Larger clutch size increases fledging success and offspring quality in a precocial species

1. We tested the hypothesis that the ability of parents to raise viable offspring limits clutch size in the greater snow goose ( Anser caerulescens atlanticus L.), a precocial bird.
2. We manipulated clutch size by exchanging complete clutches between pairs of nests to increase or decrease the clutch size by zero (control), one, two or three eggs in 314 nests over 2 years.
3. Pre-fledging survival of goslings increased in enlarged broods and decreased in reduced broods compared to control. Consequently, enlarged broods fledged more offspring and the reverse was true for reduced broods.
4. Size and mass of goslings near fledging was also higher in enlarged broods than in control, which suggests that offspring quality was also enhanced by the manipulation. This is contrary to the common trade-off between offspring numbers and quality.
5. Large families were dominant over smaller ones in feeding sites, which could explain the increased survival and growth of enlarged broods.
6. Our results suggest that the ability to raise young does not limit clutch size in this species and that parents could be more successful (i.e. increase both the number and quality of their offspring) by laying more eggs. However, the time required to lay additional eggs reduces the viability of all offspring and may explain why females do not lay more eggs.     

Parental age influences developmental stability of the progeny in Drosophila

The stochastic nature of biochemical processes is a source of variability that influences developmental stability. Developmental instability (DI) is often estimated through fluctuating asymmetry (FA), a parameter that deals with within-individual variation in bilateral structures. A relevant goal is to shed light on how environment, physiology and genotype relate to DI, thus providing a more comprehensive view of organismal development. Using Drosophila melanogaster isogenic lines, we investigated the effect of parental age, parental diet and offspring heterozygosity on DI. In this work, we have uncovered a clear relationship between parental age and offspring asymmetry. We show that asymmetry of the progeny increases concomitantly with parental age. Moreover, we demonstrate that enriching the diet of parents mitigates the effect of age on offspring symmetry. We show as well that increasing the heterozygosity of the progeny eliminates the effect of parental age on offspring symmetry. Taken together, our results suggest that diet, genotype and age of the parents interact to determine offspring DI in wild populations. These findings provide us with an avenue to understand the mechanisms underlying DI.     

Differences in the effects of parental age on offspring life history between tropical and temperate populations of milkweed bugs (Oncopeltus spp.)

Summary We compare the effects of parental age on several offspring life history traits in two milkweed bug populations: a typically univoltine population ofOncopeltus fasciatus from the Sacramento Valley of California and a typically multivoltine population ofO. cingulifer from Monteverde, Costa Rica. Reared under identical conditions (27°C, 12 h light: 12 h dark photoperiod), these bugs exhibit significant differences in the effects of parental age on offspring life history. As they age,O. fasciatus females from Sacramento lay clutches of eggs of decreasing average weight and a decreasing proportion of their eggs produce offspring that survive to adulthood. Those offspring which do survive have a significantly faster developmental rate and females have a larger body size at adult eclosion. AsO. cingulifer from Monteverde age, they also produce lighter eggs, but there is no significant change in the offspring developmental rate, survival or female adult body size. We suggest that these results are largely explicable as the consequence of different parental investment strategies associated with the predictable relationship between parental age and time of season inO. fasciatus but not inO. cingulifer. AsO. fasciatus from Sacramento age, they may be increasing their investment per developing offspring so as to increase the probability that nymphs hatching late in the season will reach a prereproductive adult diapause before the first killing frost.     

Parental conflict in birds: comparative analyses of offspring development, ecology and mating opportunities

Parents often conflict over how much care to provide to their offspring. This conflict is expected to produce a negative relationship between male and female parental care, the strength of which may be mediated by both ecological and life-history variables. Previous studies have observed such trade-offs, but it is not known how generally they occur. Traditional views of sexual conflict place great importance on ecological factors in determining levels of parental care, whereas alternative views propose that the key determinant is mating opportunity. We carried out a broad-scale comparative study of parental conflict using 193 species from 41 families of birds. Using phylogenetic comparative analysis, we establish the generality of intersexual parental care conflict. We also show that parental conflict, as indicated by the disparity in care between the male and the female, depends on offspring development and mating opportunities, since in precocial species both males and females responded to increased mating opportunities. Altricial birds, however, failed to show these relationships. We also found little influence of breeding climate on parental conflict. Taken together, our results suggest that sexual conflict is a key element in the evolution of parental care systems. They also support the view that the major correlates of the intersexual conflict are mating opportunities for both sexes, rather than the breeding environment.     

The effect of growth rate,size, and season on oocyte development and maturity of Atlantic cod (Gadus morhua L.)

