|From Etosha National Park|
Verreaux's eagle-owl, also commonly known as the milky eagle owl or giant eagle owl, (Bubo lacteus) is a member of the family Strigidae. This species is widespread in sub-Saharan Africa. A member of the Bubo genus, it is the largest African owl measuring up to 66 cm (26 in) in total length. This eagle-owl is a resident primarily of dry, wooded savanna. Verreaux's eagle-owl is mainly grey in color and is at once distinguished from other large owls by its bright pink eyelids, a feature shared with no other owl species in the world. Verreaux's eagle-owl is a highly opportunistic predator equipped with powerful talons. Just over half of its known diet is comprised by mammals but equal or even greater numbers of birds and even insects may be hunted locally, along with any other appropriately sized prey that is encountered. This species is considered of Least Concern by IUCN as it occurs over a wide range and has shown some adaptability to human-based habitation alterations and destruction and adaptability to diverse prey when a primary prey species declines in a region. As a large, highly territorial species of owl, it does however occur at fairly low densities and some regional declines have been reported.
The common name commemorates the French naturalist Jules Verreaux. The type specimen that was later described by Temminck at the Rijksmuseum van Natuurlijke Historie was collected by Verreaux while he was still in his teens.
Despite the alternate common name of giant eagle-owl, the Verreaux's eagle-owl is not the largest owl or eagle-owl in the world. It is, however, a very large and powerful owl species. This species is both the largest owl found in Africa and the world's largest owl to occur in the tropics. Among all the world's owls, it is fourth heaviest living owl, after Blakiston's fish owl (Bubo blakistoni), the Eurasian eagle-owl (Bubo bubo) and the tawny fish owl (Bubo flavipes), and is also the fourth longest living owl (measured from the bill to the tip of the tail), after the great gray (Strix nebulosa), Blakiston's fish and Eurasian eagle-owls. Based on body mass and wing chord length, Verreaux's eagle-owl is about the same size as "medium-sized" races of Eurasian eagle-owl, such as those from Central Asian steppe (B. b. turcomanus) and the Himalayas (B. b. hemachalana), slightly smaller than most northern Eurasian races, considerably smaller than Siberian and Russian eagle-owls, and somewhat larger than the smallest Eurasian eagle-owl subspecies, such as those from the Iberian Peninsula (B. b. hispanus) and the Middle East (B. b. omissus or nikolskii).
Verreaux's eagle-owl ranges from 58 to 66 cm (23 to 26 in) in total length. This species has been reported as having an average wingspan of 140 cm (4 ft 7 in), but Mikkola referenced this as the wingspan of a smaller male. The largest known wingspan from a wild female measured nearly 164 cm (5 ft 5 in). While female owls are almost always larger than males, Verreaux's eagle-owl stands out as one of the most sexually dimorphic living owl species, some studies showing the female can average 35% heavier than the male. In comparison, the females of the nominate subspecies of Eurasian eagle-owls and great horned owl (Bubo virginianus) are reported to average approximately 20% and 25% heavier than the males, respectively. The full range of reported body mass in the species ranges from 1,615 to 2,000 g (3.560 to 4.409 lb) in males against a body mass of 2,475–3,150 g (5.456–6.945 lb) in females. In one study, 4 males were found to have averaged 1,704 g (3.757 lb) while 6 females averaged 2,625 g (5.787 lb). Another study found 5 males to have averaged approximately 1,700 g (3.7 lb) while five females averaged 2,300 g (5.1 lb). Unusually large sizes have been claimed in captivity with claims that specimens measuring up to 75 cm (30 in) in length and 200 cm (79 in) but these are unverified and possibly misreported as these figures match the largest Eurasian eagle-owls. Males heavier than any in the wild have been verified in captivity to weigh up to 2,200 g (4.9 lb). Among standard measurements, the female is reported to measure from 447 to 490 mm (17.6 to 19.3 in), averaging 465 mm (18.3 in), in wing chord, 230 to 273 mm (9.1 to 10.7 in) in the tail, while the same measurements in the male are from 420 to 490 mm (17 to 19 in), averaging 448 mm (17.6 in), and from 220 to 275 mm (8.7 to 10.8 in) in tail length. In both sexes, the tarsus has measured 73 to 86 mm (2.9 to 3.4 in) and the bill (in a small sample) 51 to 54 mm (2.0 to 2.1 in). Based on wing chord size compared to body mass and other linear dimensions, the Verreaux's eagle-owl average somewhat larger in the size of its wings relative to its body size than most other eagle-owls, excluding the Asian fish owls which are also seemingly relatively long-winged.
Overall, Verreaux's eagle-owl are a fairly uniform and somewhat pale gray, with light and fine brownish vermiculations on the underside. The back is more solidly light brown with white spots on the shoulder. The oval facial disc is paler, sometimes ranging into a whitish color, than the rest of the front side of the bird with strong black borders bracketing either side. One other feature that immediately distinguished adult Verreaux's eagle-owls in good light are its pink eyelids. The ecological purpose of their colorful eyelids are not known, however Brown (1965) opined that they replace the colorful yellow to orange eyes of eagle-owls in breeding and territorial displays, since they were very conspicuous in displaying males. Their eyes are dark-brown in color and like all eagle-owls, they have ear-tufts. The ear tufts are blunter and smaller relative to those of other African eagle-owls. The ear-tufts of this species being relatively subtle of this species can be missed in the field especially if they are held lax. In appearance, they are quite easily distinguished if seen well. They are much bigger and bulkier than most other co-occurring owls. The only eagle-owl species in range that approaches its size is the Shelley's eagle-owl (Bubo shelleyi), which may (but is not confirmed to) co-exist with the Verreaux's in northern Cameroon and the southern sliver of the Central African Republic most likely in forest edge and mosaics, but that species is a much darker sooty colour overall with broad black bands on the underside. Shelley's eagle-owl also has considerable different habitat preferences, preferring deep, primary forests, and is much more rarely observed in the wild. The next largest eagle-owl in sub-Saharan Africa is the cape eagle-owl (Bubo capensis). The individual home ranges, if not habitats, of the Verreaux's and cape eagle-owls may abut in nearly every part of the latter distribution. Even in its largest race (Mackinder's eagle-owl, B. c. mackinderi) the cape eagle-owl is around 30% lighter in body mass on average than the Verreaux's eagle-owl, not to mention it being markedly different in almost all outward characteristics. Pel's fishing owl (Scotopelia peli), which occurs in west, central and inland southern Africa and may co-exist with the Verreaux's eagle-owl in much of its range (despite favoring wetland and riparian zones surrounded by wooded areas), can attain similar sizes as the Verreaux's eagle-owl but is dramatically different in color (a rather brighter rufous-cinnamon hue) and lacks ear tufts. In combination, the characteristics of their pink eyelids, dark eyes, relatively uniform plumage and extremely large size render the Verreaux's eagle-owl as nearly unmistakable.
The male's song is an exceptionally deep gwok, gwok, gwonk-gwokwokwok gwokwokwok gwonk. The depth and quality of the song makes confusion by sound more likely with a leopard (Panthera pardus) than any other bird. The song is sometimes considered unmistakable. In Kenya, the voice is considered the second deepest bird call after the southern ground hornbill (Bucorvus leadbeateri). Apparently, the song can carry up to 5 km (3.1 mi) away on quiet nights. The female's call is similar but higher pitched, as in all owls to some extent because the larger female tends to have a smaller syrinx. Like most Bubo owls, breeding pairs not infrequently call together but they are not as well-synchronized as the pair duets of cape eagle-owls (Bubo africanus) which are often found in nearby ranges. The alarm calls of both sexes are often a sonorous whok or hook but variable grunting notes and raspy screams also seem to indicate alarm. Both the female and the young engage in high, piercing calls when begging for food at the nest (at which time the male does the food capture). One other vocalizations recorded include a raspy, drawn-out shrooooo-ooo-eh apparently uttered as a distraction display mainly by the male near the nest. While sound is important to some degree for inner-species relations and hunting behaviour to all owl species, the Verreaux's eagle-owl appears to have relatively small and uncomplicated ear openings compared to several smaller types of owl, as is typical of most living eagle-owl species, this indicating auditory senses are relatively unimportant in this species compared to vision.
There are no known subspecies in the Verreaux's eagle-owl and there is remarkably little variation in their appearance across their considerable distribution. Reportedly, birds in the southern part of their range appear marginally larger on average but these size differences are quite subtle and may be considered as a mild case of Bergmann's rule. While genetic research has been untaken for this species, its closest living relative in the Bubo genus is not fully clear. At one time, the Verreaux's eagle-owl was mentioned as an owl with particularly mysterious genetic alliances among living owls. Per Konig & Weick (2008), the species with studied genetic markers found to be most closely related are a dark-eyed species pair of Asian eagle-owls, the spot-bellied (Bubo nipalensis) and barred eagle-owls (Bubo sumatranus) but these are not particularly closely related to the Verreaux's. Among species with available genomes to study for DNA characteristics, it has been revealed that the fish owls, in particular the brown fish owl (Bubo zeylonensis), is third most closely related species to the Verreaux's. Notably, Konig & Weick did not test the DNA of other African eagle-owls who may bear relation to the Verreaux's eagle-owl based largely on their solid dark brown eyes, namely Fraser's (Bubo poensis), Usambara (Bubo vosseleri), greyish (Bubo cinerascens) and Shelley's eagle-owl, as opposed to other eagle-owls which have yellow to orange irises. Fraser's and Usambara eagle-owls also have a small amount of bare skin around their eyes but this tends to bluish in color and is not nearly as extensive as the pink seen in Verreaux's. Other large owls native to Africa, the fishing owls, also have uniform dark brownish eyes and are sometimes included with the Bubo genus but how closely related they are to modern eagle-owls is unclear. Pliocene fossil Bubo owls with clear similarities based on ostelogical characteristics to the modern Verreaux's eagle-owl (most are currently classified as Bubo cf. lacteus) from South Africa and Tanzania, indicate that the Verreaux's eagle-owl descended from slightly smaller ancestors that increased in size as they diversified from related species.
