ESTABLISHMENT OF WEIGHT HIERARCHIES IN THE BROODS OF HOUSE MARTINS DELICHON URBICA

Nestling birds may differ in size and weight on the first day a clutch is fully hatched, mainly because eggs within clutches hatch over a period of several days. This asynchronous pattern of hatching is usually thought to facilitate brood reduction when the food supply is unpredictably restricted. The purpose of the study reported here was to examine the contribution of egg-weight, clutch-size, hatching spread, food supply and season to weight differences in newly hatched broods of the House Martin. At laying, heavy eggs had a greater moisture and dry weight content than light eggs and immediately before hatching there was a correlation between initial egg-weight and the dry weight of embryo and yolk. Heavier clutches also tended to give rise to heavier hatchlings. There was, however, no correlation of fresh egg-weight with the dry weight of embryos alone and the relative dry weight of embryos in a clutch was dependent on laying sequence. Hatching spread (the number of days between the emergence from the egg of the first and the last hatchling of the clutch) was 0.75 ± 0.46 days for clutches of two and increased with the size of the clutch up to 1.80 ± 0.79 days for clutches of five. When food was scarce during laying, hatching spread was greater. Weight difference in newly hatched broods was correlated with hatching spread and moreover in multivariate analysis was also correlated with periods of food scarcity during laying. It was concluded that all examples of weight hierarchies among hatchlings should not be considered adaptive; in some cases they may be imposed by food scarcity. This can lead to mortality of the runs even if food is plentiful. When the weight hierarchy is not adversely accentuated by food scarcity it may function as previously suggested, to allow brood reduction. Alternatively, particularly among House Martins, it may spread out the peak food needs of individual nestlings thereby spreading the demand on the adults.     

Factors affecting the probability of double brooding by Southern House Wrens

Seasonal fecundity of birds is influenced by clutch sizes and the number of successful breeding attempts during a breeding season. As such, understanding the factors that determine the decision to initiate multiple broods within a season and the consequences of this reproductive tactic is important. We examined the frequency of double brooding by Southern House Wrens (Troglodytes aedon musculus) in eastern Argentina. We analyzed inter‐ and intraseasonal variation in double brooding and evaluated the effect of weather conditions and laying date on the frequency and occurrence of this behavior. Finally, we assessed the effect of double brooding on the seasonal and lifetime productivity of female Southern House Wrens. During our 8‐year study, we found that ～43% (range = 17–83% each year) of breeding pairs attempted a second brood after successfully raising a first brood. The probability of females having a second brood was affected by the laying date of the first nesting attempt, but was independent of the number of young fledged. About 65% of females that started laying eggs before the first quarter of each breeding season produced a second brood, and this percentage decreased to ～40% after this period. In addition, variation in double‐brooding frequency among years was related to weather conditions, with the proportion of pairs double brooding increasing with increased precipitation early in the breeding season. More precipitation likely contributed to an increase in insect abundance. Although double brooding increased the seasonal and lifetime productivity of female Southern House Wrens, additional study of the survival and fate of fledglings from first and second broods is needed to assess the importance of multi‐brooding in the reproductive success of these wrens.     

ENVIRONMENTAL INFLUENCES ON GROWTH AND SURVIVAL OF NESTLING HOUSE MARTINS DELICHON URBICA

Growth of nestling House Martins was studied in relation to (a) conditions in the external environment and (b) aspects of their breeding biology. The dependence of growth performance on (1) hatchling weights, (2) relative difference in hatchling weights within broods, (3) brood size,(4) season, (5) earliness of breeding in relation to other pairs in the colony, (6) timing of breeding in relation to the median breeding week of the colony and (7) aerial food abundance, was investigated by step-down multiple regression analysis. Up to the stage of the peak brood weight, early laying, small brood sizes and high hatchling weights were associated with higher nestling growth rates. Large relative differences in hatchling weights however tended to depress mean brood weights and increase weight differences (= size hierarchies) within broods. These differences in hatchling weights were considered to contribute significantly to 23% of all nestling deaths, because small, late hatching nestlings suffered very high mortality even when food was abundant. The nestlings which died showed a progressive reduction on growth rates and all succumbed before the 11th nestling day. Because these differences in hatchling weights can be linked to the food supply during laying rather than immediately prior to their death, it is considered that the mortality of these nestlings can ultimately be attributed to the low quality of eggs from which they hatched. There was a tendency for pre-hatching factors to diminish in importance throughout growth, while post-hatching factors increased in importance and, with one exception, were responsible for explaining all the significant variance in the growth characteristics of fledglings. The exception was that differences in wing-lengths in broods could be linked with weight differences at hatching. Food shortages lowered average brood weights prior to fledging. Because pairs breeding during the median breeding week had lighter young, it was inferred that competition for food during this peak of breeding activity had the effect of lowering nestling growth performance, although the overall effect was considered to be small. Early breeding pairs tended to have larger broods, and these large broods showed a lowered growth performance. However, early breeding pairs had relatively smaller weight and wing-length differences, in broods of a given size, than occurred in broods of late breeders. It was therefore concluded that early breeding pairs had some attribute which tended to minimize certain disadvantages of large broods. This effect appeared to be linked to the pair, rather than to season or food supply.     

