Père David's Deer


Adult males (stags) do bear antlers and, unusually, there may be two pairs of antlers per year. The summer antlers are the larger set, and are dropped in November following the rutting season. The second set then appear in January and are lost a few weeks later. Unique among deer, this species has antlers with a main branched anterior segment, with the points extending backwards. This deer’s summer coat is reddish tan in colour and becomes woollier and dark grey in the winter. The underside is a cream colour and along the spine there is also a distinctive darker stripe. Juveniles are spotted with pale flecks.


 Did You Know

           This species of deer was first made known to Western science in 1866 by Armand David (Père David), a French missionary working in China. He obtained the carcasses of an adult male, an adult female and a young male, and sent them to Paris, where the species was named Père David's Deer by Alphonse Milne-Edwards, a French biologist.

Scientific Classification

Kingdom
Animalia
Phylum
Chordata
Class
Mammalia
Order
Cetartiodactyla
Family
Cervidae
Genus
Elaphurus
Species
davidianus

Other Names

English
Pere David's deer
French
Père David's deer
Chinese
Sibuxiang

Status

           This species is listed as Extinct in the Wild, as all populations are still under captive management. The captive population in China has increased in recent years, and the possibility remains that free-ranging populations can be established sometime in the near future.


Population

           The first conservation reintroduction of Pere David’s deer to China included two groups, of 20 deer (5 males: 15 females) and 18 deer (all females), in 1985 and 1987, respectively. All 38 deer were donated by the Marques of Tavistock of Woburn Abbey, and the transportation was sponsored by the World Wildlife Fund (WWF). The second re-introduction was carried out in August of 1986, organized by former Ministry of Forestry and WWF. A group of 39 Pere David’s deer was selected from five zoological gardens in the United Kingdom.


By the end of calving season of 2006, there were 522 E. davidianus in the Tianezhou Milu National Nature Reserve. The annual average population growth rate was 22.2%. The birth rate and population growth rate in Tianezhou were significantly higher whereas the mortality rate was significantly lower than those of the Dafeng. Currently, there are a total of 53 herds in China. Nine herds have fewer than 25 deer, 75.5% have fewer than 10 deer.

Habitat

           Studies have been carried out on the behavior, ecology and reproduction of Pere David’s deer in Beijing since 1985, in Dafeng since 1986, and in Tianezhou since 2001. This species lives in low-lying grasslands and reed beds, often in seasonally flooded areas such as the lower Yangtze River valley and coastal marshes.


Range

           During the Holocene, Pere David's deer was restricted to swamps and wetlands in the region south of 43°N and east of 110°E in mainland China. However, the distribution shrank and its population declined due to hunting and land reclamation in the swamp areas as human population expanded. Pere David's deer had largely disappeared in the wild by the late 19th century, and the last wild animal was shot near the Yellow Sea in 1939.


However, during the Qing Dynasty (1616-1911), the Nanyuang Royal Hunting Garden contained a herd of Pere David's deer in its 200 km² hunting ground. This hunting garden in the southern suburbs of Beijing was predominantly a wetland, consisting of swamps, ponds and lakes crossed by the Yongding River. However, before the demise of the royal herd of Père David’s deer in the Nanyuan Royal Hunting Garden in 1900, the deer had been introduced into private deer collections in the United Kingdom, France and Germany.

Biology

          Since this deer is so rare in the wild, the only observations of its behaviour come from captive populations. It eats grass, reeds and leaves of bushes, can swim well, and spend long periods in water. It lives in single sex ormaternal herds. Animals reach maturity during second year. This species is social and lives in large herds, except before and after the breeding season, or 'rut', in June. At these times males leave the herd to feed intensively and build up strength, and before the rut, females bunch together in several groups.


 A stag joins each group of females and engages in fights with rival males using its antlers, teeth and forelegs. The successful stags win dominance and, as the fittest males, are able to mate with the females. During the rutting season males do not feed, as every moment is spent trying to establish dominance over other males. Therefore, after leaving the females, males will begin feeding again and quickly regain weight. Gestation is 270-300 days. One, rarely two young are born. These are weaned in 10-11 months. Adults live up to 18 years. Data from the Dafeng Reserve suggests that female E. davidianus establish a home range of approximately 1 km².


