Reproductive measures and chick provisioning of Cory's Shearwater Calonectris diomedea borealis in the Azores

Capsule Timing of breeding influenced wing-length at fledging, and egg size may be an indicator of fledging weight and the amount of food received by chicks.

Aims To investigate chick growth, temporal patterns of chick food provisioning and the importance of indices of parental condition or quality, egg size and hatching date, to predict nestling body mass and wing-length at fledging, and compare breeding and chick feeding characteristics between colonies in the northeast Atlantic.

Methods A survey of Cory's Shearwater nests was carried out at Vila islet. A sample of 52 chicks, ringed and weighed at hatching, was selected to study chick growth and food provisioning.

Results Hatching success (51%) was much lower than fledging success (87%). Both hatching date and egg size contributed to explain wing-length at fledging, but hatching date, which was negatively correlated with wing-length at fledging, had the most important contribution (22%). There was some indication that egg size may explain variation in fledging weight and the amount of food received by chicks. Food delivery and feeding frequency of chicks varied throughout the chick development stage and three phases were distinguished: (1) 0–29 days, the highest feeding frequency values and a linear increase in food delivery; (2) 30–69 days, an oscillation in food delivery and medium feeding frequencies; (3) 70–90+ days, a sharp decrease in both food delivery and feeding frequency.

Conclusion Variation in food availability did not seem sufficient to override the overall importance of indices of parental quality in determining reproductive measures and chick provisioning. Breeding and feeding characteristics were similar between colonies in the northeast Atlantic, with variability in chick provisioning higher further south.     

Sensitivity of breeding parameters to food supply in Black-legged Kittiwakes Rissa tridactyla

We fed Herring Clupea pallasi to pairs of Black-legged Kittiwakes Rissa tridactyla throughout the breeding season in two years at a colony in the northern Gulf of Alaska. We measured responses to supplemental feeding in a wide array of breeding parameters to gauge their relative sensitivity to food supply, and thus their potential as indicators of natural foraging conditions. Conventional measures of success (hatching, fledging and overall productivity) were more effective as indicators of food supply than behavioural attributes such as courtship feeding, chick provisioning rates and sibling aggression. However, behaviour such as nest relief during incubation and adult attendance with older chicks were also highly responsive to supplemental food and may be useful for monitoring environmental conditions in studies of shorter duration. On average, the chick-rearing stage contained more sensitive indicators of food availability than prelaying or incubation stages. Overall, rates of hatching and fledging success, and the mean duration of incubation shifts were the most food-sensitive parameters studied.     

Breeding systems of New Zealand Snipe Coenocorypha aucklandica and Chatham Island Snipe C. pusilla; are they food limited?

New Zealand Snipe Coenocorypha aucklandica were studied over six breeding seasons on the Snares Islands. The study area (7.5 ha) held about 20 pairs at a density of 3.2 ± O.5 pairs/ha, plus 5 to 25 nonterritorial birds. Most matings were monogamous but simultaneous polygyny was recorded in one territory (by two different males) in four consecutive seasons. Males courtship fed females before egg-laying. The typical clutch was two eggs, laid three days apart. Incubation was shared equally by the sexes in monogamous pairs and took 22 days. Some females with polygynous mates attempted to incubate unaided, which took about 38 days. Broods were split at hatching, with the male caring for the first chick to leave the nest. Chicks were fed by adults for at least 41 days, and did not become independent until about 65 days old. Growth rates were slow compared to Common Snipe Gallinago gallinago and full plumage took about 54 days to attain. No pairs were double-brooded but 43% of pairs that failed during incubation or early chick-rearing renested together. Some breeders of both sexes who had lost their dependent chick bred a second time with a new mate while their first mate continued rearing the surviving chick (sequential polygyny and polyandry). Hatching success was 80%, and fledging success was 48%. Each pair produced, on average, O.6 fledglings per year. Chatham Island Snipe C. pusilla were studied on Rangatira Island during the 1983–84 breeding season. Breeding density was about 5.6 pairs/ha. The breeding system was very similar to that for C. aucklandica but chicks became independent at about 41 days old. Hatching success was 89%. Compared to Common Snipe, Coenocorypha snipes occurred at high densities, had courtship feeding, large eggs, a long interegy interval, a small clutch, shared incubation and a long incubation period. Nest desertion rates were high, but overall hatching success was also high, chick growth rates were slow, there was a long period of chick dependence and a long relaying interval following nest failure or chick loss. Survival rates of both adults and chicks were high. These differences are attributed to the absence of predation, and to intense intraspecific competition for food in a stable environment.     

