Sexually dimorphic eggs, nestling growth and sibling competition in American Kestrels Falco sparverius

1. American Kestrel ( Falco sparverius ) nestlings are sexually dimorphic, with daughters larger than sons. The larger daughters have an advantage during sibling competition for food in excess of their higher per capita food requirements, and we predicted that parents would reduce this competitive disparity by differentially enhancing the growth of sons, specifically by laying them in larger eggs.
2. In a captive breeding population, eggs producing sons were significantly larger than eggs producing daughters; laying order effects were controlled.
3. The influence of sibling egg size ratios on post-natal size relationships persisted through the nesting period, providing parents with a tool to manipulate size-related phenomena in their offspring.     

Sexual dimorphism in four species of rockfish genusSebastes (Scorpaenidae)

Synopsis Sexual dimorphisms, and factors influencing the evolution of these differences, have been investigated for four species of rockfish:Sebastes melanops, S. flavidus, S. mystinus, andS. serranoides. These four species, which have similar ecology, tend to aggregate by species with males and females staying together throughout the year. In all four species adult females reach larger sizes than males, which probably relates to their role in reproduction. The number of eggs produced increases with size, so that natural selection has favored larger females. It appears males were subjected to different selective pressures than females. It was more advantageous for males to mature quickly, to become reproductive, than to expend energy on growth. Other sexually dimorphic features include larger eyes in males of all four species and longer pectoral fin rays in males of the three piscivorous species:S. melanops, S. flavidus, andS. serranoides. The larger pectoral fins may permit smaller males to coexist with females by increasing acceleration and, together with the proportionately larger eye, enable the male to compete successfully with the female to capture elusive prey (the latter not necessarily useful for the planktivoreS. mystinus). Since the size of the eye is equivalent in both sexes of the same age, visual perception should be comparable for both sexes.     

The Relationship Among Swimming Performance, Courtship Behavior, and Carotenoid Pigmentation of Guppies in Four Rivers of Trinidad

In the laboratory, courtship behavior and carotenoid pigmentation of male guppies are condition-dependent traits, since their expression is affected by physical vigor and environmental factors such as water velocity and diet. Whether these relationships exist in guppies under field conditions is yet to be determined. We compared the swimming performance, courtship behavior, and carotenoid pigmentation of guppies from headwater and downstream localities in four rivers of Trinidad. Swimming performance and courtship behavior of males differed among rivers and between headwater and downstream sites. Guppies from headwater sites swam significantly faster and had higher display rates than those from downstream sites. Mean swimming performance across sites was positively correlated with mean water velocity, but was correlated with the number of orange color spots (carotenoid pigment) in only one river. These results indicate that the courtship behavior of Trinidadian guppies is condition-dependent because the amount of display behavior is positively correlated to swimming performance, a measure of physical endurance. The proximal cause for this condition-dependence may be predator induced variation in microhabitat use by guppies in headwater and downstream locations.     

Sex differences in recombination and mapping adaptations

Since the raw material of marker based mapping is recombination, understanding how and why recombination rates evolve, and how we can use variation in these rates will ultimately help to improve map resolution. For example, using this variation could help in discriminating between linkage and pleiotropy when QTL for several traits co-locate. It might also be used to improve QTL mapping algorithms. The goals of this chapter are: (1) to highlight differences in recombination rates between the sexes, (2) describe why we might expect these differences, and (3) explore how sex difference in recombination can be used to improve resolution in QTL mapping.     

Experimental reduction in dietary omega-3 polyunsaturated fatty acids depresses sperm competitiveness

The health benefits of diets containing rich sources of long-chain omega-3 polyunsaturated fatty acids (n-3 LC-PUFA) are well documented and include reductions in the risk of several diseases typical of Western societies. The dietary intake of n-3 LC-PUFA has also been linked to fertility, and there is abundant evidence that a range of ejaculate traits linked to fertility in humans, livestock and other animals depend on an adequate intake of n-3 LC-PUFA from dietary sources. However, relatively few studies have explored how n-3 LC-PUFA influence reproductive fitness, particularly in the context of sexual selection. Here, we show that experimental reduction in the level of n-3 LC-PUFA in the diet of guppies (Poecilia reticulata) depresses a male''s share of paternity when sperm compete for fertilization, confirming that the currently observed trend for reduced n-3 LC-PUFA in western diets has important implications for individual reproductive fitness.     

