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Monday 18 November 2013
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Bird of Paradise
The birds-of-paradise are
members of the family Paradisaeidae of the order Passeriformes. The majority of
species in this family are found on the island of New Guinea and its satellites,
with a few species occurring in the Moluccas and eastern Australia. The family
has forty species in 14 genera. The members of this family are perhaps best
known for the plumage of the males of most species, in particular highly
elongated and elaborate feathers extending from the beak, wings or head. For
the most part they are confined to dense rainforest habitat. The diet of all
species is dominated by fruit and to a lesser extent arthropods. The
birds-of-paradise have a variety of breeding systems, ranging from monogamy to
lek-based polygamy. The family is of cultural importance to the inhabitants of
New Guinea. The trade in skins and feathers of the birds-of-paradise has been
going on for two thousand years. The birds have been of considerable interest
to Western collectors, ornithologists and writers as well. A number of species
are threatened by hunting and habitat loss.
Description
Birds of paradise are
generally crow-like in general body-form, and, indeed, are the brother group to
the corvids (crows and jays). Birds-of-paradise range in size from the King
Bird-of-paradise at 50 g (1.8 oz) and 15 cm (5.9 in) to the Curl-crested
Manucode at 44 cm (17 in) and 430 g (15 oz). The male Black Sicklebill, with
its long tail, is the longest species at 110 cm (43 in). In most of the males
are larger and longer than the female, the differences ranging from slight to
extreme. The wings are rounded and in some species structurally modified on the
males in order to make sound. There is considerable variation in the family
with regard to bill shape. Bills may be long and decurved, as in the
sicklebills and riflebirds, or small and slim like the Astrapias. As with body
size on average bill size varies with sex, although species where the females
have larger bills than the male are more common, particularly in the insect
eating species. For reasons of camouflage plumage of the females typically
blends well with their habitat, unlike the bright attractive colors found on
the males.
Plumage variation between
the sexes is closely related to breeding system. The manucodes and
Paradise-crow, which are socially monogamous, are sexually monomorphic. So are
the two species of Paradigalla, which are polygamous. All these species have
generally black plumage with varying amounts of green and blue iridescence.
Habitat
and distribution
The centre of
bird-of-paradise diversity is the large island of New Guinea; all but two
genera are found in New Guinea. The two that are not are the monotypic genera
Lycocorax and Semiptera, both of which are endemic to the Moluccas, to the west
of New Guinea. Of the riflebirds in the genus Ptiloris, two are endemic to the
coastal forests of eastern Australia, one occurs in both Australia and New
Guinea, and one is only found in New Guinea. The only other genus to have a
species outside New Guinea is Manucodia, one representative of which is found
in the extreme north of Queensland. The remaining species are restricted to New
Guinea and some of the surrounding islands. Many species have highly restricted
ranges, particularly a number of species with restricted habitat types such as
mid-montane forest (like the Black Sicklebill) or island endemics (like the
Wilson's Bird-of-paradise). The majority of birds-of-paradise live in tropical
forests, including rainforest, swamps and moss forest, nearly all of them
solitary tree dwellers. Several species have been recorded in coastal
mangroves. The southernmost species, the Paradise Riflebird of Australia, lives
in sub-tropical and temperate wet forests. As a group the manucodes are the
most plastic in their habitat requirements, with in particular the
Glossy-mantled Manucode inhabiting both forest and open savanna woodland.
Mid-montane habitats are the most commonly occupied habitat, with thirty of the
forty species occurring in the 1000–2000 m altitudinal band.
Behaviour
Diet and feeding
The diet of the
birds-of-paradise is dominated by fruit and arthropods. The ratio of the two
food types varies by species, with fruit predominating in some species, and
arthropods dominating the diet in others. The ratio of the two will affect
other aspects of the behaviour of the species, for example frugivorous species
tend to feed in the forest canopy, whereas insectivores may feed lower down.
Frugivores are more social than the insectivores, which are more solitary and
territorial.
Breeding
Most species have
elaborate mating rituals, with the Paradisaea species using a lek-type mating
system. Others, such as the Cicinnurus and Parotia species, have highly
ritualised mating dances. Males are polygamous in the sexually dimorphic
species, but monogamous in at least some of the monomorphic species.
Hybridisation is frequent in these birds, suggesting the polygamous species of
bird of paradise are very closely related despite being in different genera.
