Routine Metabolic Rate Research Articles

Consumo de oxigênio pós-prandial de juvenis do pampo Trachinotus marginatus

Para determinar a viabilidade do cultivo de uma espécie, é importante o conhecimento dos fatores limitantes para sua produção. Conhecer a taxa de consumo de oxigênio pós-prandial pode auxiliar na determinação da freqüência alimentar ideal para as espécies cultivadas. O objetivo deste trabalho foi estudar a taxa de consumo de oxigênio pós-prandial para juvenis do pampo Trachinotus marginatus. A avaliação do consumo de oxigênio foi feita a 24°C e 33‰, com pampos (9,64±0,2g) alimentados com 12% da biomassa por dia com dieta NRD INVE (59% proteína). Foi observado um pico de consumo de oxigênio 30min após a alimentação (1,06mgO2 g-1 h-1) e seu retorno ao nível de jejum (0,79mgO2 g-1 h-1) depois de decorridos mais 120min. A alimentação de juvenis de pampo pode ser realizada com uma freqüência de aproximadamente oito vezes por dia, pois a cada 2,5h a taxa de consumo de oxigênio já não mostra a elevação característica da fase pós-prandial, sugerindo que os processos de digestão e assimilação dos nutrientes estejam finalizados.

Hemoglobin enhances oxygen uptake in larval zebrafish (Danio rerio) but only under conditions of extreme hypoxia

The role of hemoglobin (Hb) in O(2) uptake by zebrafish larvae ranging in age from 5 to 42 days postfertilization was assessed under conditions of normoxia, moderate hypoxia and extreme hypoxia. This was achieved by exposing larvae with and without functional Hb to continuously declining oxygen levels (P(O(2))) in closed-system respirometers. Exposure to 5% CO for 2-4 h was used to render Hb effectively non-functional in terms of its ability to transport O(2). Routine metabolic rate (rM(O(2))), critical dissolved oxygen level (P(c)) and residual oxygen level (P(r)) were determined and used, respectively, as indicators of response in normoxia, moderate hypoxia and extreme hypoxia. rM(O(2)) was defined as the average rate of O(2) uptake before O(2) became limiting (i.e. at high P(O(2))s). P(c) is the P(O(2)) at which rM(O(2)) first becomes O(2)-limited and P(r) is the P(O(2)) below which larvae are no longer able to extract O(2) from the ambient medium. CO poisoning had no significant impact on rM(O(2)) or P(c) at any age, indicating that the lack of functional Hb does not impair routine O(2) usage in normoxia or at moderate levels of hypoxia [down to at least 25-50 torr (1 torr approximately 0.133 kPa), depending on age]. P(r), however, was significantly lower overall for control larvae (6.7+/-1.1 torr; mean +/- 95%CI) than for CO-poisoned larvae (11.2+/-2.1 torr). It would appear that the presence of functional Hb allows zebrafish larvae to extract O(2) from water down to lower P(O(2))s under conditions of extreme hypoxia. This is the first documented (as opposed to inferred) benefit of Hb in developing zebrafish. However, given the relatively small magnitude of the effect it is unclear if this benefit on its own is sufficient to balance the costs associated with Hb production and maintenance.

The routine metabolic rate of mulloway ( Argyrosomus japonicus: Sciaenidae) and yellowtail kingfish ( Seriola lalandi: Carangidae) acclimated to six different temperatures

