Does daylength explain the latitudinal variation in clutch size of Pied Flycatchers Ficedula hypoleuca?

Geographical trends in breeding parameters were studied in the Pied Flycatcher Ficedula hypoleuca in the western Palaearctic. Predictions arising from the hypothesis that daylength and/or energy requirements of the brood explain latitudinal clutch size variation were tested. The nestling period decreased with latitude, but nestling mass on day 13 after hatching did not show a trend with latitude. The length of the daily activity period (working day) at the time of peak brood demand showed a quadratic relationship with latitude and did not increase linearly with daylight hours. The present study supports the hypothesis that latitudinal clutch size variation is influenced by the duration of the working day and the energy requirements of the brood. The balance between the energy requirements of the brood and the parents, in relation to the duration of working day and ambient temperature, are proposed to explain the latitudinal variation in clutch size in the Pied Flycatcher.     

Energy expenditure, nestling age, and brood size: an experimental study of parental behavior in the great tit Parus major

A brood manipulation experiment on great tits Parus major was performedto study the effects of nestling age and brood size on parentalcare and offspring survival. Daily energy expenditure (DEE)of females feeding nestlings of 6 and 12 days of age was measuredusing the doubly-labeled water technique. Females adjusted theirbrooding behavior to the age of the young. The data are consistentwith the idea that brooding behavior was determined primarilyby the thermoregulatory requirements of the brood. Female DEEdid not differ with nestling age; when differences in body masswere controlled for, it was lower during the brooding periodthan later. In enlarged broods, both parents showed significantlyhigher rates of food provisioning to the brood. Female DEE wasaffected by brood size manipulation, and it did not level offwith brood size. There was no significant effect of nestlingage on the relation between DEE and manipulation. Birds wereable to raise a larger brood than the natural brood size, althoughlarger broods suffered from increased nestling mortality ratesduring the peak demand period of the nestlings. Offspring conditionat fledging was negatively affected by brood size manipulation,but recruitment rate per brood was positively related to broodsize, suggesting that the optimal brood size exceeds the naturalbrood size in this population.     

FACTORS GOVERNING FEEDING RATE, FOOD REQUIREMENT AND BROOD SIZE OF NESTLING GREAT TITS PARUS MAJOR

SUMMARY Observations were made on feeding rates and food-consumption of nestling Great Tits Parus major mainly in Larch plantations at lake Yamanaka, Japan. Feeding frequencies were recorded by an automatic recorder. There were marked differences between early and late broods; the feeding frequencies were twice as great in early than in late broods of the same size. No clear tendency was observed in the variations of feeding frequencies in relation to brood size. There was, however, a clear inverse relationship between the frequencies and the average size of food brought to the nests. The males' share in terms of feeding frequencies is described. These figures, however, did not follow the males' contribution in terms of weight of food, which was nearly always higher than the females'. It is pointed out that feeding frequencies are far too variable to be used as a true index of food consumption by nestlings, and are not reliable. Attempts were made to measure the weight of food; the method is described. The average weight of food brought by males was lighter in early than in later broods. The total weight of food was estimated. The trend of daily food consumption per chick was similar to that of the chick's growth curve. It was found that up to about the tenth day of the nestling period daily food-intake per chick increased linearly as body weight increased. At some nests, rate of defaecation was observed. This was at first low, but it increased steeply on the third day, with a steady increase thereafter. By comparing the rates of food intake, faeces output, and weight increment of a chick, it was found that only 20–30% of digested matter (the difference between food-intake and faeces-output was used up daily (for body temperature regulation various external effort, etc.). The factors responsible for this high efficiency of growth in nestlings are discussed. There was a clear inverse relationship between the total weight of food brought per chick per day and the brood size. This is largely because the heat-loss is greater in small than in large broods, so that a chick from a small brood in fact needs more energy to maintain its body temperature after a certain age than one from a large brood. This is discussed in detail. Factors which caused variations in size of food are discussed in relation to feeding frequencies. It is pointed out that, because of the inverse relationship between energy requirement by each chick and brood size, the total food requirement by a brood as a whole did not vary directly in proportion to the brood size. An estimation showed that a b/3 still required about 75% of the total food required by a b/8. A smaller brood is less advantageous than expected to parents feeding nestlings when they encounter adverse conditions, e.g. food shortage in the habitat, or a lack of help by their mates, etc. On the other hand, it is suggested that once they have left the nest, the food-demand by a brood of fledglings the parents have to feed, so that, in the fledging period, in times of food shortage it would certainly be advantageous to have fewer young. It is suggested that, although fledglings may consume three to four times as much food as nestlings, the parents, in providing this food, would not work proportionately harder, since the parents' efficiency of providing food could be higher in feeding the fledglings, which always follow the parents as they are hunting, than in feeding the nestlings to which food has to be brought. On this basis, the adaptive significance of the length of the nestling period in nidicolous species is discussed in relation to clutch size, brood size and food requirement.     

