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.     

BREEDING BIOLOGY OF THE BEARDED VULTURE IN SOUTHERN AFRICA,PART III: THE POST-NESTLING DEPENDENCE PERIOD

Brown, C. J. 1990. Breeding biology of the Bearded Vulture in southern Africa, Part III: The post-nestling dependence period. Ostrich 6l: 43–49.

The post-nestling dependence period of the Bearded Vulture Gypaetus barbatus in southern Africa begins with the first flight of the young bird at 126 ± 2 days after latching (November-January) and ends during the pre-laying nod or the parent birds' next breeding attempt (April-June), a nod of about five months. For the first two weeks after first flit young bid remaine6 within about 200m of the nest, moving up to 800 m by the third week. By a month out of the nest young birds spent about 40% of the day in flight, moved up to 3 km from the nest, began bone-dropping and interacting with young birds from neighbouring nests. At six weeks they began to accompany their parents for part of some of their foraging trips, but returned to the nest alone, and by eight weeks they completed foraging forays with parents Pasting up to 3 h. At 2–3 months out of the nest young birds covered an area of about 42 km², excluding the foraging trips with parents, by 3–4 months, 78km² and 4–6 months, 168 km². Parent birds delivered food for at least five months after the young bird's first flight. Young birds left their natal areas of their own accord, usually during the first month of their parents' next breeding attempt.     

Breeding behaviour of the Bearded Vulture Gypaetus barbatus: minimal sexual differences in parental activities

Monogamous biparental care is expected to occur when opportunities for extra-pair copulations are rare, and both parents are required to raise the chick. Bearded Vultures Gypaetus barbatus fulfill these conditions. Contributions by male and female Bearded Vulture to nest building, nest defence, incubation, nest attendance and chick feeding were studied over five years in eight pairs from the Pyrenees [Catalonia, northeast Spain). Overall, the sexes show equal investment, although the degree of parental effort developed differs depending on the specific activities. During pre-laying, males were significantly more active than females in supplying material to the nest and in territorial defence behaviour, which increased (in both sexes) as the season advanced. Incubation was shared equally both by day and by night. During chick-rearing, the nest was attended by both sexes and the presence of both parents at the nest decreased in parallel with the growth of the chick. Activities related to chick feeding were also equally divided. These results are discussed in the context of female selection of mates and the particular ecology of this species.     

Behavioural and body mass changes before egg laying in the Barn Owl: cues for clutch size determination?

To investigate laying decision and clutch size determination in indeterminate layers, we analysed in-nest activity (nest presence, and copulation, prey deliveries, and entrance frequencies) and female body mass change, as well as their relation to clutch size variation in five Barn Owl pairs (Tyto alba) nesting in eastern France. Body mass of the female and behaviour [copulation frequency, entrance frequency, and prey delivery to the nest by the male (in number and mass)] were monitored using an automated weighing system and a video camera. There was a consistent change of behaviour and foraging activity among pairs ca. 18 days before laying indicating that the females may be tied to the nest at this time. Barn Owls being indeterminate layers have their clutch size determined at the oviposition of the first egg of the clutch. Window correlation analyses between the clutch size and the female body mass gain indicate that the clutch size might be determined no later than a few days before the laying of the first egg. Our results suggest that female Barn Owls may use the pre-laying period to determine the clutch size using cues such as the male food deliveries (a proxy for male quality).     

THE LAYING INTERVAL AND INCUBATION PERIOD OF ROCKHOPPER AND MACARONI PENGUINS

Williams, A. J. 1981. The laying interval and incubation period of Rockhopper and Macaroni Penguins. Ostrich 52: 226–229.

The laying interval and incubation period of Rockhopper Penguins Eudyptes chrysocome and Macaroni Penguins E. chrysolophus were studied at Marion Island in 1974–75 and 1976–77. On average, the laying interval was 4,4 and 4,5 days, the incubation period of second-laid eggs was 34,2 and 35,9 days and that of first-laid eggs was 39,1 and 38,0 days in Rock-hopper and Macaroni Penguins respectively. The laying interval in this genus is longer than that in other penguins. The incubation period is similar to that of most other penguins but the second-laid egg normally hatches before the first-laid egg. The long laying interval and the hatching sequence of the eggs both have important affects upon the mortality of eggs in the genus Eudyptes.     

