Offspring pay sooner,parents pay later: experimental manipulation of body mass reveals trade-offs between immune function,reproduction and survival

Introduction

Life-history theory predicts that organisms trade off survival against reproduction. However, the time scales on which various consequences become evident and the physiology mediating the cost of reproduction remain poorly understood. Yet, explaining not only which mechanisms mediate this trade-off, but also how fast or slow the mechanisms act, is crucial for an improved understanding of life-history evolution. We investigated three time scales on which an experimental increase in body mass could affect this trade-off: within broods, within season and between years. We handicapped adult skylarks (Alauda arvensis) by attaching extra weight during first broods to both adults of a pair. We measured body mass, immune function and return rates in these birds. We also measured nest success, feeding rates, diet composition, nestling size, nestling immune function and recruitment rates.

Results

When nestlings of first broods fledged, parent body condition had not changed, but experimental birds experienced higher nest failure. Depending on the year, immune parameters of nestlings from experimental parents were either higher or lower than of control nestlings. Later, when parents were feeding their second brood, the balance between self-maintenance and nest success had shifted. Control and experimental adults differed in immune function, while mass and immune function of their nestlings did not differ. Although weights were removed after breeding, immune measurements during the second brood had the capacity to predict return rates to the next breeding season. Among birds that returned the next year, body condition and reproductive performance a year after the experiment did not differ between treatment groups.

Conclusions

We conclude that the balance between current reproduction and survival shifts from affecting nestlings to affecting parents as the reproductive season progresses. Furthermore, immune function is apparently one physiological mechanism involved in this trade-off. By unravelling a physiological mechanism underlying the trade-offs between current and future reproduction and by demonstrating the different time scales on which it acts, our study represents an important step in understanding a central theory of life-history evolution.

     

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.     

Some effects of inclement weather conditions on the survival and condition of bull-headed shrike nestlings

Inclement weather struck Japan in 1993, permitting a natural experiment for examining the effect of weather conditions on nesting success and nestling growth of the bull-headed shrike, Lanius bucephalus. Aspects of the breeding biology of bull-headed shrikes in relation to weather conditions and timing of breeding in 1992 and 1993 were examined. The two breeding seasons were divided into two periods, early and late, in each year. While the probability of nest survival in nestling stages during both periods was almost equal, the probability of nest survival in the egg stage during the early period was significantly lower than that during the late period. In 1993, the probability of nestling survival during the late period was significantly lower than during the early period; the late period had larger fluctuations of precipitation and was colder than the same period in 1992. The number of disappeared nestlings positively correlated with mean precipitation per day. The greater part of the disappeared nestlings was the lightest in each brood. Late breeders fledged lighter young than the early breeders. Although shrikes adopted hatching asynchrony, the late breeders could not surmount the unpredictable inclement weather in 1993.     

Parasites favour intermediate nestling mass and brood size in cliff swallows

A challenge of life‐history theory is to explain why animal body size does not continue to increase, given various advantages of larger size. In birds, body size of nestlings and the number of nestlings produced (brood size) have occasionally been shown to be constrained by higher predation on larger nestlings and those from larger broods. Parasites also are known to have strong effects on life‐history traits in birds, but whether parasitism can be a driver for stabilizing selection on nestling body size or brood size is unknown. We studied patterns of first‐year survival in cliff swallows (Petrochelidon pyrrhonota) in western Nebraska in relation to brood size and nestling body mass in nests under natural conditions and in those in which hematophagous ectoparasites had been removed by fumigation. Birds from parasitized nests showed highest first‐year survival at the most common, intermediate brood‐size and nestling‐mass categories, but cliff swallows from nonparasitized nests had highest survival at the heaviest nestling masses and no relationship with brood size. A survival analysis suggested stabilizing selection on brood size and nestling mass in the presence (but not in the absence) of parasites. Parasites apparently favour intermediate offspring size and number in cliff swallows and produce the observed distributions of these traits, although the mechanisms are unclear. Our results emphasize the importance of parasites in life‐history evolution.     

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.     

