Reverse translation: effects of acclimation temperature and acute temperature challenges on oxygen consumption, diffusive water flux, net sodium loss rates, Q10 values and mass scaling coefficients in the rainbow trout (Oncorhynchus mykiss)

2020 ◽  
Vol 190 (2) ◽  
pp. 205-217 ◽  
Author(s):  
John O. Onukwufor ◽  
Chris M. Wood
2014 ◽  
Vol 92 (9) ◽  
pp. 777-784 ◽  
Author(s):  
M.M. Yau ◽  
E.B. Taylor

Hybridization between rainbow trout (Oncorhynchus mykiss (Walbaum, 1792)) and westslope cutthroat trout (Oncorhynchus clarkii lewisi (Girard, 1856)) occurs commonly when rainbow trout are introduced into the range of westslope cutthroat trout. Typically, hybridization is most common in warmer, lower elevation habitats, but much less common in colder, higher elevation habitats. We assessed the tolerance to cold water temperature (i.e., critical thermal minimum, CTMin) in juvenile rainbow trout and westslope cutthroat trout to test the hypothesis that westslope cutthroat trout better tolerate low water temperature, which may explain the lower prevalence of rainbow trout and interspecific hybrids in higher elevation, cold-water habitats (i.e., the “elevation refuge hypothesis”). All fish had significantly lower CTMin values (i.e., were better able to tolerate low temperatures) when they were acclimated to 15 °C (mean CTMin = 1.37 °C) versus 18 °C (mean CTMin = 1.91 °C; p < 0.001). Westslope cutthroat trout tended to have lower CTMin than rainbow trout from two populations, second–generation (F2) hybrids between two rainbow trout populations, and backcrossed rainbow trout at 15 °C (cross type × acclimation temperature interaction; p = 0.018). Differential adaptation to cold water temperatures may play a role in influencing the spatial distribution of hybridization between sympatric species of trout.


1993 ◽  
Vol 71 (11) ◽  
pp. 2167-2173 ◽  
Author(s):  
John R. Bailey ◽  
William R. Driedzic

Rainbow trout (Oncorhynchus mykiss) were acclimated to 5 and 20 °C. Oxygen consumption of isolated perfused hearts was measured at 5 or 15 °C with either glucose or palmitate as the exogenous fuel source. With glucose as the fuel there was no significant difference in oxygen consumption of hearts from either acclimation group at either temperature. With palmitate as the fuel source, hearts from fish acclimated to and tested at 5 °C had significantly higher oxygen consumption than hearts from fish acclimated to 20 °C and tested at either 5 or 15 °C. Hearts from fish both acclimated to and tested at 5 °C had a higher oxygen consumption with palmitate than when glucose was supplied. This reflects the preference for fatty acid fuels found in cold acclimated muscle tissue, and consequently the amount of oxygen required to utilize fats. Under all experimental conditions, 14CO2 production from either (6-14C)glucose or (1-14C)palmitate could account for less than 0.5% of oxygen consumption. Tissue chemical analysis showed that most of the label from (6-14C)glucose appeared in acid-soluble (glycolytic intermediates, citric acid cycle intermediates, amino acids, etc.) and lipid fractions while most of the label from (1-14C)palmitate appeared in lipid- or acid-soluble or acid precipitate (protein material) fractions. This indicates considerable dilution of exogenous fuels in endogenous pools, which could account for the discrepancy in measured O2 consumption and 14CO2 production. Glucose catabolism was little affected by either acute or chronic changes in temperature other than an increase in glucose incorporation into the glycogen pool. Hearts from fish both acclimated to and tested at 5 °C showed an increased handling of exogenous fatty acids as reflected by elevated rates of catabolism and incorporation into intracellular lipids.


1994 ◽  
Vol 72 (3) ◽  
pp. 423-426 ◽  
Author(s):  
Paul W. Webb ◽  
Hongbao Zhang

We measured reaction distance, escape velocity, and the apparent looming threshold (ALT) of heat-shocked goldfish (Carassius auratus) attacked by trout (Oncorhynchus mykiss). We tested fish at the acclimation temperature of 15 °C after heat-shocking prey for 2 min at temperatures ranging from 34 to 39 °C. Escape speeds were unaffected by heat shock. Reaction distance decreased from about 21 cm for fish shocked at 35 °C to about 6 cm for those shocked at 39 °C. ALT increased from 0.2 rad∙s−1 for controls to 0.4 rad∙s−1 for goldfish heat-shocked at 39 °C. The elusiveness of prey, E, was measured as the number of attacks required per prey capture. E was related to ALT as: E = 1.29 (±0.47)∙ALT−0.82(±0.25) (mean (±2 SE)). Factors that decrease responsiveness of prey have large effects on the ability of prey to avoid predators.


