EDITORIAL

Olver, M. D. &; Kuyper, M. A. 1978. Breeding biology of the Whitebreasted Cormorant in Natal. Ostrich 49:25-30.

From 1972–1975 Whitebreasted Cormorants Phalacrocorax carbo bred at the Cedara Dam, Natal, South Africa (29 32S, 30 17E), and from 1973 they fished for food at Midmar Dam, 5 km away and carried the food back to the nestlings. Breeding occurred from April to October and was preceded by a period of courtship. Nesting material was collected by the males and the nests built by the females. The mean clutch size for 1972–1973 was 3,1. Both parents incubated the eggs and guarded the nest and chicks. Growth of the chicks was studied in 1972–1973. The mean number of chicks reared was 1,6 per nest although seven nests contained three nestlings. At 28 days they left the nest when alarmed, but could not fly until 49 days old. The average flying age appeared to be about 53 days. The height of the nests above the ground seemed to determine the nest leaving age. Of the 186 eggs laid in the 60 nests observed over two years, 74% hatched. Fledging success was 52% of eggs laid and 69% of eggs hatched. Chick mortality seemed to be caused mainly by falling from the nests and dying of starvation.     

BREEDING BIOLOGY AND BEHAVIOUR OF THE QUAIL FINCH ORTYGOSPIZA ATRICOLUS

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.     

THE PROBLEM OF NOMENCLATURE

Whitfield, A. K. &; Blaber, S. J. M. 1978. Feeding ecology of piscivorous birds at Lake St Lucia, Part 3: Swimming birds. Ostrich 50:10-20. The diets, foraging periodicities and feeding behaviour of the Reed Cormorant Phalacrocorax africanus, Whitebreasted Cormorant Phalacrocorax carbo and White Pelican Pelecanus onocrotalus were studied at Lake St Lucia, Natal, South Africa, during 1975 and 1976. The Reed Cormorant fishes in shallow water within 100 m of the shore and mainly caught Sarotherodon mossambicus and Solea bleekeri, while the Whitebreasted Cormorant caught Mugilidae, Rhabdosargus sarba and Thryssa vitrirostris in deeper water. The diet of the White Pelican followed three distinct phases: a pre-incubation phase when the birds followed and preyed heavily on migrating Mugil cephalus shoals; an incubation and post-incubation phase when the adults flew a round trip of 200 km to the north to obtain freshwater fish, mainly cichlids, from the Pongolo pans where fishes were concentrated and densities high; and a post-fledgling phase when both adults and juveniles fed on a variety of marine species of fish in Lake St Lucia for about a month before dispersing to other areas. The feeding and breeding of Reed Cormorants and White-breasted Cormorants is discussed in relation to wind speeds, water turbidity and flooding of backwaters. The diet and long-range foraging behaviour of White Pelicans at St Lucia are compared with data from other African lakes. The breeding season of White Pelicans at St Lucia is related to availability of fish and inaccessibility of the breeding site to predators. The latter is determined by lake levels.     

1. A CENSUS AND STUDY OF BIRDS IN ALBANY OPEN THORNBUSHVELD

Williams, A. J. &; Cooper, J. 1983. The Crowned Cormorant: breeding biology, diet, and offspring reduction strategy. Ostrich 54:213-219.

Crowned Cormorants Phalacrocorax coronatus were studied at Dassen and Marcus Islands. The most frequent clutch was three eggs. Egg size varied within clutches with first-laid eggs being largest and heaviest and subsequent eggs progressively smaller and lighter, The mean laying interval was 2,2 days, the mean laying-to-hatching interval was 23,0 days, and the hatching interval was one day. The normal incubation period was 22.4 days. The weight of hatchings was related to the position of the originating egg in the laying sequence. Chicks were fed within 24 h of hatching. Chick development is described over the first 35 days. One chick could fly at 35 days. Hatching success was 48,2%. Hatching success was greatest in second-laid eggs, least in last-laid eggs. The mean number of chicks hatched at a nest was two. Mean diving time was 23,5 s. Most food was fish, particularly klipfish Clinidae and pipefish Syngnathus, 60–160 mm long. The number of offspring produced can be related to food availability by interaction of difference in egg size, hatching asynchrony, and the preferential feeding by adults of the strongest-begging chick. There is a trend towards producing two chicks, normally those from the first two eggs to be laid.     

