Respiration rate and cost of swimming for Antarctic krill,<Emphasis Type="Italic"> Euphausia superba</Emphasis>, in large groups in the laboratory

Constructing realistic energy budgets for Antarctic krill, Euphausia superba, is hampered by the lack of data on the metabolic costs associated with swimming. In this study respiration rates and pleopod beating rates were measured at six current speeds. Pleopod beating rates increased linearly with current speed, reaching a maximum of 6 beats s^–1 at 17 cm s^–1. There was a concomitant linear increase in respiration rate, from 1.8 mg O₂ g_D^–1 h^–1 at 3 cm s^–1 to 8.0 mg O₂ g_D^–1 h^–1 at 17 cm s^–1. The size of the group tested (50, 100 and 300 krill) did not have a significant effect on pleopod beating rates or oxygen consumption (ANCOVA, F=0.264; P>0.05). The cost of transport reached a maximum of 75 J g^–1 km^–1 at 5 cm s^–1, and then decreased with increasing current speed to 29 J g^–1 km^–1. When considered in light of energy budgets for E. superba, these data indicate that the cost of swimming could account for up to 73% of total daily metabolic expenditure during early summer.Communicated by G.F. Humphrey, Sydney     

Temperature and plankton

The relationship between temperature and metabolism was studied in Artic copepods with regard to the concept of metabolic cold adaptation of polar poikilotherms. Temperature tolerance and respiration rates of the dominant copepods Calanus finmarchicus (Gunnerus), C. glacialis (Jaschnov), C. hyperboreus (Krøyer) and Metridia longa (Lubbeck), collected in Fram Strait, Greenland Sea, in July 1983, were studied at different temperatures. Temperature tolerance in the boreal C. finmarchicus was slightly higher than in the three Arctic species. Respiration rates at lower temperatures followed the Arrhenius equation in all species, with values for (temperature characteristics) between 11.05 and 22.95, corresponding to a Q₁₀ between 2.05 and 4.5. This increase in metabolic rate with rising temperature was not related to an increase of swimming activity, as was shown by videoanalysis. Activity was determined as average swimming speed and as frequency of certain locomotor patterns. Average swimming speed remained unchanged at all temperatures and was ca 1 cm s^-1 for all species, when only periods of active swimming were considered. The time spent with active swimming did not change with temperature in M. longa and C. finmarchicus, but decreased in c. glacialis. In C. hyperboreus it increased at 5°C and decreased again at higher temperatures. It is suggested that the increase in oxygen consumption is fully accounted for by the basal metabolism.     

The ecophysiological complex of Bathyporeia pilosa and B. pelagica (Crustacea: Amphipoda). I. Respiration rates

The metabolic rates of high and low shore estuarine populations of Bathyporeia pilosa Lindström and an open coast population of B. pelagica (Bate) have been determined over a range of temperatures during January and February, and June and July, 1968. Changes in oxygen uptake have also been measured monthly at 15°C. During the winter, oxygen uptake was in the order: high shore B. pilosa>low shore B. pilosa>B. pelagica. During the summer, high shore B. pilosa and B. pelagica had similar metabolic rates, but both were significantly higher than low shore B. pilosa. Both populations of B. pilosa had lower metabolic rates in summer than in winter, whereas the metabolic rate of B. pelagica remained much the same. Seasonal changes in metabolic rate are closely correlated with reproductive cycles. The possible influences of environmental parameters are discussed.     

Metabolic rates of juvenile scalloped hammerhead sharks (Sphyrna lewini)

Oxygen consumption of juvenile scalloped hammerhead sharks, Sphyrna lewini, was measured in a Brett-type flume (volume=635 l) to quantify metabolic rates over a range of aerobic swimming speeds and water temperatures. Oxygen consumption (log transformed) increased at a linear rate with increases in tailbeat frequency and swimming speed. Estimates of standard metabolic rate ranged between 161 mg O₂ kg^-1 h^-1 at 21°C and 203 mg O₂ kg^-1 h^-1 at 29°C (mean-SD: 189ᆣ mg O₂ kg^-1 h^-1 at 26°C). Total metabolic rates ranged from 275 mg O₂ kg^-1 h^-1 at swimming speeds of 0.5 body lengths per second (L s^-1) to a maximum aerobic metabolic rate of 501 mg O₂ kg^-1 h^-1 at 1.4 L s^-1. Net cost of transport was highest at slower swimming speeds (0.5-0.6 L s^-1) and was lowest between 0.75 and 0.9 L s^-1. Therefore, these sharks are most energy efficient at swimming speeds between 0.75 and 0.9 L s^-1. These data indicate that tailbeat frequency and swimming speed can be used as predictors of metabolic rate of free-swimming juvenile hammerhead sharks.     

