DIVERSITY AND DEVELOPMENT OF CIRCADIAN RHYTHMS IN THE EUROPEAN RABBIT

REFERENCES

• Manning P. J., Ringler D. H., Newcomer C. E. The Biology of the Laboratory Rabbit. Academic Press, New York 1994; 483
   Google Scholar
• Thompson H. V., King C. M. The European Rabbit. Oxford University, Oxford, Press. 1994; 245
   Google Scholar
• Jilge B., Stähle H. The Internal Synchronization of Five Circadian Functions of the Rabbit. Chronobiol. Int. 1984; 1: 195–204
   PubMedGoogle Scholar
• Jilge B. The Ontogeny of Circadian Rhythms in the Rabbit. J. Biol. Rhythms 1993; 8: 247–60
   PubMed Web of Science ®Google Scholar
• Jilge B., Kuhnt B., Landerer W., Rest S. Circadian Thermoregulation in Suckling Rabbit Pups. J. Biol. Rhythms 2000; 15: 329–35
   PubMed Web of Science ®Google Scholar
• Jilge B., Kuhnt B., Landerer W., Rest S. Circadian Thermoregulation in Rabbit Pups and Their Does. Lab. Anim. 2000, in press
   Google Scholar
• Kennedy G A., Hudson R., Armstrong S. M. Circadian Wheel Running Activity Rhythms in Two Strains of Domestic Rabbit. Physiol. Behav. 1994; 55: 385–89
   PubMed Web of Science ®Google Scholar
• Hudson R., Distel H. The Pattern of Behaviour of Rabbit Pups in the Nest. Behaviour 1982; 79: 255–71
   Google Scholar
• Hudson R., Distel H. The Temporal Pattern of Suckling in Rabbit Pups: A Model of Circadian Synchrony Between Mother and Young. Development of Circadian Rhythmicity and Photoperiodism in Mammals, S. M. Reppert. Perinatology Press, Boston 1989; 83–102
   Google Scholar
• Hudson R. Potential of the Newborn Rabbit for Circadian Rhythms Research. Biol. Rhythm Res. 1998; 29: 546–55
   Web of Science ®Google Scholar
• Southern H N. Coprophagy in the Wild Rabbit. Nature 1940; 145: 262
   Google Scholar
• Southern H N. Sexual and Aggressive Behaviour in the Wild Rabbit. Behaviour 1948; 1: 173–94
   Google Scholar
• Dunnet G M. Notes on Emergence Behaviour of the Rabbit, Oryctolagus cuniculus (L.), and Its Bearing on the Validity of Sight Counts for Population Estimates. CSIRO Wildl. Res. 1957; 2: 85–89
   Google Scholar
• Myers K. Some Observations on the Use of Sight Counts in Estimating Populations of the Rabbit, Oryctolagus cuniculus (L.). CSIRO Wildl. Res. 1957; 2: 170–72
   Google Scholar
• Rowley I. Observations on Evening Rabbit Activity in Relation to Weather and Sunset. CSIRO Wildl. Res. 1957; 2: 168–69
   Google Scholar
• Mykytowycz R., Rowley I. Continuous Observations of the Activity of the Wild Rabbit, Oryctolagus cuniculus (L.) During 24-Hour Periods. CSIRO Wildl. Res. 1958; 3: 26–31
   Google Scholar
• Stoddart E., Myers K. A Comparison of Behaviour, Reproduction and Mortality of Wild and Domestic Rabbits in Confined Populations. CSIRO Wildl. Res. 1964; 9: 144–59
   Google Scholar
• Kolb H. H. Circadian Activity in the Wild Rabbit (Oryctolagus cuniculus). Mammal Rev. 1986; 16: 145–50
   Web of Science ®Google Scholar
• Wallage-Drees J. M. A Field Study on Seasonal Changes in the Circadian Activity of Rabbits. Z. Säugetierkunde 1989; 54: 22–30
   Web of Science ®Google Scholar
• Villafuerte R., Kufner M B., Delibes M., Moreno S. Environmental Factors Influencing the Seasonal Daily Activity of the European Rabbit (Oryctolagus cuniculus) in a Mediterranean Area. Mammalia 1993; 57: 341–47
   Web of Science ®Google Scholar
