بررسی رشد و نمو وابسته به دما در زنبور Telenomus busseolae، انگل‌وارۀ تخم Sesamia cretica

نوع مقاله : علمی پژوهشی-فارسی

نویسنده

دانشیار گروه حشره‌شناسی و بیماری‌های گیاهی، پردیس ابوریحان، دانشگاه تهران، ایران

چکیده

ساقه‌خواران نیشکر Sesamia cretica Lederer و S. nonagrioides Lefevere از مهم‌ترین آفات مزارع نیشکر در ایران محسوب می‌شوند. مهم‌ترین دشمن طبیعی این آفات در خوزستان، زنبور انگل‌وارۀ تخم Telenomus busseolae Gahan می‌باشد که نقش قابل توجهی را در تنظیم جمعیت آفت ایفاء می‌نماید. دما مهم‌ترین عامل محیطی است که رشد و نمو حشرات را تحت تأثیر قرار می‌دهد. به منظور بررسی ارتباط تغییرات دما و روند رشد و نمو زنبور T. busseolae تأثیر 7 دمای ثابت 15، 18، 20، 25، 30، 35 و 37 درجۀ سلسیوس بر طول دوره رشدی مراحل نابالغ زنبور هنگام فعالیت روی تخم S. cretica مورد مطالعه قرار گرفت .جهت توصیف اثر دما روی سرعت رشد و نمو مراحل نابالغ زنبور و تعیین آستانۀ دمایی از دو مدل خطی معمولی و ایکموتو و تاکای استفاده شد. نتایج حاصل از تجزیه رگرسیون بین دما و طول دوره نابالغ زنبور روی تخم میزبان نشان داد که دما به‌طور معنی‌داری در هر دو جنس نر و ماده بر طول دورۀ رشدی قبل از بلوغ زنبور تأثیر دارد. اگرچه هر دو مدل خطی قادر به توصیف داده بودند ولی مدل ایکموتو و تاکای برازش بهتری را روی داده‌ها ارائه نمود. با استفاده از مدل خطی ایکموتو و تاکای، آستانۀ دمایی در دو جنس نر و ماده زنبور روی تخمS. cretica به ترتیب 44/12 و 50/12 درجۀ سلسیوس و نیاز گرمایی 250 و 255 روز- درجه تعیین شد.

کلیدواژه‌ها


عنوان مقاله [English]

Temperature-dependent development of parasitoid wasp, Telenomus busseolae on Sesamia cretica

نویسنده [English]

  • A. Jamshidnia
Associate Professor, Department of Entomology and Plant Pathology, College of Aburaihan, University of Tehran, Iran
چکیده [English]

Background and Objectives
The sugarcane stem borers, Sesamia cretica Lederer and S. nonagrioides Lefever are the most important pests of sugarcane in Iran causing heavy losses in cane and considerable reduction in sugar yield. The egg parasitoid wasp, Telenomus busseolae Gahan is the most remarkable natural enemy of Sesamia spp. in Khuzestan province, Iran that plays an important role in regulating the populations of sugarcane stem borers. Temperature is an effective abiotic factor that influences the development of natural enemies. The present study aimed to investigate the temperature-dependent development of T. busseolae on S. cretica.
Material and Methods
The development rates and thermal constant of the immature stages of T. busseolae on S. cretica eggs were studied at seven constant temperatures (15, 18, 20, 25, 30, 35, and 37ºC), a photoperiod of 16L:8L, and 65%±5% RH. Fresh egg masses of S. cretica were exposed to the newly mated female of T. busseolae for 6 h. Afterwards, the parasitized eggs were kept at different temperatures. The parasitized eggs were checked daily until adult emergence. Development rate was modeled as a function of temperature using two mathematical models, including common and Ikemoto and Takai linear models. The linear models were analyzed using the SAS software.
Results
The results of regression analysis showed that the immature developmental period of T. busseolae decreased with elevating temperature from 18ºC to 35ºC. In 15ºC and 37ºC, no development rate was found for T. busseolae. Immature development time declined from 45 to 11 days and 46 to 12 days in male and female parasitoids, respectively. The percent of adult emergence was not affected by temperature. However, two linear models provided a satisfactory relationship between immature development rate and temperature. Based on statistical criteria, Ikemoto and Takai linear model estimated thermal constant and temperature threshold more precisely. For male and female parasitoids, the thermal constant was 250 and 255 degree-days and the low-temperature threshold was 12.44ºC and 12.5ºC on S. cretica eggs, respectively.
Conclusion
In the current study, the thermal requirement of T. busseolae on S, cretica was estimated for the first one. Information regarding the thermal requirement of T. busseolae can be useful for the rearing and application of this parasitoid in the biological control of sugarcane stem borers. This finding could be used to predict the number of T. busseolae generations and the best time for parasitoid release in sugarcane fields.

