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Maternal care in house mice

I. The weaning strategy as a means for parental manipulation of offspring quality

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Summary

This paper analyzes the flexibility of maternal care in wild house mice (Mus domesticus) under different reproductive conditions in the laboratory. All maternal activities were both qualitatively and quantitatively analyzed over a period of 28 days after birth of a litter. The standard behavior of a lactating house mouse with 7–8 young can be described as follows: During days 1–16 the offspring fully depend on the mother for nutrition. Due to rapid growth of the litter, the energetic demands of lactation reach a peak for the female during days 13–16. During days 17–22, the weaning period, the young begin to eat solid food. This period is characterized by behaviors that indicate different interests of the mother and offspring, and thus the existence of a parent-offspring conflict sensu Trivers (1974). Resting alone and remaining far from the litter indicate the female's interest in avoiding the offspring's demands, which are expressed in frequent attempts to initiate sucking. There is no aggression towards the young during weaning. House mice are weaned at 23 days. The relationship between mother and young appears free of conflict after weaning. Nursing is replaced by resting with body contact, but the offspring do not try to suck. The following results suggest that during the weaning period the offspring do not get more milk than corresponds to the maternal optimum—despite their frequent sucking attempts:

(a) When the mother is simultaneously lactating and pregnant, offspring are smaller at weaning than under standard conditions. (b) Small litters are weaned earlier than large ones. Despite a longer nursing period, offspring from large litters are lighter at weaning than those from small ones. (c) Under high energy demand, as after postpartum mating and with large litters, females wean their young at a body weight which corresponds to the earliest physiologically possible state of independence.

Parity of the female has no effect on maternal activities, nor has the presence of the father. In the latter case, however, offspring are less often left alone and unprotected.

Females seem to adjust their investment according to the body weight of the progeny by delaying or advancing the date of weaning (Table 2). This behavior allows the production of the largest possible number of offspring that can be raised to a minimal physiological threshold corresponding to a body weight of approximately 9 g. Such flexibility in parental care may enhance maternal fitness under different and unpredictable environmental conditions.

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References

  • Alexander RD (1974) The evolution of social behaviour. Ann Rev Ecol Syst 5:325–383

    Google Scholar 

  • Bateman N (1967) Reduced fertility of mice born in large families. Agric Res Council Report, Anim Breed Res Organ, pp 14–17

  • Berger J (1979) Weaning conflict in desert and mountain bighorn sheep Ovis canadensis, an ecological interpretation. Z Tierpsychol 50:188–200

    Google Scholar 

  • Berry RJ (1981) Population dynamics of the house mouse. In: Berry RJ (ed) Biology of the house mouse, Symp Zool Soc Lond 47. Academic, London, pp 395–425

    Google Scholar 

  • Berry RJ, Cuthbert A, Peters J (1982) Colonization by house mice: an experiment. J Zooh 198:329–336

    Google Scholar 

  • Berry RJ, Jakobson ME (1971) Life and death in an island population of the house mouse. Exp Gerontol 6:187–197

    Google Scholar 

  • Bronson FH (1979) The reproductive ecology of the house mouse. Q Rev Biol 54:265–299

    Google Scholar 

  • Bronson FH (1984) Energy allocation of the house mouse. Sci Am 250(3):90–97

    Google Scholar 

  • Bruce HM (1958) Suckling stimulus and lactation. Proc R Soc Lond (Biol) 149:421–423

    Google Scholar 

  • Cameron GN (1973) Effect of litter size on postnatal growth and survival in the desert woodrat. J Mammal 54:489–493

    Google Scholar 

  • Dunbar RIM (1982) Adaptation, fitness and the evolutionary tautology. In: King's College Sociobiology Group (eds) Current problems in sociobiology. Cambridge University Press, Cambridge, pp 9–28

    Google Scholar 

  • Ehret G (1976) Development of absolute auditory thresholds in the house mouse (Mus musculus). J Am Audio Soc 1:179–184