• Henning S. J., Hird F. J. Diurnal Variations in the Concentrations of Volatile Fatty Acids in the Alimentary Tracts of Wild Rabbits. Br. J. Nutr. 1972; 27: 57–64
   PubMedGoogle Scholar
• Eisermann K. Seasonal and Environmental Influences upon the Diurnal Heart-Rate Pattern in Wild Rabbits Living under Seminatural Conditions. Physiol. Behav. 1988; 43: 539–65
   PubMedGoogle Scholar
• Eisermann K., Meier B., Khaschei M., von Holst D. Ethophysiological Responses to Overwinter Food Shortage in Wild European Rabbits. Physiol. Behav. 1993; 54: 973–80
   PubMedGoogle Scholar
• Southern H. N. Periodicity of Refection in the Wild Rabbit. Nature 1942; 149: 553–54
   Google Scholar
• Stephens M. N. Seasonal Observations on the Wild Rabbit (Oryctolagus cuniculus cuniculus L) in West Wales. Proc. Zool. Soc. Lond. 1952; 122: 417–34
   Google Scholar
• Niethammer G. Ergebnisse von Markierungsversuchen an Wildkaninchen. Z. Morphol Ökol Tiere 1937; 33: 297–12
   Google Scholar
• Lloyd H. G., McCowan D. Some observations on the Breeding Burrows of the Wild Rabbit, Oryctolagus cuniculus, on the Island of Skokholm. J. Zool. (London.) 1968; 156: 540–49
   Google Scholar
• Kraft R. Vergleichende Verhaltensstudien an Wild- und Hauskaninchen. I. Das Verhaltensinventar von Wild- und Hauskaninchen. Z. Tierzüchtg Züchtungsbiol. 1979; 95: 140–62
   Google Scholar
• Broekhuizen S., Mulder J. L. Differences and Similarities in Nursing Behaviour of Hares and Rabbits. Acta Zool. Fennica 1983; 174: 61–63
   Google Scholar
• Hudson R., Schaal B., Martínez-Gómez M., Distel H. Mother–Young Relations in the European Rabbit, Physiological and Behavioral Locks and Keys. World Rabbit Sci. 2000; 8: 85–90
   Google Scholar
• Zarrow M. X., Denenberg V. M., Anderson C. O. Rabbit, Frequency of Suckling in the Pup. Science 1965; 150: 1835–36
   PubMed Web of Science ®Google Scholar
• Lincoln D. W. Suckling: A Time-Constant in the Nursing Behavior of the Rabbit. Physiol. Behav. 1974; 13: 711–14
   PubMed Web of Science ®Google Scholar
• Hudson R., Distel H. Olfactory Guidance of Nipple-Search Behaviour in Newborn Rabbits. Ontogeny of Olfaction, W. Breipohl. Springer, New York 1986; 243–54
   Google Scholar
• van Hof M. W., Rietveld W. J., Tordoir W. E.M. Influence of Illumination on Locomotor Activity of Rabbits. Acta Physiol. Pharmacol. Neerl. 1963; 12: 266–74
   PubMedGoogle Scholar
• van Hof van Duin J. Locomotor Activity in Normal and Dark-Reared Rabbits. Doc. Opthalm. 1971; 30: 317–31
   PubMedGoogle Scholar
• Horton B. J., Turley S. D., West C. E. Diurnal Variation in the Feeding Pattern of Rabbits. Life Sci. 1974; 15: 1895–1907
   Web of Science ®Google Scholar
• Jilge B. Soft Faeces Excretion and Passage Time in the Laboratory Rabbit. Lab. Anim. 1974; 8: 337–46
   PubMedGoogle Scholar
• Jilge B. The Entrainment of Circadian Soft Faeces Excretion in the Rabbit. J. Interdis. Cycle Res. 1976; 7: 229–35
   Google Scholar
• Jilge B. The Entrainment of Caecotrophy-Rhythm of the Rabbit Following 6- and 12-Hours Phase-Shifts of the Zeitgeber. Chronobiologia 1979; 6: 33–38
   PubMedGoogle Scholar
• Jilge B. Monophasic and Diphasic Patterns of the Circadian Caecotrophy-Rhythm of Rabbits. Lab. Anim. 1982; 16: 1–6
   PubMedGoogle Scholar
