Skip to main content
Log in

Attraction of the Larval Predator Elater ferrugineus to the Sex Pheromone of Its Prey, Osmoderma eremita, and Its Implication for Conservation Biology

  • Published:
Journal of Chemical Ecology Aims and scope Submit manuscript

Abstract

Elater ferrugineus is a threatened click beetle inhabiting old hollow trees. Its larvae consume larvae of other saproxylic insects including the threatened scarab beetle Osmoderma eremita. Recently, (R)-(+)-γ-decalactone was identified as a male-produced sex pheromone of O. eremita. Here we present evidence that E. ferrugineus adults use this odor as a kairomone for location of their prey. In field trapping experiments, significantly more trapping events of E. ferrugineus beetles were observed in Lindgren funnel traps baited with (R)-(+)-γ-decalactone than in control traps (20 vs. 1, respectively). Analyses of headspace collections from E. ferrugineus beetles indicate that the predator itself does not produce the substance. Both sexes were attracted to the prey pheromone, suggesting that E. ferrugineus males use the odor as an indirect cue for location of mates or of the tree hollows, which make up their habitat. When compared to pitfall traps, the Lindgren system was significantly more effective in trapping E. ferrugineus, and no difference could be established for O. eremita, showing the high potential to use odor-based systems to catch both species. We suggest that (R)-(+)-γ-decalactone could be used as a master signal in monitoring programs for these vulnerable beetle species, which are both regarded as indicators of the associated insect fauna of the threatened habitat of old hollow trees.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

REFERENCES

  • Aldrich, J. R. 1999. Predators, pp. 357–381, in J. Hardie and A. K. Minks (eds.). Pheromones of Non-Lepidopteran Insects Associated with Agricultural Plants. CAB International, New York.

    Google Scholar 

  • Anonymous, 1992. Directive 92/43 of the Council of the European Community on the Conservation of Habitats and Wild Fauna and Flora. European Community, Brussels.

  • Bakke, A. and Kvamme, T. 1981. Kairomone response in Thanasimus predators to pheromone components of Ips typographus. J. Chem. Ecol. 7:305–312.

    Google Scholar 

  • Borden, J. H. 1997. Disruption of semiochemical-mediated aggregation in bark beetles, pp. 421–438, in R. T. Cardé and A. K. Minks (eds.). Insect Pheromone Research: New Directions. Chapman and Hall, New York.

    Google Scholar 

  • Borg-Karlsson, A.-K, Ågren, L., Dobson, H., and BergstrÖm, G. 1988. Identification and electroantennographic activity of sex-specific geranyl esters in an abdominal gland of female Agriotes obscurus (L.) and A. lineatus (L.) (Coleoptera, Elateridae). Experentia 44:531–534.

    Google Scholar 

  • Dajoz, R. 2000. Insects and Forests. Intercept Publishing, London, pp. 515–533.

    Google Scholar 

  • Eliasson, P. and Nilsson, S. G. 2002. “You should hate young oaks and young noblemen”: The environmental history of oaks in eighteenth-and nineteenth-century Sweden. Environ. Hist. 7:657–675.

    Google Scholar 

  • Frazier, J. L., Nebecker, T. E., Mizell, R. F., and Calvert, W. H. 1981. Predatory behavior of the clerid beetle Thanasimus dubius (Coleoptera: Cleridae) on the southern pine beetle (Coleoptera: Scolytidae). Can. Entomol. 113:35–43.

    Google Scholar 

  • Gärdenfors, U. (ed.) 2000. RÖdlistade arter i Sverige 2000 [The 2000 Red List of Swedish Species]. ArtDatabanken, Uppsala, Sweden.

  • Hannah, L., Carr, J. L., and Lankerani, A. 1995. Human disturbance and natural habitat: A biome level analysis of a global data set. Biodivers. Conserv. 4:128–155.

    Google Scholar 

  • Hansen, V. 1966. Danmarks Fauna, Biller XXIII, Smældere of Pragtbiller. Gads Forlag, København, pp. 36–37 (in Danish).

  • Hedin, J. and Ranius, T. 2002. Using radio telemetry to study dispersal of the beetle Osmoderma eremita, an inhabitant of tree hollows. Comput. Electron. Agric. 35:171–180.

    Google Scholar 

  • Larsson, M. C., Hedin, J., Svensson, G. P., Tolasch, T., and Francke, W. 2003. Characteristic odor of Osmoderma eremita identified as a male-released pheromone. J. Chem. Ecol. 29:575–587.

