Several species of wrasse (Labridae) are used as cleaner fish to remove salmon lice from farmed Atlantic salmon. We estimated the fishery and use of wrasse in Hardangerfjord. The estimated numbers of labrids used on salmon and rainbow trout farms varied between 86,000 and 251,000 from 2002Á2006, but increased to as much as 1.1 million in 2009 and 2010. A total of 93,500 kg (around 1.54 million) labrids were reported landed during 2000Á2010. Corkwing wrasse (Symphodus melops) was by far the most important wrasse species: 52% by weight and 56% by number. Ballan wrasse (Labrus bergylta) made up 34% by weight but only 14% by number (due to its larger size). The relative proportion of species between the different sampling locations in the fjord was significantly different, as was the condition factor of some species. Goldsinny wrasse (Ctenolabrus rupestris) had the slowest growth of the labrids in this study, and did not reach the minimum commercial catch size (11 cm) before they were 4Á5 years old. Very few goldsinny caught were over that size. Corkwing reach commercial size in 1Á2 years. The results of this study indicate that wrasse should be protected during the spawning season. Species such as goldsinny grow so slowly that they will most likely be collected several times in heavily fished areas but discarded because they are smaller than the minimum allowable size. This could be avoided through the use of modified traps with escape routes for undersized fish. This study represents a first step towards establishing a knowledge-based management plan for the wrasse fishery.
The Pacific oyster (Crassostrea gigas) is an important aquaculture species world-wide. Due to its wide environmental tolerance and high growth rate, it has also become a successful invader in many areas, leading to major ecosystem changes. Low water temperatures were previously believed to restrict the establishment of Pacific oysters in Scandinavia. However, recent surveys reveal that the Pacific oyster is now established in many areas in Scandinavia. We present data on the current distribution, abundance and age-structure in Denmark, Sweden and Norway. The biomass of oysters in the Danish Wadden Sea increased from 1,056 to 6,264 tonnes between 2005 and 2007. Massive settlements were observed along the Swedish west coast in 2007, with densities [400 oysters per m -2 . In Norway, populations are established on the southern coast, and specimens have been found as far north as 60°N. The potential impacts and probable causes of this recent large-scale establishment are discussed.
Blue mussels Mytilus edulis with shell deformations and green pustules containing parasitic algae were collected at 3 coastal sites (Burøy, Norway; Bockholm, Denmark; Goose Green, Falkland Islands). A comparative study, including mussel histopathology, algal morphology, ultrastructure and phylogenetic position was performed. Green pustules were mainly located in the posterior portion of the mantle and gonad tissues and the posterior adductor muscle. Electron microscopy confirmed the presence of algal cells with similar morphology to Coccomyxa parasitica. Algae were oval shaped with a single nucleus and chloroplast, 1 or 2 mitochondria and a dense granular cytoplasm with a lipid inclusion body, Golgi apparatus and small vesicles. Partial small subunit (SSU) rRNA phylogeny confirmed the inclusion of parasitic algae into the Coccomyxa clade. However, the sequence identity between almost full SSU rRNA sequences of parasitic algae and others in this clade yielded an unexpected result. Green algae from mussels were distant from C. parasitica Culture Collection of Algae and Protozoa (CCAP) strain 216/18 (94% identity), but very similar (99% identity) to C. glaronensis (a lichen endosymbiont) and green endophytes from the tree Ginkgo biloba. The CCAP strain 216/18 was a sister sequence to Nannochloris algae, far from the Coccomyxa clade. These results suggest a misidentification or outgrowth of the original CCAP strain 216/18 by a different 'Nannochloris-like' trebouxiophycean organism. In contrast, our sequences directly obtained from infested mussels could represent the true C. parasitica responsible for the green pustules in blue mussels.
The Pacific oyster (Crassostrea gigas) is an important aquaculture species world-wide. Due to its wide environmental tolerance and high growth rate, it has also become a successful invader in many areas, leading to major ecosystem changes. Low water temperatures were previously believed to restrict the establishment of Pacific oysters in Scandinavia. However, recent surveys reveal that the Pacific oyster is now established in many areas in Scandinavia. The biomass of oysters in the Danish Wadden Sea has increased dramatically between 2005 and 2007, large numbers were observed along the Swedish west coast from settlement in 2006, and in Norway, populations are established along the southwest coast to 60°N.
During summer 2001, blue mussels Mytilus edulis with abnormal shell growth were collected near Kragerø, southern Norway. The mussels had green spots in their mantle tissues, mainly posteriorly and ventrally, and in the adductor muscle. Mussels from 4 sites had a prevalence of green spots varying from 2 to 71% that correlated well with shell deformities. Histological examination revealed the presence of round or ovoid algae, 0.9 to 1.5 × 1.2 to 2.4 µm, free within haemocytes and in the lesions, characterised by an inflammatory response and the presence of cellular debris. The alga contain a relatively large nucleus, 1 chloroplast and 1 mitochondrion. Size and morphology suggest that the alga might be a picoeucaryot green alga. Infection of mussel tissues appears to start in the posterior mantle edge, near the siphons, and spread anterior-ventrally in the mantle connective and storage tissues -occasionally spots were also found in the gonad follicles. Large infected areas were also observed in sinuses within the adductor muscle. Only mussels that were 3 yr old or more were infected. Deformations apparently resulted from years of continuous shell formation by a contracted, partly deformed mantle. Most deformed mussels had eroded shells, allowing some light penetration through the exposed, thin nacre. Young, thin-shelled mussels were not infected. The present work suggests that the alga has, at least partially, a parasitic relationship with the mussels, and is associated with pathological alterations in mussel tissues. MATERIALS AND METHODSField sampling. Mussels were sampled from 4 sites around Burøy on the island of Skåtøy, and Jomfruland, near Kragerø, southern Norway (58°50' N, 9°35' E) ( Fig. 1) in June 2002 and April 2003. Three samples (1a, 1b and 1c) were collected at Site 1, and 1 sample at each of Sites 2, 3 and 4. Each sample consisted of 150 randomly collected mussels, dredged or picked by hand. Sample 1c consisted of empty shells and shell fragments from approximately 300 mussels. Additional mussels were sampled for fixation of affected tissues. Geographical, hydrographical and biological conditions were noted at each sampling site.Gross morphology. During sampling, 20 mussels were steamed, aircooled, and opened to determine if green spots were apparent after processing. Samples 1a, 2, 3 and 4 were subsequently steamed and cooled separately. The length of each mussel shell was measured to the nearest 1 mm. Shell and tissue morphology was categorised as: shell morphology (normal/ deformed); infection site (adductor muscle/mantle edge/gonad area); and infection rate (no/low/moderate/high). Sample 1a had the highest prevalence of infected mussels, and was used for examination of the relationship between infection and shell length. Age of the mussels was estimated using Sample 1b, which was divided into mussel year-classes based on size, shell shape (fast versus slow growing specimens), presumed winter growth rings and erosion and fouling, partly according to Seed (1968). The length of each musse...
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