• Jilge B. Rate of Movement of Marker Particles in the Digestive Tract of the Rabbit. Lab. Anim. 1982; 16: 7–11
   PubMedGoogle Scholar
• Jilge B. The Phase Relation Between a Circadian Rhythm of the Rabbit and Different Light:Dark Time Ratios. Z. Versuchstierk, 26: 111–22
   PubMedGoogle Scholar
• Jilge B. The Rabbit: A Diurnal or a Nocturnal Animal. J. Exp. Anim. Sci. 1991; 34: 170–83
   PubMedGoogle Scholar
• Prud'hon M., Goussopoulos J. Comportement alimentaire du Lapin de Garenne en Captivité. Ann. Zootech. 1976; 25: 407–10
   Google Scholar
• Prud'hon M., Goussopoulos J., Reyne Y. Comportement Alimentaire du Lapin de Garenne en Captivité, II Modifications Induites par un Décalage des Périodes D'éclairement. Ann. Zootech. 1978; 27: 101–106
   Google Scholar
• Leng E., Hörnicke H. Tagesrhythmische Unterschiede in der Zusammensetzung des Blinddarminhalts von Kaninchen. Z. Versuchstierk 1975; 17: 285–99
   PubMedGoogle Scholar
• Jolivet E., Reyne Y., Teyssier J. Approche Méthodologique de la Répartition Nycthémérale des Prises D'aliment Chez le Lapin Domestique en Croissance. Reprod. Nutr. Dévelop. 1983; 23: 13–24
   PubMedGoogle Scholar
• Hörnicke H., Ruoff G., Vogt B., Clauss W., Ehrlein M-J. Phase Relationship of the Circadian Rhythms of Feed Intake, Caecal Motility and Production of Soft and Hard Faeces in Domestic Rabbits. Lab. Animals 1984; 18: 169–72
   PubMed Web of Science ®Google Scholar
• Pivik R. T., Blysma F W., Cooper P. Sleep-Wakefulness in the Rabbit. Behav. Neur. Biol. 1986; 45: 275–86
   PubMedGoogle Scholar
• Jilge B. Der Circadianrhythmus des Kaninchens im Licht-Dunkelwechsel in Abwesenheit des Zeitgebers und bei zeitrestriktiver Fötterung. Dtsch Tierörztl Wochenschr 1987; 94: 18–23
   PubMedGoogle Scholar
• Fox R. R., Laird C W. Diurnal Variations in Rabbits: Hematological Parameters. Am. J. Physiol. 1970; 218: 1609–12
   PubMed Web of Science ®Google Scholar
• Gattermann R. Zur Biorhythmik des Kaninchens (O. cuniculus (L.) f. domestica) 1. Mitteilung: Circadiane Rhythmen der lokomotorischen Aktivität der Futterund Wasseraufnahme, der Harnabgabe und des Körpergewichts. Zool. Jb. Physiol. 1978; 82: 214–33
   Google Scholar
• Gattermann R. Zur Biorhythmik des Kaninchens (O. cuniculus (L.) f. domestica) 2. Mitteilung: Circadiane Rhythmen des Hämatokrit, des Hämoglobingehalts, der Leukozytenzahl und des Blutglukosespiegels. Zool. Jb. Physiol. 1978; 82: 234–43
   Google Scholar
• Gingras J. L., Lawson E. E., McNamara M. C. Developmental Characteristics in the Daily Rhythm of Serotonin Concentration within Rabbit Brainstem Regions. Dev. Pharmacol. Ther. 1990; 14: 245–53
   PubMedGoogle Scholar
• Vernay M., Marty J. Absorption and Metabolism of Butyric Acid in Rabbit Hind Gut. Comp. Biochem. Physiol. 1984; 77A: 89–96
   Google Scholar
• Vernay M. Origin and Utilization of Volatile Fatty Acids and Lactate in the Rabbit: Influence of the Faecal Excretion Pattern. Br. J. Nutr. 1987; 57: 371–81
   PubMed Web of Science ®Google Scholar
• Bobbert A. C., Krul W. H., Brandenburg J. Diurnal Changes in the Rabbit's Visual Evoked Potential. Int. J. Chronobiol. 1978; 5: 307–25
   PubMedGoogle Scholar
• Bobbert A. C., van Wiechen R. J.M.P., Eggelmeijer F. Imitations of the Circadian Changes in Rabbit Photic Responses, Elicited by Stimulation of the Cervical Sympathetic Nerves Mediated by Means of Intraocular Adrenergic Alpha Receptors. Interdis. Cycle Res. 1990; 21: 273–88
