اثر قارچ بیمارگر (Beauveria bassiana (Ascomycota, Hypocreales بر رفتارکاوشگری زنبور پارازیتویید ( Aphidius matricariae (Hym.: Braconidae در شرایط نیمه طبیعی

نوع مقاله : مقاله پژوهشی

نویسندگان

1 دانشکدة علوم و مهندسی کشاورزی، پردیس کشاورزی و منابع طبیعی دانشگاه تهران، کرج، ایران

2 پژوهشگاه تنوع زیستی و دینامیک اکوسیستم، دانشگاه آمستردام، هلند

چکیده

در این تحقیق، اثر قارچ بیمارگر Beauveria bassiana (Ascomycota, Hypocreales) بر رفتار کاوشگری زنبور پارازیتویید Aphidius matricariae Haliday (Hym.: Braconidae) روی گیاه بادمجان کامل در شرایط نیمه طبیعی ارزیابی شد. آزمایش بویایی ­سنج Y- شکل نشان داد حضور قارچ باعث دور شدن افراد پارازیتویید و بالعکس باعث جلب آن‌ها به بازوی فاقد قارچ شد. افراد پارازیتویید به طور معنی ­دار به سمت هوای پاک (شاهد) حرکت کردند. در حالی­ که عده کمی ‌به سمت گیاه بادمجان خسارت دیده آلوده با اجساد شته حاوی قارچ جلب شدند. همچنین، آزمون غیر انتخابی اثر اجساد شته حاوی اسپور قارچ بر رفتار کاوشگری پارازیتویید ثابت کرد وجود قارچ به طور معنی­داری باعث کاهش تعداد تلاش‌های تخم­ریزی افراد ماده شد. در آزمون انتخابی، پارازیتویید مدت زمان بیشتری روی گیاه خسارت دیده سپری کرد و گیاه سالم را در مدت زمان کمتری ترک نمود. حضور یا عدم حضور قارچ بر زمان ترک کلونی شته توسط زنبور پارازیتویید اثر معنی­دار نداشت. نتایج نشان داد زنبور پارازیتویید A. matricariae قادر به تشخیص قارچ بیمارگر بود و از ورود به کلنی شته های آلوده اجتناب کرد. با این حال، زمانی که پارازیتویید به یک کلنی آلوده وارد شد از تخمریزی و تماس با قارچ خودداری کرد. نتایج نشان داد که علایم شیمیایی ارسال شده از گیاه بادمجان و قارچ بیمارگر B. bassiana جدایة EUT116 نقش مهمی را در اتخاذ تصمیم‌های بهینه برای کاوشگری و افزایش شایستگی زنبور پارازیتویید A. matricariae در جهت کنترل شته سبز هلو بازی می‌کنند. 

کلیدواژه‌ها


عنوان مقاله [English]

Effect of entomopathogenic fungus, Beauveria bassiana (Ascomycota, Hypocreales) on foraging behaviour of parasitoid wasp, Aphidius matricariae (Hym.: Braconidae)

نویسندگان [English]

  • M. Rashki 1
  • A. Kharazi-pakdel 1
  • H. Allahyari 1
  • J. van Alphen 2
1 Department of Plant Protection, College of Science and Agricultural Engineering, Campus of Agriculture and Natural Resources, University of Tehran, Karaj, Iran
2 Institute for Biodiversity and Ecosystem Dynamics, Amsterdam University, The Netherlands
چکیده [English]

