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1.
A. S. Robertson 《Ostrich》2013,84(1-3):58-66
Robertson, A. S. 1985. Observations on the post-fledging dependence period of Cape Vultures. Ostrich 56: 58–66.

Cape Vultures were observed during their post-fledging dependence period at a colony in the Cape Province, South Africa. Information is presented on the length of the period, behaviour of juveniles and of parents at the nest, survival of juveniles, aggressive interactions between parents and juveniles and retention of the nest site following breeding. At the colony, juveniles initiate contact with their parents, which supply food to their own offspring at the natal site only. Parental aggression was observed over an average period of five months after juveniles had left the nest (range 32–218 days); at two nest sites, the period overlapped with the next season's incubation period, although no transfer of food was observed during this period-of overlap.  相似文献   

2.
D. Whitelaw 《Ostrich》2013,84(4):236-241
Silbernagl, H. P. 1982. Seasonal and spatial distribution of the American Purple Gallinule in South Africa. Ostrich 53:236-240.

The American Purple Gallinule Porphyrula martinica has been recorded 21 times in the southwestern Cape Province of South Africa. Nearly all records fall in the period 22 April to 2 July and nearly all birds were juveniles. The majority of dated records for which weather data are available appear to be of birds starting their northward migration in Buenos Aires Province, Argentina, or Uruguay and caught by strong westerly winds which carry them downwind to South Africa in about five days. Most birds arrive in South Africa in an exhausted condition and markedly below normal weight. Thus it is unlikely that the American Purple Gallinule will establish a breeding population in Africa.  相似文献   

3.
R. J. Nuttall 《Ostrich》2013,84(2-3):110-117
Summary

Nuttall, R.J. 1992. Breeding biology and behaviour of the Quail Finch Ortygospiza atricollis. Ostrich 63:110-117.

During a study of the breeding biology of the Quail Finch Ortygospiza atricollis, observations of nest-building, egg-laying, incubation and nestling periods, and nestling development in a grassland near Pietermaritzburg, South Africa were supplemented with observations of breeding behaviour in captivity. Mean clutch size was 4,5 and eggs were laid at intervals of approximately one day. Incubation began after the third or fourth egg was laid. An incubation period of 15–16 days and an estimated nestling period of 18–19 days was recorded. Incubation and brooding are shared by both sexes. Breeding success was low (26,7% ?28,6%), with most losses resulting from predation during either the egg-laying or incubation stages.  相似文献   

4.
R. K. Brooke 《Ostrich》2013,84(3):164-169
Crawford, R. J. M., Cooper, J. &; Shelton, P. A. 1982. Distribution, population size, breeding and conservation of the Kelp Gull in southern Africa. Ostrich 53:164:177.

The Kelp Gull Lams dominicanus in Africa occurs coastally between Luanda, Angola and Delagoa Bay, Moçmbique. It breeds between Cape Cross Lagoon, South West Africa/Namibia and Riet River, eastern Cape, South Africa. Censuses of nests and breeding birds at all known southern African breeding localities in the period 1976–1981 indicated that 11 199 pairs bred at 52 localities; 79.5% of this population occurred in South Africa, 57,1% in the Saldanha Bay to Dassen Island region, southwestern Cape. Of the breeding pairs 83% occurred on offshore islands and rocks. Colony size at islands is related to their surface area andMayalso be influenced by food availability and the level of human disturbance. The species breeds in a wide variety of habitats ranging from cliffs and rock stacks to wooden platforms, lowlying vegetation among sand dunes and estuarine sandbars. Any available material is used in the construction of nests, whichMaybe as dense as 4/m2 Clutch size is 2–3 eggs. In 1978 breeding took place earlier in South Africa than in South West Africa/Namibia. 92% of the population breeds m sites which are legally protected. Kelp Gulls have decreased or increased in numbers at some breeding localities but there is no clear overall trend. Any increases in colony size near urban areasMayresult in added airstrike hazards.  相似文献   

5.
Mrs. J. A. Scott 《Ostrich》2013,84(3):201-207
Scott, J. A. 1975. Observations on the breeding of the Woollynecked Stork. Ostrich 46: 201–207.

