Impala

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Impala
Ram in northern Botswana
Ewe with calf at the Kruger National Park, South Africa

Least Concern  (IUCN 3.1)[1]
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Artiodactyla
Family: Bovidae
Tribe: Aepycerotini
Genus: Aepyceros
Species:
A. melampus
Binomial name
Aepyceros melampus
(
Lichtenstein
, 1812)
Subspecies
  • A. m. melampus Lichtenstein, 1812
  • A. m. petersi Bocage, 1879
Distribution:
  Black-faced impala
  Common impala
Synonyms[2]
List
  • A. holubi Lorenz, 1894
  • A. johnstoni Thomas, 1893
  • A. katangae Lönnberg, 1914
  • A. pallah (Gervais, 1841)
  • A. rendilis Lönnberg, 1912
  • A. typicus Thomas, 1893

The impala or rooibok (Aepyceros melampus) is a medium-sized

coat. The male's slender, lyre-shaped horns
are 45–92 cm (18–36 in) long.

Active mainly

oestrus. Gestation lasts six to seven months, following which a single calf is born and immediately concealed in cover. Calves are suckled
for four to six months; young males—forced out of the all-female groups—join bachelor herds, while females may stay back.

The impala is found in woodlands and sometimes on the interface (

species of least concern; the black-faced subspecies has been classified as a vulnerable species
, with fewer than 1,000 individuals remaining in the wild as of 2008.

Etymology

The first attested English name, in 1802, was palla or pallah, from the

Afrikaans name, rooibok 'red buck', is also sometimes used in English.[5]

The

Ancient Greek αἰπύς (aipus, 'high, steep') + κέρας (keras, 'horn');[6][7] the specific name melampus (lit. ‘black-foot’) from μελάς (melas, 'black') + πούς (pous, 'foot').[8]

Taxonomy and evolution

The impala is the

rRNA and β-spectrin nuclear sequence analysis in 2003 also supported an association between Aepyceros and Neotragus.[11] The following cladogram is based on the 1999 study:[10]

Sheep (Ovis aries)

Bontebok (Damaliscus pygargus)

Sable antelope (Hippotragus niger)

Klipspringer (Oreotragus oreotragus)

Bay duiker (Cephalophus dorsalis)

Impala (Aepyceros melampus)

Suni (Neotragus moschatus)

Grant's gazelle (Nanger granti)

Mountain reedbuck (Redunca fulvorufula)

Up to six subspecies have been described, although only two are generally recognised on the basis of mitochondrial data.[12] Though morphologically similar,[13] the subspecies show a significant genetic distance between them, and no hybrids between them have been reported.[13][14]

  • A. m. melampus Lichtenstein, 1812: Known as the common impala, it occurs across eastern and southern Africa. The range extends from central Kenya to South Africa and westward into southeastern Angola.
  • A. m. petersi Bocage, 1879: Known as the black-faced impala, it is restricted to southwestern Africa, occurring in northwestern Namibia and southwestern Angola.

According to Vrba, the impala evolved from an alcelaphine ancestor. She noted that while this ancestor has diverged at least 18 times into various morphologically different forms, the impala has continued in its basic form for at least five million years.[9][15] Several fossil species have been discovered, including A. datoadeni from the Pliocene of Ethiopia.[16] The oldest fossil discovered suggests its ancient ancestors were slightly smaller than the modern form, but otherwise very similar in all aspects to the latter. This implies that the impala has efficiently adapted to its environment since prehistoric times. Its gregarious nature, variety in diet, positive population trend, defence against ticks and symbiotic relationship with the tick-feeding oxpeckers could have played a role in preventing major changes in morphology and behaviour.[9]

Description

A grooming male at Serengeti National Park
Close view of a male, with characteristic lyre-shaped horns, white tail and several black markings

The impala is a medium-sized, slender-bodied antelope, comparable to the kob, puku and Grant's gazelle in size and build.[17] The head-and-body length is around 130 centimetres (51 in).[18] Males reach approximately 75–92 cm (30–36 in) at the shoulder, while females are 70–85 cm (28–33 in) tall. Males typically weigh 53–76 kilograms (117–168 lb) and females 40–53 kg (88–117 lb). Sexually dimorphic, females are hornless and smaller than males. Males grow slender, lyre-shaped horns 45–92 cm (18–36 in) long.[17] The horns, strongly ridged and divergent, are circular in section and hollow at the base. Their arch-like structure allows interlocking of horns, which helps a male throw off his opponent during fights; horns also protect the skull from damage.[13][17]

The glossy coat of the impala shows two-tone colouration – the reddish brown back and the tan flanks; these are in sharp contrast to the white underbelly. Facial features include white rings around the eyes and a light chin and snout. The ears, 17 cm (6.7 in) long, are tipped with black.[13][19] Black streaks run from the buttocks to the upper hindlegs. The bushy white tail, 30 cm (12 in) long, features a solid black stripe along the midline.[19] The impala's colouration bears a strong resemblance to the gerenuk, which has shorter horns and lacks the black thigh stripes of the impala.[13] The impala has scent glands covered by a black tuft of hair on the hindlegs. 2-Methylbutanoic Acid and 2-Nonanone have been identified from this gland.[20] Sebaceous glands concentrated on the forehead and dispersed on the torso of dominant males[17][21] are most active during the mating season, while those of females are only partially developed and do not undergo seasonal changes.[22] There are four nipples.[17]