Metabolic consequences of hard work

When an animal has to meet increased demands on its working capacity, for example, for thermoregulation or parental care, two strategies are available. The animal can reallocate energy from costly maintenance processes - such as immunological defence or DNA repair systems (compensation hypothesis) - or it may try to increase the rate of energy intake or efficiency of digestion by increasing the size of the alimentary tract (increased-intake hypothesis). By manipulating brood size, I affected parental effort among marsh tits (Parus palustris) as demonstrated by a significant increase in parental feeding rate with experimental brood size. Basal metabolic rate (BMR) increased both with manipulated brood size and individual feeding rate, supporting the predictions from the increased-intake hypothesis. Furthermore, I found a direct positive relation between BMR and energy expenditure, measured with the help of the doubly labelled water technique. The cost of achieving a higher working capacity is substantial since BMR increases more quickly than the surplus energy available for work. Since the cost of a high sustained workload was not primarily dependent on a reallocation of energy away from maintenance, such a cost should be searched for among the detrimental effects of a high metabolic rate per se, for example, an increased oxidative damage to DNA, proteins and lipids.     

An Experimental Study of Chick Provisioning in the Cooperatively Breeding Acorn Woodpecker

Acorn woodpeckers (Melanerpes formicivorus) are cooperative breeders in which groups consist of a variable number of cobreeding males, joint‐nesting females, and non‐breeding helpers of both sexes that are offspring from prior nests. We temporarily manipulated brood size of nests to determine the feeding response of birds in relation to their status (breeder or non‐breeding helper) and sex. All categories of birds responded similarly to brood size increases, adjusting their feeding rate upwards so as to maintain approximately the same per‐nestling feeding rate. Breeders, however, exhibited more flexibility with respect to brood size reductions, decreasing their feeding rate while helpers did not. This suggests that the ‘feeding rules’ of helpers are less flexible than those of breeders, a result not previously detected in other cooperative breeders that have been studied to date. Particularly surprising was the finding that helpers maintain their feeding rates when brood demand is decreased rather than when it was increased, suggesting that the flexibility they exhibit is not a result of birds using the opportunity afforded by reduced brood demand to engage in other less cooperative activities.     

Cost of reproduction, T-lymphocyte mediated immunocompetence and health status in female and nestling barn swallows Hirundo rustica

We investigate the trade-off between reproductive effort, health status and T-lymphocyte acquired immunity in female and nestling barn swallows Hirundo rustica using a brood size manipulation experiment. Maternal and total feeding effort increased with experimental brood size. Parents did not fully compensate for the increased food demand of the enlarged broods and as a consequence the per capita feeding rate of nestlings decreased with increasing experimental brood size. Body mass and a measure of T-cell mediated immunity in 12 days old nestlings also decreased with increasing experimental brood size. Different leucocyte concentrations and the heterophile/lymphocyte ratio – an index of stress – of nestlings did not change in relation to experimental brood size, suggesting that within brood competition did not affect stress to nestlings. The brood size manipulation had a significant effect on maternal T-cell mediated immunity, measured by the phytohemagglutinin skin test, but not on maternal body mass, haematocrit or differential or total white blood cell counts. Our results seem to support the prediction that under mild work stress females respond first by reducing the energetically expensive acquired immunity. Different leucocyte types and the heterophile/lymphocyte ratio appear less sensitive to parental workload.     

