References
- Abdollahi, M., Ranjbar, A., Shadnia, S., Nikfar, S., & Rezaie, A. (2004). Pesticides and oxidative stress: a review, Med. Sci. Monitor 10, Ra141-147.
- Angilletta, M. J., Steury, T. D., & Sears, M. W. (2004). Temperature, growth rate, and body size in ectotherms: fitting pieces of a life-history puzzle, Integr. Comp. Biol. 44, 498-509. https://doi.org/10.1093/icb/44.6.498
- Arrigo, A.-P. (1987). Cellular localization of HSP23 during Drosophila development and following subsequent heat shock, Dev. Biol. 122, 39-48. https://doi.org/10.1016/0012-1606(87)90330-7
- Bagchi, R., Gallery, R. E., Gripenberg, S., Gurr, S. J., Narayan, L., Addis, C. E., Freckleton, R. P., & Lewis, O. T. (2014). Pathogens and insect herbivores drive rain forest plant diversity and composition, Nature 506, 85-88. https://doi.org/10.1038/nature12911
- Balabanidou, V., Grigoraki, L., & Vontas, J. (2018). Insect cuticle: a critical determinant of insecticide resistance, Curr. Opin. Insect Sci. 27, 68-74. https://doi.org/10.1016/j.cois.2018.03.001
- Balabanidou, V., Kampouraki, A., MacLean, M., Blomquist, G. J., Tittiger, C., Juarez, M. P., Mijailovsky, S. J., Chalepakis, G., Anthousi, A., Lynd, A., Antoine, S., Hemingway, J., Ranson, H., Lycett, G. J., & Vontas, J. (2016). Cytochrome P450 associated with insecticide resistance catalyzes cuticular hydrocarbon production in Anopheles gambiae, Proc. Nat'l Acad. Sci. USA. 113, 9268-9273. https://doi.org/10.1073/pnas.1608295113
- Barrett, R. D., Paccard, A., Healy, T. M., Bergek, S., Schulte, P. M., Schluter, D., & Rogers, S. M. (2011). Rapid evolution of cold tolerance in stickleback, Proc. Biol. Sci. 278, 233-238. https://doi.org/10.1098/rspb.2010.0923
- Bauerfeind, S. S., & Fischer, K. (2014). Simulating climate change: Temperature extremes but not means diminish performance in a widespread butterfly, Popul. Ecol. 56, 239-520. https://doi.org/10.1007/s10144-013-0409-y
- Bruey, J. M., Ducasse, C., Bonniaud, P., Ravagnan, L,, Susin, S. A., Diaz-Latoud, C., Gurbuxani, S., Arrigo, A. P., Kroemer, G., Solary, E., & Garrido, C. (2000). Hsp27 negatively regulates cell death by interacting with cytochrome c, Nat. Cell Biol. 2, 645-652. https://doi.org/10.1038/35023595
- Casique-Arroyo, G., Martinez-Gallardo, N., de la Vara, L. G., & Delano-Frier, J. P. (2014). Betacyanin biosynthetic genes and enzymes are differentially induced by (a)biotic stress in Amaranthus hypochondriacus, PLOS ONE 6, e99012.
- Chowdary, T. K., Raman, B., Ramakrishna, T., & Rao, C. M. (2004). Mammalian Hsp22 is a heat-inducible small heat-shock protein with chaperone-like activity, Biochem. J. 381, 379-387. https://doi.org/10.1042/BJ20031958
- Chown, S. L., Hoffmann, A. A., Kristensen, T. N., Angilletta, M. J., Stenseth, N. C., & Pertoldi, C. (2010). Adapting to climate change: a perspective from evolutionary physiology, Climate Res. 43, 3-15. https://doi.org/10.3354/cr00879
- Chown, S. L., Terblanche, J. S., & Simpson, S. J. (2006). Physiological diversity in insects: ecological and evolutionary contexts, Adv. Insect Physiol. 33, 50-152.