This study compared the mass-specific routine metabolic rate (RMR) of similar sized mulloway ( Argyrosomus japonicus), a sedentary species, and yellowtail kingfish ( Seriola lalandi), a highly active species, acclimated at one of several temperatures ranging from 10–35 °C. Respirometry was carried out in an open-top static system and RMR corrected for seawater–atmosphere O 2 exchange using mass-balance equations. For both species RMR increased linearly with increasing temperature ( T). RMR for mulloway was 5.78 T − 29.0 mg O 2 kg − 0.8 h − 1 and for yellowtail kingfish was 12.11 T − 39.40 mg O 2 kg − 0.8 h − 1 . The factorial difference in RMR between mulloway and yellowtail kingfish ranged from 2.8 to 2.2 depending on temperature. The energetic cost of routine activity can be described as a function of temperature for mulloway as 1.93 T − 9.68 kJ kg − 0.8 day − 1 and for yellowtail kingfish as 4.04 T − 13.14 kJ kg − 0.8 day − 1 . Over the full range of temperatures tested Q 10 values were approximately 2 for both species while Q 10 responses at each temperature increment varied considerably with mulloway and yellowtail kingfish displaying thermosensitivities indicative of each species respective niche habitat. RMR for mulloway was least thermally dependent at 28.5 °C and for yellowtail kingfish at 22.8 °C. Activation energies ( E a) calculated from Arrhenius plots were not significantly different between mulloway (47.6 kJ mol − 1 ) and yellowtail kingfish (44.1 kJ mol − 1 ).

The Effect of Water Temperature on Standard and Routine Metabolic Rate in Two Different Sizes of Nile Tilapia

The Effect of Water Temperature on Standard and Routine Metabolic Rate in Two Different Sizes of Nile Tilapia

Effect of allozyme heterozygosity on basal and induced levels of heat shock protein (Hsp70), in juvenile Concholepas concholepas (Mollusca)

Organisms cope physiologically with extreme temperature by producing heat shock proteins (HSPs). Expression of Hsp70 enhances thermal tolerance and represents a key strategy for ectotherms to tolerate elevated temperature in nature. Synthesis of these proteins, together with other physiological responses to elevated temperatures, increases energy demands. A positive association between multiple and single locus heterozygosity (MLH and SLH, respectively) and individual fitness has been widely demonstrated. In molluscs, MLH can decrease routine metabolic rates and improve energetic status. Juvenile Concholepas concholepas live in the intertidal zone and are constantly exposed to temperature fluctuations. Thus, these young individuals are exposed both to thermal risks and the large metabolic costs required to cope with thermal stress. We evaluated the effects of allozyme MLH and SLH on basal (control animals) and induced (stressed animals) levels of the Hsp70 in juveniles C. concholepas. Juveniles (n = 400) were acclimated at 16 °C for 2 weeks; then 100 animals were exposed to 24 °C (stress) and 100 were kept at 16 °C (control) for 2 and 7 days. The variability of 20 loci was analyzed by starch gel electrophoresis. For SLH effects we used 7 polymorphic loci. We quantified expression of Hsp70 by Western blot analyses. Hsp70 expression increased markedly (~ 90%) with temperature. We found a positive association between MLH and basal and induced levels of Hsp70 in the 2-day exposure experiment. Regardless of temperature, Hsp70 levels increased with MLH ( r 2 = 0.7 and 0.9, for basal and induced levels, respectively) reaching maximal levels in juveniles with intermediate and high MLH levels (2 and 3 loci), and decreasing slightly (but not significantly) in juveniles with highest MLH (≥ 4 heterozygous loci). However, after 7 days of exposure to thermal stress, less heterozygous juveniles attained the same levels of Hsp70 than more heterozygous juveniles. Given the faster increment of Hsp70 in C. concholepas juveniles with intermediate-high levels of MLH, these individuals could be less affected by thermal stress in the intertidal zone. We found an association between specific loci genotype and higher Hsp70 levels (basal or induced). In comparison to homozygous juveniles, heterozygous juveniles for several loci showed higher Hsp70. However, these associations were not for the same loci in juveniles exposed to high temperature for 2 and 7 days. This suggests genotypic variation at some allozyme loci could be more important in the period of initial response to high temperature and others can be more important in the response to the chronic temperature stress.

