Length-weight relationship and condition factor of sea trout from the Słupia River (Poland), during the spawning migration

Various factors, including heavy metals, can make fish more susceptible to disease. This study investigated, inter alia, the relationship between Pb, Cd, and Hg contamination of the organs and muscles of sea trout from the river Rega (Poland) and the occurrence of UDN (ulcerative skin necrosis) symptoms. Moreover, the dietary risk of Pb, Cd, and Hg uptake from the muscles of healthy sea trout was assessed based on estimated daily intake (EDI), target hazard quotient (THQ), benchmark dose lower confidence limits (BMDL01 and BMDL10), and tolerable weekly intake (TWI). The metal concentrations varied, depending on the fish organs and the fish condition. A significantly higher amount of Pb was found in the gonads, gills, and muscles, Cd in the kidneys, and Hg in the muscles of sea trout with UDN symptoms. The lowest concentrations of Pb and Cd were detected in the muscles, and of Hg in the gonads. Dietary exposure to Pb, Cd, and Hg accounted for: 0.4% of BMDL01 and 1.0% of BMDL10, 0.56% of TWI, and 16.5% of TWI, respectively. THQs for each metal and the HI value for combined metals were below 1. The weakening of fish due to UDN-like disease probably increased the accumulation of Pb in the gonads, gills, and muscles, and of Cd in the kidneys, of the sea trout. As regards the maximum levels (MRLs), the muscles of healthy sea trout are safe for consumption. The risk assessment suggests no concern for the health of consumers.

Ulcerative dermal necrosis (UDN) in wild salmonids

Every year, ulcerative dermal necrosis (UDN) affects salmonids that spend most of their lives in the sea during their migration to the rivers of northern Poland to spawn. The clinical form of the disease manifests itself in ulcerative skin lesions, which lead to significant weakening of the fish and, in most cases, result in their death. This study was carried out on samples taken from sea trout in the Słupia River in northern Poland. In order to identify the pathogen, experiments on the transmission of the disease were carried out, and additional histopathological, microbiological and electron microscopic examinations were performed. As a result of these studies, it was possible to experimentally transfer the disease from sick to healthy fish. The results indicate a complex etiology of the disease (lack of a clearly defined pathogen), in which the change in the environment from salty to freshwater triggers the related changes in skin physiology, which are the main causes of increased susceptibility to the development of the disease.

The clinical signs and histopathological findings of an ‘ulcerative dermal necrosis’ in brown trout were compared with those observed in salmon and sea trout suffering from UDN. There were close similarities in the lesions shown by both types of fish, but more brown trout recovered and the healing process was temperature dependent.

Abstract. Continuous visual observations of the signs of development of UDN in fish kept in aquaria were correlated with light microscopical, transmission and scanning electron microscopical results. The initial signs of the disease are circles of pathologically‐changed epidermis. The tight junctions of the squamous cells within these mucus‐free areas disintegrate resulting in the loss of the protective function of the zonula occludens. Subsequently, the intercellular spaces dilate and communicate with the exterior. Necrosis of the epidermal cells due to hydromineral disturbances occur simultaneously with fungal infections and marked responses of the melanophores. It is suggested that the fungal infections are triggered by metabolites of the necrotic epidermal cells. The epidermal cells are shed and the fungus determines the further course of the disease which terminates in large ulcers covered with fungal hyphae. No substantial evidence for the presence of a virus could be recorded at any stage of the disease. It is concluded that the disease is a squames and the fungus appears as an opportunist which causes the eventual death of the fish.

Since 2007 in Poland, skin lesions have been observed in salmon (Salmo salar L.) and sea trout (Salmo trutta L.) entering Pomeranian rivers to spawn. The clinical picture of affected fish resembled ulcerative dermal necrosis (UDN), a disease of unknown etiology affecting mainly the scalps of wild salmonids. The aim of the 2009-2012 study was to determine with microbiological tests the etiological agent of the skin lesions observed in salmonids entering the Pomeranian rivers. During the study, a total of 13 species of Gram-negative bacteria belonging mainly to the Yersiniaceae, Enterobacteriaceae, and Pseudomonadaceae families were isolated and identified from the skin and kidneys of diseased fish. The Gram-positive bacteria isolated were aerobic, hemolytic granules of the genus Streptococcus. Mycological examinations on damaged fish body surfaces revealed yeasts of the genus Rhodotorula and fungi of the family Saprolegniaceae. The results of our study did not permit us to identify unequivocally the direct cause of the fish diseases analyzed since all the bacteria isolated during the study are normally found in aquatic environments. Some of the isolated bacteria identified were assumed to be potentially pathogenic to fish. The fungal infections observed were probably secondary and only exacerbated ongoing disease processes.

