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Formal properties of the circadian system underlying photoperiodic time-measurement in Japanese quail

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Summary

The photosensitive phase for the photoperiodic response of Japanese quail was delineated with 3 h main photoperiods and 0.25 h night breaks in cycles (T) of 24 and 27 h. UnderT24 there was one peak of induction of testicular growth and luteinizing hormone release, while underT27 there were two, the first of which had a phase angle which was about 1.5 h more positive than that of the peak inT24. In contrast, the phase angle of locomotor activity underT27 was 3–4 h more positive than underT24. During entrainment to 1 h photoperiods in cycles between 19.1 and 25.7 h in length the rate of testicular growth (k) remained close to zero even though the subjective night of the activity rhythm was illuminated in some treatments. The ratek also remained close to zero when quail were exposed to 3 h photoperiods in cycles between 21 and 36 h in length, and underT30 the critical daylength for photoperiodic induction was only 1.5 h shorter than that underT24. The results suggest that asT is altered the changes in the phase angle of the photoinducible phase are smaller than those of the rhythm of locomotor activity, indicating the involvement of oscillators with different entrainment properties. This hypothesis is neither supported nor excluded by consideration of the internal coincidence model.

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References

  • Adkisson PL (1964) Action of the photoperiod in controlling insect diapause. Am Nat 98:357–374

    Google Scholar 

  • Aschoff J (1965) The phase-angle difference in circadian periodicity. In: Aschoff J (ed) Circadian clocks. North-Holland, Amsterdam, pp 262–276

    Google Scholar 

  • Aschoff J, Wever R (1966) Circadian period and phase-angle difference in chaffinches (Fringilla coelebs). Comp Biochem Physiol 18:397–404

    Google Scholar 

  • Bünning E (1936) Die endogene Tagesrhythmik als Grundlage der photoperiodischen Reaktion. Ber Dtsch Bot Ges 54:590–607

    Google Scholar 

  • Bünning E (1969) Common features of photoperiodism in plants and animals. Photochem Photobiol 9:219–228

    Google Scholar 

  • Chandola A, Singh R, Thapliyal JP (1976) Evidence for a circadian oscillator in the gonadal response of the tropical weaver bird (Ploceus philippinus) to programmed photoperiod. Chronobiologia 3:219–227

    Google Scholar 

  • Davies DT, Follett BK (1975) The neuroendocrine control of gonadotrophin release in the Japanese quail. Proc R Soc Lond [Biol] 198:285–315

    Google Scholar 

  • Dumortier B, Brunnarius J (1981) Involvement of the circadian system in photoperiodism and thermoperiodism inPieris brassicae. In: Follett BK, Follett DE (eds) Biological clocks in seasonal reproductive cycles. Wright, Bristol, pp 83–99

    Google Scholar 

  • Elliott JA (1976) Circadian rhythms and photoperiodic time measurement in mammals. Fed Proc 35:2339–2346

    Google Scholar 

  • Enright JT (1965) Synchronization and ranges of entrainment. In: Aschoff J (ed) Circadian clocks. North Holland, Amsterdam, pp 112–124

    Google Scholar 

  • Eskin A (1971) Some properties of the system controlling the circadian activity rhythm of sparrows. In: Menaker M (ed) Biochronometry. Natl Acad Sci, Washington, pp 55–78

    Google Scholar 

  • Farner DS (1965) Circadian systems in the photoperiodic response of vertebrates. In: Aschoff J (ed) Circadian clocks. North Holland, Amsterdam, pp 357–369

    Google Scholar 

  • Farner DS, Donham RS, Lewis RA, Mattocks PW, Darden TR (1977) The circadian component in the photoperiodic mechanism of the house sparrow,Passer domesticus. Physiol Zool 50:247–268

    Google Scholar 

  • Follett BK (1973) Circadian rhythms and photoperiodic time measurement in birds. J Reprod Fertil [Suppl] 19:5–18

    Google Scholar 

  • Follett BK (1981) The stimulation of LH and FSH secretion in quail with complete and skeleton photoperiods. Gen Comp Endocrinol (in press)

  • Follett BK, Maung SL (1978) Rate of testicular maturation, in relation to gonadotrophin and testosterone levels, in quail exposed to various artificial photoperiods and to natural day-lengths. J Endocrinol 78:267–280

    Google Scholar 

  • Follett BK, Sharp PJ (1969) Circadian rhythmicity in photoperiodically induced gonadotrophin release and gonadal growth in the quail. Nature 223:968–971

    Google Scholar 

  • Follett BK, Scanes CG, Cunningham FJ (1972) A radioimmunoassay for avian LH. J Endocrinol 52:359–378

    Google Scholar 

  • Follett BK, Davies DT, Gledhill B (1977) Photoperiodic control of reproduction in Japanese quail: changes in gonadotrophin secretion on the first day of induction and their pharmacological blockade. J Endocrinol 74:449–460

    Google Scholar 

  • Follet BK, Robinson JE, Simpson SM, Harlow CR (1981) Photoperiodic time measurement and gonadotrophin secretion in quail. In: Follett BK, Follett DE (eds) Biological clocks in seasonal reproductive cycles. Wright, Bristol, pp 185–201

    Google Scholar 

  • Hamner WM (1968) The photo-refractory period of the house finch. Ecology 49:211–227

    Google Scholar 

  • Hamner WM, Enright JT (1967) Relationships between photoperiodism and circadian rhythms of activity in the house finch. J Exp Biol 46:43–61

