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Survival physiology and sex ratio of the Chinese white pine beetle Dendroctonus armandi (Coleoptera: Scolytinae) during host colonization and overwintering

Published online by Cambridge University Press:  29 May 2019

L. Dai ,
J. Zheng ,
Y. Wang ,
Y. Sun  and
H. Chen
L. Dai
Affiliation:
College of Forestry, Northwest A and F University, Yangling, 712100, Shaanxi, China
J. Zheng
Affiliation:
College of Forestry, Northwest A and F University, Yangling, 712100, Shaanxi, China
Y. Wang
Affiliation:
College of Forestry, Northwest A and F University, Yangling, 712100, Shaanxi, China
Y. Sun
Affiliation:
College of Forestry, Northwest A and F University, Yangling, 712100, Shaanxi, China
H. Chen*
Affiliation:
State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources (South China Agricultural University), Guangdong Key Laboratory for Innovative Development and Utilization of Forest Plant Germplasm, College of Forestry and Landscape Architecture, South China Agricultural University, Guangzhou 510642, China
*
*Author for correspondence Phone: +86-020-85280256 Fax: +86-020-85280256 E-mail: [email protected]
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Abstract

The Chinese white pine beetle Dendroctonus armandi (Coleoptera: Scolytinae) typically displays bivoltinism at altitudes below 1700 m in the Qinling Mountains, China. The periods of host colonization and larval overwintering are two important phases in the life cycle of bark beetles, as it is during these periods that they have to contend with host plant defences and periods of intense cold, respectively. Although during different seasons, the females and males of Chinese white pine beetles show varying tolerances to host plant terpenoids, the sex ratio and survival physiology condition of the two beetle generations are unknown. We investigated the sex ratio of individuals, and also examined the body mass, energy stores, and detoxication enzymes of males and females in each of the two generations in order to determine the overall population stability of each generation. We identified a female-biased sex ratio among adults in both generations. Furthermore, patterns of body mass, energy stores, and detoxication enzymes were found to differ between the two sexes and two seasons. Compared with the males, the females have a larger body mass and higher amounts of stored lipids, which are assumed to be adaptations designed to overcome host resistance and facilitate subsequent oviposition.

Keywords

Dendroctonus armandisex ratioenergy storesdetoxication enzymeshost colonization
Type
Research Paper
Information
Bulletin of Entomological Research , Volume 110 , Issue 1 , February 2020 , pp. 115 - 122
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Copyright
Copyright © Cambridge University Press 2019 