Seasonal declines in reproductive success of the common tern Sterna hirundo: timing or parental quality?

Reproductive success declines over the course of the breeding season in many bird species. Two categories of hypothesis have been evoked to explain this decline. The “timing” hypothesis suggests that seasonal declines in breeding success are attributable to the date of laying. The “parental quality” hypothesis suggests that seasonal declines result from the fact that young, inexperienced, or low quality birds breed later in the season. To evaluate the relative importance of timing and parental quality, egg exchanges and removals were used to manipulate hatching dates of common terns Sterna hirundo. Indices of quality, attendance, provisioning rates, and reproductive success of birds in three experimental groups (delayed hatch pairs, advanced hatch pairs, and pairs induced to relay) were compared to those of date‐matched controls. Pairs that hatched chicks early raised more chicks than pairs hatching chicks late in the season, regardless of initial laying date. This suggests that hatching chicks early is advantageous in itself. Our results, however, also support the parental quality hypothesis. There was a significant negative relationship between natural laying date and fledging success, independent of hatching date. Differences in chick growth and survival suggest that higher quality adults may be able to compensate for the disadvantages of late hatching dates and achieve similar reproductive success to that of pairs hatching chicks early. We found that pairs hatching chicks late in the season were subject to more incidents of kleptoparasitism than those hatching chicks early. This may be a proximate factor contributing to seasonal declines in reproductive success for common terns, although such a mechanism would not be likely in non‐colonial species. Failure to control for egg quality may have biased the results of some prior egg exchange experiments. Additionally, altered cost of incubation may be an unavoidable confounding factor in studies designed to manipulate timing of breeding.     

Behaviour of the yellow-eyed penguin chick

The ontogeny of yellow-eyed penguin ( Megadyptes antipodes ) chick behaviour follows the order of development determined by Nice (1962) for several species of birds, and by Spurr (1975) for the Adélie penguin ( Pygoscelis adeliae ). Feeding and comfort behaviours are the first to develop, followed by locomotion and aggressive behaviour.
Active solicitation of food may occur at one day of age. Chicks initially use non-visual cues to mediate begging. After their eyes open on the third or fourth day there is an increase in the use of visual stimuli, and begging occurs most often following adult nest relief. Sibling rivalry is not intense, occurring least during feeding, and in general both chicks are fed at each session.
The chicks are brooded for the first 21–25 days. At sparsely vegetated nest sites overheating may occur after 21 days and down-covered chicks will seek shade and pant in hot weather.
Throughout the 6–7 weeks of the guard phase there is a decrease in the amount of time spent resting in a prone posture, and an increase in exploratory, locomotory behaviour. During the post-guard phase, and until fledging and independence at 15 weeks after hatching, chicks may wander up to 20 m from the nest bowl during exploration, shade-seeking and feeding.
Adults feed only their own chicks, and chicks appear to beg only from their parents. Dense vegetation and long distances between nests tend to restrict contact between adults and chicks from neighbouring nests, and prevent the formation of large chick crèches.     

