Aphis gossypii Glover (Hemiptera: Aphididae)’nin Biyolojik Özelliklerine Ana Yaşının Etkileri

Year 2020, Volume: 7 Issue: 1, 60 - 65, 25.01.2020

Alime Bayındır Erol , Ali Kemal Birgücü

https://doi.org/10.30910/turkjans.679910

Cited By: 2

Abstract

Pamuk yaprakbiti, Aphis gossypii Glover (Hemiptera: Aphididae) pamuk, kabak, turunçgiller ve örtüaltı sebzelerinde önemli zararlar meydana getiren yaprak bitlerinden biridir. Bu çalışmada pamuk yaprak bitinin en iyi gelişme, üreme ve canlı kalma oranlarının hangi ana yaşında doğan yavrularından elde edildiği araştırılmıştır. Bu amaçla ana bireyin 1., 2., 3. günlerde, 7., 8., 9. günlerde ve 13., 14., 15. günlerde doğurduğu yavru bireylerden genç, orta ve yaşlı popülasyon grupları oluşturulmuştur. Her bir popülasyon grubu için yaşa bağlı yaşam çizelgesi parametreleri ayrı ayrı hesaplanmıştır. Çalışma sonucunda genç, orta ve yaşlı popülasyon gruplarının hesaplanan yaşam çizelgesi parametreleri; kalıtsal üreme yeteneği (rm) 0,292, 0,363 ve 0,305 dişi/dişi/gün, net üreme gücü (Ro) 22,207, 23,425 ve 22,881 dişi/dişi, ortalama döl süresi (To) 10,610, 8,673 ve 10,259 gün, toplam üreme oranı (GRR) 37,509, 43,174 ve 44,525 dişi/dişi, artış oranı sınırı (λ) 1,339, 1,438 ve 1,356 dişi/gün olarak bulunmuştur. Ergin ömrü 12,10, 11,14 ve 10,26 gün, preovipozisyon süresi tüm popülasyon gruplarında 0,00 gün, ovipozisyon süresi sırasıyla 14,00, 13,33 ve 14,12 gün, postovipozisyon süresi sırasıyla 1,60, 1,47 ve 1,80 gün ve döl süresi sırasıyla 7,52, 6,75 ve 7,25 gün olarak belirlenmiştir.

Keywords

Aphis gossypii, pamuk yaprakbiti

Thanks

Bu çalışma Pamukkale Üniversitesi Bilimsel Araştırma Projeleri Koordinasyon Birimi tarafından 2019KKP076 nolu proje ile desteklenmiştir.

Effects of Maternal Age on Biological Characteristics of Aphis gossypii Glover (Hemiptera: Aphididae)

Abstract

Cotton aphid, Aphis gossypii Glover (Hemiptera: Aphididae) is one of the aphids that cause significant damage to cotton, cucurbits, citrus fruits and greenhouse-grown vegetables. In this study the best developmental, reproduction and survival rates of cotton aphids were investigated from the offspring at which maternal age. For this purpose, young, middle and older-aged group populations were constituted offspring bred at the 1st, 2nd, 3rd days, 7th, 8th, 9th days and 13th, 14th, 15th days of oviposition period of maternal aphids, respectively. Age dependent life table parameters were calculated separately for each population group. As a result of the study parameters obtained for intrinsic rate of increase (rm) 0.292, 0.363 and 0.305 females/ female/ day, net reproductive rates (Ro) 22.207, 23.425 and 22.881 females/ female, mean generation time (To) 10.610, 8.673 and 10.259 days, gross reproduction rate (GRR) 37.509, 43.174 and 44.525 females/ female, finite rate of increase (λ) were found to be 1.339, 1.438, and 1.356 females/ days respectively for Aphis gossypii young, middle and older-aged population groups. The adult life times were 12.10, 11.14 and 10.26 days, the preoviposition period all population groups were 0.00 days, the oviposition period were 14.00, 13.33 and 14.12 days, the postoviposition period were 1.60, 1.47 and 1.80 days respectively and the generation time were 7.52, 6.75 and 7.25 days, respectively

