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Adult sex ratio determines the level of mate availability and intrasexual competition for each sex. Sex ratio biases have been proposed to enhance the productivity of animal rearing procedures. However, behaviour may change in response to sex ratio manipulations that may counteract potential benefits. We investigated how sex ratios affected mating behaviour of the housefly Musca domestica , a species used in the animal feed industry. We hypothesized a reduced courtship effort and mating latency and increased ejaculate allocation (copulation duration) under male-biased sex ratios, whereas female-biased sex ratios would lead to the opposite effects. However, courtship effort was reduced in female-biased groups, implying reduced male harassment. Mating latency was lower and copulation lasted longer in female-biased groups, which may reduce reproduction time and increase female fecundity and lifespan. Our results indicate that in houseflies, female-biased sex ratios cause behavioural changes in both sexes that could positively contribute to reproductive output. [ABSTRACT FROM AUTHOR]

The ability to transition between different behavioural stages is a widespread phenomenon across the animal kingdom. Such behavioural adaptations are often linked to changes in the sensitivity of those neurons that sense chemical cues associated with the respective behaviours. To identify the genetic mechanisms that regulate neuronal sensitivity, and by that behaviour, typically *omics approaches, such as RNA‐ and protein‐sequencing, are applied to sensory organs of individuals displaying differences in behaviour. In this review, we discuss these genetic mechanisms and how they impact neuronal sensitivity, summarize the correlative and functional evidence for their role in regulating behaviour and discuss future directions. As such, this review can help interpret *omics data by providing a comprehensive list of already identified genes and mechanisms that impact behaviour through changes in neuronal sensitivity. [ABSTRACT FROM AUTHOR]

Social interactions depend on individuals recognizing each other, and in this context many organisms use chemical signals to indicate species and sex (1). Cuticular hydrocarbon signals are used by insects, including Drosophila melanogaster, to distinguish conspecific individuals from others (1-3). These chemicals also contribute to intraspecific courtship and mating interactions (1-3). However, the possibility that sex and species identification are linked by common chemical signalling mechanisms has not been formally tested. Here we provide direct evidence that a single compound is used to communicate female identity among D. melanogaster, and to define a reproductive isolation barrier between D. melanogaster and sibling species. A transgenic manipulation eliminated cuticular hydrocarbons by ablating the oenocytes, specialized cells required for the expression of these chemical signals. The resulting oenocyte-less ([oe.sup.-]) females elicited the normal repertoire of courtship behaviours from males, but were actually preferred over wild-type females by courting males. In addition, wild-type males attempted to copulate with [oe.sup.-]- males. Thus, flies lacking hydrocarbons are a sexual hyperstimulus. Treatment of virgin females with the aversive male pheromone cis-vaccenyl acetate (cVA) significantly delayed mating of [oe.sup.-] females compared to wild-type females. This difference was eliminated when [oe.sup.-] females were treated with a blend of cVA and the female aphrodisiac (7Z,11Z)-heptacosadiene (7,11-HD), showing that female aphrodisiac compounds can attenuate the effects of male aversive pheromones. 7,11-HD also was shown to have a crucial role in heterospecifrc encounters. Specifically, the species barrier was lost because males of other Drosophila species courted [oe.sup.-] D. melanogaster females, and D. simulans males consistently mated with them. Treatment of [oe.sup.-] females with 7,11-HD restored the species barrier, showing that a single compound can confer species identity. These results identify a common mechanism for sexual and species recognition regulated by cuticular hydrocarbons., D. melanogaster produces hydrocarbons of various chain lengths, including unbranched alkanes, methyl-branched alkanes, alkenes and derivatives thereof. The alkenes are expressed sex-specifically, and have been associated with both sex and [...]

The fruitless (fru) gene in Drosophila melanogaster is a multifunctional gene that has sex-specific functions in the regulation of male sexual behavior and sex-nonspecific functions affecting adult viability and external morphology. While much attention has focused on fru's sex-specific roles, less is known about its sex-nonspecific functions. We have examined fru's sex-nonspecific role in embryonic neural development, fru transcripts from sex-nonspecific promoters are expressed beginning at the earliest stages of neurogenesis, and Fru proteins are present in both neurons and glia. In embryos that lack most or all fru function, FasII- and BP102-positive axons have defasciculation defects and grow along abnormal pathways in the CNS. These defects in axonal projections in fru mutants were rescued by the expression of specific UAS-fru transgenes under the control of a pan-neuronal scabrous-GAL4 driver. Our results suggest that one of fru's sex-nonspecific roles is to regulate the pathfinding ability of axons in the embryonic CNS.