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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1971 Mar;68(3):595–599. doi: 10.1073/pnas.68.3.595

Hour-Glass Behavior of the Circadian Clock Controlling Eclosion of the Silkmoth Antheraea pernyi

James W Truman 1
PMCID: PMC388997  PMID: 5276768

Abstract

The emergence of the Pernyi silkmoth from the pupal exuviae is dictated by a brain-centered, photosensitive clock. In continuous darkness the clock displays a persistent free-running rhythm. In photoperiod regimens the interaction of the clock with the daily lightdark cycle produces a characteristic time of eclosion. But, in the majority of regimens (from 23L:1D to 4L:20D), the eclosion clock undergoes a discontinuous “hourglass” behavior. Thus, during each daily cycle, the onset of darkness initiates a free-running cycle of the clock. The next “lights-on” interrupts this cycle and the clock comes to a stop late in the photophase. The moment when the Pernyi clock stops signals the release of an eclosion-stimulating hormone and is demonstrated to be a function of the time when the free-running cycle is interrupted by lights-on. Moreover, the width (duration) of the eclosion peak in a photoperiod is shown to be dependent upon the length of the dark phase, and, consequently, upon the amount of the free-running cycle that is completed. This relationship demonstrates that the free-running cycle may be divided into two parts. The attainment of maximal accuracy (and thus the narrowest eclosion peak) is dependent upon the completion of only the first 2 hr of the free-running cycle. The completion of succeeding portions of the cycle, while having an effect upon the time of eclosion, no longer affects the accuracy of the clock. A mechanistic model of the eclosion clock is presented.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. PITTENDRIGH C. S. Circadian rhythms and the circadian organization of living systems. Cold Spring Harb Symp Quant Biol. 1960;25:159–184. doi: 10.1101/sqb.1960.025.01.015. [DOI] [PubMed] [Google Scholar]
  2. Pittendrigh C., Bruce V., Kaus P. ON THE SIGNIFICANCE OF TRANSIENTS IN DAILY RHYTHMS. Proc Natl Acad Sci U S A. 1958 Sep 15;44(9):965–973. doi: 10.1073/pnas.44.9.965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Truman J. W., Riddiford L. M. Neuroendocrine control of ecdysis in silkmoths. Science. 1970 Mar 20;167(3925):1624–1626. doi: 10.1126/science.167.3925.1624. [DOI] [PubMed] [Google Scholar]
  4. Williams C. M. Photoperiodism and the endocrine aspects of insect diapause. Symp Soc Exp Biol. 1969;23:285–300. [PubMed] [Google Scholar]

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