Document Type

Article

Publication Title

Animal Behaviour

Publication Date

2-2023

Keywords

accessory gland protein, cricket, mating behaviour, nuptial food gift, oviposition, sexual conflict, sexual receptivity

Abstract

Accessory gland proteins contained within male ejaculates influence female reproduction and survival in insects. Nuptial food gifts offered by male crickets and katydids, the consumption of which may also alter female behaviour and physiology after mating, also contain accessory gland proteins. However, because nuptial feeding promotes the transfer of sperm and ejaculatory substances, it is unclear whether it is accessory gland proteins in the ejaculate, nuptial gifts or both that mediate these effects. Here we evaluate the effects of mating, nuptial gifts and accessory gland proteins on female reproduction in a gift-giving cricket (Gryllodes sigillatus) using a crossed experimental design. We injected females of varying mating experience with male accessory gland extract, permitting some females to consume the nuptial food gift, while experimentally preventing others from doing so. Mating resulted in a significant decrease in female sexual receptivity, an effect likely mediated by accessory gland proteins contained in the male's ejaculate. Consumption of the nuptial food gift resulted in the premature cessation of nuptial feeding following the female's next mating, leading to a concomitant decrease in sperm transfer by a rival male. This is a novel finding, demonstrating that fitness benefits to males of nuptial gift provisioning can also accrue over later copulations by their mates. Neither injection of accessory gland extract nor nuptial feeding influenced female oviposition; the absence of any effect of the injection of accessory gland proteins on female reproduction suggests that their efficacy may depend on their direct introduction into the female reproductive tract. More research is required to identify the specific accessory gland proteins in ejaculates and nuptial gifts that modulate female behaviour and physiology, potentially illuminating the evolution of these mechanistic tactics underlying sexual conflict.

Funding Source

This research was funded by a grant from the U.S. National Science Foundation to S.K.S., B.M.S. and J.H. (IOS 16-54028), a grant from the Australian Research Council to J.H. (DP180101708), grants from the Beta Lambda Chapter of the Phi Sigma Biological Honor Society, Society for the Study of Evolution, Animal Behavior Society, Sigma Xi and the Orthopterist's Society to I.G.R. and a Dr. Robert H. Gray Scholarship from the School of Biological Sciences, Illinois State University to I.G.R.

Comments

This is the Accepted Manuscript of an article published in Animal Behavior: https://doi.org/10.1016/j.anbehav.2022.11.008

First published in Animal Behaviour: https://doi.org/10.1016/j.anbehav.2022.11.008

Raw data are archived in the Mendeley Data Repository: https://doi.org/10.17632/dh2pdkby89.1 (Sakaluk, 2022).

Supplemental material available at https://doi.org/10.1016/j.anbehav.2022.11.008

DOI

10.1016/j.anbehav.2022.11.008

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