Many hybrids have been described as new species, and doubt remains regarding
whether some forms, such as Rothschild's Lobe-billed Bird of Paradise, are
valid. Despite the presence of hybrids, some ornithologists hypothesise that at
least some putative hybrids are valid species that may be extinct. Birds-of-paradise
build their nests from soft materials, such as leaves, ferns, and vine
tendrils, typically placed in a tree fork. Clutch size is somewhat uncertain.
In the large species, it is almost always just one egg. Smaller species may
produce clutches of 2–3. Eggs hatch after 16–22 days, and the young leave the
nest at between 16 and 30 days of age.
Taxonomy
and systematics
For many years the
birds-of-paradise were treated as being closely related to the bowerbirds.
Today while both are treated as being part of the Australasian lineage Corvida,
the two are now only thought to be distantly related. The closest evolutionary
relatives of the birds-of-paradise are the crow and jay family Corvidae, the
monarch flycatchers Monarchidae and the Australian mudnesters Struthideidae. A
2009 study examining the mitochondrial DNA of all species to examine the
relationships within the family and to its nearest relatives estimated that the
family emerged 24 million years ago, older than previous estimates. The study
identified five clades within the family, and placed the split between the
first clade, which contains the monogamous manucodes and Paradise-crow, and all
the other birds-of-paradise, to be 10 million years ago. The second clade
includes the parotias and the King of Saxony Bird-of-paradise. The third clade
provisionally contains a number of genera, Seleucidis, the Drepanornis
sicklebills, Semioptera, Ptiloris and Lophorina, but support values for some of
these is inclusions is low. The fourth clade includes the Epimachus
sicklebills, Paradigalla and the astrapias. The final clade includes the
Cicinnurus and the Paradisaea birds-of-paradise. The exact limits of the family
have been the subject of revision as well. The three species of satinbird (the
genera Cnemophilus and Loboparadisea) were treated as a subfamily of the
birds-of-paradise, Cnemophilinae. In spite of differences in the mouth, foot
morphology and nesting habits they remained in the family until a 2000 study
moved them to a separate family closer to the berrypeckers and longbills
(Melanocharitidae). The same study found that the Macgregor's Bird-of-paradise
was actually a member of the large Australasian honeyeater family. In addition
to these three species, a number of systematically enigmatic species and genera
have been considered potential members of this family. The two species in the
genus Melampitta, also from New Guinea, have been linked with the
birds-of-paradise, but their relationships remain uncertain, more recently
being linked with the Australian mudnesters. The Silktail of Fiji has been
linked with the birds-of-paradise many times since its discovery, but never
formerly assigned to the family. Recent molecular evidence now places the
species with the fantails.
Sumatran Elephant
The Sumatran Elephant
(Elephas maximus sumatranus) is one of three recognized subspecies of the Asian
Elephant, and native to Sumatra island of Indonesia. In January 2011 the
Sumatran elephant has been classified as critically endangered by IUCN as the
population has declined by at least 80% over the last three generations,
estimated to be about 75 years. The subspecies is pre-eminently threatened by
habitat loss, degradation and fragmentation; over 69% of potential elephant
habitat has been lost within the last 25 years.
Characteristics
In general, Asian
elephants are smaller than African elephants and have the highest body point on
the head. The tip of their trunk has one finger-like process. Their back is
convex or level. Females are usually smaller than males, and have short or no
tusks. Sumatran elephants reach a shoulder height of between 2 and 3.2 m (6.6
and 10.5 ft), weigh between 2,000 and 4,000 kg (4,400 and 8,800 lb), and have
20 pairs of ribs. Their skin color is lighter than of maximus and indicus with
least depigmentation.
Distribution
of populations
The Sumatran elephant was
once widespread on the island, and Riau Province was believed to have the
largest elephant population in Sumatra with over 1,600 individuals in the
1980s. In 1985, an island-wide rapid survey suggested that between 2,800 and
4,800 elephants lived in all eight mainland provinces of Sumatra in 44
populations. Twelve of these populations occurred in Lampung Province, where
only three populations were extant in 2002 according to surveys carried out between
September 2000 and March 2002. The population in Bukit Barisan Selatan National
Park was estimated at 498 individuals, while the population in Way Kambas
National Park was estimated at 180 individuals. The third population in Gunung
Rindingan–Way Waya complex was considered to be too small to be viable over the
long-term.