Neoparamoebic gill infections: host response and physiology in salmonids

Amoebic gill diseases (AGD) caused primarily by the amphizoic Neoparamoeba spp. have been identified as significant to fish health in intensive aquaculture. These diseases have consequently received significant attention with regard to disease pathophysiology. Neoparamoeba perurans has been putatively identified as the aetiological agent in salmonids, with other species such as turbot Psetta maxima and sea bass Dicentrarchus labrax also affected. Similarly, Neoparamoeba spp. have also been identified in co‐infections with other gill diseases in salmonids. While infection of the gills results in an acute multifocal hyperplastic host response, reduced gill surface area and increased mucous cell densities, ion regulation and respiration in terms of blood gasses are only marginally affected. This may be partially attributed to reserve respiratory capacity and a reduction in mucous viscosity allowing for a greater flushing of the gill, so reducing the gill mucus boundary layer. Clinical and acute infections result in significant cardiovascular compromise with increases in aortic blood pressure, and systemic vascular resistance in Atlantic salmon, Salmo salar, which are not seen in rainbow Oncorhynchus mykiss and brown trout Salmo trutta. Increases in vascular resistance appear to be due to vascular constriction potentially reducing blood flow to the heart in compromised fishes, the overall effect being to lead to a compensatory tissue remodelling and change in cardiac shape in chronically infected fishes. The combined effect of reduced gill surface area and cardiovascular compromise leads to a significant reduction in swimming performance and increases in the routine metabolic rate that lead to an increase in the overall metabolic cost of disease.

A Bioenergetics Model for Zander: Construction, Validation, and Evaluation of Uncertainty Caused by Multiple Input Parameters

AbstractA bioenergetics model for zander Sander lucioperca was constructed using data from respirometer and feeding experiments to estimate temperature and mass‐specific functions of metabolic and food consumption (C) rates. Other parameters were taken from the literature. The model, together with a previously published model for walleyes S. vitreus (Kitchell et al. 1977) and its modification for zander (Salonen et al. 1996), was validated with independent feeding experiments in the laboratory and was field evaluated in two lakes by using mercury (Hg) as a marker. Both validation procedures gave high modeling efficiency, indicating that the model was able to predict zander C under field conditions. The effect of uncertainty in 29 input parameters on Hg concentration and C was estimated using the Latin hybercube sampling technique (a modified Monte Carlo approach that uses a form of stratified sampling). The simulation results showed that our model was rather insensitive to given uncertainties in input parameters. Parameters in respiration function were responsible for producing the highest uncertainty for C. Parameters in Hg balance model produced the highest uncertainty for Hg concentration. Furthermore, both output variables were sensitive to the activity multiplier, which supported earlier results on the central role of activity in bioenergetics models. The field test of our model with different growth rates and Hg concentrations indicated that in the long term, our experimentally measured routine metabolic rate satisfactorily described the activity of fish in the field. The original walleye model and its revision for zander underestimated zander C relative to the bioenergetics model developed here. Our new model offers a validated tool for estimating C and trophic impact of the zander population.

Effects of Dissolved Oxygen Concentration on Oxygen Consumption and Development of Channel Catfish Eggs and Fry: Implications for Hatchery Management

AbstractEight channel catfish Ictalurus punctatus spawns were split into two similar portions and incubated under controlled conditions to determine the effect of dissolved oxygen (DO) concentration on the development and survival of eggs and fry. The DO concentration was 7.42 ± 0.03 mg/L (mean ± SD; 92.5% saturation) and 18.40 ± 0.28 mg/L (230% saturation) through hatching in the low‐ and high‐oxygen treatments, respectively. Eggs hatched 6 h earlier in the low‐oxygen treatment, but fry reached swim‐up stage 31 h later. Survival to the swim‐up stage in the low‐oxygen treatment was 16.4 percentage points lower than in the high‐oxygen treatment (72.5% versus 88.9%, respectively). The routine metabolic rate and limiting oxygen concentration were also determined for eggs, sac fry, and swim‐up fry. Oxygen consumption increased through swim‐up stage, as expected. However, the limiting oxygen concentration peaked during the last day of incubation at 88.1 ± 2.9% saturation and decreased to 40.1 ± 2.0% saturation upon hatching. Premature hatching observed in the low‐oxygen treatment was apparently initiated when the limiting oxygen concentration approached the ambient oxygen saturation on the last day of incubation. A survey of DO management in 26 commercial catfish hatcheries in the Mississippi Delta revealed that DO saturation in the hatching troughs ranged from 45.2% to 100.2%, with only nine hatcheries (35% of the hatcheries sampled) having a DO saturation greater than 95%. Seventeen hatcheries (65%) had a DO saturation less than that maintained in the low‐oxygen treatment in our hatching experiment and could experience greater mortality through swim‐up than we observed. We recommend that hatcheries initially run well water through a packed column and use blowers or liquid oxygen to maintain the DO concentration in hatching troughs at or above air saturation as eggs near the time of hatching.

