Morus capensis
Cape gannet

Cape gannets are found in coastal areas of sub-Saharan Africa, from the Gulf of Guinea on the west coast to South Africa and to Mozambique, occasionally Kenya, on the east coast. They breed only off the coasts of South Africa and Namibia on approximately 6 breeding islands: Lambert's Bay, Malgas, and Algoa Bay in South Africa and Mercury, Ichaboe, and Possession Islands in Namibia. (BirdLife International, 2009; del Hoyo, Elliott, and Sargatal, 1992)

Cape gannets are found in coastal and offshore waters, usually less than 120 km from land. They forage mainly over continental shelf areas but are also sometimes seen in pelagic waters. They breed in open areas on flat or gently sloping, offshore islands. (BirdLife International, 2009; del Hoyo, Elliott, and Sargatal, 1992)

Cape gannets are large seabirds, 85 to 94 cm in length and about 2600 g. Like other gannets and boobies (Sulidae), they have a characteristic sleek, but robust body, with strong, webbed feet and a long, robust bill. They have white plumage on most of the body, with yellow on the head, chin, and neck and black primary and secondary wing feathers and tail. About 10% of individuals have white feathers in the tail as well. They have a dark gular stripe on their throat, which is longer than those found in other Morus species. Their legs, feet, and webbing are black and their bills are pale yellow with black markings and black skin around the eyes. Juvenile Cape gannets have uniformly brown plumage, gradually becoming white as they mature. They can be confused with masked boobies (Sula dactylatra), which have white heads, northern gannets (Morus bassanus), which have white tails and secondary feathers, and Australasian gannets (Morus serrator), which have only the central tail feathers black. Sexual dimorphism and subspecies are not described. (BirdLife International, 2009; del Hoyo, Elliott, and Sargatal, 1992)

Longevity in Cape gannets is not reported but they are long-lived, as are other sulids. Natural adult mortality is generally low, less than 10%, and adults live from 10 to 20 years, or as high as over 40 years old. (del Hoyo, Elliott, and Sargatal, 1992)

Cape gannets are social and sedentary. Juveniles disperse long distances (~4000 km) northwards after fledging, remaining in northern areas for a year after hatching. Adults tend to stay in the same general area, typically within 500 km of their breeding island. Some adults, however, wander over 3000 km outside of the breeding season. Cape gannets are active during the day. (BirdLife International, 2009)

Home Range

Cape gannets occasionally wander widely to forage, but generally remain within 500 km of breeding islands. Nests at breeding colonies are very close together, within pecking distance of neighbors. (BirdLife International, 2009; del Hoyo, Elliott, and Sargatal, 1992)

Cape gannets are typically silent except at breeding colonies, where they make a raucous "arrah arrah" call. Boobies and gannets are social birds and use a variety of calls and visual displays, but these have not been described in Morus capensis. (BirdLife International, 2009; del Hoyo, Elliott, and Sargatal, 1992)

Cape gannets forage mainly over the continental shelf for fish, but sometimes enter pelagic waters to forage as well. They eat mainly shoaling fish, including pilchard (Sardinops ocellata, up to 90% of the diet), anchovies (Engraulis capensis), saury (Scomberesox saurus), mackerel (Scomber japonicus), and maasbankers (Trachurus). Fish are captured by plunge-diving, typically from about 20 meters high. Cape gannets also follow commercial fishing and trawling ships to take advantage of discarded fish, offal, and aggregations in nets. One study suggested that a pair of Cape gannets raising a hatchling to independence uses 246 kg of fish in a breeding season. (Adams et al., 1991; del Hoyo, Elliott, and Sargatal, 1992)

Cape gannets are preyed on by great white pelicans and humans. They are large birds that are capable of deterring predators at nests and their habit of nesting colonially on offshore islands help to reduce predation risk on eggs and young. (BirdLife International, 2009)

Cape gannets are important predators of pelagic and coastal fish off the coasts of Africa. (del Hoyo, Elliott, and Sargatal, 1992)

There are no negative impacts of Cape gannets on humans, although some fishermen persecute gannets because they are perceived to compete for fish prey. They do gather around commercial fishing and trawling boats to take advantage of fish aggregations. (del Hoyo, Elliott, and Sargatal, 1992)

Cape gannets are captured for food and fish bait, especially at breeding colonies. They continue to be collected in Angola, but are protected at breeding colonies in South Africa and Namibia. Breeding colonies have also been exploited for guano collection. (BirdLife International, 2009; del Hoyo, Elliott, and Sargatal, 1992)

Cape gannets are considered vulnerable because of their limited breeding range, population declines associated with persecution and exploitation, and continued declines in habitat quality and foraging near breeding colonies as a result of pollution and overfishing. The collapse of the Namibian sardine fishery has seriously impacted Namibian populations (Engraulis capensis). They are also sometimes entangled in fishing gear when they accompany commercial fishing operations to take advantage of discards and aggregations of fish in nets. They are sometimes captured on long lines used in fishing. Population declines of more than 30% have been documented since 1956. They are restricted to 6 breeding islands, making them vulnerable to local stochastic events and guano collection and competition with Cape fur seals (Arctocephalus pusillus) have inhibited breeding at several islands. The global population is estimated at 150,000 pairs. Breeding colonies are protected currently and Morus capensis is protected in South Africa. (BirdLife International, 2009; del Hoyo, Elliott, and Sargatal, 1992)

Cape gannets were previously known as Sula capensis and Dysporus capensis. (BirdLife International, 2009; del Hoyo, Elliott, and Sargatal, 1992)