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The black rhinoceros or hook-lipped rhinoceros (Diceros bicornis) is a species of rhinoceros, native to eastern and central Africa including Kenya, Tanzania, Cameroon, South Africa, Namibia, Zimbabwe, and Angola. Although the rhinoceros is referred to as black, its colors vary from brown to grey.
The other African rhinoceros is the white rhinoceros (Ceratotherium simum). The word "white" in the name "white rhinoceros" is a misinterpretation of the Afrikaans word wyd, itself derived from the Dutch word wijd for wide, referring to its square upper lip, as opposed to the pointed or hooked lip of the black rhinoceros. These species are now sometimes referred to as the square-lipped (for white) or hook-lipped (for black) rhinoceros.
The species was first named Rhinoceros bicornis by Carolus Linnaeus in the 10th edition of his Systema naturae in 1758. The name means "double-horned rhinoceros". There is some confusion about what exactly Linnaeus conceived under this name as this species was probably based upon the skull of a single-horned Indian rhinoceros (Rhinoceros unicornis), with a second horn artificially added by the collector. Such a skull is known to have existed and Linnaeus even mentioned India as origin of this species. However he also referred to reports from early travellers about a double-horned rhino in Africa and when it emerged that there is only one, single-horned species of rhino in India, "Rhinoceros" bicornis was used to refer to the African rhinos (the white rhino only became recognised in 1812). In 1911 this was formally fixed and the Cape of Good Hope officially declared the type locality of the species.
The intraspecific variation in the black rhinoceros has been discussed by various authors and is not finally settled. The most accepted scheme considers seven or eight subspecies, of which three became extinct in historical times and one is on the brink of extinction:
- Southern black rhinoceros or Cape rhinoceros (D. b. bicornis) – Extinct. Once abundant from the Cape of Good Hope to Transvaal, South Africa and probably into the south of Namibia, this was the largest subspecies. It became extinct due to excessive hunting and habitat destruction around 1850.
- North-eastern black rhinoceros (D. b. brucii) – Extinct. Formerly central Sudan, Eritrea, northern and southeastern Ethiopia, Djibouti and northern and southeastern Somalia. Relict populations in northern Somalia vanished during the early 20th century.
- Chobe black rhinoceros (D. b. chobiensis) – A local subspecies restricted to the Chobe Valley in southeastern Angola, Namibia (Zambezi Region) and northern Botswana. Nearly extinct, possibly only one surviving specimen in Botswana.
- Uganda black rhinoceros (D. b. ladoensis) – Former distribution from South Sudan, across Uganda into western Kenya and southwesternmost Ethiopia. Black rhinos are considered extinct across most of this area and its conservational status is unclear. Probably surviving in Kenyan reserves.
- Western black rhinoceros (D. b. longipes) – Extinct. Once lived in South Sudan, northern Central African Republic, southern Chad, northern Cameroon, northeastern Nigeria and south-eastern Niger. The range possibly stretched west to the Niger River in western Niger, though this is unconfirmed. The evidence from Liberia and Burkina Faso mainly rests upon the existence of indigenous names for the rhinoceros. A far greater former range in West Africa as proposed earlier is doubted by a 2004 study. The last known wild specimens lived in northern Cameroon. In 2006 an intensive survey across its putative range in Cameroon failed to locate any, leading to fears that it was extinct in the wild. On November 10, 2011 the IUCN declared the western black rhinoceros extinct.
- Eastern black rhinoceros (D. b. michaeli) – Had a historical distribution from South Sudan, Ethiopia, down through Kenya into north-central Tanzania. Today, its range is limited primarily to Tanzania.
- South-central black rhinoceros (D. b. minor) – Most widely distributed subspecies, characterised by a compact body, proportionally large head and prominent skin-folds. Ranged from north-eastern South Africa (KwaZulu-Natal) to northeastern Tanzania and southeastern Kenya. Preserved in reserves throughout most of its former range but probably extinct in eastern Angola, southern Democratic Republic of Congo and possibly Moçambique. Extinct but reintroduced in Malawi, Botswana, and Zambia.