BREEDING OF THE INDIAN WHITEBACKED VULTURE AT JODHPUR

Vulture populations have declined globally as well as regionally within Africa. Little is known about the status of the African White-backed Vulture Gyps africanus in Kenya, but ongoing studies indicate that its population has declined over the last two decades. A total of 32 African White-backed Vulture nests were monitored in the Masai Mara National Reserve over a five-year period between 2003 and 2007. Mean nesting success was 59%, which is comparable to that of populations from southern Africa. Nearest neighbour distances were significantly closer in wooded habitats (‘trees and shrubs savanna’) than in more open grassland habitats (‘open low shrubs’). Based on nearest neighbour distances, the estimated total breeding population within the Masai Mara National Reserve is 1 106 pairs, a figure that may be an overestimate and requires ground-truthing. Collecting baseline data on numbers of breeding pairs and regular nest monitoring are essential in order to assess the impact of various threats to vultures in Kenya, which include growing threats (elephant-mediated habitat disturbance and fire) as well as emerging threats (such as poisoning with the carbamate-based pesticide Furadan?).     

Incubation capacity contributes to constraints on maximal clutch size in Brent Geese Branta bernicla nigricans

Lack ( 1967 ) proposed that clutch size in species with precocial young was determined by nutrients available to females at the time of egg formation; since then others have suggested that regulation of clutch size in these species may be more complex. We tested whether incubation limitation contributes to ultimate constraints on maximal clutch size in Black Brent Geese (Black Brant) Branta bernicla nigricans. Specifically, we investigated the relationship between clutch size and duration of the nesting period (i.e. days between nest initiation and the first pipped egg) and the number of goslings leaving the nest. We used experimental clutch manipulations to assess these questions because they allowed us to create clutches that were larger than the typical maximum of five eggs in this species. We found that the per‐capita probability of egg success (i.e. the probability an egg hatched and the gosling left the nest) declined from 0.81 for two‐egg clutches to 0.50 for seven‐egg clutches. As a result of declining egg success, clutches containing more than five eggs produced, at best, only marginally more offspring. Manipulating clutch size at the beginning of incubation had no effect on the duration of the nesting period, but the nesting period increased with the number of eggs a female laid naturally prior to manipulation, from 25.4 days (95% CI 25.1–25.7) for three‐egg clutches to 27.7 days (95% CI 27.3–28.1) for six‐egg clutches. This delay in hatching may result in reduced gosling growth rates due to declining forage quality during the brood rearing period. Our results suggest that the strong right truncation of Brent clutches, which results in few clutches greater than five, is partially explained by the declining incubation capacity of females as clutch size increases and a delay in hatching with each additional egg laid. As a result, females laying clutches with more than five eggs would typically gain little fitness benefit above that associated with a five‐egg clutch.     

THE BREEDING OF CORY'S SHEARWATER CALONECTRIS DIOMEDEA ON THE SALVAGE ISLANDS

The breeding of Cory's Shearwater on Selvagem Grande was studied during the seasons of 1968 and 1969, on a number of specially timed visits. After a pre-laying exodus (duration not determined) the birds returned in a mass to the island on 26 May 1969 and laying began immediately reaching its peak on 31 May. Egg dimensions and weights are tabulated. In most cases the female handed over to the male immediately after laying, and the two sexes incubated in alternating spells averaging about six days. The incubation period averaged 53-8 days. The chicks reached their maximum weight at about 53 days, but the fledging period was not determined. In 1968 young birds were leaving the nest on 22–25 October, about 90 days after the 1969 mean hatching date. Herring Gulls were important egg predators, but losses of chicks were few, 29 out of a sample of 30 being alive at the age of about 60 days.     

Relationship between breeding activity and rainfall for Swainson's Spurfowl,Pternistis swainsonii,within southern Africa,with specific reference to the Springbok Flats,Limpopo Province,South Africa

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.     

A new method for catching cavity‐nesting birds during egg laying and incubation

ABSTRACT The physiological condition of female birds during the egg‐laying and incubation periods is of considerable interest and yet is relatively understudied in wild birds, primarily due to the difficulty of catching birds during this period without causing nest desertion. We therefore developed a box‐net to capture cavity‐nesting birds using sections of a mist‐net placed around a metal cubic frame. We captured female Great Tits (Parus major) as they left nest boxes during the egg‐laying and incubation periods and measured desertion rates. Using box‐nets, we captured 108 of 119 (90%) females during egg laying and 10 of 12 (83%) during incubation. Our recapture rate over two consecutive days during incubation was 50% (5 of 10). Females not captured left nest boxes before we attempted to capture them, escaped through a hole in the mist‐net, or remained in nest boxes for more than 2 h, after which we ended capture attempts. Overall, 22% of egg‐laying females deserted, with desertion rates highest early in the egg‐laying period. Desertion rates of females captured using box‐nets did not differ from those of undisturbed females. One of 10 females captured in a box‐net deserted during the incubation period. Box‐nets are portable, can be set up and taken down quickly and easily, and could potentially be used with nest boxes or natural cavities at any height. Box‐nets are easy to construct and adaptable for use with an array of cavity‐nesting birds, and can be an important tool for studying female physiology during egg laying and incubation.     

