Post-fledging brood and care division in the roseate tern (Sterna dougallii)

Extended post-fledging parental care is an important aspect of parental care in birds, although little studied due to logistic difficulties. Commonly, the brood is split physically (brood division) and/or preferential care is given to a subset of the brood by one parent or the other (care division). Among gulls and tern (Laridae), males and females generally share parental activities during the pre-fledging period, but the allocation of parental care after fledging is little documented. This study examined the behaviour of male and female roseate terns (Sterna dougallii) during the late chick-rearing and early post-fledging periods, and in particular the amount of feeds and the time spent in attendance given to individual chicks/fledglings. Pre-fledging parental care was biparental in all cases. Post-fledging parental care was dependent on the number of fledglings in the brood. Males and females continued biparental care in clutches with one surviving fledgling, while in two-fledgling clutches, males fed the A-fledgling while females fed the B-fledgling. Overall, there was no difference in attendance, only in feeds. This division of care may be influenced by the male only being certain of the paternity of the A-chick but not by chick sex.     

Paternal care and male mate-attraction effort in the European starling is adjusted to clutch size

In facultative polygynous birds with biparental care, a trade-off may occur between male parental care and attraction of additional mates. If there is a cost associated with reduced male parental care, the relative benefit of mate attraction may be predicted to decrease as the size of a male's clutch or brood increases. We tested this prediction in monogamous pairs of facultatively polygynous European starlings (Sturnus vulgaris). The larger the clutch, the more time the male spent incubating and the less time he spent attracting an additional female (i.e. singing near and carrying green nesting material into adjacent empty nest-boxes). Reduced paternal incubation resulted in lower overall incubation (the female did not compensate) and lower hatching success. Immediately after experimental reduction of clutches, males spent significantly less time incubating and more time singing and carrying greenery, and vice versa for experimentally enlarged clutches. Males with experimentally reduced clutches attracted a second female more often than males with experimentally enlarged clutches. This is the first study, to our knowledge, to provide experimental evidence for an adjustment of paternal care and male mate-attraction effort to clutch size. However, a trade-off between paternal nestling provisioning and mate attraction was not revealed, probably due to the absence of unpaired females by that time in the breeding season. Experiments showed that the relative contribution of the male and female to nestling provisioning was unrelated to brood size.     

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

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

Multiple breeding in the Great Tit. A trade-off between successive reproductive attempts?

1. Multiple breeding (raising more than one batch of young per breeding season) is a common life-history tactic that has received very little attention. A simple static optimization model was developed, applicable to iteroparous animals with parental care, that predicts: (1) when an animal should be a multiple breeder, (2) the optimal interval between successive clutches, and (3) when a clutch should be deserted.
2. More specifically, it was predicted that (I) animals should invest less in a clutch when it is followed by another clutch in the same season, and (II) as a consequence the contribution of the first clutch to the parents' fitness will be reduced.
3. These predictions were tested experimentally in a population of Great Tits ( ParusM. major L.). The experiment consisted of the removal of second clutches. When second clutches were removed, parents tended their first brood fledglings for a longer period than undisturbed control pairs, in agreement with the first prediction. Removal of second clutches did not affect fledgling survival, but recruits enjoyed higher reproductive success in their first year of breeding when the second clutch of their parents had been removed, in agreement with the second prediction.
4. It is concluded that a trade-off exists between successive reproductive attempts, which will affect the optimal rate of reproductive attempts.     

Ecological factors regulating brood attendance patterns of the Western Sandpiper Calidris mauri