    Google Scholar 

  • Hillman WS (1964) Endogenous circadian rhythms and the response ofLemna perpusilla to skeleton photoperiods. Am Nat 98:323–328

    Google Scholar 

  • Konishi T (1980) Circadian rhythm of ovipositional time. In: Tanabe Y, Tanaka K, Ookawa T (eds) Biological rhythms in birds. Neural and endocrine aspects. Springer, Berlin Heidelberg New York, pp 79–90

    Google Scholar 

  • Lees AD (1966) Photoperiodic timing mechanism in insects. Nature 203:986–989

    Google Scholar 

  • Lees AD (1973) Photoperiodic time measurement in the aphidMegoura viciae. J Insect Physiol 19:2279–2316

    Google Scholar 

  • Lofts B, Lam NL (1973) Circadian regulation of gonadotrophin secretion. J Reprod Fertil [Suppl] 19:19–34

    Google Scholar 

  • Menaker M (1965) Circadian rhythms and photoperiodism inPasser domesticus. In: Aschoff J (ed) Circadian clocks. North Holland, Amsterdam, pp 385–395

    Google Scholar 

  • Menaker M, Eskin A (1967) Circadian clock in photoperiodic time measurement: a test of the Bünning hypothesis. Science 157:1182–1185

    Google Scholar 

  • Minis DH (1965) Parallel peculiarities in the entrainment of a circadian rhythm and photoperiodic induction in the pink boll worm (Pectinophora gossypiella). In: Aschoff J (ed) Circadian clocks. North Holland, Amsterdam, pp 333–343

    Google Scholar 

  • Murton RK, Lofts B, Westwood NJ (1970) The circadian basis of photoperiodically controlled spermatogenesis in the greenfinchChloris chloris. J Zool 161:125–136

    Google Scholar 

  • Nicholls TJ, Follett BK (1974) The photoperiodic control of reproduction inCoturnix quail. The temporal pattern of LH secretion. J Comp Physiol 93:301–313

    Google Scholar 

  • Pittendrigh CS (1960) Circadian rhythms and the circadian organization of living systems. Cold Spring Harbor Symp Quant Biol 25:159–184

    Google Scholar 

  • Pittendrigh CS (1966) The circadian oscillation inDrosophila pseudoobscura: A model for the photoperiodic clock. Z Pflanzen-physiol 54:275–307

    Google Scholar 

  • Pittendrigh CS (1972) Circadian surfaces and the diversity of possible roles of circadian organization in photoperiodic induction. Proc Natl Acad Sci USA 69:2734–2737

    Google Scholar 

  • Pittendrigh CS (1974) Circadian oscillations in cells and the circadian organization of multicellular systems. In: Schmitt FO, Worden FG (eds) The neurosciences. MIT, Boston, pp 437–458

    Google Scholar 

  • Pittendrigh CS (1981) Circadian organization and the photoperiodic phenomena. In: Follett BK, Follett DE (eds) Biological clocks in seasonal reproductive cycles. Wright, Bristol, pp 1–35

    Google Scholar 

  • Pittendrigh CS, Minis DH (1964) The entrainment of circadian oscillations by light and their role as photoperiodic clocks. Am Nat 98:261–294

    Google Scholar 

  • Pittendrigh CS, Minis DH (1971) The photoperiodic time measurement inPectinophora gossypiella and its relation to the circadian system in that species. In: Menaker M (ed) Biochronometry. Natl Acad Sci, Washington, pp 215–250

    Google Scholar 

  • Saunders DS (1978) Internal and external coincidence and the apparent diversity of photoperiodic clocks in the insects. J Comp Physiol 127:197–207

    Google Scholar 

  • Saunders DS (1979) External coincidence and the photoinducible phase in theSarcophaga photoperiodic clock. J Comp Physiol 132:179–189

    Google Scholar 

  • Saunders DS (1981) Insect photoperiodism: entrainment within the circadian system as a basis for time measurement. In: Follett BK, Follett DE (eds) Biological clocks in seasonal reproductive cycles. Wright, Bristol, pp 67–81

    Google Scholar 

  • Simpson SM, Follett BK (1981) Pineal and hypothalamic pacemakers: their role in regulating circadian rhythmicity in Japanese quail. J Comp Physiol 144:381–389

    Google Scholar 

  • Simpson SM, Follett BK (1982) Formal properties of the circadian rhythm of locomotor activity in Japanese quail. J Comp Physiol 145:391–398

    Google Scholar 

  • Siopes TD, Wilson WO (1980) A circadian rhythm in photosensitivity as the basis for the testicular response of Japanese quail to intermittent light. Poult Sci 59:868–873

    Google Scholar 

  • Tyschenko VP (1966) Two-oscillatory model of the physiological mechanism of insect photoperiodic reaction. Zh Obshch Biol 27:209–222

    Google Scholar 

  • Wada M (1979) Photoperiodic control of LH secretion in Japanese quail with special reference to the photoinducible phase. Gen Comp Enocrinol 39:141–149

    Google Scholar 

  • Winer BJ (1971) Statistical principles in experimental design. McGraw-Hill Kogakusha, Tokyo

    Google Scholar 

Download references

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Simpson, S.M., Follett, B.K. Formal properties of the circadian system underlying photoperiodic time-measurement in Japanese quail. J. Comp. Physiol. 145, 381–390 (1982). https://doi.org/10.1007/BF00619342

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