Fecundity selection theory: concepts and evidence

Fitness results from an optimal balance between survival, mating success and fecundity. The interactions between these three components of fitness vary depending on the selective context, from positive covariation between them, to antagonistic pleiotropic relationships when fitness increases in one reduce the fitness of others. Therefore, elucidating the routes through which selection shapes life history and phenotypic adaptations via these fitness components is of primary significance to understanding ecological and evolutionary dynamics. However, while the fitness components mediated by natural (survival) and sexual (mating success) selection have been debated extensively from most possible perspectives, fecundity selection remains considerably less studied. Here, we review the theoretical basis, evidence and implications of fecundity selection as a driver of sex‐specific adaptive evolution. Based on accumulating literature on the life‐history, phenotypic and ecological aspects of fecundity, we (i) suggest a re‐arrangement of the concepts of fecundity, whereby we coin the term ‘transient fecundity’ to refer to brood size per reproductive episode, while ‘annual’ and ‘lifetime fecundity’ should not be used interchangeably with ‘transient fecundity’ as they represent different life‐history parameters; (ii) provide a generalized re‐definition of the concept of fecundity selection as a mechanism that encompasses any traits that influence fecundity in any direction (from high to low) and in either sex; (iii) review the (macro)ecological basis of fecundity selection (e.g. ecological pressures that influence predictable spatial variation in fecundity); (iv) suggest that most ecological theories of fecundity selection should be tested in organisms other than birds; (v) argue that the longstanding fecundity selection hypothesis of female‐biased sexual size dimorphism (SSD) has gained inconsistent support, that strong fecundity selection does not necessarily drive female‐biased SSD, and that this form of SSD can be driven by other selective pressures; and (vi) discuss cases in which fecundity selection operates on males. This conceptual analysis of the theory of fecundity selection promises to help illuminate one of the central components of fitness and its contribution to adaptive evolution.     

Independent cytoplasmic incompatibility induced by Cardinium and Wolbachia maintains endosymbiont coinfections in haplodiploid thrips populations

Cardinium and Wolbachia are common maternally inherited reproductive parasites that can coinfect arthropods, yet interactions between both bacterial endosymbionts are rarely studied. For the first time, we report their independent expression of complete cytoplasmic incompatibility (CI) in a coinfected host, and CI in a species of the haplodiploid insect order Thysanoptera. In Pezothrips kellyanus, Cardinium‐induced CI resulted in a combination of male development (MD) and embryonic female mortality (FM) of fertilized eggs. In contrast, Wolbachia‐induced CI resulted in FM together with postembryonic mortality not previously reported as a CI outcome. Both endosymbionts appeared to not influence fecundity but virgins produced more offspring than mated females. In coinfected individuals, Wolbachia density was higher than Cardinium. Wolbachia removal did not impact Cardinium density, suggesting a lack of competition within hosts. Maternal transmission was complete for Wolbachia and high for Cardinium. Our data support theoretical predictions and empirical detection of high endosymbiont prevalence in field populations of the native range of this pest thrips. However, previous findings of more frequent loss of Wolbachia than Cardinium, particularly in field populations of the host's invasive range, suggest that genetic diversity or varying environmental factors between field populations also play a role in shaping host‐endosymbiont dynamics.     

Increased reproduction by pea aphids in the presence of secondary parasitoids

1. The influence of the presence of secondary parasitoids on aphid reproduction was tested in a field experiment. 2. Single pea aphids Acyrthosiphon pisum in clip cages on potted bean plants were exposed to a collection of secondary parasitoids enclosed within a small perforated bag. The aphids were exposed to volatile chemicals released by the secondary parasitoids but there was no physical contact. 3. The production of nymphs was recorded over an 11‐day period. Aphids produced significantly more offspring in the presence of secondary parasitoids than in the absence of secondary parasitoids (36.9 vs. 31.2). 4. This is the second reported occurrence of this phenomenon, and the reasons for its occurrence and its consequences for aphid population and community ecology are discussed.     

Interactions between density-dependent processes, population dynamics and control of an invasive plant species, Tripleurospermum perforatum (scentless chamomile)

Tripleurospermum perforatum is an invasive weedy species which exhibits strong over-compensating density dependence. Interactions between density-dependent survival, probability of flowering and fecundity were modelled and their impact on the population dynamics were examined. When only fecundity was density-dependent, the dynamics were similar to those observed in the model containing all three density-dependent terms. Density-dependent survival was a stabilizing process when acting in combination with density-dependent fecundity and probability of flowering; removing density-dependent survival from the model produced two-point cycles. The addition of a seed bank was also stabilizing. Simulations of control strategies at different life-history stages indicated that full control would be difficult due to the strong over-compensating density dependence, with severe reductions in fecundity and late season survival necessary in order to reduce equilibrium seed density and biomass.     

Cancer brings forward oviposition in the fly Drosophila melanogaster

Hosts often accelerate their reproductive effort in response to a parasitic infection, especially when their chances of future reproduction decrease with time from the onset of the infection. Because malignancies usually reduce survival, and hence potentially the fitness, it is expected that hosts with early cancer could have evolved to adjust their life‐history traits to maximize their immediate reproductive effort. Despite the potential importance of these plastic responses, little attention has been devoted to explore how cancers influence animal reproduction. Here, we use an experimental setup, a colony of genetically modified flies Drosophila melanogaster which develop colorectal cancer in the anterior gut, to show the role of cancer in altering life‐history traits. Specifically, we tested whether females adapt their reproductive strategy in response to harboring cancer. We found that flies with cancer reached the peak period of oviposition significantly earlier (i.e., 2 days) than healthy ones, while no difference in the length and extent of the fecundity peak was observed between the two groups of flies. Such compensatory responses to overcome the fitness‐limiting effect of cancer could explain the persistence of inherited cancer‐causing mutant alleles in the wild.     