Energetic costs of swarming behavior for the copepod Dioithona oculata

The cyclopoid copepod Dioithona oculata forms dense swarms within shafts of sunlight that penetrate the mangrove prop-root habitat of islands off the coast of Belize. Previous studies, based on in situ video recordings and laboratory studies, have shown that D. oculata is capable of maintaining fixed-position swarms in spite of currents of up to 2 cm s⁻¹. The purpose of this study was to examine the energetic costs of maintaining these swarms, in terms of increased metabolic costs of maintaining position in currents and in terms of reduced feeding rates in densely packed swarms during the day. Using a sealed, variable-speed flow-through chamber, the respiration rates of D. oculata were measured while swarms maintained position in different current speeds. The results indicate that active metabolism (swimming at maximum speed to maintain the swarm in a current) is approximately three times greater than routine metabolism (normal swimming speeds in the absence of currents), indicating a significant metabolic cost of maintaining swarms in the presence of currents. In addition, gut-pigment analysis indicated that feeding rates of these copepods were often reduced in swarms during the day compared to when the copepods were dispersed at night. Given the high “cost” of swarming, the adaptive value of swarming in terms of reduced predation, increased opportunities for mating, and reduced dispersal, must be substantial. Received: 4 June 1997 / Accepted: 18 September 1997     

Swimming performance of three southwest Pacific fishes

The logarithm of stamina for each of Sardinops sagax (4 to 6 600 s), Scomber japonicus peruanus (16 to 27 000 s) and Odontestes regia (7 to 9 900 s), adjusted to a length of 10 cm, decreased linearly over swimming speeds of 31 to 82, 25 to 78 and 24 to 75 cm s^-1, respectively (19°C). The regression coefficient was -0.064 for both S. j. peruanus and O. regia and -0.049 for S. sagax. Critical swimming speed (60 min, 5 cm s^-1) for S. sagax (10cm), 32 cm s^-1, is within the range found for other species of similar length. The suggestion of a change in regression coefficient as swimming speed increased from prolonged to burst (Brett, 1964) was not supported by the results of this study.     

Relationship of oxygen consumption to swimming speed in Euphausia pacifica

Swimming efficiency (the ratio of thrust power required to overcome hydrodynamic drag to net metabolic energy expenditure) was calculated for the vertically migrating euphausiid Euphausia pacifica swimming at speeds of 1–20 cm s^–1 and at temperatures of 8° and 12°C. Efficiencies ranged from 0.014 to 2.8% at 8°C and 0.009 to 1.69% at 12°C. A comparison with efficiency in fishes 2–3 orders of magnitude larger in weight (efficiency range 10–25%) indicates that locomotion in E. pacifica is far less efficient, a probable result of the organism's small size (x=33.5 mg WW) and multiple-paddle mode of propulsion. Net cost of transport of E. pacifica is three to six times the cost of a hypothetical value for sockeye salmon. Low swimming efficiencies in zooplankton such as E. pacifica are responsible for the underestimation of zooplankton swimming costs. Multiple-paddle propulsion is less efficient than the undulatory mode of fishes.     

Tail beat frequency as a predictor of swimming speed and oxygen consumption of saithe (<Emphasis Type="Italic">Pollachius virens</Emphasis>) and whiting (<Emphasis Type="Italic">Merlangius merlangus</Emphasis>) during forced swimming

Oxygen consumption and tail beat frequency were measured on saithe (Pollachius virens) and whiting (Merlangius merlangus) during steady swimming. Oxygen consumption increased exponentially with swimming speed, and the relationship was described by a power function. The extrapolated standard metabolic rates (SMR) were similar for saithe and whiting, whereas the active metabolic rate (AMR) was twice as high for saithe. The higher AMR resulted in a higher scope for activity in accordance with the higher critical swimming speed (U _crit) achieved by saithe. The optimum swimming speed (U _opt) was 1.4 BL s⁻¹ for saithe and 1.0 BL s⁻¹ for whiting with a corresponding cost of transport (COT) of 0.14 and 0.15 J N⁻¹ m⁻¹. Tail beat frequency correlated strongly with swimming speed as well as with oxygen consumption. In contrast to swimming speed and oxygen consumption, measurement of tail beat frequency on individual free-ranging fish is relatively uncomplicated. Tail beat frequency may therefore serve as a predictor of swimming speed and oxygen consumption of saithe and whiting in the field.     