- Dennis, D., & Weisenburger, M. D. (1993). Human health effects of agrichemical use, Human Pathol. 24, 571-576. https://doi.org/10.1016/0046-8177(93)90234-8
- Deutsch, C. A., Tewksbury, J. J., Huey, R. B., Sheldon, K. S., Ghalambor, C. K., Haak, D. C., & Martin, P. R. (2008). Impacts of climate warming on terrestrial ectotherms across latitude, Proc. Natl. Acad. Sci. USA. 105, 6668-6672. https://doi.org/10.1073/pnas.0709472105
- Ehrnsperger, M., Graber, S., Gaestel, M., & Buchner, J. (1997). Binding of non-native protein to Hsp25 during heat shock creates a reservoir of folding intermediates for reactivation, EMBO J. 16, 221-229. https://doi.org/10.1093/emboj/16.2.221
- Enayati, A. A., Ranson, H., & Hemingway, J. (2005). Insect glutathione transferases and insecticide resistance, Insect Mol. Biol. 14, 3-8. https://doi.org/10.1111/j.1365-2583.2004.00529.x
- Goto, S., & Kimura, M. (1998). Heat- and cold-shock responses and temperature adaptations in subtropical and temperate species of Drosophila, J. Insect Physiol. 44, 1233-1239. https://doi.org/10.1016/S0022-1910(98)00101-2
- Grazyna, C., Hanna, C., Adam A., & Magdalena, B. M. (2017). Natural antioxidants in milk and dairy products, Int. J. Dairy Technol. 70, 165-178. https://doi.org/10.1111/1471-0307.12359
- Guittard, E., Blais, C., Maria, A., Parvy, J. P., Parishna, S., Lumb, C., Lafont, R., Daborn, P. J., & Dauphin-Villemant, C. (2011). CYP18A1, a key enzyme of Drosophila steroid hormone inactivation, is essential for metamorphosis, Dev. Biol. 349, 35-45. https://doi.org/10.1016/j.ydbio.2010.09.023
- Gutierrez, E. D., Wiggins, D., Fielding, B., & Gould, A. P. (2007). Specialized hepatocyte-like cells regulate Drosophila lipid metabolism, Nature 445, 275-280. https://doi.org/10.1038/nature05382
- Habig, W. H., Pabst, M. J., & Jakoby, W. B., (1974). Glutathione S-transferases. The first enzymatic step in mercapturic acid formation, J. Biol. Chem. 249, 7130-7139.
- Haslbeck, M., Walke, S., Stromer, T., Ehrnsperger, M., White, H. E., Chen, S., Saibil, H. R., & Buchner, J. (1999). Hsp26: a temperature-regulated chaperone, EMBO J. 18, 6744-6751. https://doi.org/10.1093/emboj/18.23.6744
- Hillebrand, H., Borer, E. T., Bracken, M. E. S., Cardinale, B. J., Cebrian, J., Cleland, E. E., Elser, J. J., Gruner, D. S., Harpole, W. S., Ngai, J. T., Sandin, S., Seabloom, E. W., Shurin, J. B., Smith, J. E., & Smith, M. D. (2009). Herbivore metabolism and stoichiometry each constrain herbivory at different organizational scales across ecosystems, Ecology Lett. 12, 516-527. https://doi.org/10.1111/j.1461-0248.2009.01304.x
- Hopkins, T. L., & Kramer, K. J. (1992). Insect cuticle sclerotization, Annu. Rev. Entomol. 37, 273-302. https://doi.org/10.1146/annurev.en.37.010192.001421
- Kaplanoglu, E., Chapman, P., & Scott, Donly, C. (2017). Overexpression of a cytochrome P450 and a UDP glycosyltransferase is associated with imidacloprid resistance in the Colorado potato beetle, Leptinotarsa decemlineata, Sci. Rep. 7, 1762. https://doi.org/10.1038/s41598-017-01961-4
- Kim, E., Choi, B., Park, Y., Cha, O., Jung, C., Lee, D., Kim, K., & Kim, Y. (2014). Overwintering conditions of the Diamondback moth and genetic variation of overwintering populations, Kor. J. Appl. Entomol. 53, 353-363.