Essential fatty acids influence metabolic rate and tolerance of hypoxia in Dover sole (Solea solea) larvae and juveniles

Dover sole (Solea solea, Linneaus 1758) were raised from first feeding on brine shrimp (Artemia sp.) with different contents and compositions of the essential fatty acids (EFA) arachidonic acid (ARA, 20:4n − 6); eicosapentaenoic acid (EPA, 20:5n − 3), and docosahexaenoic acid (DHA, 22:6n − 3), and their metabolic rate and tolerance to hypoxia measured prior to and following metamorphosis and settlement. Four dietary Artemia preparations were compared: (1) un-enriched; (2) enriched with a commercial EFA mixture (Easy DHA SELCO Emulsion); (3) enriched with a marine fish oil combination (VEVODAR and Incromega DHA) to provide a high ratio of ARA to DHA, and (4) enriched with these fish oils to provide a low ratio of ARA to DHA. Sole fed un-enriched Artemia were significantly less tolerant to hypoxia than the other dietary groups. Larvae from this group had significantly higher routine metabolic rate (RMR) in normoxia, and significantly higher O2 partial pressure (PO2) thresholds in progressive hypoxia for their regulation of RMR (Pcrit) and for the onset of agitation, respiratory distress and loss of equilibrium. Metamorphosis was associated with an overall decline in RMR and increase in Pcrit, but juveniles fed on un-enriched Artemia still exhibited higher Pcrit and agitation thresholds than the other groups. Sole fed un-enriched Artemia had significantly lower contents of EFA in their tissues, both before and after settlement. Thus, enriching live feeds with EFA has significant effects on the respiratory physiology of sole early life stages and improves their in vivo tolerance to hypoxia. We found no evidence, however, for any effect of the ratio of ARA to DHA.

Rate of energy depletion and overwintering mortality of juvenile walleye pollock in cold water

The winter energy deficit and mortality of juvenile walleye pollock at extremely cold temperature were examined by field observations and laboratory experiments. In the Doto area, along the northern coast of Japan, juvenile walleye pollock resided on the continental shelf despite extremely cold temperatures (mean 0·4° C) during the latter half of winter (March to April). Measurements of the rate of energy depletion (equivalent to the routine metabolic rate) revealed that juvenile walleye pollock consumed 37% less energy at 0·5° C than at 2·0° C, suggesting an energetic benefit of residence in cold water (<1·0° C) over the shelf during winter. Prior to the starvation experiments, temperatures and ration level in the holding tanks were adjusted to create two different body condition groups of fish. Under the thermal condition of the latter half of winter (0·5° C), fish with a mean condition factor of 0·6 and 0·5 suffered 19·1 and 74·5% mortality, respectively, at the end of the experiments (after 56 days). The residual analysis of total body energy demonstrated that the cause of mortality was mainly associated with the depletion of energy reserves. When a logistic regression model for mortality derived from the experiments was applied to wild fish collected in March, the estimated overwintering mortality in 2004 and 2005 was 25·4 and <2·3%, respectively, assuming no feeding during the winter. Considering that juvenile walleye pollock feed during winter as shown in previous studies, intense overwintering mortality induced by energy depletion is improbable during the latter half of winter in the Doto area.