   Google Scholar
• Schnell C. R., Debon C., Percicot C. L. Measurement of Intraocular Pressure by Telemetry in Conscious, Unrestrained Rabbits. Invest. Ophthalmol. Vis. Sci. 1996; 37: 958–65
   PubMed Web of Science ®Google Scholar
• McLaren J. W., Brubaker R. F., FitzSimon J. S. Continuous Measurement of Intraocular Pressure in Rabbits by Telemetry. Invest. Opthalmol. Vis. Sci. 1996; 37: 966–75
   PubMed Web of Science ®Google Scholar
• Deutsch J. A. Nest Building Behaviour of Domestic Rabbits under Semi-natural Conditions. Brit. J. Anim. Behav. 1957; 5: 53–54
   Google Scholar
• Venge O. The Influence of Nursing Behaviour and Milk Production on Early Growth in Rabbits. Anim. Behav. 1963; 11: 500–506
   Google Scholar
• Kraft R. Beobachtungen zur Tagesperiodik von Wild- und Hauskaninchen. Z. Säugetierkunde 1978; 43: 155–66
   Google Scholar
• Hudson R., Müller A., Kennedy G. A. Parturition in the Rabbit is Compromised by Daytime Nursing: The Role of Oxytocin. Biol. Reprod. 1995; 53: 519–24
   PubMed Web of Science ®Google Scholar
• Fuchs A-R., Dawood Y. Oxytocin Release and Uterine Activation During Parturition in Rabbits. Endocrinology 1980; 107: 1117–26
   PubMedGoogle Scholar
• Hudson R., Cruz Y., Lucio R. A., Ninomiya J., Martínez-Gómez M. Temporal and Behavioral Patterning of Parturition in Rabbits and Rats. Physiol. Behav. 1999; 66: 599–604
   PubMedGoogle Scholar
• Nimomiya J. G., Reyes-Guerrero G., Barrera-Mera B., Martínez-Merlos T., Hudson R., Guevara-Guzmán R. The Effect of Photoperiod on the Sensitivity to Oxytocin of the Uterine Horn Longitudinal Layer in the Rabbit. Abstr. Soc. Neurosci. 1999; 25: 2200
   Google Scholar
• Hudson R. Chronoendocrinology of Reproductive Behavior in the Female Rabbit (Oryctolagus cuniculus). Bericht 9. Arbeitstagung über Haltung und Krankheiten der Kaninchen, Pelztiere und Heimtiere, S. Matthes. DVG, Celle 1995; 1–11
   Google Scholar
• Hörnicke H., Batsch F. Caecotrophy in Rabbits—A Circadian Function. J. Mammal 1977; 58: 240–42
   PubMed Web of Science ®Google Scholar
• Bobbert A C., Krul W. H., Brandenburg J. Photoperiodic Programming of Diurnal Changes in Rabbit Visual Evoked Potentials. Int. J. Chronobiol. 1978; 5: 327–44
   PubMedGoogle Scholar
• Jilge B. The Effect of Two Different Light Intensities on Spontaneous Period and Phase Angle Difference of Caecotrophy-Rhythm in the Rabbit. J. Interdis. Cycle Res. 1980; 11: 41–54
   Google Scholar
• Jilge B. The Entrainment of the Circadian Caecotrophy Rhythm with Different Light–Dark Time Ratios. J. Interdis. Cycle Res. 1983; 14: 1–20
   Google Scholar
• Jilge B. Ontogeny of the Rabbit's Circadian Rhythms Without an External Zeitgeber. Physiol. Behav. 1995; 58: 131–40
   PubMed Web of Science ®Google Scholar
• Jilge B., Friess L., Stähle H. Internal Coupling of Five Functions of Rabbits Exhibiting a Bimodal Circadian Rhythm. J. Interdiscipl. Cycle Res. 1986; 17: 7–28
   Google Scholar
• Jilge B., Stähle H. Restricted Food Access and Light–Dark Impact of Conflicting Zeitgebers upon Circadian Rhythms of the Rabbit. Am. J. Physiol. 1993; 264: R708–15
   PubMed Web of Science ®Google Scholar
• Aschoff J. Exogenous and Endogenous Components in Circadian Rhythms. Cold Spr. Harb. Symp. Quant. Biol. 1960; 25: 11–28