Parental brood attendance patterns vary greatly among shorebird species. For monogamous calidridine species, biparental care with female-first brood departure is most common. It is believed that adult sandpipers balance potential individual survival costs associated with extended parental care against the benefit gained by their brood of prolonged parental care. These costs and benefits are difficult to quantify and factors affecting the termination of parental brood attendance are unclear. We compared clutch size, nesting phenology, and parental attendance patterns of Western Sandpipers Calidris mauri at Nome and Kanaryarmiut, Alaska, sites separated by three degrees of latitude. The sites differed in breeding density and duration of breeding season, but the distribution of clutch sizes did not differ between sites or between nesting attempts. Parental attendance patterns were similar between sites, suggesting that parental attendance is a highly conserved life-history trait in Western Sandpipers. Male Western Sandpipers attended broods longer than females, and the duration of parental attendance decreased at a similar rate for both sexes as the season progressed. Male and female Western Sandpipers undertake differential migrations to their non-breeding grounds, with males typically settling at more northerly locations and females at more southerly sites, a migration pattern shared by certain other monogamous calidridine species. These same species exhibit similar parental brood attendance patterns, suggesting the strong role of overall migration distance in shaping the expression of parental attendance behaviours. A contrast of more geographically disjunct sites coupled with a better understanding of the migratory connectivity between Western Sandpiper breeding and non-breeding populations would elucidate the role of cross-seasonal effects on parental brood attendance decisions.     

The significance of clutch overlap in Great Tits Parus major

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

Clutch size evolution under sexual conflict enhances the stability of mating systems.

Models of optimal clutch size often implicitly assume a situation with uniparental care. However, the evolutionary conflict between males and females over the division of parental care will have a major influence on the evolution of clutch size. Since clutch size is a female trait, a male has little possibility of directly influencing it. However, the optimal clutch size from a female's perspective will depend on the amount of paternal care her mate is expected to provide. The sexual conflict over parental care will in its turn be affected by clutch size, since a larger clutch makes male care more valuable. Hence, there will be joint evolution of mating system and clutch size. In this paper, we demonstrate that this joint evolution will tend to stabilize the mating system. In a situation with conventional sex roles, this joint evolution might result in either increased clutch size and biparental care or reduced clutch size and uniparental female care. Under some circumstances the initial conditions might determine which will be the outcome. These results demonstrate that it may be difficult to deduce whether biparental care evolved because of few opportunities for breeding males increasing their fitness by attracting additional mates or because of the importance of male care for offspring fitness by studying prevailing mating systems using, for example, male removals or manipulation of males' opportunities for finding additional mates. In general terms, we demonstrate that models of life-history evolution have to consider the social context in which they evolve.     

Females Paired with New and Heavy Mates Reduce Intra-Clutch Differences in Resource Allocation

Reproductive investment affects both offspring and parental fitness and influences the evolution of life histories. Females may vary their overall primary reproductive effort in relation to the phenotypic characteristics of their mate. However, the effects of male quality on differential resource allocation within clutches have been largely neglected despite the potential implications for mate choice and population dynamics, especially in species exhibiting biparental care and brood reduction. Female southern rockhopper penguins Eudyptes chrysocome paired with heavy mates reduced intra-clutch variation in egg and albumen masses. Females paired with new mates also reduced intra-clutch variation in yolk androgen levels. Since both an increased mass and increased androgen concentrations positively influence chick survival under sibling competition, the chances of fledging the whole clutch are likely to be higher for newly formed pairs with heavy males than for previously formed pairs with light males. Interestingly, total clutch provisioning did not vary with male quality. We show for the first time that females vary intra-clutch variation in resource allocation according to male quality. In species with brood reduction, it may be more adaptive for females to modulate the distribution of resources within the clutch according to breeding conditions, than to change their total clutch provisioning.     

Fitness cost of incubation in great tits (Parus major) is related to clutch size

Life-history theory predicts that parents produce the number of offspring that maximizes their fitness. In birds, natural selection on parental decisions regarding clutch size may act during egg laying, incubation or nestling phase. To study the fitness consequences of clutch size during the incubation phase, we manipulated the clutch sizes during this phase only in three breeding seasons and measured the fitness consequences on the short and the long term. Clutch enlargement did not affect the offspring fitness of the manipulated first clutches, but fledging probability of the subsequent clutch in the same season was reduced. Parents incubating enlarged first clutches provided adequate care for the offspring of their first clutches during the nestling phase, but paid the price when caring for the offspring of their second clutch. Parents that incubated enlarged first clutches had lower local survival in the 2 years when the population had a relatively high production of second clutches, but not in the third year when there was a very low production of second clutches. During these 2 years, the costs of incubation were strong enough to change positive selection, as established by brood size manipulations in this study population, into stabilizing selection through the negative effect of incubation on parental fitness.     