Effect of acclimation temperature on routine metabolic rate in triploid salmonids

The objective of this research was to determine whether triploid fish differ from diploids in their routine metabolic rates across a range of acclimation temperatures. Sibling diploids and triploids were acclimated to 12, 15 and 18 °C (Atlantic salmon; Salmo salar) and to 9, 12 and 15 °C (brook charr; Salvelinus fontinalis) prior to experimentation. Routine metabolic rates were then determined three times over a two-month period. Triploids of both species had higher metabolic rates than diploids at lower temperatures, and lower metabolic rates than diploids at higher temperatures, demonstrating that triploids have different (i.e., lower) thermal optima than diploids. This likely explains prior observations of high mortality of triploids at chronically elevated, but sub-lethal, rearing temperatures for sibling diploids.

Allometric scaling in centrarchid fish: origins of intra- and inter-specific variation in oxidative and glycolytic enzyme levels in muscle

The influence of body size on metabolic rate, muscle enzyme activities and the underlying patterns of mRNA for these enzymes were explored in an effort to explain the genetic basis of allometric variation in metabolic enzymes. We studied two pairs of sister species of centrarchid fish: black bass (largemouth bass Micropterus salmoides and smallmouth bass Micropterus dolomieui) and sunfish (pumpkinseed Lepomis gibbosus and bluegill Lepomis macrochirus). Our goal was to assess the regulatory basis of both intraspecific and interspecific variation relative to body size, as well as to gain insights into the evolutionary constraints within lineages. Whole animal routine metabolic rate showed scaling coefficients not significantly different from 1, ranging from (+0.87 to +0.96). However, there were significant effects of body size on the specific activities of oxidative and glycolytic enzymes. Mass-specific activity of the oxidative enzyme citrate synthase (CS) scaled negatively with body size in each species, with scaling coefficients ranging from -0.15 to -0.19, whereas the glycolytic enzyme pyruvate kinase (PK) showed positive scaling, with scaling coefficients ranging from +0.08 to +0.23. The ratio of mass-specific enzyme activity in PK to CS increased with body size, whereas the ratio of mRNA transcripts of PK to CS was unaffected, suggesting the enzyme relationships were not due simply to transcriptional regulation of both genes. The mass-dependent differences in PK activities were best explained by transcriptional regulation of the muscle PK gene; PK mRNA was a good predictor of PK specific enzyme activity within species and between species. Conversely, CS mRNA did not correlate with CS specific enzyme activities, suggesting post-transcriptional mechanisms may explain the observed inter-specific and intraspecific differences in oxidative enzymes.

Aerobic metabolic rates of swimming juvenile mako sharks, Isurus oxyrinchus

The shortfin mako shark, Isurus oxyrinchus, is a highly streamlined epipelagic predator that has several anatomical and physiological specializations hypothesized to increase aerobic swimming performance. A large swim-tunnel respirometer was used to measure oxygen consumption (MO2) in juvenile mako sharks (swimming under controlled temperature and flow conditions) to test the hypothesis that the mako shark has an elevated maintenance metabolism when compared to other sharks of similar size swimming at the same water temperature. Specimen collections were conducted off the coast of southern California, USA (32.94°N and 117.37°W) in 2001-2002 at sea-surface temperatures of 16.0–21.0°C. Swimming MO2 and tail beat frequency (TBF) were measured for nine mako sharks [77–107 cm in total length (TL) and 4.4 to 9.5 kg body mass] at speeds from 28 to 54 cm s−1 (0.27–0.65 TL s−1) and water temperatures of 16.5–19.5°C. Standard metabolic rate (SMR) was estimated from the extrapolation to 0-velocity of the linear regression through the LogMO2 and swimming speed data. The estimated LogSMR (±SE) for the pooled data was 2.0937 ± 0.058 or 124 mg O2 kg−1 h−1. The routine metabolic rate (RMR) calculated from seventeen MO2 measurements from all specimens, at all test speeds was (mean ± SE) 344 ± 22 mg O2 kg−1h−1 at 0.44 ± 0.03 TL s−1. The maximum metabolic rate (MMR) measured for any one shark in this study was 541 mg O2 kg−1h−1 at 54 cm s−1 (0.65 TL s−1). The mean (±SE) TBF for 39 observations of steady swimming at all test speeds was 1.00 ± 0.01 Hz, which agrees with field observations of 1.03 ± 0.03 Hz in four undisturbed free-swimming mako sharks observed during the same time period. These findings suggest that the estimate of SMR for juvenile makos is comparable to that recorded for other similar-sized, ram-ventilating shark species (when corrected for differences in experimental temperature). However, the mako RMR and MMR are apparently among the highest measured for any shark species.