Threats

As inhabitants of open marshland and plains, this deer was easily hunted and suffered huge population losses. In the late 19th century, the world's only herd belonged to Tongzhi, the Emperor of China. The herd was maintained in the Nanyuang Royal Hunting Garden in Nan Haizi, near Peking. In 1895, one of the walls of the hunting garden was destroyed by a heavy flood of the Yongding River, and most of the animals escaped and were killed and eaten by starving peasants. Fewer than thirty Père David's Deer remained in the garden. Then in 1900, during the Boxer Rebellion, the garden was occupied by troops and the remaining deer were shot and eaten, leaving the animal extinct in its native China.


Conservation Measures

           It is listed on the Chinese Red List as Extinct in the Wild, and on the China Key List - I.  Pere David, a French missionary, became fascinated by these animals and persuaded the Emperor to allow some deer to be sent to Europe. Shortly after this, in May 1865, there were catastrophic floods in China, killing the entire population of Pere David’s deer. Fortunately the captive populations in Europe bred well, and in 1986 a small group of 39 individuals was reintroduced to the Dafeng Nature Reserve in China.



The present reintroduced population within the Dafeng Nature Reserve is contained within enclosures, where it is subject to captive management and is protected from hunting. Over the years, this population has increased in numbers, and it is hoped that at some point in the future, a free-ranging population could be established in China. This species was saved from the brink of extinction and is making a slow but steady recovery. It is, however, dependant on conservation measures and captive management and so it is essential that these efforts are continued.

References

The Saiga Antelope


            Saiga antelope have an extremely distinctive appearance with an enlarged nose that hangs down over the mouth. Despite their common name these ungulates are thought to be intermediates between antelope and sheep. The coat is sparse and cinnamon-buff in the summer but becomes white and around 70 percent thicker in winter. The underbelly is light in colour throughout the year, and there is a small mane on the underside of the neck. Mature males have almost vertical horns; these are semi translucent and are ringed in the bottom sections.

            The saiga typically stands 0.6–0.8 m (1 ft 10 in–2 ft 7 in) at the shoulder and weighs between 36 and 63 kg (79 and 140 lb). The horned males are larger than the polled females. Their lifespans range from 6 to 10 years. The saiga is recognizable by an extremely unusual, over-sized, flexible nose structure, the proboscis.


Did You Know

            The saiga antelope is active mostly during the day, although it may rest at midday.  A nomadic species, saiga have no fixed home ranges and usually walk several dozen kilometers in a given day.  The saiga is an extremely good runner, and is able to reach speeds up to 80 kmph / 48 mph.  Populations undertake seasonal migrations, moving north in the spring to the summer grazing grounds, and returning southward in the fall. Covering 80-120 km / 48-72 miles per day, saiga march with their heads low to the ground, with their specialized noses filtering out the stirred up dust from the air.


Scientific Classification

Kingdom
Animalia
Phylum
Chordata
Class
Mammalia
Order
Cetartiodactyla
Family
Bovidae
Genus
Saiga
Species
tatarica

Other Names

English
Saiga Antelope
French
Saïga
Spanish
Antílope Saiga

Status

            Classified as Critically Endangered (CR) on the IUCN Red List 2007, and listed on Appendix II of CITES. It is also listed on Appendix II of the Convention on the Conservation of Migratory Species (CMS or Bonn Convention). Subspecies: Mongolian saiga (Saiga tatarica mongolica) classified as Endangered (EN) and the Russian saiga (S. t. tatarica) is Critically Endangered (CR) on the IUCN Red List 2007.


Population

            Historically, this was a common species in Eurasian steppes and semi-deserts. From information provided in recent references it appears that between 1991 and 1994, the global population of S. tatarica was relatively stable at just under one million animals, the majority of which were in Kazakhstan (approximately 810,00–825,000). However, the population in Kazakhstan had fallen to around 570,000 animals by 1998.


            In European Russia (Kalmykia), the Saiga population steeply declined after land reclamation of the Volga basin started, but the species remained numerous within the distribution area. In the 1970s the population recovered to ca.700,000–800,000 as a result of hunting regulation. However, since then the population has drastically declined. In 1980 there were an estimated 380,000 individuals, in 1996 there were 196,000, and by 2000 just 26,000. 2001 for annual survey results for 1980–2000). At present there are no more than 18,000 animals in Kalmykia. Sex ratio is severely skewed; the proportion of males varies from 1 to 10% in different years.