- South-western black rhinoceros (D. b. occidentalis) – A small subspecies, adapted to survival in desert and semi-desert conditions. Originally distributed in north-western Namibia and southwestern Angola, today restricted to wildlife reserves in Namibia with sporadic sightings in Angola. These populations are often erroneously referred to D. b. bicornis or D. b. minor but represent a subspecies in their own right.
The most widely adopted alternative scheme only recognizes five subspecies or "eco-types", D. b. bicornis, D. b. brucii, D. b. longipes, D. b. michaeli, and D. b. minor. This concept is also used by the IUCN, listing three surviving subspecies and recognizing D. b. brucii and D. b. longipes as extinct. The most important difference to the above scheme is the inclusion of the extant southwestern subspecies from Namibia in D. b. bicornis instead of in its own subspecies, whereupon the nominal subspecies is not considered extinct.
The rhinoceros originated in the Eocene about fifty million years ago alongside other ungulates (hooved animals). Ancestors of the black and the white rhinoceros were present in Africa by the end of the Late Miocene about ten million years ago. The two species evolved from the common ancestral species Ceratotherium neumayri during this time. The clade comprising the genus Diceros is characterised by an increased adaptation to browsing. Between four and five million years ago, the black rhinoceros diverged from the white rhinoceros. After this split, the direct ancestor of Diceros bicornis, Diceros praecox was present in the Pliocene of East Africa (Ethiopia, Kenya, Tanzania). D. bicornis evolved from this species during the Late Pliocene – Early Pleistocene.
An adult black rhinoceros stands 140–180 cm (55–71 in) high at the shoulder and is 3–3.75 m (9.8–12.3 ft) in length. An adult typically weighs from 800 to 1,400 kg (1,800 to 3,100 lb), however unusually large male specimens have been reported at up to 2,199–2,896 kg (4,848–6,385 lb). The females are smaller than the males. Two horns on the skull are made of keratin with the larger front horn typically 50 cm (20 in) long, exceptionally up to 140 cm (55 in).
The longest known black rhinoceros horn measured nearly 1.5 m (4.9 ft) in length. Sometimes, a third, smaller horn may develop. These horns are used for defense, intimidation, and digging up roots and breaking branches during feeding. The black rhino is smaller than the white rhino, and is close in size to the Javan Rhino of Indonesia. It has a pointed and prehensile upper lip, which it uses to grasp leaves and twigs when feeding. The white rhinoceros has square lips used for eating grass. The black rhinoceros can also be distinguished from the white rhinoceros by its size, smaller skull, and ears; and by the position of the head, which is held higher than the white rhinoceros, since the black rhinoceros is a browser and not a grazer. This key differentiation is further illustrated by the shape of the two species mouths (lips): the "square" lip of the white rhinoceros is an adaptation for grazing, and the "hooked" lip of the black rhinoceros is an adaptation to help browsing.
Their thick-layered skin helps to protect the rhino from thorns and sharp grasses. Their skin harbors external parasites, such as mites and ticks, which may be eaten by oxpeckers and egrets. Such behaviour was originally thought to be an example of mutualism, but recent evidence suggests that oxpeckers may be parasites instead, feeding on rhino blood. Black rhinos have poor eyesight, relying more on hearing and smell. Their ears have a relatively wide rotational range to detect sounds. An excellent sense of smell alerts rhinos to the presence of predators.
As with many other components of the African large mammal fauna, black rhinos probably had a wider range in the northern part of the continent in prehistoric times than today. However this seems to have not been as extensive as that of the white rhino. Unquestionable fossil remains have not yet been found in this area and the abundant petroglyphs found across the Sahara desert are often too schematic to unambiguously decide whether they depict black or white rhinos. Petroglyphs from the Eastern Desert of southeastern Egypt relatively convincingly show the occurrence of black rhinos in these areas in prehistoric times.
