Skip to main content
Log in

Circadian nature of the photoperiodic clock in Japanese quail

  • Published:
Journal of Comparative Physiology A Aims and scope Submit manuscript

Summary

The photoperiodic clock in quail (Coturnix colurnix japonica) is based upon a rhythm of photoinducibility (Øi) but the extent to which this rhythm is circadian remains unclear. Two types of experiment investigated this situation. In the first, gonadectomized quail were adapted to live in periods of darkness by training them on a schedule containing one short day and 3 days of darkness (SD/DD/DD/DD). They were then exposed to a single pulse of 6 or 10 h of light at different times across 3 days of darkness. The photoperiodic response, measured by the increase in LH secretion, showed clear rhythmicity, demonstrating unequivocally the circadian nature of Øi. The second set of experiments employed Nanda-Hamner cycles and varied the length of the photoperiod from 6 to 11 h. Responsiveness in a 36 h or a 60 h cycle was highly dependent upon the length of the photoperiod, something not predicted from theory. For instance, LD 6:30 was not photoperiodically inductive but LD 10:26 was clearly inductive. Close analysis of patterns of LH secretion indicated an unexpected delay before induction occurred and then a rapid rise to a stable level of induction. When LH was measured in every pulse under LD 10:26 there was no evidence that LH levels alternately increased and decreased. This is not consistent with the simplest interpretation of Nanda-Hamner experiments where alternate pulses of light are thought to “entrain” the rhythm or “induce” a photoperiodic response by coinciding with Øi. It is concluded that the quail's photoinducible rhythm is indeed based on a circadian rhythm but one that is only weakly self-sustaining. Possibly as a consequence of this, the rhythm's behaviour under abnormal photoperiodic cycles may be rather different from that found in other species and from other circadian rhythms in quail.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

Øi :

photoinducible phase

LH :

luteinizing hormone

References

  • Boissin-Agasse J, Ortavant R, Boissin J (1986) Circadian rhythm of photosensitivity and control of the annual testicular cycle in long-day (ferret) and short-day (mink) breeding mammals. In: Assenmacher I, Boissin J (eds) Endocrine regulations as adaptive mechanisms to the environment. CNRS, Paris, pp 131–142

    Google Scholar 

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

    Google Scholar 

  • Bünning E (1973) The physiological clock (3rd ed). Springer, Berlin Heidelberg

    Google Scholar 

  • Bünsow RC (1953) Über Tages- und jahresrhythmische Änderungen der photoperiodischen Lichtempfindlichkeit bei Kalanchoe blossfeldiana und ihre Beziehungen zur endogenen Tagesrhythmik. Z Bot 41:257–276

    Google Scholar 

  • Claret J, Dumortier B, Brunnarius J (1981) Mise en évidence d'une composante circadienne dans le photopériodisme de Pieris brassicae, lors de l'induction photopériodique de la diapause. CR Acad Sci Sér D 292:427–430

    Google Scholar 

  • Dumortier B, Brunnarius J (1989) Diet-dependent switch from circadian to hourglass-like operation of an insect photoperiodic clock. J Biol Rhythms 4:481–490

    Google Scholar 

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

    Google Scholar 

  • Elliott JA, Stetson MH, Menaker M (1972) Regulation of testis function in golden hamsters: A circadian clock measures photoperiodic time. Science 178:771–773

    Google Scholar 

  • Follett BK (1973) Circadian rhythms and photoperiodism in birds. J Reprod Fertil 19 (Suppl):5–18

    Google Scholar 

  • Follett BK (1981) The stimulation of luteinizing hormone and follicle stimulating hormone secretion in quail with complete and skeleton photoperiods. Gen Comp Endocrinol 45:306–316

    Google Scholar 

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

    Google Scholar 

  • Follett BK, Milette JJ (1982) Photoperiodism in quail: Testicular growth and maintenance under skeleton photoperiods. J Endocrinol 93:83–90

    Google Scholar 

  • Follett BK, Pearce-Kelly AS (1991) Photoperiodic induction in quail as a function of the period of the light-dark cycle: implications for models of time measurement. J Biol Rhythms 6:331–341

