Bongo | |
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Western/lowland bongo at the Marwell Zoo in Hampshire, England | |
An eastern/mountain bongo at the Jacksonville Zoo, Jacksonville, Duval County | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Mammalia |
Order: | Artiodactyla |
Family: | Bovidae |
Subfamily: | Bovinae |
Genus: | Tragelaphus |
Species: | T. eurycerus |
Binomial name | |
Tragelaphus eurycerus (Ogilby, 1837) | |
Subspecies | |
| |
Lowland bongo range | |
Mountain bongo range |
The bongo (Tragelaphus eurycerus) is a large, mostly nocturnal, forest-dwelling antelope, native to sub-Saharan Africa. Bongos are characterised by a striking reddish-brown coat, black and white markings, white-yellow stripes, and long slightly spiralled horns. It is the only tragelaphid in which both sexes have horns. Bongos have a complex social interaction and are found in African dense forest mosaics. They are the third-largest antelope in the world. [3]
The western or lowland bongo, T. e. eurycerus, faces an ongoing population decline, and the IUCN Antelope Specialist Group considers it to be Near Threatened on the conservation status scale. [2]
The eastern or mountain bongo, T. e. isaaci, of Kenya, has a coat even more vibrant than that of T. e. eurycerus. The mountain bongo is only found in the wild in a few mountain regions of central Kenya. This bongo is classified by the IUCN Antelope Specialist Group as Critically Endangered, with fewer individuals in the wild than in captivity (where it breeds readily). [4]
In 2000, the Association of Zoos and Aquariums in the USA (AZA) upgraded the bongo to a Species Survival Plan participant and in 2006 added the Bongo Restoration to Mount Kenya Project to its list of the Top Ten Wildlife Conservation Success Stories of the year. However, in 2013, it seems, these successes have been compromised by reports of possibly only 100 mountain bongos left in the wild due to logging and poaching.
Phylogenetic relationships of the mountain nyala from combined analysis of all molecular data (Willows-Munro et.al. 2005) |
The scientific name of the bongo is Tragelaphus eurycerus, and it belongs to the genus Tragelaphus and family Bovidae. It was first described by Irish naturalist William Ogilby in 1837. [5] The generic name Tragelaphus is composed of two Greek words: trag-, meaning a goat; and elaphos, meaning deer. [6] The specific name eurycerus originated from the fusion of eurus (broad, widespread) and keras (an animal's horn). [7] The common name "bongo" originated probably from the Kele language of Gabon. The first known use of the name "bongo" in English dates to 1861. [8]
Bongos are further classified into two subspecies: T. e. eurycerus, the lowland or western bongo, and the far rarer T. e. isaaci, the mountain or eastern bongo, restricted to the mountains of Kenya only. The eastern bongo is larger and heavier than the western bongo. Two other subspecies are described from West and Central Africa, but taxonomic clarification is required. They have been observed to live up to 19 years. [9]
Bongos are one of the largest of the forest antelopes. In addition to the deep chestnut colour of their coats, they have bright white stripes on their sides to help with camouflage.
Adults of both sexes are similar in size. Adult height is about 1.1 to 1.3 m (3.6 to 4.3 ft) at the shoulder and length is 2.15 to 3.15 m (7.1 to 10.3 ft), including a tail of 45–65 cm (18–26 in). Females weigh around 150–235 kg (331–518 lb), while males weigh about 220–405 kg (485–893 lb). Its large size puts it as the third-largest in the Bovidae tribe of Strepsicerotini, behind both the common and greater eland by about 300 kg (660 lb), and above the greater kudu by about 40 kg (88 lb). [10] [11]
Both sexes have heavy spiral horns; those of the male are longer and more massive. All bongos in captivity are from the isolated Aberdare Mountains of central Kenya.
The bongo sports a bright auburn or chestnut coat, with the neck, chest, and legs generally darker than the rest of the body, especially in males. Coats of male bongos become darker as they age until they reach a dark mahogany-brown colour. Coats of female bongos are usually more brightly coloured than those of males. The eastern bongo is darker in color than the western and this is especially pronounced in older males which tend to be chestnut brown, especially on the forepart of their bodies.
