Ecological commonalities among pelagic fishes: comparison of freshwater ciscoes and marine herring and sprat

Systematic comparisons of the ecology between functionally similar fish species from freshwater and marine aquatic systems are surprisingly rare. Here, we discuss commonalities and differences in evolutionary history, population genetics, reproduction and life history, ecological interactions, behavioural ecology and physiological ecology of temperate and Arctic freshwater coregonids (vendace and ciscoes, Coregonus spp.) and marine clupeids (herring, Clupea harengus, and sprat, Sprattus sprattus). We further elucidate potential effects of climate warming on these groups of fish based on the ecological features of coregonids and clupeids documented in the previous parts of the review. These freshwater and marine fishes share a surprisingly high number of similarities. Both groups are relatively short-lived, pelagic planktivorous fishes. The genetic differentiation of local populations is weak and seems to be in part correlated to an astonishing variability of spawning times. The discrete thermal window of each species influences habitat use, diel vertical migrations and supposedly also life history variations. Complex life cycles and preference for cool or cold water make all species vulnerable to the effects of global warming. It is suggested that future research on the functional interdependence between spawning time, life history characteristics, thermal windows and genetic differentiation may profit from a systematic comparison of the patterns found in either coregonids or clupeids

Species specificity and potential roles of Karlodinium micrum toxin

Karlodinium micrum is a toxic mixotrophic dinoflagellate that has been responsible for fish kills in coastal environments worldwide. The role that karlotoxins play in the life history of K. micrum is unknown, but maycontribute to its bloom-forming ability. We tested the hypothesis that karlotoxins could inhibit the growth of other protists depending on the sterol composition of target cell membranes. We also examined the effect of toxin addition on feeding rates of K. micrum on a flagellatedprey, Storeatula major. Dose-dependent effects of isolated karlotoxin (KmTX2) were tested in growth bioassays (24–48h) of K. micrum, three raphidophytes (Heterosigma akashiwo, Fibrocapsa japonica andChattonella subsalsa), two cryptophytes (S. major and Pyrenomonas salina), and the dinoflagellates Amphidinium carterae, Pfiesteria piscicida and P. shumwayae. Growth of K. micrum, P. salina, A. carterae and P. piscicida were not affected by karlotoxin additions up to 1 000ng ml–1. Other organisms showed growth inhibition at concentrations between 500ng ml–1 and 1 000ng ml–1. Predation by K. micrum on S. major was significantly higher in the presence of 25ng ml–1 KmTX2. Theresults are consistent with a role for karlotoxin in allelopathic inhibition of competitors and/or prey immobilisation depending on sterol composition

Antioxidant CR-6 protects against reperfusion injury after a transient episode of focal brain ischemia in rats

Oxidative and nitrosative stress are targets for intervention after ischemia/reperfusion. The aim of this study was to explore the effect of CR-6, a vitamin-E analogue that is antioxidant and scavenger of nitrogen-reactive species. Sprague–Dawley rats had the middle cerebral artery (MCA) occluded either for 90 mins or permanently. Cortical perfusion was continuously monitored by laser–Doppler flowmetry. CR-6 (100 mg/kg) was administered orally either at 2 and 8 h after MCA occlusion, or at 2 h only. Infarct volume, neurological deficit, and signs of reperfusion injury were evaluated. CR-6 was detected in plasma and brain by HPLC. CR-6 reduced glutathione consumption in the ischemic brain and superoxide generation in the isolated MCA. CR-6 decreased infarct volume and attenuated the neurological deficit at 1 and 7 days after ischemia/reperfusion, but not after permanent ischemia. Immediately after reperfusion, cortical blood flow values returned to their baseline (±20%) in several animals, whereas others showed hyper-perfusion (>20% of baseline). Reactive hyperemia was associated with adverse events such as increased cortical BBB leakage, edema, protein nitrotyrosination, COX-2 expression, and neutrophil accumulation; and with a poorer outcome, and CR-6 attenuated these effects. In conclusion, oral CR-6 administration after transient ischemia protects the brain from reperfusion injury