Annual variation in breeding biology of gentoo penguins, Pygoscelis papua, at Bird Island, South Georgia

The breeding biology of the gentoo penguin, Pygoscelis papua , was studied over a three-year period (1986–1988) at Bird Island, South Georgia, with particular reference to birds of known age or breeding experience. Laying date varied significantly between all three years, being three weeks later in 1987, when the breeding population decreased markedly. Factors involved in the timing of breeding are discussed. Within years egg-laying was highly synchronous: 95% of clutches were initiated in 14·5 days or less. The incubation period was 35 days and the laying interval, between the two eggs, 3·3–3·4 days. Chicks creched when 25–30 days old, and this varied between years, possibly related to food supply and chick growth. Chicks left the colony for the first time between 75 and 85 days of age. The breeding population at Bird Island decreased by 20% and increased by 84% in successive years during the study period. Breeding success (chicks fledged per egg laid) varied between 0·33 and 0·65 within colonies, but for the whole island was very consistent over the three years: 0·45, 0·51 and 0·47. Overall, colony differences were not correlated between years. Disturbance from Antarctic fur seals, Arctocephalus gazella , is suggested as the cause of consistently lower breeding success at one colony. Mean egg weight varied annually, and with age of the breeding bird, nest location and, in one year, with laying date. Young, first-time breeders laid smaller eggs and had lower breeding success compared to older, experienced birds, similar to other seabirds. However, they differed from other species in laying on average earlier than older birds. The relationship between age, egg weight, laying date and breeding success is discussed in relation to predation and seasonal food supply.     

Drivers of the breeding success of American Oystercatchers (Haematopus palliatus frazari) at a critical site in Sinaloa,Mexico

Understanding breeding phenology and success can elucidate population dynamics, which is especially important for species in need of conservation. We describe the factors affecting the breeding biology of American Oystercatchers (Haematopus palliatus frazari) at El Rancho Island, a critical site that contains ~ 7% of the total estimated population, on the coast of Sinaloa, Mexico. We monitored 192 nests over four years (2016–2019). The breeding season lasted from March to June and mean laying dates differed among years, with the mean laying date in 2019 an average of 20 days earlier than in 2016. Clutch sizes decreased as the breeding season progressed. Both breeding success and productivity differed among years, with the lowest values in 2016 (30% hatching success and 0.6 chicks/nest) and the highest in 2019 (66% hatching success and 1.2 chicks/nest). Hatching success was affected by year, laying date, type of habitat, and distance to the high tide line. American Oystercatchers that laid eggs earlier in the season, used mixed marsh and dune habitat, and with nests relatively close to the waterline (< 50 m) had greater breeding success. Overall, however, the breeding success of American Oystercatchers was low and influenced by a combination of several intrinsic and extrinsic factors. Management measures may be required to increase breeding success and ensure the conservation of this subspecies.     

Breeding biology of the Barn Owl Tyto alba in central Mali

Data were obtained on 178 clutches of African Barn Owls in central Mali from four breeding seasons during 1979–1983. Significantly more clutches were laid in 1979–1980 and significantly fewer in 1980– 1981 than the average for the 4 years and there were significantly more clutches laid in the middle period of the annual breeding season. The egg volume was significantly smaller at the beginning of the breeding season and significantly larger in the middle than the overall mean with eggs of second clutches being larger than those of first clutches. The clutch size was 605 eggs of which 479 hatched. The number of young fledged per successful nest was 319 and was 1 83 for all nesting attempts. The month was the only variable shown to affect significantly the clutch size, eggs hatched and fledging rate, the highest success rates being associated with the middle of the breeding period. The average interval between the hatching of eggs was 2–31 days. Survival rates (47'1%) to fledging were significantly affected by year (1981–1982 being the least) and month (mid-season birds the best). The order of hatching significantly affected age at death or disappearance, the first-hatched birds surviving the longest. The year significantly affected age at fledging, the young from the year in which most clutches were laid leaving the nest at the youngest age and those associated with the year having the least number of clutches remaining in the nest the longest. The month of hatching also affected fledging age, birds at the extremes of the breeding season fledging at older ages. The discussion compares these data with those from elsewhere.     

