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Dieback and recovery in poplar and attack by the hornet clearwing moth, Sesia apiformis (Clerck) (Lepidoptera: Sesiidae)

Published online by Cambridge University Press:  12 November 2007

N.A. Straw ,
G. Green  and
D.T. Williams
N.A. Straw*
Affiliation:
Tree Health Division, Forest Research, Alice Holt Lodge, Wrecclesham, Farnham, Surrey, GU10 4LH, UK
G. Green
Affiliation:
Tree Health Division, Forest Research, Alice Holt Lodge, Wrecclesham, Farnham, Surrey, GU10 4LH, UK
D.T. Williams
Affiliation:
Tree Health Division, Forest Research, Alice Holt Lodge, Wrecclesham, Farnham, Surrey, GU10 4LH, UK
*
*Author for correspondence Fax: 01420 23653 Email: [email protected]
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Abstract

A survey of 801 poplar trees in central east England in 1999 demonstrated a correlation between crown dieback and infestation by hornet clearwing moth (Sesia apiformis), induced by a period of drought in 1995–1996. To determine whether trees colonised by S. apiformis would subsequently deteriorate and die or whether they could recover despite infestation and damage to the stem, all trees in the original survey were re-assessed in 2001, 2003 and 2005. The repeat surveys showed that trees with 70% or less crown dieback in 1999 replaced their canopy and generally improved by 2005, irrespective of the numbers of S. apiformis in the stem, whereas trees that had 75% or more crown dieback in 1999 either died or declined further. The presence of S. apiformis did not prevent tree recovery, and there was little evidence that infestation slowed the rate of recovery. Populations of S. apiformis, measured in terms of the numbers of adult emergence holes visible in the base of the trees, decreased between 2001 and 2005 at the same time as the amount of dieback visible in the canopy of the poplars markedly decreased. However, the fall in numbers of emergence holes at this time reflected a decline in larval establishment 2–3 years earlier, and indicated that the moth population had responded to a more rapid restoration in the internal state of the trees, which was not reflected immediately by the gradual replacement of dead branches and reduction in dieback symptoms.

Keywords

crown diebackdamageplant healthPopulus×euramericanapoplarSesia apiformis
Type
Research Article
Information
Bulletin of Entomological Research , Volume 97 , Issue 6 , December 2007 , pp. 555 - 567
Copyright
Copyright © Cambridge University Press 2007