The effect of growth rate, body weight, age, and season on ovarian development and maturation was investigated for Atlantic cod (Gadus morhua L.) reared in the laboratory over 10 months, for each of two consecutive years, 1978–1980. Cod were also collected from the Gulf of St. Lawrence, the Scotian Shelf, Georges Bank, the Flemish Cap, and the N.E. Newfoundland Shelf.The state of maturity was recognized by oocyte size. Stage I oocytes did not vary in size with growth rate, season, age, or maturity, while the size of stage II oocytes was positively correlated with maturity and negatively correlated with maximum stage of development achieved. Ovarian wall thickness was positively correlated with age and maturity.The frequency distribution of stage I and II oocytes distinguished the state of maturation, with cod that would mature by the next spawning season having a minimum of 20% ($\text{x}\text{?}\text{= 42\%}$) of their oocytes at stage II or greater level of development.Maturing 3-yr-old cod had greater life specific growth rates than immature 3-yr-olds, but growth rates during the third year itself were not significantly different. A hypothesis of a three-part density-dependent mechanism controlling fecundity is postulated. Future reductions in partial recruitment and total fecundity are predicted for the Gulf of St. Lawrence cod stock based on calculated growth rates for Gulf cod in 1979.     

Seasonal variation in parental care, offspring development, and reproductive success in the burying beetle, Nicrophorus vespillo

1. Beetles of the genus Nicrophorus reproduce on small vertebrate carcasses that they bury in the soil to provide the larvae with food. Usually, both parents cooperate in brood care by feeding and guarding their progeny. 2. In pairs of the common European species N. vespillo, the duration of care depended on the time of year when the beetles reproduced. Both in 1990 and in 1991, male and female parents stayed longer with their broods when reproduction started in spring than when reproduction started in early or late summer. This was probably due to the longer development time of the larvae caused by lower temperatures in spring, because laboratory experiments suggested a strong influence of temperature on both the duration of brood care and offspring development. 3. The number of adult offspring produced by a beetle pair did not vary among different times of the year. 4. The median time required for offspring development, measured as time from burial of the carcass to emergence of young adults, was between 62 and 84 days. When the beetles reproduced in late summer, only about three-quarters of the offspring left the soil and hibernated as adults. The remaining offspring stayed underground and adults appeared on the soil surface the following spring. They still showed the flexible cuticle typical of newly-hatched beetles, suggesting that they may have overwintered in a pre-adult stage.     

Evolution of reproductive life histories in island birds worldwide

Island environments typically share characteristics such as impoverished biotas and less-seasonal climates, which should be conducive to specific adaptations by organisms. However, with the exception of morphological studies, broad-scale tests of patterns of adaptation on islands are rare. Here, I examine reproductive patterns in island birds worldwide. Reproductive life histories are influenced by latitude, which could affect the response to insularity; therefore, I additionally test this hypothesis. Island colonizers showed mostly bi-parental care, but there was a significant increase in cooperative breeding on islands. Additionally, I found support for previous suggestions of reduced fecundity, longer developmental periods and increased investment in young on islands. However, clutch size increased with latitude at a rate nearly five times faster on the mainland than on the islands revealing a substantially stronger effect of insularity at higher latitudes. Latitude and insularity may also interact to determine egg volume and incubation periods, but these effects were less clear. Analyses of reproductive success did not support an effect of reduced nest predation as a driver of reproductive change, but this requires further study. The effect of latitude detected here suggests that the evolutionary changes associated with insularity relate to environmental stability and improved adult survival.     

The short-term and long-term effects of parental age in the bean weevil (Acanthoscelides obtectus)

We examined the influence of parental age on life history traits of their offspring in the lines of bean weevil that have evolved different rates of senescence. Measurements included preadult traits (egg size, embryonic developmental time, total preadult developmental time, preadult viability) and adult traits (body weight, total realized fecundity of females, first day of egg laying, early fecundity, late fecundity and longevity). The negative parental age effects were observed for all traits except for the early and total realized fecundity. We did not detect statistically significant line×parental age interactions for either preadult- or adult-survival, so offspring survival did not change with parental age after selection for early vs. late reproduction. It seems that selection acting on the quality of offspring produced by parents of different ages has not been responsible for the evolution of senescence in bean weevil. This revised version was published online in August 2006 with corrections to the Cover Date.     

Sexual conflict over parental care promotes the evolution of sex differences in care and the ability to care

Strong asymmetries in parental care, with one sex providing more care than the other, are widespread across the animal kingdom. At present, two factors are thought to ultimately cause sex differences in care: certainty of parentage and sexual selection. By contrast, we here show that the coevolution of care and the ability to care can result in strong asymmetries in both the ability to care and the level of care, even in the absence of these factors. While the coevolution of care and the ability to care does not predict which sex evolves to care more than the other, once other factors give rise to even the slightest differences in the cost and benefits of care between the sexes (e.g. differences in certainty in parentage), a clear directionality emerges; the sex with the lower cost or higher benefit of care evolves both to be more able to care and to provide much higher levels of care than the other sex. Our findings suggest that the coevolution of levels of care and the ability to care may be a key factor underlying the evolution of sex differences in care.     