Of the subspecies, the black-faced impala is significantly larger and darker than the common impala; melanism is responsible for the black colouration.[23] Distinctive of the black-faced impala is a dark stripe, on either side of the nose, that runs upward to the eyes and thins as it reaches the forehead.[18][19] Other differences include the larger black tip on the ear, and a bushier and nearly 30% longer tail in the black-faced impala.[13]

The impala has a special dental arrangement on the front lower jaw similar to the

ectoparasites.[13][25]

Ecology and behaviour

An impala mid-air during a leap
Impala can leap up to 3 m (9.8 ft).

The impala is diurnal (active mainly during the day), though activity tends to cease during the hot midday hours; they feed and rest at night.[17] Three distinct social groups can be observed – the territorial males, bachelor herds and female herds.[26] The territorial males hold territories where they may form harems of females; territories are demarcated with urine and faeces and defended against juvenile or male intruders.[17] Bachelor herds tend to be small, with less than 30 members. Individuals maintain distances of 2.5–3 m (8.2–9.8 ft) from one another; while young and old males may interact, middle-aged males generally avoid one another except to spar. Female herds vary in size from 6 to 100; herds occupy home ranges of 80–180 ha (200–440 acres; 0.31–0.69 sq mi). The mother–calf bond is weak, and breaks soon after weaning; juveniles leave the herds of their mothers to join other herds. Female herds tend to be loose and have no obvious leadership.[17][27] Allogrooming is an important means of social interaction in bachelor and female herds; in fact, the impala appears to be the only ungulate to display self-grooming as well as allogrooming. In allogrooming, females typically groom related impalas, while males associate with unrelated ones. Each partner grooms the other six to twelve times.[28]

An impala stotting

Social behaviour is influenced by the climate and geography; as such, the impala are territorial at certain times of the year and gregarious at other times, and the length of these periods can vary broadly among populations. For instance, populations in southern Africa display territorial behaviour only during the few months of the rut, whereas in eastern African populations, territoriality is relatively minimal despite a protracted mating season. Moreover, territorial males often tolerate bachelors, and may even alternate between bachelorhood and territoriality at different times of the year. A study of impala in the Serengeti National Park showed that in 94% of the males, territoriality was observed for less than four months.[17]

The impala is an important prey species for Africa's large

predators.[13][29] At times, the impala may also conceal itself in vegetation to escape the eye of the predator.[30] The most prominent vocalisation is the loud roar, delivered through one to three loud snorts with the mouth closed, followed by two to ten deep grunts with the mouth open and the chin and tail raised; a typical roar can be heard up to 2 km (1.2 mi) away.[17] Scent gland secretions identify a territorial male.[31] Impalas are sedentary; adult and middle-aged males, in particular, can hold their territories for years.[17]

Parasites

Impala have a symbiotic relationship with oxpeckers.

Common ixodid ticks collected from impala include Amblyomma hebraeum, Boophilus decoloratus, Hyalomma marginatum, Ixodes cavipalpus, Rhipicephalus appendiculatus and R. evertsi.[32][33][34] In Zimbabwe, heavy infestation by ticks such as R. appendiculatus has proved to be a major cause behind the high mortality of ungulates, as they can lead to tick paralysis. Impala have special adaptations for grooming, such as their characteristic dental arrangement, to manage ticks before they engorge; however, the extensive grooming needed to keep the tick load under control involves the risk of dehydration during summer, lower vigilance against predators and gradual wearing out of the teeth. A study showed that impala adjust the time devoted to grooming and the number of grooming bouts according to the seasonal prevalence of ticks.[32]

Impala are symbiotically related to

udders of a female and pilfer its milk.[38]

Lice recorded from impala include Damalinia aepycerus, D. elongata, Linognathus aepycerus and L. nevilli; in a study, ivermectin (a medication against parasites) was found to have an effect on Boophilus decoloratus and Linognathus species, though not on Damalinia species.[39] In a study of impala in South Africa, the number of worms in juveniles showed an increase with age, reaching a peak when impala turned a year old. This study recorded worms of genera such as Cooperia, Cooperoides, Fasciola, Gongylonema. Haemonchus, Impalaia, Longistrongylus and Trichostrongylus; some of these showed seasonal variations in density.[40]

Impala show high frequency of

trace levels of feeding by Glossina (tsetse fly) upon impala.[41]

cross infectious to cattle: Grootenhuis et al 1975 were not able to induce cattle infection and Fawcett et al 1987 did not find it naturally occurring.[42]