   PubMedGoogle Scholar
• Wever R. A. The Circadian System of Man: Results of Experiments under Temporal Isolation. Springer Verlag, Berlin 1979; 276
   Google Scholar
• Mistlberger R. E., Houpt T. A., Moore-Ede M. C. Characteristics of Food-Entrained Circadian Rhythms in Rats During Long-Term Exposure to Constant Light. Chronobiol. Int. 1990; 7: 383–91
   PubMed Web of Science ®Google Scholar
• Depres-Brummer P., Levi F., Metzger G., Touitou Y. Light-Induced Suppression of the Rat Circadian System. Am. J. Physiol. 1995; 268: R1111–16
   PubMed Web of Science ®Google Scholar
• Lax P., Zamora S., Madrid J. A. Food-Entrained Feeding and Locomotor Circadian Rhythms in Rats under Different Lighting Conditions. Chronobiol. Int. 1999; 16: 281–91
   PubMed Web of Science ®Google Scholar
• Bobbert A. C., Bruinvel D. J. Properties of the Two Oscillators Influencing the Rabbit's Food Intake Pattern. Behav. Brain Res. 1986; 19: 193–204
   PubMed Web of Science ®Google Scholar
• Bobbert A. C., van Kempen A. P., Braakman J. N. Re-entrainment of the Rabbit's Circadian Food Intake Pattern After Inversion of 24-h Sawtooth Illuminations and Standard Light–Dark Alternations. Biol. Rhythms Res. 1994; 25: 89–105
   Web of Science ®Google Scholar
• Moore R. Y. Organization of the Primate Circadian System. J. Biol. Rhythms 1993; 8: S3–S9, Supplement
   Google Scholar
• Rusak B., Abe H., Mason R., Piggins H. D., Ying S. W. Neurophysiological Analysis of Circadian Rhythm Entrainment. J. Biol. Rhythms 1993; 8: S39–S45; Supplement
   Web of Science ®Google Scholar
• Weaver D. R. The Suprachiasmatic Nucleus: A 25-Year Retrospective. J. Biol. Rhythms 1998; 13: 100–12
   PubMed Web of Science ®Google Scholar
• Lucas R. J, Foster R. G. Photoentrainment in Mammals: A Role for Cryptochrome?. J. Biol. Rhythms 1999; 14: 4–10
   PubMed Web of Science ®Google Scholar
• Jilge B., Hörnicke H., Stähle H. Circadian Rhythms of Rabbits During Restrictive Feeding. Am. J. Physiol. 1987; 253: R46–R54
   Google Scholar
• Stephan F. K. Interaction Between Light- and Feeding-Entrainable Circadian Rhythms in the Rat. Physiol. Behav. 1986; 38: 127–33
   PubMed Web of Science ®Google Scholar
• Abe H., Kida M., Tsuli K., Mano T. Feeding Cycles Entrain Circadian Rhythms of Locomotor Activity in CS Mice but Not in C57BL/6J Mice. Physiol. Behav. 1989; 45: 397–402
   PubMed Web of Science ®Google Scholar
• Coleman G. J., O'Reilly H. M., Armstrong S. M. Food-Deprivation-Induced Phase Shifts in Smithopsis Macroura Froggatti. J. Biol. Rhythms 1989; 4: 49–60
   PubMedGoogle Scholar
• Kennedy G. A., Coleman G. J., Armstrong S. M. Restricted Feeding Entrains Circadian Wheel-Running Activity Rhythms of the Kowari. Am. J. Physiol. 1991; 261: R819–27
   PubMedGoogle Scholar
• Mistlberger R. E. Effects of Scheduled Food and Water Access on Circadian Rhythms of Hamsters in Constant Light, Dark, and Light: Dark. Physiol. Behav. 1993; 53: 509–16
   PubMed Web of Science ®Google Scholar
• Marchant E. G., Mistlberger R. E. Anticipation and Entrainment to Feeding Time in Intact and SCN-Ablated C57BL/6J Mice. Brain Res. 1997; 765: 273–82
   PubMed Web of Science ®Google Scholar
• Challet E., Solberg L. C., Turek F. W. Entrainment in Calorie-Restricted Mice: Conflicting Zeitgebers and Free-Running Conditions. Am. J. Physiol. 1998; 274: R1751–61