Many Norwegian rivers and lakes are regulated for hydropower, which affects freshwater ecosystems and anadromous fish species, such as sea trout (Salmo trutta). Lakes are an important feature of many anadromous river systems. However, there is limited knowledge on the importance of lakes as habitat for sea trout and how hydropower affects the behaviour of sea trout in lakes. To investigate this, we conducted an acoustic telemetry study. A total of 31 adult sea trout (532 ± 93 mm total length) were captured by angling in river Aurlandselva, Norway, and tagged between July 20 and August 12, 2021. The tags were instrumented with accelerometer, temperature, and depth sensors, which provided information on the sea trout’s presence and behaviour in lake Vassbygdevatnet. Our results indicate that there was a large prevalence of sea trout in the lake during the spawning migration, and that the sea trout were less active in the lake compared to the riverine habitats. An increase in activity of sea trout in the lake during autumn might indicate that sea trout spawn in the lake. However, the discharge from the high-head storage plant into the lake did not affect the depth use or activity of sea trout in the lake. Furthermore, the large prevalence of spawners in the lake during autumn will likely cause an underestimation of the size of the sea trout population in rivers with lakes during annual stock assessment. In conclusion, our results could not find evidence of a large impact of the discharge on the behaviour of sea trout in the lake.

In the present work we evaluated the effect of ulcerative dermal necrosis (UDN) syndrome on resistance of erythrocytes to haemolytic agents and lipid peroxidation level in the blood from brown trout (Salmo trutta m. trutta L.). Results showed that lipid peroxidation increased in erythrocytes, as evidenced by high thiobarbituric acid reactive substance (TBARS) levels. Compared to control group, the resistance of erythrocytes to haemolytic agents was significantly lower in UDN-positive fish. Besides, UDN increased the percent of hemolysated erythrocytes subjected to the hydrochloric acid, urea and hydrogen peroxide. Results showed that UDN led to an oxidative stress in erythrocytes able to induce enhanced lipid peroxidation level, as suggested by TBARS level and decrease of erythrocytes resistance to haemolytic agents.

Fusarium infections have been reported in aquatic animals, but are still poorly investigated in wild salmonids. The aim of the study was to determine the impact of the fungi and their toxins on the health status of brown trout (Salmo trutta morpha trutta) migrating from the Baltic Sea to the freshwater. Individuals from the wild brown trout population exhibiting ulcerative skin lesions were collected from the Słupia River in Poland and subjected to microbiological, histopathological, and hematological examinations, as well as toxicological analysis for a presence of mycotoxins. The results of microflora isolation from the brown trout skin samples revealed the presence of conditionally pathogenic bacteria and fungi classified by molecular techniques as Fusarium spp. Toxicological analysis allowed for detection of zearalenone (ZEN) in the liver, kidney, and gastrointestinal tract of the fish. In several cases, there was α-zearalenone (α-ZEL) identified at trace levels in the liver, as well as sterigmatocystin and enniatin B at low levels in the kidney and the liver. Histopathological examination revealed the presence of fungal hyphae disrupting the epidermis and penetrating into the necrotic dermis and hypodermis. The decreased values of the blood parameters, i.e., hemoglobin concentration (HGB), packed cell volume (PCV), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), and white blood cell count (WBC), were indicative of osmoregulation failure being a consequence of the skin damage. The results of the study provide new information regarding Fusarium sp. infection in brown trout and serve as the basis for further research on the potential impact of the fungi and their mycotoxins on the Baltic salmonid population, including their role in ulcerative dermal necrosis.

The objective of the present study was to investigate the importance of the antioxidant enzymes: superoxide dismutase (SOD), catalase (CAT), glutathione reductase (GR), and glutathione peroxidase (GPX) in the defense against lipid and protein oxidation in spawn from female brown trout, Salmo trutta m. trutta L. affected by ulcerative dermal necrosis (UDN). UDN induced increased lipid and protein oxidation levels. The current results show that UDN infection led to oxidative stress with the inhibition of antioxidant defense mechanisms. The inhibition of glutathione defense system activity might be responsible for this failure in cellular antioxidant defenses. UDN induces irreversible changes in proand antioxidative function which effected decreased spawn survival as well as reductions in spawning efficiency.

