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Variability and genetic basis for migratory behaviour in a spring population of the aphid, Aphis gossypii Glover in the Yangtze River Valley of China

Published online by Cambridge University Press:  16 June 2008

X.D. Liu ,
B.P. Zhai ,
X.X. Zhang  and
H.N. Gu
X.D. Liu*
Affiliation:
Department of Entomology, Nanjing Agricultural University, Nanjing 210095, China
B.P. Zhai
Affiliation:
Department of Entomology, Nanjing Agricultural University, Nanjing 210095, China
X.X. Zhang
Affiliation:
Department of Entomology, Nanjing Agricultural University, Nanjing 210095, China
H.N. Gu
Affiliation:
CSIRO Entomology, Black Mountain Laboratories, Clunies Ross Road, Canberra, ACT 2601, Australia
*
*Author for correspondence Fax: +8625 84395242 E-mail: [email protected]
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Abstract

The population dynamics, development of gonads, takeoff and flight behaviour of Aphis gossypii Glover were investigated in order to test whether there was variation of migratory ability in the spring population. Field surveys showed that not all the aphids overwintering on hibiscus migrated to the secondary host plants, and the host-alternating and host-specific life-cycle forms coexisted in Nanjing, China. Substantial variation in flight capacity of winged individuals, development of gonads and takeoff behaviour were found within the spring population. The frequency distribution of flight duration and the number of ovarioles per individual alatae exhibited two peaks, representing the migratory and sedentary genotypes, respectively. Significant response to directional selection on takeoff behaviour demonstrated the additive genetic component of this variation. Selection for ‘takeoff’ individuals caused a significant increase in takeoff angle from 39.8° in the first selection to 68.7° in the fifth; and, hence, screened out the migratory genotype (M), while selection for the sedentary individuals increased the rate of non-takeoffs significantly, and screened out the sedentary genotype (S). The reciprocal cross, M♀×S♂, produced hybrid offspring performing significantly steeper takeoff angles compared with those from the cross S♀×M♂, suggesting the presence of a maternal effect. On the other hand, takeoff rate was ranked as M♀×S♂=S♀×M♂>M>S, involving no sex-linkage and maternal effect. The coexistence of host-alternating and host-specific life-cycle forms of A. gossypii on the primary host has, as deduced from the present studies, a genetic basis.

Keywords

Aphis gossypiipopulation differentiationinheritancemigratory genotypesedentary genotypetakeoff behaviourChina
Type
Research Paper
Information
Bulletin of Entomological Research , Volume 98 , Issue 5 , October 2008 , pp. 491 - 497
Copyright
Copyright © 2008 Cambridge University Press