Mate discrimination by females in the burying beetle Nicrophorus orbicollis: the influence of male size on attractiveness to females

1. Female burying beetles behave differently towards males of different sizes, avoiding mating with large males that are not defending resources but mating with small males regardless of the presence of resources. Females of the burying beetle Nicrophorus orbicollis were therefore examined to determine whether they discriminate among males using only pheromonal signals. The influence of female size on its own mate choice was also examined. 2. Females do use male pheromonal signals to discriminate among males and these signals do appear to convey information about male body size to females. Overall, females were more likely to be attracted to larger males than to smaller males. 3. Female choice of a male was influenced by both the female's own body size and the size of the female relative to the size of the two males available to it. 4. While there is an overall mating advantage for larger males, resulting from female preferences based on odour cues, smaller males are also attractive to some females under some circumstances. 5. It is argued that there are different costs and benefits of mating with different sized males, leading to the evolution of context‐dependent mate choice for females and the need to be able to discriminate males of different sizes from a distance.     

Condition-dependent expression of red colour differs between stickleback species

Sexual isolation may arise when male mating traits and female preferences differ between species. Such divergence in mating traits is likely to occur when the strength or targets of sexual selection differ. Therefore, by comparing the traits under sexual selection in closely related species and the nature of preference for those traits, we can gain insight into when sexual selection contributes to sexual isolation and how it does so. Collecting these data is no easy undertaking. To simplify this comparison, I use the presence and extent of condition dependence in traits to determine whether directional sexual selection is acting on them. Condition dependence thus serves as a signature of sexual selection. I investigate differences in sexual selection on red nuptial colour in limnetic-benthic species pairs of three-spined sticklebacks. I evaluate condition dependence by comparing the strength of the relationship between colour and condition, and the magnitude of variance in red nuptial colour to other colour traits and to nonsexual traits. I find that limnetic males have strong condition-dependent expression of red nuptial colour whereas benthic males have at most weak condition-dependent expression. Ancestral anadromous males show no condition dependence. This suggests that colour is under strong directional sexual selection only in limnetics and that this is the derived state. Moreover, I find that the strength of female preference for red is related to the extent of condition dependence. The extent of condition dependence is also associated with the importance of colour differences to mate recognition. These results show that differences between these species in the action of sexual selection underlie their sexual isolation.     

Condition dependence of sexually dimorphic colouration and longevity in the ambush bug Phymata americana

Sexually selected traits that are costly are predicted to be more condition dependent than nonsexually selected traits. Assuming resource limitation, increased allocation to a sexually selected trait may also come at a cost to other fitness components. To test these predictions, we varied adult food ration to manipulate condition in the colour dimorphic bug, Phymata americana. We compared the degree of condition dependence in a sexually selected trait expressed in males to a nonsexually selected trait expressed in males and females. We also evaluated the effects of condition on longevity of both sexes. We found that the expression of these colour pattern traits was strongly influenced by both diet and age. As expected, the strength of condition dependence was much more pronounced in the sexually selected, male-limited trait but the nonsexual trait also exhibited significant condition dependence in both sexes. The sexually selected male trait also exhibited a higher coefficient of phenotypic variation than the nonsexually selected trait in males and females. Diet had contrasting effects on male and female longevity; increased food availability had positive effects on female lifespan but these effects were not detected in males, suggesting that males allocated limited resources preferentially to sexually selected traits. These results are consistent with the expectation that optimal allocation to various fitness components differs between the sexes.     

