Diminished social status affects ionoregulation at the gills and kidney in rainbow trout (Oncorhynchus mykiss)

2004 ◽  
Vol 61 (4) ◽  
pp. 618-626 ◽  
Author(s):  
Katherine A Sloman ◽  
Graham R Scott ◽  
D Gordon McDonald ◽  
Chris M Wood

Competition for social status can result in physiological differences between individuals, including differences in ionoregulatory ability. Subordinate rainbow trout (Oncorhynchus mykiss) had two-fold higher uptake rates of sodium across the gill and two-fold higher whole-body sodium efflux rates than the dominant fish with which they were paired. Sodium efflux was then divided into branchial and renal components, both of which were higher in subordinates. Branchial sodium efflux accounted for 95%–98% of sodium loss. Plasma sodium concentrations were more variable, although not significantly different, in subordinate fish, suggesting that the increased loss of sodium in these trout is compensated for by an increase in uptake rates. Urine flow rates and plasma cortisol concentrations were higher in subordinate fish, but there was no difference in glomerular filtration rate between dominants and subordinates. Renal sodium reabsorption was significantly reduced in subordinates. In summary, the ionoregulation of subordinate individuals was altered, most likely occurring as a result of stress-induced changes in gill permeability, resulting in a higher throughput of water and increased branchial sodium efflux. These changes in ionoregulatory ability have many physiological implications, including the increased susceptibility of subordinates to ionoregulatory challenges and an increased metabolic cost of ionoregulation.


1991 ◽  
Vol 48 (4) ◽  
pp. 583-590 ◽  
Author(s):  
Paul W. Webb

Routine swimming encompasses all volitional motions of fish. It is usually assumed to be quasi-steady, i.e. routine swimming is mechanically equivalent to steady swimming. Routine swimming of rainbow trout, Oncorhynchus mykiss, was dominated by unsteady motions of linear and centripetal (angular) acceleration. Constant-speed swimming was rare. Mean speeds and acceleration rates were small. Tail-beat frequencies were nevertheless strongly correlated with mean swimming speed, but increased more rapidly with increasing speed in routine swimming than in steady swimming. Tail-beat amplitudes and propulsive wavelengths were similar to values seen in steady swimming. The composition of routine swimming and analysis of the force balance showed that routine swimming was not quasi-steady. Therefore, forces and rates of working should be estimated from a complete description of whole-body deformation. This is impractical. Drag dominated resistance in routine swimming, such that average thrust (= resistance) may be computed from mean speed and/or averaged kinematic variables for the trailing edge with a correction factor of approximately 3. Analysis of routine swimming may permit comparisons among a wider range of vertebrates than possible with commonly used methods.



1994 ◽  
Vol 51 (2) ◽  
pp. 372-380 ◽  
Author(s):  
M. G. Rankin ◽  
D. G. Dixon

The 144-h LC50 (95% fiducial limits) of arsenite for 4.5-g rainbow trout (Oncorhynchus mykiss) was 18.5 (17.9–19.1) mg∙L−1. In a pair-fed growth study which exposed trout to 0.0, 0.76, 2.48, or 9.64 mg arsenite∙L−1 over 17 wk, growth was significantly reduced (by 55%) only at 9.64 mg∙L−1. The reduction was attributable to both reduced appetite (primarily) and direct metabolic impact (marginally). Fish at 9.64 mg∙L−1 suffered 10% mortality, usually associated with necrotic erosion of the mandibular and olfactory regions of the head. All fish exposed to 9.64 mg∙L−1 showed inflammation of the gallbladder wall, a lesion absent at lower exposure concentrations. There were no arsenite impacts on hepato- and splenosomatic index, hematocrit, hemoglobin, total plasma lipid, cholesterol, and protein or brain concentrations of norepinephrine, dopamine, and serotonin. Exposure to 0.0, 0.76, 2.48, and 9.64 mg arsenite∙L−1 for 26 wk resulted in mean (SE) equilibrium whole-body As concentrations of 0.3 (0.02), 0.2 (0.02), 0.4 (0.10), and 1.7 (0.40) μg As∙g wet weight−1, respectively, No depuration below these concentrations occurred during a 12-d period in arsenite-free water. The threshold of chronic toxicity was estimated to be 4.9 mg∙L−1.



2012 ◽  
Vol 85 (4) ◽  
pp. 309-320 ◽  
Author(s):  
Kathleen M. Gilmour ◽  
Sheryn Kirkpatrick ◽  
Andrey Massarsky ◽  
Brenda Pearce ◽  
Sarah Saliba ◽  
...  