Survival of Herring Gull Larus argentatus chicks: an experimental analysis of the need for early breeding

In 1985 and 1990, we manipulated the hatching date of Herring Gulls Larus argentatus by exchanging complete clutches between pairs which had started egg laying on different dates in the season. The aim was to investigate whether the observed seasonal decline in Hedging success can be explained by laying date. In both years, fledging success of advanced pairs followed the natural seasonal trend, supporting the date hypothesis. However, in both years, Hedging success of delayed pairs remained as high as that of control pairs with the same original hatching date as the foster parents, supporting the parental quality hypothesis. These data suggest that the delayed pairs may have compensated for less favourable environmental conditions. Although conspecific predation was the main direct cause of chick mortality, food shortage probably indirectly determined the mortality rate. A model of fledging success in relation to the timing of egg laying predicts that when food is abundant the optimal hatching date coincides with the mean hatching date of the colony (synchronization advantage). When food is less abundant, early breeders have the highest fledging success.     

Accelerated growth rates in late‐hatched Rhinoceros Auklet Cerorhinca monocerata chicks depend on food conditions and growth stage: an experimental approach

In some bird species, the survival of chicks hatching later in the season is lower than those hatched earlier due to increased risk of predation and a seasonal decline in feeding conditions. To reduce these risks, it might be advantageous for late‐hatched chicks to grow faster and hence fledge at younger age. In this experimental study, the growth rates of early‐ and late‐hatched Rhinoceros Auklet Cerorhinca monocerata chicks were compared under average and poor food supplies in captivity. Controlling for potentially confounding effects of chick mass at 10 days old, chick age and nest‐chamber temperature, late‐hatched chicks had higher wing growth rate than early‐hatched chicks before attaining the minimum wing length required for fledgling under both average and poor food supplies. After attaining the minimum wing length, however, late‐hatched chicks had a lower fledging mass, indicating a potential cost that could diminish the early advantage of fast wing growth.     

Why does the herring gull lay three eggs?

Food supplements placed daily beside the nests of herring gulls, Larus argentatus, for the first 5 days after the first chick hatched produced improved weight gains over this initial period and higher fledging success, particularly in the third chick. The fledging success of the fed group appears to be due to increased weight gain and not to increased parental protection in the supplemented period. Since there is indirect evidence that food is available this suggests that the parents are putting less effort into foraging for their chicks than they are able to, and less than is in the interests of the third chick, in the first days after hatching. On a separate colony we found that having three chicks in the brood for more than 5 days resulted in lower weight gains for the second chick, but not the first. We suggest that fledging three chicks rather than one or two greatly increases the parents' reproductive effort, and consequently interpret the third egg as primarily insurance against the loss of the first or second.     

Factors affecting fledging weight of Adélie penguin (Pygoscelis adeliae) chicks: a modeling study

An individual-based model is developed to examine mechanisms that potentially underlie the observed constancy in fledging weight (2.8-3.2 kg) of Adélie (Pygoscelis adeliae) penguin chicks, in spite of large variability in the abundance of Antarctic krill (Euphausia superba), the primary food source. The model describes the energetic requirements of the chick, with growth resulting from the difference between assimilated energy and respiration. Parameterizations of these metabolic processes are based upon experimental and field observations. Ingestion of Antarctic krill by the chick is dependent on the frequency of food delivery to the chick by the adults, which is based on measured foraging times. The mass, size, and size frequency distribution of Antarctic krill fed to the chick are specified using empirical data. The energy content of the Antarctic krill provided to the chick is taken to be constant or allowed to vary with size. The simulations show that food availability is most critical in the latter portion of chick development, when growth rates and food demands are high. Low food availability during this time must be compensated by either feeding chicks with larger krill of higher caloric value or by increased assimilation efficiency. Periods when small krill with lower caloric value dominate require more frequent feeding of the chicks in order to attain their observed fledging weight. Thus, although the total food energy given to the chick is the main factor determining chick growth, the distribution of food availability relative to chick size (i.e., different net growth rates) and food quality are also factors influencing the fledging weight of penguin chicks. The simulations provide insight into the compensating effects of food delivery, food quality, and metabolic processes that allow Adélie penguin chicks to reach their observed fledging weight in spite of considerable environmental variability in food supply.     