Little is known about the breeding of the Woollynecked Stork Ciconia episcopus in Africa. This paper discusses breeding, adult and nestling behaviour, nests and sites. Seasonal movements are discussed briefly. Eight nests were studied during 1970 to 1974. At one nest incubation was established at 30 to 31 days and the fledging period 55 to 65 days. No feeding of the young was observed at any time, though one eight hour observation period was undertaken. Few mating displays were seen and none away from the nest.  相似文献   

6.
Alan C. Kemp 《Ostrich》2013,84(2-3):61-68
Kemp, A. C. 1995. Aspects of the breeding biology and behaviour of the Secretarybird Sagittarius serpentarius near Pretoria, South Africa. Ostrich 66: 61–68.

Secretarybirds in three adjacent territories were monitored from 1977 to 1988 on grass- and croplands near Pretoria, South Africa. Most observations of breeding biology and behaviour confirmed or extended previous studies. There was no correlation between pairs in occupancy of territory, productivity or development periods of young: this confirms the flexible breeding abilities which are unusual for such a large bird. Some aspects of breeding biology (egg shape and texture, watering of chicks) and behaviour (Wings open and Up-down greeting displays) may be homologous with storks and important in understanding the phylogeny and evolution of the Sagitariidae and other diurnal raptors.  相似文献   

7.
Elliott, C. C. H. & Cooper, J. 1980. The breeding biology of an urban population of Rock Pigeons Columba guinea. Ostrich 51:198-203.

The breeding biology of the Rock Pigeon Columba guinea was studied for three seasons from 1972 to 1975 at the University of Cape Town, southwestern Cape, South Africa. Nests were visited at approximately weekly intervals. The breeding season (September to February) coincided with the end of the winter rainy season and the presence of cereal crops. Clutch size was two eggs in 99% of cases. Mean incubation period was 14,8 days. Incubation was shared as two continuous shifts per day. Growth rate was similar to that in other studies. The mean nestling period was 23,6 days. Second broods after the successful departure of chicks were frequent, the interval between nest departure and re-laying being as little as five days. Hatching success was 66%, chick rearing success 83% and overall breeding success 49%, similar to other Columba pigeons. It is suggested that the production of pigeon's milk is the limiting factor controlling the invariable clutch size.  相似文献   

8.
J. W. H. WILSON 《Ostrich》2013,84(2):108-111
Steyn, P. &; Grobler, J. H. 1981. Breeding biology of the Booted Eagle in South Africa. Ostrich 52:108-118.

The Booted Eagle Hieraaetus pennatus is a breeding visitor to the Cape Province of South Africa, wintering mostly in Namibia on present knowledge. Palaearctic birds probably also reach the Cape but arrive later. Two nests in different localities in the Cape were studied. The birds breed soon after arrival. Both sexes build the nest on a cliff ledge. Incubation, which lasts 40 days, is done mostly by the female. The female spends most of her time on the nest during the first four weeks of the nestling period, but considerably less time thereafter. The male provides nearly all the prey until near the end of the nestling period, and helps to feed the young. Details of nestling growth and behaviour and of parental care are given. The nestling period was 50 and 54 days in two cases. Post-nestling dependence is about two months. Prey preferences in the two study areas were very similar: 54% birds, 33% lizards and 13% rodents. Breeding biology in South Africa is basically the same as that of Palaearctic populations, with the main differences being the habitat and cliff nest site.  相似文献   