Cavity size, clutch-size and the breeding ecology of Tree Swallows Tachycineta bicolor

Previous studies provide evidence that cavity size influences clutch-size and reproductive success in some hole-nesting birds, because overcrowding in cavities may cause brood mortality due to trampling or hyperthermia. We tested this hypothesis with two experiments at nestbox populations of Tree Swallows Tachycineta bicolor in southeastern Ontario. Female Tree Swallows showed a preference for nesting in large boxes over small ones in the first experiment, and they laid significantly smaller clutches in small nestboxes during both experiments. Differences in clutch–size between large and small nestboxes could not be attributed to other factors known to influence clutch-size in birds (e.g. parental quality, habitat quality, laying date). Reproductive success, however, did not differ between pairs using the two box types during either experiment, nor did it differ during within-clutch-size comparisons between box types. Some measures of nestling quality were significantly lower for broods in large boxes, but during most comparisons there were no differences. These results do not support the adaptive reason for why cavity size affects clutch-size. We suggest that broods in our experiments did not experience the microhabitat conditions necessary to induce the expected differences in brood mortality.     

Intraseasonal effects of clutch manipulation on parental provisioning and residual reproductive value of eastern phoebes (Sayornis phoebe)

Summary First clutches of double-brooded eastern phoebes Sayornis phoebe were manipulated (up two eggs, down 2 eggs or no change) to test for intraseasonal reproductive tradeoffs and to test whether size of first brood influenced food delivery rates to nestlings and nestling quality in second broods.Considering all nests from both broods, rate of feeding nestlings increased linearly with brood size but nestling mass per nest decreased with increasing brood size. High nestling weights in small broods may have resulted from parents delivering better quality food, but we did not test this.Among treatment groups in first broods, nestlings from decreased broods weighed more than those in control or increased broods. Treatment did not influence the likelihood that second nests would be attempted after successful first nests nor did it alter the interval between nests. Nestlings of parents that renested weighed more than those of parents that did not, regardless of treatment, suggesting that post-fledging care may preclude renesting. Mass of individual females did not change between broods, regardless of brood size. Clutch sizes of second attempts were not affected by manipulations of first broods but increasing first broods reduced the number of nestlings parents were able to raise to day 11 in their second broods. However, manipulation of first broods did not affect mean nestling mass per nest of nestlings that survived to day 11.In phoebes, parents of small first broods are able to raise nestlings in better condition. We predict that in harsh years, parents of small first broods would be more likely to renest. Parents of enlarged first broods sacrificed quality of offspring in second broods, which seems a reasonable strategy if nestlings from second broods have lower reproductive value.     

Great tits, Parus major, lay too many eggs: experimental evidence in mid-boreal habitats

This study shows that great tits lay too large clutches in mid‐boreal habitats. First, breeding success, measured with number of fledglings or proportion of eggs that produce fledglings, in northern Finland (65°N) is much poorer than in central and western Europe. Second, brood size manipulations (ca ±30% of the natural mean) revealed that reduced broods produced equal numbers of and larger‐sized fledglings than control and enlarged broods, giving thus the best fitness value for reduced broods. Third, parents of enlarged broods could not adjust (i.e. increase) their feeding effort to the greater number of nestlings. Fourth, extra feeding (about 1/3 of the theoretical maximal needs of the nestlings) during the nestling period resulted in more numerous and larger‐sized fledglings in comparison to control broods. We suggest that the ultimate explanation for the too large clutches is gene flow from the southern population, which prevents local adaptations in the north. Consequently, the main reason for food limitation during the nestling period is that northern great tits apply “southern” decision rules for timing of breeding, clutch size and foraging behaviour. Thus, they tend to breed too early in comparison to the food abundance peak, lay too large clutches in comparison to the level of resources and, perhaps, forage on a too narrow diet (75% caterpillars). Since the late broods that matched the local food abundance peak did not succeed better than the mismatched earlier ones, the most crucial fault of northern great tits seems to be that they overestimate food abundance during peak demands and lay too large clutches. Another explanation for this could be that northern great tits have adopted a brood reduction strategy. However, the long‐term data reveal that years of high breeding success, which would maintain large clutches in the population, are very rare in the north. Therefore, it is unlikely that a brood reduction strategy per se could explain the phenomenon. Instead, it could work together with the gene flow against local adaptation for clutch adjustment.     