    Google Scholar 

  • Luce, J.-M 1996. Osmoderma eremita (Scopoli 1763), pp. 64–69, in P. J. van Helsdingen, L. Willemse, and M. C. D. Speight (eds.). Background Information on Invertebrates of the Habitats Directive and the Bern Convention. Part 1: Crustacea, Coleoptera, and Lepidoptera. Council of Europe, Strasbourg, France.

    Google Scholar 

  • Nilsson, S. G. 1997. Forests in the temperate-boreal transition: Natural and man-made features. Ecol. Bull. 46:61–71.

    Google Scholar 

  • Nilsson, S. G. and Baranowski, R. 1994. Indicators of megatree continuity—Swedish distribution of click beetles (Coleoptera, Elateridae) dependent on hollow trees. Entomol. Tidskr. 115(3):81–97 (in Swedish, English summary).

    Google Scholar 

  • Nilsson, S. G., Hedin, J., and Niklasson, M. 2001. Biodiversity and its assessment in boreal and nemoral forests. Scand. J. For. Res. 16 (Suppl. 3):10–26.

    Google Scholar 

  • Palm, T. 1959. Die Holz-und Rinden-Käfer der Süd-und Mittelschwedishen Laubbäume. Lund, Sweden: Opuscula Entomologica supplementum XVI (in German, English summary).

  • Raffa, K. F. and Dahlsten, D. L. 1995. Differential responses among natural enemies and prey to bark beetle pheromones. Oecologia 102:17–23.

    Google Scholar 

  • Ranius, T. 2001. Constancy and asynchrony of Osmoderma eremita populations in tree hollows. Oecologia 126:208–215.

    Google Scholar 

  • Ranius, T. 2002a. Osmoderma eremita as an indicator of species richness of beetles in tree hollows. Biodivers. Conserv. 11:931–941.

    Google Scholar 

  • Ranius, T. 2002b. Influence of stand size and quality of tree hollows on saproxylic beetles in Sweden. Biol. Conserv. 103:85–91.

    Google Scholar 

  • Ranius, T. and Hedin, J. 2001. The dispersal rate of a beetle, Osmoderma eremita, living in tree hollows. Oecologia 126:363–370.

    Google Scholar 

  • Ranius, T. and Nilsson, S. G. 1997. Habitat of Osmoderma eremita Scop. (Coleoptera: Scarabaeidae), a beetle living in hollow trees. J. Insect Conserv. 1:193–204.

    Google Scholar 

  • Siegel, S. and Castellan, N. J. 1998. Nonparametric Statistics for the Behavioral Sciences, 2nd edn. McGraw-Hill, New York.

    Google Scholar 

  • Svensson, G. P., Larsson, M. C., and Hedin, J. 2003. Air sampling of its pheromone to monitor the occurrence of Osmoderma eremita, a threatened beetle inhabiting hollow trees. J. Insect Conserv. 7:189–198.

    Google Scholar 

  • Tóth, M., Furlan, L., Yatsynin, V. G., Ujváry, I., Szarukán, I., Imre, Z., Subchev, M., Tolasch, T., and Francke, W. 2002. Identification of sex pheromone composition of click beetle Agriotes brevis Candeze. J. Chem. Ecol. 28:1641–1652.

    Google Scholar 

  • Weslien, J. 1994. Interaction within and between species at different densities of the bark beetle Ips typographus and its predator Thanasimus formicarius. Entomol. Exp. Appl. 71:133–143.

    Google Scholar 

  • Wood, D. L. 1982. The role of pheromones, kairomones, and allomones in the host selection behavior of bark beetles. Annu. Rev. Entomol. 27:411–446.

    Google Scholar 

  • Yatsynin, V. G., Rubanova, E. V., and Okhrimenko, N. V. 1996. Identification of female-produced sex pheromones and their geographical differences in pheromone gland extract composition from click beetles (Col., Elateridae). J. Appl. Entomol. 120:463–466.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Svensson, G.P., Larsson, M.C. & Hedin, J. Attraction of the Larval Predator Elater ferrugineus to the Sex Pheromone of Its Prey, Osmoderma eremita, and Its Implication for Conservation Biology. J Chem Ecol 30, 353–363 (2004). https://doi.org/10.1023/B:JOEC.0000017982.51642.8c

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/B:JOEC.0000017982.51642.8c

Navigation