By 2008, elephants had
become locally extinct in 23 of the 43 ranges identified in Sumatra in 1985,
indicating a very significant decline of the Sumatran elephant population up to
that time. By 2008, the elephant was locally extinct in West Sumatra Province
and at risk of being lost from North Sumatra Province too. In Riau Province
only about 350 elephants survived across nine separate ranges.
Threats
The remaining population
is threatened by habitat loss, poaching, and as a result of conflict with
humans. 65% of Sumatran elephant deaths are because of human
persecution.[citation needed] 30% of this human persecution is through
poisoning because of fear of the animal. 83% of the Sumatran elephant's former
habitat has now been turned into plantations; this means that the elephant has
to learn to adapt to new habitats if it is to live.
Conservation
Elephas maximus is listed
on CITES Appendix I. Sumatran elephants are protected under Indonesia law. In
2004, the Tesso Nilo National Park has been established in Riau province to
protect the Sumatran elephant's habitat. This forest is one of the last areas
large enough to support a viable population of elephants.
In
captivity
In 1986 the Indonesian
government started establishing Elephant Training Centers intended to capture
and train elephants for use in logging, patrol work, and tourism. Currently
there are six provincial centres on 11 separate sites, that hold approximately
400 elephants.
Population
In mid 1980s, when about
50% of natural forest remained on the island, elephant populations persisted in
44 discrete populations on all of the island’s eight provinces (Hedges et al.
2005). 1985: An island-wide rapid survey suggested that between 2,800 and 4,800
elephants lived in the wild in 44 ranges in all eight mainland provinces of
Sumatra (Blouch and Haryanto 1984). Riau Province was believed to have the
largest elephant population in Sumatra. 2002: Sumatra was still thought to
contain some of the largest populations of Asian elephants outside of India and
Sri Lanka. Rigorous dung density based surveys in Lampung Province’s two
national parks, Bukit Barisan Selatan and Way Kambas, produced population
estimates of 498 (95% CI=[373, 666]) and 180 (95% CI=[144, 225]) elephants,
respectively. But province-wide surveys at the same time also showed that by
2002 elephants had gone locally extinct in nine of 12 elephant ranges recorded
in Lampung in the early 1980s (Hedges et. al. 2005).
2007: Guesstimates
suggested that between 2,400 and 2,800 elephants live in the wild (Soehartono
et al. 2007). Given the very high number of elephants brought into captivity
since 1985 (Mikota et al. 2003), the high mortality experienced during these
government capture-and-translocation operations, and the high numbers of
elephants lost to retaliatory killing after human–elephant conflict (WWF 2008)
and poaching (based on local newspaper reports), it is highly likely that
Sumatra’s total elephant population size in 1985 might actually have been
greater than even that year’s high estimate of 4,800 elephants suggests. In any
case, in only one generation (between 1985 and 2007) Sumatra may have lost up
to 50% of its elephants. 2008: By 2008, elephants had become locally extinct in
23 of the 43 ranges identified in Sumatra in 1985, indicating a very
significant decline of the Sumatran elephant population up to that time. By
2008, the elephant was locally extinct in one of Sumatra’s eight mainland provinces
(West Sumatra) and at risk of being lost from North Sumatra Province too. Only
ca. 350 elephants survived across nine separate ranges in Riau Province, which
in 1985 was considered to have the largest elephant population in Sumatra with
over 1,600 individuals.
Post-2008: Simple
extrapolations from past population history suggests that Riau’s last surviving
elephants may soon disappear if the current trend of forest loss continues
(Uryu et al. 2008). Indeed, a 2009 survey of nine forest blocks in Riau that
had elephant herds in 2007 revealed that six herds had gone extinct (Desai and
Samsuardi 2009). Systematic study on the population of Sumatran Elephants is
lacking from most of the elephant’s distributional range. Province-wide
assessments have been conducted in Riau (Desai and Samsuardi 2009) and Lampung
(Hedges et al. 2005). However, rigorous population estimates are only available
from two protected areas in Lampung, namely Way Kambas National Park and Bukit
Barisan Selatan National Park (Hedges et al. 2005, Soehartono et al. 2007). Riau.
