Tattersall, Glenn J., James L. Blank, and Stephen C. Wood. Ventilatory and metabolic responses to hypoxia in the smallest simian primate, the pygmy marmoset. J Appl Physiol 92: 202-210, 2002; 10.1152/japplphysiol.00500.2001.-The pygmy marmoset (Cebuella pygmaea) is the smallest New World Monkey (average body mass of 120-130 g). As such, it faces possible challenges to thermoregulation. Small mammals (e.g., rats) are well known to lower body temperature and metabolism in response to hypoxia; however, small primates have not been studied in this respect nor have, in general, the interactions between metabolism and ventilation. Because little is known about these responses in small primates, it seemed of great interest to assess the hypoxiainduced metabolic depression and drop in body temperature and the associated ventilatory requirements in this species under hypoxic conditions. Exposure to graded hypoxia (30 min at each of 18, 16, 14, 12, and 10% O2) caused body temperature to drop from the normoxic value of 39 to 37°C. This was accompanied by a marked metabolic depression (O2 consumption was ϳ68% of the normoxic value, implying a suppression of metabolism greater than that predicted from a typical value of the effect of 10°C change on metabolism of 2-3 times). Minute ventilation declined in parallel to metabolism, maintaining a constant air-convection requirement during hypoxia; thus this species did not show the typical mammalian hyperventilation. Acute exposure to 10% O2 led to a similar overall decline in metabolism and body temperature and qualitative differences in the timing of these changes. The pygmy marmoset shares some similarities in its hypoxic metabolic response with other mammals of similar size yet appears to be unique in its much diminished ventilatory response to hypoxia. body temperature; thermoregulation; hypoxic ventilatory response; hypothermia; metabolic depression MANY ANIMALS RESPOND TO HYPOXIA by reducing body temperature (T b ) and metabolic rate (46). Since the 1950s, this was known to occur in a broad range of small mammals (18) and in neonates of larger mammals, including humans (10, 25). This hypoxia-induced drop in T b and metabolic depression serves a protective role by reducing O 2 demand, eliminating costly thermogenesis, improving blood O 2 affinity, and reducing the costs of ventilation (14,27,36,38,47,48). Furthermore, numerous studies support the conclusion that hypoxia resets the hypothalamic thermoregulatory set point to a lower level (9,(15)(16)(17)34), suggesting that this is a regulated process.Metabolism and thermoregulation affect ventilatory control (13, 30). Pulmonary ventilation is controlled so that O 2 delivery matches metabolic rate under varying states of metabolic demand (24). Thus breathing during hypoxic exposure is complicated by reduced metabolism and T b in small mammals. Lowered T b and metabolic rate decrease the metabolic drive to breathe (13), whereas hypoxia serves to increase the chemical drive to breathe. These drives for breathing conflict with o...