for lion bone. However, considering the
sharp and continuing increases in
demand from Asia for lion bone, there
is potential for demand to surpass the
availability of legally obtained lion bone
and, consequently, result in poaching of
wild lions to meet demand.
In addition, recent evidence strongly
suggests live lions are being used to
supply the lion bone trade (Williams et
al. 2015, pp. ix, 2–3, 42–44). In August
2006 a live Asiatic lion was observed in
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a market in Mong La, Myanmar (Oswell,
2010, p. 12). The town, known for
incidents of wildlife trafficking, is less
than 2km from the Chinese border. Up
to 2006/2007, Williams et al. (2015, p.
x, Table 11, Figure 24) noted:
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‘‘The combined quantity of live lions and
lion parts and derivatives exported to East–
Southeast Asia from South Africa was
minimal in the broader global trade. From
2008, however, the quantities exported
increased almost six-fold from the previous
year. Not only did the number of live lions
exported to East–Southeast Asia reach record
levels from this time, but also the first
permits to export lion skeletons were issued.
The demand for lion parts and derivatives
appears to have coincided with the
strengthened conservation measures adopted
in 2006–2007 to protect tigers and Asian big
cats. Accordingly, tiger parts were
increasingly substituted with lion parts
obtained from Africa. The trade in lion parts
and derivatives to Lao PDR dominates the
exports. Since 1998, but especially after
2007, China, Viet Nam, Lao PDR, Myanmar
and Thailand have imported increasing
amounts of live lions, lion bodies and bones
from South Africa.’’
Evidence also indicates ‘‘well
established’’ links between South
Africa’s legal lion bone trade and the
Xaysavang Network, an international
wildlife trafficking syndicate that is also
involved in the illicit rhino horn trade
in South Africa (Williams et al. 2015,
pp. 7–10, 59; Environmental
Investigative Agency 2014, p. 13; U.S.
Department of State 2013, unpaginated).
The U.S. Department of State has issued
a $1 million reward for information
leading to the dismantling of this
network. According to the U.S.
Department of State, the Xaysavang
Network facilitates the killing of
endangered species in Africa and
elsewhere and smuggles them to Laos
for export to other Asian countries (U.S.
Department of State 2013, unpaginated).
During 2008–2011, the vast majority
(85%) of the permits issued by South
Africa to export lion skeletons or
carcasses were issued for exports to
Laos (Williams et al. 2015, pp. x, 46)
and, for the only 2 years for which data
were available (2009 and 2010), over
half of the consignments destined for
Laos were listed as imported by Vixay
Keosavang, believed by the U.S.
Department of State to be the leader of
the Xaysavang network (U.S.
Department of State 2013, unpaginated;
Williams et al. 2015, pp.8–10). The
involvement of the Xaysavang Network
in South Africa’s lion bone trade
indicates there are well-established
avenues for laundering of illegally
obtained lion bones, such as those
obtained from poached wild lions, into
the legal trade.
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Lastly, evidence suggests incentive to
poach wild lions for the bone trade may
currently exist. According to Williams
et al. (2015, p. x), the 2013 price paid
to South African game farmers and
landowners for lion bones was $1,260–
2,100 USD per skeleton. In many lion
range states this exceeds per capita GDP
(gross domestic product) (World Bank
2015, unpaginated). Thus, the current
price paid for lion bone appears to
provide incentive in some countries to
poach wild lions.
While the lion bone trade appears to
currently be based primarily in South
Africa’s captive-bred lion hunting
industry, the trade appears to be having
little or no impact on wild lion
populations in South Africa at this
time—lion populations in South Africa
are stable or increasing and there is little
poaching of wild lions in the country
(Funston and Levendal 2014, pp. 1, 26;
Williams et al. 2015, pp. 79–80).
However, the impact of the lion bone
trade on lion populations outside South
Africa is unknown, and most wild lions
occur outside South Africa (see
Distribution and Abundance). Based on
the effect of the tiger bone trade on tiger
populations, if current conditions—for
example, rapidly increasing demand
and involvement of an international
crime syndicate—continue unchanged,
then there is considerable potential for
extensive poaching of wild lions to
occur in order to meet demand.
Disease
Wild lions are known to be infected
with various pathogens (Hunter et al.
2012, p. 2; Craft 2008, p. 6; Michel et al.
2006, p. 92; Hofmann-Lehmann et al.
1996, pp. 559–561). However,
information on the extent of infections
and impacts of diseases on lion
populations is limited. We found one
study documenting disease in a single
wild lion in India that died from
trypanosomiasis in 2007; analysis of
tissue samples also detected peste des
petits ruminants virus (PPRV), which is
not known to cause disease in
carnivores (LionAid 2013, unpaginated;
Balamurugan et al. 2012, pp. 203, 205).
Information on the presence of disease
and impacts to lions come from a few
long-term studies that have been
conducted in Africa, including
Serengeti National Park, Ngorongoro
Crater, and Kruger National Park.
As a result of human population
expansion into lion habitat, lions are
increasingly exposed to diseases from
domestic animals (IUCN 2006b, p. 26).
Because lions are a top predator, they
are at a particularly high risk of
exposure to pathogens (Keet et al. 2009,
p. 11). Some pathogens are endemic,
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meaning they are constantly present, but
often do not cause disease. Others are
epidemic and cause a sudden severe
outbreak with the potential to cause
high mortality (Craft 2008, pp. 5, 6). The
association between disease, age,
nutritional health and other factors that
could predispose a lion to morbidity
and, eventually, mortality is complex. It
is often difficult to determine whether
mortality was due to a single factor or
a combination. Lions could be infected
with and become debilitated by a
disease, but the actual cause of death
could be other factors, such as fighting
with other lions or large predators
(LionAid 2014a, p. 4).
Feline calicivirus, feline herpesvirus,
feline parvovirus, feline coronavirus,
and feline leukemia virus are endemic
viruses known to occur in lions of
Serengeti National Park, Ngorongoro
Crater, Lake Manyara National Park,
Kruger National Park, and Etosha
National Park (but not all viruses are
known in all parks). However, these
diseases are not known to affect lion
survival (Hunter et al. 2012, p. 2; Craft
2008, p. 6; Hofmann-Lehmann 1996, pp.
559, 561).
Lions within Kruger National Park
and Hluhluwe-iMfolozi Park, South
Africa, and Serengeti National Park,
Tanzania, are known to be infected with
Mycobacterium bovis, a pathogen that
causes bovine tuberculosis (bTB). This
pathogen is not endemic to African
wildlife and was likely introduced from
cattle imported from Europe. M. bovis is
transmitted to ungulates, such as
African buffalo (Syncerus caffer) and
wildebeest (Connochaetes taurinus),
from domestic cattle located on the
periphery of the parks (Maas et al. 2012,
p. 4206; Keet et al. 2009, pp. 4, 11;
Renwick et al. 2007, p. 532; Michel et
al. 2006, pp. 92, 93; Cleaveland et al.
2005, pp. 446, 449, 450). Spillover of the
disease from buffalo to other lion prey
species, such as kudu (Tragelaphus
strepsiceros) and warthog
(Phacochoerus africanus), has also been
documented (Keet et al. 2009, pp. 4, 11;
Renwick et al. 2007, p. 535; Cleaveland
et al. 2005, p. 450). Because the lion’s
primary prey are infected with bTB,
they are frequently exposed to large
amounts of infected tissue and are at
risk of infection (Keet et al. 2009, pp. 4,
6; Renwick et al. 2007, pp. 532, 536;
Michel et al. 2006, p. 93; Cleaveland et
al. 2005, pp. 450, 451). Furthermore,
predators prey on weak animals and
scavenge on carcasses, increasing their
likelihood of being exposed to M. bovis
(Renwick et al. 2007, p. 536; Michel et
al. 2006, p. 93). Transmission may also
occur among lions via scratching and
biting (Keet et al. 2009, p. 7; Renwick
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et al. 2007, pp. 532–533). M. bovis is a
pathogen that causes the infected
animal to remain infectious and,
therefore, a source of infection, until it
dies (Renwick et al. 2007, p. 531). Miller
et al. (2014, pp. 495, 496) found
respiratory shedding of viable M. bovis
in living lions, meaning that lions could
transmit bTB and serve as maintenance
hosts.
The social behavior of buffalo and
lions allows M. bovis to spread to larger
areas and facilitates the transmission
within and between prides. Drought
conditions may also encourage the
spread of this pathogen as herds must
move into new areas in search of forage,
potentially putting them in contact with
new, uninfected herds (Keet et al. 2009,
pp. 4, 6; Renwick et al. 2007, p. 533;
Michel et al. 2006, p. 93). In Kruger
National Park, bTB was introduced in
the southeastern corner of the park
between 1950 and 1960. It gradually
made a northern progress and reached
the park’s northern boundary in 2006. In
2009, the disease was found in buffalo
across the river boundary in Zimbabwe
(Keet et al. 2009, pp. 6, 11; Renwick et
al. 2007, pp. 532, 533; Michel et al.
2006, pp. 92, 96, 98). A study from
Kruger National Park indicated that bTB
spreads quickly through lion
populations; in an area with high herd
prevalence of M. bovis, 90 percent of
lions became infected (Cleaveland et al.
2005, p. 451). In time it will likely
spread to Mozambique (Keet et al. 2009,
p. 6). In Serengeti National Park,
infection may be widespread due to the
large, migratory wildebeest population
that ranges throughout the Serengeti
ecosystem, including Maasai Mara
National Reserve (Cleaveland et al.
2005, p. 450). Although an eradication
program has been implemented for
cattle in South Africa, once an infection
is established in a free-ranging
maintenance host, like buffalo, it is
unlikely to be eradicated (Keet et al.
2009, p. 11; Renwick et al. 2007, pp.
537, 538; Michel et al. 2006, p. 96). In
fact, modeling has predicted that
prevalence could reach as high as 90
percent over the next 25 years, with
similar consequences for predators
(Renwick et al. 2007, p. 535).
Clinical signs of bTB in lions include
emaciation, respiratory complications,
swollen lymph nodes, draining sinuses,
ataxia, and lameness (Keet et al. 2009,
p. 13; Renwick et al. 2007, pp. 533, 534;
Cleaveland et al. 2005, p. 450), although
some lions may be subclinically
infected but remain asymptomatic until
they experience another bTB infection,
suffer from poor nutrition or advancing
age, or become super-infected with
other diseases that may exacerbate the
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infection (Renwick et al. 2007, p. 533).
The impact of bTB on lions is largely
unknown. Researchers suggest that bTB
may lower breeding success, reduce
resiliency, and be a mortality factor
based on data that indicate survival is
shortened in infected lions, with death
ranging between 2 and 5 years after
infection (Maas et al. 2012, p. 4212;
Renwick et al. 2007, p. 536; Keet,
unpublished data in Michel et al. 2006,
p. 93; Cleaveland et al. 2005, pp. 450,
451). In addition to clinical effects of
bTB that may lead to mortality, this
disease has also led to social changes
with lower lion survival and breeding
success with more frequent male
coalition turnover and, consequently,
higher infanticide (Keet, unpublished
data in Michel et al. 2006, p. 93).
Research has shown adverse effects to
lion individuals and subpopulations,
but effects at the species population
level are developing slowly (Michel et
al. 2006, p. 97). Studies have shown that
impacts of bTB on lion numbers vary
between populations. For example, 30
percent of the inbred populations in
Hluhluwe-iMfolozi Park died due to a
combination of bTB and malnutrition
(Hunter et al. 2012, p. 3). However,
despite bTB infection and a high
prevalence in prey species, the lion
population in Kruger National Park has
remained stable (Ferreira and Funston
2010, p. 201).
Epidemics of canine distemper virus
(CDV) are known to have occurred in
the Serengeti-Mara Ecosystem, an area
that encompasses the Serengeti National
Park, Ngorongoro Conservation Area,
and Maasai Mara National Reserve
(Craft 2008, pp. 13–14; Cleaveland et al.
2007, pp. 613, 616, 618). CDV is a
common pathogen in the large
population of domestic dogs (Canis
lupus familiaris) around the SerengetiMara Ecosystem, which are believed to
be the source of CDV in lions
(Cleaveland et al. 2007, pp. 613, 617).
CDV is assumed to be transferred to
lions by the sharing of food sources with
spotted hyenas (Crocuta crocuta) or
jackals (Canis spp.) that become
infected by consuming the infected
carcasses of domestic dogs (Craft et al.
2009, p. 1783; Craft 2008, p. 13). Viana
et al. (2015, pp. 1466, 1467) recently
discovered that domestic dogs are not
the sole source of CDV in the Serengeti,
but rather there is likely a larger,
multihost community of wildlife that
contribute to outbreaks. Lions may also
transmit CDV among themselves via
sharing food, fights, and mating (Craft et
al. 2009, pp. 1778, 1783; Craft 2008, pp.
13, 18, 71).
CDV generally lacks clinical signs or
measurable mortality in lions, and most
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CDV events have been harmless.
However, in 1994 and 2001, CDV
epidemics in the Serengeti National
Park/Maasai Mara National Reserve and
Ngorongoro Crater, respectively,
resulted in unusually high mortality
rates (Hunter et al. 2012, p. 2; Craft
2008, p. 14; Munson et al. 2008, pp. 1,
2; Cleaveland et al. 2007, pp. 613, 618;
Roelke-Parker et al. 1996, pp. 441, 443).
These outbreaks coincided with climate
extremes that resulted in a higher
number of Babesia, a tick-borne
parasite, infections (Munson et al. 2008,
pp. 2, 5). Babesia is common in lions,
but typically at low levels with no
measurable impacts on their health
(Craft 2008, p. 14; Munson et al. 2008,
p. 3). However, droughts in 1993 and
2000 in Serengeti National Park/Maasai
Mara National Reserve and Ngorongoro
Crater, respectively, led to large-scale
starvation and widespread die-offs of
buffalo. This situation combined with
resumption of rains and fire suppression
in Ngorongoro Crater favored
propagation of ticks, vectors of Babesia,
leading to unusually high tick burdens.
The compromised health of buffalo
allowed lions to feed on an inordinate
number of tick-infested prey (Craft 2008,
p. 14; Munson et al. 2008, pp. 2, 4, 5).
Exposure to either CDV or Babesia
singly is not typically associated with a
compromise in health or an increase in
mortality (Craft 2008, p. 14; Munson et
al. 2008, pp. 1, 2, 3). However, the
Babesia infections were exacerbated by
the immunosuppressive effects of CDV
and led to the unusually high mortality
rates (Craft 2008, p. 14; Munson et al.
2008, p. 5). The Serengeti National Park/
Maasai Mara National Reserve lion
population lost 30 percent of its
population (approximately 1,000 lions),
but has recovered to its pre-epidemic
population levels (Craft 2008, pp. v, 14,
41; Munson et al. 2008, p. 1; Cleaveland
et al. 2007, pp. 613, 617; Roelke-Parker
et al. 1996, p. 444). Thirty-four percent
of the Ngorongoro Crater lion
population was killed, but frequent
outbreaks of disease have prevented this
population from recovering back to its
carrying capacity (Craft 2008, p. 14;
Munson et al. 2008, pp. 1, 2; Cleaveland
et al. 2007, p. 617). The difference in
recovery is likely due to the highly
inbred nature of the Ngorongoro Crater
lion population, compared to the
Serengeti population, and its greater
susceptibility to parasitic and viral
infections (Hunter et al. 2012, p. 2;
Munson et al. 2008, p. 5; Brown et al.
1994, pp. 5953–5954).
Feline immunodeficiency virus (FIV)
is an endemic pathogen in many lion
populations of southern and eastern
Africa (Maas et al. 2012, p. 4206; Adams
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et al. 2011, p. 173; Pecon-Slattery et al.
2008, p. 2; Hofmann-Lehmann et al.
1996, pp. 555, 558; Brown et al. 1994,
p. 5966). FIV is believed to have been
present in lions since the late Pliocene
(O’Brien et al. 2012, p. 243; Troyer et al.
2011, p. 2; Roelke et al. 2009, p. 3;
Pecon-Slattery et al. 2008, p. 8). There
are 6 subtypes of FIV, A through F, each
with a distinct geographic area of
endemnicity (Adams et al. 2011, p. 174;
Troyer et al. 2011, p. 2; Roelke et al.
2009, p. 3; Pecon-Slattery et al. 2008, p.
4; O’Brien et al. 2006, p. 262) and
differing levels of virulency (LionAid
2014b, unpaginated). The social nature
of lions allows for viral transmission
within and between prides through
saliva when biting (Maas et al. 2012, p.
4210; Pecon-Slattery et al. 2008, p. 5;
Brown et al. 1994, p. 5953). Prevalence
of FIV often approaches 100 percent of
adults in infected lion populations,
including the few remaining
populations in Botswana, South Africa,
and Tanzania, (LionAid 2014b,
unpaginated; O’Brien et al. 2012, p. 243;
Troyer et al. 2011, p. 2; Roelke et al.
2009, p. 3; O’Brien et al. 2006, p. 262;
Hofmann-Lehmann et al. 1996, p. 559).
FIV causes immune deficiencies that
allow for opportunistic infections in the
host (Roelke et al. 2009, p. 1; Brown et
al. 1994, p. 5,953). With an impaired
immune system, lions may not have an
appropriate and effective immune
response to various pathogens to which
they are consistently exposed (LionAid
2014a, p. 6). There may also be
unrecognized immunological
consequences (Roelke et al. 2006, p.
234) and adverse clinical and
pathological outcomes (Roelke et al.
2009, p. 1). Chronic effects of FIV are
important to long-term survival and
differ according to subtype (Troyer et al.
2011, p. 6). Studies have indicated that
lions may exhibit signs of opportunistic
infection associated with AIDS, such as
swollen lymph nodes, gingivitis, tongue
papillomas, dehydration, poor coat
condition, and abnormal red blood cell
parameters, and in some cases death
(Troyer et al. 2011, p. 2; Roelke et al.
2009, pp. 2, 3–6). Lions in Botswana
and Tanzania have demonstrated
multiple clinical features of chronic
immune depletion similar to HIV and
domestic cat AIDS (Troyer et al. 2011,
pp. 2–3). However, there is no evidence
that FIV itself poses a threat to wild
populations (Frank et al. 2006, p. 1); FIV
does not appear to be impacting lions in
Kruger National Park (Maas et al. 2012,
p. 4212), and no evidence of AIDS-like
illnesses or decreased lifespan has been
found in FIV lion populations in the
Serengeti (O’Brien et al. 2006, p. 263).
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The role of disease in determining
survival and reproductive potential in
lions is almost completely unknown. It
is often difficult to determine whether
mortality was due to a single or
combination of factors. Lions could be
infected with and become debilitated by
a disease, but the cause of death could
ultimately be due to other factors
(LionAid 2014a, pp. 4–5). Available
studies do not indicate that infection
with a single disease is causing
detrimental impacts to lions at the
species level, although general body
condition, health, and lifespan may be
compromised and result in negative
impacts at the individual or population
level.
Co-infections, however, could have
synergistic effects that lead to greater
impacts on lions than a single infection.
Lions impacted by the 1994 CDV
outbreak in Serengeti National Park/
Maasai Mara National Reserve may have
been more susceptible to CDV due to
depleted immunity caused by FIV
(O’Brien et al. 2006, p. 263). Troyer et
al. (2011, pp. 5–6) found that survival
during the CDV/Babesia outbreak in
Serengeti National Park/Maasai Mara
National Reserve was significantly less
for lions infected with FIV A and/or C
than FIV B. This finding suggests that
FIV A and C may predispose carriers to
CDV pathogenesis and may increase the
risk of mortality (O’Brien et al. 2012, p.
243). Impacts of co-infections of FIV
with FCV, FPV, FHV, and FCoV on
individual lions are negligible and do
not endanger the lion population, at
least in the absence of other aggravating
cofactors (Hofmann-Lehmann et al.
1996, p. 561).
Pathogen–pathogen interactions may
become more important when lions are
under additional stress (e.g., increased
parasite load or low prey density) (Maas
et al. 2012, p. 4212). Certain
environmental conditions may
exacerbate the effects of an otherwise
innocuous infection. For example, as
discussed above, CDV and Babesia
infections generally have no measurable
impacts on lion health, but climatic
conditions increased exposure of lions
to Babesia infections, which were
exacerbated by the immunosuppressive
effects of CDV and led to unusually high
mortality rates (Craft 2008, p. 14;
Munson et al. 2008, p. 5). Some lions
infected with bTB may remain
asymptomatic until conditions change
and they suffer from poor nutrition due
to low prey density, advancing age, or
become super-infected with other
diseases that may exacerbate the
infection (Renwick et al. 2007, p. 533).
Species with reduced genetic
variation may be less able to mount an
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effective immune response against an
emerging pathogen (O’Brien et al. 2006,
p. 255). For example, the inbred
populations in Hluhluwe-iMfolozi Park
lost 30 percent of lions due to a
combination of bTB and malnutrition
(Hunter et al. 2012, p. 3). The
Ngorongoro Crater lions have not
recovered to pre-outbreak numbers due
to their inbred nature and greater
susceptibility to parasitic and viral
infections (Hunter et al. 2012, p. 2;
Munson et al. 2008, p. 5; Brown et al.
1994, pp. 5953–5954). Additionally,
disease outbreaks can lead to extirpation
in small, isolated populations (Gilpin
and Soule 1986 and Paul-Murphy et al.
1994 in Harvell et al. 2002). Although
we found no information indicating
presence of disease in the Indian
population, the small, isolated nature
makes the population more vulnerable
to disease outbreaks and could have a
detrimental impact on the population
(Banerjee and Jhala 2012, p. 1427;
Meena 2010, p. 209; Johnsingh et al.
2007, p. 93). This principle also applies
to the small, isolated populations
throughout Africa.
Although disease is known in several
populations, the impacts are known in
only a few populations where disease
has been frequently studied. Precise
estimates of lions lost to disease are
lacking, due to the difficulty in
detection. However, disease appears to
be a secondary factor influencing the
decline of lions when co-infections
occur or when disease is combined with
other factors, including environmental
changes, reduced prey density, and
inbreeding depression. Diseases weaken
individuals and allow them to succumb
to other diseases or factors. Although
disease does not appear to be a major
driver in the status of the lion,
populations can suffer significant losses;
some may recover to pre-outbreak
levels, others may not. Given the small
and declining lion populations that
remain, any loss of individuals from the
populations could be detrimental.
The risk of disease may increase with
time due to loss of genetic variation
associated with continued
fragmentation of populations, whether
by habitat loss or fencing of habitat, and
increased proximity to humans and
domestic livestock that may expose
lions to new diseases (IUCN 2006b, pp.
19, 26). Additionally, changes in climate
may increase disease outbreaks in prey
species, as well as lions (See Climate
Change). Climate change could
potentially increase the likelihood of
lethal co-infections (The Heinz Center
2012, p. 12), similar to the co-infections
of CDV and Babesia in Serengeti
National Park/Maasai Mara National
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Reserve and Ngorongoro Crater lions
following drought events.
Deleterious Effects Due to Small
Population Sizes
The risk of extinction is related to the
moment when a declining population
becomes a small population and is often
estimated using minimum viable
population (MVP) sizes (Traill et al.
2010, p. 28). The viability of a lion
population is complex, but it partly
depends on the number of prides and
ability of males to disperse and interact
with other prides, which affects
¨
exchange of genetic material (Bjorklund
2003, p. 518). Without genetic exchange,
or variation, individual fitness is
reduced and species are less able to
adapt to environmental changes and
stress, increasing the risk of extinction
(Bijlsma and Loeschcke 2012, pp. 117,
119; Segelbacher et al. 2010, p. 2; Traill
¨
et al. 2010, p. 31; Bjorklund 2003, p.
515).
¨
Bjorklund (2003, p. 520) found that
the most important determining factors
for the level of inbreeding in lions is the
number of prides and male dispersal.
The MVP for lions has not been formally
established and agreed upon by species
experts (Riggio et al. 2011, p. 5; CITES
¨
2004a, p. 2; Bjorklund 2003, p. 521);
however, it has been suggested that to
conserve genetic diversity, populations
of at least 50 prides, but preferably 100
prides (250 to 500 individuals), with no
limits to dispersal, are necessary (Bauer
et al. 2008 in Riggio et al. 2013, p. 32;
¨
Bjorklund 2003, pp. 515, 518).
¨
Bjorklund (2003, p. 518) found that
inbreeding decreased rapidly with the
number of prides. For example, if there
are less than 10 prides the likelihood of
genetic effects due to inbreeding
increased from 0 in the beginning to 26–
45 percent after 30 generations, whereas
if 100 prides are present, the likelihood
is only 5 percent assuming no migration
¨
into the population (Bjorklund 2003, p.
515). Additionally, it appears that
inbreeding rapidly increases when the
number of prides falls below 50
¨
(Bjorklund 2003, p. 518, Figure 2).
Riggio et al. (2013, pp. 20, 22) used the
¨
threshold described by Bjorklund (2003)
to define, in part, lion strongholds.
Stronghold populations of lions were
considered to be those that meet the
necessary requirements for long-term
viability and were defined, in part, as
containing at least 500 individuals (100
prides). Potential strongholds were
described, broadly, as areas where
immediate interventions might create a
viable population and were defined, in
part, as populations that contained at
least 250 lions. However, the threshold
¨
described by Bjorklund (2003) and used
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by Riggio et al. (2013) may be smaller
for P. l. leo as pride sizes are generally
smaller than those for P. l. melanochaita
(Riggio et al. 2013, p. 32; Meena 2009,
p. 7; Nowell and Jackson 1996, p. 37).
Male dispersal also plays an
important role in determining the level
of inbreeding in lion populations. Even
if only a fraction of males do not
disperse, inbreeding rapidly increases
with each generation (approximately 5
¨
years) (Bjorklund 2003, pp. 518, 520).
Even when migration rates of males is
as high as 95 or 99 percent, the
likelihood of inbreeding is clearly
higher than if 100 percent of males
disperse. Using a 95 percent dispersal
rate, the probability of inbreeding
reached 57 percent and 20 percent for
10 and 100 prides within 30 generations
¨
(150 years) (Bjorklund 2003, pp. 518–
519). One example is the lion
population in Ngorongoro Crater. New
males rarely migrate into the population
due to physical barriers, and inbreeding
has been shown to occur (Packer et al.
¨
1991b in Bjorklund 2003, p. 521). The
fewer number of males present to
contribute genes to the next generation,
the more inbred the population will be
(Riggio et al. 2013, p. 32). Therefore, not
only does dispersal impact inbreeding,
so does the loss of male lions due to
excessive trophy hunting and
infanticide (see Trophy Hunting).
Because the number of prides and
male dispersal are the most important
factors for maintaining viability,
sufficient areas are needed to support at
least 50 prides, but preferably 100
prides, and allow unrestricted male
¨
dispersal (Bjorklund 2003, p. 521).
Unfortunately, few lion populations
meet these criteria as almost all lion
populations in Africa that historically
exceeded 500 individuals are declining,
and few protected areas are large
enough to support viable populations
(Bauer et al. 2015a, unpaginated; Bauer
et al. 2015b, p. 1; Bauer et al. 2008,
unpaginated; Riggio 2011, p. 5; Hazzah
2006, p. 2; Bauer and Van Der Merwe
¨
2004, pp. 28–30; Bjorklund 2003, p.
521). Even within large areas,
inbreeding will increase if dispersal is
¨
limited, (Bjorklund 2003, pp. 521–522).
Furthermore, research indicates that
there is a general lack of gene flow in
most lion conservation units (Dubach et
al. 2013, pp. 749, 750; Bertola et al.
2011, p. 1364; Chardonnet et al. 2009,
p. 54).
Small populations (e.g., fewer than 50
lions) can persist in the wild for some
time; however, the lack of dispersal and
genetic variation can negatively impact
the reproductive fitness of lions in these
populations and local extirpation is
likely (Traill et al. 2010, p. 30; O’Brien
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1994, p. 5748). Loss of fecundity leads
to a decrease in population size, fewer
prides in a population, and increased
inbreeding which contributes to a
decline in the population and increases
¨
the risk of extinction (Bjorklund 2003,
p. 521). Additionally, lack of genetic
variation can impact the ability of lions
to withstand stochastic events. For
example, the inbred populations in
Hluhluwe-iMfolozi Park were unable to
mount an effective immune response
and lost 30 percent of lions due to a
combination of bTB and malnutrition
(Hunter et al. 2012, p. 3). Additionally,
the lions of Ngorongoro Crater never
recovered to pre-outbreak numbers due
its inbred nature and greater
susceptibility to parasitic and viral
infections (Hunter et al. 2012, p. 2;
Munson et al. 2008, p. 5; Brown et al.
1994, pp. 5953–5954). Reductions in
genetic variations may also limit the
lion’s ability to evolve responses to
climate change (The Heinz Center 2012,
p. 12).
The lion population in India is one of
the few populations that are increasing
(Bauer et al. 2015a, unpaginated; BBC
2015, unpaginated; The Guardian 2015,
unpaginated; Banerjee and Jhala 2012,
p. 1427) and could be considered a
stronghold according to the criteria set
by Riggio et al. (2013, p. 22). Despite
being genetically less diverse, Banerjee
and Jhala (2012, pp. 1424–1425) found
no evidence of depressed demographic
parameters in the lions of India.
However, intense management,
including healthcare interventions, may
interfere with natural selection
processes by ensuring the survival of
unfit lions which facilitates the
propagation of deleterious genes in the
population (Banerjee and Jahala 2012, p.
1427). This population is also running
out of area to expand. Being a small,
isolated population and less genetically
diverse, it is more vulnerable to the loss
of any individuals due to environmental
and stochastic events, and more prone
to local extinction events (Banerjee and
Jhala 2012, p. 1428; Meena 2010, p. 209;
Johnsingh et al. 2007, p. 93; Thuiller et
al. 2006, pp. 434–435).
The establishment of another freeranging population geographically
separate from Gir would reduce the risk
of extinction of this population due to
stochastic events (e.g., disease outbreaks
or floods). In the early 1990s, a second
population was proposed at Kuno
Wildlife Sanctuary in Madhya Pradesh
State (Johnsingh et al. 2007, p. 93).
However, the Government of Gujarat has
refused to allow any lions from Gir to
be transferred to the Kuno Wildlife
Sanctuary, despite a ruling by India’s
Supreme Court (The Economic Times
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2015, unpaginated; Duerr 2014,
unpaginated; Meena 2014, p. 29).
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Regulatory Mechanisms
Regulatory mechanisms in place to
provide protections to African lions
vary substantially throughout Africa.
The lion species (Panthera leo) is listed
in Appendix II of CITES; however, the
former Asiatic lion (P. l. persica) is
listed in Appendix I. With the exception
of South Sudan, all of the lion range
states are Parties to CITES. According to
the draft CITES Periodic Review of the
Status of African Lions (CITES 2014, pp.
14–15) outside of CITES, lions have no
legal protections in four countries:
Burundi, Guinea Bissau, Lesotho, and
Swaziland. However, CITES 2014 (p. 15)
states that most of the southern and
eastern lion range states have regulatory
mechanisms in place to protect lions.
We found that most of the range states
have national environmental legislation
to establish national parks and
conservation areas, and to conserve and
regulate the take, hunting, and trade of
wildlife, including parts and products,
but could find no legislation specific to
lions, or to the main threats affecting
lions: habitat loss, human–lion conflict,
and loss of prey base (Ecolex 1
information last accessed November 6,
2015).
National and international
conservation strategies rely on protected
areas to protect natural resources from
negative impacts of human populations
(Craigie et al. 2010, p. 2221). The lion
is largely limited to protected areas;
therefore, effective management is
crucial to the survival of the species.
However, weak management of
protected areas has been documented
across its range, especially in western
Africa where most protected areas are
experiencing severe management
deficiencies (Henschel et al. 2015,
unpaginated; Henschel et al. 2014, pp.
´
5, 7; Brugiere 2012 in Henschel et al.
2014, p. 7; Craigie et al. 2010, entire).
The WAP complex in western Africa
had received high scores for
management effectiveness (Henschel et
al. 2015, p. 7).
Effective management requires
adequate funding, resources, and staff.
Packer et al. (2013a, pp. 638–639) found
that lion densities were highest in
protected areas with the highest
1 ECOLEX is a comprehensive database on
environmental law, maintained by the International
Union for Conservation of Nature (IUCN), the
United Nations Environment Programme (UNEP),
and the Food and Agriculture Organization of the
United Nations (FAO). Our search terms used with
respect to wildlife laws were ‘‘African lion,’’
‘‘Asiatic lion,’’ ‘‘Panthera leo leo,’’ ‘‘Panthera leo
persica,’’ and ‘‘country,’’ e.g., ‘‘Angola,’’ ‘‘Benin,’’
etc. Information accessed at https://ecolex.org.
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management budgets. Cost estimates for
maintaining lion populations in
protected areas range from an annual
budget of $500 USD per km2 in smaller
fenced reserves to $2,000 USD per km2
for unfenced reserves (Packer et al.
2013, p. 640). This includes but is not
limited to costs associated with
permanent and temporary staff, fencing
installation and maintenance (fences
can cost $3,000 USD per km to install),
infrastructure maintenance, antipoaching activities such as surveillance
and snare/trap removal, wildlife
restocking fees (both for lions killed by
illegal poaching/snares as well as other
trophy species killed by lions on the
reserves), community outreach, and
compensation for loss of livestock in
surrounding communities. However,
many management areas lack adequate
funding (Packer et al. 2013, p. 640;
Groom 2013, pp. 4–5; Barnett and
Patterson 2005, p. 82).
Of 12 protected areas assessed in
western Africa, 6 had no budget for
management activities or the budget was
too low to conserve lion populations;
nine reported having either no law
enforcement activity or major
deficiencies in staff and resources to
´
conduct patrols. In Comoe National
Park, the staff was found to be too small
for the size of the park (Henschel et al.
2014, p. 7). Protected areas in Guinea
are essentially parks on paper only.
They have no staff, management plan, or
´
operating budget (Brugiere 2012 in
Henschel et al. 2014, p. 7). Although the
WAP complex has received high scores
for management effectiveness, the
presence of 50,000 head of cattle inside
W National Park indicates weak
management. Livestock are rare in ArlyPendjari, and lion density is higher; a
higher management budget allocation is
suspected to be the cause of the
observed differences (Henschel et al.
2014, pp. 5–6). Across the lion’s range,
Africa’s protected areas have generally
failed to mitigate threats to large
mammal populations, including the lion
and its prey (Craigie et al. 2010, entire).
Poor management leads to many of
the threats that lions face, including
encroachment by pastoralists, increased
poaching pressure, collapse of prey
populations, and persecution by
´
pastoralists (Brugiere et al. 2015, pp.
519–520; Henschel et al. 2015,
unpaginated; Henschel et al. 2014, pp.
5, 7; Henschel et al. 2010, p. 38).
Therefore, it can be said that
management of protected areas that still
harbor lions is inadequate to address the
threats impacting lions, especially those
in western Africa (Henschel 2015,
unpaginated). Overall, investment in
conservation activities is extremely low
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in western Africa, compared to central,
eastern, and southern Africa. Countries
in the former or current western Africa
lion range are among the 50 poorest
countries in the world, and six are
classified as least developed countries.
These countries will likely be unable to
generate the resources required to
secure their remaining lion populations
(Henschel et al. 2014, pp. 7–8).
Investment from the international
community is needed to increase
management effectiveness of these
protected areas (Henschel et al. 2015,
unpaginated).
In India, most lions occur within five
designated protected areas: Gir National
Park and Gir Wildlife Sanctuary (Gir
Protected Area) and Pania, Mitiyala, and
Girnar sanctuaries (Bauer et al. 2015a,
unpaginated; Banerjee and Jhala 2012,
p. 1421; Singh and Gibson 2011, p.
1754; Jhala et al. 2009, pp. 3384, 3385;
Nowell and Jackson 1996, p. 38). Under
India’s Wild Life Protection Act of 1972
(Act No. 53 of 1972; Chapter IV, sections
27, 28, 33, 35), entry into protected
areas is regulated and certain activities
are controlled and managed, including
security of wild animals and grazing of
livestock. In 2012, India’s Ministry of
Environment and Forests (2012, p. 22)
declared the area 5 km from the
boundary of Girnar Wildlife Sanctuary
an Eco-sensitive Zone for the long-term
protection and conservation of the lion.
This designation prohibits certain
activities within the designated zone,
such as mining, unregulated tourism,
polluting industries, and unregulated
felling of trees.
Because of the protections afforded by
the Government of Gujarat, threats that
contributed to the decline of this
population have been ameliorated and
most threats faced by lions are not an
immediate threat. Protections ensure
food security, water availability, habitat
suitability, and safety for these lions
(Meena 2014, p. 26). However, because
this population is small and isolated, it
is vulnerable to extinction from
stochastic events. Although a second
location has been proposed to establish
another free-ranging population
geographically separate from Gir to
reduce the risk of extinction of this
population, translocation of lions from
Gujarat are still pending (see Deleterious
Effects Due to Small Population Sizes).
Climate Change
Consideration of ongoing and
projected climate change is a
component of our analysis under the
Act. The term ‘‘climate change’’ refers to
a change in the mean, variability, or
seasonality of climate variables over
time periods of decades or hundreds of
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years (Intergovernmental Panel on
Climate Change (IPCC) 2013, p. 1255).
Climate change models, like all other
scientific models, produce projections
that have some uncertainty because of
the assumptions used, the data
available, and the specific model
features. The science supporting climate
model projections as well as models
assessing their impacts on species and
habitats will continue to be refined as
more information becomes available.
Temperature and Precipitation Trends
Within the past 50–100 years, the
surface temperature in Africa and Asia
has increased (Hijioka et al. 2014a, p.
1333; Niang et al. 2014, p. 1206). Across
Africa, surface temperature has
increased by 0.5 °C over the past
century (Niang et al. 2014, p. 1206),
although there are regional differences.
For example, decadal warming rates in
South Africa have ranged from 0.1 °C to
0.3 °C (Chidumayo et al. 2011, p. 18)
and 0.23 °C in Tanzania (Carr et al.
2013, p. 16). The mean annual
temperature in Burundi has increased
by 0.7–0.9 °C since the 1930s, while the
mean annual temperature in Uganda has
increased by 1.3 °C since 1960 (Carr et
al. 2013, p. 16). In India, annual mean
temperatures increased by 0.56 °C
during the 20th century (Hijioka et al.
2014a, p. 133; Hijioka et al. 2014b, p.
SM24–2).
Across Africa, trends in annual
precipitation indicate a small but
statistically significant decline in
rainfall (Niang et al. 2014, p. 1209;
Chidumayo et al. 2011, p. 20). Eastern
Africa has experienced an increase in
extreme precipitation changes, with
increasingly frequent droughts followed
by increasingly intense heavy rainfall,
for the last 30 to 60 years; however,
overall levels of precipitation have been
declining. The intense rainfall events
have caused more frequent flooding and
soil erosion and degradation (Niang et
al. 2014, pp. 1209, 1211; Carr et al.
2013, p.16). Attri and Tyagi (2010 in
Hijioka et al. 2014b, p. SM24–3) report
no significant national trends in
precipitation for India, although there
has been a decrease in the number of
monsoon depressions and an increase in
the number of monsoon break days,
which is consistent with an overall
decrease in seasonal mean rainfall
(Hijioka et al. 2014a, p. 1333).
Throughout the 20th century, droughts
were frequent in the Gir area. However,
in the last two decades average rainfall
has increased due to increased western
monsoons (Singh and Gibson 2011, p.
1756).
Overall, projections indicate
temperatures will continue to increase
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in Africa and Asia and rainfall will
continue to decrease in Africa but
increase in India, although regional
variations exist (Hijioka et al. 2014a, p.
1334; Peterson et al. 2014, p. 562;
Gosling et al. 2011, pp. 64–65).
Warming in Africa is expected to be
greater than the global annual mean
warming throughout the continent and
all seasons (Chidumayo et al. 2011, p.
22). Future projections expect the
average temperature in Africa to be
higher by 1.5–3 °C by 2050 (Niang et al.
2014, p. 1206; Carr et al. 2013, p. 16;
UENP 2007, p. 2), while temperatures in
Gujarat are expected to increase
between 3.0 and 3.5 °C by 2100 (Gosling
et al. 2011, pp. 64–65).
Annual precipitation shows greater
regional variations, although predictions
of precipitation contain high levels of
uncertainty. Generally speaking, both
Africa and Asia are expected to
experience harsher drought and stronger
floods during the wet season (Hijioka et
al. 2014a, p. 1334; Carr et al. 2013, p.
12). Precipitation has been projected to
decline in western, central, and
southern Africa. The areas of southern
Africa expected to experience a decline
in precipitation is projected to expand
during the second half of the 21st
century (Niang et al. 2014, p. 1210;
Hijioka et al. 2014a, p. 1333; Carr et al.
2013, pp. 12, 14; The Heinz Center
2012, p. 13).
In contrast, eastern Africa and
northern India are expected to
experience an increase in mean annual
precipitation (Niang et al. 2010, p. 1210;
Hijioka et al. 2014a, p. 1334; Carr et al.
2013, pp. 12, 14; Gosling et al. 2011, p.
65). Some General Circulation Models
predict that, by the end of the 21st
century, eastern Africa will have a
wetter climate with more, intense wet
seasons and less severe droughts from
October to December and March
through May, a reverse in observed
trends described above. Other models
suggest drying in most parts of Uganda,
Kenya, and South Sudan in August and
September by the end of the 21st
century (Niang et al. 2014, p. 1210). Carr
et al. (2013, p. 15) state that levels of
increased precipitation predicted for the
Albertine Rift, located mainly within
the eastern African region, are not
predicted to be sufficient to counter the
effects of warming temperatures;
therefore, an overall drying effect is
likely to occur, which will be more
pronounced between February and May.
They also state that November and
December will experience the largest
increases in precipitation.
In South Asia, including India, future
declines in the number of rainy days
and increases in extreme precipitation
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events related to monsoons are very
likely (Hijioka et al. 2014a, p. 1334;
Gosling et al. 2011, pp. 123–124).
Increases in precipitation are expected
by the 2030s and all regions of India are
expected to experience between 10 and
30 percent increases in magnitude of
pluvial flooding (flooding derived
directly from heavy rainfall and results
in overland flow) and an average across
India of approximately 50 percent
greater risk of fluvial flooding (floods as
a result of river flows exceeding river
channel capacity, breaking through
riverbanks, and inundating the
floodplain) (Gosling et al. 2011, pp. 122,
123, 126, 130). Gosling et al. (2011, pp.
65–66) predict increases in average
annual rainfall of up to 20 percent in
Gujarat by 2100.
Impacts of Climate Change
Climate change is likely to become a
main driver of change in large mammal
populations in the future (Scholte 2011,
p. 7). In the mid-Holocene, mammals
responded rapidly to climate change
with a series of local extinctions and
near-extinctions, driving a decrease in
species richness, and a dramatic
increase in xerophytic taxa (Grayson
2000 and Graham 1992 in Thuiller et al.
2006, p. 425). It is likely that many
species and ecosystems will endure
similar impacts in response to predicted
climate change in the 21st century,
which will act synergistically with the
predicted increase in anthropogenic
pressures (Fischlin et al. 2007, in Carr
et al. 2013, p. 10; Thuiller et al. 2006,
p. 425). For lion, impacts described
above from existing and predicted
anthropogenic pressures on the species
and its habitat are likely to be
exacerbated by climate change. The
general warming and drying trend
projected for Africa could further reduce
lion range, numbers, and prey base.
Lions may also have to travel greater
distances to find food or shift their diet
to livestock, increasing conflict with
humans and the risk of retaliatory
killings (Peterson et al. 2014, pp. 562–
563; Tuqa et al. 2014, p. 8; Tumenta et
al. 2013, p. 240). Additionally, changes
in climate may increase the number and
intensity of disease outbreaks in lions
and its prey (Peterson et al. 2014, pp.
562–563; The Heinz Center 2012, p. 12;
Baylis 2006, p. 4).
Peterson et al. (2014, pp. 555, 561–
562) evaluated the magnitude of
potential changes in lion distribution in
Africa under different climate change
scenarios between the years 2040 and
2070. They found little optimism for the
future of lions. No broad new areas will
become suitable for lion. Southern
Africa, where the broadest areas of
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suitable conditions occur, is projected to
become less suitable because of climate
change. Specifically, park areas,
including the ‘‘Etosha Pan, Lake
Opnono, Cuvelai Drainage, Kalahari
Gemsbok, and Kgalagadi Transfrontier
Park areas’’ are projected to decline
substantially in suitability for lions. A
broad swath of potential distributional
area in western Africa is projected to
become ‘‘distinctly less suitable or even
uninhabitable.’’ A decrease in the lion’s
range could mean that stochastic events
impact a larger portion of the whole
species, especially when the species and
its habitat are fragmented (Thuiller et al.
2006, p. 434). Additionally, reductions
in populations and geographic range
may limit the lion’s ability to respond
to climate change (The Heinz Center
2012, p. 12). However, climate change
effects on potential lion distribution are
projected to be more neutral in eastern
Africa than across the entire range.
Reserves in this region are more likely
to sustain lion populations under
climate change scenarios (Peterson et al.
2014, pp. 555, 561–562).
In India, an increase in average
rainfall in the past two decades has
resulted in the conversion of dry
savanna to forestland (Hijioka et al.
2014a, p. 1333; Singh and Gibson 2011,
p. 1756). However, the lion population
in India has shown to be able to use
both forestlands and savannas (Singh
and Gibson 2010, p. 1753). Therefore,
this type of habitat conversion due to
changes in climate may not be as
detrimental to lions in India population.
However, increased risks of flooding
could pose problems for lions.
Following a recent flood in Gujarat, nine
lions drowned in a stream that flows
alongside Gir Wildlife Santuary.
Additionally, lions could face serious
threats following flood events, such as
an outbreak of a disease epidemic (The
Economic Times 2015, unpaginated).
This population of lions is small,
isolated, and less genetically diverse;
therefore, it is more vulnerable to
stochastic events such as disease
outbreaks and flooding and more prone
to local extinction events (Banerjee and
Jhala 2012, p. 1428; Meena 2010, p. 209;
Johnsingh et al. 2007, p. 93).
Current lion habitat and suitable
habitat predicted to remain under
climate change scenarios will be under
increasing pressure due to land
conversions to meet the needs of the
growing human population. As stated
earlier, and supported by Carr et al.
(2013, p. 20), demand for agricultural
land is likely to increase to meet the
needs of the growing human population,
putting pressure on natural landscapes.
Projected changes in Africa’s climate
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will increase this pressure as land
becomes more arid and food security
concerns are exacerbated (Carr et al.
2013, p. 20). Impacts to the socioeconomic and physical well-being of
humans will cause adaptive responses,
eliciting changes in the way much of the
land is used, including further
encroachment of urban environments
and agricultural land into existing
natural habitats (Carr et al. 2013, pp. 10,
19), including protected areas where
lions occur. Additionally, land
conversion restructures the landscape
and may disrupt prey migrations that
are induced by climate change (Thuiller
et al. 2006, p. 425), decreasing or
altering prey available to the lion.
Although lions occur in a variety of
temperature and precipitation regimes,
suggesting the species may be tolerant of
some climatic changes (The Heinz
Center 2012, p. 13), lions appear to
thrive under specific climate parameters
(Leighton-Jones 2004 in Celesia et al.
2009, p. 63) and abundance is
significantly determined by temperature
and rainfall (Celesia et al. 2009, pp. 67,
68). Large felids, including lions, occur
in biomes with an average annual
temperature of 13 °C or higher; lion
demography is best when mean annual
temperatures are 16–18 °C (Celesia et al.
2009, p. 68). Lion density is influenced
by multiple natural ecological factors
including herbivore biomass, annual
mean rainfall, soil nutrients, annual
mean temperature, and interactive
effects between rainfall and soil
nutrients (Celesia et al. 2009, pp. 67,
69). These factors explain regional
variations in lion densities, where low
densities are found in desert or semidesert ecosystems and higher densities
in moist savannas (Celesia et al. 2009,
p. 67). Lion densities decrease with
increasing mean temperature and
decreasing rainfall. Therefore, lion
density, or carrying capacity of
protected areas, in sub-Saharan Africa is
likely to decline with climate warming
and drying (Chidumayo et al. 2011, p.
144).
Lion demography is also influenced
by environmental factors. Many
variables are associated with aspects of
demography, but the strongest
associations are with rainfall,
temperature, and landscape features
(e.g., elevation, slope, direction of slope,
and compound topographic index)
(Celesia et al. 2009, pp. 63, 68). Impacts
to lion demography have been noted
with the longer dry spells occurring. For
example, when prey become scarce at
the end of the dry season, subadult
females may be forced out of prides.
Furthermore, older lions and cubs may
die of starvation (Celesia et al. 2009, p.
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68). Additionally, Van Vuuren et al.
(2005 in Celesia et al. 2009, p. 68) found
in a study of Kgalagadi Transfrontier
Park that adult and cub mortality
reached 70 to 90 percent in poor years
(defined as years in which average
annual rainfall in the previous 2 years
was less than 165 mm). Mortality
decreased to 10 to 40 percent in good
years (years in which average annual
rainfall in the previous 2 years was
greater than or equal to 237 mm). These
impacts on demography result in
reduced numbers of lions and pride
sizes (Celesia et al. 2009, p. 68). Given
the predicted warming and drying trend
for the 21st century, additional lions
could be lost and pride sizes reduced.
Furthermore, loss of these lions reduces
reproductive potential and recruitment,
further contributing to the decline of
existing populations. The loss of lions
could also mean the loss of genetic
variation. Combined with declining
populations, the risk of inbreeding and
associated complications could
increase.
Drought conditions can also
contribute to reduced prey availability
by altering the timing of migration
(Peterson et al. 2014, p. 562). For
migratory species such as the wildebeest
or zebra, an earlier and more frequent
onset of the dry season may lead to the
species undertaking more migrations,
which can lead to increases in mortality
and disruption of seasonal hunting
patterns of lion (The Heinz Center 2012,
p. 42). Climate change may already be
having an impact on the wildebeest as
Dobson (2009, as cited in Chidumayo et
al. 2011, p. 144) found that, due to the
wet season slowly getting drier and the
dry season getting wetter, the species is
migrating 2 months earlier than usual,
throwing off timing of migrations and
conception times that are set by lunar
cycles. If the wet season rains are
diminishing there will be a reduction in
high-quality forage needed to support
lactation. This reduction has a
detrimental effect not only on the
survival of the calf but also for the
population as a whole (Dobson 2009, as
cited in Chidumayo et al. 2011, pp. 144–
145).
Climate conditions also influence
prey abundance. In Kruger Park, South
Africa, almost all ungulate species are
extremely sensitive to lack of rainfall
during the dry season, which is
predicted to increase in the future. This
factor may be important to retain green
forage during a period when the risk of
malnutrition is higher (Thuiller et al.
2006, p. 432). Similarly, reproduction in
Cape buffalo is strongly related to
season. Changes in the timing,
frequency, or intensity of seasonal rains
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could negatively affect reproduction.
This species is also sensitive to rainfall
due to its high water consumption rate
(up to 30–40 liters per animal per day)
(Du Troit 2005, as cited in The Heinz
Center 2012, p. 15; Whyte et al. 1995,
pp. 84–85). Variation in the buffalo
population then is tied to rainfall
conditions year-to-year. Funston and
Mills (2006, p. 20) observed that the
buffalo population increases only
during periods of average to aboveaverage rainfall, which means that
climate projections for a drier Africa
will have detrimental impacts on the
buffalo population. Lions are
opportunistic predators that feed on a
variety of prey. This flexibility in prey
may aid lions in exhibiting some
resiliency to changes in prey
populations (The Heinz Center 2012, p.
12). However, as discussed under Loss
of Prey Base and Human–Lion Conflict,
the loss of prey species can result in
lions shifting their diet towards
livestock which may increase retaliatory
killings by humans (Bauer and Kari
2001, as cited in Tumenta et al. 2013,
p. 241; Whyte et al. 1995, p. 85).
Variation in lion home ranges may
have an impact on the frequency of
human–lion conflict especially in
situations where lion home ranges
expand into areas inhabited by humans
(Peterson et al. 2014, p. 562). The
interplay between the types of climate,
the density of prey, and seasonal
variation in temperature and
precipitation all affect lion home range.
Areas with a more arid climate and
small prey density are associated with
larger home ranges, while temperate or
tropical regions with higher prey
density are associated with smaller
home ranges. In addition, prey living in
an arid climate tend to disperse, while
prey in a wetter climate are more
concentrated, leading to a larger and
smaller home range, respectively (Tuqa
et al. 2014, p. 2; Celesia et al. 2010, pp.
63, 67; Sogbohossou 2011, p. 17;
Loveridge et al. 2009, p. 953). In
southern Africa, where most of the lion
populations are enclosed (fenced),
variation in the species’ home range
may be more limited. Lion home ranges
are also influenced by the season with
ranges being smaller during the dry
season and larger during the wet season.
During the dry season, prey congregate
around the few remaining water
sources, concentrating prey species in a
smaller area, shrinking the home range
needed by the lion to find food.
Conversely, home ranges expand during
the wet season due to prey dispersal
(Tuqa et al. 2014, p. 8).
Climate projections point toward a
drier climate for western, central, and
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southern Africa (Niang et al. 2014, p.
1209; Hijioka et al. 2014a, p. 1333; Carr
et al. 2013, p. 14; Chidumayo et al.
2011, p. 21). Drought in the western and
central African regions is expected to
increase by a rate of 5–8 percent by 2080
(UNEP 2007, p. 2). Although drier
conditions might initially lead to the
lion home range shrinking as prey
congregate around remaining water
sources (Sogbohoussou 2011, p. 133),
Tuqa et al. (2014, p. 8) found that lion
home ranges expand in the time after a
drought. The reason for this expansion
may be that, as prey populations around
water sources are depleted, the lion has
to travel greater distances to find prey.
In addition, researchers found that lions
move beyond reserve boundaries and
into communal ranches where there will
be greater conflict with humans (Tuqa et
al. 2014, p. 9). It is likely that lions prey
on livestock, which will intensify
human–lion conflict. To compound the
issue, pastoralists in sub-Saharan Africa
will often lead their herds into protected
areas where lions occur during a
drought in search of water, which
increases the risk of lion predation
(Tumenta et al. 2013, p. 240).
When lion prey on livestock, they
primarily focus on cattle (Patterson et al.
2004, p. 510). Out of all livestock that
are domesticated in Africa, cattle have
the highest monetary value, which
means the loss of cattle to lion predation
will have the most adverse effect on
pastoralists (Tumenta et al. 2013, p.
240). Additionally, droughts affect the
survival of livestock (Peterson et al.
2014, p. 562). A study of the drought
that occurred in Kenya in 2008–2009
found that mortality rates among the
cattle population varied between 57 and
64 percent in six districts (Dolrenry
2013, p. 47; Zwaagstra et al. 2010, p.
21). Such high mortality may make
pastoralists less tolerant of lion
predation and may increase the
frequency of retaliatory killings
(Peterson et al. 2014, p. 562).
Climate change may increase the
number and intensity of disease
outbreaks in lion prey species, as well
as lions (The Heinz Center 2012, p. 12;
Baylis 2006, p. 4). Diseases can be
directly and indirectly affected by
climate change by impacting
distribution, the timing of outbreaks,
and the intensity of outbreaks (Baylis
2006, p. 4). Higher temperatures may
increase the rates of development of
pathogens and parasites, shorten
generation times, and increase the
number of generations per year,
increasing the population (Baylis 2006,
p. 8; Thuiller et al. 2006, p. 435).
Temperatures can have impacts on
vectors (e.g., ticks and mosquitoes) and
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hosts that may further influence the
spread of diseases (Baylis 2006, pp. 9,
11) and increase risks of extinctions
(Thuiller et al. 2006, p. 435).
Additionally, rainfall conditions also
affect the susceptibility of animals to
disease outbreaks (Thuiller et al. 2006,
p. 435). Munson et al. (2008) concluded
that severe climate change could
synchronize temporal and spatial
convergence of multiple infectious
agents, triggering epidemics with greater
mortality than infections from a single
pathogen.
Conservation Measures in Place To
Protect Lions
There has been awareness for several
years that conservation strategies need
to be implemented for the lion due to
the apparent decrease in its population
numbers (Hamunyela et al. 2013, p. 1;
Henschel et al. 2010, p. 34; Gebresenbet
et al. 2009, p. 5; IUCN 2006a, b, entire).
Prior to 2006, institutional
inconsistencies throughout the lion’s
African range resulted in poor lion
conservation policies and little to no
enforcement of existing laws (IUCN
2006b, p. 18). As mentioned, in 2005
and 2006, nongovernmental
organizations (NGOs) and several
governments at various levels organized
two regional lion conservation
workshops. Species specialists, wildlife
managers, and government officials
attended these regional workshops in
order to provide range country
governments with frameworks for
developing their own national action
plans for the conservation of lions. Over
50 lion specialists, representing all lion
range countries, participated in these
workshops (Henschel et al. 2010, p. 34).
During the workshops, lion experts
collectively assessed what they believed
to be the then-current status of African
lions based on a variety of information,
and subsequently identified 86 African
LCUs. This information was then used
as a framework to identify lion areas,
strongholds, and potential strongholds
by Riggio et al. (2013, p. 32).
Many African countries with very
small lion populations have developed
or updated their conservation plans for
the lion. Some of these include Benin,
Cameroon, Uganda, and Malawi. Some
range countries participate in
transboundary conservation projects
and are collaborating on transboundary
lion conservation initiatives for shared
lion populations. Most range countries
have a national lion action plan or
strategies in place, particularly if there
are economic incentives for them to
have viable lion populations (Groom
2013, p. 4; Namibia 2013, pp. 11–12;
Zambia Wildlife Authority 2012, p.3;
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LionAid 2011, pp. 1–2; Mesochina et al.
2010a, pp. 40–49; Mesochina et al.
2010b, pp. 33–38; Government of
Tanzania 2010, pp. 3–17; Begg and Begg
2010, entire). Range states have also
implemented a number of conservation
strategies designed to conserve habitat,
reduce human–lion conflict, and
preserve the lion’s prey-base.
Conservation Measures To Stem Habitat
Loss
Habitat loss represents one of the
main threats facing lions in Africa
(Bauer et al. 2008, unpaginated).
Attempts by range countries to address
this decline in habitat are manifested in
a number of ways, such as the creation
of protected areas and the establishment
of wildlife corridors to connect
fragmented habitats.
Two conservation tools used by
African range countries for lions include
the establishment of protected areas and
the enforcement of protections in these
areas (Mesochina et al. 2010a and b;
Treves et al. 2009, pp. 60, 64). However,
several problems have emerged. For
example, certain land-tenure systems do
not recognize community ownership of
land and wildlife and undermine the
extent to which benefits are converted
into incentives for conservation.
Protected-area ‘‘boundaries’’ are not
always visible. Additionally, law
enforcement in protected areas can be
sporadic, and parks are often
understaffed (Pfeifer et al. 2012, pp. 1,
7). More recent evidence suggests that
some protected areas are being more
commonly encroached upon as human
populations expand and search for
resources.
Despite encroachment, protected
areas are somewhat effective at
protecting wildlife and habitat as rates
of habitat loss tend to be lower in
protected areas than outside them
(Green et al. 2013, p. 70; Pfeifer et al.
2012, p. 2). African countries are
realizing the benefits of managing their
wildlife populations and parks for
tourism; however, conservation of vast
areas of land for megafauna such as the
lion is not only complex, but also
expensive. As an example, the 28-km
(17-mi) elephant corridor, completed in
2011 in Kenya, cost $1 million USD
(The Nature Conservancy 2013,
unpaginated). Additionally, the overall
costs of anti-poaching and
compensation is expected to increase in
range states concurrently with growing
human populations, declining
purchasing power of external funds, and
corruption (Garnett et al. 2011, pp. 1–2;
Wittemyer et al. 2008, pp. 123, 125).
Another mechanism for protecting
habitat is to reconnect fragmented
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habitat across national boundaries.
Corridors are being restored, fences are
being removed, and protected areas are
being connected. Restoration of these
corridors allows wildlife to travel
between areas of suitable habitat (Jones
et al. 2012, pp. 469–470). In some areas,
fences have been constructed to protect
grazing resources for domestic livestock
as well as to provide barriers to disease
(Gadd 2012, pp. 153, 176). One aspect
of these fences is that they separate
lions from their prey. In southern
Africa, fences are being taken down to
increase the size of connected habitat
and link it to reserves and national
parks (IUCN 2009, p. 101; IUCN 2008,
various). The Limpopo Transfrontier
Park is another example of where this
practice is being implemented
(Newmark 2008, p. 327). Boundary
fences along national borders that
separate many reserves are being
removed to form a 35,000-km2 park.
Limpopo National Park (formerly
known as Coutada 16) in Mozambique,
Kruger National Park in South Africa,
and Gonarezhou National Park, Manjinji
Pan Sanctuary, and Malipati Safari Area
in Zimbabwe will all be connected, as
will be the area between Kruger and
Gonarezhou, and the Sengwe communal
land in Zimbabwe and the Makuleke
region in South Africa (Newmark 2008,
p. 327). However, in some locations,
areas that have previously been
designated as corridors have been
encroached upon by human settlements
and agriculture (Estes et al. 2012, pp.
258–261; Jones et al. 2012, p. 469).
Tanzania is an example of a country
attempting to reconnect habitat. As of
2002, the Tanzanian Government, with
donor and NGO support, was
reconnecting the nine largest blocks of
forest in the East Usambara Mountains
using wildlife corridors (Newmark 2002,
various). Additionally, the 2009
Wildlife Act of Tanzania allows the
Minister, in consultation with relevant
local authorities, to designate wildlife
corridors, dispersal areas, buffer zones,
and migratory routes. The 2010–2015
National Elephant Management Plan of
Tanzania indicates that corridors are the
primary objective of the plan, and
although primarily designed for
elephants, these corridors allow for
continuity of populations of other large
mammal species such as lions (Jones et
al. 2012, p. 470).
In 2011, Kenya (which neighbors
Tanzania to the North), completed a 28km corridor through an area that had
been heavily impacted by human–
wildlife conflict. The purpose of the
corridor was primarily to reduce
human–elephant conflict and appears to
have been successful (Mount Kenya
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allows other wildlife such as lions to
disperse through habitat that otherwise
would have been unfavorable for
wildlife to travel through (Mount Kenya
Trust 2011, p. 1). It was an expensive
project, but the effort appears to have
served its purpose: Elephants are using
the corridor on a regular basis
(particularly an underpass under a
highway), and humans are reporting less
human–wildlife conflict (Mount Kenya
Trust 2011, p. 1).
However, connectivity alone does not
ensure the dispersal of animals (Roever
et al. 2013, pp. 19–21). The Tanzania
Wildlife Research Institute (TAWIRI) is
an organization under Tanzania’s
Ministry of Natural Resources and
Tourism, and is responsible for
conducting and coordinating wildlife
research activities in Tanzania. In this
role, TAWIRI has been actively involved
in promoting the development of and
monitoring the use of wildlife corridors
in Tanzania. Surveys conducted in 2009
and 2010 suggest that the Nyanganje
Corridor in Tanzania is no longer being
used by elephants and other wildlife.
This corridor is at a narrow passage in
the Kilombero Valley and is the shortest
distance for animals to cross between
the Udzungwa and Selous ecosystems.
Despite efforts in place, much of the
corridor is being encroached upon by
conversion of land to rice farming and
cattle grazing (Jones et al. 2012, p. 469).
Because these activities often deter
wildlife from passing through, the
corridor is ineffective (Jones et al. 2012,
p. 469).
In the latter half of the 20th century,
lions in India were on the verge of
extinction. However, conservation
measures were put in place to protect
lion habitat. In 1965, Gir Wildlife
Sanctuary was created and became the
first protected area in Gujarat. In 1972,
the Gir Lion Sanctuary Project began.
Two-thirds of the pastoral families
living in the Sanctuary, and their
livestock, were relocated outside Gir
forests (Singh and Gibson 2011, p.
1754). The area of Gir Wildlife
Sanctuary was expanded and the core
area designated as Gir National Park in
1975.
Following these actions, habitat began
to recover, the wild ungulate population
increased, and, subsequently, lion
numbers increased (Singh and Gibson
2011, pp. 1754, 1755). Habitat adjacent
to Gir was also declared a Sanctuary
(Pania Sanctuary) in 1989. This area and
surrounding community lands were
declared protected forests to serve as a
buffer area to the Gir Forests (Singh and
Gibson 2011, p. 1754). As the lion
population began to increase, lion
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dispersed into satellite forest patches.
These reclaimed patches of habitat were
protected and the Mitiyala Sanctuary
was created in 2002, and the Girnar
Sanctuary, in 2007 (Singh and Gibson
2011, p. 1754).
After 40 years, the protected areas of
India have experienced habitat recovery,
a 10-fold increase in ungulates, and an
increase in lion numbers (Singh and
Gibson 2011, pp. 1754, 1756). Since
1968, India’s Forest Department has
conducted wildlife censuses every 5
years (Singh and Gibson 2011, p. 1754),
documenting a steady increase in the
lion population. Community pride and
love of lions, the media, and political
pressure has ensured efforts are made to
protect these lions. When problems
arise, they are quickly assessed and a
solution found. For example, when 6
lions were hit and killed by trains,
immediate action was taken to rectify
the problem (Meena 2014, p. 26).
Because of these actions, lions in India
now number 523 (BBC 2015,
unpaginated).
Conservation Measures in Place To
Stem the Loss of Prey Base
Lions, like most large carnivores, prey
upon a variety of species including
buffalo, plains zebra, wildebeest, giraffe,
gemsbok, kob, and warthog (Kenya
Wildlife Service 2013, p. 13; Beg and
Beg 2011, p. 4; Nowell and Jackson
1996, p. 18). Depletion of these prey
species due to competition with humans
represents a threat to the lion
(Chardonnet et al. 2005, pp. 8–9). As
noted, the increase in the human
population in Africa is a major
contributor to the increase in demand
for bushmeat, which in turn increases
human encroachment into wildlife
territory (Lindsey et al. 2012b, p. 36). In
addition to the increase in the human
population, lack of an alternative
livelihood, lack of alternate food
sources, and lack of clear rights over
land or wildlife are contributing factors
toward the increase in demand for
bushmeat (Lindsey et al. 2012b, pp. 36–
41). The advent of automatic weapons
in the bushmeat trade impacts the lion’s
prey base, which is being hunted at
unsustainable levels.
Reconnecting fragmented habitat has
the additive effects of not only
conserving the biodiversity of the lion’s
habitat, but also that of its prey base
(Lindsey et al. 2012b, p. 43). These
types of restoration practices enhance
the health of species by allowing genetic
interchange to occur and, thus, conserve
the genetic diversity of all wildlife.
Wildlife management entities are
linking many of the major protected
areas by removing boundary fences
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along national borders that separate
many reserves in addition to creating or
improving corridors to link good-quality
habitat for wildlife (Gadd 2012, p. 179;
Newmark 2008, pp. 323–324).
To address the increasing
consumption of bushmeat, host
countries have employed a variety of
different strategies, including the
development of alternative industries
for communities. Helping local
communities develop alternate
industries represents one of the ways
range countries can reduce their
dependence on bushmeat. Throughout
Africa, several ideas have been
attempted with varying levels of
success. For example, the Anne Kent
Taylor Fund (AKTF) helps local Maasai
women to buy beads and other supplies
to produce traditional items for the local
tourist industry (AKTF 2012, p. 7;
Lindsey et al. 2012b, p. 45; van Vliet
2011, p. 17). In addition, AKTF helps
organize local men into anti-poaching
and de-snaring teams (AKTF 2012, p. 5;
van Vliet 2011, p. 17). By creating
programs targeting both men and
women, AKTF creates an environment
that provides communities with
financial stability as well as direct
community interest in protecting local
wildlife. With 13 years assisting local
communities, the AKTF represents one
of the more successful attempts to
encourage locals to shift away from
relying on bushmeat.