Responses to hypoxia and recovery: repayment of oxygen debt is not associated with compensatory protein synthesis in the Amazonian cichlid,Astronotus ocellatus

Oxygen consumption, as an indicator of routine metabolic rate (RoMR), and tissue-specific changes in protein synthesis, as measured by (3)H-labelled phenylalanine incorporation rates, were determined in Astronotus ocellatus to investigate the cellular mechanisms behind hypoxia-induced metabolic depression and recovery. RoMR was significantly depressed, by approximately 50%, when dissolved oxygen levels reached 10% saturation (0.67+/-0.01 mg l(-1) at 28+/-1 degrees C). This depression in RoMR was accompanied by a 50-60% decrease in liver, heart and gill protein synthesis, but only a 30% decrease in brain protein synthesis. During recovery from hypoxia, an overshoot in RoMR to 270% of the normoxic rate was observed, indicating the accumulation of an oxygen debt during hypoxia. This conclusion was consistent with significant increase in plasma lactate levels during the hypoxic exposure, and the fact that lactate levels rapidly returned to pre-hypoxic levels. In contrast, a hyperactivation of protein synthesis did not occur, suggesting the overshoot in oxygen consumption during recovery is attributed to an increase in cellular processes other than protein synthesis.

Comparison of metabolic rates and feed nutrient digestibility in conventional, genetically improved (GIFT) and genetically male (GMNT) Nile tilapia, Oreochromis niloticus (L.)

Various aspects of energy metabolism and feed digestibility were evaluated in two reportedly improved strains of Nile tilapia (Oreochromis niloticus) namely GIFT (genetically improved farmed tilapia) and GMNT (genetically male Nile tilapia) and compared with those of CNT (conventional Nile tilapia). Fish were stocked individually in a computer-controlled respirometer system at 27+/-0.1 degrees C for 10 weeks. Metabolic rates were measured at three different feeding levels: starved, maintenance (3.0 g kg(-0.8) day(-1)) and growth (7.5 g kg(-0.8) day(-1)) using a fishmeal based feed containing TiO2 marker (41% crude protein, 9% crude lipid and 19 kJ (g DM)(-1) gross energy). The standard metabolic rate (SMR), measured at the beginning of the experiment (45.4+/-4.6, 52.4+/-7.7 and 46.8+/-4.6 mg O2 kg(-0.8) h(-1) respectively for GIFT, GMNT and CNT), did not differ significantly between the groups (p<0.05). Similarly, non-significant differences were also observed in the routine metabolic rates under starved, maintenance and growth conditions but the variability was higher in the case of GMNT and CNT than in GIFT. The latter group showed a significantly lower active metabolic rate (145 mg O2 kg(-0.8) h(-1)) compared to GMNT and CNT (232 and 253 mg O2 kg(-0.8) h(-1), respectively) at maintenance feeding level. The specific dynamic action (% offered feed energy) showed no significant differences among the groups. Digestibility coefficients of feed dry matter, protein, lipid and energy for the three tilapia groups also did not differ significantly. Therefore, we concluded that the genetic improvement or modification in the GIFT or GMNT might not upgrade the inherent physiological potential compared to CNT as far as energy metabolism and digestion efficiencies are concerned.

