• Journal of Photoscience
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• v.9 no.2
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• pp.252-254
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• 2002

Djungarian hamsters show distinct seasonal rhythms in several physiological parameters. One of them is daily torpor that occurs in winter with decreased body temperature (about 1O-20$^{\circ}$C) during daytime. Daily torpor is induced by short-day photoperiod, food restriction and castration. But the mechanism to induce daily torpor has not been clarified. In the present study, we tried to clarify the process of daily torpor induction in detail. Adult male hamsters were kept in long photoperiod and high temperature (LP-HT) before the experiment and, thereafter, the animals were transferred to short photoperiod and low temperature (SP-LT), and they were kept in this condition for about six months. The daily rhythms of locomotor activity and body temperature were recorded every three-minutes by using the Minimitter telemetry system. Locomotor activity and body temperature showed very closely synchronized rhythms. All animals under LP-HT showed daily rhythms with higher locomotor activity and body temperature in nighttime than in daytime. Under SP-LT, there were two types of animals with and without showing daily torpor. Thus, they have individual differences in the response to SP -LT.

• Journal of Life Science
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• v.16 no.4
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• pp.618-625
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• 2006

Patterns of induced daily torpor were measured in the striped field mouse, Apodemus agrarius, in response to low temperature, food deprivation and various photoperiods using implanted data loggers. A total of 8 of 21 females entered daily torpor in response to low outside ambient temperature (Ta) during winter and spring, constant low Ta $(4^{\circ}C)$ or food deprivation $(23^{\circ}C)$ during summer, but 2 of 23 males did only in response to low outside Ta during winter. This fact indicates that torpor is an adaptive hypothermia to unpredictable environment in both some males and females, as well as that torpor was inhibited in males in the reproductive season as in other mammals, which is regarded as a strategy not to reduce the chance of copulation. As for females, however, torpor was employed in response to unpredictable environment even in the reproductive season, suggesting that alternative strategies other than keeping the chance of copulation maybe hired by females to keep the population. Torpor bout generally began at $6{\sim}12$ AM, but the decrease of body temperature $(T_b)$ began mainly at $4{\sim}6$ AM at any conditions, the time when Ta is lowest. This strategy might be also adopted for reducing heat loss to unpredictable environment. Minimum $T_b$ of both males and females during torpor did not fall below $16.5^{\circ}C$. Photoperiod had no influence on the incidence and timing of daily torpor in either males and females. The similar timing of torpor bout in response to the 3 different photoperiods (24D, 16L:8D or 8L:16D) under the constant temperatures $(4^{\circ}C\;or\;23{\pm}2^{\circ}C)$ suggests that entering time of torpor might be controlled by the circadian rhythm of the mice rather than by the photoperiod.