Disseminated Intravascular Coagulation in “Hitra Disease” (Hemorrhagic Syndrome) in Farmed Atlantic Salmon

1987 ◽  
Vol 24 (5) ◽  
pp. 378-385 ◽  
Author(s):  
R. Salte ◽  
P. Nafstad ◽  
T. Åsgård

Necropsy findings in adult salmon with subclinical “Hitra disease” (hemorrhagic syndrome) varied from negligible to hemorrhagic diathesis with generalized edema. By light microscopy, minute vessels were dilated, arterioles had mural necrosis, and thrombi were present. Occlusions consisted of fused erythrocytes and fibrin. Ultrastructurally, endothelial nuclei were pyknotic with condensed chromatin. The cytoplasm contained numerous laminar structures and electron-dense particles. Damaged erythrocytes adhered to the degenerated endothelium, and coalesced erythrocytes had formed mural thrombi or filled the vascular lumen. Microthrombi were frequently seen. There were no thrombocytes in the thrombi, which consisted of erythrocytes or reticulocytes. Clinically healthy farmed salmon parr showed the same disorders as did adults, but to a far lesser degree. Wild salmon parr had normal microvasculature. Results indicate that disseminated intravascular coagulation (DIC) occurs in “Hitra disease” in farmed Atlantic salmon.

2016 ◽  
Vol 73 (10) ◽  
pp. 2488-2498 ◽  
Author(s):  
Sten Karlsson ◽  
Ola H. Diserud ◽  
Peder Fiske ◽  
Kjetil Hindar ◽  

Abstract Farmed Atlantic salmon (Salmo salar) escape from net pens and enter rivers to spawn, potentially resulting in genetic introgression and reduced fitness of wild salmon. Here, we quantify genetic introgression of farmed to wild salmon, using molecular genetic markers, in populations from 147 salmon rivers, representing three-quarters of the total wild salmon spawning population in Norway. For 109 rivers with adult modern samples and sample sizes of 20 or more, the average level of farmed genetic introgression was 6.4% (median = 2.3%), with a range between 0.0% and 42.2%. Fifty-one of these rivers showed significant farmed genetic introgression when compared with historical reference samples. We observed a highly significant correlation between estimated farmed introgression and average proportion of escaped farmed salmon. We quantify levels of introgression as unweighted averages or weighted by population sizes, to compare geographical regions and to compare levels of introgression in rivers and fjords designated as locations deserving a high level of protection. We found a generally lower level of introgression in National Salmon Rivers and National Salmon Fjords subjected to formal protection by parliament. We conclude that farmed to wild genetic introgression is high in a large proportion of Norwegian salmon rivers, with the highest levels found in the most intensive areas of salmon farming. The extensive genetic introgression documented here poses a serious challenge to the management of farmed and wild Atlantic salmon in Norway and, in all likelihood, in other regions where farmed-salmon escape events occur with regularity


2006 ◽  
Vol 63 (7) ◽  
pp. 1224-1233 ◽  
Author(s):  
Øystein Skaala ◽  
Vidar Wennevik ◽  
Kevin A. Glover

Abstract A large number of farmed Atlantic salmon escape from sea cages and hatcheries annually. Selection programmes and domestication have changed the genetic composition of farmed salmon to improve their performance in the culture environment, which apparently occurs at the cost of their fitness in the natural environment. Therefore, gene flow from farmed salmon to wild salmon populations may have altered the genetic composition of wild salmon populations. To investigate the temporal genetic stability in seven wild Norwegian salmon populations, genetic profiles were produced from historical and contemporary scale samples. Historical and contemporary samples of salmon from the Namsen, Etne, Opo, Vosso, Granvin, Eio, and Hå Rivers were genotyped at the following eight microsatellite loci: Ssa13.37, Ssa28, SsOSL85, Ssa197, Ssa20.19, SsaF43, Ssa202, and Ssa85. A significant change in genetic profiles was observed over time in the Opo, Vosso, and Eio Rivers, but no changes in genetic profiles were observed in the Namsen, Etne, Granvin, and Hå Rivers. A small reduction in FST values and genetic distances among populations was observed in the contemporary samples compared with the historical samples, indicating a eduction in population differentiation over time.