- Kim, S. M., Hur, J. H., Han, D. S., Cho, J. M., & Kim, K. J., 2001. Diamondback moth (Plutella xylostella L.) resistance to organophosphorus and carbamate insecticides in Kangwon alpine vegetable croplands, Kor. Soc. Pestic. Sci. 5, 24-30.
- Kim, T. M., Underwood, N., & Inouye, B. D., 2013. Insect herbivores change the outcome of plant competition through both inter- and intraspecific processes, Ecology 94, 1753-1763. https://doi.org/10.1890/12-1261.1
- Kriehuber, T., Rattei, T., Weinmaier, T., Bepperling, A., Haslbeck, M., & Buchner, J. (2010). Independent evolution of the core domain and its flanking sequences in small heat shock proteins, FASEB J. 24, 3633-3642. https://doi.org/10.1096/fj.10-156992
- Lavoie, J. N., Gingras-Breton, G., Tanguay, R. M., & Landry, J. (1993). Induction of Chinese hamster HSP27 gene expression in mouse cells confers resistance to heat shock. HSP27 stabilization of the microfilament organization, J. Biol. Chem. 268, 3420-3429.
- Leal, M., & Gunderson, A. R. (2012). Rapid change in the thermal tolerance of a tropical lizard, Am Nat. 180, 815-822. https://doi.org/10.1086/668077
- Lee, S. C., Cho, Y. S., Kim, D. I. (1993). Comparative study of toxicological methods and field resistance to insecticides in diamondback moth (Lepidoptera: Plutellidae), Kor. J. Appl. Entomol. 32, 323-329.
- Lee, S. H., Kang, J. S., Min, J. S., Yoon, K. S., Strycharz, J. P., Johnson, R., Mittapalli, O., Margam, V. M., Sun, W., Li, H. M., Xie, J., Wu, J., Kirkness, E. F., Berenbaum, M. R., Pittendrigh, B. R., & Clark, J. M. (2010). Decreased detoxification genes and genome size make the human body louse an efficient model to study xenobiotic metabolism, Insect Mol. Biol. 19, 599-615. https://doi.org/10.1111/j.1365-2583.2010.01024.x
- Lemoine, N. P., & Burkepile, D. E. (2012). Temperatureinduced mismatches between consumption and metabolism reduce consumer fitness, Ecology 93, 2483-2489. https://doi.org/10.1890/12-0375.1
- Lemoine, N. P., Drews, W. A., Burkepile, D. E., & Parker, J. D. (2013). Increased temperature alters feeding behavior of a generalist herbivore, Oikos 122, 1669-1678. https://doi.org/10.1111/j.1600-0706.2013.00457.x
- Li, X., Schuler, M. A., & Berenbaum, M. R. (2007). Molecular mechanisms of metabolic resistance to synthetic and natural xenobiotics, Annu. Rev. Entomol. 52,231-253. https://doi.org/10.1146/annurev.ento.51.110104.151104
- Li, X., Zhu, B., Gao, X., & Liang, P. (2017). Over-expression of UDP-glycosyltransferase gene UGT2B17 is involved in chlorantraniliprole resistance in Plutella xylostella (L.), Pest Manag. Sci. 73, 1402-1409. https://doi.org/10.1002/ps.4469
- Lindmark-Mansson, H., & Akesson, B. (2000). Antioxidative factors in milk, Br. J. Nutr. 84, 103-110. https://doi.org/10.1017/S0007114500002324
- Lumjuan, N., McCarroll, L., Prapanthadara, L. A., Hemingway, J., & Ranson, H. (2005). Elevated activity of an Epsilon class glutathione transferase confers DDT resistance in the dengue vector, Aedes aegypti, Insect Biochem. Mol. Biol. 35,861-871. https://doi.org/10.1016/j.ibmb.2005.03.008
- Maibeche-Coisne, M. L., Monti-Dedieu, S., Aragon, S., & Dayphin-Villemant, C. (2000). A new cytochrome P450 from Drosophila melanogaster, CYP4G15, expressed in the nervous system, Biochem. Biophys. Res. Commun. 273, 1132-1137. https://doi.org/10.1006/bbrc.2000.3058
- Mannervik, B. (1985). The isoenzymes of glutathione transferase, Adv. Enzymol. Relat, Areas Mol. Biol. 57, 357-417.
