Growing seasons of Nordic mountain birch in northernmost Europe as indicated by long-term field studies and analyses of satellite images.

The phenophases first greening (bud burst) and yellowing of Nordic mountain birch (Betula pubescens ssp.tortuosa, also called B. p. ssp. czerepanovii) were observed at three sites on the Kola Peninsula in northernmost Europe during the period 1964-2003, and at two sites in the trans-boundary Pasvik-Enare region during 1994-2003. The field observations were compared with satellite images based on the GIMMS-NDVI dataset covering 1982-2002 at the start and end of the growing season. A trend for a delay of first greening was observed at only one of the sites (Kandalaksha) over the 40 year period. This fits well with the delayed onset of the growing season for that site based on satellite images. No significant changes in time of greening at the other sites were found with either field observations or satellite analyses throughout the study period. These results differ from the earlier spring generally observed in other parts of Europe in recent decades. In the coldest regions of Europe, e.g. in northern high mountains and the northernmost continental areas, increased precipitation associated with the generally positive North Atlantic Oscillation in the last few decades has often fallen as snow. Increased snow may delay the time of onset of the growing season, although increased temperature generally causes earlier spring phenophases. Autumn yellowing of birch leaves tends towards an earlier date at all sites. Due to both later birch greening and earlier yellowing at the Kandalaksha site, the growing season there has also become significantly shorter during the years observed. The sites showing the most advanced yellowing in the field throughout the study period fit well with areas showing an earlier end of the growing season from satellite images covering 1982-2002. The earlier yellowing is highly correlated with a trend at the sites in autumn for earlier decreasing air temperature over the study period, indicating that this environmental factor is important also for autumn phenophases.

Sealworm (Pseudoterranova decipiens) infection in common seals (Phoca vitulina) and potential intermediate fish hosts from the outer Oslofjord.

Infection with Pseudoterranova decipiens in 45 common seals (Phoca vitulina) from the outer Oslofjord was investigated. Seals were collected before and during the phocine distemper virus epizootic in 1988 when the seal population in the area was reduced from about 350 to 100. In 1989, cod (Gadus morhua) and other fish species were sampled for comparison with earlier investigations on prevalence and abundance of P. decipiens infection in fishes from the outer Oslofjord. Seventy-two per cent of cod were infected with P. decipiens larvae in shallow waters between the seal skerries; the corresponding abundance was 2.2. At other fishing sites at increasing distances from the seal colony, abundance dropped to 0.05-0.20. Otoliths recovered from stomachs and scats indicated that gadids (Micromesistius poutassu, Trisopterus esmarkii and G. morhua) made up more than 80% of the seal diet. Bullrout (Myxocephalus scorpius) was also heavily infected with P. decipiens (prevalence 93% and abundance 8.4), but was not found in the seal diet. However, uninfected cod that enter shallow water from the surrounding deep waters became infected when they feed on bullrout. Recruitment to mature stock of P. decipiens occurs when highly infected cod are eaten by seals. The number of reproducing P. decipiens is very low in common seals. Only 2 seals (i.e. less than 5% of the sample) were simultaneously infected with mature worms of both sexes. The dramatic reduction of the seal stock in the outer Oslofjord by the epizootic did not seem to affect the abundance of P. decipiens in its intermediate hosts.

Lung-worms (Nematoda: Pseudaliidae) of harbour porpoises (Phocoena phocoena) in Norwegian waters: patterns of colonization.

We studied the component community of lung-worms of the harbour porpoise, attempting to establish the relative importance of ecological and evolutionary factors on its development. The lungs of 64 porpoises by-caught in Norwegian waters were examined for helminths. Three pseudaliid species were detected. The porpoises appear to be readily colonized by lung-worms, the structure of the component community of calves being fairly similar to that of the remainder. Prenatal and/or transmammary infections might partly account for these early infections. However, host age was correlated with the number of lung-worm species, suggesting that the lung-worms may have heteroxenous cycles similar to other metastrongyloids. The lung-worm species tended to co-occur more often than expected by chance. This pattern is commonly observed in communities formed by phylogenetic relatives. Mean species richness of lung nematodes differed significantly among mammalian orders. However, species richness of marine species seemed very similar to those of most terrestrial species. This evidence suggests that phylogenetic factors seem more important than ecological ones in determining the number of lung-worm species in mammals.

Mercury and selenium in arctic and coastal seals off the coast of Norway.

Mercury and selenium concentrations (wet weight) have been determined in samples of liver, kidney and brain of grey seal (Halichoerus grypus), harbour seal (Phoca vitulina), harp seal (Phoca groenlandica) and ringed seal (Phoca hispida) caught along the Norwegian coast, 114 individuals in all. Significant differences have been found in mercury contamination between the 4 species caught in the same coastal area, Jarfjord, located at the north-east of the Norwegian coast close to the Russian border. Very low hepatic mercury levels were found in the arctic species, ringed and harp seals, ranging from 0.20 to 0.67 and 0.04 to 1.0 microg g(-1), respectively, while in the coastal seal species the concentrations were 10 to 40 times higher. The corresponding ranges were 0.7 to 48.3 microg g(-1) in grey seals and 0.2 to 19.0 microg g(-1) in harbour seals. The median values were 13.5 and 0.7 microg g(-1), respectively. The highest levels were found in grey seals, indicating that particularly the stock frequenting the waters of the north-east coast of Norway and north-west coast of Russia had received a substantial mercury exposure. Fifty-five percent of these grey seals from Jarfjord had hepatic mercury levels above 10 microg g(-1) and 21% had levels above 20 microg g(-1). By a one-way analysis of covariance, sex and age were found to explain 28 and 30%, respectively, of the total variability in the mercury concentration in grey seal from Jarfjord. Significant differences in mercury concentrations were also found between stocks of harbour seals caught at different sites along the Norwegian coast, and decreasing concentration from the south to the north-east coast of Norway was revealed. The renal mercury levels in the arctic seals ranged from 0.08 to 0.45 microg g(-1), and about five times higher levels were found in grey seals and harbour seals. The mercury levels in the brain ranged from the detection level (0.01 microg g(-1)) to about 0.1 microg g(-1). The hepatic selenium levels in the arctic seal species ranged from 0.8 to 3.7 microg g(-1). The corresponding ranges in grey seals and harbour seals were 1.0 to 23.3 microg g(-1). The renal selenium levels were lower, and the levels in the brain were below the detection level (0.01 microg g(-1)). The mercury/selenium ratio was close to unity for mercury concentrations greater than 15 microg g(-1), and a nonlinear, concave relationship was found between the ratio of the hepatic mol concentrations of mercury and selenium and the hepatic mol concentrations of mercury.