Thermal tolerance of larvae of Pollicipes elegans, a marine species with an antitropical distribution

For the antitropical gooseneck barnacle Pollicipes elegans, population-specific physiological temperature tolerance of larvae may serve as a barrier to larval dispersal across the warmest regions of the tropical Pacific Ocean. Thermal tolerance ranges of larvae of three different populations of P. elegans sampled in 2011 and 2012 (Mexico [MX], El Salvador [ES], and Peru [PE]) were investigated by measuring three indicators of physiological performance: swimming activity, oxygen consumption, and lethality or LT₅₀. The thermal tolerance profiles, which include measurable optimum (maximum aerobic performance), pejus (“getting worse”) and pessimum (worst aerobic performance) ranges, of larvae from the three populations were consistent with their characteristic environmental temperatures. In MX, larvae live close to the upper border of their optimum during warm months and so have a limited capacity to tolerate higher-than-normal temperatures. Larvae from the ES population likewise appear to live within their optimum temperature range, but these larvae lack a detectable pessimum range, suggesting they would be unable to cope with temperatures above their pejus range. Larvae from PE have a broad optimum but no pejus range. Different thermal tolerance ranges provide strong evidence for population-dependent physiological adaptations in P. elegans. For the southern (PE) and northern (MX) P. elegans populations, high tropical temperatures are likely to be a strong direct physiological barrier to larval survival and dispersal, which is in contrast to the more thermally tolerant ES population.     

Environmental parameters affecting induction of hatching in halibut (Hippoglossus hippoglossus) embryos

The influence of some environmental parameters in the regulation of hatching of halibut (Hippoglossus hippoglossus) embryos is reported. The progress of hatching was observed when light, oxygen and turbulence were varied. Environmental parameters influenced the induction of hatching, while the exit mechanism of halibut embryos was unaltered. Light arrests hatching of halibut eggs, and transfer of such eggs to darkness resulted in rapid and synchronous hatching. Hatching under different oxic conditions shows that better oxygen availability does not postpone the time of hatching in halibut. Oxygen seems therefore to have a minor role in the regulation of hatching in halibut. Induction of hatching was delayed under hypoxic conditions (15 mm Hg) compared to higher oxygen levels, but this probably reflects a minimal oxygen level needed for metabolism during hatching. Non-stationary water conditions delayed hatching for 1.5 d both in eggs incubated in turbulence, and in eggs subjected to turbulence at the time of hatching. Turbulence had an immediate inhibitory effect on hatching, but this inhibition was reversible under stationary conditions, under which hatching resumed after 150 to 250 min. We conclude that hatching in halibut occurs after sensory input from environmental factors which are integrated by the embryo before proceeding to hatch.