THE BIOLOGY OF THE WAVED ALBATROSS DIOMEDEA IRRORATA OF HOOD ISLAND, GALAPAGOS

As a nesting species, the Waved Albatross Diomedea irrorata is restricted to Hood Island in the Galapagos archipelago where 12,000 pairs bred in 1971. Outside the islands the species occurs over the northern parts of the Humboldt Current. Two colonies were studied in detail (1970–1971). At the start of a season, males returned first to the colonies and defended a small territory. Copulation occurred without any elaborate ceremony and the female spent little time on land before laying. There was no fixed nest-site, even within a season, and birds moved their eggs considerable distances. This resulted in heavy egg losses. Younger birds bred later than older birds and laid longer but narrower eggs. The average incubation spell varied from four to five days at the extremes of the incubation period to 19 days in the middle. The average incubation and fledging periods were 60 and 167 days respectively. Pairs which lost an egg sometimes adopted the abandoned egg of another bird and successfully reared the chick. Most pairs nested in both seasons. Nesting success was extremely variable, both between years and between colonies. Between 1961 and 1971 at Punta Suarez, virtually no young were reared in four seasons. Even in 1970–71, where nesting success was good, some groups of birds deserted their eggs en masse whereas in neighbouring areas up to 80% of the pairs reared young. The main foods of the young were squid and fish. Birds did not moult wing and tail feathers at the breeding colonies, and about 50% retained some primaries for more than one season, suggesting that successful pairs had difficulty in fitting in a complete moult between breeding attempts. Old feathers were normally found among the inner primaries and at the next moult were preferentially replaced, though adjacent newer feathers were sometimes retained for another season. Some birds bred in their fourth years, but most not until a year or two older. Immatures were present at the colonies late in the breeding cycle, the youngest returning latest and remaining until the last young fledged. Survival of adults and young averaged at least 95% and 93% per annum over many years. Adults and young ringed in 1961 survived equally well. The significance of the timing of the return of immatures and of the large-scale desertion of eggs, apparently not due to food shortage or disturbance, is discussed.     

Breeding biology and success of the Bearded Vulture Gypaetus barbatus in the eastern Pyrenees

We present data from an extensive study of Bearded Vulture Gypaetus barbatus breeding biology in the Pyrenees from 1992 to 1999. Average laying date was 6 January (range 11 December to 12 February, n  = 69) with no significant differences between years. Eighty per cent of clutches were of two eggs ( n  = 20) and average incubation was 54 days (range 52–56, n  = 14). Hatching occurred on average between 21 February and 3 March (range 5 February–7 April) and the first and last chicks fledged in 21–27 May and 20 July, respectively. The average chick age at fledging was 123 days (range 103–133, n  = 20). Bearded Vulture density increased significantly during the study period. Breeding success and productivity declined apparently as a consequence of the increase in the percentage of breeding failures during incubation and chick rearing, most during the hatching period. The factors that may determine breeding failure and the decline in breeding performance are analysed and management recommendations for more effective conservation measures are discussed.     

Partial incubation during egg laying reduces eggshell microbial loads in a temperate‐breeding passerine

Incubation prior to clutch completion may be adaptive if it maintains egg viability by inhibiting eggshell microbial growth, thus reducing the likelihood that the embryo becomes infected. To test this hypothesis, we examined the effect of partial incubation during egg laying on eggshell microbial loads in eastern bluebirds Sialia sialis breeding at a temperate‐zone site. We sampled eggshell microbes prior to and following four days of exposure to either partial incubation during the laying period or ambient environmental conditions without incubation (experimental eggs). Microbial colony counts declined significantly for eggs left in the nest during the laying period but did not vary significantly for eggs exposed to ambient conditions. Initial microbial loads were more similar to those previously reported from tropical than temperate environments, and microbes from potentially pathogenic groups were detected on 88% of first‐laid eggs on the day of laying. Egg viability was maintained when eggs were held indoors for four days without incubation but declined sharply thereafter. Our results suggest that partial incubation during egg laying may enhance egg viability in eastern bluebirds by reducing eggshell microbial loads; these effects appear stronger than those usually reported from the temperate zone.     