9.
Several species of migratory swifts breed in the Western Palearctic, but they differ in reproductive traits and nonbreeding areas explored in Africa. We examined survival and recapture probabilities of two species of swifts by capture–mark–recapture data collected in northern Italy (Pallid Swift Apus pallidus in Carmagnola, Turin, and Common Swift Apus apus in Guiglia, Modena) in the breeding season (May–July). Apparent survival rates were relatively high (>71%), comparable to other studies of European swifts, but showed marked annual variations. We used geolocators to establish the exact wintering areas of birds breeding in our study colonies. Common Swifts explored the Sahel zone during migration and spent the winter in SE Africa, while the Pallid Swifts remained in the Sahel zone for a longer time, shifting locations southeast down to Cameroun and Nigeria later in winter. These movements followed the seasonal rains from north to south (October to December). In both species, we found large yearly differences in survival probabilities related to different climatic indices. In the Pallid Swift, wintering in Western Africa, the Sahel rainfall index best explained survival, with driest seasons associated with reduced survival. In the Common Swift, wintering in SE Africa, the El Niño–Southern Oscillation (ENSO) cycle performed significantly better than Sahel rainfall or North Atlantic Oscillation (NAO). Extreme events and precipitation anomalies in Eastern Africa during La Niña events resulted in reduced survival probabilities in Common Swifts. Our study shows that the two species of swifts have similar average annual survival, but their survival varies between years and is strongly affected by different climatic drivers associated with their respective wintering areas. This finding could suggest important ecological diversification that should be taken into account when comparing survival and area use of similar species that migrate between temperate breeding areas and tropical wintering areas.  相似文献   

10.
D. C. H. Plowes 《Ostrich》2013,84(3):133-144
Olver, M.D. 1984. Breeding biology of the Reed Cormorant. Ostrich 55:133-140.

The breeding biology of the Reed Cormorant Phalacrocorax africanus was studied at Cedara Dam, Natal, South Africa, from 1973 to 1975. Breeding occurred from November to February and was preceded by a period of courtship. Mean clutch size was 3,6 eggs and mean egg measurements were 44,2 x 29,5 mm. The average incubation period was 23,3 days. Young leave the nest at 28 days when alarmed but cannot fly until 35 days old. Hatching success was 84,1%, and fledging success 60,6%.  相似文献   

11.
Warwick Fraser 《Ostrich》2013,84(3):150-155
Fraser, W. 1983. Foraging patterns of some South African flycatchers. Ostrich 54:150-155.

The foraging behaviour of eight species of flycatchers found in South Africa was studied. Four feeding techniques were recognized: hawking, hawking-gleaning, gleaning and pouncing. The Chinspot Batis Batis molitor, Pririt Batis Batis pririt, Paradise Flycatcher Terpsiphone viridis and the Leadcoloured Flycatcher Myioparus plumbeus use hawking-gleaning as their main feeding technique and forage predominantly within the canopy of the vegetation. The Fiscal Flycatcher Sigelus silens, Black Flycatcher Melaenornis pammelaina and Marico Flycatcher Melaenornis mariquensis use pouncing as their main feeding technique and forage outside the canopy. The Spotted Flycatcher Muscicapa striata uses hawking as its main feeding technique and also forages outside the vegetation. While foraging the canopy-feeders are active and continually on the move through the vegetation in their search for prey whereas those foraging outside the vegetation are far less active and employ still-hunting, waiting for their prey to appear.  相似文献   

12.
ABSTRACT South of Mexico, little is known about the fall migration patterns of most Neotropical migrants. I studied the migration of Empidonax flycatchers using mist‐net surveys in northwestern Colombia from late September to mid‐October in 4 yr (2003–2005, 2008). Empidonax species were identified using linear measurements and color patterns. About 62% of captured individuals were reliably identified to species, with 86% identified as Willow Flycatchers (Empidonax traillii) and 14% as Alder Flycatchers (E. alnorum). No Acadian Flycatchers (E. virescens) were identified. Most birds captured were adults (84.9%) and, due to overlap in measurements, I was only able to determine the sex of 16.3% of the birds. Most Empidonax flycatchers migrated through northwestern Colombia during September and October, with individuals migrating through my study area over a period of at least 1 mo. Willow Flycatchers tended to migrate earlier than Alder Flycatchers, a pattern consistent with the fall movements of these two species at other locations. No captured flycatchers were molting either remiges or rectrices, and most (89%) had either no or slight traces of subcutaneous fat. No Empidonax flycatchers were recaptured, suggesting that stopover duration at my study site was brief. My results show that many Empidonax flycatchers can be identified as Willow and Alder flycatchers during the nonbreeding period, and such identification will enhance our knowledge of their geographical distribution and improve our understanding of possible patterns of segregation on their wintering grounds.  相似文献   