Historical and extant range
The natural range of the black rhino included most of southern and eastern Africa, but it did not occur in the Congo Basin, the tropical rainforest areas along the Bight of Benin, the Ethiopian Highlands, and the Horn of Africa. Its former native occurrence in the extremely dry parts of the Kalahari desert of southwestern Botswana and northwestern South Africa is uncertain. In western Africa it was abundant in an area stretching east to west from Eritrea and Sudan through South Sudan to southeastern Niger, and especially around Lake Chad. Its occurrence further to the west is questionable, though often purported to in literature. Today it is totally restricted to protected nature reserves and has vanished from many countries in which it once thrived, especially in the west and north of its former range. The remaining populations are highly scattered. Some specimens have been relocated from their habitat to better protected locations, sometimes across national frontiers. The black rhino has been successfully reintroduced to Malawi since 1993, where it became extinct in 1990. Similarly it was reintroduced to Zambia (North Luangwa National Park) in 2008, where it had become extinct in 1998, and to Botswana (extinct in 1992, reintroduced in 2003).
Black rhinoceros are generally thought to be solitary, with the only strong bond between a mother and her calf. In addition, males and females have a consort relationship during mating, also subadults and young adults frequently form loose associations with older individuals of either sex. They are not very territorial and often intersect other rhino territories. Home ranges vary depending on season and the availability of food and water. Generally they have smaller home ranges and larger density in habitats that have plenty of food and water available, and vice versa if resources are not readily available. Sex and age of an individual black rhino influence home range and size, with ranges of females larger than those of males, especially when accompanied by a calf. In the Serengeti home ranges are around 70 to 100 km2 (27 to 39 sq mi), while in the Ngorongoro it is between 2.6 to 58.0 km2 (1.0 to 22.4 sq mi). Black rhinos have also been observed to have a certain area they tend to visit and rest frequently called "houses" which are usually on a high ground level. These "home" ranges can vary from 2.6 km2 to 133 km2 with smaller home ranges having more abundant resources than larger home ranges.
Black rhinoceros in captivity and reservations sleep patterns have been recently studied to show that males sleep longer on average than females by nearly double the time. Other factors that play a role in their sleeping patterns is the location of where they decide to sleep. Although they do not sleep any longer in captivity, they do sleep at different times due to their location in captivity, or section of the park.
The black rhino has a reputation for being extremely aggressive, and charges readily at perceived threats. They have even been observed to charge tree trunks and termite mounds. Black rhinos will fight each other, and they have the highest rates of mortal combat recorded for any mammal: about 50% of males and 30% of females die from combat-related injuries. Adult rhinos normally have no natural predators, thanks to their imposing size as well as their thick skin and deadly horns. However, adult black rhinos have fallen prey to crocodiles in exceptional circumstances. Calves and, very seldom, small sub-adults may be preyed upon by lions as well.
Black rhinoceros follow the same trails that elephants use to get from foraging areas to water holes. They also use smaller trails when they are browsing. They are very fast and can get up to speeds of 55 kilometres per hour (34 mph) running on their toes.
The black rhinoceros is a herbivorous browser that eats leafy plants, branches, shoots, thorny wood bushes, and fruit. The optimum habitat seems to be one consisting of thick scrub and bushland, often with some woodland, which supports the highest densities. Their diet can reduce the amount of woody plants, which may benefit grazers (who focus on leaves and stems of grass), but not competing browsers (who focus on leaves, stems of trees, shrubs or herbs). It has been known to eat up to 220 species of plants. They have a significantly restricted diet with a preference for a few key plant species and a tendency to select leafy species in the dry season. The plant species they seem to be most attracted to when not in dry season are the woody plants. There are 18 species of woody plants known to the diet of the black rhinoceros, and 11 species that could possibly be a part of their diet too. Black rhinoceros also have a tendency to choose food based on quality over quantity, where researchers find more populations in areas where the food has better quality. In accordance with their feeding habit, adaptations of the chewing apparatus have been described for rhinos. D. Bicornis has a twophased chewing activity with a cutting ectoloph and more grinding lophs on the lingual side. The black rhinoceros can also be considered a more challenging herbivore to feed in captivity compared to its grazing relatives. It can live up to 5 days without water during drought. Black rhinos live in several habitats including bushlands, Riverine woodland, marshes, and their least favorable, grasslands. Habitat preferences are shown in two ways, the amount of sign found in the different habitats, and the habitat content of home ranges and core areas. Habitat types are also identified based on the composition of dominant plant types in each area. Different subspecies live in different bushlands including, Acacia bushlands, Euclea bushlands, mixed bushlands, and dense euclea bushland. They browse for food in the morning and evening. They are selective browsers but, studies done in Kenya show that they do add the selection material with availability in order to satisfy their nutritional requirements. In the hottest part of the day they are most inactive- resting, sleeping, and wallowing in mud. Wallowing helps cool down body temperature during the day and protects against parasites. When black rhinos browse they use their lips to strip the branches of their leaves. Competition with elephants is causing the black rhinoceros to shift its diet. The black rhinoceros alters its selectivity with the absence of the elephant.