Aerobic metabolic rates of swimming juvenile mako sharks, <Emphasis Type="Italic">Isurus oxyrinchus</Emphasis>

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.     

Comparative thermal metabolic patterns in Euterpina acutifrons dimorphic males

Thermal metabolic acclimation patterns have been determined for cold-and warm-acclimated dimorphic males of the copepod Euterpina acutifrons. The copepods were acclimated either to 15° or 25°C. Metabolic measurements were made at the two acclimation temperatures. At 25 °C, the small males had a higher rate than the large ones. At 15 °C, the large males had the higher rate. The metabolic pattern of thermal acclimation is also distinctive in the two forms. Small males showed metabolic adaptation at the lower acclimation temperature (15 °C), but not at the higher acclimation temperature (25 °C). In the large males the acclimation patterns were reversed, i. e., these males acclimated at the higher temperature, not at the lower. The acclimation patterns based on Precht's (1958) scheme of acclimation are entirely different in the two forms.Supported by PHS grant 5-SO5-FR-07070-02.     

Critical swimming speeds of late-stage coral reef fish larvae: variation within species,among species and between locations

The swimming abilities of larval fishes are important for their survival, potentially affecting their ability to avoid predators, obtain food and control dispersal patterns. Near settlement swimming abilities may also influence spatial and temporal patterns of recruitment. We examined Critical speed (U-crit) swimming ability in late stage larvae of 89 species of coral reef fishes from the Great Barrier Reef and the Caribbean. Coefficients of variation in U-crit calculated at the individual level were high (28.4%), and this was not explained by differences in size or condition factor of these same larvae. Among species U-crit ranged from 5.5 cm s⁻¹ to 100.8 cm s⁻¹ (mean=37.3 cm s⁻¹), with 95% of species able to swim faster than the average current speed around Lizard Island, suggesting that most species should be capable of influencing their spatial and temporal patterns of settlement. Inter-specific differences in swimming ability (at both the family and species levels) were significantly correlated with size and larval morphology. Correlations were found between swimming performance and propulsive area, fineness ratio and aspect ratio, and these morphological parameters may prove useful for predicting swimming ability in other taxa. Overall, the swimming speeds of larvae from the same families at the two locations were relatively similar, although the Lutjanidae and Acanthuridae from the Caribbean were significantly slower than those from the great barrier reef. Differences in swimming speed and body form among late stage larvae suggests that they will respond differently to factors influencing survival and transport during their pelagic phase, as well as habitat use following settlement.     

In situ ontogeny of behaviour in pelagic larvae of three temperate, marine, demersal fishes

The ontogeny of behaviour relevant to dispersal was studied in situ with reared pelagic larvae of three warm temperate, marine, demersal fishes: Argyrosomus japonicus (Sciaenidae), Acanthopagrus australis and Pagrus auratus (both Sparidae). Larvae of 5–14 mm SL were released in the sea, and their swimming speed, depth and direction were observed by divers. Behaviour differed among species, and to some extent, among locations. Swimming speed increased linearly at 0.4–2.0 cm s⁻¹ per mm size, depending on species. The sciaenid was slower than the sparids by 2–6 cm s⁻¹ at any size, but uniquely, it swam faster in a sheltered bay than in the ocean. Mean speeds were 4–10 body lengths s⁻¹. At settlement size, mean speed was 5–10 cm s⁻¹, and the best performing individuals swam up to twice the mean speed. In situ swimming speed was linearly correlated (R ²=0.72) with a laboratory measure of swimming speed (critical speed): the slope of the relationship was 0.32, but due to a non-zero intercept, overall, in situ speed was 25% of critical speed. Ontogenetic vertical migrations of several metres were found in all three species: the sciaenid and one sparid descended, whereas the other sparid ascended to the surface. Overall, 74–84% of individual larvae swam in a non-random way, and the frequency of directional individuals did not change ontogenetically. Indications of ontogenetic change in orientated swimming (i.e. the direction of non-random swimming) were found in all three species, with orientated swimming having developed in the sparids by about 8 mm. One sparid swam W (towards shore) when <10 mm, and changed direction towards NE (parallel to shore) when >10 mm. These results are consistent with limited in situ observations of settlement-stage wild larvae of the two sparids. In situ, larvae of these three species have swimming, depth determination and orientation behaviour sufficiently well developed to substantially influence dispersal trajectories for most of their pelagic period.     