- Metcalf, D. B., Asner, G. P., Martin, R. E., Espejo, J. E. S., Huasco, W. H., Amezquita, F. F. F., Carranza-Jimenez, L., Cabrera, D. F. G., Baca, L. D., Sinca, F., Quispe, L. P. H,, Taype, I. A., Mora, L. E., Davila, A. R., Solorzano, M. M., Vilca, B. L. P., Roman, J. M. L., Bustios, P. C. G., Revilla, N. S., Tupayachi, R., Girardin, C. A. J., Doughty, C. E., & Malhi, Y. (2014). Herbivory makes major contributions to ecosystem carbon and nutrient cycling in tropical forests. Ecol. Lett. 17, 324-332. https://doi.org/10.1111/ele.12233
- O'Connor, M. I. (2009). Warming strengthens an herbivore- plant interaction, Ecology 90, 388-398. https://doi.org/10.1890/08-0034.1
- O'Connor, M. I., Piehler, M. F., Leech, D. M., Anton, A., & Bruno, J. F. (2009). Warming and resource availability shift food web structure and metabolism, PLOS Biol. 7, e1000178. https://doi.org/10.1371/journal.pbio.1000178
- Pan, Y., Tian, F., Wei, X., Wu, Y., Gao, X., Xi, J., & Shang, Q. (2018). Thiamethoxam resistance in Aphis gossypii Glover relies on multiple UDP-glucuronosyltransferases, Front. Physiol. 9, 322. https://doi.org/10.3389/fphys.2018.00322
- Pavlidi, N., Vontas, J., & Van Leeuwen, T. (2018). The role of glutathione S-transferases (GSTs) in insecticide resistance in crop pests and disease vectors, Curr. Opin. Insect Sci. 27, 97-102. https://doi.org/10.1016/j.cois.2018.04.007
- Peyser, R. D., Lanno, S. M., Shimshak, S. J., & Coolon, J. D. (2017). Analysis of cytochrome P450 contribution to evolved plant toxin resistance in Drosophila sechellia, Insect Mol. Biol. 26, 715-720. https://doi.org/10.1111/imb.12329
- Rewitz, K. F., & Gilbert, L. I. (2008). Daphnia Halloween genes that encode cytochrome P450s mediating the synthesis of the arthropod molting hormone: evolutionary implications, BMC Evol. Biol. 8, 60. https://doi.org/10.1186/1471-2148-8-60
- Riveron, J. M., Yunta, C., Ibrahim, S. S., Djouaka, R., Irving, H., Menze, B. D., Ismail, H. M., Hemingway, J., Ranson, H., Albert, A., & Wondji, C. S. (2014). A single mutation in the GSTe2 gene allows tracking of metabolically based insecticide resistance in a major malaria vector, Genome Biol. 2014, 15.
- Sable, M. G., & Rana, D. K. (2016). Impact of global warming on insect behavior - A review, Agricultural Rev. 37, 81-84.
