Pre-incubation feeding activities and energy budgets of Snow Geese: can food on the breeding grounds influence fecundity?

The potential contribution of early spring feeding conditions in the Arctic to clutch size variation was examined in a population of Lesser Snow Geese Anser caerulescens caerulescens. Behavioural observations were combined with energetic analyses of food material to derive an estimate of the energy budgets of pre-laying and laying females. Food intake of females between arrival on the breeding grounds and incubation was considerable; estimated energy gains in this period were in the same magnitude as the cost of one or several eggs. The pre-laying period spent on the breeding grounds can thus be energetically beneficial rather than costly. Accumulation of resources for reproduction in Snow Geese is a continual process including the breeding grounds, and nutrient limitation after arrival in the Arctic cannot sufficiently explain the environmental component of clutch size variation. The timing of migration and follicle development is such that clutch size decisions are sometimes made during the late stages of migration and some-times after arrival. In the latter case food conditions on the breeding grounds may greatly influence clutch size; in the former case they may still influence readjustments of clutch size after the initial decision. The universal negative correlation between clutch size and laying date in Snow Geese can be explained by negative fitness consequences of late hatching, which outweigh the benefits of delayed laying and further nutrient accumulation. Food shortage on the breeding grounds may sometimes be a secondary factor contributing to seasonal clutch size decline.     

Differences in size between first and replacement clutches match the seasonal decline in single clutches in Tree Swallows Tachycineta bicolor

The seasonal decline in clutch size in birds can be a response to the environmentally conditioned decrease in prospects for offspring or a consequence of a lower physical ability of late‐breeding females. To find out which of the explanations apply in Tree Swallows Tachycineta bicolor, we assessed whether replacement clutch size in this species is affected by an individual female's ability to lay a certain number of eggs. To do this, we measured the decline in clutch size as a function of laying date between first and replacement clutches in individuals that re‐nested following natural failure, and compared this with the rate of decline in clutch size with laying date for Tree Swallows that laid only a single clutch in that season. Additionally, we assessed whether the clutch size and the rate of its seasonal decline varied across years. We accounted for the truncated and under‐dispersed nature of clutch size data by using a Bayesian approach in the analysis. We found little variation in the rate of clutch size decline across years at our breeding site. Accounting for this seasonal decline in clutch size, mean clutch size was similar between single‐time breeding females and those that laid replacement clutches, implying that the number of eggs laid on the second attempt by female Tree Swallows is determined by laying date, rather than by the female's physical ability to produce a clutch of a certain size.     

Effect of food abundance on laying date and clutch size in the White Stork Ciconia ciconia

CapsuleFood independently affects both laying date and clutch size, suggesting that seasonal decline in clutch size is related to a decrease in food availability.

Aim To test the effect of food abundance on laying date and clutch size of the White Stork and identify the cause of seasonal decline in the number of eggs laid.

Methods During 1991 and 1996 we recorded clutch size and laying date of pairs breeding next to rubbish dumps (food abundant and constant throughout the breeding season) and birds breeding far from rubbish dumps (using natural food sources).

Results In 1991 there was no difference in mean laying date between pairs nesting at rubbish dumps and control pairs. Clutch size was significantly larger at rubbish dump nests. In contrast, mean laying date was earlier in control pairs in 1996 and there was no significant differences in clutch sizes, even when controlling for laying date effect.

Conclusion The results support the hypothesis that food availability independently affects both laying date and clutch size. The seasonal decline in clutch size close to rubbish dumps was negligible (1991) or much smaller than in the control zone (1996) suggesting that a progressive deterioration of natural food sources is the most probable reason for a decline in clutch size as the season advances.     

