Effect of hydration, photoperiod and temperature on diapause termination in eggs ofPetrobia (Tetranychina) harti (Acari: Tetranychidae)

Experimental and Applied Acarology - Tập 11 - Trang 111-123 - 1991
D. S. Koveos1, M. E. Tzanakakis1
1Laboratory of Applied Zoology and Parasitology, Faculty of Agriculture, University of Thessaloniki, Thessaloniki, Greece

Tóm tắt

Petrobia harti (Ewing) displays a facultative summer diapause in the egg stage. An adult female will lay only either diapause or non-diapause eggs throughout her life. In the laboratory, diapause eggs are laid by females which develop on detachedOxalis articulata leaves under long-day photoperiods and a relatively low temperature of 19±1°C. Diapause occurs in a stage of advanced embryonic development, in which the embryo appears U-shaped when observed from the egg's ventral side. Embryonic development ceased at this stage, and no further growth occurred when the eggs were kept under a relative humidity of about 70% in various photoperiod and temperature conditions. However, when the eggs were hydrated by placing them on wet cotton wool, development in some embryos (apparently in those which had completed their diapause development) proceeded beyond the U-stage at a rate similar to that in non-diapause embryos and the eggs hatched. Under LD 16∶8 and 19±1°C or 26±1°C, the later from oviposition the period of egg hydration started, the higher the percentage of diapause termination. Under LD 16∶8 and 26±1°C, diapause termination occurred mostly during the first week of hydration, while at 19±1°C mostly during the second and third week. At 26±1°C, in eggs hydrated 15 days but not 30 days from oviposition, the percentage of diapause termination was higher under a long-day than under a short-day photoperiod. Under LD 16∶8, when the eggs were hydrated continuously from oviposition or starting 15, 30 and 45 days from it, the percentage of diapause termination was higher at 26±1°C than at 19±1°C. The percentage of diapause-laying adult females and the intensity of egg diapause were higher when the pre-imaginal mites grew at LD 12∶12 and 19±1°C, than when they grew at LD 16∶8 and 26±1°C. This maternal effect on egg diapause intensity was expressed when the eggs were maintained at LD 12∶12 and 19±1°C but not at LD 16∶8 and 26±1°C.

Tài liệu tham khảo

Ando, Y., 1972. Eggs diapause and water absorption in the false melon beetle,Atrachya menetriesi Feldermann (Coleoptera: Chrysomelidae). Appl. Entomol. Zool., 7: 142–154. Beck, S.D., 1967. Water intake and the termination of diapause in the european corn borer,Ostrinia nubilalis. J. Insect Physiol., 13: 739–750. Beck, S.D., 1980. Insect Photoperiodism (2nd ed.). Academic, New York, 387 pp. Brooking, B.C. Jr., 1957. A study of the evocation and termination of diapause inPetrobia apicalis (Banks) (Acarina: Tetranychidae). Master's Thesis, Louisiana State Univ., Baton Rouge, 45 pp. Dubitzki, E. and Gerson, U., 1987. The natural history ofPetrobia (Tetranychina) harti (Ewing) andPetrobia (Mesotetranychus) tunisiae Manson (Acari: Tetranychidae) in the laboratory. Exp. Appl. Acarol., 3: 91–94. Garcia Mari, F. and del Rivero, J.M., 1982. El ácaroTetranychina harti (Ewing) en Espana. Bol. Serv. Def. Plagas, 8: 55–62. Glancey, B.M., 1958. Studies of embryonic diapause in the legume mitePetrobia apicalis (Banks). Master's Thesis, Louisiana State Univ., Baton Rouge, 66 pp. Gutierrez, J. and Helle, W., 1985. Evolutionary changes in the Tetranychidae. In: W. Helle and M.W. Sabelis (Editors), Spider Mites, Their Biology, Natural Enemies and Control, Vol. A. Elsevier, Amsterdam, pp. 91–107. Hatzinikolis, E.N., 1968. Mites of the subfamily Bryobiinae noticed on cultivated plants in Greece. Ann. Inst. Phytopathol. Benaki, 8: 170–171 (in Greek). Jeppson, L.R., Keifer, H.H. and Baker, E.W., 1975. Mites Injurious to Economic Plants. Univ. California Press, Berkeley, 614 pp. Koveos, D.S. and Tzanakakis, M.E., 1989. Influence of photoperiod, temperature and host plant on the production of diapause eggs inPetrobia (Tetranychina) harti (Acari: Tetranychidae). Exp. Appl. Acarol., 6: 327–342. Krysan, J.L., 1978. Diapause, quiescence, and moisture in the egg of the western corn rootwormDiabrotica virgifera. J. Insect Physiol., 24: 535–540. Lees, A.D., 1961. On the structure of the egg shell in the mitePetrobia latens Muller (Acarina: Tetranychidae). J. Insect Physiol., 6: 141–151. Masaki, S., 1980. Summer diapause. Annu. Rev. Entomol., 25: 1–25. Moriarty, F., 1969. Egg diapause and water absorption in the grasshopperChorthippus brunneus. J. Insect Physiol., 15: 2069–2074. Reddy, A.S. and Chippendale, G.M., 1973. Water involvement in diapause and the resumption of morphogenesis of the southwestern corn borer,Diatraea grandiosella. Entomol. Exp. Appl., 16: 445–454. Slifer, E.H., 1946. The effects of xylol and other solvents on diapause in the grasshopper egg, together with a possible explanation for the action of these agents. J. Exp. Zool., 102: 333–356. Sokal, R.R. and Rohlf, F.J., 1969. Biometry. The Principles and Practice of Statistics in Biological Research. W.H. Freeman, San Francisco, 776 pp. Tauber, M.J., Tauber, C.A. and Masaki, S., 1986. Seasonal Adaptations in Insects. Oxford Univ. Press, New York, 411 pp. Usua, E.J., 1970. Diapause in the maize stemborer. J. Econ. Entomol., 63: 1605–1610. Wallace, M.M.H., 1970. Diapause in the aestivating eggs ofHalotydeus destructor (Acari: Eupodidae). Aust. J. Zool., 18: 295–313. Wallace, M.M.H., 1971. The influence of temperature and moisture on diapause development in the eggs ofBdellodes lapidaria (Acari: Bdellidae). J. Aust. Entomol. Soc., 10: 276–280.