The objective of the current research was to evaluate the effect of the entomopathogenic fungus, Beauveria bassiana (Ascomycota, Hypocreales), on foraging behaviour of the parasitoid wasp, Aphidius matricariae Haliday (Hym.: Braconidae), on whole eggplant under microcosm conditions. A Y-tube olfactometer experiment showed the presence of the fungus caused avoidance of the parasitoid and conversely, its attraction towards the empty arm. Although most of A. matricariae significantly moved towards clean air (control), but a few were attracted to damaged eggplants infested with the sporulating aphid cadavers. Moreover, no-choice test for the effect of sporulating aphid cadaver on foraging behaviour of the A. matricariae revealed that the presence of the fungus significantly reduced the number of ovipositional attempts. In choice test, the parasitoid spent more time on damaged plants than on intact ones. The presence or absence of the fungus had no impact on allocation time of the parasitoid in an aphid colony. The results indicated that the parasitoid wasp, A. matricariae, was able to distinguish the entomopathogenic fungus and avoided entering the infected aphid colony. Nevertheless, when the parasitoid entered to an infected colony, it avoided contacting with the fungus or ovipositing. The results indicated thatthe released chemical cues of eggplant and also those of the entomopathogenic fungus, B. bassiana isolate EUT116, play an important role in the foraging decision making and also for increasing itsfitnessto control the green peach aphid.

کلیدواژه‌ها [English]