Selection for synchronous breeding in the European starling

Colonial birds often demonstrate considerable breeding synchrony. In southern Sweden the semi-colonial European starling initiated the vast majority of clutches within one week. Laying dates were positively skewed so that many birds initiated clutches at similar dates early in the season. Breeding was further synchronised by a particularly strong clutch-size reduction equivalent to one third of an egg per day during the first part of the breeding season. The decline in clutch size with season also held true for separate age-classes of females, for individual females laying at different times at different years and for individual females laying at different times the same year. Trends in breeding success during nestling rearing were unlikely to explain the high degree of breeding synchrony or the seasonal decline in clutch size; nestling survival and growth were weakly related or unrelated to reproductive timing. In contrast recruitment success of fledged offspring declined sharply with season. Even within the synchronous laying period, defined as clutches initiated during the first week each year, local recruitment success declined. It is suggested that the early seasonal decline is caused by selection for synchronous fledging permitting the immediate formation of flocks after fledging, whereas the late seasonal trends may be caused by either population differences in female quality or deteriorating conditions for raising young.     

Is there a trade-off between egg weight and clutch size in wild Lesser Snow Geese (Anser c. caerulescens)?

Previous studies of arctic nesting geese suggest that laying is limited by the size of a female's body reserves and that larger eggs contain more nutrients. These observations imply a life-history trade-off between egg size and clutch size which may give rise to a negative genetic correlation between the two characters. We estimated the genetic correlation between egg weight and clutch size using measurements from mothers and their daughters in a wild population of Lesser Snow Geese Anser caerulescens caerulescens. Between 65 and 80 % of the variance in egg weight is attributable to differences between individuals, and heritability of egg weight is about 60 %. In contrast, 10–20 % of the variance in clutch size is attributable to differences between individuals, and heritability of clutch size is about 15 %. The genetic correlation coefficient between egg weight and clutch size ranges from 0.09 to 0.32 and does not differ significantly from zero. We discuss the possible reasons for the lack of the expected negative genetic correlation.     

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.     

Photoperiodic control of reproduction and molt in the kestrel, Falco tinnunculus

An adaptive decline in average clutch size with progressive date of laying is characteristic of most bird species with a single clutch of variable size per year. The effect of photoperiod on timing of laying, clutch size, and subsequent molt was investigated in kestrel pairs breeding and raising their young in captivity. In natural daylight (nLD), clutch size, under ad libitum feeding, showed the same decline with date as in nature. Birds breeding later also started molt later and molted faster (more feathers simultaneously), so that all birds completed molt more or less at the same time. Constant long days (LD 17.5:6.5 and LD 13:11) from December 1 onward advanced both reproduction and molt. The LD 17.5:6.5 group developed the reproductive system faster, had a shorter courtship period, and laid eggs earlier than the LD 13:11 group. In both photoperiods there was a decrease in clutch size with progressive laying date, similar to that in nLD. Molt started in both groups at about the end of the laying period and slowed down in the longer photoperiod, especially in males. Plasma luteinizing hormone (LH) changes in the two photoperiods were different for males and females. Males showed the expected slower LH response in the shorter photoperiod, but the initial LH response by females was the same in both photoperiods. Data on LH, reproductive behavior, and body mass suggest that females have a wider annual reproductive window than males. Data on time of laying and number of eggs suggest that clutch size in the kestrel is determined by laying date itself, following an endogenous rhythm that is phase-locked to the reproductive cycle.     

Life history of breeding partners alters age‐related changes of reproductive traits in a natural population of blue tits

Reproductive senescence, an intra‐individual decline in reproductive function with age, is widespread, but proximate factors determining its rate remain largely unknown. Most studies of reproductive senescence focus on females, leaving senescence in male function and its implications for female function largely understudied. We constructed linear mixed models to explore the interactive effects of paternal and maternal age and a life‐history trait (i.e. age at first reproduction) on four fitness components (i.e. laying date, clutch size, number of fledglings and number of recruits) measured in a wild, breeding population of blue tits Cyanistes caeruleus ogliastrae where individual breeding success has been followed for over 30 years (our dataset spanned 29 years). Previous studies have shown that, across female lifespan, laying date decreases and subsequently increases; earlier laying dates result in higher fitness because hatchlings have greater access to a seasonal food source. Our analyses reveal that females that initiate reproduction early in life show a greater delay in laying date with old age. In addition to delayed laying dates, older females lay smaller clutches. However, the magnitude of female age effects was influenced by the age at first reproduction of their breeding partners. Senescence of laying date and clutch size was reduced when females mated with males that reproduced early in life compared to males that delayed reproduction. We confirmed that both laying date and clutch size were significantly correlated with reproductive fitness suggesting that these dynamics early in the breeding cycle can have long‐term consequences. These complex phenotypic interactions shed light on the proximate mechanisms underlying reproductive senescence in nature and highlight the potential importance of cross‐sex age by life‐history interactions.     