Studies compiled by Hazzah (2013
pp. 1, 8) have shown that local
communities who live near protected
areas with more lenient policies have a
more positive attitude and relationship
with both the manager and the protected
area as a whole. This open approach to
protected area management reflects a
trend in recent years to bring in local
communities to assist in the
management of protected areas (Lindsey
et al. 2012b, p. 53). Wildlife
management programs run by local
communities are defined by two goals:
conserving wildlife and providing
economic aids to the community
(Bandyopadhyay et al. 2010, p. 5). With
regard to discouraging the consumption
of bushmeat, this new approach is seen
in the creation of community-based
wildlife management programs (van
Vliet 2011, p. 26). The purpose of these
programs is to give the local community
a direct stake in the management of
wildlife areas. One use for these areas is
to turn them into game ranches. These
areas are used both for legal bushmeat
production as well as trophy hunting
and ecotourism.
Namibia has had great success in
setting up community-run
conservancies. After gaining
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independence in 1990, Namibia began
to turn over ownership of wildlife areas
to local communities (van Vliet 2011, p.
29; Bandyopadhyay et al. 2010, p. 6). By
2011, Namibia had 64 communities that
covered 17 percent of the country total
area (van Vliet 2011, p. 29; Connif 2011,
unpaginated; NASCO 2011, p. 4). The
majority of the incomes from these
conservancies come from ecotourism,
followed by trophy hunting (NASCO
2011, p. 22). These incomes are then
used to support infrastructure
improvement in the community. In
addition, legal bushmeat acquired
within conservancy lands is distributed
to local families (NASCO 2011, p. 25).
The success of the program in Namibia
has been attributed to Namibia’s unique
characteristics, including low
population density and favorable
seasonal rain, which helps prey species
recover (van Vliet 2011, p. 30). Despite
the successes in Namibia, the country’s
unique characteristics mean that
adapting Namibia’s success to other,
more densely populated countries will
be difficult.
Conservation Measures to Stem HumanLion Conflict
As the human population expands,
the potential for conflict with wildlife
increases. In Africa, conflict between
villagers and lions, who prey upon
livestock, represent a threat to the
species (Chardonnet et al. 2010, p. 12;
Moghari 2009, p. 14; IUCN 2006a, p.
23). In addition, habitat loss due to
conversion of land increases the chance
of villagers coming into direct contact
with lions (Chardonnet et al. 2010, p.
24). In an attempt to address these
problems, range countries have
employed a variety of different
strategies to help the lion. Such
strategies involve education, an effective
conservation plan, and interacting with
the local community.
Historically, range countries seek to
mitigate human-lion conflict through
controlling rather than conserving the
predator population. In countries such
as Malawi, for example, the Department
of Game, Fish and Tsetse Control would
shoot large carnivores that preyed upon
livestock. Because of this policy, more
than 560 predators (which include
lions) were killed in the country
between 1948 and 1961, (Mesochina et
al. 2010b, p. 35). While this department
was disbanded in 1963 and jurisdiction
shifted to the new Department of
Forestry, crop and livestock protection
still remains an important part of its
function. Despite the department
focusing on protecting crops and
livestock, the number of lions killed in
the country has declined. Between 1977
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and 1982, eight lions were killed,
whereas six lions were killed between
1998 and 2007 (Mesochina et al. 2010b,
p. 35). While fewer lions are being
killed than in the previous decades,
problems remain, including lack of
resources, lack of manpower, and
corruption within the range countries.
Current governmental management of
lions in countries such as Malawi,
Tanzania, and Zambia are managed by
the Problem Animal Control units
(Mesochina et al. 2010a, p. 41;
Mesochina et al. 2010b, p. 36). When
lion attack incidents occur, Problem
Animal Control dispatches officials to
investigate the problems. If the problem
lion is located, it is either removed or
eliminated. When properly funded, this
program has helped in reducing not
only conflicts between lions and
humans but also has driven down the
numbers of lions killed. Between 2005
and 2009, there were 116 reported cases
of lions killed, with the number of lions
killed being less than 50 per year in
Tanzania (Mesochina et al. 2010a, p.
41). However, limitations of resources
(including both manpower and funds)
have hampered the effectiveness of
these officials in responding to these
incidents. In addition, many Problem
Animal Control interventions resulted
in the death of the lion (Mesochina et
al. 2010a, p. 41; Chardonnet et al. 2009,
p. 36). Even in cases of translocation,
the lions that were being transported
often end up injured or continue to pose
problems to the community (Bauer et al.
2007, p. 91).
NGOs are also assisting in protecting
lions. Intervention by NGOs often takes
the form of interacting with the local
community (Winterbach et al. 2010, p.
98). Lion Guardians, which operates in
Kenya and Tanzania, recruits and
educates local young men to monitor
and track lion movement and warn
herders of lion presence in the area,
recover lost livestock, reinforce
protective fencing, and intervene to stop
lion hunting parties, thereby mitigating
or preventing possible human-lion
conflict (Hazzah et al. 2014, p. 853; Lion
Guardians 2013, p. 7; Lion Guardians
2012, p. 3). From 2010 to 2013, Lion
Guardians maintained a recovery rate of
lost livestock of more than 85, totaling
over $1.5 million USD; in 2014 alone,
more than 20,000 livestock (93 percent)
were recovered (Lion Guardians 2014, p.
7; Lion Guardians 2013, p. 6). Since
2010, 1,700 bomas have been reinforced
to reduce depredation of livestock. Endof-year sampling shows that more than
90 percent of reinforced bomas sampled
did not experience further depredation
(Lion Guardians 2014, p. 7; Lion
Guardians 2013, p. 6). Additionally, 103
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lion hunts were stopped or prevented
between 2010 and 2014 (Lion Guardians
2014, p. 6; Lion Guardians 2013, p. 5).
Lastly, in the years of Lion Guardians
operations, lion kills have decreased by
95 percent and the number of lions has
steadily increased; a total of 286 lions
have been documented in the AmboseliTsavo ecosystem (Lion Guardians 2014,
p. 6; Lion Guardians 2013, p. 5).
In addition, Lion Guardians work
with tribal elders to dissuade young
men from killing lions for ceremonial
purposes. Historically, the killing of
lions through ritualized lion hunts
called ilmurran is rewarded with gifting
of cows and other rewards (Lion
Guardians 2012, p. 5; Goldman et al.
2010, p. 334). After introducing village
elders to the Lion Guardians program
first hand, many return home to their
village and give their blessings to the
project. This education led to significant
results; on August 11, 2013, two Lion
Guardians stopped a group of hunters
who were planning to hunt a lion in
retaliation for the lion preying on their
livestock. The local village elders fined
the potential hunters two cattle each for
going on a lion hunt, marking a gradual
but significant shift in the cultural
attitudes regarding the lion (Hazzah et
al. 2014, p. 858; Lion Guardians 2013,
p. 20). Between 2007 and 2014, only
five lions had been killed in territories
where Lion Guardians operates, in
contrast to more than 100 lions killed in
adjacent areas (Lion Guardians 2013, p.
5). Furthermore, reduced lion mortality
was sustained across multiple years,
resulting in the reserve having one of
the highest lion densities in Africa
(Hazzah et al. 2014, p. 857; Schuette et
al. 2013, p. 149). Despite the success of
this program, retaliatory as well as
ceremonial killings of lions outside the
program areas remain a threat to the
species.
We found that many of the lion range
states are trying to address lion
conservation through the establishment
of protected areas, wildlife management
areas, wildlife corridors, and
reconnecting habitat. In some areas,
creating incentives for lion conservation
is occurring through community
conservation programs in range
countries. In other cases, participatory
strategies have been implemented to
enhance local tolerance for large
carnivores in Africa. An increasing
number of programs encourage local
communities to solve problems that
arise from human–lion conflict without
killing lions. However, the effectiveness
of these measures still ranges from
successful to unsuccessful, due in part
to lack of resources, political will, and
infighting. It is imperative that range
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countries continue to recognize and
support the role that local communities
play in lion conservation. Greater
support by countries to address the
needs of local communities, and thereby
address the needs of lions, may be the
single-most important role these
countries can play in changing the
trajectory of lion declines.
Finding
Section 4 of the Act (16 U.S.C. 1533)
and implementing regulations (50 CFR
part 424) set forth procedures for adding
species to, removing species from, or
reclassifying species on the Federal
Lists of Endangered and Threatened
Wildlife and Plants. Under section
4(a)(1) of the Act, a species may be
determined to be an endangered species
or a threatened species based on any 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.
A species is ‘‘endangered’’ for
purposes of the Act if it is in danger of
extinction throughout all or a significant
portion of its range and is ‘‘threatened’’
if it is likely to become endangered
within the foreseeable future throughout
all or a significant portion of its range.
The ‘‘foreseeable future’’ is the period of
time over which events or effects
reasonably can or should be anticipated,
or trends extrapolated.
As required by the Act, we conducted
a review of the status of the species and
considered the five factors in assessing
whether the lion is in danger of
extinction throughout all or a significant
portion of its range or likely to become
endangered within the foreseeable
future 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
lion. We reviewed the petition,
information available in our files, other
available published and unpublished
information, and comments received
from peer reviewers and the general
public.
When considering what factors might
constitute threats to a species, we must
look beyond the mere exposure of the
species to a factor to evaluate whether
the species may respond to the factor in
a way that causes actual impacts to the
species. If there is exposure to a factor
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and the species responds negatively, the
factor may be a threat and we attempt
to determine how significant a threat it
is. The threat is significant if it drives,
or contributes to, the risk of extinction
of the species such that the species may
warrant listing as endangered or
threatened as those terms are defined in
the Act.
Overall, the lion population has
declined and is expected to continue to
decline. Across its range, the lion is
facing threats stemming from human
population growth. We find a number of
factors are currently impacting the
species and will impact the species in
the future. In general, these factors
include: Habitat fragmentation,
degradation, and loss (Factor A);
excessive mortality due to trophy
hunting and trade in lion bone (Factor
B); disease (Factor C); loss of prey base,
retaliatory killing due to human–lion
conflict, deleterious effects due to small
populations, and climate change (Factor
E); and inadequate regulatory
mechanisms and weak management of
protected areas (Factor D).
Overall, the lion population has
decreased by 43 percent over the last 21
years. Regional variations indicate an 8
percent increase in southern Africa and
a 55 percent increase in India; however,
the eastern region and western and
central region (combined) decreased by
59 and 66 percent, respectively, in the
past 21 years. Furthermore, almost all
lion populations in Africa that
historically exceeded 500 individuals,
the minimum number estimated to
constitute a viable population, are
declining.
Human population growth has led to
a substantial decrease in lion habitat
over the past 50 years. Current savanna
habitat that is suitable for lions is
fragmented and totals only 25 percent of
African savanna habitat. This loss of
habitat has resulted in local and
regional lion population extirpations,
reduced lion densities, and a
dramatically reduced range; this
decrease in habitat also partially
explains why lions are now largely
limited to protected areas. Due to good
protection and management, lions in
India have dispersed to additional
forested habitat outside the protected
area, extending their range. Lion habitat
in Africa, however, continues to be
threatened by expansion of human
settlements, despite occurring within
protected areas.
Expansion of human settlements,
agriculture, and/or livestock grazing are
reported as occurring in or on the
periphery of several areas identified by
Riggio et al. (2013, suppl. 1) as lion
strongholds (viable populations) and
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potential strongholds, and are
particularly a threat in western, central,
and eastern Africa and some parts of
southern Africa. Lions are generally
incompatible with humans and humancaused habitat alteration and loss; they
are the least successful large African
carnivore outside conservation areas. In
order to survive, they require larger
contiguous habitats with fewer negative
human impacts than other more
resilient species. Expansion of human
settlements and activities into lion
habitat renders it unsuitable for lions,
primarily because human expansion
results in reduced availability of wild
prey and lion mortality due to increases
in human–lion conflict. Both of these
factors influence the distribution and
population viability of lions.
Furthermore, fragmentation and
isolation of lion habitat and populations
can also impact dispersal and genetic
viability.
Prey availability is essential to lion
survival as it affects reproduction,
recruitment, and foraging behavior and,
therefore, also impacts lion movement,
abundance, and population viability.
Prey abundance does not appear to be
a concern for lion populations in India.
Conservation initiatives have ensured
that ample prey is available, and the
pastoral communities that cohabitate
with lions are primarily vegetarian;
therefore, there is no competition for
food and no demand for bushmeat. In
Africa, lions are under serious threat
due to decreased prey abundance.
Widespread decreases in prey species
have been driven by human population
growth and unsustainable, increasingly
commercialized bushmeat hunting in
and around protected areas.
Bushmeat is an important source of
protein and livelihood in Africa. The
growing human population increases
the demand for bushmeat, fueling trade,
urban markets, and international
markets. Bushmeat sold at elevated
prices increases commercialization and
the number of hunters. These hunters,
who are often poor, are enticed by the
quick income to find more efficient
hunting methods, putting
unprecedented pressure on wildlife.
Bushmeat contributes significantly to
food security, and is often the most
important source of protein in rural
areas. It comprises between 6 percent
(southern Africa) and 55 percent (CAR)
of a human’s diet within the lion’s
African range. In western Africa,
bushmeat is a secondary source of
protein, with fish being the primary
source. However, when widespread loss
of jobs and income occurs due to poor
fish harvests, bushmeat becomes an
important source of income and
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sustenance, leading to increased
presence of hunters in protected areas
and higher than average declines in
wildlife.
Due to growing demand and
availability of modern weapons, many
wildlife species, including the lion’s
prey base, have become depleted in
many areas. Hunters are increasingly
focusing on protected areas since
wildlife has been depleted in nonprotected areas. Bushmeat hunting is
illegal, yet weak management and
inadequate law enforcement have
facilitated poaching of bushmeat in
protected areas. Significant decreases in
large mammal populations, including
lion prey species, have occurred in
protected areas throughout Africa.
Overall, the large mammal population
has declined 59 percent. Regional
differences in herbivore population
abundance were also detected. Because
prey availability is an important factor
for lions, decreases in prey densities
result in decreases in lion density.
Expansion of human settlements and
agricultural and pastoral activities into
protected areas not only decreases prey
availability, it increases exposure of
livestock and humans to lions, thus
resulting in human-lion conflict. Most
conflict occurs at protected area
boundaries where villages are
established and human encroachment
occurs, which increases the chance of
human-lion encounters. Furthermore,
cattle herders enter protected areas, and
lions move beyond the borders of
protected areas in search of food,
increasing interactions between humans
and lions and the risk of human-lion
conflict.
The most significant cause of humanlion conflict is livestock depredation
and, to a lesser extent, attacks on
humans. As a result of prey species
becoming depleted in many areas, lions
will seek out livestock. Additionally,
when pastoralists graze increasing
numbers of livestock in and adjacent to
protected areas and cultivate land up to
and within the boundaries of protected
areas, humans and livestock are
subjected to lions, and the risk of
predation and the number of livestock
lost to predation increases. Conversion
of rangeland to agricultural land has
blocked migratory prey routes, forcing
lions to rely more on livestock.
Additionally, because most protected
areas are too small to support a lion’s
large home range, adjacent dispersal
areas are often used by lions in search
of prey, putting them into greater
contact with livestock and humans.
Conditions worsen as livestock numbers
and areas under cultivation increase,
leading to overgrazing, further habitat
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destruction, and greater depredation
rates. Attacks on humans appear to be
more frequent in southern and eastern
Africa and rare in western and central
Africa.
Livestock provide an economic value
to humans, particularly those in extreme
poverty. When lions have no economic
value to local communities and they kill
or are perceived to kill livestock, the
economic impact to local communities
can be significant. Impacts on victims of
lion attacks create resentment towards
lions and lion conservation, and a
greater likelihood of retaliation. The
most common solution to lion attacks is
retaliatory killing. Spearing, shooting,
trapping, and poisoning of lions occur
regularly. Retaliatory killings have been
reported as a significant threat to lion
populations in protected areas of
western and central Africa, Botswana,
South Africa, Cameroon, Kenya,
Tanzania, and Zimbabwe. Despite close
occupation of India’s lion population
with human settlements, increased
predation on livestock, and some
retaliatory killing of lions, human-lion
conflict and associated retaliatory
killing is not a major source of lion
mortality for that population.
Every year, human-lion conflicts
intensify due to habitat loss, poor
livestock management, and decreased
availability of wild prey. Because most
human-lion conflict occurs at the
borders of protected areas, only those
prides that occur near the borders are
subjected to human-lion conflict.
However, when these lions are removed
via retaliatory killing, territorial gaps are
then filled with lions that may have
occurred closer to the core of protected
areas, causing these border areas to
serve as population sinks and exposing
more lions to human-lion conflict and
retaliation. Retaliatory killing of lions
continues in many areas, and this
practice impacts the viability of lion
populations across their range. The
killing of lions due to human-lion
conflict is enough to result in the local
extirpation of lion populations.
Lions are a key species in sport
hunting, or trophy hunting, which is
carried out in a number of range
countries. If managed correctly, trophy
hunting can be an important
management tool for conserving land
and providing financial resources for
lion conservation. However,
management programs are not always
sufficient to deter unsustainable
offtakes, which has resulted in declines
in lion populations in many areas. The
main problem with mismanaged trophy
hunting stems from excessive harvests
because of impacts associated with
removal of males.
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Six management weaknesses have
been identified in the current
management of lion hunting. These
weaknesses include: (1) A lack of
scientifically based quotas, which
results in excessive harvests; (2) a lack
of enforcement in age restrictions,
which leads to unsustainable harvests,
increased rates of infanticide, and
population declines; (3) hunting of
female lion in Namibia, which decreases
reproduction success, thereby
decreasing males available for trophy
hunting; (4) the use of fixed quotas that,
which encourages hunters to be
unselective in their take of a trophy (i.e.,
they will kill younger, less desirable
males); (5) a lack of minimum hunt
lengths or minimum lengths that are too
short to allow hunter the time needed to
be more selective in their take of
trophies; and (6) general problems
associated with management of trophy
hunting, including corruption,
allocation of concessions, and lack of
benefits to communities and recognition
of the important role they play in
conservation.
Documented declines in lion
populations of Africa are a result, in
part, of mismanaged trophy hunting.
Multiple researchers have documented
declines in lion populations across the
range of the species as a result of
mismanaged trophy hunting.
Specifically, negative impacts to lions
from excessive offtakes have been
documented in Benin, Cameroon,
Tanzania, Zambia, and Zimbabwe.
Additionally, the effects of overharvesting can extend into adjacent
national parks where hunting is
prohibited.
Except in Mozambique, trophy
hunting quotas are higher than the
recommended maximum harvest of 1
lion per 2,000 km2. Additionally, the
mean actual harvests in Burkina Faso,
Zambia, Namibia, and Zimbabwe are
higher than the recommended 1 lion per
2,000 km2 offtake.
In the absence of reliable population
estimates, age restriction on trophy
harvests can ensure sustainability. If
offtake is restricted to males older than
6 years of age, trophy hunting will likely
have minimal impact on the pride’s
social structure and young. By removing
only males 6 years of age or older,
younger males remain in residence long
enough to rear a cohort of cubs
(allowing their genes to enter the gene
pool; increasing the overall genetic
diversity); recruitment of these cubs
ensures lion population growth and,
therefore, sustainability. However,
harvesting males that are too young
causes male replacements, which results
in increased infanticide rates and death
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of the surviving male coalition.
Additionally, a study found a 100
percent fatality rate for males that are
prematurely forced to disperse due to a
new male takeover. A lack of mature
males dispersing, whether it’s due to
trophy hunting or retaliatory killing,
reduces the genetic viability of
populations and may contribute to local
population extinctions.
Lion experts recommend age-based
strategies be incorporated into lion
management action plans. Although the
6-year method has the potential to
reduce the rate of infanticide in lion
populations subject to trophy hunting,
the issue of incorporating this strategy
into each country’s conservation
strategy and/or action plan, and
following up with implementation,
enforcement, and transparency, has yet
to be observed in many of the lion’s
range countries. Lack of implementation
of age-based strategies may undermine
the successful use of trophy hunting as
a sustainable conservation strategy.
Trade in lion parts and products are
common in western and central Africa.
Lion populations in these regions are
small and declining and, therefore, the
common use of lions in these regions for
their parts and products is likely
unsustainable. Further, there seems to
be a burgeoning trade in lion bone to
supplement or replace tiger bone. There
is potential that the current legal trade
in lion bone will eventually not be
enough to supply demand, resulting in
poaching of lions in the future for the
Asian medicinal trade.
As a result of human population
expansion into lion habitat, lions are
increasingly exposed to diseases from
domestic animals. Because lions are a
top predator, they are at a particularly
high risk of exposure to pathogens.
Available studies do not indicate that
infection with a single disease is
causing detrimental impacts to lions at
the species level, although general body
condition, health, and lifespan may be
compromised and result in negative
impacts at the individual or population
level. Co-infections, however, could
have synergistic effects that lead to
greater impacts on lions than a single
infection.
Disease appears to be a secondary
factor influencing the decline of lions
when co-infections occur or when
disease is combined with other factors,
including environmental changes,
reduced prey density, and inbreeding
depression. Diseases weaken
individuals and allow them to succumb
to other diseases or factors. Although
disease does not appear to be a major
driver in the status of the lion,
populations can suffer significant losses;
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some may recover to pre-outbreak
levels, others may not. Given the small
and declining lion populations that
remain, any loss of individuals from the
populations could be highly
detrimental.
The viability of a lion population
partly depends on the number of prides
and ability of males to disperse and
interact with other prides, which affects
exchange of genetic material. Without
genetic exchange, or variation,
individual fitness is reduced and
species are less able to adapt to
environmental changes and stress,
increasing the risk of extinction.
Male dispersal plays an important
role in determining the level of
inbreeding in lion populations. The
fewer number of males present to
contribute genes to the next generation,
the more inbred the population will be.
Therefore, not only does dispersal
impact inbreeding, so does the loss of
male lions due to excessive trophy
hunting and infanticide. Because the
number of prides and male dispersal are
the most important factors for
maintaining viability, sufficient areas
are needed to support at least 50 prides,
but preferably 100 prides, and allow
unrestricted male dispersal.
Unfortunately, few lion populations
meet these criteria as almost all lion
populations in Africa that historically
exceeded 500 individuals are declining,
and few protected areas are large
enough to support viable populations.
Furthermore, research indicates that
there is a general lack of gene flow in
most lion conservation units.
Lack of dispersal and genetic
variation can negatively impact the
reproductive fitness of lions in these
populations and local extirpation is
likely. Loss of fecundity leads to a
decrease in population size, fewer
prides in a population, and increased
inbreeding which contributes to a
decline in the population and increases
the risk of extinction. Additionally, lack
of genetic variation can impact the
ability of lions to withstand stochastic
events or limit the lion’s ability to
evolve responses to climate change.
India’s lion population is isolated and
genetically less diverse. Currently, there
is no evidence of depressed
demographic parameters. However,
intense management may interfere with
natural selection by ensuring survival of
unfit lions, which facilitates the
propagation of deleterious genes in the
population. Being a small, isolated
population and less genetically diverse,
therefore, it is more vulnerable to the
loss of any individuals due to
environmental and stochastic events,
and more prone to local extinction
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events. The establishment of another
geographically separated, free-ranging
population would reduce the risk of
extinction. Establishment of a new
population at Kuno Wildlife Sanctuary
in Madhya Pradesh State has been
proposed. However, the Government of
Gujarat has refused to allow any lions
from Gir to be transferred.
As human populations continue to
rise in sub-Saharan Africa, the amount
of land required to meet the expanding
human population’s needs is constantly
increasing. Lions are increasingly
limited to protected areas, and human
population growth rates around
protected areas in Africa tend to be
higher than the average rural growth
rate. Considering the majority of the
human population in sub-Saharan
Africa is rural, and land supports the
livelihood of most of the population,
loss and degradation of lion habitat, loss
of prey base, and increased human-lion
conflict can reasonably be expected to
accompany the rapid growth in subSaharan Africa’s human population into
the foreseeable future.
Impacts described above from existing
and predicted anthropogenic pressures
on the species and its habitat are likely
to be exacerbated by climate change.
The general warming and drying trend
projected for Africa could further reduce
lion range, numbers, and prey base.
Lions may also have to travel greater
distances to find food or shift their diet
to livestock, increasing conflict with
humans and the risk of retaliatory
killings. Additionally, changes in
climate may increase the number and
intensity of disease outbreaks in lions
and their prey.
Under different climate change
scenarios between the years 2040 and
2070, no broad new areas will become
suitable for lion. Southern Africa, where
the broadest areas of suitable conditions
occur, is projected to become less
suitable because of climate change. A
broad swath of potential distributional
area in western Africa is projected to
become ‘‘distinctly less suitable or even
uninhabitable.’’ A decrease in the lion’s
range could mean that stochastic events
impact a larger portion of the whole
species, especially if it occurs where the
species and its habitat occur.
Additionally, reductions in populations
and geographic range may limit the
lion’s ability to respond to climate
change. Conversely, climate change
effects on potential lion distribution are
projected to be more neutral in eastern
Africa than across the entire range.
Reserves in this region are more likely
to sustain lion populations under
climate change scenarios in the
medium-term.
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Increases in average rainfall in the
past 20 years have resulted in the
conversion of dry savanna to forestland
in India; however, these lions have used
both habitats. Therefore, habitat
conversion due to climate change may
not be as detrimental to lions in India.
However, increased risks of flooding
could pose a problem for lions.
Additionally, lions could face threats
following flood events, such as an
outbreak of disease. Because this
population is small, isolated, and less
genetically diverse, it is more vulnerable
to stochastic events and more prone to
local extinction events.
Current lion habitat and suitable
habitat predicted to remain under
climate change scenarios will be under
increasing pressure due to land
conversions to meet the needs of the
growing human population. Projected
changes in Africa’s climate will increase
this pressure as land becomes more arid
and food security concerns are
exacerbated. Adaptive responses may
result in further encroachment into
natural habitats. Land conversion will
restructure the landscape, disrupt prey
migration, and decrease prey available
to lion. Lion densities decrease with
increasing mean temperature and
decreasing rainfall. Therefore, lion
density, or carrying capacity of
protected areas, in sub-Saharan Africa is
likely to decline with climate warming
and drying.
The loss of lions could also mean the
loss of genetic variation. Combined with
declining populations, the risk of
inbreeding and associated
complications could increase. Drought
conditions can also contribute to
reduced prey availability by altering the
timing of migration. Climate conditions
also influence prey abundance, and the
loss of prey species can result in lions
shifting their diet towards livestock,
which may increase retaliatory killings
by humans.
Diseases can be directly and
indirectly affected by climate change by
impacting distribution, the timing of
outbreaks, and the intensity of
outbreaks. Severe climate change could
synchronize temporal and spatial
convergence of multiple infectious
agents, triggering epidemics with greater
mortality than infections from a single
pathogen.
National and international
conservation strategies rely on protected
areas to protect natural resources from
negative impacts of human populations.
The lion is largely limited to protected
areas; therefore, effective management is
crucial to the survival of the species.
However, weak management of
protected areas has been documented
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across its range, especially in western
Africa where most protected areas are
experiencing severe management
deficiencies.
Based on the best scientific and
commercial information, we find that
several factors are negatively impacting
the lion and contributing to the risk of
extinction. However, we find there is a
substantial difference in the magnitude
of these threats to the risk of extinction
between the subspecies P. l. leo and P.
l. melanochaita. Based on current
population estimates, projected
population trends, and the threats
described herein, we find that the
subspecies P. l. leo and P. l.
melanochaita qualify for different
statuses under the Act.
Finding for Panthera leo leo
The range of P. l. leo includes the
western and central African regions and
India. This subspecies has experienced
a reduction in range, a reduction in total
number of populations, and a reduction
in number of lions. There are
approximately 1,500 lions distributed
among 15 populations; 14 in Africa and
1 in India. The population in western
and central Africa has declined by 66
percent since 1993. The current
population estimate for this portion of
its range is approximately 915 lions.
None of the lion populations in these
regions meet the MVP, although we do
note that the WAP complex qualifies as
a potential stronghold where a viable
population could occur if immediate
interventions are implemented. Between
1993 and 2014, the Indian population
increased by 55 percent. A census
conducted in 2015 indicates the
population has increased by 27 percent
since 2010, with lions now numbering
523. Although this population is found
within a protected area, its single, small
population of 523 animals continues to
be highly vulnerable to disease and
other stochastic events. Due to weak
management in Africa and small
populations throughout its range, this
subspecies continues to face threats.
Remaining African populations are
particularly threatened by expansion of
human settlements, agriculture, and/or
livestock grazing. Expansion of
agriculture and livestock grazing are
reported in or around two of the larger
African populations of P. l. leo, WAP
Complex and a Chad–CAR population;
management in portions of both
protected areas is reported as weak,
raising concern for the persistence of
lions and their habitat. Expansion of
human settlements and activities into
lion habitat renders it unsuitable for
lions, primarily because human
expansion results in reduced
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availability of wild prey and lion
mortality due to increases in human–
lion conflict. Both of these factors
influence the distribution and
population viability of lions.
Significant decreases in prey
abundance have occurred in protected
areas throughout Africa. In western
Africa, specifically, herbivore
populations have decreased by 85
percent. As a result of prey species
becoming depleted in many areas, lions
seek out livestock for food; attacks on
livestock occur at the highest frequency
in areas where natural prey abundance
is lowest. Traditional livestock
husbandry practices can reduce
depredation rates, but these traditional
practices are being replaced with less
diligent practices. For example, in the
Pendjari area of Benin, traditional
enclosures are low with few branches.
These structures and the lack of
enclosures encourage livestock
predation. People do not invest much
into improving enclosures even though
they appear to be economically efficient,
ecologically effective, and culturally
acceptable. Even enclosures that were
built as part of a conservation project
were not used full time due to lack of
labor and, in some cases, the herd being
too large for the enclosures. When lions
in Africa cause or are perceived to cause
damage to livestock, property, or
people, the response is generally to kill
them. Retaliatory killings are reported to
be a significant threat to lion
populations in western and central
Africa.
Some countries in the African range
of this subspecies allow hunting of P. l.
leo. Management programs do not
appear to be sufficient to deter
unsustainable offtakes, which has
resulted in declines in lion populations
in many areas. Specifically, negative
impacts to lions from excessive offtakes
have been documented in Benin and
Cameroon. Additionally, hunting quotas
in Benin and Burkina Faso are too high
for sustainability, although Burkina
Faso has proposed to reduce their quota
in the 2015–2016 season. Actual
harvests in Burkina Faso were also
found to be higher than recommended
levels. Although experts recommend
age-based strategies be incorporated into
lion management plans to reduce
excessive harvests and reduce the rate of
infanticide, Benin and Burkina Faso
have yet to implement an age-based
strategy. As a result, species experts
agree that there is no level of offtake that
would be sustainable for P. l. leo
populations in their current condition.
Trade in lion parts and products is
very common in western and central
Africa. Many African countries,
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including Nigeria, Burkina Faso, and
Cameroon, maintain local markets in
lion products. Trade in lion skins and
partial skins is described as ‘‘frequent’’
ˆ
in street markets in Abidjan, Cote
d’Ivoire, and the scale of domestic trade
in illegal lion products is described as
‘‘massive’’ in Nigeria. In the central
African country of Cameroon, the
estimated value of a single lion carcass
exceeds the trophy fee, and at a lion
conservation conference, the
Government of Cameroon identified
trade in lion skins as a major cause of
the decline in lion populations in
western and central Africa. Trade in
lion skins is most likely one of the
biggest threats to lion survival in
western Africa due to the rarity of lions
in the region, the extent of the trade,
and the high price of lion skins. Lion
populations in western and central
Africa are small and declining and,
therefore, the common use of lions in
these regions for their parts and
products is likely unsustainable.
The viability of a lion population
partly depends on the number of prides
and the ability of males to disperse and
interact with other prides, which affects
exchange of genetic material. Without
genetic exchange, or variation, the more
inbred the population will be,
individual fitness is reduced,
reproductive fitness is reduced, and
species are less able to adapt to
environmental changes and stress or
stochastic events. Loss of fecundity
leads to a decrease in population size,
fewer prides in a population, and
increased inbreeding which contributes
to a decline in the population and may
result in local extirpation. The entire P.
l. leo subspecies comprises small,
isolated populations. Research indicates
that there is a general lack of gene flow
in most lion conservation units.
Furthermore, the suggested minimum
number of lions estimated to constitute
a viable population is at least 250 lions,
but preferably 500 lions, or 50–100
prides. This threshold may be smaller
for P. l. leo as pride sizes are generally
smaller than those for P. l.
melanochaita. However, given the size
of the remaining populations, few could
be considered potentially viable.
Additionally, few protected areas are
large enough to support viable
populations.
Although there are laws meant to
protect wildlife, including lions and
their prey species, the drastic and
continuing decline of the species and its
prey indicate these regulatory
mechanisms are not adequate to
ameliorate threats to P. l. leo.
Furthermore, national and international
conservation strategies rely on protected
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areas to protect natural resources from
negative impacts of human populations.
However, weak management of
protected areas has been documented
across the lion’s range, especially in
western Africa where most protected
areas are experiencing severe
management deficiencies, including the
lack of a budget or a budget insufficient
to carry out management activities.
The lion population in India is one
population of P. l. leo that is increasing
and could potentially be considered a
viable population based on the number
of lions. However, intense management,
including healthcare interventions, may
interfere with natural selection
processes by ensuring the survival of
unfit lions, which facilitates the
propagation of deleterious genes in the
population. This population is also
running out of area to expand. Being a
small, isolated population and less
genetically diverse, it is more vulnerable
to the loss of any individuals due to
environmental and stochastic events,
and more prone to local extinction
events.
As previously stated, threats to the
lion are expected to continue or increase
in conjunction with predicted human
population growth. The human
population, and thus negative impacts
to lions, as well as decreases in lion
populations, associated with human
population growth, is expected to
increase substantially by 2050. If
regional trends continue at their current
rate, western and central Africa will
likely lose a third of its population in 5
years and half the population in 10
years. Lion bone may be increasingly
used as a replacement for tiger bone in
traditional Asian medicine and in Asian
luxury products. Therefore, trade in lion
bone could become lucrative, spur
considerable demand from suppliers of
the black market, result in extensive
poaching of wild lions, and have
significant impacts to lion populations.
Additionally, future development in
India could alter habitat vital for
dispersal. Tolerance to loss of livestock
may also wane as traditional beliefs and
traditional value systems are rapidly
changing under the influence of
globalization. Furthermore, effects of
climate change on lion habitat are
projected to manifest as early as 2040.
Under climate change scenarios, a broad
swath of potential distributional area in
western Africa is projected to become
distinctly less suitable or even
uninhabitable. Increases in rainfall
predicted for India may not have
detrimental impacts on lion habitat;
however, increased risks of flooding
could result in increased mortality, and
post-flooding conditions could be
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conducive to disease outbreaks and are
a serious concern to the persistence of
the lion population as this population is
more vulnerable to stochastic events
and local extinction.
Threats acting on P. l. leo have
contributed to large reductions in the
subspecies’ range and suitable habitat,
abundance, and number and
connectivity of populations. The
subspecies has reached critically low
numbers of individuals and potentially
viable populations. Furthermore, while
one small population may be increasing,
we are not aware of any information
indicating that the overall trend of large
declines in the subspecies range,
abundance, and connectivity, will
reverse course.
Threats continue to act on this
subspecies. Due to small population size
and lack of connectivity between
populations, most populations are not
able to recover from the loss of suitable
habitat or individuals. Furthermore,
because all populations are small and
isolated, the subspecies lacks resiliency
to recover from stochastic or
catastrophic events and is thus highly
vulnerable to extirpation. Threats are
currently affecting the subspecies and
the impacts on the subspecies are
expected to continue or even intensify
over time as the human population
increases and as climate change
progresses, negatively impacting
availability of suitable habitat, lion
distribution, and lion numbers. Based
on the current distribution and size of
P. l. leo populations, the current threats
acting on this subspecies, the impacts of
those threats, and the impacts of future
threats and climate change on lion
distribution, lion numbers, habitat, prey
availability, susceptibility to disease,
loss of lions via human–lion conflict
and trophy hunting, and resiliency to
stochastic and catastrophic events, we
find that the viability of this subspecies
is compromised and will not be
resistant or resilient to ongoing and
future threats. Therefore, we find that P.
l. leo is in danger of extinction
throughout its range and list the
subspecies as endangered.
Finding for Panthera leo melanochaita
The range of P. l. melanochaita
includes the southern and eastern
African regions. Although this
subspecies has experienced range
reduction, a decline in the number of
populations, and a decline in the
number of lions, it remains relatively
widespread. Currently, there are
approximately 17,730 P. l. melanochaita
lions distributed among 68 protected
areas, with larger populations in
Botswana, Kenya, Namibia, South
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80041
Africa, Tanzania, Zambia, and
Zimbabwe. Between 1993 and 2014, the
lion population in eastern Africa
declined by 59 percent. In southern
Africa the lion population increased by
8 percent during the same time period.
Most of the increasing populations
contributing to this trend are small,
fenced reserves. However, one of the
largest populations in southern Africa,
Okavango, and populations in 6
unfenced reserves in Botswana,
Namibia, and Zimbabwe declined.
Although there are larger populations of
P. l. melanochaita that may meet the
suggested MVP, almost all lion
populations in Africa that historically
exceeded 500 individuals, are declining.
Expansion of human settlements,
agriculture, and/or livestock grazing is
occurring in or on the major populations
and is particularly a threat in eastern
Africa and some parts of southern
Africa. In particular, expansion of
agriculture and livestock grazing is
occurring in or around major
populations in Kenya, Tanzania, and
Zambia and both are major threats to
lion survival in these countries.
Expansion of human settlements and
activities into lion habitat renders it
unsuitable for lions, primarily because
human expansion results in reduced
availability of wild prey and lion
mortality due to increases in human–
lion conflict. Both of these factors
influence the distribution and
population viability of lions. However,
in some parts of southern Africa, lions
are repopulating areas where lions were
recently extirpated due to adequate
protection of habitat and prey.
Significant decreases in prey
abundance have occurred in protected
areas throughout Africa, including
Botswana, Kenya, Mozambique, Sudan,
Zambia, and Zimbabwe. Herbivore
populations have decreased by 52
percent in eastern Africa, although they
have increased by 24 percent in
southern Africa. Protected areas in
Ethiopia, Mozambique, Tanzania, and
Zambia are increasingly settled;
decreases in prey abundance in African
protected areas are driven by human
population growth, especially along the
boundaries of protected areas where
human population growth rates are
high, encroachment and habitat loss
occurs, and people are dependent on
bushmeat. Additionally, many
communities lack the rights over land
and in most cases in Botswana,
Tanzania, Zambia, and Zimbabwe, the
government retains a significant portion
of revenue from wildlife; therefore,
those that bear the costs of wildlife do
not receive benefits, and bushmeat
hunting is the only way to benefit from
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wildlife. Furthermore, conversion of
rangeland to agricultural use has
blocked several migratory routes for
Tanzania’s wildebeest and zebra
populations, which likely forces lions to
rely more on livestock.
As a result of prey species becoming
depleted in many areas, lions seek out
livestock for food; attacks on livestock
occur at the highest frequency in areas
where natural prey abundance is lowest.
Additionally, traditional livestock
husbandry practices can reduce
depredation rates, but these traditional
practices are being replaced with less
diligent practices. In Kenya and
Tanzania, social changes are altering
traditional Maasai pastoral livelihoods,
reducing dependency on livestock, and
reducing traditional livestock care and
management, leaving livestock more
vulnerable to predation. Although lions
generally avoid people, they will
occasionally prey on humans, causing
serious injury or death. Attacks on
humans appear to be more frequent in
the range of P. l. melanochaita than P.
l. leo. When lions cause or are perceived
to cause damage to livestock, property,
or people, the response is generally to
kill them. Retaliatory killings are
reported to be a significant threat to lion
populations in Botswana, South Africa,
Kenya, Tanzania, and Zimbabwe.
Some P. l. melanochaita range
countries allow hunting of lions.
Although some management programs
appear to follow recommended
practices for sustainability, most do not
appear to be sufficient to deter
unsustainable offtakes, which has
resulted in declines in lion populations
in many areas. Specifically, negative
impacts to lions from excessive offtakes
have been documented in Tanzania,
Zambia, and Zimbabwe. Additionally,
hunting quotas in most countries are
higher than the recommended offtake
for sustainability. Actual harvests in
Namibia, Zambia, and Zimbabwe were
also found to be higher than
recommended levels. Experts
recommend age-based strategies be
incorporated into lion management
plans to reduce excessive harvests and
reduce the rate of infanticide and
several countries, including
Mozambique (only Niassa National
Reserve), Tanzania, and Zimbabwe have
committed to implementing an agebased strategy. Of these, only Niassa
National Reserve and Zimbabwe have
fully implemented age restrictions and
shown reductions in offtake. Tanzania
has implemented age restrictions and
shown reductions in offtake; however,
transparency (in terms of trophy quality
data) and the scientific objectivity of the
evaluating body has been questioned.
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Lack of implementation of age-based
strategies may undermine the successful
use of trophy hunting as a sustainable
conservation strategy.
The captive-breeding industry has
publicized captive breeding and
reintroduction of captive-born species
into the wild as a potential solution to
the decrease in wild lion populations.
However, lions raised in captivity often
develop a variety of issues that make
them unsuitable for reintroduction, and
reintroduction efforts have not been
shown to address the underlying causes
of population declines throughout the
species’ range. Existing research has
generally found that captive-raised lions
are not as able to adapt successfully to
conditions out of captivity and,
therefore, the success rate is much
reduced compared to the use of wildcaught lions.
While it is argued that South Africa’s
captive-bred lion industry may reduce
pressures of trophy hunting on wild
South African populations, there is no
substantial or peer-reviewed science to
support such a claim. Likewise, there is
no record or evidence to support claims
that the captive-bred lion industry is
supporting reintroduction into the wild
in any significant way. However, future
efforts to control hunting of captive-bred
lions could potentially increase the
demand for wild lion trophies and
result in excessive harvests.
Additionally, trade in bones of captive
lions could stimulate harvest of wild
lions to supply a growing bone trade.
Hunting of captive lions could also
potentially undermine the price of wild
hunts and reduce incentives for
conservation of wild lions in other
African countries.
Lion parts and products are used in
many African countries as medicine,
nutrition, talismans, and decorations,
and in traditional ceremonies and
rituals. Kenya and Somalia maintain
local markets in lion products. Lion
skins and canines are also described as
‘‘easily found’’ in the markets of Dakar,
Senegal. In southern and eastern Africa,
trade in lion parts, particularly lion
bone, to Asia is generally considered a
severe potential threat to the species.
According to CITES, there is ‘‘clear
scope for the international trade in lion
body parts for [traditional Chinese
medicine and traditional African
medicine] to grow uncontrollably, as it
has done for other big cats.’’ According
to Kenya, the declared exports of bones,
skulls, and skeletons derived from wild
lions also show an increasing trend
through the period 2003–2012, with
total declared specimens in 2012 more
than ten times those in 2003. Evidence
suggests incentive to poach wild lions
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for the bone trade may currently exist as
prices paid to South African game
farmers and landowners for lion bones
exceeded the per capita GDP (gross
domestic product) in many lion range
states. Thus, the current price paid for
lion bone appears to provide incentive
in some countries to poach wild lions.
The viability of a lion population
partly depends on the number of prides
and ability of males to disperse and
interact with other prides, which affects
the exchange of genetic material.
Without genetic exchange, or variation,
the more inbred the population will be,
individual fitness is reduced,
reproductive fitness is reduced, and
species are less able to adapt to
environmental changes and stress or
stochastic events. Loss of fecundity
leads to a decrease in population size,
fewer prides in a population, and
increased inbreeding, which contributes
to a decline in the population and local
extirpation. Research indicates that
there is a general lack of gene flow in
most lion conservation units.
Furthermore, the suggested minimum
number of lions estimated to constitute
a viable population is at least 250 lions,
but preferably 500 lions, or 50–100
prides. Almost all lion populations in
Africa that historically exceeded 500
individuals are declining, and few
protected areas are large enough to
support viable populations.
While the lion bone trade appears to
currently be based primarily in South
Africa’s captive-bred lion hunting
industry, the trade appears to be having
little or no impact on wild lion
populations in South Africa at this
time—lion populations in South Africa
are stable or increasing and there is little
poaching of wild lions in the country
(Funston and Levendal 2014, pp. 1, 26;
Williams et al. 2015, pp. 79–80).
However, the impact of the lion bone
trade on lion populations outside South
Africa is unknown and most wild lions
occur outside South Africa (see
Distribution and Abundance). While
wild tiger populations are declining, the
demand for tiger parts in Asia is
increasing. With tigers difficult to
obtain, lion bone may be increasingly
used as a replacement for tiger bone.
Considering the sharp and continuing
increases in demand from Asia for lion
bone and the effect of the tiger bone
trade on tiger populations, there is
potential for demand to surpass the
availability of legally obtained lion
bone. Therefore, trade in lion bone
could become lucrative, spur
considerable demand from suppliers of
the black market, result in extensive
poaching and unsustainable harvest of
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wild lions to meet demand, and have
significant impacts to lion populations.
Although there are laws in place in
lion range countries that are meant to
protect wildlife, including lions and
their prey species, the drastic and
continuing decline of the species and its
prey in some parts of its range indicate
these regulatory mechanisms are not
adequate to ameliorate threats to the P.
l. melanochaita throughout its range.
Furthermore, national and international
conservation strategies rely on protected
areas to protect natural resources from
negative impacts of human populations.
However, weak management of
protected areas has been documented
across the lion’s range.
As indicated above, P. l. melanochaita
remains relatively widespread and some
remaining populations are large enough
to be considered viable. Therefore, due
to the size of some populations, the
number of remaining populations, and
the stability or increasing status of some
populations, we find that P. l.
melanochaita is not currently in danger
of extinction. However, the overall
population of the subspecies continues
to decline and threats to the lion are
expected to continue or increase in the
future in conjunction with predicted
human population growth. If regional
trends in lion populations continue at
the current rate, eastern Africa will lose
a third of its lion population in 20 years
and half the population in 30 years.
Effects of climate change on lion habitat
are projected to manifest as early as
2040. Although climate change effects
on potential lion distribution are
projected to be more neutral in eastern
Africa than across the entire range,
southern Africa, where the broadest
areas of suitable conditions occur, is
projected to become less suitable
because of climate change. Specifically,
park areas, including the ‘‘Etosha Pan,
Lake Opnono, Cuvelai Drainage,
Kalahari Gemsbok, and Kgalagadi
Transfrontier Park areas’’ are projected
to decline substantially in suitability for
lions. In addition, reforms to trophy
hunting have been made to ensure
sustainability of trophy hunting, but
these reforms have been implemented in
only a few places. Furthermore, demand
for lion bone is expected to increase in
the future and high prices for lion bone
provide incentive to poach wild lions.
As a result of the likely impacts of these
threats, it is reasonable to conclude that
the population of P. l. melanochaita is
likely to be drastically reduced and
fragmented in the foreseeable future,
limiting the ability of the subspecies to
recover from stochastic and catastrophic
events. Therefore, we find that this
subspecies is likely to become an
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endangered species within the
foreseeable future and we are listing P.
l. melanochaita as a threatened species.
Significant Portion of Its Range
Under the Act and our implementing
regulations, a species may warrant
listing if it is endangered or threatened
throughout all or a significant portion of
its range. The term ‘‘species’’ includes
‘‘any subspecies of fish or wildlife or
plants, and any distinct population
segment [DPS] of any species of
vertebrate fish or wildlife which
interbreeds when mature.’’ We
published a final policy interpreting the
phrase ‘‘Significant Portion of its
Range’’ (SPR) (79 FR 37578, July 1,
2014). The final policy states that (1) if
a species is found to be endangered or
threatened throughout a significant
portion of its range, the entire species is
listed as endangered or threatened,
respectively, and the Act’s protections
apply to all individuals of the species
wherever found; (2) a portion of the
range of a species is ‘‘significant’’ if the
species is not currently endangered or
threatened throughout all of its range,
but the portion’s contribution to the
viability of the species is so important
that, without the members in that
portion, the species would be in danger
of extinction, or likely to become so in
the foreseeable future, throughout all of
its range; (3) the range of a species is
considered to be the general
geographical area within which that
species can be found at the time the
Service or the National Marine Fisheries
Service makes any particular status
determination; and (4) if a vertebrate
species is endangered or threatened
throughout an SPR, and the population
in that significant portion is a valid
DPS, we will list the DPS rather than the
entire taxonomic species or subspecies.
We found the lion subspecies P. l. leo
to be in danger of extinction throughout
its range, and the subspecies P. l.
melanochaita likely to become
endangered within the foreseeable
future throughout its range. Therefore,
no portions of the species’ range are
‘‘significant’’ as defined in our SPR
policy, and no additional SPR analysis
is required.
4(d) Rule for Panthera leo
melanochaita
The purposes of the ESA are to
provide a means whereby the
ecosystems upon which endangered
species and threatened species depend
may be conserved, to provide a program
for the conservation of such endangered
species and threatened species, and to
take such steps as may be appropriate to
achieve the purposes of the treaties and
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80043
conventions set forth in the ESA. When
a species is listed as endangered, certain
actions are prohibited under section 9 of
the ESA and are implemented through
our regulations in 50 CFR 17.21. These
include, among others, prohibitions on
take within the United States, within
the territorial seas of the United States,
or upon the high seas; import; export;
and shipment in interstate or foreign
commerce in the course of a commercial
activity. Exceptions to the prohibitions
for endangered species may be granted
in accordance with section 10 of the
ESA and our regulations at 50 CFR
17.22.
The ESA does not specify particular
prohibitions and exceptions to those
prohibitions for threatened species.
Instead, under section 4(d) of the ESA,
the Secretary, as well as the Secretary of
Commerce depending on the species,
was given the discretion to issue such
regulations as deemed necessary and
advisable to provide for the
conservation of such species. The
Secretary also has the discretion to
prohibit by regulation with respect to
any threatened species any act
prohibited under section 9(a)(1) of the
ESA. Exercising this discretion, the
Service has developed general
prohibitions in the ESA regulations (50
CFR 17.31) and exceptions to those
prohibitions (50 CFR 17.32) that apply
to most threatened species. Under 50
CFR 17.32, permits may be issued to
allow persons to engage in otherwise
prohibited acts for certain purposes.
Under section 4(d) of the ESA, the
Secretary, who has delegated this
authority to the Service, may also
develop specific prohibitions and
exceptions tailored to the particular
conservation needs of a threatened
species. In such cases, the Service issues
a 4(d) rule that may include some or all
of the prohibitions and authorizations
set out in 50 CFR 17.31 and 17.32, but
which also may be more or less
restrictive than the general provisions at
50 CFR 17.31 and 17.32. For P. l.
melanochaita, the Service has
determined that a 4(d) rule is necessary
and advisable.
We are adding a 4(d) (special) rule for
P. l. melanochaita at 50 CFR 17.40(r).
This 4(d) rule maintains all of the
prohibitions and exceptions codified in
50 CFR 17.31 and 17.32 with regard to
this subspecies and supersedes the
import exemption found in 50 CFR 17.8
for threatened wildlife listed in
Appendix II of CITES, such that a
threatened species import permit under
50 CFR 17.32 is now required for the
importation of all P. l. melanochaita
specimens. Therefore, through the
promulgation of this 4(d) rule, the
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presumption of legality provided under
section 9(c)(2) of the Act for the
otherwise lawful importation of wildlife
listed in Appendix II of CITES that is
not an endangered species listed
pursuant to section 4 of the Act does not
apply to this subspecies. Thus, under
this 4(d) rule, all otherwise prohibited
activities, including all imports of P. l.
melanochaita specimens, require prior
authorization or permits under the Act.
Under our regulations at 50 CFR 17.32,
permits or authorization to carry out an
otherwise prohibited activity could be
issued for scientific purposes, the
enhancement of propagation or survival
of the species, economic hardship,
zoological exhibitions, educational
purposes, or special purposes consistent
with the purposes of the Act.
Applications for these activities are
available from either https://www.fws.
gov/forms/3-200-20.pdf or https://www.
fws.gov/forms/3-200-37.pdf.
The intent of this 4(d) rule is to
provide for the conservation of P. l.
melanochaita consistent with the
purposes of the Act. Under this 4(d)
rule, the prohibitions, 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 or foreign
commerce, by any means whatsoever, in
the course of commercial activity; or sell
or offer for sale in interstate or foreign
commerce any P. l. melanochaita
specimens. It would also be illegal to
possess, sell, deliver, carry, transport, or
ship any such wildlife that has been
taken in violation of the Act. We find
that these protections, including the
requirement for a permit for the import,
export, interstate and foreign commerce
and take for all P. l. melanochaita
specimens, will support and encourage
conservation actions for P. l.
melanochaita and require that permitted
activities involving this subspecies are
carried out in a manner that is
consistent with the purposes of the Act
and our implementing regulations.
In connection with this 4(d) rule, the
Service notes that P. l. melanochaita is
listed in Appendix II of CITES and,
without this 4(d) rule, could be
imported into the United States
pursuant to section 9(c)(2) of the Act
upon the presentation of a proper CITES
export permit from the country of
export, if such importation is not made
in the course of a commercial activity.
Section 9(c)(2) of the Act provides that
the otherwise lawful importation of
wildlife that is not an endangered
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species listed pursuant to section 4 of
the Act, but that is listed in Appendix
II of CITES, shall be presumed to be in
compliance with provisions of the Act
and implementing regulations if the
importation is not made in the course of
a commercial activity. While there has
been question as to whether this
provision of the Act might automatically
require allowing the importation of a
species that is both listed as threatened
and in Appendix II, and preclude the
issuance of more restrictive 4(d) rules
covering importation, the Service has
concluded that such 4(d) rules may be
issued to provide for the conservation of
the involved species. Section 9(c)(2)
does not expressly refer to threatened
species or prevent the issuance of
appropriate 4(d) rules and could not
logically have been intended to allow
the addition of a species to an appendix
of an international convention to
override the needs of U.S. law, where
there is reliable evidence to affect the
presumption of validity. Finally, the
term ‘‘presumed’’ implies that the
established presumption is rebuttable
under certain circumstances, including
through the promulgation of a protective
regulation pursuant to section 4(d) of
the Act.
In the case of the P. l. melanochaita,
there are substantive grounds on which
to challenge the presumption. For the
import of sport-hunted trophies, while
there is evidence that some range
countries are implementing lion
management programs, the best
available information indicates that not
all lion hunting programs are well
managed or provide enhancement to
survival of the subspecies (see Trophy
Hunting section), Namely, mismanaged
trophy hunting is reported to contribute
to documented declines in lion
populations of Africa (Rosenblatt et al.
2014, entire; Sogbohossou et al. 2014,
entire; Becker et al. 2013, entire;
Lindsey et al. 2013a, entire; Packer et al.
2013, p. 636; Croes et al. 2011, entire;
Packer et al. 2011, entire; Loveridge et
al. 2007, entire). Depending on how
trophy hunting is regulated and
managed, trophy hunting can be a tool
for conservation, but may also have
negative impacts on lions (Bauer et al.
2015a, unpaginated; Lindsey et al.
2013a, p. 1; Whitman et al. 2004, pp.
176–177; Loveridge et al. 2007, p. 548).
We want to encourage and support
efforts by range countries to develop
programs that are based on sound
scientific information. As noted, the
4(d) rule for P. l. melanochaita would
provide for the importation into the
United States of trophies taken legally
in range countries upon the issuance of
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a threatened species import permit.
While the Service cannot control
hunting of foreign species such as P. l.
melanochaita, we can regulate their
importation and thereby require that
U.S. imports of sport-hunted P. l.
melanochaita trophy specimens are
obtained in a manner that is consistent
with the purposes of the Act and the
conservation of the subspecies in the
wild, by allowing importation from
range countries that have scientifically
sound management programs that
address the threats that are facing lions
and are enhancing the survival of the
species in the wild within that country
(see further discussion below on
enhancement of propagation or survival
with regard to authorizing the import of
sport-hunted trophies of P. l.
melanochaita). Further, for the import
of parts or products, there is evidence
that trade in lion parts, particularly
bones, is fast becoming a substitute for
tiger bones in traditional Asian
medicine and Asian luxury products
(see Traditional Use of Lion Parts and
Products section). While the primary
source of the current bone trade appears
to be from captive-bred lions from South
Africa, considering the sharp and
continuing increases in demand from
Asia for lion bone, there is potential for
demand to surpass the availability of
legally obtained lion bone and,
consequently, result in poaching and
unsustainable harvest of wild lions to
meet demand. Based on the effect of the
tiger bone trade on tiger populations, if
current conditions continue unchanged,
there is considerable potential for
extensive poaching of wild lions to
occur in order to meet demand. Given
the current threats to the subspecies,
unsustainable harvest to supply a trade
in parts could contribute to the further
decline of the subspecies.
Finally, due to our concerns about the
increasing trade in lion bones and
evidence that live lions are being
exported to Asia, presumably for the
bone trade, we find that unregulated
trade and the taking of live lions could
further contribute to the lion bone trade.
Further, the noncommercial imports of
live lions could be a cover for the
establishment of lion bone trade within
the United States. As with captive tigers
and the use of live animals for the bone
trade, the Service finds that the
unregulated movement of lions within
the United States, as well as the import
or export of these animals is reasonably
likely to be used as a loophole for the
bone trade and serve as cover for the
establishment of lion bone trade within
the United States. By requiring permits
for all otherwise prohibited activities
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under the Act, such as import, export,
interstate and foreign commerce and
take, including noncommercial imports
of live lions, we can ensure that live
lions are not used to supplement the
trade in lion bones.
Therefore, we find that regulation of
the importation of all P. l. melanochaita
parts and products, including live
animals and sport-hunted trophies, will
ensure that imported specimens are
obtained in a manner that is consistent
with the purposes of the Act and the
conservation of the subspecies in the
wild.
Our threatened species permitting
regulations at 50 CFR 17.32 provide
issuance criteria for threatened species
permits (50 CFR 17.32(a)(2)), but do not
specify what would constitute the
enhancement of propagation or survival
with regard to authorizing the import of
parts or products of P. l. melanochaita,
including sport-hunted trophies.
Therefore, when making a
determination of whether an otherwise
prohibited activity enhances the
propagation or survival of P. l.
melanochaita, the Service will examine
the overall conservation and
management of the subspecies in the
country where the specimen originated
and whether that management of the
subspecies addresses the threats to the
subspecies (i.e., that it is based on sound
scientific principles and that the
management program is actively
addressing the current and longer term
threats to the subspecies). In that
review, we will evaluate whether the
import contributes to the overall
conservation of the species by
considering whether the biological,
social, and economic aspects of a
program from which the specimen was
obtained provide a net benefit to the
subspecies and its ecosystem.
The Service will evaluate any
application received that involves P. l.
melanochaita in the context of
enhancement of propagation or survival
permitting in accordance with our
threatened species permitting
regulations at 50 CFR 17.32 and
issuance criteria for threatened species
permits (50 CFR 17.32(a)(2)). These
include, in addition to the general
permitting criteria in 50 CFR 13.21(b):
(i) Whether the purpose for which the
permit is required is adequate to justify
removing from the wild or otherwise
changing the status of the wildlife sought to
be covered by the permit;
(ii) The probable direct and indirect effect
that issuing the permit would have on the
wild populations of the wildlife sought to be
covered by the permit;
(iii) Whether the permit, if issued, would
in any way, directly or indirectly, conflict
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with any known program intended to
enhance the survival probabilities of the
population from which the wildlife sought to
be covered by the permit was or would be
removed;
(iv) Whether the purpose for which the
permit is required would be likely to reduce
the threat of extinction facing the species of
wildlife sought to be covered by the permit;
(v) The opinions or views of scientists or
other persons or organizations having
expertise concerning the wildlife or other
matters germane to the application; and
(vi) Whether the expertise, facilities, or
other resources available to the applicant
appear adequate to successfully accomplish
the objectives stated in the application.
In addition to these factors,
particularly in relation to sport hunting,
we find the IUCN Species Survival
Commission (SSC) Guiding Principles
on Trophy Hunting as a Tool for
Creating Conservation Incentives, Ver.
1.0 (IUCN SSC 2012), to provide useful
principles, which, considered in
conjunction with our threatened species
issuance criteria, will aid the Service
when making an enhancement finding
for importation of sport-hunted trophies
of P. l. melanochaita. This document
sets out guidance from experts in the
field on the use of trophy hunting as a
tool for ‘‘creating incentives for the
conservation of species and their
habitats and for the equitable sharing of
the benefits of use of natural resources’’
(IUCN SSC 2012, p. 2) and recognizes
that recreational hunting, particularly
trophy hunting, can contribute to
biodiversity conservation and more
specifically, the conservation of the
hunted species.
The SSC document lays out five
guiding principles that, considered in
conjunction with our threatened species
issuance criteria, will aid the Service
when making an enhancement finding
for importation of sport-hunted trophies
of P. l. melanochaita:
(a) Biological sustainability: The hunting
program cannot contribute to the long-term
decline of the hunted species. It should not
alter natural selection and ecological
function of the hunted species or any other
species that share the habitat. The program
should not inadvertently facilitate poaching
or illegal trade in wildlife by acting as a cover
for such illegal activities. The hunting
program should also not manipulate the
ecosystem or its component elements in a
way that alters the native biodiversity.
(b) Net Conservation Benefit: The
biologically sustainable hunting program
should be based on laws, regulations, and
scientifically based quotas, established with
local input, that are transparent and
periodically reviewed. The program should
produce income, employment, and other
benefits to create incentives for reducing the
pressure on the target species. The program
should create benefits for local residents to
co-exist with the target species and other
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species. It is also imperative that the program
is part of a legally recognized governance
system that supports conservation.
(c) Socio-Economic-Cultural Benefit: A
well-managed hunting program can serve as
a conservation tool when it respects the local
cultural values and practices. It should be
accepted by most members of the
community, involving and benefiting local
residents in an equitable manner. The
program should also adopt business practices
that promote long-term economic
sustainability.
(d) Adaptive Management: Planning,
Monitoring, and Reporting: Hunting can
enhance the species when it is based on
appropriate resource assessments and
monitoring (e.g., population counts, trend
data), upon which specific science-based
quotas and hunting programs can be
established. Resource assessments should be
objective, well documented, and use the best
science available. Adaptive management of
quotas and programs based on the results of
resource assessments and monitoring is
essential. The program should monitor
hunting activities to ensure that quotas and
sex/age restrictions of harvested animals are
met. The program should also generate
reliable documentation of its biological
sustainability and conservation benefits.
(e) Accountable and Effective Governance:
A biologically sustainable trophy-hunting
program should be subject to a governance
structure that clearly allocates management
responsibilities. The program should account
for revenues in a transparent manner and
distribute net revenues to conservation and
community beneficiaries according to
properly agreed decisions. All necessary
steps to eliminate corruption should be taken
and to ensure compliance with all relevant
national and international requirements and
regulations by relevant bodies such as
administrators, regulators and hunters.
The Service’s approach to
enhancement findings for the
importation of sport-hunted trophies of
P. l. melanochaita is consistent with the
purpose and intent of the Endangered
Species Act. Before we will authorize
the importation of a sport-hunted
trophy, we must determine that the
trophy hunting program is managed to
ensure the long-term survival of the
species. In many parts of the world,
wildlife exists outside of protected areas
and must share the same habitat and
compete with humans living in these
areas for space and resources. If
communities that share these resources
with wildlife do not perceive any
benefits from the presence of wildlife,
they may be less willing to tolerate the
wildlife. However, under certain
circumstances, trophy hunting can
address this problem by making wildlife
more valuable to the local communities
and encourage community support for
managing and conserving the hunted
species, as well as other species.
When evaluating whether the
importation of a trophy of P. l.
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melanochaita would be authorized
pursuant to 50 CFR 17.32, in accordance
with our threatened species issuance
criteria, we will examine how a
country’s management program for lions
addresses the three main threats that
have led to the decline of the
subspecies: Habitat loss, loss of prey
base, and human-lion conflict. When
examining a management program and
whether trophies taken as part of that
program meet the issuance criteria, we
would study a number of factors. Some
of the factors we would consider
include whether the program is based
on sound scientific information and
identifies mechanisms that would arrest
the loss of habitat or increase available
habitat (i.e., by establishing protected
areas and ensuring adequate protection
from human encroachment). We would
consider whether the management
program actively address the loss of the
lion’s prey base by addressing poaching
or unsustainable offtake within the
country. A component of a management
plan from which trophy imports would
meet the issuance criteria would be
whether there are government
incentives in place that encourage
habitat protection by private
landowners and communities and
incentives to local communities to
reduce the incursion of livestock into
protected areas or to actively manage
livestock to reduce conflicts with lions.
We would examine if the hunting
component of the management program
supports all of these efforts by looking
at whether hunting concessions/tracts
are managed to ensure the long-term
survival of the lion, its prey base, and
habitat. As stated previously, hunting
can generate significant economic
benefits if properly conducted. In
looking at whether we would be able to
authorize the import of a trophy under
the issuance criteria of 50 CFR 17.32, we
would examine if the trophy hunting
provides financial assistance to the
wildlife department to carry out
elements of the management program
and if there is a compensation scheme
or other incentives to benefit local
communities that may be impacted by
lion predation. We would also consider
how a U.S. hunter’s participation in the
hunting program contributes to the
overall management of lions within a
country.
Management programs for P. l.
melanochaita would be expected to
address, but are not limited to,
evaluating population levels and trends;
the biological needs of the species;
quotas; management practices; legal
protection; local community
involvement; and use of hunting fees for
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conservation. In evaluating these
factors, we will work closely with the
range countries and interested parties to
obtain the information. By allowing
entry into the United States of P. l.
melanochaita trophies from range
countries that have science-based
management programs, we anticipate
that other range countries would be
encouraged to adopt and financially
support the sustainable management of
lions that benefits both the species and
local communities. In addition to
addressing the biological needs of the
subspecies, a scientifically based
management program would provide
economic incentives for local
communities to protect and expand P. l.
melanochaita habitat.
As stated, under this 4(d) rule any
person wishing to conduct an otherwise
prohibited activity, including all
imports of P. l. melanochaita
specimens, must first obtain a permit
under 50 CFR 17.32. As with all permit
applications submitted under 50 CFR
17.32, the individual requesting
authorization to import a sport-hunted
trophy of P. l. melanochaita bears the
burden of providing information in their
application showing that the activity
meets the requirements for issuance
criteria under 50 CFR 17.32. In some
cases for imports, such as sport-hunted
trophies, it is not always possible for the
applicant to provide all of the necessary
information needed by the Service to
make a positive determination under the
Act to authorize the activity. For the
import of sport-hunted trophies of P. l.
melanochaita, the Service will typically
consult with the range country to the
extent practicable and other interested
parties to obtain necessary information.
The Service has the discretion to make
the required findings on sport-hunted
trophy imports of P. l. melanochaita on
a country-wide basis, although
individual import permits will be
evaluated and issued or denied for each
applicant. While the Service may make
enhancement findings for sport-hunted
trophy imports of P. l. melanochaita on
a country-wide basis, the Service
encourages the submission of
information from individual applicants.
We would rely on the information
available to the Service and may rely on
information from sources other than the
applicant when making a permitting
decision.
Effects of This Rule
This action revises the taxonomic
classification of the Asiatic lion
(currently classified as P. l. persica and
listed as an endangered species under
the Act) to P. l. leo based on a
taxonomic change. This rule revises 50
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CFR 17.11(h) to add P. l. leo subspecies
and the P. l. melanochaita subspecies to
the List of Endangered and Threatened
Wildlife as an endangered species and
a threatened species, respectively. This
rule establishes a 4(d) rule for P. l.
melanochaita, which implements all of
the prohibitions and exceptions under
50 CFR 17.31 and 17.32 and requires a
threatened species import permit under
50 CFR 17.32 for the importation of all
P. l. melanochaita specimens. Under the
4(d) rule, the import exemption found
in 50 CFR 17.8 for threatened wildlife
listed in Appendix II of CITES does not
apply to this subspecies. Therefore,
through the promulgation of this 4(d)
rule, the presumption of legality
provided under section 9(c)(2) of the
Act for the otherwise lawful importation
of wildlife listed in Appendix II of
CITES that is not an endangered species
listed pursuant to section 4 of the Act
does not apply to this subspecies (See:
4(d) Rule for Panthera leo
melanochaita).
Available Conservation Measures
Conservation measures provided to
species listed as endangered or
threatened under the Act include
recognition of conservation status,
requirements for Federal protection, and
prohibitions against certain practices.
