Sex pheromones have been characterized only for species in the subfamilies Rutelinae and Melolonthinae; aggregation pheromones have been identified for two species in the Dynastinae. Melolonthines utilize mainly amino acid derivatives and terpenoid compounds, but sex pheromones of rutelines are fatty acid derivatives. Various other species utilize japonilure-type lactones that are produced by d...

Schizophyllum commune has thousands of mating types defined in part by numerous lipopeptide pheromones and their G-protein-coupled receptors. These molecules are encoded within multiple versions of two redundantly functioning B mating-type loci, B alpha and B beta. Compatible combinations of pheromones and receptors, produced by individuals of different B mating types, trigger a pathway of fert...

Mosquitoes of various species mate in swarms comprised of tens of thousands of flying males. In this study, we examined Aedes aegypti swarming behavior and identified associated chemical cues. Novel evidence is provided that Ae. aegypti females aggregate by means of olfactory cues, such as aggregation pheromones. Isolation of Ae. aegypti aggregation pheromones was achieved by aeration of confin...

Animals often use sex pheromones for mate choice and reproduction. As for other signals, the genetic control of the emission and perception of sex pheromones must be tightly coadapted, and yet we still have no worked-out example of how these two aspects interact. Most models suggest that emission and perception rely on separate genetic control. We have identified a Drosophila melanogaster gene,...

Intercellular chemical signaling in bacteria, commonly referred to as quorum sensing (QS), relies on the production and detection of compounds known as pheromones to elicit coordinated responses among members of a community. Pheromones produced by Gram-positive bacteria are comprised of small peptides. Based on both peptide structure and sensory system architectures, Gram-positive bacterial sig...

Many insects deposit marking pheromones following egg-laying that signal an occupied and thus sub-optimal resource. Herbivorous insects mark host fruit or other vegetative plant parts after depositing eggs, while insect parasitoids deposit such pheromones directly on the cuticle of a particular life stage of their prey. These oviposition marking pheromones (OMPs) are then recognized by conspeci...

Two anatomically and neurochemically distinct zones within the vomeronasal organ (VNO) and accessory olfactory bulb (AOB) have been identified that are responsible for the detection of pheromones. Using markers to distinguish between apical and basal neurons of the VNO neuroepithelium and rostral versus caudal AOB glomeruli, we examined immediate early gene immunoreactivity (IEG-IR) in gonadect...

Worker sterility in honeybees is neither absolute nor irreversible. Whether under queen or worker control, it is likely to be mediated by pheromones. Queen-specific pheromones are not exclusive to queens; workers with activated ovaries also produce them. The association between ovarian activation and queen-like pheromone occurrence suggests the latter as providing a reliable signal of reproduct...

Olfactory cues play an integral role in the organization of events that mediate reproductive success. In a variety of species, priming pheromones, in particular, are important for ensuring reproductive fitness. To date, very little research has focused on how male-emitted priming pheromones, such as those that regulate the onset of puberty and estrus synchronization in females, affect the repro...

Many species of female moths produce sex pheromones to attract conspecific males. Most moth species utilize Type I pheromones that consist of straight-chain compounds 10–18 carbons in length with a functional group of a primary alcohol, aldehyde, or acetate ester, and usually with several double bonds. Studies over the past three decades have demonstrated that female moths usually produce sex p...