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Weissflog, J.

Publications and source records attributed to Weissflog, J..

3 recordsLinked to original sources

Offspring chemical control of adult reproductive transitions in a social insect

Parental care enhances offspring survival and growth but often entails a trade-off in which caregivers temporarily suppress their own reproduction to invest in existing young. In vertebrates, these parental reproductive cycles are controlled by offspring-derived cues that reduce or suppress parental fertility. While many insects display obligate parental care, the role of offspring cues in regulating adult reproduction remains unresolved outside advanced eusocial taxa, where reproductive cycles have largely been lost. Here, we investigate reproductive cycles in the clonal raider ant Ooceraea biroi, in which totipotent females alternate between caring for larvae and laying eggs. Using custom behavioral assays, we show that larvae inhibit adult reproduction without physical contact, implicating volatile cues. Chemical analyses identified a previously undescribed larva-specific compound, methyl 3-ethyl-2-hydroxy-4-methylpentanoate (MEHMP), which is absent from other developmental stages and ant species. Exposure to synthetic MEHMP recapitulated the inhibitory effect of larval volatiles, confirming its role as a pheromone that suppresses adult egg laying. To our knowledge, this is the first brood pheromone described in ants. By providing a direct chemical link between offspring presence and parental reproductive suppression, our findings underscore the central role of offspring signals in mediating parental reproductive investment across animals that care for their young. Significance StatementParental care enhances offspring survival but induces profound physiological changes in caregivers. A common feature across animals is that adults temporarily suppress their own reproduction while caring for the young. The offspring cues enforcing these cycles remain poorly understood, especially in insects. Using the clonal raider ant Ooceraea biroi, in which all females alternate between reproduction and brood care, we identify a larval pheromone that suppresses adult egg laying. This pheromone is a previously undescribed volatile chemical compound, and exposure to its synthetic version mimics the full biological effect of larvae volatiles. By providing a direct link between offspring presence and adult reproductive suppression, our work highlights how offspring can chemically control the reproduction of their caregivers.

animal behavior and cognition↗

Large-scale characterization of sex pheromone communication systems in Drosophila

Insects use sex pheromones as a reproductive isolating mechanism to attract conspecifics and repel heterospecifics. Despite the profound knowledge of sex pheromones, little is known about the coevolutionary mechanisms and constraints on their production and detection. Using whole-genome sequences to infer the kinship among 99 drosophilids, we investigate how phylogenetic and chemical traits have interacted at a wide evolutionary timescale. Through a series of chemical syntheses and electrophysiological recordings, we identify 51 sex-specific compounds, many of which are detected via olfaction. Behavioral analyses reveal that many of the 42 male-specific compounds are transferred to the female during copulation and mediate female receptivity and/or male courtship inhibition. Measurement of phylogenetic signals demonstrates that sex pheromones and their cognate olfactory channels evolve rapidly and independently over evolutionary time to guarantee efficient intra- and inter-specific communication systems. Our results show how sexual isolation barriers between species can be reinforced by species-specific olfactory signals.

evolutionary biology↗

Mate discrimination among subspecies through a conserved olfactory pathway

Signaling mechanisms underlying the sexual isolation of species are poorly understood. Using four subspecies of Drosophila mojavensis as a model, we identify two behaviorally active male-specific pheromones. One functions as a conserved male anti-aphrodisiac in all subspecies and acts via gustation. The second induces female receptivity via olfaction exclusively in the two subspecies that produce it. Genetic analysis of the cognate receptor for the olfactory pheromone indicates an important role for this sensory pathway in promoting sexual isolation of subspecies, in collaboration with auditory signals. Surprisingly, the peripheral sensory pathway detecting this pheromone is conserved molecularly, physiologically and anatomically across subspecies. These observations imply that subspecies-specific behaviors arise from differential interpretation of the same peripheral cue, reminiscent of sexually conserved detection but dimorphic interpretation of male pheromones in D. melanogaster. Our results reveal that, during incipient speciation, pheromone production, detection and interpretation do not necessarily evolve in a coordinate manner.

neuroscience↗