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Varanus niloticus Print E-mail

During the dry season in tropical Africa and in the cooler months in temperate regions activity is reduced or suspended (Cowles 1930, Cisse 1971). Juveniles are better at climbing than adults, but even large Nile monitors will climb readily. However they lack the dexterity to be classed as truly arboreal: Loveridge (1923) reports that specimens sleeping in trees have been known to loose their grip and plummet to their deaths. They are, of course, superb swimmers. In the wild Nile monitors can remain underwater for more than an hour (Ingleton 1929). Experiments with small specimens (1.4-4.8kg) in captivity have shown that most dives last for 12-15 minutes, never more than half an hour. During these dives heart rate and blood pressure drop (Wood & Johansen 1974). Hirth & Latif (1984) recorded an average body temperature of 28.8oC, with a range from 20-37.2oC with activity above 26oC. An active specimen caught in the late afternoon had a cloacal temperature of 32oC whilst ambient temperature was 25.3oC (pers. obs.).

Population densities of 40-60 Nile monitors per km2 have been recorded in northern Kenya (Western 1974). Our preliminary studies suggest that populations are equally high in parts of Ghana, where this species is completely protected. Very high densities are recorded for heavily exploited populations around Lake Chad (Buffrenil 1992). However despite its abundance, size and economic importance the Nile monitor is a very poorly studied animal. The most complete published* study of their ecology is from Natal, South Africa (Cowles 1928, 1930). Here they were found close to water between September and March and were relatively inactive during the rest of the year, sheltering in abandoned termite mounds. Cowles was also the first person to note the use of active termite mounds as nest sites. The nests used are large mounds, usually situated close to water. The female tears open the nest and deposits her eggs without attempting to cover them. The termites quickly repair the nest and the eggs are incubated safely, with constant heat and humidity, providing the mound remains occupied by termites. Cowles (1930) suggested an incubation period of about 300 days, based on his observations of hatchlings emerging in November and December and estimated that eggs were laid during the hottest part of the year (December to February). However Branch & Erasmus (1982) record a female in Transvaal seen depositing her eggs in August (at the end of the winter) and considering known incubation times in captivity (see below) it seems likely that the duration of incubation is less than half, or even a third, of that suggested by Cowles. In more northern parts of Africa suitable termitaria appear to be unavailable and eggs are deposited in burrows. In Sudan eggs may be laid burrows dug into the clay walls of irrigation canals (Cloudsley-Thompson 1967). In Senegal eggs are laid from late October to late December during the wet season. Gravid females have been found in Tanganyika during November (Barbour & Loveridge 1928) and during early July in Zanzibar (Pakenham 1983). In Ghana we have found what appeared to be gravid females in August and September.

Large female Nile monitors can lay enormous clutches of eggs. According to Loveridge (1934) up to 60 eggs are produced in a single clutch, Borquin (1991) found 63 eggs in a termite mound and there are many records of clutches containing over 35 eggs (e.g. Barbour & Loveridge 1928, Pakenham 1983, Boycott & Morgan 1988). According to Buffrenil (1992) females mature at around 120cm TL around Lake Chad and initially produce only about ten eggs per year. Like other African monitor lizards, the Nile monitor enhances its chances of survival by producing large numbers of eggs that hatch comparatively quickly. Most eggs weigh 46-52g and measure about 6x4cm. Therefore the weight of a clutch of eggs from a large female can approach 3,000g! It appears that females spend most of the spring and summer feeding heavily and accumulating massive fat reserves which are then converted into egg yolk in the liver during the long period of inactivity during the winter. In less temperate parts of Africa the period of activity occurs during the dry season and may be shorter in duration (Buffrenil 1992). This is reflected by the apparent smaller clutches of females from West Africa (e.g. Cisse 1976). The need for females to accumulate large fat deposits and then greatly reduce activity during ovagenesis appears to be important in a number of both temperate and tropical varanids. It is discussed further in the following chapters.