Habitat

            Saigas typically inhabit open dry steppe and semi desert grasslands of Central Asia and Pre-Caspian region. They prefer open areas free from dense vegetation where they can avoid predators such as wolves and humans.


Range

            Saiga tatarica inhabited the steppes and semi-desert regions of south-eastern Europe and Central Asia from the Precaspian steppes to Mongolia and western China. Currently, there is one population in Russia (Kalmykia) and three in Kazakhstan, although in winter some animals reach Uzbekistan and even northern Turkmenistan. A distinctive subspecies occurs in western Mongolia. Saiga became extinct in China by the 1960s, and in Ukraine in the 18th century.


Biology

            Saiga is nomadic animals and undertakes seasonal migrations from summer pastures in steppe grassland to winter pastures in desert areas. Large groups of saiga migrate southwards to the winter grounds, covering up to 72 miles in a day. The rut begins in late November and males gather groups of around 30 females in ‘harems’, which they defend aggressively. During the rut, males’ noses swell up and the hair tufts below the eyes are covered in a sticky secretion. Males do not feed much during the rutting season, when they take part in violent fights that often end in death. The male mortality rate can reach 90 percent during this time, due to exhaustion. Surviving males begin to migrate north at the end of April.


            Females give birth at this time, usually to two young, which are initially concealed in vegetation; all the females within the herd will give birth within a week of each other. Once the calves are a few days old, the whole herd breaks into smaller herds which head northwards to the summer feeding grounds. Once there, smaller groups break off, reforming again for the journey south the following autumn.


            Saiga grazes on a number of different grasses, herbs and shrubs. The unusual swollen nose is thought to filter out airborne dust during the dry summer migrations and to enable cold winter air to be warmed before it reaches the lungs.

Threats

            All the saiga populations have suffered from habitat degradation, poaching and disturbance. Droughts or severe winters, diseases and predation pressure from wolves can also act as threats of saiga populations, although these are unlikely to be major causes of the decline.

            Saiga within the former Soviet Union was the subject of concerted conservation programmes, so much so that the population reached almost one million individuals. Management of the species has now broken down however and illegal poaching is rife. Saiga horns are highly valued in traditional Chinese medicine as cures for illnesses such as strokes. Only the males of the species bear horns and poaching thus produces a population where there are far more females than males. The average life span of saiga is only around three to four years and if females do not mate every year the species can rapidly decline.


            Another main cause of the saiga's decline is the overgrazing of its pastures, general habitat degradation and construction of roads and canals. Before 1991 numbers of livestock, particularly sheep increased enormously. As a result the quality of the pastures for saiga has deteriorated

Conservation Measures

            The saiga antelope’s listing on Appendix II of the Convention on International Trade in Endangered Species (CITES) means that any trade in this species should be carefully monitored. Hunting is banned throughout the saiga’s range. Further research into saiga reproductive behaviour is needed to assess the impact of hunting and this may be used to produce an effective conservation action plan.


            In order to conserve this species, protected areas for lambing and rutting should be established where saiga populations are present. Given that poaching for domestic consumption is now a major threat, strengthening of anti-poaching law enforcement is crucial. It is considered to be more important to fund national conservation action than to improve the international trade control

References

http://en.wikipedia.org/wiki/Saiga_antelope
http://www.fws.gov/international/animals/saiga-antelope.html
http://www.edgeofexistence.org/mammals/species_info.php?id=62
http://www.ultimateungulate.com/artiodactyla/saiga_tatarica.html
http://kids.nationalgeographic.co.in/kids/stories/animalsnature/saiga/
http://wwf.panda.org/what_we_do/endangered_species/saiga_antelope/

The Himalayan Monal



            A stunningly colourful member of the pheasant family, the Himalayan monal is the national bird of Nepal. The iridescent rainbow-like plumage of the male is surpassed only by the slightly larger Chinese monal (Lophophorus lhuysii). The male Himalayan monal possesses a wiry, metallic green head-crest that is absent in other monal species, as well as a chestnut brown tail, light brown wings and a white rump that is visible in flight. The head is bright green, the eyes ringed with blue and the neck reddish brown. At the nape of the neck is a yellow patch which forms the top edge of the bluish black wings and the purplish black back. The breast is dark brown and the tail feathers are light brown.