On the evolutionary pathway of parental care in mouth-brooding cichlid fishes

Evolutionary theory predicts that differences in parental care patterns among species arose from interspecific differences in the costs and benefits of care for each sex. In Galilee St Peter''s fish, Sarotherodon galilaeus (Cichlidae), male care, female care and biparental care all occur in the same population. We exploit this unusual variability to isolate conditions favouring biparental versus uniparental mouth-brooding by males or females. We first review a game-theoretic model of parental care evolution, predictions of which we test experimentally in this paper. Manipulations of the operational sex ratio show that males and females desert their offspring more frequently when the costs of care are high (in terms of lost mating opportunities). Breeding trials with males of different sizes show that small fathers desert more frequently than large fathers. We attribute this to the associated difference in the fitness benefit of biparental care relative to female-only care. Our experimental results confirm that in St Peter''s fish the probability of caring is determined facultatively according to current conditions at each spawn. The experiments and model together suggest that interspecific variation in remating opportunities and clutch size may be responsible for differences in care patterns within the sub-family Tilapiini. Our results support the hypothesis that biparental mouth-brooding was the ancestral state of both male and female uniparental mouth-brooding in cichlid fishes.     

Costs of large communal clutches for male and female Greater Rheas Rhea americana

The breeding system of the Greater Rhea Rhea americana is almost unique among birds as it combines harem polygyny and sequential polyandry, with communal egg-laying and uniparental male care. In this species, large communal clutches (more than 30 eggs) are rare and have a lower hatching success than smaller clutches. Here we analyse the proximate causes of hatching failures and the costs of large communal clutches (and therefore the costs of extensive polygyny) for males and females. We evaluated if length of the nesting period, egg viability, egg losses during incubation and male parental activity at the nest were affected by clutch size. We also evaluated if chicks hatched from large clutches have a lower survival during the first 2 months after hatching. Large clutches had longer nesting period and lower hatching success, mainly as a result of bacterial contamination of the eggs and increased hatching asynchrony. In addition, large clutches tended to lose more eggs as a result of accidental breakage or predation. Male activity at the nest and chick survival were not related to clutch size. Low hatching success, nest predation risk and energetic costs associated with large clutches penalize females that join large harems and males that accept additional eggs into the nest.     

Decline in the frequency and benefits of multiple brooding in great tits as a consequence of a changing environment

For multiple-brooded species, the number of reproductive events per year is a major determinant of an individual''s fitness. Where multiple brooding is facultative, its occurrence is likely to change with environmental conditions, and, as a consequence, the current rates of environmental change could have substantial impacts on breeding patterns. Here we examine temporal population-level trends in the proportion of female great tits (Parus major) producing two clutches per year (‘double brooding’) in four long-term study populations in The Netherlands, and show that the proportion of females that double brood has declined in all populations, with the strongest decline taking place in the last 30 years of the study. For one of the populations, for which we have data on caterpillar abundance, we show that the probability that a female produces a second clutch was related to the timing of her first clutch relative to the peak in caterpillar abundance, and that the probability of double brooding declined over the study period. We further show that the number of recruits from the second clutch decreased significantly over the period 1973–2004 in all populations. Our results indicate that adjustment to changing climatic conditions may involve shifts in life-history traits other than simply the timing of breeding.     

A more informative method for analyzing reproductive success

ABSTRACT.   Few investigators have examined how a female's prior history (i.e., number of clutches laid previously and whether those nesting attempts were successful or not) might influence the success of a particular clutch. Our objective was to determine the seasonal change in the mean number of fledglings successfully leaving nests in a population of Prairie Warblers ( Dendroica discolor ). To do so, we calculated the success of each clutch in the laying sequence (i.e., first, second, third, …, n ^th) and sorted them further by whether they were laid before (first-brood clutches) or after (second-brood clutches) the first brood fledged. In our sample population of 70 females we knew the fate of all clutches laid during a breeding season. Although the number of fledglings per successful clutch varied slightly, the probability that a clutch would be successful (i.e., produce at least one fledgling) and the number of fledglings per nest attempt increased during the breeding season. Thus, later clutches were more productive than earlier clutches. The low probability of producing a successful first clutch early in the breeding season would seem to favor selection for females that wait until later in the season to begin breeding. However, the seasonal reproductive success of females may be more dependent on breeding early (increasing the number of clutches laid in a season) than on the higher probability of success with later clutches. Our results indicate that further study of seasonal changes in reproductive success and their causes is needed.     

