Seasonal variations of opisthaptoral hard parts of Gyrodactylus salaris Malmberg, 1957 (Monogenea: Gyrodactylidae) on parr of Atlantic salmon Salmo salar L. in the River Batnfjordselva,Norway

Seasonal variations in size and shape of the marginal hooks, the anchors and the ventral bar of the opisthaptor of Gyrodactylus salaris Malmberg, 1957 were studied. The G. salaris specimens were collected from parr of Atlantic salmon Salmo salar L. in the River Batnfjordselva, north-western Norway. Samples were taken at roughly monthly intervals during a two-year period. The marginal hooks, the anchors and the ventral bar showed considerable seasonal variation in size, but varied only slightly in shape. The variation in 12 of the 14 characters measured showed a significant regression to the variation in the water temperature. The total length of the marginal hooks of G. salaris can be considerably longer than the previously reported maximum of 40 m for the species.     

Variations of opisthaptoral hard parts of Gyrodactylus salaris Malmberg, 1957 (Monogenea: Gyrodactylidae) on parr of Atlantic Salmon Salmo salar L. in laboratory experiments

On parr of Atlantic salmon Salmo salar L. in laboratory experiments at different water temperatures, opisthaptoral hard parts of Gyrodactylus salaris Malmberg, 1957 differed in size. Their shape, on the other hand, varied only slightly. The opisthaptoral hard parts were largest at the lowest water temperatures and decreased in size with increasing water temperatures (1.5°C to 20.0°C). At both 18.0°C and 20.0°C the opisthaptoral hard parts of G. salaris were smaller than has been found under natural conditions. In the experiments, the mean size of the opisthaptor in the G. salaris micropopulation at each water temperature gradually increased or decreased compared to the mean size at the start of the experiments. At the end of the experiments the mean size of the opisthaptoral hard parts in the G. salaris micropopulations showed a significant regression to the different water temperatures.     

<Emphasis Type="Italic">Gyrodactylus salaris</Emphasis> (Monogenea,Gyrodactylidae) infections on resident Arctic charr (<Emphasis Type="Italic">Salvelinus alpinus</Emphasis>) in southern Norway

This study surveys the distribution of Gyrodactylus salaris on resident Arctic charr, Salvelinus alpinus, in lakes connected to three south-Norwegian watercourses: Numedalsvassdraget, Skiensvassdraget and Hallingdalsvassdraget. Gyrodactylus salaris infected charr was only recorded in Numedalsvassdraget. The parasites had the same mitochondrial haplotype as those previously reported on charr in Lake Pålsbufjorden, which is part of Numedalsvassdraget. Since the G. salaris-charr association is persistent in Pålsbufjorden and has a wide distribution above the stretches of the watercourse inhabited by anadromous salmonids, this is considered a stable, although perhaps relatively young, host-parasite system. More detailed analyses of these interactions revealed seasonal variations in the parasite population dynamics between late summer and late autumn, with heavier infections occurring in males and older fish in October. This is explained by the combined action of seasonal differences in temperature and physiology and ecology of host cohorts. It is assumed that the occurrence of G. salaris on charr in Pålsbufjorden resulted from a host switch to charr from rainbow trout, Onchorynchus mykiss. Host switches may cause significant expansions of the geographical range of pathogenic variants of G. salaris. Therefore, observations of frequently occurring G. salaris on charr have implications for the diagnosis, management and control of salmonid gyrodactylosis.     

Incorporation of 1-14C-acetate into fatty acids and sterols by isolated hepatocytes of thermally acclimated rainbow trout (Salmo gairdneri)