The smooth coat is marked with 10–15 vertical white-yellow stripes, spread along the back from the base of the neck to the rump. The number of stripes on each side is rarely the same. It also has a short, bristly, brown ridge of dorsal hair from the shoulder to the rump; the white stripes run into this ridge.
A white chevron appears between the eyes, with two large white spots on each cheek. Another white chevron occurs where the neck meets the chest. Bongos have no special secretion glands, so rely likely less on scent to find one another than do other similar antelopes. The lips of a bongo are white, topped with a black muzzle.
Bongos have two heavy and slightly spiralled horns that slope over their backs. Bongo males have larger backswept horns, while females have smaller, thinner, and more parallel horns. The size of the horns range between 75 and 99 cm (29.5 and 39 in). The horns of bongos are spiraled, and share this trait with those of the related antelope species of nyalas, sitatungas, bushbucks, kudus, and elands. The horns of bongos twist once.
Unlike deer, which have branched antlers shed annually, bongos and other antelopes have unbranched horns they keep throughout their lives.
Like all other horns of antelopes, the core of a bongo's horn is hollow and the outer layer of the horn is made of keratin, the same material that makes up human fingernails, toenails, and hair. The bongo runs gracefully and at full speed through even the thickest tangles of lianas, laying its heavy spiralled horns on its back so the brush cannot impede its flight. Bongos are hunted for their horns by humans. [12]
Like other forest ungulates, bongos are seldom seen in large groups. Males, called bulls, tend to be solitary, while females with young live in groups of six to eight. Bongos have seldom been seen in herds of more than 20. Gestation is about 285 days (9.5 months), with one young per birth, and weaning occurs at six months. Sexual maturity is reached at 24–27 months. The preferred habitat of this species is so dense and difficult to operate in, that few Europeans or Americans observed this species until the 1960s. As young males mature and leave their maternal groups, they most often remain solitary, although rarely they join an older male. Adult males of similar size/age tend to avoid one another. Occasionally, they meet and spar with their horns in a ritualised manner and it is rare for serious fights to take place. However, such fights are usually discouraged by visual displays, in which the males bulge their necks, roll their eyes, and hold their horns in a vertical position while slowly pacing back and forth in front of the other male. They seek out females only during mating time. [13] When they are with a herd of females, males do not coerce them or try to restrict their movements as do some other antelopes.
Although mostly nocturnal, they are occasionally active during the day. However, like deer, bongos may exhibit crepuscular behaviour. [14] Bongos are both timid and easily frightened; after a scare, a bongo moves away at considerable speed, even through dense undergrowth. Once they find cover, they stay alert and face away from the disturbance, but peek every now and then to check the situation. [9] The bongo's hindquarters are less conspicuous than the forequarters, and from this position the animal can quickly flee.
When in distress, the bongo emits a bleat. It uses a limited number of vocalisations, mostly grunts and snorts; females have a weak mooing contact-call for their young. Females prefer to use traditional calving grounds restricted to certain areas, while newborn calves lie in hiding for a week or more, receiving short visits by the mother to suckle. [15]
The calves grow rapidly and can soon accompany their mothers in the nursery herds. Their horns grow rapidly and begin to show in 3.5 months. They are weaned after six months and reach sexual maturity at about 20 months.
Bongos are found in tropical jungles with dense undergrowth up to an altitude of 4,000 m (13,000 ft) in Central Africa, with isolated populations in Kenya, and these West African countries: Cameroon, the Central African Republic, the Republic of the Congo, the Democratic Republic of Congo, the Ivory Coast, Equatorial Guinea, Gabon, Ghana, Guinea, Liberia, Sierra Leone, South Sudan.
Historically, bongos are found in three disjunct parts of Africa: East, Central, and West. Today, all three populations' ranges have shrunk in size due to habitat loss for agriculture and uncontrolled timber cutting, as well as hunting for meat.
Bongos favour disturbed forest mosaics that provide fresh, low-level green vegetation. Such habitats may be promoted by heavy browsing by elephants, fires, flooding, tree-felling (natural or by logging), and fallowing. Mass bamboo die-off provides ideal habitat in East Africa. They can live in bamboo forests.
Like many forest ungulates, bongos are herbivorous browsers and feed on leaves, bushes, vines, bark (bark and pith of rotting trees, grasses/herbs, roots, cereals, and fruits.