Breeding biology of the endangered Dupont’s Lark Chersophilus duponti in two separate Spanish shrub-steppes

Capsule: The Dupont’s Lark Chersophilus duponti in Iberia has relatively high breeding success in both core and fragmented habitats, so population declines are more likely to be the result of low juvenile or adult survival.

Aims: To measure important aspects of the reproductive biology of one of the most endangered and least known larks: the Dupont’s Lark C. duponti.

Methods: We monitored 36 nests in 2 Spanish shrub-steppes, one holding one of the largest European populations (250 pairs) and one composed by fragmented habitat patches holding a smaller population (50 pairs).

Results: The breeding season went from late-March to early July. Overall mean (±sd) clutch size was 3.47?±?0.56, and the number of fledglings per successful nest was 3.0?±?1.15. Mean nestling period was short (8.2 days). Nests showed similar daily survival rate during the incubation period (0.9750?±?0.0110) as during the nestling period (0.9545?±?0.0168), with a mean breeding success of 50%. Predation was the main cause of complete nest failure (83.3% of failed nests in both localities).

Conclusion: Breeding parameters did show no significant variation between populations. Breeding success in both sites was generally higher than recorded in previous studies of this and most other lark species, which suggests that breeding success does not compromise long-term viability of these populations. The decline of the studied populations should be explained by other causes, such as a general decrease in habitat quality, habitat loss or habitat fragmentation.     

BIOLOGY OF THE BANK CORMORANT,PART 1: DISTRIBUTION,POPULATION SIZE,MOVEMENTS AND CONSERVATION

Cooper, J. 1981. Biology of the Bank Cormorant, Part 1: Distribution, population size, movements and conservation. Ostrich 52: 208–215.

The Bank Cormorant Phalacrocorax neglectus is a marine species, endemic to southern Africa. Its non-breeding range extends from Walvis Bay to Cape Agulhas. Breeding range extends from Hollamsbird Island to Quoin Rock. Its distribution is broadly similar to that of kelp beds Ecklonia maxima. A total of 44 breeding localities supports approximately 18 000 adult birds; 12 800 (71%) occur on two islands (Ichaboe and Mercury) north of large kelp beds. Adult Bank Cormorants are resident but juveniles may disperse several hundred kilometres. The species is not considered to be seriously at risk to disturbance at most breeding localities. However, modern expansion of fishing activities may affect the very large populations of Ichaboe and Mercury Islands.     

THE INFLUENCE OF THE ENVIRONMENT ON BREEDING SUCCESS OF A SUBURBAN POPULATION OF CRESTED BARBETS TRACHYPHONUS VAILLANTII

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.     

THE BREEDING BIOLOGY OF AN URBAN POPULATION OF ROCK PIGEONS COLUMBA GUINEA

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.     

Aspects of population dynamics and feeding by piscivorous birds in the intermittently open Riet River estuary,Eastern Cape,South Africa

Aspects of the population dynamics and feeding activity of piscivorous birds in the small (c. 5 ha) intermittently open Riet River estuary, on the south-eastern coastline of South Africa, were investigated monthly from August 2005 to July 2006. A total of 188 birds of 13 species were recorded, of which six were wading piscivores, four aerial divers and three were pursuit swimmers. The Reed Cormorant (Phalacrocorax africanus) was the numerically dominant species, with a mean of 8.25 (SD ± 7.90) individuals per count. Mean numbers of the Pied Kingfisher (Ceryle rudis) and Giant Kingfisher (Megaceryle maximus) were 3.42 (SD ± 1.20) and 1.17 (SD ± 0.60) individuals per count, respectively. The remaining 10 species revealed mean values <0.5 individuals per count. Breaching events were associated with a change in feeding groups from waders to pursuit feeders, and a decrease in total bird numbers, most likely due to loss of potential littoral zone foraging habitat for waders resulting from reduced water levels. The highest bird numbers were recorded in winter reflecting the migration of large numbers of Reed Cormorant into the system. Monthly food consumption by all piscivorous birds showed large temporal variability, ranging from 26.35 to 140.58 kg per month.     

BREEDING BIOLOGY OF THE BEARDED VULTURE IN SOUTHERN AFRICA,PART II: THE NESTLING PERIOD

Brown, C. J. 1990. Breeding biology of the Bearded Vulture in southern Africa, Part I: The nestling period. Ostrich 61: 24–32.