ASPECTS OF THE BIOLOGY OF THE FOREST BUZZARD

Palmer, N. G., Norton, P. M. & Robertson, A. S. 1985. Aspects of the biology of the Forest Buzzard, Ostrich 56: 67–73.

Aspects of the biology of the Forest Buzzard Buteo oreophilus in the southern Cape Province were studied. Information was obtained from eight nests, one of which was visited several times during the nesting period, and from a hand-reared free-living bird. Details of nest structure and locality, egg measurements, hatching period (late October to early December), nestling period (50 days ± 5 days), food intake, growth rate and development are given. Probable Cainism was observed at one nest; prey remains collected from this nest included rodents, moles, birds, snakes and insects. The use of pine trees for nesting is discussed.     

Breeding adaptations of Franklin's gull (larus pipixcan) to a marsh habitat

The behaviour and ecology of Franklin's gull were studied at Agassiz National Wildlife Refuge in northwestern Minnesota to determine the adaptations of the species for nesting in marshes. Two factors seemed to be important in colony site selection: cattail dispersion pattern and cattail density. Franklin's gulls prefer to nest in cattail areas closest to open water. The number of nests per unit area decreased as cattail density increased. Nest site selection is dependent on aggression and visibility. Visibility from nest level is the result of cattail placement and height. The distance between nests was directly correlated with visibility. Aggression by gulls on nests was lowered experimentally by decreasing visibility and raised by increasing visibility. Nest platforms were constructed of cattail material, and were attached to cattail stems. Nest material was added to the nests throughout the incubation and brooding period. Material was usually added following nest relief. The egg laying period was from 6 to 28 May. There was more synchrony of egg laying in sub-areas of the colony than in the colony as a whole. Successive eggs in clutches were laid at 24- to 48-hr intervals. The distance between nests decreased during the season as pairs filled in areas that were not defended. Territorial pairs defended an area up to 10 m from their stations prior to egg laying, but defended only the area within 3 m of their nests during incubation. Both members of pairs incubated the eggs and cared for the young. The incubation period was 24 days. The primary predators on adults and young were marsh hawk, great horned owl and mink. Franklin's gulls do not eat eggs or young of gulls. Adults fed on earthworms, insects and grain. Most marked adults fed within 16 km of the colony. Chicks were fed primarily on earthworms. The hatching period was from 30 May to 21 June. Chicks of all ages tested on a visual cliff apparatus were able to perceive the drop. Chicks tested on a 30-degree incline apparatus walked up it when 6 days old and younger, and walked down at 12 days of age and older. Brood mobility was less than in ground nesting species of gulls. In an undisturbed colony the chicks remained on the nest platforms until they were 25 to 30 days old although they were capable of swimming shortly after hatching. Individual recognition between parents and chicks appeared later in this species than in ground-nesting gulls. Adults accepted alien chicks (experimentally exchanged) that were younger than about 14 days old until their own chicks were over that age. Adults accepted larger and older broods than their own, as well as broods of mixed ages. Chicks began to react differently to strange adults at about 16 days of age. The breeding chronology of Franklin's gull is compressed when compared to that of other gulls. Possible selection pressures affecting this synchrony are discussed. The behaviour of the marsh-nesting Franklin's gull is compared with that of typical ground-and cliffnesting gulls; the possibility that the ancestral gull may have been a marsh nester is discussed.     