Intraclutch egg-size variation and offspring survival in the Kentish Plover Charadrius alexandrinus

We studied the consequences of intraclutch egg-size variation in Kentish Plovers Charadrius alexandrinus in southern Spain to test the hypothesis that females allocate resources preferentially to eggs with the greatest survival potential. Second eggs were larger and had a greater hatching success than the other eggs in a clutch. However, we did not find unequivocal support for the differential allocation hypothesis, because egg failures according to laying order were not due to the causes predicted by the hypothesis, and the change in egg-size with laying order was not consistent between successive clutches of renesting females. This suggests that nutrient availability during egg formation could act as a proximate factor affecting egg-size independently of laying order. Larger eggs produced heavier chicks and, within broods, heavier chicks were most likely to be recruited into the breeding population. By laying clutches with a larger mean egg volume in replacement clutches, females took longer to lay again after failure of the first clutch. Thus, opposing selective forces may act to increase and decrease egg volume. Although a trade-off between egg-size and clutch-size has not been found in precocial birds, our results suggest that there may be a trade-off between egg-size and fecundity, since an increase in the size of eggs within clutches may limit the time remaining within the season to lay second or replacement clutches.     

The significance of clutch overlap in Great Tits Parus major

We studied the effects of manipulation of the size of first broods in the Great Tit Parus major on the size and breeding success of second clutches and its relation to the degree of clutch overlap. The rearing of first brood fledglings always overlapped with the laying of the second clutch and in most cases also with the incubation period of the latter. The degree of clutch overlap depended on the size of the first brood, being less when the first brood was large. Clutch overlap also increased with season. Mechanisms affecting the timing of laying of second clutches are discussed. A large first brood imposed reproductive costs. It affected the size of the second clutch by causing it to be delayed; second clutch size decreases with season. It affected the post-fledging survival of second brood young as, in this population, this decreases with fledging date. The breeding success of second clutches was, however, not affected by the size of the first brood, but instead by the weight of the female when rearing the first brood.     

Direct and indirect effects of an insect outbreak increase the reproductive output for an avian insectivore and nest‐cavity excavator,the red‐breasted nuthatch Sitta canadensis

Community‐wide food pulses may ameliorate food constraints but may also result in increased competition for other resources and predation rates. In cavity‐nesting vertebrate communities, where the availability of tree cavities can limit reproduction and the reuse of cavities can increase nest predation by squirrels, excavators may maximize their fecundity by creating new cavities in competitor‐ and predator‐rich habitats that undergo food pulses. The reproductive cost associated with excavation (i.e. increased energy allocation early in the breeding season that often delays laying and thereby reduces clutch size), may be reduced if food pulses allow for a longer breeding season and larger clutches. A large‐scale mountain pine beetle Dendroctonus ponderosae outbreak that occurred during our long‐term study (1995–2009) provided a natural food supplementation experiment across 27 sites in British Columbia, Canada. We examined the effects of a reduction in food constraints accompanied with increases in excavation rates, conspecific density and nest predation risk on the fecundity of a facultative excavator, the red‐breasted nuthatch Sitta canadensis. We found a total of 420 nests in tree cavities. Nuthatch clutch sizes ranged from two to nine eggs, and broods from one to nine fledglings per nest. Later clutches were larger at sites and in years with high beetle abundance (mean clutch size of six eggs did not decline later in the season), second broods were produced in outbreak years (usually only one nesting attempt/normal year), and the number of fledglings per successful nest increased with increasing beetle abundance and nuthatch densities, but declined with increased squirrel densities. Since fecundity did not differ between new and reused cavities, the costs and benefits of excavation versus cavity reuse may be neutralized for nuthatches during strong resource pulses. Overall, the beetle outbreak reduced food constraints for nuthatches and provided alternate food for nest predators, allowing increased annual fecundity.     