Effects of current speed on filtration during suspension feeding in Oligometra serripinna (Echinodermata: Crinoidea)

Suspension feeding by the crinod Oligometra serripinna was studied at Lizard Island, Australia, in 1986. Video recordings were made of 90-m particles interacting with the filter of the crinoid in a laboratory flow chamber. A complete census of particles was possible because both the capture event and the filter area could be defined unequivocally. Also, because O. serripinna is a passive suspension feeder, a census of partcles could be made at different ambient current speeds without interference due to active pumping by the crinoid. Experiments were run at seven current speeds from 0.9 to 13.3 cm s^-1. Particles approaching the filter: (1) were captured, (2) passed through the filter without triggering a capture event, (3) passed through the filter after escaping from an unsuccessful capture event, or (4) were deflected around the filter. With increasing current speed, the proportion of deflections declined and the proportion of particles passing through rose: these results could be partially explained by the progressive widening of the spaces within the filter due to distortion of filter parts by the current. The proportion of captures (normalized to approaches) was comparatively low at 0.9 cm s^-1, rose to a relatively constant maximum from 1.7 to 6.4 cm s^-1, and then declined progressively at 9.5 and 13.3 cm s^-1. These proportions were translated into capture rates for whole crinoids by taking into consideration both the encounters with particles and the reduction of filter area by distortion of body parts at higher speeds. When plotted against current speed, capture rate peaked at 6.4 cm s^-1, which was close to the mean current speed that we measured on the reef in the microhabitat of O. serripinna.     

Energetics of underwater swimming in the great cormorant (Phalacrocorax carbo sinensis)

Resting metabolic rate (RMR), energy requirements and body core temperature were measured during underwater swimming in great cormorants (Phalacrocorax carbo sinensis) at the zoological garden in Neumünster, Germany, using gas respirometry and stomach temperature loggers. We used a 13 m long still water canal equipped with a respiration chamber at each end. Birds swam voluntarily in the canal at a mean speed of 1.51 ms^-1. Power input during underwater swimming averaged 31.4 W kg^-1. Minimal costs of transport of 19.1 J kg^-1 m^-1 were observed at a speed of 1.92 m s^-1. Body core temperature was stable in all birds within the first 60 min spent in the canal. After that, body temperature dropped at a rate of 0.14°C min^-1 until the birds voluntarily left the water. Our data indicate that great cormorants spend 2.7 times more energy than Adélie penguins (Pygoscelis adeliae) during underwater swimming. This can be essentially attributed to their poor insulation, their mode of locomotion underwater and differences in streamlining. RMR on land was related to body mass via VO₂=0.691 M^0.755 (where VO₂ is O₂-consumption in litre h^-1 and M is body mass in kg). In order to quantify the effects of external devices on energy consumption during underwater swimming, we tested a dummy data logger attached to the back of the cormorants as well as a ring on the leg. The ring had no apparent influence on the swimming energetics of the cormorants. In birds equipped with dummy loggers, swimming speed was not significantly influenced, but both power input and costs of transport increased by a mean of 19% for swimming speeds between 1.4 and 1.8 m s^-1.     

Effect of hatching time on larval mortality and survival of the prawn Macrobrachium idae

The prawn Macrobrachium idae Heller carries 40 to 160 eggs depending upon the body size of the mother animal. After incubation, 63, 35 and 2% eggs are hatched on the first, second and third hatching nights, respectively. Mean dry weight of a single larva relased on the first night is 420 g (equivalent to 2.86 cal). Larvae released on the second or third hatching nights weighed 380 g (=2.56 cal) or 308 g (=2.02 cal). The total reserve yolk-energy available in a larva hatched on the first night is 1 cal. There is a definite shift from protein to fat metabolism as hatching is delayed. Oxygen consumption of developing eggs awaiting release on the first or second hatching night is 1.9 l/mg dry weight/h. In comparison to larvae released on the first night, those released on the second night exhibit 2% increase in total body-length and 2.4 or 14.3% decrease in the lengths of the 6th abdominal segment or the orbit. Larvae released on the first, second or third hatching nights, on exposure to starvation stress, survive for 3.8, 2.3 or 1.5 days. The swimming speed of larvae released on the first or second night is 1.0 or 0.6 cm/sec. Larvae released on the subsequent hatching nights committed nearly 2 times greater number of mistakes per cm distance in the horizontal plane. Since hatching of all developing eggs simultaneously on the first hatching night is possible by means of artificial technique(s), it is possible to improve survival rate of decapod larvae.     

