Reproductive Effort and Costs

Predictions about life-history evolution are intellectually bereft without a consideration of trade-offs. Benefits derived from making one life-history ‘decision’ are made at a cost of not realizing potential benefits associated with alternative decisions. These trade-offs are the inevitable product of constraints, often driven by an individual’s differential allocation of fixed resources to reproduction versus survival or growth. These allocations prevent multiple positive outcomes from being simultaneously realized. Reproductive effort is the proportion of total energy or resources allocated to all elements of reproduction. Reproductive effort generates reproductive costs. Increases in current reproductive effort reduce future reproductive success by affecting survival, growth, and/or fecundity. The causal mechanisms of these costs can be energetic, ecological, behavioural, or genetic. Evidence for reproductive costs is widespread. Instances where the evidence of costs is equivocal are usually caused by using among-individual correlations to study what is a within-individual phenomenon.

Flying males mediate oviposition and migration in female Mythimna separata (Lepidoptera: Noctuidae)

In recent decades, the oriental armyworm, Mythimna separata (Walker), has caused severe damage to staple grains in China. However, little is known about when M. separata begin their first migration and the role of males in reproduction and migration. Here, the migratory benefits and reproductive costs of flight frequency were examined in adults under laboratory conditions. We found that flying males had a positive effect on ovarian and reproductive development in females who flew for 1–2 nights by comparing two treatment groups (flying and nonflying male groups). Moreover, flying males decreased the flight capacity and flight propensity of females. In contrast, flight for more than two nights by males significantly inhibited ovarian and reproductive development in adult females. Compared with the controls (0 night), male flight for 1–2 nights significantly shortened the preoviposition period but significantly increased ovarian and reproductive development in females. However, male flight for more than three nights significantly inhibited female reproduction and flight capacity. These results indicate that M. separata begin their first migration within 2 days after emergence and fly for two nights. Prolonged flight times can result in significant reproductive costs. Females initiated their first migration earlier than males due to a stronger flight capacity. These observed findings will be useful for forecasting and monitoring population dynamics to prevent outbreaks of M. separata and reduce crop losses.

Sex, mating and repeatability of Drosophila melanogaster longevity

Costs of reproduction are seemingly ubiquitous across the animal kingdom, and these reproductive costs are generally defined by increased reproduction leading to decreases in other fitness components, often longevity. However, some recent reports question whether reproductive costs exist in every species or population. To provide insight on this issue, we sought to determine the extent to which genetic variation might play a role in one type of reproductive cost—survival—using Drosophila melanogaster . We found, surprisingly, no costs of reproduction nor sex differences in longevity across all 15 genetic backgrounds in two cohorts. We did find significant variation within some genotypes, though these were much smaller than expected. We also observed that small laboratory changes lead to significant changes in longevity within genotypes, suggesting that longevity repeatability in flies may be difficult. We finally compared our results to previously published longevities and found that reproducibility is similar to what we saw in our own laboratory, further suggesting that stochasticity is a strong component of fruit fly lifespan. Overall, our results suggest that there are still large gaps in our knowledge about the effects of sex and mating, as well as genetic background and laboratory conditions on lifespan reproducibility.

Parental reactions to a dying marmoset infant: conditional investment by the mother, but not the father

The reproductive costs of cooperatively breeding callitrichid mothers are remarkable, and they have to rely on fathers and other group members to raise their offspring. Consequently, maternal responsiveness to and investment in infants tends to be conditional, and especially sensitive to infant cues and signals of vigour. Since fathers do not bear the same excessive reproductive costs, their threshold to invest in a dying immature may be lower than in mothers. We present an anecdotal report of reactions of a first-time breeding pair of captive common marmosets (Callithrix jacchus) to their dying infant. We found a male bias in all interactions with the dying infant that did not show typical cues of infant vigour. These results show that the dying infant elicited more investment by the father than the mother. Because of this conditional maternal investment, infants of cooperatively breeding primates may be under selection to advertise their viability, in particular to their mothers.

Sex-biased genes and metabolites explain morphologically sexual dimorphism and reproductive costs in Salix paraplesia catkins

Dioecious species evolved from species with monomorphic sex systems in order to achieve overall fitness gains by separating male and female functions. As reproductive organs, unisexual flowers have different reproductive roles and exhibit conspicuous sexual dimorphism. To date, little is known about the temporal variations in and molecular mechanisms underlying the morphology and reproductive costs of dioecious flowers. We investigated male and female flowers of Salix paraplesia in three flowering stages before pollination (the early, blooming and late stages) via transcriptional sequencing as well as metabolite content and phenotypic analysis. We found that a large number of sex-biased genes, rather than sex-limited genes, were responsible for sexual dimorphism in S. paraplesia flowers and that the variation in gene expression in male flowers intensified this situation throughout flower development. The temporal dynamics of sex-biased genes derived from changes in reproductive function during the different flowering stages. Sexually differentiated metabolites related to respiration and flavonoid biosynthesis exhibited the same bias directions as the sex-biased genes. These sex-biased genes were involved mainly in signal transduction, photosynthesis, respiration, cell proliferation, phytochrome biosynthesis, and phenol metabolism; therefore, they resulted in more biomass accumulation and higher energy consumption in male catkins. Our results indicated that sex-biased gene expression in S. paraplesia flowers is associated with different reproductive investments in unisexual flowers; male flowers require a greater reproductive investment to meet their higher biomass accumulation and energy consumption needs.