The nestling period of the Bearded Vulture Gypaetus barbatus in southern Africa was 124–128 days. The hatching interval between the normal two-egg. clutch was usually 3–6 days (range 2–9 days Only one nestling per clutch survived to the third day. Tittle sibling aggression and no infanticide took place, but the older nestling dominated the younger which obtained no food. For the first 40 days the nestling was closely brooded. The nest duties were evenly shared by both parents, but females brooded at night. Food was brought to the nest usually once or twice per day by both parents, and was stored behind the nest. During days 41–90 parental attendance steadily decreased. Dunng this stage the female spent more time in the nesting area (57%) and on the nest (91%) than the male. Towards the end of this stage the nestlin started to feed itself but preferred to be fed by a parent. From da 91 to first flight the nestling was left unattended and was visited by its parents only to provide food, which it fed from itself. All pars monitored (40 pair-years) attempted to breed every year. The breeding success (n = 18 pair-years) was 0,89 young fledged per pair per year.     

4. UNUSUAL EXPERIENCES WITH BIRDS

Earlé, R. A. 1989. Breeding biology of the Redbreasted Swallow Hirundo semirufa. Ostrich 60: 13–21.

The two races of the Redbreasted Swallow Hirundo semirufa seem to have separate breeding seasons with the northern race H. s. gordoni breeding April-July, while most records for the nominate race fall in October-February. All nests studied were in concrete culverts less than 1 m high. Eggs laid in second clutches by individual females weighed significantly less than eggs laid in first clutches. Eggs hatched on average 16,2 days after incubation started or 18–21 days after the eggs were laid. Only females incubated. Chicks fledged 23–25 days after hatching and reached a maximum body mass of about 31,5 g on day 18 before a steady decline in mass until fledging. Most nesting failures resulted from infertile eggs or starvation of young in the nest (16,2% of all young starved). Overall breeding success was 60,6%. In all, 81,8% of first clutches produced fledglings but only 44,4% of second clutches. Over a three year period 4,9 young were produced per pair breeding in the area (1,6 young/pair/breeding season).     

DO NEST SITE CHARACTERISTICS AFFECT THE BREEDING SUCCESS OF RED BISHOPS EUPLECTES ORIX?

Summary

Ferguson, J.W.H. 1994. Do nest site characteristics affect the breeding success of Red Bishops Euplectes orix? Ostrich 65:274-280.

A colony of Red Bishop birds Euplectes orix in a reed bed near Pretoria was studied during two breeding seasons. Breeding activity was greater during the second year, following increased rainfall. Predation was the most important source of mortality with 25–30% of the nests yielding fledglings. Between 7 and 11% of the nests were parasitised by Diederik Cuckoos. Reed height and distance from the edge of the reed bed were strongly correlated with nest density. From a temporal perspective breeding success was highest in late January following the peak in breeding activity. These observations suggest that overall breeding success is higher when nest densities are low. The mean fledging rate per nest was lower in areas of high nest density. This was, however, a statistical artifact. Multivariate analyses could not identify any environmental factors as predictors of breeding success within a colony.     

4. GAME RESERVES IN SOUTHERN AFRICA

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.     

The importance of observer effort on the accuracy of breeding success estimates in the Common Guillemot Uria aalge

ABSTRACT

Capsule: A data-thinning approach was used to assess the effects of reducing the frequency of nest-checks on estimates of breeding success of Common Guillemots Uria aalge. Inter-year and inter-colony differences in fledging age and their implications for setting a minimum age after which a chick could be assumed to have fledged were evaluated.

Aims: To assess the consequences of reducing sampling frequency on the estimation of breeding success, and on the robustness of the assumption that breeding has been successful if a chick survives to 15 days old.

Methods: Breeding success, ages at fledging and loss of chicks were estimated from daily checks at two Scottish colonies over a six-year period. Data-thinning was used to assess the consequences of reducing checks from daily to every two or three days. Breeding success was recalculated assuming that all chicks surviving to 15 days fledged.

Results: Reducing the frequency of checks from daily to every second or third day resulted in a small but statistically significant increase in the estimate of success. Between 20% and 25% of chick losses occurred when chicks were ≥15 days old. Assuming that these chicks had fledged resulted in significant increases in breeding success.

