The impala (/ɪmˈpɑːlə, -ˈpælə/, Aepyceros melampus) is a medium-sized antelope found in eastern and southern Africa. The sole member of the genus Aepyceros, it was first described to European audiences by German zoologist Hinrich Lichtenstein in 1812. Two subspecies are recognised—the common impala, and the larger and darker black-faced impala. The impala reaches 70–92 centimetres (28–36 inches) at the shoulder and weighs 40–76 kg (88–168 lb). It features a glossy, reddish brown coat. The male's slender, lyre-shaped horns are 45–92 centimetres (18–36 inches) long.
Active mainly during the day, the impala may be gregarious or territorial depending upon the climate and geography. Three distinct social groups can be observed: the territorial males, bachelor herds and female herds. The impala is known for two characteristic leaps that constitute an anti-predator strategy. Browsers as well as grazers, impala feed on monocots, dicots, forbs, fruits and acacia pods (whenever available). An annual, three-week-long rut takes place toward the end of the wet season, typically in May. Rutting males fight over dominance, and the victorious male courts female in 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 (ecotone) between woodlands and savannahs; it inhabits places close to water. While the black-faced impala is confined to southwestern Angola and Kaokoland in northwestern Namibia, the common impala is widespread across its range and has been reintroduced in Gabon and southern Africa. The International Union for Conservation of Nature (IUCN) classifies the impala as a species of least concern; the black-faced subspecies has been classified as a vulnerable species, with less than 1,000 individuals remaining in the wild as of 2008.
Description & appearance
The impala is a medium-sized, slender antelope similar to the kob or Grant's gazelle in build. The head-and-body length is around 130 centimetres (51 in). Males reach approximately 75–92 centimetres (30–36 in) at the shoulder, while females are 70–85 centimetres (28–33 in) tall. Males typically weigh 53–76 kilograms (117–168 lb) and females 40–53 kilograms (88–117 lb). Sexually dimorphic, females are hornless and smaller than males. Males grow slender, lyre-shaped horns 45–92 centimetres (18–36 in) long. 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. 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 centimetres (6.7 in) long, are tipped with black. Black streaks run from the buttocks to the upper hindlegs. The bushy white tail, 30 centimetres (12 in) long, features a solid black stripe along the midline. The impala's colouration bears a strong resemblance to the gerenuk, which has shorter horns and lacks the black thigh stripes of the impala. The impala has scent glands covered by a black tuft of hair on the hindlegs. Sebaceous glands concentrated on the forehead and dispersed on the torso of dominant males are most active during the mating season, while those of females are only partially developed and do not undergo seasonal changes. There are four nipples.
Of the subspecies, the black-faced impala is significantly larger and darker than the common impala; melanism is responsible for the black colouration. 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. Other differences include the larger black tip on the ear, and a bushier and nearly 30% longer tail in the black-faced impala.
The impala has a special dental arrangement on the front lower jaw similar to the toothcomb seen in strepsirrhine primates, which is used during allogrooming to comb the fur on the head and the neck and remove ectoparasites.
Distribution & habitat
The impala inhabits woodlands due to its preference for shade; it can also occur on the interface (ecotone) between woodlands and savannahs. Places close to water sources are preferred. In southern Africa, populations tend to be associated with Colophospermum mopane and Acacia woodlands. Habitat choices differ seasonally – Acacia senegal woodlands are preferred in the wet season, and A. drepanolobium savannahs in the dry season. Another factor that could influence habitat choice is vulnerability to predators; impala tend to keep away from areas with tall grasses as predators could be concealed there. A study found that the reduction of woodland cover and creation of shrublands by the African bush elephants has favoured impala population by increasing the availability of more dry season browse. Earlier, the Baikiaea woodland, which has now declined due to elephants, provided minimum browsing for impala. The newly formed Capparis shrubland, on the other hand, could be a key browsing habitat. Impala are generally not associated with montane habitats; however, in KwaZulu-Natal, impala have been recorded at altitudes of up to 1,400 metres (4,600 ft) above sea level.
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. Food
Impala browse as well as graze; either may predominate, depending upon the availability of resources. The diet comprises monocots, dicots, forbs, fruits and acacia pods (whenever available). Impala prefer places close to water sources, and resort to succulent vegetation if water is scarce. 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. 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. Another study showed that the dicot proportion in the diet is much higher in bachelors and females than in territorial males.
Impala feed on soft and nutritious grasses such as Digitaria macroblephara; tough, tall grasses, such as Heteropogon contortus and Themeda triandra, are typically avoided. 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. 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%). Reproduction
Males are sexually mature by the time they are a year old, though successful mating generally occurs only after four years. Mature males start establishing territories and try to gain access to females. Females can conceive after they are a year and a half old; oestrus lasts for 24 to 48 hours, and occurs every 12–29 days in non-pregnant females. 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. The bulbourethral glands are heavier, testosterone levels are nearly twice as high in territorial males as in bachelors, 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.
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; the male checks the female's urine to ensure that she is in oestrus. 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.
Gestation lasts six to seven months. Births generally occur in the midday; the female will isolate herself from the herd when labour pain begins. The perception that females can delay giving birth for an additional month if conditions are harsh may however not be realistic.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.