Range and Habitat
Verreaux's eagle-owl is found through most of sub-Saharan Africa, though it is absent from most of the deep rainforests. The species is found at the highest densities in eastern and southern Africa. Due to the avoidance in this species of primary forests, they are found very spottily in west Africa. They reach their western distribution in The Gambia, Senegal, Guinea and Sierra Leone. Eastward from those countries, the species is distributed in a narrow transitional zone between the Sahara and rainforests to all the way south to the Central African Republic. Seemingly isolated populations occur in central Nigeria and central Mali. In south-western Africa, they range up to as far north as the southern parts of the Republic of the Congo and the Democratic Republic of the Congo down to most of Namibia (excluding the coastal regions) and northern South Africa. In east Africa their distribution is more or less continuous from southern Sudan, Eritrea and inland Somalia down to South Africa as far as the region of the city of Durban.
This species inhabit mainly savanna with scattered trees and thorny vegetation. Verreaux's eagle-owls mainly inhabit rather dry regions, some bordering into arid areas such as semi-desert. In central Mali, for example, near the extreme northwestern limit of the species range, the habitat that hosts these owls averages less than 55 cm (22 in) of rainfall annually. They also range into riverine forest adjacent to savanna and small, semi-open woodland surrounded by open country, though they are less likely to inhabit heavily wooded habitats. South African eagle-owls are not infrequent found around floodplains and marshes with floodplains may provide the primary nesting habitat in some areas. In Uganda, they are largely associated with riparian woodlands. Verreaux's eagle-owl may live at nearly all elevations, from sea-level to near the snow line, at around 3,000 m (9,800 ft) in elevation, in some central African slopes. However, in general, they only sporadically inhabit rocky areas and so are generally very scarce in mountainous regions. The bushveld of southern Africa is near ideal habitat for Verreaux's eagle-owl and the species may be found at near peak numbers here. The species was historically rare to absent from the Kalahari desert which makes up the heart of South Africa, but the introduction by man of invasive trees like conifers, eucalyptus and acacias, irrigation areas and prey species closely tied to man has allowed them to spottily occupy this region.
Verreaux's eagle-owls are nocturnal birds and roost by day in trees, with large, shaded horizontal branches of tall, old trees being preferred. In Kenya, the most often used perch trees were Croton megalocarpus and invasive Eucalypts. Elsewhere, Acacia trees may be used habitually. Despite normally choosing dense foliage to rest in, sometimes they may sit wherever their hunting path ends from the prior night, including relatively exposed perches. They reportedly will sleep rather lightly and will awaken very quickly to defend themselves from attack in daylight hours. Family groups consisting of breeding pairs and their offspring frequently roost together and may engage in allopreening during this time. Reportedly some family groups include eagle-owls that had hatched up to three years prior, which if accurate is exceptional for any type of large owl species. During extremely hot days, this species may flutter its throat for cooling purposes and has been known to bathe in rain and shallow water during extreme heat in the middle of the afternoon but usually drinks when possible during nighttime. Each breeding pair of Verreaux's eagle-owl defends a territory and these may be extremely large, ranging in size up to 7,000 ha.
Verreaux's eagle-owl is considered an avian apex predator, meaning it is at or near the top of the food chain and healthy adults normally have no natural predators. In many known aspects of its hunting behaviour, it is typical of the members of the Bubo genus. This species hunt predominantly in early evening, however they have been observed to swoop on prey during daylight. The owls usually fly to a different perch from their daytime roost to use as their habitual hunting perch. Verreaux's eagle-owls mainly hunt by gliding down on their prey from a perch. However hunting on the wing has been reported, even of flying insects. On occasion, they hunt by flying low over a bush to catch prey by surprise or dash on the wing into dense foliage or through forests to catch a galago or other arboreal prey item. They will also sometimes run after prey on the ground, flapping their wings rapidly as they walk, or wade into shallow waters to pin down fish. The wing size of eagle-owls in general limits their flying speed and abilities in the open and so they require perches to execute most of their hunting behaviour.
Even among the Bubo owls, most species of which are known to be highly opportunistic predators with indiscriminating diets, the Verreaux's eagle-owl is a particularly opportunistic predator. While earlier studies characterized great horned owl, one of the most well-studied members of the Bubo genus, has been as hunting whatever random species they first come across, more modern dietary studies have contrarily shown their prey selection is not completely random and that regionally they selected cottontails and hares as prey instead of other foods regardless of prey population trends and become regional specialists on such prey, to such an extent that it predictably causes owl population declines at times when leporid numbers decline. Furthermore, species-wide, great horned owls may select mammals as prey nearly 88% of the time. In contrast, studies have indicated that for the Verreaux's eagle-owl only around 56% of its diet is comprised by mammals and no single prey type predictably dominates their prey selection by biomass in multiple regions. To date, more than 100 prey species have been counted for this eagle-owl and, with only about half a dozen comprehensive dietary studies known to have been conducted, this probably only represents a small portion of the total prey selected. Estimated prey size for the species has ranged from insects weighing less than 5 g (0.18 oz) to ungulates weighing at least 10,000 g (22 lb). This is the second broadest size range positively attributed to a single owl species for prey items after the Eurasian eagle-owl and the largest exceptional upper prey-size also after the Eurasian species.
The prey type most often associated with Verreaux's eagle-owl are hedgehogs. It appears that this species is the only routine predator of hedgehogs in Africa, most other predators of small-to-medium-sized mammals choosing to pursue other abundant mammals without the hedgehog's prickly defenses. In both the southernmost, from the western cape of South Africa, and northernmost, a partial study of the foods at nests in central Mali, food studies for this species have found hedgehogs to be the most significant contributor of biomass in Verreaux's eagle-owl nests. The two known hedgehog prey species taken are the four-toed hedgehog (Atelerix albiventris), which averages 335 g (11.8 oz) in adults, in the north and the southern African hedgehog (Atelerix frontalis), which averages 350 g (12 oz) in adults, in the south. When capturing hedgehogs, the eagle-owl descends silently with its soft-comb wings and ambushes the hedgehog by imbedding its talons about the face. After death, the hedgehog is skinned of its prickly back before being consumed by either the eagle-owl itself or the young at the nest. This may result in over a dozen hedgehog skins being found around Verreaux's eagle-owl roosts near their nests. The same method of dealing with hedgehogs is utilized by the Eurasian eagle-owl, which is likewise reported as the only routine predator of hedgehogs in its native continent. Other studies have shown that, while hedgehogs are seemingly taken opportunistically, they are at best secondary as contributors of prey both in quantity and biomass.
In general, the diet of Verreaux's eagle-owl is seemingly random and highly variable. Eagle-owl species from temperate zones may have no choice but to predate rodents which are rather small and this may require a nesting pair to hunt up to a dozen rodents nightly. In comparison, the diversity and abundance of rodents is considerably greater in wild areas of sub-Saharan Africa and the Verreaux's eagle-owl seemingly ignores most small rodent species, with no rodent prey species known to average under 30 g (1.1 oz) in adult body mass. In Kenya, the most often recorded prey locally were Tachyoryctes mole-rats, however these were recorded only slightly more often than other genera or species, including non-mammals. Several species of blesmol, a separate family also sometimes referred to as mole-rats, have also been recorded as prey. Several murid species have been hunted ranging in size from the 31 g (1.1 oz) southern multimammate mouse (Mastomys coucha) to the two non-native Rattus species, including the 360 g (13 oz) brown rat (Rattus norvegicus). Some larger rodents they’ve hunted have included the 529 g (1.166 lb) cape ground squirrel (Xerus inauris), the 786 g (1.733 lb) Gambian pouched rat (Cricetomys qambianus) and the 1,900 g (4.2 lb) lesser cane rat (Thryonomys gregorianus). The largest known rodent prey is the South African springhare (Pedetes capensis) at an average adult weight of 3,040 g (6.70 lb). Avery, et al. (1985) opined that springhares may be only taken as carrion as they claim it be too large for the eagle-owl to overpower and indeed at least one South African springhare was fed on as roadkilled carrion. However Avery, et al. (1985) also acknowledge that adult monkeys of larger size are taken alive by the eagle-owls, so it certainly should not be ruled out that they also take live springhares.
Many other mammals taken as prey by Verreaux's eagle-owl are seemingly any encountered except the much larger species, especially those that show a propensity for nocturnal or crepuscular activity. This species has hunted bats in several cases from the 8.1 g (0.29 oz) Lander's horseshoe bat (Rhinolophus landeri), the smallest known vertebrate prey species known for this eagle-owl, to Rousettus fruit bats that weigh over 150 g (5.3 oz). Most other mammalian prey recorded or inferred as hunted by Verreaux's eagle-owl tend to be considerably larger. Both the scrub hare (Lepus saxatilis) and the cape hare (Lepus capensis) have been reported as food, the scrub species estimated to average 2,740 g (6.04 lb) when taken. In parts of Kenya, the scrub hare can be a particularly significant contributor of biomass to the eagle-owl's diet. Other assorted mammalian prey species include the 540 g (1.19 lb) golden-rumped elephant shrew (Rhynchocyon chrysopygus) and the 3,800 g (8.4 lb) cape hyrax (Procavia capensis), although it is possible that juvenile hyraxes are rather more commonly taken than adults.