Behaviour that influences dispersal and connectivity in the small,young larvae of a reef fish

Determining the scale of larval dispersal and population connectivity in demersal fishes is a major challenge in marine ecology. Historically, considerations of larval dispersal have ignored the possible contributions of larval behaviour, but we show here that even young, small larvae have swimming, orientation and vertical positioning capabilities that can strongly influence dispersal outcomes. Using young (11–15 days), relatively poorly developed (8–10 mm), larvae of the pomacentrid damselfish, Amblyglyphidodon curacao (identified using mitochondrial DNA), we studied behaviour relevant to dispersal in the laboratory and sea on windward and leeward sides of Lizard Island, Great Barrier Reef. Behaviour varied little with size over the narrow size range examined. Critical speed was 27.5 ± 1.0 cm s⁻¹ (30.9 BL s⁻¹), and in situ speed was 13.6 ± 0.6 cm s⁻¹. Fastest individuals were 44.6 and 25.0 cm s⁻¹, for critical and in situ speeds, respectively. In situ speed was about 50% of critical speed and equalled mean current speed. Unfed larvae swam 172 ± 29 h at 8–10 cm s⁻¹ (52.0 ± 8.6 km), and lost 25% wet weight over that time. Vertical distribution differed between locations: modal depth was 2.5–5.0 and 10.0–12.5 m at leeward and windward sites, respectively. Over 80% of 71 larvae observed in situ had directional swimming trajectories. Larvae avoided NW bearings, with an overall mean SE swimming direction, regardless of the direction to nearest settlement habitat. Larvae made smaller changes between sequential bearings of swimming direction when swimming SE than in other directions, making it more likely they would continue to swim SE. When swimming NW, 62% of turns were left (more than in other directions), which would quickly result in swimming direction changing away from NW. This demonstrates the larvae knew the direction in which they were swimming and provides insight into how they achieved SE swimming direction. Although the cues used for orientation are unclear, some possibilities seemingly can be eliminated. Thus, A. curacao larvae near Lizard Island, on average swam into the average current at a speed equivalent to it, could do this for many hours, and chose different depths in different locations. These behaviours will strongly influence dispersal, and are similar to behaviour of other settlement-stage pomacentrid larvae that are older and larger.     

Life in a warm deep sea: routine activity and burst swimming performance of the shrimp<Emphasis Type="Italic"> Acanthephyra eximia</Emphasis> in the abyssal Mediterranean

Measurements of routine swimming speed, tail-flip escape responses, and oxygen consumptions were made of the deep-sea shrimp Acanthephyra eximia using autonomous landers in the Rhodos Basin at depths of up to 4,400 m and temperatures of 13–14.5°C. Routine swimming speeds at 4,200 m averaged 0.18 m s^–1 or 3.09 body lengths s^–1, approximately double those of functionally similar oceanic scavengers. During escape responses peak accelerations of 23 m s^–2 or 630.6 body lengths s^–2 were recorded, with animals reaching speeds of 1.61 m s^–1 or 34.8 body lengths s^–2. When compared to shallow-water decapods at similar temperatures these values are low for a lightly calcified shrimp such as A. eximia despite a maximum muscle mass specific power output of 90.0 W kg^–1. A preliminary oxygen consumption measurement indicated similar rates to those of oceanic crustacean scavengers and shallower-living Mediterranean crustaceans once size and temperature had been taken into account. These animals appear to have high routine swimming speeds but low burst muscle performances. This suite of traits can be accounted for by high competition for limited resources in the eastern Mediterranean, but low selective pressure for burst swimming due to reductions in predator pressure.Communicated by J.P. Thorpe, Port Erin     

Foraging behavior in early Atlantic cod larvae (Gadus morhua) feeding on a protozoan (Balanionsp.) and a copepod nauplius (Pseudodiaptomussp.)