What the hen can tell about her eggs: egg development on the basis of energy budgets

By a simple model involving the state variables size and storage, it is possible to describe a wide variety of observations on the feeding, growth, energy storage and reproduction of animals. The model is based on the assumption that reproduction, growth as well as maintenance depend on the stored energy only and not directly on feeding. If an egg is thought of as a non-feeding animal, the model predicts the respiration ontogeny and growth of the embryo inside the egg. These predictions seem to hold well for published data on the development of eggs of fish and ratite, precocial and altricial birds. The latter two are known to follow different respiration ontogenies, but both are described well, differing only in one (compound) parameter value. The model explains why the incubation times of eggs of different species tend to increase linearly with egg size to the power 1/4, and why kiwis and petrels, which lay relatively large eggs, have to brood them much longer than larger birds with eggs of the same size. Conversely, it explains why the small eggs of the (parasitic) European cuckoo, hatch earlier than the still smaller eggs of their tiny hosts.Furthermore, it has been shown how the maintenance rate constant, which frequently appears in the microbial literature, can be obtained from measurements on the respiration and weight ontogeny in embryos, so linking independent lines of research. Application of the model shows an increase of the maintenance rate constant from bacteria, crustaceans, up to fish and birds, and a decrease from bacteria to green algae, suggesting lines of evolutionary development.     

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.     

HATCHING ASYNCHRONY IN ALTRICIAL BIRDS

1. The review aims to provide a simple conceptual framework on which to place recent studies of hatching asynchrony in altricial birds and to assess the evidence used in support of specific hypotheses. 2. Hatching asynchrony arises bsecause parents start incubation before laying is complete, but the precision of parental control is largely unknown. 3. Hypothesses concerning the functional significance of hatching asynchrony fall into four broad types. Hatching asynchrony might: (i) arise because of selection on the timing of events during the nesting period; (ii) facilitate the adaptive reduction in brood size; (iii) increase the energetic efficiency of raising the brood, or (iv) result from environmental or phylogenetic constraints. 4. The incubation pattern could function to minimize the losses of eggs, nestlings or adults to predators (or climatic sources of mortality), particularly in species which cannot actively defend their nest. The best evidence comes from comparative studies of hatching asynchrony. Early incubation might also be favoured if the food supply declines sharply through the breeding season, although the evidence is weak and indirect, or if there is a risk of brood parasitism. In species in which only the female incubates, early incubation could ‘force’ the male to invest more in the nestlings, but this idea remains to be tested. Males may be constrained by the risk of cuckoldry to delay incubation until laying is complete. 5. Hatching asynchrony could be adaptive by enabling the efficient reduction of brood size if food proves short after hatching (primarily because of a shortage of food in the environment or possibly because of a large proportion of ‘expensive’ nestlings in the brood in species which are sexually dimorphic). Observational evidence is often consistent with this hypothesis but few experimental studies provide adequate tests. Brood reduction could be adaptive in species (primarily eagles and pelecaniformes) which lay an extra egg to act as insurance against hatching failure, and again hatching asynchrony might facilitate brood reduction, although there are few experimental tests on such species. Hatching asynchrony might also enable sex ratio manipulation through selective brood reduction, although there is as yet no clear supportive evidence. 6. Ins species in which young have a marked peak in energy demand during the period of parental care, hatching asynchrony can reduce the peak demand of the brood, which might allow the parents to raise more healthy young. In many species such savings are likely to be small or absent. There is some behavioural evidence that hatching asynchrony can reduce fighting amongst nestlings and therefore lead to the more efficient use of energy by the brood. In general this effect seems small and the only energetic study found no difference in the energy requirements of synchronous and asynchronous broods. Other possible energetic advantages to hatching asynchrony have not been tested. 7. Environmental conditions during laying can influence both egg size and laying interval in aerial insectivores, and might directly influence incubation in this and other groups. Thus some variation in hatching asynchrony and the relative size of siblings is probably non-adaptive. The variability of incubation pattern within and across species suggests that hatching asynchrony is not under strong phylogenetic constraint. 8. The hypotheses about the adaptive significance of hatching asynchrony are complementary rather than mutually exclusive: within a species, several selective pressures could influence the optimal incubation pattern, and the relative importance of selective pressures will differ among species. Furthermore one should expect that the incubation pattern and parent–offspring interactions will be coadapted to maximize brood productivity.     