The breeding biology of the White-spectacled Bulbul,Pycnonotus xanthopygos,at the northwestern edge of its distribution range

The White-spectacled Bulbul, Pycnonotus xanthopygos, is an abundant and possibly invasive species in Turkey, where it has gradually expanded its distribution and breeding range in both western and southeastern directions. This study focused on its breeding biology, which is still poorly known. The breeding activity extends from February until September. The preferred nesting areas are mainly gardens and maquis groves, where 24 different nesting tree species have been identified. The clutch size is 3.3 ± 0.8 eggs per pair, nesting success 68%, hatching success 94%, fledgling success 95%, and overall breeding success 89%. While nesting success differs significantly between the years, we found no significant differences in hatching, fledging, and overall breeding success between the years studied. Despite favourable climatic conditions in the Mediterranean region, the species makes only one brood per year in a relatively extended breeding season extending over seven months, and has a relatively a high reproduction rate per nest.     

Annual variation in reproductive parameters of Adélie penguins at Edmonson Point,Victoria Land,Antarctica

Annual egg and chick production and breeding success at the Adélie penguin (Pygoscelis adeliae) colony Edmonson Point (74°21′S–165°10′E), Victoria Land, is presented for eight breeding seasons between 1995 and 2005. During this period the colony consisted of 10–13 subcolonies and averaged 2098 ± 278 breeding pairs. A sample of over 100 nests (114–150), belonging to two subcolonies, was monitored each year. Some breeding parameters remained constant while others showed substantial annual variation. Laying date showed little variation, and laying was highly synchronous: 82.5% of clutches were initiated in a 10-day period, 9–18 November. In contrast, clutch size (1.77–1.97) and incubation period (34.4 ± 2.5) varied significantly. Variation among years was also recorded in hatching success (from 58 to 86%) and breeding success. This last parameter, measured as number of chicks reared to crèche per nest with eggs, varied between 0.34 and 0.97.     

Clutch size, brood size and brood emergence in the Marbled Teal Marmaronetta angustirostris in the Marismas del Guadalquivir, southwestern Spain

The first detailed study of the breeding biology of the globally threatened Marbled Teal Marmaronetta angustirostris is presented, using data from the Marismas del Guadalquivir in southwestern Spain. Complete clutches, with 9–20 eggs, were recorded from 28 April to 27 July. Excluding clutches of over 14 eggs (likely to be intraspecifically parasitized), the mean clutch size was 11.8, larger than that reported for almost all other Anatidae species. Broods hatched from May to early August (later than sympatric duck species), with a peak in mid-late June and significant annual variation in date. Brood sizes were exceptionally high, declining from a mean of 10.9 in the first week of age to 8.5 when fully feathered (at 42 days or more). Duckling mortality was concentrated in the first 2 weeks after hatching. Nine percent of broods had 15–23 ducklings, largely as a result of nest parasitism. Brood size decreased strongly with hatching date and varied significantly between years. Data from across the species' range showed that breeding occurs later at more northerly latitudes. A recent decline in the Marbled Teal in the Marismas is linked with its late breeding season. Anthropogenic changes have reduced the duration of flooding in the natural marshes of Donana National Park, which now dry out by August, before this species has completed breeding     

The origin of out‐of‐range pelicans in Europe: wild bird dispersal or zoo escapes?

We tested whether spatial and annual patterns of occurrence of out-of-range Great White Pelecanus onocrotalus , Dalmatian Pelecanus crispus and Pink-backed Pelicans Pelecanus rufescens recorded in Europe between 1980 and 2004 supported a natural vagrancy theory. Candidate variables tested were those likely to influence dispersal and escape probability (distance to the usual breeding/wintering range, national captive stock), and wild breeding population sizes and their movements (size of breeding colonies, climate conditions on wintering grounds or during dispersal). Spatial vagrancy patterns supported the hypothesis of wild birds dispersing from their normal range, with decreasing national totals with increasing distance to the usual range for the three species. Annual out-of-range numbers of Great White Pelican were predicted by breeding colony size and breeding success in Greece, with a further effect of Sahel rainfall during the previous year. Annual numbers of Dalmatian Pelican were related to the North Atlantic Oscillation index and to breeding success in Greece. Finally, annual numbers of Pink-backed Pelican were predicted by summer Sahel rainfall, which is known to drive dispersal of the species northwards into the sub-Sahelian steppes during wet summers there. Hence, annual vagrancy patterns in Europe were well predicted for all three species by population size indices, reproductive success and/or climatic components, which presumably influence survival and/or dispersal. We therefore consider that vagrancy patterns were driven by wild birds, whereas escapes – even if potentially numerous – do not create sufficient 'noise' to hide these patterns.     

