Abstract

BackgroundLife history theory predicts that an individualʼs current reproductive investment should depend on its future reproductive value. A variety of intrinsic biotic and extrinsic factors influence reproductive value, including age, health status and current environmental conditions. Phenotypic plastic reproductive decisions are particularly crucial in species with limited mating and breeding opportunities. In the malaria mosquito Anopheles coluzzii, the combination of male-male competition and female monandry results in male reproductive success being dependent on limited mating opportunities and sperm reserves. Short life spans combined with 3–4 day gonotrophic cycles imply that females can produce only a limited number of egg-batches in their lifetime and rely on a single maleʼs insemination to do so. Here we experimentally tested the effect of hydric stress on male sperm transfer and female sperm maintenance in this important vector species.MethodsVirgin males and females were stressed prior to mating to simulate environmental uncertainty, hence the prospect of a decreased lifespan. They were then paired overnight with non-stressed mates in standardized mating assays. Sperm transfer, uptake and maintenance were quantified using qPCR, and sperm activity determined via video recording.ResultsWhen exposed to hydric stress, males responded by increasing their current reproductive investment and transferred significantly larger amounts of sperm to females. There was no significant increase in the mean number of females inseminated overnight by stressed males. In contrast, females did not significantly change their sperm uptake following stress nor did they alter their sperm maintenance strategy after 7-day post-mating hydric stress as measured through sperm activity level and sperm cells quantification.ConclusionsAs predicted by life-history theory, pre-mating hydric stress was associated with an increase in male current reproductive effort in the form of increased sperm transfer. In contrast, pre and post-mating hydric stress had no impact on sperm uptake and maintenance by females, which is compatible with the prediction that females maximize their reproductive value by withstanding stress periods until a blood meal opportunity and maintain sperm quality towards future egg production.

Highlights

  • Life history theory predicts that an individuals current reproductive investment should depend on its future reproductive value

  • Effect of pre‐mating hydric stress on male current reproductive effort Across all hydric stress treatment groups, an average of 52.6% of virgin females were inseminated by males overnight and no significant difference was observed in insemination frequency among treatment groups (χ2 = 0.04, df = 2, P = 0.978, n = 587)

  • The level of hydric stress strongly affected the amount of sperm cells transferred to females by males (ANOVA: F(2,117) = 58.2, P < 0.001) (Table 1)

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Summary

Introduction

Life history theory predicts that an individuals current reproductive investment should depend on its future reproductive value. Empirical studies have demonstrated this important trade-off by measuring the negative impact of an increase in current reproductive effort on survival and future reproduction. Depending on their life-cycle, parasites can affect the costs of current or future reproduction differentially [3,4,5]. Adult blue tits, Parus caeruleus, with nests experimentally infested by hen fleas, Ceratophyllus gallinae, compensated for the fleasnegative effects on nestling growth by increasing nestling feeding rates [6] This increase in current reproductive effort resulted in decreased adult survival and smaller eggbatches the following year [7]. Biomphalaria glabrata snails infected with Schistosoma mansoni, a trematode known to shorten its hosts lifespan, increased egg production upon experimental infection [5]

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