Diet

A herd grazing in Maasai Mara

Impala

acacia pods (whenever available). Impala prefer places close to water sources, and resort to succulent vegetation if water is scarce.[17] An analysis showed that the diet of impala is composed of 45% monocots, 45% dicots and 10% fruits; the proportion of grasses in the diet increases significantly (to as high as 90%) after the first rains, but declines in the dry season.[44] Browsing predominates in the late wet and dry season, and diets are nutritionally poor in the mid-dry season, when impala feed mostly on woody dicots.[13][45] Another study showed that the dicot proportion in the diet is much higher in bachelors and females than in territorial males.[46]

Impala feed on soft and nutritious grasses such as Digitaria macroblephara; tough, tall grasses, such as Heteropogon contortus and Themeda triandra, are typically avoided.[47] Impala on the periphery of the herds are generally more vigilant against predators than those feeding in the centre; a foraging individual will try to defend the patch it is feeding on by lowering its head.[48] A study revealed that time spent in foraging reaches a maximum of 75.5% of the day in the late dry season, decreases through the rainy season, and is minimal in the early dry season (57.8%).[49]

Reproduction

dominance

Males are

oestrus lasts for 24 to 48 hours, and occurs every 12–29 days in non-pregnant females.[30] The annual three-week-long rut (breeding season) begins toward the end of the wet season, typically in May. Gonadal growth and hormone production in males begin a few months before the breeding season, resulting in greater aggressiveness and territoriality.[17] The bulbourethral glands are heavier, testosterone levels are nearly twice as high in territorial males as in bachelors,[50] and the neck of a territorial male tends to be thicker than that of a bachelor during the rut. Mating tends to take place between full moons.[17]

Sounds of rutting male

Rutting males fight over dominance, often giving out noisy roars and chasing one another; they walk stiffly and display their neck and horns. Males desist from feeding and allogrooming during the rut, probably to devote more time to garnering females in oestrus;[51] the male checks the female's urine to ensure that she is in oestrus.[52][51] On coming across such a female, the excited male begins the courtship by pursuing her, keeping a distance of 3–5 metres (9.8–16.4 ft) from her. The male flicks his tongue and may nod vigorously; the female allows him to lick her vulva, and holds her tail to one side. The male tries mounting the female, holding his head high and clasping her sides with his forelegs. Mounting attempts may be repeated every few seconds to every minute or two. The male loses interest in the female after the first copulation, though she is still active and can mate with other males.[17][26]

Gestation lasts six to seven months. Births generally occur in the midday; the female will isolate herself from the herd when labour pain begins.[53] The perception that females can delay giving birth for an additional month if conditions are harsh may however not be realistic.[54] A single calf is born, and is immediately concealed in cover for the first few weeks of its birth. The fawn then joins a nursery group within its mother's herd. Calves are suckled for four to six months; young males, forced out of the group, join bachelor herds, while females may stay back.[17]

Distribution and habitat

A herd in Tanzania
Impala inhabit woodlands.

The impala inhabits woodlands due to its preference for shade; it can also be found on the interface (ecotone) between woodlands and savannahs. Places near water sources are preferred. In southern Africa, populations tend to be associated with

above sea level.[43]

The historical range of the impala – spanning across southern and eastern Africa – has remained intact to a great extent, although it has disappeared from a few places, such as Burundi. The range extends from central and southern Kenya and northeastern Uganda in the east to northern KwaZulu-Natal in the south, and westward up to Namibia and southern Angola. The black-faced impala is confined to southwestern Angola and Kaokoland in northwestern Namibia; the status of this subspecies has not been monitored since the 2000s. The common impala has a wider distribution, and has been introduced in protected areas in Gabon and across southern Africa.[1]

Threats and conservation

Impalas of Kruger National Park, RSA
Impala tracks

The

species of least concern overall.[1] The black-faced impala, however, is classified as a vulnerable species; as of 2008, fewer than 1,000 were estimated in the wild.[56] Though there are no major threats to the survival of the common impala, poaching and natural calamities have significantly contributed to the decline of the black-faced impala. As of 2008, the population of the common impala has been estimated at around two million.[1] According to some studies, translocation of the black-faced impala can be highly beneficial in its conservation.[57][58]

Around a quarter of the common impala populations occur in protected areas, such as the

Zambezi Valley (Zimbabwe). The rare black-faced impala has been introduced into private farms in Namibia and the Etosha National Park. Population densities vary largely from place to place; from less than one impala per square kilometre in Mkomazi National Park (Tanzania) to as high as 135 per square kilometre near Lake Kariba (Zimbabwe).[1][59]

References

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  34. ^ Hussain Kanchwala (2022). "How Did We Start Drinking Milk Of The Ruminants? Are We The Only Species To Drink Milk Of Other Species?". ScienceABC.
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  48. ^ Hart, Lynette A., and Benjamin L. Hart. "Species-specific patterns of urine investigation and flehmen in Grant's gazelle (Gazella granti), Thomson's gazelle (G. thomsoni), impala (Aepyceros melampus), and eland (Taurotragus oryx)." Journal of Comparative Psychology 101.4 (1987): 299.
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