13.
《Ostrich》2013,84(3-4):190-194
We collated the literature available on the breeding activity of the Swainson's Spurfowl Pternistis swainsonii and made use of reliable unpublished reports, nest record cards and field observations within the Springbok Flats, Limpopo Province, South Africa to establish breeding seasons and pairing behaviour. The onset of breeding (egg laying) is closely associated with rainfall, with male gonad development, population density and covey size (pairing behaviour), all correlated with rainfall. Peak breeding activity is from January–April in South Africa, February–May in Zimbabwe and March–June in Botswana. Egg laying has been recorded in all months and sporadic egg laying in the winter months is most likely the result of isolated rainfall. Mean clutch size is 5.2 eggs/hen (n = 140) with an incubation period of 23 days and brood hatching success and chick survival of 69.4% over the southern African sub-region. Current hunting seasons within Limpopo Province are in line with the recommended hunting season for this region and should remain unchanged: 15 June–30 September. The success of this phasianid can be attributed to its extended breeding season, high survival rate of hatchlings and the potential of birds to breed within their first year.  相似文献   

14.
15.
Earle, R.A. &; Oatley, T.B. 1983. Populations, ecology and breeding of the Orange Thrush at two sites in eastern South Africa. Ostrich 54:205-212.

The two populations of the Orange Thrush Turdus gurneyi studied represented two races, the nominate gurneyi in Natal and disruptans in Transvaal. In the Transvaal there was a large influx of individuals during the winter but numbers stayed constant during the breeding season with one pair/ha. Natal birds were more sedentary. Food seemed to be a major factor in regulating the winter population size of both the Orange Thrush and the Olive Thrush T. olivaceus in the Transvaal forest as the number of earthworms showed a peak just before the bird numbers peaked. In Natal the Orange Thrush showed a higher degree of specialization in diet than the Olive Thrush which his a mixed diet. Clutches consisted of two eggs and incubation lasted IS days. Chicks were brooded frequently, virtually to the time of fledging, thus protecting them from the cool, wet conditions of the forest. The nestling period was 15–18 days. The Orange Thrush preferred areas in the forest where little vegetation occurred at 1,0-1,5 m and where a good layer of leaf litter was present.  相似文献   

16.

The two species of yellow-nosed albatross, Atlantic (Thalassarche chlororhynchos) and Indian (T. carteri), are morphologically similar, but they differ in breeding behaviour and distribution. Both species are listed as endangered by the IUCN due to the limited number of breeding sites, threats from introduced predators and diseases, and impact of commercial fishing. We quantified genetic variation between and within the two species. Using nuclear (microsatellites and two nuclear sequences) and mitochondrial (control region) markers, we analysed 354 samples from four breeding islands (Atlantic: Nightingale, Inaccessible, and Gough; Indian: Amsterdam) and bycatch samples from South Africa and New Zealand. In addition to all markers separating the two species, nuclear markers showed Atlantic yellow-nosed albatrosses from Gough Island are genetically distinct from those breeding at Nightingale and Inaccessible Islands in the Tristan da Cunha archipelago. Nuclear markers confirmed that all bycatch samples were Indian yellow-nosed albatrosses, however, the bycatch birds from South Africa and New Zealand were distinct from each other and from birds breeding on Amsterdam Island, suggesting colony specific dispersal at sea. Our study supports the current recognition of two yellow-nosed albatross species and recognises genetically distinct groups of both Atlantic and Indian yellow-nosed albatross breeding on different islands, which is important for their conservation and management.