BREEDING OF THE ADÉLIE PENGUIN PYGOSCELIS ADELIAE AT CAPE BIRD

Observations were made during four seasons (1967–68, 1968–69, 1969–70, 1970–71) on the breeding of Adelie Penguins at Cape Bird, Ross Island, Antarctica. Breeding data from individuals were related to date of return, laying date, clutch-size, nest location, and change of mate. Some females consistently laid near the mean date of laying, while others were consistently early or late layers. Laying date may be under direct genetic control, or may reflect feeding ability. The mean clutch-size was smaller in peripheral compared to central nests, and smallest of all in isolated nests. Clutches laid late in the season were smaller than those laid near the peak date, and small, late clutches were laid in peripheral rather than central nests. These differences may reflect age and/or feeding ability. Penguins that are better able to find food will return earlier, obtain central sites, and have larger clutches than those with a lesser ability. The two main causes of egg and chick losses were predation and parental failure. Losses were highest in single-egg clutches, at isolated and peripheral nests, and among eggs laid late in the season. These results may be partly related to the age and experience of the penguins. However, regardless of age, peripheral nesting and late laying were always disadvantageous. The sex ratio of adults in the colonies was 117♂:100♀. This may be explained by the higher mortality of females. Some males could not find partners, but females that did not breed had probably been unable to obtain sufficient food for gonad development. The return of penguins, incidence of non-breeding, adult mortality, clutch-size, and breeding success at Cape Bird were all markedly different in 1968–69 compared to the other three seasons studied. This season was marked by the persistence of sea-ice along the northwestern shores of Ross Island. The low reproductive output in 1968–69 was thought to result from a shortage of food for egg-laying and incubation.     

Timing of breeding of Tengmalm's Owl Aegolius funereus in relation to vole dynamics in western Finland

Timing of breeding in Tengmalm's Owl was studied in western Finland for 13 years. During 1973-85, half of the females started laying before 4 April, near the seasonal low of main food abundance (voles), and earlier than in southern Finland or as early as in southeastern Norway. The reason for this latitudinal trend is the shallow snow cover of the study area. The annual variation in the median laying dates was one month and was negatively correlated with the spring abundance of Microtus voles. The mean clutch size was related to the start of laying with early clutches being larger than late ones. These findings accord with the 'food limitation hypothesis', which states that laying begins as soon as the female can accumulate enough energy stores for forming eggs. Early breeding is adaptive, since juveniles of early clutches probably survive better during their first winter. In adults, early nesting improves the chances of rearing two broods per year, allows them to moult after breeding and gives more time to accumulate fat reserves to survive the winter. Tengmalm's Owl is one of the earliest breeders among North European birds. This is possible because of its hole-nesting and resident habits, small body-size in relation to the main prey and the greatest sexual size dimorphism among European owls.     

Breeding biology of the White-rumped Swallow Tachycineta leucorrhoa in Buenos Aires Province, Argentina

We conducted a study of the breeding biology of the White-rumped Swallow Tachycineta leucorrhoa nesting in nestboxes in a flat, farming landscape in Buenos Aires Province, Argentina. White-rumped Swallow nesting attempts were detected from the end of September to mid December, with most clutches laid during October. Birds laid clutches of 4–6 eggs with a mode of five eggs; most broods hatched synchronously (58%), but hatching spread could last up to 4 days. Nestling growth curves adjust well to logistic functions, and at day 15 nestlings attain the asymptotic weight of 21.6 g. Clutch size in White-rumped Swallows declined significantly as the season progressed. In addition, late-season eggs were smaller and late-season nestlings had a shorter nestling period and lower weight at day 15, probably leaving the nest lighter than early-season nestlings. These data suggest that the Swallows would benefit greatly from laying early in the season, which would provide nestlings with better survival prospects. However, both major sources of nest mortality, interspecific competition for nest-sites and nestling mortality during bad weather, decreased through the season. White-rumped Swallows follow the pattern found for other southern species, as it has smaller clutch size, lower growth rate and remains longer at the nest than its Northern Hemisphere congener the Tree Swallow Tachycineta bicolor .     

