Hatching asynchrony and brood reduction influence immune response in Common Kestrel Falco tinnunculus nestlings

The onset of incubation before the end of laying imposes asynchrony at hatching and, therefore, a size hierarchy in the brood. It has been argued that hatching asynchrony might be a strategy to improve reproductive output in terms of quality or quantity of offspring. However, little is known about the mediating effect of hatching asynchrony on offspring quality when brood reduction occurs. Here, we investigate the relationship between phenotypic quality and hatching asynchrony in Common Kestrel Falco tinnunculus nestlings in Spain. Hatching asynchrony did not increase breeding success or nestling quality. Furthermore, hatching asynchrony and brood reduction had different effects on nestlings’ phytohaematogglutinin (PHA)‐mediated immune response and nestling growth. In asynchronous and reduced broods (in which at least one nestling died), nestlings showed a stronger PHA‐mediated immune response and tended to have a smaller body size compared with nestlings raised in synchronous and reduced broods. When brood reduction occurred in broods hatched synchronously, there was no effect on nestling size, but nestlings had a relatively poor PHA‐mediated immune response compared with nestlings raised in asynchronous and reduced broods. We suggest that resources for growth can be directed to immune function only in asynchronously hatched broods, resulting in improved nestling quality, as suggested by their immune response. We also found that males produced a greater PHA‐mediated immune response than females only in brood‐reduced nests without any effect on nestling size or condition, suggesting that females may trade off immune activities and body condition, size or weight. Overall, our results suggest that hatching pattern and brood reduction may mediate resource allocation to different fitness traits. They also highlight that the resolution of immune‐related trade‐offs when brood reduction occurs may differ between male and female nestlings.     

Siblicide, starvation and nestling growth in the laughing kookaburra

I examined the growth of surviving nestlings in broods of the cooperatively breeding laughing kookaburra Dacelo novaeguineae , which has complex patterns of brood reduction. Laughing kookaburras usually lay three eggs that hatch asynchronously. Brood reduction occurs in nearly half of all broods and always affects the youngest nestling. In most cases, the youngest nestling is killed within a few days of hatching by aggressive attacks from its older siblings. In a smaller proportion of nests, the youngest nestling dies from starvation, rather than physical attack, much later in the nestling period when nestling growth rates and adult feeding rates peak (about 20 days post-hatching). These mechanistically and temporally distinct episodes of brood reduction were associated with very different patterns of growth in the senior nestlings. Seniors that killed their youngest sibling reached higher asymptotic weights than seniors that did not commit siblicide. In contrast, if the youngest nestling was not killed by its older siblings, but later starved to death, the surviving seniors were skeletally smaller and had retarded feather development compared to seniors from other broods. These differences in nestling growth may have longer-term fitness consequences, because kookaburra fledging weight is positively associated with both juvenile survival and successful recruitment into the breeding population. Therefore, although parents of broods without mortality produce the highest number of fledglings and also the highest number of independent juveniles, if parents are unable to raise a full brood, early siblicide may represent the best brood reduction option. Early siblicide is at least associated with high quality young that have enhanced survival and recruitment prospects. In contrast, the poor growth of seniors in broods where the youngest nestling starved suggests that parents overestimated the size of the brood they could provision.     

Optimal brood size and its limiting factors in the Rufous Turtle DoveStreptopelia orientalis

Optimal brood size and its limiting factors of the Rufous Turtle Dove,Streptopelia orientalis, were studied at the campus of the University of Tsukuba, Japan, during the breeding season in 1990–92. The dove usually lays two eggs in a nest. I made nests of a brood size of one and three by transferring a hatchling from one nest to the other, and compared their fledging success, factors of breeding failure, weight and tarsus length at fledging, growth rate and nestling period with those of a brood of two. The index of fitness (fledgling weight multiplied by average number of fledglings per nest) was almost the same in broods of two and three. However, the highest variation in fledging weight within the brood and the extension of nestling period were observed in broods of three, which caused the extension of inter-brood interval and consequently the smaller number of broods in the total breeding season. Therefore, broods of three would not have an advantage in producing more offspring than broods of two. Crop milk production had an effect on the growth of nestlings in the early phase of the nestling period, but the rapid growth in the granivorous phase compensated for the growth delay of the smallest nestling in broods of three. Small brood size and a large number of broods in a season would also be more effective under high predation pressure.     