Harboring extensive flat lowland forest that is a prime habitat for elephant,
Riau province was one of the strongholds for elephant conservation. However,
elephant numbers in this province dropped by 84% in less than 25 years (Uryu et
al. 2007). The population declined from
ca. 1,342 in 1984 to ca. 210 in 2007. Due to habitat fragmentation, the number
of fragmented elephant populations (“pockets”) increased from nine in 1984 to
16 in 1999. By 2007, mainly due to removal and killings related to conflicts,
elephants were completely extirpated in several “pockets” including Rokan
Hilir, Kerumutan, Koto Panjang, Bukit Rimbang Baling, Tanjung Pauh and Bukit
Suligi. Thorough population estimates are not yet available the latest assessment indicates that all but two of these fragmented elephant
populations are unlikely to survive over the long term. West Sumatra. Elephants
have been completely extirpated from this province.
Lampung. Twelve of the 44
Sumatran elephant populations identified in the mid-1989s occurred in Lampung
Province. But, according to surveys conducted in 2001 and 2002 only three were
still extant in 2002, and one of those was not considered viable (Hedges et al.
2005). Surveys in the early 2000s using dung density based methods in Lampung
Province’s two national parks, Bukit Barisan Selatan and Way Kambas, produced
population estimates of 498 (95% CI=[373, 666]) and 180 (95% CI=[144, 225])
elephants, respectively (Hedges et al. 2005). New field surveys using fecal DNA
based capture–recapture methods are currently underway in the two national
parks (S. Hedges pers comm).
Sumatran Tiger
The Sumatran tiger
(Panthera tigris sumatrae) is a tiger subspecies that inhabits the Indonesian
island of Sumatra and has been classified as critically endangered by IUCN in
2008 as the population is projected to be 441 to 679 individuals, with no
subpopulation having an effective population size larger than 50 individuals,
with a declining trend. The Sumatran tiger is the only surviving member of the
Sunda Islands group of tigers that included the now extinct Bali tiger and
Javan tiger. Sequences from complete mitochondrial genes of 34 tigers support
the hypothesis that Sumatran tigers are diagnostically distinct from mainland
populations.
Characteristics
The Sumatran tiger is the
smallest of the tiger subspecies as compared to the Siberian tiger which is the
largest. Sumatran male tigers average 8 feet (2.438m) in length from head to
tail and weigh about 265 lbs.(120.2 kg). Females average 7 feet (2.134 m) in
length and weigh about 200 lbs (90.718 kg). The smaller size of the Sumatran
tiger makes it easier to move quickly through the jungle. Also, their stripes
are narrower than other tiger species. The tiger's patterned coloring is an
adaptation for camouflage in their natural habitat, which is often tall grass.
The males, especially, have a more bearded and maned appearance in which neck
and cheek hair are well developed. Webbing between their toes, when spread,
enables the Sumatran tiger to be a very fast swimmer. It will, if given the
chance, run hoofed prey, who are much slower swimmers, into the water. The
white spots on the back of the tiger's ears are called "eye spots" or
"predator spots." These spots are believed to function as false eyes
as well as to make it look larger to any predator approaching from behind. This
is particularly helpful in keeping cubs safe.
Genetics
and evolution
Analysis of DNA is
consistent with the hypothesis that Sumatran tigers have been isolated from
other tiger populations after a rise in sea level that occurred at the
Pleistocene to Holocene border (about 12,000-6,000 years ago). In agreement
with this evolutionary history, the Sumatran tiger is genetically isolated from
all living mainland tigers, which form a distinct group closely related to each
other.
The Sumatran tiger
represents a uniquely hopeful opportunity for the survival of an individual
subspecies of tiger in the wild. Specifically, the animal is isolated
geographically to the island of Sumatra in Indonesia. This is important for
many reasons. First, the animal has been genetically isolated. This offers
felid biologists the opportunity to study the effects of such genetic isolation
on a particular subspecies, unlike other surviving subspecies, which until the
beginning of the last century, could roam among and between the realms of
neighboring subspecies.
Wild Sumatran tigers have
survived within the isolated and somewhat continuous political environment of
the Island of Sumatra. This has afforded researchers, such as The Sumatran
Tiger Project team, an opportunity to study these animals' genetic status in
their natural habitat over an extended period of time. As a result, important
first-hand field data has been generated which is relevant to all the surviving
tiger subspecies.
