Oocyte composition can directly influence offspring fitness, particularly in oviparous species such as most insects, where it is the primary form of parental investment. Oocyte production is also energetically costly, dependent on female condition and responsive to external cues. Here, we investigated whether mating influences mature oocyte composition in
Parental investment by solitary nest‐building wasps and bees is predicted to be plastic, responding to variation in the sex of the offspring, the availability of food used as provisions (‘resource limitation’), the female's inventory of mature oocytes (‘egg limitation’), and risk imposed by nest parasites. I observed nest provisioning by Neither the hunting time required to capture the first caterpillar prey nor the female's inventory of oocytes predicted a female's likelihood of adding a second caterpillar to a nest. Variation in oocyte inventory across females was minimal; all females examined had a mature or nearly mature oocyte remaining in the ovaries immediately after laying an egg. Although many nest parasites have evolved adaptations to avoid detection by their hosts, oviposition by
- PAR ID:
- 10264324
- Publisher / Repository:
- Wiley-Blackwell
- Date Published:
- Journal Name:
- Ecological Entomology
- Volume:
- 46
- Issue:
- 2
- ISSN:
- 0307-6946
- Page Range / eLocation ID:
- p. 394-405
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract Drosophila melanogaster using a quantitative proteomic approach. Our analyses robustly identified 4,485 oocyte proteins and revealed that stage-14 oocytes from mated females differed significantly in protein composition relative to oocytes from unmated females. Proteins forming a highly interconnected network enriched for translational machinery and transmembrane proteins were increased in oocytes from mated females, including calcium binding and transport proteins. This mating-induced modulation of oocyte maturation was also significantly associated with proteome changes that are known to be triggered by egg activation. We propose that these compositional changes are likely to have fitness consequences and adaptive implications given the importance of oocyte protein composition, rather than active gene expression, to the maternal-to-zygotic transition and early embryogenesis. -
Abstract Developmental responses can help young animals reduce predation risk but can also yield costs to performance and survival in subsequent life stages with major implications for lifetime fitness. Compensatory mechanisms may evolve to offset such costs, but evidence from natural systems is largely lacking.
In songbirds, increased nest predation risk should favour reduced provisioning, but also young that fledge (leave their nest) at an earlier age. Both responses can result in fledglings with shorter wings, reduced mobility and decreased survival. Young may compensate for shorter wings developmentally by reallocating resources towards feather development or behaviourally by adjusting flight kinematics or habitat use. However, underfed young may lack the capacity to express these phenotypes due to insufficient resources or an inability to adjust allocation of resources.
Using predation risk experiments and 29 years of observational field data, we test whether increased nest predation risk reduces flight performance and survival during the fledgling stage and explore potential mechanisms that might underlie these effects. We show that young from high‐risk nests did not leave the nest earlier on average, but wing growth was slower likely due to observed reductions in parental feeding rates. Wings were shorter in high‐risk nests when fledglings left the nest early. Yet, fledglings from high‐risk nests showed improved flight performance for a given wing length such that flight performance at fledging did not differ between young from high‐risk and low‐risk nests. Young from high‐risk nests may have offset the costs of shorter wings on flight performance by accelerating the emergence of flight feathers from their sheaths to reduce wing porosity, though evidence for this mechanism was mixed. Fledglings from high‐risk nests also selected habitat with denser woody vegetation compared with young from low‐risk nests.
Together, these developmental and behavioural responses seem to mitigate the expected effects of increased nest predation risk on fledgling survival. Ultimately, our results show that offspring predation risk can affect parental provisioning and offspring morphology without major implications for performance and survival in subsequent life stages.
A free
Plain Language Summary can be found within the Supporting Information of this article. -
Abstract Co‐parasitism is ubiquitous and has important consequences for the ecology and evolution of wild host populations. Studies of parasite co‐infections remain limited in scope, with few experimental tests of the fitness consequences of multiple parasites, especially in natural populations.