The upstream spawning migrations of brown trout and sea trout were studied using stationary traps placed in Kirk Burn, a tributary of the upper Tweed. The sea trout spawning period extended from early November to the first week of December, while that of brown trout occurred from the middle of October to the third week of December. Sea trout were predominantly maiden spawners of ages 2.1+ and 3.1+ while brown trout were mostly age 2+ and 3+. Male‐female sex ratios approximated 1:1.4 in sea trout but 6 : 1 in brown trout. Brown trout males participated in the spawning activities of sea trout. Low water conditions in Kirk Burn hindered the upstream movement of spawning sea trout, while sudden increases in water level appeared to stimulate the upstream migration of both brown trout and sea trout. The suggestion is advanced that the freshwater resident brown trout of the Tweed which migrate upstream into the smaller tributaries to spawn is wholly, or at least partially, the progeny of anadromous parents.

The effect of the introduction of fry of anadromous sea trout, Salmo trutta L., on the genetic integrity of landlocked brown trout populations was evaluated. Samples were taken from six brown trout populations from streams above impassable waterfalls in the Conwy river system (North Wales, U.K.) in 1989 and 1990. Three of these streams had no known stocking history and three had been stocked with sea trout fry from the lower Conwy system over the last few years. Representatives of these sea trout were collected from two streams in the lower Conwy system and from a hatchery. Allele frequencies at 13 loci, six of which were polymorphic, were determined by starch gel electrophoresis.The stocked populations were intermediate in their allele frequencies between unstocked brown trout and sea trout samples. A principal component analysis suggested significant numbers of hybrids in all of the stocked streams. This shows that some of the introduced sea trout did not migrate down the falls to the sea, but stayed in fresh water and hybridized with the local population. The significance of this finding for the conservation of the genetic resource of brown trout stocks is discussed.

– Sea trout (Salmo trutta) originating from small coastal streams can be found at sea throughout the year, in contrast to conspecifics from larger rivers, which typically spend the autumn and winter in fresh water. Such an extended marine stay has been observed in coastal Skagerrak. We studied the seasonal variation in marine growth of Skagerrak sea trout based on scale increment patterns and body lengths of 563 individuals captured at sea. Growth, measured as increased body length, was rapid during summer while there was no evidence for continued growth during autumn and winter. Growth decreased with increasing age of the fish. Our results suggest that coastal Skagerrak is an important feeding area for sea trout during summer, and that an extended marine stay during autumn and winter may have trade‐off benefits other than somatic growth. Alternative benefits might be increased winter survival and decreased migratory costs of juvenile fish.

Anadromous and freshwater populations of Salvelinus fontinalis have been compared to determine the taxonomic relationship of the sea trout and brook trout. Sea trout and freshwater trout differ seasonally in coloration and flesh colour but these differences appear to be environmental in origin rather than hereditary. Freshwater trout reared to hatching at 5.5 °C. had larger head parts, deeper and wider bodies, longer fins, more pectoral rays, dorsal rays, and branchiostegals but fewer scale rows and anal rays than those of common parentage reared at 0.9 °C. Sea trout and freshwater trout from the same river differ less in body form than trout of common parentage reared at different temperatures and less than four populations of freshwater trout. Differential development of the secondary sexual characteristics accounts for most of the differences in body form between sea and freshwater trout. Sea trout and freshwater trout from different rivers reared under the same conditions differed less in body form than any of the other populations compared. Sea and freshwater trout did not differ significantly in any of the meristic structures counted. Seasonal differences in weight-length relationship related to spawning and feeding habits were observed. Sea trout grow rapidly during the year in which they first migrate to the sea but subsequent growth is not appreciably faster than freshwater trout from the same river. Exposure of freshwater trout to sea water indicates that some could survive typical sea trout migrations. No evidence was obtained to indicate hereditary differences in migratory behaviour. Evidence available indicates that sea and freshwater trout of Moser River, Nova Scotia, constitute one taxonomic unit.

Management of multiple exploited stocks of anadromous salmonids in large catchments requires understanding of movement and catchment use by the migrating fish and of their harvesting. The spawning migration of sea trout (Salmo trutta) and Atlantic salmon (Salmo salar) was studied in the River Tweed, UK, using acoustic telemetry to complement exploitation rate data and to quantify catchment penetration. Salmon (n = 79) and sea trout (n = 65) were tagged in the tidal-influenced Tweed in summer–autumn. No tagged salmon left the river before spawning, but 3% (2010) and 8% (2011) of pre-spawning sea trout dropped out. Combined tag regurgitation/fish mortality in salmon was 12.5%, while trout mortality was 6% (2010) and 0% (2011). The estimated spawning positions of salmon and sea trout differed; tagged salmon were mostly in the main channel while trout occurred mostly in the upper Tweed and tributaries. Early fish migrated upstream slower than later fish, but sea trout moved through the lower-middle river more quickly than salmon, partly supporting the hypothesis that the lower exploitation rate in autumn of trout (1 vs 3.3% for salmon) there is generated by differences in migration behaviour.