THE OCCURRENCE AND SIGNIFICANCE OF ANOMALOUS REPRODUCTIVE ACTIVITIES IN TWO NORTH AMERICAN NON-PARASITIC CUCKOOS COCCYZUS SPP.

Among the unusual breeding habits of the non-parasitic Yellow-billed and Black-billed Cuckoos of North America are great variability in clutch size and rate of laying, initiation of incubation long before the clutch is complete, occasional laying in nests of other species, annual irregularity in the timing of the breeding season, and semi-nomadic post-migratory movements into breeding areas where food is abundant. These facts, in addition to their peculiar diet and the very large size of their eggs, suggest that cuckoos have extraordinary problems in obtaining adequate energy for reproduction. At Bloomington, Indiana (U.S.A.), during a 15-year period, anomalies in the reproductive activities of cuckoos were concentrated into two years in which food was abundant. This was particularly true of one of these years, when there was a vast emergence of periodical cicadas: the Yellow-billed Cuckoo advanced its normal schedule and bred during peak cicada abundance, laid unusually large clutches, and parasitized Black-billed Cuckoo nests. Some females may have resumed laying in nests in which, having already deposited clutches of normal size, they had been incubating for long periods; the alternative possibility is that there was intraspecific brood parasitism. The erratic egg-laying behaviour of these cuckoos is attributed to the evolution of mechanisms permitting very quick exploitation of a favourable feeding situation. It is suggested that reproductive behaviour has become so responsive to an abundance of food that normal ordering and integration of the stages of breeding have been lost in some females. Such a loss could be responsible for the laying of eggs in alien nests, and it may have been the antecedent of obligate brood parasitism in parasitic cuckoo species.     

FACTORS AFFECTING THE EGG SIZE OF RED-BILLED GULLS LARUS NOVAEHOLLANDIAE SCOPULINUS

The factors influencing the egg size of the Red-billed Gull Larus novaehollandiae scopulinus were studied at Kaikoura, New Zealand, between 1964 and 1972. In two- and three-egg clutches there was a trend for the eggs to become smaller in the sequence of laying. Length, breadth and volume of eggs of one-, two- and three-egg clutches declined significantly as the season progressed. The size of eggs from single-egg clutches tended to be smaller than eggs from two-egg clutches laid at the same time. There were correlations between the proportions of one-egg and of three-egg clutches being laid at a given period and the mean egg volume of two-egg clutches. When the mean egg volume of two-egg clutches increased there was a corresponding increase in the proportion of two- and three-egg clutches laid. When the mean egg volume of two-egg clutches decreased there was an increase in the proportion of single-egg clutches laid. The egg size of the Red-billed Gull showed no direct correlation with the abundance or availability of food; the largest eggs were produced early in the season when food was in short supply. In spite of an increase in the food supply in the middle of the breeding season, birds laying at this time produced smaller eggs than birds which laid earlier in the season. However, early breeders which relayed at the peak in food abundance on average produced a larger replacement clutch than originals laid early in the season. It is suggested that the birds nesting early in the season are able to produce the largest eggs because they are the most efficient foragers for food, and those which nest later in the season produce smaller eggs, even at peak food abundance, because of their inefficiency or inexperience. Early breeders laying replacement clutches tended to lay larger eggs and larger clutches than birds which are producing their first clutches at the same time. Two-year-old females laid eggs which were significantly shorter than older aged birds while the breadth and volume of the egg increased with the age of the female up to the fifth year. There was a trend for females to lay larger eggs when mated with older rather than younger males. No statistical differences in egg size were detected between females changing or retaining the partner of the previous season. Female body weight and egg volume were positively correlated in females weighing less than 275 g but not for heavier females. It is suggested that the seasonal decline in egg size and clutch size results from a decrease in the availability of food and the ability of the individual to exploit the resource.     

The cost of incubation in relation to clutch-size in the Collared Flycatcher Ficedula albicollis