NESTLING SURVIVAL AND NESTLING WEIGHTS IN THE HOUSE SPARROW AND TREE SPARROW PASSER SPP. AT OXFORD

Nestling survival and nestling weights in P. domesticus and P. montanus were studied in 1961 and 1963–64 at Oxford. This paper concludes a study of factors influencing the reproductive rate. Taking all losses into account, P. domesticus reared an average of 1^.6 nestlings per brood (45%) and P. montanus 2.7 nestlings per brood (59%). About a third of all broods of both species failed completely to survive the nestling period. In P. domesticus these failures were most numerous in the middle part of the breeding season and are attributed to nutritional deficiencies derived from unsuitable food provided as a consequence of a seasonal food shortage, but in P. montanus complete brood failures occurred mostly in the second half of the nestling period and are attributed to predation. 43 broods of P. domesticus and one brood of P. montanus were weighed daily. Those of P. domesticus were classified as (1) successful broods—in these some nestlings died in the larger brood-sizes, apparently through starvation; (2) long-lived unsuccessful broods—in these the nestlings died at intervals and failure was attributed to nutritional deficiencies; and (3) short-lived unsuccessful broods. A slight decrease in the weights of nestlings in successful broods at the end of the nestling period is attributed to the utilization of insulating fat facilitated by the completion of the feather covering. Nestlings of both species left the nest at 88–89% of the adult weight. Taking all “successful” broods together, the percentage survival rates on nestling day 13¹/₂ (day of hatching = day ¹/₂) in P. domesticus were 81–82% in b/2–3, 70% in b/4 and 56% in b/5 (a situation paralleled in this respect by P. hispaniolensis), but in P. montanus they were c. 82% in all brood-sizes. Hence, in P. domesticus b/4 probably gave rise to the largest number of nestlings reared per brood, while in P. montanus most nestlings were produced by the largest brood-size. Weighings of many broods on day 13¹/₂ showed two trends in the weight of the nestlings: (1) in both species the weight of the nestling decreased as the number of survivors from each initial brood-size decreased; (2) between successive initial brood-sizes the weight of the nestling of P. domesticus decreased with increasing brood-size but in P. montanus there was no change. The losses in the larger broods of P. domesticus occurred mostly in the first half of the nestling period—apparently in association with the asynchronous hatching of the eggs and as a consequence of the limitation on the feeding frequency of the adults. Nestling survival was lowest in the larger broods in the middle of the breeding season and contrasted with the mid-season increase in mean clutch-size. It is suggested that in the study area there was a (possibly unnatural) shortage of food suitable for nestlings in the middle of the season. It is suggested that in P. domesticus the unexpectedly low feeding frequencies of the adults with large broods, apparently causing their low survival rates, may be an adaptation evolved to obtain the maximum amount of food in the presence of other adults which would be attracted to a food source by higher rates of activity. The breeding success calculated from data derived from the whole of this study was 35% for P. domesticus and 49% for P. montanus (2.9 and 3.9 nestlings per breeding pair per year respectively). It is suggested that the population of P. domesticus was much closer to a critical limiting factor, e.g. food supply, than that of P. montanus. This may account for the striking differences between the two species in their nestling survival rates and their nestling weights in relation to brood-size; in particular, the success of the larger broods of P. montanus may have been a temporary phenomenon.     

An experimental approach to the brood reduction hypothesis in Magellanic penguins

In many bird species, eggs in a brood hatch within days of each other, leading to a size asymmetry detrimental to younger siblings. Hatching asynchrony is often thought of as an adaptive strategy, and the most widely studied hypothesis in relation to this is the ‘brood reduction hypothesis’. This hypothesis states that when food resources are unpredictable, hatching asynchrony will allow the adjustment of the brood size maximizing fledging success and benefitting parents. The Magellanic penguin Spheniscus magellanicus is an appropriate species to test this hypothesis because it has a 2‐egg clutch that hatches over a 2‐d interval with a broad range of variation (–1 to 4 d), it shows facultative brood reduction, and food abundance between breeding seasons is variable. We performed a manipulative study at Isla Quiroga, Argentina, during three breeding seasons (2010–2012) by forcing broods to hatch synchronously (0 d) or asynchronously (2 or 4 d). Years were categorized based on estimated food abundance. Our study provided mixed results because in the low estimated food abundance year asynchronous broods did not have higher nestling survival than synchronous broods, and the second‐hatchling in asynchronous broods did not die more often than those in synchronous broods. On the other hand, younger siblings of 4‐d asynchronous broods starved earlier than those of synchronous broods, and 2‐d asynchronous broods fledged heavier young than synchronous broods. Asynchronous hatching would seem to benefit reproduction in this species, not with respect to survival, but in terms of the advantages it can accord to nestlings and, in terms of lower costs, for parents raising nestlings.     