Recognition through listing encourages
and results in public awareness and
conservation actions by Federal and
State governments in the United States,
foreign governments, private agencies
and groups, and individuals.
Section 7(a) of the Act, as amended,
and as implemented by regulations at 50
CFR part 402, requires Federal agencies
to evaluate their actions that are to be
conducted within the United States or
upon the high seas, with respect to any
species that is proposed to be listed or
is listed as endangered or threatened.
Because P. l. leo and P. l. melanochaita
are not native to the United States, no
critical habitat is being proposed for
designation with this rule. Regulations
implementing the interagency
cooperation provision of the Act are
codified at 50 CFR part 402. Section
7(a)(2) of the Act requires Federal
agencies to ensure that activities they
authorize, fund, or carry out are not
likely to jeopardize the continued
existence of a listed species or to
destroy or adversely modify its critical
habitat. If a proposed Federal action
may adversely affect a listed species, the
responsible Federal agency must enter
into formal consultation with the
Service. Currently, with respect to the
lion, no Federal activities are known
that would require consultation.
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Section 8(a) of the Act authorizes the
provision of limited financial assistance
for the development and management of
programs that the Secretary of the
Interior determines to be necessary or
useful for the conservation of
endangered or threatened species in
foreign countries. Sections 8(b) and 8(c)
of the Act authorize the Secretary to
encourage conservation programs for
foreign listed species, and to provide
assistance for such programs, in the
form of personnel and the training of
personnel.
Section 9 of the Act and our
implementing regulations at 50 CFR
17.21 and 50 CFR 17.31 set forth a series
of general prohibitions that apply to all
endangered and threatened wildlife,
respectively, except where a 4(d) rule
applies to threatened wildlife, in which
case the 4(d) rule contains all the
applicable prohibitions and exceptions.
Under the 4(d) rule for P. l.
melanochaita, all of the prohibitions
under 50 CFR 17.31 apply to P. l.
melanochaita specimens. 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 or foreign commerce, by any
means whatsoever, in the course of
commercial activity; or sell or offer for
sale in interstate or foreign commerce
any lion specimens. It also is illegal to
possess, sell, deliver, carry, transport, or
ship any such wildlife that has been
taken in violation of the Act. 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, such as P. l. leo, are
codified at 50 CFR 17.22. Regulations
governing permits for threatened
species, such as P. l. melanochaita, are
codified at 50 CFR 17.32. Certain
exceptions apply to agents of the
Service and State conservation agencies.
Summary of Comments and
Recommendations
We based this action on a review of
the best scientific and commercial
information available, including all
information received during the public
comment period. In the October 2014
proposed rule, we requested that all
interested parties submit information
that might contribute to development of
a final rule. We also contacted
appropriate scientific experts and
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organizations and invited them to
comment on the proposed listing. We
received tens of thousands of comments.
We reviewed all comments we
received from the public for substantive
issues and new information regarding
the proposed listing of this species, and
we address those comments below.
Overall, most commenters supported
the proposed listing, but did not provide
additional scientific or commercial data
for consideration. We have not included
responses to comments that supported
the listing decision but did not provide
specific information for consideration.
Most of the commenters that did not
support the proposed listing were
affiliated with the trophy hunting
industry and opposed the rule due to
potential impacts on importing trophies.
These comments are addressed below.
Peer Review
In accordance with our policy
published on July 1, 1994 (59 FR
34270), we solicited expert opinions
from ten individuals with scientific
expertise that included familiarity with
the species, the geographic region in
which wild members of the species
occur, and conservation biology
principles. We received responses from
five of the peer reviewers from whom
we requested comments. The peer
reviewers generally supported our rule;
however, they provided updated
information on taxonomy, current
population estimates, and population
trends. They also found our analysis of
some of the threats to be inaccurate.
Specifically, they provided comments
and additional information on loss of
prey base, trophy hunting, infanticide,
corruption, and trade in lion bones. In
some cases, a correction is indicated in
the citations by ‘‘personal
communication’’ (pers. comm.), which
could indicate either an email or
telephone conversation; in other cases,
the research citation is provided.
Peer Reviewer Comments
(1) Comment: Several peer reviewers
commented on our section of the
proposed rule regarding the taxonomic
classification of lion. These peer
reviewers confirmed that the IUCN Cat
Specialist Group recommended a twosubspecies classification: Panthera leo
leo for lions of India and western and
central Africa, and P. l. melanochaita
for lions in eastern and southern Africa.
Our Response: We have reviewed the
2015 IUCN Red List Assessment for the
lion, which proposes the new
classification as recommended by the
IUCN Cat Specialist Group, and the
genetic studies supporting this
classification. We found this
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information to be the best available
scientific and commercial information;
therefore, we have accepted this
taxonomic change and incorporated this
decision into this document under the
Taxonomy section of this document. As
a result, our assessment is of the status
of the lion species (both P. l. leo and P.
l. melanochaita), including the lion
population in India.
(2) Comment: Several peer reviewers
provided updated information on
population estimates and trends. Based
on a time trend analysis of scientific
census data for 46 well-monitored
populations, an overall 43 percent
decline in lion populations across
Africa was inferred. Furthermore,
regional trends emerged, showing that,
while populations in southern African
increased by 22 percent, populations in
eastern and western and central Africa
combined decreased by 57 percent and
66 percent, respectively. The peer
reviewers also indicated that the actual
number of lions in Africa is much lower
than previous estimates. Application of
regional trends to lion estimates made
in 2002 resulted in an estimate of fewer
than 20,000 lions, a significant
difference from the previous estimate of
32,000.
Our Response: We considered this
information and note that this
information was also included in the
IUCN Red List Assessment for the lion.
Information on population estimates
and trends was incorporated into the
Species Information section of this
document. Assessment of this
information led us, in part, to conclude
that the status of the lion is more serious
than previously indicated, especially in
the western and central regions of Africa
(P. l. leo).
(3) Comment: One peer reviewer
commented that the section on prey loss
does not address the issue of prey loss
in protected areas where most lions
occur.
Our Response: The peer reviewer
provided a list of literature on the
patterns and trends of prey loss in
protected areas that were recently or are
currently occupied by lions. We have
reviewed these articles and have
incorporated the findings in this
document (under Loss of Prey Base).
This information did not change our
determination, but rather further
supported our determination that prey
loss has occurred throughout the
African range countries and is one of the
major threats to lion.
(4) Comment: One peer reviewer
stated that although most lions in Africa
persist inside protected areas, the
majority of the protected areas should
be uninhabited by humans; therefore,
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only prides located at the edge of these
protected areas should come into
conflict with humans. Because the
proportion of lions subjected to conflict
with humans is small, it is wrong to
state that the greatest threat to lions in
Africa is human-lion conflict.
Our Response: We have considered
the peer reviewer’s comments and have
altered our discussion of threats to lions
from human-lion conflict by clarifying
that it is the lions that persist at the
boundary, or just outside, of protected
areas that are most subjected to this
threat. This information did not change
our determination; human-lion conflict
remains a threat to lion persistence.
(5) Comment: Three peer reviewers
indicated that our assessment of
corruption within lion range countries
was not realistic; that corruption in
most of Africa is extensive and
worsening. They pointed out oversights
and errors pertaining to this subject in
our proposed rule and provided
additional citations on the topic.
Our Response: We reexamined the
information available to us during the
drafting of the proposed rule and
reviewed information in additional
citations, and agree that our section on
corruption did not accurately reflect
corruption in lion range countries.
Based on peer reviewer comments and
available information, we have revised
this section accordingly.
(6) Comment: Two peer reviewers and
three NGO stakeholders indicated
concern that trade in lion parts,
particularly lion bone, from Africa to
Asia may pose a potential threat to the
species.
Our Response: We agree and have
revised this rule to include information
on the lion bone trade.
(7) Comment: A peer reviewer
identified inaccuracies in our review of
information on traditional use of lion
parts and products in west and central
Africa, and also indicated that trade in
lion parts and products is very common
in these regions.
Our Response: We appreciate the peer
reviewer’s input. We reviewed the
available information and revised the
section of this rule pertaining to
traditional use of lion parts and
products in west and central Africa
accordingly.
(8) Comment: One peer reviewer
questioned whether ‘‘any lion
specimen’’ referred to in the 4(d) rule
would include Asiatic lion and/or
scientific samples.
Our Response: The 4(d) rule applies
only to the threatened subspecies, P. l.
melanochaita. Scientific samples of P. l.
melanochaita will require permits
pursuant to 50 CFR 17.32. The former
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Asiatic lion (Panthera leo persica) is
now classified as Panthera leo leo
which is now listed as endangered
under the Act. Scientific samples of P.
l. leo will require permits pursuant to 50
CFR 17.22.
(9) Comment: Several peer reviewers
commented that the information
provided in the proposed rule regarding
quotas and offtake trends was incorrect;
specifically, several peer reviewers
noted several publications pertinent to
quotas that should be re-examined and
more thoroughly discussed.
Our Response: We reexamined the
information available to us during the
drafting of the proposed rule and
reviewed the citations provided during
the public comment period. We
consider these publications to be the
best available science regarding quota
setting in the interim while other
strategies are more fully developed (i.e.
age-based strategies, adaptive
management systems, etc.). We have
revised this section to include more
discussion accordingly.
(10) Comment: Several peer reviewers
provided additional information on
country-specific management trends;
specifically, information was provided
on the progress of the commitment to
and implementation of the age-based
strategy.
Our Response: We appreciate the peer
reviewers input and have incorporated
this information into the section of the
rule accordingly.
(11) Comment: One peer reviewer
commented that, although species
experts do generally support trophy
hunting as a management tool,
additional discussion was needed
regarding the recommended reforms
species experts submitted during the
drafting of the proposed rule.
Our Response: We reexamined the
recommendations as provided by
species experts and agree that additional
discussion was needed. We have
incorporated the additional discussion
in the section as appropriate.
(12) Comment: Four of the peer
reviewers commented that although
species experts support trophy hunting
as a management tool, it needs to be
conducted in a sustainable manner that
would require reforms to the current
practices. Peer reviewers stated that the
quotas set throughout most range states
are above sustainable levels (Packer et
al. 2011) and that quotas should be
science-based and sustainable.
Our Response: We agree that current
quotas are currently set higher than
those recommended by Packer et al.
(2011). Species experts recommend the
implementation of an adaptive
management quota system that would
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ensure quotas would be based on the
best available science. We have revised
this section accordingly.
(13) Comment: Several peer reviewers
commented that the information
provided in the proposed rule regarding
quotas and offtake trends was incorrect;
several of the peer reviewers provided
additional information (and citations)
on country-specific quota trends,
current quotas, and offtake trends. One
peer reviewer noted that clarification
was needed regarding the difference
between quotas and offtake rates.
Additionally, two peer reviewers
provided additional information on
moratoriums in two of the range
countries.
Our Response: We reexamined the
information available to us during the
drafting of the proposed rule and
reviewed information in additional
citations provided during the public
comment period. We agree that
clarification was needed, and, based
upon peer review comments and
additional information, we have revised
this section accordingly.
(14) Comment: One peer reviewer
commented that lion trophy hunting
could remain as an additive threat if
hunting reforms are not implemented
and suggested that ‘‘USFWS and
equivalent bodies in the EU and
elsewhere could mediate such reforms
by imposing reduced quotas, best
practices and the adherence to age
restrictions on countries wishing to
export trophies.’’
Our Response: It is not appropriate to
establish specific criteria, such as a set
quota number, in this final rule because
this may not allow for the countries to
implement an adaptive management
strategy based on the current status of
the species within the country. During
the public comment period we received
new information regarding infanticide
and the effects of hunting younger male
lions on pride structure. Therefore, we
agree with the peer reviewer that the
Service is in a position to proactively
engage with countries to assure
exported trophies fulfill minimum age
requirements, and we will consider
these factors in making our
enhancement findings.
(15) Comment: Two peer reviewers
stated that populations in West and
Central Africa are small and isolated,
and, as a result, sustainable offtake was
not possible. Several peer reviewers also
provided additional information and
citations on documented lion
population declines resulting from
excessive lion quotas and poor
management of trophy hunting.
Our Response: We reexamined the
information available to us during the
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Our Response: We agree that if
hunting concessions maintained
sustainable levels of harvest, the
situation of harvesting males from
neighboring protected areas would not
be expected to occur. Species experts
have recommended best practices for
sustainable development of quotas and
offtake (Packer et al. 2011, p. 151) while
other methods are developed (adaptive
quota management based upon
scientific data with an enforceable
monitoring program, (Lindsey et al.
(2013a, pp. 8–9) and Hunter et al. (2013,
unpaginated)); these recommended
reforms have been incorporated as
appropriate. Additionally, based on
information provided during the public
comment period, there currently is no
level of offtake that would be
sustainable in West and Central Africa
at this time. We have incorporated this
information into our rule. For Panthera
leo melanochaita, we have developed a
4(d) rule and clarified factors we will
Public Comments
consider when making an enhancement
(17) Comment: One commenter noted finding for importation of sport-hunted
trophies of P. l. melanochaita (see 4(d)
that there are very few reliable or
Rule for Panthera leo melanochaita,
scientifically credible lion population
surveys in Africa and as a result, quotas above).
(20) Comment: Several commenters
are not scientifically derived.
stated that populations in West and
Additionally, the commenter noted that
quota allocations are largely based upon Central Africa are small and isolated
and as a result, sustainable offtake was
concession operators’ opinions.
not possible. Several commenters also
Our Response: We consider Packer et
provided additional information and
al. (2011) to be the best available science
citations on documented lion
regarding quota setting in the interim
population declines resulting from
while other strategies are more fully
excessive lion quotas and poor
developed (i.e., age-based strategies,
management of trophy hunting.
adaptive management systems, etc.). We
Our Response: We reexamined the
have re-examined information provided information available to us during the
during the development of the proposed drafting of the proposed rule and
rule and reviewed new information
reviewed the citations provided during
provided during the public comment
the public comment period. With the
period on quotas, scientific quota
new population estimates, in
development, and adaptive quota
combination with the literature and
management systems. As a result, we
citations provided during the public
have incorporated this information into
comment period, we agree that given the
our rule accordingly.
current state of the populations in West
(18) Comment: One commenter noted and Central Africa (Panthera leo leo),
that the proposed rule addressed only
sustainable offtake is not possible. As a
CITES Trade Data exports under the
result, we have found that, in their
‘‘trophy’’ category and that many are
current condition, sustainable offtake
exported under the ‘‘skins’’ category.
for Panthera leo leo is not possible.
Our Response: We have reviewed the
Therefore, we find that trophy hunting
U.S. imports of ‘‘skins’’ for 2013 and
does rise to a level of threat for Panthera
have incorporated this information into
leo leo. We have incorporated the new
our rule.
information accordingly.
(19) Comment: One commenter states
(21) Comment: Several range
that lion trophies exported are almost
countries provided additional
exclusively males and subadult males,
information on their progress in
and as such, are targeted by hunters at
implementing the best recommended
unsustainable levels. Additionally, the
practices and reforms as outlined by
commenters note that the situation of
species experts.
Our Response: We appreciate the
harvesting males from neighboring
information provided by the range
protected areas would not be expected
countries. We have incorporated
to occur if the males were being
relevant portions of this information
harvested at sustainable levels.
asabaliauskas on DSK5VPTVN1PROD with RULES
drafting of the proposed rule and
reviewed the citations provided during
the public comment period. We have
incorporated the new information
accordingly.
(16) Comment: One peer reviewer
commented that our review of
infanticide as a result of trophy hunting
was incomplete and provided additional
literature and citation on the subject for
our consideration.
Our Response: We agree that
additional discussion was appropriate
regarding the impacts of infanticide,
including a review of the new studies
provided on evolutionary adaptions and
impacts of subadult early dispersal on
the species. We agree that infanticide
and associated factors relating to trophy
hunting of males may have additive
impacts on the decline of certain
populations. Therefore, we have
incorporated this information into our
final rule.
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80049
into our rule accordingly. It should be
noted, however, that, with this finding,
Panthera leo leo meets our definition of
an endangered species and, therefore,
will be subject to the provisions and
regulations of the Act for endangered
species. Import of sport-hunted trophies
of Panthera leo melanochaita will
require issuance of a threatened species
import permit under 50 CFR 17.32,
which will require an enhancement
finding (see 4(d) Rule for Panthera leo
melanochaita, above).
(22) Comment: One commenter noted
that, although the proposed rule offers
concrete examples of the role of trophy
hunting in lion conservation, the
proposal offers only limited support of
trophy hunting benefits. Additionally,
one commenter notes that the hunting
community has been a leader in lion
conservation in terms of habitat
conservation and states that the success
of certain populations is largely in part
to contributions from the hunting
community.
Our Response: Based on information
received during the formation of the
proposed rule and based on additional
information received during the public
comment period, we agree that trophy
hunting, if managed in a sustainable and
scientific manner, can provide benefits
to both local communities as well as to
lion conservation. We also agree that
trophy hunting has conserved a
considerable portion of lion habitat.
However, species experts have
identified several areas across the range
of the species where hunting has
contributed to the decline of lion
populations. Species experts have
outlined these flaws and have
developed and introduced several
recommended reforms to assure that
offtake is sustainable and scientific. We
have incorporated these key issues and
the recommended reforms into this rule
as appropriate. Although we
acknowledge the role trophy hunting
has played in lion conservation, we also
have reviewed additional literature
provided that documents the decline of
lion populations as a result of
mismanaged trophy hunting. At this
time, based on information received
during the public comment period,
based on the current trends of lion
populations in West and Central Africa
(Panthera leo leo), experts suggest that
there is no level of offtake that is
considered sustainable in these regions.
Regardless, import of sport-hunted
trophies of Panthera leo leo will require
issuance of an endangered species
import permit under 50 CFR 17.22,
which will require an enhancement
finding. Import of sport-hunted trophies
of Panthera leo melanochaita will
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require issuance of a threatened species
import permit under 50 CFR 17.32,
which will require an enhancement
finding (see 4(d) Rule for Panthera leo
melanochaita, above).
(23) Comment: Several commenters
noted that excessive lion quotas and
offtake was the primary driver for
declines in lion abundance.
Our Response: We reviewed the new
literature provided and agree that the
excessive offtake contributed to the
decline of some lion populations
throughout their range. We have
incorporated this information into our
rule and addressed the recommended
reforms as provided by Hunter et al.
(2013, entire) and Lindsey (2013a, pp.
8–9).
(24) Comment: Several commenters
noted that current practices, unless
reformed according to best
recommendations, should be considered
a potential threat to lion. Species
experts recommend a maximum
science-based offtake of no more than
<1 lion/2,000 km2 of hunting block until
age restrictions are enforced.
Our Response: We have reexamined
information provided during the
formation of the proposed rule and have
reviewed new literature submitted
during the public comment period
regarding the best scientific information
available regarding quota setting for
lions. We agree and have incorporated
this information in our rule as
appropriate.
(25) Comment: Three commenters
provided additional information on the
biological impacts of trophy hunting.
New information was provided
regarding (1) the evolutionary impacts
of selective removal of specimens
displaying key traits; (2) biological and
genetic results of infanticide as it relates
to subadult dispersal and survival; and
(3) the role of adult male range and
dispersal requirements in genetic
variation and isolated populations.
Our Response: We reexamined the
information available to us during the
drafting of the proposed rule and
reviewed the citations and peer review
input provided during the public
comment period. We agree that
additional discussion was required
regarding the impacts of infanticide,
including a review of the studies the
commenters submitted. We agree that
infanticide and associated factors
relating to trophy hunting of males may
have additive impacts on the decline of
certain populations. Therefore, we have
incorporated this information into our
final rule.
(26) Comment: Several commenters
noted that many range countries are in
the process of reforming their lion
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hunting regulations. Other commenters
note that these reforms have only been
fully implemented in some countries
and additional reforms are needed
throughout the range. An additional
commenter noted that the information
presented in the proposed rule on range
countries implementation of best
practices is overly optimistic with
regard to what has actually been
achieved.
Our Response: Several commenters
provided updates regarding the progress
of range countries’ reforms to hunting
regulations. Although multiple
countries have begun to implement the
reforms as outlined in this document,
only two locations (Mozambique, in
Niassa Reserve, and Zimbabwe) have
fully implemented the process and are
completely transparent. However, many
countries are still in the earliest stages
of implementation, and their progress is
still pending. After a review of this
information, we concur that most range
countries have multiple barriers (e.g.
corruption and poverty) that will have
to be addressed concurrently with the
establishment of a transparent and
scientific-based, adaptive management
system. This information has been
incorporated into the rule. Import of
sport-hunted trophies of Panthera leo
melanochaita, will require issuance of a
threatened species import permit under
50 CFR 17.32, which will require an
enhancement finding (see 4(d) Rule for
Panthera leo melanochaita, above).
(27) Comment: One commenter noted
that recent scientific knowledge has
established that hunting males aged five
and older does not affect lion
population dynamics.
Our Response: We have reviewed the
literature provided and have
incorporated the recommended strategy
into our rule. Whitman et al. (2004, pp.
175–177) found that if offtake is
restricted to males older than 6 years of
age, then trophy hunting will likely
have minimal impact on the pride’s
social structure and young. Restricting
offtake to males over 6 years of age will
decrease the frequency of maletakeovers, and reduce the potential for
infanticide and delayed infanticide by
allowing younger males a chance to sire
and raise a cohort of young, and by
allowing the subadults to stay within
their pride longer (thus allowing them
to mature prior to dispersal) (Elliot
2014, p. 1054; Packer et al. 2006, p. 6).
(28) Comment: One commenter stated
that the validity of the so-called 6-year
age approach has been questioned.
Our Response: The 6-year approach is
a relatively new development based on
research conducted by Whitman (2004,
p. 175–177). Like all new concepts,
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technical issues will arise during the
implementation phase. Species experts
have been working through these issues
by providing research and outreach
materials detailing the most current
aging techniques, and by providing
training to concession operators and
communities (Begg and Begg 2010, pp.
8, 14; Packer and Whitman 2006,
entire). We anticipate additional
research will emerge as this strategy is
implemented across the species range.
(29) Comment: Several commenters
noted that the existing age limit for ‘old
males’ is not enforced.
Our Response: Enforcement of
wildlife crime continues to be an issue
for many countries in Africa as
evidenced by the rising rate of poaching
epidemics and corruption across the
African continent. Enforcement of
trophy hunting regulations across the
range of the species is a critical issue.
Currently, only two places within the
African continent have completely
implemented the recommendations as
set forth in this rule. Several other
countries have committed to
implementing this strategy, but their
progress is currently pending. We must
note here that enforcement is complex;
it is only one component of a multitiered regulatory system. Successful
enforcement will rely on a variety of
other factors related to management.
Countries will have to address
corruption in order to ensure their
monitoring and management systems
are transparent.
(30) Comment: During the public
comment period, several commenters
expressed concern that local
communities do not actually benefit
from the revenue derived from trophy
hunting. Specifically, comments were
focused on three issues (see Potential
Impacts of Trophy Hunting): (1)
Corruption of concession operators and
corrupt practices surrounding
concession allocation prevent local
communities from benefitting from
trophy derived revenue; (2) financial
contributions to local communities from
trophy hunting is often exaggerated and
bears little connection to conservation
of the species (local communities
receive only 3–5 percent of revenues);
and (3) that benefits have never been
independently evaluated and
communities involved in hunting
concessions have not been adequately
surveyed as to their satisfaction of land
use for trophy hunting.
Our Response: Corruption occurs
throughout the range of the species, and
it likely has an impact on the actual
benefits received by local communities.
Although many countries have
incorporated incentives into their
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trophy hunting policies, land
management policies, and national lion
action strategies, most countries are still
in the earliest stages of implementing
the strategies discussed in the rule.
Therefore, we have incorporated this
information into our final rule.
(31) Comment: One commenter stated
that there is no evidence to support that
trophy hunting might provide sufficient
money to motivate communities in
hunting regions to protect lions against
other threats such as retaliatory killings
for livestock losses.
Our Response: Although there is
limited data on the motivations of
individuals who kill lions (see Hazzah
2013), we recognize that human-lion
conflict resulting in retaliatory killing is
a major threat. Although not the only
mechanism for increasing tolerance,
incentives are an important aspect of
changing individuals’ perceptions of
lions, especially for communities who
live close to lion populations.
According to Packer et al. (2011, p. 152,
citing e.g., Baker 1997, Hurt and Ravn
2000, Child 2004, Lindsey et al. 2006,
and Dickson et al. 2009), ‘‘trophy
hunting has been considered essential
for providing economic incentives to
conserve large carnivores.’’ For
example, Kenya banned trophy hunting
in 1977 due to questionable ethics and
poor management. Since then, ‘‘wildlife
populations outside of parks have
declined by at least 60%, due partly to
the inability of local people to benefit
from wildlife’’ (Lindsey et al. 2006,
citing Child, 2000, 2005).
Recently, Hazzah et al. (2014, entire)
conducted research in Kenya in the
Amboseli ecosystem, where it was
estimated that 55 percent of lion killings
were retaliatory in nature. In this area,
two programs are used to provide
incentives to locals to prevent these
types of killing. First, there is a Predator
Compensation Fund (PCF) wherein
local people are compensated for
depredated livestock and the system is
carefully designed with a system of
verification processes, payments, and
violation penalties (2014, p. 852).
Second, the Lion Guardians (LG)
program uses traditional techniques to
incorporate community value and belief
systems to improve local perceptions.
According to Hazzah et al. (2014, pp.
857–858), compensation alone showed a
73 percent reduction in lion killing.
Combining this with the LG program (in
2007) further reduced the decline by 91
percent (less than one killed per year).
Hazzah et al. estimated that the PFC
program cost an estimated $250,000
USD annually and employed 30
community members. The LG program
was estimated to have cost $140,000
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USD annually and employed 38
community members. It is important to
note, however, that the authors are
uncertain regarding the sustainability of
long-term payments and questioned
what would happen if the compensation
stopped. In other countries within the
range of lion, systems like these are not
necessarily in place. Experts believe the
revenue from trophy hunting, if well
managed in a transparent way, could
potentially fund similar programs
throughout the species’ range, thus
reducing retaliatory killings and
benefitting the local population
simultaneously.
(32) Comment: One commenter
suggested non-consumptive uses such
as eco-tourism could provide the
promise of sustainable enterprise.
Our Response: We agree in part, but
ecotourism and the trophy hunting
community need to come together to
support the African countries in lion
conservation. Non-consumptive uses of
wildlife such as eco-tourism have been
practiced in many regions throughout
Africa. Lindsey et al. (2007, entire)
studied viewing preferences among
visitors in protected areas in South
Africa. Most tourists, especially firsttime and foreign visitors, were generally
focused on charismatic mega-species
that are generally confined to protected
areas; African visitors had more interest
in bird and plant diversity, scenery, and
other rare species. Lindsey et al. (2007)
acknowledge that ecotourism may align
with conservation objectives and
provide incentives for the development
of tour operations geared away from the
‘big five.’ However, ecotourism as a
replacement to trophy hunting will have
to be researched further. Information
provided by Hunter et al. (2013,
unpaginated citing Norton-Griffiths
2007) indicates that ‘‘a significant
portion of the land where trophy
hunting occurs is unlikely to be viable
for alternate wildlife-based land uses
such as photo- or ecotourism due to
remoteness, lack of infrastructure
including integration in established
tourism circuits, lack of spectacular
scenery or lack of high densities of
viewable wildlife.’’ Additionally,
according to Hunter et al. (2013,
unpaginated citing Packer et al. 2007;
Groom 2013, pp. 2–3) ecotourism is
highly dependent on political stability.
As a result, ecotourism is unlikely to be
able to provide the revenue potential
that is currently associated with trophy
hunting, although we agree there is
potential for growth in this industry.
(33) Comment: Several commenters
state that hunting is able to generate
revenues for a larger proportion of areas
that are unsuitable for ecotourism (e.g.,
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remote areas lacking infrastructure,
attractive scenery, or high densities of
viewable wildlife). Additionally, the
commenters state that trophy hunting
revenue provides a means of preserving
natural habitat despite strong pressure
to convert habitat into agriculture or
rangelands.
Our Response: We agree that trophy
hunting revenue provides conservation
value at many levels, especially in terms
of lion habitat, conservation programs,
anti-poaching programs, equipment, and
poaching patrols. However, lion experts
have documented the decline of many
populations of lion resulting from
mismanagement of trophy hunting
(Rosenblatt et al. 2014, p. entire;
Sogbohossou et al. 2014, entire; Becker
et al. 2013, entire; Lindsey et al. 2013,
entire; Croes et al. 2011, entire; Packer
2011, entire; Loveridge et al. 2007,
entire). Additionally, the high revenue
potential associated with trophy
hunting makes it a target for corruption.
As a result, we have reviewed the
recommended best practices as
provided by species experts to
encourage countries to establish a
transparent, science-based, adaptive
quota management system. Import of
sport-hunted trophies of Panthera leo
leo will require issuance of an
endangered species import permit under
50 CFR 17.22, which will require an
enhancement finding. Import of sporthunted trophies of Panthera leo
melanochaita will require issuance of a
threatened species import permit under
50 CFR 17.32, which will require an
enhancement finding (see 4(d) Rule for
Panthera leo melanochaita, above).
(34) Comment: One commenter noted
that that the estimates of revenue from
trophy hunting presented in the
proposed rule were not believed to be
the best scientific information available.
Specifically, they questioned the
objectivity of one source (Jackson 2013)
and provided additional information
analyzing Lindsey et al. (2012a).
Our Response: The new literature
provided by the commenter (Campbell
2012, entire) identifies some analysis
and data flaws in Lindsey (2012a). We
have reviewed the information
presented and updated this rule using
the best available scientific information.
We have removed information we used
from Jackson (2013) and Lindsey et al.
(2012) and rely upon information from
Groom (2013) and Barnett and Patterson
(2005), which was also presented in the
proposed rule.
(35) Comment: One commenter noted
that the discussion as presented in the
proposed rule was biased toward the
hunting industry and did not discuss
the body of research documenting the
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potential negative impacts of trophy
hunting. A peer reviewer requested a
more thorough discussion be included
to address (1) the major flaws in current
management practices, and (2)
recommendations for how these issues
can be addressed to account for
sustainability.
Our Response: We reexamined the
information available to us during the
drafting of the proposed rule and
reviewed the citations and peer review
input provided during the public
comment period. As a result, we have
incorporated this information into the
rule.
(36) Comment: Three range countries
provided information on the occurrence
of human-lion conflict. All three
countries indicated that human-lion
conflict is a serious problem.
Our Response: We incorporated this
information into our discussion of
human-lion conflict. The information
further supported our conclusion that
human-lion conflict constitutes a threat
to lion persistence.
(37) Comment: One commenter agrees
that human-lion conflict is a threat to
remaining lion populations, but asserts
that it does not constitute a level of
threat in eastern and southern Africa to
warrant a listing under the Act. The
commenter further asserts that the lion
has been secured from the negative
impacts of human-lion conflict where
90 percent of its population exists and
that human-lion conflict can be
controlled and reduced.
Our Response: We agree that there are
populations of lions where adequate
management has reduced the
occurrence and impacts of human-lion
conflict. However, the best available
information indicates that retaliatory
killing is a rangewide occurrence, and
given the limited number of lions
remaining, any loss of lions to
retaliatory killing, or other actions, can
have a detrimental impact on the
species.
(38) Comment: One commenter
disagreed with our conclusion that
disease was not a significant threat to
the lion and provided additional
information on FIV, bTB, and CDV and
discussed difficulties in determining the
role of disease in lion mortality. The
commenter requested that we reconsider
our determination based on
consequences of diseases to the immune
system.
Our Response: As mentioned in their
comment, the role of disease in lion
mortality and reproductive potential is
almost completely unknown in lion
populations. Except for a few
populations that have been studied,
there are no estimates of the number of
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lions lost to diseases. Some populations
were able to recover to pre-outbreak
levels, but for others, factors such as an
inbred population prevented
populations from recovering to preoutbreak levels. We found no
information indicating the loss of lions
to disease is a significant driver of the
status to the species. However, we
acknowledge that diseases can debilitate
rather than cause mortality, but
debilitation may cause an individual to
succumb to other factors. Furthermore,
due to the prevalence of some diseases
in lion populations and current stressors
on lions, it is likely that disease
contributes to lion mortality. The
information provided by the commenter
did not alter our finding that disease is
not a significant threat to the species;
however, we have altered the discussion
of disease to clarify that disease is a
secondary factor that is exacerbated by
other threats the lion faces.
(39) Comment: Several commenters
stated that climate change has a
detrimental impact on the species and
that the Service did not incorporate
recent climate trend data into our
analysis.
Our Response: We have incorporated
climate change data and its effect on the
species into our analysis.
(40) Comment: One commenter
specifically commented that the 4(d)
rule is appropriate and needed for the
conservation of the species. A second
commenter applauded the Service for
recognizing the importance of regulated
hunting and the conservation of the
African lion and the need for a system
that allows U.S. hunters to import
trophies.
Our Response: The Service agrees that
the 4(d) rule is necessary and advisable
for the conservation of the subspecies P.
l. melanochaita. The Service has
recognized that a well-managed,
scientifically based hunting program
can provide for the conservation of a
species and benefit local communities.
By establishing the 4(d) rule that
encourages range countries to effectively
manage their lion populations, U.S.
hunters can continue to contribute to
the long-term conservation of the
subspecies.
(41) Comment: Four commenters
stated that the Service lacks the
authority to rebut the Act’s section
9(c)(2) with a blanket finding applicable
to lions throughout Africa, for an
indefinite time period. Section 9(c)(2)
states that any importation shall ‘‘be
presumed to be an importation not in
violation’’ of any provision of the Act or
implementing regulation for species not
listed as endangered but listed on
Appendix II of CITES. The commenters
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stated that African lions, because they
are currently listed in CITES Appendix
II, would be covered by the presumption
provided by section 9(c)(2) if they are
listed as threatened. One of the
commenters noted a disparity between
the 4(d) rule for lions and a 4(d) rule for
another species that was commonly
hunted. This commenter felt that
because both species are listed in
Appendix II of CITES that their
treatment under the Act should be
similar.
Our Response: While there has been
question as to whether section 9(c)(2) of
the Act might automatically require
allowing the importation of a species
that is both listed as threatened and in
Appendix II, and preclude the issuance
of more restrictive 4(d) rules covering
importation, the Service has concluded
that such 4(d) rules may be issued to
provide for the conservation of the
involved species. Section 9(c)(2) does
not expressly refer to threatened species
or prevent the issuance of appropriate
4(d) rules and could not logically have
been intended to allow for an
international convention to override
U.S. law, where there is reliable
evidence to affect the presumption of
validity. Finally, the term ‘‘presumed’’
implies that the established
presumption is rebuttable under certain
circumstances, including through the
promulgation of a protective regulation
pursuant to section 4(d) of the Act.
(42) Comment: Two commenters
stated that, even if the Service had the
authority to promulgate a regulation that
establishes the manner in which African
lions are imported, it cannot use the
regulation to essentially shift to the
hunter/importer the burden of proving
enhancement or survival of the species
criteria.
Our Response: The burden of showing
that an ‘‘otherwise prohibited activity’’
meets the issuance criteria under 50
CFR 17.32 is on the applicant. In some
cases for imports, such as sport-hunted
trophies, it is not always possible for the
applicant to provide all of the necessary
information needed by the Service to
make a positive determination under the
Act to authorize the activity. For the
import of sport-hunted trophies of P. l.
melanochaita, the Service will typically
consult with the range country to the
extent practicable and other interested
parties to obtain necessary information.
The Service has the discretion to make
the required findings on sport-hunted
trophy imports of P. l. melanochaita on
a country-wide basis, although
individual import permits will be
evaluated and issued or denied for each
applicant. While the Service may make
enhancement findings for sport-hunted
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trophy imports of P. l. melanochaita on
a country-wide basis, the Service
encourages the submission of
information from individual applicants.
We would rely on the information
available to the Service and may rely on
information from sources other than the
applicant when making a permitting
decision.
(43) Comment: Two commenters
stated the Service has offered nothing to
demonstrate why limitations on the
importation of sport-hunted African
lions from throughout the subspecies’
range is necessary and advisable to
provide for the conservation of the
subspecies or sufficient to overcome the
Congressional conclusion that such
imports would normally (i.e.,
presumptively) benefit the conservation
of the species. Further, these
commenters did not feel that the
Service’s proposed rule for African lion
supported a conclusion that a 4(d) rule
requiring import permits for trophies
was necessary and advisable for the
conservation of the subspecies.
Our Response: For the import of
sport-hunted trophies, while there is
evidence that many of the range
countries have lion management plans,
we have little information indicating
that the plans are being implemented,
and we received new information
during the public comment period
indicating that some hunting programs
are not scientifically based or providing
adequate conservation benefits to the
species. We want to encourage U.S.
hunters to take advantage of one of the
conservation tools available, wellregulated hunting programs, to improve
the long-term survival of the subspecies.
The 4(d) rule will support implementing
well-managed plans by encouraging
countries that have insufficient lion
management plans to develop plans that
are based on sound scientific
information that would generate
revenue in support of communities and
conservation. As noted, the proposed
4(d) rule for African lion would provide
for the importation into the United
States of trophies taken legally in range
countries upon the issuance of a
threatened species import permit. While
the Service cannot control hunting of
foreign species such as African lion, we
can regulate their importation and
thereby require that U.S. imports of
sport-hunted African lion trophy
specimens are obtained in a manner that
is consistent with the purposes of the
Act and the conservation of the
subspecies in the wild, by allowing
importation from range countries that
have management plans that are based
on scientifically sound data and are
being implemented to address the
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threats that are facing lions within that
country.
(44) Comment: Three commenters, a
peer reviewer and comments from a
consortium of seven range countries felt
that the proposed 4(d) rule did not
adequately explain the criteria used by
the Service to determine whether the
importation of any sport-hunted lion
would enhance the survival of the
species. The commenter expressed
concern that because the Service has not
adequately explained the criteria for
enhancement or made an enhancement
finding for lions in Africa, U.S. hunters
will be barred from importing their lion
trophy. The peer reviewer expressed a
need for the Service to elaborate
concrete requirements to which
countries must adhere as a minimum
standard in order for imports of sporthunted lion trophies from a country to
qualify for the export of lion trophies,
including quotas of less than one male
per 2000 km2 with a minimum age
requirement.
Our Response: We recognize that the
preambular language of the proposed
4(d) rule was general, and we have
addressed this issue in this final rule.
However, we did not find that it was
appropriate to establish specific criteria,
such as a set quota number, in this final
rule because this may not allow for the
countries to implement an adaptive
management strategy based on the
current status of the species within the
country. During the public comment
period we received new information
regarding infanticide and the effects of
hunting younger male lions on pride
structure. Therefore, we agree with the
peer reviewer that the Service is in a
position to proactively engage with
countries to ensure exported trophies
fulfill minimum age requirements and
we will consider these factors in making
our enhancement findings.
(45) Comment: Two commenters
recommended that the Service should
not adopt a 4(d) rule until it makes
specific enhancement-of-survival
findings for each of the countries for
which lions can be hunted, or delay the
implementation of the 4(d) rule for 1
year. These two commenters, as well as
a third commenter, stated that
implementing the 4(d) rule at this time
would impact hunters who had already
booked trophy hunts months or even
years in advance, resulting in the loss of
money invested that could not be
recovered ‘‘in the event of a sudden
change in the rules governing the
importation of sport-hunted trophies.’’
Our Response: In the proposed rule,
the Service found that hunting, if well
managed, may provide a benefit to the
subspecies. However, the best available
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information, obtained by the Service
during the public comment period,
indicates that not all hunting programs
are well managed or provide
enhancement to survival of the
subspecies. Delaying the
implementation of a 4(d) rule may result
in U.S. hunters participating in poorly
managed hunting programs, which
would be counter to the purposes of the
Act. We do not agree that such a delay
would be appropriate for the
conservation of the subspecies.
Regarding the potential loss of deposits
for previously booked trophy hunts,
hunters were notified of a potential
regulatory change when the proposed
rule with a 4(d) rule was published on
October 29, 2014 (79 FR 64472). The
availability of the proposed rule would
have given hunters the opportunity to
use that information to minimize
financial losses.
(46) Comment: One commenter urged
the Service to adjust the rule to ensure
that imports are not stopped, and that
the benefits generated by U.S. hunters in
foreign countries continue while the
Service is making determinations
regarding the countries’ lion
management program. This commenter
suggested that the Service issue U.S.
import permits for all lion trophies until
such time as the Service deems that the
import from a particular country would
not enhance the survival of the
subspecies. It is the commenter’s belief
that there are beneficial aspects of
hunting (benefits to local communities,
dollars coming into the country, etc.)
that should not be interrupted while the
Service is making its determinations.
The commenter expressed concern that
the Service has insufficient resources to
make timely country-by-country
determinations.
Our Response: Import of sport-hunted
trophies of Panthera leo leo will require
issuance of an endangered species
import permit under 50 CFR 17.22,
which will require an enhancement
finding. Import of sport-hunted trophies
of Panthera leo melanochaita will
require issuance of a threatened species
import permit under 50 CFR 17.32,
which will require an enhancement
finding (see 4(d) Rule for Panthera leo
melanochaita, above). We would be
unable to issue import permits until we
made such determinations. The Service
recognizes that making these findings
may be time consuming given our
current resources. We appreciate the
commenter’s willingness to use their
own resources to obtain information on
the range countries’ management and
assist the Service in making timely
findings. We encourage the commenter
and others to work with us by
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submitting any information they may
have to make these determinations.
(47) Comment: One commenter stated
that the Service should only apply a
permitting requirement on lions taken
after the listing and 4(d) rule go into
effect.
Our Response: For lions held in
captivity or a controlled environment on
the date of the listing under the Act, no
import permit will be required, if the
lion meets all the requirements to be
considered ‘‘pre-Act’’ (Section 9(b)(1) of
the Act). Accordingly, lions hunted after
the listing would require permits, and
those hunters who have booked hunts,
but have not yet hunted a lion, would
require a U.S. import permit prior to
importation.
(48) Comment: Two commenters
stated their belief that most of the lion
range countries do not have national
lion conservation plans in place, or have
plans with quotas in place that are
based on inaccurate population
numbers. One commenter spoke of lion
conservation conferences in 2005 and
2006 that established conference
resolutions, very few of which have
been adequately addressed by the lion
range states. This commenter felt there
is an urgent need to conduct
independent and scientifically valid
lion population assessments throughout
the range of the lion. This commenter
urged the Service to impose an import
moratorium until these population
assessments have been conducted. The
second commenter recommended that
prior to the import of trophies, there
needs to be evidence of recovery and
stability, as well as clearly identified
governmental reforms and their
implementation in some of the range
states.
Our Response: New information
received during the public comment
period raises questions about whether
some of the range countries have
adequate management programs in
place, and this information has been
incorporated in this final rule. The
Service is not imposing a moratorium;
however, permits will be required for all
imports. Import of sport-hunted trophies
of Panthera leo leo will require issuance
of an endangered species import permit
under 50 CFR 17.22, which will require
an enhancement finding. Import of
sport-hunted trophies of Panthera leo
melanochaita will require issuance of a
threatened species import permit under
50 CFR 17.32, which will require an
enhancement finding (see 4(d) Rule for
Panthera leo melanochaita, above). The
import of lions hunted in countries that
do not meet the criteria for
enhancement will not be permitted.
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(49) Comment: Several lion range
countries as well as two commenters
expressed that successful conservation
of African lion relies upon a thoughtful
strategy that includes sustainable use.
There was concern that the inability to
import lions into the United States
would result in the increase of threats
we identified in the proposed rule (e.g.,
human-lion conflict and habitat loss).
The countries expressed that if U.S.
hunters are unable to import sporthunted trophies, the economic value of
lions within the country would be
reduced or eliminated, resulting in
retaliatory killing of lions by local
communities because of real or
perceived perceptions that lions kill
people and livestock. In addition, two
countries noted that, without an
economic value, safari companies
would not support lions in hunting
concessions because lions prey upon
other valued trophy species, such as
hartebeest and buffalo. One country
noted that if hunting companies were
unable to export to the United States,
they would abandon their hunting areas
to agro-pastoral uses, resulting in
‘‘unavoidable extinction of wildlife and
collapse of ecosystem services.’’ These
countries expressed that hunting zones
often provide a buffer to protected areas
as well as provide ecological corridors
between protected areas. They
expressed that the removal of lions from
these hunting zones would decrease the
range of the subspecies and result in
overall lion population declines.
Further, the loss of legal income from
lion hunting, which supports antipoaching efforts, will negatively affect
lion conservation and increase
poaching.
Our Response: The Service recognizes
the benefits that a well-managed trophy
hunting program can provide by
increasing revenue for local
communities, providing jobs, and
supporting local microbusinesses.
Revenue is often used to build and
maintain fences, pay for security
personnel, and provide resources for
anti-poaching activities, habitat
acquisition, and wildlife management.
Our 4(d) rule for P. l. melanochaita
will support and encourage
conservation actions for this subspecies
and ensure that U.S. imports of sporthunted lion trophy specimens are
obtained in a manner that is consistent
with the purposes of the Act and the
conservation of the P. l. melanochaita in
the wild. By ensuring that imports of
lions occur only from range countries
that have management plans based on
scientifically sound data which are
being implemented to address the
threats facing lions within that country,
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U.S. hunters will continue to support
the good efforts of the range countries,
while encouraging those countries that
have not fully implemented a lion
management plan to do so in order to
receive business from U.S. hunters.
(50) Comment: Several countries and
one commenter provided a combined
comment expressing concern that the
Service’s 4(d) rule surpasses the
regulatory requirements they are already
following under CITES, and that such
restrictions undermine CITES and
increase the regulatory burden to lion
range states by adding additional
reporting requirements. These countries
noted that under CITES exports of
trophies must not be detrimental to the
survival of the species and expressed
that proving their management
programs enhance the survival of the
subspecies is an added administrative
burden on their wildlife management
authorities that are already limited on
staff, resources, and time. Further, they
felt the 4(d) rule would penalize
countries that are already working hard
to achieve success in wildlife
management.
Our Response: As these countries
noted in their comments, CITES allows
for stricter domestic measures, such as
the Act and our 4(d) rule for P. l.
melanochaita promulgated under the
Act. The Service recognizes that the 4(d)
rule for P. l. melanochaita has stricter
requirements than CITES Appendix-II
requirements. We find that our 4(d) rule
for P. l. melanochaita will support and
encourage countries to carry out strong
conservation programs for P. l.
melanochaita and ensure that U.S.
imports of sport-hunted lion trophy
specimens are obtained in a manner that
is consistent with the purposes of the
Act and the conservation of the P. l.
melanochaita in the wild. We do not
anticipate a significant burden on the
lion range countries to provide
documentation that should already exist
for well-managed lion programs, and we
will work with the countries in order to
make our determinations under the Act
in a timely manner. The 4(d) rule is in
place to support countries that have
achieved success in managing their
lions.
(51) Comment: Several countries and
one commenter disagreed with how
trade in captive-bred lions would be
subject to the prohibitions under the
Act. These countries expressed that
trade in captive-bred lion does not have
an adverse effect on wild lion
populations. They felt that the Act’s
treatment of captive lions in the same
manner as wild lions is inconsistent
with CITES regulations and that the 4(d)
rule should exempt captive-bred lions.
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Our Response: In analyzing threats to
the species, we focused our analysis on
threats acting upon wild specimens
within the native range of the species,
because the goal of the Act is survival
and recovery of the species within its
native ecosystem. We did not separately
analyze ‘‘threats’’ to captive-held
specimens because the statutory five
factors under section 4 (16 U.S.C. 1533)
are not well-suited to consideration of
specimens in captivity and captive-held
specimens are not eligible for separate
consideration for listing. However, we
did consider the extent to which
specimens held in captivity create,
contribute to, reduce, or remove threats
to the species. See the Captive Lions
and Traditional Use of Lion Parts and
Products sections above. Under CITES,
captive specimens are still listed the
same as their wild counterparts;
however, the Convention does allow for
different treatment of captive-bred
specimens in regard to permitting. As
stated earlier, CITES also provides for
stricter domestic measures, and the
protections afforded to all specimens of
the subspecies through listing under the
ESA and the 4(d) rule would constitute
such a measure.
(52) Comment: A joint comment from
the petitioners asked us to scrutinize
applications for the import of lion
trophies or parts to ensure that they
were obtained within a scientifically
based management program that
promotes the conservation of the
subspecies and provided suggestions for
criteria to consider when making an
enhancement finding. The comment
included a number of suggestions for
establishing a formal internal guidance
on how we would evaluate each
application. Finally, the petitioners
called on the Service to publish the
receipt of threatened species permit
applications in the Federal Register and
allow for a 30-day comment period.
Another commenter questioned
establishing findings on a country-wide
basis instead of specific regions/hunting
programs within a country.
Our Response: We appreciate the
input regarding publishing the receipt of
threatened species applications,
establishing formal internal guidance on
how we will evaluate each application,
and consideration of making
enhancement findings on a specific
region/hunting program scale. We will
consider these suggestions; however,
this issue is outside the scope of this
rulemaking process. In regard to the
suggested criteria for making
enhancement findings, we have
expanded the discussion of
enhancement within this final rule, and
many of the suggestions have been
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addressed in the preambular language of
the 4(d) rule.
(53) Comment: The petitioners also
asserted that we should not authorize
imports of lions from western Africa,
Tanzania or Zimbabwe; imports of
trophies from females or males under 6
years of age; or trophies obtained from
captive-hunting facilities, or authorize
imports, interstate commerce or foreign
commerce in lion parts.
Our Response: While the comments
are outside the scope of this rulemaking,
the Service must make a finding that an
‘‘otherwise prohibited activity,’’ such as
import, export, interstate and foreign
commerce, must meet the issuance
criteria under 50 CFR 17.32. We cannot
make any determination of whether a
particular permit application can be
approved or denied until the
application is reviewed.
(54) Comment: One commenter called
on the Service to specifically prohibit
the importation of sport-hunted lions in
the 4(d) rule, citing that there is no
documented evidence that trophy
hunting supports conservation of the
subspecies. In addition, the commenter
felt that allowing for legal trade of sporthunted lions would support the illegal
harvest of the subspecies.
Our Response: We found no evidence
that allowing legal import of lion
trophies would stimulate illegal trade
into the United States. In evaluating the
best available scientific and commercial
information, we concluded that a wellmanaged, scientifically based lion
management program can provide a
benefit to the species. While we
obtained new information indicating
that some hunting programs are not
scientifically based or providing
adequate conservation benefits to the
species, this 4(d) rule will support
implementing well-managed plans by
encouraging countries that have
insufficient lion management plans to
develop plans that are based on sound
scientific information that would
generate revenue in support of
communities and conservation.
Therefore, we are not prohibiting the
import of sport-hunted trophies. Import
of sport-hunted trophies of Panthera leo
melanochaita will require issuance of a
threatened species import permit under
50 CFR 17.32, which will require an
enhancement finding (see 4(d) Rule for
Panthera leo melanochaita, above). The
import of lions hunted in countries that
do not meet the criteria for
enhancement will not be permitted.
(55) Comment: One commenter stated
that the Service has failed to comply
with the National Environmental Policy
Act (NEPA) in regard to promulgating
the 4(d) rule.
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Our Response: 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). Furthermore, under our 1983
policy, we determined that we do not
need to prepare an environmental
assessment in connection with
regulations adopted under section 4(a)
of the Act, including 4(d) rules that
accompany listings of threatened
species.
Because we are listing P. l.
melanochaita as threatened and are
finalizing this 4(d) rule simultaneously
with our final listing determination, we
consider this 4(d) rule to be part of the
listing determination for the purposes of
National Environmental Policy Act
compliance.
(56) Comment: One commenter stated
that lions do not lend themselves to
population surveying due to the boom
and bust nature and high fecundity of
lion populations. The commenter felt
that population surveys have long been
considered impractical, and as such,
quotas can never be set scientifically
and, therefore questioned how the
Service can make this a criteria for
determining enhancement. Finally, the
commenter was concerned that having
countries have an understanding of lion
population numbers and developing
lion management plans would be cost
prohibitive to many of the range
countries.
Our Response: We are not requiring
an exact count of the lions within each
country before being able to make a
determination of whether imports could
occur. However, we need to consider
what methods countries are using to
establish quotas, such as population
trend data, in order to determine if the
offtake by U.S. hunters is sustainable
and meets the criteria under 50 CFR
17.32.
(57) Comment: One commenter stated
that lions have an extraordinary high
fecundity, which contributes to its boom
or bust population characteristic and
helps ensure its long-term existence,
making it far less vulnerable to
endangerment.
Our Response: We agree that lions
have high fecundity and in absence of
stressors populations can rapidly
increase. However, across most of its
range, the lion is not without stressors,
and given the threats the lion is
currently facing, natural fecundity is
reduced. One of the greater stressors on
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lions, excessive harvests of lions for
trophies, can negatively impact the
reproduction of a lion such that it
causes local extirpations. Harvesting
males that are too young causes male
replacements, which results in
increased infanticide rates, death of the
surviving male coalition, and a 100
percent fatality rate for males that are
prematurely forced to disperse.
Furthermore, the population will be
driven to extinction as female
populations collapse as they eventually
are unable to mate. The species is
largely not able to rapidly recover from
population declines. This is evidenced
by long-term population trends that
indicate an overall 43 percent decline in
lions over 21 years and higher regional
rates of decline in western and eastern
Africa.
(58) Comment: One commenter stated
that the Service should use its power to
list Distinct Population Segments
(DPSs), rather than the entire African
lion subspecies in light of the recent
ruling in Humane Society of the United
States v. Jewell, No. CV 13–186 (BAH),
2014 WL 7237702 (D.D.C. Dec. 19,
2014)..
Our Response: We disagree with this
conclusion. Pursuant to 50 CFR
17.11(g), all populations are included in
the listing.
Required Determinations
National Environmental Policy Act (42
U.S.C. 4321 et seq.)
We have determined that we do not
need to prepare an environmental
assessment, as defined under the
authority of the National Environmental
Policy Act of 1969, in connection with
regulations adopted under section 4(a)
of the Act for the listing, delisting, or
reclassification of species. We published
a notice outlining our reasons for this
determination in the Federal Register
on October 25, 1983 (48 FR 49244).
References Cited
A list of all references cited in this
document is available at https://
www.regulations.gov at Docket No.
FWS–R9–ES–2012–0025, or upon
request from the U.S. Fish and Wildlife
Service, Endangered Species Program,
Branch of Foreign Species (see FOR
FURTHER INFORMATION CONTACT).
Authors
The primary authors of this rule are
staff of the Branch of Foreign Species,
Ecological Services, U.S. Fish and
Wildlife Service.
Historic range
Common name
Vertebrate
population where
endangered or
threatened
*
Africa, Asia .............
Africa ......................
*
Entire ......................
Entire ......................
Scientific name
Regulation Promulgation
Accordingly, we 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; 1531–
1544; and 4201–4245; unless otherwise
noted.
2. Amend § 17.11(h), the List of
Endangered and Threatened Wildlife,
by:
■ a. Removing the entry for ‘‘Lion,
Asiatic (Panthera leo persica)’’; and
■ b. Adding entries for ‘‘Lion (Panthera
leo leo)’’ and ‘‘Lion (Panthera leo
melanochaita)’’ in alphabetic order
under MAMMALS to read as set forth
below:
■
§ 17.11 Endangered and threatened
wildlife.
List of Subjects in 50 CFR Part 17
Endangered and threatened species,
Exports, Imports, Reporting and
Species
recordkeeping requirements,
Transportation.
*
Status
*
*
(h) * * *
*
When listed
*
Critical
habitat
Special
rules
MAMMALS
*
Lion ..........................
Lion ..........................
*
*
Panthera leo leo .....
Panthera leo
melanochaita.
*
*
*
*
*
*
*
3. Amend § 17.40 by adding paragraph
(r) to read as follows:
■
§ 17.40
Special rules—mammals.
*
*
*
*
(r) Lion (Panthera leo melanochaita).
(1) General requirements. All
prohibitions and provisions of §§ 17.31
and 17.32 apply to this subspecies.
asabaliauskas on DSK5VPTVN1PROD with RULES
*
VerDate Sep<11>2014
18:43 Dec 22, 2015
Jkt 238001
*
862
862
*
*
*
E
T
*
(2) The import exemption found in
§ 17.8 for threatened wildlife listed in
Appendix II of the Convention on
International Trade in Endangered
Species of Wild Fauna and Flora
(CITES) does not apply to this
subspecies. A threatened species import
permit under § 17.32 is required for the
importation of all specimens of
Panthera leo melanochaita.
PO 00000
Frm 00058
Fmt 4701
Sfmt 9990
*
NA
NA
NA
17.40(r)
*
(3) All applicable provisions of 50
CFR parts 13, 14, 17, and 23 must be
met.
Dated: December 10, 2015.
Daniel M. Ashe,
Director, Fish and Wildlife Service.
[FR Doc. 2015–31958 Filed 12–21–15; 4:15 pm]
BILLING CODE 4333–15–P
E:\FR\FM\23DER2.SGM
23DER2
Agencies
[Federal Register Volume 80, Number 246 (Wednesday, December 23, 2015)]
[Rules and Regulations]
[Pages 79999-80056]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-31958]
[[Page 79999]]
Vol. 80
Wednesday,
No. 246
December 23, 2015
Part II
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; Listing Two Lion
Subspecies; Final Rule
Federal Register / Vol. 80 , No. 246 / Wednesday, December 23, 2015 /
Rules and Regulations
[[Page 80000]]
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DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R9-ES-2012-0025; 450 003 0115]
RIN 1018-BA29
Endangered and Threatened Wildlife and Plants; Listing Two Lion
Subspecies
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), determine
endangered status for the lion subspecies Panthera leo leo and
threatened status for P. l. melanochaita under the Endangered Species
Act of 1973, as amended (Act). We are also publishing a concurrent rule
under section 4(d) of the Act. This rule provides for conservation
measures for P. l. melanochaita.
DATES: This rule is effective January 22, 2016.
ADDRESSES: This final rule is available on the Internet at https://www.regulations.gov and comments and materials received, as well as
supporting documentation used in the preparation of this rule, will be
available for public inspection, by appointment, during normal business
hours at: U.S. Fish and Wildlife Service; 5275 Leesburg Pike; Falls
Church, VA 22041.
FOR FURTHER INFORMATION CONTACT: Branch of Foreign Species, Ecological
Services, U.S. Fish and Wildlife Service, MS: ES, 5275 Leesburg Pike,
Falls Church, VA 22041-3803; telephone, 703-358-2171; facsimile, 703-
358-1735. If you use a telecommunications device for the deaf (TDD),
call the Federal Information Relay Service (FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Executive Summary
I. Purpose of the Regulatory Action
We are listing two subspecies of lion, Panthera leo leo and P. l.
melanochaita, under the Endangered Species Act of 1973, as amended
(Act). We are listing the P. l. leo subspecies as an endangered species
and the P. l. melanochaita subspecies as a threatened species under the
Act. We are also finalizing a rule under section 4(d) of the Act that
will provide for conservation measures for P. l. melanochaita.
II. Major Provision of the Regulatory Action
This action revises the taxonomic classification of the Asiatic
lion (currently classified as P. l. persica and listed as an endangered
species under the Act) to P. l. leo based on a taxonomic change. The P.
l. leo subspecies will be listed as an endangered species and the P. l.
melanochaita subspecies will be listed as a threatened species in the
List of Endangered and Threatened Wildlife in title 50 of the Code of
Federal Regulations (CFR) at 50 CFR 17.11(h). This action will also add
a rule under section 4(d) of the Act for P. l. melanochaita which is
set forth at 50 CFR 17.40(r).
Background
The Endangered Species Act of 1973, as amended (Act) (16 U.S.C.
1531 et seq.), is a law that was passed to prevent extinction of
species by providing measures to help alleviate the loss of species and
their habitats. Before a plant or animal species can receive the
protection provided by the Act, it must first be added to the Federal
List of Endangered and Threatened Wildlife or the Federal List of
Endangered and Threatened Plants in part 17 of title 50 of the Code of
Federal Regulations (CFR). Section 4 of the Act and its implementing
regulations at 50 CFR part 424 set forth the procedures for adding
species to these lists.
Previous Federal Actions
In a final rule published in the Federal Register on June 2, 1970
(35 FR 8491), the Asiatic lion (currently listed under the Act as
Panthera leo persica) was listed under the Act's precursor, the
Endangered Species Conservation Act of 1969, as an endangered species
and has remained listed as an endangered species under the Act.
On March 1, 2011, we received a petition dated the same day from
the International Fund for Animal Welfare, the Humane Society of the
United States, Humane Society International, the Born Free Foundation/
Born Free USA, Defenders of Wildlife, and the Fund for Animals
requesting that the African lion subspecies be listed as endangered
under the Act. The petition identified itself as such and included the
information as required by 50 CFR 424.14(a). On November 27, 2012, we
published a ``positive'' 90-day finding (77 FR 70727) indicating that
we would initiate a status review of the African lion.
On October 29, 2014 (79 FR 64472) we published in the Federal
Register a finding that listing the African lion subspecies (Panthera
leo leo) as a threatened species was warranted and proposed to list the
subspecies as a threatened species under the Act. We also proposed a
rule under section 4(d) of the Act to provide conservation measures for
the African lion.
Summary of Changes From the Proposed Rule
We fully considered comments from the public and the peer reviewers
on the proposed rule to determine our final listing status of lion.
This final rule incorporates changes to our proposed rule based on the
comments we received that are discussed under Summary of Comments and
Responses and newly available scientific and commercial information
that became available after the close of the comment period. We accept
the taxonomy as recommended by the International Union for Conservation
of Nature (IUCN) Species Survival Commission Cat Classification Task
Force: P. l. leo (Asia and western, central, and northern Africa) and
P. l. melanochaita (southern and eastern Africa). Here we evaluate the
status of the lion species (P. leo), which includes the previously
unreviewed population of P. l. leo in India (formerly P. l. persica).
Additionally, we have incorporated new population estimates and
population trends for the lion into our Species Information section.
Based on comments by peer reviewers and others, we revised the
section on trophy hunting, providing additional information on the
practices that experts have identified as undermining the
sustainability of trophy hunting, recommended best practices and
reforms, biological impacts of trophy hunting on lion populations, and
corruption in range countries, and expanded our assessment of the level
of threat that trophy hunting presents to the species. Additionally, we
have incorporated information on infanticide, corruption, traditional
use of lion parts and products, disease, and climate change. Under the
discussion of the 4(d) rule in the preamble, we further clarify factors
we will consider when making an enhancement finding for importation of
sport-hunted trophies of P. l. melanochaita.
Based on the information we received and our assessment of that
information, we have altered our finding. Some of the information we
received indicated threats may be worse than previously indicated. Due
to significant differences in the impacts of threats within the
species, we found that P. l. leo and P. l. melanochaita qualify for
different statuses under the Act.
[[Page 80001]]
Species Information
Taxonomy
The lion (Panthera leo) was first described by Linnaeus (1758, in
Haas et al. 2005, p. 1), who gave it the name Felis leo. It was later
placed in the genus Panthera (Pocock 1930, in Haas et al. 2005, p. 1).
Although the classification of the modern lion as P. leo is accepted
within the scientific community, there was a lack of consensus
regarding lion intraspecific taxonomy (Mazak 2010, p. 194; Barnett et
al. 2006b, p. 2120).
Based on morphology, traditional classifications recognize anywhere
from zero subspecies (classifying lions as one monotypic species) up to
nine subspecies (Mazak 2010, p. 194, citing several sources). The most
widely referenced of the morphology-based taxonomies is an eight-
subspecies (six extant) classification provided by Hemmer (1974, in
Nowell and Jackson 1996, p. 312; Barnett et al. 2006a, p. 507; Barnett
et al. 2006b, p. 2120), which is recognized by the Integrated Taxonomic
Information System (ITIS) (ITIS 2013, unpaginated). It divides the lion
species into: Panthera leo persica (India); P. l. leo, commonly
referred to as the Barbary lion (Morocco through Tunisia, extinct); P.
l. senegalensis (West Africa east to the Central African Republic
(CAR)); P. l. azandica (northern Zaire); P. l. bleyenberghi (southern
Zaire and presumably neighboring areas of Zambia and Angola); P. l.
nubica (East Africa); P. l. krugeri (Kalahari region east to the
Transvaal and Natal regions of South Africa), and P. l. melanochaita,
also called the Cape lion (Cape region of South Africa, extinct)
(Nowell and Jackson 1996, p. 312).
In 1987, O'Brien (1987a, entire; 1987b, entire) reported the first
results of genetic studies conducted on lion samples from some, but not
all, regions of the species' range using early genetic techniques.
Lions in India differed from lions in Africa, supporting a two-
subspecies classification for extant lions: P. l. leo and P. l.
persica, the African and Asiatic lion, respectively (O'Brien et al.
1987, Meester and Setzer 1971, Ellerman et al. 1953, in Dubach 2005, p.
16). According to Dubach (2005, p. 16), most taxonomic authorities
recognize this two-subspecies taxonomy. This taxonomy was also
recognized by the International Union for Conservation of Nature (IUCN)
(Bauer et al. 2012, unpaginated) and, consequently, by several
international organizations and governing bodies. As a result, this is
the classification on which the conservation of the species is largely
based. However, results of recent genetic research call into question
this classification.
In recent years, several genetic studies have provided evidence of
an evolutionary division within lions in Africa (see Barnett et al.
2014, p. 6; Dubach et al. 2013, p. 746; Bertola et al. 2011 (entire);
Antunes et al. 2008 (entire); Barnett et al. 2006a, pp. 511-512). These
studies include analysis of DNA samples from all major regions of the
species' range, though some regions are sparsely represented. A major
genetic subdivision among lions occurs in Africa, with lions in
southern and eastern Africa being distinct from and more diverse than
lions elsewhere (western and central Africa and Asia) (Figure 1). Lions
in western and central Africa (as well as now-extinct North African
lions) are more closely related to lions in India than to lions in
southern and eastern Africa (Barnett et al. 2014, pp. 4-8; Dubach et
al. 2013, pp. 741, 746-747, 750-751; Bertola et al. 2011, entire).
According to Dubach et al. (2013, p. 753), current range collapse and
fragmentation is too recent a phenomenon to explain the reduced genetic
variability in these regions. Rather, the low genetic diversity in and
between western and central African lion populations suggests they have
a shorter evolutionary history than the more genetically diverse lions
in southern and eastern Africa (Bertola et al. 2011, p. 1362). Several
authors argue that the origin of these genetically distinct groups may
be the result of regional extinctions and recolonizations during major
climate (and consequently biome) fluctuations during the Pleistocene
Epoch (Barnett et al. 2014, pp. 5-8; Bertola et al. 2011, pp. 1362-
1364).
These findings on lion genetic relationships are based primarily on
analysis of mitochondrial DNA (mtDNA), which is inherited only from the
mother. Because lions display sex-biased dispersal, in which males
leave their natal range and females tend to remain in their natal
range, one would expect gene flow in females to be lower than in males,
resulting in greater geographic differentiation in females (Mazak 2010,
p. 204). Consequently, some authors state that results of mtDNA
analyses should be backed up by studies on nuclear DNA (nDNA, inherited
from both parents) and morphological traits before assigning taxonomic
importance to them (Barnett et al. 2014, pp. 1, 8).
Recently, Mazak (2010, entire) examined morphological
characteristics of 255 skulls of wild lions and found considerable
variation throughout the species' range, with variation being greater
within populations than between them. However, according to Dubach et
al. (2013, p. 742), the genetic distinction of lions in southern and
eastern Africa from those elsewhere in the species' range is confirmed
by results of studies by Antunes et al. (2008, entire) which, in
addition to analysis of mtDNA, also included analysis of nDNA sequence
and microsatellite variation.
The recent results of genetic research renewed the debate on lion
taxonomy among the experts. For this reason, the IUCN Species Survival
Commission Cat Specialist Group commissioned a Cat Classification Task
Force from among its expert members to reach a consensus on taxonomy
for the group. As we explained in our proposed rule, until the results
of the IUCN Cat Classification Task Force became available, we
concluded that the taxonomy of the species was unresolved, but, as
required by the Act, we based our status review in our proposed rule on
the best available scientific and commercial information, which was the
taxonomy that was most widely recognized by taxonomic experts: P. leo
leo (African lion) and P. leo persica (Asiatic lion) and reviewed the
status of the petitioned entity, the African lion.