Summary Rates of 1-¹⁴C-acetate incorporation into specific fatty acids and sterol fractions were determined at assay temperatures of 5°C and 20°C in hepatocytes isolated from warm (20°C)- and cold (5°C)- acclimated rainbow trout (Salmo gairdneri). Rates of sterol lipogenesis were 2.5- to 3-fold higher in hepatocytes from cold-acclimated trout. Rates of acetate oxidation and of total fatty acid lipogenesis did not differ significantly between acclimation groups. Fatty acid compositions did not change significantly during the experiment (9–12 h), but hepatocytes from cold-acclimated trout possessed significantly higher levels of polyunsaturates and unsaturates of the linolenic acid (n-3) family, and significantly lower levels of monounsaturates than did hepatocytes from warm-acclimated animals. Hepatocytes from cold-acclimated trout channeled a larger percentage of their total acetate incorporation into unsaturated fatty acids at 5°C than at 20°C due primarily to increased recovery of acetate in polyunsaturates and monoenes at 5°C. In contrast, hepatocytes from warm-acclimated trout channeled a slightly smaller percentage of their total acetate incorporation into unsaturates at 5°C than at 20°C. Hepatocytes from warm-acclimated trout incorporated significantly more 1-¹⁴C-acetate into the unsaturated fatty acid fraction (due primarily to incorporation into the diene fraction and less importantly all other classes of unsaturates) and significantly less into the saturated fatty acid fraction than hepatocytes from cold-acclimated trout when assayed at 20°C; similar but less dramatic differences were observed at 5°C. Consequently, unsaturated/saturated ratios for acetate incorporation ranked: warm-acclimated at 20°Cwarm-acclimated at 5°Ccold-acclimated at 5°C>cold-acclimated at 20°C. These results suggest that regulation of the relative rates of unsaturated and saturated fatty acid synthesis is involved in lipid restructuringduring adaptation from one temperature regime to another, but that other mechanisms must be invoked to explain the maintenance of observed steady state differences between the fatty acid compositions of warm- and cold-acclimated trout.This work was supported by grant PCM-76-04313-AO1 from the National Science Foundation     

Seasonal variations of the opisthaptoral hard parts of Gyrodactylus derjavini Mikailov, 1975 (Monogenea: Gyrodactylidae) on brown trout Salmo trutta L. parr and Atlantic salmon S. salar L. parr in the River Sandvikselva,Norway

Seasonal variations in the size and shape of the marginal hooks, anchors and ventral bar of the opisthaptor of Gyrodactylus derjavini Mikailov, 1975 were studied. The G. derjavini specimens were collected from brown trout Salmo trutta L. parr and Atlantic salmon S. salar L. parr in the River Sandvikselva, southeastern Norway. Samples were taken at roughly monthly intervals during a 13-month period. The marginal hooks, anchors and ventral bars showed considerable seasonal variation in size, but varied very little in shape. The size increased when the water temperature decreased and vice versa.     

Evidence of genetic and environmental influences on meristic variation in the rainbow trout,Salmo gairdneri Richardson

Synopsis An investigation of the effect of parentage and temperature on the expression of selected meristic characters of rainbow trout, Salmo gairdneri, reveals statistical differences in the number of vertebrae, dorsal fin rays and anal fin rays among test batches of progeny of different parentage. Batches of fertilized ova of the same stock or parentage, when incubated at 9.5 °C and 14.8 °C, produced lower mean dorsal and anal fin ray counts and a higher mean pectoral fin ray count at the higher temperature. Incubation temperature had no significant effect on the number of vertebrae.Significant statistical differences occurring in various characters among groups of rainbow trout of different parental origin provide convincing evidence of genetic inputs into meristic expression. However, the existence of both environmental and genetic inputs into meristic expression in rainbow trout necessitates further investigation before the meaning of observed meristic plasticity in rainbow trout can be resolved.     

Cardiac force-interval relationship,adrenaline and sarcoplasmic reticulum in rainbow trout

The force-interval relationship was examined at 20 and 10 °C in electrically paced atrial and ventricular tissue of rainbow trout,Oncorhynchus mykiss, regarding dependence on the sarcoplasmic reticulum and influence of adrenaline. In both tissues, adrenaline (10^-6 mol·l^-1) doubled control force developed at 0.5 Hz. In atrial but not in ventricular tissue it also shortened the diastolic interval needed for recovery of a given fraction of the control force. In atrial tissue and in ventricular tissue at 20 °C, the fraction of force recovered in the presence of adrenaline was diminished by 10 mol·l^-1 of ryanodine, a specific inhibitor of the sarcoplasmic reticulum. In atrial tissue not exposed to adrenaline and in ventricular tissue at 10 °C irrespective of adrenaline, ryanodine did not affect recovery. In atrial but not in ventricular tissue it also diminished control force. In conclusion, the cardiac sarcoplasmic reticulum of trout seems to support force development during adrenaline dependent increases in heart rate, and in atrial tissue also the force at steady state.Abbreviations E-C coupling excitation-contraction coupling - P-R potential - SR sarcoplasmic reticulum - SE standard error of the mean     

