Hostname: page-component-78c5997874-m6dg7 Total loading time: 0 Render date: 2024-11-13T03:33:15.119Z Has data issue: false hasContentIssue false

Maturation feeding and reproductive development in adult pine weevil, Hylobius abietis (Coleoptera: Curculionidae)

Published online by Cambridge University Press:  09 March 2007

D. Wainhouse*
Affiliation:
Forest Research, Alice Holt Lodge, Wrecclesham, Farnham, GU10 4LH,Surrey, UK
R. Boswell
Affiliation:
Forest Research, Alice Holt Lodge, Wrecclesham, Farnham, GU10 4LH,Surrey, UK
R. Ashburner
Affiliation:
Forest Research, Alice Holt Lodge, Wrecclesham, Farnham, GU10 4LH,Surrey, UK
*
*Fax: 01420 23653 E-mail: david.wainhouse@forestry.gsi.gov.uk

Abstract

Maturation feeding on conifer bark by newly emerged Hylobius abietis(Linnaeus) is essential for reproductive development. When feeding occurs on young conifer transplants, this weevil causes significant economic damage. Between emergence and oviposition however, weevils feed on bark from different sources but of unknown nutritional ‘quality’. The factors influencing the rate of feeding by males and females and female reproductive development were determined in laboratory bioassays using two contrasting food sources – the bark on different species of seedling conifer and on logs of mature trees. The nutritional ‘quality’ of bark was characterized by the concentration of nitrogen, total sugars, total polyphenols and resin. Regression models were used to show that overall, the rate of feeding on the bark of both seedlings and logs increased with weevil size and was negatively related to nitrogen concentration. The nitrogen concentration in seedling bark (mean 1.1%) was about three times higher than that of logs (mean 0.4%). The rate of reproductive development increased with nitrogen intake during feeding and the preoviposition period for weevils feeding on seedlings and logs was ~ 13 days and 46 days, respectively. Analysis of weevil mortality and of the weight gain of surviving weevils suggests that a nitrogen content of around 0.3% may be limiting for H. abietis. The possibility that nutritionally adequate food resources may be limiting for H. abietis is briefly discussed.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2004

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Genstat 5 Committee of the Statistics Department, Rothamsted Experimental Station, (1993) Genstat 5 Release 3 Reference manual. Oxford, Clarendon Press.Google Scholar
Långström, B. (1982) Abundance and seasonal activity of adult Hylobius-weevils in reforestation areas during first years following final felling. Communicationes Instituti Forestalis Fenniae 106, 122.Google Scholar
LeatherS.R., S.R.,Day, K.R. & Salisbury, A.N. (1999) The biology and ecology of the large pine weevil, Hylobius abietis (Coleoptera: Curculionidae): a problem of dispersal? Bulletin of Entomological Research, 89, 316.Google Scholar
Mole, S. & Waterman, P.G. (1987) A critical analysis of techniques for measuring tannins in ecological studies. I. Techniques for chemically defining tannins. Oecologia 72, 137147.Google Scholar
Munro, J.W. (1928) The biology and control of Hylobius abietis L. Forestry, 2, 3139.Google Scholar
Nordenhem, H. (1989) Age, sexual development, and seasonal occurrence of the pine weevil Hylobius abietis (L.). Journal of Applied Entomology, 108, 260270.CrossRefGoogle Scholar
ÖrlanderG., G.,NordlanderG., G.,Wallertz, K. & Nordenhem, H. (2000) Feeding in the crowns of Scots pine trees by the pine weevil Hylobius abietis. Scandinavian Journal of Forest Research 15, 194201.Google Scholar
ÖrlanderG., G.,Nordlander, G. & Wallertz, K. (2001) Extra food supply decreases damage by the pine weevil Hylobius abietis. Scandinavian Journal of Forest Research, 16, 450454.Google Scholar
SauvestyA., A.,Page, F. & Huot, J. (1992) A simple method for extracting plant phenolic compounds. Canadian Journal of Forest Research 22, 654659Google Scholar
Slansky, F. (1993) Nutritional ecology: the fundamental quest for nutrients. pp. 2991in Stamp, N.E. & Casey, T.M. (Eds) Caterpillars: ecological and evolutionary constraints on foraging. New York, Chapman and Hall.Google Scholar
StatSoft (1995) Statistica for Windows. 2nd edn. Tulsa, Oklahoma, StatSoft Inc.Google Scholar
Wainhouse, D. & Ashburner, R. (1996) The influence of genetic and environmental factors on a quantitative defensive trait in spruce. Functional Ecology 10 137143.Google Scholar
WainhouseD., D.,AshburnerR., R.,Ward, E. & Rose, J. (1998) The effect of variation in light and nitrogen on growth and defence in young Sitka spruce. Functional Ecology 12, 561572.Google Scholar
WainhouseD., D.,Ashburner, R. & Boswell, R. (2001) Reproductive development and maternal effects in the pine weevil Hylobius abietis. Ecological Entomology 26, 655661.Google Scholar
Ward, E. & Deans, J.D. (1993) A simple method for the routine extraction and quantification of non-structural sugars in tree tissues. Forestry 66, 171180.Google Scholar