- Strode, C., Wondji, C. S., David, J. P., Hawkes, N. J., Lumjuan, N., Nelson, D. R., Drane, D. R., Karunaratne, S. H., Hemingway, J., Black, W. C., & Ranson, H. (2008). Genomic analysis of detoxification genes in the mosquito Aedes aegypti, Insect Biochem. Mol. Biol. 38, 113-123. https://doi.org/10.1016/j.ibmb.2007.09.007
- Sunday, J. M., Bates, A. E., & Dulvy, N. K. (2012). Thermal tolerance and the global redistribution of animals, Nat. Clim. Chang. 2, 686-690. https://doi.org/10.1038/nclimate1539
- Sunday, J. M., Bates, A. E., Kearney, M. R., Colwell, R. K., Dulvy, N. K., Longino, J. T., & Huey, R. B. (2014). Thermal-safety margins and the necessity of thermoregulatory behavior across latitude and elevation, Proc. Natl. Acad. Sci. USA. 111, 5610-5615. https://doi.org/10.1073/pnas.1316145111
- Talekar, N., & Shelton, A. (1993). Biology, ecology, and management of the diamondback moth. Annu. Rev. Entomol. 38, 275-301. https://doi.org/10.1146/annurev.en.38.010193.001423
- Taylor, R. P., & Benjamin, I. J. (2005). Small heat shock proteins: a new classification scheme in mammals, J. Mol. Cell. Cardiol. 38, 433-444. https://doi.org/10.1016/j.yjmcc.2004.12.014
- Thomas, J. H. (2007). Rapid birth-death evolution specific to xenobiotic cytochrome P450 genes in vertebrates, PLOS Genet. 3, e67. https://doi.org/10.1371/journal.pgen.0030067
- Tissieres, A., Mitchell, H. K., & Tracy, U. M. (1974). Protein synthesis in salivary glands of Drosophila melanogaster: relation to chromosome puffs, J. Mol. Biol. 84, 389-398. https://doi.org/10.1016/0022-2836(74)90447-1
- Vucic-Pestic, O., Ehnes, R. B., Rall, B. C., & Brose, U. (2011). Warming up the system: higher predator feeding rates but lower energetic efficiencies, Global Change Biol. 17, 1301-1310. https://doi.org/10.1111/j.1365-2486.2010.02329.x
- Watson, G. S., Watson, J. A., & Cribb, B. W. (2017). Diversity of cuticular micro- and nanostructures on insects: properties, functions, and potential applications, Annu. Rev. Entomol. 62, 185-205. https://doi.org/10.1146/annurev-ento-031616-035020
- Wilding, C. S., Weetman, D., Rippon, E. J., Steen, K., Mawejje, H. D., Barsukov, I., & Donnelly, M. J. (2015). Parallel evolution or purifying selection, not introgression, explains similarity in the pyrethroid detoxification linked GSTE4 of Anopheles gambiae and An. Arabiensis, Mol. Genet. Genomics 290, 201-215. https://doi.org/10.1007/s00438-014-0910-9
- Xu, Z.-B., Zou, X.-P., Zhang, N., Feng, Q.-L., & Zheng, S.-C. (2015). Detoxification of insecticides, allelochemicals and heavy metals by glutathione S-transferase SlGSTE1 in the gut of Spodoptera litura, Insect Sci. 22, 503-511. https://doi.org/10.1111/1744-7917.12142
- Yamamoto, K., Nagaoka, S., Banno, Y., & Aso, Y. (2009). Biochemical properties of an omega-class glutathione S-transferase of the silkmoth, Bombyx mori, Comp. Biochem. Physiol. C Toxicol. Pharmacol. 149, 461-467. https://doi.org/10.1016/j.cbpc.2008.10.108
- Yamamoto, K., & Yamada, N. (2016). Identification of a diazinon metabolizing glutathione S-transferase in the silkworm, Bombyx mori, Sci. Rep. 6.
- Zhang, X., Wu, M., Yao, H., Yang, Y., Cui, M., Tu, Z., Stallones, L., & Xiang, H. (2016). Pesticide poisoning and neurobehavioral function among farm workers in Jiangsu, People's Republic of China, Cortex 74, 396-404. https://doi.org/10.1016/j.cortex.2015.09.006