Age effects on clutch size and laying dates of individual female Lesser Snow Geese Anser caerulescens

It is well known in many species of birds that mean clutch size increases and laying date advances with increasing age of the female. This has been interpreted widely as being due to some maturation process in which the performance of individual birds improves as they age. There are two alternative explanations, however. Birds which lay small clutches and lay late may have a higher mortality and be under-represented in the later year samples, or birds with a propensity to lay large and early clutches may enter the breeding population at a later age. In an attempt to discriminate between these alternatives, the reproductive performances of individual Snow Geese were examined over a series of years. Clutch size increased and laying date advanced for these individuals as it did for the population as a whole, thus confirming the maturation hypothesis.     

Timing of current reproduction directly affects future reproductive output in European coots

Life-history theory suggests that the variation in the seasonal timing of reproduction within populations may be explained on the basis of individual optimization. Optimal breeding times would vary between individuals as a result of trade-offs between fitness components. The existence of such trade-offs has seldom been tested empirically. We experimentally investigated the consequences of altered timing of current reproduction for future reproductive output in the European coot (Fulica atra). First clutches of different laying date were cross-fostered between nests, and parents thereby experienced a delay or an advance in the hatching date. The probability and success of a second brood, adult survival until and reproduction in the next season were then compared to the natural variation among control pairs. Among control pairs the probability of a second brood declined with the progress of season. Delayed pairs were less likely and advanced pairs were more likely to produce a second brood. These changes were quantitatively as predicted from the natural seasonal decline. The number of eggs in the second clutch was positively related to egg number in the first clutch and negatively related to laying date. Compared to the natural variation, delayed females had more and advanced females had fewer eggs in their second clutch. The size of the second brood declined with season, but there was no significant effect of delay or advance. Local adult survival was higher following a delay and reduced following an advance. The effect of the experiment on adult survival was independent of sex. Laying date and clutch size of females breeding in the next year were not affected by treatment. The study demonstrates the existence of a trade-off between increased probability of a second brood and decreased parental survival for early breeding. Timing-dependent effects of current reproduction on future reproductive output may thus play an important role in the evolution of the seasonal timing of reproduction.     

Producing extra eggs does not deplete macronutrient reserves in European Starlings Sturnus vulgaris

Recent studies have suggested that the size of avian clutches may be determined in part by the costs of egg production, which are thought to involve the depletion of endogenous nutrient reserves. I tested the hypothesis that producing extra eggs would deplete protein and lipid reserves in a passerine species, the European Starling Sturnus vulgaris . The first three eggs of clutches were removed on the days they were laid to induce females to lay extra eggs. Females responded to this manipulation by laying, on average, 1.3 eggs more than controls. However, based on the distribution of clutch sizes, it appears that some females responded to the removal of three eggs by producing more than one extra egg, whereas others responded by laying no extra eggs or by deserting. In unmanipulated females, the lean dry mass of the flight muscles and total body lipid were found to decline throughout breeding, an observation which is often interpreted as evidence that egg production depletes endogenous reserves. However, females experimentally induced to produce an extra egg did not have reduced stores of protein or lipid at clutch completion. No effect was observed in starlings even though this study had substantial (80%) power to detect a change in protein reserves of the same magnitude as that observed in a previous study of gulls. The decrease in flight muscle mass that has frequently been observed during breeding in passerines may not be due simply to mobilization of endogenous protein reserves.     