So far as is known, Verreaux's eagle-owl is the only living owl who predates multiple species of primate, although isolated incidents of predation (normally on young primates) has been reported in two to three other large, tropical owls. Multiple cases of predation against galagos have been reported, unsurprisingly as they represent all nocturnal primates in Africa, although they are seldom identified to species. Known galago prey species have ranged from the 85.3 g (3.01 oz) Thomas's bushbaby (Galagoides thomasi) to the 1,098.2 g (2.421 lb) brown greater galago (Otolemur crassicaudatus). Monkeys are also predated opportunistically. Particularly often reported in foods of the Verreaux's eagle-owl as primates go is the vervet monkey (Chlorocebus pygerythrus). Incidents of successful predation have included vervets that were half-grown, which the eagle-owl was able to fly off with (despite being about as heavy as the eagle-owl itself), and an adult vervet of an estimated weight of 4,000 to 5,000 g (8.8 to 11.0 lb), which an eagle-owl took on the ground and subsequently dismembered. However, considering the formidable gauntlet of predators that vervet monkeys face, the Verreaux's eagle-owl is one of its more minor predators and attacks on them may be considered incidental, due in part to the monkey's primarily diurnal activities. Other monkey species believed to be occasionally vulnerable to attacks include the blue monkey (Cercopithecus mitis), which is similar in size to the vervet, patas monkeys (Erythrocebus patas) and the young of the chacma baboon (Papio ursinus). Adult patas monkeys, averaging some 8,633 g (19.033 lb), can be even larger than vervet monkeys but whether they take prime adults of the species is questionable. There are a few verified cases of Verreaux's eagle-owls feeding on ungulates, however some authors such as Avery, et al. (1985) feel that these generally represent cases of scavenging on carrion. The remains of an adult grysbok (Raphicerus melanotis), weighing an estimated 10,670 g (23.52 lb), was opined with certainty to have been taken as carrion per this study. However, Steyn (1982) accepted that this species could take live prey weighing up to 10,000 g (22 lb) on rare occasions, however he stated in a case of an adult common duiker (Sylvicapra grimmia) being fed on by an eagle-owl that the duiker was likely roadkill. Scavenging on carrion is generally a rare behaviour in owls and has been reported in only a few cases where large owls are exceptionally hungry. Live ungulates verified to have been hunted have included piglets of common warthogs (Phacochoerus africanus), which have an average birth weight of only 665 g (1.466 lb) but grow to over 2,000 g (4.4 lb) in just a couple weeks. Adult Kirk's dik-diks (Madoqua kirkii), one of the smallest antelope species at an average of 4,590 g (10.12 lb) have also been hunted by Verreaux's eagle-owl.
Among mammalian carnivores the bulk of predatory incidents have reportedly involved mongooses. Common, social species from savanna-edge such as the 710 g (1.57 lb) yellow mongoose (Cynictis penicillata) and the 725 g (1.598 lb) meerkats (Suricata suricatta) have been attacked, as well as larger, shy forest dwellers such as the 2,500 g (5.5 lb) Jackson's mongoose (Bdeogale jacksoni). An adult Meller's mongoose (Rhynchogale melleri) weighing about 2,200 g (4.9 lb) which was taken by a Verreaux's eagle-owl on the wing represents the second heaviest known object successfully flown with this species after the aforementioned half-grown vervet monkey. Other smallish carnivores known to fall prey to Verreaux's eagle-owls include the 292 g (10.3 oz) African striped weasel (Poecilogale albinucha) and its larger cousin, the 817.5 g (1.802 lb) striped polecat (Ictonyx striatus), which in one nest from the border of the Kalahari represented the sole prey species for a pair of eagle-owls. In southern Africa, both the cape genet (Genetta tigrina), averaging 1,732 g (3.818 lb), and the 1,600 g (3.5 lb) black-footed cat (Felis nigripes), the smallest felid in Africa, have been included amongst their prey. The Verreaux's eagle-owl is thought to be a threat to even larger carnivores, including the 4,150 g (9.15 lb) bat-eared fox (Otocyon megalotis) and the 10,000 g (22 lb) aardwolf (Proteles cristata), although whether healthy adults of the latter are in danger is doubtful. An scientifically-observed attack on an adult African wildcat (Felis silvestris cafra), which averages about 4,000 g (8.8 lb), was aborted after the eagle-owl apparently deemed that the felid was too heavy to take flight with. However, domesticated cats of any size may fall prey to Verreaux's eagle-owl. At Lake Baringo Country Club in Kenya, this eagle-owl has apparently taken to habitually hunting outdoor cats, reportedly making the cats on the grounds highly skittish.
Verreaux's eagle-owl takes a diverse range of birds as prey. More than 50 avian prey species have been identified and they may locally exceed mammals in importance in the diet, somewhat unusually for eagle-owls. No one type of bird can be said to be predictably favored as prey and any avian species unfortunate enough to have a nighttime roost or nest that happens to be in an eagle-owl's foraging path may fall victim to this species. Many cases of predation involve nest robbery, with nestlings or fledglings being taken, although adult birds may be taken just as often, especially for species with less conspicuous nests. In South Africa's De Hoop Nature Reserve, it was found that birds were somewhat better represented by both number, 43.3% of remains, and biomass, 57.84% of remains, than mammals or any other prey group. The species best represented in biomass in the prior study was the black-headed heron (Ardea melanocephala) with several adults estimated to average 1,260 g (2.78 lb) being found among the prey remains. Other fairly common, largish herons are also known to fall prey at night to Verreaux's eagle-owl including the 873 g (1.925 lb) great egret (Ardea alba), the 1,443 g (3.181 lb) grey heron (Ardea cinerea) and the 975 g (2.150 lb) purple heron (Ardea purpurea). Other medium-sized water birds known to have been represented in this species diet include the 1,008 g (2.222 lb) yellow-billed duck (Anas undulata), the 983 g (2.167 lb) African black duck (Anas sparsa), the 596 g (1.314 lb) African swamphen (Porphyrio madagascariensis) and the 825 g (1.819 lb) red-knobbed coot (Fulica cristata). Besides herons, another well-represented group of birds in the diet are galliforms. Perhaps the most widely prey species reported from this group is the 1,229 g (2.709 lb) helmeted guineafowl (Numida meleagris), which may seasonally dominate the eagle-owl's food in Kenya. More modestly sized wild galliform species reported in the diet including the 96 g (3.4 oz) common quail (Coturnix coturnix) and the 390 g (14 oz) grey-winged francolin (Francolinus africanus). Domestic fowl, especially those allowed back to a semi-feral state and thus sleeping in the open as is prevalent in Africa, are taken when encountered, including chickens and peafowls.
Various upland birds recorded as prey include the 177 g (6.2 oz) Namaqua sandgrouse (Pterocles namaqua), the 350 g (12 oz) rock pigeon (Columba livia), the 84 g (3.0 oz) laughing dove (Streptopelia senegalensis), the 169 g (6.0 oz) Senegal coucal (Centropus senegalensis), the 49 g (1.7 oz) scaly-throated honeyguide (Indicator variegatus) and several species of hornbill, ranging in size from the 139 g (4.9 oz) northern red-billed hornbill (Tockus erythrorhynchus) to the 1,235 g (2.723 lb) silvery-cheeked hornbill (Bycanistes brevis). Among passerines, the most frequently taken are likely to be corvids, which are often favored by Bubo owls from around the world due to their large size, relatively open nests and frequently easy-to-find, communal nocturnal roosts. To date the cape crow (Corvus capensis) and pied crow (Corvus albus) are the corvids reported in dietary studies but in Ethiopia thick-billed ravens (Corvus crassirostris), which at 1,500 g (3.3 lb) are possible the heaviest corvid species in the world, mobbed them vigorously and seemed to consider them a primary threat. Smaller passerines are by no means ignored. White-eyes are among the more frequently taken smaller passerines, with the 10.9 g (0.38 oz) African yellow white-eye (Zosterops senegalensis) being the smallest identified avian prey species, although penduline tits (Anthoscopus ssp.) (thus far unidentified to species) are likely to be even smaller. The largest bird to be hunted to Verreaux's eagle-owl is complicated by the fact that they often take relatively small nestlings of larger species, such as ostriches (Struthio camelus) and grey crowned cranes (Balearica regulorum). The only avian prey items successfully attacked larger than other types of birds of prey (reviewed later) are likely bustards. Most predation records have reported on relatively small bustards, namely northern (Afrotis afraoides) and southern black korhaans (Afrotis afra), which average only 745 g (1.642 lb) and 690 g (1.52 lb), respectively. Larger species of bustard thought to be threatened by Verreaux's eagle-owl are the 4,790 g (10.56 lb) Denham's bustard (Neotis denhami) and the 8,430 g (18.58 lb) kori bustard (Ardeotis kori), although it is not clear whether adults (especially males) are attacked in the latter species.