   PubMed Web of Science ®Google Scholar
• Mistlberger R. E., Marchant E. G. Enhanced Food-Anticipatory Circadian Rhythms in the Genetically Obese Zucker Rat. Physiol. Behav. 1999; 66: 329–35
   Google Scholar
• Stephan F. K., Swann J. M., Sisk C. L. Anticipation of 24 h Feeding Schedules in Rats with Lesions of the Suprachiasmatic Nucleus. Behav. Neural Biol. 1979; 25: 345–63
   Google Scholar
• Clarke J. D., Coleman G. J. Persistent Meal-Associated Rhythms in SCN-Lesioned Rats. Physiol. Behav. 1986; 36: 105–13
   PubMed Web of Science ®Google Scholar
• Mistlberger R. E. Nonphotic Entrainment of Circadian Activity Rhythms in Suprachiasmatic Nuclei-Ablated Hamsters. Behav. Neurosci. 1992; 106: 192–202
   PubMed Web of Science ®Google Scholar
• Choi S., Wong L. S., Yamat C., Dallmann M. F. Hypothalamic Ventromedial Nuclei Amplify Circadian Rhythms: Do They Contain a Food-Entrained Endogenous Oscillator?. J. Neurosci. 1998; 18: 3843–52
   PubMed Web of Science ®Google Scholar
• Stephan F. K. Calories Affect Zeitgeber Properties of the Feeding-Entrained Circadian Oscillator. Physiol. Behav. 1997; 62: 995–1002
   PubMed Web of Science ®Google Scholar
• Stephan F. K., Davidson A. J. Glucose, but Not Fat, Phase Shifts the Feeding-Entrained Circadian Clock. Physiol. Behav. 1998; 65: 277–88
   PubMed Web of Science ®Google Scholar
• Escobar C., Diaz-Muñoz M., Encinas F., Aguilar-Roblero R. Persistence of Metabolic Rhythmicity During Fasting and Its Entrainment by Restricted Feeding Schedules in Rats. Am. J. Physiol. 1998; 274: R1309–16
   PubMed Web of Science ®Google Scholar
• Findlay A. L.R. Nursing Behavior and the Condition of the Mammary Gland in the Rabbit. J. Comp. Physiol. Psychol. 1969; 69: 115–18
   PubMedGoogle Scholar
• Findlay A. L.R., Roth L. L. Long-Term Dissociation of Nursing Behavior and the Condition of the Mammary Gland in the Rabbit. J. Comp. Physiol. Psychol. 1970; 72: 341–44
   PubMedGoogle Scholar
• Findlay A. L.R., Tallal P. A. Effect of Reduced Suckling Stimulation on the Duration of Nursing in the Rabbit. J. Comp. Physiol. Psychol. 1971; 76: 236–41
   PubMedGoogle Scholar
• Davis F. C. Ontogeny of Circadian Rhythms. Handbook of Behavioral Neurobiology, J. Aschoff. Plenum Press, New York 1981; 4: 257–74
   Google Scholar
• Reppert S. M. Development of Circadian Rhythmicity and Photoperiodism in Mammals. Perinatology Press, Boston 1989; 262
   Google Scholar
• Hudson R., Distel H. Nipple Location by Newborn Rabbits: Behavioural Evidence for Pheromonal Guidance. Behaviour 1983; 85: 260–75
   Google Scholar
• Hudson R., Distel H. On the Nature and Action of the Rabbit Nipple-Search Pheromone: A Review. Chemical Signals in Vertebrates VII, R. Apfelbach, D. Müller-Schwarze, K. Reuter, E. Weiler. Elsevier, Oxford 1995; 223–32
   Google Scholar
• Hull J., Hull D. Behavioral thermoregulation in Newborn Rabbits. J. Comp. Physiol. Psychol. 1982; 96: 143–47
   PubMedGoogle Scholar
• Hull D., Segall M. M. The Contribution of Brown Adipose Tissue to Heat Production in the Newborn Rabbit. J. Physiol. 1965; 181: 449–57
   PubMed Web of Science ®Google Scholar
• Hull D., Segall M. M. Sympathetic Nervous Control of Brown Adipose Tissue and Heat Production in the Newborn Rabbit. J. Physiol. 1965; 181: 458–67