Thermal adaptation in biological membranes: interacting effects of temperature and pH

Summary The interacting effects of pH and temperature on membrane fluidity were studied in plasma membranes isolated from liver of rainbow trout (Oncorhynchus mykiss) acclimated to 5 and 20°C. Fluidity was determined as a function of temperature under conditions of both constant (in potassium phosphate buffer) and variable pH (in imidazole buffer, consistent with imidazole alphastat regulation) from the fluorescence anisotropy of two probes: 1,6-diphenyl-1,3,5-hexatriene, which intercalates into the bilayer interior, and 1-(4-trimethylammoniumphenyl)-6-phenyl-1,3,5-hexatriene which is anchored at the membrane/water interface. The temperature dependence of the anisotropy parameter for 1,6-diphenyl-1,3,5-hexatriene in plasma membranes of 20°C-acclimated trout was greater when determined in phosphate (AP per °C=-0.047) than in imidazole buffer (AP per °C=-0.022); similar, but less significant, trends were noted with 1-(4-trimethylammoniumphenyl)-6-phenyl-1,3,5-hexatriene. In contrast, the temperature dependence of fluidity (AP/°C in the range-0.0222 to-0.027) did not vary with buffer composition in membranes of 5°C-acclimated trout. In phosphate buffer, anisotropy parameter values for 1,6-diphenyl-1,3,5-hexatriene were significantly lower in 5°C-than 20°C-acclimated trout, indicating a less restricted probe environment following cold acclimation and nearly perfect compensation (91%) of fluidity. Temperature-dependent patterns of acid-base regulation were estimated to account for 11–40% of the fluidization evident in membranes of 5°C-trout, but a period of cold acclimation was required for complete fluidity compensation. In contrast, no homeoviscous adaptation was evident in imidazole buffer, indicating that membrane fluidity is sensitive to buffer composition. Accordingly, vesicles of bovine brain phosphatidylcholine, suspensions of triolein, and plasma membranes of 5°C-acclimated trout were consistently more fluid in imidazole than phosphate buffer. Membranes of 5°C-acclimated trout were enriched in molecular species of phosphatidylcholine containing 22:6n3 (at the expense of species containing 18:1n9 and 18:2n6) compared to membranes of 20°C-trout; consequently, the unsaturation index was significantly higher (3.29 versus 2.73) in trout maintained at 5 as opposed to 20°C. It is concluded that: 1) the chemical composition of the internal milieu can significantly influence the physical properties of membrane lipids; 2) temperature-dependent patterns of intracellular pH regulation may partially offset the ordering effect of low temperature on membrane fluidity in 20°C-acclimated trout transferred to 5°C, but not in 5°C-acclimated trout transferred to warmer temperatures; 3) the majority of the thermal compensation of plasma membrane fluidity resulting from a period of temperature acclimation most likely reflects differences in membrane composition between acclimation groups; 4) imidazole apparently interacts with trout hepatocyte plasma membranes in a unique way.Abbreviations _im netcharge stateofproteins - AP anisotropyparameter - bw body weight - DPH 1,6-diphenyl-1,3,5-hexatriene - HEPES N-2-hydroxyethylpiperazine-N-2-ethanesulphonicacid - PC phosphatidylcholine - pH_e pHofarterial blood - pH_i intracellular pH - TMA-DPH 1-(4-trimethylammoniumphenyl)-6-phenyl-1,3,5-hexatriene - TRIS tris(hydroxymethyl)aminomethane     

Effect of acclimation temperature on the elongation step of protein synthesis in different organs of rainbow trout

