Physiology &Behavior, Vol.52, pp. 1-5, 1992 0031-9384/92 $5.00+ .00
Printedin the USA. Copyright© 1992PergamonPressLtd.
Sex Differences in the Play Fighting Activity
of Golden Hamster Infants
ROGERIO F. GUERRA, l MAURO L. VIEIRA, EMILIO TAKASE AND SIMONE GASPARETTO
Universidade Federal de Santa Catarina, Departamento de Psicologia, Laboratrrio de Psicologia Experimental,
Campus Universitrrio da Trindade, 88049, Florianrpolis, S.C., Brasil
Received 13 December 1990
GUERRA, R. F., M. L. VIEIRA, E. TAKASE AND S. GASPARETTO. Sex differences in the play fighting activity of golden
hamster infants. PHYSIOL BEHAV 52(1) 1-5, 1992.--Play fightingof homosexual and heterosexual dyads in golden hamsters
was studied. The behaviors of male-male (MM), female-female (FF), male-female (MF) and female-male (FM) dyads were
recorded from the 25th to the 31st day of age. Play fightingactivity of heterosexual dyads was depressed since MF and FM dyads
exhibited a significantly high physical contact time and engaged in less play fighting,with a significantly lower time spent on such
activity. Alternation ratio in the pinning posture was very high and subjects did not differ in the mean number of active (top)
and passivepinning(under) in each dyad, showingan inexistenceof sex dominance. In most cases, differences in the performances
of MM and FF dyads were not significant. We have concluded that play fighting in golden hamsters may be predominantly
modulated by environmental stimuli (sex of the partner) rather than by endogenous stimuli (androgen level).
Play fighting sex differences androgen pinning postures locomotion Physical contact
Golden hamster
PLAY fighting occurs in many species of rodents. This behavior
is very easy to discern, but its definitions and functions are very
difficult to characterize (4,10,19,25). In fact, when playing, infant
rodents may behave in many ways as they do during serious
encounters. In rats, play fighting may be discerned from real
fighting since snout or oral contact is directed to the partner's
nape of the neck, whereas during real fighting bites are directed
to the opponent's rump (20). In golden hamsters, the infants
attack and defend the cheeks and cheek pouches during play
fighting, whereas they attack and defend the rump and lower
flanks during real fighting (22). Play fighting begins around the
15th day of age and becomes more frequent as the infant grows
older (5,7).
Sex differences in play-fighting behavior have already been
mentioned for many species of mammals (13). In fact, play en-
counters between juvenile male rats are more frequent than be-
tween females, and also males are more likely to engage with
other males than with females (12) and to initiate more play
than do females (8). Male rats engage in more rough-and-tumble
than do females of the same age, and female pups submitted to
a testosterone treatment during their early development exhibit
an increased play-fighting behavior comparable to that of males
(15). It has already been concluded that androgen level of infant
rats appears to promote the sexual differentiation of some CNS
structures during early development which, in turn, mediate sex
differences in play fighting, independent of later testosterone
levels (11,14). The present article examined sex differences in
play-fighting activity of homosexual and heterosexual dyads of
golden hamster infants.
METHOD
Subjects
Eighty juvenile golden hamsters (Mesocricetus auratus) were
used as subjects. The animals were obtained from the stock of
the Laborat6rio de Psicologia Experimental at the Universidade
Federal de Santa Catarina.
Equipment
The animals were housed in polypropylene home cages (40
X 30 X 17 cm). Chronometers and standard sheet notes were
utilized during the experimental sessions for recording of be-
haviors.
Procedure
On the 24th day of age, the infants were removed from the
mother's cage and seperately housed in 40 x 30 Ă— 17 cm home
cages in four different groups of male-male (MM), female-fe-
male (FF), male-female (MF) and female-male (FM). Each
group was formed by 20 subjects, or 10 dyads, each dyad was
formed by infants of different litters. The focal-infant (FInf) of
each dyad was notched in its right ear and the partner-infant
(PInf) in its left ear. The animals were observed from the 25th
Requests for reprints should be addressed to Dr. Rogerio F. Guerra.