  • searching
  • fitness
  • patch
  • plant condition
Baverstock, J. 2004. Interactions between aphids, their insect and fungal natural enemies and the host plant. Ph.D. thesis. The University of Nottingham.
Baverstock, J., Alderson, P. G. and Pell, J. K. 2005. Influence of the aphid pathogen Pandora neoaphidis on the foraging behaviour of the aphid parasitoid Aphidius ervi. Ecological Entomology 30: 665-672.
Blande, J. D., Pickett, J. A. and Poppy, G. M. 2007. A comparison of semiochemically mediated interactions involving specialist and generalist brassica-feeding aphids and the braconid parasitoid Diaeretiella rapae. Journal of Chemical Ecology 33:767-779.
Bottrell, D. G. and Barbosa, P. 1998. Manipulating natural enemies by plant variety selection and modification: A realistic strategy? Annual Review of Entomology 43: 347-67.
Brobyn, P. J., Clark, S. J. and Wilding, N. 1988. The effect of fungus infection of Metopolophium dirhodum (Hom.: Aphididae) on the oviposition behaviour on the aphid parasitoid Aphidius rhopalosiphi (Hym.: Aphidiidae). Entomophaga 33: 333-338.
Burger, J. M. S., Huang, Y., Hemerik, L., van Lenteren, J. C. and Vet, L. E. M. 2006. Flexible use of patch-leaving mechanisms in a parasitoid wasp.Journal of Insect Behavior 19(2): 155-170. 
Couchoux, C. and van Nouhuys, S. 2014 Effects of Intraspecific competition and host-parasitoid developmental timing on foraging behavior of a parasitoid wasp. Journal of Insect Behavior 27: 283-301.
Crespo, R., Pedrinia, N., Juareza, M. P. and Dal Bellob, G. M. 2008. Volatile organic compounds released by the entomopathogenic fungus Beauveria bassiana. Microbiological Research 163: 148-151.
De Farias, A. M. I. and Hopper, K. R. 1999. Oviposition behavior of Aphelinus asychis (Hymenoptera: Aphelinidae) and Aphidius matricariae (Hymenoptera: Aphidiidae) and defense behavior of their host Diuraphis noxia (Homoptera: Aphididae). Environmental Entomology 28: 858-862.
Dicke, M. and Baldwin, I. T. 2010. The evolutionary context for herbivore-induced plant volatiles: beyond the cry for help’. Trends in Plant Science15: 167-175.
Driessen, G. and Bernstein, C. 1999. Patch departure mechanisms and optimal host exploitation in an insect parasitoid. Journal of Animal Ecology 68: 445-459.
Fazeli-Dinan, M., Talaei-Hassanloui, R., Allahyari, H., Kharazi-Pakdel, A. and Mohammadi, H. 2015.Olfactometric responses of Encarsia formosa (Hym.:Aphelinidae) to odors of infested greenhouse whitefly Trialeurodes vaporariorum (Hem.: Aleyrodidae), by Lecanicillium longisporum treated on cucumber leaves. Plant Pests Research 5(1): 1-12.
Fellowes, M. D. E., van Alphen, J. J. M. and Jervis, M. A. 2005. Foraging behaviour. In Jervis, M. A. (Ed.). Foraging behaviour. Insects as natural enemies: A practical perspective. Springer, Dordrecht, The Netherlands. pp. 1-71.
Hardy, I. C. W., Goubault, M. and Batchelor, T. P. 2013. Hymenopteran contests and agonistic behaviour. In: Hardy, I. C. W. and Briffa, M. (Ed.). Animal contests. Cambridge University Press, UK, pp. 5-32.
Furlong, M. J. and Pell, J. K. 1996. Interactions between the fungal entomopathogen Zoophthora radicans Brefeld (Entomophthorales) and two hymenopteran parasitoidsattacking the diamondback moth, Plutella xylostella L. Journal of Invertebrate Pathology 68:15-21.
Giri, M. K., Pass, B. C., Yeargan, K. V. and Parr, J. C. 1982. Behavior, net reproduction, longevity, and mummy-stage survival of Aphidius matricariae (Hym. Aphididae). Entomophaga 27: 147-153.
Girling, R. D., Hassall, M., Turner, J. G. and Poppy, G. M. 2006. Behavioural responses of the aphid parasitoid Diaeretiella rapae to volatiles from Arabidopsis thaliana induced by Myzus persicae. Entomologia Experimentalis et Applicata 120: 1-9.
Grasswitz, T. R. 1998. Effect of adult experience on the host-location behavior of the aphid parasitoid Aphidius colemani Viereck (Hymenoptera: Aphidiidae). Biological Control 12: 177-181.
Hansen, L. S. and Steenberg, T. 2007. Combining larval parasitoids and an entomopathogenic fungus for biological control of Sitophilus granaries (Coleoptera: Curculionidae) in stored grain. Biological Control 40: 237–242.
Hochberg, M. E. and Lawton, J. H. 1990. Competition between kingdoms. Trends in Ecology and Evolution 5: 367-371.
Hilker, M. and McNeil, J. 2008. Chemical and behavioral ecology in insect parasitoids: how to behave optimally in a complex odorous environment. In: Wajnberg E., Bernstein C., van Alphen J., (Eds.) Behavioral Ecology of Insect Parasitoids. Blackwell Publishing, Oxford, UK. pp. 92-112.