  相似文献   

17.
Largemouth bass Micropterus salmoides are among the world's 100 worst invaders and negatively affect aquatic biodiversity in many regions worldwide. In South Africa there is a paucity of empirical studies describing their impacts. The impact of M. salmoides on the fish community in the Groot Marico River catchment, an otherwise near-pristine river ecosystem and a freshwater ecosystem priority area, was assessed from surveys conducted in 2012. Fish presence and abundance were enumerated using multiple survey techniques, and their association with key habitat variables and the presence or absence of M. salmoides were assessed. A total of 14 native fish species were recorded, besides introduced M. salmoides, which occupied the majority of the mainstem and several tributaries downstream of barriers to upstream movement. Canonical correspondence analysis showed that only one native species, the Marico barb Barbus motebensis, had a negative spatial association with M. salmoides. Assessment of relative distributions showed this species to be excluded from M. salmoides-invaded river reaches, whereas the other native species were not visibly affected by the invader. This species-specificity of the impact of M. salmoides indicates that their impacts in South African streams may be dependent on predator-naiveté of prey.  相似文献   

18.
J. D. Macdonald 《Ostrich》2013,84(3):160-161
Williams, A. J. 1980. Aspects of the breeding biology of the Subantarctic Skua at Marion Island. Ostrich 51:160-167.

The breeding biology of the Subantarctic Skua Catharacta antarctica lonnbergi was studied in two austral summers at Marion Island. Eggs were laid between 23 October and 19 December. The clutch size was one (6%) or two (94%) eggs. The laying interval was two (20%) or three (80%) days and the incubation period was 29 days. Chicks could fly at 50–65 days after hatching. Chicks from first and second hatched eggs in the same brood had similar growth rates. Chicks in one- and two-chick broods had similar growth rates until 50 days after hatching when chicks reared singly were heavier. Egg mortality was 15,8%, chick mortality was 34,8% and the overall breeding success was 50,9%. The results are discussed in comparison with previous studies of Subantarctic and South Polar C. maccormicki Skuas.  相似文献   

19.
A. J. Van Zyl 《Ostrich》2013,84(3-4):291-296
Van Zyl, A.J. 1994. The influence of the environment on the breeding success of a suburban population of Crested Barbets Trachyphonus vaillantii. Ostrich 65: 291–296.

I studied the breeding biology of the Crested Barbet Trachyphonus vaillantii in Colbyn, a suburb east of Pretoria, South Africa, for nine breeding seasons from 1981 to 1989 to examine patterns in annual breeding success, breeding attempt success in multiple broods, and rainfall. The modal incubation period was 14 days and the nestling period ranged from 28 to 31 days. Average clutch size for all the years was 3,3 eggs/clutch and there was no significant difference in clutch size or number of young fledged/nest between years. On average, Crested Barbet pairs made 2,4 breeding attempts/season. There was no difference in clutch size or breeding success between the breeding attempts. Crested Barbets nesting in natural nests laid on average larger clutches than those in artificial nestboxes, but had non-signficantly lower breeding success. Failure to raise Crested Barbet chicks was attributed to parasitism by Lesser Honeyguides Indicator minor, bee swarms occupying nestboxes, and flooding of natural nests. Breeding performance was not correlated with rainfall or adult body size. The suburban environment may be less variable than a natural environment, resulting in a stable breeding Crested Barbet population.  相似文献   

20.
W. L. N. Tickell  R. Pinder 《Ibis》1975,117(4):433-451
The two small albatrosses Diomedea melanophris and Diomedea chrysostoma were studied during five summers and one winter at Bird Island, South Georgia. Although superficially similar in habit small but consistent differences in breeding biology were demonstrated between the two species and may be related to differences in breeding frequency. The breeding season of D. chrysostoma was longer than that of D. melanophris and each species favoured slightly different colony sites. The development time (incubation+fledging) of D. chrysostoma (213 days) was substantially longer than that of D. melanophris (184 days). The eggs of D. chrysostoma were slightly larger than those of D. melanophris and there was marked difference in the behaviour of those breeding adults who lost eggs or chicks. D. chrysostoma departed to sea straight away whereas D. melanophris continued to visit the colony for some weeks before going. Daily weighings of nestlings suggested that chrysostoma bring in less food per a given time than melanophris, and this may account for the longer fledgling period.  相似文献   

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