Recent studies have suggested that Paleozoic hyperoxia enabled animal gigantism, and the subsequent hypoxia drove a reduction in animal size. This evolutionary hypothesis depends on the argument that gas exchange in many invertebrates and skin-breathing vertebrates becomes compromised at large sizes because of distance effects on diffusion. In contrast to vertebrates, which use respiratory and circulatory systems in series, gas exchange in insects is almost exclusively determined by the tracheal system, providing a particularly suitable model to investigate possible limitations of oxygen delivery on size. In this study, we used synchrotron x-ray phase-contrast imaging to visualize the tracheal system and quantify its dimensions in four species of darkling beetles varying in mass by 3 orders of magnitude. We document that, in striking contrast to the pattern observed in vertebrates, larger insects devote a greater fraction of their body to the respiratory system, as tracheal volume scaled with mass 1.29 . The trend is greatest in the legs; the cross-sectional area of the trachea penetrating the leg orifice scaled with mass 1.02 , whereas the cross-sectional area of the leg orifice scaled with mass 0.77 . These trends suggest the space available for tracheae within the leg may ultimately limit the maximum size of extant beetles. Because the size of the tracheal system can be reduced when oxygen supply is increased, hyperoxia, as occurred during late Carboniferous and early Permian, may have facilitated the evolution of giant insects by allowing limbs to reach larger sizes before the tracheal system became limited by spatial constraints. allometric scaling ͉ hyperoxia ͉ Tenebrionidae ͉ tracheal system
Laboratories that study Drosophila melanogaster or other insects commonly use carbon dioxide (CO2) anaesthesia for sorting or other work. Unfortunately, the use of CO2 has potential unwanted physiological effects, including altered respiratory and muscle physiology, which impact motor function behaviours. The effects of CO2 at different levels and exposure times were examined on the subsequent recovery of motor function as assessed by climbing and flight assays. With as little as a five minute exposure to 100% CO2, D. melanogaster exhibited climbing deficits up to 24 hours after exposure. Any exposure length over five minutes produced climbing deficits that lasted for days. Flight behaviour was also impaired following CO2 exposure. Overall, there was a positive correlation between CO2 exposure length and recovery time for both behaviours. Furthermore, exposure to as little as 65% CO2 affected the motor capability of D. melanogaster. These negative effects are due to both a CO2-specific mechanism and an anoxic effect. These results indicate a heretofore unconsidered impact of CO2 anaesthesia on subsequent behavioural tests revealing the importance of monitoring and accounting for CO2 exposure when performing physiological or behavioural studies in insects.
The respiratory physiology and water relations of three harvester ant species (Pogonomyrmex rugosus Emery, P. occidentalis[Cresson] and P. californicus[Buckley]) were examined at three temperatures (15, 25 and 35°C) using a flow‐through respirometry system. As intact ants tended to be active during testing, we performed a parallel set of experiments on individuals rendered motionless by decapitation. Both intact and decapitated ants exhibited discontinuous ventilation. Decapitation caused metabolic rate (V˙CO2) and burst frequency to decrease in all three species. Burst volume either remained constant or increased after removal of the head, though mass‐specific V˙CO2 was unaffected except in P. rugosus. Mass‐specific V˙CO2s of headless harvesters were comparable with published values derived from motionless specimens of other ant species. The mean Q10 for intact ants of all three species was 2.37; for decapitated insects the mean was 2.32. Respiratory water constituted a small (< 5%) fraction of total loss, and we believe that discontinuous ventilation does not act to conserve water in these organisms, although it may serve other functions.
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