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Canada's Policy for Conservation of Wild Pacific Salmon has been heralded as a transformative approach to the management of wild salmon whereby conservation is the highest priority. Given that changes to the Policy are under consideration, it is timely that we understand whether our state of knowledge and the status of wild salmon in Canada have indeed improved after its adoption in 2005. To answer these questions, we used two indices of improvement: ( i) monitoring effort and ( ii) abundance of spawning adults. Our results, based on data for all species from British Columbia's north and central coasts, show that monitoring effort has continued to erode, abundance of spawning adults has significantly declined for several species, the status of many salmon Conservation Units are in zones of concern, and 42% of the Conservation Units that we assessed as Red (threatened) would have improved in status had the Canadian fishery been reduced. We conclude with recommendations to help improve our knowledge of the status of salmon and enable a robust and successfully implemented Wild Salmon Policy for the future. [ABSTRACT FROM AUTHOR]

Through analysis of a cDNA library and third-party annotation of available database sequences, we characterized the full-length coding regions of rainbow trout (Oncorhynchus mykiss) Type I, Onmy-ARG01, and Type II, Onmy-ARG02, arginase genes. Two partial related arginase sequences, Onmy-ARG01b and Onmy-ARG02b, and a full-length zebrafish arginase coding region (Danio rerio), Dare-ARG02, are also reported. Comparison of vertebrate arginase sequences shows that both Type I and Type II genes in bony fishes contain a mitochondrial targeting N-terminal domain. This suggests that the cytosolic Type I arginase found in ureotelic vertebrates arose in the common ancestor of amphibia and mammals. Onmy-ARG01 and Onmy-ARG02 mRNA was detected in liver, kidney, gill, intestine, red muscle and heart tissues. Onmy-ARG01 was expressed at a significantly higher level relative to Onmy-ARG02 in liver and red muscle tissue. To investigate whether there was differential regulation of Onmy-ARG01 and Onmy-ARG02, juvenile trout were fasted for 6 weeks and hepatic enzyme activities and mRNA levels were compared with those of fed control fish. There was a 3-fold increase in liver arginase activity and a 2-fold increase in Onmy-ARG02 mRNA levels but no change in Onmy-ARG01 mRNA levels in fasted fish relative to fed fish. These findings indicate that both types of arginase genes are present and expressed in rainbow trout and that the pattern of expression varies between tissues. The increase in liver arginase activity after a 6-week fast is due, in part, to an increase in the expression of Onmy-ARG02 mRNA levels. [ABSTRACT FROM AUTHOR]