Sex pheromones play a central role in intersexual communication for reproduction in many organisms. Particularly in insects, reproductive isolation that leads to speciation is often achieved by shifts of pheromone chemistries. However, the divergence and evolution of pheromones remain largely unknown. This study reveals a unique evolutionary consequence for terpenoid pheromones in coccoid insects. Coccoids, such as mealybugs, show clear sexual dimorphism: males are dwarf and short-lived, whereas females are wingless and almost immobile. Female pheromones are therefore indispensable for males to navigate for sexual reproduction, but some females can reproduce asexually. Interestingly, a derived asexual lineage that reproduces by parthenogenesis coexists with its ancestral lineage that reproduces sexually in a population of the pineapple mealybug, Here, we isolated, characterized and synthesized a novel monoterpene, (-)-(-1,2-dimethyl-3-methylenecyclopentyl)acetaldehyde, as a pheromone of the sexual females of This monoterpene aldehyde, with an irregular linkage of isoprene units, is notable, because all mealybug pheromones previously reported are carboxylic esters of terpenols. This compound was, however, never produced by the asexual females. As a consequence of acquiring parthenogenetic reproduction, the asexual females appear to have abandoned the production of the sex pheromone, which had been essential to attracting males in their ancestors.
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http://dx.doi.org/10.1098/rsif.2017.0027 | DOI Listing |
J Chem Ecol
January 2025
Embrapa Recursos Genéticos e Biotecnologia, Laboratório de Semioquímicos, Brasília, DF, 70297-400, Brazil.
The small black stem bug, Paratibraca (= Glyphepomis) spinosa (Campos and Grazia 1998), is a rice pest in Brazil and is part of a complex of stink bugs that includes Oebalus poecilus (Dallas) and Tibraca limbativentris Stål. Together, these pentatomid species pose a serious threat to rice crops throughout South America. In this study, we identified the sex pheromone of P.
View Article and Find Full Text PDFInsects
January 2025
Department of Environmental Management, Institute of Environmental Engineering, RUDN University, 6 Miklukho-Maklaya St., Moscow 117198, Russia.
Tomato leaf miner (Meyrick) (Lepidoptera: Gelechiidae) has gained the status of major pest globally. Integrated pest management (IPM) consists of different control methods. This field study was conducted to evaluate the influence of different pheromone-based traps to attract the male population and the potential of sticky pads of four different colors in capturing the adults in the absence of pheromone lures.
View Article and Find Full Text PDFInsects
December 2024
Institute of Chemistry, Pontificia Universidad Católica de Valparaíso, Valparaíso 2340000, Chile.
The poplar moth, (Lepidoptera: Lyonetiidae), is widely distributed across Europe, Asia, and parts of Africa. It was first identified in Chile in 2015 and has since become a significant pest in the agricultural sector. Additionally, economic losses are further aggravated by the presence of pupae in nearby fruit orchards.
View Article and Find Full Text PDFInsects
December 2024
Nature Research Centre, Akademijos St. 2, LT-08412 Vilnius, Lithuania.
The pheromones of crane flies (Tipulidae), one of the largest families within the order Diptera (over 15,000 species), are unknown. The aim of our study was to identify the chemical compounds involved in communication in , a representative species of the family. Female cuticular washes were found to be attractive to males in a bioassay.
View Article and Find Full Text PDFInt J Mol Sci
January 2025
Pheromone Production Center, "Raluca Ripan" Institute for Research in Chemistry, "Babes-Bolyai" University, 30 Fantanele Street, 400294 Cluj-Napoca, Romania.
The nun moth, L. (Linnaeus, 1758), is one of the most important defoliators of coniferous forests in Europe and Asia. In sexual communication, females produce three epoxides and an alkene: (-)-disparlure [(7,8)--7,8-epoxy-2-methyloctadecane], (+)-monachalure [(7,8)--7,8-epoxyoctadecane], (-)-monachalure [(7,8)--7,8-epoxyoctadecane], and their corresponding olefins.
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