The effect of maternal age and experience on egg-size and hatching success in Wandering Albatrosses Diomedea exulans

The roles of maternal age and experience, on the one hand, and individual, year and random effects on the other, in influencing avian egg-size and hatching success have been much debated but seldom studied comprehensively. We investigated these topics with Wandering Albatrosses Diomedea exulans of known age (7–30 years) and experience (1–8 breeding attempts) over a 10-year period. Older and more experienced birds laid larger eggs. After allowing for year and controlling for experience, significant age effects remained; after controlling for age, no detectable experience effects remained. However, age accounted for only 6% of the overall egg-size variation. Egg-size varied significantly between years and has increased over the last decade. Individuals laid eggs of consistent sizes; 55% of the random variation in egg-weight was due to such effects. Egg- and hatchling-weight were very closely linked; larger eggs also had higher hatching success. The latter was influenced significantly by age and experience but neither remained significant after controlling for the other. Year effects were also detectable.
That there are significant effects of age, experience, year and individual on egg-weight (and hatching success) is probably typical of seabirds generally, though with different balances between factors depending on species and situation; however, insufficient data exist to examine this critically. Our finding that age was a more important influence than breeding experience does not support recent suggestions that hatching success is mainly influenced by experience and that experience will have a greater effect on reproductive success in long-lived species with high mate-fidelity. However, Wandering Albatrosses may have acquired much relevant experience before even starting to breed.     

Decision analysis for conservation breeding: Maximizing production for reintroduction of whooping cranes

Captive breeding is key to management of severely endangered species, but maximizing captive production can be challenging because of poor knowledge of species breeding biology and the complexity of evaluating different management options. In the face of uncertainty and complexity, decision-analytic approaches can be used to identify optimal management options for maximizing captive production. Building decision-analytic models requires iterations of model conception, data analysis, model building and evaluation, identification of remaining uncertainty, further research and monitoring to reduce uncertainty, and integration of new data into the model. We initiated such a process to maximize captive production of the whooping crane (Grus americana), the world's most endangered crane, which is managed through captive breeding and reintroduction. We collected 15 years of captive breeding data from 3 institutions and used Bayesian analysis and model selection to identify predictors of whooping crane hatching success. The strongest predictor, and that with clear management relevance, was incubation environment. The incubation period of whooping crane eggs is split across two environments: crane nests and artificial incubators. Although artificial incubators are useful for allowing breeding pairs to produce multiple clutches, our results indicate that crane incubation is most effective at promoting hatching success. Hatching probability increased the longer an egg spent in a crane nest, from 40% hatching probability for eggs receiving 1 day of crane incubation to 95% for those receiving 30 days (time incubated in each environment varied independently of total incubation period). Because birds will lay fewer eggs when they are incubating longer, a tradeoff exists between the number of clutches produced and egg hatching probability. We developed a decision-analytic model that estimated 16 to be the optimal number of days of crane incubation needed to maximize the number of offspring produced. These results show that using decision-analytic tools to account for uncertainty in captive breeding can improve the rate at which such programs contribute to wildlife reintroductions. © 2011 The Wildlife Society.     

