High Blood Flow Into the Femur Indicates Elevated Aerobic Capacity in Synapsids Since the Synapsida-Sauropsida Split

Varanids are the only non-avian sauropsids that are known to approach the warm-blooded mammals in stamina. Furthermore, a much higher maximum metabolic rate (MMR) gives endotherms (including birds) higher stamina than crocodiles, turtles, and non-varanid lepidosaurs. This has led researchers to hypothesize that mammalian endothermy evolved as a second step after the acquisition of elevated MMR in non-mammalian therapsids from a plesiomorphic state of low metabolic rates. In recent amniotes, MMR correlates with the index of blood flow into the femur (Qi), which is calculated from femoral length and the cross-sectional area of the nutrient foramen. Thus, Qi may serve as an indicator of MMR range in extinct animals. Using the Qi proxy and phylogenetic eigenvector maps, here we show that elevated MMRs evolved near the base of Synapsida. Non-mammalian synapsids, including caseids, edaphosaurids, sphenacodontids, dicynodonts, gorgonopsids, and non-mammalian cynodonts, show Qi values in the range of recent endotherms and varanids, suggesting that raised MMRs either evolved in synapsids shortly after the Synapsida-Sauropsida split in the Mississippian or that the low MMR of lepidosaurs and turtles is apomorphic, as has been postulated for crocodiles.

Energetic costs of ectoparasite infection in Atlantic salmon

Parasites are widespread in nature where they affect energy budgets of hosts, and depending on the imposed pathogenic severity, this may reduce host fitness. However, the energetic costs of parasite infections are rarely quantified. In this study, we measured metabolic rates in recently seawater adapted Atlantic salmon (Salmo salar) infected with the ectoparasitic copepod Lepeophtheirus salmonis and used an aerobic scope framework to assess the potential ecological impact of this parasite-host interaction. The early chalimus stages of L. salmonis did not affect either standard or maximum metabolic rates. However, the later mobile pre-adult stages caused an increase in both standard and maximum metabolic rate yielding a preserved aerobic scope. Notably, standard metabolic rates were elevated by 26%, presumably caused by increased osmoregulatory burdens and costs of mobilizing immune responses. The positive impact on maximum metabolic rates was unexpected and suggests that fish are able to transiently overcompensate energy production to endure the burden of parasites and thus allow for continuation of normal activities. However, infected fish are known to suffer reduced growth, and this suggests that a trade-off exists in acquisition and assimilation of resources despite of an uncompromised aerobic scope. As such, when assessing impacts of environmental or biotic factors, we suggest that elevated routine costs may be a stronger predictor of reduced fitness than the available aerobic scope. Furthermore, studying effects on parasitized fish in an ecophysiological context deserves more attention, especially considering interacting effects of other stressors in the Anthropocene.

Correlation between Metabolic Rate and Salinity Tolerance and Metabolic Response to Salinity in Grass Carp (Ctenopharyngodon idella)

The metabolic rate could be one of the factors affecting the salinity tolerance capacity of fish. Experiment I tested whether metabolic rates correlate with the upper salinity tolerance limit among individual grass carp by daily increasing salinity (1 g kg−1 day−1). The feeding dropped sharply as the salinity reached 10 g kg−1 and ceased when salinities exceeded 11 g kg−1. The ventilation frequency decreased weakly as salinity increased from 0 to 12 g kg−1 and then increased rapidly as salinity reached 14 g kg−1. The fish survived at salinities lower than 14 g kg−1, and all fish died when salinity reached 17 g kg−1. The upper salinity tolerance limit was not correlated with metabolic rates. Therefore, a lower metabolic rate may not necessarily allow for better salinity tolerance capacity. Experiment II tested how different salinities (0, 0.375, 0.75, 1.5, 3, and 6 g kg−1 for 2 weeks) affect the metabolic parameters of grass carp. The changes in the resting metabolic rate with increasing salinity could be explained by the relative changes in interlamellar cell mass and protruding lamellae. The maximum metabolic rate remained constant, suggesting that the salinity-induced changes in the gill surface had a minor effect on oxygen uptake capacity.