Reptiles and amphibians are occasional prey for Verreaux's eagle-owls. Various snakes have been included in their diet ranging from the small, innocuous brown house snake (Boaedon fuliginosus) at 31 g (1.1 oz) to large and venomous Egyptian cobras (Naja haje) weighing over 454 g (1.001 lb). Frogs were amongst the prominent prey recorded for suburban-breeding eagle-owls in South Africa, namely the African red toad (Schismaderma carens) and the guttural toad (Amietophrynus gutturalis). Unidentified frogs were fairly significant in the diet from Kenya. The largest herpetological prey known is the Nile monitor (Varanus niloticus), at a mean mature mass of 5,850 g (12.90 lb), these primarily diurnal reptiles can provide a fulfilling meal but can be hard to subdue even if ambushed unaware. Predation on fish has been reported but no fish have been observed firsthand in dietary studies. A surprisingly wide range of invertebrates have been reported in the diet for this species. In some cases, they may prey on insects as small as termites and even smaller invertebrates have been recorded in pellets such as orbatid mites and Sarcophaga flies, but are likely consumed incidentally while eating a larger item, either from carrion or the stomach of the prey itself. Unidentified scorpions, spiders and millipedes have also been reported in their foods. Most attacks on insects involve large ground beetles or dung beetles. Verreaux's eagle-owl has been known to feed on dung beetles among herds of African buffalo (Syncerus caffer) by night, boldly diving below the massive bovids’ legs, and will readily feed on beetles among elephant dung when available.
Interspecies predatory relations
Sub-Saharan Africa has many species of owl, although there is less species diversity than in some areas of similar latitude in the neotropics and south Asia. It also hosts the most species of eagle-owl with approximately eight "typical" Bubo species and all three fishing owl species as well. Due to the diversity here, there are a number of distinctions between habitat preference, primary prey types and body size among the eagle-owls of Africa. The three smallest species of this genus reside solely in Africa, the akun eagle-owl (Bubo leucostictus), the greyish eagle-owl (Bubo cinerascens) and the spotted eagle-owl (Bubo africanus), in rough order of increasing size. These species are all primarily insectivores and are much reduced in the size and strength of their feet and talons compared to most other contemporary species, although the spotted eagle-owl can be locally specialized to feed on small rodents as well. While the akun is a primary forest-dweller as are the medium-sized Fraser's and Usambara eagle-owl and large Shelley's eagle-owl and thus is not likely to co-exist with Verreaux's eagle-owls except in rare cases, the northerly-distributed greyish eagle-owl (which was at one point considered merely a subspecies of the spotted) and the southerly-distributed spotted eagle-owl have much more similar habitat preferences to the Verreaux's species. Of the non-piscovorous owls in Africa, the cape eagle-owl can have a somewhat broad diet and a capability to take large prey but is more specialized to feed on a narrow range of mammals, mole-rats often supplemented with rock hyrax, than the Verreaux's eagle-owl. The cape eagle-owl has a fairly strong preference for nesting and hunting within the confines of rocky and mountainous habitats, whereas the Verreaux's is at best sporadic in such areas. In east Africa and South Africa, habitat degradation has allowed the more adaptable Verreaux's eagle-owl to move into areas inhabited by cape eagle-owls and has presented the possible issue of the Verreaux's competitively excluding the smaller species.
Outside of the Bubo genus, other owls in Africa are much smaller than Verreaux's eagle-owls and are more likely to be viewed as prey than competition. Among the small-to-mid-sized owls that have fallen prey to this species including the barn owl (Tyto alba) and the African grass owl (Tyto capensis), both of which average around 419 g (14.8 oz) in body mass in Africa, the 334 g (11.8 oz) marsh owl (Asio capensis) and the 216 g (7.6 oz) southern white-faced owl (Ptilopsis granti). The only verified interactions with other typical eagle-owls have been predatory, as the 645 g (1.422 lb) spotted eagle-owl has been recorded among their prey in a few cases. There are several owls was broadly similar habitat preferences from African scops owls (Otus senegalensis) to African wood owls (Strix woodfordii) that have not been reported as food but are almost certainly occasionally threatened by Verreaux's eagle-owls. As is commonly the case with eagle-owls, the Verreaux's eagle-owl is perhaps the most serious predatory threat to diurnal raptors in its range, most often ambushing raptors on their prominent nests upon nightfall and freely killing birds of prey of any age from nestlings to adults. Such prey is not quantitatively significant as a food source but since raptors as a rule are sparsely distributed the habitual visitation of a single or pair of Verreaux's eagle-owl can potentially be devastating to a local population. Among the species known to be attacked have included, among small-to-medium-sized raptors, include the 638 g (1.407 lb) African harrier-hawk (Polyboroides typus), the 675 g (1.488 lb) pale chanting goshawk (Melierax canorus), the 507 g (1.118 lb) African marsh harrier (Circus ranivorus), the 110 g (3.9 oz) scissor-tailed kite (Chelictinia riocourii), the 291.5 g (0.643 lb) African goshawk (Accipiter tachiro) the 875 g (1.929 lb) common buzzard (Buteo buteo) and the 640 g (1.41 lb) Wahlberg's eagle (Hieraaetus wahlbergi).
There are reports of Verreaux's eagle-owls attacking even larger raptorial birds. A case of the Verreaux's eagle-owl killing an adult Pel's fishing owl in Botswana was verified. At roughly 2,000 g (4.4 lb) in body mass, the fishing owl is of nearly the same size as the eagle-owl. Cases where they’ve attacked the nests of particularly large diurnal birds of prey have sometimes involved only nestlings being victimized, such as attacks on the hooded vulture (Necrosyrtes monachus) and the bateleur (Terathopius ecaudatus), none of the adults, which are about the same average adult body mass as the Verreaux's eagle-owls, have been reported as prey. However, in some even larger birds of prey, adults as well as nestlings and fledglings have been killed. Successful nighttime attacks have been reported on adults of the 2,810 g (6.19 lb) African fish eagle (Haliaeetus vocifer) and the 4,017 g (8.856 lb) secretarybird (Sagittarius serpentarius). In the Matobo Hills of Zimbabwe, the Verreaux's eagle-owl has been considered as one of the inferred predators of 4,195 g (9.248 lb) Verreaux's eagle (Aquila verreauxii), although whether adults or only nestlings are vulnerable is not definitely clear.
Other than these rare cases, larger birds of prey such eagles are not usually harassed by Verreaux's eagle-owl and are more aptly viewed as competitors. In fact, the martial eagle (Polemaetus bellicosus), in most regards the largest eagle in Africa, is sometimes regarded as the diurnal ecological equivalent of the Verreaux's eagle-owl. The martial eagle has rather similar habitat preferences to the eagle-owl and has a similarly broad, opportunistic diet. At roughly 4,200 g (9.3 lb) in average body mass, the martial eagle is roughly twice as heavy so Verreaux's eagle-owl and takes correspondingly large prey, its average prey weight range being 1,000 to 5,000 g (2.2 to 11.0 lb) and the eagles are capable of exceptionally taking prey up to nearly nine times their own weight, whereas quantitatively most of the eagle-owls prey does not exceed 1,000 to 1,500 g (2.2 to 3.3 lb). Verreaux's eagle-owl are likely to give martial eagles a respectful amount of space during daytime and there are no records of the two species harassing one another. Another particularly large and aggressive eagle, the crowned eagle (Stephanoaetus coronatus), is largely a forest-dweller and so is less directly a diurnal equivalent. There a single recorded instance of an immature crowned eagle being aggressively displaced at night by an adult Verreaux's eagle-owl when it happen to encroach on the eagle-owl's territory but without bloodshed and eagle-owls would do well to avoid the exceptionally powerful eagle. Taken together, the Verreaux's, the Shelley's and the cape eagle-owls could be seen as nocturnally replacing the eagle species of martial, crowned and Verreaux's eagles in the respective habitats of savanna, forest and rocky areas but their increasingly diminishing size in comparison to the diurnal eagles means that, generally speaking, less large-bodied prey is likely to be attacked. Despite its place near the top of the nocturnal avian food chain, in 2013 a remote wildlife camera videotaped a black-backed jackal (Canis mesomelas) attacking and killing a Verreaux's eagle owl at a watering hole. Similar rare successful attacks on great horned owls and Eurasian eagle-owls by smaller red foxes (Vulpes vulpes) have been reported but in these cases the owls were mysteriously grounded in the horned owl and distracted by nesting into too-easily accessed sea cliffs in the eagle-owl. More often foxes are prey rather than predators for northern Bubo owls. Given that the Verreaux's eagle-owl is surprisingly bold about coming to their ground to, among other things capture beetles, feed on prey too large to carry in flight or, as is likely the case in the jackal attack, drink water, it is possible that the jackal was simply able to ambush an incautious eagle-owl rather than a grounded one.
In the heart of their distribution, i.e. east Africa, breeding activity in this species can peak any time from February to September, but can occur nearly any month at the species level. The timing of breeding is said to be correspondent roughly to the regional dry season, so averages earlier in the northern part of the range (before February) and later (July to September) in the southern part of the range such as Kenya and South Africa. In the northern part of the range, breeding season commenced in November in Mali, in November and December in Senegal, December in Equatorial Guinea and January in Nigeria. The monogamous pair is quite stable, most likely mating for life. As in most owls, a courtship display is both to establish mates for a newly mature pair of eagle-owls or to strength pair bonds prior to nesting. Vocalizations during courtship displays consist of relatively rapid and excited calling, hooting and whining. The pair during courtship will bow to one another, flick open their wings and preen each other's feathers, with the male taking the more active part in the courtship ritual. Like all raptorial birds, Verreaux's eagle-owls are strongly territorial. The pair will defend their territory by their song and sometimes (though rarely) through duets. The territories of Verreaux's eagle-owls can range up to 7,000 hectares in size, although average territory sizes are seemingly unknown.