2008 ◽  
Vol 65 (12) ◽  
pp. 2807-2826 ◽  
Author(s):  
Matthew R.J. Morris ◽  
Dylan J. Fraser ◽  
Anthony J. Heggelin ◽  
Frederick G. Whoriskey ◽  
Jonathan W. Carr ◽  
...  

Knowledge of the prevalence of escaped farmed fishes in the wild is an essential first step to assessing the risk resulting from interactions between farmed and wild fishes. This is especially important in eastern North America, where Atlantic salmon ( Salmo salar ) aquaculture occurs near wild Atlantic salmon rivers and where many wild salmon populations are severely depressed. Here, we review the literature on the incidence of escaped farmed salmon in eastern North American rivers, for which there has been no comprehensive compilation to date. Escaped farmed salmon have been found in 54 of 62 (87%) rivers investigated within a 300 km radius of the aquaculture industry since 1984, including 11 rivers that contain endangered salmon populations. Averaged among all investigations, the proportional representation of farmed salmon among adults entering the rivers from the sea was 9.2% (range 0% to 100%). Where data were sufficient to examine temporal trends, farmed salmon proportions varied considerably over time, suggesting that escape events are episodic in nature. We conclude that escaped farmed salmon are sufficiently prevalent in eastern North American rivers to pose a potentially serious risk to the persistence of wild salmon populations, especially in those rivers that are adjacent to existing aquaculture sites.


1995 ◽  
Vol 31 (11) ◽  
pp. 259-264 ◽  
Author(s):  
L. J. Farmer ◽  
J. M. McConnell ◽  
T. D. J. Hagan ◽  
D. B. Harper

Sensory profiling techniques were used to investigate the odour and flavour of Atlantic salmon (Salmo salar) from six sources in order to determine (i) whether there was any scientific basis for reports of off-flavours in salmon from certain sources and (ii) whether farmed and wild salmon differed in terms of flavour attributes. There were no consistent differences in odour or flavour between sea-caught wild salmon and farmed salmon. However, river-caught wild salmon showed enhanced ‘earthy’ flavour and odour; GC-odour assessment studies have indicated that 2-methylisoborneol and geosmin contribute to these attributes. For a short period, wild river salmon from one source also suffered from a manure-like off-flavour which has been shown to be due to the presence of skatole. The source of this compound remains uncertain.


2020 ◽  
Vol 12 ◽  
pp. 371-383
Author(s):  
T Aronsen ◽  
EM Ulvan ◽  
TF Næsje ◽  
P Fiske

To gain more knowledge about escaped farmed salmon Salmo salar in the wild, we investigated the proportion of escapees, body length at escape, proportion escaped as smolts/post-smolts (≤300 mm) and number of winters in the wild (winter zones in the growth pattern in the scale samples) in catches on the Norwegian coast and in an adjacent fjord from 2013 to 2017. The mean proportion of escapees was higher on the coast (26%) than in the fjord (4%), and escapees caught on the coast had a slightly larger mean body length at escape (607 mm) than in the fjord (557 mm). However, the mean proportion escaped as smolts/post-smolts did not differ significantly between the coast (8%) and the fjord (11%). There was also no significant difference in the mean proportion of farmed salmon with 1 or more winter zones after escape (50% on the coast and 56% in the fjord). The proportions of escapees with 1, 2, 3 or 4 winter zones after escape were 28, 20, 2 and 0.4% in catches on the coast and 30, 21 and 4% in catches in the fjord, respectively. This study found that the proportion of escapees was considerably higher in coastal waters than in the fjord. Escapees consisted of farmed salmon from several escape events over several years, and approximately 50% of the escapees had one or more winter zones after escape. Thus, escaped farmed salmon may pose a threat to wild salmon populations for several years after the escape event.


