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a b s t r a c tPolar cod (Boreogadus saida) is the dominant forage fish in Arctic seas and the main prey of the ringed seal (Pusa hispida), the beluga (Delphinapterus leucas) and several seabird species. Changes in the abundance of polar cod will have cascading effects on arctic marine ecosystems. We tested the hypothesis that an earlier sea ice breakup and warmer sea surface temperatures (SST) in spring-summer result in the higher recruitment of juvenile polar cod in late summer. The density (number m À2 ) and biomass (mg m À2 ) of age-0 polar cod in August and September, estimated by hydroacoustics over 9 years in 9 areas of the Canadian Arctic, were negatively correlated to ice breakup week and positively correlated to SST. The timing of the ice breakup was the main determinant of recruitment, with mean juvenile biomass in September up to 11 times greater for early breakup (late May) than for late breakup (early September). Early ice breakup in spring increased juvenile biomass in August and September by allowing the survival of larvae hatched in winter and spring. Since 1979, ice breakup has occurred earlier by as much as 9.3 days per decade in some areas. We thus forecast a transient increase in polar cod biomass over the first part of the present century. Thereafter, the relaxation of extreme climatic conditions in Arctic seas should harbinger the replacement of the hyper-specialized polar cod by subarctic and boreal forage fish.Crown

Mambalgins are peptides isolated from mamba venom that specifically inhibit a set of acid-sensing ion channels (ASICs) to relieve pain. We show here the first full stepwise solid phase peptide synthesis of mambalgin-1 and confirm the biological activity of the synthetic toxin both in vitro and in vivo. We also report the determination of its three-dimensional crystal structure showing differences with previously described NMR structures. Finally, the functional domain by which the toxin inhibits ASIC1a channels was identified in its loop II and more precisely in the face containing Phe-27, Leu-32, and Leu-34 residues. Moreover, proximity between Leu-32 in mambalgin-1 and Phe-350 in rASIC1a was proposed from double mutant cycle analysis. These data provide information on the structure and on the pharmacophore for ASIC channel inhibition by mambalgins that could have therapeutic value against pain and probably other neurological disorders.

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