This study examines the importance of avian incubation costs as determinants of clutch-size variation by performing clutch-size and brood-size manipulations in the same population of Collared Flycatchers Ficedula albicollis during the same breeding season. In 2 5 cases when three or more clutches of the same size were completed on the same day, we moved two eggs on the day after the last egg had been laid from one randomly selected clutch (C) to another (C) and moved two other eggs from this to a third clutch (C⁺). In 20 other cases of simultaneously completed clutches of the same size, we moved two randomly selected young from one brood to a second and from that moved two other young to a third (B, B and B⁺groups). Most females were weighed the day after completion of the clutch and 1–4 days before hatching of the young, and some of them also 10–14 days after hatching of the young. We measured the daily energy expenditure of females incubating manipulated clutches of 4, 6 and 8 eggs by means of the doubly-labelled water (D₂¹⁸O) technique and also recorded their nest attendance. Hatching success of fertilized eggs was reduced in the enlarged clutches compared with control and reduced clutches. Females expired on average 3142.6 ml CO₂ and expended 78.6 kJ per day while incubating, which corresponds to a metabolic intensity of 3.3 times BMR. Daily energy expenditure increased with clutch-size due to higher costs while incubating, and not because of changed activity patterns. There were no significant differences in length of incubation, female mass or mass changes between phases for the C, C and C⁺groups. In both the C and B groups, enlarged broods produced significantly more fledged young than control broods, and those significantly more than reduced broods. Fledgling tarsus-length and mass did not differ significantly between treatments in either the C or B groups. There was no significant difference in breeding success between clutch and brood manipulations. In this season, incubation costs did not entail significant fitness losses, expressed either as fledgling production or female condition. Also, control females could have raised more young to fledging age than they did with no apparent costs.     

Hatching asynchrony that maintains egg viability also reduces brood reduction in a subtropical bird

In birds, hatching failure is pervasive and incurs an energetic and reproductive cost to breeding individuals. The egg viability hypothesis posits that exposure to warm temperatures prior to incubation decreases viability of early laid eggs and predicts that females in warm environments minimize hatching failure by beginning incubation earlier in the laying period, laying smaller clutches, or both. However, beginning incubation prior to clutch completion may incur a cost by increasing hatching asynchrony and possibly brood reduction. We examined whether Florida scrub jays (Aphelocoma coerulescens) began incubation earlier relative to clutch completion when laying larger clutches or when ambient temperatures increased, and whether variation in incubation onset influenced subsequent patterns of hatching asynchrony and brood reduction. We compared these patterns between a suburban and wildland site because site-specific differences in hatching failure match a priori predictions of the egg viability hypothesis. Females at both sites began incubation earlier relative to clutch completion when laying larger clutches and as ambient temperatures increased. Incubation onset was correlated with patterns of hatching asynchrony at both sites; however, brood reduction increased only in the suburbs, where nestling food is limiting, and only during the late nestling period. Hatching asynchrony may be an unintended consequence of beginning incubation early to minimize hatching failure of early laid eggs. Food limitation in the suburbs appears to result in increased brood reduction in large clutches that hatch asynchronously. Therefore, site-specific rates of brood reduction may be a consequence of asynchronous hatching patterns that result from parental effort to minimize hatching failure in first-laid eggs. This illustrates how anthropogenic change, such as urbanization, can lead to loss of fitness when animals use behavioral strategies intended to maximize fitness in natural landscapes.     

Seasonal changes in cell‐mediated immunocompetence and mass gain in nestling barn swallows: a parasite‐mediated effect?

Reproduction in seasonal environments is usually timed so peak demand for food by offspring coincides with peak availability. Hence, late breeders will encounter a scarcity of food. Since parasite populations grow during the reproductive season of their hosts, late reproducing animals will also face an increasing challenge by parasites. We hypothesised that seasonal decrease in food availability and seasonal increase in parasite abundance will cause a trade-off between growth and immune function. This prediction was tested in nestling barn swallows ( Hirundo rustica ) from first and second broods. Nestlings from second broods mounted stronger T cell mediated immune responses to a challenge with a novel antigen, but had lower rates of mass gain, than nestlings from first broods, consistent with the prediction. Broods in which at least one nestling died had lower levels of T cell mediated immune response, but not lower rates of mass gain, than broods without mortality, suggesting that brood reduction is mediated through an inability of offspring to defend themselves against parasites rather than an inability to grow. Possible mechanisms include scarcity of specific nutrients needed for immune responses, and/or parasites being concentrated on a single or few nestlings.     