Summary Cytosolic extracts of liver, kidney, spleen, gill, red and white muscle from rainbow trout acclimated to 4 and 17°C, respectively, have been investigated in vitro with respect to their enzymic activity in stimulating the growth of nascent peptide chains (labelled polyphenylalanine) at assay temperatures from 5 to 25°C using polyuracil as messenger RNA. The elongation step of protein synthesis is characterized by aQ ₁₀ value of about 2.4 (range 10–25°C) in all organs from both, 4 and 17°C acclimated fish.Except for the red muscle, the organs of cold acclimated trout, however, exhibit significantly higher specific elongation rates (mol phenylalanine polymerized/(g wet weight·h)) at any experimental temperature than those of warm acclimated fish. This increase of the elongation rates varies between the organs and ranges from +29% (liver) to +60% in the gill. The specific acylation rate (mol phenylalanyl-tRNA formed/(g wet weight·h)) surpasses the specific elongation rate by a factor of at least 8.5. Moreover, the specific acylation rate per mg protein is independent of acclimation temperature.It is concluded that the increased specific elongation rates in 4°C acclimated trout are not due to altered pool sizes of the precursor phenylalanyl-tRNA, but reflect an effective enhancement of enzymic elongation factor activities.In accordance with data taken from literature, this finding suggests a compensatory enhancement of in vivo protein synthesis to occur in trout during cold acclimation.Abbreviations E _a apparent activation energy - EF elongation factor - HEPES N-2-hydroxyethylpiperazine-N-2-ethane sulfonic acid - PHE phenylalanine - PHE-tRNA phenylalanyl transfer ribonucleic acid - POLY (U) poly-uracil - Q ₁₀ van't Hoff's temperature coefficient - T _accl acclimation temperature - T _exp experimental temperature - TRITON X-100 octylphenol-polyethylene-glycolether     

The effects of assay temperature upon the pH optima of enzymes from poikilotherms: A test of the imidazole alphastat hypothesis

Summary A study of the thermal responses of Na-ATPase and NaK-ATPase activities in microsomes prepared from gill tissue of rainbow trout (Salmo gairdneri) revealed further evidence that the two activities are distinct from one another. Arrhenius plots of the NaK-ATPase from sea water-adapted fish and the Na-ATPase from fresh water-adapted fish were linear (Fig. 4) with estimated activation energies of 19.5 and 7.7 kcal/mole, respectively. The Na-ATPase and NaK-ATPase both showed optimum activity at 45°C (Figs. 2 and 3). The Mg-ATPase from fresh water fish showed a distinct temperature optimum at 24°C (Fig. 1) while Mg-ATPase activity from sea water fish was optimum at temperatures of about 15–24 °C (Fig. 3). The Na⁺ dependence of the Na-ATPase and the NaK-ATPase was examined at an assay temperature of 37 °C (Fig. 5) and the results compared with those obtained at 13 °C. No apparent differences were noted for the Na-ATPase, but with the NaK-ATPase both theK _0.5 for Na⁺ and optimum Na⁺ concentration increased at the higher assay temperature. Finally, evidence is presented showing the Na-ATPase to be distinct from Mg-ATPase activity in fresh water trout gill microsomes.Abbreviation HEPES N-2-hydroxyethylpiperazine-N-2-ethane-sulfonic acid     

Preconditioning stimuli do not benefit the myocardium of hypoxia-tolerant rainbow trout (<Emphasis Type="Italic">Oncorhynchus mykiss)</Emphasis>