Sources and timing of calcium intake during reproduction in flycatchers

Calcium availability may limit the reproductive output of birds and snail shells are considered to be the main source of calcium in many passerine species. This study of collared (Ficedula albicollis) and pied (F. hypoleuca) flycatchers evaluates calcium intake of a natural diet in Central Europe, and sex differences in the utilization of experimentally supplemented sources of calcium during the entire breeding period in aviary birds. The study provides the first evidence that successful reproduction of these species depends on the availability of woodlice (Isopoda) and millipedes (Diplopoda). Each of these two components provided about 3 times more calcium than the snail shells contained in a natural nestling diet. The breeding performance of aviary birds was poor when only snail shells and the fragments of eggshells were provided in food, i.e., irregular laying, smaller clutches, eggshell defects (25 of 53 eggs), and eggs dried-up during incubation. In contrast, no defective eggshell or dried-up eggs were found and the overall breeding performance increased 2–3 times when woodlice were added to the food. Females increased their intake of woodlice during both the pre-laying and laying periods, and both sexes did so during the nestling period. Both sexes took more woodlice in the evening than in the morning, independent of the nesting stage. Intake by females was low until 4 days before laying the first egg, then increased to the highest level, dropping immediately after laying the last egg. Intake of woodlice by both sexes increased steadily from hatching until the nestling age of about 10–12 days decreasing thereafter, which corresponds with the period of rapid skeletal growth. In contrast, the intake of mealworms increased until the nestling age of 13–14 days leveling off thereafter which corresponds with the growth curve of nestling body mass.Due to an error in the citation line, this revised PDF (published in December 2003) deviates from the printed version, and is the correct and authoritative version of the paper.     

MINUTES OF THE ANNUAL GENERAL MEETING OF THE SOUTH AFRICAN ORNITHOLOGICAL SOCIETY,HELD AT CAPE TOWN, 26 JUNE 1959

Brown, C. J. 1989. Plumages and measurements of the Bearded Vulture in southern Africa. Ostrich 60: 165–171.

Four different age classes of the southern African Bearded Vulture Gypaetus barbatus are recognized and their plumages described: juvenile (3–24 months old), immature (24–45 months), subadult (45–60 months) and adult (60+ months). There was no significant difference in size between adult male and female birds. Adults were larger than juvenile birds in bill width, beard length, wingspan and mass, and had a higher aspect ratio and wing loading, while juvenile birds were larger than adults in the length of their outer rectrices, tail area, wing breadth and wing area. These features are considered to be adaptive to young birds inexperienced in flying. Immature and subadult birds were intermediate in size between juveniles and adults. Bearded Vultures differ from other large raptors in two sets of physical characteristics, (a) those adapted to cold, mountainous habitat, e.g. feathered head and face, unusually long wings, a high aspect ratio and a particularly long tail, and (b) those adapted to their diet of mainly bones, e.g. wide gape, beard and relatively long talons for carrying food.     

吉林白城地区草原栗斑腹(巫鸟)窝卵数、营巢成功率和繁殖成功率的研究

对分布于吉林白城地区草原生境中栗斑腹巫鸟的窝卵数、营巢成功率和繁殖成功率的初步研究结果表明 ,繁殖期栗斑腹巫鸟种群的平均窝卵数为 5 .0 9± 0 .5 8枚 /巢 ;窝卵数与产卵期、出巢数与产卵期、窝卵数与卵大小之间呈负相关 ,产卵期与孵化率之间存在极显著的负相关关系 ,巢外径与窝卵数之间存在显著的正相关关系 ,巢的其余指标均与窝卵数呈正相关 ;平均孵化期为 12± 0 .4 9d ,孵化率为 36 .3% ,繁殖成功率为 11.11% ;7日龄以上的雏鸟群体大小为 2 .5 6± 1.5 3只 ,栗斑腹巫鸟的雏鸟存活率为 2 7.6 9% .     

FIELD OBSERVATIONS ON CENTROPUS TOULOU INSULARIS ON ALDABRA ATOLL

Frith, C. B. 1975. Field observations on Centropus toulou insularis on Aldabra Atoll. Ostrich 46:251-257.

Details are presented of the nesting of a pair of Malagasy Coucals on Aldabra, with incidental observations of other pairs and nests. Courtship and copulation behaviour is very similar to that of the black Coucal Centropus grillii of Africa. Both sexes net build and incubate the eggs but these activities are performed very predominately by the male. Eggs are white and average 27,5 x 23.5 mm and 8,3 g. Two complete clutches of two and one of thee egg; were found and a doubtful early record of a four egg clutch is considered unlikely. There was an interval of at least 9 days between the laying of the two egg;, which hatched 7–8 days apart, incubation commencing with the first egg. The incubation of the second egg was 14 days, and the fledging period of both young about 19 days. Nestlings in the chamber produce a snake-like hissing noise, excrete a foul-smelling sticky fluid when handled and burst through the rear chamber wall as means of avoiding predation.

Both members of the pair were in the brown plumage generally considered to be the non-breeding plumage. It is suggested that the plumages of the Aldabran population of Centropus toulou are possibly more complex than previously considered or that the population may be dimorphic.