Seasonal clutch size decline and individual variation in the timing of breeding are related to female body condition in a non-migratory species, the Upland Goose Chloephaga picta leucoptera

Several studies have shown that waterfowl females in good condition lay larger clutches and start egg-laying earlier in a breeding season. However, most of these studies lack corresponding data on individual condition and timing of breeding in different years. We analysed data on clutch size, egg size, hatching date and female body condition of a non-migratory species, the Upland Goose Chloephaga picta leucoptera, recorded in three seasons on New Island, Falkand Islands. We found a strong seasonal decline in both egg and clutch size. Egg size increased with clutch size. The mean egg volume and total clutch volume increased with female body condition and hatching date was earlier for females in higher body condition. Chicks hatched from nests with higher mean egg volume had higher early body condition. We also compared individual females between different study years and found that individual body condition showed a significant repeatability between years, whereas hatching date did not. While female aging did not systematically affect hatching date, females produced clutches that hatched earlier in years of higher body condition. We could thus show for the first time that the frequently reported negative relationship between female condition and hatching date also holds true on an individual basis. To our knowledge, this is the first study on seasonal clutch size decline in sheldgeese and one of a few in waterfowl comparing condition and timing of breeding within individuals between different years.     

Body condition,migration, and timing of reproduction in snow geese: a test of the condition-dependent model of optimal clutch size

The seasonal decline of avian clutch size may result from the conflict between the advantage of early breeding (greater offspring value) and the advantage of a delay in lay date (improved body condition and hence clutch size). We tested predictions of a condition-dependent individual optimization model based on this trade-off (Rowe et al. 1994) in a long-distance migrant, the greater snow goose (Chen caerulescens atlantica), using data on condition, migration, and reproductive decisions of individuals. We closely tracked radio-marked females at their main spring staging area and on their breeding grounds. Our results were consistent with predictions of the model. Early-arriving females had a longer prelaying period and initiated their nests earlier than late arrivals. After controlling statistically for arrival date, we determined that females with high premigration condition had an earlier lay date than those in low condition. After controlling for the seasonal decline (i.e., lay date), we observed that clutch size was not related to premigration condition. Moreover, we took advantage of an unplanned manipulation of the prebreeding condition that occurred during our long-term study. We found that a reduction in condition caused a delay in lay date. However, after controlling for the seasonal decline, it did not affect clutch size. Our study indicates that geese simultaneously adjust their lay date and clutch size according to their premigration condition and migratory behavior as predicted by the condition-dependent optimization model.     

Absence of seasonal variation in great tit offspring sex ratios

When the timing of breeding affects the reproductive value of sons and daughters differently, parents are expected to increase their fitness by changing the offspring sex ratio during the course of the breeding season. Previous studies have shown that in great tits Parus major hatching date has a stronger effect on the fitness of juvenile males than on that of juvenile females. We tested whether this difference was reflected in a seasonal decline in the proportion of sons per breeding attempt. Although offspring sex ratio was more variable than would be expected from a binomial distribution, there was no significant relationship between the proportion of sons and the laying date of the clutch. Moreover, individual females did not adjust the sex ratio of their offspring following an experimental delay of breeding. This study therefore fails to demonstrate adaptive seasonal variation in great tit offspring sex ratios.     

Foraging time and dietary intake by breeding Ross's and Lesser Snow Geese

We compared foraging times of female Ross's (Chen rossii) and Lesser Snow Geese (Chen caerulescens caerulescens) breeding at Karrak Lake, NT, Canada and examined variation due to time of day and reproductive stage. We subsequently collected female geese that had foraged for known duration and we estimated mass of foods consumed during foraging bouts. Female Ross's Geese spent more time foraging (mean % - SE =28.4ǃ.3%; P=0.0002), on average, than did female Lesser Snow Geese (21.5 - 1.4%). Foraging time by female geese differed among reproductive stages, but differences were not consistent among time periods (stage-by-time block interaction, P=0.0003). Females spent considerably more time foraging during prelaying and laying than during incubation. Ross's Geese also spent a greater percent of time feeding (83.0DŽ.8%) during incubation recesses than did Lesser Snow Geese (60.9Dž.6%). Consumption of organic matter during foraging bouts was minimal; estimated consumption averaged 9.6dž.0 and 12.4dž.6 g (mean - SE) dry mass/day before incubation and 5.9DŽ.0 and 5.7DŽ.1 g dry mass/day during incubation for Lesser Snow and Ross's Geese, respectively. Diets consisted primarily of mosses (bryophytes), Chickweed (Stellaria spp.) and Sedges (Carex spp.). Before incubation, eggshell consumption was estimated as 4.3Dž.2 and 0.4ǂ.3 g dry mass/day for Lesser Snow and Ross's Geese, respectively; neither species consumed eggshell during incubation. We conclude that eggshell from nests of previous years is likely an important source of dietary calcium used to meet mineral demands of eggshell formation at Karrak Lake. Our findings of wide disparities between foraging time and food intake indicate that results from studies that do not directly measure intake rates remain equivocal. Finally, we propose four hypotheses accounting for foraging effort that evidently yields little nutritional or energetic benefit to geese nesting at Karrak Lake.     