   PubMedGoogle Scholar
• Hudson R., Bilkó Á, Altbäcker V. Nursing, Weaning and the Development of Independent Feeding in the Rabbit. Z. Säugetierkunde 1996; 61: 36–48
   Google Scholar
• Cowie A. T. Variations in the Yield and Composition of Milk During Lactation in the Rabbit and the Galactopoietic Effect of Prolactin. J. Endocrinol. 1969; 44: 437–50
   PubMedGoogle Scholar
• Escobar C., Hudson R., Martínez-Gómez M., Aguilar-Roblero R. Metabolic Correlates of the Circadian Pattern of Suckling-Associated Arousal in Young Rabbits. J. Comp. Physiol. A 2000; 186: 33–38
   PubMed Web of Science ®Google Scholar
• Kleitmann N., Engelmann T. G. Sleep characteristics of infants. J Appl. Physiol. 1953; 6: 269–82
   PubMedGoogle Scholar
• Meier-Koll A., Hall U., Hellwig U., Kott G., Meier-Koll V. A Biological Oscillator System and the Development of Sleep-Waking Behavior During Early Infancy. Chronobiologia 1978; 5: 424–40
   Google Scholar
• Tenrerio S., Dowse H. B., D'Souza S., Minors D., Chiswick M., Simms D., Waterhouse J. The Development of Ultradian Rhythms in Premature Babies Maintained in Constant Conditions. Early Hum. Dev. 1991; 27: 33–52
   PubMedGoogle Scholar
• Schuh J., Börnert D. Zur Genesis zeitlich rhythmischer Ordnung im biologischen System: Modelluntersuchungen am Kaninchen. Nova Acta Leopoldina: Die Zeit und das Leben, H. J. Scharf, H. von Mayersbach. Deutsche Akad. Naturf. Leopoldina, Halle 1977; 561–72
   Google Scholar
• Distel H., Hudson R. The Contribution of the Olfactory and Tactile Modalities to the Nipple-Search Behaviour of Newborn Rabbits. J. Comp. Physiol. A 1985; 157: 599–605
   PubMedGoogle Scholar
• Hudson R. Do Newborn Rabbits Learn the Odor Stimuli Releasing Nipple-Search Behavior?. Dev. Psychobiol. 1985; 18: 575–85
   PubMed Web of Science ®Google Scholar
• Hudson R., Distel H. Regional Autonomy in the Peripheral Processing of Odor Signals in Newborn Rabbits. Brain Res. 1987; 421: 85–94
   PubMed Web of Science ®Google Scholar
• Hudson R., Mendoza-Soylovna A., Labra-Cardero D., Pacheco-Cobos L., Rosetti-Sciutto M. F. Maternal Stimuli Contributing to Olfactory Learning in the Newborn Rabbit. Chem. Senses, in press
   Google Scholar
• Allingham K., von Saldern C., Brennan P. A., Distel H., Hudson R. Endogenous Expression of c-Fos in Hypothalamic Nuclei of Neonatal Rabbits Coincides with Their Circadian Pattern of Suckling-Associated Arousal. Brain Res. 1998; 783: 210–18
   PubMedGoogle Scholar
• Pongrácz P., Altbäcker V. The Effect of Early Handling is Dependent upon the State of the Rabbit (Oryctolagus cuniculus) Pups Around Nursing. Dev. Psychobiol. 1999; 35: 241–51
   PubMed Web of Science ®Google Scholar
• Pittendrigh C. S. Circadian Rhythms and the Circadian Organization of Living Systems. Cold Spr. Harb. Symp. Quant. Biol. 1960; 25: 159–84
   PubMedGoogle Scholar
• Pittendrigh C. S., Daan S. A Functional Analysis of Circadian Pacemakers in Nocturnal Rodents I. The Stability and Lability of Spontaneous Frequency. J. Comp. Physiol. A 1976; 106: 223–52
   Web of Science ®Google Scholar
• Pittendrigh C. S., Daan S. A Functional Analysis of Circadian Pacemakers in Nocturnal Rodents IV. Entrainment: Pacemaker as Clock. J. Comp. Physiol. A 1976; 106: 291–31
   Web of Science ®Google Scholar