Bongos require salt in their diets, and are known to regularly visit natural salt licks. Bongos are also known to eat burnt wood after a storm, as a rich source of salt and minerals. [16] [17] This behavior is believed to be a means of getting salts and minerals into their diets. This behavior has also been reported in the okapi. Another similarity to the okapi, though the bongo is unrelated, is that the bongo has a long prehensile tongue which it uses to grasp grasses and leaves.
Suitable habitats for bongos must have permanent water available. [18] As a large animal, the bongo requires an ample amount of food, and is restricted to areas with abundant year-round growth of herbs and low shrubs.
Few estimates of population density are available. Assuming average population densities of 0.25 animals per km2 in regions where it is known to be common or abundant, and 0.02 per km2 elsewhere, and with a total area of occupancy of 327,000 km2, a total population estimate of around 28,000 is suggested. Only about 60% are in protected areas, suggesting the actual numbers of the lowland subspecies may only be in the low tens of thousands. In Kenya, their numbers have declined significantly and on Mount Kenya, they were extirpated within the last decade due to illegal hunting with dogs. Although information on their status in the wild is lacking, lowland bongos are not presently considered endangered.
Bongos are susceptible to diseases such as rinderpest, which almost exterminated the species during the 1890s. Tragelaphus eurycerus may suffer from goitre. Over the course of the disease, the thyroid glands greatly enlarge (up to 10 x 20 cm) and may become polycystic. Pathogenesis of goiter in the bongo may reflect a mixture of genetic predisposition coupled with environmental factors, including a period of exposure to a goitrogen. [19] Leopards and spotted hyenas are the primary natural predators (lions are seldom encountered due to differing habitat preferences); pythons sometimes eat bongo calves. Humans prey on them for their pelts, horns, and meat, with the species being a common local source for "bush meat". [5] Bongo populations have been greatly reduced by hunting, poaching, and animal trapping, although some bongo refuges exist.
Although bongos are quite easy for humans to catch using snares, many people native to the bongos' habitat believed that if they ate or touched bongo, they would have spasms similar to epileptic seizures. Because of this superstition, bongos were less harmed in their native ranges than expected. However, these taboos are said no longer to exist, which may account for increased hunting by humans in recent times.
An international studbook is maintained to help manage animals held in captivity. Because of its bright colour, it is very popular in zoos and private collections. In North America, over 400 individuals are thought to be held, a population that probably exceeds that of the mountain bongo in the wild.
In 2000, the Association of Zoos and Aquariums (AZA) upgraded the bongo to a Species Survival Plan participant, which works to improve the genetic diversity of managed animal populations. The target population for participating zoos and private collections in North America is 250 animals. Through the efforts of zoos in North America, a reintroduction to the population in Kenya is being developed.
At least one collaborative effort for reintroduction between North American wildlife facilities has already been carried out. In 2004, 18 eastern bongos born in North American zoos gathered at White Oak Conservation in Yulee, Florida for release in Kenya. White Oak staff members traveled with the bongos to a Mount Kenya holding facility, where they stayed until being reintroduced. [20]
In the last few decades, a rapid decline in the numbers of wild mountain bongo has occurred due to poaching and human pressure on their habitat, with local extinctions reported in Cherangani and Chepalungu hills, Kenya.
The Bongo Surveillance Programme, working alongside the Kenya Wildlife Service, have recorded photos of bongos at remote salt licks in the Aberdare Forests using camera traps, and, by analyzing DNA extracted from dung, have confirmed the presence of bongo in Mount Kenya, Eburru, and Mau forests. The programme estimate as few as 140 animals left in the wild – spread across four isolated populations. Whilst captive breeding programmes can be viewed as having been successful in ensuring survival of this species in Europe and North America, the situation in the wild has been less promising. Evidence exists of bongo surviving in Kenya. However, these populations are believed to be small, fragmented, and vulnerable to extinction.
Animal populations with impoverished genetic diversity are inherently less able to adapt to changes in their environments (such as climate change, disease outbreaks, habitat change, etc.). The isolation of the four remaining small bongo populations, which themselves would appear to be in decline, means a substantial amount of genetic material is lost each generation. Whilst the population remains small, the impact of transfers will be greater, so the establishment of a "metapopulation management plan" occurs concurrently with conservation initiatives to enhance in situ population growth, and this initiative is both urgent and fundamental to the future survival of mountain bongo in the wild.