Density dependence of avian clutch size in resident and migrant species: is there a constraint on the predictability of competitor density?

The presence of density dependence of clutch size is tested in 57 long-term population studies of 10 passerine bird species. In about half of the studies of tit species Parus spp. density dependence of clutch size was found, while none was found in studies of two flycatcher species Ficedula spp. One hypothesis explaining this difference is that migrants are less able to predict the final competitor density, because new pairs are still settling when the first females start laying eggs. Such unpredictability is only a problem for early laying females. If this explanation is true, the commonly observed negative correlation between clutch size and laying date should be stronger in high-density years. I tested this prediction in three populations of Pied Flycatcher Ficedula hypoleuca , and compared the results with three populations of Great Tit Parus major . In none of the six populations was there a significant correlation between the strength of the seasonal decline in clutch size and population density. Thus the lack of density dependence of clutch size in Pied Flycatchers was not consistent with the idea that this is caused by the unpredictability of final density at the time of egg-laying of the earliest females in the population. Furthermore, density does not have any adverse effect on reproductive output of Pied Flycatchers, and therefore they do not adjust clutch size to density.     

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.     

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% .     

Time-dependent reproductive decisions in the blue tit

Many breeding attempts in birds do not result in any fledged young due to predation on eggs or young. Consequently, the influence of time constraints on reproductive decisions are integrated parts of the reproductive behaviour of birds breeding within short, seasonal climate zones. In this study, I mimicked nest predation by removing blue tit (Parus caeruleus) clutches shortly after completion. Around 75% of the removed clutches were followed by a repeat clutch. Females producing their first clutch early in the season and females with an early onset of incubation in the laying sequence (an indication of high parental or territory quality) were most likely to initiate a repeat clutch. A trade‐off between the benefits of a repeat clutch and survival likely stopped late females in bad condition from investing more in the current reproductive season. Females producing a repeat clutch laid fewer eggs, had an earlier onset of incubation in the laying sequence and produced larger eggs than they did when producing their original first clutch. Eggs produced after the onset of incubation were especially large in the repeat clutches. Since food availability was presumably higher when the female produced her repeat clutch compared with her first clutch, females made a strategical decision when reducing clutch size, whereas onset of incubation and egg size may have been energetically constrained when producing the first clutch. Females that produced a relatively large clutch, had a relatively early onset of incubation, and laid relatively large eggs in their first clutch also did so when producing a repeat clutch, indicating that some of the variation in breeding parameters are due to differences in parental or territory quality. Differences between years in the temperature‐dependent development rate of caterpillars seem to affect the time constraints on breeding. A year with a predicted early seasonal decline in caterpillars resulted in short intervals between removal and relaying, small clutches and an early onset of incubation.     

Breeding performance of kestrels at Eskdalemuir, south Scotland

The performance of 144 pairs of European kestrels breeding in upland young conifer plantations was studied from 1976 to 1979. Laying started between 15 April and 1 June, and was 14 days later, on average, in the poor vole year of 1977 than in the other years. Some 38% of pairs failed to fledge young, mainly because they deserted clutches during incubation. The proportion of pairs that failed was positively correlated with total rainfall in May, but apparently not with estimated spring vole numbers. There was a marked seasonal decline in both clutch size and the probability of breeding successfully, so that early laying pairs fledged 2.7 times as many young per attempt as did late pairs. Within years, there was considerable variation in the laying date between pairs. On the available data, environmental factors, such as the habitat or vole numbers around the nest, appeared to have less influence on this variation than did the age of the pair members, their pairing date or their previous breeding experience.