Change in body mass in relation to breeding phase in bull-headed shrikes

Changes in body mass of both sexes of the bull-headed shrike, Lanius bucephalus, were investigated over the six breeding phases of this species. Standardized body mass (SBM), which was defined as body mass divided by the length of the tarsus, of the males was relatively constant over the phrases, while the SBM of the females changed drastically. In the females, the SBM during egg-laying was higher than the SBM in all the other breeding phases. The SBM of the females did not differ between the incubation and early-nestling phases, and was lowest during the fledgling phase. Mass loss in bull-headed shrikes did not correspond to an adaptive adjustment of body mass to permit a reduction in the power required for flight in the nestling period. It is likely that incubating females constantly maintain their body mass to invest in parental efforts from the incubating to nestling periods.     

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.     

Fitness-related consequences of egg mass in nestling house wrens

The fitness-related consequences of egg mass, independent of confounding influences associated with parental quality, remain poorly understood for wild birds in general and for passerines in particular. We performed cross-fostering experiments to test the hypothesis that egg mass, independent of parental quality, is the primary determinant of fitness-related traits in nestling house wrens (Troglodytes aedon), an insectivorous passerine. Nestling mass was significantly correlated with the mass of the eggs from which nestlings hatched early but not late in the nestling period in early-season broods. In contrast, in late-season broods, nestling mass was correlated with egg mass until nestlings achieved asymptotic mass. Neither nestling growth nor survival to nest leaving was related to egg mass in either early- or late-season broods; however, nestlings in late-season broods grew more slowly than did nestlings in early-season broods. We propose that nestling mass and egg mass remained correlated throughout the nestling period in late-season broods because decreased arthropod food resources late in the breeding season constrain parents'' ability to provision nestlings. We conclude that female house wrens in this population trade-off clutch size for greater egg mass to maximise reproductive success in late-season broods.     

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.     

Effects of temperature and nest heat exposure on nestling growth,dehydration and survival in a Mediterranean hole‐nesting passerine

Variable environments impose constraints on adaptation by modifying selection gradients unpredictably. Optimal bird development requires an adequate thermal range, outside which temperatures can alter nestling physiology, condition and survival. We studied the effect of temperature and nest heat exposure on the reproductive success of a population of double‐brooded Spotless Starlings Sturnus unicolor breeding in a nestbox colony in central Spain with a marked intra‐seasonal variation in temperature. We assessed whether the effect of temperature differed between first and second broods, thus constraining optimal nest‐site choice. Ambient temperature changed greatly during the chick‐rearing period and had a strong influence on nestling mass and all body size measures we recorded, although patterns of clutch size or nestling mortality were not influenced. This effect differed between first and second broods: nestlings were found to have longer wings and bills with increasing temperature in first broods, whereas the effect was the opposite in second broods. Ambient temperature was not related to nestling body mass or tarsus‐length in first broods, but in second broods, nestlings were lighter and had smaller tarsi with higher ambient temperatures. The exposure of nestboxes to heat influenced nestling morphology: heat exposure index was negatively related to nestling body mass and wing‐length in second broods, but not in first broods. Furthermore, there was a positive relationship between nest heat exposure and nestling dehydration. Our results suggest that optimal nest choice is constrained by varying environmental conditions in birds breeding over prolonged periods, and that there should be selection for parents to switch from sun‐exposed to sun‐protected nest‐sites as the season progresses. However, nest‐site availability and competition for sites are likely to impose constraints on this choice.     

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.     

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

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

Ectoparasites and reproductive trade-offs in the barn swallow (Hirundo rustica)

Parents are predicted to trade offspring number and quality against the costs of reproduction. In altricial birds, parasites can mediate these costs because intensity of parasitism may increase with parental effort. In addition, parasites may mediate a trade-off between offspring number and quality because nestlings in large broods may have reduced anti-parasite immune defence. In this study, we experimentally analysed the effect of brood size on infestation by an ectoparasitic mite in nests of barn swallows (Hirundo rustica). Nests with an enlarged brood had larger prevalence and intensity of infestation than those with a reduced brood. Importantly, each nestling in enlarged broods was exposed to a larger number of mites, even when measured on a per nestling basis, than in reduced broods. Nestlings in enlarged broods had smaller body mass and T-cell-mediated immune response compared to reduced broods. T-cell-mediated immune response and feather growth were negatively correlated with per nestling intensity of infestation in enlarged but not in reduced broods. The results suggest that nestlings in enlarged broods have depressed immunity leading to larger per nestling mite infestation. Hence, exposure to parasites of offspring and parents increases with brood size, and parasitism can thus mediate trade-offs between reproduction and number and quality of the progeny in the barn swallow.     