The western/lowland bongo faces an ongoing population decline as habitat destruction and hunting pressures increase with the relentless expansion of human settlement. Its long-term survival will only be assured in areas which receive active protection and management. At present, such areas comprise about 30,000 km2, and several are in countries where political stability is fragile. So, a realistic possibility exists whereby its status could decline to Threatened in the near future.
As the largest and most spectacular forest antelope, the western/lowland bongo is both an important flagship species for protected areas such as national parks, and a major trophy species which has been taken in increasing numbers in Central Africa by sport hunters during the 1990s. [21] Both of these factors are strong incentives to provide effective protection and management of populations. [22]
Trophy hunting has the potential to provide economic justification for the preservation of larger areas of bongo habitat than national parks, especially in remote regions of Central Africa, where possibilities for commercially successful tourism are very limited. [21]
The eastern/mountain bongo's survival in the wild is dependent on more effective protection of the surviving remnant populations in Kenya. If this does not occur, it will eventually become extinct in the wild. The existence of a healthy captive population of this subspecies offers the potential for its reintroduction. [23]
In 2004, Dr. Jake Veasey, the head of the Department of Animal Management and Conservation at Woburn Safari Park and a member of the European Association of Zoos and Aquariums Population Management Advisory Group, with the assistance of Lindsay Banks, took over responsibility for the management and coordination of the European Endangered Species Programme for the eastern bongo. This includes some 250 animals across Europe and the Middle East.
Along with the Rothschild giraffe, the eastern bongo is arguably one of the most threatened large mammals in Africa, with recent estimates numbering less than 140 animals, below a minimum sustainable viable population. The situation is exacerbated because these animals are spread across four isolated populations. Whilst the bongo endangered species program can be viewed as having been successful in ensuring survival of this species in Europe, it has not yet become actively involved in the conservation of this species in the wild in a coordinated fashion. The plan is to engage in conservation activities in Kenya to assist in reversing the decline of the eastern bongo populations and genetic diversity in Africa, and in particular, applying population management expertise to help ensure the persistence of genetic diversity in the free ranging wild populations.
To illustrate significance of genetic diversity loss, assume the average metapopulation size is 35 animals based on 140 animals spread across four populations (140/4=35). Assuming stable populations, these populations will lose 8% of their genetic diversity every decade. By managing all four populations as one, through strategic transfers, gene loss is reduced from 8% to 2% per decade, without any increase in bongo numbers in Kenya. By managing the European and African populations as one – by strategic exports from Europe combined with in situ transfers, gene loss is reduced to 0.72% every 100 years, with both populations remaining stable. If populations in Kenya are allowed to grow through the implementation of effective conservation, including strategic transfers, gene loss can be effectively halted in this species and its future secured in the wild.
The initial aims of the project are:
If effective protection were implemented immediately and bongo populations allowed to expand without transfers, then this would create a bigger population of genetically impoverished bongos. These animals would be less able to adapt to a dynamic environment. Whilst the population remains small, the impact of transfers will be greater. For this reason, the 'metapopulation management plan' must occur concurrently with conservation strategies to enhance in situ population growth. This initiative is both urgent and fundamental to the future survival of the mountain bongo in the wild.
In 2013, SafariCom telecommunications donated money to the Bongo Surveillance Programme [24] to try to keep tabs on what are thought to be the last 100 eastern bongos left in the wild in the Mau Eburu Forest in central Kenya, whose numbers are still declining due to logging of their habitat and illegal poaching. [25]
Mount Kenya Wildlife Conservancy runs a bongo rehabilitation program in collaboration with the Kenya Wildlife Service. [26] The Conservancy aims to prevent extinction of the bongo through breeding and release back into the wild. [27] [28]
The IUCN Antelope Specialist Group considers the western or lowland bongo, T. e. eurycerus, to be Lower Risk (Near Threatened) [2] and the eastern or mountain bongo, T. e. isaaci, of Kenya, to be Critically Endangered. [4] These bongos may be endangered due to human environmental interaction, as well as hunting and illegal actions towards wildlife.
CITES lists bongos as an Appendix III species, only regulating their exportation from a single country, Ghana. It is not protected by the US Endangered Species Act and is not listed by the USFWS.
