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Nine samples of Antarctic krill collected at seven localities in the Palmer Archipelago and Bransfield Strait west of the Antarctic Peninsula were analysed for genetic variation at eight enzyme loci. Despite significant among sample heterogeneity in allele frequencies, no convincing evidence was found to support the hypothesis of distinct genetic stocks of Euphausia superba in the investigated area. Allele frequency distributions could not be correlated to regional differences in size patterns. Allelic proportions at the PGI locus did not indicate that the investigated krill was genetically different from E. superba from the Weddell Sea region (from earlier investigations). Deviations of genotypes, or allele frequencies from those expected under Hardy-Weinberg equilibrium, however, may indicate regional, or yearly variation due to occasional selection.

Krill was sampled in the Weddell Sea, farther south than ever before, and off Bouvet-öya. Five species were found: Euphausia superba, E. crystallorophias, E. frigida, E. triacantha, and Thysanoessa macrura. E. superba and E. crystallorophias were the most abundant species north and south of 74° S respectively. Length frequency analyses suggest that E. superba from the inner Weddell Sea takes three years to reach maturity. This population differed in several aspects from the populations farther north. E. crystallorophias and T. macrura were registered south to 77°45′ S, the southernmost localisation investigated. The material gives no clear evidence whether these species take one or two years to reach maturity. Their spawning activity seems to start earlier in the season than for E. superba. E. frigida and E. triacantha were only-found off Bouvetöya. Continuous echosounder recordings revealed that the total abundance of krill in the southern parts of the Weddell Sea was low, as was also the abundance on the route between the South Orkney Islands and Dronning Maud Land.

In the austral summer 1978/79 samples of krill were taken off Bouvetøya and in the southern Weddell Sea. Off Bouvetøya Euphausia superba Dana was the dominant species, but the population pattern indicates that the individuals found there were expatriates from other areas. For the first time larvae of E. superba were found in significant amounts in the southern Weddell Sea. Except from shallow water and the most southern position, they were equal in abundance to the larvae of E. crystallorophias Holt & Tattersall. Larval stages of the latter are described as is the successive spawning that takes place among the three species of krill found in the southern Weddell Sea.

Development of a comprehensive picture of the genetic population structure of the Antarctic krill (Euphausia superba) has been hampered by a lack of genetic data from two major areas of the species' distribution, the Bellingshausen Sea and the Ross Sea. Evidence from earlier studies of a discrete “Bellingshausen Sea” population was based on anomalous allele frequencies in two sample sets that were collected near the west coast of the Antarctic Peninsula rather than in the Bellingshausen Sea proper. In this paper we describe the first biochemical genetic data obtained on krill from the central Bellingshausen Sea and from the Ross Sea. Analyses of eight polymorphic loci in samples from these two areas have failed to provide any evidence of population structuring within the Pacific sector of the Southern Ocean, and have indicated that Pacific sector krill cannot be genetically discriminated from Atlantic sector krill or Indian Ocean sector krill. These findings further support the hypothesis of a single circumpolar breeding population of Antarctic krill.

Electrophoretic analyses of allele distributions at nine polymorphic gene loci were conducted in samples of Euphausia superba from the Bransfield Strait, off the South Orkney Islands, and from the south-eastern part of the Weddell Sea. The aim was to determine whether reported phenotypic differences between krill stocks from these areas could be linked to genotypic differences. Despite minor deviations of genotype distributions from Hardy-Weinberg expectations, the data gave no evidence of genetic heterogeneity over the sampled area, and the hypothesis of a single genetically homogeneous krill population could not be rejected. Genetic data for four selected loci were verified by using two different electrophoretic methods. Results from these two techniques yielded no discrepancies in interpretation of the data.

The bacterial flora of two species of Antarctic krill, Euphausia superba Dana and E. crystallorophias Holt & Tattersall, was studied with the aim of investigating the role played by bacteria during the claimed rapid deterioration of these animals. The number of bacteria on fresh krill was characterized as low, but started to increase exponentially after a few days of storage at low temperatures. Dominant species were of the genera Moraxella, Pseudomonas, and Alteromonas. Comparing the low initial number of bacteria with the high autolytic activity it is suggested that the rapid degradation of krill during the first days of storage is induced by autolysis and not by bacterial activity.

By means of enzyme electrophoretical assays three samples of Euphausia superba, all from the Atlantic sector of the Antarctic Ocean, were examined to see whether or not they represent genetically separated populations. The same samples were also compared with E. superba from off the Western coast of the Antarctic Peninsula, representing the Pacific sector. The latter animals have previously been studied by other authors. One sample of a second species of Antarctic krill, E. crystallorophias, was likewise examined. Thirty-five loci were studied in E. superba, and it is concluded that the three samples from the Atlantic sector most probably do not represent reproductively isolated populations. Their average heterozygosity, about 10%, is however greater than the value previously found for the ‘Pacific’ E. superba, 5.8 %. Calculations of the genetic identity and genetic distance between the Atlantic and ‘Pacific’ samples of E. superba suggest they represent separate populations. The average heterozygosity of E. crystallorophias was estimated to be between 9.1 and 9.4 %, from studies of 33 loci. The genetic distance between this species and E. superba was estimated at 0.989. The results are finally discussed in terms of postulated theories on genetic variability versus environmental heterogeneity.

In the austral summer of 1983, schools of krill from Bransfield Strait and Palmer Archipelago were analyzed for composition in terms of size frequencies and maturity stages. Juveniles dominated in all schools, and mature animals never exceeded 6.8% of the animals at any sampling site. Gravid females were encountered in only four out of 15 schools and were never more frequent than 1.8% of the animals in any school. Among subadults and juveniles the largest animals were found on the inside of Palmer Archipelago. Smaller nonreproductive animals were on the outside and in Bransfield Strait. A second group of juveniles, in a size range of 12-15 mm, was more pronounced north of Crocker Passage than south of the Passage. Their potential origin from a more slowly growing and later spawning Southern Weddell Sea population is discussed. Lack of reproductive animals in the Bransfield/South Shetlands vicinity may reflect yearly variation in this region. A hypothesis is put forward on the basis of this study that Palmer Archipelago is a nursery ground for krill spawned elsewhere. The sites of origin of this krill could be ascertained on the basis of studies of enzyme polymorphism in these populations.