Abstract

This study investigated interactions of temperature and hypoxia on metabolic plasticity and regulation in zebrafish, Danio rerio, in the first week of development. Larval morphometry, oxygen consumption, and metabolic responses to acute changes in temperature and oxygen were measured in larvae reared under four conditions, including control (28°C and partial pressures of oxygen [PO2] of 21kPa), high temperature (31°C), hypoxia (11kPa), and the two stressors combined. Rearing conditions did not result in consistent morphometric changes; substantial metabolic adjustments, however, were evident. While acute temperature increase resulted in elevated oxygen consumption, with a Q10 of 2.2 ± 0.08, early-staged larvae were able to compensate to chronic temperature rise as routine metabolic rates did not differ between 28°C and 31°C chronic treatments. In contrast, larval responses to chronic and acute hypoxia were similar, with ∼30% decrease in metabolic rates from normoxic values at both temperatures. Further, prior exposure to chronic hypoxia in conjunction with acute high temperature increased Q10 by a factor of 2.5 from 2.2 ± 0.08 to 5.6 ± 0.19. Metabolic suppression by acute hypoxia was independent of any prior exposure conditions. In short, results from this study showed that zebrafish larvae exhibited surprising temperature resilience and metabolic plasticity to a 3°C temperature rise even in their first week of life. Yet exposure to a second stressor (hypoxia) resulted in elevated sensitivity to temperature change that may lead to bioenergetic imbalance due to synergetic effects of temperature and hypoxia on metabolic rates.

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