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References

Blackmer, J.L. & Byme, D.N. (1993) Flight behaviour of Bemisia tabaci in a vertical flight chamber: Effect of time of day, sex, age and host quality. Physiological Entomology 18, 223–232.CrossRefGoogle Scholar
Blackmer, J.L., Byrne, D.N. & Tu, Z. (1995) Behavioural, morphological, and physiological traits associated with migratory Bemisia tabaci (Homoptera: Aleyrodidae). Journal of Insect Behavior 8, 251–267.CrossRefGoogle Scholar
Blackman, R.L. & Eastop, V.F. (1984) Aphids on the World's Crops: An Identification and Information Guide. 466 pp. Chichester, UK, John Wiley.Google Scholar
Blackman, R.L. & Eastop, V.F. (1994) Aphids on the World's Trees. 987 pp. Wallingford, UK, CAB International.CrossRefGoogle Scholar
Byrne, D.N., Buchmann, S.L. & Spangler, H.G. (1988) Relationship between wing loading, wing beat frequency and body mass in homopterous insects. Journal of Experimental Biology 135, 9–23.CrossRefGoogle Scholar
Ding, J.H. & Su, J.Y. (2002) Agricultural Entomology. pp. 242–244. Beijing, Agricultural Press of China.Google Scholar
Dixon, A.F.G. (1998) Aphid Ecology. 2nd edn. pp. 128–186. London, Chapman & Hall.Google Scholar
Ferrari, R. & Nicoli, G. (1994) Life cycle and natural enemies of Aphis gossypii Glover: first observations. Informatore Fitopatologico 44, 59–62.Google Scholar
Fuller, S.J., Chavigny, P., Lapchin, L. & Valerberghe-Masutti, F. (1999) Variation in clonal diversity in glasshouse infestations of the aphid, Aphis gossypii Glover, in southern France. Molecular Ecology 8, 1867–1877.CrossRefGoogle ScholarPubMed
Gatehouse, A.G. (1997) Behaviour and ecological genetics of wind-borne migration by insects. Annual Review of Entomology 42, 475–502.CrossRefGoogle ScholarPubMed
Gong, P. & Zhang, X.X. (2001) The inducement of temperature and photoperiod to produce sexuals of Aphis gossypii Glover. Acta Phytophylacica Sinica 28, 318–324.Google Scholar
Isard, S.A., Irwin, M.E. & Hollinger, S.E. (1990) Vertical distribution of aphids (Homoptera: Aphididae) in the planetary boundary layer. Environmental Entomology 19, 1473–1484.CrossRefGoogle Scholar
Kidd, N.A.C. & Cleaver, A.M. (1984) The relationship between pre-flight reproduction and migratory urge in alatae of Aphis fabae Scopoli (Hemiptera: Aphididae). Bulletin of Entomological Research 74, 517–527.CrossRefGoogle Scholar
Kidd, N.A.C. & Cleaver, A.M. (1986) The control of migratory urge in Aphis fabae Scopoli (Hemiptera: Aphididae). Bulletin of Entomological Research 76, 77–87.CrossRefGoogle Scholar
Liu, X.D., Zhai, B.P., Zhang, X.X. & Xiong, F. (2003a) The relationship between flight behaviour and ovary development in Aphis gossypii Glover. Entomological Knowledge 40, 39–42.Google Scholar
Liu, X.D., Zhang, X.X. & Zhai, B.P. (2003b) Flight activity rhythm of Aphis gossypii Glover in Nanjing and its flight capacity. Acta Entomologica Sinica 46, 489–493.Google Scholar
Liu, X.D., Zhai, B.P., Liang, S.A., Xu, X.H. & Gong, Q.H. (2006) Migratory and sedentary strains of Aphis gossypii Glover and the flight characteristics of their hybridized offspring. Acta Entomologica Sinica 49, 619–624.Google Scholar
Loxdale, H.D. & Lushai, G. (1999) Slaves of the environment: the movement of insects in relation to their ecology and genotype. Philosophical Transactions of the Royal Society of London Series B: Biological Science 354, 1479–1495.CrossRefGoogle Scholar
Loxdale, H.D., Hardie, J., Halbert, S., Foottit, R., Kidd, N.A.C. & Carter, C.I. (1993) The relative importance of short- and long-range movement of flying aphids. Biological Reviews 68, 291–311.CrossRefGoogle Scholar
Loxdale, H.D., Brookes, C.P., Wynne, I.R. & Clark, S.J. (1998) Genetic variability within and between English populations of the damson-hop aphid, Phorodon humuli (Hemiptera: Aphididae), with special reference to esterases associated with insecticide resistance. Bulletin of Entomological Research 88, 513–526.CrossRefGoogle Scholar
Messina, F.J. (1987) Genetic contribution to the dispersal polymorphism of the cowpea weevil (Coleoptera: Bruchidae). Annual Entomology Society of American 80, 12–16.CrossRefGoogle Scholar
Reynolds, D.R., Mukhopadhyay, S., Riley, J.R., Das, B.K., Nath, P.S. & Mandal, S.K. (1999) Seasonal variation in the windborne movement of insect pests over northeast India. International Journal of Pest Management 45, 195–205.CrossRefGoogle Scholar
Riley, J.R., Downham, M.C.A. & Cooter, R.J. (1997) Comparison of the performance of Cicadulina leafhoppers on flight mills with that to be expected in free flight. Entomologia Experimentalis et Applicata 83, 317–322.CrossRefGoogle Scholar
Rufus, I., Willis, M. & Byrne, D. (1999) Modulation of whitefly takeoff and flight orientation by wind speed and visual cues. Physiological Entomology 24, 311–318.Google Scholar
SAS Institute Inc. (2001) JMP user's guide, ver. 4. Cary, NC, USA, SAS Institute Inc.Google Scholar
SPSS Inc. (2000) TableCurve 2D 5.0 for Windows. Chicago, IL, USA, SPSS Inc.Google Scholar
Sunnucks, P., De Barro, J., Lushai, G., Maclean, N. & Hales, D. (1997) Genetic structure of an aphid studied using microsatellites: cyclic parthenogenesis, differentiated lines and host specialization. Molecular Ecology 6, 1059–1073.CrossRefGoogle Scholar
Sunnucks, P., Chisholm, D., Turak, E. & Hales, D. (1998) Evolution of an ecological trait in parthenogenetic Sitobion aphids. Heredity, 81, 638–647.CrossRefGoogle Scholar
Taylor, L.R., Woiwod, I.P. & Taylor, R.A.J. (1979) The migratory ambit of the hop aphid and its significance in aphid population dynamics. Journal of Animal Ecology 48, 955–972.CrossRefGoogle Scholar
Walters, K.F.A. & Dixon, A.F.G. (1983) Migratory urge and reproductive investment in aphids: variation within clones. Oecologia 58, 70–75.CrossRefGoogle ScholarPubMed
Walters, K.F.A. & Dixon, A.F.G. (1984) The effect of temperature and wind on the flight activity of cereal aphids. Annals of Applied Biology 104, 17–26.CrossRefGoogle Scholar
Wang, Q., Du, J.G. & Cheng, X.N. (1997) Genetics studies on wing dimorphism of brown planthopper, Nilaparvata lugens (Homoptera: Delphacidae). Acta Entomologica Sinica 40, 343–348.Google Scholar
Wright, L.C., Pike, K.S., Allison, D. & Cone, W.W. (1995) Seasonal occurrence of alate hop aphids (Homoptera, Aphididae) in Washington-state. Journal of Agricultural Entomology 12, 9–20.Google Scholar
Zhang, X.X. & Wang, M.T. (1991) Studies on the relationship between variation of ovary canal number and the takeoff behaviour in green peach aphid. Acta Phytophylacica Sinica 18, 161–166.Google Scholar