    Google Scholar 

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

    Google Scholar 

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

    Google Scholar 

  • Follett BK, Mattocks PW, Farner DS (1974) Circadian function in the photoperiodic induction of gonadotrophin secretion in the white-crowned sparrow. Proc Natl Acad Sci USA 71:1666–1669

    Google Scholar 

  • Follett BK, Robinson JE, Simpson SM, Harlow CR (1981) Photoperiodic time measurement and gonadotrophin secretion in quail. In: Biological clocks in seasonal reproductive cycles. Scientechnica, Bristol, pp 185–202

    Google Scholar 

  • Hamner WM (1963) Diurnal rhythms and photoperiodism in testicular recrudescence of the house finch. Science 142:1294–1295

    Google Scholar 

  • Kumar V, Tewary PD (1982) Photoperiodic regulation of the gonadal recrudescence in common Indian rosefinch: Dependence on circadian rhythms. J Exp Zool 223:37–40

    Google Scholar 

  • Kumar V, Follett BK, Juss TS (1993) An interpretation based upon physiological data of how Nanda-Hamner resonance cycles lead to photoperiodic induction in Japanese quail. J Biol Rhythms, submitted

  • Lees AJ (1973) Photoperiodic time measurement in the aphid, Megoura viciae. J Insect Physiol 19:2279–2316

    Google Scholar 

  • Nanda KK, Hamner KC (1958) Studies on the nature of the endogenous rhythm affecting photoperiodic response of Biloxi soybean. Bot Gaz 120:14–25

    Google Scholar 

  • Nicholls TJ, Follett BK, Robinson JE (1983) A photoperiodic response in gonadectomized quail exposed to a single long day. J Endocrinol 97:121–126

    Google Scholar 

  • Pittendrigh CS (1981) Circadian organization and the photoperiodic phenomena. In: Biological clocks in seasonal reproductive cycles. Scientechnica, Bristol, pp 1–36

    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 

  • Saiovici MS, Nicholls TJ, Follett BK (1987) Rapid photoperiodic responses in Japanese quail: Is daylength measurement based upon a circadian system? J Biol Rhythms 2:139–152

    Google Scholar 

  • Saunders DS (1982) Insect clocks (2nd ed). Pergamon Press, Oxford

    Google Scholar 

  • Simpson SM, Follett BK (1982) Formal properties of the circadian system underlying photoperiodic time-measurement in Japanese quail. J Comp Physiol 145:381–390

    Google Scholar 

  • Tewary PD, Kumar V (1981) Circadian periodicity and the initiation of gonadal growth in male blackheaded buntings (Emberiza melanocephala). J Comp Physiol 144:201–203

    Google Scholar 

  • Turek FW (1974) Circadian rhythmicity and the initiation of gonadal growth in sparrows. J Comp Physiol 92:59–64

    Google Scholar 

  • Underwood H (1983) Circadian organization in the lizard Anolis carolinensis: A multioscillator system. J Comp Physiol 152:265–274

    Google Scholar 

  • Underwood H, Hall D (1982) Photoperiodic control of reproduction in the male lizard Anolis carolinensis. J Comp Physiol 146:485–492

    Google Scholar 

  • Underwood H, Hyde LL (1990) A circadian clock measures photoperiodic time in the male lizard Anolis carolinensis. J Comp Physiol A 167:231–243

    Google Scholar 

  • Urbanski HU, Follett BK (1982) Photoperiodic modulation of gonadotrophin secretion in castrated Japanese quail. J Endocrinol 92:73–83

    Google Scholar 

  • Vaz Nunes M, Hardie J (1987) An instantly damping oscillator model for photoperiodic time measurement in the aphid Aphis fabae. J Insect Physiol 33:831–841

    Google Scholar 

  • Veerman A, Beekman M, Veenendaal RL (1988) Photoperiodic induction in the large white butterfly, Pieris brassicae: Evidence for hourglass time measurement. J Insect Physiol 34:1063–1069

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Follett, B.K., Kumar, V. & Juss, T.S. Circadian nature of the photoperiodic clock in Japanese quail. J Comp Physiol A 171, 533–540 (1992). https://doi.org/10.1007/BF00194586

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00194586

Key words

Navigation