THE BREEDING OF THE GREATER FLAMINGO AND GREAT WHITE PELICAN IN EAST AFRICA

This paper brings together observations on the breeding of the Greater Flamingo Phoenicopterus ruber and Great White Pelican Pelecanus onocrotalus, mainly at Lake Elmenteita, Kenya, 1951–1971. The Greater Flamingo bred at Lakes Elmenteita and Nakuru in 11/21 observed years and at Lakes Natron and Magadi in 5/12 observed years. On average, it breeds about every second year, but a succession of breeding years is followed by several years in which no breeding occurs. A history of 21 years' breeding at Lakes Nakuru and Elmenteita is given. At Elmenteita three sites have been used, the main site in every breeding year, the others less often. The number of pairs breeding in any year has varied from 500–9,250, but in 1968 flamingos bred three times, involving perhaps 8,500 pairs which made about 15,700 nests, some pairs perhaps laying twice or even thrice in a year. Losses of eggs (38.2% overall) were caused by rising water (16.2%), competition for nest space with Great White Pelicans (6.9%, after 1968 only), human interference (3.5%), Marabou Stork predation (1.8%) and other natural causes (9.8%). Losses among chicks totalled 68.3% overall and were mainly due to Marabou Storks (36.5%), undiagnosed disease (8.6%), and rising water (6.6%). Disease caused serious loss only in 1966, and after 1968 losses from Marabous rose from 2.7% to 76.5%, resulting in an increase in overall mortality from 48.7 to 92%. This was perhaps associated with the establishment of a fish factory at Lake Naivasha. When attacking flamingo colonies Marabous did not actually eat many eggs or chicks, but simply caused wholesale desertion by alarming the flamingos. In 1968 total desertion of a colony of 4,500 pairs was caused between 18 and 26 March by a maximum of 17 Marabous, and similar wholesale desertion was caused in later years. The overall breeding success among Greater Flamingos at Elmenteita was about 19% of eggs laid, but without the excessive post-1968 Marabou predation would have been about 30%. At such a rate Greater Flamingos require at least 24 years of adult life to replace themselves, but if the mortality caused by Marabous since 1968 continues they will require about 58 years, and the population will inevitably decline. Breeding success at Lakes Magadi and Natron has been higher, about 44% of eggs laid; but figures available are much more approximate than at Elmenteita. Some new data on display, nest-site selection, laying dates, clutch-size, hatching and creche behaviour are given for the Greater Flamingo. The Great White Pelican bred at Lake Elmenteita from 1968 to 1971 without a break, some birds laying in every month, but with reduced laying November–December. They bred on the same islands as, and in association with the Greater Flamingo, and caused heavy losses among the latter, not through aggressiveness, but simply because of their superior size and weight. Although food supply must ultimately have controlled the pelican's ability to breed, an adequate food supply was available for 6 years before they did and continued after they had ceased. Their breeding was finally triggered by the Greater Flamingo colonies, with which the pelicans associated. When a flamingo colony was deserted because of Marabou Storks the pelicans, unafraid themselves of the Marabous, also deserted. They also associated with, and wiped out, a colony of Sacred Ibis. From July 1968 to June 1969 about 2,600 pairs of pelicans bred at Elmenteita, rearing about 2,200 young to the flying stage. The breeding colony apparently comprised most of the adults from Lake Nakuru and Lake Naivasha, the main feeding areas. From July 1968 to January 1971 certainly 7,200 and probably 8,000 pairs of pelicans bred at Elmenteita. Some pairs may have bred twice or thrice in this period. Breeding ceased suddenly in January 1971, eggs, and small and large young being alike abandoned for no established reason, although food supply was certainly still plentiful. Additional information on pair formation, incubation and fledging periods, nest-relief, etc. is given. The best available record of the incubation period is 35–36 days. Nest relief takes place on average about once every 48 hrs, and is dependent on thermal activity enabling the pelicans to soar. At Elmenteita large young ate quantities of putrefying matter, including the corpses of other young pelicans. They also ate living young hatching from eggs, and up to 14 days old. Touch probably plays an important part in helping them to locate possible food in opaque water.     

