High-quality Females (high-quality + female)

Distribution by Scientific Domains


Selected Abstracts


Mating Effort and Cryptic Sperm Choice in Scorpionflies: Male Investment Strategy vs.

ETHOLOGY, Issue 12 2008
Female Control
In this study, we examined which sex controls sperm transfer during copulation in scorpionflies. Therefore male scorpionflies were doubly mated to females of high and low fecundity to explore whether they allocate sperm according to female quality. While mating order had no effect males transferred sperm at higher rates when mating with low-quality instead of high-quality females. As there is no obvious benefit from providing low-fecundity females with more sperm, we suggest a condition-dependent female ability to counteract sperm transfer. Therefore, we disabled females at the beginning of copulations using the insecticide Propoxur which leads to total paralysis caused by tremors. While the provoked muscle contractions led to significantly smaller numbers of sperm transferred, Propoxur treatment had no effect on males. We suggest female counteracting of sperm transfer to be adaptive by decreasing the relative amount of sperm transferred by low-quality males and increasing the proportion of offspring sired by high-quality males. [source]


Egg Colour Covaries with Female Expression of a Male Ornament in the Spotless Starling (Sturnus unicolor)

ETHOLOGY, Issue 10 2007
Isabel López-Rull
The sexually selected egg colour hypothesis (SSECH) proposes that egg colouration is as a post-mating sexually selected signal of female phenotypic quality, maintained by a higher allocation of paternal care. Similarly, some female traits can reflect genetic quality or condition and males could use this information in mate choice or in modulating parental investment. In our study, we examined the correlation of individual variation in egg colouration with female expression of a male ornament and how male feeding covaried with these two female traits in the spotless starling, in which egg colour varies widely between clutches and where both sexes possess showy throat feathers that are age dependent and that may signal individual quality. According to the SSECH, high-quality females (females with longer throat feathers) are expected to lay more colourful eggs than low-quality females and males should modify their feeding behaviour accordingly. By means of a principal component analysis, we found that most of the variation in egg colouration was due to brightness differences, and in a lower proportion to chromatic variation. Chromatic variation reflected a ultraviolet (UV) vs. greenness trade-off and was positively associated with throat feather length: females with larger throat feathers laid eggs with higher UV and lower green reflectance. However, egg brightness was not related to female feather length, as the SSECH would predict. Male feedings were positively related to female throat feather length and negatively related to chromatic variation, meaning that males contributed more to nests of females with long throat feathers who laid eggs with higher UV and lower green reflectance. In conclusion, our data provide mixed support for the SSECH: although egg chromatic variation was related to female expression of a male ornament and male parental care, we found no evidence that egg brightness was involved in these processes. [source]


Within- and between-year variation in the juvenile survival of Common Guillemots Uria aalge

IBIS, Issue 3 2007
MICHAEL P. HARRIS
We studied juvenile survival of 20 cohorts of Common Guillemot Uria aalge chicks colour-ringed on the Isle of May, Scotland, using both live observations at the colony and dead recoveries, allowing estimation of fidelity to the colony as well as survival. In this seabird, chicks leave the colony when only partly grown and are cared for by the male parent for several weeks afterwards. First-year survival varied strongly between cohorts, with a mean of 56% (range 30,91%). We did not identify any covariates which could explain this variation, whether relating to climate, population size or prey density. Survival was low during two regime shift episodes in the North Sea (1987,90 and 2000 onwards). Early hatched chicks were substantially more likely to survive than those hatching later in most years, whereas body condition at ringing had no detectable effect. Ringing recoveries indicated that mortality was highest in mid-winter, i.e. well after the cessation of paternal care. These results do not support the hypothesis that variation in prey quantity or energy content before fledging is a primary driver of variation in juvenile survival. Rather, it seems that chicks of high-quality parents are more likely to survive, as high-quality females tend to lay earlier in the season, and high-quality males presumably are better able to prepare their chicks to survive their first winter at sea. Very few (4%) Guillemots emigrated permanently before age 3 years, but from age 5 onwards 25,30% of birds annually left the colony or otherwise became unobservable. [source]


Individual variation in reproductive costs of reproduction: high-quality females always do better

JOURNAL OF ANIMAL ECOLOGY, Issue 1 2009
Sandra Hamel
Summary 1Although life-history theory predicts substantial costs of reproduction, individuals often show positive correlations among life-history traits, rather than trade-offs. The apparent absence of reproductive costs may result from heterogeneity in individual quality. 2Using detailed longitudinal data from three contrasted ungulate populations (mountain goats, Oreamnos americanus; bighorn sheep, Ovis canadensis; and roe deer, Capreolus capreolus), we assessed how individual quality affects the probability of detecting a cost of current reproduction on future reproduction for females. We used a composite measure of individual quality based on variations in longevity (all species), success in the last breeding opportunity before death (goats and sheep), adult mass (all species), and social rank (goats only). 3In all species, high-quality females consistently had a higher probability of reproduction, irrespective of previous reproductive status. In mountain goats, we detected a cost of reproduction only after accounting for differences in individual quality. Only low-quality female goats were less likely to reproduce following years of breeding than of nonbreeding. Offspring survival was lower in bighorn ewes following years of successful breeding than after years when no lamb was produced, but only for low-quality females, suggesting that a cost of reproduction only occurred for low-quality females. 4Because costs of reproduction differ among females, studies of life-history evolution must account for heterogeneity in individual quality. [source]