Breeding patterns of great tits ( Parus major ) in pine forests along the Portuguese west coast

The breeding biology of great tits (Parus major) was studied in two forests of maritime pine (Pinus pinaster) on the west coast of Portugal, 200 km apart: Leiria (north) and Aposti?a (south). These two forests are located in a transition zone between Atlantic climate in the north, and Mediterranean climate in the south. Breeding onset was, on average, in the second and third week of March, which are the earliest records of breeding for this species. The southern population started to breed earlier than the northern one and produced a larger first clutch, 8.3 and 7.4 eggs, respectively. Corresponding to larger clutch sizes, we also found a higher first brood fledgling production in Aposti?a compared to Leiria, 6.1 and 5.4 fledglings, respectively. However, the total number of fledglings produced per pair was higher in Leiria (8.3) than in Aposti?a (7.7), due to higher productivity of second clutches (4.7 and 2.7 fledglings, respectively). Accordingly, the allocation of eggs between successive breeding attempts was more equal in Leiria. Results are discussed in accordance to the different climatic patterns in the two areas. It is suggested that the timing of breeding and different allocation of reproductive investment between successive breeding attempts play an important role in optimizing breeding tactics in this facultative multiple-brooded passerine in different climatic areas.     

Repeated parallel evolution of parental care strategies within Xenotilapia, a genus of cichlid fishes from Lake Tanganyika

The factors promoting the evolution of parental care strategies have been extensively studied in experiment and theory. However, most attempts to examine parental care in an evolutionary context have evaluated broad taxonomic categories. The explosive and recent diversifications of East African cichlid fishes offer exceptional opportunities to study the evolution of various life history traits based on species-level phylogenies. The Xenotilapia lineage within the endemic Lake Tanganyika cichlid tribe Ectodini comprises species that display either biparental or maternal only brood care and hence offers a unique opportunity to study the evolution of distinct parental care strategies in a phylogenetic framework. In order to reconstruct the evolutionary relationships among 16 species of this lineage we scored 2,478 Amplified Fragment Length Polymorphisms (AFLPs) across the genome. We find that the Ectodini genus Enantiopus is embedded within the genus Xenotilapia and that during 2.5 to 3 million years of evolution within the Xenotilapia clade there have been 3-5 transitions from maternal only to biparental care. While most previous models suggest that uniparental care (maternal or paternal) arose from biparental care, we conclude from our species-level analysis that the evolution of parental care strategies is not only remarkably fast, but much more labile than previously expected.     

Interval between clutches, fitness, and climate change

Timing of optimal reproduction can be affected by the presenceof multiple broods, with multi-brooded species breeding earlier(and later) than the optimal timing of breeding as comparedwith single-brooded species that only need to optimize the timingof a single brood. Approximately two-thirds of barn swallowsHirundo rustica produce 2 broods per year, and I tested whetherthe constraints on timing of reproduction were affected by climatechange because climatic amelioration would allow both an earlierstart and a later termination of reproduction. The durationof the interval between first and second clutches and the variancein the duration increased during 1971–2005 when temperatureduring spring, but not summer, increased rapidly. Interclutchinterval was shorter when mean date of breeding was late andalso among late-breeding individuals during individual years.When clutch size and brood size of the first clutch were large,interval until the second brood increased. Pairs with a longinterval produced more fledglings than pairs with a short interval.Pairs with first broods with strong mean T-cell–mediatedimmune responses took shorter time to start their second clutch,whereas mean body mass or tarsus length of first broods werenot significantly related to interclutch interval. Interclutchinterval increased with the size of a secondary sexual character,the length of the outermost tail feathers of adult male barnswallows, but not with tail length of females, or with sizeof several other phenotypic characters in either sex. Thesefindings are consistent with the hypothesis that the durationof the interclutch interval is determined by a combination ofenvironmental conditions, reproductive effort, and sexual selection.     

