Hostname: page-component-cc8bf7c57-hbs24 Total loading time: 0 Render date: 2024-12-11T22:08:33.636Z Has data issue: false hasContentIssue false
  • English
  • Français

Longitudinal study of Caribbean pine elucidates the role of 4-allylanisole in patterns of chemical resistance to bark beetle attack

Published online by Cambridge University Press:  20 January 2020

Austin J. Hammer ,
Nathan W. Bower Open the ORCID record for Nathan W. Bower [Opens in a new window] ,
Aaron I. Snyder ,
Zachary N. Snyder ,
Fredy L. Archila  and
Marc A. Snyder
Austin J. Hammer
Affiliation:
Chemistry and Biochemistry, Colorado College, Colorado Springs, CO, 80903, USA
Nathan W. Bower*
Affiliation:
Chemistry and Biochemistry, Colorado College, Colorado Springs, CO, 80903, USA
Aaron I. Snyder
Affiliation:
Chemistry and Biochemistry, Colorado College, Colorado Springs, CO, 80903, USA
Zachary N. Snyder
Affiliation:
Chemistry and Biochemistry, Colorado College, Colorado Springs, CO, 80903, USA
Fredy L. Archila
Affiliation:
Herbario BIGU, Universidad de San Carlos de Guatemala, Guatemala, 01012
Marc A. Snyder*
Affiliation:
Organismal Biology and Ecology, Colorado College, Colorado Springs, CO, 80903, USA
*
Authors for correspondence: *Nathan W. Bower, Email: [email protected]; Marc A. Snyder, Email: [email protected]
Authors for correspondence: *Nathan W. Bower, Email: [email protected]; Marc A. Snyder, Email: [email protected]
Get access Rights & Permissions [Opens in a new window]

Abstract

Southern pine beetles (Dendroctonus frontalis Zimmermann) and symbiotic fungi are associated with mass mortality in stands of Caribbean pine (Pinus caribaea Morelet). This study provides a 12.7-year assessment of semiochemical mediation between southern pine beetle and Caribbean pine in relation to concentrations of 4-allylanisole (estragole, methyl chavicol) and monoterpenes measured by gas chromatography–mass spectrometry in different seasons in premontane and coastal pine stands of Belize and Guatemala. Individual trees and stands with >2.5% (relative mass %) of 4-allylanisole in the xylem oleoresin exhibited significantly less beetle-induced mortality than those with <2.5%. Changes in relative levels of 4-allylanisole and monoterpenes during this study are consistent with seasonal temperature and cumulative water deficit effects and suggest bark beetle attack of P. caribaea may intensify in the future.

Keywords

4-allylanisoleBelizeclimate changeDendroctonus frontalisGuatemalamonoterpenesPinus caribaea
Type
Research Article
Information
Journal of Tropical Ecology , Volume 36 , Issue 2 , March 2020 , pp. 43 - 46
Copyright
© The Author(s) 2020. Published by Cambridge University Press

