Arnfinn Langeland

Reproductive investment and energy allocation in an alpine Arctic charr, Salvelinus alpinus, population

Reproductive investment was determined in a population of stunted Arctic charr, Salvelinus alpinus, living in an ultra-oligotrophic alpine lake (altitude 1100 m) in central Norway (62°51′W). No reductions in somatic energy content (carcass and intestines) were detected during the spawning period. Post-spawning somatic lipid, protein and total energy content did not differ between male spawners, female spawners and immatures. The recorded reproductive output consisted of gonad tissue equivalent to 13% of total pre-spawning energy in females and 4% in males, respectively. Mean stored somatic lipid reserves were as low as 2.8% and did not change significantly from pre- (30 June) to post-spawning (1% October) samples. Female fecundity varied between 41 and 84 (mean 60) eggs, with a corresponding body length varying between 110 to 160 mm (mean 13%). Mean yearly survival rate after maturation was 70% for females and 64% for males, respectively. This particularly low reproductive investment is discussed in relation to environmental conditions and low resource availability.

The relevance of individual size to management of Arctic charr, Salvelinus alpinus, populations

Arctic charr, Salvelinus alpinus, tend to form stunted populations presumably due to competition for limited resources. In this context a long-term intensive fishery programme aiming at reducing charr density, and thereby increasing growth and harvestable sizes, was initiated in the early 1980s in a Norwegian alpine lake. Here we present long-term data on catch statistics and changes in mean weights of charr caught with gill nets on spawning grounds, as well as changes in mean weight of juvenile charr caught with funnel traps during the 1990s. Furthermore, we present results from shorter-term studies on growth, size- and age-distribution, and size-related habitat and resource utilisation of Arctic charr and brown trout, Salmo trutta, in this lake. Mean weight (±SD) of charr caught on the spawning grounds increased significantly from 129.8 g (±11.9) in the years 1982–1990 to 213.1 g (±37.8) in the years 1996–1999, whereas catch per unit of effort decreased significantly. Mean weight of juveniles caught in funnel traps increased significantly from 21.2 g (±6.9) in 1993 to 41.9 g (±14.8) in 1999. Apparently the increase in weight of spawning charr coincided with the onset of trap fishing for juvenile dim Compared to generally shallow dwelling trout, charr grew rapidly and were generally found in deeper areas of the lake. Charr went through a distinct size-related niche shift from mainly consuming small zooplankton in the pelagic to consuming large benthic prey in shallower waters. Resource and habitat utilisation in different size-groups of charr and trout are discussed with respect to possible competitive and predatory intra- and interspecific interactions, and with regard to management of charr populations.

Mitochondrial DNA inference between European populations of Tanymastix stagnalis and their glacial survival in Scandinavia

The early observation from 1914 of Tanymastix stagnalis in Norway was not repeated recently, showing a rare and restricted distribution of this species. All four sampled localities were concentrated in the same area of the Trollheimen Mountains with altitudes of 900–1244 m above sea level. In March 2002, a new population of T. stagnalis was observed at about 50 km north of Madrid at an altitude of 1350 m. In general, all habitats with T. stagnalis were fishless shallow ponds and varied in size from 1 to about 300 m2. Natural variability of the global temperature is well accepted, but recent climate models have predicted increases in global average temperature. Based on the new biogeographical distribution, diurnal temperature variations, and biological evidence (inference with the analysis of mitochondria DNA), the immigration history of T. stagnalis was considered on the basis of two opposing immigration theories and in relation to the implications of global climate change. Two immigration theories, namely – the Tabula rasa and Nunatak, have prevailed in explaining the present distribution of plants and animals in Scandinavia. It was concluded that the rare occurrence of T. stagnalis in Norway fits into the Nunatak theory and that the species probably survived, at least, the last glaciation on Nunataks or coast refuges located in central northwestern Norway at Møre mountain and coast areas.