Like great horned owls, but unlike Eurasian eagle-owls, the Verreaux's eagle-owls normally uses old nests built other birds as their own nests. Usage of a nest site other than those constructed by other birds is considered rarer even than in the horned owl and is viewed as almost exceptional in some parts of this species range. Existent reports of this species building its own nest are certain to be dubious, as no known living owl builds a nest and only a small handful of owl species have been verified adding a small amount of nesting material to an existing surface or nest. They variety of bird nests they use is extreme. Large stick nests in sturdy trees are generally used. In southern Africa, recorded nest heights have ranged from 6 to 25 m (19 ft 8 in to 82 ft 0 in) off the ground. Like other Bubo owls, the large nest of large-bodied accipitirids are often popular for use, due to the often huge size and sturdiness of construction typical in this family, with the nest builders devoting up to four months to their construction. However, perhaps the constructor of nests that most often host Verreaux's eagle-owls are hamerkops (Scopus umbretta). In everywhere from Mali to South Africa the eagle-owl has been recorded using old nests built by this species. The unusual, massive nest is an enclosed circle of sticks with a side entrance that are often very large relative to the size of the hamerkop, a smallish, compact wading bird. Usually the eagle-owls nest on the flat top of the hamerkop nest rather than the interior which is usually too small for the eagle-owls to enter and this can provide a rather safe structure for the eagle-owl family to call home. Other nest builders which are popular as hosts are vultures, eagles (at least eight species have built nests used by these eagle-owls), secretarybirds, crows and even much smaller birds such as weavers, which build huge communal nest structures which the eagle-owls then similarly nest on top of. Most nests are already abandoned when the Verreaux's eagle-owl take over it, in large accipitrids for example, many build alternate nests which are not used for years on end. However, if the nest is occupied, the Verreaux's eagle-owl pair readily displaces the occupants and sometimes feeds on the birds in them. Species known to be successfully displaced from their nests have ranged up in size to lappet-faced vultures (Torgos tracheliotos), which are more than three times heavier on average than the Verreaux's eagle-owl. In some cases, hamerkops have been known to try to defend their nest from the eagle-owls but are usually chased away. Verreaux's eagle-owls have been known to displace other opportunistic nest usurpers such as other owls and falcons in order to take over nest structures for themselves. In one case, a pair of eagle-owls nesting on top of a hamerkop nest while the interior of the nest was occupied by Egyptian geese (Alopochen aegyptiacus), an unusual aggressive species of waterfowl that uses nests built by other species. In rare cases, Verreaux's eagle-owls have been recorded using large, old hollows, the stem of a palm tree or on a very dense tangle of creepers or orchids instead of birds’ nests as a nesting site.
On average, the female lays two white eggs, which typically measure 62.6 mm × 51.4 mm (2.46 in × 2.02 in), with a range in height of 58 to 66 mm (2.3 to 2.6 in) and a range in width of 48 to 54 mm (1.9 to 2.1 in). The eggs weigh from 93 to 101.6 g (3.28 to 3.58 oz), the upper weight being the mean mass of the first egg and the lower weight being the mean mass of the second egg. The eggs are reportedly laid at up to 7 day intervals and may take up nearly seven days as well between hatching. Most nest reportedly contain two eggs, but some may contain only one, and no more than two has been recorded in this species. The adult female incubates the eggs for 33 to 39 days, the incubation stage being slightly longer than those of most other eagle-owls, at least the more northern species. On average at hatching, the young weigh about 60 to 70 g (2.1 to 2.5 oz). The weight of the nestling can triple within five days after hatching. Due to the extreme interval between the hatching of the first and the second egg, the older owlet is always considerably larger than the second. As is widely reported in different kinds of raptorial birds, the smaller chick usually dies in the nest. This may be due to starvation upon being outcompeted for food by the older chick or the smaller chick may be being attacked and killed by its older sibling. Usually the smaller chick is gone within two weeks after hatching in this species. In rare cases, both chicks are reared and survive to leave the nest, although there are no known cases of two fledglings resulting from a Verreaux's eagle-owl nest in southern Africa. The young are covered in off-white down from hatching on and the pink eyelids may become apparent within the first week of life. By three weeks of age, the chicks down will thicken and darken to a greyish colour with some barring present. By six weeks, the young eagle-owl will start to somewhat resemble an adult, replete with the blackish brackets on the facial disc of the adult but still being fairly downy, particularly about the head. Only a week later, almost all the down is likely to be moulted.
The mother Verreaux's eagle-owl remains on the nest for nearly the entire incubation period while the male hunts for food for both of them. During the brooding stage, which lasts about 20 days after hatching, the female is still fed by the male, but resumes hunting thereafter. During the incubation and brooding stage, the male usually roosts near the nest during the day while the female continually sits about the nest. After the brooding stage, the female normally takes to a perch within a dozen or so metres of the nest. Both parents may use a favor perch near the nest at which they dismantle prey into pieces that can be more easily consumed by their young, these may be called "plucking" perches where birds are more commonly eaten or "peeling" perches where hedgehogs are the most regular prey. Most dietary studies for the species have been from researching the pellets and skins under such perches. The female is an extremely tight sitter both while incubating and brooding, and may not even be displaced from the nest even if shouted at or the tree is struck. When intruders approach too closely, including other eagle-owls, potential predators and humans, the most common response of the parent Verreaux's eagle-owl is to grunt lowly, often raising its ear-tufts and bill-clapping. Both sexes may engage in distraction displays when the area near the nest is encroached, but it usually the male and most displays occur during nighttime but are possible at any time of day or night. During such displays, the adult will fly lover the ground with drooping wings, or alights and drags its wings and flaps about, often while bill-clacking and calling. Similar injury-feigning distraction displays have been recorded in the Eurasian eagle-owl and smaller owl species but are not known in most other Bubo species. In one case, feral dogs were successfully lured away from a young Verreaux's eagle-owl by its parents’ distraction display after the young bird had fallen to the ground. In rare cases, the parent eagle-owls will attack interlopers. In one such case, a person who picked up a young eagle-owl on the ground was several injured after both parents attacked him.
On average, the young Verreaux's eagle-owl leaves the nest at around 62–63 days but cannot fly at this point. It may take roughly anywhere from another two weeks to a month after this before the fledgling is a competent flier. After leaving the nest, the fledgling is "remarkably inactive", making a minimum of effort to fly, and usually selecting a roost within a few feet of the nest which it has awkwardly climbed to will drop to a large bush below the nest. In the nest, the chick will beg for food with a shrill or chittering noise, sometimes bobbing its head or swaying about and transferring its weight between its feet (sometimes called a "hunger dance") and it continues to rely on its parents for food well after leaving the nest. Sometimes after leaving the nest, the young eagle-owls are often mobbed as are adults by other birds of prey and crows during the day, which is often heatedly directed at this species as adult eagle-owls regularly kill these birds at night. The young eagle-owl may dodge to denser branches to avoid being wounded during such attacks. Young Verreaux's eagle-owls may fall to the ground, often as a result of mobbing. If the young bird is discovered on the ground, it may feign death, lying prone with its head lax and its eyes closed. Even if picked up while death-shamming, the young eagle-owl may remain moribund. Upon being left without disturbance after "playing dead", the young Verreaux's eagle-owl will gradually open its eyes and return to a normal state. It is not until they are about 5 months old do most young Verreaux's eagle-owl show the ability to capture prey for themselves. However, the stage at which the young of this species becomes independent appears to remarkably variable. One ringed 9-month-old moved 24 km (15 mi) away from its nest area and was thus seemingly fully independent. On the other hand, Verreaux's eagle-owls of over half-a-year in age who presumably can fly and hunt on their owl have been seen to linger and continue to beg its parents to be fed into the next breeding season and may even be feed by their father while he is also feeding the mother and a new nestling. In Kenya, when a biologists fed a wild juvenile eagle-owl mole-rats and chicken heads in its nest area, the young eagle-owl apparently became remarkably confiding towards the person. The tendency of young eagle-owls to linger into the next breeding season sometimes results in "family groups" being seen roosting together, a very unusual occurrence for an eagle-owl species. One such group consisted of five birds together, including two parents and three owls from the preceding past three years and apparently the younger eagle-owls even helped bring food for the chick once the egg hatched.
On average, sexual maturity in Verreaux's eagle-owls appears to be attained at three to four years of age. In most cases, a pair of Verreaux's eagle-owl is able to nest annually, however in some cases they may nest only every two to three years, in probable situations of extreme food shortages. Annual mortality appears to be fairly low in this large owl species. Few species have been reported to hunt Verreaux's eagle-owls short of the aforementioned jackal attack, even nests have rarely been seen to be predated, although they may on rare occasions run afoul of some predators such as larger felids with the ability to climb, although such cases are as yet unverified. That young birds usually leave the nest before they can fly would appear to endanger them but the threat and distraction display of parent eagle-owls are apparently often successful. Adult eagle-owls can appear nearly fearless, as they have been reported to stand their ground and engage in threat displays when encountered on or near the ground against much larger animals such as rhinoceroses and lions and in such cases are apparently not approached further by the bigger animals although the eagle-owls could easily be killed by such animals if contact was made. The lifespan in the wild is not known to have been researched, however in captivity the species can live for over 15 years, possibly up to 30 years in some cases.