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

Literature cited

Armendáriz-Toledano, F, Niño, A, Sullivan, BT, Kirkendall, LR and Zúñiga, G (2015) A new species of bark beetle, Dendroctonus mesoamericanus sp. nov. (Curculionidae: Scolytinae), in Southern Mexico and Central America. Annals of the Entomological Society of America 108, 403–414.CrossRefGoogle Scholar
Bentz, BJ and Jönsson, AM (2015) Modeling bark beetle responses to climate change. In Vega, FE and Hofstetter, RW (eds), Bark Beetles: Biology and Ecology of Native and Invasive Species. London: Academic Press, pp. 533–553.CrossRefGoogle Scholar
Blanche, CA, Lorio, Jr PL, Sommers, RA, Hodges, JD and Nebeker, TE (1992) Seasonal cambial growth and development of loblolly pine: xylem formation, inner bark chemistry, resin ducts, and resin flow. Forest Ecology and Management 49, 151–165.CrossRefGoogle Scholar
Cobb, FW Jr, Zavarin, E and Bergot, J (1972) Effect of air pollution on the volatile oil from leaves of Pinus ponderosa. Phytochemistry 11, 1815–1818.CrossRefGoogle Scholar
Coppen, JJW, Gay, C, James, DJ, Robinson, JM and Mullin, LJ (1993) Xylem resin composition and chemotaxonomy of three varieties of P. caribaea. Phytochemistry 33, 1103–1111.CrossRefGoogle Scholar
Emerick, JJ, Snyder, AI, Bower, NW and Snyder, MA (2008) Mountain Pine Beetle attack associated with low levels of 4-allylanisole in Ponderosa pine. Environmental Entomology 37, 871–875.CrossRefGoogle ScholarPubMed
Ferrenberg, S, Langenhan, JM, Loskot, SA, Rozal, LM and Mitton, JB (2017) Resin monoterpene defenses decline within three widespread species of pine (Pinus) along a 1530‐m elevational gradient. Ecosphere 8, e01975.CrossRefGoogle Scholar
Glare, TR, Reay, SD and Etxebeste, I (2011) Options for control of scolytid beetles that attack pines. CAB Reviews: Perspectives in Agriculture, Veterinary Science, Nutrition and Natural Resources 6(No. 051), 1–17.CrossRefGoogle Scholar
Hayes, JL, Strom, BL, Roton, LM and Ingram, LL Jr (1994) Repellent properties of the host compound 4-allylanisole to the southern pine beetle. Journal of Chemical Ecology 20, 1595–1615.CrossRefGoogle ScholarPubMed
Hobson, KR (1995) Host compounds as semiochemicals for bark beetles. In Salom SM and Hobson KR (eds), Application of Semiochemicals for Management of Bark Beetle Infestations – Proceedings of an Informal Conference. Annual meeting of the Entomological Society of America, 12-16 December 1993; Indianapolis, IN. Gen. Tech. Rep. INT-GTR-318. Ogden, UT: U.S. Department of Agriculture, Forest Service, Intermountain Research Station.Google Scholar
Hofstetter, RW, Mahfouz, JB, Klepzig, KD and Ayres, MP (2005) Effects of tree phytochemistry on the interactions among endophloedic fungi associated with the southern pine beetle. Journal of Chemical Ecology 31, 539–560.CrossRefGoogle ScholarPubMed
Katz, C (2017) Small Pests, Big Problems: The Global Spread of Bark Beetles. Yale E360. Yale School of Forestry & Environmental Studies. https://e360.yale.edu/features/small-pests-big-problems-the-global-spread-of-bark-beetles.Google Scholar
Kurz, WA, Dymond, C, Stinson, G, Rampley, G, Neilson, E, Carroll, A, Ebata, T and Safranyik, L (2008) Mountain pine beetle and forest carbon feedback to climate change. Nature 452, 987–990.CrossRefGoogle ScholarPubMed
Marei, GIK, Rasoul, MAAR and Abdelgaleil, SAM (2012) Comparative antifungal activities and biochemical effects of monoterpenes on plant pathogenic fungi. Pesticide Biochemistry and Physiology 103, 56–61.CrossRefGoogle Scholar
Richards, LA, Dyer, LA, Forister, ML, Smilanich, AM, Dodson, CD, Leonard, MD and Jeffrey, CS (2015) Phytochemical diversity drives plant–insect community diversity. Proceedings of the National Academy of Sciences USA 112(15), 10973–10978.CrossRefGoogle ScholarPubMed
Richardson, RB (2009) Belize and Climate Change: The Costs of Inaction. Human Development Issues Paper. Belmopan, Belize: United Nations Development Programme, pp. 14–19.Google Scholar
Six, DL, Vegobbi, C and Cutter, M (2018) Are survivors different? Genetic-based selection of trees by mountain pine beetle during a climate change-driven outbreak in a high-elevation pine forest. Frontiers in Plant Science 9, Article 993.CrossRefGoogle Scholar
Snyder, MA and Bower, NW (2005) Resistance to bark beetle attack in Caribbean pine: potential role of 4-allylanisole. Biotropica 37, 702–705.CrossRefGoogle Scholar
Sullivan, BT (2016) Semiochemicals in the natural history of southern pine beetle Dendroctonus frontalis Zimmermann and their role in pest management. Advances in Insect Physiology 50, 129–193.CrossRefGoogle Scholar
Werner, R (1995) Toxicity and repellency of 4-allylanisole and monoterpenes from white spruce and tamarack to the spruce beetle and eastern larch beetle (Coleoptera: Scolytidae). Environmental Entomology 24, 372–379.CrossRefGoogle Scholar
World Bank Group (2019) Climate Change Knowledge Portal. http://sdwebx.worldbank.org/climateportal/index.cfm.Google Scholar