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.     

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     

Body condition variation in kestrel (<Emphasis Type="Italic">Falco tinnunculus</Emphasis>) nestlings in relation to breeding conditions

The body condition index (i.e., body mass corrected for age or size differences) is commonly used to investigate offspring condition in nestling birds. The body condition index reflects different parameters related to the general nutritional state of nestlings and may predict survival prospects. Since conditions experienced during the growth period can affect the fitness of nestlings in adulthood, we investigated proximate and ultimate factors underlying body condition index variation in kestrel (Falco tinnunculus) nestlings in a 9-year field study and we carried out two cross-fostering experiments to disentangle the origin (genetics plus maternal effects) and rearing (environment effect) components of body condition index variation. In total, we sampled 2,065 nestlings from 464 broods and used 121 nestlings from 24 broods in the cross-fostering experiments. We found that nestlings from larger broods had higher body condition index than nestlings from smaller ones, but this pattern did not emerge in two of the 9 years of study; nestlings born later in the breeding season had lower body condition index in some years but not in others; the decrease of body condition index over the breeding season emerged in all but three-chick broods; males and females did not differ neither in body condition index nor in the covariation between body mass and wing length, while this result was limited to one of the nine field study years; the annual mean value of body condition index did not covary with the total rainfall; both the origin and rearing components explained body condition index variation, but their relative contributions varied from a year to another. Overall, these results suggest that the brood size is not a good predictor of body condition index; the rule “nesting early in the season is better” is less general than previously thought; the body condition index may contain origin variance, whose expression may be modulated by environmental conditions.     

Nestlings’ carotenoid feather ornament affects parental allocation strategy and reduces maternal survival

In some birds, feather ornaments are expressed in nestlings well before sexual maturation, possibly in response to parental favouritism towards high‐quality offspring. In species with synchronous hatching, in which nestling ornaments may vary more among than within broods, parents may use this information to adjust their parental allocation to the current brood accordingly. We tested this hypothesis in the rock sparrow, in which a sexually selected yellow feather ornament is also expressed in nestlings. We experimentally enlarged nestlings’ breast patch in a group of broods and sham‐manipulated another group of control broods. Nestlings with enlarged ornament were fed more frequently and defended more actively from a dummy predator than their control counterparts. Mothers from the enlarged group were more likely to lay a second clutch and showed a reduced survival to the next breeding season. These results provide one of the first evidences of differential parental allocation among different broods based directly on nestlings’ ornamentation, and the first, to our knowledge, to show a reduction in maternal survival.     

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.     

Body-Mass, Composition, and Survival of Nestling and Fledgling Starlings (

Earlier studies of the starling (Sturnus vulgaris) population at Belmont, Lower Hutt, New Zealand, showed that nest productivity was low compared with other populations in New Zealand and elsewhere. Therefore, we investigated possible trade-offs between offspring number and quality (as measured by body mass and composition). We also compared these measures of offspring condition with pre- and post-fledging survival. Nestling mass did not significantly differ with clutch size or brood size at any age. In starlings about to leave the nest, lean (i.e., fat-free) dry mass and water mass increased with body mass, but lipid mass increased approximately twice as much. When the effects of the other variables were controlled in a partial correlation analysis, lean dry mass, water mass, lipid mass, and mass of stomach contents were positively correlated with mass at nest-leaving; brood size was not correlated with mass at nest-leaving. Nest success was independent of clutch size and brood size, but lighter broods were more likely to fail totally than were heavier broods early in the nestling period. Nestling survival early, but not late, in the nestling period was positively correlated with nestling mass. The likelihood that a nestling raised in 1973-1979 would be recruited as a breeder was independent of its mass at brood- day 12. Thus, unlike some other passerines, larger, heavier starling nestlings did not seem to survive better than average ones. Low productivity was not accompanied by a decrease in body condition of those nestlings that survived the nestling period. Therefore, starlings at Belmont reduced offspring number rather than offspring quality when they encountered unfavourable conditions.     

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.