Verreaux's eagle-owl is a seldom-encountered species, occurring at low densities and needing large territories for hunting and breeding purposes. The threats faced by this species are sadly typical of many large birds of prey from around the world. Not infrequently, they are locally rare due to persecution. The normal cause of persecution is their possible status of predators of small domestic stock, though this is certain to be rare, at least in areas with substantial wild prey populations. An additional threat is the residual effects of pesticides, as poison (usually through rodenticide or poisoned carcasses left out for scavengers such as jackals) consumed through prey may badly affect them. They may be killed by flying into novel man-made objects, including wires and massive dams along reservoirs. Habitat destruction can also affect them, as they require ample trees with large bird nests in order to take residence in a given area. In some areas, however, they’ve been shown to be able to nest in peri-urban or suburban areas, showing greater adaptability to human based land changes than many other large birds of prey. In Swaziland, the species is considered Near Threatened and the species has been recommended for threatened status in southern Africa overall. In west Africa and central Africa, the habitat is often marginal for this species, the distribution is sporadic and thus this eagle-owl is only encountered either uncommonly or rarely. The greatest regional stronghold for Verreaux's eagle-owls is seemingly east Africa, in countries such as Kenya, which may have numbers comparable to pre-colonial times. At the species level, they are widespread and to date are not currently considered to be threatened with extinction.
- BirdLife International (2012). "Bubo lacteus". IUCN Red List of Threatened Species. Version 2013.2. International Union for Conservation of Nature. Retrieved 26 November 2013.
- Giant Eagle-Owl, Arkive
- König, C., & Weick, F. (2008). Owls of the World. A&C Black. ISBN 9780300142273.
- Brown, L. H. (1965). "Observations on Verreaux's Eagle Owl Bubo lacteus (Temminck) in Kenya". Journal of the East African Natural History Society, 25, 101-107.
- Avery, G., Robertson, A. S., Palmer, N. G., & Prins, A. J. (1985). "Prey of giant eagle owls in the de Hoop nature reserve, Cape province, and some observations on hunting strategy". Ostrich, 56(1-3), 117-122.
- Beolens, Bo; Watkins, Michael (2003). Whose Bird? Men and Women Commemorated in the Common Names of Birds. London: Christopher Helm. pp. 350–351.
- Hume, R. (1991). Owls of the world. Running Press, Philadelphia. 1991.
- CRC Handbook of Avian Body Masses, 2nd Edition by John B. Dunning Jr. (Editor). CRC Press (2008), ISBN 978-1-4200-6444-5.
- Tana, P. G., Vazquez, A., & Chavez, C. (1997). "Notes on a nest of the Tawny Fish Owl (Ketupa flavipes) at Sakatang Stream, Taiwan.". Wilson Bulletin, 66, 135-136.
- Bull, E. L., & Duncan, J. R. (1993). Great Gray Owl: Strix nebulosa. American Ornithologists' Union.
- Vaurie, C. (1960). Systematic notes on Palearctic birds. No. 41, Strigidae, the genus Bubo. American Museum novitates; no. 2000.
- Rothschild, W. & Hartert, E. "Notes on eagle-owls". Novitates Zoologicae, A Journal of Zoology.
- Vaurie, C. (1963). Systematic notes on Palearctic birds. No. 52, Supplementary notes on Bubo bubo. American Museum novitates; no. 2132.
- Qinghu C., Jianping S. & Zhigang J. (2008). "Summer diet of two sympatric species of raptors upland buzzard (Buteo hemilasius) and Eurasian eagle owl (Bubo bubo) in Alpine meadow: Problem of coexistence". Pol. J. Ecol, 56(1), 173-179.
- "Our big breeding owls". Owl Breeder Wings. Retrieved 2015. Check date values in:
- Field Guide to the Birds of East Africa: Kenya, Tanzania, Uganda, Rwanda, Burundi by Stevenson & Fanshawe. Elsevier Science (2001), ISBN 978-0856610790
- J. del Hoyo, A. Elliott and J. Sargatal, eds. Handbook of the birds of the world. Volume 5. Barn-owls to Hummingbird. Barcelona: Lynx Edicions.
- Owls of the World: A Photographic Guide by Mikkola, H. Firefly Books (2012), ISBN 9781770851368
- Mendelsohn, J. M., Kemp, A. C., Biggs, H. C., Biggs, R., & Brown, C. J. (1989). Wing areas, wing loadings and wing spans of 66 species of African raptors. Ostrich, 60(1), 35-42.
- Earhart, C. M. and N. K. Johnson. 1970. Size dimorphism and food habits of North American Owls. Condor 72:251-264.
- Weick, F. (2007). Owls (Strigiformes): annotated and illustrated checklist. Springer Science & Business Media.
- Biggs, H.C., Kemp, A.C., Mendelsohn, H.P., & Mendelsohn, J.M. (1979) Weights of South African raptors and owls. Durban Museum Novitas, 12: 73-81.
- Musindo, P. T. (2006). Morphological variation in bills and claws in relation to Prey type in Southern African Birds of Prey (Orders Falconiformes and Strigiformes) (Doctoral dissertation, University of Zimbabwe).
- Animal Photo Album. Animal Pictures Archive. Retrieved on 2012-08-24.
- Barlow, C., Wacher, T., & Disley, T. (2005). A field guide to birds of The Gambia and Senegal. Yale University Press.
- Voous, K.H. 1988. Owls of the Northern Hemisphere. The MIT Press, 0262220350.
- Benson, C. W. (1948). Geographical voice-variation in African birds. Ibis, 90(1), 48-71.
- Kelso, L. (1940). Variation of the external ear-opening in the Strigidae. The Wilson Bulletin, 24-29.
- Andersson, C. J. (1872). Notes on the birds of Damara Land and the adjacent countries of South-West Africa. J. van Voorst.
- Olsen, Jery; Wink, Michael; Sauer-Gürth, Heidi & Trost, Susan (2002). A new Ninox owl from Sumba, Indonesia. Emu 102 (3): 223–231.
- Penhallurick, J. M. (2002). The taxonomy and conservation status of the owls of the world: a review. Ecology and conservation of Owls. CSIRO Publishing, Australia, 343-354.
- Brodkorb, P., & Mourer-Chauviré, C. (1984). Fossil owls from early man sites of Olduvai Gorge, Tanzania. Ostrich, 55(1), 17-27.
- Pavia, M., Manegold, A., & Haarhoff, P. (2014). New early Pliocene owls from Langebaanweg, South Africa, with first evidence of Athene south of the Sahara and a new species of Tyto. Acta Palaeontologica Polonica, 60(4), 815-828.
- Buxton, P. A. (1935). Notes on birds from northern Nigeria. Ibis, 77(1), 101-110.
- Wilson, R. T., & Wilson, M. P. (1981). Notes on the Giant Eagle Owl Bubo lacteus in central Mali. Ardea, 69, 205-208.
- Layard, E. L. (1884). The birds of South Africa. Bernard Quaritch.
- Lynesc, A. H. (1925). XV.— On the Birds of North arid Central Darfur, with Notes on the West‐Central Kordofan and North Nuba Provinces of British Sudan (Part IV.). Ibis, 67(2), 344-416.
- Wilhelmi, F. K., & Kaariye, H. Y. Bird observation in the Ogaden Region Somali Regional State,/Ethiopia A Contribution to the Identification of Important Bird Areas.
- South Africa Bird Atlas Project 2 (January, 2010)
- Seavy, N. E. (2004). "Calling activity in Kibale National Park, Uganda". Journal of Raptor Res., 38(3), 208-213.
- Bowdler Sharpe, R. (1892). XLV.—On the "Birds collected by Mr. FJ Jackson, FZS, during his recent Expedition to Uganda through the Territory of the Imperial British East‐African Company". Ibis, 34(4), 534-555.
- Herholdt, J. J. (1993). "Status of the Giant Eagle Owl Bubo lacteus in the Kalahari Gemsbok National Park, South Africa". Gabar, 8, 17-20.
- Maclean, G. L. (1969). "The breeding seasons of birds in the south-western Kalahari". Ostrich, 40(S1), 179-192.
- Pitman, C., & Adamson, J. (1978). "Notes on the ecology and ethology of the giant eagle owl, Bubo lacteus". Honeyguide, 95: 26-43.
- Steyn, P. (1983). Birds of prey of southern Africa: Their identification and life histories. Croom Helm, Beckenham (UK). 1983.
- Errington, P.L. 1932. Studies on the Behavior of the Great Horned Owl. Wilson Bulletin, 12: 212-220.
- Marti, C. D. (1974). Feeding ecology of four sympatric owls. Condor, 45-61.
- Adamcik, R. S., A. W. Todd, and L. B. Keith. 1978. "Demographic and dietary responses of Great Horned Owls during a snowshoe hare cycle". Canadian Field-Naturalist, 92:156-166.
- Andrews, Peter (1990) Owls, Caves, and Fossils: Predation, Preservation, and Accumulation of Small Mammal Bones in Caves, with an Analysis of the Pleistocene Cave Faunas from Westbury-sub-Mendip, Somerset, UK University of Chicago Press. 231 pg.
