The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.
The Role of Host Plant Resistance in the Colonization Behavior and Ecology of Bark Beetles (Coleoptera: Scolytidae)
Abstract
Unlike most phytophagous insects, the reproduction of primary bark beetles (Coleoptera: Scolytidae) is contingent on host mortality. Consequently, there have been intense selective pressures on trees for properties which confer resistance to attack, and likewise, on the insect for increased behavioral complexity by which to overcome these defenses. In this study, we examined the relationship between the physiology of Pinus contorta var. latifolia and the behavior of the bark beetle, Dendroctonus ponderosae. Host mortality is a discrete outcome which is contingent on the quantitative interaction between host resistance and beetle numbers. At low attack densities, trees respond by confining beetles and their associated fungi within necrotic lesions containing toxic or inhibitory compounds. Beyond a critical "threshold of attack," however, the defensive capacity of the tree is exhausted, and mortality occurs. This threshold occurred at °40 galleries/m 2 in our experimental stands. The reproductive success of the bark beetle is directly related to the depletion of host defenses through concentrated attack. At sufficiently high attack densities, °80 galleries/m 2, the potential suppressive effect of the host on brood development is not manifested. Increased beetle numbers, however, cause an exponential decline in brood production due to intraspecific competition. Consequently, there is an optimal density, °62 attacks/m 2 at which reproduction and survival of the beetle is maximized. Dendroctonus ponderosae utilize defensive secretions as precursors and synergists of aggregation pheromones, and thereby, elicit maximum responses from flying beetles while the host's production of toxins is at its maximum. This mechanism also ensures that the attack will terminate once the tree has been rendered suitable for brood development and, thus, minimizes the deleterious effect of intraspecific competition. Such an interaction, in which all trees could theoretically be colonized regardless of their resistance capacity, cannot result in a stable host—parasite system. Conifers, however, seem to be able to interfere with bark beetle communication. Pheromone synthesis within the hindgut and emission from the entrance site are distinct events, and beetles contained within a copious flow of resin seem unable to elicit attraction. This ability to interrupt the beetles' communication sequence, however, is inversely related to the number of beetles initiating localized attacks. Consequently, the colonization sequence reflects the outcome of a dynamic interaction between the tree and the initial "pioneer" beetles.
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Cites
Rudinsky, J. A. (1962) · Annual Review of Entomology · doi:10.1146/annurev.en.07.010162.001551 · Cited by 300
REACTIONS OF LODGEPOLE PINE TO ATTACK BY DENDROCTONUS PONDEROSAE HOPKINS AND BLUE STAIN FUNGI
Reid, R. W., Whitney, H. S., & Watson, J. A. (1967) · Canadian Journal of Botany · doi:10.1139/b67-116 · Cited by 252
Raffa, K. F., & Berryman, A. A. (1982) · Environmental Entomology · doi:10.1093/ee/11.2.486 · Cited by 221
Self-citationPHEROMONES IN IPS(COLEOPTERA: SCOLYTIDAE): OCCURRENCE AND PRODUCTION
Vité, J. P., Bakke, A., & Renwick, J. A. A. (1972) · The Canadian Entomologist · doi:10.4039/ent1041967-12 · Cited by 213
Hodges, J. D., Elam, W. W., Watson, W. F., & Nebeker, T. E. (1979) · The Canadian Entomologist · doi:10.4039/ent111889-8 · Cited by 189
Production of verbenol pheromone by a bacterium isolated from bark beetles
Brand, J. M., Bracke, J. W., Markovetz, A. J., WOOD, D. L., & Browne, L. E. (1975) · Nature · doi:10.1038/254136a0 · Cited by 185
Mountain Pine Beetle Brood Production in Relation to Thickness of Lodgepole Pine Phloem1
Amman, G. D. (1972) · Journal of Economic Entomology · doi:10.1093/jee/65.1.138 · Cited by 173
MONOTERPENE VARIATION IN PONDEROSA PINE XYLEM RESIN RELATED TO WESTERN PINE BEETLE PREDATION
Sturgeon, K. B. (1979) · Evolution · doi:10.1111/j.1558-5646.1979.tb04736.x · Cited by 156
Moeck, H. A., Wood, D. L., & Lindahl, K. Q. (1981) · Journal of Chemical Ecology · doi:10.1007/bf00988635 · Cited by 149
Bark Beetle Attractants: Trans-verbenol isolated from Dendroctonus
Pitman, G. B., Vite, J. P., Kinzer, G. W., et al. (1968) · Nature · doi:10.1038/218168a0 · Cited by 129
Cited by
Anatomical and chemical defenses of conifer bark against bark beetles and other pests
Franceschi, V. R., Krokene, P., Christiansen, E., & Krekling, T. (2005) · New Phytologist · doi:10.1111/j.1469-8137.2005.01436.x · Cited by 1,120
The interdependence of mechanisms underlying climate-driven vegetation mortality
McDowell, N. G., Beerling, D. J., Breshears, D. D., Fisher, R. A., Raffa, K. F., & Stitt, M. (2011) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2011.06.003 · Cited by 1,020
Self-citationFettig, C. J., Klepzig, K. D., Billings, R. F., Munson, A. S., Nebeker, T. E., Negrón, J. F., & Nowak, J. T. (2007) · Forest Ecology and Management · doi:10.1016/j.foreco.2006.10.011 · Cited by 529
Observed and anticipated impacts of drought on forest insects and diseases in the United States
Kolb, T. E., Fettig, C. J., Ayres, M. P., Bentz, B. J., Hicke, J. A., Mathiasen, R., Stewart, J. E., & Weed, A. S. (2016) · Forest Ecology and Management · doi:10.1016/j.foreco.2016.04.051 · Cited by 409
Raffa, K. F., & Berryman, A. A. (1983) · The Canadian Entomologist · doi:10.4039/ent115723-7 · Cited by 167
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Metadata
- Authors
- Raffa, K. F., & Berryman, A. A.
- Venue
- Ecological Monographs
- Publisher
- Wiley
- Published
- 1983-03
- Volume
- 53
- Issue
- 1
- Pages
- 27-49
- ISSN
- 0012-9615 (ISSN-L)
- 1557-7015
- OpenAlex
- W2062374893
- Cited by
- 668
- References
- 24
- FWCI
- 13.25
- Type
- journal article
- Language
- en
- Open access
- closed
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