References
- Mitchell KA, Boardman L, Clusella-Trullas S, et al. Effects of nutrients and water restriction on thermal tolerance: a test of mechanisms and hypotheses. Comparative Biochemistry and Physiology Part A, 2012:15–11. https://www.sciencedirect.com/science/article/pii/S1095643317301411?via%3Dihub
- Beaman JE, White CR, Seebacher F. Evolution of plasticity: mechanistic link between development and reversible acclimation. Trends Ecol Evol. 2016;31(3):237–249. https://www.sciencedirect.com/science/article/pii/S0169534716000185?via%3Dihub
- Little CM, Chapman TW, Hillier NK. Plasticity is key to success of Drosophila suzukii (Diptera: drosophilidae) invasion. Journal of Insect Sciences. 20:1–8. 2020;https://academic.oup.com/jinsectscience/article/20/3/5/5837529
- Nestel D, Papadopoulos NT, Pascacio-Villafan C, et al. Resource allocation and compensation during development in holometabolous insects. J Insect Physiol. 2016;95:78–88 https://doi.org/10.1016/j.jinsphys.2016.09.010.
- Andersen, S. O. (2010). Insect cuticular sclerotization: a review. Insect biochemistry and molecular biology, 40(3), 166-178. https://www.sciencedirect.com/science/article/pii/S0965174809001544
- Weldon CW, Mnguni S, Demares F, et al. Adult diet does not compensate for impact of a poor larval diet on stress resistance of a tephritid fruit fly. J Exp Biol. 2019;222:11.
- Weldon CW, Díaz-Fleischer F, Pérez-Staples D. Desiccation resistance of tephritid flies. Area-Wide Management of Fruit Fly Pests. (2019b);27. https://www.taylorfrancis.com/chapters/oa-edit/10.1201/9780429355738-4/desiccation-resistance-tephritid-flies-christopher-weldon-francisco-d%C3%ADaz-fleischer-diana-p%C3%A9rez-staples
- Nyamukondiwa C, Terblanche JS. Thermal tolerance in adult Mediterranean and natal fruit flies (Ceratitis capitata and Ceratitis rosa): effect of age, gender and feeding status.J Therm Biol. 2009;34(8):406–414.
- Colinet H, Renault D. Dietary live yeast alters metabolic profiles, protein biosynthesis and thermal stress tolerance of Drosophila melanogaster. Comparative Biochemistry and Physiology, Part A. 2014;170:6–14. https://www.sciencedirect.com/science/article/pii/S1095643314000038?via%3Dihub
- Andersen LH, Kristensen TN, Loeschcke V, et al. Protein and carbohydrate composition of larval food affects tolerance to thermal stress and desiccation in adult Drosophila melanogaster. J Insect Physiol. 2010;56(4):336–340. https://www.sciencedirect.com/science/article/pii/S002219100900359X?via%3Dihub
- Hoffmann AA. Rapid adaptation of invertebrate pests to climatic stress? Curr Opin Insect Sci. 2017;21:7–13.
- Terblanche JS, Hoffmann AA. Validating measurements of acclimation for climate change adaptations. Curr Opin Insect Sci. 2020;41:7–16. Doi: https://www.sciencedirect.com/science/article/pii/S2214574520300511?via%3Dihub.
- Kellerman V, Heerwaarden BV, Sgro CM, et al. Fundamental evolutionary limits in ecological traits drive Drosophila species distributions. Science. 2009;325(5945):1244–1246.
- White IM, Elson-Harris MM. Fruit flies of economic importance: their identification and bionomics. Oxon UK: CAB International; 1992. p. 601.
- Zingore KM, Sithole G, Abdel-Rahman EM, et al. Global risk of invasion by Bactrocera zonata: implications on horticultural crop production under changing climatic conditions. PLoS One. 2020;15(12):e0243047. https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0243047.
- Jang EB, Enkerlin W, Miller C, et al. Trapping related to phytosanitary status and trade. In: Shelly B, Epsky, N, Jang, EB, Reyes-Flores, J, Vargas, R, et al., editors. Trapping and the detection, control, and regulation of Tephritidae fruit flies. Dondrecht: Springer Science+Bussiness Media; 2014. p. 589–608. DOI: 10.1007/978-94-017-9193-9_2
- EPPO Bulletin. PM 9/11 (1): bactrocera zonata: procedure for official control. EPPO Bull. 2010; 40(3):390–395. https://onlinelibrary.wiley.com/doi/10.1111/j.1365-2338.2010.02421.x
- Ben-Yosef M, Verykouki E, Altman Y, et al. Effect of thermal acclimation on the tolerance of Bactrocera zonata (Diptera: tephritidae) to hydric stress. Frontiers in Physiology. 2021;12:686424. https://www.frontiersin.org/articles/10.3389/fphys.2021.686424/full
- Gazit Y, Akiva R. Toxicity of malathion and spinosad to bactrocera zonata and ceratitis capitata (Diptera: tephritidae). Fl Entomol. 2017;100(2):385–389. doi:10.1653/024.100.0240.