In many vertebrates, a short episode of oxygen lack protects against myocardial necrosis during a subsequent, longer period of oxygen deprivation. This protective effect, termed preconditioning, also improves the functional recovery. Improved functional recovery has been reported for hypoxia-sensitive, in situ perfused rainbow trout hearts, but appears absent in another strain of rainbow trout that has a more hypoxia-tolerant heart. The results for the hypoxia-tolerant rainbow trout heart, however, might have occurred because the preconditioning stimuli were insufficient in either intensity or type to elicit cardioprotective effects. In the present study, we attempted to induce preconditioning in in situ perfused hearts from hypoxia-tolerant rainbow trout (Oncorhynchus mykiss), acclimated and tested at 10 °C, by either doubling the anoxic preconditioning stimulus (PO₂ of the perfusate <0.5 kPa) relative to earlier studies or by using short exposures to high concentrations of adrenaline. In addition, anoxic-preconditioning experiments were conducted at an acutely elevated temperature (15 °C) to increase myocardial sensitivity to oxygen lack. The effect of preconditioning stimuli was assessed by measuring cardiac performance before and after exposure to a 20-min anoxic challenge. In addition, myocardial condition was evaluated at the termination of the experiment by measuring myocardial concentrations of glycogen, high energy phosphates and lactate, as well as activities of pyruvate kinase and lactate dehydrogenase. Maximal cardiac performance in oxygenated control hearts was unchanged by the 2-h experimental protocol, whereas inclusion of a 20-min period of anoxia led to 25 and 35% reductions in maximal cardiac performance at 10 and 15 °C, respectively. Reduced contractility, however, could not be ascribed to myocardial necrosis, as the biochemical and energy state of the hearts was unaffected. Hence, anoxic exposure merely stunned the myocardium. At 10 °C, neither the anoxic nor adrenergic preconditioning protocols improved post-anoxic cardiac performance. Further, the preconditioning protocols did not reduce post-anoxic myocardial dysfunction at 15 °C, despite the increased cardiac sensitivity to anoxia at this temperature. Thus, despite using strong and different preconditioning stimuli compared with earlier studies, the cardio-protective effect of preconditioning seems to be absent in rainbow trout hearts that are inherently more hypoxia-tolerant.     

Isolation and characterization of the receptor for vitellogenin from follicles of the rainbow trout,Oncorhynchus mykiss

The isolation and characterization of the receptor for vitellogenin from follicle membranes of the rainbow trout, Oncorhynchus mykiss, is described. Follicle membrane proteins subjected to SDS-polyacrylamide gel electrophoresis and subsequently to either protein staining or ligand blotting with radiolabelled vitellogenin (¹²⁵iodine-vitellogenin) demonstrated that the vitellogenin receptor has an apparent molecular mass of 200 kD (probably comprising of two 100-kD subunits) under non-reducing conditions. The vitellogenin binding sites were identified as specific receptors: binding was saturable and the binding sites were both tissue specific to follicle membranes and exhibited ligand specificity. Scatchard analyses of specific binding data revealed a single class of binding sites with a high affinity for rainbow trout vitellogenin (K _d=8.2·10^-9 mol·1^-1). Both brown trout, Salmo trutta, vitellogenin and carp, Cyprinus carpio, vitellogenin were able to displace the radiolabelled rainbow trout vitellogenin from its receptor, although they were less effective than rainbow trout vitellogenin.Abbreviations B _max maximum number of binding sites available - BSA bovine serum albumin - bt-VTG brown trout vitellogenin - c-VTG earp vitellogenin - HEPES N-2-hydroxyethylpiperazine-N-2-ethanesulfonic acid - K _d dissociatian constant - NCM nitrocellulose membranes - PMSF phenylmethylsulphonylfluoride - rt-VTG rainbow trout vitellogenin - VTG vitellogenin     

Seasonal dynamics and persistence of Gyrodactylus salaris in two riverine anadromous Arctic charr populations

The seasonal occurrence of the monogenean ectoparasite Gyrodactylus salaris Malmberg infecting Arctic charr, Salvelinus alpinus (L.) in the two rivers Skibotnelva and Signaldalselva in northern Norway was studied in the period from autumn 2003 to autumn 2005. Skibotnelva has been infected with the parasite since 1979, and treated with rotenone twice. Most likely resident Arctic charr avoided the rotenone treatment in small tributary streams, and thus was the source of the repeated re-infection of this river. G. salaris was first recorded in Signaldalselva in the year 2000 and it is still untreated. Unlike Atlantic salmon, which is highly susceptible to G. salaris, Arctic charr can display a wide range of host-responses to G. salaris infections. Arctic charr were sampled by electro fishing with a total sample of 681 Arctic charr. The results from this study demonstrate an evident seasonal dynamic in G. salaris infection in charr in both rivers. Parasite intensities fluctuated with the rise and fall in temperature through the year, with an autumn high and spring low. There was a significantly lower prevalence and mean intensity of G. salaris in Skibotnelva than in Signaldalselva. There were also a lower prevalence and intensity of G. salaris in the older than in the youngest charr. The different history of infection and treatment in the two rivers might be the underlying cause of these observed dissimilarities. The current study indicates that Arctic charr is a good natural host for G. salaris.     