In June 2015, after the close of the comment period on our proposed
rule, IUCN posted an updated Red List Assessment for lion. In this
assessment, a new two-subspecies classification is proposed based on
the recommendation of the IUCN Cat Classification Task Force: P. l. leo
of Asia (India) and western, central, and northern Africa, and P. l.
melanochaita for southern and eastern Africa (Bauer et al. 2015a,
unpaginated) (Figure 1), which is supported by Barnett et al. (2014, p.
6), Dubach et al. (2013, p. 746), Bertola et al. (2011, entire),
Antunes et al. (2008, entire), and Barnett et al. (2006a, pp. 511-512).
[[Page 80002]]
[GRAPHIC] [TIFF OMITTED] TR23DE15.000
As required by the Act, and as explained in our proposed rule, we
base our listing determinations on the best available scientific and
commercial information. We accept the taxonomy as recommended by the
IUCN Cat Classification Task Force, which is supported by mtDNA
analysis, as well as analysis of nDNA sequence and microsatellite
variation: P. l. leo (Asia and western, central, and northern Africa)
and P. l. melanochaita (southern and eastern Africa) (Figure 1) as the
best available scientific and commercial information. Because this new
classification for lion includes subspecies whose ranges span two
continents, we assessed the status of the entire lion species (P. leo).
Currently, the Asiatic lion (P. l. persica) is listed as an
endangered species under the Act. Based on the new taxonomic
classification for lions, we are revising the List of Endangered and
Threatened Wildlife at 50 CFR 17.11(h). In the Regulation Promulgation
section of this document, we implement a taxonomic change by removing
the invalid subspecies P. l. persica. This entity is now included in
the assessment of the lion species (P. leo).
Species Description
The lion is the second-largest extant cat species (second in size
only to the tiger) and the largest carnivore in Africa (Ray et al.
2005, p. 67). As with other widely distributed large cats, there is
considerable morphological variation within the species as a result of
sexual selection, regional environmental adaptations, and gene flow
(Mazak 2010, p. 194). These include, among others, variation in size,
coat color and thickness, mane color and form, and skull
characteristics (Mazak 2010, p. 194, citing several sources; Hollister
1917, in Dubach 2005, p. 15). They are described in the Convention on
International Trade in Endangered Species of Wild Fauna and Flora
(CITES) Periodic Review of the Status of African Lion Across Its Range
(CITES 2014, p. 3) as follows:
Characteristics include sharp, retractile claws, a short neck, a
broad face with prominent whiskers, rounded ears and a muscular
body. Lions are typically a tawny color with black on the backs of
the ears and white on the abdomen and inner legs. Males usually have
a mane around the head, neck and chest. Lions are sexually
dimorphic, with males weighing about 20-27 percent more than
females. Adult males, on average, weigh about 188 kilograms (kg)
(414 pounds (lbs)) with the heaviest male on record weighing 272 kg
(600 lbs). Females are smaller, weighing, on average, 126 kg (278
lbs). The male body length, not including the tail, ranges from 1.7
meters (m) to 2.5 m (5.6 feet (ft to 8.2 ft) with a tail from 0.9 m
to 1 m (3 ft to 3.2 ft) (Nowell and Jackson, 1996).
Lions in India tend to be smaller than those in Africa. Adult males
weigh between 160-190 kg (353-419 lb), while females weigh between 110-
120 kg (243-265 lb) (Chellam in litt. in Nowell and Jackson 1996, p.
37). The record total length for a male lion in India, including the
tail, is 2.92 m (9.6 ft) (Sinha 1987 in Nowell and Jackson 1996, p.
37). One characteristic unique to lions in India is a longitudinal fold
[[Page 80003]]
of skin that runs along the belly (O'Brien et al. 1987, p. 100).
Additionally, male lions in India do not have as large and full a mane
as those in Africa, allowing their ears to always be visible, whereas
the manes of male lions in Africa completely hide the ears (Nowell and
Jackson 1996, p. 37; O'Brien et al. 1987, p. 100).
Habitat
Historically, the species occurred in all habitats in Africa,
except rainforest and the hyper-arid interior of the Sahara (Ray et al.
2005, p. 66). Today they are found primarily in savannas, although
there are some remnant populations in other habitat types (Riggio et
al. 2013, p. 19). According to Nowell and Jackson (1996, p. 19),
optimal habitat appears to be open woodlands and thick bush, scrub, and
grass complexes, where sufficient cover is provided for hunting and
denning. The highest lion densities are reached in savanna woodlands
plains mosaics of southern and eastern Africa (Ray et al. 2005, p. 66).
The species is intolerant of anthropogenic (human-caused) habitat
conversion, such as farming or overgrazing by livestock (Ray et al.
2005, p. 66). In India, the lion occurs in dry deciduous forests (Meena
et al. 2014, p. 121). Moist mixed and mixed forest habitats are
critical to lions as they seek moist shady habitats that provide
shelter from the heat and cover to hide during peak times of human
activities (Jhala et al. 2009, p. 3391).
General Biology
Lions are well studied. Much information exists on habits,
behavior, and ecology of lions in Africa. CITES (2014, p. 3) provides a
general overview as follows:
Lions are generalist, cooperative hunters, with foraging
preferences changing with season and with lion group size. Lions
live in groups called ``prides,'' which are ``fission-fusion''
social units with a stable membership that sometimes divide into
small groups throughout the range. Lions have no fixed breeding
season. Females give birth every 20 months if they raise their cubs
to maturity, but the interval can be as short as 4-6 months if their
litter is lost. Gestation lasts 110 days, litter size ranges 1-4
cubs, and sex ratio at birth is 1:1. At about 4 years of age,
females will have their first litter and males will become resident
in a pride. Pride takeovers by male lions and subsequent infanticide
of cubs sired by the ousted male lions greatly influences
reproductive success. Lionesses defending their cubs from the
victorious males are sometimes killed during the takeover.
Infanticide accounts for 27 percent of cub mortality. Adult
mortality is typically caused by humans, starvation, disease, or
attacks from other lions. Injury and death can also occur during
hunting attempts on some of their larger prey.
Haas et al. (2005, entire) provide a summary of information on lion,
including the following:
Prides vary in size and structure, but typically contain 5-9
adult females (range, 1-18), their dependent offspring, and a
coalition of 2-6 immigrant males (Heinsohn and Packer 1995; Packer
et al. 1991). . . . Pride sizes are smallest in arid environments
with limited prey species (Elliott and Cowan 1977; Hanby and Bygott
1979; Ruggiero 1991; Schaller 1972; Stander 1992b; Wright 1960). . .
. Males reside in a pride for [approximately] 2 years before being
replaced by another group of males (Packer et al. 1988). . . . In
the absence of a pride takeover, males generally leave their natal
pride when 2-4 years old (Bertram 1975b; Pusey and Packer 1987).
Most females are incorporated into their natal prides (Pusey and
Packer 1987; Van Orsdol et al. 1985). . . . A small proportion of
lions is nomadic, including young and adult males without a pride.
Nomadic lions follow the migrations of prey and hunt and scavenge
cooperatively (Bertram 1975a; Bygott et al. 1979; Schaller 1968,
1969; Van Orsdol et al. 1985).
. . . Lion productivity (measured as number of surviving cubs)
is limited by food. . . . Cub mortality is high in lions and is
linked to periods of prey scarcity and infanticide by male lions
during pride takeovers (Packer and Pusey 1983b; Schaller 1972; Van
Orsdol et al. 1985; Whitman and Packer 1997).
. . . Lions are mainly active at night. . . . [They] usually
hunt in groups; males hunt less frequently than do females, but
males are stronger and can gain access to kills made by females
(Bertram 1975a; Scheel and Packer 1991). Prey selection is related
to seasonal weather patterns and the migration of large herbivores
in some parts of Africa (Hanby et al. 1995). . . . Lions exhibit
individual preferences in prey selection within and between prides
in the same area (Rudnai 1973b; Van Orsdol 1984).
Lion prides in India tend to be smaller than those in Africa; most
prides in India contain an average of two females, with the largest
having five. Coalitions of males will defend home ranges that contain
one or more groups of females, but unlike lions in Africa, in India
male lions only associate with pride females when mating or on a large
kill (Meena 2009, p. 7; Nowell and Jackson 1996, p. 37). Females are
approximately 4 years old at first reproduction, males 5-8 years
(Banerjee and Jhala 2012, p. 1424; Nowell and Jackson 1996, p. 37).
Banerjee and Jhala (2012, p. 1424) found that mating occurred
throughout the year, but mostly in winter. Gestation lasts 110 days;
births peaked in the summer (April-May). Average litter size is 2.5
cubs, but as many as 5 have been observed (Banerjee and Jhala 2012, pp.
1424, 1427; Nowell and Jackson 1996, p. 37). Lion reproduction in India
appears to coincide with the fawning peak of chital deer (Axis axis)
between December and January or with the rutting season of chital and
peak fawning for sambar deer (Cervus unicolor) between May and June.
Breeding lionesses may cue into these times of increased availability
of food sources to time births for maximum survival of cubs (Banerjee
and Jhala 2012, p. 1427). Average interbirth interval is estimated to
be 1.37 years; however, if cubs of the previous litter survived to
independence, it could be higher. After territorial takeovers and
infanticides, females mated within an average 4.8 months (Banerjee and
Jhala 2012, p. 1424). Banjeree and Jhala (2012, p. 1424) found that the
major cause of cub mortality is infanticide due to territorial
takeovers by adult males. Most observed adult mortalities (54.5
percent) were due to natural causes and 43 percent were due to human
causes; remaining mortalities were due to unknown causes.
Diet and Prey
Lions are opportunistic hunters and scavengers. As scavengers,
lions are dominant and can usually readily displace other predators
from their kills (Packer 1986, Schaller 1972, in Haas et al. 2005, pp.
4-5). As hunters, they are known to take a variety of prey. However,
they are also the largest carnivore in Africa and, as a result, require
large prey to survive. Ray et al. (2005, pp. 66-67) summarizes lion
prey in Africa as follows:
Lions are generalists and have been recorded to consume
virtually every mammal species larger than 1 kg in their range, as
well as a wide variety of larger reptiles and birds (Nowell &
Jackson 1996; Sunquist & Sunquist 2002). The constraints of large
physical size and extended social groups, however, bind them to
large-bodied prey, and their diet is dominated by medium-large
ungulates. In fact, only a few species of large ungulates comprise a
majority of their diet wherever they occur (Schaller 1972; Stander
1992; Packer et al. 1995), and they are unable to persist in areas
without large-bodied prey. The threshold of this requirement is
perhaps represented at Etosha National Park, Namibia, where Stander
(1992) showed that lions hunting in pairs met their minimum
requirements hunting springboks which, at < 50 kg, are the smallest
preferred prey species recorded.
In India, the lion's diet is comprised of both small and medium
prey, as well as vulnerable livestock (Meena et al. 2011, p. 61; Singh
and Gibson 2011, p. 1753; Meena 2009, p. 8). The most commonly taken
species is chital, which weighs approximately 50 kg (110 lb), and a
larger species, the sambar deer
[[Page 80004]]
(Meena et al. 2011, p. 63; Nowell and Jackson 1996, p. 37). The smaller
size of the prey available in India may be responsible for the smaller
lion group sizes and less interaction between male and female groups
(Meena 2009, p. 8; Nowell and Jackson 1996, p. 37). Historically,
domestic cattle also constituted a major portion of the lion's diet
(Nowell and Jackson 1996, p. 37) and remains a significant portion
today (Meena et al. 2011, pp. 63, 64; Singh and Gibson 2011, pp. 1753-
1754). The proportion of wild prey and domestic livestock in a lion's
diet may vary by season and between protected areas and peripheral
areas (Meena et al. 2011, pp. 64, 65).
Prey availability affects the reproduction, recruitment, and
foraging behavior of lions and, as a result, strongly influences lion
movements, abundance, and population viability (Winterbach et al. 2012,
p. 7, citing several sources). Lion densities are directly dependent on
prey biomass (Van Orsdol et al. 1985, in Packer et al. 2013, p. 636;
Hayward et al. 2007, entire). In Africa, lion densities range from 8-13
lions per 100 square kilometers (km\2\) in Selous Game Reserve and up
to 18 per 100 km\2\ in protected areas of eastern Africa and South
Africa (Creel and Creel 1997, Nowell and Jackson 1996, in Haas et al.
2005, p. 4). In India, densities are estimated to be 15 lions per 100
km\2\ in Gir Protected Area, 6 per 100 km\2\ in Girnar Wildlife
Sanctuary, and 2 per 100 km\2\ in the surrounding agro-pastoral land
(Banerjee and Jhala 2012, p. 1421; Banerjee et al. 2010, p. 249). Aside
from human-related mortality, prey availability is likely the primary
determinant of lion density in Africa (Fuller and Sievert 2001, in
Winterbach et al. 2012, p. 7). In areas of low natural prey density, or
high human contact, lions may prey on livestock (see Human-Lion
Conflict).
Movements/Home Range
Availability of prey is perhaps the primary factor that determines
the ranging behavior of large carnivores (Gittleman & Harvey 1982, Van
Orsdol et al. 1985, Grant et al. 2005, Hayward et al. 2009, in
Winterbach et al. 2012, p. 4). Home-range sizes of lion prides
correlate with lean-season prey biomass (Van Orsdol et al. 1985, in
Haas et al. 2005, p. 4) and, therefore, vary widely among habitats.
Average range sizes of lion prides in Africa are 26-226 km\2\, but can
be considerably larger (Stander 1992b; Van Orsdol et al. 1985; Viljoen
1993, in Haas et al. 2005, p. 4). In areas of low or variable prey
biomass, annual range requirements for a single lion pride can exceed
1,000 km\2\ (Packer et al. 2013, p. 636). Funston (2011, p. 5) found
the home ranges of lion prides in the dune-savanna habitat of Kgalagadi
Transfrontier Park to range from 1,762 to 4,532 km\2\. In India,
however, Jhala et al. (2009, p. 3391) found the average home range of a
breeding group of lionesses to be 33 km\2\. Similarly, Meena (2009, pp.
7-8) found home ranges of females and males to be 35 km\2\ and 85
km\2\, respectively.
Range
The historical range of the lion included most current continental
African countries (Chardonnet 2002, pp. 25-28) and extended from Greece
through eastern Europe, southwest Asia (the Middle East), and India
(Bauer et al. 2015a, unpaginated; Nowell and Jackson 1996, p. 38).
Lions have undergone dramatic range retraction from this historical
distribution (Ray et al. 2005, p. 67). Extirpation of lions in Europe
occurred almost 2,000 years ago. The species was extirpated from
southwest Asia within the last 150 years and northern Africa in the
1940s (Bauer et al. 2015a, unpaginated; Black et al. 2013, p. 1; Nowell
and Jackson 1996, p. 38). Today, lions occur only in Asia and sub-
Saharan Africa (Table 1). In Asia, P. l. leo only remains in the Gir
Forests of India. Within sub-Saharan Africa, P. l. leo and P. l.
melanochaita remain in 34 range countries (35 with South Sudan, which
gained its independence as a country in July 2011) and have been
recently extirpated from 12 African range countries and potentially
extirpated from another 4 (Bauer et al. 2015a, unpaginated) (Table 1).
Table 1--Range Countries of P. l. leo and P. l. melanochaita
[Information derived from Bauer et al. 2015a, unpaginated, IUCN 2006a,
IUCN 2006b, and Chardonnet 2002]
------------------------------------------------------------------------
Subspecies Countries
------------------------------------------------------------------------
Panthera leo leo.................. Algeria \1\, Benin, Burkina Faso,
Cameroon, CAR, Chad, Congo \2\,
C[ocirc]te d'Ivoire \2\, DRC, Egypt
\1\, Gabon \2\, Gambia \2\, Ghana
\3\, Guinea \3\, Guinea-Bissau \2\,
India, Liberia, Libya \1\, Mali
\2\, Mauritania \2\, Morocco \1\,
Niger, Nigeria, Senegal, Sierra
Leone \2\, Togo \3\, Tunisia \1\.
Panthera leo melanochaita......... Angola, Botswana, Burundi \2\,
Djibouti \2\, Eritrea \2\,
Ethiopia, Kenya, Lesotho \2\,
Malawi, Mozambique, Namibia, Rwanda
\3\, Somalia, South Africa, Sudan/
South Sudan, Swaziland, Tanzania,
Uganda, Zambia, Zimbabwe.
------------------------------------------------------------------------
\1\ Lions extirpated.
\2\ Lions considered recently extirpated (Bauer et al. 2015a).
\3\ Lions considered possibly extirpated (Bauer et al. 2015a).
The confirmed lion range in western Africa (the total size of
protected areas where lions were confirmed) is estimated at 49,000
km\2\, or 1.1 percent of the historic range (Henschel et al. 2014, p.
5). The most recent estimate of the lion's range throughout Africa
comes from Bauer et al. (2015a, unpaginated) who estimate the extant
lion range (areas reasonably confident that lions persist based on
recent records) to be approximately 1.6 million km\2\ (617,763 mi\2\),
or 8 percent of the historical range in Africa. The areas classified by
Bauer et al. (2015, unpaginted) as possibly extinct total approximately
1.8 million km\2\ (694,984 mi\2\), which is over half (52 percent) of
the range classified as extant by the previous estimate conducted by
Riggio et al. (2013, p. 26), which was based on estimates of savanna
habitat. The lion's range in Asia is estimated to be approximately
10,500 km\2\ (4,054 mi\2\), which occurs within the Gir National Park
and Wildlife Sanctuary (Gir Protected Area), Girnar Wildlife Sanctuary,
and surrounding agro-pastoral land (Bauer et al. 2015a, unpaginated;
Banerjee and Jhala 2012, p. 1421; Jhala et al. 2009, pp. 3384, 3385;
Nowell and Jackson 1996, p. 38).
Distribution and Abundance
The general distribution of lions in Africa is summarized by Ray et
al. (2005, p. 67) as follows:
Currently, lions are restricted mainly to protected areas and
surrounding conservancies or `game management areas,' with the
largest populations in East and southern Africa. Where protection is
poor, particularly outside protected areas, range
[[Page 80005]]
loss or population decreases can be significant. Declines have been
most severe in West and Central Africa, with only small, isolated
populations scattered chiefly through the Sahel. Lions in the region
are declining in some protected areas and, with the exception of
southern Chad and northern Central African Republic, are virtually
absent from unprotected areas (Bauer 2003).
Estimates of lion abundance on a large geographical scale are few
in number. For a variety of reasons--including low densities, large
ranges, cryptic coloration, nocturnal and wary habits--lions are
difficult to count (Riggio et al. 2013, p. 31; Bauer et al. 2005, p.
6). There are large areas of the species' range in which no data are
available on lion occurrence or abundance (IUCN 2006b, pp. 12-13).
Species experts recognize that estimating the size of the lion
population in Africa is an ambitious task, involving many uncertainties
(Bauer et al. 2012, unpaginated). Estimates, particularly throughout
Africa or broad region-wide estimates tend to rely to a considerable
extent on expert opinion or inference (Riggio et al. 2013, p. 21;
Chardonnet 2002, p. 19). Consequently, there is a large degree of
uncertainty in these estimates. In addition, to date all efforts to
estimate the number of lions in Africa have used different methods;
therefore, the results of earlier estimates cannot be directly compared
to those of later estimates to determine population trend.
The earliest estimates of lion abundance in Africa were educated
guesses made during the latter half of the 20th Century. Bauer et al.
(2008, unpaginated) summarize the information as follows:
There have been few efforts in the past to estimate the number
of lions in Africa. Myers (1975) wrote, ``Since 1950, their [lion]
numbers may well have been cut in half, perhaps to as low as 200,000
in all or even less.'' Later, Myers (1986) wrote, ``In light of
evidence from all the main countries of its range, the lion has been
undergoing decline in both range and numbers, often an accelerating
decline, during the past two decades.'' In the early 1990s, IUCN SSC
Cat Specialist Group members made educated ``guesstimates'' of
30,000 to 100,000 for the African Lion population (Nowell and
Jackson 1996).
Ferreras and Cousins (1996, entire) provided the first
quantitatively derived estimate of lion abundance in Africa using a
GIS-based model calibrated with information obtained from lion experts.
Ferreras and Cousins predicted lion abundance in Africa in 1980 to be
75,800. Later, four additional efforts--Chardonnet (2002), Bauer and
Van Der Merwe (2004), IUCN (2006a, 2006b), and Riggio et al. (2013)--
estimated lion population sizes ranging from 23,000 to 40,000 (Table
2).
Between 2006 and 2012, Henschel et al. (2014, p. 2) conducted field
surveys in protected areas within designated Lion Conservation Units
(LCUs) of western Africa to confirm lion presence where evidence of
occurrence was lacking and to establish population estimates where
lions occurred. Lions were absent from protected areas in 5 of the 10
countries in western Africa where lions were considered to be present
(Henschel et al. 2014, p. 4). Henschel et al. (2014, p. 5) estimated
only 400 lions remain in the entire western region, with most (about
350, or 88 percent) concentrated in a single population.
Bauer et al. (2015a, unpaginated) attempted to correct for outdated
sources in Riggio et al. (2013) by applying regional trends (discussed
below) to 2002 population estimates for central, eastern, and southern
Africa from Bauer and Van Der Merwe (2004) and Chardonnet (2002);
estimates for western Africa were taken from Henschel et al. (2014)
because of the greater precision of their estimate. Applying regional
trends to Bauer and Van Der Merwe (2004) lion populations estimates,
Bauer et al. (2015a, unpaginated; supporting information, Table 7)
estimated lions in central Africa to be 590, eastern Africa to be
7,345, and southern Africa to be 10,385 (Table 2). When regional trends
were applied to Chardonnet (2002) lion estimates, Bauer et al. (2015,
unpaginated; supporting information, Table 7) estimated lions in
central Africa to be 1,748, eastern Africa to be 13,316, and in
southern Africa to be 15,925 (Table 2). In total, Bauer et al. (2015,
unpaginated) estimate the lion population in Africa to be between
18,841 and 31,394. However, the authors found that the study by Bauer
and Van Der Merwe (2004) was more conservative and stricter on data
quality; therefore they have a greater confidence in an estimate closer
to 20,000 lions in Africa. Additionally, the lion population in India
was estimated to be 445 by Bauer et al. (2015a, unpaginated). In 2015,
the Government of Gujarat completed its latest census, estimating 523
lions in India (BBC 2015, unpaginated) (Table 2).
Table 2--Estimates of Lion Abundance
[Rows may not tally due to rounding]
--------------------------------------------------------------------------------------------------------------------------------------------------------
Western Africa Central Africa Eastern Africa Southern Africa
Source (percent of total) (percent of total) (percent of total) (percent of total) India Total
--------------------------------------------------------------------------------------------------------------------------------------------------------
Ferreras & Cousins 1996 (estimate .................... ................... ................... ................... ........... 75,800 (18,600 in
for lion abundance in 1980). protected areas).
Chardonnet 2002.................. 1,163 (3 percent)... 2,815 (7 percent).. 15,744 (40 percent) 19,651 (50 percent) ........... 39,373
Bauer & Van Der Merwe 2004....... 850 (4 percent)..... 950 (4 percent).... 11,000 (48 percent) 10,000 (44 percent) ........... 23,000
IUCN 2006 \1\ (as calculated by 1,640 (5 percent)... 2,410 (7 percent).. 17,290 (52 percent) 11,820 (37 percent) ........... 33,160
Riggio et al. 2013).
Riggio 2013 (based on estimates 480 (1 percent)..... 2,419 (7 percent).. 19,972 (57 percent) 12,036 (34 percent) ........... 34,907
of savanna habitat).
Henschel et al. 2014............. 406 (n/a)........... ................... ................... ................... ........... ...................
Bauer et al. 2015a (trends .................... 590 (3 percent).... 7,345 (39 percent). 10,385 (55 percent) ........... 18,726 *
applied to Bauer and Van Der
Merwe 2004).
Bauer et al. 2015a (trends .................... 1,748 (6 percent).. 13,316 (42 percent) 15,925 (51 percent) ........... 31,394 *
applied to Chardonnet 2002).
Bauer et al. 2015a............... .................... ................... ................... ................... 445 ...................
[[Page 80006]]
Government of Gujarat 2015 **.... .................... ................... ................... ................... 523 ...................
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ Estimates were made for individual Lion Conservation Units (defined management units), and were given as population size classes rather than
specific figures. As calculated by Riggio et al.
* Total includes estimate for western Africa taken from Henschel et al. (2014).
** As reported in BBC 2015, unpaginated.
As previously stated, extant lion populations are limited to
protected areas. These populations are largely isolated and many are
small. P. l. leo (totaling approximately 1,500 lions), is divided into
15 populations in and around protected areas; of these, 14 are
remaining populations from a total of 38 historical occurrences in
western and central Africa, while one occurs in India (Bauer et al.
2015a, unpaginated; Henschel et al. 2015b, unpaginated; Brugi[eacute]re
et al. 2015, p. 515; Henschel et al. 2014, pp. 4-5; Jhala et al. 2009,
p. 3384). Nearly 90 percent of the lions in western Africa persist in a
single population, the W-Arly-Pendjari (WAP) Complex (Henschel et al.
2014, p. 5). Based on Bauer et al. (2015a, unpaginated; Supporting
Information, Table 3) and Bauer and Van Der Merwe (2004, pp. 28-30),
most P. l. melanochaita occur in approximately 68 protected areas
throughout southern and eastern Africa, with larger populations
occurring in Botswana, Kenya, Namibia, South Africa, Tanzania, Zambia,
and Zimbabwe.
Population Trends
Based on the best available information, lion range and numbers
have clearly declined over the past several decades. However, not all
lion populations have declined--some have increased or remained stable,
and some have been restored to areas from which they were previously
extirpated (Bauer et al. 2015a, unpaginated; Packer et al. 2013, p.
636; Funston 2011, p. 3; Ferreira and Funston 2010, pp. 201, 203).
Bauer et al. (2015a, unpaginated), using a time trend analysis of
census data, determined the trend of lion populations from 1993 to
2014. Overall, these lion populations decreased by 43 percent in 21
years (Table 3). However, the authors found significant regional
differences. In Asia, the single population increased by 55 percent
(Bauer et al. 2015a, unpaginated). The population inside the protected
area has stabilized and expanded into surrounding agro-pastoral land
(Bauer et al. 2015b, p. 2; Breitenmoser et al. 2008, unpaginated).
Additionally, the 2015 census of Gir Sanctuary and surrounding forest
areas showed a 27 percent increase from the 2010 census (The Guardian
2015, unpaginated). In southern Africa, the sample populations overall
increased by 8 percent (Bauer et al. 2015a, unpaginated). However, one
of the largest populations, Okavango, and populations of 6 unfenced
reserves are declining (Bauer et al. 2015a, unpaginated, supporting
information Table 3; Bauer et al. 2015b, p. 1). Fifteen of the 23
sample populations in southern Africa were fenced; none experienced
sharp declines and many small fenced populations are increasing (Bauer
et al. 2015a, unpaginated, supporting information Table 3; Bauer et al.
2015b, p. 1). South Africa was the only African country with growth in
every population. However, these were all fenced populations, and most
were reestablished in the past 20 years and quickly reached capacity
(Bauer et al. 2015b, pp. 1-2). Populations in eastern Africa decreased
overall by 59 percent (Bauer et al. 2015a, unpaginated). The Serengeti
population was the only large population surveyed that did not
decrease. Katavi National Park experienced complete loss of lions from
an estimated 1,118 in 1993 to zero in 2014 (Bauer et al. 2015a,
unpaginated, supporting information Table 3; Bauer et al. 2015b, p. 1).
Western and central Africa (combined) experienced the largest decline
at 66 percent (Table 3). All populations are declining, except the
population in Pendjari; populations in Como[eacute] and Mole are now
likely extinct (Bauer et al. 2015a, unpaginated, supporting information
Table 3; Bauer et al. 2015b, p. 1). Furthermore, almost all lion
populations in Africa that historically exceeded 500 individuals, the
minimum number estimated to constitute a viable population (according
to Riggio et al. 2013, p. 32 and Bj[ouml]rklund in Riggio et al. 2013,
p. 32), are declining (Bauer et al. 2015b, p. 1).
Although these trends are based on 47 sample populations, they
comprise a substantial portion of the total remaining lion populations;
therefore, the authors are confident in applying the observed trends to
regions and the species as a whole (Bauer et al. 2015a, unpaginated).
Table 3--Regional Trends for 47 Monitored Lion Populations From 1993-2014
[Bauer et al. 2015a, unpaginated; supporting information Table 7].
----------------------------------------------------------------------------------------------------------------
Estimated lions in sample
populations
Region -------------------------------- Percent change
1993 2014
----------------------------------------------------------------------------------------------------------------
Asia............................................................ 312 485 +55
Southern Africa................................................. 4,887 5,265 +8
Eastern Africa.................................................. 3,112 1,266 -59
Western and Central Africa...................................... 1,304 439 -66
=================
Total....................................................... 9,615 7,455 -22%
----------------------------------------------------------------------------------------------------------------
[[Page 80007]]
Using these rates of change, the authors calculated that the
population in 5 countries (Botswana, India, Namibia, South Africa, and
Zimbabwe), or 25 percent of the lion's range, increased by 12 percent,
while the population in the remaining 75 percent of the range decreased
by 60 percent (Bauer et al. 2015a, unpaginated), resulting in a 43
percent population decrease of the entire lion species between 1993 and
2014.
The growth rate estimates discussed above are the best available
information on global trends for lion populations, although Bauer et
al. (2015b, p. 2) caution that these numbers are rough estimates.
However, it is unlikely that regional declines are a product of
differences in methodological shortcomings. Sample populations are all
monitored with at least partial protection. Research sites are known to
be generally avoided by poachers and encroachers. Therefore, the
estimated growth rates may be less optimistic. It is likely that
unmonitored, unfenced populations will have suffered greater rates of
decline than reported since lack of management generally means a lack
of conservation effort (Bauer et al. 2015b, p. 3).
The work of Packer et al. (2013a, pp. 639-640) predicts future
declines within a number of protected areas. Bauer et al. (2015b, p. 2)
found that if regional trends remain unchanged in the future, lions in
western and central Africa would likely lose a third of their
population in 5 years and half of their population in 10 years. The
population in eastern Africa is likely to decline by a third in 20
years and half in 30 years. The Okavago population, Botswana, will also
likely decline by a third in 20 years (Bauer et al. 2015b, p. 2). Many
lion populations are expected to disappear within the next few decades
such that the intensely managed populations in southern Africa will
replace savanna landscapes as sites for the most successful
conservation of lions.
Summary of Threats
Today, lions are mainly restricted to protected areas; however,
they still face serious threats that stem from inadequate management of
those areas and increasing pressure on natural resources to meet the
needs of a growing human population. Habitat loss has been extensive
throughout the range of the lion, resulting in local and regional lion
population extirpations and a dramatically reduced range with isolated
lion populations that are increasingly limited to protected areas. As
the human population increases, the protected areas where lions occur
will be under increased pressure as more land is needed to satisfy the
agricultural needs of the human population.
Inadequate management and law enforcement has led to poaching of
the lion's prey base in Africa for bushmeat, which has been critically
depleted. Additionally, human population growth in Africa has led to
human-lion conflict, particularly on the edge of protected areas, when
pastoralists invade protected areas to allow their herds to graze or
when lions move out of protected areas in search of prey, often preying
on domestic livestock. Human-lion conflict leads to indiscriminate
killing of lions, primarily as a result of retaliatory or preemptive
actions to protect livestock and human lives. The close proximity of
lions to humans and domestic livestock throughout their range exposes
them to diseases, mainly transmitted through livestock and domestic
dogs, which can impact general fitness, reproduction, and lifespan.
These are in addition to diseases that naturally occur in lion
populations in Africa. Furthermore, in some areas of Africa improper
management has resulted in reduced lion numbers due to excessive lion
harvests from trophy hunting. Subsequently, some lion populations are
negatively impacted by infanticide following pride takeovers by new
males.
Because habitat loss has resulted in small, isolated populations
across its range, lions face threats from stochastic events, such as a
disease epidemic and inbreeding depression. An emerging threat to lions
is trade in bones and other body parts for traditional medicine. These
causes of lion population declines are widespread and likely to
continue. The impacts of these threats are likely to be exacerbated by
climate change. Projected changes indicate negative impacts to
available habitat and, therefore, the range of the lion, prey
availability, and the number of disease outbreaks as well as
susceptibility to those diseases.
Habitat Loss
Habitat destruction and degradation have been extensive throughout
the range of the lion, resulting in local and regional lion population
extirpations, reduced lion densities, a dramatically reduced range (see
Range), and small, fragmented, and isolated lion populations that are
increasingly limited to protected areas (see Distribution and
Abundance) (Singh 2007, in Jhala et al. 2009, p. 3384; Ray et al. 2005,
p. 69; Bauer and Van der Merwe 2004, pp. 29-30; Nowell and Jackson
1996, pp. 20-21). In India, habitat loss is partly responsible for the
decline of lions to a single population in a protected area. However,
due to good protection and management, lions have dispersed to forested
areas outside the protected area, extending their range from an initial
1,883 km\2\ to 10,500 km\2\ (Johningh et al. 2007, Singh 2007, and
Divyabhanusinh 2005, in Banerjee et al. 2010, p. 248; Singh 2007, in
Jhala et al. 2009, p. 3384). Farming has been encouraged in the area
and has flourished. Cultivated areas have created refuge areas and
corridors for lion movement (Vijayan and Pati 2001 in Meena et al.
2014, p. 124). At this time, no information indicates habitat loss is
currently threatening the lion population in India. In Africa, however,
despite lions being mainly found in protected areas, habitat loss and
degradation continue to be among the main threats to lions (IUCN 2006a,
p. 18; Ray et al. 2005, pp. 68-69).
The main cause of lion habitat loss and degradation is expansion of
human settlements and activities, particularly due to agriculture and
intensive livestock grazing (IUCN 2006a, p. 18; IUCN 2006b, p. 23; Ray
et al. 2005, pp. 68-69; Chardonnet 2002, pp. 103-106). From 1970 to
2000, the human population in sub-Saharan Africa increased by 126
percent (from 282 million to 639 million) (United Nations (UN) 2013, p.
9), while at about the same time (1975 to 2000), agriculture area
increased by 57 percent (from just over 200 million ha to almost 340
million ha) and natural vegetation in the region decreased by 21
percent (Brink and Eva 2009, p. 507). In 2009, approximately 1.2
billion ha, or 40 percent, of Africa's land area was in permanent
pasture or crops, with the vast majority (31 percent) in pasture (UNEP
2012b, p. 68). Riggio et al. (2013, p. 29) estimate the original extent
of savanna habitat in Africa to be approximately 13.5 million km\2\.
Based on an analysis of land-use conversion and human population
densities, Riggio et al. (2013, p. 29) found current savanna habitat
that is suitable for lions to be fragmented and to total about 3.4
million km\2\ (or 25 percent of African savanna habitat). This
indicates a substantial decrease in lion habitat over the past 50 years
and explains, in part, why lions are limited to protected areas.
Based on a comparison of land-use and human population data, Riggio
et al. (2013, p. 23) determined that a density of 25 or more people per
km\2\ served as a proxy for the extent of land-use conversion that
would render habitat unsuitable for lions. Woodroffe (2000, p. 167)
analyzed the impact of people on predators by relating local
[[Page 80008]]
carnivore extinctions to past and projected human population densities
and estimated 26 people per km\2\ as the mean human density at which
lions went locally or regionally extinct. In 1960, 11.9 million km\2\
of the original 13.5 million km\2\ of savanna habitat had fewer than 25
people per km\2\; however, in 2000 that number decreased to 9.7 million
km\2\ (Riggio et al. 2013, p. 29).
Expansion of human settlements, agriculture, and/or livestock
grazing are reported as occurring in or on the periphery of several
areas identified by Riggio et al. (2013, suppl. 1) as lion strongholds
(viable populations) and potential strongholds (IUCN 2006a, p. 16; IUCN
2006b, pp. 20-22), and are particularly a threat in western, central,
and eastern Africa and some parts of southern Africa. Expansion of
agriculture and livestock grazing are reported in or around two of the
larger populations of P. l. leo in Africa, WAP Complex and a Chad-CAR
population (Heschel et al. 2014, pp. 5-6; Houessou et al. 2013, entire;
Chardonnet et al. 2010, pp. 24-26; IUCN 2008, pp. 8, 28-29); management
in portions of both is reported as weak (Heschel et al. 2014, pp. 5-6;
IUCN 2008, p. 8). Eastern Africa contains approximately 40 percent of
all the lions in Africa (Table 2). Seven of the seventeen major P. l.
melanochaita populations identified by Riggio et al. occur in eastern
Africa; six of which occur in Tanzania and Kenya. Between 1990 and
2010, Kenya's human population grew from 23 million (40/km\2\) to 41
million (70/km\2\), whereas Tanzania's grew from 25 million (27/km\2\)
to 45 million (48/km\2\) (UN 2013, pp. 421, 798). Not unexpectedly,
expansion of agriculture and livestock grazing is occurring in these
countries (Brink et al. 2014, entire; UNEP 2009, p. 91; Mesochina et
al. 2010a, p. 74), including in or around these major populations
(Ogutu et al. 2011, entire; Mesochina et al. 2010a, pp. 71-74, 76;
Packer et al. 2010, pp. 8-9; UNEP 2009, pp. 98-99; Newmark 2008, pp.
322-324; IUCN 2006b, pp. 20-22; Ogutu et al. 2005, entire). Mesochina
et al. (2010a, p. 74) state that widespread destruction of wildlife
habitat and human encroachment in wildlife corridors are major threats
to lion conservation in Tanzania and consider loss of suitable habitat
as a top threat to lion survival in the country. The Kenya Wildlife
Service indicates that habitat loss due to land-use changes and human
encroachment into previously wild areas is having a major impact on
lion range size in Kenya (Kenya's National Large Carnivore Task Force
2010, p. 21).
In southern Africa, the extent of current habitat destruction and
degradation appears to vary widely. For example, according to the
Zambia Wildlife Authority (2009 pp. 4-5), unplanned human settlement
and other land-use activities in game management areas are a major
threat to the long-term survival of the lion in Zambia. They note that
conversion of natural habitat in game management areas for cropping and
grazing of livestock has led to habitat destruction and indicate that
elimination of tsetse flies and subsequent increase in pastoralist
activities in game management areas places the lion under renewed
direct conflict with humans. On the other hand, according to Funston
(2008, pp. 123-126), in several areas of southern Africa where lions
were recently extirpated, lions are reestablishing as a result of,
among other factors, adequate protection of habitat and prey.
Projections of future growth in human populations, areas converted
to agriculture, and livestock numbers suggest suitable lion habitat
will continue to decrease across its range into the foreseeable future.
Between 2015 and 2050, half of the world's population growth is
expected to occur in 9 countries, 6 of which are within the lion's
range (India, Nigeria, Democratic Republic of the Congo (DRC),
Ethiopia, Tanzania, and Uganda (UN 2015, p. 4). Africa has the fastest
population growth rate in the world (UN 2015, pp. 3, 9; UNEP 2012a, p.
2), and future population growth in sub-Saharan Africa is projected to
be large and rapid (UN 2013, p. 9). By 2100, Angola, Burundi, DRC,
Malawi, Mali, Niger, Somalia, Uganda, Tanzania and Zambia are projected
to increase by at least five-fold (UN 2015, p. 9).
By 2050, the UN projects the human population of Tanzania to almost
triple its 2010 population, reaching a density of 137 people per km\2\,
whereas Kenya's population is projected to more than double, reaching a
density of 167 people per km\2\ (Table 4). Human population growth, and
resulting pressures exerted on habitat, are also expected to vary
widely in the southern region. Population increases from 2010 to 2050
are projected to range from about 23 percent (South Africa) to well
over 200 percent (Zambia), with 2050 densities in the region ranging
from 5 people per km\2\ (Botswana and Namibia) to 432 people per km\2\
(Uganda) (Table 4). The human populations of most other current and
recent lion range countries are also expected to have very high growth
rates (Table 4). The country-wide human population densities provided
here (and in Table 4) are not directly comparable to the density
thresholds determined by Riggio et al. (discussed above) due to the
differences in scale at which they were made. However, country-wide
population densities relate the number of humans to land area and,
consequently, are indicative of the level of pressure that will exist
to convert land to uses that will meet the needs of the human
population. This situation is particularly the case given that much of
sub-Saharan Africa is rural and locals depend on agriculture for their
livelihood.
Table 4--Human Population Projections in Countries Containing the 47 Sample Lion Populations Used by Bauer et
al. (2015), Except C[ocirc]te D'ivoire and Ghana Where Lions Are Considered Extirpated
[Population data is from UN 2013]
----------------------------------------------------------------------------------------------------------------
UN Population estimate, in thousands (people/km\2\)
Subspecies Country ---------------------------------------------------------------
1950 2010 2050 2100
----------------------------------------------------------------------------------------------------------------
P. l. leo.................... India............ 376,325 1,205,625 1,620,051 1,546,833
(114) (367) (493) (471)
Benin............ 2,255 9,510 22,137 32,944
(20) (84) (197) (293)
Burkino Faso..... 4,284 15,540 40,932 75,274
(16) (57) (149) (275)
Cameroon......... 4,467 20,624 48,599 82,393
(9) (43) (102) (173)
Nigeria.......... 37,860 159,708 440,355 913,834
[[Page 80009]]
(41) (173) (477) (989)
Senegal.......... 2,477 12,951 32,933 58,180
(13) (66) (167) (296)
P. l. melanochaita........... Kenya............ 6,077 40,909 97,173 160,423
(10) (70) (167) (276)
Tanzania......... 7,650 44,973 129,417 275,624
(8) (48) (137) (292)
Botswana......... 413 1,969 2,780 3,025
(1) (3) (5) (5)
Mozambique....... 6,442 23,967 59,929 112,018
(8) (30) (75) (140)
Namibia.......... 485 2,179 3,744 4,263
(1) (3) (5) (5)
South Africa..... 13,683 51,452 63,405 64,135
(11) (42) (52) (53)
Uganda........... 5,158 33,987 104,078 204,596
(21) (141) (432) (849)
Zambia........... 2,372 13,217 44,206 124,302
(3) (18) (59) (165)
Zimbabwe......... 2,747 13,077 26,254 32,608
(7) (33) (67) (83)
----------------------------------------------------------------------------------------------------------------
Although urbanization is increasing in sub-Saharan Africa, the
majority of the population is rural (UN 2014, p. 20). About 60-70
percent of the sub-Saharan population relies on agriculture and
livestock for their livelihood (UNEP 2006, pp. 82, 100, 106; IAASTD
2009, p. 2). Much of the agriculture and livestock-raising is at
subsistence level (IAASTD 2009, pp. 8, 28). As a result, a large
portion of the growing population will depend directly on expansion of
agriculture and livestock grazing to survive. Between 2010 and 2050,
the population of sub-Saharan Africa is projected to more than double
to more than 2 billion (from 831 million to 2.1 billion) (UN 2013, p.
9). During about this same time period (2005 to 2050), the area of
cultivated land is projected to increase by 51 million ha
(approximately 21 percent) (Alexandratos and Bruinsma 2012, p. 107).
However, this figure does not include range land, and the majority of
agricultural land in Africa is devoted to grazing (UNEP 2012b, p. 68).
The number of livestock (cattle, sheep, and goats) in sub-Saharan
Africa is projected to increase about 73 percent, from 688 million to
1.2 billion, by 2050 (Alexandratos and Bruinsma 2012, p. 133).
Expansion of human settlements and activities into lion habitat
renders the habitat unsuitable for lions primarily because it results
in reduced availability of the wild prey that lions depend on for
survival (see Loss of Prey Base) and increased human-lion conflict
resulting in lion mortality (see Human-Lion Conflict)--two of the main
factors that influence the distribution and population viability of
large carnivores such as lions (Winterbach et al. 2014, p. 1; Riggio et
al. 2013, p. 18). Ray et al. (2005, p. 69) note that, although lions
have a wide tolerance for habitats, they are generally incompatible
with humans and human-caused habitat alteration and loss; they are the
least successful large African carnivore outside conservation areas
(Woodroffe 2001, in Winterbach et al. 2012, p. 6). Further
fragmentation and isolation of lion habitat and populations can also
impact dispersal and genetic viability (see Deleterious Effects Due to
Small Population Sizes).
Large carnivores with low potential for cohabitation with humans
have a high risk of local extinction. In order to survive, they require
larger contiguous habitats with fewer negative human impacts than do
more resilient species (Winterbach et al. 2012, p. 5). As human
populations continue to rise in sub-Saharan Africa, the amount of land
required to meet the needs of those populations is constantly
increasing (Brink et al. 2014, entire; Brink and Eva 2009, entire; Eva
et al. 2006, p. 4), a problem accentuated by slow rates of
technological progress in food production and land degradation from
both overuse and natural causes (United Nations Environment Programme
(UNEP) 2012a, p. 3; Chardonnet et al. 2010a, p. 19; International
Assessment of Agricultural Knowledge, Science and Technology for
Development (IAASTD) 2009, pp. 3-4, 8; United Nations Economic
Commission for Africa 2008, pp. 3-5). The result of this process is
accelerated transformation of natural landscapes at the expense of
wilderness that sustains species such as lions and their prey
(Chardonnet et al. 2010a, p. 19).
Urbanization is also increasing in India, but like sub-Saharan
Africa, the majority of the population is rural (UN 2014, p. 22; Swain
et al. 2012, p. 1). In the State of Gujarat, 70 percent of all workers
are rural based, with almost 52 percent being cultivators and
agricultural laborers (Swain et al. 2012, p. 1). Suitable lion habitat
within the Gir Protected Area appears to be secure; however, habitat
outside this area that is vital for dispersal may experience increasing
pressure in the future. Dispersal corridors and resource-rich habitats
outside the protected area are important to avoid inbreeding depression
and extirpation of the lion population from stochastic events. Due to
the population growth of lions in India, there is increased movement,
dispersal, and establishment of lion in natural habitats outside the
protected area. Twenty-five percent of the lion population is found in
Girnar Wildlife Sanctuary, coastal areas, and natural
[[Page 80010]]
habitats along the Shetrunji River northeast of Gir (Meena 2014, p.
27). Additionally, the size of the Gir Protected Area implies that
dispersing lions will inevitably cross the protected area boundaries
(Meena 2010, p. 212). When lions move, they must cross heavily
populated human settlements and agricultural fields (Meena 2010, p.
209). Traditional land uses are quickly changing in the region due to
limestone mine and infrastructure development (Banerjee et al. 2010, p.
250). Additionally, tourist activities (safaris to see the lions and
religious pilgrimages to visit temples located within and on the border
of protected areas) can have detrimental impacts to wildlife if not
carefully planned. For example, construction of a road has been
proposed to circle the outside of the whole Gir Protected Area System
(Meena 2014, p. 28). Altering this habitat would result in land-use
changes, promoting rapid development and urbanization and thereby
disconnecting corridors for lion movement (Meena 2014, p. 28; Banerjee
et al. 2010, p. 250). Furthermore, crossing these areas renders lions
more vulnerable to disease transmission (See Disease below) and
conflict with humans (see Human-Lion Conflict below). Because lions are
social and territorial, they need adequate space to survive. Lack of
adequate habitat will have a bearing on the lion's ecology, behavior,
and population structure (Meena 2014, p. 28).
Growing human populations have been associated with declines in
large carnivore populations all over the world, and high human density
is strongly associated with local extirpation of large carnivores
(Linnell et al. 2001, Woodroffe 2001, in Woodroffe and Frank 2005, p.
91; Woodroffe 2000, entire). Chardonnet et al. (2002, p.103) indicate
that the distribution maps of lion subpopulations tend to confirm a
direct inverse correlation of lion density and numbers with human
activity and presence. Further, Packer et al. (2013a, entire) found
that lions in unfenced reserves are highly sensitive to human
population densities in surrounding communities.
Loss of Prey Base
One of the most important requirements for carnivore survival,
including lion, is prey availability, as it affects reproduction,
recruitment, and foraging behavior and, therefore, also impacts lion
movement, abundance, and population viability (Winterbach et al. 2012,
p. 7, citing several sources). In India, prey abundance does not appear
to be a concern for the lion population as conservation initiatives
have ensured availability of ample prey (Banerjee et al. 2010, p. 249;
Khan et al. 1996 and Singh and Kamboj 1996 in Meena 2010, p. 209; Jhala
et al. 2009, p. 3384). The semi-nomadic pastoral communities that
inhabit the Gir Forests are primarily vegetarian (Banerjee et al. 2013,
p. 2); therefore, there is no great demand for bushmeat. However, in
most African countries, large carnivores such as lions are under
serious threat through decreased prey abundance (Bauer et al. 2014, p.
97) due to unsustainable and increasingly commercialized bushmeat
hunting in and around protected areas (Bauer et al. 2015a, unpaginated;
Henschel et al. 2015, unpaginated; Henschel et al. 2014, p. 5; Lindsey
et al. 2013b, p. 84; Lindsey and Bento 2012, pp. 1-2, 61; Scholte 2011,
p. 7; Bouch[eacute] et al. 2010, pp. 1000, 1001; Cragie et al. 2010, p.
2227; Brashares et al. 2004, p. 1181; Fischer and Linsenmair 2001, pp.
132, 133).
Humans in Africa rely on protein obtained from bushmeat, resulting
in direct competition for prey between humans and lions, and commercial
poaching of wildlife is becoming a significant threat to many species,
including those that lions rely upon for food. Subsistence hunting was
traditionally carried out with the use of spears, which had minimal
impact to wildlife populations. Spears have since been replaced by
automatic weaponry (Chardonnet et al. 2010, p. 27) and snares, which
are most commonly used (Lindsey et al. 2013b, p. 83). These methods
allow for poaching of large numbers of animals for the bushmeat trade,
particularly snares, which are cheap, difficult to detect, and
unselective as they can kill nontarget animals ranging from rodents to
elephants (Lindsey et al. 2013b, p. 83).
The human population in a majority of African countries within the
range of the lion has quadrupled since the 1960s (Riggio et al. 2013,
p. 29; IUCN 2009, p. 15), increasing the demand for bushmeat. Bushmeat
contributes significantly to food security, and is often the most
important source of protein in rural areas (Nasi et al. 2008 in Lindsey
et al. 2013b, p. 82). It comprises between 6 percent (southern Africa)
and 55 percent (CAR) of a human's diet within the lion's range in
Africa (Chardonnet et al. 2005, p. 9; IUCN 2006b, p. 19). In western
Africa, bushmeat is a secondary source of protein, with fish being the
primary source. However, when widespread loss of jobs and income occurs
due to poor fish harvests, bushmeat becomes an important source of
income and sustenance, leading to increased presence of hunters in
protected areas and higher than average declines in wildlife (Brashares
et al. 2004, pp. 1180-1181).
The sale of bushmeat is an important livelihood in Africa
(Chardonnet et al. 2010, p. 27; Mesochina et al. 2010a, p. 38; Abwe and
Morgan 2008, p. 26; Bennett et al. 2007, p. 885; Fa et al. 2006, p.
507). The little meat produced from domestic livestock is unaffordable
for common people (Bouch[eacute] et al. 2010, p. 1001). Bushmeat
hunting is rarely practiced solely for subsistence. It supplies meat
for local consumption and trade, urban markets, and even international
markets (Lindsey et al. 2013b, pp. 86-87). Outlets for the sale of
bushmeat have arisen in some areas, and full-time commercial bushmeat
traders occur in most southern and eastern African countries (Lindsey
et al. 2013b, p. 86). Significant distribution of bushmeat to Europe
and the United States, where it is sold at elevated prices, drives
increasing commercialization of trade, a greater number of hunters,
adoption of more efficient hunting methods, and an unprecedented
pressure on wildlife populations (Stiles 2011 and Barnett 2000 in
Lindsey et al. 2013b, p. 88). Many illegal hunters are poor (Barnett
2000 in Lindsey et al. 2013b, p. 88; Lindsey and Bento 2012, p. 37;
Scholte 2011, p. 7). Bushmeat trade can provide a quick income to
purchase other food and essentials (Lindsey et al. 2013b, p. 82;
Lindsey and Bento 2012, p. 62). Hunters are wealthier than non-hunters
(Knapp 2007 in Lindsey et al. 2013b, p. 86) and enjoy elevated social
status.
This growing demand and the availability of modern weapons have led
to many African wildlife species being hunted at unsustainable levels
and the lion prey base becoming depleted in many areas (Hoppe-Dominik
et al. 2011, p. 452; Chardonnet et al. 2010, pp. 6, 13-14, 27; Packer
et al. 2010, p. 8; Frank et al. 2006, p. 12). Because wildlife has been
depleted in non-protected areas, illegal bushmeat hunters are
increasingly focusing efforts on protected areas (Lindsey et al. 2013b,
p. 84). Weak management effectiveness and inadequate law enforcement
have facilitated poaching for bushmeat in protected areas and resulted
in a widespread decrease in large mammal populations, including lion
prey, in these areas (Henschel et al. 2015b, unpaginated; Henschel et
al. 2014, pp. 5, 7; Lindsey et al. 2013b, pp. 84, 88; Lindsey and Bento
2012, p. 61; Scholte 2011, p. 7; Bouch[eacute] et al. 2010, pp. 99,
1001; Brashares et al. 2004 in Craigie et
[[Page 80011]]
al. 2010, p. 2227; Fischer and Linsenmair 2001, p. 134).
Significant decreases in prey abundance have occurred in protected
areas throughout Africa (Lindsey et al. 2013b, pp. 84, 85; Scholte
2011, pp. 2, 8; Craigie et al. 2010, p. 2225); Botswana (Bauer et al.
2014, pp. 101, 103); CAR (Bouch[eacute] et al. 2010, pp. 99, 1000;
Roulet 2004 in Bouch[eacute] et al. 2010, p. 1002); Chad (Potgieter et
al. 2009 in Bouch[eacute] et al. 2010, p. 1002); C[ocirc]te d'Ivoire
(Fischer and Linsenmair 2001, p. 134); DRC (Martin and Hillman-Smith
1999 in Bouch[eacute] et al. 2010, pp. 1001-1002); Ghana (Brashares et
al. 2004, p. 1182); Kenya (Western et al. 2009, pp. 2, 3, 4);
Mozambique (Lindsey and Bento 2012, p. 63); Sudan (UNEP 2006 in
Bouch[eacute] et al. 2010, p. 1001); Zambia (Simasiku et al. 2008 in
Lindsey et al. 2013b, p. 84); and Zimbabwe (Zimbabwe Parks and Wildlife
Management Authority 2015, p. 9). Bouch[eacute] et al. (2010, p. 1001)
found that large wilderness areas spanning the boundaries of Chad, CAR,
DRC, and Sudan suffered depleted wildlife abundance. Lindsey et al.
(2013b, p. 84) concluded that the case studies represented only a tiny
fraction of the areas in savannas that are severely impacted by
bushmeat hunting. Craigie et al. (2010, p. 2226) stated their study
might underestimate the extent of decline that has occurred in Africa's
protected areas because data came from sites with resources to carry
out long-term monitoring programs and increased management may be
associated with greater capacity to address threats.
Low lion population densities have been found to correspond with
low prey densities (Van Orsdol et al. 1985, Hayward et al. 2007 in
Bauer et al. 2015a, unpaginated; Bauer et al. 2014, p. 103; Bauer et
al. 2010, p. 363). Regional trends in lion populations, as discussed
above, mirror regional trends in herbivore populations in western,
eastern, and southern Africa between 1970 and 2005 (Bauer et al. 2015a,
unpaginated; Henschel et al. 2015, unpaginated). Overall, Craigie et
al. (2010, p. 2225) found a 59 percent decline in large mammal
populations. Regional differences in herbivore population abundance
were also detected. While population sizes in southern Africa increased
by 24 percent, they declined by 52 percent and 85 percent in eastern
and western Africa, respectively (Craigie et al. 2010, p. 2225).
Continent-wide decreases in prey abundance in African protected
areas are driven by human population growth (Craigie et al. 2010, p.
2225), especially along the boundaries of protected areas where human
population growth rates are high, encroachment and habitat loss occurs,
and people are dependent on bushmeat. Protected areas in Ethiopia,
Mozambique, Tanzania, and Zambia are increasingly settled (Lindsey et
al. 2013b, pp. 87, 88; Lindsey and Bento 2012, p. 64; Scholte 2011, p.
7). Hunting is more prevalent close to borders and near human
settlements as the longer the distance, the more time, effort, and cost
is needed to find and transport meat; the chances of detection are also
increased with distance (Lindsey et al. 2013b, pp. 84, 88; Brashares et
al. 2001, p. 2475). Additionally, communities often retain livestock as
assets and rely on bushmeat for daily protein needs (Barnett 2000 in
Lindsey et al. 2013b, p. 88). Furthermore, many communities lack the
rights over land and in most cases in Botswana, Tanzania, Zambia, and
Zimbabwe, the government retains a significant portion of revenue from
wildlife; therefore, those that bear the costs of wildlife do not
receive benefits, and bushmeat hunting is the only way to benefit from
wildlife (Lindsey et al. 2013b, p. 88).
Throughout the African range countries, hunting of wildlife is
regulated by various laws and regulations and harvests are controlled
through permitting systems and quotas (Lindsey et al. 2013b, pp. 82-
83). In many countries, the use of snares, poison, and automatic
weapons, among other methods, is prohibited. Single-shot firearms,
muzzle-loading firearms, shot guns, and bows and arrows are legal under
certain circumstances when permitted, and in some cases specific
calibers and bow strengths are given depending on the species being
hunted (Lindsey et al. 2013b, p. 82). Hunting laws also specify hunting
seasons and prohibit hunting in certain protected areas, hunting
certain species, and hunting young or pregnant animals. Therefore,
bushmeat hunting is illegal in most situations due to violations of one
or more of these restrictions (Lindsey et al. 2013b, p. 83). However,
penalties for violations are inadequate and do not inhibit illegal
bushmeat hunting. Penalties typically comprise warnings, community
service, or fines that are often lower than the value of the meat, or
the hunter is not penalized at all. Many governments lack the will and
most state wildlife agencies lack the resources or expertise to
effectively enforce laws (Lindsey et al. 2013b, p.88). Some government
officials and police are known to purchase bushmeat, despite it coming
from an illegal source, which further contributes to ineffective
regulation of illegal hunting (Lindsey and Bento 2012, p. 63). Given
the widespread and significant decrease in lion prey throughout its
range in Africa, it is apparent that enforcement of laws and
regulations is not adequate. Additionally, weak management of protected
areas has caused declining prey populations (Henschel et al. 2015,
unpaginated; Henschel et al. 2014, pp. 5-6; Craigie et al. 2010,
entire).
The human population in the developing world is projected to
increase rapidly, suggesting human pressure on protected areas will
also increase (Lindsey et al. 2013b, p. 84; Brashares et al. 2001, p.
2475). Without intervention, wildlife resources will be lost in many
areas with severe ecological impacts (Lindsey et al. 2013b, p. 84).
Because lion densities closely mirror prey densities, we can expect
that lion populations will also be lost in Africa.
Human-Lion Conflict
The lion population in and around the Gir Protected Area, India,
lives among and is surrounded by many pastoral and forest settlements
(Banerjee and Jhala 2012, p. 1421; Singh and Gibson 2011 in Banerjee
and Jhala 2012, p. 1421; Banerjee et al. 2010, p. 249; Singh 2007 in
Jhala et al. 2009, p. 3385). The lion population of Gir has increased
and dispersed into the large agro-pastoral area adjacent to the
protected area. Only 10 percent of lions in India occur in the human-
free portion of Gir National Park (Banerjee et al. 2013, p. 8).
Conflict there, like in Africa, arises from predation of livestock and
associated threats to security of pastoral livelihoods (Karanth and
Chellam in Banerjee et al. 2013, p. 1). The lion's diet there includes
livestock (Banerjee et al. 2013, p. 6; Meena et al. 2011, pp. 63-65).
Between 2001 and 2010 the number of villages reporting depredation of
livestock increased (Meena et al. 2014, pp. 122-123). Additionally,
Meena (2012, p. 36) found that in all Forest Divisions, except Gir
West, annual livestock predation increased more than 100 percent in 5
years. However, despite the lion's close occupation with human
settlements and increased predation on livestock, human-lion conflict
and associated retaliatory killing was not found to be a major source
of lion mortality (Pathak et al. 2002 in Banerjee and Jhala 2012, p.
1427), mainly due to low economic losses via certain husbandry
practices and a compensation scheme (Meena et al. 2014, pp. 123, 124;
Banerjee et al. 2013, pp. 6-7, 8), cultural ethics (Raval 1991 in
Banerjee et al. 2013, p. 2; Banerjee et al. 2013, p. 8), and strict
legal enforcement (Banerjee et al. 2013, p. 8).
[[Page 80012]]
Although some lions have been killed (Meena 2008 and Meena et al. 2007
in Meena 2010, p. 211), the lion population remained stable between
2001 and 2010 (Meena et al. 2014, p. 123).
Although human-lion conflict is not currently considered a threat
to the lion population in India due to tolerance of lion presence by
the pastoralist community (Banerjee et al. 2013, pp. 1-2, 8; Pathak et
al. 2002 in Banerjee and Jhala 2012, p. 1427), human-caused mortality
is likely to increase in the future due to increased human-lion
conflict and will be a major threat to the persistence of the lion
population (Banerjee and Jhala 2012, p. 1428). Similar to the observed
transition in the Maasai community in eastern Africa, traditional value
systems of pastoralists in India are rapidly changing under the
influence of globalization and free markets. The younger generation is
becoming less tolerant to even small monetary losses. These changes in
attitudes will likely result in less tolerance of livestock loss to
lions (Banerjee et al. 2013, p. 8). An indefinite increase in humans
and livestock within Gir Forests would upset the current balance by
altering forest composition or population dynamics of prey species and
would be detrimental to conservation (Banerjee et al. 2013, p. 8).
Furthermore, with an expanding lion population that disperses and uses
habitat in agro-pastoral areas densely populated with human villages,
there is an increased potential for human-lion conflict (Meena 2010 and
Singh 2007 in Meena et al. 2014, pp. 120, 121). Due to high human
density and demand for land, most human-free protected areas in India,
and elsewhere, are too small to hold viable populations of large
carnivores for the long term (Narain et al. 2005 and Karanth 2003 in
Banerjee et al. 2013, p. 8).
Human-lion conflict and associated retaliatory killing of lions has
played a major role in the reduction of lion populations throughout
Africa (Lion Guardians 2013, p. 1; Lion Guardians 2011, p. 2; Hazzah
and Dolrenry 2007, p. 21; Frank et al. 2006, p. 1; Patterson et al.
2004, p. 508) and is a threat to remaining lion populations (Bauer et
al. 2010, p. 363; Hazzah et al. 2009, p. 2428; Moghari 2009, p. 31;
Kissui 2008, p. 422; Frank et al. 2006, pp. 1, 3, 10; Ray et al. 2005
in Hazzah 2006, p. 2; IUCN 2006b, p. 18). Conflict between humans and
wildlife has been linked to population declines, reduction in range,
impacts to small population demographics, and even species extinctions
(Dickman 2013, p. 377; Sogbohossou et al. 2011, p. 61; Begg and Begg
2010, p. 2; Hazzah et al. 2009, p. 2428; Moghari 2009, p. 36; Kissui
2008, p. 422; Hazzah 2006, pp. 15, 23, 25).
Human-lion conflict stems from human population growth and the
resulting overlap of humans and wildlife habitat, with associated
livestock encroachment and decreasing availability of prey (Hoppe-
Dominik et al. 2011, p. 452; Chardonnet et al. 2010, pp. 6, 13-14;
Frank et al. 2006, p. 12; Hazzah 2006, pp. 14, 15). Lion populations
are increasingly restricted to protected areas due to human expansion
and associated expansion of livestock husbandry and agricultural
activities. Despite being within protected areas, lions, due to their
large home range, often range beyond protected area borders where they
are exposed to and impacted by people living on adjacent land.
Therefore, most conflict occurs at protected area boundaries (Henschel
2015, pers. comm.; Woodroffe and Ginsberg 1998, p. 2126). It is along
these borders that villages are often established and human
encroachment occurs due to conversion of natural habitats for
agriculture and grazing livestock, which increases the chance of human-
lion encounters (Sogbohossou et al. 2011, pp. 51, 62; Chardonnet et al.
2010, p. 23; Mesochina et al. 2010a, p. 39; Mesochina et al. 2010b, p.
33; Moghari 2009, p. 14). Furthermore, cattle herders enter the
protected areas, and lions move beyond the borders of protected areas
in search of food, increasing interactions between humans and lions and
the risk of human-lion conflict (Burkina Faso 2014, pp. 19-20, 21;
Hazzah et al. 2013, p. 1; Republic of Namibia 2013, p. 13; Bauer et al.
2010, p. 365; Chardonnet et al. 2010, pp. 11-12; Mesochina et al.
2010a, p. 39; Mesochina et al. 2010b, p. 33; Packer et al. 2010, pp. 2,
6; Gebresenbet et al. 2009, p. 9; Moghari 2009, pp. 1, 14, 25, 26, 78;
Kissui 2008, p. 422; Hazzah 2006, p. 2). Hunting zones are thought to
serve as buffers; however, these areas are not adequate as a low
density of competitors in these areas may attract wildlife, including
lions, which further disperse into villages, causing conflicts
(Sogbohossou et al. 2011, p. 51). Lion attacks can have various impacts
on those communities that coexist with conflict-causing animals,
generating resentment towards them. When lions in Africa cause or are
perceived to cause damage to livestock, property, or people, the
response is generally to kill them (Dickman 2013, pp. 378-379; Moghari
2009, p. 25; Frank et al. 2006, p. 1).
Attacks on Livestock in Africa
The most significant cause of human-lion conflict is livestock
depredation. In addition to bushmeat trade, the demand for food to meet
increasing needs of a growing population has been met by intensified
agriculture and livestock practices (Chardonnet et al. 2010, p. 19). As
natural habitats are converted to agricultural or pastoral land, the
lion's natural prey base is further reduced (Chardonnet et al. 2010, p.
27; Gebresenbet et al. 2009, p. 9). As a result of prey species
becoming depleted in many areas, lions seek out livestock (and in some
cases, humans) for food (Zimbabwe Parks and Wildlife Management
Authority 2015, p. 9; Burkina Faso 2014, p. 20; Hoppe-Dominik et al.
2011, p. 452; Chardonnet et al. 2010, pp. 6, 13-14, 27; Gebresenbet et
al. 2009, p. 9; Moghari 2009, pp. 78, 83; Frank et al. 2006, p. 12;
Hazzah 2006, pp. 17-18; Patterson et al. 2004, pp. 507, 514).
Therefore, lion attacks occur at the highest frequency in areas where
natural prey abundance is lowest (Packer et al. 2010, p. 9; Frank et
al. 2006, pp. 9, 12; Patterson et al. 2004, p. 507).
Pastoralists allow increasing numbers of livestock to graze in and
adjacent to protected areas, and villagers farm up to the boundaries of
protected areas, subjecting livestock and humans to lions and
increasing the risk of predation and the number of livestock lost to
predation (Brugi[eacute]re et al. 2015, p. 514; Bauer et al. 2014, p.
98; Burkina Faso 2014, pp. 19-22; Hazzah 2013, p. 1; Chardonnet et al.
2010, pp. 11-12; Uganda Wildlife Authority 2010, p. 27; Moghari 2009,
pp. 1, 90). Additionally, poor husbandry practices and grazing of
livestock within or adjacent to protected areas increase exposure of
livestock to lions and increase livestock loss (Uganda Wildlife
Authority 2010, p. 27; Woodroffe and Frank 2005 in Moghari 2009, p. 35;
Hazzah and Dolrenry 2007, pp. 22-23). Furthermore, conversion of
rangeland to agricultural use has blocked several migratory routes for
Tanzania's wildebeest and zebra populations, which likely forces lions
to rely more on livestock (Packer et al. 2010, p. 9). Because most
protected areas are too small to support a lion's large home range,
adjacent dispersal areas are often used for supplementary food, putting
them in greater contact with livestock and humans (Kissui 2009, p. 422;
Moghari 2009, p. 27). Conditions worsen as livestock numbers and area
under cultivation increase, leading to overgrazing, further habitat
destruction, and greater depredation rates (Gebresenbet et al. 2009, p.
