6. SHORT NOTES

Schmitt, M. B. 1975. Observations on the Black Crake in the Southern Transvaal. Ostrich 46:129-138.

During a four-year study period, several pairs of Black Crakes Porzana flavirostris and their progeny have been studied on a vlei in the southern Transvaal. Morphological differences between male and female are discussed, a double-brooded breeding season is indicated, the development of chicks is described, and the moult cycle is indicated. The Black Crake moults all flight feathers simultaneously and during its breeding season.     

7. SHORT NOTES

Raseroka, B. H. 1974. Diet of the Hadedah Ibis. Ostrich 45:51-54.

The diet of the Hadedah Ibis in Victoria East, Cape Province is described. 60% of the weight of the diet is composed of animals obtainable from the surface of the soil, indicating that the birds can survive in dry areas where the hardness of the ground would prevent probing for the collection of food.     

6. SHORT NOTES

Feare, Christopher J. 1981. Breeding schedules and feeding strategies of Seychelles sea-birds. Ostrich 52:179–185.

A comparison of the breeding schedules of Seychelles seabirds with their feeding strategies showed no relation between synchronous breeding and the ranges over which the birds forage, but there was a relation with flock feeding. Flock feeding birds are largely dependent upon schools of predatory fishes that drive prey species to the surface, and food is thus localized and transient. Synchronous colonial breeding probably helps individuals to locate these localized food sources, but species that are dependent mainly on dispersed prey would derive no benefit from synchrony, and they do, in fact, breed throughout the year.

Within shoals of prey, food is probably superabundant, but feeding space may be limiting. The dark backs of flock feeding birds render them inconspicuous to foraging birds (conspecifics and other species), thereby tending to reduce competition for space within the feeding flocks. The white plumage of species that feed on dispersed prey appears to act as a spacing out mechanism, reducing interference between feeding birds.     

7. SHORT NOTES

Randall, R. and Ross, G. J. B. 1979. Increasing population of Cape Gannets on Bird Island, Algoa Bay, and observations on breeding success. Ostrich 50:168-175.

The South African Gannet Sula capensis on Bird Island has doubled in numbers between 1956 and 1974 and the process is continuing. The increase is similar to that of the two closely related species S. serrator and S. bassana. We estimated from the colony surface area and nest density that the number of birds with nests in 1974/5 was approximately 77 000. Making allowance for non-breeders, there were about 100 000 adults in 1974/5. Guano harvests from 1938–75 show considerable annual fluctuations with an overall downward trend. Poor agreement was found when relating guano harvests to population estimates, when the latter are gauged by colony surface area. We suggest that guano harvests are not good indicators of gannet population trends on Bird Island, primarily because of harvesting methods and environmental conditions. The number of chicks which fledged in the 1976/7 season in a section of the colony was far fewer than expected, even when allowances were made for egg-loss and chick mortality. A combination of heavier-than-usual rainfall and poor management techniques have resulted in high egg-loss and low chick numbers.     

SHORT NOTES

Laycock, H. T. 1982. Moulting and plumage changes in the Thickbilled Weaver. Ostrich 53:91-101.

Thickoilled Weavers were studied in captivity, in the wild and as museum specimens. Moulting follows the normal passerine pattern, but a difference from related species is that there is no post-fledging moult of the flight feathers. Methods were devised for identifying isolated feathers and for aging trapped birds, this being easier in the male. After the breeding season the male undergoes eclipse, which has apparently not been described before, and loses his white forehead patches. Adult males and females moult about the same time, but second-year males moult six or eight weeks earlier. The duration of post-nuptial moult is about four months and is timed to occur during the season when there is maximum food availability. The use of a “moult score” is avoided in this account and the timing of feather loss substituted as having more real meaning.     

SHORT NOTES

Earlé, R. A. 1981. Factors governing avian breeding in Acacia savanna, Pietermaritzburg, Part 3: Breeding success, recruitment and clutch size. Ostrich 52:235-243.

The clutch size and breeding success of eight species of birds were monitored over a two year period in Acacia savanna. The mean clutch size fluctuated within the breeding season and four patterns of clutch size variation were noted. A smaller proportion of large clutches were laid in the 1979 season when less food was available. Breeding success was higher in the dry 1979 season but fewer breeding attempts were made and the overall recruitment was thus lower. At the peak of the breeding season, in mid-November, breeding success was at its lowest. Predation on nests was the greatest factor reducing breeding success although rain and strong winds affected some species.