Pair formation in social insects mostly happens early in adult life and away from the social colony context, which precludes promiscuity in the usual sense. Termite males have continuous sperm production, but males of social Hymenoptera have fixed complements of sperm, except for a few species that mate before female dispersal and show male-fighting and lifelong sperm production. We develop an evolutionary framework for testing sexual selection and sperm competition theory across the advanced eusocial insects (ants, wasps, bees, termites) and highlight two areas related to premating sexual selection (sexual dimorphism and male mate number) that have remained understudied and in which considerable progress can be achieved with relatively simple approaches. We also infer that mating plugs may be relatively common, and we review further possibilities for postmating sexual selection, which gradually become less likely in termite evolution, but for which eusocial Hymenoptera provide unusual opportunities because they have clonal ejaculates and store viable sperm for up to several decades.

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Ejaculates contain sperm but also seminal fluid, which is increasingly recognized to be of central importance for reproductive success. However, a detailed biochemical composition and physiological understanding of seminal fluid is still elusive. We have used MS to identify the 57 most abundant proteins within the ejaculated seminal fluid of the honeybee Apis mellifera. Their amino acid sequences revealed the presence of diverse functional categories of enzymes, regulators and structural proteins. A number have known or predicted roles in maintaining sperm viability, protecting sperm from microbial infections or interacting with the physiology of the female. A range of putative glycoproteins or glycosylation enzymes were detected among the 57, subsequent fluorescent staining of glycolysation revealed several prominent glycoproteins in seminal fluid, while no glycoproteins were detected in sperm samples. Many of the abundant proteins that accumulate in the seminal fluid did not contain predictable tags for secretion for the cell. Comparison of the honeybee seminal fluid proteins with Drosophila seminal fluid proteins (including secreted accessory gland proteins known as ACPs), and with the human seminal fluid proteome revealed the bee protein set contains a range of newly identified seminal fluid proteins and we noted more similarity of the bee protein set with the current human seminal fluid protein set than with the known Drosophila seminal fluid proteins. The honeybee seminal fluid proteome thus represents an important addition to available data for comparative studies of seminal fluid proteomes in insects.

Honeybee queen sperm storage

A proteomic and metabolic network analysis of honeybee queen spermathecal fluid provides insights into female long-term sperm storage mechanisms.

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-Honey bees in the genus Apis share many reproductive features with other social insects, but have also a number of highly derived mating characteristics, such as obligatory polyandry and -in at least two species -males who deposit their ejaculates directly into the spermathecal duct. These characteristics make the honeybees highly interesting and a special model system for studying sexual selection. Furthermore, the numerical sex ratio of Apis bees is extremely male biased and males die during their first and only copulation. This review updates our present knowledge of the mating biology of Apis bees and places this information into a broader concept of sexual selection. I concentrate on two intensively studied aspects of sexual selection: Sperm competition and cryptic female choice. I present evidence that sperm competition is likely to occur during the egg fertilization process, whereas cryptic female choice is likely to operate shortly after insemination when ejaculates of many males get stored in the spermatheca of the queen.Apis / honeybee / polyandry / sperm storage / sperm use / sperm competition / cryptic female choice

Sperm Wars Some female insects mate on only one day of their life, but then they may mate with multiple males and store the sperm, sometimes for years. But as the mates compete for mates, so their sperm compete for ova, and competition between ejaculates can result in the destruction of sperm inside multiply mated females. But females need to select the sperm they want and to maintain stores of viable sperm to ensure a lifetime's fertility. Den Boer et al. (p. 1506 ) compared species of bees and ants with queens that either mate once or mate multiple times, and found that sperm competition has driven the evolution of compounds in the male accessory gland that protect a male's own sperm while damaging another male's sperm. To counteract the male effect, queens produce compounds that mitigate sperm destruction and maximize the number of her offspring.

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