Effect of nesting environment on incubation temperature and hatching success of Morelet's crocodile (Crocodylus moreletii) in an urban lake of Southeastern Mexico

Incubation temperature is an important aspect in terms of biological performance among crocodiles, and several controlled experiments have demonstrated a significant relationship between incubation temperature, success in hatching and survival of hatchlings. However, a few studies have tested these relationships in the wild. The objective of this study was to determine the relationship of nest characteristics and environment (hatch year, nest basal area and height, clutch size, distance to shore line, and vegetation cover), to incubation temperature and hatching success among Morelet's crocodile (Crocodylus moreletii). The study was carried out during the nesting seasons of Morelet's crocodile, from 2007 to 2009 in the Laguna de Las Ilusiones, an urban lake located in Villahermosa, Tabasco, Mexico. We physically characterized 18 nests and inserted a temperature data logger in each nest chamber. At the end of the nesting season and prior to hatching, we recovered the crocodile eggs and data loggers and calculated hatching success, under laboratory conditions. We related the environmental variables of the nest with the mean and fluctuation (standard deviation) of nest temperature, using linear models. We also related the environmental variables affecting the nest, to mean nest temperature and fluctuation in incubation temperature and to hatching success, using linear models. Although we found differences in incubation temperature between nests, mean incubation temperature did not differ between years, but there were differences in nest thermal fluctuation between years. The mean incubation temperature for 11 nests (61.1%) was lower than the suggested Female–Male pivotal temperature (producing 50% of each sex) for this species, and all hatchlings obtained were males. There were no differences in clutch size between years, but hatching success varied. Our study indicates that hatching success depends on certain environmental variables and nest conditions to which the eggs are subjected, including season, nest size and clutch size. We also discuss the importance of the fluctuation of incubation temperature on hatching success and sex determination.     

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% .     

Annual and seasonal reproductive trends in the Lesser Spotted Woodpecker Dendrocopos minor

Annual and seasonal variation in reproductive timing and performance were studied in a population of the Lesser Spotted Woodpecker Dendrocopos minor over 10 years in southern Sweden. The median laying date of the first egg varied by up to 17 days between years, being generally larger than the variation of laying dates within years. Neither clutch size, brood size in successful nests, fledging success in successful nests nor mean nestling weight differed significantly between years. There was no trend for mean clutch size to vary between early and late years. In spite of a more than threefold variation in population size, no reproductive variable demonstrated an apparent density-dependence. Within the season, clutch size declined steeply with increasing clutch initiation date, whereas fledging success and nesting success did not, leading to a trend in brood size almost identical to the trend in clutch size. The survival prospects of fledged young declined with increasing clutch initiation date, and it is argued that the clutch size laid is a strategic adjustment to laying date. Out of 124 breeding attempts, 34% did not produce fledged young. In 9% of the breeding attempts, pairs laid no eggs. At least 20% of the breeding attempts failed after egg-laying. The most common cause of breeding failure was loss of the breeding partner followed by nest abandonment (40% of the failures). Only 16–28% of the failures were due to predation on the nest. Most complete failures, and also partial losses from nests, occurred at the early breeding stages. It is argued that the early nestling phase may be a critical stage, which the woodpeckers adjust to coincide with the seasonal food peak, explaining the strikingly late breeding season compared with other non-migrant species.     

The comparative breeding behaviour of two sympatric cuckoos, Horsfield's Bronze-Cuckoo Chrysococcyx basalts and the Shining Bronze-Cuckoo C. lucidus, in Western Australia: a new model for the evolution of egg morphology and host specificity in avian brood parasites

The breeding behaviour of two similarly sized sympatric cuckoos, Horsfield's Bronze-Cuckoo Chrysococcyx basalts and the Shining Bronze-Cuckoo C. lucidus, was studied over four breeding seasons at Gooseberry Hill, Western Australia. Both cuckoos usually began laying in late August; Shining Bronze-Cuckoos laid for up to 13 weeks and Horsfield's Bronze-Cuckoos for up to 15 weeks. Four host species were parasitized and major hosts were parasitized throughout most of their laying periods. The frequency of parasitism varied between hosts and between years, but Splendid Fairy-wrens Malurus splendens and Yellow-rumped Thornbills Acanthiza chrysorrhoa (major hosts) were always parasitized more heavily than Western Thornbills A. inornata and Scarlet Robins Petroica multicolor. Western Thornbills were parasitized by both cuckoos. Horsfield's and Shining Bronze-Cuckoos laid monomorphic eggs; those of Horsfield's Bronze-Cuckoos were highly mimetic whereas those of Shining Bronze-Cuckoos were non-mimetic and dark in colour. Both cuckoos laid one egg per host nest, deposited eggs directly into the nest, laid very quickly in the early morning, removed at least one host egg at laying, laid eggs small for the size of the birds, hatched after 12 days and evicted nest companions shortly after hatching. Laying was well synchronized with the start of incubation by hosts. Field observations and experiments with egg models indicated that neither of the major hosts, nor the secondary host in common, discriminate against foreign eggs. The nestling period for Horsfield's Bronze-Cuckoo was 17 days, and for the Shining Bronze-Cuckoo 20 days. There was a corresponding difference in nestling growth rate between the cuckoo species. About 50% of cuckoo eggs produced fledglings. Reproductive success for both cuckoos was highest in nests of the secondary host in common, the Western Thornbill. Young cuckoos reached independence 5–6 weeks after hatching. The adaptive significance of competition between cuckoos as a selective agent for cuckoo egg morphology and host specificity is discussed.     