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.     

BREEDING BIOLOGY OF HOUSE MARTINS DELICHON URBICA IN RELATION TO AERIAL INSECT ABUNDANCE

The breeding biology of House Martins nesting in artificial boxes was examined in relation to aerial insect abundance and weather. The insect food supply was continuously monitored with a suction-trap at 40 ft above ground level. Aerial insect abundance started to rise from the winter level in April and reached a high stable state in June. Insects remained abundant until September; the subsequent decline continued at least until the end of October. The size of first clutches (mean size 3.87) was correlated with the abundance of aphids in spring, though not with temperature. It is suggested that this was an adaptive response because high food levels in May were associated with high levels in the main nesting period. Clutch-size declined through the season but was not matched by changes in food abundance. Second clutches (mean size 2–95) were most frequent following a high food level in June. No correlation was found between egg-weight and preceding food conditions, nor with season, clutch-size or order of laying within clutches. If food was scarce on the day of laying of the first egg, these clutches suffered a suspension of laying of subsequent eggs. Some of the young in these nests showed a reduced growth rate. The duration of incubation (mean 14.6 ± 1.1 days) was not apparently correlated with food abundance, however it must have been potentially extended by extreme shortages because incubation duties were neglected at such times. Infertility was probably the main cause of hatching failure (14.2%). A model was used to predict the date of onset of laying. It was based on the assumption that nestling tissue was produced with the same energetic efficiency as eggs. The model indicated that House Martins could collect enough food to lay eggs earlier than the observed date in most years. The high probability of food shortage before the laying period, however, appeared to discourage laying at this time. The observed onset of laying coincided with the appearance of aphids in the air, probably because they comprised an abundant and stable food source for egg formation. Breeding generally occurred in the period of highest food abundance. Pairs rearing only a single brood each year did so in July when food levels were highest. The growth of first brood nestlings was more closely associated with food levels than any other factor investigated, while in second broods, rainfall was found to have the greatest influence. The total variance in growth explained by environmental factors in the first broods (41%) was greater than in second broods (22%). This relative independence of second broods from adverse environments probably arose from more abundant food and the feeding of some of these broods by the young of first broods. An exceptionally late brood showed an extended nestling period indicating deteriorating conditions later in the breeding season. It is proposed that the spread of laying may reflect differences in the feeding efficiency of nesting House Martins, because the growth of two early first broods was more rapid at given food levels than two late broods. Laying patterns conformed to a distribution based on a progressive threshold mechanism. The more efficient pairs may be able to attain breeding condition and lay at low levels of food abundance, and hence breed earlier in the season. Subsequent layings are facilitated by the rise in food levels in early summer. Mortality within the nest was low (5.8%) and associated with food shortage. Nestling periods (mean 30.6 ± 2.3 days) were not shown to be correlated with food abundance; they were more dependent on brood-size. Recruitment into House Martin populations is thus widely influenced by food supply, particularly through an influence on clutch-size, the occurrence of second clutches and nestling mortality.     

Differential Begging and Locomotory Behaviour by Early and Late Hatched Nestlings Affecting the Distribution of Food in Asynchronously Hatched Broods of Altricial Birds

Distribution of food to early and late hatched nestlings was studied in asynchronously hatched broods of the great tit Parus major, the blackbird Turdus merula, and the fieldfare T. pilaris. Food distribution is related to the locomotory and begging behaviour and positions in the nest of these nestlings. Late hatched (small) nestlings were found to beg more often per feed than bigger nestlings and move more towards favoured positions in the nest to counteract selective feeding of bigger young. The functional significance of these differences in the behaviour of early and late hatched nestlings are discussed. It is argued that they are adaptive by 1) ensuring that each nestling survives when food supplies are ample, and 2) by mediating an optimal brood reduction when food is insufficient to raise the entire brood. The roles of asynchronous hatching, and selective feeding which follows from differential behaviour of early and late hatched young are discussed in relation to food conditions during the breeding season.     