Influence of photoperiod,temperature and host plant on the production of diapause eggs inPetrobia (Tetranychina) harti (Acari: Tetranychidae)

Petrobia harti (Ewing) diapauses in the egg stage. Adult females lay either diapause or nondiapause eggs. On the University of Thessaloniki campus (41°N), the mite was found to develop on leaves ofOxalis corniculata L. throughout the year, while no mites were found on leaves ofOxalis articulata Savigny growing in the same area. In the laboratory the mite could be maintained equally well on detached leaves of both plant species, kept on wet cotton-wool.Forty to 90% females laying diapause eggs (dlf) were produced when the mites developed under LD 1212 and 19±1 °C, or LD 168 and 19±1 °C or 25±1 °C on leaves ofO. articulata detached from plants grown in the open in various seasons. Under the same conditions, a very low to zero percentage ofdlf was produced onO. corniculata. By rearing certain feeding stages on one of these twoOxalis hosts, and the other feeding stages on the other host, various percentages ofdlf were obtained. These percentages were the net effect of the antagonistic action of the twoOxalis species.By rearing the mites at LD 8.515.5, LD 1212 or LD 168 and a temperature of 19±1 °C onO. articulata leaves renewed every 3 days, or every 16–18 days, or not at all, it could be shown that diapause induction or aversion is caused by the direct effect of photoperiod on the mites, and not by an effect through the host leaves.When wholeO. articulata plants were grown under LD 168 and 19±1 °C in the laboratory, or developed in the open during April and May, flowers were produced, while under LD 1212 no flowering occurred. In the laboratory under diapause-inducing conditions, higher percentages ofdlf were produced on leaves detached from flowering plants than on leaves detached from plants not flowering.OnO. articulata leaves at 20 °C, photoperiods with photophases equal to or longer than 12 h induced from 70 to 80%dlf, while photoperiods with photophases equal to or shorter than 10.9 h induced very low to zero percentages. By transferring different chrysalis stages from a diapause-inducing (LD 1212) to a diapause-averting (LD 8.515.5) photoperiod, and vice versa, it was found that the nymphochrysalis through deutonymph stages were sensitive to photoperiod, the deutochrysalis and deutonymph being the most sensitive.Under an LD 1212 photoperiod, a temperature of 20 °C induced diapause, whereas 25 °C, 30 °C, or a daynight thermoperiod of 25 °C18 °C suppressed it.     

The recovery and hematological rehabilitation of chlorine stressed adult rainbow trout (Salmo gairdneri)

Synopsis The ability of adult rainbow trout (Salmo gairdneri) to recover from acute chlorine exposure was tested. Six separate tests were carried out in duplicate. Blood was collected from each duplicate group of fish at the beginning of the test, at the appearance of the chlorine-distress symptoms, and at 24 and 48 h after exposures. The total residual chlorine (TRC) concentrations used in these six tests were 1.67, 3.50, 1.10, 1.25, 1.02 and 0.0 mg 1^–1, at water temperatures of 13.5, 14.6, 17.2, 22.6, 23.0 and 26.0° C, respectively. The cumulative fish mortality for these six tests at 48 h after exposure were 11.5, 100, 0.0, 67.1, 36.1 and 100 percent. Blood of chlorine stressed fish exhibited signs of hemoconcentration and hemolysis. All blood parameters with the exception of hemolysis returned to control levels within 24 hours after exporsure. High TRC concentrations in the range of 3.5 mg 1^–1 at 14.0° C, and TRC of 1.25 and 1.02 mg 1^–1 TRC at 23° C, significantly diminished the rainbow trout recovery.     

