SUMMARYThe life strategy of the anadromous Arctic charr (Salvelinus alpinus) includes several months of voluntary fasting during overwintering in freshwater, leading to emaciation prior to seawater migration in spring. In this study we compared changes in condition, substrate utilization and liver metabolism between captive anadromous charr subjected to food deprivation during late winter and spring, and conspecifics fed in excess. In March, nine out of the 10 sampled fed fish had not eaten, indicating that they were in a voluntary anorexic state. In June, the fed fish were eating and all had higher body mass, condition factor and adiposity than in March. In fasted fish there were only small decreases in body mass, condition factor and adiposity between March and May, but all these parameters decreased markedly from May to June. The fasted fish were depleted in fat and glycogen in June, had suppressed activity of hepatic enzymes involved in lipid metabolism (G6PDH and HOAD) and seemed to rely on proteinderived glucose as a major energy source. This was associated with upregulated liver gene expression of leptin A1, leptin A2, SOCS1, SOCS2 and SOCS3, and reduced IGF-I expression. In an in vitro study with liver slices it was shown that recombinant rainbow trout leptin stimulated SOCS1 and SOCS3 expression, but not SOCS2, IGF-I or genes of enzymes involved in lipid (G6PDH) and amino acid (AspAT) metabolism. It is concluded that liver leptin interacts with SOCS in a paracrine fashion to suppress lipolytic pathways and depress metabolism when fat stores are depleted. Supplementary material available online at

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Methane emissions from reindeer (Rangifer tarandus tarandus) fed lichens (mainly Cladonia stellaris) and a concentrate feed were determined using open-circuit respirometry. The lichen diet was low in crude protein (< 2.6% of dry matter [DM]), starch (6.0% DM) and acid detergent lignin (2.0% DM) compared to the concentrate feed (12.7, 22.5 and 7.2% DM, respectively), and high in neutral detergent fibre (82.2% DM versus 34.8% DM in concentrate feed). The feeds were offered in equal amounts (ca. 0.440 kg DM) 2 h after initiating methane recordings in the respiration chamber. The reindeer were adapted to these diets for > 4 weeks prior to experiments and methane emissions recorded for two separate 23 h periods for each diet. Methane emissions increased on average by 0.93 g/h (or by 5.8 times) in the first hour after feeding the concentrate feed, while emissions remained unchanged after the intake of lichens. Mean methane emissions from reindeer (n = 5) were 7.5 ± 0.54 (SE) g CH 4 day −1 when fed lichens, compared to a higher emission (p = 0.001) of 11.2 ± 0.54 g CH 4 day −1 on the concentrate diet. The mean proportion of gross energy intake lost as methane was 5.2 ± 0.37% on the lichens and 7.6 ± 0.37%, or some 50% higher, on the concentrate feed. This difference was significant (p < 0.001). Our results suggest that it is of environmental importance to preserve the lichens on the tundra and minimize supplementary feeding with concentrate diets, in order to reduce methane emission.

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