Bovines comprise a diverse group of 10 genera of medium to large-sized ungulates, including cattle, bison, African buffalo, water buffalos, and the four-horned and spiral-horned antelopes. The evolutionary relationship between the members of the group is still debated, and their classification into loose tribes rather than formal subgroups reflects this uncertainty. General characteristics include cloven hooves and usually at least one of the sexes of a species having true horns. The largest extant bovine is the gaur.
The lowland nyala or simply nyala is a spiral-horned artiodactyl antelope native to Southern Africa. The species is part of the family Bovidae and the genus Tragelaphus. It was first described in 1849 by George French Angas and exhibits the highest sexual dimorphism among the spiral-horned antelopes. It is not to be confused with the endangered mountain nyala living in the Bale region of Ethiopia.
The sitatunga or marshbuck is a swamp-dwelling medium-sized antelope found throughout central Africa, centering on the Democratic Republic of the Congo, the Republic of the Congo, Cameroon, parts of Southern Sudan, Equatorial Guinea, Burundi, Ghana, Botswana, Rwanda, Zambia, Gabon, the Central African Republic, Tanzania, Uganda and Kenya. The sitatunga is mostly confined to swampy and marshy habitats. Here they occur in tall and dense vegetation as well as seasonal swamps, marshy clearings in forests, riparian thickets and mangrove swamps.
The mountain nyala or balbok, is a large antelope found in high altitude woodlands in a small part of central Ethiopia. It is a monotypic species first described by English naturalist Richard Lydekker in 1910. The males are typically 120–135 cm (47–53 in) tall while females stand 90–100 cm (35–39 in) at the shoulder. Males weigh 180–300 kg (400–660 lb) and females weigh 150–200 kg (330–440 lb). The coat is grey to brown, marked with two to five poorly defined white strips extending from the back to the underside, and a row of six to ten white spots. White markings are present on the face, throat and legs as well. Males have a short dark erect crest, about 10 cm (3.9 in) high, running along the middle of the back. Only males possess horns.
The lesser kudu is a medium-sized bushland antelope found in East Africa. The species is a part of the ungulate genus Tragelaphus, along with several other related species of striped, spiral-horned African bovids, including the related greater kudu, the bongo, bushbuck, common and giant elands, nyala and sitatunga. It was first scientifically described by English zoologist Edward Blyth (1869).
The greater kudu is a large woodland antelope, found throughout eastern and southern Africa. Despite occupying such widespread territory, they are sparsely populated in most areas due to declining habitat, deforestation, and poaching. The greater kudu is one of two species commonly known as kudu, the other being the lesser kudu, T. imberbis.
The common eland, also known as the southern eland or eland antelope, is a large-sized savannah and plains antelope found in East and Southern Africa. An adult male is around 1.6 m (5.2 ft) tall at the shoulder and can weigh up to 942 kg (2,077 lb) with a typical range of 500–600 kg (1,100–1,300 lb). Females are around 1.4 m (4.6 ft) tall and weigh 340–445 kg (750–981 lb). It is the second-largest antelope in the world, being slightly smaller on average than the giant eland. It was scientifically described by Peter Simon Pallas in 1766.
The giant eland, also known as the Lord Derby's eland and greater eland, is an open-forest and savanna antelope. A species of the family Bovidae and genus Taurotragus, it was described in 1847 by John Edward Gray. The giant eland is the largest species of antelope, with a body length ranging from 220–290 cm (7.2–9.5 ft). There are two subspecies: T. d. derbianus and T. d. gigas.
The sable antelope is a large antelope which inhabits wooded savanna in East and Southern Africa, from the south of Kenya to South Africa, with a separated population in Angola.
The scimitar oryx, also known as the scimitar-horned oryx and the Sahara oryx, is an Oryx species that was once widespread across North Africa and parts of West Africa and Central Africa. In 2000, it was declared extinct in the wild on the IUCN Red List, but in 2023 it was downlisted to endangered, with a reintroduced population in Chad. This particular oryx is adapted to harsh desert conditions and can survive for months or even years without drinking water. A grazing animal, it derives most of its daily moisture intake from plants.
