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Determining the age of adults of Stomoxys calcitrans (L.) (Diptera: Muscidae)

Published online by Cambridge University Press:  10 July 2009

T. S. Mail
Affiliation:
School of Animal Biology, University College of North Wales, Bangor, Gwynedd LL57 2UW, UK.
J. Chadwick
Affiliation:
School of Animal Biology, University College of North Wales, Bangor, Gwynedd LL57 2UW, UK.
M. J. Lehane
Affiliation:
School of Animal Biology, University College of North Wales, Bangor, Gwynedd LL57 2UW, UK.

Abstract

A preliminary investigation to find an easily assayable biochemical character, varying reproducibly with age which would give a more accurate assessment of insect age than the best methods then available, had revealed the fluorescent eye pigments, the pteridines, as a promising candidate. Stomoxys calcitrans (L.) was chosen as a model. Double-blind laboratory experiments in which the age post-eclosion of females was predicted from a standard laboratory curve of pteridine accumulation with age post-eclosion, showed the method to be accurate on average to ±1·49 days. Further laboratory experiments defined the relationships between temperature and pteridine accumulation in males and females of S. calcitrans such that the method could be modified for field use. Field observations in the UK indicated that the temperature of adults in the wild is determined by ambient temperature, the number of sunlight hours and the flies' own physiological and/or behavioural capabilities. From this information, equations for the accumulation of pteridines with temperature and age post-eclosion in males and females of S. calcitrans were constructed. To test the accuracy of these equations, approximately 19 600 marked flies of known age were released in a farmyard; 126 females were recaptured over 22 days and 90 males over 19 days. The average errors of predicted age using the pteridine accumulation method were ±190 days for females and ±137 days for males over the life-span of the recaptured insects.

Type
Original Articles
Copyright
Copyright © Cambridge University Press 1983

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References

Chadwick, J. (1983). Age determination studies on Stomoxys calcitrans. — M.Sc. thesis, Univ. Wales.Google Scholar
Davies, J. B., Corbet, P. S., Gillies, M. T., McCrae, A. W. R. (1971). Parous rates in some Amazonian mosquitoes collected by three different methods. — Bull. ent. Res. 61, 125132.CrossRefGoogle Scholar
Detinova, T. S. (1962). Age–grouping methods in Diptera of medical importance with special reference to some vectors of malaria. — Monograph Ser. W.H.O. no. 47, 216 pp.Google ScholarPubMed
Johnston, J. S., Ellison, J. R. (1982). Exact age determination in laboratory and field-caught Drosophila. — J. Insect Physiol. 28, 773779.CrossRefGoogle Scholar
Kuzina, O. S. (1942). On the gonotrophic relationships in horseflies (Stomoxys calcitrans and Haematobia irritans) [in Russian]. — Medskaya Parazit. 11, 70.Google Scholar
Michener, C. D., Cross, E. A., Daly, H. V., Rettenmeyer, C. W., Wille, A. (1955). Additional techniques for studying the behaviour of wild bees (I). Insectes soc. 2, 237246.CrossRefGoogle Scholar
Neville, A. C. (1963). Daily growth layers in locust rubber-like cuticle influenced by an external rhythm. — Insect Physiol. 9, 177186.CrossRefGoogle Scholar
Neville, A. C. (1970). Cuticle ultrastructure in relation to the whole insect. — pp. 1739 in Neville, A. C. (Ed.). Insect ultrastructure. —Symp. R. entomol. Soc. Lond. no. 5, 185 pp.Google Scholar
Nieschulz, O. (1933). éber die Bestimmung der Vorzugstemperatur von Insekten (besonders von Fliegen und Miicken). — Zool. Anz. 103, 2129.Google Scholar
Perry, E. L. (1912). Malaria in the Jeypore Hill tract and djoining coastland. — Paludism 5, 32.Google Scholar
Polovodova, V. P. (1949). Determination of the physiological age of female Anopheles ‘in Russian’. — Medskaya Parazit. 18, 352.Google Scholar
Saunders, D. S.(1962). Age determination for female tsetse flies and the age compositions of samples of Glossina pallidipes Aust., G. palpalis fuscipes Newst. and G. brevipalpis Newst. — Bull. ent. Res. 53, 579595.CrossRefGoogle Scholar
Saunders, D. S. (1964). Age–changes in the ovaries of the sheep ked, Melophagus ovinus (L.)(Diptera: Hippoboscidae). — Proc. R. ent. Soc. Lond. (A) 39, 6872.Google Scholar
Schlein, Y. (1979). Age grouping of anopheline malaria vectors (Diptera: Culicidae) by the cuticular growth lines. — J. med. Entomol. 16, 502506.CrossRefGoogle Scholar
Schlein, Y., Gratz, N. G. (1972). Age determination of some flies and mosquitos by daily growth layers of skeletal apodemes. — Bull. Wld Hlth Org. 47, 7176.Google ScholarPubMed
Schlein, Y., Gratz, N. G. (1973). Determination of the age of some anopheline mosquitos by daily growth layers of skeletal apodemes. — Bull. Wld Hlth Org. 49, 371375.Google ScholarPubMed
Southwood, T. R. E. (1978). Ecological methods. —524 pp. London, Chapman & Hall.Google Scholar
Stones, L. C. (1976). The stablefly. —pp. 561569 in The U.F.A.W. handbook on the care and management of laboratory animals. —1015 pp. London, E.&S. Livingstone.Google Scholar
Tyndale-Biscoe, M., Kitching, R. L. (1974). Cuticular bands as age criteria in the sheep blowfly Lucilia cuprina (Wied.) (Diptera, Calliphoridae). — Bull. ent. Res. 64, 161174.CrossRefGoogle Scholar
Willmer, P. G. (1982). Microclimate and the environmental physiology of insects. —Adv. Insect Physiol. 16, 157.CrossRefGoogle Scholar
Ziegler, I., Harmsen, R. (1969). The biology of pteridines in insects. — Adv. Insect Physiol. 6, 139203.CrossRefGoogle Scholar