- Curry-Lindahl, K. Photographic Studies of Some Less Familiar Birds: LXXXIV. Eagle Owl. British Birds, L: 486-490.
- Kingdon, J., Happold, D., Butynski, T., Hoffmann, M., Happold, M., & Kalina, J. (2013). Mammals of Africa, Volume IV: Hedgehogs, Shrews and Bats. A&C Black.
- Hallam, S. L. (2011). Heterothermy and seasonal patterns of metabolic rate in the southern African hedgehog (Atelerix frontalis) (Doctoral dissertation, MSc thesis, Nelson Mandela Metropolitan University, Port Elizabeth).
- Santana, E. M., Jantz, H. E., & Best, T. L. (2010). "Atelerix albiventris (Erinaceomorpha: Erinaceidae)". Mammalian Species, 42(1), 99-110.
- Reeve, N. (1994). Hedgehogs. London: T. & AD Poyser.
- Wassink, G. (2010). Het dieet van de Oehoe in Nederland en enkele aangrenzende gebieden in Duitsland. Limosa. 83: 97-108.
- Marti, C. D., Korpimäki, E., & Jaksić, F. M. (1993). "Trophic structure of raptor communities: a three-continent comparison and synthesis". In Current Ornithology (pp. 47-137). Springer US.
- Craighead, J. J. and F. C. Craighead, Jr. 1956. Hawks, owls and wildlife. Stackpole Co. Harrisburg, Pennsylvania.
- Bennett, N. C., & Jarvis, J. U. (1988). "The social structure and reproductive biology of colonies of the mole-rat, Cryptomys damarensis (Rodentia, Bathyergidae)". Journal of Mammalogy, 69(2), 293-302.
- Avery, D. M. (1985). "The dispersal of brown rats Rattus norvegicus and new specimens from 19 th century Cape Town". Mammalia, 49(4), 573-576.
- Happold, D. C., & Kingdon, J. (Eds.). (2013). Mammals of Africa. Volume 3, Rodents, hares and rabbits. Bloomsbury.
- Dave Taylor's African Safari: Trophic Level IV: Large Carnivores – Verreaux's Eagle Owl – Page 2. sensesofwildness.com
- Brain, C. K. (1983). The hunters or the hunted?: an introduction to African cave taphonomy. University of Chicago Press.
- Mikula, P., & Hromada, M. (2015). "Short Communication: True bats (Microchiroptera) in the diet of Verreaux's Eagle Owl Bubo lacteus". Scopus, 35(1), 50-51.
- Short, L. L., & Horne, J. F. (2006). The Avifauna of an Upland Seasonal Woodland in Central Kenya: Ecology, Behavior, Breeding (No. 53). Zoologisches Forschungsmuseum Alexander Koenig.
- Rathbun, G. B. (1979). "Rhynchocyon chrysopygus. VII. Interspecific Ecology". Advances in Ethology, 49: 51–54. doi: 10.1111/j.1439-0310.1979.tb00150.x.
- Badenhorst, S., van Niekerk, K. L., & Henshilwood, C. S. (2014). "Rock Hyraxes (Procavia capensis) from Middle Stone Age Levels at Blombos Cave, South Africa". African Archaeological Review, 31(1), 25-43.
- Olds, M. & Soshani, J. (1982). "Procavia capensis". Mammalian Species, 171: 1-7.
- Hart, D. (2007). "Predation on primates: a biogeographical analysis". In Primate anti-predator strategies (pp. 27-59). Springer US.
- T. M. Butynski, J. Kingdon, J. Kalina (eds.). 2013. Mammals of Africa. Volume II: Primates. Bloomsbury Publishing, London, United Kingdom, 556 pp. ISBN 978-1-4081-2252-5 (print).
- Seyfarth, R., & Cheney, D. (1990). "The assessment by vervet monkeys of their own and another species' alarm calls". Animal Behaviour, 40(4), 754-764.
- Struhsaker, T. T. (1967). "Ecology of vervet monkeys (Cercopithecus aethiops) in the Masai-Amboseli game reserve, Kenya". Ecology, 892-904.
- Seyfarth, R. M., Cheney, D. L., & Marler, P. (1980). Vervet monkey alarm calls: semantic communication in a free-ranging primate. Animal Behaviour, 28(4), 1070–1094.
- Pasternak, G. M. (2011). Environmental effects on group structure and vigilance in vervet monkeys (Doctoral dissertation, Lethbridge, Alta.: University of Lethbridge, Dept. of Psychology, c2011).
- Josephs, N. (2015). Social and spatial structure of vervet monkey troops (Doctoral dissertation, Lethbridge, Alta.: University of Lethbridge, Dept. of Psychology).
- Ducheminsky, N., Henzi, S. P., & Barrett, L. (2014). "Responses of vervet monkeys in large troops to terrestrial and aerial predator alarm calls". Behavioral Ecology, 25(6), 1474–1484.
- Coleman, B. (2013). Spatial and temporal determinants of samango monkey (Cercopithecus mitis erythrarchus) resource acquisition and predation avoidance behaviour (Doctoral dissertation, Durham University).
- Comparison of play behaviour of four guenon species: Diana monkey (Cercopithecus diana), de Brazza monkey (Cercopithecus neglectus), Patas monkey (Erythrocebus patas) and Vervet (Chlorocebus pygerythus) with regard to self-handicapping; diploma thesis [in English] – 57 pp. Faculty of Natural Sciences, University of South Bohemia, České Budějovice, Czech Republic.
- MacLean, G. (1969) Proceedings of the Third Pan-African Ornithological Congress held at Pretoriuskop, Kruger National Park. pp. 182.
- Steyn, P. (2010). A delight of owls: African owls observed. Jacana Media.
- Common Warthog (Phacochoerus africanus) Fact Sheet, 2015. c2015. San Diego (CA): San Diego Zoo Global; [accessed 2016]. http://ielc.libguides.com/sdzg/factsheets/warthog_com.
- Kingswood, S. C., & Kumamoto, A. T. (1997). Madoqua kirkii. Mammalian Species Archive, 569, 1-10.
- Madoqua, Volume 19, Issue 2 South-west Africa. Nature Conservation and Tourism of the South West Africa Administration., 1997 Cornell University.
- J. Kingdon, M. Hoffmann (eds.). 2013. Mammals of Africa. Volume V: Carnivores, Pangolins, Equids and Rhinoceroses. Bloomsbury Publishing, London, United Kingdom, 544 pp. ISBN 978-1-4081-2255-6
- Taylor, P.J. & Meester, J. (1993). "Cynictis penicillata". Mammal Species, 432: 1-7.
- Larivière, S. (2001). "Poecilogale albinucha". Mammalian Species, 681(1), 1-4.
- Larivière, S. (2002). "Ictonyx striatus". Mammalian Species, 1-5.
- Rasa, O.A.E. (2007). "Diet of a Verreaux's Eagle-Owl in the Kalahari". Gabar, 18: 1.
- "Verreaux's eagle-owl". Cannudrum. Retrieved 2016. Check date values in:
- Stuart, C. T. (1981). "Notes on the mammalian carnivores of the Cape Province, South Africa". Bontebok 1: 1–58.
- Renard, A., Lavoie, M., Pitt, J. A., & Larivière, S. (2015). "Felis nigripes (Carnivora: Felidae)". Mammalian Species, 47(925), 78-83.
- Olbricht, G., & Sliwa, A. (1997). "In situ and ex situ observations and management of Black‐footed cats Felis nigripes". International Zoo Yearbook, 35(1), 81-89.
- Clark Jr, H. O. (2005). "Otocyon megalotis". Mammalian Species, 1-5.
- Bat-eared fox, Otocyon megalotis, J.A.J. Nel and B. Maas, Sillero-Zubiri, C., Hoffmann, M. and Macdonald, D.W. (eds). 2004. Canids: Foxes, Wolves, Jackals and Dogs. Status Survey and Conservation Action Plan. IUCN/SSC Canid Specialist Group. Gland, Switzerland and Cambridge, UK. x + 430 pp.
- Sliwa, A. (1996). A functional analysis of scent marking and mating behaviour in the aardwolf (Doctoral dissertation, University of Pretoria).
- Kingdon, J. (2015). The Kingdon field guide to African mammals. Bloomsbury Publishing.
- Herbst, M., & Mills, M. G. (2010). "Techniques used in the study of African wildcat, Felis silvestris cafra, in the Kgalagadi Transfrontier Park (South Africa/Botswana)". Koedoe, 52(1), 1-6.
- Paul; Helen Harris & Kenya Birds. "Bubo lacteus". Ecoport. Retrieved 2016. Check date values in:
- Tomlinson, D. N. S. (1974). "Studies of the Purple Heron, Part 1: Heronry structure, nesting habits and reproductive success". Ostrich, 45(3), 175-181.
- Hancock, P., & Weiersbye, I. (2015). Birds of Botswana. Princeton University Press.
- Chittenden, H. (2014). "Prey items of Verreaux's Eagle-Owl Bubo lacteus breeding in suburbia". Gabar 25: 15–16..
- Kemp, A. C. (1976). A study of the ecology, behaviour and systematics of Tockus hornbills:(Aves: Bucerotidae) (No. 20). Transvaal Museum.
- Moreau, R. E. (1936). "The breeding biology of certain East African hornbills (Bucerotidae)." Jour. East Africa and Uganda Nat. Hist. Soc, 13, 1-28.