Nest size predicts the effect of food supplementation to magpie nestlings on their immunocompetence: an experimental test of nest size indicating parental ability

Post-mating sexually selected signals are expected to indicateparental quality. The good parent model assumes that expressionof the sexual character positively reflects parental ability,resulting in a potential link between the exaggeration of thecharacter and nestling-fitness traits. We tested this predictionin a population of a monogamous passerine, the magpie (Picapica), for which nest size is known to act as a post-matingsexually selected signal. We provided a food supplement to halfof the magpie nestlings in each nest, keeping the other halfas control nestlings. We found that food-supplemented nestlingsexperienced a significantly higher T-cell-mediated immune responseand a tendency to an increased condition index. In accordancewith the good parent model, we found that nest size was positivelyrelated to T-cell mediated immune response for control magpie,whereas this relationship was nonexistent in food-supplementednestlings. In addition, the difference in T-cell mediated immuneresponse between food-supplemented and control nestlings ofthe same nest was principally explained by nest size. Basedon our results, we discuss that magpie pairs with large nestsprovided their nestlings with higher quality food as comparedto pairs with smaller nests, nest size thereby being an indicatorof parental ability. To our knowledge, this is the first studyshowing a link between a post-mating sexually selected signaland nestling immunocompetence, a trait closely related to fitnessin birds.     

Sex-biased survival predicts adult sex ratio variation in wild birds

Adult sex ratio (ASR) is a central concept in population demography and breeding system evolution, and has implications for population viability and biodiversity conservation. ASR exhibits immense interspecific variation in wild populations, although the causes of this variation have remained elusive. Using phylogenetic analyses of 187 avian species from 59 families, we show that neither hatching sex ratios nor fledging sex ratios correlate with ASR. However, sex-biased adult mortality is a significant predictor of ASR, and this relationship is robust to 100 alternative phylogenetic hypotheses, and potential ecological and life-history confounds. A significant component of adult mortality bias is sexual selection acting on males, whereas increased reproductive output predicts higher mortality in females. These results provide the most comprehensive insights into ASR variation to date, and suggest that ASR is an outcome of selective processes operating differentially on adult males and females. Therefore, revealing the causes of ASR variation in wild populations is essential for understanding breeding systems and population dynamics.     

Does the badge of status influence parental care and investment in house sparrows? An experimental test

Theory predicts that traits which signal parental quality might evolve in males of species with biparental care. In avian species, male ornaments may be the most likely candidates for such signals. Male house sparrows (Passer domesticus) possess a black throat patch often referred to as a “badge” or a “badge of status”. By assuming a trade-off between male attractiveness (reflected in male ornaments) and parental care under the differential allocation hypothesis, we predicted that badge size would be negatively correlated with male parental investment. An experiment in which the badge was enlarged in one group and unchanged in a control group was conducted. Our manipulation was predicted to affect female as well as male parental investment. However, we found that eight variables associated with parental investment—the start date for breeding, clutch size, male and female incubation time, male and female food provisioning rate, and average chick weight and the number of fledglings—barely differed between treatments. Also, little evidence for correlations between natural variation in badge size and any of these eight variables was found. Instead, the start date for breeding and the number of fledglings were significantly correlated with both male and female age, while clutch size increased with female age. Female condition was a positive predictor of clutch size and number of fledglings. Female tarsus length, unexpectedly, is related to both male and female incubation time. Badge size was also positively correlated with male age. However, parental age (male or female) was not related to parental care. We conclude that badge size does not signal parental quality, but that the ages of both sexes and the condition of the female play significant roles in the reproductive performance of this species.     

Will male advertisement be a reliable indicator of paternal care,if offspring survival depends on male care?

Existing theory predicts that male signalling can be an unreliable indicator of paternal care, but assumes that males with high levels of mating success can have high current reproductive success, without providing any parental care. As a result, this theory does not hold for the many species where offspring survival depends on male parental care. We modelled male allocation of resources between advertisement and care for species with male care where males vary in quality, and the effect of care and advertisement on male fitness is multiplicative rather than additive. Our model predicts that males will allocate proportionally more of their resources to whichever trait (advertisement or paternal care) is more fitness limiting. In contrast to previous theory, we find that male advertisement is always a reliable indicator of paternal care and male phenotypic quality (e.g. males with higher levels of advertisement never allocate less to care than males with lower levels of advertisement). Our model shows that the predicted pattern of male allocation and the reliability of male signalling depend very strongly on whether paternal care is assumed to be necessary for offspring survival and how male care affects offspring survival and male fitness.