scholarly journals Polymorphism and multiple correlated characters: Do flatfish asymmetry morphs also differ in swimming performance and metabolic rate?

2019 ◽  
Vol 9 (8) ◽  
pp. 4772-4782
Author(s):  
Carolyn A. Bergstrom ◽  
JoMarie Alba ◽  
Julienne Pacheco ◽  
Trevor Fritz ◽  
Sherry L. Tamone
1978 ◽  
Vol 35 (6) ◽  
pp. 816-821 ◽  
Author(s):  
J. R. Brett ◽  
J. M. Blackburn

The metabolic rate of spiny dogfish, Squalus acanthias, was determined in both a tunnel respirometer and a large, covered, circular tank (mass respirometer). Swimming performance was very poor in the respirometer, so that a power–performance curve could not be established. Instead, resting metabolic rates were determined, with higher rates induced by causing heavy thrashing (active metabolism). Routine metabolic rates were measured for the spontaneous activity characterizing behavior in the circular tank. For fish of 2 kg mean weight, the metabolic rates at 10 °C were 32.4 ± 2.6 SE (resting), 49.2 ± 5.0 SE (routine), and 88.4 ± 4.6 SE (active) mg O2∙kg−1∙h−1. Assuming that the routine rate represents a general energy expenditure in nature, this is equivalent to metabolizing about 3.8 kcal∙kg−1∙d−1 (15.9 × 103 J∙kg−1∙d−1). Key words: dogfish, metabolic rates, energetics, respiration


1998 ◽  
Vol 201 (24) ◽  
pp. 3355-3366
Author(s):  
C Swanson

The euryhaline milkfish (Chanos chanos) is an excellent subject for studies of the physiological and behavioral processes involved in salinity adaptation. In this study, energy partitioning for metabolism, activity and growth, maximal activity performance and blood osmotic concentrations were assessed at two activity levels in juvenile milkfish fed equal rations and maintained at a relatively constant temperature (262 C) and at salinities(15, 35 and 55 ?) that represented a wide range of osmoregulatory challenges. Changes in the measured parameters were not consistently related to the magnitude of the trans-integumentary osmotic gradients. Routine oxygen consumption rates were high in 35 ? salinity (mean 1 s.e.m. 1678 mg O2 kg-1 h-1) and comparably low in 15 and 55 ? salinity (1336 and 1273 mg O2 kg-1 h-1, respectively). Routine activity levels (relative swimming velocity) were highest in 35 ? salinity (0. 960.04 L s-1), where L is standard length, intermediate in 15 ? salinity (0.770.03 L s-1) and lowest in 55 ? salinity (0.670.03 L s-1). Growth was significantly higher in 55 ? salinity (3.40.2 % increase in wet body mass per day) than in 35 ?salinity (2.40.2 % increase per day) and intermediate in 15 ? salinity(2.90.5 % increase per day). Maximum swimming velocities decreased with increases in salinity, from 9.90.7 L s-1 in 15 ? salinity to 6.60. 5 L s-1 in 55 ? salinity. Sustained swimming activity above routine levels for 2 h resulted in an increase in blood osmotic concentrations in milkfish in 55 ?salinity, but osmoregulation was re-established during the second 2 h of activity. Thus, patterns of variation in metabolic rate and growth were largely parallel to variations in routine activity although, comparing 15 and 55 ? salinity, elevated maintenance costs for osmoregulation at the high salinity were detectable. Reduced osmoregulatory abilities and reductions in maximal swimming performance suggest that high salinity may constrain activity. The results demonstrate that investigations of salinity adaptation in euryhaline fishes should take into account the interactive effects of salinity on physiology and behavior.


1996 ◽  
Vol 199 (6) ◽  
pp. 1295-1309 ◽  
Author(s):  
J Nelson ◽  
Y Tang ◽  
R Boutilier

The objective of this study was to determine whether differences in exercise physiology between Atlantic cod (Gadus morhua) populations from different salinity environments could be changed by acclimating individuals of each population to the natural salinity of the comparison population. The exercise-associated blood chemistry of cod from the brackish Bras d'Or lakes, which had previously been shown to be quite different from that of 'open-ocean' cod, changed to resemble the blood chemistry of their oceanic relatives after only 2 months of acclimation to full-strength salinity. In contrast, the blood chemistry of cod from the Scotian Shelf of the Northwest Atlantic Ocean showed little change after 2 months of acclimation to brackish water. These results demonstrate that the degree of osmoconformity to changes in environmental salinity is a population-specific not a species-specific trait. The blood chemistry differences between populations and salinities did not translate into differences in exercise performance: i.e. critical swimming speeds were statistically uniform across all combinations of population and salinity, although performance was more varied in fish swimming in 'non-native' waters. Other 'whole-animal' physiological characteristics, such as metabolic rate and the aerobic cost of transport, were dependent upon both population origin and the environmental salinity. Vigorous swimming was more energetically expensive at full-strength salinity than at 20 salinity, yet estimates of standard (i.e. resting) metabolic rate were lower for full-strength salinity. Environmental salinity also influenced the relative appearance of lactate and metabolic acid in the extracellular fluid compartment, with full-strength salinity favouring the relative appearance of lactate in the blood. Multivariate statistical analyses of this data set showed that, in contrast to other fish species and studies, differences in blood oxygen transport appear to account for some of the swimming performance differences seen in Atlantic cod at 2 °C. The two experimental populations were cleanly separated by a principal components analysis, regardless of the salinity to which they were acclimated, confirming our earlier contention that these cod populations are physiologically distinct. A key feature of that distinctness is the greater phenotypic plasticity exhibited by the population from the more euryhaline, more eurythermal environment.