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References

Amman, G.D. & Cole, W.E. (1983) Mountain pine beetle dynamics in lodgepole pine forests. Part II: Population dynamics. General Technical Report, Intermountain Forest and Range Experiment Station, USDA Forest Service, INT-145.Google Scholar
Arrese, E.L. & Soulages, J.L. (2010) Insect fat body: energy, metabolism, and regulation. Annual Review of Entomology 55, 207–225.Google Scholar
Athenstaedt, K. & Daum, G. (2006) The life cycle of neutral lipids: synthesis, storage and degradation. Cellular and Molecular Life Sciences 63, 1355–1369.Google Scholar
Cano-Ramírez, C., López, M.F., Cesar-Ayala, A.K., Pineda-Martínez, V., Sullivan, B.T. & Zúñiga, G. (2013) Isolation and expression of cytochrome P450 genes in the antennae and gut of pine beetle Dendroctonus rhizophagus (Curculionidae: Scolytinae) following exposure to host monoterpenes. Gene 520, 47–63.Google Scholar
Chen, H. & Yuan, F. (2000) Chinese White Pine Bark Beetle Ecosystem and Integrated Pest Management in Qinling Mountain. Beijing, China Forestry Publishing House.Google Scholar
Chen, H. & Yuan, F. (2002) Resistance of host trees and existance strategy evolution of bark beetles. Scientia Silvae Sinicae 38(5), 147–151.Google Scholar
Chen, H. & Tang, M. (2007) Spatial and temporal dynamics of bark beetles in Chinese white pine in qinling mountains of shaanxi province, China. Environmental Entomology 36(5), 1124–1130.Google Scholar
Chen, H., Li, Z. & Tang, M. (2010) Laboratory evaluation of flight activity of Dendroctonus armandi (Coleoptera: Curculionidae: Scolytinae). Canadian Entomologist 142, 378–387.Google Scholar
Chiu, C.C., Keeling, C.I. & Bohlmann, J. (2017) Toxicity of pine monoterpenes to mountain pine beetle. Scientific Reports 7(1), 8858.Google Scholar
Cole, W.E., Amman, G.D. & Jensen, C.E. (1976) Mathematical models for the mountain pine beetle–lodgepole pine interaction. Environmental Entomology 5, 11–19.Google Scholar
Dai, L., Ma, M., Wang, C., Shi, Q., Zhang, R. & Chen, H. (2015) Cytochrome P450s from the Chinese white pine beetle, Dendroctonus armandi (Curculionidae: Scolytinae): expression profiles of different stages and responses to host allelochemicals. Insect Biochemistry and Molecular Biology 65, 35–46.Google Scholar
Dai, L., Ma, J., Ma, M., Zhang, H., Shi, Q., Zhang, R. & Chen, H. (2016) Characterisation of GST genes from the Chinese white pine beetle Dendroctonus armandi (Curculionidae: Scolytinae) and their response to host chemical defence. Pest Management Science 72, 816–827.Google Scholar
Dinneen, L.C. & Blakesley, B.C. (1973) Algorithm AS 62: a generator for the sampling distribution of the Mann- Whitney U Statistic. Journal of the Royal Statistical Society 22(2), 269–273.Google Scholar
Folch, J., Lees, M. & Sloane Stanley, G.H. (1957) A simple method for the isolation and purification of total lipids from animal tissues. Journal of Biological Chemistry 226(1), 497–509.Google Scholar
Gunasekaran, K., Muthukumaravel, S., Sahu, S.S., Vijayakumar, T. & Jambulingam, P. (2011) Glutathione S-transferase activity in Indian vectors of malaria: a defense mechanism against DDT. J. Journal of Medical Entomology 48, 561–569.Google Scholar
Huber, D.P.W. & Robert, J.A. (2016) ‘‘The proteomics and transcriptomics of early host colonization and overwintering physiology in the mountain pine beetle, Dendroctonus ponderosae Hopkins (Coleoptera: Curculionidae),’’ in Pine Bark Beetle. Advances in Insect Physiology 50, 101–128.Google Scholar
Jakoby, W.B. & Ziegler, D.M. (1990) The enzymes of detoxication. Journal of Biological Chemistry 265, 20 715–20 718.Google Scholar
James, P.M.A., Janes, J.K., Roe, A.D. & Cooke, B.J. (2016) Modeling landscape-level spatial variation in sex ratio skew in the Mountain Pine Beetle (Coleoptera: Curculionidae). Environmental Entomology 45(4), 790–801.Google Scholar
Keeling, C.I., Henderson, H., Li, M., Yuen, M., Clark, E.L., Fraser, J.D., Huber, D.P.W., Liao, N.Y., Docking, T.R., Birol, I., Chan, S.K., Taylor, G.A., Palmquist, D., Jones, S.J.M. & Bohlmann, J. (2012) Transcriptome and full-length cDNA resources for the mountain pine beetle, Dendroctonus ponderosae Hopkins, a major insect pest of pine forests. Insect Biochemistry and Molecular Biology 42(8), 525–536.Google Scholar
Keeling, C.I., Yuen, M.M.S., Liao, N.Y., Docking, T.R., Chan, S.K., Taylor, G.A., Palmquist, D.L., Jackman, S.D., Nguyen, A., Li, M., Henderson, H., Janes, J.K., Zhao, Y.J., Pandoh, P., Moore, R., Sperling, F.A.H., Huber, D.P.W., Birol, I., Jones, S.J.M. & Bohlmann, J. (2013) Draft genome of the mountain pine beetle, Dendroctonus ponderosae Hopkins, a major forest pest. Genome Biology 14, R27.Google Scholar
Lachowsky, L.E. & Reid, M.L. (2014) Developmental mortality increases sex ratio bias of a size-dimorphic bark beetle. Ecological Entomology 39, 300–308.Google Scholar
Latty, T. & Reid, M. (2009) First in line or first in time? Effects of settlement order and arrival date on reproduction in a group-living beetle Dendroctonus ponderosae. Journal of Animal Ecology 78, 549–555.Google Scholar
Li, K. & Zhou, J. (1992) Dendroctonus armandi, in Xiao, G. (Ed.) Forest Insects of China. pp. 616–618, Beijing, China Forestry Publishing House.Google Scholar
Li, X., Schuler, M.A. & Berenbaum, M.R. (2007) Molecular mechanisms of metabolic resistance to synthetic and natural xenobiotics. Annual Review of Entomology 52, 231–253.Google Scholar