2018 ◽  
Vol 75 (4) ◽  
pp. 506-512 ◽  
Author(s):  
Freya Keyser ◽  
Brendan F. Wringe ◽  
Nicholas W. Jeffery ◽  
J. Brian Dempson ◽  
Steven Duffy ◽  
...  

The escape of Atlantic salmon (Salmo salar) from aquaculture facilities can result in both negative genetic and ecological interactions with wild populations, yet the ability to predict the associated risk to wild populations has remained elusive. Here we assess the potential of a spatiotemporal database of aquaculture facility locations, production estimates, and escape events to predict the distribution of escaped farmed salmon and genetic impacts on wild populations in the Northwest Atlantic. Industry production data, reported escape events, and in-river detections of escaped farmed salmon were collected from across the Northwest Atlantic. Genetic estimates of impact were obtained using single nucleotide polymorphisms (95 loci) representing aquaculture and wild salmon throughout the region (30 populations, 3048 individuals). Both the number of escaped farmed salmon detected at counting facilities and the magnitude of genetic impacts were positively correlated with a cumulative spatial measure of aquaculture production. Our results suggest that the risk of escapees and genetic introgression from wild–farmed salmon interactions can be assessed using information on farm production characteristics. This represents a first step in predicting the impact of existing cage-based farms on wild Atlantic salmon.


2006 ◽  
Vol 63 (7) ◽  
pp. 1218-1223 ◽  
Author(s):  
Frederick G. Whoriskey ◽  
Paul Brooking ◽  
Gino Doucette ◽  
Stephen Tinker ◽  
Jonathan W. Carr

Abstract We sonically tagged and released farmed Atlantic salmon (Salmo salar) from a cage site in Cobscook Bay, Maine, USA. The fish were released in January (n = 75) and in April and May (n = 198) 2004 to study their movement patterns and survival and to assess the possibility of recapturing them. Inshore and offshore waters in this region are subject to intense tidal currents. Tagged salmon dispersed >1 km from the cage site within a few hours of their release. Mortality was high within Cobscook Bay and the surrounding coastal region (56% of the winter (January) releases; 84% of the spring (March) releases), probably the result of seal predation. Most surviving fish exited the coastal zone and entered the Bay of Fundy along the routes of the dominant tidal currents, passing through Canadian waters. No tagged fish were detected during the wild salmon spawning season in autumn 2004 in any of the 43 monitored salmon rivers draining into the Bay of Fundy, or during 2005 either in the Magaguadavic River, the site of the hatchery in which the fish were reared to the smolt stage, or by a limited coastal receiver array.


1998 ◽  
Vol 55 (2) ◽  
pp. 507-514 ◽  
Author(s):  
Arnulf Soleng ◽  
Tor A Bakke ◽  
Lars P Hansen

Population growth of Gyrodactylus salaris increased exponentially on Atlantic salmon (Salmo salar) smolts in laboratory experiments conducted at 12.0°C. Furthermore, G. salaris was transmitted successfully from salmon smolt to parr at 0.0, 7.5, 10.0, and 20.0%° salinity and reproduced in fresh water after direct transfer from 7.5%° (16 days), 20.0%° (4 and 8 h), and 33.0%° (5, 15, and 30 min). No G. salaris were observed on salmon parr exposed to 33.0%° for 60 min. The prevalence of G. salaris on wild salmon smolts caught approximately 25 km from the river mouth in the Drammensfjord (surface salinity 2.0-3.5%°) was 71.2% compared with 88.0% on those from the neighbouring River Lierelva. Adult wild salmon caught as prespawners, spawners, and postspawners (kelts) in the River Drammenselva were infected with G. salaris. The prevalence and abundance increased from autumn to spring, in contrast with earlier studies on salmon parr, demonstrating the possible importance of adult salmon as reservoirs for G. salaris during winter. The results support the hypothesis of brackish water dispersal of G. salaris by infected salmonids migrating in estuaries and fjords. The use of salt as a disinfectant against G. salaris in hatcheries, and the stocking of possibly infected fish into brackish and seawater, should also be reexamined.


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