The breeding biology and aspects of the feeding ecology of brown noddies Anous stolidus nesting near Culebra, Puerto Rico, 1985–1989

We have studied brown noddies Anous stolidus breeding on Cayo Noroeste in the Culebra National Wildlife Refuge for the past five years (1985–1989). Daily visits during our residence there each year permitted collection of precise data on arrival chronology, egg-laying and incubation patterns, egg morphometries, chick growth rates, food delivered to chicks and breeding success. Over 150 adults are now individually colour-banded, and each annual chick cohort has been uniquely marked. Some features of the breeding biology of Culebran brown noddies were similar to those reported for pairs at Atlantic and Pacific Ocean colonies; these included duration of egg development, mass of newly hatched chicks, chick growth rates and fledging periods. Other features appear unique to Culebra. These include a tightly synchronous arrival (range of first egg dates: 29 April-4 May) and short egg-laying period (about six weeks), a consistently high breeding success each year (average 84% hatching success, 88% chicks fledged from eggs hatched, 0.79 chicks fledged per pair), and an unusually narrow range of food items (two fish species) taken by adults for their own needs and those of chicks. Observations of the direction taken by adults departing the colony suggest a predictable and productive foraging area along a prominent east-west shelf-break located c. 20 km to the north. We conclude that during these five years, brown noddies on Cayo Noroeste were not limited by food during the breeding season.     

Investigator disturbance reduces reproductive success in Short‐tailed Shearwaters Puffinus tenuirostris

Research procedures can have a detrimental effect on the reproductive success of the study species. In this study, the frequency of investigator disturbance on Short‐tailed Shearwaters Puffinus tenuirostris was examined experimentally throughout the incubation period to assess whether disturbance influences hatching success, pre‐fledging chick survival and chick body size. Handling of incubating birds every day, every 3 days and once a week reduced hatching success by 100, 61 and 39%, respectively, compared with pairs that were not disturbed. Most failures resulted from egg abandonment by the parents, particularly during the early stage of incubation. Chick survival did not differ between treatment groups, but control chicks were significantly heavier and had larger bill depths and longer wings. The difference in chick body mass and size observed between the control and disturbed chicks might be due to physiological or behavioural mechanisms in adults or carry‐over effects from the incubation stage to the next life‐history stage. Reduced offspring quality has the potential to affect post‐fledging survival and recruitment. These findings are significant in broader terms because any investigator disturbance that reduces reproductive success, survival and offspring fitness could interfere with the accurate assessment of demographic parameters and exacerbate population declines.     

A long-term large-scale study of the breeding biology of the Spanish imperial eagle (Aquila adalberti)

We present data from a 17-year study of the population biology of a growing population of Spanish imperial eagles Aquila adalberti across most of its breeding range. The objective of this study was to analyse the effects of age, supplemental feeding and rabbit haemorrhagic disease (RHD) on several breeding parameters of this population of eagles. Average clutch size was 2.2 eggs per clutch, and the average incubation time was 41.7 days per clutch. Fledging occurred an average of 76.8 days after hatching, the length of the fledgling period was not correlated to clutch size. The annual average percentage of pairs laying eggs was 88%. A significant reduction in the percentage of pairs laying eggs in the period 1992–1994 (from 91 to 81%) coincided with most of the eagles’ territories being affected by the rabbit epizootic disease, RHD, which reduced their food supply significantly. Average productivity was 1.23 chicks per monitored territory, average breeding success was 1.40 chicks in a clutch per territory and the average fledging rate was 1.69 chicks per territory with hatching success. The main known causes of breeding failure during incubation were nest collapse and human disturbance. During chick-rearing, total or partial chick losses were mainly caused by siblicide, disease, malnutrition or nest collapse. In 26.2% of the 1372 monitored breeding attempts, at least one of the breeding birds was a subadult (the male in 56.1% of the cases, the female in 15.5% and both sexes in 28.4% of cases). In cases of mixed-aged pairs (n = 205), 70.7% were the result of a substitution, and 29.3% were the result of the forming of a new pair. Egg laying took place significantly earlier and breeding success was higher in territories occupied by adults than in those occupied by subadults. Breeding parameters were higher in high-quality (rabbit-rich) territories than in low-quality (rabbit-poor) territories, but only for those territories occupied by adults. The values obtained in the territories occupied by adults were only significantly higher than in those of the subadults in high-quality territories. Age and territory quality thus simultaneously affected reproductive output.     