Surprisingly there are few published accounts of interactive behaviours such as ritual combat or courtship in Nile monitors. This can be attributed to the secretive behaviour of these huge lizards. Adults have been seen wrestling on the ground (presumed to be courtship by Clements (1968) but interpreted as ritual combat by Horn (1985). They have also been observed standing on their hind legs (Wearne 1962), but bipedal combat has not been observed to occur in this species. The Nile monitor makes great use of its tail for defence and the battered condition of these appendages in old specimens is attributed to its regular use as a club with which to deter aggressors. A number of unusual behaviours have been noted amongst Nile monitors. A young monitor lizard that fell into a enclosure full of young (30cm) crocodiles seized several of the crocodiles and turned them onto their backs before being removed. The crocodiles were estimated to weigh twice as much as the lizard (Pooley 1968). According to Stevenson-Hamilton (1947) a monitor surrounded by four large lion cubs kept perfectly motionless apart from occasionally twitching its tail tip. The lion cubs watched closely, but appeared to interpret the movements as that of a snake and eventually wandered away. The same author reports that an eagle which seized a Nile monitor was in turn seized by the thigh by the lizards, which steadfastly refused to let go. When found by a ranger the bird was in a state of utter exhaustion.

There are few lizards less suited to life in captivity than the Nile monitor. Buffrenil (1992) considered that, when fighting for its life, a Nile monitor was a more dangerous adversary than a crocodile of a similar size. Their care presents particular problems on account of the lizards' enormous size and lively dispositions. Very few of the people who buy brightly-coloured baby Nile monitors can be aware that, within a couple of  years, their purchase will have turned into an enormous, ferocious carnivore, quite capable of breaking the family cat's neck with a single snap and swallowing it whole. An enormous enclosure (at least 8m2 and 2.5m high) is needed to keep these animals properly, furnished with a sizeable pool of water and plenty of  tree trunks for the lizards to climb on. A period of inactivity during the cool winter or hot dry season (depending on the origins of the animals) is desirable. Nile monitors are prone to obesity and the diet should include significant quantities of non-mammalian food. A temperature range of 18-30oC is suitable with basking spots up to 45oC. Very few records of captive breeding are available (Enright 1989). Animals should be housed apart except at breeding time. The small size of females suggests that finding a compatible pair could be particularly problematic. Best results would be obtained by obtaining a group of young, unrelated, animals and rearing them to adulthood. Eggs collected in the wild or laid by wild caught females hatch after 141-150 days at 27-30.5oC, 120-137 days at 30oC and 92 days at 32oC (Boycott & Morgan 1988, Branch & Erasmus 1982, Olmstead 1987, Enright 1989). In captivity they are known to practise cannibalism (Charlton 1973). Animal dealers who sell Nile monitors under the pretence that they can be kept as pets are a despicable breed, but given spacious surroundings and suitable furnishings Nile monitors can be very rewarding animals to keep in captivity.

Nile monitors are eaten in many areas and their organs and tissues used for medicinal purposes (Anon 1937). The skin is very durable and beautiful. Between 1980 and 1985 trade in live specimens averaged 816 specimens per year whilst trade in skins averaged over 400,000 per year. In 1988 more than 700,000 skins were exported (Luxmoore & Groombridge 1990; Buffrenil 1992). Most skins are exported from Mali, Nigeria, Cameroon and Sudan to Europe, particularly France. The uses of monitor lizards and the effects of exploitation for meat and skins around Lake Chad is documented by Buffrenil (1992, 1993, et al 1994). In Ghana the Nile monitor is known as mampan tintin, in Zambia as mbulu, nabulwe, hopani, nsamba or imbulu (Broadley 1971). An extensive list of  the common names of African monitor lizards can be found in Auerbach (1995).



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Varanus bitatawa

Varanus bitatawa is the third species of  monitor lizard to be recognised by science that belongs to the "Pandan Biawak" group,  all of which are of at least as great a conservation concern as the Komodo dragon, but receive virtually none of the attention. Pandan Biawak occur only in lowland dipterocarp forest. The first species (Varanus olivaceus or Butaan) was discovered in 1845 and not seen alive by a scientist until the late 1970s. The next species (Varanus mabitang or Mabitang) was discovered in 2001 and in 2010 Varanus bitatawa (Butikaw or Bitatawa) was described. Other species of frugivorous monitor lizards may remain undescribed, but many may have  gone extinct without ever having been recognised.




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