Seasonal variation in reproductive measures of tropical Roseate Terns Sterna dougallih previously undescribed breeding patterns in a seabird

Seasonal variation in egg-laying, egg size, hatching success, hatchling mass, fledging success and chick growth of Roseate Terms Sterna dougallii breeding on Aride Island (Seychelles), Indian Ocean, were studied in 1997 and 1998. I investigated to what extent two patterns, common in a range of species, were followed by tropical Roseate Terns: (a) seasonal decrease in clutch size, egg size and breeding success and (b) an increase in breeding success with increasing egg weight. In 1997 (a poor year), the earliest nesting birds laid significantly smaller eggs, and chicks were lighter at hatching than those of peak nesting birds. The mean clutch size, of 1.04 eggs, showed no seasonal variation and no 'b'-eggs hatched. In 1998 (a good year) the earliest nesting birds laid eggs of similar size and their chicks were of similar weight to those of peak nesting birds. Mean clutch size, of 1.25 eggs, increased significantly through the season and about 60% of the 'b'-eggs hatched. In 1997, hatching success was 57% whereas in 1998 it was 80%. In both years, breeding success declined significantly through the season. The fact that the earliest breeding birds laid smaller eggs in a poor year and smaller clutches in a good year is in marked contrast to a range of other species, and to temperate-nesting Roseate Terns. Egg volume explained about half of the variance in hatchling mass in both years, but only 15% of the variation in linear growth rate. Hatching date was the only variable with a significant effect on fledging success. Roseate Terns on Aride seemed to sacrifice egg size and clutch size for earliness of laying. Presumably it is a strategy of older birds to lay as early as possible and may be regarded as a response of tropical Roseate Terns to breeding under relatively poor, and seasonally declining, food conditions.     

Aspects of breeding ecology of the eastern olivaceous warbler (Hippolais pallida)

The breeding ecology of eastern olivaceous warblers Hippolais pallida is poorly known. In this study, we provide data on nest site selection and breeding parameters of the species in a population in northwestern Bulgaria, the only one known to be regularly and heavily parasitized by the common cuckoo Cuculus canorus (hereafter cuckoo). Eastern olivaceous warblers only bred within human settlements of the study area, avoiding seemingly suitable habitat outside them. Nests were built in a wide range of plant taxa but ailanthuses Ailanthus altissima and mulberries Morus spp. were most frequently used (21%). After taking into account the availability of vegetation, there was an apparent preference for several plant taxa but not for mulberries. Mean nest height was 1.65 ± 0.98 (0.53–7.60) m, n = 217, and it varied significantly among different types of nesting substrate. Laying date and clutch size of first breeding attempts averaged 10 June ± 0.98 days, n = 101 and 3.9 ± 0.07 (2–5) eggs, n = 72, respectively. Hatching success, fledging success, and breeding success were 42.5, 86.4, and 36.7%, respectively. The main sources of nest mortality were predation and cuckoo parasitism, with no significant difference in the proportion of nests lost to each. Cuckoo parasitism seemed responsible for the relatively low hatching success in this population.     