Conclusion: Assumptions about whether or not a chick fledged had a greater impact on the estimate of breeding success than reducing the frequency of nest-checks from daily to every second or third day. There was no threshold age after which a chick could be assumed to have fledged. These findings are relevant to other monitoring schemes where there is pressure to reduce input. Sampling methods used in monitoring schemes need to be clearly stated and changes in protocols documented so that sampling effects can be incorporated into future analyses.     

VARIATION IN THE CAPPED WHEATEAR

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.     

2. COLLETOPTERA AFFINIS AT THE NEST

Research into the effect of environmental variables on reproductive success of tropical raptors is often constrained by the lack of information on breeding biology. We provide the first detailed information of the breeding biology and nestling development of the Grasshopper Buzzard Butastur rufipennis, an Afrotropical migratory raptor threatened by extensive land transformation in its breeding range. Breeding coincided with the transition from the dry to the wet season. The mean incubation period was 30 d and mean fledging period 36 d. The breeding period was characterised by rapid establishment of territories and short post-fledging dependency periods related to the onset of migration shortly after breeding. Growth rate of body mass, tarsus, wing and primary feathers were similar between sexes, which showed significant but moderate body mass dimorphism at fledging (♂85–90% of ♀). Second hatchlings were smaller in body mass and structural dimensions compared to similarly-aged first hatchlings and singles of the same sex. Survival of second hatchlings was related to body mass ratio with first hatchlings, whereas brood reduction occurred through food competition and siblicide. We provide ageing formulae and photographic records to facilitate further studies of Grasshopper Buzzard nestling development and reproductive success in the region.     

Survival of Reed Warbler Acrocephalus scirpaceus clutches in relation to nest position

Nest survival was studied in relation to nest position of 164 nests of the Reed Warbler Acrocephalus scirpaceus in the Southeastern part of the Czech Republic in 1993. Breeding was successful in 91 (55.5%) cases, whereas 40 (24.4%) were predated, 19 (11.6%) were parasitized by the Cuckoo Cuculus canorus and 14 (8.5%) were destroyed by other causes. Of the predated nests, small mammals accounted for 26 (65.0%) and unknown predators for 14 (35.0%) nests. Rates of predation and parasitism varied in relation to a series of habitat factors and Reed Warblers avoided nest sites most vulnerable to predation or parasitism. Concealed places in the vegetation far away from trees were the safest nest sites.     

CORMORANT AND DARTER PREY SIZE SELECTION UNDER EXPERIMENTAL CONDITIONS

Hustler, 1995. Cormorant and Darter prey size selection under experimental conditions. Ostrich 66:109-113.

The most profitable sized cichlid fish for Reed Phalacrocorax africanus and Whitebreasted Cormorants P. carbo lucidus and Darter Anhinga melanogaster were determined experimentally. A range of sizes was fed to all three species in captivity to determine whether, given a choice, they would choose the most profitable fish. All species chose certain sizes of fish preferentially, but not in accordance with their profitability. The hunger status of the birds at the time of the experiment and the way in which the experiments were designed and carried out probably influenced the size of fish chosen by the birds.     

BIOLOGY OF THE BANK CORMORANT,PART 3: FORAGING BEHAVIOUR

Cooper, J. 1985. Biology of the Bank Cormorant, Part 3: Foraging behaviour. Ostrich 56: 86–95.

The Bank Cormorant Phalacrocorax neglectus, endemic to southern Africa, is primarily a solitary inshore forager. Bank Cormorants forage Primarily on the bottom among kelp beds but also may forage over shingle or coarse sand substrates or in midwater. Breeding birds forage up to 9 km from their colony. Little is known of foraging depth but birds may dive as deep as 28 m. Mean dive duration was 44,9 s and ratio of dives to surface rests was 2,18. In most cases prey is swallowed under water, presumably to avoid kleptoparasitism. Bank Cormorants foraged during daylight hours from before sunrise to after sunset. Birds did not forage in exceptionally rough seas. Mean female foraging bout duration (84,3 min) was significantly longer than that of males (68,4 min) in breeding individuals. Breeding males undertook significantly more foraging bouts (3,47 boutdday) than did females (3,02 bouts/day). No significant differences were found between the sexes when total time spent foraging/day by breeding birds was compared. It is not clear why males foraged more often, but for shorter periods, than did females, but the differences may be related to sexual dimorphism, males being larger than females.     

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.