Kessler, A. and Heil, M. 2011. Evolutionary ecology of plant defenses.The multiple faces of indirect defenses and their agents of natural selection. Functional Ecology 25: 348-357.
Lacey, L. A., Mesquita, A. L. M., Mercadier, G., Debire, R., Kazmer, D. J. and Leclant, F. 1997. Acute and sublethal activity of the entomopathogenic fungus Paecilomyces fumosoroseus (Deuteromycotina: Hyphomycetes) on adult Aphelinus asychis (Hymenoptera : Aphelinidae). Environmental Entomology 26 (6): 1452-1460.
Lord, J. C. 2001. Response of the wasp Cephalonomia tarsalis (Hymenoptera: Bethylidae) to Beauveria bassiana (Hyphomycetes: Moniliales) as free conidia or infection in its host, the sawtoothed grain beetle, Oryzaephilus surinamensis (Coleoptera: Silvanidae). Biological Control 21: 300-304.
Meiners, T. and Peri, E. 2013. Chemical ecology of insect parasitoids: essential elements for developing effective biological control programmes. In: Wajnberg, E. and Colazza, S. (Eds.). Chemical ecology of insect parasitoids. Wiley- Blackwell, Oxford, UK, pp.193-224.
Meyling, N. V. and Pell, J. K. 2006.  Detection and avoidance of an entomopathogenic fungus by a generalist insect predator. Ecological Entomology 31: 162–171.
Milner, R. J. 1997. Prospects for biopesticides for aphid control. Entomophaga42: 227-239.
Muratori, F., Boivin, G. and Hance, T. 2008. The impact of patch encounter rate on patch residence time of female parasitoids increases with patch quality. Ecological Entomology 33: 422-427.
Pell, J. K., Pluke, R., Clark, S. J., Kenward, M. G. and Alderson, P. G. 1997. Interactions between two aphid natural enemies, the entomopathogenic fungus Erynia neoaphidis Remaudie` re & Hennebert (Zygomycetes: Entomophthorales) and the predatory beetle Coccinella septempunctata L. (Coleoptera: Coccinellidae). Journal of Invertebrate Pathology 69: 261-268.
Powell, W., Pennacchio, F., Poppy, G. M. and Tremblay, E. 1998. Strategies involved in the location of hosts by the parasitoid Aphidius ervi Haliday (Hymenoptera: Braconidae: Aphidiinae). Biological Control 11: 104-112.
Rännbäcka, L. M., Cotesa, B., Andersonb, P., Rämerta, B.and Meyling, N. V. 2015. Mortality risk from entomopathogenic fungi affects oviposition behavior in the parasitoid wasp Trybliographa rapae. Journal of Invertebrate Pathology 124: 78-86.
Roy, H. E., Steinkraus, D. C., Eilenberg, J., Hajek, A. E. and Pell, J. K. 2006. Bizarre interactions and endgames: entomopathogenic fungi and their arthropod hosts. Annual Review of Entomology 51: 331-357.
SAS 1989. SAS/STAT Users Guide, version 6, Vols. 1 and 2. SAS Institute Inc. Cary, NC.
Sewify, G. H. and El Arnaouty, S. A. 1998. The effect of the entomopathogenic fungus Verticillium lecanii (Zimm.) Viegas on mature larvae of Chrysoperla carnea Stephens (Neuroptera, Chrysopidae) in the laboratory. Acta Zoologica Fennica 209: 233-237.
Stockermans, B. C. and Hardy, I. C. W. 2013. Subjective and objective components of resource value additively increase aggression in parasitoid contests. Biology Letters9: 4.
Storeck, A., Powell, W., Rehman, A., Poppy, G. M. and van Emden H. F. 2000. The role of plant chemical cues in determining host preference in the aphid parasitoids Praon myzophagum and Aphidius colemani. Entomologia Experimentalis et Applicata 97: 41-46.
Tentelier, C., Wajnberg, E. and Fauvergue, X. 2005. Parasitoids use herbivore-induced information to adapt patch exploitation behaviour. Ecological Entomology 30: 739–744.
Todorova, S. I., Coderre, D. and Cote, J. C. 2000. Pathogenicity of Beauveria bassiana isolates toward Leptinotarsa decemlineata (Coleoptera: Chrysomelidae), Myzus persicae (Homoptera: Aphididae) and their predator Coleomegilla maculata lengi (Coleoptera: Coccinellidae). Phytoprotection 81: 15–22.
Wajnberg, E. 2006. Time allocation strategies in insect parasitoids: from ultimate predictions to proximate behavioral machanisms. Behavioral Ecology and Sociobiology 60: 589-611.
Weisser, W. W. 1995. Within-patch foraging behaviour of the aphid parasitoid Aphidius funebris:plant architecture, host behaviour, and individual variation.Entomologia Experimentalis et Applicata76: 133-141.
Yeo, H., Pell, J. K., Alderson, P. G., Clark, S. J. and Pye, B. J. 2003. Laboratory evaluation of temperature effects on the germination and growth of entomopathogenic fungi and on their pathogenicity to two aphid species. Pest Management Science 59:156-165.
Zimmermann, G. 2007. Review on safety of the entomopathogenic fungi Beauveria bassiana and Beauveria brongniartii. Biocontrol Science and Technology 17: 553-596.