            Females do not share the same splendour as males, with overall dark brown feathers, except for a white throat and rump patch, and the bright blue circle around the eyes. The female also has a crest, but whereas the male’s is green and has spoon-shaped feathers, the female’s is shorter, and brown with ordinary feathers.


Did You Know
            The Himalayan Monal undertakes an annual migration, but to a lesser degree. During winter this species can be located at the lower end of its altitude distribution. The Western Tragopan and the Himalayan Monal occupy the same blocks of forest and can be observed together throughout the year. It is unlikely that there is a high degree of competition as their feeding and nesting biology differs slightly, permitting the two species to co-inhabit.



Scientific Classification

Kingdom
Animalia
Phylum
Chordata
Class
Aves
Order
Galliformes
Family
Phasianidae
Genus
Lophophorus
Species
L. impejanus

Other Names
English
Himalayan Monal
Local Name
Impeyan Pheasant

Status
                     Classified as Least Concern (LC) on the IUCN Red List 2006 and listed on Appendix I of CITES.

Population
           The population size has not been quantified, but it is not believed to approach the thresholds for Vulnerable under the population size criterion (<10,000 mature individuals with a continuing decline estimated to be >10% in ten years or three generations, or with a specified population structure). For these reasons the species is evaluated as Least Concern.


Habitat
            During the summer months, the Himalayan monal ventures above the tree-line to wander on the grassy slopes, but during winter it is found in coniferous and mixed forests with a high proportion of rhododendrons and bamboo, where it shelters from the weather. It is a high-altitude species, remaining between 2,100 and 4,500 metres above sea level



Range
            Found in the Himalayas from eastern Afghanistan to Bhutan, northeast India and southern Tibet; the Himalayan monal has also been reported from Burma.
           

Biology
            A highly communicative bird, the Himalayan monal uses several different call types to express meaning to its mate, other birds in its foraging group, or intruding birds. Males also use body displays to attract females; bobbing the head-crest and fanning their tail feathers. The breeding season begins in April when the monals are at higher altitudes. The male switches from calling only in the early morning to calling throughout the day. 


              Once a female notices his display they mate and shortly afterwards she scrapes a nest in the ground and lays between three and five eggs. The female must incubate the eggs alone, but the male will stand guard throughout the 27-day incubation period and until fledging to protect the eggs and chicks from predators. After six months the young are completely independent and must search for food and mates alone.


            Like many of the pheasants, quails and partridges in the Phasianidae family, the Himalayan monal has very strong legs and a long, curved beak which together enable it to dig into the hard soil of the mountains to uncover seeds, tubers, shoots, berries, and insects. This method of foraging leaves conspicuous areas of turned over soil up to 25 cm deep on hillsides



Threats
            The specific requirements of the Himalayan monal make it important to conserve its habitat, but currently this beautiful bird is not seriously threatened. In many parts of its range tree harvesting takes place and additionally this pheasant is hunted for food. It is also hunted for the colourful plumes of its headdress by the inhabitants of Kulu Valley, but this practice appears to have declined significantly in the last ten years. For now the Himalayan monal is not facing any serious threat.


Conservation Measures
            The Himalayan monal’s status as the national bird of Nepal helps to raise awareness of this stunning bird and its needs, and it is hoped that this may keep the species safe in the future. It is currently common and has been recorded in many protected areas in its range, as well as many areas that are not suffering degradation. It is listed on Appendix I of the Convention on International Trade in Endangered Species of Fauna and Flora which prevents unlicensed export of the species or its body parts. This listing prevents the possibility that such an extraordinary bird might find popularity as a pet


References
http://en.wikipedia.org/wiki/Himalayan_Monal
http://www.birdlife.org/datazone/speciesfactsheet.php?id=243
http://www.arkive.org/himalayan-monal/lophophorus-impejanus/
http://www.gbwf.org/pheasants/monal.html
http://whozoo.org/Intro2003/AprilStJ/AS_himalayanMonalfinal.html