9;
[[Page 80013]]
Hazzah 2006, p. 61; Frank et al. 2005, Ntiati 2002, Mishra 1997,
Meriggi and Lovari 1996, Rao 1996, Mech et al. 1988 in Hazzah 2006, p.
18).
The use of fences to subdivide rangeland interferes with
traditional wet and dry season grazing schedules for livestock and
wildlife (Hazzah 2006, pp. 58-59). Restricting wildlife movement
reduces wild prey and, when combined with an increase in livestock
numbers, increases the rate of human-lion conflict (Hazzah 2006, pp.
59, 61). Although well-built bomas (a livestock enclosure) can
effectively constrain cattle and keep predators out (Frank et al. 2006,
p. 8), they are traditionally built to keep livestock confined, but do
not offer effective protection from predators (Moghari 2009, p. 35). In
the absence of reliable methods for protecting livestock, some amount
of depredation can be expected, and some lions can become habitual
livestock killers (Frank et al. 2006, p. 9).
Rates of livestock depredation vary with regional rainfall that
correlate with prey availability, including changes in herding
strategies, movement of prey, and movement of lions (Lion Guardians
2011, p. 6; Moghari 2009, p. 32; Hazzah 2006, pp. 17, 18; Patterson et
al. 2004, p. 514). For example, in some parts of Zimbabwe, Kenya, and
Tanzania, livestock losses occur during the dry season. During this
time, herders travel farther for forage and water, they use temporary
bomas that are typically weak, they are unfamiliar with carnivore
movements in these new areas, and livestock are weak due to disease,
which makes them more vulnerable to predator attacks by lions (Hazzah
2006, p. 17). Additionally, herders are dependent on resources within
protected areas, and livestock may be left to wander for days or weeks
during a prolonged drought to find forage, increasing opportunities for
attacks on livestock by lions (Sogbohossou et al. 2011, p. 44;
Chardonnet et al. 2010, p. 24; Frank et al. 2006, p. 6). In Benin,
other parts of Kenya, the Maasai Steppe region of Tanzania, and Queen
Elizabeth National Park, Uganda, livestock losses were greater during
or following the rainy season (Sogbohossou et al. 2011, p. 49; Moghari
2009, p. 88; Kissui 2008, pp. 427, 428; Frank et al. 2006, p. 6;
Patterson et al. 2004, pp. 510, 514). Weakened prey and readily
available carcasses provide easy meals during times of drought, and
wild herbivores tend to concentrate near available water sources,
making them easier to prey on and leading to fewer livestock attacks.
However, when rains return, the abundant grass makes wild prey harder
to catch, and lions may turn to livestock. Migratory prey species such
as zebra and wildebeest will move to other areas for forage and
replenished water sources, leaving lions to turn to livestock as an
alternate food source. Migratory prey may also move outside of
protected areas. Opportunities for livestock predation on communal land
increase when lions follow migratory prey out of protected areas
(Sogbohossou et al. 2011, p. 50; Packer et al. 2010, p. 9; Kissui 2008,
p. 427; Patterson et al. 2004, p. 514; Frank et al. 2006, p. 6).
Traditional livestock husbandry practices are effective at reducing
depredation of livestock by lions (Chardonnet et al. 2010, p. 35;
Moghari 2009, p. 35; Frank et al. 2006, p. 2; Hazzah 2006, p. 22).
These practices include livestock being closely herded by men and dogs
during the day and being brought into bomas at night with people living
in huts around them (Frank et al. 2006, p. 4). However, traditional
practices are being replaced by less diligent husbandry practices,
which is increasing conflict (Woodroffe and Frank 2005 in Moghari 2009,
p. 35; Frank et al. 2006, pp. 2, 10; Hazzah and Dolrenry 2007, p. 23).
In Botswana, livestock are often left to wander outside bomas at night
(Frank et al. 2006, p. 5). In Kenya and Tanzania, social changes are
altering traditional Maasai pastoral livelihoods, reducing dependency
on livestock, and reducing traditional livestock care and management,
leaving livestock more vulnerable to predation (Chardonnet et al. 2010,
p. 35; Hazzah and Dolrenry 2007, pp. 22-23). Young Maasai boys
traditionally guarded herds at night; however, increased access to
schools has left herds unattended to wander into predator areas at
night (Chardonnet et al. 2010, p. 35).
In the Pendjari area of Benin, traditional enclosures are low with
few branches. These structures and the lack of enclosures encourage
livestock predation (Butler 2000, Mazzolli et al. 2002, and Wang and
Macdonald 2006 in Sogbohossou et al. 2011, p. 51). Surveillance of a
main pasture area south of Waza National Park in Cameroon and improved
enclosures around Waza National Park and Pendjari National Park, Benin,
led to a significant decrease in depredation (Bauer et al. 2010, p.
365). However, people do not invest much into improving enclosures even
though they appear to be economically efficient, ecologically
effective, and culturally acceptable. Even enclosures that were built
as part of a conservation project were not used full time due to lack
of labor and, in some cases, the herd being too large for the
enclosures (Bauer et al. 2010, p. 365).
Attacks on Humans in Africa
Although lions generally avoid people, they will occasionally prey
on humans, causing serious injury or death (Dickman 2013, pp. 380, 384;
Chardonnet et al. 2010, pp. 11, 12, 13; Moghari 2009, pp. 14, 49, 26,
88; Bauer et al. 2001 in Moghari 2009, pp. 31, 78, 84; Frank et al.
2006, p. 1; Hazzah 2006, pp. 14, 17; Patterson et al. 2004, p. 507).
Attacks on humans appear to be more frequent in southern and eastern
Africa and rare in western and central Africa (Bauer et al. 2010, p.
363; Chardonnet et al. 2010, pp. 12, 13; Mesochina et al. 2010a, pp.
29-30; Frank et al. 2006, pp. 1, 10), although attacks on humans have
been reported in Burkina Faso (Burkina Faso 2014, pp. 19, 22).
Environmental factors such as vegetative cover, habitat, climate,
seasonality, and prey availability may affect the rate of attacks on
humans. A certain amount of vegetative cover is crucial for lion's
hunting success; however, in some cases, the vegetative cover may make
it more difficult to catch prey, leading to more attacks on humans.
Additionally, dense cover near settlements allows lions to hide or
stalk humans at a close distance (Mesochina et al. 2010a, p. 39;
Moghari 2009, p. 85; Frank et al. 2006, p. 12).
Provoked attacks on humans are usually associated with someone
approaching a lion too closely or trying to injure or kill it and
stealing a lion's prey for bushmeat (Chardonnet et al. 2010, p. 14;
Uganda Wildlife Authority 2010, p. 27). Unprovoked attacks are usually
associated with old, sick, or injured lions that turn to humans as easy
prey. Additionally, there are risks of unprovoked attacks associated
with certain human activities. These activities include walking alone
at night, sleeping outside, and surprising a lion, particularly if it
has cubs (Begg and Begg 2010, pp. 3, 21; Chardonnet et al. 2010, pp.
14, 15; Mesochina et al. 2010a, pp. 38, 39; Mesochina et al. 2010b, p.
32; Uganda Wildlife Authority 2010, p. 27; Moghari 2009, p. 85; Frank
et al. 2006, pp. 11, 12). The most common context for attacks on humans
occurs during harvest, due to prey dispersal during the wet season,
bush pig attraction to crops, and because humans are particularly
vulnerable in makeshift tents while protecting crops (Frank et al.
2006, p. 12).
Retaliatory Killing of Lions in Africa
Livestock provide an economic value to humans, particularly those
in extreme
[[Page 80014]]
poverty who rely solely on livestock for their protein source and
livelihood. When lions have no economic value to local communities and
they kill or are perceived to kill livestock, the economic impact can
be significant (Bauer et al. 2015a, unpaginated; Hazzah et al. 2014, p.
852; Chardonnet et al. 2010, p. 12; Mesochina et al. 2010a, p. 38;
Mesochina et al. 2010b, p. 33; Gebresenbet et al. 2009, p. 9; Moghari
2009, pp. 4, 25, 49; Kissui 2008, pp. 423, 429; Hazzah 2006, p. 24;
IUCN 2006a, pp. 23, 24; IUCN 2006b. pp. 18-19; Frank et al. 2006, p.
3). Subsequently, those lions that reside on the edge and outside of
protected areas, where there is an increased risk of exposure to humans
and livestock, are subject to retaliatory killing across Africa.
Boundary transgression leads to lions predating on livestock, and in
turn, be subject to pre-emptive or retaliatory killing (Bauer et al.
2014, pp. 98, 103; Funston 2011, pp. 1, 3, 5, 6-7); however, this type
of killing of lions also occurs within protected areas (Henschel et al.
2015, unpaginated; Zimbabwe Parks and Wildlife Management Authority
2015, p. 10; Burkina Faso 2014, pp. 19, 21, 22; Tumenta et al. 2009 and
Henschel et al. 2010 in Sogbohossou et al. 2011, p. 100; Moghari 2009,
p. 49). Furthermore, killing of lions outside of protected areas may
disrupt movement of lions to other areas that could contribute to the
viability of larger resident populations (White 2015, pers. comm.).
This occurrence greatly impacts already-dwindling lion populations.
Even if mortality occurs outside of protected areas, population
dynamics inside protected areas are negatively impacted. When lions
outside of protected areas are removed, either through retaliatory
killings or trophy hunting, territorial gaps that are left are filled
by lions from closer to the core of the protected area, exposing more
lions to human-lion conflict along the borders of the protected area
and creating a population sink (Brugi[eacute]re et al. 2015, p. 514;
Sogbohossou 2014, p. 3; Loveridge et al. 2007, pp. 552, 555; Woodroffe
and Ginsberg 1998, p. 2162).
The availability of guns and poison makes killing suspected
predators cheaper and easier than other control methods, such as
reinforcing bomas (Hazzah et al. 2009, p. 2429; Moghari 2009, p. 35;
Frank et al. 2006, p. 14; Hazzah 2006, p. 3). Spearing, shooting,
trapping, and poisoning of lions, as either a preventive measure or in
retaliation for livestock and human attacks, occurs regularly
(Brugi[eacute]re et al. 2015, p. 519; Bauer et al. 2015a, unpaginated;
Tanzania 2015, p. 13; Republic of Namibia 2013, pp. 12, 13-14; Begg and
Begg 2010, p. 15; Chardonnet et al. 2010, pp. 41-42; Packer et al.
2010, pp. 9-10; Uganda Wildlife Authority 2010, pp. 13, 42;
Gebrensenbet et al. 2009, p. 7; Hazzah et al. 2009, p. 2429; Moghari
2009, pp. 52, 89, 91; Ikanda 2008, pp. 5-6; Hazzah and Dolrenry 2007,
p. 21; Frank et al. 2006, pp. 2-4, 7; Hazzah 2006, p. 52; IUCN 2006b,
p. 15). Retaliatory killings have been reported as a significant threat
to lion populations in protected areas of western and central Africa
(Tumenta et al. 2009 and Henschel et al. 2010 in Sogbohossou et al.
2011, p. 100), Botswana (Bauer et al. 2014, pp. 98, 103), Botswana and
South Africa (Kgaladi Transfrontier Park; Funston 2011, p. 1), Cameroon
(Delongh et al. 2009 and Tumenta et al. 2010 in Sogbohossou et al.
2011, p. 60), Kenya (Patterson et al. 2004, Kolowski and Holekamp 2006,
and Hazzah et al. 2009 in Sogbohossou et al. 2011, p. 60), Tanzania
(Tanzania 2015, p. 13; Kissui 2008 in Sogbohossou et al. 2011, p. 60),
and Zimbabwe (Zimbabwe Parks and Wildlife Management Authority 2015, p.
10).
In areas of high conflict, identifying the responsible animal is
often difficult, and a token animal may be killed instead (Hazzah 2006,
p. 25), leaving the problem lion to continue to attack and the
potential for additional retaliatory killings. In Tanzania, game
officers kill numerous lions each year in retaliation for attacks
(Frank et al. 2006, p. 12). Whereas shooting or spearing target
specific problem animals, poisoning is indiscriminate and is known to
remove entire prides at once (Frank et al. 2006, pp. 2, 10, Living with
Lions no date, unpaginated). In the absence of reliable methods for
protecting livestock, rural people often turn to indiscriminant
methods, like poisoning, to control livestock depredation. Poisoning is
an easy method for lethal control since it is readily available, and
reinforcing bomas or more carefully tending livestock requires time and
effort. The use of Furadan, a widely available and cheap agricultural
pesticide, is particularly lethal to wildlife and is increasingly being
used to kill predators in small pastoralist areas of Kenya and
Tanzania. Livestock carcasses are doused with the poison, killing
predators and scavengers that feed on them (Frank et al. 2006, pp. 2,
10, Living with Lions no date, unpaginated). Poisoning of bush pig
carcasses to kill lions is not uncommon after attacks on humans. These
practices have serious negative impacts on lion populations (Frank et
al. 2006, p. 9).
Studies have shown that lion populations are declining in areas
where pastoralism persists and the presence of mobile pastoralists are
a good indicator of lion extinction (Brugi[eacute]re et al. 2015, p.
519; Hazzah et al. 2009, p. 2428). Within protected areas, human-
wildlife conflict is likely under-reported because cattle herders are
within the protected areas illegally and, therefore, unlikely to report
it (Chardonnet et al. 2010, p. 14; Mesochina et al. 2010b, p. 34). For
example, Etosha National Park and Caprivi Game Park have the highest
rates of lions killed per 100 km\2\, yet it may be that just under half
of the lions that are killed are reported (Republic of Namibia 2013, p.
14). Although we do not have information on human-lion conflict from
all lion range countries, it is reasonable to conclude that lions are
being killed as a result of conflict in all major African range
countries, due to their depredation on livestock (Frank et al. 2006, p.
4).
Factors That Drive Retaliation in Africa
Several anthropogenic factors drive the level of resentment towards
lions and the extent of retaliatory killing (Dickman 2013, pp. 379,
385), including the extent of the loss caused by the lions and the
wealth and security of the people affected (Dickman 2013, p. 381;
Mesochina et al. 2010b, p. 54; Moghari 2009, pp. 14, 25; Hazzah 2006,
p. 81). Depending on alternative assets or incomes, the economic impact
of lions killing livestock can be significant. Domestic livestock can
provide manure, milk, and meat, and are the basis of many family
incomes, savings, and social standing; losses can amount to a large
proportion of a subsistence herder's annual income. These losses are
generally uncompensated, reinforcing negative community attitudes
toward lions and causing retaliation (Dickman 2013, pp. 380, 381;
Chardonnet et al. 2010, pp. 11, 12, 18, 29; Hazzah et al. 2009, p.
2428; Moghari 2009, pp. 14, 25, 27, 36; Kissui 2008, pp. 422-423).
Furthermore, a common perception among local communities is that lions
are conserved at the cost of community safety and uncompensated
financial losses. When the people who suffer significant costs from
wildlife feel that the wildlife's needs are being put before their own
needs, their frustration can lead to retaliatory killings (Dickman
2013, p. 382). Additionally, government officials and local tour and
hunting operators experience economic gain from lions, whereas the
communities bear the costs in livestock losses
[[Page 80015]]
(Hazzah et al. 2014, p. 852). This situation further contributes to
negative attitudes toward lion conservation programs (Moghari 2009, p.
37).
Lions are particularly vulnerable to retributive killing because
they are often driven by a perceived level of lion predation on
livestock rather than actual levels of conflict. In some locations,
other predators (e.g., baboons (Papio ursinus), spotted hyenas (Crocuta
crocuta), and leopards (Panthera pardus)) as well as disease are
responsible for the majority of livestock losses and human casualties,
yet it is lions that are sought and killed more often. In the Pendjari
Biosphere Reserve, Sogbohossou et al. (2011, p. 74) found that just one
case of a nonlethal attack on a human in a decade and mere rumors of
attacks in other regions was enough to cause people to perceive lions
as a threat. Negative perceptions of lions may be based on an over-
estimated number of lions in a community or protected area and an over-
estimated number of human-lion conflicts (Dickman 2013, p. 380; Begg
and Begg 2010, p. 20; Chardonnet et al. 2010, pp. 12, 21-22; Hazzah et
al. 2009, p. 2436; Maclennan et al. 2009 in Hazzah et al. 2009, p.
2429; Moghari 2009, pp. 77-78, 107, 150; Holmern et al. 2007 in Moghari
2009, p. 34; Butler 2001 in Moghari 2009, p. 34; Kissui 2008, pp. 426,
428, 429; Hazzah 2006, pp. 18-19, 83-85, 96, 98, 107, 111; Patterson et
al. 2004, pp. 514, 515). One cause for the disproportionate blame put
on lions is that the lion is a highly visible species. It is a large-
bodied species that lives in groups and has cultural significance.
Because of its physical presence, there is often a hyper-awareness of
the potential risk for lion attacks and lions may be blamed simply
because they have been seen in an area (Dickman 2013, pp. 380-381).
Cultural beliefs and traditions can have a negative impact on
lions. Because cattle are of great cultural significance to Maasai,
their loss can impose social or cultural costs and incite greater
resentment and higher levels of retributive killing (Dickman 2013, p.
384; Kissui 2008, p. 429; Hazzah 2006, p. 99). Cultural beliefs still
motivate ritual lion hunts for young Maasai warriors. Despite being
outlawed, this practice persists due to community secrecy. However, it
is easily disguised as retaliatory killings for livestock predation.
The prohibition of ritual lion hunts provides a greater incentive for
participating in retaliatory hunts (Hazzah et al. 2014, p. 852; Packer
et al. 2010, p. 10; Moghari 2009, pp. 13-14, 28; Ikanda 2008, pp. 5, 6;
Kissui 2008, p. 423; Frank et al. 2006, p. 10; Hazzah 2006, p. 99). In
some areas of Africa, locals believe in ``spirit lions,'' a lion whose
body is overtaken by evil to kill rivals or their livestock (West 2001
in Dickman 2013, pp. 381-382). Because people believe spirit lions are
created by their enemies, the number of perceived spirit lions, and
killing of these lions, increases during times of social tension
(Dickman 2013, p. 382.)
Cultural beliefs can also have a positive impact on lions. An
association with a totem is an important component of certain cultures
and could explain why retaliatory killing is uncommon in some areas
despite negative perceptions. However, the positive impact may not
continue as cultural beliefs dwindle due to urbanization and
modernization (Sogbohossou et al. 2011, pp. 73, 75).
Social tensions within tribes and between local communities and
other communities, the government, park officials, or tourists can lead
to conflict and retributive killing of lions (Dickman 2013, p. 382;
Hazzah 2006, p. 75). Locals often report that wildlife authorities do
not react effectively when chronic livestock raiders are reported
(Frank et al. 2006, p. 9). Significant numbers of lions have been
killed when promised benefits were not received or adequate
compensation was not provided for livestock and human losses (Dickman
2013, p. 383; Hazzah 2006, p. 45).
Trophy Hunting
Lions are a key species in sport hunting, or trophy hunting, as
they are considered one of the ``big five'' African species (lion,
leopard, elephant, rhino, and cape buffalo) touted to be the most
challenging to hunt due to their nimbleness, speed, and behavioral
unpredictability (Lindsey et al. 2012a, p. 2). However, with the
documented decline in lion population numbers throughout Africa, sport
hunting of lions for trophies has become a highly complex issue.
Trophy hunting is carried out in a number of range countries and is
considered an important management tool for conserving land and
providing financial resources for lion conservation. However,
management programs are not always sufficient to deter unsustainable
off takes (harvests), which has occurred in many areas (Lindsey et al.
2013a, pp. 8-9; Packer et al. 2006 in Bauer et al. 2015a, unpaginated).
Documented declines in lion populations of Africa are a result, in
part, of mismanaged trophy hunting (Rosenblatt et al. 2014, entire;
Sogbohossou et al. 2014, entire; Becker et al. 2013, entire; Lindsey et
al. 2013a, entire; Packer et al. 2013, p. 636; Croes et al. 2011,
entire; Packer et al. 2011, entire; Loveridge et al. 2007, entire).
Depending on how trophy hunting is regulated and managed, trophy
hunting can be a tool for conservation, but may also have negative
impacts on lions (Bauer et al. 2015a, unpaginated; Lindsey et al.
2013a, p. 1; Whitman et al. 2004, pp. 176-177; Loveridge et al. 2007,
p. 548).
In response to growing international recognition of reduced
population numbers, many countries began implementing moratoriums
banning the sport hunting of lions. In this document we use the terms
moratorium and ban interchangeably. A ban or moratorium can be
permanent, long term, or temporary, and can occur in countries that
have hunting quotas in place (e.g., Botswana and Zambia). Having both a
moratorium and a quota in place at the same time means that, although
the country may have a hunting quota, the country has halted
authorization of trophy hunting pursuant to that quota until some later
date or until some further action is taken, as prescribed by that
country.
Trophy hunting is currently banned in 12 range countries: Angola,
Botswana, Congo, Gabon, Ghana, India, Kenya, Malawi, Mauritania, Niger,
Nigeria, and Rwanda (CITES 2014, p. 14; Meena 2014, p. 26; Lindsey et
al. 2013a, entire; Lindsey 2013, pers. comm.; Jackson 2013, pp. 7-8).
In 1977, Kenya banned all sport hunting (Elliot and Mwangi 1998, p. 3).
Botswana banned lion hunting between 2001 and 2004, and then again from
2008 to the present (Davison et al. 2011, p. 114). Benin imposed a 2-
year moratorium, and CAR a 3-year moratorium, in the early 2000s
(Lindsey et al. 2013a, p. 4). In January of 2013, Zambia placed a
moratorium on sport hunting in 19 game management areas. While a few
other game management areas and private game ranches in Zambia remain
open for sport hunting for other species, the nationwide moratorium on
sport hunting of cats remains in place (White 2015, pers. comm.; ABC
News 2014, unpaginated; Flocken 2013, unpaginated). Trophy hunting is
restricted to problem or dangerous animals in Ethiopia and Uganda
(Lindsey 2008, p. 42). In our proposed rule, we had conflicting
information regarding whether Cameroon had or has a lion hunting
moratorium (CITES 2014, p. 14; Lindsey 2013, pers. comm.; Jackson 2013,
p. 8). During the public comment period, a peer reviewer confirmed that
Cameroon has not put a moratorium in place for lions, either in the
past or present (Bauer 2015, pers. comm.). Additionally, Zimbabwe has
[[Page 80016]]
suspended trophy hunting in the Gonarezhou area (Conservation Force
2015, pers. comm.).
As of May 2014, approximately 18 countries in Africa allowed legal
hunting of lions for trophies: Benin, Burkina Faso, CAR, DRC, Ethiopia,
C[ocirc]te d'Ivoire, Mali, Mozambique, Namibia, Senegal, Somalia, RSA,
Sudan, Tanzania, Togo, Uganda, Zambia (nationwide moratorium on sport
hunting of cats is currently in place), and Zimbabwe. However, in 2013
lion trophy hunting was documented to occur in only 8 countries,
specifically Benin, Burkina Faso, CAR, Mozambique, Namibia, South
Africa (RSA), Tanzania, and Zimbabwe (Lindsey 2013, pers. comm.). Four
countries, Burundi, Guinea Bissau, Lesotho, and Swaziland, provide no
legal protection for lions (CITES 2014, p. 14).
Where trophy hunting occurs, quotas are set by the government for
the purpose of limiting the actual number of lions killed (offtake)
during a given timeframe. A scientifically based quota is the maximum
number of a given species that can be removed from a specific
population without damaging the biological integrity and sustainability
of that population (World Wildlife Fund (WWF) 1997, p. 9). Two primary
concerns have been raised by the scientific and international community
with regard to current lion quotas. These are that (1) existing quotas
are set above sustainable levels, and (2) the data used for setting
quotas is inconsistent and not scientifically based (Hunter et al.
2013, unpaginated; Lindsey et al. 2006, p. 284) (see Potential Impacts
of Trophy Hunting). For example, recent quotas do not appear to address
safeguards for sustainability nor has a systematic approach been
established for setting lion quotas (Hunter et al. 2013, p. 2; Lindsey
et al. 2013b, p. 8). Additionally, it has been noted that previous
quotas in Namibia, Mozambique, and Zimbabwe may have been influenced by
human-lion conflict, with higher quotas being allocated to locations
with reportedly higher levels of human-lion conflict (Lindsey et al.
2013b, p. 4).
Generally, the conservation principle behind scientifically based
quotas is to limit total offtake of the species to either equal or
slightly lower than the growth rate of the target specimens (e.g.,
males vs. female), such that damage to the integrity and sustainability
of that population is prevented. Scientifically based quotas do not
apply solely to sport hunting, but set the limits for total offtake for
a particular timeframe; other potential offtake includes problem-animal
control (to reduce human-wildlife conflict), translocation (to expand
conservation), culling (reducing population pressures), and local
hunting (for protein/meat or employment) (WWF 1997, pp. 8-10). For
quotas to be sustainable, scientists and policy makers must evaluate a
multitude of factors including the species' biological factors (i.e.,
reproductive rate, gender ratios, age, and behavior), as well as
community and client objectives (WWF 1997, pp. 14-19).
Creel and Creel (1997, p. 83, executive summary) suggest that, for
a quota to be considered sustainable for lions, it should be limited to
no more than 5 percent of the population. Distinct from the quota,
Packer et al. (2011, p. 151) recommend actual lion offtake should not
exceed more than 1 lion per 2,000 km\2\ (Bauer 2015, pers. comm.;
Henschel 2015, pers. comm.; Packer et al. 2015, per comm.; Creel and
Creel 1997, p. 83, executive summary). However, most range countries
have their quotas set well above these recommendations (Bauer 2015,
pers. comm.; Henschel 2015, pers. comm.; Packer 2015, pers. comm.).
Specifically, Lindsey et al. (2013a, p. 8) found that of the nine
countries allowing trophy hunting of lions in 2013 (including data from
Zambia prior to the moratorium in 2013), eight have quotas set higher
than current recommendations by Packer et al. (2011, p. 151) and five
have quotas set to more than double Packer's recommendations.
Mozambique is the only country with a lion quota less than the
recommended 1 lion per 2,000 km\2\. It should be noted that although
quotas are currently set higher than recommended, the actual offtake
for each of the countries overall has been consistently lower than the
set quota (Table 5). However, in Burkina Faso, Zambia, Namibia, and
Zimbabwe, the actual harvests are greater than Packer's recommended
offtake (Lindsey et al. 2013a, p. 8). For instance, five countries
maintain quotas to allow for 5-31 lion trophies to be taken per year:
Benin (5), Burkina Faso (20), Cameroon (30), CAR (31), and Namibia
(15). Only Mozambique currently has a quota lower than the
recommendation of Packer et al. (2001, p. 1651). In 2013, the quota was
set at 42-60 lions, which translates to 1 lion per 2,400km\2\ (or 0.8
lions per 2,000km\2\). Between 2011 and 2012, Tanzania maintained the
highest quota for lions at 315 (Lindsey et al. 2013a, p. 6).
Several countries have begun to reduce their quotas as they have
begun implementing recommendations as outlined by Lindsey et al.
(2013a, pp. 8-9), Hunter et al. (2013, unpaginated), and Packer et al.
(2011, p. 151) (Bauer 2015, pers. comm.; Henschel 2015, pers. comm.;
White 2015, pers. comm.; Tanzania 2015, pers. comm. Zimbabwe 2015,
pers. comm.). In 2011, Zimbabwe's quota was set at 101 lions; in 2014,
it was reduced to 50 lions following the implementation of age
restrictions (Henschel 2015, pers. comm.). Following pressure from the
European Union to ban lion trophies if their quota remained higher than
the 1 lion per 2,000 km\2\ recommendation, Burkina Faso proposed to
reduce the set quota of 20 lions in the 2014/2015 season to 6 in the
2015/2016 season (Henschel 2015, pers. comm.). South Africa has not set
a quota for the take of wild lions since 99 percent of the trophy-
hunted lions are reportedly not of wild origin but captive born (Hunter
et al. 2013, p. 2; RSA 2013, pp. 5, 7) (Table 5).
Table 5--Annual Trophy Quotas and Offtake by Country (Approximate) as of 2013*
----------------------------------------------------------------------------------------------------------------
Annual lion Year(s) of Annual Year(s) of
Country trophy quotas data offtakes data
----------------------------------------------------------------------------------------------------------------
Panthera leo leo
Benin........................................... 5.00 minus>0.4
Burkina Faso.................................... 20.00 minus>1.45
Cameroon........................................ 29.22 minus>1.0
CAR............................................. 31 2009 13.76.9
Panthera leo melanochaita .............. .............. .............. ..............
Mozambique...................................... 42-60 2013 19.27.3
Namibia......................................... 14.5 2010 14.03.2
Tanzania........................................ 315 2011-2012 85 2011-2012
Zambia (moratorium) \1\......................... 74(50 \2\) 2012 47 2012
[[Page 80017]]
Zimbabwe........................................ 101(50\3\) 2011 42.57.5
----------------------------------------------------------------------------------------------------------------
* Source: Lindsey et al. 2013a. p.6.
\1\ Zambia enacted a moratorium on sport hunting in 19 game management units. Sport hunting remained open in
other game management units and on some private game ranches. Sport hunting of all cats is currently banned
throughout Zambia (White 2015, pers. comm.).
\2\ Approximate average quota for Zambia in the few years prior to the moratorium placed on cat hunting in 2013.
(White 2015, pers. comm.).
\3\ In 2014, Zimbabwe reduced its quota to 50 due to implementation of age restrictions (Henschel 2015, pers.
comm., citing Lindsey pers. comm.)
Potential Benefits of Trophy Hunting
Proponents and most lion experts support trophy hunting as a
conservation tool for the lion if it is practiced in a sustainable and
scientifically based manner (Henschel 2015, pers. comm.; Hunter 2011,
entire; van der Merwe 2013, entire; Hunter et al. 2013, entire) because
it can provide: (1) Incentives for the conservation of large tracts of
prime habitat, and (2) funding for park and reserve management, anti-
poaching activities, and security activities.
As habitat loss has been identified as one of the primary threats
to lion populations, it is notable that the total amount of land set
aside for hunting throughout Africa, although not ameliorating threats
to habitat loss, exceeds the total area of the national parks,
accounting for approximately half of the amount of viable habitat
currently available to lions (Chardonnet et al. 2010, p. 34; Packer et
al. 2006, pp. 9-10). For example, in Tanzania, 25-33 percent of the
total area, covering over 247,000 km\2\ and encompassing 190 hunting
units, has been set aside for sport hunting purposes; this has resulted
in an area 5.1 times greater than Tanzania's fully protected and
gazetted parks (Jackson 2013, p. 6; Barnett and Patterson 2005, p. 61).
Tanzania also has land set aside for sport hunting in the form of
safari areas, communal land, and privately owned properties that make
up 23.9 percent of the total land base (Barnett and Patterson 2005, pp.
76-77).
In Botswana, despite the current ban on lion hunting, the country
currently has over 128,000 km\2\ of gazetted wildlife management areas
and controlled hunting areas set aside for hunting purposes, which
equates to 22.1 percent of the country's total area. This amount is in
addition to 111,000 km\2\ (or 19.1 percent of the country's total area)
set aside as habitat in the form of national parks, game reserves, and
forest reserves (Barnett and Patterson 2005, p. 7). In 2000, five
countries in southern Africa (Botswana, Namibia, South Africa,
Tanzania, and Zimbabwe) set aside a combined 420,000 km\2\ of communal
land, 188,000 km\2\ of commercial land, and 420,089 km\2\ of state land
totaling over 1,028,000 km\2\ for sport hunting purposes (Barnett and
Patterson 2005, p. iii).
As a species with a considerable range (up to 1,000 km\2\) (Packer
et al. 2013, p. 636; Haas et al. 2005, p. 4), suitable habitat is
important to the survival of the species, and the marked decline in
suitable habitat is a significant threat to the species (see Habitat
Loss). The land currently designated in Africa for use in sport hunting
has helped to reduce, but not eliminate, the impact of habitat loss on
the lion.
If trophy hunting is part of a scientifically based management
program, it may provide direct economic benefits to the local
communities and may potentially create incentives for local communities
to conserve lions, reduce the pressure on lion habitat, and reduce
retaliatory killing, primarily because lions are viewed as having
value. Conversely, lack of incentives could cause declines in lion
populations because lions are viewed as lacking value and they kill
livestock, which are of great value to communities (see Human-lion
Conflict).
Over the last few decades, conservationists and range countries
have realized the integral role local communities play in the
conservation of lions and their habitat; when communities benefit from
a species, they have incentive to protect it. Therefore, using wildlife
as a source of income for rural populations has increasingly been
employed throughout the lion's range countries in Africa. Many of these
countries are classified as ``developing'' nations; specifically, seven
of the ten countries (we include Cameroon here) where trophy hunting is
permitted have 27-64 percent of their human populations living in
severe poverty (United Nations Development Programme's (UNDP) 2014,
unpaginated; Barnett and Patterson 2005, p. iii). These countries often
have high population growth, high unemployment, limited industry, and a
Gross Domestic Product (GDP) per capita lower than the poverty level
(Barnett and Patterson 2005, p. iii). These combined challenges
highlight the need for innovative solutions. Conservationists and range
countries recognize the value of the wildlife sector; if managed
sustainably, there is potential to contribute to rural economic
development while simultaneously protecting the unique ecological
habitats and species contained therein (Chardonnet et al. 2010, p. 33;
Kiss 1990, pp. 1, 5-15).
For species such as the lion to persist, local communities must
benefit from or receive a percentage of funds generated from tourism
such as wildlife viewing, photography, or trophy hunting (White 2013,
p. 21; Martin 2012, p. 57; Kiss [editor] 1990, pp. 1, 5-15). The
economic value of a species, such as lion, can encourage range
countries to develop management and conservation programs that involve
local communities and which would ultimately discourage indiscriminate
killings by local communities (Groom 2013, pp. 3, 5; Hazzah et al.
2013, p. 1; White 2013, p. 21; Martin 2012, p. 49). If local
communities see no benefit of lions being present in their communal
areas, sustainable use of lions becomes less competitive with other
land-use options, such as grazing and livestock management, and local
communities become unwilling and unable to manage their wildlife
heritage (Barnett and Patterson 2005, p. iii). When the value of lions
in areas outside national parks is diminished, those areas are likely
to be converted to forms of land use less suitable for lions, such as
agriculture, livestock pastures, or areas of resource extraction,
making lions even more vulnerable to expanding human settlement (Van
der Merwe 2013, p. 2).
Community conservancies that benefit from trophy hunting have
specifically been formed as a way to protect wildlife and habitat. As
an example, in Namibia, 160,000 km\2\ of community conservancies were
established in part due to revenue from trophy hunting. These
conservancies benefit the local communities, which in turn protect lion
habitat. In 2012, the Sav[eacute] Valley
[[Page 80018]]
Conservancy (Zimbabwe) ``provided over $100,000 USD worth of support to
adjacent villages or farmers in the resettled areas. Assistance
included drilling boreholes, maintaining boreholes, dredging of dams,
building clinics and schools, assisting with repairs, maintenance and
materials for schools, education initiatives, school field trips,
provision of computer equipment in schools, and craft programs'' (Groom
2013, p. 5). Connecting conservation to community benefits can provide
a value for wildlife, including lions, where there was previously
resentment or indifference, helping to instill a sense of importance
for lion conservation. Additionally an estimated 125,000 kg of game
meat is provided annually to rural communities by trophy hunters in
Zambia at an estimated value of $250,000 USD per year, which is
considerable for rural locations where severe poverty and malnutrition
exists (White 2013, p. 21), further providing a value for wildlife,
including lions. As stated above, local communities can benefit from
the trophy hunting industry by additional employment opportunities and
revenue generated for local microbusinesses.
Many range countries have recognized the need to incorporate
incentives and local community benefits into their trophy hunting
regulations, land management policies, and lion conservation action
plans (Lindsey et al. 2013a, pp. 2-3; Zambia Wildlife Authority 2009,
p. 10; Windhoek 2008, p. 18; IUCN 2006a, pp. 22, 24; IUCN 2006b, pp.
23, 28; Zimbabwe Parks and Wildlife Management Authority 2006,
unpaginated). Of the ten countries where lion trophy hunting currently
occurs (we are including Cameroon and South Africa here), seven have
developed National Poverty Reduction Strategies in partnership with the
International Monetary Fund (for a complete list, see https://www.imf.org/external/np/prsp/prsp.aspx). Each of these countries has
incorporated sustainable natural resource development as a priority and
discussed benefit distribution and management to rural communities
(Benin 2000, unpaginated; Burkina Faso 2000, unpaginated; CAR 2000, p.
45; United Republic of Tanzania 2000, pp. 13, 21; Zambia 2000,
unpaginated). Although we acknowledge the steps many countries have
taken to address local community incentives, most of the countries are
currently not transparent about the benefits provided to local
communities, and due to the high revenue potential, are subject to
corruption (Packer 2015, pers. comm.; see Potential Impacts of Trophy
Hunting).
Many range countries rely heavily on tourism (predominantly
ecotourism and safari hunting) to provide funding for wildlife
management (IUCN 2006a, p. 24). Additionally, revenue generated from
these industries provides jobs, such as game guards, cooks, drivers,
and security personnel and often brings in revenue for local
microbusinesses that sell art, jewelry, and other crafts. Revenue
generated from scientifically based management programs can be used to
build and maintain fences, provide security personnel with weapons and
vehicles, provide resources for anti-poaching activities, and provides
resources for habitat acquisition and management (Chardonnet et al.
2010, pp. 33-34; Newmark 2008, p. 321). For example, trophy hunting
revenue in the Sav[eacute] Valley Conservancy in Zimbabwe has enabled
$150,000-$250,000 USD to be invested in anti-poaching activities,
including the removal of wire-snares (Groom 2013, p. 5). Revenue from
trophy hunting can also increase the ability of many African countries
to manage wildlife populations both within and adjacent to reserves;
many of these hunting areas are geographically linked to national parks
and reserves, providing wildlife corridors and buffer zones (Chardonnet
et al. 2010, p. 34; Newmark 2008, p. 321).
Depending on the country in which a hunter visits, there may be
several different fees associated with trophy hunts, including game
fees, observer fees, conservation fees, permit fees, trophy handling
fees, and government payments in terms of taxes, as well as safari
operator fees (Barnett and Patterson 2005, p. 71). In the late 1990s,
Tanzania reported annual revenue of $29.9 million USD from all trophy
hunting, South Africa $28.4 million USD, Zimbabwe $23.9 million USD,
Botswana $12.6 million USD, and Namibia $11.5 million USD; the revenue
generated solely from lion hunting was not broken out (Barnett and
Patterson 2005, p. iv). According to Groom (2013, p. 4), a 21-day lion
hunt in Sav[eacute] Valley Conservancy, Zimbabwe, may be sold for
approximately $2,500 USD per day, with an additional trophy fee of
approximately $10,000 USD. Between 2005 and 2011, lion hunting in
Sav[eacute] Valley Conservancy provided an estimated net income (based
on 26 lions) of approximately $1,365,000 USD in per-night charges and
roughly $260,000 USD in trophy fees (Groom 2013, p. 4). In the past,
government and private landowners were the primary beneficiaries of the
revenue gained; currently, efforts are being made in many range
countries to incorporate incentives at the local level (Barnett and
Patterson 2005, p. vi).
In summary, if part of a scientifically based management program
(including a scientifically based quota), trophy hunting of lions can
provide direct benefits to the species and its habitat, both at the
national and local levels. Trophy hunting and the revenue generated
from trophy hunting are tools that range countries can use to
facilitate maintaining habitat to sustain large ungulates and other
lion prey, protecting habitat for lions, supporting the management of
lion habitat, and protecting both lions and their prey base through
anti-poaching efforts. While scientifically based trophy hunting alone
will not address all of the issues that are contributing to the
declined status of the lion, it can provide benefits to the species.
Potential Impacts of Trophy Hunting
An issue critical to the conservation of lions is sustainable
management of trophy hunting by lion range countries. Lion experts
agree that, if trophy hunting is well regulated and managed, it can be
a tool for conservation (Bauer et al. 2015a, unpaginated; Lindsey et
al. 2013a, p. 1; Whitman et al. 2004, pp. 176-177; Loveridge et al.
2007, p. 548). However, problems with the current management of lion
hunting increase the likelihood of negative impacts on the species
(note that because 99 percent of hunted lions in South Africa are
captive-bred, we exclude them from this discussion) (Hunter et al.
2013, p. 2). Lindsey et al. (2013a, pp. 8-9) and Hunter et al. (2013,
p. 2) identified six key practices undermining sustainable management
of lions:
Arbitrary establishment of quotas and excessive harvest
lack of age-restriction implementation
fixed quotas
hunting of females
lack of minimum hunt lengths in some countries
general problems associated with management of trophy hunting
As discussed above, one of the primary practices experts identify
as undermining sustainable trophy hunting is the use of non-scientific
information underlying the development of quotas (Lindsey et al. 2013a,
p. 8). The best available monitoring data should be used to set quotas
if they are to be scientifically based and sustainable. However,
monitoring data are often lacking (Barnett and Patterson 2005, p. 102).
A limited number of independent, scientific population counts of lions
[[Page 80019]]
have occurred across their range, especially in hunting concessions
(LionAid 2014a, pers. comm.; Packer 2015, pers. comm.; Packer et al.
2011, p. 143). While some existing quota allocations have been derived
from information provided by hunting concession operators, it has been
noted that many hunting concession operators have not allowed
independent population studies to take place, possibly as a result of
illegal activity and corruption (LionAid 2014a, pers. comm.; Packer
2015, pers. comm.). Lion experts also describe an over-reliance on
subjective opinions, including input from concession operators, in the
process of developing quotas (Lindsey et al. 2013a, p. 8). As a result,
information underlying current quotas in much of the species' range has
been inconsistent, biased, and/or lacking. It is difficult to predict
with accuracy what level of offtake would be appropriate to ensure a
quota is sustainable for a given population without accurate
information on the size of the resource (LionAid 2014a, pers. comm.;
Barnett and Patterson 2005, p. 102). Therefore, quotas not
scientifically based are often too high to maintain sustainability and
overharvest occurs.
Lions are particularly vulnerable to excessive harvests due to
impacts associated with the removal of males (Hunter et al. 2013, p.
2). As stated before, except in Mozambique, quotas are higher than the
recommended maximum harvest of 1 lion per 2,000 km\2\. Additionally,
mean actual harvests are higher than the recommended 1 lion per 2,000
km\2\ offtake in Burkina Faso, Zambia, Namibia, and Zimbabwe (Lindsey
et al. 2013, p. 8). Multiple researchers have documented declines in
lion populations across the range of the species as a result of
mismanaged trophy hunting. Specifically, negative impacts to lions from
excessive offtakes have been documented in Benin (Sogbohossou et al.
2014, entire), Cameroon (Croes et al. 2011, entire), Tanzania (Packer
2011, entire), Zambia (Rosenblatt et al. 2014, p. entire; Becker et al.
2013, entire), and Zimbabwe (Groom et al. 2014, entire; Davidson et al.
2011, entire; Loveridge et al. 2007, entire). Additionally, the effects
of over-harvesting can extend into adjacent national parks where
hunting does not occur (Packer et al. 2013, p. 636).
Most experts consider the recommendation by Packer et al. (2011, p.
151) to limit offtake to no more than 1 lion per 2,000 km\2\ throughout
its range (or 1 per 1,000 km\2\ in areas with high density of lions) to
be the best available science and recommend each country impose a quota
cap at those levels to ensure sustainability while other methods are
being developed and refined. According to Hunter et al. (2013, p. 5),
``such caps provide a short-term means of reducing the risk of negative
population impacts while more robust methods are being implemented.
Areas that are smaller than 1,000 km\2\ should be granted the
equivalent fraction of 0.5 lions per year: For example, an area of 200
km\2\ would be allocated 0.1 lions per year, or one tag every ten
years. Such a system would reduce the extent to which hunting in small
concessions adjacent to protected areas affects protected populations,
as in Zambia and Zimbabwe.''
Species experts also recommend, as part of reforming trophy
hunting, adoption by range countries of an adaptive quota management
system that would allow for quotas to fluctuate annually based on the
population trends of the species. An adaptive quota management system
would not only prevent over-harvesting of lions, but would also prevent
excessively conservative quotas (Hunter et al. 2013, p. 5).
Recognizing the inconsistencies in the process of setting a quota
and the information on which they are based, range countries and
conservationists have been working to establish a set of best practices
in order to create a more consistent, scientifically based approach to
determining quotas. The recommended best practices include: (1)
establishing processes and procedures that are clearly outlined,
transparent, and accountable; (2) establishing processes and procedures
that are CITES compliant; (3) demonstrating management capacity; (4)
standardizing information sources; (5) establishing monitoring systems
for critical data; (6) recording and analyzing trophy hunting data; (7)
conducting data collection and analysis for each hunting block and
concession; and (8) establishing a primary body who will approve quotas
(Burnett and Patterson 2005, p. 103).
Each country that allows trophy hunting has some data collection
system in place; most countries have a central wildlife authority that
requires operators to submit data collection forms or questionnaires
providing details of each of their hunts. However, according to the
authors, these guidelines have not been followed throughout much of the
range countries, which has led to a variety of compliance issues. Some
systems have been overly complex and cumbersome. ``In 2000, Zimbabwe,
for example, had nine different forms, which contain essentially the
same information, that had to be completed by safari operators for each
client and submitted to different government departments'' (Barnett and
Patterson 2005, p. 100). Additionally, governmental bodies have
sometimes failed to analyze data and provide feedback to operators;
experts agree this failure undermines the purpose of the system and
encourages noncompliance.
In the absence of reliable population estimates, age restriction on
trophy harvests can ensure sustainability (Lindsey et al. 2013a, p. 8;
Packer et al. 2006, pp. 6-8). Whitman et al. (2004, pp. 176-177) found
that if offtake is restricted to males older than 6 years of age,
trophy hunting will likely have minimal impact on the pride's social
structure and young. By removing only males 6 years of age or older,
younger males remain in residence long enough to rear a cohort of cubs
(allowing their genes to enter the gene pool; increasing the overall
genetic diversity); recruitment of these cubs ensures lion population
growth and therefore, sustainability. Simulations indicate that
populations with quotas of more than two male lions of minimum eligible
age of 3-4 years were more likely to experience extinction events than
populations with hunting restricted to a minimum eligible age of 5-6-
year-old males (Whitman et al. 2004, p. 176). Additionally, full
implementation and enforcement of this age-based strategy could
potentially cause the need for quotas to become irrelevant or
eliminated entirely. Age restrictions will naturally restrict offtake
to a limited number of individuals that meet the age criteria
(Loveridge et al. 2007, p. 549; Whitman et al. 2004, p. 177).
Implementing this approach in the field involves conducting an age
assessment of male lions using identification techniques, such as mane
development, facial markings, nose pigmentation, and tooth-aging to
establish the relative age of the target lion. Tooth wear on incisors,
yellowing and chipping of teeth, coupled with scars, head size, mane
length and color, and thinning hair on the face, as well as other
factors can be an indicator of advanced age in lions (Whitman and
Packer 2006, entire).
Whitman et al. (2004, p. 176) postulated that ``the most reliable
index in the Serengeti/Ngorongoro lions is the extent of dark
pigmentation in the tip of the nose, which becomes increasingly
freckled with age. Individual variation in nose coloration is
sufficiently low that age can be estimated up to 8-9 years. The noses
of 5-yr-old males are 50 [percent] black so the rule of thumb would be
to restrict all trophy hunting to males with noses that are more than
[[Page 80020]]
half black.'' Although this varies individually and regionally,
recommended best practices could be regionally tailored. Packer et al.
(2006, p. 7) note that males in South Africa require an additional 1-2
years to become competitive with other males, and suggest a 7-year
minimum might be judicious for some regions. Therefore, there is
concurrence by species experts that national or regional guidelines
should be developed to accompany those produced in Tanzania and Zambia
(Lindsey et al. 2013a, p. 8; Packer and Whitman 2006, entire).
According to Lindsey et al. (2013a, p. 8), some operators were
uncertain of their ability to age lions; however, based on research
conducted in Niassa National Reserve, Mozambique, hunters can be taught
to age lions effectively. While experts agree it may be difficult to
determine the exact age of a lion, broader categories based on age have
been developed to assist officials. For example, Tanzania officials
have ``aging sessions'' wherein each concession operator is required to
bring in the skulls of their trophies for examination. Each skull is
then classified as ``acceptable'' (6+ years old), ``accepted with
penalties'' (4-5 years old), and ``not accepted with deterrent
penalties'' (<4 years) (Tanzania 2015, pp. 23-24). Tanzania reports
that this step is required prior to any issuance of a CITES export
permit.
Species experts place high emphasis on the requirement for both
enforcement and transparency in the strategy. A fully transparent quota
allocation system would be one in which a quota allocation system is
based on scientific data received from all hunting areas and concession
units annually, and would require trophies to be independently
evaluated, data on the trophies (e.g. age, sex, origin) be available
nationally and internationally, and quotas based upon data obtained
from the previous hunting season (Henschel pers. comm. 2015).
Lion experts recommend age-based strategies be incorporated into
lion management action plans (Hunter et al. 2013, pp. 4-5; Lindsey et
al. 2013a, p. 8). Although the 6-year method has potential to reduce
the rate of infanticide in lion populations used for trophy hunting
(Hunter et al. 2013, p. 4-5; Lindsey et al. 2013a, p. 8), the issue of
incorporating this strategy into each country's conservation strategy
and/or action plan, and following up with implementation, enforcement,
and transparency has yet to be observed in many of the lion's range
countries (Henschel 2015, pers. comm.). While several countries,
including Benin, Burkina Faso, Mozambique (only in Niassa National
Reserve), Tanzania, and Zimbabwe have committed to implementing the
age-based strategy (White 2013, p. 14; Davidson et al. 2011, p. 114;
Whitman et al. 2004, p. 176), only two have fully implemented it
(Henschel 2015, pers. comm.). Thus far, Mozambique and Zimbabwe have
implemented this strategy and shown a reduction in total offtake
(Henschel 2015, pers. comm.). They also appear to be transparent in
their implementation. Tanzania has implemented age restrictions and
shown reductions in offtake; however, there is concern related to
transparency (in terms of trophy quality data) and the scientific
objectivity of the evaluating body has been questioned. Benin and
Burkina Faso committed to implementing age restrictions in 2014; their
progress is currently pending. Lastly, Mozambique, excluding Niassa
National Reserve and Cameroon have not yet instituted or committed to
the strategy (Henschel 2015, pers. comm.). Lack of implementation of
age-based strategies may undermine the successful use of trophy hunting
as a sustainable conservation strategy.
Additionally, experts believe that importing countries should have
the ability to ascertain that the imported trophies originated from
hunting concessions that fully comply with best practices. According to
Lindsey et al. (2007, p. 3; Lindsey et al. 2006, pp. 285, 288), there
is a market in the United States for conservation-based hunting. ``In a
survey of prospective clients 45-99 percent were unwilling to hunt
under various scenarios if conservation objectives would be
compromised, and 86 percent were more willing to purchase a hunt if
local communities would benefit'' (Lindsey et al. 2007, p. 3). Experts
agree that a fully transparent system would allow hunters to choose
operators who have demonstrated a commitment to conservation
principles; this system could provide incentives for operators to
comply with the recommended best practices.
Harvesting of males that are too young can have devastating impacts
to the population. If male lions are harvested too young (even as old
as 3 years of age), combined with quotas that are too high, the
population will be driven to extinction as female populations collapse
as they eventually are unable to mate (Whitman et al. 2004, p. 176).
Additionally, excessive trophy hunting and taking of males under a
certain age cause male replacements and increased infanticide rates
(when males kill young lion cubs sired by other males) (Whitman et al.
2004, p. 175). Packer (2001, p. 829, citing Bertram 1975, Packer and
Pusey 1984, and Pusey and Packer 1994) demonstrated that cub mortality
increases when a new male joins a pride. Infanticide is a common
practice among many species, including lions (Hausfater et al. 1984,
pp. 31, 145, 173, 487). Removing a younger male lion allows another
male of the pride to take over and kill the former patriarch's cubs;
offspring younger than 2 years of age are generally unable to defend
themselves and may be killed or forced to disperse from the pride
prematurely, which also often leads to death (Elliot et al. 2014, p.
1054; Packer 2001, p. 829; Pusey and Packer 1984, p. 279). This
behavior is believed to be advantageous to the incoming male as it
increases and accelerates the opportunity for the new male to sire a
cohort of cubs. When females give birth to cubs, the female generally
does not return to estrus until the cubs are around 18-24 months old
(Pusey and Packer 1984, p. 281). Following the loss of her cubs,
however, a female will return to estrus rather quickly; females will
resume mating within days or weeks, thus increasing the likelihood that
the new male will have the chance to sire the next cohort. Pusey and
Packer (1984, p. 279) calculated that infant fatality during male
takeovers accounted for 27 percent of all cub fatalities under the age
of 12 months.
Further, when an adult male lion in a pride is killed, surviving
males who form the pride's coalition are vulnerable to takeover by
other male coalitions, and this often results in injury or death of the
remaining males (Davidson et al. 2011, p. 115).
Recently, Elliot (2014, p. 1054) postulated that the impacts of
male takeovers due to trophy hunting may be more severe than previously
recognized. Specifically, when a pride male is removed and a new male
takes over, subadults may be forced to disperse from the pride. These
males are then at a disadvantage as they are often inexperienced and
physically smaller which may prevent them from being able to compete
with older males for territory. In the study, Elliot found 100 percent
fatality for all males who dispersed earlier than 31 months old. The
study concluded that dispersal of subadults is highly related to the
presence of incoming males, resulting in a type of delayed infanticide,
as many of the subadults do not survive the dispersal. This effect may
be amplified in populations that have a high offtake rate. Therefore,
the author concluded that age restriction and reducing offtake could
reduce takeover rates by new males, allowing subadults a longer period
to mature prior to dispersal and
[[Page 80021]]
thus, reducing the number of subadult deaths (Elliot et al. 2014, p.
1055).
A lack of mature males dispersing reduces the genetic viability of
populations and may contribute to local population extinctions (See
Deleterious Effects Due to Small Population Sizes). Selective offtake
of large males may also modify the genetic evolution of lions.
Allendorf and Hard (2009, p. 9987) and Loveridge et al. (2007, p. 553)
consider the genetic and evolutionary role of selective hunting on
wildlife populations. As individuals who display certain
characteristics (such as largest size) are more likely to be harvested,
this type of selective removal will bring about genetic change in
future generations. Specifically, removing the males with the most
desirable traits from a population ultimately affects upcoming
generations as those individuals are no longer contributing to the gene
pool. ``For example, the frequency of elephants (Loxodonta africana)
without tusks increased from 10 percent to 38 percent in South Luangwa
National Park, Zambia, apparently brought about by poaching of
elephants for their ivory'' (Jachmann et al. 1995 in Allendorf and Hard
2009, p. 9987). This comparison relates to lion as the removal of the
largest males consequentially results in females breeding with less
desirable males and thus, perpetuating the production of less desirable
individuals. Selective offtake based on gender also has the potential
to skew sex ratios and impact breeding success, as has been the case
for lions (Allendorf and Hard 2009, p. 9991; Loveridge et al. 2007, p.
553). The authors state that in order to maintain the highest yield and
viability of the most desirable males, one option is to be less
selective (Allendorf and Hard 2009, p. 9991). Specifically as related
to lions, this would mean implementing age restrictions so that the
more desirable males are not harvested prior to successful
reproduction.
Whitman et al. (2004, pp. 175-177) found that if offtake is
restricted to males 6 years of age or older, the impacts of trophy
hunting are likely to be minimal on the prides social structure and
reproduction. Therefore, experts recommend that a 6-year age
restriction should be implemented for all hunting concessions
throughout the lion's range.
Species experts have suggested an additional mechanism that could
help reduce infanticide. In concessions where operators can distinguish
between resident and solitary individuals, removal of the nomadic males
may reduce the likelihood of a possible conflict and take-over (Packer
et al. 2006, p. 7; Whitman 2004, p. 177). If concession operators
selectively remove males in a manner that promotes healthy population
growth, the lion population could yield more males in the long term
(Davidson et al. 2011, p. 114; Packer et al. 2006, p. 7; Whitman et al.
2004, p. 176).
Hunter et al. (2013, pp. 2, 5) and Lindsey et al. (2013a, p. 9)
identified hunting of female lions to be another aspect of trophy
hunting that is harmful to lion populations. Specifically, females are
the most productive portion of a population; if females are removed
from a pride, there is inherent risk that dependent cubs will die and
the overall breeding success of the pride will be reduced. Packer et
al. (2001 in Packer et al. 2006, pp. 5, 7) report that ``large prides
out-compete smaller prides and per capita reproduction is lowest in
prides of only 1-2 females.'' Lindsey et al. (2013a, pp. 2, 4, 9)
indicate that a loss of a female increases a pride's vulnerability to
territory loss. As a result, removing females has injurious effects on
the overall success of the population and, ultimately, the number of
harvestable males.
Lindsey et al. (2013a, pp. 2, 4, 9) indicate that quotas are
currently available for female lions in some locations within Namibia,
and between 1990 and 2011, in Zimbabwe (Packer et al. 2006, p. 4).
Between 1998 and 2004, Zimbabwe maintained a mean quota of 0.3 0.1/100 km\2\ for female lions; during the same period, actual
offtake was lower at 0.08 0.1/100 km\2\, or a mean of 30.6
percent of the quota actually harvested (Loveridge et al. 2007, p.
551). Zimbabwe discontinued issuing quotas for females in 2011. Female
hunting is not allowed elsewhere within the range of the species
(Lindsey et al. 2013a, p. 2). Species experts recommend that the trophy
hunting of females be prohibited, unless the management plan is
specifically to control the size of the lion population (Hunter et al.
2013, p. 5; Lindsey et al. 2013a, p. 9).
Another deficiency in current trophy hunting management is the use
of fixed quotas. There are two primary types of quotas, ``fixed'' and
``optional.'' Trophy fees for fixed quotas require the payment of a
portion (40-100 percent) of the lion trophy fee, regardless of whether
the hunt is successful, whereas optional quotas are paid by operators
only when the lion is shot. Until 1999, male lions were typically on
fixed quotas, whereas female lions were under optional quotas.
According to Lindsey et al. (2013a, pp. 2-3), Mozambique, Benin,
Burkino Faso, and Cameroon all have optional quotas in place, thereby,
hunters only pay for animals hunted. Other range countries continue to
have fixed quotas in place and charge a percentage of the quota
regardless of success (CAR charges 50 percent; Namibia 100 percent;
Tanzania 40 percent; Zambia 60 percent; Zimbabwe 30 percent). This
approach facilitates harvesting of trophies even if a sufficiently old
lion is not found (Hunter et al. 2013, p. 6). Therefore, harvested
lions are often of lower quality, younger, and less desirable male
lions, as operators and hunters, who had already paid the trophy fee,
had no incentive to be selective. Abolishing fixed-quota fees and only
allowing optional quotas will encourage and reward operators who are
selective and follow age restrictions (Lindsey et al. 2013a, p. 9;
Packer et al. 2006, pp. 5, 9).
To ensure hunters have adequate time to be selective in trophies
harvested, and to ensure the revenue earning potential is maximized,
experts recommend that a minimum stipulated hunt length be set at 21
days. However, many countries either have no limits on length of
hunting safaris or have too short a minimum length (Lindsey et al.
2013a, p. 9). Currently, there are no set lengths for hunting safaris
in Mozambique, Namibia, Zambia, and Zimbabwe. Burkino Faso has a
minimum requirement of 12 days, and Benin and Cameroon require 12 to 14
days. Tanzania has a minimum length of 21 days while CAR varies from 12
to 21 days (Lindsey et al. 2013a, pp. 2-3).
Several other problems with current management of lion trophy
hunting are likely to worsen negative impacts associated with hunting
of lions and undermine conservation incentives. Corruption, allocation
of hunting concessions, and lack of benefits and recognition of the
role communities play in conservation have been identified (Lindsey et
al. 2013a, pp. 2-3, 9).
Corruption is widespread within the range of the lion (Transparency
International 2014, unpaginated). All but one lion range country
(Botswana) scored below 50 (out of 100) on Transparency International's
2014 Corruption Perception Index (CPI), which measures perceived levels
of public sector corruption based on expert opinion and is based on a
scale of 0 (highly corrupt) to 100 (very clean). Approximately half of
the current lion range countries--including Tanzania and Kenya, where
more than half of all wild lions occur--are among the most corrupt
countries in the world, ranking in the lower 30 percent of 174
countries
[[Page 80022]]
assessed (Transparency International 2014, unpaginated).
Corruption is particularly prevalent in areas with extreme poverty
(Transparency International 2014, unpaginated; Michler 2013, pp. 1-3;
Kimati 2012, p. 1; Garnett et al. 2011, p. 1; IUCN 2009, p. 89; Leader-
Williams et al. 2009, pp. 296-298; Kideghesho 2008, pp. 16-17). Certain
circumstances tend to promote corruption, such as opportunity for
financial gain, weak rule of law, abnormal concentrations of power in
one individual or institution, no counter-balancing mechanisms in place
among different government agencies, and reliance on discretionary
powers for allocation of permits, licenses, or activities (Smith et al.
2015, p. 953; Nelson 2009, unpaginated; Luo 2005 in Smith et al. 2015,
p. 953).
Corruption manifests itself in several ways, such as embezzling of
public funds, fraud, demanding or accepting bribes to overlook illegal
activities, interference in decisions to implement conservation
measures, and offering patronage, nepotism, and political influence
(Vargas-Hernandez 2013 in Smith et al. 2015, p. 953; Garnett et al.
2011, p. 1; Leader-Williams et al. 2009, p. 301; Kaufmann 1997 in
Leader-Williams et al. 2009, p. 297). With respect to lion management,
it may include, for example: Infringement of hunting regulations in the
field; acceptance of bribes to overlook illegal activities such as
poaching; interference or mismanagement in monitoring and setting of
hunting quotas and in issuing of licenses; misappropriation of hunting
fees; allocation of hunting blocks based on patronage and nepotism or
to persons presumably considered to be of financial or other strategic
importance; and allocation of hunting blocks at less than competitive
prices (see Leader-Williams et al. 2009, pp. 301-305; Nelson 2009,
unpaginated).
Peh and Dori (2010, pp. 336-337) show that global indices of
corruption and governance are highly correlated with those of
environmental performance--countries with high levels of corruption
have lower levels of environmental performance. Further, Smith et al.
(2003, entire) found strong associations between changes (declines) in
elephant and rhinoceros numbers and governance scores. Governance
scores, which were based largely on Transparency International's CPI,
explained observed changes in numbers of elephants and rhinoceroses
better than per capita GDP, Human Development Index scores, and human
population density. These results suggest that political corruption may
play a significant role in determining the success of national
strategies to conserve these species (Smith et al. 2003, p. 69).
Corruption can reduce the effectiveness of conservation programs by
reducing the funding, law enforcement, and political support available
for conservation, and also by acting as an incentive for the
overexploitation of resources (Garnett et al. 2011, p. 1, citing
several sources; Smith and Walpole 2005, p. 252). Given the financial
gains to be made from lion trophy hunting, and the high level of
corruption in many lion range countries (Packer 2015, pers. comm.;
Transparency International 2014, unpaginated), it is reasonable to
conclude that corruption and the inability to control it are having
negative impacts on decisions made about lion management in many areas
of the species' range and on lion populations, and undermine steps to
reform hunting of lions. The impacts highlight the importance of
transparency within the hunting industry and independent verification
of processes such as quota setting, trophy monitoring, and concession
allocation (Lindsey et al. 2013a, p. 9).
In recent years, leadership in several African lion range countries
has taken steps to address corruption, or activities that facilitate
corruption, associated with wildlife management. For example, in 2013,
the Tourism Minister of Zambia banned hunting in 19 game management
areas for 1 year due to allegations of corruption and malpractice among
the hunting companies and various government departments. Some game
management areas and privately owned game ranches were not included in
the ban, but lion hunting appears to be prohibited throughout the
country (Michler 2013, pp. 1-3). Whether recent reforms taken by
various lion range countries will reduce the effect of corruption on
lion management and, therefore, lion populations is as yet unknown.
Most concessions in the African range of the lion use a closed-
tender process for land management. A closed-tender system is the
process of selling a product by inviting a specific group of potential
buyers to provide a written offer by a specified date. In the case of a
hunting concession, the owner of the property thus sells a lease on a
property for a given length of time. Countries that use this process
for state-owned lands include Benin (lease is for 5 years); Burkina
Faso (20 years); Cameroon (10 years, renewable); CAR (10 years
(renewable); Mozambique (10+ years); Tanzania (5 years); and Zambia
(10-15 years based on status of wildlife). In Namibia, state
concessions lease land by public auctions for 3-year periods, while
community conservancies lease for a 5-year period via a closed-tender
process. Zimbabwe holds a public auction for state safari areas, with
the option to extend 5 years based on performance. Communal Areas
Management Programme for Indigenous Resources (CAMPFIRE) areas are
leased on 3-10 year-period using a closed-tender process (Lindsey et
al. 2013a, pp. 2-3).
The chief complaint regarding this system is that concession areas
are leased to operators without regard for the operators' track record
in conservation. Zimbabwe is the only country that renews based on
operator performance (Lindsey et al. 2013a, pp. 2, 9). Lindsey et al.
(2007, p. 2) found that various countries have problems with their
allocation process, ``with the effect that they are sometimes sold too
cheaply, allocated for periods too short to promote responsible
custodianship, and occasionally given to unlicensed operators. . .. In
several countries large citizen quotas are provided to urban residents
at low prices, reducing revenues from trophy hunting and reducing
incentives for communities to conserve wildlife.'' Experts believe that
basing the ability to renew a concession lease on operators' past
performance records could be an incentive for operators to comply with
best practices. Thus, experts recommend concession allocation should
base concession lease renewals on operator performance in regard to
best practices compliance.
As discussed under Human-lion Conflict, the risk of retaliatory
killing is elevated in many cases due to the fact that communities
living in close proximity to lion populations often bear the cost of
that proximity (e.g., loss of valuable livestock due to lion
depredation), but receive little of the benefits generated by the
presence of lion in the trophy hunting and ecotourism industries
(Lindsey et al. 2013a, p. 9). Trophy hunting can generate millions of
dollars in annual revenue (see Potential Benefits of Trophy Hunting).
In the past, government and private land owners were the primary
beneficiaries of the revenue gained; currently efforts are being made
in many range countries to incorporate incentives at the local level
(Barnett and Patterson 2005, p. vi). Many range countries are now
recognizing the need to incorporate incentives and local community
benefits into their trophy hunting regulations, land management
policies, and lion conservation action plans. Most countries that allow
lion trophy hunting have developed National Poverty Reduction
Strategies and
[[Page 80023]]
discussed benefit distribution and management to rural communities (see
Potential Benefits of Trophy Hunting). Although positive steps are
being taken to address local community incentives, most of the
countries are currently not transparent about the benefits provided to
local communities, and due to the high revenue potential are subject to
corruption.
Captive Lions
In analyzing threats to a species, we focus our analysis on threats
acting upon wild specimens within the native range of the species,
because the goal of the Act is survival and recovery of the species
within its native ecosystem. We do not separately analyze ``threats''
to captive-held specimens because the statutory five factors under
section 4 (16 U.S.C. 1533) are not well-suited to consideration of
specimens in captivity, and captive-held specimens are not eligible for
separate consideration for listing. However, we do consider the extent
to which specimens held in captivity create, contribute to, reduce, or
remove threats to the species.
In 2009, approximately 3,600 captive-held lions were managed for
trophy hunting across 174 breeding facilities in South Africa ((Lindsey
et al. 2012, p. 18, citing Taijaard 2009; Barnett et al. 2006a, p.
513). The captive-breeding industry often publicizes captive breeding
and reintroduction of captive-born species into the wild as a potential
solution to the decrease in wild lion populations. However, lions
raised in captivity often develop a variety of issues that make them
unsuitable for reintroduction. Captive lions in general are not
suitable for reintroduction due to their uncertain genetic origins
(Barnett et al. 2006a, p. 513; Hunter et al. 2012, p. 3), potential
maladaptive behaviors, and higher failure risk compared to translocated
individuals (Hunter et al. 2012, pp. 2-3). Research has indicated that
restoration efforts using wild-caught individuals have a much higher
rate of success than those using captive-raised individuals for a large
variety of species (Hunter et al. 2012, p. 21). Currently,
reintroduction efforts of captive-raised lions have not been shown to
address the underlying causes of populations' declines throughout the
species range.