Hatching Asynchrony Decreases the Magnitude of Parental Care in Domesticated Zebra Finches: Empirical Support for the Peak Load Reduction Hypothesis

Parent–offspring conflict over the supply of parental care results in offspring attempting to exert control using begging behaviours and parents attempting to exert control by manipulating brood sizes and hatching patterns. The peak load reduction hypothesis proposes that parents can exert control via hatching asynchrony, as the level of competition amongst siblings is determined by their age differences and not by their growth rates. Theoretically, this benefits the parents by reducing both the peak load of the offspring's demand and their overall demand for food and benefits the offspring by reducing the amplification of their competition. However, the peak load reduction hypothesis has only received mixed support. Here, we describe an experiment where we manipulated the hatching patterns of domesticated zebra finch Taeniopygia guttata broods and quantified patterns of nestling begging and parental feeding effort. There was no difference in the begging intensity of nestlings raised in asynchronous or experimentally synchronous broods, yet parental feeding effort was lower when provisioning asynchronous broods and particularly so when levels of nestling begging were low. Further, both parents acted in unison, as there was no evidence of parentally biased favouritism in relation to hatching pattern. Therefore, our study provided empirical support for the prediction that hatching asynchrony reduces the feeding effort of parents, thereby providing empirical support for the peak load reduction hypothesis.     

PATTERNS OF GROWTH IN BIRDS

Parameters used to characterize the course of growth are described, and calculated growth parameters are presented for 105 species of birds of many taxonomic groups from a wide range of geographical localities. Growth parameters are found to exhibit as much as 20% variation within a species with respect to geographic locality and time of the nesting season. There is also considerable local variation, irrespective of season and locality, which is related to nutrition and perhaps to an inherited variability. The application of curve-fitting as a method of analysing intraspecific variation is discussed briefly, and the importance of comparative growth studies is emphasized. Growth patterns are correlated with other parameters of the life-history to evaluate the extent of diversity in the course of growth. Low rates of growth and prolonged growth periods occur primarily in species large for their families and in oceanic species. In most others, high rates of growth are maintained for longer periods of time. The shape of the growth curve is not related to the mode of development (i.e. whether precocial or altricial). Overall relative, or weight-specific growth rates, as measured by the constants of fitted growth equations, are most highly correlated with the adult body size of the species, changing as the -0–278 power of adult body weight. Smaller variations in the rate of growth appear to be correlated with differences in nesting success; open-nesting passerines grow faster than hole-nesting species of a similar size. Growth rate is further correlated with brood size. Oceanic species with single egg clutches and tropical land-birds with small clutches have low growth rates. The asymptote of the growth curve of the young (in relation to the adult weight) is related to the foraging behaviour of the adults. Aerial feeders generally have high asymptotes while those of ground feeding species are usually below adult weight. These differences are related to the need in the former for well-developed flight at the time of fledging. The diversity of growth patterns is related to evolutionary trends which are the result of (1) selective forces acting at stages of the life-history cycle other than development, (2) factors which affect the survival of offspring during the growth period, and (3) adjustments made to balance the energy budget of the family group. The last trend is discussed in detail in relation to the correlations found in the analysis. Two hypotheses are presented. Firstly, in species which cannot gather enough food to support even one young at a normal growth rate, the pace of development is reduced to decrease the energetic requirements of the young. Secondly, in species with small clutches, where adjustments to feeding capacities are not readily made by changing brood size, growth rate may be adjusted to accomplish this. The lack of critical energetic data to test these hypotheses is emphasized as a major deficiency in our understanding of the breeding biology of birds.     

Flexibility in the Foraging Behavior of Blue Tits in Response to Short‐Term Manipulations of Brood Size

Previous work suggests that short‐term changes in feeding rate are usually produced by the parent‐offspring interaction. However, few studies have properly tested this assumption. In this study, we attempt to explore the short‐term consequences of daily (within‐pair) brood size manipulations (reduced, original, and enlarged) on feeding behavior (provisioning rates, prey size, and prey type) of Mediterranean blue tits Cyanistes caeruleus. Total provisioning rates were lowest when broods were reduced in size and greatest when broods were enlarged. Mean prey size was also affected by the brood size changes: parents tended to bring larger prey when confronted with low brood demand reinforcing the view that a trade‐off exists between minimizing foraging time and maximizing food quantity. Such differences in feeding frequencies and the load sizes delivered may be explained by changes in the parents’ foraging tactic. Increase of brood size compelled parents to work harder and be less selective in prey choice; we found that stressed birds with a high level of feeding responsibility (hungry nestlings) opted to concentrate on more readily available food items (Tortricids). On the other hand, their immediate reaction when faced with a low level of feeding responsibility was to decrease this prey type in the diet, so that the percentage of other preys (Noctuids) in the diet increased. There was no intersexual difference in the way in which parents responded to the manipulation. In sum, our results revealed a flexibility in foraging strategies of blue tits to cope with changing scenarios, which supports the idea that provisioning behavior is largely governed by nestling demand.     