- Pascacio-Villafán C, Righini N, Nestel D, et al. Diet quality and conspecific larval density predicts functional trait variation and performance in a polyphagous frugivorous fly. Funct Ecol. 2022;36(5):1163–1176.
- FAO/IAEA/USDA. Product Quality Control for Sterile Mass-Reared and Released Tephritid Fruit Flies, Version 6.0. Vienna Austria: International Atomic Energy Agency; 2014. p. 164.
- Romanyukha AA, Carey JR, Karkach AS, et al. (2004). The impact of diet switching on resource allocation to reproduction and longevity in Mediterranean fruit flies. Proceedings of the Royal Society of London, 271, 1319–1324. https://royalsocietypublishing.org/doi/10.1098/rspb.2004.2719
- Nestel D, Nemny-Lavy E, Chang CL. Lipid and protein loads in pupating larvae and emerging adults as affected by composition of Mediterranean fruit fly (Ceratitis capitata) meridic larval diets. Arch Insect Biochem Physiol. 2004;56:97–109.
- Moraiti CA, Verykouki E, Papadopoulos NT. Chill coma recovery of Ceratitis capitata adults across the Northern Hemisphere. Sci Rep. 2022;12(1):17555. https://www.nature.com/articles/s41598-022-21340-y
- Weldon CW, Nyamukondiwa C, Karsten M, et al. Geographic variation and plasticity in climate stress resistance among Southern Africa populations of Ceratitis capitata (Wiedmann) (Diptera:Tephritidae). Sci Rep. 2018;8(1):8–9849. https://www.nature.com/articles/s41598-018-28259-3
- Nestel D, Nemni-Lavi E. Nutrient balance in medfly, Ceratitis capitata, larval diets affects the ability of the developing insect to incorporate lipid and protein reserves. Entomologia Experimentalis et Applicatta. 2007;126:53–60. https://onlinelibrary.wiley.com/doi/full/10.1111/j.1570-7458.2007.00639.x
- Balandran-Quintana RR, Mercado-Ruiz JN, Mendoza-Wilson AM. Wheat bran proteins: a review of their uses and potential. Food Rev Int. 2015;31(3):279–293. https://www.tandfonline.com/doi/full/10.1080/87559129.2015.1015137
- Hemndane S, Jacobs PJ, Dornez E, et al. Comprehensive Reviews in Food Science and Food Safety. 2015;15:28–42. https://ift.onlinelibrary.wiley.com/doi/10.1111/1541-4337.12176
- Hemdane S, Jacobs P J, Dornez E, Verspreet J, Delcour J A and Courtin C M. (2016). Wheat (Triticum aestivum L .) Bran in Bread Making: A Critical Review. COMPREHENSIVE REVIEWS IN FOOD SCIENCE AND FOOD SAFETY, 15(1), 28–42. 10.1111/1541-4337.12176
- Chang CL. Effect of amino acids on larvae and adults of Ceratitis capitata (Diptera: tephritidae). Ann Entomol Soc Am. 2004;97(3):529–535. https://academic.oup.com/aesa/article/97/3/529/70302
- Pascacio-Villafán C, Williams T, Birke A, et al. Nutritional and non-nutritional food components modulate phenotypic variation but not physiological trade-offs in insects. Sci Rep. 2016;6(1):29413. https://www.nature.com/articles/srep29413
- Chang CL, Kurashima R, Albrecht C. Effect of limiting concentrations of growth factors in mass rearing diets for Ceratitis capitata larvae (Diptera: tephritidae). Ann Entomol Soc Am. 2000;93(4):898–903. https://academic.oup.com/aesa/article/93/4/898/22677
- Kaspi R, Mossinson S, Drezner T, Kamensky B and Yuval B. Effects of larval diet on development rates and reproductive maturation of male and female Mediterranean fruit flies. Physiol Entomol, 2002;27(1), 29–38. 10.1046/j.1365-3032.2001.00264.x
- Nestel D, Nemny-Lavy E and Chang C Ling. (2004). Lipid and protein loads in pupating larvae and emerging adults as affected by the composition of Mediterranean fruit fly (Ceratitis capitata) meridic larval diets. Arch. Insect Biochem. Physiol., 56(3), 97–109. 10.1002/arch.20000
- Nestel D, Nemny-Lavy E and Chang C Ling. (2004). Lipid and protein loads in pupating larvae and emerging adults as affected by the composition of Mediterranean fruit fly (Ceratitis capitata) meridic larval diets. Arch. Insect Biochem. Physiol., 56(3), 97–109. 10.1002/arch.20000
- Kristensen TN, Henningsen AK, Aastrup C, et al. Fitness components of Drosophila melanogaster developed on a standard laboratory diet or a typical natural food source. Insect Sci. 2016;23(5):771–779. https://onlinelibrary.wiley.com/doi/epdf/10.1111/1744-7917.12239
- Henry Y, Overgaard J, Colinet H. Dietary nutrient balance shapes phenotypic traits of Drosophila melanogaster in interaction with gut microbiota. Comp Biochem Physiol Part A. 2020;241:110626.