Major histocompatibility class II genes in rainbow trout (Oncorhynchus mykiss) exhibit temperature dependent downregulation

Major histocompatibility (MH) class II receptors are expressed on the surface of specialized antigen-presenting cells in vertebrate immune systems. Their function is to present peptides derived from exogenous pathogens to CD4+ T cells. Variation in the level of expression of these genes has been linked to pathogenesis in various diseases. Very little has been published on the function of MH class II receptors in teleost fish to date. In this study, we have produced polyclonal antibodies recognizing MH class II alpha and beta proteins of rainbow trout and employed them to characterize the expression pattern of these genes. Deglycosylation using N-glycosidase F and endoglycosidase H showed that MH class II alpha is glycosylated in rainbow trout. MH class II beta was also found to be glycosylated as reported previously. Results from Northern blotting revealed that the expression of these genes was not affected by exposure of rainbow trout to temperature of 5°C. However, at 2°C, downregulation of MH class II alpha and beta genes was evident at both the mRNA and protein levels as assessed by Northern and Western blotting, respectively. Because MH class II antigens play an important role in generating an immune response to bacterial and fungal pathogens, downregulation of these genes at low temperature could account for the susceptibility of fish to low temperature-related diseases such as bacterial cold-water disease and winter saprolegniosis.     

Potential Effects of Climate Warming on Fish Habitats in Temperate Zone Lakes with Special Reference to Lake 239 of the Experimental Lakes Area (ELA), North-Western Ontario

We used simple statistics (e.g. mean temperature, degree days, cumulative volume days) to describe present thermal habitats for cool water (yellow perch, Perca flavescens) and cold water (lake trout, Salvelinus namaycush) fish of a small boreal lake. We then modelled changes in the vertical and temporal extent of these habitats under various scenarios of climatic change that included increases in air temperature of 2°C, 4°C, and 9°C, and positive and negative deviations from present levels of 10% in solar radiation and relative humidity, and 20% in wind speed and the lake water extinction coefficient. Model simulations indicated pronounced changes in the temporal and vertical availability of fish thermal niche space. These changes were mainly driven by the large increases in mean mixed layer temperatures that corresponded to 85% of the increases in air temperature, but, in particular, changes in light attenuation also resulted in some non-linear, unexpected effects in the distribution and seasonal availability of thermal niche space. As expected, classical lake trout thermal habitat (5–15°C) was progressively reduced and almost disappeared in littoral areas in spring and early summer. Perch thermal niche space expanded for air temperature increases of up to 4°C, but largely disappeared for the 9°C increase. We discuss changes in thermal habitat with regard to the life history of lake trout and yellow perch, and include other determinants of fish habitat to evaluate the potential of these species for long-term ecological success under climatic warming.     

Temperature dependent development and survival of two sympatric species, Galerucella calmariensis and G. pusilla, on purple loosestrife

Two sympatric Europeanbeetles, Galerucella calmariensis (L.)and G. pusilla (Duft.) (Coleoptera:Chrysomelidae), have been released in NorthAmerica for biological control of purpleloosestrife, Lythrum salicaria L.(Lythraceae). Because establishment isaffected by environmental conditions, studieswere conducted at temperatures ranging from12.5 to 30 °C to determine differencesin rate of development and survival between thetwo species. No egg hatch occurred at12.5 °C for both species. Eggdevelopment was faster for G.calmariensis than for G. pusilla attemperatures 15 °C. Theminimum threshold temperature for eggdevelopment was lower for G. calmariensisthan G. pusilla. At 12.5 °C, G. calmariensis larvae developed 1.6 daysfaster than G. pusilla, but at 15, 20,25, and 27.5 °C G. pusilla developed2.9, 1.2, 1.1, and 0.6 days faster,respectively, than G. calmariensis. Nodifferences in developmental rate of pupa andtotal development time from egg to adulteclosion were observed for the two species. However, survival of G. calmariensisgenerally was higher than that of G.pusilla at lower temperatures. No differencewas observed in the preoviposition periodbetween the two species except at27.5 °C. The preoviposition period forboth species at 12.5 and 15 °C exceeded50 days and was much higher than for20 °C and above. The long preovipositionperiod suggests that temperatures below15 °C induce reproductive diapause. At15 °C, G. pusilla females livedlonger and also had a longer oviposition periodthan G. calmariensis. However, fasteregg and larval development, and higher survivalat 12.5 °C may give G. calmariensisa competitive advantage over G. pusillain cooler climates.     