Is hatching asynchrony beneficial for the brood?

Many hypotheses have been proposed to explain why female birdsstart to incubate before clutch completion (IBCC). Some of thosesuggest that the resulting hatching asynchrony (HA) is adaptivebecause it increases the size hierarchy among offspring andin turn reduces nestling competition and energy demands duringthe peak feeding period. Others argue that IBCC is a good strategyin unpredictable environments. When food conditions deteriorate,the large size hierarchy quickly results in the death of thelast hatched nestlings, allowing the remaining ones to surviveand fledge in better condition. In comparison, under favorableconditions, all nestlings can fledge independent of hatchingorder. To test these hypotheses, we performed a brood size manipulationexperiment (as a simulation of good and bad years) in collaredflycatchers Ficedula albicollis and examined the effect of sizehierarchy on offspring and brood performance. We found thatchicks with an initial size disadvantage experienced reducedbody mass growth and had shorter feathers at fledging in bothreduced and enlarged broods. In enlarged broods, they also fledgedwith a smaller skeletal size. Although broods on average orparents could possibly still benefit from HA when food is scarce,this was not seen in the current study. Parental survival wasnot related to the size hierarchy in the broods, and the averagebody mass growth of the nestlings was slower in broods witha high initial size variance. We therefore conclude that HAand the resulting size hierarchy are probably detrimental forthe growth of nestlings in both good and bad years, at leastin species where nestling mortality does not occur early inlife.     

Horned larks on the Tibetan Plateau adjust the breeding strategy according to the seasonal changes in the risk of nest predation and food availability

Songbirds in seasonal environments often adjust their breeding strategy according to spatial or temporal changes in breeding conditions. Here we investigate how horned larks Eremophila alpestris, a multi‐brooded songbird on the Tibetan Plateau, responded to the changing risk of nest predation and food availability across breeding attempts. We showed that both nest concealment and food supply increased with plant growth, and horned larks adjusted their breeding strategies accordingly. First they selected nest‐sites where predator density was low, which enhanced nest survival. Second, clutch size increased with improving breeding conditions. They did not adopt an ‘egg‐size’ strategy as egg size did not change with laying sequence or breeding attempt. Instead, they adopted the ‘brood survival (feeding later‐hatched nestlings more)’ and ‘brood reduction (feeding early‐hatched nestlings more)’ strategies during early and later attempts. Moreover, nestlings’ growth varied with breeding attempt: more energy was invested into the growth of body mass during the first attempt but more energy was expended on the growth of linear structures during later attempts. This difference in energy allocation reflected changing food availability. We suggest that temporal changes of environmental factors are also the important force driving the evolution of avian breeding strategies.     

The benefit of large broods in barnacle geese: a study using natural and experimental manipulations

1. In precocial birds, where the young feed themselves, the costs and benefits of brood size are still poorly understood. An experimental manipulation of brood size was employed to examine the effects of brood size on both parents and young in a wild population of barnacle geese [ Branta leucopsis (Bechstein)] during brood-rearing on Svalbard.
2. Social dominance of the family unit, the amount of vigilance behaviour of the parents, the growth of the goslings in the family unit and an index of body condition for female parents during moult were all positively correlated with brood size.
3. When brood size changed as a result of natural events (i.e. predation or adoption) or experimental manipulation, rates of dominance, parental vigilance, gosling growth and female parent condition changed in a similar direction to the observed relation between the variable and brood size in unchanged broods.
4. After fledging, the fast-growing goslings in large broods survived better during autumn migration, while there was no apparent net cost in survival or next-year breeding for the parents.
5. Via a direct effect of brood size on dominance of the family unit, large broods were beneficial for both parent and young in a situation where there was strong intraspecific competition for the available food resources.
6. This study provides a clear demonstration of a causal relationship between brood size and various components of both gosling and adult fitness and is of direct relevance to the phenomenon of adoption and the evolution of brood size in this species.     