We note that while the captive-lion industry may not be
contributing to the conservation of the species in the wild via
reintroduction, the captive-lion industry in South Africa may reduce
the pressures of trophy hunting on the wild populations in South Africa
(Hargreaves 2010b in Lindsey et al. 2012, p. 12; Lindsey et al. 2012,
p. 19), which is evidenced by the fact that 99 percent of lion trophies
from South Africa are of captive origin. Lindsey et al. (2012, p. 21)
warn that future efforts to control hunting of captive-bred lions could
potentially increase the demand for wild lion trophies and result in
excessive harvests. However, we also note that trade in bones of
captive lions could stimulate harvest of wild lions to supply a growing
bone trade (Lindsey et al. 2012, p. 20). Hunting of captive lions could
also potentially undermine the price of wild hunts and reduce
incentives for conservation of wild lions in other African countries
(Lindsey et al. 2012, p. 12).
Limited research has been conducted on the use of captive-raised
lions for reintroduction purposes. Existing research has generally
found that captive-raised lions are not as able to successfully adapt
to conditions out of captivity and therefore, the success rate is much
reduced compared to the use of wild-caught lions. Although some
potential exists that the captive-lion industry in South Africa may
benefit some local wild populations, additional research would be
needed to verify this claim. As a result, we do not believe that the
captive-lion industry currently contributes to, reduces, or removes
threats to the species.
Summary of Trophy Hunting
If trophy hunting of lions is part of a scientifically based
management program, it can provide considerable benefits to the species
by reducing or removing incentives to kill lions in retaliation for
livestock losses, and by reducing the conversion of lion habitat to
agriculture. Trophy hunting, if managed well and with local communities
in mind, can bring in needed revenue, jobs, and a much-needed protein
source to impoverished local communities, demonstrating the value of
lions (Groom 2013, pp. 1-3; Lindsey et al. 2006, pp. 283, 289). In
addition, the amount of habitat that has been set aside by range
countries specifically for trophy hunting has greatly increased the
range and habitat of lions and their prey base, which contrasts the
overall ongoing rate of habitat destruction occurring in Africa. The
total amount of land set aside for trophy hunting throughout Africa
exceeds the total area of the national parks, providing half the amount
of viable lion habitat (Chardonnet et al. 2010, p. 34; Packer et al.
2006, pp. 9-10).
The main problem with mismanaged trophy hunting stems from
excessive harvests and impacts associated with removal of males (Hunter
et al. 2013, p. 2). Researchers have documented declines in populations
across the range of the species that were a direct result of mismanaged
trophy hunting (Rosenblatt et al. 2014, p. entire; Sogbohossou et al.
2014, entire; Becker et al. 2013, entire; Lindsey et al. 2013, entire;
Croes et al. 2011, entire; Packer 2011, entire; Loveridge et al. 2007,
entire). Six management weaknesses have been identified in the current
management of lion hunting. These weaknesses include: (1) A lack of
scientifically based quota that results in excessive harvests; (2) a
lack of enforcement in age restrictions, which leads to unsustainable
harvests, increased rates of infanticide, and population declines; (3)
hunting of female lions in Namibia, which decreases reproduction
success, thereby decreasing males available for trophy hunting; (4) the
use of fixed quotas, which encourages hunters to be unselective in
their take of a trophy (i.e., they will kill younger, less desirable
males); (5) a lack of minimum hunt lengths or minimum lengths that are
too short to allow hunters the time needed to be more selective in
their take of trophies; and (6) general problems associated with
management of trophy hunting, including corruption, allocation of
concessions, and lack of benefits to communities and recognition of the
important role they play in conservation.
Most P. l. leo populations are extremely small, isolated, and
rapidly declining. Of the 18 countries documented to allow lion trophy
hunting, 8 are in the range of P. l. leo. However, we note that due to
the lack of lions in some of these countries, it is unlikely that all
of these countries could conduct lion trophy hunts. A study found that
quotas in Benin and Burkina Faso are too high for sustainability,
although Burkina Faso has proposed to reduce their quota in the 2015-
2016 season (Henschel 2015, pers. comm.; Lindsey et al. 2013a, p. 6).
Actual harvests in Burkina Faso were also found to be higher than the
level recommended by Packer et al. (2011, p. 151). Additionally, Benin
and Burkina Faso have committed to implementing an age-based strategy,
but have yet to implement it. As a result, species experts agree that
there is no level of offtake that would be sustainable for P. l. leo
populations in their current condition (Bauer 2015, pers. comm.;
Henschel et al. 2014, entire; Henschel et al. 2010, entire).
Of the 18 countries documented to allow lion trophy hunting, 10 are
in the range of P. l. melanochaita. However, we note that, like the
situation with P.
[[Page 80024]]
l. leo, due to a lack of lion populations in some of these countries,
it is likely that fewer countries could conduct lion trophy hunts. A
study found that Namibia, Tanzania, Zambia, and Zimbabwe all had quotas
higher than the recommended level for sustainability; however, Zimbabwe
has reduced their quota. Mozambique (Niassa National Reserve) is the
only location found to have a quota below the recommended level. Age-
based strategies have been implemented and shown to reduce offtakes in
Mozambique (only in Niassa National Reserve, excludes the rest of the
country), Tanzania, and Zimbabwe. Furthermore, Zimbabwe and Niassa
National Reserve are the only two locations that have fully implemented
an age-based strategy with transparency, an element experts say is
critical to a quota allocation system. Several other countries have
made commitments to implement the age-restrictions strategy but their
progress is pending. In South Africa, 99 percent of the lion trophies
are captive bred, and, therefore, were not the result of removing lions
from the wild.
Unless reforms are made to the current management of trophy
hunting, we expect the declines specifically documented from excessive
offtakes in Benin, Cameroon, Tanzania, Zambia, and Zimbabwe to
continue. Furthermore, we expect excessive harvests to further
contribute to declines in the species across its African range.
Import/Export of Lion Trophies
The lion species (Panthera leo) is listed in Appendix II of CITES;
however, the former Asiatic lion (P. l. persica) is listed in Appendix
I. CITES is an international agreement through which member countries
work together to protect against over-exploitation of animal and plant
species found in international trade. Parties regulate and monitor
international trade in CITES-listed species--that is, their import,
export, and reexport, and introduction from the sea--through a system
of permits and certificates. CITES lists species in one of three
appendices--Appendix I, II, or III.
An Appendix-I listing includes species threatened with extinction
whose trade is permitted only under exceptional circumstances, which
generally precludes commercial trade. The import of specimens (both
live and dead, as well as parts and products) of an Appendix-I species
generally requires the issuance of both an import and export permit
under CITES. 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 commercial purposes. For live specimens, a finding
must also be made that the recipient is suitably equipped to house and
care for the specimens (CITES Article III(3)). Export permits are
issued only if findings are made that the specimen was legally acquired
and the export is not detrimental to the survival of the species in the
wild, and that a living specimen will be so prepared and shipped as to
minimize the risk of injury, damage to health, or cruel treatment, and
that the CITES Management Authority of the exporting country is
satisfied that an import permit has been granted for the specimen
(CITES Article III(2)).
CITES Appendix II includes species that are less vulnerable to
extinction than species listed in Appendix I, and ``although not
necessarily now threatened with extinction, may become so unless trade
in specimens of such species is subject to strict regulation in order
to avoid utilization incompatible with their survival.'' Species listed
in Appendix II of CITES may be commercially traded, subject to several
restrictions.
Although each country has its own method of regulating trophy
hunting, international trade of lion trophies must adhere to CITES.
International trade of lion parts and products (including trophies) are
reported by both the exporting and importing countries and tracked by
the United Nations Environment Programme World Conservation Monitoring
Centre (UNEP-WCMC).
According to the UNEP-WCMC CITES Trade Database, between 2005 and
2012, exports of lion trophies demonstrated a decreasing trend, if
exports of captive-born lions from South Africa are excluded (UNEP-WCMC
2014, unpaginated). UNEP-WCMC indicates that 521 lion trophies were
exported (excluding South Africa) in 2005 and 303 were reported
(excluding South Africa) in 2012.
It should be noted that there are limitations to interpreting the
above reported information. The 2004 guide to using the CITES Trade
Database indicates that the outputs produced by the CITES Trade
Database can be easily misinterpreted if one is not familiar with it
(CITES 2004b, p. 5). The number of ``trophies'' reported does not
necessarily equate to the number of lions hunted. Additionally, the
number of trophies reported for a given year in the trade report does
not equate directly to the number of animals hunted in that given year
(CITES export permits are generally valid for 6 months, and a trophy
could in theory be exported the year after it was hunted). The second
limitation to interpreting this information is that, although many
permits may indicate that an animal is of wild origin (source code
``W''), these permits may be incorrectly coded. This is true for South
Africa, where during the period of 2000 to 2009, animals that were
captive born and released into private reserve systems were assigned an
incorrect source code of ``W.'' South Africa has since requested their
provincial authorities to use the correct source code for ``captive
bred'' in order to correctly reflect the source of sport-hunted lion
trophies; however, some provinces are not complying (RSA 2013, pp. 8-
9). Based on South African trade data, the bulk of lion exports and
their parts and products (including trophies) are from captive-born
lions (RSA 2013, p. 7).
Tanzania, with one of the largest lion populations (Hamunyela et
al. 2013, pp. 29, 283; Riggio et al. 2013, p. 32; Ikanda 2008, p. 4;
Baldus 2004, pp. 5, 6), was the largest exporter of wild-origin lion
trophies, but their exports have decreased significantly since 2008. In
2008, approximately 138 trophies were exported from Tanzania; in 2010,
128 were exported; in 2011, 55 were exported; in 2012, 62 were exported
(it should be noted that in 2012 Tanzania established an annual quota
to limit trophy hunting to no more than 50 animals (Jackson 2013, p.
7); and in 2013, 11 were exported (UNEP-WCMC 2014, unpaginated). Again,
it should be noted that there may be discrepancies between the annual
quota and the actual number of trophies exported in a given year (see
https://www.cites.org/common/resources/TradeDatabaseGuide.pdf for
additional information). Regardless, the numbers of lion trophies
exported by Tanzania according to the UNEP-WCMC CITES Trade Database
suggest a decreasing trend.
Additionally, some trophies are exported from source countries
under the ``skins'' category. According to the most recent data
available, the United States imported skins of wild origin from four
African countries in 2013; 9 from Mozambique, 5 from Tanzania, 2 from
South Africa, and 22 from Zimbabwe. The purpose code for these imports
was ``Trophy Hunt,'' except for the two skins from South Africa which
were coded as ``Commercial.''
For 2013, the most recent year for which complete CITES trade data
are available, U.S. CITES Annual Report trade data indicate that the
United States allowed the direct import of lion
[[Page 80025]]
trophies from seven African countries, as follows:
Botswana = 1 trophy (originated from Mozambique)
Burkino Faso = 3 trophies
Mozambique = 5 trophies
Namibia = 9 trophies
South Africa = 545 trophies (the majority of which are reported to be
of captive-born origin; additionally 2 captive trophies originated in
South Africa, imported to Canada, and then imported into the United
States)
Tanzania = 3 trophies
Zambia = 17 trophies
Zimbabwe = 44 trophies
Based on CITES trade data, lion trophy exports have decreased
throughout most of the lion's range, including Tanzania, which has one
of the largest lion populations. South Africa is the only country where
exports have increased because most of these trophies are of captive
origin.
Traditional Use of Lion Parts and Products
Lion parts and products are used in many African countries as
medicine, nutrition, talismans, and decorations, and in traditional
ceremonies and rituals (CITES 2014, p. 7; Burton et al. 2010, p. 4).
CITES (2014, p. 8) reports that many African countries, including
Somalia, Nigeria, Burkina Faso, Kenya, and Cameroon, maintain local
markets in lion products. Parts used include skin, teeth, claws, fat,
whiskers, bone, bile, testicles, meat, and tails. In addition, lion
bone is also used in Asia as a substitute for tiger bone in traditional
Asian medicine (Williams et al. 2015, pp. 2, 62).
While quantitative data is lacking, according to a peer reviewer
(Bauer 2015, pers. comm.), trade in lion parts and products is very
common within western and central Africa. Responses to the CITES
periodic review consultation process support this claim: Trade in lion
skins and partial skins is described as ``frequent'' in street markets
in Abidjan, C[ocirc]te d'Ivoire; lion skins and canines are described
as ``easily found'' in the markets of Dakar, Senegal; and the scale of
domestic trade in illegal lion products is described as ``massive'' in
Nigeria (CITES 2014, pp. 5-6). Further, in the central African country
of Cameroon, the estimated value of a single lion carcass exceeds the
trophy fee, and at a lion conservation conference the Government of
Cameroon identified trade in lion skins as a major cause of the decline
in lion populations in western and central Africa (LAGA pers. comm., in
CITES 2014, p. 12). According to Henschel (in CITES 2014, p. 12), the
trade in lion skins is most likely one of the biggest threats to lion
survival in western Africa due to the rarity of lions in the region,
the extent of the trade, and the high price of lion skins.
In southern and eastern Africa, trade in lion parts, particularly
lion bone, to Asia is generally considered a severe potential threat to
the species (Bauer 2015, pers. comm.). According to CITES (2014, p.
14), there is ``clear scope for the international trade in lion body
parts for [traditional Chinese medicine and traditional African
medicine] to grow uncontrollably, as it has done for other big cats.''
Lion bones are used as a substitute for tiger (Panthera tigris)
bone in traditional Asian medicine and in Asian luxury products
(Williams et al. 2015, pp. 2-3, 5; Graham-Rowe 2011, pp. s101-s102).
Lion bones are difficult to distinguish from tiger bones (Williams et
al. 2015, pp. 8, 102; Wildlife Protection Society of India 2007,
unpaginated), and are sold into Asian markets as tiger bone fakes
(Williams et al. 2015, pp. 2-3, 62, citing several sources). Tiger bone
is highly valued in Asia, primarily in China and Vietnam, and there is
considerable demand for it (Williams et al. 2015, p. 1; Gratwicke et
al. 2008, pp. 2-5; Graham-Rowe 2011, pp. s101-s102). Consequently,
tiger bones are one of the most lucrative products on the illegal
wildlife market (Haken 2011, in Williams et al. 2015, p. 1)--the retail
price of raw tiger bone can reach $1,250-3,750 USD per kilogram (Nowell
and Ling 2007, p. 23).
Tigers are categorized by IUCN as endangered (Goodrich 2015, p. 2).
Globally, the tiger population has declined from what is believed to
have been 100,000 at the turn of the 19th century (Jackson 1993, in
Nijman and Shepherd 2015, p. 1) to an estimated 5,000-7,000 in 1998, to
3,159 tigers in 2014 (Goodrich 2015, p. 7; Seidensticker et al. 1999,
in Goodrich et al. 2015, p. 7). Poaching for the illegal trade in tiger
parts, especially bone has become a major driver in the species'
decline (Goodrich et al. 2015, p. 9; Williams et al. 2015, p. 1; Nowell
and Ling 2007, p. v). While wild tiger populations are declining, the
demand for tiger parts in Asia is increasing (Williams et al. 2015, p.
5; United Nations Office on Drugs and Crime 2013, p. 81; United Nations
Office on Drugs and Crime 2010, pp. 10, 17; Nowell and Ling 2007, p.
4). This increasing demand for tiger parts has led to the rise of tiger
farms, where live captive bred tigers appear to be utilized to supply
the bone trade within China (Denyer 2015, unpaginated). With tigers
difficult to obtain, lion bone may be increasingly used as a
replacement for tiger bone. Thus, the lion bone trade could potentially
follow the same course as the tiger bone trade: Become lucrative, spur
considerable demand from suppliers of the black market, result in
extensive poaching of wild individuals, and have significant impacts to
wild populations.
Certain aspects of the current lion bone trade suggest that the
potential for the trade to impact wild lion populations may be high.
For example, evidence suggests that demand from Asia for lion bone is
increasing rapidly. Based on Williams (2015, pp. ix-x, 46), during
1982-2000, only nine lion skeletons were exported from worldwide
sources, destined primarily to Europe. CITES permit records show only
three exported from South Africa prior to 2008, destined for Denmark.
In 2008, South Africa began issuing CITES permits for the export of
skeletons of captive-bred lions to Asia. These exports currently appear
to come primarily from South Africa's captive-bred lion hunting
industry as a byproduct of trophy hunting. The number of lion skeletons
for which South Africa issued permits for export to Asia (China, Viet
Nam, Thailand and Lao PDR) increased tenfold from 2008 to 2011, from
about 50 to about 573 skeletons, respectively, representing a total of
1,160 skeletons or about 10.8 metric tons (11.9 US tons) of lion bone
in 4 years (Williams 2015, pp. ix-x, 46). Further, according to the
Government of Kenya (2015, p. 3), the declared exports of bones,
skulls, and skeletons derived from wild lions also show an increasing
trend through the period 2003-2012, with total declared specimens in
2012 more than ten times those in 2003. With respect to meeting demand
for lion bone, Lindsey et al. (2012, p. 20) state that there are likely
to be large numbers of lion bones available for export from game farms,
from lionesses and non-trophy males, and as byproducts from animals
shot as trophies. In addition, Williams et al. (2015, p. 41) report
that there may be between 1,400 and 6,200 lion skeletons from past
trophy hunts on South African game farms that could potentially be used
to supply demand for lion bone. However, considering the sharp and
continuing increases in demand from Asia for lion bone, there is
potential for demand to surpass the availability of legally obtained
lion bone and, consequently, result in poaching of wild lions to meet
demand.
In addition, recent evidence strongly suggests live lions are being
used to supply the lion bone trade (Williams et al. 2015, pp. ix, 2-3,
42-44). In August 2006 a live Asiatic lion was observed in
[[Page 80026]]
a market in Mong La, Myanmar (Oswell, 2010, p. 12). The town, known for
incidents of wildlife trafficking, is less than 2km from the Chinese
border. Up to 2006/2007, Williams et al. (2015, p. x, Table 11, Figure
24) noted:
``The combined quantity of live lions and lion parts and derivatives
exported to East-Southeast Asia from South Africa was minimal in the
broader global trade. From 2008, however, the quantities exported
increased almost six-fold from the previous year. Not only did the
number of live lions exported to East-Southeast Asia reach record
levels from this time, but also the first permits to export lion
skeletons were issued. The demand for lion parts and derivatives
appears to have coincided with the strengthened conservation
measures adopted in 2006-2007 to protect tigers and Asian big cats.
Accordingly, tiger parts were increasingly substituted with lion
parts obtained from Africa. The trade in lion parts and derivatives
to Lao PDR dominates the exports. Since 1998, but especially after
2007, China, Viet Nam, Lao PDR, Myanmar and Thailand have imported
increasing amounts of live lions, lion bodies and bones from South
Africa.''
Evidence also indicates ``well established'' links between South
Africa's legal lion bone trade and the Xaysavang Network, an
international wildlife trafficking syndicate that is also involved in
the illicit rhino horn trade in South Africa (Williams et al. 2015, pp.
7-10, 59; Environmental Investigative Agency 2014, p. 13; U.S.
Department of State 2013, unpaginated). The U.S. Department of State
has issued a $1 million reward for information leading to the
dismantling of this network. According to the U.S. Department of State,
the Xaysavang Network facilitates the killing of endangered species in
Africa and elsewhere and smuggles them to Laos for export to other
Asian countries (U.S. Department of State 2013, unpaginated). During
2008-2011, the vast majority (85%) of the permits issued by South
Africa to export lion skeletons or carcasses were issued for exports to
Laos (Williams et al. 2015, pp. x, 46) and, for the only 2 years for
which data were available (2009 and 2010), over half of the
consignments destined for Laos were listed as imported by Vixay
Keosavang, believed by the U.S. Department of State to be the leader of
the Xaysavang network (U.S. Department of State 2013, unpaginated;
Williams et al. 2015, pp.8-10). The involvement of the Xaysavang
Network in South Africa's lion bone trade indicates there are well-
established avenues for laundering of illegally obtained lion bones,
such as those obtained from poached wild lions, into the legal trade.
Lastly, evidence suggests incentive to poach wild lions for the
bone trade may currently exist. According to Williams et al. (2015, p.
x), the 2013 price paid to South African game farmers and landowners
for lion bones was $1,260-2,100 USD per skeleton. In many lion range
states this exceeds per capita GDP (gross domestic product) (World Bank
2015, unpaginated). Thus, the current price paid for lion bone appears
to provide incentive in some countries to poach wild lions.
While the lion bone trade appears to currently be based primarily
in South Africa's captive-bred lion hunting industry, the trade appears
to be having little or no impact on wild lion populations in South
Africa at this time--lion populations in South Africa are stable or
increasing and there is little poaching of wild lions in the country
(Funston and Levendal 2014, pp. 1, 26; Williams et al. 2015, pp. 79-
80). However, the impact of the lion bone trade on lion populations
outside South Africa is unknown, and most wild lions occur outside
South Africa (see Distribution and Abundance). Based on the effect of
the tiger bone trade on tiger populations, if current conditions--for
example, rapidly increasing demand and involvement of an international
crime syndicate--continue unchanged, then there is considerable
potential for extensive poaching of wild lions to occur in order to
meet demand.
Disease
Wild lions are known to be infected with various pathogens (Hunter
et al. 2012, p. 2; Craft 2008, p. 6; Michel et al. 2006, p. 92;
Hofmann-Lehmann et al. 1996, pp. 559-561). However, information on the
extent of infections and impacts of diseases on lion populations is
limited. We found one study documenting disease in a single wild lion
in India that died from trypanosomiasis in 2007; analysis of tissue
samples also detected peste des petits ruminants virus (PPRV), which is
not known to cause disease in carnivores (LionAid 2013, unpaginated;
Balamurugan et al. 2012, pp. 203, 205). Information on the presence of
disease and impacts to lions come from a few long-term studies that
have been conducted in Africa, including Serengeti National Park,
Ngorongoro Crater, and Kruger National Park.
As a result of human population expansion into lion habitat, lions
are increasingly exposed to diseases from domestic animals (IUCN 2006b,
p. 26). Because lions are a top predator, they are at a particularly
high risk of exposure to pathogens (Keet et al. 2009, p. 11). Some
pathogens are endemic, meaning they are constantly present, but often
do not cause disease. Others are epidemic and cause a sudden severe
outbreak with the potential to cause high mortality (Craft 2008, pp. 5,
6). The association between disease, age, nutritional health and other
factors that could predispose a lion to morbidity and, eventually,
mortality is complex. It is often difficult to determine whether
mortality was due to a single factor or a combination. Lions could be
infected with and become debilitated by a disease, but the actual cause
of death could be other factors, such as fighting with other lions or
large predators (LionAid 2014a, p. 4).
Feline calicivirus, feline herpesvirus, feline parvovirus, feline
coronavirus, and feline leukemia virus are endemic viruses known to
occur in lions of Serengeti National Park, Ngorongoro Crater, Lake
Manyara National Park, Kruger National Park, and Etosha National Park
(but not all viruses are known in all parks). However, these diseases
are not known to affect lion survival (Hunter et al. 2012, p. 2; Craft
2008, p. 6; Hofmann-Lehmann 1996, pp. 559, 561).
Lions within Kruger National Park and Hluhluwe-iMfolozi Park, South
Africa, and Serengeti National Park, Tanzania, are known to be infected
with Mycobacterium bovis, a pathogen that causes bovine tuberculosis
(bTB). This pathogen is not endemic to African wildlife and was likely
introduced from cattle imported from Europe. M. bovis is transmitted to
ungulates, such as African buffalo (Syncerus caffer) and wildebeest
(Connochaetes taurinus), from domestic cattle located on the periphery
of the parks (Maas et al. 2012, p. 4206; Keet et al. 2009, pp. 4, 11;
Renwick et al. 2007, p. 532; Michel et al. 2006, pp. 92, 93; Cleaveland
et al. 2005, pp. 446, 449, 450). Spillover of the disease from buffalo
to other lion prey species, such as kudu (Tragelaphus strepsiceros) and
warthog (Phacochoerus africanus), has also been documented (Keet et al.
2009, pp. 4, 11; Renwick et al. 2007, p. 535; Cleaveland et al. 2005,
p. 450). Because the lion's primary prey are infected with bTB, they
are frequently exposed to large amounts of infected tissue and are at
risk of infection (Keet et al. 2009, pp. 4, 6; Renwick et al. 2007, pp.
532, 536; Michel et al. 2006, p. 93; Cleaveland et al. 2005, pp. 450,
451). Furthermore, predators prey on weak animals and scavenge on
carcasses, increasing their likelihood of being exposed to M. bovis
(Renwick et al. 2007, p. 536; Michel et al. 2006, p. 93). Transmission
may also occur among lions via scratching and biting (Keet et al. 2009,
p. 7; Renwick
[[Page 80027]]
et al. 2007, pp. 532-533). M. bovis is a pathogen that causes the
infected animal to remain infectious and, therefore, a source of
infection, until it dies (Renwick et al. 2007, p. 531). Miller et al.
(2014, pp. 495, 496) found respiratory shedding of viable M. bovis in
living lions, meaning that lions could transmit bTB and serve as
maintenance hosts.
The social behavior of buffalo and lions allows M. bovis to spread
to larger areas and facilitates the transmission within and between
prides. Drought conditions may also encourage the spread of this
pathogen as herds must move into new areas in search of forage,
potentially putting them in contact with new, uninfected herds (Keet et
al. 2009, pp. 4, 6; Renwick et al. 2007, p. 533; Michel et al. 2006, p.
93). In Kruger National Park, bTB was introduced in the southeastern
corner of the park between 1950 and 1960. It gradually made a northern
progress and reached the park's northern boundary in 2006. In 2009, the
disease was found in buffalo across the river boundary in Zimbabwe
(Keet et al. 2009, pp. 6, 11; Renwick et al. 2007, pp. 532, 533; Michel
et al. 2006, pp. 92, 96, 98). A study from Kruger National Park
indicated that bTB spreads quickly through lion populations; in an area
with high herd prevalence of M. bovis, 90 percent of lions became
infected (Cleaveland et al. 2005, p. 451). In time it will likely
spread to Mozambique (Keet et al. 2009, p. 6). In Serengeti National
Park, infection may be widespread due to the large, migratory
wildebeest population that ranges throughout the Serengeti ecosystem,
including Maasai Mara National Reserve (Cleaveland et al. 2005, p.
450). Although an eradication program has been implemented for cattle
in South Africa, once an infection is established in a free-ranging
maintenance host, like buffalo, it is unlikely to be eradicated (Keet
et al. 2009, p. 11; Renwick et al. 2007, pp. 537, 538; Michel et al.
2006, p. 96). In fact, modeling has predicted that prevalence could
reach as high as 90 percent over the next 25 years, with similar
consequences for predators (Renwick et al. 2007, p. 535).
Clinical signs of bTB in lions include emaciation, respiratory
complications, swollen lymph nodes, draining sinuses, ataxia, and
lameness (Keet et al. 2009, p. 13; Renwick et al. 2007, pp. 533, 534;
Cleaveland et al. 2005, p. 450), although some lions may be
subclinically infected but remain asymptomatic until they experience
another bTB infection, suffer from poor nutrition or advancing age, or
become super-infected with other diseases that may exacerbate the
infection (Renwick et al. 2007, p. 533). The impact of bTB on lions is
largely unknown. Researchers suggest that bTB may lower breeding
success, reduce resiliency, and be a mortality factor based on data
that indicate survival is shortened in infected lions, with death
ranging between 2 and 5 years after infection (Maas et al. 2012, p.
4212; Renwick et al. 2007, p. 536; Keet, unpublished data in Michel et
al. 2006, p. 93; Cleaveland et al. 2005, pp. 450, 451). In addition to
clinical effects of bTB that may lead to mortality, this disease has
also led to social changes with lower lion survival and breeding
success with more frequent male coalition turnover and, consequently,
higher infanticide (Keet, unpublished data in Michel et al. 2006, p.
93). Research has shown adverse effects to lion individuals and
subpopulations, but effects at the species population level are
developing slowly (Michel et al. 2006, p. 97). Studies have shown that
impacts of bTB on lion numbers vary between populations. For example,
30 percent of the inbred populations in Hluhluwe-iMfolozi Park died due
to a combination of bTB and malnutrition (Hunter et al. 2012, p. 3).
However, despite bTB infection and a high prevalence in prey species,
the lion population in Kruger National Park has remained stable
(Ferreira and Funston 2010, p. 201).
Epidemics of canine distemper virus (CDV) are known to have
occurred in the Serengeti-Mara Ecosystem, an area that encompasses the
Serengeti National Park, Ngorongoro Conservation Area, and Maasai Mara
National Reserve (Craft 2008, pp. 13-14; Cleaveland et al. 2007, pp.
613, 616, 618). CDV is a common pathogen in the large population of
domestic dogs (Canis lupus familiaris) around the Serengeti-Mara
Ecosystem, which are believed to be the source of CDV in lions
(Cleaveland et al. 2007, pp. 613, 617). CDV is assumed to be
transferred to lions by the sharing of food sources with spotted hyenas
(Crocuta crocuta) or jackals (Canis spp.) that become infected by
consuming the infected carcasses of domestic dogs (Craft et al. 2009,
p. 1783; Craft 2008, p. 13). Viana et al. (2015, pp. 1466, 1467)
recently discovered that domestic dogs are not the sole source of CDV
in the Serengeti, but rather there is likely a larger, multihost
community of wildlife that contribute to outbreaks. Lions may also
transmit CDV among themselves via sharing food, fights, and mating
(Craft et al. 2009, pp. 1778, 1783; Craft 2008, pp. 13, 18, 71).
CDV generally lacks clinical signs or measurable mortality in
lions, and most CDV events have been harmless. However, in 1994 and
2001, CDV epidemics in the Serengeti National Park/Maasai Mara National
Reserve and Ngorongoro Crater, respectively, resulted in unusually high
mortality rates (Hunter et al. 2012, p. 2; Craft 2008, p. 14; Munson et
al. 2008, pp. 1, 2; Cleaveland et al. 2007, pp. 613, 618; Roelke-Parker
et al. 1996, pp. 441, 443). These outbreaks coincided with climate
extremes that resulted in a higher number of Babesia, a tick-borne
parasite, infections (Munson et al. 2008, pp. 2, 5). Babesia is common
in lions, but typically at low levels with no measurable impacts on
their health (Craft 2008, p. 14; Munson et al. 2008, p. 3). However,
droughts in 1993 and 2000 in Serengeti National Park/Maasai Mara
National Reserve and Ngorongoro Crater, respectively, led to large-
scale starvation and widespread die-offs of buffalo. This situation
combined with resumption of rains and fire suppression in Ngorongoro
Crater favored propagation of ticks, vectors of Babesia, leading to
unusually high tick burdens. The compromised health of buffalo allowed
lions to feed on an inordinate number of tick-infested prey (Craft
2008, p. 14; Munson et al. 2008, pp. 2, 4, 5).
Exposure to either CDV or Babesia singly is not typically
associated with a compromise in health or an increase in mortality
(Craft 2008, p. 14; Munson et al. 2008, pp. 1, 2, 3). However, the
Babesia infections were exacerbated by the immunosuppressive effects of
CDV and led to the unusually high mortality rates (Craft 2008, p. 14;
Munson et al. 2008, p. 5). The Serengeti National Park/Maasai Mara
National Reserve lion population lost 30 percent of its population
(approximately 1,000 lions), but has recovered to its pre-epidemic
population levels (Craft 2008, pp. v, 14, 41; Munson et al. 2008, p. 1;
Cleaveland et al. 2007, pp. 613, 617; Roelke-Parker et al. 1996, p.
444). Thirty-four percent of the Ngorongoro Crater lion population was
killed, but frequent outbreaks of disease have prevented this
population from recovering back to its carrying capacity (Craft 2008,
p. 14; Munson et al. 2008, pp. 1, 2; Cleaveland et al. 2007, p. 617).
The difference in recovery is likely due to the highly inbred nature of
the Ngorongoro Crater lion population, compared to the Serengeti
population, and its greater susceptibility to parasitic and viral
infections (Hunter et al. 2012, p. 2; Munson et al. 2008, p. 5; Brown
et al. 1994, pp. 5953-5954).
Feline immunodeficiency virus (FIV) is an endemic pathogen in many
lion populations of southern and eastern Africa (Maas et al. 2012, p.
4206; Adams
[[Page 80028]]
et al. 2011, p. 173; Pecon-Slattery et al. 2008, p. 2; Hofmann-Lehmann
et al. 1996, pp. 555, 558; Brown et al. 1994, p. 5966). FIV is believed
to have been present in lions since the late Pliocene (O'Brien et al.
2012, p. 243; Troyer et al. 2011, p. 2; Roelke et al. 2009, p. 3;
Pecon-Slattery et al. 2008, p. 8). There are 6 subtypes of FIV, A
through F, each with a distinct geographic area of endemnicity (Adams
et al. 2011, p. 174; Troyer et al. 2011, p. 2; Roelke et al. 2009, p.
3; Pecon-Slattery et al. 2008, p. 4; O'Brien et al. 2006, p. 262) and
differing levels of virulency (LionAid 2014b, unpaginated). The social
nature of lions allows for viral transmission within and between prides
through saliva when biting (Maas et al. 2012, p. 4210; Pecon-Slattery
et al. 2008, p. 5; Brown et al. 1994, p. 5953). Prevalence of FIV often
approaches 100 percent of adults in infected lion populations,
including the few remaining populations in Botswana, South Africa, and
Tanzania, (LionAid 2014b, unpaginated; O'Brien et al. 2012, p. 243;
Troyer et al. 2011, p. 2; Roelke et al. 2009, p. 3; O'Brien et al.
2006, p. 262; Hofmann-Lehmann et al. 1996, p. 559).
FIV causes immune deficiencies that allow for opportunistic
infections in the host (Roelke et al. 2009, p. 1; Brown et al. 1994, p.
5,953). With an impaired immune system, lions may not have an
appropriate and effective immune response to various pathogens to which
they are consistently exposed (LionAid 2014a, p. 6). There may also be
unrecognized immunological consequences (Roelke et al. 2006, p. 234)
and adverse clinical and pathological outcomes (Roelke et al. 2009, p.
1). Chronic effects of FIV are important to long-term survival and
differ according to subtype (Troyer et al. 2011, p. 6). Studies have
indicated that lions may exhibit signs of opportunistic infection
associated with AIDS, such as swollen lymph nodes, gingivitis, tongue
papillomas, dehydration, poor coat condition, and abnormal red blood
cell parameters, and in some cases death (Troyer et al. 2011, p. 2;
Roelke et al. 2009, pp. 2, 3-6). Lions in Botswana and Tanzania have
demonstrated multiple clinical features of chronic immune depletion
similar to HIV and domestic cat AIDS (Troyer et al. 2011, pp. 2-3).
However, there is no evidence that FIV itself poses a threat to wild
populations (Frank et al. 2006, p. 1); FIV does not appear to be
impacting lions in Kruger National Park (Maas et al. 2012, p. 4212),
and no evidence of AIDS-like illnesses or decreased lifespan has been
found in FIV lion populations in the Serengeti (O'Brien et al. 2006, p.
263).
The role of disease in determining survival and reproductive
potential in lions is almost completely unknown. It is often difficult
to determine whether mortality was due to a single or combination of
factors. Lions could be infected with and become debilitated by a
disease, but the cause of death could ultimately be due to other
factors (LionAid 2014a, pp. 4-5). Available studies do not indicate
that infection with a single disease is causing detrimental impacts to
lions at the species level, although general body condition, health,
and lifespan may be compromised and result in negative impacts at the
individual or population level.
Co-infections, however, could have synergistic effects that lead to
greater impacts on lions than a single infection. Lions impacted by the
1994 CDV outbreak in Serengeti National Park/Maasai Mara National
Reserve may have been more susceptible to CDV due to depleted immunity
caused by FIV (O'Brien et al. 2006, p. 263). Troyer et al. (2011, pp.
5-6) found that survival during the CDV/Babesia outbreak in Serengeti
National Park/Maasai Mara National Reserve was significantly less for
lions infected with FIV A and/or C than FIV B. This finding suggests
that FIV A and C may predispose carriers to CDV pathogenesis and may
increase the risk of mortality (O'Brien et al. 2012, p. 243). Impacts
of co-infections of FIV with FCV, FPV, FHV, and FCoV on individual
lions are negligible and do not endanger the lion population, at least
in the absence of other aggravating cofactors (Hofmann-Lehmann et al.
1996, p. 561).
Pathogen-pathogen interactions may become more important when lions
are under additional stress (e.g., increased parasite load or low prey
density) (Maas et al. 2012, p. 4212). Certain environmental conditions
may exacerbate the effects of an otherwise innocuous infection. For
example, as discussed above, CDV and Babesia infections generally have
no measurable impacts on lion health, but climatic conditions increased
exposure of lions to Babesia infections, which were exacerbated by the
immunosuppressive effects of CDV and led to unusually high mortality
rates (Craft 2008, p. 14; Munson et al. 2008, p. 5). Some lions
infected with bTB may remain asymptomatic until conditions change and
they suffer from poor nutrition due to low prey density, advancing age,
or become super-infected with other diseases that may exacerbate the
infection (Renwick et al. 2007, p. 533).
Species with reduced genetic variation may be less able to mount an
effective immune response against an emerging pathogen (O'Brien et al.
2006, p. 255). For example, the inbred populations in Hluhluwe-iMfolozi
Park lost 30 percent of lions due to a combination of bTB and
malnutrition (Hunter et al. 2012, p. 3). The Ngorongoro Crater lions
have not recovered to pre-outbreak numbers due to their inbred nature
and greater susceptibility to parasitic and viral infections (Hunter et
al. 2012, p. 2; Munson et al. 2008, p. 5; Brown et al. 1994, pp. 5953-
5954). Additionally, disease outbreaks can lead to extirpation in
small, isolated populations (Gilpin and Soule 1986 and Paul-Murphy et
al. 1994 in Harvell et al. 2002). Although we found no information
indicating presence of disease in the Indian population, the small,
isolated nature makes the population more vulnerable to disease
outbreaks and could have a detrimental impact on the population
(Banerjee and Jhala 2012, p. 1427; Meena 2010, p. 209; Johnsingh et al.
2007, p. 93). This principle also applies to the small, isolated
populations throughout Africa.
Although disease is known in several populations, the impacts are
known in only a few populations where disease has been frequently
studied. Precise estimates of lions lost to disease are lacking, due to
the difficulty in detection. However, disease appears to be a secondary
factor influencing the decline of lions when co-infections occur or
when disease is combined with other factors, including environmental
changes, reduced prey density, and inbreeding depression. Diseases
weaken individuals and allow them to succumb to other diseases or
factors. Although disease does not appear to be a major driver in the
status of the lion, populations can suffer significant losses; some may
recover to pre-outbreak levels, others may not. Given the small and
declining lion populations that remain, any loss of individuals from
the populations could be detrimental.
The risk of disease may increase with time due to loss of genetic
variation associated with continued fragmentation of populations,
whether by habitat loss or fencing of habitat, and increased proximity
to humans and domestic livestock that may expose lions to new diseases
(IUCN 2006b, pp. 19, 26). Additionally, changes in climate may increase
disease outbreaks in prey species, as well as lions (See Climate
Change). Climate change could potentially increase the likelihood of
lethal co-infections (The Heinz Center 2012, p. 12), similar to the co-
infections of CDV and Babesia in Serengeti National Park/Maasai Mara
National
[[Page 80029]]
Reserve and Ngorongoro Crater lions following drought events.
Deleterious Effects Due to Small Population Sizes
The risk of extinction is related to the moment when a declining
population becomes a small population and is often estimated using
minimum viable population (MVP) sizes (Traill et al. 2010, p. 28). The
viability of a lion population is complex, but it partly depends on the
number of prides and ability of males to disperse and interact with
other prides, which affects exchange of genetic material
(Bj[ouml]rklund 2003, p. 518). Without genetic exchange, or variation,
individual fitness is reduced and species are less able to adapt to
environmental changes and stress, increasing the risk of extinction
(Bijlsma and Loeschcke 2012, pp. 117, 119; Segelbacher et al. 2010, p.
2; Traill et al. 2010, p. 31; Bj[ouml]rklund 2003, p. 515).
Bj[ouml]rklund (2003, p. 520) found that the most important
determining factors for the level of inbreeding in lions is the number
of prides and male dispersal. The MVP for lions has not been formally
established and agreed upon by species experts (Riggio et al. 2011, p.
5; CITES 2004a, p. 2; Bj[ouml]rklund 2003, p. 521); however, it has
been suggested that to conserve genetic diversity, populations of at
least 50 prides, but preferably 100 prides (250 to 500 individuals),
with no limits to dispersal, are necessary (Bauer et al. 2008 in Riggio
et al. 2013, p. 32; Bj[ouml]rklund 2003, pp. 515, 518). Bj[ouml]rklund
(2003, p. 518) found that inbreeding decreased rapidly with the number
of prides. For example, if there are less than 10 prides the likelihood
of genetic effects due to inbreeding increased from 0 in the beginning
to 26-45 percent after 30 generations, whereas if 100 prides are
present, the likelihood is only 5 percent assuming no migration into
the population (Bj[ouml]rklund 2003, p. 515). Additionally, it appears
that inbreeding rapidly increases when the number of prides falls below
50 (Bj[ouml]rklund 2003, p. 518, Figure 2). Riggio et al. (2013, pp.
20, 22) used the threshold described by Bj[ouml]rklund (2003) to
define, in part, lion strongholds. Stronghold populations of lions were
considered to be those that meet the necessary requirements for long-
term viability and were defined, in part, as containing at least 500
individuals (100 prides). Potential strongholds were described,
broadly, as areas where immediate interventions might create a viable
population and were defined, in part, as populations that contained at
least 250 lions. However, the threshold described by Bj[ouml]rklund
(2003) and used by Riggio et al. (2013) may be smaller for P. l. leo as
pride sizes are generally smaller than those for P. l. melanochaita
(Riggio et al. 2013, p. 32; Meena 2009, p. 7; Nowell and Jackson 1996,
p. 37).
Male dispersal also plays an important role in determining the
level of inbreeding in lion populations. Even if only a fraction of
males do not disperse, inbreeding rapidly increases with each
generation (approximately 5 years) (Bj[ouml]rklund 2003, pp. 518, 520).
Even when migration rates of males is as high as 95 or 99 percent, the
likelihood of inbreeding is clearly higher than if 100 percent of males
disperse. Using a 95 percent dispersal rate, the probability of
inbreeding reached 57 percent and 20 percent for 10 and 100 prides
within 30 generations (150 years) (Bj[ouml]rklund 2003, pp. 518-519).
One example is the lion population in Ngorongoro Crater. New males
rarely migrate into the population due to physical barriers, and
inbreeding has been shown to occur (Packer et al. 1991b in
Bj[ouml]rklund 2003, p. 521). The fewer number of males present to
contribute genes to the next generation, the more inbred the population
will be (Riggio et al. 2013, p. 32). Therefore, not only does dispersal
impact inbreeding, so does the loss of male lions due to excessive
trophy hunting and infanticide (see Trophy Hunting).
Because the number of prides and male dispersal are the most
important factors for maintaining viability, sufficient areas are
needed to support at least 50 prides, but preferably 100 prides, and
allow unrestricted male dispersal (Bj[ouml]rklund 2003, p. 521).
Unfortunately, few lion populations meet these criteria as almost all
lion populations in Africa that historically exceeded 500 individuals
are declining, and few protected areas are large enough to support
viable populations (Bauer et al. 2015a, unpaginated; Bauer et al.
2015b, p. 1; Bauer et al. 2008, unpaginated; Riggio 2011, p. 5; Hazzah
2006, p. 2; Bauer and Van Der Merwe 2004, pp. 28-30; Bj[ouml]rklund
2003, p. 521). Even within large areas, inbreeding will increase if
dispersal is limited, (Bj[ouml]rklund 2003, pp. 521-522). Furthermore,
research indicates that there is a general lack of gene flow in most
lion conservation units (Dubach et al. 2013, pp. 749, 750; Bertola et
al. 2011, p. 1364; Chardonnet et al. 2009, p. 54).
Small populations (e.g., fewer than 50 lions) can persist in the
wild for some time; however, the lack of dispersal and genetic
variation can negatively impact the reproductive fitness of lions in
these populations and local extirpation is likely (Traill et al. 2010,
p. 30; O'Brien 1994, p. 5748). Loss of fecundity leads to a decrease in
population size, fewer prides in a population, and increased inbreeding
which contributes to a decline in the population and increases the risk
of extinction (Bj[ouml]rklund 2003, p. 521). Additionally, lack of
genetic variation can impact the ability of lions to withstand
stochastic events. For example, the inbred populations in Hluhluwe-
iMfolozi Park were unable to mount an effective immune response and
lost 30 percent of lions due to a combination of bTB and malnutrition
(Hunter et al. 2012, p. 3). Additionally, the lions of Ngorongoro
Crater never recovered to pre-outbreak numbers due its inbred nature
and greater susceptibility to parasitic and viral infections (Hunter et
al. 2012, p. 2; Munson et al. 2008, p. 5; Brown et al. 1994, pp. 5953-
5954). Reductions in genetic variations may also limit the lion's
ability to evolve responses to climate change (The Heinz Center 2012,
p. 12).
The lion population in India is one of the few populations that are
increasing (Bauer et al. 2015a, unpaginated; BBC 2015, unpaginated; The
Guardian 2015, unpaginated; Banerjee and Jhala 2012, p. 1427) and could
be considered a stronghold according to the criteria set by Riggio et
al. (2013, p. 22). Despite being genetically less diverse, Banerjee and
Jhala (2012, pp. 1424-1425) found no evidence of depressed demographic
parameters in the lions of India. However, intense management,
including healthcare interventions, may interfere with natural
selection processes by ensuring the survival of unfit lions which
facilitates the propagation of deleterious genes in the population
(Banerjee and Jahala 2012, p. 1427). This population is also running
out of area to expand. Being a small, isolated population and less
genetically diverse, it is more vulnerable to the loss of any
individuals due to environmental and stochastic events, and more prone
to local extinction events (Banerjee and Jhala 2012, p. 1428; Meena
2010, p. 209; Johnsingh et al. 2007, p. 93; Thuiller et al. 2006, pp.
434-435).
The establishment of another free-ranging population geographically
separate from Gir would reduce the risk of extinction of this
population due to stochastic events (e.g., disease outbreaks or
floods). In the early 1990s, a second population was proposed at Kuno
Wildlife Sanctuary in Madhya Pradesh State (Johnsingh et al. 2007, p.
93). However, the Government of Gujarat has refused to allow any lions
from Gir to be transferred to the Kuno Wildlife Sanctuary, despite a
ruling by India's Supreme Court (The Economic Times
[[Page 80030]]
2015, unpaginated; Duerr 2014, unpaginated; Meena 2014, p. 29).
Regulatory Mechanisms
Regulatory mechanisms in place to provide protections to African
lions vary substantially throughout Africa. The lion species (Panthera
leo) is listed in Appendix II of CITES; however, the former Asiatic
lion (P. l. persica) is listed in Appendix I. With the exception of
South Sudan, all of the lion range states are Parties to CITES.
According to the draft CITES Periodic Review of the Status of African
Lions (CITES 2014, pp. 14-15) outside of CITES, lions have no legal
protections in four countries: Burundi, Guinea Bissau, Lesotho, and
Swaziland. However, CITES 2014 (p. 15) states that most of the southern
and eastern lion range states have regulatory mechanisms in place to
protect lions. We found that most of the range states have national
environmental legislation to establish national parks and conservation
areas, and to conserve and regulate the take, hunting, and trade of
wildlife, including parts and products, but could find no legislation
specific to lions, or to the main threats affecting lions: habitat
loss, human-lion conflict, and loss of prey base (Ecolex \1\
information last accessed November 6, 2015).
---------------------------------------------------------------------------
\1\ ECOLEX is a comprehensive database on environmental law,
maintained by the International Union for Conservation of Nature
(IUCN), the United Nations Environment Programme (UNEP), and the
Food and Agriculture Organization of the United Nations (FAO). Our
search terms used with respect to wildlife laws were ``African
lion,'' ``Asiatic lion,'' ``Panthera leo leo,'' ``Panthera leo
persica,'' and ``country,'' e.g., ``Angola,'' ``Benin,'' etc.
Information accessed at https://ecolex.org.
---------------------------------------------------------------------------
National and international conservation strategies rely on
protected areas to protect natural resources from negative impacts of
human populations (Craigie et al. 2010, p. 2221). The lion is largely
limited to protected areas; therefore, effective management is crucial
to the survival of the species. However, weak management of protected
areas has been documented across its range, especially in western
Africa where most protected areas are experiencing severe management
deficiencies (Henschel et al. 2015, unpaginated; Henschel et al. 2014,
pp. 5, 7; Brugi[eacute]re 2012 in Henschel et al. 2014, p. 7; Craigie
et al. 2010, entire). The WAP complex in western Africa had received
high scores for management effectiveness (Henschel et al. 2015, p. 7).
Effective management requires adequate funding, resources, and
staff. Packer et al. (2013a, pp. 638-639) found that lion densities
were highest in protected areas with the highest management budgets.
Cost estimates for maintaining lion populations in protected areas
range from an annual budget of $500 USD per km\2\ in smaller fenced
reserves to $2,000 USD per km\2\ for unfenced reserves (Packer et al.
2013, p. 640). This includes but is not limited to costs associated
with permanent and temporary staff, fencing installation and
maintenance (fences can cost $3,000 USD per km to install),
infrastructure maintenance, anti-poaching activities such as
surveillance and snare/trap removal, wildlife restocking fees (both for
lions killed by illegal poaching/snares as well as other trophy species
killed by lions on the reserves), community outreach, and compensation
for loss of livestock in surrounding communities. However, many
management areas lack adequate funding (Packer et al. 2013, p. 640;
Groom 2013, pp. 4-5; Barnett and Patterson 2005, p. 82).
Of 12 protected areas assessed in western Africa, 6 had no budget
for management activities or the budget was too low to conserve lion
populations; nine reported having either no law enforcement activity or
major deficiencies in staff and resources to conduct patrols. In
Como[eacute] National Park, the staff was found to be too small for the
size of the park (Henschel et al. 2014, p. 7). Protected areas in
Guinea are essentially parks on paper only. They have no staff,
management plan, or operating budget (Brugi[eacute]re 2012 in Henschel
et al. 2014, p. 7). Although the WAP complex has received high scores
for management effectiveness, the presence of 50,000 head of cattle
inside W National Park indicates weak management. Livestock are rare in
Arly-Pendjari, and lion density is higher; a higher management budget
allocation is suspected to be the cause of the observed differences
(Henschel et al. 2014, pp. 5-6). Across the lion's range, Africa's
protected areas have generally failed to mitigate threats to large
mammal populations, including the lion and its prey (Craigie et al.
2010, entire).
Poor management leads to many of the threats that lions face,
including encroachment by pastoralists, increased poaching pressure,
collapse of prey populations, and persecution by pastoralists
(Brugi[eacute]re et al. 2015, pp. 519-520; Henschel et al. 2015,
unpaginated; Henschel et al. 2014, pp. 5, 7; Henschel et al. 2010, p.
38). Therefore, it can be said that management of protected areas that
still harbor lions is inadequate to address the threats impacting
lions, especially those in western Africa (Henschel 2015, unpaginated).
Overall, investment in conservation activities is extremely low in
western Africa, compared to central, eastern, and southern Africa.
Countries in the former or current western Africa lion range are among
the 50 poorest countries in the world, and six are classified as least
developed countries. These countries will likely be unable to generate
the resources required to secure their remaining lion populations
(Henschel et al. 2014, pp. 7-8). Investment from the international
community is needed to increase management effectiveness of these
protected areas (Henschel et al. 2015, unpaginated).
In India, most lions occur within five designated protected areas:
Gir National Park and Gir Wildlife Sanctuary (Gir Protected Area) and
Pania, Mitiyala, and Girnar sanctuaries (Bauer et al. 2015a,
unpaginated; Banerjee and Jhala 2012, p. 1421; Singh and Gibson 2011,
p. 1754; Jhala et al. 2009, pp. 3384, 3385; Nowell and Jackson 1996, p.
38). Under India's Wild Life Protection Act of 1972 (Act No. 53 of
1972; Chapter IV, sections 27, 28, 33, 35), entry into protected areas
is regulated and certain activities are controlled and managed,
including security of wild animals and grazing of livestock. In 2012,
India's Ministry of Environment and Forests (2012, p. 22) declared the
area 5 km from the boundary of Girnar Wildlife Sanctuary an Eco-
sensitive Zone for the long-term protection and conservation of the
lion. This designation prohibits certain activities within the
designated zone, such as mining, unregulated tourism, polluting
industries, and unregulated felling of trees.
Because of the protections afforded by the Government of Gujarat,
threats that contributed to the decline of this population have been
ameliorated and most threats faced by lions are not an immediate
threat. Protections ensure food security, water availability, habitat
suitability, and safety for these lions (Meena 2014, p. 26). However,
because this population is small and isolated, it is vulnerable to
extinction from stochastic events. Although a second location has been
proposed to establish another free-ranging population geographically
separate from Gir to reduce the risk of extinction of this population,
translocation of lions from Gujarat are still pending (see Deleterious
Effects Due to Small Population Sizes).
Climate Change
Consideration of ongoing and projected climate change is a
component of our analysis under the Act. The term ``climate change''
refers to a change in the mean, variability, or seasonality of climate
variables over time periods of decades or hundreds of
[[Page 80031]]
years (Intergovernmental Panel on Climate Change (IPCC) 2013, p. 1255).
Climate change models, like all other scientific models, produce
projections that have some uncertainty because of the assumptions used,
the data available, and the specific model features. The science
supporting climate model projections as well as models assessing their
impacts on species and habitats will continue to be refined as more
information becomes available.
Temperature and Precipitation Trends
Within the past 50-100 years, the surface temperature in Africa and
Asia has increased (Hijioka et al. 2014a, p. 1333; Niang et al. 2014,
p. 1206). Across Africa, surface temperature has increased by 0.5
[deg]C over the past century (Niang et al. 2014, p. 1206), although
there are regional differences. For example, decadal warming rates in
South Africa have ranged from 0.1 [deg]C to 0.3 [deg]C (Chidumayo et
al. 2011, p. 18) and 0.23 [deg]C in Tanzania (Carr et al. 2013, p. 16).
The mean annual temperature in Burundi has increased by 0.7-0.9 [deg]C
since the 1930s, while the mean annual temperature in Uganda has
increased by 1.3 [deg]C since 1960 (Carr et al. 2013, p. 16). In India,
annual mean temperatures increased by 0.56 [deg]C during the 20th
century (Hijioka et al. 2014a, p. 133; Hijioka et al. 2014b, p. SM24-
2).
Across Africa, trends in annual precipitation indicate a small but
statistically significant decline in rainfall (Niang et al. 2014, p.
1209; Chidumayo et al. 2011, p. 20). Eastern Africa has experienced an
increase in extreme precipitation changes, with increasingly frequent
droughts followed by increasingly intense heavy rainfall, for the last
30 to 60 years; however, overall levels of precipitation have been
declining. The intense rainfall events have caused more frequent
flooding and soil erosion and degradation (Niang et al. 2014, pp. 1209,
1211; Carr et al. 2013, p.16). Attri and Tyagi (2010 in Hijioka et al.
2014b, p. SM24-3) report no significant national trends in
precipitation for India, although there has been a decrease in the
number of monsoon depressions and an increase in the number of monsoon
break days, which is consistent with an overall decrease in seasonal
mean rainfall (Hijioka et al. 2014a, p. 1333). Throughout the 20th
century, droughts were frequent in the Gir area. However, in the last
two decades average rainfall has increased due to increased western
monsoons (Singh and Gibson 2011, p. 1756).
Overall, projections indicate temperatures will continue to
increase in Africa and Asia and rainfall will continue to decrease in
Africa but increase in India, although regional variations exist
(Hijioka et al. 2014a, p. 1334; Peterson et al. 2014, p. 562; Gosling
et al. 2011, pp. 64-65). Warming in Africa is expected to be greater
than the global annual mean warming throughout the continent and all
seasons (Chidumayo et al. 2011, p. 22). Future projections expect the
average temperature in Africa to be higher by 1.5-3 [deg]C by 2050
(Niang et al. 2014, p. 1206; Carr et al. 2013, p. 16; UENP 2007, p. 2),
while temperatures in Gujarat are expected to increase between 3.0 and
3.5 [deg]C by 2100 (Gosling et al. 2011, pp. 64-65).
Annual precipitation shows greater regional variations, although
predictions of precipitation contain high levels of uncertainty.
Generally speaking, both Africa and Asia are expected to experience
harsher drought and stronger floods during the wet season (Hijioka et
al. 2014a, p. 1334; Carr et al. 2013, p. 12). Precipitation has been
projected to decline in western, central, and southern Africa. The
areas of southern Africa expected to experience a decline in
precipitation is projected to expand during the second half of the 21st
century (Niang et al. 2014, p. 1210; Hijioka et al. 2014a, p. 1333;
Carr et al. 2013, pp. 12, 14; The Heinz Center 2012, p. 13).
In contrast, eastern Africa and northern India are expected to
experience an increase in mean annual precipitation (Niang et al. 2010,
p. 1210; Hijioka et al. 2014a, p. 1334; Carr et al. 2013, pp. 12, 14;
Gosling et al. 2011, p. 65). Some General Circulation Models predict
that, by the end of the 21st century, eastern Africa will have a wetter
climate with more, intense wet seasons and less severe droughts from
October to December and March through May, a reverse in observed trends
described above. Other models suggest drying in most parts of Uganda,
Kenya, and South Sudan in August and September by the end of the 21st
century (Niang et al. 2014, p. 1210). Carr et al. (2013, p. 15) state
that levels of increased precipitation predicted for the Albertine
Rift, located mainly within the eastern African region, are not
predicted to be sufficient to counter the effects of warming
temperatures; therefore, an overall drying effect is likely to occur,
which will be more pronounced between February and May. They also state
that November and December will experience the largest increases in
precipitation.
In South Asia, including India, future declines in the number of
rainy days and increases in extreme precipitation events related to
monsoons are very likely (Hijioka et al. 2014a, p. 1334; Gosling et al.
2011, pp. 123-124). Increases in precipitation are expected by the
2030s and all regions of India are expected to experience between 10
and 30 percent increases in magnitude of pluvial flooding (flooding
derived directly from heavy rainfall and results in overland flow) and
an average across India of approximately 50 percent greater risk of
fluvial flooding (floods as a result of river flows exceeding river
channel capacity, breaking through riverbanks, and inundating the
floodplain) (Gosling et al. 2011, pp. 122, 123, 126, 130). Gosling et
al. (2011, pp. 65-66) predict increases in average annual rainfall of
up to 20 percent in Gujarat by 2100.
Impacts of Climate Change
Climate change is likely to become a main driver of change in large
mammal populations in the future (Scholte 2011, p. 7). In the mid-
Holocene, mammals responded rapidly to climate change with a series of
local extinctions and near-extinctions, driving a decrease in species
richness, and a dramatic increase in xerophytic taxa (Grayson 2000 and
Graham 1992 in Thuiller et al. 2006, p. 425). It is likely that many
species and ecosystems will endure similar impacts in response to
predicted climate change in the 21st century, which will act
synergistically with the predicted increase in anthropogenic pressures
(Fischlin et al. 2007, in Carr et al. 2013, p. 10; Thuiller et al.
2006, p. 425). For lion, impacts described above from existing and
predicted anthropogenic pressures on the species and its habitat are
likely to be exacerbated by climate change. The general warming and
drying trend projected for Africa could further reduce lion range,
numbers, and prey base. Lions may also have to travel greater distances
to find food or shift their diet to livestock, increasing conflict with
humans and the risk of retaliatory killings (Peterson et al. 2014, pp.
562-563; Tuqa et al. 2014, p. 8; Tumenta et al. 2013, p. 240).
Additionally, changes in climate may increase the number and intensity
of disease outbreaks in lions and its prey (Peterson et al. 2014, pp.
562-563; The Heinz Center 2012, p. 12; Baylis 2006, p. 4).
Peterson et al. (2014, pp. 555, 561-562) evaluated the magnitude of
potential changes in lion distribution in Africa under different
climate change scenarios between the years 2040 and 2070. They found
little optimism for the future of lions. No broad new areas will become
suitable for lion. Southern Africa, where the broadest areas of
[[Page 80032]]
suitable conditions occur, is projected to become less suitable because
of climate change. Specifically, park areas, including the ``Etosha
Pan, Lake Opnono, Cuvelai Drainage, Kalahari Gemsbok, and Kgalagadi
Transfrontier Park areas'' are projected to decline substantially in
suitability for lions. A broad swath of potential distributional area
in western Africa is projected to become ``distinctly less suitable or
even uninhabitable.'' A decrease in the lion's range could mean that
stochastic events impact a larger portion of the whole species,
especially when the species and its habitat are fragmented (Thuiller et
al. 2006, p. 434). Additionally, reductions in populations and
geographic range may limit the lion's ability to respond to climate
change (The Heinz Center 2012, p. 12). However, climate change effects
on potential lion distribution are projected to be more neutral in
eastern Africa than across the entire range. Reserves in this region
are more likely to sustain lion populations under climate change
scenarios (Peterson et al. 2014, pp. 555, 561-562).
In India, an increase in average rainfall in the past two decades
has resulted in the conversion of dry savanna to forestland (Hijioka et
al. 2014a, p. 1333; Singh and Gibson 2011, p. 1756). However, the lion
population in India has shown to be able to use both forestlands and
savannas (Singh and Gibson 2010, p. 1753). Therefore, this type of
habitat conversion due to changes in climate may not be as detrimental
to lions in India population. However, increased risks of flooding
could pose problems for lions. Following a recent flood in Gujarat,
nine lions drowned in a stream that flows alongside Gir Wildlife
Santuary. Additionally, lions could face serious threats following
flood events, such as an outbreak of a disease epidemic (The Economic
Times 2015, unpaginated). This population of lions is small, isolated,
and less genetically diverse; therefore, it is more vulnerable to
stochastic events such as disease outbreaks and flooding and more prone
to local extinction events (Banerjee and Jhala 2012, p. 1428; Meena
2010, p. 209; Johnsingh et al. 2007, p. 93).
Current lion habitat and suitable habitat predicted to remain under
climate change scenarios will be under increasing pressure due to land
conversions to meet the needs of the growing human population. As
stated earlier, and supported by Carr et al. (2013, p. 20), demand for
agricultural land is likely to increase to meet the needs of the
growing human population, putting pressure on natural landscapes.
Projected changes in Africa's climate will increase this pressure as
land becomes more arid and food security concerns are exacerbated (Carr
et al. 2013, p. 20). Impacts to the socio-economic and physical well-
being of humans will cause adaptive responses, eliciting changes in the
way much of the land is used, including further encroachment of urban
environments and agricultural land into existing natural habitats (Carr
et al. 2013, pp. 10, 19), including protected areas where lions occur.
Additionally, land conversion restructures the landscape and may
disrupt prey migrations that are induced by climate change (Thuiller et
al. 2006, p. 425), decreasing or altering prey available to the lion.
Although lions occur in a variety of temperature and precipitation
regimes, suggesting the species may be tolerant of some climatic
changes (The Heinz Center 2012, p. 13), lions appear to thrive under
specific climate parameters (Leighton-Jones 2004 in Celesia et al.
2009, p. 63) and abundance is significantly determined by temperature
and rainfall (Celesia et al. 2009, pp. 67, 68). Large felids, including
lions, occur in biomes with an average annual temperature of 13 [deg]C
or higher; lion demography is best when mean annual temperatures are
16-18 [deg]C (Celesia et al. 2009, p. 68). Lion density is influenced
by multiple natural ecological factors including herbivore biomass,
annual mean rainfall, soil nutrients, annual mean temperature, and
interactive effects between rainfall and soil nutrients (Celesia et al.
2009, pp. 67, 69). These factors explain regional variations in lion
densities, where low densities are found in desert or semi-desert
ecosystems and higher densities in moist savannas (Celesia et al. 2009,
p. 67). Lion densities decrease with increasing mean temperature and
decreasing rainfall. Therefore, lion density, or carrying capacity of
protected areas, in sub-Saharan Africa is likely to decline with
climate warming and drying (Chidumayo et al. 2011, p. 144).
Lion demography is also influenced by environmental factors. Many
variables are associated with aspects of demography, but the strongest
associations are with rainfall, temperature, and landscape features
(e.g., elevation, slope, direction of slope, and compound topographic
index) (Celesia et al. 2009, pp. 63, 68). Impacts to lion demography
have been noted with the longer dry spells occurring. For example, when
prey become scarce at the end of the dry season, subadult females may
be forced out of prides. Furthermore, older lions and cubs may die of
starvation (Celesia et al. 2009, p. 68). Additionally, Van Vuuren et
al. (2005 in Celesia et al. 2009, p. 68) found in a study of Kgalagadi
Transfrontier Park that adult and cub mortality reached 70 to 90
percent in poor years (defined as years in which average annual
rainfall in the previous 2 years was less than 165 mm). Mortality
decreased to 10 to 40 percent in good years (years in which average
annual rainfall in the previous 2 years was greater than or equal to
237 mm). These impacts on demography result in reduced numbers of lions
and pride sizes (Celesia et al. 2009, p. 68). Given the predicted
warming and drying trend for the 21st century, additional lions could
be lost and pride sizes reduced. Furthermore, loss of these lions
reduces reproductive potential and recruitment, further contributing to
the decline of existing populations. The loss of lions could also mean
the loss of genetic variation. Combined with declining populations, the
risk of inbreeding and associated complications could increase.
Drought conditions can also contribute to reduced prey availability
by altering the timing of migration (Peterson et al. 2014, p. 562). For
migratory species such as the wildebeest or zebra, an earlier and more
frequent onset of the dry season may lead to the species undertaking
more migrations, which can lead to increases in mortality and
disruption of seasonal hunting patterns of lion (The Heinz Center 2012,
p. 42). Climate change may already be having an impact on the
wildebeest as Dobson (2009, as cited in Chidumayo et al. 2011, p. 144)
found that, due to the wet season slowly getting drier and the dry
season getting wetter, the species is migrating 2 months earlier than
usual, throwing off timing of migrations and conception times that are
set by lunar cycles. If the wet season rains are diminishing there will
be a reduction in high-quality forage needed to support lactation. This
reduction has a detrimental effect not only on the survival of the calf
but also for the population as a whole (Dobson 2009, as cited in
Chidumayo et al. 2011, pp. 144-145).
Climate conditions also influence prey abundance. In Kruger Park,
South Africa, almost all ungulate species are extremely sensitive to
lack of rainfall during the dry season, which is predicted to increase
in the future. This factor may be important to retain green forage
during a period when the risk of malnutrition is higher (Thuiller et
al. 2006, p. 432). Similarly, reproduction in Cape buffalo is strongly
related to season. Changes in the timing, frequency, or intensity of
seasonal rains
[[Page 80033]]
could negatively affect reproduction. This species is also sensitive to
rainfall due to its high water consumption rate (up to 30-40 liters per
animal per day) (Du Troit 2005, as cited in The Heinz Center 2012, p.
15; Whyte et al. 1995, pp. 84-85). Variation in the buffalo population
then is tied to rainfall conditions year-to-year. Funston and Mills
(2006, p. 20) observed that the buffalo population increases only
during periods of average to above-average rainfall, which means that
climate projections for a drier Africa will have detrimental impacts on
the buffalo population. Lions are opportunistic predators that feed on
a variety of prey. This flexibility in prey may aid lions in exhibiting
some resiliency to changes in prey populations (The Heinz Center 2012,
p. 12). However, as discussed under Loss of Prey Base and Human-Lion
Conflict, the loss of prey species can result in lions shifting their
diet towards livestock which may increase retaliatory killings by
humans (Bauer and Kari 2001, as cited in Tumenta et al. 2013, p. 241;
Whyte et al. 1995, p. 85).