- Littler AS, Garcia MJ, Teets NM. Laboratory diet influences cold tolerance in a genotype-dependent manner in Drosophila melanogaster. Comp Biochem Physiol Part A. 2021;257:110948.
- Morey AC, Venette RC, Nystrom Santacruz EC, et al. Host‐mediated shift in the cold tolerance of an invasive insect. Ecol Evol. 2016;6(22):8267–8275.
- Mutamiswa R, Machekano H, Nyamukondiwa C, et al. Host plant-related responses on the thermal fitness of Chilo partellus (Swinhoe) (Lepidoptera: crambidae). Arthropod Plant Interact. 2020;14(4):463–471. https://link.springer.com/article/10.1007/s11829-020-09762-9
- Koštál V, Šimek P, Zahradníčková H, et al. Conversion of the chill susceptible fruit fly larva (Drosophila melanogaster) to a freeze tolerant organism. Proc Nat Acad Sci. 2012;109(9):3270–3274.
- Yerushalmi GY, Misyura L, Donini A, et al. Chronic dietary salt stress mitigates hyperkalemia and facilitates chill coma recovery in Drosophila melanogaster. J Insect Physiol. 2016;95:89–97.
- Raza MF, Wang Y, Cai Z, et al. Gut microbiota promotes host resistance to low-temperature stress by stimulating its arginine and proline metabolism pathway in adult Bactrocera dorsalis. PLoS Pathog. 2020;16(4):e1008441. https://pubmed.ncbi.nlm.nih.gov/32294136/
- Shreve SM, Yi SX, Lee RE. Increased dietary cholesterol enhances cold tolerance in Drosophila melanogaster. Cryoletters. 2007;28(1):33–37.
- Andersen SO. Insect cuticular sclerotization: a review. Insect Biochem Mol Biol. 2010;40(3):166–178. https://www.sciencedirect.com/science/article/pii/S0965174809001544
- Gibbs AG, Rajpurohit S. Cuticular lipids and water balance. Insect hydrocarbons: biology, biochemistry, and chemical ecology. 2010;100–120. https://books.google.co.il/books?hl=en&lr=&id=brc3SLVzo-oC&oi=fnd&pg=PA100&dq=Gibbs+cuticular+&ots=3CrZFtsJ2J&sig=1AJQ9GTX-g4rAIoPkAFlNBSd56s&redir_esc=y#v=onepage&q=Gibbs%20cuticular&f=false
- Lindquist S, Craig EA. The heat-shock proteins. Annu Rev Genet. 1988;22(1):631–677. https://web.archive.org/web/20170809032227id_/http://lindquistlab.wi.mit.edu/PDFs/LindquistCraig1988ARG.pdf
- Ballard JWO, Melvin RG, Simpson SJ. Starvation resistance is positively correlated with body lipid proportion in five wild caught Drosophila simulans populations. J Insect Physiol. 2008;54(9):1371–1376. https://www.sciencedirect.com/science/article/pii/S0022191008001406
- Gibbs AG, Chippindale AK, Rose MR. Physiological mechanisms of evolved desiccation resistance in Drosophila melanogaster. J Exp Biol. 1997;200(12):1821–1832. https://pubmed.ncbi.nlm.nih.gov/9225453/