Worker brood survival in honeybees

The brood survival in honeybee workers was measured in order to obtain the data basic to the preparation of life tables. Under normal condition, that is, at the center of brood area, the survival is high. The survival/stage function runs 100.0 eggs, 94.2 unsealed brood (=feeding larvae), 86.4 sealed brood (=post-feeding larvae and pupae) and 85.1 adults. The total duration of immature stages is 20 days in 87.1%, 21 days in 8.3% and 19 days or more than 22 days in the residual fraction of successfully emerging workers. The survival remarkably decreases at peripheral areas within the hive. Various factors affecting the brood survival are discussed and the importance of a dense worker cover on the brood area is stressed in relation to the maintenance of thermal conditions optimal to the brood. The occurrence of one factor, which is not expected in solitary animals, the self-control of population by egg eating, is pointed out.     

Energy requirements for growth and maintenance in macaroni and rockhopper Penguins

Summary Energy requirements for growth and maintenance of macaroni and rockhopper penguin chicks at Marion Island, southern Indian Ocean, were estimated from rates of oxygen consumption and body composition analysis. Mass-specific energy expenditures of both species increased to levels 1.5 times that of hatchlings within 14–21 days of hatching and subsequently decreased. Lipid was initially accumulated slowly but the rate of accumulation increased after 30 days of age when male parents joined the females in feeding the chicks. Lipid, however, decreased markedly after 45 days of age and was presumably metabolized. Protein was laid down throughout the growth period, but doubled its initial rate of accumulation between 22 and 35 days of age. Thereafter the rate decreased until independence. Daily energy requirements of macaroni and rockhopper penguins increased from 417 and 211 kJ d^-1, respectively, in the first week after hatching to peaks of 1540 and 1170 kJ d^-1 about halfway through the growth period before decreasing until independence. Total energy requirement for growth and maintenance was estimated to be 76200 kJ for macaroni penguins and 59400 kJ for rockhopper penguins, of which growth energy comprised 38% and 28%, respectively. Based on the energy requirements and population data, macaroni and rockhopper penguin chicks at Marion Island consume an estimated 4200 and 700 t of food, respectively, each year.     

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.     

Maternal investment in a spider with suicidal maternal care, Stegodyphus lineatus (Araneae, Eresidae)

Providing parental care is costly for the parent, but generally beneficial for the young whose survival, growth and reproductive value can be increased. Selection should strongly favour an optimal distribution of parental resources, depending on the relationship between the costs and benefits for parents and their offspring. Parental care is characterized by trade offs in investment, for example between egg size and number of young or providing resources at the egg stage versus the post-hatching stage. Females of the spider Stegodyphus lineatus (Eresidae) produce a single small brood with small eggs and provide the young with regurgitated fluid and later, with their body contents via matriphagy. We asked whether females adjust the investment of resources differentially into eggs, regurgitation feeding and matriphagy, and how maternal investment affects the size of the young at dispersal. We followed the growth of young of broods in the lab and in the field and manipulated brood size in order to determine the pattern of resource allocation. We found that brood size was positively correlated with body mass: larger females had larger broods. Females provided 95% of their body mass to the young, allocating more resources to regurgitation than to matriphagy. Females provided regurgitated food to the young according to the brood size, providing less food when the brood was reduced. Maternal resources had a large influence on offspring mass at dispersal, which is likely to affect their future fitness. The study shows the importance of the female's body mass and her resource allocation decisions for her reproductive outcome.     

Long-term effects of manipulated natal brood size on metabolic rate in zebra finches

Long-term effects of developmental conditions on health, longevity and other fitness components in humans are drawing increasing attention. In evolutionary ecology, such effects are of similar importance because of their role in the trade-off between quantity and quality of offspring. The central role of energy consumption is well documented for some long-term health effects in humans (e.g. obesity), but little is known of the long-term effects of rearing conditions on energy requirements later in life. We manipulated the rearing conditions in zebra finches (Taeniopygia guttata) using brood size manipulation and cross-fostering. It has previously been shown in this species that being reared in a large brood has negative fitness consequences, and that such effects are stronger in daughters than in sons. We show that, independent of mass, standard metabolic rate of 1-year-old birds was higher when they had been reared in a large brood, and this is to our knowledge the first demonstration of such an effect. Furthermore, the brood size effect was stronger in daughters than in sons. This suggests that metabolic efficiency may play a role in mediating the long-term fitness consequences of rearing conditions.