We measured the separate and combined effects of
Philornis seguyi nest flies and shiny cowbirdsMolothrus bonariensis on the fitness of a shared host, the chalk‐browed mockingbird (Mimus saturninus ) in Argentina.Using a two‐factor experimental approach, we manipulated the presence of nest flies and cowbirds in mockingbird nests and assessed their effects on mockingbird haemoglobin levels, begging and provisioning rates, body size, and fledging success. We also monitored rates of nest predation in relation to parasitism by flies and cowbirds.
Nest flies reduced the haemoglobin concentration, body size, and fledging success of mockingbirds, likely because mockingbirds did not compensate for parasitism by begging more or feeding their nestlings more. Cowbirds also reduced the fledging success of mockingbirds, even though they had no detectable effect on haemoglobin or body size. Nests with cowbirds, which beg more than mockingbirds, attracted more nest predators. There was no significant interaction between the effects of flies and cowbirds on any component of mockingbird fitness. The combined effects of nest flies and cowbirds were strictly additive.
In summary, we show that nest flies and cowbirds both reduce host fitness, but do not have interactive effects in co‐parasitized nests. Our results further suggest that predators exacerbate the effects of nest flies and cowbirds on their hosts. Our study shows that the fitness consequences of co‐parasitism are complex, especially in the context of community‐level interactions.
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Abstract Offspring mortality varies dramatically among species with critical demographic and evolutionary ramifications, yet the causes of this variation remain unclear. Nests are widely used for breeding across taxa and thought to influence offspring mortality risk. Traditionally, more complex, enclosed nest structures are thought to reduce offspring predation by reducing the visibility of nest contents and muffling offspring sounds compared to open nests. Direct tests of the functional bases for nest structure influence on predation risk are lacking.
We used experiments and 10 years of observational data to examine how nest structure influences nest predation risk in a diverse community of tropical songbirds. First, we examined how nest size was related to nest structure and nest predation rates across species. Second, we assessed how nest structure influences the detectability of nestling begging calls both in field and in laboratory settings. Finally, we examined how the acoustic properties of different nest structures influence nest predation risk. Specifically, we experimentally broadcast begging calls from open and enclosed nests to determine how auditory cues and nest structure interact to affect predation on plasticine and quail eggs. We also tested whether nest structure was associated with differences in nest predation rates between the incubation (no begging cues) and nestling (begging cues) stages.
We found that enclosed nests are larger than open nests after accounting for adult size, and larger nests had increased predation rates. Moreover, enclosed nests did not consistently alter nestling begging calls in ways that reduce the likelihood of predation compared to open nests. Indeed, begging cues increased predation rates for enclosed but not open‐cup nests in our playback experiment, and nest predation rates showed greater increases after hatching in enclosed than open‐cup nests.
Ultimately, enclosed nests do not necessarily provide greater predation benefits than open nests in contrast to long‐standing theory.
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Abstract Elucidating factors that limit the number of offspring produced is fundamental to understanding life‐history evolution. Here, we examine the hypothesis that parental ability to maintain an optimal physical developmental environment for all offspring constrains clutch size via effects on offspring quality.
Experimental laboratory studies of birds have shown that a <1°C difference in average incubation temperature has diverse effects on fitness‐related post‐hatching offspring phenotypes. Thus, the inability of parents to maintain optimal incubation temperatures could constrain clutch sizes.
A fundamental question that has not been sufficiently addressed is whether larger clutch sizes lead to
within nest variation in egg temperature that is large enough to produce offspring with different phenotypes within a brood. This could lead to differential survival among offspring, and could create a trade‐off between offspring number and quality.We manipulated clutch size in nests of free‐living wood ducks and measured incubation temperature among and within clutches using multiple temperature loggers.
As clutch size increased, average incubation temperatures were lower and more variable, and eggs took longer to hatch. Notably, the range in
average incubation temperature among eggswithin nests increased with clutch size and exceeded 1°C in large clutches. Clutch size did not affect hatch success.In conjunction with our companion laboratory studies that used artificial incubation to document the effects of temperature variation on fitness‐related traits in this species, our work suggests that suboptimal incubation temperatures could be a factor that limits clutch size through diminishing returns on post‐hatch offspring quality.
A free
plain language summary can be found within the Supporting Information of this article.