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References

Arundell, J.C. & Straw, N.A. (2001) Hornet clearwing moth (Sesia apiformis [Clerck]) and dieback of poplars in eastern England. Arboricultural Journal 25, 235–253.CrossRefGoogle Scholar
Binns, W.O. (1980) Trees and Water. Arboriculture Leaflet No. 6. 19 pp. London, HMSO.Google Scholar
Bouchet, J. (1962) Attacks of Sesia apiformis on poplars in Anjou and the Department des Deux-Sèvres. Phytoma 14, 29–31.Google Scholar
Cedervind, J. & Långstrom, B. (2003) Tree mortality, foliage recovery and top-kill in stands of Scots pine (Pinus sylvestris) subsequent to defoliation by the pine looper (Bupalus piniaria). Scandinavian Journal of Forest Research 18, 505–513.CrossRefGoogle Scholar
Chrystal, R.N. (1937) Insects of the British Woodlands. 370 pp. London, Frederick Warne & Co. Ltd.Google Scholar
Coleman, D.A. & Boyle, M.K. (2000) The status and ecology of the hornet moth, Sesia apiformis (Clerck) (Lepidoptera: Sesiidae), in suburban south London. British Journal of Entomology and Natural History 13, 99–106.Google Scholar
Escherich, K. (1931) Die Forstinsekten Mitteleuropas, Band 3. 825 pp. Berlin, Paul Parey.Google Scholar
Gibbs, J.N. & Greig, J.W. (1997) Biotic and abiotic factors affecting the dying back of pedunculate oak Quercus robur L. Forestry 70, 399–406.CrossRefGoogle Scholar
Hanks, L.M., Paine, T.D. & Millar, J.G. (1991) Mechanisms of resistance in Eucalyptus against larvae of the Eucalypus longhorned borer (Coleoptera: Cerambycidae). Environmental Entomology 20, 1583–1588.CrossRefGoogle Scholar
Heath, J. & Emmet, A.M. (Eds) (1985) The Moths and Butterflies of Great Britain and Ireland. Vol. 2 Cossidae – Heliodinidae. 460 pp. Colchester, UK, Harley Books Ltd.Google Scholar
Huberty, A.F. & Denno, R.F. (2004) Plant water stress and its consequences for herbivorous insects: a new synthesis. Ecology 85, 1383–1398.CrossRefGoogle Scholar
Innes, J.L. (1990) Assessment of Tree Condition. Forestry Commission Field Book 12. 96 pp. London, HMSO.Google Scholar
Jobling, J. (1990) Poplars for Wood Production and Amenity. Forestry Commission Bulletin No. 92. 84 pp. London, HMSO.Google Scholar
Kolomoets, T.P., Sinel-Nikova, A.M., Kovalenko, V.M. & Danilkina, N.V. (1978) The great poplar clearwing. Zashchita Rastenii 1, 1–36.Google Scholar
Koricheva, J., Larsson, S. & Haukioja, E. (1998) Insect performance on experimentally stressed woody plants: a meta-analysis. Annual Review of Entomology 43, 195–216.CrossRefGoogle ScholarPubMed
Kozlowski, T.T. & Pallardy, S.G. (1997) Growth Control in Woody Plants. 641 pp. London, Academic Press.Google Scholar
Kozlowski, T.T., Kramer, P.J. & Pallardy, S.G. (1991) The Physiological Ecology of Woody Plants. 657 pp. London, Academic Press.Google Scholar
Larsson, S. (1989) Stressful times for the plant stress – insect performance hypothesis. Oikos 56, 277–283.CrossRefGoogle Scholar
Larsson, S. & Tenow, O. (1984) Areal distribution of a Neodiprion sertifer (Hym., Diprionidae) outbreak on Scots pine as related to stand condition. Holarctic Ecology 7, 81–90.Google Scholar
Mattson, W.J. & Haack, R.A. (1987) The role of drought stress in provoking outbreaks of phytophagous insects pp. 365–407in Barbosa, P. & Schultze, J.C. (Eds) Insect Outbreaks. London, Academic Press.CrossRefGoogle Scholar
Parker, J. (1970) Effects of defoliation and drought on root food reserves in sugar maple seedling. US Department Agriculture Forest Service Research Paper NE-169.Google Scholar
Parker, J. & Patton, R.L. (1975) Effects of drought and defoliation on some metabolites on roots of black oak seedlings. Canadian Journal of Forest Research 5, 457–463.CrossRefGoogle Scholar
Payne, R., Murray, D., Harding, S., Baird, D., Soutar, D. & Lane, P. (2002) GenStat® for Windows™ (6th Edition). Oxford, VSN International.Google Scholar
Peace, T.R. (1962) Pathology of Trees and Shrubs. 723 pp. Oxford, Clarendon Press.Google Scholar
Phillips, D.H. & Burdekin, D.A. (1992) Diseases of Forest and Ornamental Trees. 581 pp. London, MacMillan Press Ltd.CrossRefGoogle Scholar
Schnaiderowa, J. (1974) Aegeria apiformis, Aegeriidae, Lep. Prace Instytutu Badawczego Lesnictwa 427–432, 63–90.Google Scholar
Schwenke, W. (1978) Die Forstschädlinge Europas. 467 pp. Berlin, Paul Parey.Google Scholar
South, R. (1961) The Moths of the British Isles, Series I. 379 pp. London, Frederick Warne & Co. Ltd.Google Scholar
Speight, M.R. (1986) Tree pests – 13. Goat and clearwing moths. (Lepidoptera: Cossidae and Sesiidae). Arboricultural Journal 10, 113–116.CrossRefGoogle Scholar
Šrot, M. (1963) Widespread outbreaks of Paranthrene [Sciapteron] tabaniformis and Aegeria [Sesia] apiformis in poplar stands throughout Czechoslovakia. Lesnický Časopis Ročník, Praha 9, 145–158.Google Scholar
Šrot, M. (1969) New data on the bionomics of Aegeria apiformis Cl. and its possible control in Czechoslovakia. Práce Výzkumného Ústavu Lesního Hospodářství a Myslivosti 38, 5–24.Google Scholar
Tattar, T.A. (1978) Diseases of Shade Trees. 361 pp. London, Academic Press.Google Scholar
Thomas, F.M., Blank, R. & Hartmann, G. (2002) Abiotic and biotic factors and their interactions as causes of oak decline in Central Europe. Forest Pathology 32, 277–307.CrossRefGoogle Scholar
Vuola, M. & Korpela, S. (1976) The biology of the Finnish species of Sesiidae and Cossidae (Lepidoptera). I. Aegeria apiformis and A. melanocephala. Notulae Entomologicae 56, 121–126.Google Scholar
Wargo, P.M. (1972) Defoliation-induced chemical changes in sugar maple roots stimulate growth of Armillaria mellea. Phytopathology 62, 1278–1282.CrossRefGoogle Scholar
Wargo, P.M. (1984) How stress predisposes trees to attack by Armillaria mellea – a hypothesis. pp. 115–121in Kile, G.A. (Ed.) Root and Butt Rots of Forest Trees. Melbourne, CSIRO.Google Scholar
West, C. (1985) Factors underlying the late seasonal appearance of the lepidopterous leaf-mining guild on oak. Ecological Entomology 10, 111–120.CrossRefGoogle Scholar
White, T.C.R. (1984) The abundance of invertebrate herbivores in relation to the availability of nitrogen in stressed food plants. Oecologia 63, 90–105.CrossRefGoogle Scholar
White, T.C.R. (1993) The Inadequate Environment: Nitrogen and the Abundance of Animals. 425 pp. Berlin, Springer-Verlag.CrossRefGoogle Scholar