Effects of environmental factors on circadian activity in the flesh fly, Sarcophaga crassipalpis

Abstract.The diel locomotor activity patterns of wandering larvae in the flesh fly, Sarcophaga crassipalpis Macquart (Diptera: Sarcophagidae), were examined using a novel apparatus and shown to be primarily diurnal, but with a minority (37%) showing nocturnal activity. In response to the environmental stress of heat shock, a significantly larger proportion (72%) of the larvae became nocturnal. In comparison, adult circadian activity also was predominantly diurnal, but not correlated with the larval activity patterns. In addition, adult patterns showed age‐related changes in entrainment and free running period. Finally, the phase of circadian‐gated adult eclosion was shown to be entrained by a 3‐day exposure to light–dark cycles delivered prior to pupariation, with the phase maintained throughout pupal–adult metamorphosis under constant dark conditions. These results demonstrate that environmental changes may have profound effects on the expression of 24‐h activity patterns and circadian rhythms during different life stages throughout development.

[1]  D. Denlinger,et al.  Upregulation of a 23 kDa small heat shock protein transcript during pupal diapause in the flesh fly, Sarcophaga, crassipalpis. , 1998, Insect biochemistry and molecular biology.

[2]  Ronald D. Flannagan,et al.  Diapause-specific gene expression in pupae of the flesh fly Sarcophaga crassipalpis. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[3]  T. Arai,et al.  Effects of photoperiod and aging on locomotor activity rhythms in the onion fly, Delia antiqua. , 1997, Journal of insect physiology.

[4]  C. Monnerjahn,et al.  Heat shock proteins and circadian rhythms. , 1996, Chronobiology international.

[5]  J. Brady,et al.  Circadian activity pattern in the stable fly, Stomoxys calcitrans , 1996 .

[6]  D. Denlinger,et al.  Changes in temperature, not photoperiod, control the pattern of adult eclosion in the tsetse, Glossina morsitans , 1995 .

[7]  L. Rensing,et al.  Heat Shock Effects on the Circadian Rhythm of Protein Synthesis and Phosphorylation of Ribosomal Proteins in Gonyaulax polyedra , 1995 .

[8]  R. D. Lewis,et al.  Circadian locomotor activity rhythms and their entrainment to light-dark cycles continue in flies (Calliphora vicina) surgically deprived of their optic lobes , 1994 .

[9]  D. Denlinger,et al.  Alteration of the eclosion rhythm and eclosion behavior in the flesh fly, Sarcophaga crassipalpis, by low and high temperature stress , 1994 .

[10]  A. Sehgal,et al.  Ontogeny of a biological clock in Drosophila melanogaster. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[11]  D. Saunders,et al.  Adult Locomotor Rhythmicity as "Hands" of the Maternal Photoperiodic Clock Regulating Larval Diapause in the Blowfly, Calliphora vicina , 1991, Journal of biological rhythms.

[12]  D. Denlinger,et al.  Developmental and tissue specific control of the heat shock induced 70 kDa related proteins in the flesh fly, Sarcophaga crassipalpis , 1990 .

[13]  D. Denlinger,et al.  Diapause specific proteins expressed by the brain during the pupal diapause of the flesh fly, Sarcophaga crassipalpis. , 1990 .

[14]  M. Rosbash,et al.  The period gene of Drosophila carries species‐specific behavioral instructions. , 1988, The EMBO journal.

[15]  D. Denlinger,et al.  Role of the brain and ring gland in regulation of pupal diapause in the flesh fly Sarcophaga crassipalpis , 1986 .

[16]  Peter H. Smith Responsiveness to light of the circadian clock controlling eclosion in the blowfly, Lucilia cuprina , 1985 .

[17]  D. Moore,et al.  Circadian locomotor rhythms in individual honeybees , 1985 .

[18]  D. Denlinger 11 – Hormonal Control of Diapause , 1985 .

[19]  J. Aschoff Freerunning and Entrained Circadian Rhythms , 1981 .

[20]  D. Saunders The circadian eclosion rhythm in Sarcophaga argyrostoma: delineation of the responsive period for entrainment , 1979 .

[21]  D. Saunders Thermoperiodic Control of Diapause in an Insect: Theory of Internal Coincidence , 1973, Science.

[22]  G. Fraenkel,et al.  Rates and cycles of oxygen consumption during pupal diapause in Sarcophaga flesh flies. , 1972, Journal of insect physiology.