- de Castro, J. J., & de Castro, M. (2014). "Verreaux's Eagle Owl Bubo lacteus attacked by Thick-billed Ravens Corvus crassirostris". Scopus, 32(1), 51-52.
- "Crows and Jays – General characteristics". jrank.org.
- Thiollay, J.-M. Natural predation on quelea. Quelea quelea. Africa's Bird Pest (1989): 216-229.
- Raihani, N. J., Nelson‐Flower, M. J., Moyes, K., Browning, L. E., & Ridley, A. R. (2010). "Synchronous provisioning increases brood survival in cooperatively breeding pied babblers". Journal of Animal Ecology, 79(1), 44-52.
- Bubo lacteus (Verreaux's eagle-owl, Giant eagle owl) Archived December 9, 2011, at the Wayback Machine.. Biodiversityexplorer.org. Retrieved on 2012-08-24.
- Hockey PAR, Dean WRJ and Ryan PG (eds) 2005. Roberts – Birds of southern Africa, VIIth ed. The Trustees of the John Voelcker Bird Book Fund, Cape Town.
- Piersma, T., del Hoyo, J., Elliot, A., & Sangatal, J. (1996). Handbook of the birds of the world: Hoatzin to Auks
- Feldman, A., & Meiri, S. (2013). "Length–mass allometry in snakes". Biological Journal of the Linnean Society, 108(1), 161-172.
- Vawda, A., Burger, F. J., & Smit, A. L. (1981). "Glucose tolerance in the toad Bufo gutturalis (Power)". South African Journal of Zoology, 16(3), 156-162.
- Condon, K. (1987). A kinematic analysis of mesokinesis in the Nile monitor (Varanus niloticus). Experimental biology, 47(2), 73.
- Bartlett, R., P. Bartlett. 1996. Monitors, Tegus, and Related Lizards. Hauppauge, New York: Barron's Educational Series, Inc.
- Vernon, C.J. 1980. "Prey of six species of owl at the Zimbabwe Ruins – 1970-1975". Honeyguide 101: 26-28.
- Pretorius, M. & Wolfaardt, V. (2014). "Verreaux's Eagle-Owl Bubo lacteus feeding on dung beetles". Gabar, 25 (2): 69-70.
- Friedmann, H. & Stager, K. E. (1967) Results of the 1966 Cheney expedition to the Samburu district, Kenya. Los Angeles County Museum of Natural History.
- Benson, C. W. (1962). "The food of the Spotted Eagle-owl Bubo africanus". Ostrich, 33(4).
- Mendelsohn, J. M. (1989). "Habitat preferences, population size, food and breeding of six owl species in the Springbok Flats, South Africa". Ostrich, 60(4), 183-190.
- Riegert, J., Sedláček, O., & Hutterer, R. (2008). "Diet of sympatric African grass owl (Tyto capensis) and spotted eagle owl (Bubo africanus) in the Bamenda Highlands, NW Cameroon". African Journal of Ecology, 46(3), 428-431.
- Ogada, D. L., & Kibuthu, P. M. (2009). "Impacts of Agriculture on the Diet and Productivity of Mackinder's Eagle Owls (Bubo capensis mackinderi) in Kenya". Biotropica, 41(4), 485-492.
- Voous, K. H. (1966). "The distribution of owls in Africa in relation to general zoogeographical problems". Ostrich, 37(S1), 499-506.
- Ogada, D. L., & Kibuthu, P. M. (2012). "Breeding ecology of Mackinder's Eagle-Owls (Bubo capensis mackinderi) in farmlands of central Kenya". Journal of Raptor Research, 46(4), 327-335.
- Jackson, H. D. (1973). "The Cape eagle owl Bubo capensis in Mozambique". Bulletin of the British Ornithologists' Club, 93(10).
- Ogada, D. L., & Kibuthu, P. M. (2008). "Conserving Mackinder's eagle owls in farmlands of Kenya: assessing the influence of pesticide use, tourism and local knowledge of owl habits in protecting a culturally loathed species". Environmental Conservation, 35(03), 252-260.
- Fry, C. H., Keith, S. & Urban, E. K. 1988. The Birds of Africa Vol. 3. Academic Press, London.
- Wright, D., & Hancock, P. (2008). "Pel's Fishing-Owl Scotopelia peli falls prey to Verreaux's Eagle-Owk Bubo lacteus in the Okavango Delta". Gabar, 19(2), 73-74.
- Watson, R. T. (1988). "he influence of nestling predation on nest site selection and behaviour of the bateleur". South African Journal of Zoology, 23(3), 143-149.
- Gargett, V. (1969). "Black Eagle survey, Rhodes Matopos National Park: a population study, 1964–1968". Ostrich, 40(S1), 397-414.
- Cottrell, J.A. (1970). Black eagle fly free. Cornell University (Purnell).
- Boshoff, A. F., & Palmer, N. G. (1980). "Macro-analysis of prey remains from martial eagle nests in the Cape Province". Ostrich, 51(1), 7-13.
- Boshoff, A. F., Palmer, N. G., & Avery, G. (1990). "Regional variation in the diet of martial eagles in the Cape Province, South Africa". S. Afr. J. Wildl. Res, 20, 57-68.
- Ferguson-Lees, J., & Christie, D. A. (2001). Raptors of the world. Houghton Mifflin Harcourt.
- Brown, L. H. (1982). "The prey of the crowned eagle Stephanoaetus coronatus in Central Kenya". Scopus, 6, 91-94.
- Newton, I. (2010). Population ecology of raptors. A&C Black.
- "GRAPHIC: Jackal Kills Giant Eagle Owl at Pete's Pond 7-11-2013". YouTube. Retrieved 2014-12-02.
- Mils, C.T. A Great Horned Owl killed by a Red Fox. Wisconsin Department of Natural Resources, pp. 158.
- Jaume, S. (2000). "Depredaciones de Zorro Vulpes vulpes sobre Búho Real Bubo bubo en un área del litoral Ibérico". Ardeola, 47(1), 97-99.
- ref name= Jaksic>Jaksić, F. M., & Marti, C. D. (1984). Comparative food habits of Bubo owls in Mediterranean-type ecosystems. Condor, 288-296.
- Leditznig, C., Leditznig, W., & Gossow, H. (2001). "15 Jahre Untersuchungen am Uhu (Bubo bubo) im Mostviertel Niederösterreichs-Stand und Entwicklungstendenzen". Egretta, 44: 45-73.
- Storm, G. L., Andrews, R. D., Phillips, R. L., Bishop, R. A., Siniff, D. B., & Tester, J. R. (1976). "Morphology, reproduction, dispersal, and mortality of midwestern red fox populations". Wildlife Monographs, 3-82.
- Verreaux's Eagle-Owl. Owls.org (2012-08-19). Retrieved on 2012-08-24.
- Mackworth-Praed, C. W., & Grant, C. H. B. (1970). Birds of West Central Africa Vol I.
- Collias, N. E., & Collias, E. C. (2014). Nest building and bird behavior. Princeton University Press.
- Tarboton, W. R., & Erasmus, R. (1998). Sasol Owls & Owling in Southern Africa. Struik.
- Archer, G. and Goodman, EM (1961) The birds of British Somaliland and the Gulf of Aden. Vol. III. Oliver & Boyd, Edinburgh.
- Moreau, R. E. (1944). "Clutch‐size: a comparative study, with special reference to African birds". Ibis, 86(3), 286-347.
- Simmons, R. (1988). "Offspring quality and the evolution of cainism". Ibis, 130(3), 339-357.
- Witherby, H. F., Jourdian, F.C.R., Ticehurst, N. F., and Tucker, B. W (1943). The Handbook of British Birds. Nature, 140, 199-200.
- Enriquez, P. A., & Mikkola, H. (1997). Comparative study of general public owl knowledge in Costa Rica, Central America and Malawi, Africa.
- Herholdt, J. J. (1998). "Survival threats and conservation management of raptors in the Kgalagadi Transfrontier Park". Transactions of the Royal Society of South Africa, 53(2), 201-218.
- Cooper, J. E. (1973). "Post-mortem findings in East African birds of prey". Journal of wildlife diseases, 9(4), 368-375.
- van Rooyen, C. & Diamond, M. (2008). "Wildlife-Powerline Interaction Management". Indwa, 6: 7-16.
- Anderson, M. D., Maritz, A. W., & Oosthuysen, E. (1999). "Raptors drowning in farm reservoirs in South Africa". Ostrich, 70(2), 139-144.
- Herremans, M. (1998). "Conservation status of birds in Botswana in relation to land use". Biological Conservation, 86(2), 139-160.
- Monadjem, A., Boycott, R.C., Parker, V., & Culverwell, J. 2003. Threatened vertebrates of Swaziland. Swaziland Red Data Book: fishes, amphibians, reptiles, birds and mammals. Ministry of Tourism, Environment and Communications, Mbabane, Swaziland.
- Monadjem, A., & Rasmussen, M. W. (2008). "Nest distribution and conservation status of eagles, selected hawks and owls in Swaziland". Gabar, 18, 1-22.
- Jenkins, A. R. (2008). A proposed new list of the threatened raptors of southern Africa. Gabar, 19(1), 27-40.
|Wikimedia Commons has media related to Bubo lacteus.|
|Wikispecies has information related to: Bubo lacteus|
- (Giant Eagle-Owl =) Verreaux's Eagle-Owl – Species text in The Atlas of Southern African Birds.
- Verreaux's Eagle-Owl videos, photos & sounds on the Internet Bird Collection