کلیدواژه‌ها [English]

  • linear model
  • thermal requirement
  • temperature threshold
Abrol, D.P. 2012. Pollination biology. Biodiversity conservation and agricultural production, Springer.
Aizen, M.A., Garibaldi, L.A., Cunningham, S.A., and Klein, A.M. 2008. Long-term global trends in crop yield and production reveal no current pollination shortage but increasing pollinator dependency. Current Biology, 18: 1572-1575.
Biesmeijer,  J.C.,  Roberts,  S. P. M.,  Reemer,  M.,  Ohlemuller,  R.,  Edwards,  M.,  and Peeters, T. 2006. Parallel declines in pollinators and insect-pollinated plants in Britain and the Netherlands. Science, 313: 351-354.
Blevins, D., and M. Lukaszewski. 1998. Boron in plant structure and function. Annual Reviews of Plant Physiology and Plant Molecular Biology, 49:481-500.
Bolanos, L., Lukaszewski, K., Bonilla, I., and Blevins, D. 2004. Why boron? Plant Physiology and Biochemistry, 42: 907-912.
Chandra, B.S., Sudheer Kumar, S., Ranganatha, A., and Dudhe, M.Y. 2010. Inheritance of the fertility restoration for different CMS sources in sunflower (Helianthus annuus L.). SABRAO Journal of Breeding and Genetics, 42(1): 46-50.
Dag, A., Lior, E., and Afik, O. 2002. Pollination of confection sunflowers (Heliantus annuus L.) by honey bees (Apis mellifera L.). American Bee Journal, 142(6): 443-445.
Dell, B., and Huang, L. 1997. Physiological response of plants to low boron. Plant and Soil. 193:103-120.
Eagleton, G., Sandover, S., and Dickson. 1988. Research report sunflower (1981-1986). Western Australia. pp.182.
Elmhmoud Altayeb, O.A., and Abdalla Nagi, S.K. 2015. Efficiency of honeybees (Apis mellifera) on the production of sunflower (Helianthus annus L.) seeds in the Sudan. Journal of Experimental Biology and Agricultural Sciences, 3(2): 191-195.
Free, J.B. 1993. Insect Pollination of Crops. Academic Press, London, UK. with permission from Elsevier. 
Freund, D.E., and Furgula, B. 1982. Effect of pollination by insects on the seed set and yield of ten oil seed sunflower cultivars. American Bee Journal, 122(4): 648-652.
Greenleaf, S.S., and Kremen, C. 2006. Wild bees enhance honey bees pollination of hybrid sunflower. Proceedings of the National Academy of Sciences of the United States of America, 103: 13890-13895.
Guo, S., Ge, Y., and Na Jom, K. 2017. A review of phytochemistry, metabolite changes, and medicinal uses of the common sunflower seed and sprouts (Helianthus annuus L.). Chemistry Central journal, 11(1): 95.
Lehtilä, K., and Syrjänen, K. 1995. Positive Effects of Pollination on Subsequent Size, Reproduction, and Survival of Primula Veris. Ecology, 76(4): 1084-1098.
Moreti, A.C., Silva R.M.B., Silva, E.C.A., Alves, M.L.T.M.F., and Otsuk, I.P. 1996. Increase of sunflower (Helianthus annuus) seed production by pollinating insect action. Scientia Agricola, 53: 280-284 (in Portuguese, with abstract in English).
Müller, A., Diener, S., Schnyder, S., Stutz, K., Sedivy, C., and Dorn, S. 2006. Quantitative pollen requirements of solitary bees: implications for bee conservation and the evolution of bee-flower relationships. Biological Conservation, 130: 604-615.  
Porto, W.S., Carvalho, C.G.P., and Pinto, R.J.B. 2007. Adaptability and stability as selection criteria for sunflower genotypes. Pesquisa Agropecuária Brasileira, 42: 491-499 (in Portuguese with abstract in English). 
Prasifka, J.R., Mallinger, R.E., Portlas, Z.M., Hulke, B.S., Fugate, K.K., Paradis, T., Hampton, M.E., and Carter, C.J. 2018. Using nectar-related traits to enhance crop-pollinator interactions. Frontiers in plant science, 9: 8-12.
Primack, R.B., and Inouye, D.W. 1993. Factors affecting pollinator visitation rates: A biogeographic comparison. Current Science, 65(3): 257-262.
Rojarsi, M., Kanakadurga, k., Durga Rani, V., and Anuradha, Ch. 2012. Honey bees-potential pollinators in hybrid seed production of sunflower. International Journal of Applied Biology and Pharmaceutical technology. 3(2): 216-221.
Sarah, S., Greenleaf, and Claire Kremen. 2006 . Wild bees enhance honey bees’ pollination of hybrid sunflower. PNAS, 103(37): 13890-13895.
Schutte, K.H. 1964. The biology of the trace elements; their role in nutrition. Crosby Lock-wood and Son Ltd., London.
Seltman, H.J. 2018. Experimental design and analysis. Chapter 11: Two-way Aova; available at: http://www.stat.cmu.edu/∼hseltman/309/Book/Book.pdf
Shireen, F., Nawaz, M.A., Chen, C., Zhang, Q., Zhang, Z., Sohail, H., Sun, J., Cao, H., Huang, Y., and Bie, Z. 2018. Boron: functions and approaches to enhance its availability in plants for sustainable agriculture. International Journal of Molecular Sciences, 19(7): 1856.
Sotomayor, C., Norambuena, P., and Ruiz, R. 2010. Boron dynamics related to fruit growth and seed production in kiwifruit (Actinida deliciosa, cv. Hayward). Ciencia e Investigación Agraria, 37(1): 133-141.
SPSS Inc. Released 2008. SPSS Statistics for Windows, Version 17.0. Chicago: SPSS Inc.
Van der Sluijs, J.P., and Vaage, N.S. 2016. Pollinators and global food security: the need for holistic global stewardship. Food Ethics, 1: 75-91.
Wittmann, D. 2007. Bee pollinators and economic importance of pollination in crop production, case of kakamage, Westera Kenya. Department of entomology and wildlife. University of cape coast, ULB. 93P.