Keywords

Aphis gossypii, cotton aphid

References

• Beckerman, A., Benton, T.G., Ranta, E., Kaitala, V., Lundberg, P. 2002. Population dynamic consequences of delayed life-history effects. Trends in Ecology Evolotion, 17 (6), 263-269.
• Benton, T.G., Plaistow, S.J., Beckerman, A.P., Lapsley, C.T., Littlejohns, S. 2005. Changes in maternal investment in eggs can affect population dynamics. Proceedings of the Royal Society B: Biological Sciences, 272 (1570), 1351-1356.
• Birch, L.C. 1948. The intrinsic rate of natural increase of an insect population. Journal of Animal Ecology, 17 (1), 15-26.
• Carey, J.R. 1993. Applied Demography for Biologists with Special Emphasis on Insects. Oxford University Press, Oxford, UK, 206p.
• Fox, C.W. 1993. The influence of maternal age and mating frequency on egg size and offspring performance in Callosobruchus maculatus (Coleoptera: Bruchidae). Oecologia, 96 (1), 139-146.
• Fox, C.W., Dingle, H. 1994. Dietary mediation of maternal age effects of offspring performance in seed beetle (Coleoptera: Bruchidae). Functional Ecology, 8, 600-606.
• Fox, C.W., Czesak, M.E. 2000. Evolutionary ecology of progeny size in arthropods. Annual Review of Entomologi, 45, 341-369.
• Hercus, M.J., Hoffmann, A.A. 2000. Maternal and grandmaternal age influence offspring fitness in Drosophila. Proceeding of the Royal Society B: Biological Sciences, 267 (1457), 2105–2110.
• Imura, O. 1987. Demographic attributes of Tribolium freemani Hinton (Coleoptera: Tenebrionidae). Applied Entomology and Zoology, 22 (4), 449-455.
• Jann, P., Ward, P.I. 1999. Maternal effects and their consequences for offspring fitness in the yellow dung fly. Functional Ecology, 13 (1), 51-58.
• Kairo, M.T.K., Murphy, S.T. 1995. The life history of Rodolia iceryae Janson (Coleoptera: Coccinellidae) and the potential for use in innoculative releases against Icerya pattersoni Newstead (Homoptera: Margarodidae) on coffee. Journal of Applied Entomology, 119, 487-491.
• Kern, S., M. Ackermann, Stearns, S.C., Kawecki, T.J. 2001. Decline in offspring viability as a manifestation of aging in Drosophila melanogaster. Evolution, 55 (9), 1822- 1831.
• Mills, A., Hardmann-Goldstein, I. 1985. Maternal age, development time, position effect variegation in Drosophila melanogaster. Genetic Selection Evolotion, 17 (1), 171–178.
• Mishra, G., Omkar. 2004. Influence of parental age on reproductive performance of an aphidophagous ladybird, Propylea dissecta (Mulsant). Journal of Applied Entomology, 128 (9-10), 605–609.
• Mohaghegh, J., DeClercq, P., Tirry, L. 1998. Effects of maternal age and egg weight on developmental time and body weight of offspring of Podisus maculiventris (Heteroptera: Pentatomidae). Annals of Entomological Society of America, 91 (3), 315–322.
• Moore P.J., Harris, W.E. 2003. Is a decline in offspring quality a necessary consequence of maternal age. Proceeding of the Royal Society B: Biological Sciences, 270 (2), 192–194.
• Muller, D., Giron, D., Desouhant, E., Rey, B., Casas, J., Lefrique, N., Visser, B. 2017. Maternal age affects offspring nutrient dynamics. Journal of Insect Physiology, 101, 123–131.
• Obata, S. 1987. Mating behaviour and sperm transfer in the ladybird beetle, Harmonia axyridis Pallas (Coleoptera: Coccinellidae). Applied Entomology and Zoology, 22 (4), 434–442.
• Opit, G.P., Throne, J. E. 2007. Influence of maternal age on the fitness of progeny in the rice weevil, Sitophilus oryzae (Coleoptera: Curculionidae). Environmental Entomology, 36 (1), 83-89.
• Özgökçe, M.S., Karaca, İ. 2010. Yaşam Çizelgesi: Temel Prensipler ve Uygulamalar. Türkiye Entomoloji Derneği 1. Çalıştayı, Ekoloji Çalışma Grubu, 11-12 Haziran 2010, Isparta.
• Pandey, P., Omkar. 2013. Age based mate choice improves reproductive performance and offspring attributes in parthenium beetle, Zygogramma bicolorata (Coleoptera: Chrysomelidae). Canadian Entomolojist, 145 (3), 292–301.
• Perez-Mendoza, J., Throne, J.E., Baker, J.E. 2004. Ovarian physiology and age- grading in the rice weevil Sitophilus oryzae (Coleoptera: Curculionidae). Journal of Stored Product Research, 40 (2), 179-196.
• Priest, N.K., Mackowiak, B., Promislow, D.E.L. 2002. The role of parental age effects on the evolution of aging. Evolution 56 (5), 927-935.
• Rahsepar, A., Haghani , M., Sedaratian-Jahromi, A., Ghane-Jahromi, M., Farrar, N. 2016. Different cucumber (Cucumis sativus) varieties could affects biological performance of cotton aphid, Aphis gossypii Glover (Hemiptera: Aphididae), a case study at laboratory condition. Entomofauna, 37 (21), 353-364.
• Southwood, T.R.E. 1978. Ecological methods. Halsted Press, Chapman and Hall. London, 524 pp.
• Tanaka, Y. 1990. Age specificity of inbreeding depression during a life of Callosobruchus chinensis (Coleoptera: Bruchidae). Researches on Population Ecology, 32 (2), 329-335.
• Yanagi, S.I., Miyatake, T. 2002. Effects of maternal age on reproductive traits and fitness components of the offspring in the bruchid beetle, Callosobruchus chinensis (Coleoptera: Bruchidae). Physiological Entomology, 27 (4), 261-266.