Exclusion of ground predators improves Northern Lapwing Vanellus vanellus chick survival

Many farmland‐breeding wader species have declined across Europe, probably due to reductions in reproductive output caused by high nest losses as a result of agriculture or predation, or low chick survival between hatching and fledging. Most studies have focused on nest failures, and the factors affecting post‐hatching survival of chicks are poorly known. In an experimental approach, we fenced parts of the arable foraging areas of Northern Lapwing Vanellus vanellus families to quantify chick survival simultaneously in the presence and absence of ground predators. Lapwing chicks were radiotagged to estimate survival probabilities by daily locations, applying multistate capture–recapture models. During the night, chick survival was considerably lower outside fenced plots than within. During the day, chick survival was higher than at night and did not differ between protected and unprotected plots. This suggests that nocturnal ground predators such as Red Foxes Vulpes vulpes were responsible for a significant proportion of chick mortality. Cumulative survival probability from hatching to fledging was 0.24 in chicks within fenced plots, but virtually zero in chicks outside fenced plots. In farmland, temporary electric fences can be effective in minimizing the impact of ground predators and offer a promising short‐term method to increase fledging success of precocial birds.     

Effect of brood size and hatching sequence on prefledging mortality of Sandwich terns: why lay two eggs?

The mortality of Sandwich tern Sterna sandvicensis chicks held in enclosures was studied in colonies on Griend, in the Dutch Wadden Sea, from 1992 to 1999, and on Hirsholm, in the Danish Kattegat, in 1997. Survival of chicks until fledging was 73% for chicks hatching from first-laid eggs or single-egg clutches and 59–64% for partially hatched two-egg clutches, whereas 6% of second hatchlings survived until fledging. Less than 2% of all two-chick broods actually fledged two chicks. Because 18% of the two-egg clutches only hatched one egg, 7% of fledglings of two-egg clutches originated from a second-laid egg. In nests where both eggs hatched, the number of chicks was usually reduced soon after hatching. Within five days of hatching more than 50% of the second hatchlings died of starvation or were preyed upon. It seems that overproduction commonly occurs in Sandwich terns and that investment in a surplus egg mainly serves as an insurance mechanism. On Griend and Hirsholm, chick productivity of two-egg clutches was somewhat higher than for one-egg clutches. Undernourishment was an important cause of death, either directly by starvation or by selective predation of chicks in poor condition. This, in combination with earlier, studies suggests that Sandwich tern parents on Griend are exposed to severe food stress.     

Rates and consequences of relaying in Cassin's auklets Ptychoramphus aleuticus and rhinoceros auklets Cerorhinca monocerata breeding in a seasonal environment