Genetic and environmental components of growth in nestling blue tits (Parus caeruleus)

We investigated the effect of brood‐size mediated food availability on the genetic and environmental components of nestling growth in the blue tit (Parus caeruleus), using a cross‐fostering technique. We found genetic variation for body size at most nestling ages, and for duration of mass increase, but not of tarsus growth. Hence, nestling growth in our study population seems to have the potential to evolve further. Furthermore, significant genotype–environment interactions indicated heritable variation in reaction norms of growth rates and growth periods, i.e. that our study population had a heritable plasticity in the growth response to environmental conditions. The decreasing phenotypic variance with nestling age indicated compensatory growth in all body traits. Furthermore, the period of weight increase was longer for nestlings growing up in enlarged broods, while there was no difference to reduced broods in the period of tarsus growth. At fledging, birds in enlarged broods had shorter tarsi and lower weights than birds in reduced broods, but there was no difference in wing length or body condition between the two experimental groups. The observed flexibility in nestling growth suggests that growing nestlings are able to respond adaptively to food constraint by protecting the growth of ecologically important traits.     

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.     

Unusual pattern of sex‐specific mortality in relation to initial brood sex composition in the black‐billed magpie Pica pica

In sexually size‐dimorphic species, brood sex composition may exert differential effects on sex‐specific mortality. We investigated the sex‐specific mortality and body condition in relation to brood sex composition in nestlings of the black‐billed magpie Pica pica. Neither significantly sex‐biased production at hatching nor overall sex‐biased mortality during the nestling period was found. Sex‐specific mortality as a function of brood sex composition, however, differed between female and male nestlings. We found higher mortality for females in male‐biased broods and higher mortality for males in female‐biased broods, a phenomenon that we call ‘rarer‐sex disadvantage’. As a result, fledging sex ratios became more biased in the direction of bias at hatching, a phenomenon that cannot be readily explained by previous hypotheses for sex‐specific mortality. Two temporal variables, fledging date and laying date, were also correlated with sex‐specific mortality: female nestlings in earlier broods experienced higher mortality than male nestlings whereas male nestlings in later broods experienced higher mortality. We suggest that this unusual pattern of mortality may be explained by adaptive adjustments of brood sex composition by parents, either through the effects of a slight sex difference in offspring dispersal patterns on parental fitness, or owing to sex differences as regards the benefits of early fledging.     

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.     

Brood size and begging intensity in nestling birds

Theoretical models suggest that sibling competition should selectfor conspicuous begging signals. If so, begging intensity mightbe expected to increase with the number of competitiors. Thepurpose of our study was to examine the relationship betweenbegging intensity and brood size using nestling tree swallows(Tachycineta bicolor) as our model. Over 2 years, we videotapedbegging behavior in unmanipulated broods of different sizes.We found that begging intensity increased with brood size. Theaverage weight of nestlings in each brood did not vary withbrood size, but feeding rate per nestling decreased with broodsize, suggesting that nestlings in larger broods begged moreintensively, possibly because they were hungrier. We also conductedan experiment to examine the effect of nest mates on beggingin different-sized broods. We found that nestlings with similarweights, previous competitive environments, and food deprivationbegged more intensively in large broods than in small broods.Overall, our study indicates that begging intensity increaseswith brood size in tree swallows. This relationship may resultfrom interactions among brood mates rather than from lower feeding rates to individual nestlings in larger broods.     

Hatching asynchrony and growth trade‐offs within domesticated and wild zebra finch,Taeniopygia guttata,broods

The Australian zebra finch, Taeniopygia guttata, is a widely used model organism, yet few studies have compared domesticated and wild birds with the aim of examining its relevance as an evolutionary model species. Domestic and wild broods hatch over approximately 4 and 2 days, respectively, which is important given that nestlings can fledge after as little as 12 days, although 16–18 days is common. We aimed to evaluate the extent to which the greater hatching asynchrony in domestic stock may effect reproductive success through greater variance in size hierarchies, variance in within‐brood growth rates, and partial brood mortality. Therefore, by simultaneously controlling brood sizes and experimentally manipulating hatching intervals in both domesticated and wild birds, we investigated the consequences of hatching intervals for fledging success and nestling growth patterns, as well as trade‐offs. Fledging success was similarly high in domestic and wild broods of either hatching pattern. Nonetheless, between‐brood analyses revealed that domestic nestlings had significantly higher masses, larger skeletal characters, and longer wings than their wild counterparts, although wild nestlings had comparable wing lengths at the pre‐fledging stage. Moreover, within‐brood analyses revealed only negligible differences between domestic and wild nestlings, and larger effects of hatching order and hatching pattern. Therefore, despite significant differences in the hatching intervals, and the ultimate size achieved by nestlings, the domestication process does not appear to have significantly altered nestling growth trade‐offs. The present study provides reassuring evidence that studies involving domesticated zebra finches, or other domesticated model organisms, may provide reasonable adaptive explanations in behavioural and evolutionary ecology. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 100 , 763–773.     

