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Spatial patterns of within-tree Enaphalodes rufulus (Coleoptera: Cerambycidae) attacks during outbreak conditions in the Ozark National Forest in Arkansas, United States of America

Published online by Cambridge University Press:  21 August 2019

Jessica A. Hartshorn*
Affiliation:
Department of Forestry and Environmental Conservation, Clemson University, Clemson, South Carolina, 29630, United States of America
Larry D. Galligan
Affiliation:
Department of Entomology, University of Arkansas, Fayetteville, Arkansas, 72701, United States of America
Fred M. Stephen
Affiliation:
Department of Entomology, University of Arkansas, Fayetteville, Arkansas, 72701, United States of America
*
1Corresponding author (e-mail: jhartsh@clemson.edu)

Abstract

Enaphalodes rufulus (Haldeman) (red oak borer; Coleoptera: Cerambycidae) is a native wood borer that colonises and develops in oaks (Quercus Linnaeus; Fagaceae) across southeastern Canada and the eastern United States of America. It is rarely considered a pest because it normally occurs at low population density levels in stressed or dying oak trees. In the late 1990s and early 2000s there was a large, historically unique outbreak of E. rufulus in the Ozark mountains of Arkansas and Missouri, United States of America. This outbreak provided an opportunity to investigate within-tree spatial distribution of attacks during unusually high insect population levels. Fifty trees from northern Arkansas were felled and destructively sampled. The locations of attack sites by female E. rufulus were standardised across varying heights and diameters for comparison across trees. Attack sites showed a significant clustered pattern within trees. Attack sites were aggregated towards the lower and middle bole, and on the south-facing side of trees. This pattern has been seen in other insects, including wood borers, and is potentially related to differences in temperature. These patterns of ovipositional behaviour in outbreak situations have implications for E. rufulus resource partitioning and facultative intraguild predation among larvae.