2001 ◽  
Vol 58 (6) ◽  
pp. 1104-1112 ◽  
Author(s):  
D J McKenzie ◽  
E Cataldi ◽  
P Romano ◽  
S F Owen ◽  
E W Taylor ◽  
...  

Specific growth rates, exercise respirometry, and swimming performance were compared in young-of-the-year Adriatic sturgeon (Acipenser naccarii) maintained in freshwater (FW) or acclimated to brackish water (BW) that was slightly hypertonic to sturgeon plasma, at a salinity of 11 g·L–1. Specific growth rate was significantly (17%) lower in BW than in FW. Sturgeon in BW also had a significantly (30%) higher standard metabolic rate than those in FW. In both groups, the relationship between swimming speed and oxygen uptake was described equally well by a linear or exponential equation, with a power relationship between swimming speed and net cost of locomotion and a linear relationship between tailbeat frequency and swimming speed. However, sturgeon in BW exhibited higher mean total oxygen uptake, net costs, and tailbeat frequencies than the FW group at any given swimming speed. There were, however, no differences in aerobic scope or maximum sustainable swimming speed between the FW and BW groups because the BW group exhibited a compensatory increase in active metabolic rate and maximum tailbeat frequency. The results indicate that FW is a more suitable environment than mildly hypertonic BW for young-of-the-year Adriatic sturgeon.


1985 ◽  
Vol 42 (9) ◽  
pp. 1522-1529 ◽  
Author(s):  
Louis Bernatchez ◽  
Julian J. Dodson

We tested the influence of temperature and water velocity on metabolic rate and swimming performance of lake whitefish (Coregonus clupeaformis) and Cisco (C. artedii) using respirometry techniques. Tests were conducted at 5, 12, and 17 °C (speed range 20–102 cm∙s−1) for fake whitefish and at 12 °C (speed range 20–63 cm∙s−1) for cisco. Fish lengths ranged from 10 to 39 cm (TL). The net aerobic cost of swimming, obtained by subtracting standard from total oxygen consumption, was twice as high for cisco as that for lake whitefish at any swimming speed. However, the standard metabolic rate of lake whitefish was almost the double that of cisco acclimated to the same temperature. Values of metabolic scope for activity coupled with the net cost of swimming showed that coregonines were not good performers compared with most salmonids. The active metabolic rate, scope for activity, and critical swimming speed for lake whitefish were maximal at 12 °C and minimal at 5 °C. Swimming endurance of lake whitefish decreased logarithmically with swimming speed and was reduced at low temperature, the distance traversed at any given swimming speed being minimal at 5 °C. Our results support the hypothesis that the combined effect of high water velocities and low ambient temperature on coregonines' metabolism and swimming performance may be a more important factor than specific spawning temperature in the timing of the early reproductive migration of anadromous coregonines in the Eastmain River, James Bay.


PeerJ ◽  
2018 ◽  
Vol 6 ◽  
pp. e5719 ◽  
Author(s):  
Marcio S. Ferreira ◽  
Paulo H.R. Aride ◽  
Adalberto L. Val

Background In the wild, matrinchã (Brycon amazonicus) and tambaqui (Colossoma macropomum) rely strongly on their swimming capacity to perform feeding, migration and reproductive activities. Sustained swimming speed in fishes is performed almost exclusively by aerobic red muscles. The white muscle has high contraction power, but fatigue quickly, being used mainly in sprints and bursts, with a maximum duration of few seconds. The Ucrit test, an incremental velocity procedure, is mainly a measure of the aerobic capacity of a fish, but with a high participation of anaerobic metabolism close to the velocity of fatigue. Our previous study has indicated a high swimming performance of matrinchã (Ucrit) after hypoxia exposure, despite increased levels of lactate in plasma. In contrast, tambaqui with high lactate levels in plasma presented very low swimming performance. Therefore, we aimed to study the resistance of matrinchã and tambaqui to the increased lactate levels in muscle over an incremental velocity test (Ucrit). As a secondary aim, we analyzed the differences in anaerobic metabolism in response to environmental hypoxia, which could also support the better swimming performance of matrinchã, compared to tambaqui. Methods We measured, over incremented velocities in both species, the metabolic rate (the oxygen consumption by the fish; MO2), and the concentrations of lactate and nitrites and nitrates (NOx) in muscles. NOx was measured as an indicator of nitric oxide and its possible role in improving cardiorespiratory capacity in these fishes, which could postpone the use of anaerobic metabolism and lactate production during the swimming test. Also, we submitted fishes until fatigue and hypoxia (0.5 mg L−1) and measured, in addition to the previous parameters, lactate dehydrogenase activity (LDH; the enzyme responsible for lactate production), since that swimming performance could also be explained by the anaerobic capacity of producing ATP. Results Matrinchã exhibited a better swimming performance and higher oxygen consumption rates. Lactate levels were higher in matrinchã only at the moment of fatigue. Under hypoxia, LDH activity increased in the white muscle only in tambaqui, but averages were always higher in matrinchã. Discussion and conclusions The results suggest that matrinchã is more resistant than tambaqui regarding lactate accumulation in muscle at the Ucrit test, but it is not clear how much it contributes to postpone fatigue. The higher metabolic rate possibly allows the accumulated lactate to be used as aerobic fuel by the matrinchã, improving swimming performance. More studies are needed regarding matrinchã’s ability to oxidize lactate, the effects of exercise on muscle acidification, and the hydrodynamics of these species, to clarify why matrinchã is a better swimmer than tambaqui.


Sign in / Sign up

Export Citation Format

Share Document