Livak, K.J. & Schmittgen, T.D. (2008) Analyzing real-time PCR data by the comparative CT method. Nature Protocols 3, 1101–1108.Google Scholar
Lockey, K.H. (1988) Lipids of the insect cuticle-origin, composition and function. Comparative Biochemistry and Physiology B 89, 595–645.Google Scholar
López, M.F., Cano-Ramírez, C., Cesar-Ayala, A.K., Ruiz, E.A. & Zúñiga, G. (2013) Diversity and expression of P450 genes from Dendroctonus valens LeConte (Curculionidae: Scolytinae) in response to different kairomones. Insect Biochemistry and Molecular Biology 43, 417–432.Google Scholar
Lyon, R.L. (1958) Useful secondary sex character in Dendroctonus bark Beetles. Canadian Entomologist 90, 552–558.Google Scholar
Overgaard, J., Malmendal, A., Søorensen, J.G., Bundy, J.G., Loeschcke, V., Nielsen, N.C. & Holmstrup, M. (2007) Metabolomic profiling of rapid cold hardening and cold shock in Drosophila melanogaster. Journal of Insect Physiology 53, 1218–1232.Google Scholar
Patel, R., Patel, M., Tsai, R., Lin, V., Bookout, A.L., Zhang, Y., Magomedova, L., Li, T.T., Chan, JF., Budd, C., Mangelsdorf, D.J. & Cummins, C.L. (2011) LXR is required for glucocorticoid-induced hyperglycemia and hepatosteatosis in mice. Journal of Clinical Investigation 121, 431–441.Google Scholar
Paumi, C.M., Smitherman, P.K., Townsend, A.J. & Morrow, C.S. (2004) Glutathione S-transferases (GSTs) inhibit transcriptional activation by the peroxisomal proliferator-activated receptor gamma (PPAR gamma) ligand, 15-deoxy-delta 12,14prostaglandin J2 (15-d-PGJ2). Biochemistry 43, 2345–2352.Google Scholar
Reid, R. (1958) The behaviour of the mountain pine beetle, Dendroctonus monticolae Hopk., during mating, egg laying, and gallery construction. Canadian Entomologist 90, 505–509.Google Scholar
Reid, M.L. & Purcell, J.R.C. (2011) Condition-dependent tolerance of monoterpenes in an insect herbivore. Arthropod-Plant Interactions 5, 331–337.Google Scholar
Sequeira, A.S., Normark, B.B. & Farrell, B.D. (2000) Evolutionary assembly of the conifer fauna: distinguishing ancient from recent associations in bark beetles. Proceedings of the Royal Society of London. Series B, Biological Sciences 267, 2359–2366.Google Scholar
Sheehan, D., Meade, G., Fole, Y.V.M. & Dowd, C.A. (2001) Structure, function and evolution of glutathione transferases: implications for classification of non-mammalian members of an ancient enzyme superfamily. Biochemical Journal 360, 1–16.Google Scholar
Smith, L.J. & Anderson, J. (1992) Oxygen-induced lung damage: Relationship to lung mitochondrial glutathione levels. American Review of Respiratory Disease 146(6), 1452–1457.Google Scholar
Stanley, D. (2006) Prostaglandins and other eicosanoids in insects: biological significance. Annual Review of Entomology 51, 25–44.Google Scholar
Steele, J.E. (1982) Glycogen-phosphorylase in insects. Insect Biochemistry 12, 131–147.Google Scholar
Storey, K.B. (1997) Organic solutes in freezing tolerance. Comparative Biochemistry & Physiology A 117, 319–326.Google Scholar
Takeshita, M., Yubisui, T., Tanishima, K. & Yoneyama, Y. (1980) A simple enzymatic microdetermination of cytochrome b5 in erythrocytes. Analytical Biochemistry 107(2), 305–310.Google Scholar
Thompson, S.N. (2003) ‘‘Trehalose: the insect ‘blood’ sugar,’’ in Comprehensive review on trehalose in insects. Advances in Insect Physiology 31, 205–285.Google Scholar
Van Asperen, K. (1962) A study of house fly esterase by means of a sensitive colorimetric method. Journal of Insect Physiology 8, 401–416.Google Scholar
Van Handel, E. (1985) Rapid determination of glycogen and sugars in mosquitoes. Journal of the American Mosquito Control Association 1, 299–301.Google Scholar
Van Handel, E. & Day, J.F. (1988) Assay of lipids, glycogen and sugars in individual mosquitoes: correlations with wing length in field collected Aedes vexans. Journal of the American Mosquito Control Association 4, 549–550.Google Scholar
Vanin, S., Bubacco, L. & Beltramini, M. (2008) Seasonal variation of trehalose and glycerol concentrations in winter snow-active insects. Cryo Letters 29, 485–491.Google Scholar
Wallin, K.F. & Raffa, K.F. (2000) Influences of host chemicals and internal physiology on the multiple steps of post landing host acceptance behavior of Ips pini (Coleoptera: Scolytidae). Environmental Entomology 29, 442–453.Google Scholar
Wallin, K.F. & Raffa, K.F. (2002) Density-mediated responses of bark beetles to host allelochemicals: a link between individual behaviour and population dynamics. Ecological Entomology 27, 484–492.Google Scholar
Wallin, K.F. & Raffa, K.F. (2004) Feedback between individual host selection behavior and population dynamics in an eruptive herbivore. Ecological Monographs 74, 101–116.Google Scholar
Wang, J., Gao, G., Zhang, R., Dai, L. & Chen, H. (2017) Metabolism and cold tolerance of Chinese white pine beetle Dendroctonus armandi (Coleoptera: Curculionidae: Scolytinae) during the overwintering period. Agricultural and Forest Entomology 19, 10–22.Google Scholar
Yin, H.F., Huang, F.S. & Li, Z.L. (1984) Coleoptera. Scolytidae, in Editorial Committee of Fauna, Academia Sinica (Eds) Economic Insect Fauna of China. Vol. 29, pp. 57–58. Beijing, Science Press.Google Scholar
Ziegler, R. & Ibrahim, M.M. (2001) Formation of lipid reserves in fat body and eggs of the yellow fever mosquito, Aedes aegypti. Journal of Insect Physiology 47, 623–627.Google Scholar
Ziegler, R. & Van Antwerpen, R. (2006) Lipid uptake by insect oocytes. Insect Biochemistry and Molecular Biology 36, 264–272.Google Scholar