Similarity in the begging calls of nestling Red‐winged Blackbirds

ABSTRACT Although individually distinct begging calls may permit parents to recognize their offspring, birds nesting in dense breeding colonies where fledglings intermingle might benefit from additional adaptations. For example, if the calls of all nestlings in a brood were similar, parents would need to recognize only one brood call instead of the identity calls of each nestling. We recorded nestling Red‐winged Blackbirds (Agelaius phoeniceus) to determine whether their calls function to identify individuals (identity call hypothesis) or broods (brood call hypothesis). We used spectrogram cross‐correlation and dynamic time warping as well as call duration, peak frequency, and frequency range to estimate the similarity of begging calls of nestling Red‐winged Blackbirds. We recorded individual nestlings on day 5 and on day 9 of the nestling period to determine whether calls of individuals were more similar than calls of different nestlings, and whether calls of broodmates were more similar than calls of nestlings from different broods. We found that calls of 8‐d‐old individuals were more similar than calls of different nestlings, but the calls of broodmates were not more similar than those of nestlings from different broods. These results were consistent with the identity call hypothesis. We then compared begging calls of pairs of nestlings recorded separately and together on day 9. We found that the calls of 8‐d‐old nestlings recorded together were more similar than when they were recorded separately. In addition, using playback of begging calls from normal broods and artificial “broods” constructed from the calls of single nestlings, we found that females returned with food sooner in response to the calls of single nestlings (with enhanced call similarity) than to those of normal broods. Our results suggest that similar begging calls may be beneficial for both nestlings and parents, with broodmates fed at higher rates when their calls are more similar and, after fledging, parents needing to recognize only one brood call instead of the identity calls of each fledgling.     

Supplementary feeding increases nestling feather corticosterone early in the breeding season in house sparrows

Several studies on birds have proposed that a lack of invertebrate prey in urbanized areas could be the main cause for generally lower levels of breeding success compared to rural habitats. Previous work on house sparrows Passer domesticus found that supplemental feeding in urbanized areas increased breeding success but did not contribute to population growth. Here, we hypothesize that supplementary feeding allows house sparrows to achieve higher breeding success but at the cost of lower nestling quality. As abundant food supplies may permit both high‐ and low‐quality nestlings to survive, we also predict that within‐brood variation in proxies of nestling quality would be larger for supplemental food broods than for unfed broods. As proxies of nestling quality, we considered feather corticosterone (CORT_f), body condition (scaled mass index, SMI), and tarsus‐based fluctuating asymmetry (FA). Our hypothesis was only partially supported as we did not find an overall effect of food supplementation on FA or SMI. Rather, food supplementation affected nestling phenotype only early in the breeding season in terms of elevated CORT_f levels and a tendency for more variable within‐brood CORT_f and FA. Early food supplemented nests therefore seemed to include at least some nestlings that faced increased stressors during development, possibly due to harsher environmental (e.g., related to food and temperature) conditions early in the breeding season that would increase sibling competition, especially in larger broods. The fact that CORT_f was positively, rather than inversely, related to nestling SMI further suggests that factors influencing CORT_f and SMI are likely operating over different periods or, alternatively, that nestlings in good nutritional condition also invest in high‐quality feathers.     

Influence of hatching asynchrony and within-brood parental investment on size, condition, and immunocompetence in nestling red-billed choughs

Studies of hatching asynchrony have rarely assessed the effect of parental investment strategies on the development of intra-brood hierarchies using indicators of nestling quality. The influence of hatching asynchrony and other variables related to parental investment on immunocompetence was evaluated measuring T-cell mediated immune response in broods of red-billed choughs ( Pyrrhocorax pyrrhocorax ), a large long-living passerine with a pronounced sexual size dimorphism. The results showed that T-cell mediated immune response depends on parental effects as shown by the differences between broods on hatching asynchrony. Male nestlings were both heavier and larger than female nestlings, but there was no effect of hatching order on these traits, nor on sex differences in immunocompetence. Differential investment strategy in relation to laying order did not favour older offspring or either of the sexes. Successful reproduction in this species might be so unpredictable and infrequent that strategies of parental investment in the brood could have evolved to attempt to maximize the survival of all nestlings by avoiding within-brood hierachies of size, body condition, and immunocompetence.  © 2008 The Linnean Society of London, Biological Journal of the Linnean Society , 2008, 94 , 675–684.     