We removed first eggs from early‐laying females to measure rates and consequences of relaying in Cassin's auklets Ptychoramphus aleuticus and rhinoceros auklets Cerorhinca monocerata at Triangle Island, British Columbia, Canada. Based on egg size and composition, the investment that Cassin's auklets made in first eggs was very close to that predicted from adult body mass, whereas rhinoceros auklets invested more. In both species, a high percentage of females relaid (90% of Cassin's and 87% of rhinoceros auklets). Breeding success declined weakly with later laying among control Cassin's auklet pairs, but pairs that we induced to relay bred more successfully than naturally late pairs, and similar to values predicted from laying dates of their first eggs. Their chicks also fledged heavier and younger than late control chicks, and similar to values in early control chicks, but followed the population‐wide seasonal decline in wing length at fledging. Nestling diets were dominated by Neocalanus copepods until late in the season, a sign that feeding conditions remained favourable until late. In contrast, rhinoceros auklet pairs induced to relay followed the population‐wide seasonal decline in breeding success, which was driven by a decline in hatching success. Pacific sandlance Ammodytes hexapterus, thought to be a preferred prey species, virtually disappeared from nestling diets in mid‐to‐late season, yet there was no seasonal decline in fledging mass. However, chicks from replacement eggs followed the declines among control chicks in both age and wing length at fledging. Despite the female having produced a replacement egg, and despite delayed breeding, there appeared to be little immediate consequence associated with relaying for Cassin's auklets, except for a tendency for their chicks to fledge with short wings. Consequences were more marked in rhinoceros auklets (greatly reduced hatching success, and having their chicks fledge with short wings), and this may have been due to the large investment made in eggs, and/or to delayed breeding. Results of this study show that attributes of Cassin's and rhinoceros auklets that lay at different times in the season can be important in driving seasonal declines in breeding performance, as found in studies on other Alcidae. They also show how decisions taken during the egg stage can have variable yet potentially important implications for fitness, even in relatively long‐lived species that lay single‐egg clutches.     

Behaviour of young Ringed Plovers Charadrius hiaticula and its relationship to growth and survival to reproductive age

The behaviour, growth and survival of Ringed Plover chicks were studied in 1974 at Mestersvig, northeast Greenland, and from 1973 to 1976 at Lindisfarne, northeast England. Post-fledging survival, dispersal and recruitment were also investigated for the Lindisfarne population. Growth rates were similar in both study areas, and to those reported from other sites. A diurnal rhythm in feeding activity was more evident in the Arctic than at temperate latitudes, despite continuous daylight in the former area. This was correlated with low nocturnal temperatures and prey availability. It is concluded that food supply did not limit growth or chick survival in either study area. Brooding decreased progressively during the pre-fledging period; the relationship of brooding period to age, environmental conditions and area was investigated. The adaptations of feeding and brooding behaviour for arctic and temperate breeding Ringed Plovers are discussed. Survival from hatching to fledging varied between 40% and 60% in different areas and years, and at least 59% of birds survived from fledging to about one year old. Minimum survival from one to two years old was only 57%. but year-to-year survival of older birds was higher, that of breeding adults being at least so?;. Most birds returned to the breeding area and attempted to breed when one year old. The extent of dispersal from Lindisfarne and the wintering areas of the Lindisfarne-breeding birds are investigated.     

Rates and consequences of relaying in little auks Alle alle breeding in the High Arctic an experimental study with egg removal

Most seabirds have a small clutch size. Thus, replacement of a clutch after loss can make important contributions to an individual’s lifetime reproductive success. However, in the condition of short polar summer, relaying propensity may be time‐constrained. In this study, we investigated rates and consequences of relaying in a small High Arctic seabird, the little auk Alle alle. We performed an experiment in which we removed the single egg from 20 nests of early‐laying breeders. We measured relaying rates, and compared chick body mass and breeding success between the experimental and control nests. Despite the narrow window of the Arctic summer and the closely synchronized breeding, 75% of females produced a replacement egg just 2.7% smaller in volume than the first egg. This indicates that in little auks, the demographic effects of disruptions to breeding attempts (by predators, adverse weather or human activity) may be mitigated to some extent by replacement clutches. However, peak body mass and fledging body mass were lower in the experimental than the control chicks. This effect was rather a consequence of late hatching – chicks from replacement clutches followed seasonal decline in peak body mass and fledging mass. Finally, breeding success and chick survival up to 20 d in the experimental nests were respectively 34 and 37% lower than in the control nests. Thus, the quality and post‐fledging survival of chicks from the replacement clutches were probably lower compared to the chicks hatched from the first‐laid eggs.     