    Google Scholar 

  • Fisher RA (1930) The genetical theorie of natural selection. Clarendon Press, Oxford

    Google Scholar 

  • Fuchs S (1981) Consequences of premature weaning on the reproduction of mothers and offspring in laboratory mice. Z Tierpsychol 55:19–32

    Google Scholar 

  • Fuchs S (1982) Optimality of parental investment: the influence of nursing on reproductive success of mother and female young house mice. Behav Ecol Sociobiol 10:39–51

    Google Scholar 

  • Fuller JT, Wimer RE (1966) Neural, sensory, and motor functions. In: Green EL (ed) Biology of the laboratory mouse. McGraw-Hill, New York, pp 609–629

    Google Scholar 

  • Jans JE, Leon M (1983) Determinants of mother-young contact in Norway rats. Physiol Behav 30:919–935

    Google Scholar 

  • König B (1985) Die Brutpflegestrategie der Mäusemutter (Mus musculus: Eltern-Nachkommen Konflikt, Toleranz gegen fremde Junge und Reaktion auf Nahrungsmangel. Ph D thesis, University of Konstanz

  • MacDowell EC, Gates WH, MacDowell GG (1930) The influence of the quantity of nutrition upon the growth of the suckling mouse. J Gen Physiol 13:529–546

    Google Scholar 

  • Martin P (1984) The meaning of weaning. Anim Behav 32:1257–1259

    Google Scholar 

  • McLaren A, Mitchie D (1963) Nature of the systematic effect of litter size on gestation period in mice. J Reprod Fertil 6:139–141

    Google Scholar 

  • Nicoll CS, Meites J (1959) Prolongation of lactation in the rat by litter replacement. Proc Soc Exp Biol Med 101:81–82

    Google Scholar 

  • Noirot E (1964) Responsiveness to young in the adult mouse. Anim Behav 12:52–58

    Google Scholar 

  • Noirot E (1965) Changes in responsiveness to young in the adult mouse: III. The effect of immediately preceding performances. Behaviour 24:318–325

    Google Scholar 

  • Petras ML (1967a) Studies of natural populations of Mus: I. Biochemical polymorphisms and their bearing on breeding structure. Evolution 21:259–274

    Google Scholar 

  • Petras ML (1967b) Studies of natural populations of Mus: II. Polymorphism at the T locus. Evolution 21:466–478

    Google Scholar 

  • Priestnall R (1972) Effects of litter size on the behaviour of lactating female mice (Mus musculus). Anim Behav 20:386–394

    Google Scholar 

  • Priestnall R (1983) Postpartum changes in maternal behaviour. In: Elwood RW (ed) Parental behaviour in rodents. Wiley, New York, pp 67–93

    Google Scholar 

  • Priestnall R, Young S (1978) An observational study of caretaking behaviour of male and female mice housed together. Dev Psychobiol 11:23–30

    Google Scholar 

  • Sachs L (1978) Angewandte Statistik. Springer-Verlag, Berlin Heidelberg New York

    Google Scholar 

  • Taber S, Thomas P (1982) Calf development and mother-calf spatial relationships in Southern right whales. Anim Behav 30:1072–1083

    Google Scholar 

  • Trivers RL (1972) Parental investment and sexual selection. In: Campbell B (ed) Sexual selection and the descent of man. Aldine, Chicago, pp 136–179

    Google Scholar 

  • Trivers RL (1974) Parent-offspring conflict. Am Zool 14:249–264

    Google Scholar 

  • Woodside B, Pelchat R, Leon M (1980) Acute elevation of the heat load of mother rats curtails maternal nest bouts. J Comp Physiol Psychol 94:61–68

    Google Scholar 

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König, B., Markl, H. Maternal care in house mice. Behav Ecol Sociobiol 20, 1–9 (1987). https://doi.org/10.1007/BF00292161

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