Design and Testing of a Closed, Stirring Respirometer for Measuring Oxygen Consumption of Channel Catfish Eggs

AbstractA closed, stirring respirometer was designed to agitate small egg mass samples of channel catfish Ictalurus punctatus while measuring oxygen consumption by the eggs. Egg mass samples ranging in size from 15 to 46 g were placed on a screen platform above a magnetic stir bar in the respirometer; the degree of agitation was controlled with a magnetic stir plate. Dissolved oxygen (DO) concentration and temperature were measured with a luminescent DO sensor and meter. The respirometer was used to determine routine metabolic rate and limiting oxygen concentration (the presumed hypometabolic transition zone) on egg mass samples from 10 different spawns at 0 to 5 d postfertilization. Routine metabolic rate increased from 4.8 ± 1.3 (0 d postfertilization) to 174.0 ± 7.8 mg O2·kg−1·h−1 (5 d postfertilization). The limiting oxygen concentration increased similarly up to 87.0% ± 2.7% (maximum individual value = 95.9%) air saturation by 5 d postfertilization. The respirometer described could not be used for sac fry, but it proved effective with clumped channel catfish eggs. Preliminary channel catfish hatchery management recommendations are to maintain DO concentrations in hatchery troughs at air saturation at least during the last day of egg development.

The energetic consequence of specific dynamic action in southern bluefin tunaThunnus maccoyii

The effect of feeding on the rate of oxygen consumption (M(O2)) of four groups of three southern bluefin tuna Thunnus maccoyii (SBT) was examined in a large static respirometer at water temperatures of 18.2-20.3 degrees C. Six feeding events of rations between 2.1-8.5% body mass (%M(b)) of Australian sardines (Sardinops neopilchardus) were recorded (two of the groups were fed twice). Before feeding, fish swam between 0.71 and 1.4 body lengths s(-1) (BL s(-1)) and the routine metabolic rate (RMR) was 366+/-32.5 mg kg(-1) h(-1) (mean +/- s.e.m.). For all trials, M(O2) was elevated post feeding, presumably as a result of specific dynamic action (SDA). Swimming velocity was also elevated post feeding for periods similar to that of M(O2) (between 20-45 h, longest for the largest rations). Post feeding swimming velocity increased to between 0.87-2.6 BL s(-1) and was also dependent on ration consumed. It is suggested that the purpose of increased post-feeding swimming velocity was to increase ventilation volume as a response to the enhanced metabolic demand associated with SDA. Peak post-prandial M(O2) increased linearly with ration size to a maximum of 1290 mg kg(-1) h(-1), corresponding to 2.8 times the RMR. When converted to its energy equivalent, total magnitude of SDA was linearly correlated with ration size to a maximum of 192 kJ kg(-1) h(-1), and as a proportion of gross energy ingested (SDA coefficient), it averaged 35+/-2.2%. These results demonstrate that, although the factorial increase of SDA in SBT is similar to that of other fish species, the absolute energetic cost of SDA is much higher. These results support the contention that tuna are energy speculators, gambling high rates of energy expenditure for potentially higher rates of energy returns. The ration that southern bluefin tuna require to equal the combined metabolic costs of SDA and RMR is estimated in this study to be 3.5%M(b) of Australian sardines per day.