The hirola, also called the Hunter's hartebeest or Hunter's antelope, is a critically endangered antelope species found as of now, only in Kenya along the border of Somalia. It was first described by the big game hunter and zoologist H.C.V. Hunter in 1888. It is the only living member of the genus Beatragus, though other species are known from the fossil record. The global hirola population is estimated at 300–500 animals and there are none in captivity. According to a document produced by the International Union for Conservation of Nature "the loss of the hirola would be the first extinction of a mammalian genus on mainland Africa in modern human history".
The hartebeest, also known as kongoni or kaama, is an African antelope. It is the only member of the genus Alcelaphus. Eight subspecies have been described, including two sometimes considered to be independent species. A large antelope, the hartebeest stands just over 1 m at the shoulder, and has a typical head-and-body length of 200 to 250 cm. The weight ranges from 100 to 200 kg. It has a particularly elongated forehead and oddly-shaped horns, a short neck, and pointed ears. Its legs, which often have black markings, are unusually long. The coat is generally short and shiny. Coat colour varies by the subspecies, from the sandy brown of the western hartebeest to the chocolate brown of the Swayne's hartebeest. Both sexes of all subspecies have horns, with those of females being more slender. Horns can reach lengths of 45–70 cm (18–28 in). Apart from its long face, the large chest and the sharply sloping back differentiate the hartebeest from other antelopes. A conspicuous hump over the shoulders is due to the long dorsal processes of the vertebrae in this region.
The mountain gazelle, also called the true gazelle or the Palestine mountain gazelle, is a species of gazelle that is widely but unevenly distributed.
The bohor reedbuck is an antelope native to central Africa. The animal is placed under the genus Redunca and in the family Bovidae. It was first described by German zoologist and botanist Peter Simon Pallas in 1767. The bohor reedbuck has five subspecies. The head-and-body length of this medium-sized antelope is typically between 100–135 cm (39–53 in). Males reach approximately 75–89 cm (30–35 in) at the shoulder, while females reach 69–76 cm (27–30 in). Males typically weigh 43–65 kg (95–143 lb) and females 35–45 kg (77–99 lb). This sturdily built antelope has a yellow to grayish brown coat. Only the males possess horns which measure about 25–35 cm (9.8–13.8 in) long.
The mountain reedbuck is an antelope found in mountainous areas of much of sub-Saharan Africa.
Taurotragus is a genus of giant antelopes of the African savanna, commonly known as elands. It contains two species: the common eland T. oryx and the giant eland T. derbianus.
The long-tailed goral or Amur goral is a species of ungulate of the family Bovidae found in the mountains of eastern and northern Asia, including Russia, China, and Korea. A population of this species exists in the Korean Demilitarized Zone, near the tracks of the Donghae Bukbu Line. The species is classified as endangered in South Korea, with an estimated population less than 250. It has been designated South Korean natural monument 217. In 2003, the species was reported as being present in Arunachal Pradesh, in northeast India.
Damaliscus lunatus is a large African antelope of the genus Damaliscus and subfamily Alcelaphinae in the family Bovidae, with a number of recognised geographic subspecies. Some authorities have split the different populations of the species into different species, although this is seen as controversial. Common names include topi, sassaby, tiang and tsessebe.
The tribe Tragelaphini, or the spiral-horned antelopes, are bovines that are endemic to sub-Saharan Africa. These include the bushbucks, kudus, and the elands. The scientific name is in reference to the mythical creature the tragelaph, a Chimera with the body of a stag and the head of a goat. They are medium-to-large, tall, long-legged antelopes characterized by their iconic twisted horns and striking pelage coloration patterns.
The Kahuzi-Biega National Park is a protected area near Bukavu town in eastern Democratic Republic of the Congo. It is situated near the western bank of Lake Kivu and the Rwandan border. Established in 1970 by the Belgian photographer and conservationist Adrien Deschryver, the park is named after two dormant volcanoes, Mount Kahuzi and Mount Biega, which are within its limits. With an area of 6,000 square kilometres (2,300 sq mi), Kahuzi-Biega is one of the biggest national parks in the country. Set in both mountainous and lowland terrain, it is one of the last refuges of the rare species of Eastern lowland gorilla, an endangered category under the IUCN Red List. The park is a UNESCO World Heritage Site, inscribed in 1980 for its unique biodiversity of rainforest habitat and its eastern lowland gorillas. In 1997, it was listed on the List of World Heritage in Danger because of the political instability of the region, an influx of refugees, and increasing wildlife exploitation.