Do Uniparental Sanderlings Calidris alba Increase Egg Heat Input to Compensate for Low Nest Attentiveness?

Birds breeding in cold environments regularly have to interrupt incubation to forage, causing a trade-off between two mutually exclusive behaviours. Earlier studies showed that uniparental Arctic sandpipers overall spend less time incubating their eggs than biparental species, but interspecific differences in size and ecology were potential confounding factors. This study reports on a within-species comparison of breeding schedules and metal egg temperatures in uni- and biparental sanderlings (Calidris alba) in Northeast Greenland in relation to ambient temperature. We recorded incubation schedules with nest temperature loggers in 34 sanderling clutches (13 uniparentals, 21 biparentals). The temperature of a metal egg placed within the clutch of 17 incubating birds (6 uniparentals, 9 biparentals) was measured as an indicator of the heat put into eggs. Recess frequency, recess duration and total recess time were higher in uniparentals than in biparentals and positively correlated with ambient temperatures in uniparentals only. Uniparental sanderlings maintained significantly higher metal egg temperatures during incubation than biparentals (1.4°C difference on average). Our results suggest that uniparental sanderlings compensate for the lower nest attendance, which may prolong the duration of the incubation period and negatively affect the condition of the hatchlings, by maintaining a higher heat flux into the eggs.     

THE SOCIABLE WEAVER,PART 3: BREEDING BIOLOGY AND MOULT

Maclean, G. L. 1973. The Sociable Weaver, Part 3: Breeding biology and moult. Ostrich 44: 219–240.

Rain or some associated phenomenon is the principal Zeitgeber releasing breeding in the Sociable Weaver. The species does not breed in the absence of rain. The same nest chambers are used for breeding as are used for roosting throughout the year. The Sociable Weaver is monogamous. The clutch size varies from two to six eggs, larger clutches being more common after good rains than in relatively poorer breeding periods. Food supply may therefore be the proximate factor regulating clutch size. Replacement clutches are not necessarily smaller than first clutches. The mean clutch size within a breeding period decreases with an apparent decrease in food supply. The parents share parental duties about equally. Up to four successive broods may be raised in a single breeding period; a breeding period may last up to nine months and may occur at any time of the year according to the somewhat erratic rainfall which averages about 226 mm per year in the study area.

First broods help their parents to feed later broods; fourth brood chicks may therefore be fed by as many as 11 birds (nine young and two parents). This has survival value especially toward the end of a breeding period when food is scarce. Of similar value is the habit of starting incubation with the first or second egg of the clutch; in a relatively poor season older chicks will survive while younger ones will starve, thereby effectively and quickly reducing brood size. Young birds moult into adult plumage at four months, but do not normally leave the home colony. The sexes are indistinguishable at all ages, but there is an approximate ratio of eight males to five females in the study area.

Wing moult is slow: each remex takes about a month for replacement. Body moult occurs within the space of a month, usually after rain while the birds are breeding. Primary remiges are moulted proximo-distally from 1 to 9; secondaries are moulted disto-proximally from 1 to 6. Body moult is antero-posterior with the dorsal surface slightly in advance of the ventral surface.     

The benefits of uniparental versus biparental mouth brooding in Galilee St. Peter's fish

In Galilee St. Peter's fish Sarotherodon galilaeus the care system is naturally labile; biparental, male-only and female-only care all exist in one population. This unusual flexibility facilitates comparisons between the forms of care. The costs of parental care were considered in a previous study. Here, the benefits of parental care were quantified by observing wild fish, both held in pond enclosures and free-swimming in Lake Kinneret, Israel. Parental care was shown to be essential for offspring survival in St. Peter's fish. The reproductive success of parents who shared incubation duties was nearly twice as high as that of parents caring alone. However, per brood (or mouth cavity) reproductive success was 20% higher for uniparental parents. Both sexes were equally capable and efficient in care; when both sexes cared, they each incubated a similar number of eggs and released a similar number of fry. The results are discussed in terms of the relationship between caring Strategies and clutch size.