There is some variance in the exact chemical composition of rhinoceros horns. This variation is directly linked to diet and can be used as a means of rhino identification. Horn composition has helped scientists pinpoint the original location of individual rhinos, allowing for law enforcement to more accurately and more frequently identify and penalize poachers.
Rhinos use several forms of communication. Due to their bad eyesight and solitary nature, scent marking is often used to identify themselves to other black rhinos. Urine spraying occurs on trees and bushes, around water holes and feeding areas. Females urine spray more often when receptive for breeding. Defecation sometimes occurs in the same spot used by different rhinos, such as around feeding stations and watering tracks. Coming upon these spots, rhinos will smell to see who is in the area and add their own marking. When presented with adult feces, male and female rhinoceroses respond differently than when they are presented with subadult feces. The urine and feces of one black rhinoceros helps other black rhinoceroses to determine its age, sex, and identity. Less commonly they will rub their heads or horns against tree trunks to scent-mark.
To compensate for its poor eyesight, the black rhino has powerful tube-shaped ears that can freely rotate in all directions. This highly developed sense of hearing allows black rhinos to detect sound over vast distances.
The adults are solitary in nature, coming together only for mating. Mating does not have a seasonal pattern but births tend to be towards the end of the rainy season in more arid environments.
When in season the females will mark dung piles. Males will follow females when they are in season; when she defecates he will scrape and spread the dung, making it more difficult for rival adult males to pick up her scent trail.
Courtship behaviors before mating include snorting and sparring with the horns among males. Another courtship behavior is called bluff and bluster, where the rhino will snort and swing its head from side to side aggressively before running away repeatedly. Breeding pairs stay together for 2–3 days and sometimes even weeks. They mate several times a day over this time and copulation lasts for a half hour.
The gestation period is 15 to 16 months. The single calf weighs about 35–50 kilograms (80–110 lb) at birth, and can follow its mother around after just three days. Weaning occurs at around 2 years of age for the offspring. The mother and calf stay together for 2–3 years until the next calf is born; female calves may stay longer, forming small groups. The young are occasionally taken by hyenas and lions. Sexual maturity is reached from 5 to 7 years old for females, and 7 to 8 years for males. The life expectancy in natural conditions (without poaching pressure) is from 35 to 50 years.
For most of the 20th century the continental black rhino was the most numerous of all rhino species. Around 1900 there were probably several hundred thousand living in Africa. During the latter half of the 20th century their numbers were severely reduced from an estimated 70,000 in the late 1960s to only 10,000 to 15,000 in 1981. In the early 1990s the number dipped below 2,500, and in 2004 it was reported that only 2,410 black rhinos remained. According to the International Rhino Foundation—housed in Yulee, Florida at White Oak Conservation, which breeds black rhinos—the total African population had recovered to 4,240 by 2008 (which suggests that the 2004 number was low). In 1992, nine rhinoceros were brought from Chete National Park, Zimbabwe to Australia via Cocos Island. After the natural deaths of the males in the group, 4 males were brought in from USA and have since adapted well to captivity and new climate. Calves and some subadults are preyed on by lions, but predation is rarely taken into account in managing the Black Rhinoceros. This is a major flaw because predation should be considered when attributing cause to the poor performance of the Black Rhinoceros population. In 2002 only 10 West African rhinos remained in Cameroon, and in 2006 intensive surveys across its putative range failed to locate any, leading to fears that this subspecies was extinct. In 2011 the IUCN declared the Western black rhino extinct.
