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Environmental factors associated with fluctuations in the numbers of natural enemies of a population of citrus red scale, Aonidiella aurantü (Maskell) (Hemiptera: Diaspididae)

Published online by Cambridge University Press:  10 July 2009

P. R. Atkinson
Affiliation:
South Africa Sugar Association Experiment Station, Mount Edgecomber 4300, South Africa.

Abstract

Natural enemies of Aonidiella aurantü (Mask.) were counted in suction-machine samples taken fortnightly over 41 months from an orchard of orange trees in the Swaziland lowlands, a region where biological control of the scale is difficult. Changes in the log population intensity/‘twig’ (Δ log N) of four species were, in each case, calculated over four thermal constants of 5000, 10 000, 15 000 and 20 000 hour– degrees above 12°C (h°>12C). The middle two constants were assumed to approximate to the thermal constants of the generation times of the natural enemies. For each natural enemy, Δ log N measured over each thermal constant was related by regression analysis to climatic and biotic indices to see how the interval over which population change was measured affected the conclusions. The longer the interval, the greater was the percentage of the explained variation in Δ log N, and the greater the number of indices that became significant. However at 20 000 h°>12°C, population change was measured over rather long intervals for short–lived species like Aphytis. At both 10 000 and 15 000 h°>12°C, the number and the identity of the significant indices in the regression tended to be the same. Consequently, conclusions about the factors affecting the natural enemies were based on these regression results. A. africanus Qued–nau, Comperiella bifasciata How. and Rhyzobius lophanthae (Blaisd.) responded directly to changes in their host's numbers, but Habrolepis rouxi Comp. responded inversely and was unlikely to have been effective. Furthermore, it was sensitive to high summer temperatures, as was A. africanus and possibly R. lophanthae. C. bifasciata was not sensitive to high summer temperatures but was adversely affected by the hyperparasitoid Marietta javensis (How.). None of the natural enemies was affected by prevailing saturation deficits.

Type
Original Articles
Copyright
Copyright © Cambridge University Press 1983

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References

Abdelrahman, I. (1974 a). The effect of extreme temperatures on California red scale, Aonidiella aurantü (Mask.) (Hemiptera: Diaspididae), and its natural enemies. — Aust. J. Zool. 22, 203212.Google Scholar
Abdelrahman, I. (1974 b). Growth, development and innate capacity for increase in Aphytis chrysomphali Mercet and A. melinus DeBach, parasites of California red scale, Aonidiella aurantü (Mask), in relation to temperature. — Aust. J. Zool. 22, 213230.CrossRefGoogle Scholar
Atkinson, P. R. (1977). Preliminary analysis of a field population of citrus red scale, Aonidiella aurantü (Maskell), and the measurement and expression of stage duration and reproduction for life tables.— Bull. em. Res. 67, 6587.Google Scholar
Atkinson, P. R. (1983). Estimates of natural mortality related to environmental factors in a population of citrus red scale, Aonidiella aurantü (Maskell) (Hemiptera: Diaspididae). — Bull. em. Res. 73, 239258.Google Scholar
Catling, H. D. (1971). Studies on the citrus red scale, Aonidiella aurantü (Mask.), and its biological control in Swaziland. — J. em. Soc. sth. Afr. 34, 393411.Google Scholar
Cilliers, C. J. (1971). Observations on circular purple scale Chrysomphalus aonidum (Linn.), and two introduced parasites in western Transvaal citrus orchards. — Entomophaga. 16, 269284.Google Scholar
Compere, H. (1961). Red scale and its insect enemies. — Hilgardia 31, 173278.CrossRefGoogle Scholar
Flanders, S. E. (1944). Observations on Comperiella bifasciata, an endoparasite of diaspine coccidsAnn. ent. Soc. Am. 37, 365371.Google Scholar
Morris, R. F. (1959). Single–factor analysis in population dynamics. — Ecology. 40, 580588.CrossRefGoogle Scholar
Nel, J. J. C., De Lange, L. & Van Ark, H. (1979). Resistance of citrus red scale, Aonidiella aurantü (Mask.), to insecticides. — J. ent. Soc. sth. Afr. 42, 275281.Google Scholar
Quednau, F. W. (1965). A technique for identifying mixed populations of six species of Aphytis parasitic on red scale Aonidiella aurantü (Mask), for recognition after recovery from scales collected in citrus orchards (Hymenoptera, Aphelinidae). — S. Afr. J. agric. Sci. 8, 4356.Google Scholar
Southwood, T. R. E. (1978). Ecological methods with particular reference to the study of insect populations. — 524 pp. London, Chapman & Hall.Google Scholar
Varley, G. C. & Gradwell, G. R. (1960). Key factors in population studies. — J. Anim. Ecol. 29, 399401.CrossRefGoogle Scholar
Varley, G. C., Gradwell, G. R. & Hassell, M. P. (1973). Insect population ecology, an analytical approach. — 212 pp. Oxford, Blackwell Scientific Publications.Google Scholar
Waterhouse, F. L. & Amos, T. G. (1968). The measurement of temperature, humidity and carbon dioxide/oxygen level amongst stored food products. — pp. 3346 in Wadsworth, R. M. (Ed). The measurement of environmental factors in terrestrial ecology.— 314 pp. Oxford, Blac–well Scientific Publications.Google Scholar
Williamson, M. H. (1972). The analysis of biological populations. — 180 pp. London, Edward Arnold.Google Scholar