Respiration Rates of Eurasian Perch Perca fluviatilis and Ruffe: Lower Energy Costs in Groups

AbstractThe effect of group size on the routine metabolic rate and activity of the two shoaling percids, Eurasian perch Perca fluviatilis and ruffe Gymnocephalus cernuus, was studied by using twin‐flow intermittent respirometry and time‐lapse video techniques. In both species, we found a clear group effect. In isolated fish, oxygen consumption was as much as twice that in groups of eight fish, with intermediate values in groups of four fish. The routine metabolic rate was highest during twilight in both species, irrespective of group size. Eurasian perch consumed more oxygen and were more active during the day than during the night, whereas the oxygen consumption and activity of ruffe were higher during the night than during the day. With increasing group size, the differences between day and night decreased and the diel cycle was less pronounced. Individual fish may benefit from the presence of conspecifics through a calming effect that reduces their energetic costs. We advise that the social behavior of a species be more thoroughly considered when planning behavioral, growth, and respiration experiments. Because bioenergetic model parameters for many species are based on data gained from isolated fish, we conclude that without considering group size the results of bioenergetic modeling may be seriously biased.

The importance of the cost of swimming to the foraging behavior and ecology of larval cod (Gadus morhua) on Georges Bank

Abstract Energy expenditure by larval cod, Gadus morhua , during foraging was quantified based upon laboratory observations of search behavior and measurements of the cost of swimming. A large-volume (250-L) observation system employing stereo-paired video cameras was developed to record foraging behavior in three dimensions, and a respirometry system was developed to measure the cost of swimming of individual larvae. Application of the derived cost of swimming model to activity levels observed within the large observation tank showed that activity was a substantial and variable component of a larval cod's total bioenergetic budget. The estimated routine metabolic rate of the freely swimming larvae was 3.8–5 times greater than the measured basal rate depending upon their activity level. This is greater than the range of routine factorial scopes previously reported for larval fish in general. Future trophodynamic models developed for small marine fish larvae should consider these greater scaling factors when estimating the active metabolic rate of larvae foraging in the ocean. A trophodynamic model for larval cod on Georges Bank was developed incorporating observed foraging behavior, measured swimming costs, and the theoretical effect of turbulence on predator–prey contact rates. This model was used to estimate the prey density required to meet the estimated minimum daily metabolic demand. The estimated nauplius and copepodite concentrations required for the survival of small larvae were within the range of mean homogeneous springtime concentrations observed on Georges Bank. However, for the smallest post-yolk-sac larvae (5 mm), favorable low-turbulence foraging conditions, encountering patches of high prey density, or exploitation of alternative prey sources such as protozoans may be necessary.

Allometry of thermal limitation in the cephalopod Sepia officinalis

Cuttlefish (Sepia officinalis) routine metabolic rate was determined in response to acute thermal changes at a rate of 1 degrees C h(-1) for a variety of animal sizes (15-496 g wet mass, laboratory reared at 15 degrees C). In a thermal frame of 11 to 23 degrees C, oxygen consumption rates (MO(2), in mumol O(2) g(-1) min(-1)) were observed to rise with increasing temperature (T, in degrees C) and to decline with increasing body mass (m, in g), according to the formula: ln MO(2)=-3.3+0.0945T-0.215 ln m (R(2)=0.93). Outside the above thermal window, animals were not able to increase MO(2) at similar rates, indicating a beginning oxygen limitation of metabolism. Large animals (>100 g body mass) already displayed lower than expected MO(2) values at 8 and 26 degrees C, while smaller animals (15 g wet mass) were characterized by a wider thermal window (MO(2) values deviated from expected rates at 5 and 29 degrees C). Morphometric data of cuttlefish mantle skin area was obtained to discuss size - related effects of skin respiration potential on thermal tolerance. Cuttlefish growth was observed to be isometric, as constant 'Vogel numbers' of 4.2 indicated (animal body masses: 11 to 401 g). In the same mass range, specific mantle surface area declined three-fold from 10.7 (0.24) (means+/-SD) to 3.3 (0.52) cm(2) g(-1). Thus, increased thermal tolerance in smaller animals may be enabled by a higher skin respiration potential due to higher specific skin surface areas. An elevated fraction of MO(2) provided by means of skin respiration in small animals could relieve the cardiovascular system, which previously has been found a major limiting component during acute thermal stress in cuttlefish.