1998 ◽  
Vol 201 (22) ◽  
pp. 3123-3133 ◽  
Author(s):  
JD Kieffer ◽  
D Alsop ◽  
CM Wood

Instantaneous fuel usage at 5 degreesC or 15 degreesC was assessed by measurement of rates of O2 consumption (O2), CO2 excretion (CO2) and nitrogenous waste excretion (nitrogen =ammonia-N + urea-N) in juvenile rainbow trout (Oncorhynchus mykiss) at rest and during swimming at 45 % and 75 % of aerobic capacity (Ucrit). After 2 weeks of training at approximately 1 body length s-1 (BL s-1), critical swimming speeds (approximately 3.0 BL s-1) and whole-body energy stores (total protein, lipids and carbohydrates) were identical in fish acclimated to 5 degreesC or 15 degreesC. O2 and CO2 increased with swimming speed at both temperatures and were higher at 15 degreesC than at 5 degreesC at all speeds, but the overall Q10 values (1.23-1.48) were low in these long-term (6 weeks) acclimated fish. The respiratory quotient (CO2/O2, approximately 0.85) was independent of both temperature and swimming speed. In contrast to O2 and CO2, the rate of ammonia excretion was independent of swimming speed, but more strongly influenced by temperature (Q10 1. 4-2.8). Urea excretion accounted for 15-20 % of nitrogen, was unaffected by swimming speed and showed a tendency (P&lt;0.07) to be positively influenced by temperature at one speed only (45 % Ucrit). Nitrogen quotients (NQ nitrogen/O2) were generally higher in warm-acclimated fish, remaining independent of swimming speed at 15 degreesC (0.08), but decreased from about 0.08 at rest to 0.04 during swimming at 5 degreesC. Instantaneous aerobic fuel use calculations based on standard respirometric theory showed that both acclimation temperature and swimming speed markedly influenced the relative and absolute use of carbohydrates, lipids and proteins by trout. At rest, cold-acclimated trout used similar proportions of carbohydrates and lipids and only 27 % protein. During swimming, protein use decreased to 15 % at both speeds while the relative contributions of both lipid and carbohydrate increased (to more than 40 %). On an absolute basis, carbohydrate was the most important fuel for fish swimming at 5 degreesC. In contrast, resting fish acclimated to 15 degreesC utilized 55 % lipid, 30 % protein and only 15 % carbohydrate. However, as swimming speed increased, the relative contribution of carbohydrate increased to 25 %, while the protein contribution remained unchanged at approximately 30 %, and lipid use decreased slightly (to 45 %). On an absolute basis, lipid remained the most important fuel in fish swimming at 15 degreesC. These results support the concept that lipids are a major fuel of aerobic exercise in fish, but demonstrate that the contribution of protein oxidation is much smaller than commonly believed, while that of carbohydrate oxidation is much larger, especially at higher swimming speeds and colder temperature.


1990 ◽  
Vol 68 (7) ◽  
pp. 1499-1504
Author(s):  
Moira M. Ferguson ◽  
Roy G. Danzmann ◽  
Fred W. Allendorf ◽  
Kathy L. Knudsen

We examined the lengths, weights, condition factors, and hepatosomatic indices of juvenile rainbow trout (Oncorhynchus mykiss) from four full-sib families, each segregating at the temporal regulatory locus Pgm1-t, and the concentrations of RNA, DNA, and protein in their livers and white muscle. In three families, fish with phosphoglucomutase-1 (PGM1) activity in liver (Pgm1-t(b) fish) are significantly longer than their full-sibs lacking activity for liver PGM1 (Pgm1-t(a) fish). Hepatosomatic indices tend to be higher in the Pgm1-t(b) fish than in their Pgm1-t(a) siblings. RNA/DNA ratios in the liver of Pgm1-t(b) fish are significantly higher than those of Pgm1-t(a) fish in two families and marginal in a third. However, no significant differences were detected in a parallel analysis of nucleic acids and protein in white muscle, where PGM1 is expressed in all fish. In a separate experiment, Pgm1-t(b) fish were significantly heavier in all five families, had significantly higher condition factors in two families, and had marginally lower standardized oxygen consumption rates in three families.


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