Happy to breed in the city? Urban food resources limit reproductive output in Western Jackdaws

Urban areas expand worldwide, transforming landscapes and creating new challenging habitats. Some bird species, mainly omnivorous feeding on human waste and cavity nesters, commonly breed in these habitats and are, therefore, regarded as urban‐adapted. Although urban areas may provide new nesting sites and abundant human waste, the low breeding success found in some of these species suggests that the poor protein content in human waste might limit breeding parameters. We investigated whether the breeding success of a cavity nester and omnivorous species commonly breeding in urban areas, the Western Jackdaw (Corvus monedula), depended on the availability of good‐quality non‐urban food. We approached the objective by combining a literature review and experiments in the field. With the literature review, we compared jackdaw populations in different habitats across Europe and found that clutch size and number of fledglings per pair decreased with distance to non‐urban foraging grounds, even after controlling for the effect of colony size, latitude, and climate. In two experiments, we tested whether the breeding success of urban pairs could be increased by supplementing high‐quality food, first only during egg formation and second also until chick fledging. Food supplementation during egg formation led to larger eggs and higher hatching success than in urban control nests, but this did not result in higher chick survival. However, when food supplementation was prolonged until fledging in the second experiment, we observed a significant increase of nestling survival. These findings highlight that research and management actions should not only focus on species displaced by urbanization, but also on “urban‐adapted” species, as they might be suffering from a mismatch between availability of nesting sites in buildings and adequate non‐urban food resources. In these cases, nest sites should be provided in or close to adequate food resources.     

Brood reduction in the Red-necked Grebe Podiceps grisegena

Brood reduction in Red-necked Grebes Podiceps grisegena breeding on fish ponds in south-eastern Poland occurred either through the desertion of the last-laid eggs after partial hatching of the clutch and/or the selective starvation of the smallest chicks. Abandonment of unhatched eggs was not influenced by the number of young already hatched or by the breeding date, but it was more likely in larger clutches and in families suffering chick starvation. Chicks from the largest broods had a higher probability of survival until fledging than those from single-chick broods. Larger chicks obtained food more successfully through better positioning during food delivery. In families that did not suffer brood reduction, chicks were better provisioned with food than in reduced broods. Although allocation of food among chicks in reduced broods was more skewed to the disadvantage of the younger siblings, dominant chicks obtained less food prior to brood reduction than dominant siblings in unreduced broods. Sibling aggression did not differ between unreduced and reduced broods before death of the weakest chicks. Post-laying adjustment of the number of offspring to prevailing feeding conditions occurred at two stages: by parental manipulation of the number of hatched eggs at the time when parents and chicks leave the nest and by competition between chicks. It is suggested that late egg desertion may be an adaptive mechanism of brood-size adjustment, when elimination of the weakest chicks through sibling competition is not very efficient.     

Effects of electromagnetic fields on the reproductive success of American kestrels

Reduced reproductive success of birds nesting near power lines has been documented but never directly attributed to electromagnetic fields (EMFs). Laboratory studies have identified EMF effects on embryonic development, but reproductive success of wild birds is dependent on additional factors, including fertility, egg size, hatching, and fledging success. We tested whether EMFs affect reproductive success of birds. Captive American kestrels (Falco sparverius) were bred for one season per year for 2 yr under either controlled or EMF conditions. EMF exposure was equivalent to that experienced by wild reproducing kestrels and was weakly associated with reduced egg laying in 1 yr only. In both years fertility was higher, but hatching success was lower in EMF pairs than control pairs. Fledging success was higher in EMF pairs than control pairs in 1995 only. Egg composition and embryonic development were examined in 1 yr only, but hatchlings were measured in both years. EMF eggs were larger, with more yolk, albumen, and water, but had thinner egg shells than control eggs. Late-term EMF embryos were larger and longer than control embryos, although hatchlings were similar in body mass and size. EMF exposure affected reproductive success of kestrels, increasing fertility, egg size, embryonic development, and fledging success but reducing hatching success.