Haemoglobin concentration and body condition of nestling Great Tits Parus major : a comparison of first and second broods in two contrasting seasons

The physiological condition of nestling altricial birds depends on the quantity and quality of food delivered to them by parents. One indicator of the condition of Great Tit Parus major nestlings is the haemoglobin concentration in their blood. The present study demonstrates the influence of weather conditions (temperature and rainfall) on nestling haemoglobin concentrations during two consecutive breeding seasons in two different habitat types (parkland vs. woodland) in the city of Łódź in Central Poland. This influence probably results from the effects of weather on the trophic base of the Tits. Dry, hot weather strongly affected bush and herbal foliage later in the breeding season (mid-June to mid-July) in 2006, presumably by interfering with the development of herbivorous arthropod populations. This in turn caused food shortages for second broods of Great Tits, which resulted in nestlings having low haemoglobin levels. In the following year, temperature was on average lower, and rainfall was regular but not very heavy. These conditions enabled the development of arthropod assemblages, and the trophic base for birds was much richer. Haemoglobin concentrations in the blood of nestlings from second broods were significantly higher than those of first broods and, unexpectedly, second-brood nestlings in 2007 were on average in better physiological state than first-brood nestlings in 2006 in both habitats. The relationship between haemoglobin concentration, brood category and year was very similar to that for nestling body mass. However, it was independent of both body mass and brood size. In some years and under certain conditions, second broods can be more successful than first broods.     

Tawny Owls Strix aluco with reliable food supply produce male-biased broods

Tawny Owls Strix aluco have been reported to skew the sex ratio of their offspring towards males when facing food shortage during the nestling period (and vice versa), because female fitness is more compromised by food shortage during development than male fitness. To test the generality of these results we used a DNA marker technique to determine the sex ratio in broods of Tawny Owls in Danish deciduous woodland during two years of ample food supply (rodent population outbreak) and two years of poor food supply. Of 268 nestlings, 59% were males (95% CI: 53–65%). This proportion was higher than previously reported for the species (49% in Northumberland, UK, and 52% in Hungary), but consistent with Fisherian sex allocation, which predicts a male bias of c . 57% based on inferred differences in energy requirements of male and female chicks. Contrary to previous results, brood sex ratios were not correlated with the resource abundance during the breeding seasons, despite considerable variation in breeding frequency, brood size or hatching date across years. Brood sex ratios were unaffected by brood reduction prior to DNA sampling, and nestling mortality rates after DNA sampling were not related to gender. The inconsistency between the sex ratio allocation patterns in our study and previous investigations suggests that adaptive sex allocation strategies differ across populations. These differences may relate to reproductive constraints in our population, where reproductive decisions seem primarily to concern whether to lay eggs at all, rather than adjust the sex ratio to differences in starvation risk of nestlings.     

Immune function and survival of great tit nestlings in relation to growth conditions

Life history theory predicts a trade-off between number and quality of offspring. Reduced quality with increasing brood size may arise from a decrease in body condition or in immunocompetence that would be important in fighting off virulent parasites by immunologically naive offspring. We tested the effect of rearing conditions on immune function of nestling great tits (Parus major) by reducing or increasing broods by two hatchlings. In the middle of the nestling period (on day 8), nestlings from enlarged broods developed lower T cell responses [as measured from the cutaneous swelling reaction to injection with phytohaemagglutinin (PHA)] and tended to have lower total leukocyte and lymphocyte concentrations in their peripheral blood than nestlings from reduced broods. Brood size manipulation affected the PHA response of nestlings most strongly in small clutches, suggesting that nestling immune function was dependent on their parents’ condition, as estimated by original clutch size. Intra-brood differences in nestling mortality were unrelated to immune parameters, but nestlings in broods without mortality had a stronger PHA response, higher concentration of lymphocytes and higher body mass on day 15 than nestlings in broods with mortality. These results support the prediction that the immune function of altricial birds is affected by rearing conditions, and that growth and immune parameters are related to inter-brood differences in nestling survival. Received: 1 February 1999 / Accepted: 19. July 1999