In burying beetles, Nicrophorus spp. (Coleoptera: Silphidae: Nicrophorinae) mate finding is mediated by male produced volatile compounds. To date, pheromone components of only two species have been identified. In an attempt to better understand the evolution of male pheromone signaling in burying beetles, we investigated the male released volatiles of ten Nicrophorus species and one closely related nicrophorine species, Ptomascopus mori. Volatiles emitted by calling males were collected in the laboratory by means of solid phase micro extraction and analyzed using gas chromatography coupled with mass spectrometry. Identified volatiles included short chain esters of 4-methylcarboxylic acids, terpenoids, and some other aliphatic compounds. The long-range volatile signals of the burying beetle species included in this study are blends of two to seven components. We found that methyl or ethyl esters of 4-methylheptanoic acid and 4-methyloctanoic acid are produced by eight of the ten investigated Nicrophorus species. These esters may play a key role in chemical communication. Their widespread occurrence suggests that these compounds did not evolve recently, but appeared relatively early in the phylogeny of the genus. Although Ptomascopus is considered the sister genus of Nicrophorus, P. morio males do not produce any of the Nicrophorus compounds, but release 3-methylalkan-2-ones, which are absent in Nicrophorus. A better understanding of the evolution of burying beetle pheromones, however, will only be possible once more species have been studied.
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http://dx.doi.org/10.1007/s10886-017-0892-2 | DOI Listing |
PLoS One
January 2025
Department of Entomology and Plant Pathology, Oklahoma State University, Stillwater, OK, United States of America.
Among the most immediate drivers of American burying beetle (Nicrophorus americanus Olivier) declines, nontarget toxicity to pesticides is poorly understood. Acute, episodic exposure to neonicotinoid insecticides at environmentally relevant concentrations is linked to negative impacts on beneficial terrestrial insect taxa. Beyond mortality, behavioral indicators of toxicity are often better suited to assess sublethal effects of residual concentrations in the environment.
View Article and Find Full Text PDFEcol Evol
January 2025
Henan Field Observation and Research Station of Headwork Wetland Ecosystem of the Central Route of South-To-North Water Diversion Project College of Life Sciences, Nanyang Normal University Nanyang China.
Resource availability should have consequences for life-history functions and trade-offs among them because it influences the amounts of resources allocated to different functions. Nutritional status during a key developmental window (sexual maturation) may also have an important impact on life-history functions and such trade-offs. However, less is known about whether and how they interact to influence the resource allocation of individuals.
View Article and Find Full Text PDFNeotrop Entomol
December 2024
Depto de Zoologia, Instituto de Ciências Biológicas, Univ de Brasília, Brasília, Distrito Federal, Brazil.
The present study reports new behavioral records for Oxysternon palemo Castelnau, 1840 in Cerrado. According to its nesting habits and resource allocation, this species of dung beetle is traditionally classified as coprophagous and paracoprid, transporting portions of dung through tunnels excavated below the resource. We observed a male individual moving a pequi seed (Caryocar brasiliensis Cambess.
View Article and Find Full Text PDFEcol Evol
November 2024
Institute of Ecology and Evolution, School of Biological Sciences University of Edinburgh Edinburgh UK.
The existence of life-history trade-offs is a fundamental assumption of evolutionary biology and behavioural ecology, yet empirical studies have found mixed evidence for this. Such trade-offs are expected when individuals vary in how they allocate their limited resource budgets between different life-history functions (variation in resource allocation), but they may be masked when individuals vary in how many resources they have acquired that they can later allocate to life-history functions (variation in resource acquisition). We currently lack studies on the extent to which individual differences in behaviour reflect variation between individuals in resource acquisition and resource allocation.
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