MicroRNA loci support conspecificity of Gyrodactylus salaris and Gyrodactylus thymalli (Platyhelminthes: Monogenea)

The monogenean flatworm Gyrodactylus salaris is a serious threat to wild and farmed Atlantic salmon stocks in Norway. Morphologically, the closely related but harmless Gyrodactylus thymalli on grayling can hardly be distinguished from G. salaris. Until now, molecular approaches could not resolve unambiguously whether G. salaris and G. thymalli represent just one polytypic species, two polytypic species or a complex of more than two species. In the first known genome-wide analysis utilizing 37 conserved microRNA loci, the genetic differentiation of seven populations of G. salaris and G. thymalli was assessed. The concatenated alignment spanned 21,742 bp including 62 variable positions. A neighbor-joining cluster analysis did not support any host-based or mitochondrial haplotype-based grouping of strains. We conclude that a two species concept for G. salaris and G. thymalli does not reflect meaningful biological entities. Instead, G. salaris and G. thymalli are just one species comprising several pathogenic and non-pathogenic strains on various primary hosts. Following the International Code for Zoological Nomenclature, G. salaris Malmberg, 1957 is the valid species name with G. thymalli ?itňan, 1960 becoming the junior synonym. Accordingly, the range of G. salaris is significantly increased, given that formerly G. salaris-free countries such as e.g., Great Britain are now within the species’ natural range. The synonymization of G. salaris and G. thymalli implies severe challenges to current disease management routines, which assume that G. salaris and G. thymalli are readily distinguishable. Protocols for reliable identification of pathogenic and non-pathogenic strains of G. salaris need to be developed.     

Seasonal variations in the immune system of the tench,Tinca tinca (Cyprinidae): proliferative response of lymphocytes induced by mitogens

The proliferation of tench lymphocytes induced by mitogens was studied during the four seasons of the year. Fish were maintained under natural conditions of photoperiod and temperature (mean ± SD: 12±2°C in winter, 22±3°C in spring, 30±3°C in summer and 21±3°C in autumn). Cultures were performed in vitro at 22°C in all seasons and the results were compared. Subsequently, in seasons with extreme water temperatures, cultures in vitro were performed at the same temperature as that of the water (12°C in winter and 30°C in summer) and the results were compared seasonally at the seasonal temperature, i.e. at 22°C in spring, 30°C in summer, 22°C in autumn and 12°C in winter. Phytohemagglutinin, concanavalin A, lipolisaccharide from E. coli and pokeweed mitogen were used as mitogens. Studies performed at 22°C as assay temperature in all seasons showed profound seasonal changes: while in spring, summer and autumn the mitogenic response of lymphocytes to phytohemagglutinin, concanavalin A, lipolisaccharide from E. coli and pokeweed mitogen was very low, during winter the results obtained were significantly higher. However, when the assays were performed at the corresponding seasonal temperature the differences were not as pronounced between the different seasons, and the mitogenic responses of lymphocytes were found to be the lowest during the winter and the highest during the summer with all mitogens used. This fact suggests that immunosuppression occurs in winter and an immunostimulation occurs in summer. However, the higher response found in winter when assaying at 22°C suggests that this property of lymphocytes needs an assay temperature higher than the in vivo temperature in order to observe accurate mitogenic responses.Abbreviations Con A concanavalin A - cpm counts per minute - LPS E. coli lipolisaccharide - MS222 tricainemethane sulphonate - PBS phosphate-buffered saline - PHA phytohemagglutinin - PWM pokeweed mitogen - SI stimulation index