Variation in lion home ranges may have an impact on the frequency
of human-lion conflict especially in situations where lion home ranges
expand into areas inhabited by humans (Peterson et al. 2014, p. 562).
The interplay between the types of climate, the density of prey, and
seasonal variation in temperature and precipitation all affect lion
home range. Areas with a more arid climate and small prey density are
associated with larger home ranges, while temperate or tropical regions
with higher prey density are associated with smaller home ranges. In
addition, prey living in an arid climate tend to disperse, while prey
in a wetter climate are more concentrated, leading to a larger and
smaller home range, respectively (Tuqa et al. 2014, p. 2; Celesia et
al. 2010, pp. 63, 67; Sogbohossou 2011, p. 17; Loveridge et al. 2009,
p. 953). In southern Africa, where most of the lion populations are
enclosed (fenced), variation in the species' home range may be more
limited. Lion home ranges are also influenced by the season with ranges
being smaller during the dry season and larger during the wet season.
During the dry season, prey congregate around the few remaining water
sources, concentrating prey species in a smaller area, shrinking the
home range needed by the lion to find food. Conversely, home ranges
expand during the wet season due to prey dispersal (Tuqa et al. 2014,
p. 8).
Climate projections point toward a drier climate for western,
central, and southern Africa (Niang et al. 2014, p. 1209; Hijioka et
al. 2014a, p. 1333; Carr et al. 2013, p. 14; Chidumayo et al. 2011, p.
21). Drought in the western and central African regions is expected to
increase by a rate of 5-8 percent by 2080 (UNEP 2007, p. 2). Although
drier conditions might initially lead to the lion home range shrinking
as prey congregate around remaining water sources (Sogbohoussou 2011,
p. 133), Tuqa et al. (2014, p. 8) found that lion home ranges expand in
the time after a drought. The reason for this expansion may be that, as
prey populations around water sources are depleted, the lion has to
travel greater distances to find prey. In addition, researchers found
that lions move beyond reserve boundaries and into communal ranches
where there will be greater conflict with humans (Tuqa et al. 2014, p.
9). It is likely that lions prey on livestock, which will intensify
human-lion conflict. To compound the issue, pastoralists in sub-Saharan
Africa will often lead their herds into protected areas where lions
occur during a drought in search of water, which increases the risk of
lion predation (Tumenta et al. 2013, p. 240).
When lion prey on livestock, they primarily focus on cattle
(Patterson et al. 2004, p. 510). Out of all livestock that are
domesticated in Africa, cattle have the highest monetary value, which
means the loss of cattle to lion predation will have the most adverse
effect on pastoralists (Tumenta et al. 2013, p. 240). Additionally,
droughts affect the survival of livestock (Peterson et al. 2014, p.
562). A study of the drought that occurred in Kenya in 2008-2009 found
that mortality rates among the cattle population varied between 57 and
64 percent in six districts (Dolrenry 2013, p. 47; Zwaagstra et al.
2010, p. 21). Such high mortality may make pastoralists less tolerant
of lion predation and may increase the frequency of retaliatory
killings (Peterson et al. 2014, p. 562).
Climate change may increase the number and intensity of disease
outbreaks in lion prey species, as well as lions (The Heinz Center
2012, p. 12; Baylis 2006, p. 4). Diseases can be directly and
indirectly affected by climate change by impacting distribution, the
timing of outbreaks, and the intensity of outbreaks (Baylis 2006, p.
4). Higher temperatures may increase the rates of development of
pathogens and parasites, shorten generation times, and increase the
number of generations per year, increasing the population (Baylis 2006,
p. 8; Thuiller et al. 2006, p. 435). Temperatures can have impacts on
vectors (e.g., ticks and mosquitoes) and hosts that may further
influence the spread of diseases (Baylis 2006, pp. 9, 11) and increase
risks of extinctions (Thuiller et al. 2006, p. 435). Additionally,
rainfall conditions also affect the susceptibility of animals to
disease outbreaks (Thuiller et al. 2006, p. 435). Munson et al. (2008)
concluded that severe climate change could synchronize temporal and
spatial convergence of multiple infectious agents, triggering epidemics
with greater mortality than infections from a single pathogen.
Conservation Measures in Place To Protect Lions
There has been awareness for several years that conservation
strategies need to be implemented for the lion due to the apparent
decrease in its population numbers (Hamunyela et al. 2013, p. 1;
Henschel et al. 2010, p. 34; Gebresenbet et al. 2009, p. 5; IUCN 2006a,
b, entire). Prior to 2006, institutional inconsistencies throughout the
lion's African range resulted in poor lion conservation policies and
little to no enforcement of existing laws (IUCN 2006b, p. 18). As
mentioned, in 2005 and 2006, nongovernmental organizations (NGOs) and
several governments at various levels organized two regional lion
conservation workshops. Species specialists, wildlife managers, and
government officials attended these regional workshops in order to
provide range country governments with frameworks for developing their
own national action plans for the conservation of lions. Over 50 lion
specialists, representing all lion range countries, participated in
these workshops (Henschel et al. 2010, p. 34). During the workshops,
lion experts collectively assessed what they believed to be the then-
current status of African lions based on a variety of information, and
subsequently identified 86 African LCUs. This information was then used
as a framework to identify lion areas, strongholds, and potential
strongholds by Riggio et al. (2013, p. 32).
Many African countries with very small lion populations have
developed or updated their conservation plans for the lion. Some of
these include Benin, Cameroon, Uganda, and Malawi. Some range countries
participate in transboundary conservation projects and are
collaborating on transboundary lion conservation initiatives for shared
lion populations. Most range countries have a national lion action plan
or strategies in place, particularly if there are economic incentives
for them to have viable lion populations (Groom 2013, p. 4; Namibia
2013, pp. 11-12; Zambia Wildlife Authority 2012, p.3;
[[Page 80034]]
LionAid 2011, pp. 1-2; Mesochina et al. 2010a, pp. 40-49; Mesochina et
al. 2010b, pp. 33-38; Government of Tanzania 2010, pp. 3-17; Begg and
Begg 2010, entire). Range states have also implemented a number of
conservation strategies designed to conserve habitat, reduce human-lion
conflict, and preserve the lion's prey-base.
Conservation Measures To Stem Habitat Loss
Habitat loss represents one of the main threats facing lions in
Africa (Bauer et al. 2008, unpaginated). Attempts by range countries to
address this decline in habitat are manifested in a number of ways,
such as the creation of protected areas and the establishment of
wildlife corridors to connect fragmented habitats.
Two conservation tools used by African range countries for lions
include the establishment of protected areas and the enforcement of
protections in these areas (Mesochina et al. 2010a and b; Treves et al.
2009, pp. 60, 64). However, several problems have emerged. For example,
certain land-tenure systems do not recognize community ownership of
land and wildlife and undermine the extent to which benefits are
converted into incentives for conservation. Protected-area
``boundaries'' are not always visible. Additionally, law enforcement in
protected areas can be sporadic, and parks are often understaffed
(Pfeifer et al. 2012, pp. 1, 7). More recent evidence suggests that
some protected areas are being more commonly encroached upon as human
populations expand and search for resources.
Despite encroachment, protected areas are somewhat effective at
protecting wildlife and habitat as rates of habitat loss tend to be
lower in protected areas than outside them (Green et al. 2013, p. 70;
Pfeifer et al. 2012, p. 2). African countries are realizing the
benefits of managing their wildlife populations and parks for tourism;
however, conservation of vast areas of land for megafauna such as the
lion is not only complex, but also expensive. As an example, the 28-km
(17-mi) elephant corridor, completed in 2011 in Kenya, cost $1 million
USD (The Nature Conservancy 2013, unpaginated). Additionally, the
overall costs of anti-poaching and compensation is expected to increase
in range states concurrently with growing human populations, declining
purchasing power of external funds, and corruption (Garnett et al.
2011, pp. 1-2; Wittemyer et al. 2008, pp. 123, 125).
Another mechanism for protecting habitat is to reconnect fragmented
habitat across national boundaries. Corridors are being restored,
fences are being removed, and protected areas are being connected.
Restoration of these corridors allows wildlife to travel between areas
of suitable habitat (Jones et al. 2012, pp. 469-470). In some areas,
fences have been constructed to protect grazing resources for domestic
livestock as well as to provide barriers to disease (Gadd 2012, pp.
153, 176). One aspect of these fences is that they separate lions from
their prey. In southern Africa, fences are being taken down to increase
the size of connected habitat and link it to reserves and national
parks (IUCN 2009, p. 101; IUCN 2008, various). The Limpopo
Transfrontier Park is another example of where this practice is being
implemented (Newmark 2008, p. 327). Boundary fences along national
borders that separate many reserves are being removed to form a 35,000-
km\2\ park. Limpopo National Park (formerly known as Coutada 16) in
Mozambique, Kruger National Park in South Africa, and Gonarezhou
National Park, Manjinji Pan Sanctuary, and Malipati Safari Area in
Zimbabwe will all be connected, as will be the area between Kruger and
Gonarezhou, and the Sengwe communal land in Zimbabwe and the Makuleke
region in South Africa (Newmark 2008, p. 327). However, in some
locations, areas that have previously been designated as corridors have
been encroached upon by human settlements and agriculture (Estes et al.
2012, pp. 258-261; Jones et al. 2012, p. 469).
Tanzania is an example of a country attempting to reconnect
habitat. As of 2002, the Tanzanian Government, with donor and NGO
support, was reconnecting the nine largest blocks of forest in the East
Usambara Mountains using wildlife corridors (Newmark 2002, various).
Additionally, the 2009 Wildlife Act of Tanzania allows the Minister, in
consultation with relevant local authorities, to designate wildlife
corridors, dispersal areas, buffer zones, and migratory routes. The
2010-2015 National Elephant Management Plan of Tanzania indicates that
corridors are the primary objective of the plan, and although primarily
designed for elephants, these corridors allow for continuity of
populations of other large mammal species such as lions (Jones et al.
2012, p. 470).
In 2011, Kenya (which neighbors Tanzania to the North), completed a
28-km corridor through an area that had been heavily impacted by human-
wildlife conflict. The purpose of the corridor was primarily to reduce
human-elephant conflict and appears to have been successful (Mount
Kenya Trust 2011, p. 1). The corridor also allows other wildlife such
as lions to disperse through habitat that otherwise would have been
unfavorable for wildlife to travel through (Mount Kenya Trust 2011, p.
1). It was an expensive project, but the effort appears to have served
its purpose: Elephants are using the corridor on a regular basis
(particularly an underpass under a highway), and humans are reporting
less human-wildlife conflict (Mount Kenya Trust 2011, p. 1).
However, connectivity alone does not ensure the dispersal of
animals (Roever et al. 2013, pp. 19-21). The Tanzania Wildlife Research
Institute (TAWIRI) is an organization under Tanzania's Ministry of
Natural Resources and Tourism, and is responsible for conducting and
coordinating wildlife research activities in Tanzania. In this role,
TAWIRI has been actively involved in promoting the development of and
monitoring the use of wildlife corridors in Tanzania. Surveys conducted
in 2009 and 2010 suggest that the Nyanganje Corridor in Tanzania is no
longer being used by elephants and other wildlife. This corridor is at
a narrow passage in the Kilombero Valley and is the shortest distance
for animals to cross between the Udzungwa and Selous ecosystems.
Despite efforts in place, much of the corridor is being encroached upon
by conversion of land to rice farming and cattle grazing (Jones et al.
2012, p. 469). Because these activities often deter wildlife from
passing through, the corridor is ineffective (Jones et al. 2012, p.
469).
In the latter half of the 20th century, lions in India were on the
verge of extinction. However, conservation measures were put in place
to protect lion habitat. In 1965, Gir Wildlife Sanctuary was created
and became the first protected area in Gujarat. In 1972, the Gir Lion
Sanctuary Project began. Two-thirds of the pastoral families living in
the Sanctuary, and their livestock, were relocated outside Gir forests
(Singh and Gibson 2011, p. 1754). The area of Gir Wildlife Sanctuary
was expanded and the core area designated as Gir National Park in 1975.
Following these actions, habitat began to recover, the wild
ungulate population increased, and, subsequently, lion numbers
increased (Singh and Gibson 2011, pp. 1754, 1755). Habitat adjacent to
Gir was also declared a Sanctuary (Pania Sanctuary) in 1989. This area
and surrounding community lands were declared protected forests to
serve as a buffer area to the Gir Forests (Singh and Gibson 2011, p.
1754). As the lion population began to increase, lion
[[Page 80035]]
dispersed into satellite forest patches. These reclaimed patches of
habitat were protected and the Mitiyala Sanctuary was created in 2002,
and the Girnar Sanctuary, in 2007 (Singh and Gibson 2011, p. 1754).
After 40 years, the protected areas of India have experienced
habitat recovery, a 10-fold increase in ungulates, and an increase in
lion numbers (Singh and Gibson 2011, pp. 1754, 1756). Since 1968,
India's Forest Department has conducted wildlife censuses every 5 years
(Singh and Gibson 2011, p. 1754), documenting a steady increase in the
lion population. Community pride and love of lions, the media, and
political pressure has ensured efforts are made to protect these lions.
When problems arise, they are quickly assessed and a solution found.
For example, when 6 lions were hit and killed by trains, immediate
action was taken to rectify the problem (Meena 2014, p. 26). Because of
these actions, lions in India now number 523 (BBC 2015, unpaginated).
Conservation Measures in Place To Stem the Loss of Prey Base
Lions, like most large carnivores, prey upon a variety of species
including buffalo, plains zebra, wildebeest, giraffe, gemsbok, kob, and
warthog (Kenya Wildlife Service 2013, p. 13; Beg and Beg 2011, p. 4;
Nowell and Jackson 1996, p. 18). Depletion of these prey species due to
competition with humans represents a threat to the lion (Chardonnet et
al. 2005, pp. 8-9). As noted, the increase in the human population in
Africa is a major contributor to the increase in demand for bushmeat,
which in turn increases human encroachment into wildlife territory
(Lindsey et al. 2012b, p. 36). In addition to the increase in the human
population, lack of an alternative livelihood, lack of alternate food
sources, and lack of clear rights over land or wildlife are
contributing factors toward the increase in demand for bushmeat
(Lindsey et al. 2012b, pp. 36-41). The advent of automatic weapons in
the bushmeat trade impacts the lion's prey base, which is being hunted
at unsustainable levels.
Reconnecting fragmented habitat has the additive effects of not
only conserving the biodiversity of the lion's habitat, but also that
of its prey base (Lindsey et al. 2012b, p. 43). These types of
restoration practices enhance the health of species by allowing genetic
interchange to occur and, thus, conserve the genetic diversity of all
wildlife. Wildlife management entities are linking many of the major
protected areas by removing boundary fences along national borders that
separate many reserves in addition to creating or improving corridors
to link good-quality habitat for wildlife (Gadd 2012, p. 179; Newmark
2008, pp. 323-324).
To address the increasing consumption of bushmeat, host countries
have employed a variety of different strategies, including the
development of alternative industries for communities. Helping local
communities develop alternate industries represents one of the ways
range countries can reduce their dependence on bushmeat. Throughout
Africa, several ideas have been attempted with varying levels of
success. For example, the Anne Kent Taylor Fund (AKTF) helps local
Maasai women to buy beads and other supplies to produce traditional
items for the local tourist industry (AKTF 2012, p. 7; Lindsey et al.
2012b, p. 45; van Vliet 2011, p. 17). In addition, AKTF helps organize
local men into anti-poaching and de-snaring teams (AKTF 2012, p. 5; van
Vliet 2011, p. 17). By creating programs targeting both men and women,
AKTF creates an environment that provides communities with financial
stability as well as direct community interest in protecting local
wildlife. With 13 years assisting local communities, the AKTF
represents one of the more successful attempts to encourage locals to
shift away from relying on bushmeat.
Studies compiled by Hazzah (2013 pp. 1, 8) have shown that local
communities who live near protected areas with more lenient policies
have a more positive attitude and relationship with both the manager
and the protected area as a whole. This open approach to protected area
management reflects a trend in recent years to bring in local
communities to assist in the management of protected areas (Lindsey et
al. 2012b, p. 53). Wildlife management programs run by local
communities are defined by two goals: conserving wildlife and providing
economic aids to the community (Bandyopadhyay et al. 2010, p. 5). With
regard to discouraging the consumption of bushmeat, this new approach
is seen in the creation of community-based wildlife management programs
(van Vliet 2011, p. 26). The purpose of these programs is to give the
local community a direct stake in the management of wildlife areas. One
use for these areas is to turn them into game ranches. These areas are
used both for legal bushmeat production as well as trophy hunting and
ecotourism.
Namibia has had great success in setting up community-run
conservancies. After gaining independence in 1990, Namibia began to
turn over ownership of wildlife areas to local communities (van Vliet
2011, p. 29; Bandyopadhyay et al. 2010, p. 6). By 2011, Namibia had 64
communities that covered 17 percent of the country total area (van
Vliet 2011, p. 29; Connif 2011, unpaginated; NASCO 2011, p. 4). The
majority of the incomes from these conservancies come from ecotourism,
followed by trophy hunting (NASCO 2011, p. 22). These incomes are then
used to support infrastructure improvement in the community. In
addition, legal bushmeat acquired within conservancy lands is
distributed to local families (NASCO 2011, p. 25). The success of the
program in Namibia has been attributed to Namibia's unique
characteristics, including low population density and favorable
seasonal rain, which helps prey species recover (van Vliet 2011, p.
30). Despite the successes in Namibia, the country's unique
characteristics mean that adapting Namibia's success to other, more
densely populated countries will be difficult.
Conservation Measures to Stem Human-Lion Conflict
As the human population expands, the potential for conflict with
wildlife increases. In Africa, conflict between villagers and lions,
who prey upon livestock, represent a threat to the species (Chardonnet
et al. 2010, p. 12; Moghari 2009, p. 14; IUCN 2006a, p. 23). In
addition, habitat loss due to conversion of land increases the chance
of villagers coming into direct contact with lions (Chardonnet et al.
2010, p. 24). In an attempt to address these problems, range countries
have employed a variety of different strategies to help the lion. Such
strategies involve education, an effective conservation plan, and
interacting with the local community.
Historically, range countries seek to mitigate human-lion conflict
through controlling rather than conserving the predator population. In
countries such as Malawi, for example, the Department of Game, Fish and
Tsetse Control would shoot large carnivores that preyed upon livestock.
Because of this policy, more than 560 predators (which include lions)
were killed in the country between 1948 and 1961, (Mesochina et al.
2010b, p. 35). While this department was disbanded in 1963 and
jurisdiction shifted to the new Department of Forestry, crop and
livestock protection still remains an important part of its function.
Despite the department focusing on protecting crops and livestock, the
number of lions killed in the country has declined. Between 1977
[[Page 80036]]
and 1982, eight lions were killed, whereas six lions were killed
between 1998 and 2007 (Mesochina et al. 2010b, p. 35). While fewer
lions are being killed than in the previous decades, problems remain,
including lack of resources, lack of manpower, and corruption within
the range countries.
Current governmental management of lions in countries such as
Malawi, Tanzania, and Zambia are managed by the Problem Animal Control
units (Mesochina et al. 2010a, p. 41; Mesochina et al. 2010b, p. 36).
When lion attack incidents occur, Problem Animal Control dispatches
officials to investigate the problems. If the problem lion is located,
it is either removed or eliminated. When properly funded, this program
has helped in reducing not only conflicts between lions and humans but
also has driven down the numbers of lions killed. Between 2005 and
2009, there were 116 reported cases of lions killed, with the number of
lions killed being less than 50 per year in Tanzania (Mesochina et al.
2010a, p. 41). However, limitations of resources (including both
manpower and funds) have hampered the effectiveness of these officials
in responding to these incidents. In addition, many Problem Animal
Control interventions resulted in the death of the lion (Mesochina et
al. 2010a, p. 41; Chardonnet et al. 2009, p. 36). Even in cases of
translocation, the lions that were being transported often end up
injured or continue to pose problems to the community (Bauer et al.
2007, p. 91).
NGOs are also assisting in protecting lions. Intervention by NGOs
often takes the form of interacting with the local community
(Winterbach et al. 2010, p. 98). Lion Guardians, which operates in
Kenya and Tanzania, recruits and educates local young men to monitor
and track lion movement and warn herders of lion presence in the area,
recover lost livestock, reinforce protective fencing, and intervene to
stop lion hunting parties, thereby mitigating or preventing possible
human-lion conflict (Hazzah et al. 2014, p. 853; Lion Guardians 2013,
p. 7; Lion Guardians 2012, p. 3). From 2010 to 2013, Lion Guardians
maintained a recovery rate of lost livestock of more than 85, totaling
over $1.5 million USD; in 2014 alone, more than 20,000 livestock (93
percent) were recovered (Lion Guardians 2014, p. 7; Lion Guardians
2013, p. 6). Since 2010, 1,700 bomas have been reinforced to reduce
depredation of livestock. End-of-year sampling shows that more than 90
percent of reinforced bomas sampled did not experience further
depredation (Lion Guardians 2014, p. 7; Lion Guardians 2013, p. 6).
Additionally, 103 lion hunts were stopped or prevented between 2010 and
2014 (Lion Guardians 2014, p. 6; Lion Guardians 2013, p. 5). Lastly, in
the years of Lion Guardians operations, lion kills have decreased by 95
percent and the number of lions has steadily increased; a total of 286
lions have been documented in the Amboseli-Tsavo ecosystem (Lion
Guardians 2014, p. 6; Lion Guardians 2013, p. 5).
In addition, Lion Guardians work with tribal elders to dissuade
young men from killing lions for ceremonial purposes. Historically, the
killing of lions through ritualized lion hunts called ilmurran is
rewarded with gifting of cows and other rewards (Lion Guardians 2012,
p. 5; Goldman et al. 2010, p. 334). After introducing village elders to
the Lion Guardians program first hand, many return home to their
village and give their blessings to the project. This education led to
significant results; on August 11, 2013, two Lion Guardians stopped a
group of hunters who were planning to hunt a lion in retaliation for
the lion preying on their livestock. The local village elders fined the
potential hunters two cattle each for going on a lion hunt, marking a
gradual but significant shift in the cultural attitudes regarding the
lion (Hazzah et al. 2014, p. 858; Lion Guardians 2013, p. 20). Between
2007 and 2014, only five lions had been killed in territories where
Lion Guardians operates, in contrast to more than 100 lions killed in
adjacent areas (Lion Guardians 2013, p. 5). Furthermore, reduced lion
mortality was sustained across multiple years, resulting in the reserve
having one of the highest lion densities in Africa (Hazzah et al. 2014,
p. 857; Schuette et al. 2013, p. 149). Despite the success of this
program, retaliatory as well as ceremonial killings of lions outside
the program areas remain a threat to the species.
We found that many of the lion range states are trying to address
lion conservation through the establishment of protected areas,
wildlife management areas, wildlife corridors, and reconnecting
habitat. In some areas, creating incentives for lion conservation is
occurring through community conservation programs in range countries.
In other cases, participatory strategies have been implemented to
enhance local tolerance for large carnivores in Africa. An increasing
number of programs encourage local communities to solve problems that
arise from human-lion conflict without killing lions. However, the
effectiveness of these measures still ranges from successful to
unsuccessful, due in part to lack of resources, political will, and
infighting. It is imperative that range countries continue to recognize
and support the role that local communities play in lion conservation.
Greater support by countries to address the needs of local communities,
and thereby address the needs of lions, may be the single-most
important role these countries can play in changing the trajectory of
lion declines.
Finding
Section 4 of the Act (16 U.S.C. 1533) and implementing regulations
(50 CFR part 424) set forth procedures for adding species to, removing
species from, or reclassifying species on the Federal Lists of
Endangered and Threatened Wildlife and Plants. Under section 4(a)(1) of
the Act, a species may be determined to be an endangered species or a
threatened species based on any 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.
A species is ``endangered'' for purposes of the Act if it is in
danger of extinction throughout all or a significant portion of its
range and is ``threatened'' if it is likely to become endangered within
the foreseeable future throughout all or a significant portion of its
range. The ``foreseeable future'' is the period of time over which
events or effects reasonably can or should be anticipated, or trends
extrapolated.
As required by the Act, we conducted a review of the status of the
species and considered the five factors in assessing whether the lion
is in danger of extinction throughout all or a significant portion of
its range or likely to become endangered within the foreseeable future
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 lion. We reviewed the
petition, information available in our files, other available published
and unpublished information, and comments received from peer reviewers
and the general public.
When considering what factors might constitute threats to a
species, we must look beyond the mere exposure of the species to a
factor to evaluate whether the species may respond to the factor in a
way that causes actual impacts to the species. If there is exposure to
a factor
[[Page 80037]]
and the species responds negatively, the factor may be a threat and we
attempt to determine how significant a threat it is. The threat is
significant if it drives, or contributes to, the risk of extinction of
the species such that the species may warrant listing as endangered or
threatened as those terms are defined in the Act.
Overall, the lion population has declined and is expected to
continue to decline. Across its range, the lion is facing threats
stemming from human population growth. We find a number of factors are
currently impacting the species and will impact the species in the
future. In general, these factors include: Habitat fragmentation,
degradation, and loss (Factor A); excessive mortality due to trophy
hunting and trade in lion bone (Factor B); disease (Factor C); loss of
prey base, retaliatory killing due to human-lion conflict, deleterious
effects due to small populations, and climate change (Factor E); and
inadequate regulatory mechanisms and weak management of protected areas
(Factor D).
Overall, the lion population has decreased by 43 percent over the
last 21 years. Regional variations indicate an 8 percent increase in
southern Africa and a 55 percent increase in India; however, the
eastern region and western and central region (combined) decreased by
59 and 66 percent, respectively, in the past 21 years. Furthermore,
almost all lion populations in Africa that historically exceeded 500
individuals, the minimum number estimated to constitute a viable
population, are declining.
Human population growth has led to a substantial decrease in lion
habitat over the past 50 years. Current savanna habitat that is
suitable for lions is fragmented and totals only 25 percent of African
savanna habitat. This loss of habitat has resulted in local and
regional lion population extirpations, reduced lion densities, and a
dramatically reduced range; this decrease in habitat also partially
explains why lions are now largely limited to protected areas. Due to
good protection and management, lions in India have dispersed to
additional forested habitat outside the protected area, extending their
range. Lion habitat in Africa, however, continues to be threatened by
expansion of human settlements, despite occurring within protected
areas.
Expansion of human settlements, agriculture, and/or livestock
grazing are reported as occurring in or on the periphery of several
areas identified by Riggio et al. (2013, suppl. 1) as lion strongholds
(viable populations) and potential strongholds, and are particularly a
threat in western, central, and eastern Africa and some parts of
southern Africa. Lions are generally incompatible with humans and
human-caused habitat alteration and loss; they are the least successful
large African carnivore outside conservation areas. In order to
survive, they require larger contiguous habitats with fewer negative
human impacts than other more resilient species. Expansion of human
settlements and activities into lion habitat renders it unsuitable for
lions, primarily because human expansion results in reduced
availability of wild prey and lion mortality due to increases in human-
lion conflict. Both of these factors influence the distribution and
population viability of lions. Furthermore, fragmentation and isolation
of lion habitat and populations can also impact dispersal and genetic
viability.
Prey availability is essential to lion survival as it affects
reproduction, recruitment, and foraging behavior and, therefore, also
impacts lion movement, abundance, and population viability. Prey
abundance does not appear to be a concern for lion populations in
India. Conservation initiatives have ensured that ample prey is
available, and the pastoral communities that cohabitate with lions are
primarily vegetarian; therefore, there is no competition for food and
no demand for bushmeat. In Africa, lions are under serious threat due
to decreased prey abundance. Widespread decreases in prey species have
been driven by human population growth and unsustainable, increasingly
commercialized bushmeat hunting in and around protected areas.
Bushmeat is an important source of protein and livelihood in
Africa. The growing human population increases the demand for bushmeat,
fueling trade, urban markets, and international markets. Bushmeat sold
at elevated prices increases commercialization and the number of
hunters. These hunters, who are often poor, are enticed by the quick
income to find more efficient hunting methods, putting unprecedented
pressure on wildlife. Bushmeat contributes significantly to food
security, and is often the most important source of protein in rural
areas. It comprises between 6 percent (southern Africa) and 55 percent
(CAR) of a human's diet within the lion's African range. In western
Africa, bushmeat is a secondary source of protein, with fish being the
primary source. However, when widespread loss of jobs and income occurs
due to poor fish harvests, bushmeat becomes an important source of
income and sustenance, leading to increased presence of hunters in
protected areas and higher than average declines in wildlife.
Due to growing demand and availability of modern weapons, many
wildlife species, including the lion's prey base, have become depleted
in many areas. Hunters are increasingly focusing on protected areas
since wildlife has been depleted in non-protected areas. Bushmeat
hunting is illegal, yet weak management and inadequate law enforcement
have facilitated poaching of bushmeat in protected areas. Significant
decreases in large mammal populations, including lion prey species,
have occurred in protected areas throughout Africa. Overall, the large
mammal population has declined 59 percent. Regional differences in
herbivore population abundance were also detected. Because prey
availability is an important factor for lions, decreases in prey
densities result in decreases in lion density.
Expansion of human settlements and agricultural and pastoral
activities into protected areas not only decreases prey availability,
it increases exposure of livestock and humans to lions, thus resulting
in human-lion conflict. Most conflict occurs at protected area
boundaries where villages are established and human encroachment
occurs, which increases the chance of human-lion encounters.
Furthermore, cattle herders enter protected areas, and lions move
beyond the borders of protected areas in search of food, increasing
interactions between humans and lions and the risk of human-lion
conflict.
The most significant cause of human-lion conflict is livestock
depredation and, to a lesser extent, attacks on humans. As a result of
prey species becoming depleted in many areas, lions will seek out
livestock. Additionally, when pastoralists graze increasing numbers of
livestock in and adjacent to protected areas and cultivate land up to
and within the boundaries of protected areas, humans and livestock are
subjected to lions, and the risk of predation and the number of
livestock lost to predation increases. Conversion of rangeland to
agricultural land has blocked migratory prey routes, forcing lions to
rely more on livestock. Additionally, because most protected areas are
too small to support a lion's large home range, adjacent dispersal
areas are often used by lions in search of prey, putting them into
greater contact with livestock and humans. Conditions worsen as
livestock numbers and areas under cultivation increase, leading to
overgrazing, further habitat
[[Page 80038]]
destruction, and greater depredation rates. Attacks on humans appear to
be more frequent in southern and eastern Africa and rare in western and
central Africa.
Livestock provide an economic value to humans, particularly those
in extreme poverty. When lions have no economic value to local
communities and they kill or are perceived to kill livestock, the
economic impact to local communities can be significant. Impacts on
victims of lion attacks create resentment towards lions and lion
conservation, and a greater likelihood of retaliation. The most common
solution to lion attacks is retaliatory killing. Spearing, shooting,
trapping, and poisoning of lions occur regularly. Retaliatory killings
have been reported as a significant threat to lion populations in
protected areas of western and central Africa, Botswana, South Africa,
Cameroon, Kenya, Tanzania, and Zimbabwe. Despite close occupation of
India's lion population with human settlements, increased predation on
livestock, and some retaliatory killing of lions, human-lion conflict
and associated retaliatory killing is not a major source of lion
mortality for that population.
Every year, human-lion conflicts intensify due to habitat loss,
poor livestock management, and decreased availability of wild prey.
Because most human-lion conflict occurs at the borders of protected
areas, only those prides that occur near the borders are subjected to
human-lion conflict. However, when these lions are removed via
retaliatory killing, territorial gaps are then filled with lions that
may have occurred closer to the core of protected areas, causing these
border areas to serve as population sinks and exposing more lions to
human-lion conflict and retaliation. Retaliatory killing of lions
continues in many areas, and this practice impacts the viability of
lion populations across their range. The killing of lions due to human-
lion conflict is enough to result in the local extirpation of lion
populations.
Lions are a key species in sport hunting, or trophy hunting, which
is carried out in a number of range countries. If managed correctly,
trophy hunting can be an important management tool for conserving land
and providing financial resources for lion conservation. However,
management programs are not always sufficient to deter unsustainable
offtakes, which has resulted in declines in lion populations in many
areas. The main problem with mismanaged trophy hunting stems from
excessive harvests because of impacts associated with removal of males.
Six management weaknesses have been identified in the current
management of lion hunting. These weaknesses include: (1) A lack of
scientifically based quotas, which results in excessive harvests; (2) a
lack of enforcement in age restrictions, which leads to unsustainable
harvests, increased rates of infanticide, and population declines; (3)
hunting of female lion in Namibia, which decreases reproduction
success, thereby decreasing males available for trophy hunting; (4) the
use of fixed quotas that, which encourages hunters to be unselective in
their take of a trophy (i.e., they will kill younger, less desirable
males); (5) a lack of minimum hunt lengths or minimum lengths that are
too short to allow hunter the time needed to be more selective in their
take of trophies; and (6) general problems associated with management
of trophy hunting, including corruption, allocation of concessions, and
lack of benefits to communities and recognition of the important role
they play in conservation.
Documented declines in lion populations of Africa are a result, in
part, of mismanaged trophy hunting. Multiple researchers have
documented declines in lion populations across the range of the species
as a result of mismanaged trophy hunting. Specifically, negative
impacts to lions from excessive offtakes have been documented in Benin,
Cameroon, Tanzania, Zambia, and Zimbabwe. Additionally, the effects of
over-harvesting can extend into adjacent national parks where hunting
is prohibited.
Except in Mozambique, trophy hunting quotas are higher than the
recommended maximum harvest of 1 lion per 2,000 km\2\. Additionally,
the mean actual harvests in Burkina Faso, Zambia, Namibia, and Zimbabwe
are higher than the recommended 1 lion per 2,000 km\2\ offtake.
In the absence of reliable population estimates, age restriction on
trophy harvests can ensure sustainability. If offtake is restricted to
males older than 6 years of age, trophy hunting will likely have
minimal impact on the pride's social structure and young. By removing
only males 6 years of age or older, younger males remain in residence
long enough to rear a cohort of cubs (allowing their genes to enter the
gene pool; increasing the overall genetic diversity); recruitment of
these cubs ensures lion population growth and, therefore,
sustainability. However, harvesting males that are too young causes
male replacements, which results in increased infanticide rates and
death of the surviving male coalition. Additionally, a study found a
100 percent fatality rate for males that are prematurely forced to
disperse due to a new male takeover. A lack of mature males dispersing,
whether it's due to trophy hunting or retaliatory killing, reduces the
genetic viability of populations and may contribute to local population
extinctions.
Lion experts recommend age-based strategies be incorporated into
lion management action plans. Although the 6-year method has the
potential to reduce the rate of infanticide in lion populations subject
to trophy hunting, the issue of incorporating this strategy into each
country's conservation strategy and/or action plan, and following up
with implementation, enforcement, and transparency, has yet to be
observed in many of the lion's range countries. Lack of implementation
of age-based strategies may undermine the successful use of trophy
hunting as a sustainable conservation strategy.
Trade in lion parts and products are common in western and central
Africa. Lion populations in these regions are small and declining and,
therefore, the common use of lions in these regions for their parts and
products is likely unsustainable. Further, there seems to be a
burgeoning trade in lion bone to supplement or replace tiger bone.
There is potential that the current legal trade in lion bone will
eventually not be enough to supply demand, resulting in poaching of
lions in the future for the Asian medicinal trade.
As a result of human population expansion into lion habitat, lions
are increasingly exposed to diseases from domestic animals. Because
lions are a top predator, they are at a particularly high risk of
exposure to pathogens. Available studies do not indicate that infection
with a single disease is causing detrimental impacts to lions at the
species level, although general body condition, health, and lifespan
may be compromised and result in negative impacts at the individual or
population level. Co-infections, however, could have synergistic
effects that lead to greater impacts on lions than a single infection.
Disease appears to be a secondary factor influencing the decline of
lions when co-infections occur or when disease is combined with other
factors, including environmental changes, reduced prey density, and
inbreeding depression. Diseases weaken individuals and allow them to
succumb to other diseases or factors. Although disease does not appear
to be a major driver in the status of the lion, populations can suffer
significant losses;
[[Page 80039]]
some may recover to pre-outbreak levels, others may not. Given the
small and declining lion populations that remain, any loss of
individuals from the populations could be highly detrimental.
The viability of a lion population partly depends on the number of
prides and ability of males to disperse and interact with other prides,
which affects exchange of genetic material. Without genetic exchange,
or variation, individual fitness is reduced and species are less able
to adapt to environmental changes and stress, increasing the risk of
extinction.
Male dispersal plays an important role in determining the level of
inbreeding in lion populations. The fewer number of males present to
contribute genes to the next generation, the more inbred the population
will be. Therefore, not only does dispersal impact inbreeding, so does
the loss of male lions due to excessive trophy hunting and infanticide.
Because the number of prides and male dispersal are the most important
factors for maintaining viability, sufficient areas are needed to
support at least 50 prides, but preferably 100 prides, and allow
unrestricted male dispersal. Unfortunately, few lion populations meet
these criteria as almost all lion populations in Africa that
historically exceeded 500 individuals are declining, and few protected
areas are large enough to support viable populations. Furthermore,
research indicates that there is a general lack of gene flow in most
lion conservation units.
Lack of dispersal and genetic variation can negatively impact the
reproductive fitness of lions in these populations and local
extirpation is likely. Loss of fecundity leads to a decrease in
population size, fewer prides in a population, and increased inbreeding
which contributes to a decline in the population and increases the risk
of extinction. Additionally, lack of genetic variation can impact the
ability of lions to withstand stochastic events or limit the lion's
ability to evolve responses to climate change.
India's lion population is isolated and genetically less diverse.
Currently, there is no evidence of depressed demographic parameters.
However, intense management may interfere with natural selection by
ensuring survival of unfit lions, which facilitates the propagation of
deleterious genes in the population. Being a small, isolated population
and less genetically diverse, therefore, it is more vulnerable to the
loss of any individuals due to environmental and stochastic events, and
more prone to local extinction events. The establishment of another
geographically separated, free-ranging population would reduce the risk
of extinction. Establishment of a new population at Kuno Wildlife
Sanctuary in Madhya Pradesh State has been proposed. However, the
Government of Gujarat has refused to allow any lions from Gir to be
transferred.
As human populations continue to rise in sub-Saharan Africa, the
amount of land required to meet the expanding human population's needs
is constantly increasing. Lions are increasingly limited to protected
areas, and human population growth rates around protected areas in
Africa tend to be higher than the average rural growth rate.
Considering the majority of the human population in sub-Saharan Africa
is rural, and land supports the livelihood of most of the population,
loss and degradation of lion habitat, loss of prey base, and increased
human-lion conflict can reasonably be expected to accompany the rapid
growth in sub-Saharan Africa's human population into the foreseeable
future.
Impacts described above from existing and predicted anthropogenic
pressures on the species and its habitat are likely to be exacerbated
by climate change. The general warming and drying trend projected for
Africa could further reduce lion range, numbers, and prey base. Lions
may also have to travel greater distances to find food or shift their
diet to livestock, increasing conflict with humans and the risk of
retaliatory killings. Additionally, changes in climate may increase the
number and intensity of disease outbreaks in lions and their prey.
Under different climate change scenarios between the years 2040 and
2070, no broad new areas will become suitable for lion. Southern
Africa, where the broadest areas of suitable conditions occur, is
projected to become less suitable because of climate change. A broad
swath of potential distributional area in western Africa is projected
to become ``distinctly less suitable or even uninhabitable.'' A
decrease in the lion's range could mean that stochastic events impact a
larger portion of the whole species, especially if it occurs where the
species and its habitat occur. Additionally, reductions in populations
and geographic range may limit the lion's ability to respond to climate
change. Conversely, climate change effects on potential lion
distribution are projected to be more neutral in eastern Africa than
across the entire range. Reserves in this region are more likely to
sustain lion populations under climate change scenarios in the medium-
term.
Increases in average rainfall in the past 20 years have resulted in
the conversion of dry savanna to forestland in India; however, these
lions have used both habitats. Therefore, habitat conversion due to
climate change may not be as detrimental to lions in India. However,
increased risks of flooding could pose a problem for lions.
Additionally, lions could face threats following flood events, such as
an outbreak of disease. Because this population is small, isolated, and
less genetically diverse, it is more vulnerable to stochastic events
and more prone to local extinction events.
Current lion habitat and suitable habitat predicted to remain under
climate change scenarios will be under increasing pressure due to land
conversions to meet the needs of the growing human population.
Projected changes in Africa's climate will increase this pressure as
land becomes more arid and food security concerns are exacerbated.
Adaptive responses may result in further encroachment into natural
habitats. Land conversion will restructure the landscape, disrupt prey
migration, and decrease prey available to lion. Lion densities decrease
with increasing mean temperature and decreasing rainfall. Therefore,
lion density, or carrying capacity of protected areas, in sub-Saharan
Africa is likely to decline with climate warming and drying.
The loss of lions could also mean the loss of genetic variation.
Combined with declining populations, the risk of inbreeding and
associated complications could increase. Drought conditions can also
contribute to reduced prey availability by altering the timing of
migration. Climate conditions also influence prey abundance, and the
loss of prey species can result in lions shifting their diet towards
livestock, which may increase retaliatory killings by humans.
Diseases can be directly and indirectly affected by climate change
by impacting distribution, the timing of outbreaks, and the intensity
of outbreaks. Severe climate change could synchronize temporal and
spatial convergence of multiple infectious agents, triggering epidemics
with greater mortality than infections from a single pathogen.
National and international conservation strategies rely on
protected areas to protect natural resources from negative impacts of
human populations. The lion is largely limited to protected areas;
therefore, effective management is crucial to the survival of the
species. However, weak management of protected areas has been
documented
[[Page 80040]]
across its range, especially in western Africa where most protected
areas are experiencing severe management deficiencies.
Based on the best scientific and commercial information, we find
that several factors are negatively impacting the lion and contributing
to the risk of extinction. However, we find there is a substantial
difference in the magnitude of these threats to the risk of extinction
between the subspecies P. l. leo and P. l. melanochaita. Based on
current population estimates, projected population trends, and the
threats described herein, we find that the subspecies P. l. leo and P.
l. melanochaita qualify for different statuses under the Act.
Finding for Panthera leo leo
The range of P. l. leo includes the western and central African
regions and India. This subspecies has experienced a reduction in
range, a reduction in total number of populations, and a reduction in
number of lions. There are approximately 1,500 lions distributed among
15 populations; 14 in Africa and 1 in India. The population in western
and central Africa has declined by 66 percent since 1993. The current
population estimate for this portion of its range is approximately 915
lions. None of the lion populations in these regions meet the MVP,
although we do note that the WAP complex qualifies as a potential
stronghold where a viable population could occur if immediate
interventions are implemented. Between 1993 and 2014, the Indian
population increased by 55 percent. A census conducted in 2015
indicates the population has increased by 27 percent since 2010, with
lions now numbering 523. Although this population is found within a
protected area, its single, small population of 523 animals continues
to be highly vulnerable to disease and other stochastic events. Due to
weak management in Africa and small populations throughout its range,
this subspecies continues to face threats.
Remaining African populations are particularly threatened by
expansion of human settlements, agriculture, and/or livestock grazing.
Expansion of agriculture and livestock grazing are reported in or
around two of the larger African populations of P. l. leo, WAP Complex
and a Chad-CAR population; management in portions of both protected
areas is reported as weak, raising concern for the persistence of lions
and their habitat. Expansion of human settlements and activities into
lion habitat renders it unsuitable for lions, primarily because human
expansion results in reduced availability of wild prey and lion
mortality due to increases in human-lion conflict. Both of these
factors influence the distribution and population viability of lions.
Significant decreases in prey abundance have occurred in protected
areas throughout Africa. In western Africa, specifically, herbivore
populations have decreased by 85 percent. As a result of prey species
becoming depleted in many areas, lions seek out livestock for food;
attacks on livestock occur at the highest frequency in areas where
natural prey abundance is lowest. Traditional livestock husbandry
practices can reduce depredation rates, but these traditional practices
are being replaced with less diligent practices. For example, in the
Pendjari area of Benin, traditional enclosures are low with few
branches. These structures and the lack of enclosures encourage
livestock predation. People do not invest much into improving
enclosures even though they appear to be economically efficient,
ecologically effective, and culturally acceptable. Even enclosures that
were built as part of a conservation project were not used full time
due to lack of labor and, in some cases, the herd being too large for
the enclosures. When lions in Africa cause or are perceived to cause
damage to livestock, property, or people, the response is generally to
kill them. Retaliatory killings are reported to be a significant threat
to lion populations in western and central Africa.
Some countries in the African range of this subspecies allow
hunting of P. l. leo. Management programs do not appear to be
sufficient to deter unsustainable offtakes, which has resulted in
declines in lion populations in many areas. Specifically, negative
impacts to lions from excessive offtakes have been documented in Benin
and Cameroon. Additionally, hunting quotas in Benin and Burkina Faso
are too high for sustainability, although Burkina Faso has proposed to
reduce their quota in the 2015-2016 season. Actual harvests in Burkina
Faso were also found to be higher than recommended levels. Although
experts recommend age-based strategies be incorporated into lion
management plans to reduce excessive harvests and reduce the rate of
infanticide, Benin and Burkina Faso have yet to implement an age-based
strategy. As a result, species experts agree that there is no level of
offtake that would be sustainable for P. l. leo populations in their
current condition.
Trade in lion parts and products is very common in western and
central Africa. Many African countries, including Nigeria, Burkina
Faso, and Cameroon, maintain local markets in lion products. Trade in
lion skins and partial skins is described as ``frequent'' in street
markets in Abidjan, C[ocirc]te d'Ivoire, and the scale of domestic
trade in illegal lion products is described as ``massive'' in Nigeria.
In the central African country of Cameroon, the estimated value of a
single lion carcass exceeds the trophy fee, and at a lion conservation
conference, the Government of Cameroon identified trade in lion skins
as a major cause of the decline in lion populations in western and
central Africa. Trade in lion skins is most likely one of the biggest
threats to lion survival in western Africa due to the rarity of lions
in the region, the extent of the trade, and the high price of lion
skins. Lion populations in western and central Africa are small and
declining and, therefore, the common use of lions in these regions for
their parts and products is likely unsustainable.
The viability of a lion population partly depends on the number of
prides and the ability of males to disperse and interact with other
prides, which affects exchange of genetic material. Without genetic
exchange, or variation, the more inbred the population will be,
individual fitness is reduced, reproductive fitness is reduced, and
species are less able to adapt to environmental changes and stress or
stochastic events. Loss of fecundity leads to a decrease in population
size, fewer prides in a population, and increased inbreeding which
contributes to a decline in the population and may result in local
extirpation. The entire P. l. leo subspecies comprises small, isolated
populations. Research indicates that there is a general lack of gene
flow in most lion conservation units. Furthermore, the suggested
minimum number of lions estimated to constitute a viable population is
at least 250 lions, but preferably 500 lions, or 50-100 prides. This
threshold may be smaller for P. l. leo as pride sizes are generally
smaller than those for P. l. melanochaita. However, given the size of
the remaining populations, few could be considered potentially viable.
Additionally, few protected areas are large enough to support viable
populations.
Although there are laws meant to protect wildlife, including lions
and their prey species, the drastic and continuing decline of the
species and its prey indicate these regulatory mechanisms are not
adequate to ameliorate threats to P. l. leo. Furthermore, national and
international conservation strategies rely on protected
[[Page 80041]]
areas to protect natural resources from negative impacts of human
populations. However, weak management of protected areas has been
documented across the lion's range, especially in western Africa where
most protected areas are experiencing severe management deficiencies,
including the lack of a budget or a budget insufficient to carry out
management activities.
The lion population in India is one population of P. l. leo that is
increasing and could potentially be considered a viable population
based on the number of lions. However, intense management, including
healthcare interventions, may interfere with natural selection
processes by ensuring the survival of unfit lions, which facilitates
the propagation of deleterious genes in the population. This population
is also running out of area to expand. Being a small, isolated
population and less genetically diverse, it is more vulnerable to the
loss of any individuals due to environmental and stochastic events, and
more prone to local extinction events.
As previously stated, threats to the lion are expected to continue
or increase in conjunction with predicted human population growth. The
human population, and thus negative impacts to lions, as well as
decreases in lion populations, associated with human population growth,
is expected to increase substantially by 2050. If regional trends
continue at their current rate, western and central Africa will likely
lose a third of its population in 5 years and half the population in 10
years. Lion bone may be increasingly used as a replacement for tiger
bone in traditional Asian medicine and in Asian luxury products.
Therefore, trade in lion bone could become lucrative, spur considerable
demand from suppliers of the black market, result in extensive poaching
of wild lions, and have significant impacts to lion populations.
Additionally, future development in India could alter habitat vital for
dispersal. Tolerance to loss of livestock may also wane as traditional
beliefs and traditional value systems are rapidly changing under the
influence of globalization. Furthermore, effects of climate change on
lion habitat are projected to manifest as early as 2040. Under climate
change scenarios, a broad swath of potential distributional area in
western Africa is projected to become distinctly less suitable or even
uninhabitable. Increases in rainfall predicted for India may not have
detrimental impacts on lion habitat; however, increased risks of
flooding could result in increased mortality, and post-flooding
conditions could be conducive to disease outbreaks and are a serious
concern to the persistence of the lion population as this population is
more vulnerable to stochastic events and local extinction.
Threats acting on P. l. leo have contributed to large reductions in
the subspecies' range and suitable habitat, abundance, and number and
connectivity of populations. The subspecies has reached critically low
numbers of individuals and potentially viable populations. Furthermore,
while one small population may be increasing, we are not aware of any
information indicating that the overall trend of large declines in the
subspecies range, abundance, and connectivity, will reverse course.
Threats continue to act on this subspecies. Due to small population
size and lack of connectivity between populations, most populations are
not able to recover from the loss of suitable habitat or individuals.
Furthermore, because all populations are small and isolated, the
subspecies lacks resiliency to recover from stochastic or catastrophic
events and is thus highly vulnerable to extirpation. Threats are
currently affecting the subspecies and the impacts on the subspecies
are expected to continue or even intensify over time as the human
population increases and as climate change progresses, negatively
impacting availability of suitable habitat, lion distribution, and lion
numbers. Based on the current distribution and size of P. l. leo
populations, the current threats acting on this subspecies, the impacts
of those threats, and the impacts of future threats and climate change
on lion distribution, lion numbers, habitat, prey availability,
susceptibility to disease, loss of lions via human-lion conflict and
trophy hunting, and resiliency to stochastic and catastrophic events,
we find that the viability of this subspecies is compromised and will
not be resistant or resilient to ongoing and future threats. Therefore,
we find that P. l. leo is in danger of extinction throughout its range
and list the subspecies as endangered.
Finding for Panthera leo melanochaita
The range of P. l. melanochaita includes the southern and eastern
African regions. Although this subspecies has experienced range
reduction, a decline in the number of populations, and a decline in the
number of lions, it remains relatively widespread. Currently, there are
approximately 17,730 P. l. melanochaita lions distributed among 68
protected areas, with larger populations in Botswana, Kenya, Namibia,
South Africa, Tanzania, Zambia, and Zimbabwe. Between 1993 and 2014,
the lion population in eastern Africa declined by 59 percent. In
southern Africa the lion population increased by 8 percent during the
same time period. Most of the increasing populations contributing to
this trend are small, fenced reserves. However, one of the largest
populations in southern Africa, Okavango, and populations in 6 unfenced
reserves in Botswana, Namibia, and Zimbabwe declined. Although there
are larger populations of P. l. melanochaita that may meet the
suggested MVP, almost all lion populations in Africa that historically
exceeded 500 individuals, are declining.
Expansion of human settlements, agriculture, and/or livestock
grazing is occurring in or on the major populations and is particularly
a threat in eastern Africa and some parts of southern Africa. In
particular, expansion of agriculture and livestock grazing is occurring
in or around major populations in Kenya, Tanzania, and Zambia and both
are major threats to lion survival in these countries. Expansion of
human settlements and activities into lion habitat renders it
unsuitable for lions, primarily because human expansion results in
reduced availability of wild prey and lion mortality due to increases
in human-lion conflict. Both of these factors influence the
distribution and population viability of lions. However, in some parts
of southern Africa, lions are repopulating areas where lions were
recently extirpated due to adequate protection of habitat and prey.
Significant decreases in prey abundance have occurred in protected
areas throughout Africa, including Botswana, Kenya, Mozambique, Sudan,
Zambia, and Zimbabwe. Herbivore populations have decreased by 52
percent in eastern Africa, although they have increased by 24 percent
in southern Africa. Protected areas in Ethiopia, Mozambique, Tanzania,
and Zambia are increasingly settled; decreases in prey abundance in
African protected areas are driven by human population growth,
especially along the boundaries of protected areas where human
population growth rates are high, encroachment and habitat loss occurs,
and people are dependent on bushmeat. Additionally, many communities
lack the rights over land and in most cases in Botswana, Tanzania,
Zambia, and Zimbabwe, the government retains a significant portion of
revenue from wildlife; therefore, those that bear the costs of wildlife
do not receive benefits, and bushmeat hunting is the only way to
benefit from
[[Page 80042]]
wildlife. Furthermore, conversion of rangeland to agricultural use has
blocked several migratory routes for Tanzania's wildebeest and zebra
populations, which likely forces lions to rely more on livestock.
As a result of prey species becoming depleted in many areas, lions
seek out livestock for food; attacks on livestock occur at the highest
frequency in areas where natural prey abundance is lowest.
Additionally, traditional livestock husbandry practices can reduce
depredation rates, but these traditional practices are being replaced
with less diligent practices. In Kenya and Tanzania, social changes are
altering traditional Maasai pastoral livelihoods, reducing dependency
on livestock, and reducing traditional livestock care and management,
leaving livestock more vulnerable to predation. Although lions
generally avoid people, they will occasionally prey on humans, causing
serious injury or death. Attacks on humans appear to be more frequent
in the range of P. l. melanochaita than P. l. leo. When lions cause or
are perceived to cause damage to livestock, property, or people, the
response is generally to kill them. Retaliatory killings are reported
to be a significant threat to lion populations in Botswana, South
Africa, Kenya, Tanzania, and Zimbabwe.
Some P. l. melanochaita range countries allow hunting of lions.
Although some management programs appear to follow recommended
practices for sustainability, most do not appear to be sufficient to
deter unsustainable offtakes, which has resulted in declines in lion
populations in many areas. Specifically, negative impacts to lions from
excessive offtakes have been documented in Tanzania, Zambia, and
Zimbabwe. Additionally, hunting quotas in most countries are higher
than the recommended offtake for sustainability. Actual harvests in
Namibia, Zambia, and Zimbabwe were also found to be higher than
recommended levels. Experts recommend age-based strategies be
incorporated into lion management plans to reduce excessive harvests
and reduce the rate of infanticide and several countries, including
Mozambique (only Niassa National Reserve), Tanzania, and Zimbabwe have
committed to implementing an age-based strategy. Of these, only Niassa
National Reserve and Zimbabwe have fully implemented age restrictions
and shown reductions in offtake. Tanzania has implemented age
restrictions and shown reductions in offtake; however, transparency (in
terms of trophy quality data) and the scientific objectivity of the
evaluating body has been questioned. Lack of implementation of age-
based strategies may undermine the successful use of trophy hunting as
a sustainable conservation strategy.
The captive-breeding industry has publicized captive breeding and
reintroduction of captive-born species into the wild as a potential
solution to the decrease in wild lion populations. However, lions
raised in captivity often develop a variety of issues that make them
unsuitable for reintroduction, and reintroduction efforts have not been
shown to address the underlying causes of population declines
throughout the species' range. Existing research has generally found
that captive-raised lions are not as able to adapt successfully to
conditions out of captivity and, therefore, the success rate is much
reduced compared to the use of wild-caught lions.
While it is argued that South Africa's captive-bred lion industry
may reduce pressures of trophy hunting on wild South African
populations, there is no substantial or peer-reviewed science to
support such a claim. Likewise, there is no record or evidence to
support claims that the captive-bred lion industry is supporting
reintroduction into the wild in any significant way. However, future
efforts to control hunting of captive-bred lions could potentially
increase the demand for wild lion trophies and result in excessive
harvests. Additionally, trade in bones of captive lions could stimulate
harvest of wild lions to supply a growing bone trade. Hunting of
captive lions could also potentially undermine the price of wild hunts
and reduce incentives for conservation of wild lions in other African
countries.
Lion parts and products are used in many African countries as
medicine, nutrition, talismans, and decorations, and in traditional
ceremonies and rituals. Kenya and Somalia maintain local markets in
lion products. Lion skins and canines are also described as ``easily
found'' in the markets of Dakar, Senegal. In southern and eastern
Africa, trade in lion parts, particularly lion bone, to Asia is
generally considered a severe potential threat to the species.
According to CITES, there is ``clear scope for the international trade
in lion body parts for [traditional Chinese medicine and traditional
African medicine] to grow uncontrollably, as it has done for other big
cats.'' According to Kenya, the declared exports of bones, skulls, and
skeletons derived from wild lions also show an increasing trend through
the period 2003-2012, with total declared specimens in 2012 more than
ten times those in 2003. Evidence suggests incentive to poach wild
lions for the bone trade may currently exist as prices paid to South
African game farmers and landowners for lion bones exceeded the per
capita GDP (gross domestic product) in many lion range states. Thus,
the current price paid for lion bone appears to provide incentive in
some countries to poach wild lions.
The viability of a lion population partly depends on the number of
prides and ability of males to disperse and interact with other prides,
which affects the exchange of genetic material. Without genetic
exchange, or variation, the more inbred the population will be,
individual fitness is reduced, reproductive fitness is reduced, and
species are less able to adapt to environmental changes and stress or
stochastic events. Loss of fecundity leads to a decrease in population
size, fewer prides in a population, and increased inbreeding, which
contributes to a decline in the population and local extirpation.
Research indicates that there is a general lack of gene flow in most
lion conservation units. Furthermore, the suggested minimum number of
lions estimated to constitute a viable population is at least 250
lions, but preferably 500 lions, or 50-100 prides. Almost all lion
populations in Africa that historically exceeded 500 individuals are
declining, and few protected areas are large enough to support viable
populations.
While the lion bone trade appears to currently be based primarily
in South Africa's captive-bred lion hunting industry, the trade appears
to be having little or no impact on wild lion populations in South
Africa at this time--lion populations in South Africa are stable or
increasing and there is little poaching of wild lions in the country
(Funston and Levendal 2014, pp. 1, 26; Williams et al. 2015, pp. 79-
80). However, the impact of the lion bone trade on lion populations
outside South Africa is unknown and most wild lions occur outside South
Africa (see Distribution and Abundance). While wild tiger populations
are declining, the demand for tiger parts in Asia is increasing. With
tigers difficult to obtain, lion bone may be increasingly used as a
replacement for tiger bone. Considering the sharp and continuing
increases in demand from Asia for lion bone and the effect of the tiger
bone trade on tiger populations, there is potential for demand to
surpass the availability of legally obtained lion bone. Therefore,
trade in lion bone could become lucrative, spur considerable demand
from suppliers of the black market, result in extensive poaching and
unsustainable harvest of
[[Page 80043]]
wild lions to meet demand, and have significant impacts to lion
populations.
Although there are laws in place in lion range countries that are
meant to protect wildlife, including lions and their prey species, the
drastic and continuing decline of the species and its prey in some
parts of its range indicate these regulatory mechanisms are not
adequate to ameliorate threats to the P. l. melanochaita throughout its
range. Furthermore, national and international conservation strategies
rely on protected areas to protect natural resources from negative
impacts of human populations. However, weak management of protected
areas has been documented across the lion's range.
As indicated above, P. l. melanochaita remains relatively
widespread and some remaining populations are large enough to be
considered viable. Therefore, due to the size of some populations, the
number of remaining populations, and the stability or increasing status
of some populations, we find that P. l. melanochaita is not currently
in danger of extinction. However, the overall population of the
subspecies continues to decline and threats to the lion are expected to
continue or increase in the future in conjunction with predicted human
population growth. If regional trends in lion populations continue at
the current rate, eastern Africa will lose a third of its lion
population in 20 years and half the population in 30 years. Effects of
climate change on lion habitat are projected to manifest as early as
2040. Although climate change effects on potential lion distribution
are projected to be more neutral in eastern Africa than across the
entire range, southern Africa, where the broadest areas of suitable
conditions occur, is projected to become less suitable because of
climate change. Specifically, park areas, including the ``Etosha Pan,
Lake Opnono, Cuvelai Drainage, Kalahari Gemsbok, and Kgalagadi
Transfrontier Park areas'' are projected to decline substantially in
suitability for lions. In addition, reforms to trophy hunting have been
made to ensure sustainability of trophy hunting, but these reforms have
been implemented in only a few places. Furthermore, demand for lion
bone is expected to increase in the future and high prices for lion
bone provide incentive to poach wild lions. As a result of the likely
impacts of these threats, it is reasonable to conclude that the
population of P. l. melanochaita is likely to be drastically reduced
and fragmented in the foreseeable future, limiting the ability of the
subspecies to recover from stochastic and catastrophic events.
Therefore, we find that this subspecies is likely to become an
endangered species within the foreseeable future and we are listing P.
l. melanochaita as a threatened species.
Significant Portion of Its Range
Under the Act and our implementing regulations, a species may
warrant listing if it is endangered or threatened throughout all or a
significant portion of its range. The term ``species'' includes ``any
subspecies of fish or wildlife or plants, and any distinct population
segment [DPS] of any species of vertebrate fish or wildlife which
interbreeds when mature.'' We published a final policy interpreting the
phrase ``Significant Portion of its Range'' (SPR) (79 FR 37578, July 1,
2014). The final policy states that (1) if a species is found to be
endangered or threatened throughout a significant portion of its range,
the entire species is listed as endangered or threatened, respectively,
and the Act's protections apply to all individuals of the species
wherever found; (2) a portion of the range of a species is
``significant'' if the species is not currently endangered or
threatened throughout all of its range, but the portion's contribution
to the viability of the species is so important that, without the
members in that portion, the species would be in danger of extinction,
or likely to become so in the foreseeable future, throughout all of its
range; (3) the range of a species is considered to be the general
geographical area within which that species can be found at the time
the Service or the National Marine Fisheries Service makes any
particular status determination; and (4) if a vertebrate species is
endangered or threatened throughout an SPR, and the population in that
significant portion is a valid DPS, we will list the DPS rather than
the entire taxonomic species or subspecies.
We found the lion subspecies P. l. leo to be in danger of
extinction throughout its range, and the subspecies P. l. melanochaita
likely to become endangered within the foreseeable future throughout
its range. Therefore, no portions of the species' range are
``significant'' as defined in our SPR policy, and no additional SPR
analysis is required.
4(d) Rule for Panthera leo melanochaita
The purposes of the ESA are to provide a means whereby the
ecosystems upon which endangered species and threatened species depend
may be conserved, to provide a program for the conservation of such
endangered species and threatened species, and to take such steps as
may be appropriate to achieve the purposes of the treaties and
conventions set forth in the ESA. When a species is listed as
endangered, certain actions are prohibited under section 9 of the ESA
and are implemented through our regulations in 50 CFR 17.21. These
include, among others, prohibitions on take within the United States,
within the territorial seas of the United States, or upon the high
seas; import; export; and shipment in interstate or foreign commerce in
the course of a commercial activity. Exceptions to the prohibitions for
endangered species may be granted in accordance with section 10 of the
ESA and our regulations at 50 CFR 17.22.
The ESA does not specify particular prohibitions and exceptions to
those prohibitions for threatened species. Instead, under section 4(d)
of the ESA, the Secretary, as well as the Secretary of Commerce
depending on the species, was given the discretion to issue such
regulations as deemed necessary and advisable to provide for the
conservation of such species. The Secretary also has the discretion to
prohibit by regulation with respect to any threatened species any act
prohibited under section 9(a)(1) of the ESA. Exercising this
discretion, the Service has developed general prohibitions in the ESA
regulations (50 CFR 17.31) and exceptions to those prohibitions (50 CFR
17.32) that apply to most threatened species. Under 50 CFR 17.32,
permits may be issued to allow persons to engage in otherwise
prohibited acts for certain purposes.
Under section 4(d) of the ESA, the Secretary, who has delegated
this authority to the Service, may also develop specific prohibitions
and exceptions tailored to the particular conservation needs of a
threatened species. In such cases, the Service issues a 4(d) rule that
may include some or all of the prohibitions and authorizations set out
in 50 CFR 17.31 and 17.32, but which also may be more or less
restrictive than the general provisions at 50 CFR 17.31 and 17.32. For
P. l. melanochaita, the Service has determined that a 4(d) rule is
necessary and advisable.
We are adding a 4(d) (special) rule for P. l. melanochaita at 50
CFR 17.40(r). This 4(d) rule maintains all of the prohibitions and
exceptions codified in 50 CFR 17.31 and 17.32 with regard to this
subspecies and supersedes the import exemption found in 50 CFR 17.8 for
threatened wildlife listed in Appendix II of CITES, such that a
threatened species import permit under 50 CFR 17.32 is now required for
the importation of all P. l. melanochaita specimens. Therefore, through
the promulgation of this 4(d) rule, the
[[Page 80044]]
presumption of legality provided under section 9(c)(2) of the Act for
the otherwise lawful importation of wildlife listed in Appendix II of
CITES that is not an endangered species listed pursuant to section 4 of
the Act does not apply to this subspecies. Thus, under this 4(d) rule,
all otherwise prohibited activities, including all imports of P. l.
melanochaita specimens, require prior authorization or permits under
the Act. Under our regulations at 50 CFR 17.32, permits or
authorization to carry out an otherwise prohibited activity could be
issued for scientific purposes, the enhancement of propagation or
survival of the species, economic hardship, zoological exhibitions,
educational purposes, or special purposes consistent with the purposes
of the Act. Applications for these activities are available from either
https://www.fws.gov/forms/3-200-20.pdf or https://www.fws.gov/forms/3-200-37.pdf.
The intent of this 4(d) rule is to provide for the conservation of
P. l. melanochaita consistent with the purposes of the Act. Under this
4(d) rule, the prohibitions, 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 or foreign commerce, by any means whatsoever, in the course
of commercial activity; or sell or offer for sale in interstate or
foreign commerce any P. l. melanochaita specimens. It would also be
illegal to possess, sell, deliver, carry, transport, or ship any such
wildlife that has been taken in violation of the Act. We find that
these protections, including the requirement for a permit for the
import, export, interstate and foreign commerce and take for all P. l.
melanochaita specimens, will support and encourage conservation actions
for P. l. melanochaita and require that permitted activities involving
this subspecies are carried out in a manner that is consistent with the
purposes of the Act and our implementing regulations.
In connection with this 4(d) rule, the Service notes that P. l.
melanochaita is listed in Appendix II of CITES and, without this 4(d)
rule, could be imported into the United States pursuant to section
9(c)(2) of the Act upon the presentation of a proper CITES export
permit from the country of export, if such importation is not made in
the course of a commercial activity. Section 9(c)(2) of the Act
provides that the otherwise lawful importation of wildlife that is not
an endangered species listed pursuant to section 4 of the Act, but that
is listed in Appendix II of CITES, shall be presumed to be in
compliance with provisions of the Act and implementing regulations if
the importation is not made in the course of a commercial activity.
While there has been question as to whether this provision of the Act
might automatically require allowing the importation of a species that
is both listed as threatened and in Appendix II, and preclude the
issuance of more restrictive 4(d) rules covering importation, the
Service has concluded that such 4(d) rules may be issued to provide for
the conservation of the involved species. Section 9(c)(2) does not
expressly refer to threatened species or prevent the issuance of
appropriate 4(d) rules and could not logically have been intended to
allow the addition of a species to an appendix of an international
convention to override the needs of U.S. law, where there is reliable
evidence to affect the presumption of validity. Finally, the term
``presumed'' implies that the established presumption is rebuttable
under certain circumstances, including through the promulgation of a
protective regulation pursuant to section 4(d) of the Act.
In the case of the P. l. melanochaita, there are substantive
grounds on which to challenge the presumption. For the import of sport-
hunted trophies, while there is evidence that some range countries are
implementing lion management programs, the best available information
indicates that not all lion hunting programs are well managed or
provide enhancement to survival of the subspecies (see Trophy Hunting
section), Namely, mismanaged trophy hunting is reported to contribute
to documented declines in lion populations of Africa (Rosenblatt et al.