Under CITES Appendix I all international commercial trade of the black rhino horn is prohibited since 1977. China though having joined CITES since April 8, 1981 is the largest importer of black rhino horns. However, this is a trade in which not only do the actors benefit, but so do the nation states ignoring them as well. Nonetheless, we continue to remove the rhino from its natural environment and allow for a dependence on human beings to save them from endangerment. Parks and reserves have been made for protecting the rhinos with armed guards keeping watch, but even still many poachers get through and harm the rhinos for their horns. Many have considered extracting rhino horns in order to deter poachers from slaughtering these animals or potentially bringing them to other breeding grounds such as the US and Australia. This method of extracting the horn known as dehorning consists of tranquilizing the rhino then sawing the horn almost completely off to decrease initiative for poaching. However, rhinos use their horns to protect their young against predators and this method has been proven to be less successful because it did not decrease poaching numbers and is very expensive.
The only rhino that has recovered somewhat from the brink of extinction is the southern white whose numbers now are estimated around 14,500, up from fewer than 50 in the first decade of the 20th century. But there seems to be hope for the black rhinoceros in recovering their gametes from dead rhinos in captivity. This shows promising results for producing black rhinoceros embryos, which can be used for testing sperm in vitro.
A 2014 auction for a permit to hunt an African black rhinoceros in Namibia sold for $350,000 at a fundraiser to raise money for conservation efforts. The auction drew considerable criticism, as well as death threats.
Today, there are various threats posed to the black rhinoceros today including habitat changes, illegal poaching, and competing species. Civil disturbances such as war have made mentionably negative effects on the black rhinoceros populations in since the 1960s in countries including, but not limited to, Chad, Cameroon, Rwanda, Mozambique, and Somalia. In the Addo Elephant National Park in South Africa, the African elephant Loxotonta africana is posing slight concern involving the black rhinoceroses who also inhabit the area. Both animals are browsers however the elephant's diet consists of a wider variety of foraging capacity while the rhinoceros primarily sticks to dwarf shrubs. The black rhinoceros has been found to eat grass as well, however the shortening of its range of available food could be potentially problematic.
Black rhinoceros face problems associated with the minerals they ingest. They have become adjusted to ingesting less iron in the wild due to their evolutionary progression, which poses a problem when placed in captivity. These rhinoceros can overload on iron, which leads to build up in the lungs, liver, spleen, and small intestine. Not only do these rhinoceros face threats being in the wild, but in captivity too. Black rhinoceros have become more susceptible to disease in captivity with high rates of mortality.
Illegal poaching for the international rhino horn trade is the main and most detrimental threat. The killing of these animals is not unique to modern day society. The Chinese have maintained reliable documents of these happenings dating back to 1200 B.C. The ancient Chinese often hunted rhino horn for the making of wine cups as well as the rhino's skin to manufacture imperial crowns and belts and armor for soldiers. A major market for rhino horn has historically been in the Middle East nations to make ornately carved handles for ceremonial daggers called jambiyas. Demand for these exploded in the 1970s causing the black rhinoceros population to decline 96% between 1970 and 1992. The horn is also used in traditional Chinese medicine, and is said by herbalists to be able to revive comatose patients, facilitate exorcisms and various methods of detoxification, cure fevers, and aid male sexual stamina and fertility. It is also hunted for the superstitious belief that the horns allow direct access to heaven due to their unique location and hollow nature. The purported effectiveness of the use of rhino horn in treating any illness has not been confirmed or even suggested by medical science. In June 2007, the first-ever documented case of the medicinal sale of black rhino horn in the United States (confirmed by genetic testing of the confiscated horn) occurred at a traditional Chinese medicine supply store in Portland, Oregon's Chinatown. With rhino horn selling for nearly US$30,000 per pound, it has been argued that legalization of trade would allow horn from captive-bred rhinos to reduce the price and thus the incentive for poaching. However, most[who?] doubt that this would be successful in reducing the number of rhinos killed.
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