2017 ◽  
Vol 63 (1) ◽  
pp. 13 ◽  
Author(s):  
U. İspir ◽  
M. Kirici ◽  
M. E. Yonar ◽  
S. Mişe Yonar


1997 ◽  
Vol 75 (11) ◽  
pp. 1916-1922 ◽  
Author(s):  
Grant E. Brown ◽  
R. Jan F. Smith

We investigated, under laboratory conditions, the presence of chemical alarm signals in juvenile rainbow trout (Oncorhynchus mykiss). In an initial experiment, we exposed trout to a whole-body extract from conspecifics or a distilled-water control. When exposed to whole-body extract, trout significantly (i) decreased time spent swimming, (ii) increased time taken to resume foraging, and (iii) decreased the number of food items eaten. These data indicate a significant chemically mediated antipredator response. A second experiment was conducted to determine (i) if this is a generalized response to injured fish or a specific response to injured conspecifics, and (ii) if the chemical signal is localized in the skin. We exposed juvenile trout to one of three chemical stimuli: (1) trout skin extract, (2) trout body extract, or (3) swordtail (Xiphophorus helleri) skin extract. Significant antipredator responses were observed in trout exposed to conspecific skin extract, but responses of those exposed to conspecific body extract or swordtail skin extract did not differ from those of distilled-water controls. These data strongly suggest that juvenile rainbow trout possess a chemical alarm signal, localized in the skin, that elicits antipredator behaviour when detected.by conspecifics.



1994 ◽  
Vol 51 (8) ◽  
pp. 1728-1736 ◽  
Author(s):  
Mark D. Powell ◽  
David J. Speare ◽  
Neil MacNair

Chloramine-T is a commonly used therapeutic agent for the treatment of bacterial gill and skin diseases in the intensive aquaculture of salmonids; however, little is known about its effects on healthy fish. Juvenile rainbow trout (Oncorhynchus mykiss) were exposed weekly to 5, 10, and 20 mg active chloramine-T ingredient∙L−1 in a 20-tank replicate flow-through facility. Control fish were treated with tank water only. Growth parameters and haematocrits were taken twice weekly and serum biochemistry was measured on termination of the experiment. Absolute growth rates were suppressed but only statistically significantly in fish treated with 20 mg chloramine-T∙L−1 compared with controls. Fish exposed to 10 and 20 mg chloramine-T∙L−1 showed significant predisposition to an erosive dermatitis of the caudal fin which appeared to be caused by opportunistic pathogens of the genus Pseudomonas spp. and Flavobacter spp. Haematocrits decreased in controls and ail treatments. A significant concentration-dependent decrease in plasma sodium and chloride was observed. Plasma glucose levels did not vary and were similar to those reported for unstressed trout. We recommend that care be taken when using chloramine-T prophylactically and that concentrations of less than 10 mg∙L−1 be used.



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<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.



2002 ◽  
Vol 59 (5) ◽  
pp. 768-777 ◽  
Author(s):  
H A Campbell ◽  
R D Handy ◽  
D W Sims

This study tests the hypothesis that rainbow trout (Oncorhynchus mykiss) compensate for the metabolic cost of dietary Cu exposure by reducing swimming activity at particular times during the diel cycle. Fish were exposed to excess dietary Cu for three months (726 mg Cu·kg–1 dry weight) and simultaneously oxygen consumption (MO2) and spontaneous swimming activity were measured. Rhythmicity in swimming activity was examined by videorecording fish behaviours for 48 h. Standard metabolic rate estimates (RS) of 7.2 and 8.7 mmol O2·kg–1·h–1 (15°C) were measured for control and Cu-exposed fish, respectively. MO2 was higher in Cu-exposed fish at any chosen speed compared with control Cu-exposed trout, which decreased activity (mean speed) by at least 75%, spent more time at lower speeds, and lost circadian periodicity in these parameters compared with controls. Mean growth rates were normal, although Cu-exposed fish showed a narrower range of body weights and fewer mortalities than control groups, suggesting a suppression in social behaviour in Cu-exposed fish. Overall, the increased metabolic cost of swimming in Cu-exposed fish was fully compensated by a reduction in activity, particularly at night and dawn. However, this behavioural strategy suggests that spatial and temporal aspects of ecologically important social behaviours may be compromised in Cu-exposed fish.



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