Sumatran tigers are
especially well represented in zoos around the world, most of which participate
in sophisticated global conservation breeding programs. More than 270 Sumatran
tigers are now documented in formal studbooks and are involved in captive
breeding programs aimed at preserving their genetic uniqueness. This captive
population is occasionally supplemented by wild Sumatran tigers, which are
captured when they come into conflict with their surrounding human populations,
or are rescued from situations that preclude them from living in the wild.
Thanks to the presence of a one-of-a-kind research facility at Taman Safari on
the island of Java, these tigers and their extremely rare genes can be
preserved instead of being exterminated like most other problem tigers. Through
an important scientific, community and political collaboration, these tigers
have been spared so that their precious genes may bolster breeding programs for
the Sumatran subspecies.
Unfortunately, the
political stability that has benefited Sumatran tiger research has been
interrupted recently by the violent demise of the Suharto regime. Foreign
nationals conducting tiger-related research in Indonesia were forced to flee
for the sake of their personal safety. The Indonesian researchers left behind
faced tremendous obstacles in perpetuating their delicate work, even to the
point where many of the tigers involved in the conservation breeding program at
Taman Safari could not be properly fed. In a happy turn of events, the civil
unrest associated with the destabilization of the Indonesian political situation
has been largely settled. Negotiations are underway to establish a new
framework for the conservation efforts and scientific research that has been
conducted by The Sumatran Tiger project.
Distribution
and habitat
The Sumatran tiger is
found only on the Indonesian island of Sumatra in habitat that ranges from
lowland forest to sub-mountain and mountain forest including some peat moss
forests. According to the Tiger Information Center and the World Wildlife Fund
there are no more than 500 of these tigers left in the wild with some estimates
considerably lower. Sumatra has undergone much agricultural growth and as a
result, tiger habitat has become fragmented with about 400 tigers inhabiting
five National Parks and two Game Reserves. The largest populations live in the
Kerinci Seblat National Park and Gunung Leuser National Park. Another 100 live
in unprotected areas that will soon be lost to agriculture. The tigers that
live in unprotected areas are very vulnerable to poaching as well as the
killing of problem animals that come in contact with villagers encroaching upon
the animals' habitat.
Ecology
and behaviour
Sumatran tigers commonly
prey on larger ungulates like wild pig, Malayan Tapir, and deer, and sometimes
also smaller animals such as fowl, monkeys, and fish. Orangutans could be prey,
but since they spend a minimal amount of time on the ground, tigers rarely
catch one. Sumatran tigers will sometimes prey upon mice and other small
mammals when larger prey is scarce.
Threats
The continuing loss of
habitat is intensifying the crises to save this tiger. Deforestation resulting
from the production of palm oil is a major threat to the Sumatran Tiger.[4] The
reserves also do not provide safety, as many tigers are killed by poachers each
year despite conservation efforts. Sun bears and sloth bears have been known to
be very dangerous opponents for tigers in lower asian countries. They have
overwhelmed tigers on ocassions.
Conservation
In 2006 the Indonesia
Forestry Service, the Natural Resources and Conservational Agency (BKSDA) and
the Sumatran Tiger Conservation Program sat down with commercial concession
holders and Asia Pulp & Paper and set the foundations for the Senepis
Buluhala Tiger Sanctuary, an area that covered 106,000 hectares in Riau by
2008. These organizations formed The Tiger Conservation Working Group with
other interested parties and the project is recognised as a pioneering
initiative. Current studies include the identifying of feeding behavior of
tigers to develop strategies that will help protect both tigers and human
settlements.
In 2007, the Indonesian
Forestry Ministry and Safari Park established cooperation with the Australia
Zoo for the conservation of Sumatran Tigers and other endangered species. The
cooperation agreement was marked by the signing of a Letter of Intent on
'Sumatran Tiger and other Endangered Species Conservation Program and the
Establishment of a Sister Zoo Relationship between Taman Safari and Australia
Zoo' at the Indonesian Forestry Ministry office on July 31, 2007. The program
includes conserving Sumatran Tigers and other endangered species in the wild,
efforts to reduce conflicts between tigers and humans and rehabilitating
Sumatran Tigers and reintroducing them to their natural habitat.
The Tambling Wildlife
Nature Conservation with a rehabilitation center has been set up in a 110,000
acre conservation area abutting a national park on the southern tip of Sumatra
(Lampung).[5] On October 26, 2011 a tigress which had been captured with an
injured leg in early October delivered three male cubs in a temporary cage,
while waiting for release after its recovery.
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