2014, entire; Sogbohossou et al. 2014, entire; Becker et al. 2013,
entire; Lindsey et al. 2013a, entire; Packer et al. 2013, p. 636; Croes
et al. 2011, entire; Packer et al. 2011, entire; Loveridge et al. 2007,
entire). Depending on how trophy hunting is regulated and managed,
trophy hunting can be a tool for conservation, but may also have
negative impacts on lions (Bauer et al. 2015a, unpaginated; Lindsey et
al. 2013a, p. 1; Whitman et al. 2004, pp. 176-177; Loveridge et al.
2007, p. 548). We want to encourage and support efforts by range
countries to develop programs that are based on sound scientific
information. As noted, the 4(d) rule for P. l. melanochaita would
provide for the importation into the United States of trophies taken
legally in range countries upon the issuance of a threatened species
import permit. While the Service cannot control hunting of foreign
species such as P. l. melanochaita, we can regulate their importation
and thereby require that U.S. imports of sport-hunted P. l.
melanochaita trophy specimens are obtained in a manner that is
consistent with the purposes of the Act and the conservation of the
subspecies in the wild, by allowing importation from range countries
that have scientifically sound management programs that address the
threats that are facing lions and are enhancing the survival of the
species in the wild within that country (see further discussion below
on enhancement of propagation or survival with regard to authorizing
the import of sport-hunted trophies of P. l. melanochaita). Further,
for the import of parts or products, there is evidence that trade in
lion parts, particularly bones, is fast becoming a substitute for tiger
bones in traditional Asian medicine and Asian luxury products (see
Traditional Use of Lion Parts and Products section). While the primary
source of the current bone trade appears to be from captive-bred lions
from South Africa, considering the sharp and continuing increases in
demand from Asia for lion bone, there is potential for demand to
surpass the availability of legally obtained lion bone and,
consequently, result in poaching and unsustainable harvest of wild
lions to meet demand. Based on the effect of the tiger bone trade on
tiger populations, if current conditions continue unchanged, there is
considerable potential for extensive poaching of wild lions to occur in
order to meet demand. Given the current threats to the subspecies,
unsustainable harvest to supply a trade in parts could contribute to
the further decline of the subspecies.
Finally, due to our concerns about the increasing trade in lion
bones and evidence that live lions are being exported to Asia,
presumably for the bone trade, we find that unregulated trade and the
taking of live lions could further contribute to the lion bone trade.
Further, the noncommercial imports of live lions could be a cover for
the establishment of lion bone trade within the United States. As with
captive tigers and the use of live animals for the bone trade, the
Service finds that the unregulated movement of lions within the United
States, as well as the import or export of these animals is reasonably
likely to be used as a loophole for the bone trade and serve as cover
for the establishment of lion bone trade within the United States. By
requiring permits for all otherwise prohibited activities
[[Page 80045]]
under the Act, such as import, export, interstate and foreign commerce
and take, including noncommercial imports of live lions, we can ensure
that live lions are not used to supplement the trade in lion bones.
Therefore, we find that regulation of the importation of all P. l.
melanochaita parts and products, including live animals and sport-
hunted trophies, will ensure that imported specimens are obtained in a
manner that is consistent with the purposes of the Act and the
conservation of the subspecies in the wild.
Our threatened species permitting regulations at 50 CFR 17.32
provide issuance criteria for threatened species permits (50 CFR
17.32(a)(2)), but do not specify what would constitute the enhancement
of propagation or survival with regard to authorizing the import of
parts or products of P. l. melanochaita, including sport-hunted
trophies. Therefore, when making a determination of whether an
otherwise prohibited activity enhances the propagation or survival of
P. l. melanochaita, the Service will examine the overall conservation
and management of the subspecies in the country where the specimen
originated and whether that management of the subspecies addresses the
threats to the subspecies (i.e., that it is based on sound scientific
principles and that the management program is actively addressing the
current and longer term threats to the subspecies). In that review, we
will evaluate whether the import contributes to the overall
conservation of the species by considering whether the biological,
social, and economic aspects of a program from which the specimen was
obtained provide a net benefit to the subspecies and its ecosystem.
The Service will evaluate any application received that involves P.
l. melanochaita in the context of enhancement of propagation or
survival permitting in accordance with our threatened species
permitting regulations at 50 CFR 17.32 and issuance criteria for
threatened species permits (50 CFR 17.32(a)(2)). These include, in
addition to the general permitting criteria in 50 CFR 13.21(b):
(i) Whether the purpose for which the permit is required is
adequate to justify removing from the wild or otherwise changing the
status of the wildlife sought to be covered by the permit;
(ii) The probable direct and indirect effect that issuing the
permit would have on the wild populations of the wildlife sought to
be covered by the permit;
(iii) Whether the permit, if issued, would in any way, directly
or indirectly, conflict with any known program intended to enhance
the survival probabilities of the population from which the wildlife
sought to be covered by the permit was or would be removed;
(iv) Whether the purpose for which the permit is required would
be likely to reduce the threat of extinction facing the species of
wildlife sought to be covered by the permit;
(v) The opinions or views of scientists or other persons or
organizations having expertise concerning the wildlife or other
matters germane to the application; and
(vi) Whether the expertise, facilities, or other resources
available to the applicant appear adequate to successfully
accomplish the objectives stated in the application.
In addition to these factors, particularly in relation to sport
hunting, we find the IUCN Species Survival Commission (SSC) Guiding
Principles on Trophy Hunting as a Tool for Creating Conservation
Incentives, Ver. 1.0 (IUCN SSC 2012), to provide useful principles,
which, considered in conjunction with our threatened species issuance
criteria, will aid the Service when making an enhancement finding for
importation of sport-hunted trophies of P. l. melanochaita. This
document sets out guidance from experts in the field on the use of
trophy hunting as a tool for ``creating incentives for the conservation
of species and their habitats and for the equitable sharing of the
benefits of use of natural resources'' (IUCN SSC 2012, p. 2) and
recognizes that recreational hunting, particularly trophy hunting, can
contribute to biodiversity conservation and more specifically, the
conservation of the hunted species.
The SSC document lays out five guiding principles that, considered
in conjunction with our threatened species issuance criteria, will aid
the Service when making an enhancement finding for importation of
sport-hunted trophies of P. l. melanochaita:
(a) Biological sustainability: The hunting program cannot
contribute to the long-term decline of the hunted species. It should
not alter natural selection and ecological function of the hunted
species or any other species that share the habitat. The program
should not inadvertently facilitate poaching or illegal trade in
wildlife by acting as a cover for such illegal activities. The
hunting program should also not manipulate the ecosystem or its
component elements in a way that alters the native biodiversity.
(b) Net Conservation Benefit: The biologically sustainable
hunting program should be based on laws, regulations, and
scientifically based quotas, established with local input, that are
transparent and periodically reviewed. The program should produce
income, employment, and other benefits to create incentives for
reducing the pressure on the target species. The program should
create benefits for local residents to co-exist with the target
species and other species. It is also imperative that the program is
part of a legally recognized governance system that supports
conservation.
(c) Socio-Economic-Cultural Benefit: A well-managed hunting
program can serve as a conservation tool when it respects the local
cultural values and practices. It should be accepted by most members
of the community, involving and benefiting local residents in an
equitable manner. The program should also adopt business practices
that promote long-term economic sustainability.
(d) Adaptive Management: Planning, Monitoring, and Reporting:
Hunting can enhance the species when it is based on appropriate
resource assessments and monitoring (e.g., population counts, trend
data), upon which specific science-based quotas and hunting programs
can be established. Resource assessments should be objective, well
documented, and use the best science available. Adaptive management
of quotas and programs based on the results of resource assessments
and monitoring is essential. The program should monitor hunting
activities to ensure that quotas and sex/age restrictions of
harvested animals are met. The program should also generate reliable
documentation of its biological sustainability and conservation
benefits.
(e) Accountable and Effective Governance: A biologically
sustainable trophy-hunting program should be subject to a governance
structure that clearly allocates management responsibilities. The
program should account for revenues in a transparent manner and
distribute net revenues to conservation and community beneficiaries
according to properly agreed decisions. All necessary steps to
eliminate corruption should be taken and to ensure compliance with
all relevant national and international requirements and regulations
by relevant bodies such as administrators, regulators and hunters.
The Service's approach to enhancement findings for the importation
of sport-hunted trophies of P. l. melanochaita is consistent with the
purpose and intent of the Endangered Species Act. Before we will
authorize the importation of a sport-hunted trophy, we must determine
that the trophy hunting program is managed to ensure the long-term
survival of the species. In many parts of the world, wildlife exists
outside of protected areas and must share the same habitat and compete
with humans living in these areas for space and resources. If
communities that share these resources with wildlife do not perceive
any benefits from the presence of wildlife, they may be less willing to
tolerate the wildlife. However, under certain circumstances, trophy
hunting can address this problem by making wildlife more valuable to
the local communities and encourage community support for managing and
conserving the hunted species, as well as other species.
When evaluating whether the importation of a trophy of P. l.
[[Page 80046]]
melanochaita would be authorized pursuant to 50 CFR 17.32, in
accordance with our threatened species issuance criteria, we will
examine how a country's management program for lions addresses the
three main threats that have led to the decline of the subspecies:
Habitat loss, loss of prey base, and human-lion conflict. When
examining a management program and whether trophies taken as part of
that program meet the issuance criteria, we would study a number of
factors. Some of the factors we would consider include whether the
program is based on sound scientific information and identifies
mechanisms that would arrest the loss of habitat or increase available
habitat (i.e., by establishing protected areas and ensuring adequate
protection from human encroachment). We would consider whether the
management program actively address the loss of the lion's prey base by
addressing poaching or unsustainable offtake within the country. A
component of a management plan from which trophy imports would meet the
issuance criteria would be whether there are government incentives in
place that encourage habitat protection by private landowners and
communities and incentives to local communities to reduce the incursion
of livestock into protected areas or to actively manage livestock to
reduce conflicts with lions. We would examine if the hunting component
of the management program supports all of these efforts by looking at
whether hunting concessions/tracts are managed to ensure the long-term
survival of the lion, its prey base, and habitat. As stated previously,
hunting can generate significant economic benefits if properly
conducted. In looking at whether we would be able to authorize the
import of a trophy under the issuance criteria of 50 CFR 17.32, we
would examine if the trophy hunting provides financial assistance to
the wildlife department to carry out elements of the management program
and if there is a compensation scheme or other incentives to benefit
local communities that may be impacted by lion predation. We would also
consider how a U.S. hunter's participation in the hunting program
contributes to the overall management of lions within a country.
Management programs for P. l. melanochaita would be expected to
address, but are not limited to, evaluating population levels and
trends; the biological needs of the species; quotas; management
practices; legal protection; local community involvement; and use of
hunting fees for conservation. In evaluating these factors, we will
work closely with the range countries and interested parties to obtain
the information. By allowing entry into the United States of P. l.
melanochaita trophies from range countries that have science-based
management programs, we anticipate that other range countries would be
encouraged to adopt and financially support the sustainable management
of lions that benefits both the species and local communities. In
addition to addressing the biological needs of the subspecies, a
scientifically based management program would provide economic
incentives for local communities to protect and expand P. l.
melanochaita habitat.
As stated, under this 4(d) rule any person wishing to conduct an
otherwise prohibited activity, including all imports of P. l.
melanochaita specimens, must first obtain a permit under 50 CFR 17.32.
As with all permit applications submitted under 50 CFR 17.32, the
individual requesting authorization to import a sport-hunted trophy of
P. l. melanochaita bears the burden of providing information in their
application showing that the activity meets the requirements for
issuance criteria under 50 CFR 17.32. In some cases for imports, such
as sport-hunted trophies, it is not always possible for the applicant
to provide all of the necessary information needed by the Service to
make a positive determination under the Act to authorize the activity.
For the import of sport-hunted trophies of P. l. melanochaita, the
Service will typically consult with the range country to the extent
practicable and other interested parties to obtain necessary
information. The Service has the discretion to make the required
findings on sport-hunted trophy imports of P. l. melanochaita on a
country-wide basis, although individual import permits will be
evaluated and issued or denied for each applicant. While the Service
may make enhancement findings for sport-hunted trophy imports of P. l.
melanochaita on a country-wide basis, the Service encourages the
submission of information from individual applicants. We would rely on
the information available to the Service and may rely on information
from sources other than the applicant when making a permitting
decision.
Effects of This Rule
This action revises the taxonomic classification of the Asiatic
lion (currently classified as P. l. persica and listed as an endangered
species under the Act) to P. l. leo based on a taxonomic change. This
rule revises 50 CFR 17.11(h) to add P. l. leo subspecies and the P. l.
melanochaita subspecies to the List of Endangered and Threatened
Wildlife as an endangered species and a threatened species,
respectively. This rule establishes a 4(d) rule for P. l. melanochaita,
which implements all of the prohibitions and exceptions under 50 CFR
17.31 and 17.32 and requires a threatened species import permit under
50 CFR 17.32 for the importation of all P. l. melanochaita specimens.
Under the 4(d) rule, the import exemption found in 50 CFR 17.8 for
threatened wildlife listed in Appendix II of CITES does not apply to
this subspecies. Therefore, through the promulgation of this 4(d) rule,
the presumption of legality provided under section 9(c)(2) of the Act
for the otherwise lawful importation of wildlife listed in Appendix II
of CITES that is not an endangered species listed pursuant to section 4
of the Act does not apply to this subspecies (See: 4(d) Rule for
Panthera leo melanochaita).
Available Conservation Measures
Conservation measures provided to species listed as endangered or
threatened under the Act include recognition of conservation status,
requirements for Federal protection, and prohibitions against certain
practices. Recognition through listing encourages and results in public
awareness and conservation actions by Federal and State governments in
the United States, foreign governments, private agencies and groups,
and individuals.
Section 7(a) of the Act, as amended, and as implemented by
regulations at 50 CFR part 402, requires Federal agencies to evaluate
their actions that are to be conducted within the United States or upon
the high seas, with respect to any species that is proposed to be
listed or is listed as endangered or threatened. Because P. l. leo and
P. l. melanochaita are not native to the United States, no critical
habitat is being proposed for designation with this rule. Regulations
implementing the interagency cooperation provision of the Act are
codified at 50 CFR part 402. Section 7(a)(2) of the Act requires
Federal agencies to ensure that activities they authorize, fund, or
carry out are not likely to jeopardize the continued existence of a
listed species or to destroy or adversely modify its critical habitat.
If a proposed Federal action may adversely affect a listed species, the
responsible Federal agency must enter into formal consultation with the
Service. Currently, with respect to the lion, no Federal activities are
known that would require consultation.
[[Page 80047]]
Section 8(a) of the Act authorizes the provision of limited
financial assistance for the development and management of programs
that the Secretary of the Interior determines to be necessary or useful
for the conservation of endangered or threatened species in foreign
countries. Sections 8(b) and 8(c) of the Act authorize the Secretary to
encourage conservation programs for foreign listed species, and to
provide assistance for such programs, in the form of personnel and the
training of personnel.
Section 9 of the Act and our implementing regulations at 50 CFR
17.21 and 50 CFR 17.31 set forth a series of general prohibitions that
apply to all endangered and threatened wildlife, respectively, except
where a 4(d) rule applies to threatened wildlife, in which case the
4(d) rule contains all the applicable prohibitions and exceptions.
Under the 4(d) rule for P. l. melanochaita, all of the prohibitions
under 50 CFR 17.31 apply to P. l. melanochaita specimens. 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 or foreign commerce, by any means whatsoever, in the
course of commercial activity; or sell or offer for sale in interstate
or foreign commerce any lion specimens. It also is illegal to possess,
sell, deliver, carry, transport, or ship any such wildlife that has
been taken in violation of the Act. 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, such as P. l. leo, are codified at 50
CFR 17.22. Regulations governing permits for threatened species, such
as P. l. melanochaita, are codified at 50 CFR 17.32. Certain exceptions
apply to agents of the Service and State conservation agencies.
Summary of Comments and Recommendations
We based this action on a review of the best scientific and
commercial information available, including all information received
during the public comment period. In the October 2014 proposed rule, we
requested that all interested parties submit information that might
contribute to development of a final rule. We also contacted
appropriate scientific experts and organizations and invited them to
comment on the proposed listing. We received tens of thousands of
comments.
We reviewed all comments we received from the public for
substantive issues and new information regarding the proposed listing
of this species, and we address those comments below. Overall, most
commenters supported the proposed listing, but did not provide
additional scientific or commercial data for consideration. We have not
included responses to comments that supported the listing decision but
did not provide specific information for consideration. Most of the
commenters that did not support the proposed listing were affiliated
with the trophy hunting industry and opposed the rule due to potential
impacts on importing trophies. These comments are addressed below.
Peer Review
In accordance with our policy published on July 1, 1994 (59 FR
34270), we solicited expert opinions from ten individuals with
scientific expertise that included familiarity with the species, the
geographic region in which wild members of the species occur, and
conservation biology principles. We received responses from five of the
peer reviewers from whom we requested comments. The peer reviewers
generally supported our rule; however, they provided updated
information on taxonomy, current population estimates, and population
trends. They also found our analysis of some of the threats to be
inaccurate. Specifically, they provided comments and additional
information on loss of prey base, trophy hunting, infanticide,
corruption, and trade in lion bones. In some cases, a correction is
indicated in the citations by ``personal communication'' (pers. comm.),
which could indicate either an email or telephone conversation; in
other cases, the research citation is provided.
Peer Reviewer Comments
(1) Comment: Several peer reviewers commented on our section of the
proposed rule regarding the taxonomic classification of lion. These
peer reviewers confirmed that the IUCN Cat Specialist Group recommended
a two-subspecies classification: Panthera leo leo for lions of India
and western and central Africa, and P. l. melanochaita for lions in
eastern and southern Africa.
Our Response: We have reviewed the 2015 IUCN Red List Assessment
for the lion, which proposes the new classification as recommended by
the IUCN Cat Specialist Group, and the genetic studies supporting this
classification. We found this information to be the best available
scientific and commercial information; therefore, we have accepted this
taxonomic change and incorporated this decision into this document
under the Taxonomy section of this document. As a result, our
assessment is of the status of the lion species (both P. l. leo and P.
l. melanochaita), including the lion population in India.
(2) Comment: Several peer reviewers provided updated information on
population estimates and trends. Based on a time trend analysis of
scientific census data for 46 well-monitored populations, an overall 43
percent decline in lion populations across Africa was inferred.
Furthermore, regional trends emerged, showing that, while populations
in southern African increased by 22 percent, populations in eastern and
western and central Africa combined decreased by 57 percent and 66
percent, respectively. The peer reviewers also indicated that the
actual number of lions in Africa is much lower than previous estimates.
Application of regional trends to lion estimates made in 2002 resulted
in an estimate of fewer than 20,000 lions, a significant difference
from the previous estimate of 32,000.
Our Response: We considered this information and note that this
information was also included in the IUCN Red List Assessment for the
lion. Information on population estimates and trends was incorporated
into the Species Information section of this document. Assessment of
this information led us, in part, to conclude that the status of the
lion is more serious than previously indicated, especially in the
western and central regions of Africa (P. l. leo).
(3) Comment: One peer reviewer commented that the section on prey
loss does not address the issue of prey loss in protected areas where
most lions occur.
Our Response: The peer reviewer provided a list of literature on
the patterns and trends of prey loss in protected areas that were
recently or are currently occupied by lions. We have reviewed these
articles and have incorporated the findings in this document (under
Loss of Prey Base). This information did not change our determination,
but rather further supported our determination that prey loss has
occurred throughout the African range countries and is one of the major
threats to lion.
(4) Comment: One peer reviewer stated that although most lions in
Africa persist inside protected areas, the majority of the protected
areas should be uninhabited by humans; therefore,
[[Page 80048]]
only prides located at the edge of these protected areas should come
into conflict with humans. Because the proportion of lions subjected to
conflict with humans is small, it is wrong to state that the greatest
threat to lions in Africa is human-lion conflict.
Our Response: We have considered the peer reviewer's comments and
have altered our discussion of threats to lions from human-lion
conflict by clarifying that it is the lions that persist at the
boundary, or just outside, of protected areas that are most subjected
to this threat. This information did not change our determination;
human-lion conflict remains a threat to lion persistence.
(5) Comment: Three peer reviewers indicated that our assessment of
corruption within lion range countries was not realistic; that
corruption in most of Africa is extensive and worsening. They pointed
out oversights and errors pertaining to this subject in our proposed
rule and provided additional citations on the topic.
Our Response: We reexamined the information available to us during
the drafting of the proposed rule and reviewed information in
additional citations, and agree that our section on corruption did not
accurately reflect corruption in lion range countries. Based on peer
reviewer comments and available information, we have revised this
section accordingly.
(6) Comment: Two peer reviewers and three NGO stakeholders
indicated concern that trade in lion parts, particularly lion bone,
from Africa to Asia may pose a potential threat to the species.
Our Response: We agree and have revised this rule to include
information on the lion bone trade.
(7) Comment: A peer reviewer identified inaccuracies in our review
of information on traditional use of lion parts and products in west
and central Africa, and also indicated that trade in lion parts and
products is very common in these regions.
Our Response: We appreciate the peer reviewer's input. We reviewed
the available information and revised the section of this rule
pertaining to traditional use of lion parts and products in west and
central Africa accordingly.
(8) Comment: One peer reviewer questioned whether ``any lion
specimen'' referred to in the 4(d) rule would include Asiatic lion and/
or scientific samples.
Our Response: The 4(d) rule applies only to the threatened
subspecies, P. l. melanochaita. Scientific samples of P. l.
melanochaita will require permits pursuant to 50 CFR 17.32. The former
Asiatic lion (Panthera leo persica) is now classified as Panthera leo
leo which is now listed as endangered under the Act. Scientific samples
of P. l. leo will require permits pursuant to 50 CFR 17.22.
(9) Comment: Several peer reviewers commented that the information
provided in the proposed rule regarding quotas and offtake trends was
incorrect; specifically, several peer reviewers noted several
publications pertinent to quotas that should be re-examined and more
thoroughly discussed.
Our Response: We reexamined the information available to us during
the drafting of the proposed rule and reviewed the citations provided
during the public comment period. We consider these publications to be
the best available science regarding quota setting in the interim while
other strategies are more fully developed (i.e. age-based strategies,
adaptive management systems, etc.). We have revised this section to
include more discussion accordingly.
(10) Comment: Several peer reviewers provided additional
information on country-specific management trends; specifically,
information was provided on the progress of the commitment to and
implementation of the age-based strategy.
Our Response: We appreciate the peer reviewers input and have
incorporated this information into the section of the rule accordingly.
(11) Comment: One peer reviewer commented that, although species
experts do generally support trophy hunting as a management tool,
additional discussion was needed regarding the recommended reforms
species experts submitted during the drafting of the proposed rule.
Our Response: We reexamined the recommendations as provided by
species experts and agree that additional discussion was needed. We
have incorporated the additional discussion in the section as
appropriate.
(12) Comment: Four of the peer reviewers commented that although
species experts support trophy hunting as a management tool, it needs
to be conducted in a sustainable manner that would require reforms to
the current practices. Peer reviewers stated that the quotas set
throughout most range states are above sustainable levels (Packer et
al. 2011) and that quotas should be science-based and sustainable.
Our Response: We agree that current quotas are currently set higher
than those recommended by Packer et al. (2011). Species experts
recommend the implementation of an adaptive management quota system
that would ensure quotas would be based on the best available science.
We have revised this section accordingly.
(13) Comment: Several peer reviewers commented that the information
provided in the proposed rule regarding quotas and offtake trends was
incorrect; several of the peer reviewers provided additional
information (and citations) on country-specific quota trends, current
quotas, and offtake trends. One peer reviewer noted that clarification
was needed regarding the difference between quotas and offtake rates.
Additionally, two peer reviewers provided additional information on
moratoriums in two of the range countries.
Our Response: We reexamined the information available to us during
the drafting of the proposed rule and reviewed information in
additional citations provided during the public comment period. We
agree that clarification was needed, and, based upon peer review
comments and additional information, we have revised this section
accordingly.
(14) Comment: One peer reviewer commented that lion trophy hunting
could remain as an additive threat if hunting reforms are not
implemented and suggested that ``USFWS and equivalent bodies in the EU
and elsewhere could mediate such reforms by imposing reduced quotas,
best practices and the adherence to age restrictions on countries
wishing to export trophies.''
Our Response: It is not appropriate to establish specific criteria,
such as a set quota number, in this final rule because this may not
allow for the countries to implement an adaptive management strategy
based on the current status of the species within the country. During
the public comment period we received new information regarding
infanticide and the effects of hunting younger male lions on pride
structure. Therefore, we agree with the peer reviewer that the Service
is in a position to proactively engage with countries to assure
exported trophies fulfill minimum age requirements, and we will
consider these factors in making our enhancement findings.
(15) Comment: Two peer reviewers stated that populations in West
and Central Africa are small and isolated, and, as a result,
sustainable offtake was not possible. Several peer reviewers also
provided additional information and citations on documented lion
population declines resulting from excessive lion quotas and poor
management of trophy hunting.
Our Response: We reexamined the information available to us during
the
[[Page 80049]]
drafting of the proposed rule and reviewed the citations provided
during the public comment period. We have incorporated the new
information accordingly.
(16) Comment: One peer reviewer commented that our review of
infanticide as a result of trophy hunting was incomplete and provided
additional literature and citation on the subject for our
consideration.
Our Response: We agree that additional discussion was appropriate
regarding the impacts of infanticide, including a review of the new
studies provided on evolutionary adaptions and impacts of subadult
early dispersal on the species. We agree that infanticide and
associated factors relating to trophy hunting of males may have
additive impacts on the decline of certain populations. Therefore, we
have incorporated this information into our final rule.
Public Comments
(17) Comment: One commenter noted that there are very few reliable
or scientifically credible lion population surveys in Africa and as a
result, quotas are not scientifically derived. Additionally, the
commenter noted that quota allocations are largely based upon
concession operators' opinions.
Our Response: We consider Packer et al. (2011) to be the best
available science regarding quota setting in the interim while other
strategies are more fully developed (i.e., age-based strategies,
adaptive management systems, etc.). We have re-examined information
provided during the development of the proposed rule and reviewed new
information provided during the public comment period on quotas,
scientific quota development, and adaptive quota management systems. As
a result, we have incorporated this information into our rule
accordingly.
(18) Comment: One commenter noted that the proposed rule addressed
only CITES Trade Data exports under the ``trophy'' category and that
many are exported under the ``skins'' category.
Our Response: We have reviewed the U.S. imports of ``skins'' for
2013 and have incorporated this information into our rule.
(19) Comment: One commenter states that lion trophies exported are
almost exclusively males and subadult males, and as such, are targeted
by hunters at unsustainable levels. Additionally, the commenters note
that the situation of harvesting males from neighboring protected areas
would not be expected to occur if the males were being harvested at
sustainable levels.
Our Response: We agree that if hunting concessions maintained
sustainable levels of harvest, the situation of harvesting males from
neighboring protected areas would not be expected to occur. Species
experts have recommended best practices for sustainable development of
quotas and offtake (Packer et al. 2011, p. 151) while other methods are
developed (adaptive quota management based upon scientific data with an
enforceable monitoring program, (Lindsey et al. (2013a, pp. 8-9) and
Hunter et al. (2013, unpaginated)); these recommended reforms have been
incorporated as appropriate. Additionally, based on information
provided during the public comment period, there currently is no level
of offtake that would be sustainable in West and Central Africa at this
time. We have incorporated this information into our rule. For Panthera
leo melanochaita, we have developed a 4(d) rule and clarified factors
we will consider when making an enhancement finding for importation of
sport-hunted trophies of P. l. melanochaita (see 4(d) Rule for Panthera
leo melanochaita, above).
(20) Comment: Several commenters stated that populations in West
and Central Africa are small and isolated and as a result, sustainable
offtake was not possible. Several commenters also provided additional
information and citations on documented lion population declines
resulting from excessive lion quotas and poor management of trophy
hunting.
Our Response: We reexamined the information available to us during
the drafting of the proposed rule and reviewed the citations provided
during the public comment period. With the new population estimates, in
combination with the literature and citations provided during the
public comment period, we agree that given the current state of the
populations in West and Central Africa (Panthera leo leo), sustainable
offtake is not possible. As a result, we have found that, in their
current condition, sustainable offtake for Panthera leo leo is not
possible. Therefore, we find that trophy hunting does rise to a level
of threat for Panthera leo leo. We have incorporated the new
information accordingly.
(21) Comment: Several range countries provided additional
information on their progress in implementing the best recommended
practices and reforms as outlined by species experts.
Our Response: We appreciate the information provided by the range
countries. We have incorporated relevant portions of this information
into our rule accordingly. It should be noted, however, that, with this
finding, Panthera leo leo meets our definition of an endangered species
and, therefore, will be subject to the provisions and regulations of
the Act for endangered species. Import of sport-hunted trophies of
Panthera leo melanochaita will require issuance of a threatened species
import permit under 50 CFR 17.32, which will require an enhancement
finding (see 4(d) Rule for Panthera leo melanochaita, above).
(22) Comment: One commenter noted that, although the proposed rule
offers concrete examples of the role of trophy hunting in lion
conservation, the proposal offers only limited support of trophy
hunting benefits. Additionally, one commenter notes that the hunting
community has been a leader in lion conservation in terms of habitat
conservation and states that the success of certain populations is
largely in part to contributions from the hunting community.
Our Response: Based on information received during the formation of
the proposed rule and based on additional information received during
the public comment period, we agree that trophy hunting, if managed in
a sustainable and scientific manner, can provide benefits to both local
communities as well as to lion conservation. We also agree that trophy
hunting has conserved a considerable portion of lion habitat. However,
species experts have identified several areas across the range of the
species where hunting has contributed to the decline of lion
populations. Species experts have outlined these flaws and have
developed and introduced several recommended reforms to assure that
offtake is sustainable and scientific. We have incorporated these key
issues and the recommended reforms into this rule as appropriate.
Although we acknowledge the role trophy hunting has played in lion
conservation, we also have reviewed additional literature provided that
documents the decline of lion populations as a result of mismanaged
trophy hunting. At this time, based on information received during the
public comment period, based on the current trends of lion populations
in West and Central Africa (Panthera leo leo), experts suggest that
there is no level of offtake that is considered sustainable in these
regions. Regardless, import of sport-hunted trophies of Panthera leo
leo will require issuance of an endangered species import permit under
50 CFR 17.22, which will require an enhancement finding. Import of
sport-hunted trophies of Panthera leo melanochaita will
[[Page 80050]]
require issuance of a threatened species import permit under 50 CFR
17.32, which will require an enhancement finding (see 4(d) Rule for
Panthera leo melanochaita, above).
(23) Comment: Several commenters noted that excessive lion quotas
and offtake was the primary driver for declines in lion abundance.
Our Response: We reviewed the new literature provided and agree
that the excessive offtake contributed to the decline of some lion
populations throughout their range. We have incorporated this
information into our rule and addressed the recommended reforms as
provided by Hunter et al. (2013, entire) and Lindsey (2013a, pp. 8-9).
(24) Comment: Several commenters noted that current practices,
unless reformed according to best recommendations, should be considered
a potential threat to lion. Species experts recommend a maximum
science-based offtake of no more than <1 lion/2,000 km\2\ of hunting
block until age restrictions are enforced.
Our Response: We have reexamined information provided during the
formation of the proposed rule and have reviewed new literature
submitted during the public comment period regarding the best
scientific information available regarding quota setting for lions. We
agree and have incorporated this information in our rule as
appropriate.
(25) Comment: Three commenters provided additional information on
the biological impacts of trophy hunting. New information was provided
regarding (1) the evolutionary impacts of selective removal of
specimens displaying key traits; (2) biological and genetic results of
infanticide as it relates to subadult dispersal and survival; and (3)
the role of adult male range and dispersal requirements in genetic
variation and isolated populations.
Our Response: We reexamined the information available to us during
the drafting of the proposed rule and reviewed the citations and peer
review input provided during the public comment period. We agree that
additional discussion was required regarding the impacts of
infanticide, including a review of the studies the commenters
submitted. We agree that infanticide and associated factors relating to
trophy hunting of males may have additive impacts on the decline of
certain populations. Therefore, we have incorporated this information
into our final rule.
(26) Comment: Several commenters noted that many range countries
are in the process of reforming their lion hunting regulations. Other
commenters note that these reforms have only been fully implemented in
some countries and additional reforms are needed throughout the range.
An additional commenter noted that the information presented in the
proposed rule on range countries implementation of best practices is
overly optimistic with regard to what has actually been achieved.
Our Response: Several commenters provided updates regarding the
progress of range countries' reforms to hunting regulations. Although
multiple countries have begun to implement the reforms as outlined in
this document, only two locations (Mozambique, in Niassa Reserve, and
Zimbabwe) have fully implemented the process and are completely
transparent. However, many countries are still in the earliest stages
of implementation, and their progress is still pending. After a review
of this information, we concur that most range countries have multiple
barriers (e.g. corruption and poverty) that will have to be addressed
concurrently with the establishment of a transparent and scientific-
based, adaptive management system. This information has been
incorporated into the rule. Import of sport-hunted trophies of Panthera
leo melanochaita, will require issuance of a threatened species import
permit under 50 CFR 17.32, which will require an enhancement finding
(see 4(d) Rule for Panthera leo melanochaita, above).
(27) Comment: One commenter noted that recent scientific knowledge
has established that hunting males aged five and older does not affect
lion population dynamics.
Our Response: We have reviewed the literature provided and have
incorporated the recommended strategy into our rule. Whitman et al.
(2004, pp. 175-177) found that if offtake is restricted to males older
than 6 years of age, then trophy hunting will likely have minimal
impact on the pride's social structure and young. Restricting offtake
to males over 6 years of age will decrease the frequency of male-
takeovers, and reduce the potential for infanticide and delayed
infanticide by allowing younger males a chance to sire and raise a
cohort of young, and by allowing the subadults to stay within their
pride longer (thus allowing them to mature prior to dispersal) (Elliot
2014, p. 1054; Packer et al. 2006, p. 6).
(28) Comment: One commenter stated that the validity of the so-
called 6-year age approach has been questioned.
Our Response: The 6-year approach is a relatively new development
based on research conducted by Whitman (2004, p. 175-177). Like all new
concepts, technical issues will arise during the implementation phase.
Species experts have been working through these issues by providing
research and outreach materials detailing the most current aging
techniques, and by providing training to concession operators and
communities (Begg and Begg 2010, pp. 8, 14; Packer and Whitman 2006,
entire). We anticipate additional research will emerge as this strategy
is implemented across the species range.
(29) Comment: Several commenters noted that the existing age limit
for `old males' is not enforced.
Our Response: Enforcement of wildlife crime continues to be an
issue for many countries in Africa as evidenced by the rising rate of
poaching epidemics and corruption across the African continent.
Enforcement of trophy hunting regulations across the range of the
species is a critical issue. Currently, only two places within the
African continent have completely implemented the recommendations as
set forth in this rule. Several other countries have committed to
implementing this strategy, but their progress is currently pending. We
must note here that enforcement is complex; it is only one component of
a multi-tiered regulatory system. Successful enforcement will rely on a
variety of other factors related to management. Countries will have to
address corruption in order to ensure their monitoring and management
systems are transparent.
(30) Comment: During the public comment period, several commenters
expressed concern that local communities do not actually benefit from
the revenue derived from trophy hunting. Specifically, comments were
focused on three issues (see Potential Impacts of Trophy Hunting): (1)
Corruption of concession operators and corrupt practices surrounding
concession allocation prevent local communities from benefitting from
trophy derived revenue; (2) financial contributions to local
communities from trophy hunting is often exaggerated and bears little
connection to conservation of the species (local communities receive
only 3-5 percent of revenues); and (3) that benefits have never been
independently evaluated and communities involved in hunting concessions
have not been adequately surveyed as to their satisfaction of land use
for trophy hunting.
Our Response: Corruption occurs throughout the range of the
species, and it likely has an impact on the actual benefits received by
local communities. Although many countries have incorporated incentives
into their
[[Page 80051]]
trophy hunting policies, land management policies, and national lion
action strategies, most countries are still in the earliest stages of
implementing the strategies discussed in the rule. Therefore, we have
incorporated this information into our final rule.
(31) Comment: One commenter stated that there is no evidence to
support that trophy hunting might provide sufficient money to motivate
communities in hunting regions to protect lions against other threats
such as retaliatory killings for livestock losses.
Our Response: Although there is limited data on the motivations of
individuals who kill lions (see Hazzah 2013), we recognize that human-
lion conflict resulting in retaliatory killing is a major threat.
Although not the only mechanism for increasing tolerance, incentives
are an important aspect of changing individuals' perceptions of lions,
especially for communities who live close to lion populations.
According to Packer et al. (2011, p. 152, citing e.g., Baker 1997, Hurt
and Ravn 2000, Child 2004, Lindsey et al. 2006, and Dickson et al.
2009), ``trophy hunting has been considered essential for providing
economic incentives to conserve large carnivores.'' For example, Kenya
banned trophy hunting in 1977 due to questionable ethics and poor
management. Since then, ``wildlife populations outside of parks have
declined by at least 60%, due partly to the inability of local people
to benefit from wildlife'' (Lindsey et al. 2006, citing Child, 2000,
2005).
Recently, Hazzah et al. (2014, entire) conducted research in Kenya
in the Amboseli ecosystem, where it was estimated that 55 percent of
lion killings were retaliatory in nature. In this area, two programs
are used to provide incentives to locals to prevent these types of
killing. First, there is a Predator Compensation Fund (PCF) wherein
local people are compensated for depredated livestock and the system is
carefully designed with a system of verification processes, payments,
and violation penalties (2014, p. 852). Second, the Lion Guardians (LG)
program uses traditional techniques to incorporate community value and
belief systems to improve local perceptions. According to Hazzah et al.
(2014, pp. 857-858), compensation alone showed a 73 percent reduction
in lion killing. Combining this with the LG program (in 2007) further
reduced the decline by 91 percent (less than one killed per year).
Hazzah et al. estimated that the PFC program cost an estimated $250,000
USD annually and employed 30 community members. The LG program was
estimated to have cost $140,000 USD annually and employed 38 community
members. It is important to note, however, that the authors are
uncertain regarding the sustainability of long-term payments and
questioned what would happen if the compensation stopped. In other
countries within the range of lion, systems like these are not
necessarily in place. Experts believe the revenue from trophy hunting,
if well managed in a transparent way, could potentially fund similar
programs throughout the species' range, thus reducing retaliatory
killings and benefitting the local population simultaneously.
(32) Comment: One commenter suggested non-consumptive uses such as
eco-tourism could provide the promise of sustainable enterprise.
Our Response: We agree in part, but ecotourism and the trophy
hunting community need to come together to support the African
countries in lion conservation. Non-consumptive uses of wildlife such
as eco-tourism have been practiced in many regions throughout Africa.
Lindsey et al. (2007, entire) studied viewing preferences among
visitors in protected areas in South Africa. Most tourists, especially
first-time and foreign visitors, were generally focused on charismatic
mega-species that are generally confined to protected areas; African
visitors had more interest in bird and plant diversity, scenery, and
other rare species. Lindsey et al. (2007) acknowledge that ecotourism
may align with conservation objectives and provide incentives for the
development of tour operations geared away from the `big five.'
However, ecotourism as a replacement to trophy hunting will have to be
researched further. Information provided by Hunter et al. (2013,
unpaginated citing Norton-Griffiths 2007) indicates that ``a
significant portion of the land where trophy hunting occurs is unlikely
to be viable for alternate wildlife-based land uses such as photo- or
ecotourism due to remoteness, lack of infrastructure including
integration in established tourism circuits, lack of spectacular
scenery or lack of high densities of viewable wildlife.'' Additionally,
according to Hunter et al. (2013, unpaginated citing Packer et al.
2007; Groom 2013, pp. 2-3) ecotourism is highly dependent on political
stability. As a result, ecotourism is unlikely to be able to provide
the revenue potential that is currently associated with trophy hunting,
although we agree there is potential for growth in this industry.
(33) Comment: Several commenters state that hunting is able to
generate revenues for a larger proportion of areas that are unsuitable
for ecotourism (e.g., remote areas lacking infrastructure, attractive
scenery, or high densities of viewable wildlife). Additionally, the
commenters state that trophy hunting revenue provides a means of
preserving natural habitat despite strong pressure to convert habitat
into agriculture or rangelands.
Our Response: We agree that trophy hunting revenue provides
conservation value at many levels, especially in terms of lion habitat,
conservation programs, anti-poaching programs, equipment, and poaching
patrols. However, lion experts have documented the decline of many
populations of lion resulting from mismanagement of trophy hunting
(Rosenblatt et al. 2014, p. entire; Sogbohossou et al. 2014, entire;
Becker et al. 2013, entire; Lindsey et al. 2013, entire; Croes et al.
2011, entire; Packer 2011, entire; Loveridge et al. 2007, entire).
Additionally, the high revenue potential associated with trophy hunting
makes it a target for corruption. As a result, we have reviewed the
recommended best practices as provided by species experts to encourage
countries to establish a transparent, science-based, adaptive quota
management system. Import of sport-hunted trophies of Panthera leo leo
will require issuance of an endangered species import permit under 50
CFR 17.22, which will require an enhancement finding. Import of sport-
hunted trophies of Panthera leo melanochaita will require issuance of a
threatened species import permit under 50 CFR 17.32, which will require
an enhancement finding (see 4(d) Rule for Panthera leo melanochaita,
above).
(34) Comment: One commenter noted that that the estimates of
revenue from trophy hunting presented in the proposed rule were not
believed to be the best scientific information available. Specifically,
they questioned the objectivity of one source (Jackson 2013) and
provided additional information analyzing Lindsey et al. (2012a).
Our Response: The new literature provided by the commenter
(Campbell 2012, entire) identifies some analysis and data flaws in
Lindsey (2012a). We have reviewed the information presented and updated
this rule using the best available scientific information. We have
removed information we used from Jackson (2013) and Lindsey et al.
(2012) and rely upon information from Groom (2013) and Barnett and
Patterson (2005), which was also presented in the proposed rule.
(35) Comment: One commenter noted that the discussion as presented
in the proposed rule was biased toward the hunting industry and did not
discuss the body of research documenting the
[[Page 80052]]
potential negative impacts of trophy hunting. A peer reviewer requested
a more thorough discussion be included to address (1) the major flaws
in current management practices, and (2) recommendations for how these
issues can be addressed to account for sustainability.
Our Response: We reexamined the information available to us during
the drafting of the proposed rule and reviewed the citations and peer
review input provided during the public comment period. As a result, we
have incorporated this information into the rule.
(36) Comment: Three range countries provided information on the
occurrence of human-lion conflict. All three countries indicated that
human-lion conflict is a serious problem.
Our Response: We incorporated this information into our discussion
of human-lion conflict. The information further supported our
conclusion that human-lion conflict constitutes a threat to lion
persistence.
(37) Comment: One commenter agrees that human-lion conflict is a
threat to remaining lion populations, but asserts that it does not
constitute a level of threat in eastern and southern Africa to warrant
a listing under the Act. The commenter further asserts that the lion
has been secured from the negative impacts of human-lion conflict where
90 percent of its population exists and that human-lion conflict can be
controlled and reduced.
Our Response: We agree that there are populations of lions where
adequate management has reduced the occurrence and impacts of human-
lion conflict. However, the best available information indicates that
retaliatory killing is a rangewide occurrence, and given the limited
number of lions remaining, any loss of lions to retaliatory killing, or
other actions, can have a detrimental impact on the species.
(38) Comment: One commenter disagreed with our conclusion that
disease was not a significant threat to the lion and provided
additional information on FIV, bTB, and CDV and discussed difficulties
in determining the role of disease in lion mortality. The commenter
requested that we reconsider our determination based on consequences of
diseases to the immune system.
Our Response: As mentioned in their comment, the role of disease in
lion mortality and reproductive potential is almost completely unknown
in lion populations. Except for a few populations that have been
studied, there are no estimates of the number of lions lost to
diseases. Some populations were able to recover to pre-outbreak levels,
but for others, factors such as an inbred population prevented
populations from recovering to pre-outbreak levels. We found no
information indicating the loss of lions to disease is a significant
driver of the status to the species. However, we acknowledge that
diseases can debilitate rather than cause mortality, but debilitation
may cause an individual to succumb to other factors. Furthermore, due
to the prevalence of some diseases in lion populations and current
stressors on lions, it is likely that disease contributes to lion
mortality. The information provided by the commenter did not alter our
finding that disease is not a significant threat to the species;
however, we have altered the discussion of disease to clarify that
disease is a secondary factor that is exacerbated by other threats the
lion faces.
(39) Comment: Several commenters stated that climate change has a
detrimental impact on the species and that the Service did not
incorporate recent climate trend data into our analysis.
Our Response: We have incorporated climate change data and its
effect on the species into our analysis.
(40) Comment: One commenter specifically commented that the 4(d)
rule is appropriate and needed for the conservation of the species. A
second commenter applauded the Service for recognizing the importance
of regulated hunting and the conservation of the African lion and the
need for a system that allows U.S. hunters to import trophies.
Our Response: The Service agrees that the 4(d) rule is necessary
and advisable for the conservation of the subspecies P. l.
melanochaita. The Service has recognized that a well-managed,
scientifically based hunting program can provide for the conservation
of a species and benefit local communities. By establishing the 4(d)
rule that encourages range countries to effectively manage their lion
populations, U.S. hunters can continue to contribute to the long-term
conservation of the subspecies.
(41) Comment: Four commenters stated that the Service lacks the
authority to rebut the Act's section 9(c)(2) with a blanket finding
applicable to lions throughout Africa, for an indefinite time period.
Section 9(c)(2) states that any importation shall ``be presumed to be
an importation not in violation'' of any provision of the Act or
implementing regulation for species not listed as endangered but listed
on Appendix II of CITES. The commenters stated that African lions,
because they are currently listed in CITES Appendix II, would be
covered by the presumption provided by section 9(c)(2) if they are
listed as threatened. One of the commenters noted a disparity between
the 4(d) rule for lions and a 4(d) rule for another species that was
commonly hunted. This commenter felt that because both species are
listed in Appendix II of CITES that their treatment under the Act
should be similar.
Our Response: While there has been question as to whether section
9(c)(2) of the Act might automatically require allowing the importation
of a species that is both listed as threatened and in Appendix II, and
preclude the issuance of more restrictive 4(d) rules covering
importation, the Service has concluded that such 4(d) rules may be
issued to provide for the conservation of the involved species. Section
9(c)(2) does not expressly refer to threatened species or prevent the
issuance of appropriate 4(d) rules and could not logically have been
intended to allow for an international convention to override U.S. law,
where there is reliable evidence to affect the presumption of validity.
Finally, the term ``presumed'' implies that the established presumption
is rebuttable under certain circumstances, including through the
promulgation of a protective regulation pursuant to section 4(d) of the
Act.
(42) Comment: Two commenters stated that, even if the Service had
the authority to promulgate a regulation that establishes the manner in
which African lions are imported, it cannot use the regulation to
essentially shift to the hunter/importer the burden of proving
enhancement or survival of the species criteria.
Our Response: The burden of showing that an ``otherwise prohibited
activity'' meets the issuance criteria under 50 CFR 17.32 is on the
applicant. In some cases for imports, such as sport-hunted trophies, it
is not always possible for the applicant to provide all of the
necessary information needed by the Service to make a positive
determination under the Act to authorize the activity. For the import
of sport-hunted trophies of P. l. melanochaita, the Service will
typically consult with the range country to the extent practicable and
other interested parties to obtain necessary information. The Service
has the discretion to make the required findings on sport-hunted trophy
imports of P. l. melanochaita on a country-wide basis, although
individual import permits will be evaluated and issued or denied for
each applicant. While the Service may make enhancement findings for
sport-hunted
[[Page 80053]]
trophy imports of P. l. melanochaita on a country-wide basis, the
Service encourages the submission of information from individual
applicants. We would rely on the information available to the Service
and may rely on information from sources other than the applicant when
making a permitting decision.
(43) Comment: Two commenters stated the Service has offered nothing
to demonstrate why limitations on the importation of sport-hunted
African lions from throughout the subspecies' range is necessary and
advisable to provide for the conservation of the subspecies or
sufficient to overcome the Congressional conclusion that such imports
would normally (i.e., presumptively) benefit the conservation of the
species. Further, these commenters did not feel that the Service's
proposed rule for African lion supported a conclusion that a 4(d) rule
requiring import permits for trophies was necessary and advisable for
the conservation of the subspecies.
Our Response: For the import of sport-hunted trophies, while there
is evidence that many of the range countries have lion management
plans, we have little information indicating that the plans are being
implemented, and we received new information during the public comment
period indicating that some hunting programs are not scientifically
based or providing adequate conservation benefits to the species. We
want to encourage U.S. hunters to take advantage of one of the
conservation tools available, well-regulated hunting programs, to
improve the long-term survival of the subspecies. The 4(d) rule will
support implementing well-managed plans by encouraging countries that
have insufficient lion management plans to develop plans that are based
on sound scientific information that would generate revenue in support
of communities and conservation. As noted, the proposed 4(d) rule for
African lion would provide for the importation into the United States
of trophies taken legally in range countries upon the issuance of a
threatened species import permit. While the Service cannot control
hunting of foreign species such as African lion, we can regulate their
importation and thereby require that U.S. imports of sport-hunted
African lion trophy specimens are obtained in a manner that is
consistent with the purposes of the Act and the conservation of the
subspecies in the wild, by allowing importation from range countries
that have management plans that are based on scientifically sound data
and are being implemented to address the threats that are facing lions
within that country.
(44) Comment: Three commenters, a peer reviewer and comments from a
consortium of seven range countries felt that the proposed 4(d) rule
did not adequately explain the criteria used by the Service to
determine whether the importation of any sport-hunted lion would
enhance the survival of the species. The commenter expressed concern
that because the Service has not adequately explained the criteria for
enhancement or made an enhancement finding for lions in Africa, U.S.
hunters will be barred from importing their lion trophy. The peer
reviewer expressed a need for the Service to elaborate concrete
requirements to which countries must adhere as a minimum standard in
order for imports of sport-hunted lion trophies from a country to
qualify for the export of lion trophies, including quotas of less than
one male per 2000 km\2\ with a minimum age requirement.
Our Response: We recognize that the preambular language of the
proposed 4(d) rule was general, and we have addressed this issue in
this final rule. However, we did not find that it was appropriate to
establish specific criteria, such as a set quota number, in this final
rule because this may not allow for the countries to implement an
adaptive management strategy based on the current status of the species
within the country. During the public comment period we received new
information regarding infanticide and the effects of hunting younger
male lions on pride structure. Therefore, we agree with the peer
reviewer that the Service is in a position to proactively engage with
countries to ensure exported trophies fulfill minimum age requirements
and we will consider these factors in making our enhancement findings.
(45) Comment: Two commenters recommended that the Service should
not adopt a 4(d) rule until it makes specific enhancement-of-survival
findings for each of the countries for which lions can be hunted, or
delay the implementation of the 4(d) rule for 1 year. These two
commenters, as well as a third commenter, stated that implementing the
4(d) rule at this time would impact hunters who had already booked
trophy hunts months or even years in advance, resulting in the loss of
money invested that could not be recovered ``in the event of a sudden
change in the rules governing the importation of sport-hunted
trophies.''
Our Response: In the proposed rule, the Service found that hunting,
if well managed, may provide a benefit to the subspecies. However, the
best available information, obtained by the Service during the public
comment period, indicates that not all hunting programs are well
managed or provide enhancement to survival of the subspecies. Delaying
the implementation of a 4(d) rule may result in U.S. hunters
participating in poorly managed hunting programs, which would be
counter to the purposes of the Act. We do not agree that such a delay
would be appropriate for the conservation of the subspecies. Regarding
the potential loss of deposits for previously booked trophy hunts,
hunters were notified of a potential regulatory change when the
proposed rule with a 4(d) rule was published on October 29, 2014 (79 FR
64472). The availability of the proposed rule would have given hunters
the opportunity to use that information to minimize financial losses.
(46) Comment: One commenter urged the Service to adjust the rule to
ensure that imports are not stopped, and that the benefits generated by
U.S. hunters in foreign countries continue while the Service is making
determinations regarding the countries' lion management program. This
commenter suggested that the Service issue U.S. import permits for all
lion trophies until such time as the Service deems that the import from
a particular country would not enhance the survival of the subspecies.
It is the commenter's belief that there are beneficial aspects of
hunting (benefits to local communities, dollars coming into the
country, etc.) that should not be interrupted while the Service is
making its determinations. The commenter expressed concern that the
Service has insufficient resources to make timely country-by-country
determinations.
Our Response: Import of sport-hunted trophies of Panthera leo leo
will require issuance of an endangered species import permit under 50
CFR 17.22, which will require an enhancement finding. Import of sport-
hunted trophies of Panthera leo melanochaita will require issuance of a
threatened species import permit under 50 CFR 17.32, which will require
an enhancement finding (see 4(d) Rule for Panthera leo melanochaita,
above). We would be unable to issue import permits until we made such
determinations. The Service recognizes that making these findings may
be time consuming given our current resources. We appreciate the
commenter's willingness to use their own resources to obtain
information on the range countries' management and assist the Service
in making timely findings. We encourage the commenter and others to
work with us by
[[Page 80054]]
submitting any information they may have to make these determinations.
(47) Comment: One commenter stated that the Service should only
apply a permitting requirement on lions taken after the listing and
4(d) rule go into effect.
Our Response: For lions held in captivity or a controlled
environment on the date of the listing under the Act, no import permit
will be required, if the lion meets all the requirements to be
considered ``pre-Act'' (Section 9(b)(1) of the Act). Accordingly, lions
hunted after the listing would require permits, and those hunters who
have booked hunts, but have not yet hunted a lion, would require a U.S.
import permit prior to importation.
(48) Comment: Two commenters stated their belief that most of the
lion range countries do not have national lion conservation plans in
place, or have plans with quotas in place that are based on inaccurate
population numbers. One commenter spoke of lion conservation
conferences in 2005 and 2006 that established conference resolutions,
very few of which have been adequately addressed by the lion range
states. This commenter felt there is an urgent need to conduct
independent and scientifically valid lion population assessments
throughout the range of the lion. This commenter urged the Service to
impose an import moratorium until these population assessments have
been conducted. The second commenter recommended that prior to the
import of trophies, there needs to be evidence of recovery and
stability, as well as clearly identified governmental reforms and their
implementation in some of the range states.
Our Response: New information received during the public comment
period raises questions about whether some of the range countries have
adequate management programs in place, and this information has been
incorporated in this final rule. The Service is not imposing a
moratorium; however, permits will be required for all imports. Import
of sport-hunted trophies of Panthera leo leo will require issuance of
an endangered species import permit under 50 CFR 17.22, which will
require an enhancement finding. Import of sport-hunted trophies of
Panthera leo melanochaita will require issuance of a threatened species
import permit under 50 CFR 17.32, which will require an enhancement
finding (see 4(d) Rule for Panthera leo melanochaita, above). The
import of lions hunted in countries that do not meet the criteria for
enhancement will not be permitted.
(49) Comment: Several lion range countries as well as two
commenters expressed that successful conservation of African lion
relies upon a thoughtful strategy that includes sustainable use. There
was concern that the inability to import lions into the United States
would result in the increase of threats we identified in the proposed
rule (e.g., human-lion conflict and habitat loss). The countries
expressed that if U.S. hunters are unable to import sport-hunted
trophies, the economic value of lions within the country would be
reduced or eliminated, resulting in retaliatory killing of lions by
local communities because of real or perceived perceptions that lions
kill people and livestock. In addition, two countries noted that,
without an economic value, safari companies would not support lions in
hunting concessions because lions prey upon other valued trophy
species, such as hartebeest and buffalo. One country noted that if
hunting companies were unable to export to the United States, they
would abandon their hunting areas to agro-pastoral uses, resulting in
``unavoidable extinction of wildlife and collapse of ecosystem
services.'' These countries expressed that hunting zones often provide
a buffer to protected areas as well as provide ecological corridors
between protected areas. They expressed that the removal of lions from
these hunting zones would decrease the range of the subspecies and
result in overall lion population declines. Further, the loss of legal
income from lion hunting, which supports anti-poaching efforts, will
negatively affect lion conservation and increase poaching.
Our Response: The Service recognizes the benefits that a well-
managed trophy hunting program can provide by increasing revenue for
local communities, providing jobs, and supporting local
microbusinesses. Revenue is often used to build and maintain fences,
pay for security personnel, and provide resources for anti-poaching
activities, habitat acquisition, and wildlife management.
Our 4(d) rule for P. l. melanochaita will support and encourage
conservation actions for this subspecies and ensure that U.S. imports
of sport-hunted lion trophy specimens are obtained in a manner that is
consistent with the purposes of the Act and the conservation of the P.
l. melanochaita in the wild. By ensuring that imports of lions occur
only from range countries that have management plans based on
scientifically sound data which are being implemented to address the
threats facing lions within that country, U.S. hunters will continue to
support the good efforts of the range countries, while encouraging
those countries that have not fully implemented a lion management plan
to do so in order to receive business from U.S. hunters.
(50) Comment: Several countries and one commenter provided a
combined comment expressing concern that the Service's 4(d) rule
surpasses the regulatory requirements they are already following under
CITES, and that such restrictions undermine CITES and increase the
regulatory burden to lion range states by adding additional reporting
requirements. These countries noted that under CITES exports of
trophies must not be detrimental to the survival of the species and
expressed that proving their management programs enhance the survival
of the subspecies is an added administrative burden on their wildlife
management authorities that are already limited on staff, resources,
and time. Further, they felt the 4(d) rule would penalize countries
that are already working hard to achieve success in wildlife
management.
Our Response: As these countries noted in their comments, CITES
allows for stricter domestic measures, such as the Act and our 4(d)
rule for P. l. melanochaita promulgated under the Act. The Service
recognizes that the 4(d) rule for P. l. melanochaita has stricter
requirements than CITES Appendix-II requirements. We find that our 4(d)
rule for P. l. melanochaita will support and encourage countries to
carry out strong conservation programs for P. l. melanochaita and
ensure that U.S. imports of sport-hunted lion trophy specimens are
obtained in a manner that is consistent with the purposes of the Act
and the conservation of the P. l. melanochaita in the wild. We do not
anticipate a significant burden on the lion range countries to provide
documentation that should already exist for well-managed lion programs,
and we will work with the countries in order to make our determinations
under the Act in a timely manner. The 4(d) rule is in place to support
countries that have achieved success in managing their lions.
(51) Comment: Several countries and one commenter disagreed with
how trade in captive-bred lions would be subject to the prohibitions
under the Act. These countries expressed that trade in captive-bred
lion does not have an adverse effect on wild lion populations. They
felt that the Act's treatment of captive lions in the same manner as
wild lions is inconsistent with CITES regulations and that the 4(d)
rule should exempt captive-bred lions.
[[Page 80055]]
Our Response: In analyzing threats to the species, we focused our
analysis on threats acting upon wild specimens within the native range
of the species, because the goal of the Act is survival and recovery of
the species within its native ecosystem. We did not separately analyze
``threats'' to captive-held specimens because the statutory five
factors under section 4 (16 U.S.C. 1533) are not well-suited to
consideration of specimens in captivity and captive-held specimens are
not eligible for separate consideration for listing. However, we did
consider the extent to which specimens held in captivity create,
contribute to, reduce, or remove threats to the species. See the
Captive Lions and Traditional Use of Lion Parts and Products sections
above. Under CITES, captive specimens are still listed the same as
their wild counterparts; however, the Convention does allow for
different treatment of captive-bred specimens in regard to permitting.
As stated earlier, CITES also provides for stricter domestic measures,
and the protections afforded to all specimens of the subspecies through
listing under the ESA and the 4(d) rule would constitute such a
measure.
(52) Comment: A joint comment from the petitioners asked us to
scrutinize applications for the import of lion trophies or parts to
ensure that they were obtained within a scientifically based management
program that promotes the conservation of the subspecies and provided
suggestions for criteria to consider when making an enhancement
finding. The comment included a number of suggestions for establishing
a formal internal guidance on how we would evaluate each application.
Finally, the petitioners called on the Service to publish the receipt
of threatened species permit applications in the Federal Register and
allow for a 30-day comment period. Another commenter questioned
establishing findings on a country-wide basis instead of specific
regions/hunting programs within a country.
Our Response: We appreciate the input regarding publishing the
receipt of threatened species applications, establishing formal
internal guidance on how we will evaluate each application, and
consideration of making enhancement findings on a specific region/
hunting program scale. We will consider these suggestions; however,
this issue is outside the scope of this rulemaking process. In regard
to the suggested criteria for making enhancement findings, we have
expanded the discussion of enhancement within this final rule, and many
of the suggestions have been addressed in the preambular language of
the 4(d) rule.
(53) Comment: The petitioners also asserted that we should not
authorize imports of lions from western Africa, Tanzania or Zimbabwe;
imports of trophies from females or males under 6 years of age; or
trophies obtained from captive-hunting facilities, or authorize
imports, interstate commerce or foreign commerce in lion parts.
Our Response: While the comments are outside the scope of this
rulemaking, the Service must make a finding that an ``otherwise
prohibited activity,'' such as import, export, interstate and foreign
commerce, must meet the issuance criteria under 50 CFR 17.32. We cannot
make any determination of whether a particular permit application can
be approved or denied until the application is reviewed.
(54) Comment: One commenter called on the Service to specifically
prohibit the importation of sport-hunted lions in the 4(d) rule, citing
that there is no documented evidence that trophy hunting supports
conservation of the subspecies. In addition, the commenter felt that
allowing for legal trade of sport-hunted lions would support the
illegal harvest of the subspecies.
Our Response: We found no evidence that allowing legal import of
lion trophies would stimulate illegal trade into the United States. In
evaluating the best available scientific and commercial information, we
concluded that a well-managed, scientifically based lion management
program can provide a benefit to the species. While we obtained new
information indicating that some hunting programs are not
scientifically based or providing adequate conservation benefits to the
species, this 4(d) rule will support implementing well-managed plans by
encouraging countries that have insufficient lion management plans to
develop plans that are based on sound scientific information that would
generate revenue in support of communities and conservation. Therefore,
we are not prohibiting the import of sport-hunted trophies. Import of
sport-hunted trophies of Panthera leo melanochaita will require
issuance of a threatened species import permit under 50 CFR 17.32,
which will require an enhancement finding (see 4(d) Rule for Panthera
leo melanochaita, above). The import of lions hunted in countries that
do not meet the criteria for enhancement will not be permitted.
(55) Comment: One commenter stated that the Service has failed to
comply with the National Environmental Policy Act (NEPA) in regard to
promulgating the 4(d) rule.
Our Response: 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). Furthermore, under our 1983
policy, we determined that we do not need to prepare an environmental
assessment in connection with regulations adopted under section 4(a) of
the Act, including 4(d) rules that accompany listings of threatened
species.
Because we are listing P. l. melanochaita as threatened and are
finalizing this 4(d) rule simultaneously with our final listing
determination, we consider this 4(d) rule to be part of the listing
determination for the purposes of National Environmental Policy Act
compliance.
(56) Comment: One commenter stated that lions do not lend
themselves to population surveying due to the boom and bust nature and
high fecundity of lion populations. The commenter felt that population
surveys have long been considered impractical, and as such, quotas can
never be set scientifically and, therefore questioned how the Service
can make this a criteria for determining enhancement. Finally, the
commenter was concerned that having countries have an understanding of
lion population numbers and developing lion management plans would be
cost prohibitive to many of the range countries.
Our Response: We are not requiring an exact count of the lions
within each country before being able to make a determination of
whether imports could occur. However, we need to consider what methods
countries are using to establish quotas, such as population trend data,
in order to determine if the offtake by U.S. hunters is sustainable and
meets the criteria under 50 CFR 17.32.
(57) Comment: One commenter stated that lions have an extraordinary
high fecundity, which contributes to its boom or bust population
characteristic and helps ensure its long-term existence, making it far
less vulnerable to endangerment.
Our Response: We agree that lions have high fecundity and in
absence of stressors populations can rapidly increase. However, across
most of its range, the lion is not without stressors, and given the
threats the lion is currently facing, natural fecundity is reduced. One
of the greater stressors on
[[Page 80056]]
lions, excessive harvests of lions for trophies, can negatively impact
the reproduction of a lion such that it causes local extirpations.
Harvesting males that are too young causes male replacements, which
results in increased infanticide rates, death of the surviving male
coalition, and a 100 percent fatality rate for males that are
prematurely forced to disperse. Furthermore, the population will be
driven to extinction as female populations collapse as they eventually
are unable to mate. The species is largely not able to rapidly recover
from population declines. This is evidenced by long-term population
trends that indicate an overall 43 percent decline in lions over 21
years and higher regional rates of decline in western and eastern
Africa.
(58) Comment: One commenter stated that the Service should use its
power to list Distinct Population Segments (DPSs), rather than the
entire African lion subspecies in light of the recent ruling in Humane
Society of the United States v. Jewell, No. CV 13-186 (BAH), 2014 WL
7237702 (D.D.C. Dec. 19, 2014)..
Our Response: We disagree with this conclusion. Pursuant to 50 CFR
17.11(g), all populations are included in the listing.
Required Determinations
National Environmental Policy Act (42 U.S.C. 4321 et seq.)
We have determined that we do not need to prepare an environmental
assessment, as defined under the authority of the National
Environmental Policy Act of 1969, in connection with regulations
adopted under section 4(a) of the Act for the listing, delisting, or
reclassification of species. We published a notice outlining our
reasons for this determination in the Federal Register on October 25,
1983 (48 FR 49244).
References Cited
A list of all references cited in this document is available at
https://www.regulations.gov at Docket No. FWS-R9-ES-2012-0025, or upon
request from the U.S. Fish and Wildlife Service, Endangered Species
Program, Branch of Foreign Species (see FOR FURTHER INFORMATION
CONTACT).
Authors
The primary authors of this rule are staff of the Branch of Foreign
Species, Ecological Services, 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.
Regulation Promulgation
Accordingly, we amend part 17, subchapter B of chapter I, title 50
of the Code of Federal Regulations, as set forth below:
PART 17--[AMENDED]
0
1. The authority citation for part 17 continues to read as follows:
Authority: 16 U.S.C. 1361-1407; 1531-1544; and 4201-4245;
unless otherwise noted.
0
2. Amend Sec. 17.11(h), the List of Endangered and Threatened
Wildlife, by:
0
a. Removing the entry for ``Lion, Asiatic (Panthera leo persica)''; and
0
b. Adding entries for ``Lion (Panthera leo leo)'' and ``Lion (Panthera
leo melanochaita)'' in alphabetic order under Mammals to read as set
forth below:
Sec. 17.11 Endangered and threatened wildlife.
* * * * *
(h) * * *
--------------------------------------------------------------------------------------------------------------------------------------------------------
Species Vertebrate
-------------------------------------------------------- population where Critical Special
Historic range endangered or Status When listed habitat rules
Common name Scientific name threatened
--------------------------------------------------------------------------------------------------------------------------------------------------------
MAMMALS
* * * * * * *
Lion............................. Panthera leo leo.... Africa, Asia....... Entire............. E 862 NA NA
Lion............................. Panthera leo Africa............. Entire............. T 862 NA 17.40(r)
melanochaita.
* * * * * * *
--------------------------------------------------------------------------------------------------------------------------------------------------------
* * * * *
0
3. Amend Sec. 17.40 by adding paragraph (r) to read as follows:
Sec. 17.40 Special rules--mammals.
* * * * *
(r) Lion (Panthera leo melanochaita).
(1) General requirements. All prohibitions and provisions of
Sec. Sec. 17.31 and 17.32 apply to this subspecies.
(2) The import exemption found in Sec. 17.8 for threatened
wildlife listed in Appendix II of the Convention on International Trade
in Endangered Species of Wild Fauna and Flora (CITES) does not apply to
this subspecies. A threatened species import permit under Sec. 17.32
is required for the importation of all specimens of Panthera leo
melanochaita.
(3) All applicable provisions of 50 CFR parts 13, 14, 17, and 23
must be met.
Dated: December 10, 2015.
Daniel M. Ashe,
Director, Fish and Wildlife Service.
[FR Doc. 2015-31958 Filed 12-21-15; 4:15 pm]
BILLING CODE 4333-15-P