Brood size and body condition in the House Sparrow Passer domesticus: the influence of brooding behaviour

In many bird species, females undergo a marked decline in body condition during the first days of the nestling period. This decline may be because brooding young chicks reduces the time available for foraging. Alternatively, it might be viewed as an adaptive way to reduce flight costs when the food demand of the brood is highest. To test these hypotheses we modified the brooding commitment of House Sparrows Passer domesticus by manipulating brood size to see if changes in time spent brooding affects adult body condition. During the nestling period, females provided on average three times as much brooding as males. Reduced broods received 14% more brooding than large broods and time spent brooding declined with brood size and chick age according to an exponential decay function. Male body condition was unaffected by brood size and remained stable throughout the reproductive period. Body condition of females with enlarged broods decreased gradually during the nestling period, whereas that of females tending reduced broods dropped abruptly and significantly upon hatching. This resulted in females with reduced broods having lower body condition during the first half of the nestling period than those with enlarged broods. The sharp drop in body condition of females with reduced broods coincided with the period that brooding was most intensive. Indeed, female body condition at the end of the nestling period was negatively correlated with the proportion of time they spent brooding during the first half of the nestling period. Thus, the probable lower homeothermic capacities of reduced broods implies a higher brooding commitment for female House Sparrows that, in turn, may reduce their opportunity to forage and consequently also their body condition.     

BREEDING OF THE GREY WARBLER GERYGONE IGATA AT KAIKOURA, NEW ZEALAND

I studied the breeding of Grey Warblers Gerygone igata (Muscicapidae: Acanthizinae) in forest near Kaikoura, New Zealand, between 1976 and 1979. Only males sang and singing occurred all year. From late July to January pairs defended self-contained territories of 0·25–1·73 ha but they occupied larger home ranges when not breeding. Territorial adults were strictly sedentary all year. The average annual mortality of breeding adults was 18·5% and the predicted life-expectancy 4·9 years, which is remarkable in a bird weighing 6–7 g. The breeding season from first building to last fledging was six months long and it began early. Exceptionally, Grey Warblers may build and lay before the shortest day. As the season progressed warblers nested lower on average, both in absolute terms and relative to the tree nested in and canopy at the site. Warblers built in 7–27 days then delayed up to eight days before laying. Only females built and at no stage of breeding did males feed their mates. Both sexes fed the young. Grey Warblers laid for 15–16 weeks of the year and first clutches were laid asynchronously during 5–6 weeks. Eggs of a clutch appeared at two-day intervals and each egg weighed 1·5 g when fresh (23% of mean adult weight). Clutch size was nearly constant (mean 3·9, mode 4, range 3–5). The incubation period was 17–21 days (mean 19·5 days) and the nestling period 15–19 days (mean 17·2 days). On average the clutch hatched over 1·4 days, even though incubation commenced with the laying of the last egg. Nestlings reached maximum weight on Days 13–14 on average and then receded in weight by 4%, apparently through loss of water. All healthy nestlings exceeded mean adult weight during development by up to 39%. Nestlings from broods of two were at first lighter on average than those from larger broods, but in the second half of the nestling period twins were significantly the heaviest. Grey Warblers were fed for 28–35 days after fledging and they survived well while dependent on parents. Fledglings dispersed up to 3 km or more at independence and only 5% per annum joined the breeding population. Of nests that received eggs, 42% produced at least one fledgling. On average each breeding adult raised 2·0 fledglings per season. Of 265 eggs in 73 nests 70% hatched and 38% produced fledglings. Of 185 nestlings 54% fledged. Probably the main cause of mortality of eggs and nestlings was predation by introduced rodents and mustelids. Grey Warblers raise two small broods slowly during a long breeding season, rather than investing in one large quickly-reared brood. In New Zealand's mild climate the warbler's food supply may not decline severely in winter, and the population of warblers may remain so close to the limit set by food that extra for breeding is hard to obtain. Thus the breeding strategy may be adapted to a restricted food supply.     

NESTING DENSITY AND BREEDING SUCCESS IN THE HERRING GULL LARUS ARGENTATUS

The relationship between nesting density and breeding success of Herring Gulls Larus argentatus was studied on the Isle of May, Scotland, in 1968. Herring Gulls nesting at the most common density started laying earlier in the season than those nesting at lower or higher densities. Therefore, although the overall spacing of nests was uniform, the nest density of birds laying later in the season progressively approached a random distribution. The onset of laying occurred in synchronized groups within the colony. Late-laid clutches were commonly situated on the periphery of the colony where the density of nests was lowest. When the laying period was divided into four time periods, in each period the tendancy was for birds nesting at the most common density to have the highest clutch-size, hatching and fledging success, and to rear the most chicks per pair to fledging. In addition, birds which spaced their nests most uniformly, presumably as a consequence of territorial behaviour, were the most successful parents.