Breeding ecology of an amphidromous goby of the genusRhinogobius

Field observations of markedRhinogobius sp. DA (Dark type) individuals and monthly sampling in the Kashiwa River, Shikoku Island, Japan, indicated the breeding season of the species to be from mid-April to early July, peaking in May. Mark-and-recapture data showed that at least half of the females spawned more than once in one breeding season. Although eggs in male-guarded nests were all at the same developmental stage, their mean number exceeded that of pre-spawning yolk stage oocytes per female, suggesting that at least some guarding males received eggs from more than one female. The physical condition of both sexes deteriorated considerably during the breeding season, the hepatosomatic index of guarding males decreasing concurrently with the development of eggs. The decline in physical condition of guarding males was attributed mainly to their restricted feeding opportunities.     

濒危植物裂叶沙参种群生殖力表的研究

本文分别以当年产种子数量和一年生幼苗数量为基础,编制了裂叶沙参种群(总和)和海拔2300-2400m, 2700-2900m, 2900-3100m, 3100-3400m 4个不同海拔区域种群的生殖力表,分析了不同种群两种生殖表的种群内禀增长率(r_m),周限增殖率(λ),净增长率(R₀),毛增长率(G)等动态参数与种群动态的关系;比较了两种生殖力表的特点和利弊;讨论了裂叶沙参种群生殖生态学特性和种群发展趋势及其与环境因素的关系。以种子数量为基础编制的生殖力表的各种群动态参数表明,裂叶沙参具有较强的产生种子的能力,特别是在生境条件较好的海拔2700-3100m区域,种群个体结实量可达到很高的水平。以一年生幼苗数量为基础编制的生殖力表表明,裂叶沙参种群从整体上呈衰退趋势。但不同种群间存在差异:在海拔2300-2400m,水份条件较好的特殊生境和海拔2900-3100m的种群呈稳定特征;而海拔2700-2900m,3100-3400m的种群呈缓慢衰退特征。以种子数量为基础编制的生殖力表可以反映裂叶沙参种群产生种子的能力和生殖生态学特征;而以一年生幼苗数量为基础编制的生殖力表包含了种子库的生态学过程,能较好的反映种群动态特征。在实践中,两种生殖力表应配合使用,才能全面刻划种群生殖生态学和种群动态特征。     

Thermotolerance and rapid cold hardening ameliorate the negative effects of brief exposures to high or low temperatures on fecundity in the flesh fly, Sarcophaga crassipalpis

Although the immediate effects of temperature stress are well documented, the longer‐term effects of such stresses are more poorly known. In these experiments, we investigate the effects of suboptimal and supraoptimal temperatures during pharate adult development on fecundity in the flesh fly, Sarcophaga crassipalpis Macquart. A 1 h cold shock at ?10°C during the red‐eye pharate adult stage decreases the fecundity of both sexes. Induction of rapid cold hardening by pre‐treatment at 0°C for 2 h partially prevents reproductive impairment. Heat shock of pharate adults for 1 h at 45°C also reduces fecundity in both sexes, but inducing thermotolerance by pre‐treatment at 40°C for 2 h affords protection only to females. Males heat shocked at 45°C or first pre‐treated at 40°C consistently fail to transfer sperm to the females. The injury inflicted on males by heat shock is most pronounced when the stress is administered to pharate adults or adults; wandering larvae and true pupae are unaffected. The implications of these data for naturally occurring populations are discussed.     

Reproductive performance of clonal and sexual bark beetles (Coleoptera: Scolytidae) in the field

In Ips acuminatus (Gyll.) parthenogenetic females occur together with sexual females and with sexual males upon which they depend for sperm. In a reciprocal‐transplant experiment, I studied fecundity differences among parthenogenetic and sexual females from two populations that differ dramatically in the proportion of clonal females. In a second experiment, I studied competition between larvae from different mothers and between females from the two source populations. Fecundity measured by the number of eggs per egg tunnel was influenced by the ambient environment at the sites of the experiment as well as the origin of the female, and was generally higher for clonal than for sexual females at both sites. In experimental groups where larvae competed with larvae from their own population (pure treatments), the number of surviving pupae was significantly lower than in groups where females from the two source populations were mixed. The high fecundity of clonal females makes coexistence of the two types of females difficult to explain. It makes the reproductive advantage associated with clonality in I. acuminatus even higher than the two‐fold difference due to asexuality per sé. The significant differences in the number of pupae in mixed vs. pure groups suggest ecological divergence between sexual and clonal females. This would make the mortality of larvae not only density dependent, but also frequency dependent, which could explain the coexistence of sexual and clonal females.     

Trade‐offs between growth and reproduction: an analysis of the quantitative genetic evidence

The assumption of a trade‐off between development time and fecundity, resulting from a positive correlation between body size and fecundity and between body size and development time, is a common feature of life history models. The present paper examines the evidence for such a trade‐off as indicated by genetic correlations between traits. The genetic covariances between traits are derived using a model in which maturation occurs when the organism achieves a genetically variable size threshold, and fecundity is an allometric function of body size with one genetically variable parameter (excluding body size itself). This model predicts that the heritabilities of the life history traits (growth rate, development time, fecundity) will not necessarily be less than the heritability of adult size (i.e. morphological traits). It is shown that if growth rate is genetically correlated with adult size then it is not possible, in general, to predict the sign of the genetic correlation between development time and fecundity. For particular cases the signs of the covariances between traits can be predicted. These predictions are tested using data drawn from the literature.