Costs of large communal clutches for male and female Greater Rheas Rhea americana

The breeding system of the Greater Rhea Rhea americana is almost unique among birds as it combines harem polygyny and sequential polyandry, with communal egg-laying and uniparental male care. In this species, large communal clutches (more than 30 eggs) are rare and have a lower hatching success than smaller clutches. Here we analyse the proximate causes of hatching failures and the costs of large communal clutches (and therefore the costs of extensive polygyny) for males and females. We evaluated if length of the nesting period, egg viability, egg losses during incubation and male parental activity at the nest were affected by clutch size. We also evaluated if chicks hatched from large clutches have a lower survival during the first 2 months after hatching. Large clutches had longer nesting period and lower hatching success, mainly as a result of bacterial contamination of the eggs and increased hatching asynchrony. In addition, large clutches tended to lose more eggs as a result of accidental breakage or predation. Male activity at the nest and chick survival were not related to clutch size. Low hatching success, nest predation risk and energetic costs associated with large clutches penalize females that join large harems and males that accept additional eggs into the nest.     

Breeding success and chronology of Wood Storks Mycteria americana in northern and central Florida, U.S.A.

The breeding success and chronology of Wood Storks Mycteria americana were studied at eight colonies in northern and central Florida during 1981–1985. Mean ± s.d. clutch size for all colony-years was 3.07 ± 0.56 (n = 2694 nests), with three-egg clutches (72%) most frequent. Mean clutch size among all colonies and years ranged from 2.73 ± 0.55 to 3.41 ± 0.61. Many colonies exhibited significant negative trends in clutch size with, hatching date because of a proportional decrease in four-egg clutches later in the season. Mean colony clutch size was not correlated with nest numbers, nesting density or mean hatching date within most years. Mean ± s.d. number of fledglings for all colonies and years was 1.29 ± 1.16 fledglings per nest (n = 2812 nests). Mean annual fledging rates in colonies ranged from 0 (colony failed) to 2.66 fledglings per nest. Most breeding failure occurred prior to egg hatching, and the second highest mortality occurred between hatching and 2 weeks of age. Four-egg clutches fledged more storks than three-egg clutches, which in turn were more successful than two-egg clutches. However, all clutch sizes showed similar fledgling per egg rates. The seasonal decline in productivity was associated proportionally with smaller clutch sizes later in the breeding season. An increase in mean hatching date was correlated with an increase in latitude. There was greater within-year breeding synchrony among colonies than interyear breeding synchrony within each colony. Breeding synchrony was not correlated with mean hatching date, latitude, longitude, nest numbers or nesting density.     

THE BIRDS OF LANGEBAAN LAGOON

Data are presented on breeding success of Red Bishops (Euplectes orix) collected over four breeding seasons at a colony in the Addo Elephant National Park, Eastern Cape, South Africa. Overall hatching and fledging success were 53.8% and 26.0% of all eggs laid, respectively, and the overall mean number of fledglings per breeding attempt was 0.77. Hatching and fledging success varied significantly among seasons, with both clutch and brood losses due to predation being the main reason for the observed differences. Hatching success also differed significantly among clutch sizes, being highest for four-egg clutches (63.2%), intermediate for three-egg clutches (55.5%) and lowest for two-egg clutches and five-egg clutches (33.2% and 34.3%, respectively). However, fledging success was not significantly different among clutch sizes. The mean number of fledglings per breeding attempt was 0.44 for two-egg clutches, 0.80 for three-egg clutches, 1.10 for four-egg clutches, and 0.57 for five-egg clutches. The height of accepted nests (i.e.nests in which at least one egg was laid) was significantly lower than the height of nests not accepted. In addition, accepted nests in which eggs hatched and young fledged were significantly lower than accepted nests in which no eggs hatched and no young fledged. These overall effects of nest height on nest acceptance and hatching and fledging success were, however, due only to nests built above water, since no such effects were found when nests built above ground (i.e.on dry land) were analysed separately. I detected no effect of nest coverage on the probability of a nest being accepted, nor was there any effect of nest coverage on hatching or fledging success. Nests above water were significantly more likely to be accepted than nests above ground; however, hatching and fledging success of nests that were accepted did not differ significantly between nests built above water and those built above ground.