Food limitation is likely to be a source of mortality for fish larvae in the first few weeks after hatching. In the laboratory, we analyzed all aspects of foraging in cod larvae (Gadus morhua Linnaeus) from 5 to 20 d post-hatching using protozoa (Balanion sp.) and copepod nauplii (Pseudodiaptomus sp.) as prey. A camera acquisition system with two orthogonal cameras and a digital image analysis program was used to observe patterns of foraging. Digitization provided three-dimensional speeds, distances, and angles for each foraging event, and determined prey and fish larval head and tail positions. Larval cod swimming speeds, perception distances, angles, and volumes increased with larval fish size. Larval cod swam in a series of short intense bursts interspersed with slower gliding sequences. In 94% of all foraging events prey items were perceived during glides. Larval cod foraging has three possible outcomes: unsuccessful attacks, aborted attacks, and successful attacks. The percentage of successful attacks increased with fish size. In all larval fish size classes, successful attacks had smaller attack distances and faster attack speeds than unsuccessful attacks. Among prey items slowly swimming protozoans were the preferred food of first-feeding cod larvae; larger larvae had higher swimming speeds and captured larger, faster copepod nauplii. Protozoans may be an important prey item for first-feeding larvae providing essential resources for growth to a size at which copepod nauplii are captured. Received: 20 April 1999 / Accepted: 12 January 2000     

A laboratory study of predation by Aurelia aurita on larval herring (Clupea harengus): Experimental observations compared with model predictions

Predation by the medusa Aurelia aurita L. on early first-feeding stage larvae of the herring clupea harengus L. was studied in the laboratory. The medusae were captured in Loch Etive, Scotland. Herring larvae were reared from the extificially fertilized eggs of spawning Clyde herring caught in March, 1982. Swimming speeds, volume searched”, capture efficiency and predation rates increased as medusa size increased. Predation rates on fish larvae increased with prey density, but appeared to approach a maximum at high prey densities; in 1 h experiments, a maximum rate of predation of 6.64 larvae h^-1 was estimated by fitting an Ivlev function. A model to predict predation rates was constructed from swimming speeds, sizes and densities of medusae and larvae, and capture efficiency. The rates of predation predicted from the model fell within the range of experimental data, but tended to underestimate rates and did not account for saturation of medusae. Swimming patterns of medusae changed after prey capture: (a) before capture, encounter rates were low and medusae were relatively less active; (b) after capture of 1 larva, encounter rates doubled, with the stimulated medusae exhibiting increased activity and an aftered “searching” path; and (c) after capture of many larvae, swimming speeds and encounter rates of medusae decreased.     

Activity and metabolism of larval Atlantic cod (Gadus morhua) from Scotian Shelf and Newfoundland source populations

Patterns of activity and metabolism were investigated in larval Atlantic cod (Gadus morhua L.) between December 1991 and July 1992: (1) throughout larval development; (2) between two genetically discrete populations (Scotian Shelf and Newfoundland) and (3) as a function of two different culture temperatures. During the yolk-sac stage (0 to 5 d post-hatch), changes in swimming speed were not related to mass-specific metabolic rates; no portion of the mass-specific oxygen consumption could be explained by changes in activity. In the mixed feeding stage (6 to 14 d posthatch), there was a tendency for oxygen consumption to be related to changes in swimming speed. In the exogenous feeding stage (>14 d post-hatch), oxygen consumption significantly increased with swimming speed. These ontogenetic patterns of activity and metabolism were the same for larvae from the Scotian Shelf and Newfoundland populations. However, over the entire larval life and among ontogenetic stages, the metabolic cost of activity (mass-specific O₂ consumption/swimming speed) of Scotian Shelf larvae was significantly higher than that of Newfoundland larvae. When cod larvae, that had developed at 5°C, were acutely exposed to 10°C, Scotian Shelf larvae had a higher intrinsic cost of activity than Newfoundland larvae, over the entire larval life. During the exogenous feeding stage, the mean metabolic cost of activity for Newfoundland larvae raised at 10°C and tested at 10°C was significantly higher and more variable than that of larvae raised at lower temperatures. However, the metabolic cost of activity of larvae raised and tested at 10°C was not significantly different between source populations. Together these findings suggest that differences in swimming energetics reflect changing energy requirements for activity among ontogenetic stages, and reflect adaptation to regional environments among genetically discrete populations.