Type
Behaviour and Ecology
Copyright
© Entomological Society of Canada 2019 

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Footnotes

Subject editor: Barbara Bentz

References

Baddeley, A., Rubak, E., and Turner, R. 2015. Spatial point patterns: methodology and applications with R. CRC Press, Boca Raton, Florida, United States of America.CrossRefGoogle Scholar
Cárdenas, A.M. and Gallardo, P. 2013. The effects of oviposition site on the development of the wood borer Coraebus florentinus (Coleoptera: Cerambycidae). European Journal of Entomology, 110: 135144.CrossRefGoogle Scholar
Crook, D.J., Fierke, M.K., Mauromoustakos, A., Kinney, D.L., and Stephen, F.M. 2007. Optimization of sampling methods for within-tree populations of red oak borer, Enaphalodes rufulus (Haldeman) (Coleoptera: Cerambycidae). Environmental Entomology, 36: 589594.CrossRefGoogle Scholar
Donley, D.E. 1978. Oviposition by the red oak borer, Enaphalodes rufulus (Coleoptera: Cerambycidae). Annals of the Entomological Society of America, 71: 496498.CrossRefGoogle Scholar
Donley, D.E. and Rast, E. 1984. Vertical distribution of the red oak borer, Enaphalodes rufulus (Coleoptera: Cerambycidae), in red oak. Environmental Entomology, 13: 4144.CrossRefGoogle Scholar
Dunn, J.P., Kimmerer, T.W., and Nordin, G.L. 1986. The role of host tree condition in attack of white oaks by the twolined chestnut borer, Agrilus bilineatus (Weber) (Coleoptera: Buprestidae). Oecologia, 70: 596600.CrossRefGoogle Scholar
Dunn, J.P., and Potter, D.A. 1991. Synergistic effects of oak volatiles with ethanol in the capture of saprophagous wood borers. Journal of Entomological Science, 26: 425429.CrossRefGoogle Scholar
Fierke, M.K., Kelley, M.B., and Stephen, F.M. 2007. Site and stand variables influencing red oak borer, Enaphalodes rufulus (Coleoptera: Cerambycidae), population densities and tree mortality. Forest Ecology and Management, 247: 227236.CrossRefGoogle Scholar
Fierke, M.K., Kinney, D.L., Salisbury, V.B., Crook, D.J., and Stephen, F.M. 2005a. Development and comparison of intensive and extensive sampling methods and preliminary within-tree population estimates of red oak borer (Coleoptera: Cerambycidae) in the Ozark Mountains of Arkansas. Environmental Entomology, 34: 184192.CrossRefGoogle Scholar
Fierke, M.K., Kinney, D.L., Salisbury, V.B., Crook, D.J., and Stephen, F.M. 2005b. A rapid estimation procedure for within-tree populations of red oak borer (Coleoptera: Cerambycidae). Forest Ecology & Management, 215: 163168.CrossRefGoogle Scholar
Fierke, M.K. and Stephen, F.M. 2008. Callus formation and bark moisture as potential physical defenses of northern red oak, Quercus rubra, against red oak borer, Enaphalodes rufulus (Coleoptera: Cerambycidae). The Canadian Entomologist, 140: 149157.CrossRefGoogle Scholar
Fierke, M.K. and Stephen, F.M. 2010. Dendroentomological evidence associated with an outbreak of the native wood-boring beetle Enaphalodes rufulus . Canadian Journal of Forest Research, 40: 679686.CrossRefGoogle Scholar
Galford, J.R. 1985. Role of predators on an artificially planted red oak borer population. Research note NE-331. United States Department of Agriculture Forest Service, Broomall, Pennsylvania, United States of America.Google Scholar
Haavik, L.J., Billings, S.A., Guldin, J.M., and Stephen, F.M. 2015. Emergent insects, pathogens and drought shape changing patterns in oak decline in North America and Europe. Forest Ecology and Management, 354: 190205.CrossRefGoogle Scholar
Haavik, L.J., Crook, D.J., Fierke, M.K., Galligan, L.D., and Stephen, F.M. 2012a. Partial life tables from three generations of Enaphalodes rufulus (Coleoptera: Cerambycidae). Environmental Entomology, 41: 13111321.CrossRefGoogle Scholar
Haavik, L.J., Jones, J.S., Galligan, L.D., Guldin, J.M., and Stephen, F.M. 2012b. Oak decline and red oak borer outbreak: impact in upland oak-hickory forests of Arkansas, USA. Forestry, 85: 341352.CrossRefGoogle Scholar
Haavik, L.J. and Stephen, F.M. 2011. Optimal cross-sectional sampling strategy for red oak borer (Coleoptera: Cerambycidae) scars within northern red oaks. Southern Journal of Applied Forestry, 35: 4449.CrossRefGoogle Scholar
Haavik, L.J., Stephen, F.M., Fierke, M.K., Salisbury, V.B., Leavitt, S.W., and Billings, S.A. 2008. Dendrochronological parameters of northern red oak (Quercus rubra L. (Fagaceae)) infested with red oak borer (Enaphalodes rufulus (Haldeman) (Coleoptera: Cerambycidae)). Forest Ecology and Management, 255: 15011509.CrossRefGoogle Scholar
Hanks, L.M. and Millar, J.G. 2016. Sex and aggregation-sex pheromones of cerambycid beetles: basic science and practical applications. Journal of Chemical Ecology, 42: 631654.CrossRefGoogle ScholarPubMed
Hay, C.J. 1972a. Red oak borer (Coleoptera: Cerambycidae) emergence from oak in Ohio. Annals of the Entomological Society of America, 65: 12431244.CrossRefGoogle Scholar
Hay, C.J. 1972b. Woodpecker predation on red oak borer in black, scarlet, and northern red oak. Annals of the Entomological Society of America, 65: 14211423.CrossRefGoogle Scholar
Hay, C.J. 1974. Survival and mortality of red oak borer larvae on black, scarlet, and northern red oak in eastern Kentucky. Annals of the Entomological Society of America, 67: 981986.CrossRefGoogle Scholar
Holt, R.D. 1984. Spatial heterogeneity, indirect interactions, and the coexistence of prey species. The American Naturalist, 124: 377406.CrossRefGoogle ScholarPubMed
Muilenburg, V.L., Goggin, F.L., Hebert, S.L., Jia, L., and Stephen, F.M. 2008. Ant predation on red oak borer confirmed by field observation and molecular gut-content analysis. Agricultural and Forest Entomology, 10: 205213.CrossRefGoogle Scholar
Pajares, J.A., Ibeas, F., Diez, J.J., and Gallego, D. 2004. Attractive responses by Monochams galloprovincialis (Col.; Cerambycidae) to host and bark beetle semiochemicals. Journal of Applied Entomology, 128: 633638.CrossRefGoogle Scholar
Riggins, J.J., Galligan, L.D., and Stephen, F.M. 2009. Rise and fall of red oak borer (Coleoptera: Cerambycidae) in the Ozark mountains of Arkansas, USA. Florida Entomologist, 92: 426433.CrossRefGoogle Scholar
Stephen, F.M., Salisbury, V.B., and Oliveria, F.L. 2001. Red oak borer, Enaphalodes rufulus (Coleoptera: Cerambycidae), in the Ozark mountains of Arkansas, U.S.A.: an unexpected and remarkable forest disturbance. Integrated Pest Management Reviews, 6: 247252.CrossRefGoogle Scholar
Timms, L.L., Smith, S.M., and de Groot, P. 2006. Patterns in the within-tree distribution of the emerald ash borer Agrilus planipennis (Fairmaire) in young, green-ash plantations of south-western Ontario, Canada. Agricultural and Forest Entomology, 8: 313321.CrossRefGoogle Scholar
Torres-Vila, L., Zugasti- Martínez, C., Mendiola-Díaz, F., De-Juan-Murillo, J., Sánchez-González, Á., Conejo-Rodríguez, Y., et al. 2017. Larval assemblages of large saproxylic cerambycids in Iberian oak forests: wood quality and host preference shape resource partitioning. Population Ecology, 59: 315328.CrossRefGoogle Scholar
Vansteenkiste, D., Tirry, L., Van Acker, J., and Stevens, M. 2004. Predispositions and symptoms of Agrilus borer attack in declining oak trees. Annals of Forest Science, 61: 815823.CrossRefGoogle Scholar
Ware, V.L. and Stephen, F.M. 2006. Facultative intraguild predation of red oak borer larvae (Coleoptera: Cerambycidae). Environmental Entomology, 35: 443447.CrossRefGoogle Scholar