Estimating expenditure on male and female offspring in a sexually size-dimorphic bird: a comparison of different methods

The parents of sexually size-dimorphic offspring are often assumed to invest more resources producing individuals of the larger sex. A range of different methods have been employed to estimate relative expenditure on the sexes, including quantifying sex-specific offspring growth, food intake, energy expenditure and energy intake, in addition to measures of parental food provisioning and energy expenditure. These methods all have the potential to provide useful estimates of relative investment, but each has particular problems of interpretation, and few studies have compared the estimates derived concurrently from more than two of these measures. In this study we compared these surrogate measures of parental investment in the brown songlark Cinclorhamphus cruralis, which exhibits one of the most extreme cases of sexual size dimorphism among birds. At 10 days of age we found that male chicks, on average, were 49% heavier, received 42% more prey items, expended 44% more energy and ingested 50% more metabolizable energy than their sisters. Furthermore, we created, experimentally, both all-male and all-female broods of 10-day-old chicks and found that mothers delivered 43% more prey items and expended 27% more energy when provisioning all-male broods, providing the first direct evidence for a change in parental energy expenditure in relation to brood sex ratio. These data reveal remarkable agreement between these estimates of investment and suggest that all may provide quantitatively useful information on sex allocation. However, the lower variance associated with estimates of relative mass and energy intake suggest that these methods may be of greater utility, although this may primarily reflect the shorter period over which our provisioning data were collected.     

Macrogeographic clines in fecundity, reproductive allocation, and offspring size of the forest tent caterpillar Malacosoma disstria

1. The fecundity of the forest tent caterpillar varies considerably across its geographic range. Field data indicate that populations in the southern United States (Gulf States) produce nearly twice as many eggs as females from Canada or the Lake States, with little or no difference in the size of adult females. 2. In controlled rearing experiments, female forest tent caterpillar from the southern United States (Louisiana) had much larger clutch sizes than same sized females from northern populations in Michigan or Manitoba, Canada. Increased fecundity in Louisiana females was achieved through a significant reduction in egg size and a concomitant increase in the allocation of resources to egg production. 3. Comparison of 10 forest tent caterpillar populations spanning a 27° latitudinal gradient, validated the results of detailed comparisons among the three populations above by confirming the strong negative correlation between latitude and clutch size. 4. Neonate forest tent caterpillars from Manitoba were significantly larger than larvae from either Michigan or Louisiana. Michigan larvae were intermediate in size. It is postulated that large neonates are advantageous in thermally limiting environments. More than three times as many degree‐days are available to Louisiana neonates during the first 2 weeks after hatching. A consistently favourable climate during the vulnerable post‐hatching period may have allowed the evolution of larger clutches at the expense of neonate size in southern populations.     

Multiple resources and the optimal balance between size and number of offspring

Summary We extend the classical Smith-Fretwell model for the optimal size of an offspring to the case of allocation of two or more fitness enhancing resources. Unlike the results of the single-resource model, the new model predicts that the optimal allocations will depend on the resource pool sizes. We apply this new model to the problem of carbon and nitrogen allocation to seeds and conclude (1) that the optimal seed size (carbon allocation) should be positively correlated with the ratio of the size of the carbon and nitrogen pools available for investment to offspring (C/N ratio) and (2) that there should be a negative correlation between seed size and absolute seed nitrogen content. These results may account for some of the within- and between-plant variation in resource allocation to seeds.     

Age structure, growth and reproduction of Leuciscus pyrenaicus in an intermittent stream in the Guadalquivir river basin, southern Spain

The age, growth and reproduction of Leuciscus pyrenaicus (Günther, 1868), an endemic cyprinid from the Iberian Peninsula, was studied from November 1987 to September 1989 in a small seasonal tributary of the Guadalquivir river basin. Maximum fork lengths observed were a 160 mm male with six scale annuli and a 171 mm female aged 7 +. Maximum ages observed were 7 + in males and 8 + in females. There were no significant differences in the annual growth increments between sexes. Seasonal growth period started in March and continued for 5 to 6 months. Mean lengths of 1 + specimens onwards diminished during summer and/or autumn. Males and females matured in their third and fourth year of life respectively. The overall sex ratio (272 males: 310 females) differed significantly from equality. Spawning began in May and ended in July. L. pyrenaicus is a multiple spawner that releases a minimum of two batches of eggs per female each year. Eggs in each batch were similar in both size (egg diameter) and number released. The relationship between fecundity (Fee) and fork length (mm) was represented by the formula: Fec=1.96 10⁻³ L^2.50.