Über den Einfluß der Nahrungskonzentration und anderer Faktoren auf Filtrierleistung und Nahrungsausnutzung der Muscheln Arctica islandica und Modiolus modiolus

Filtration rates and the extent of phagocytosed food particles were determined in the offshore lamellibranchs Artica islandica and Modiolus modiolus in relation to particle concentration, body size and temperature. Pure cultures of the algae Chlamydomonas sp. and Dunaliella sp. were used as food. A new method for determining filtration rates was developed by modifying the classical indirect method. The concentration of the experimental medium (100%) was kept constant to ±1%. Whenever the bivalves removed algae from the medium, additional algae were added and the filtration rate of the bivalves expressed in terms of percentage amount of algae added per unit time. The concentration of the experimental medium was measured continuously by a flow colorimeter. By keeping the concentration constant, filtration rates could be determined even in relation to different definite concentrations and over long periods of time. The amount of phagocytosed food was measured by employing the biuret-method (algae cells ingested minus algae cells in faeces). Filtration rates vary continuously. As a rule, however, during a period of 24 h, two phases of high food consumption alternate with two phases of low food consumption during which the mussels' activities are almost exclusively occupied by food digestion. Filtration rate and amount of phagocytosed algae increase with increasing body size. Specimens of A. islandica with a body length of 33 to 83 mm filter between 0.7 to 71/h (30–280 mg dry weight of algae/24 h) and phagocytose 21 to 122 mg dry weight of algae during a period of 24 h. The extent of food utilization declines from 75 to 43% with increasing body size. In M. modiolus of 40 to 88 mm body length, the corresponding values of filtration rate and amount of phagocytosed algae range between 0.5 and 2.5 l/h (20–100 mg dry weight of algae) and 17 to 90 mg dry weight of algae, respectively; the percentage of food utilization does not vary much and lies near 87%. Filtration rate and amount of phagocytosed algae follow the allometric equation y=a·x ^b. In this equation, y represents the filtration rate (or the amount of phagocytosed algae), a the specific capacity of a mussel of 1 g soft parts (wet weight), x the wet weight of the bivalves' soft parts, and b the specific form of relationship between body size and filtration rate (or the amount of phagocytosed algae). The values obtained for b lie within a range which indicates that the filtration rate (or the amount of phagocytosed algae) is sometimes more or less proportional to body surface area, sometimes to body weight. Temperature coefficients for the filtration rate are in Arctica islandica Q₁₀ (4°–14°C)=2.05 and Q₁₀ (10°–20°C)=1.23, in Modiolus modiolus Q₁₀ (4°–14°C)=2.33 and Q₁₀ (10°–20°C)=1.63. In A. islandica, temperature coefficients for the amount of phagocytosed algae amount to Q₁₀ (4°–14°C)=2.15 and Q₁₀ (10°–20°C)=1.55, in M. modiolus to Q₁₀ (4°–14°C)=2.54 and Q₁₀ (10°–20°C)=1.92. Upon a temperature decrease from 12° to 4°C, filtration rate and amount of phagocytosed algae are reduced to 50%. At the increasing concentrations of 10×10⁶, 20×10⁶ and 40×10⁶ cells of Chlamydomonas/l offered, filtration rates of both mollusc species decrease at the ratios 3:2:1. At 12°C, pseudofaeces production occurs in both species in a suspension of 40×10⁶, at 20°C in 60×10⁶ cells of Chlamydomonas/l. At 12°C and 10–20×10⁶ cells of Chlamydomonas/l, the maximum amount of algae is phagocytosed. At 40×10⁶ cells/l, the amount of phagocytosed cells is reduced by 26% as a consequence of low filtration rates and intensive production of pseudofaeces. At 20°C and 20–50×10⁶ cells of Chlamydomonas/l, the maximum amount of algae is sieved out and phagocytosed; the concentration of 10×10⁶ cells/l is too low and cannot be compensated for by increased activity of the molluscs. With increasing temperatures, the amount of suspended matter, allowing higher rates of filtration and food utilization, shifts toward higher particle concentrations; but at each temperature a threshold exists, above which increase in particle density is not followed by increase in the amount of particles ingested. Based on theoretical considerations and facts known from literature, 7 different levels of food concentration are distinguishable. Experiments with Chlamydomonas sp. and Dunaliella sp. used as food, reveal the combined influence of particle concentration and particle size on filtration rate. Supplementary experiments with Mytilus edulis resulted in filtration rates similar to those obtained for M. modiolus, whereas, experiments with Cardium edule, Mya arenaria, Mya truncata and Venerupis pullastra revealed low filtration rates. These species, inhabiting waters with high seston contents, seem to be adapted to higher food concentrations, and unable to compensate for low concentrations by higher filtration activities. Adaptation to higher food concentrations makes it possible to ingest large amounts of particles even at low filtration rates. Suspension feeding bivalves are subdivided into four groups on the basis of their different food filtration behaviour.     

Metabolic responses of the sympagic amphipodsGammarus wilkitzkii andOnisimus glacialis to acute temperature variations

Acutely elevated seawater temperatures had pronounced metabolic effect on the Arctic under-ice amphipodsGammarus wilkitzkii andOnisimus glacialis, collected in May 1986 and 1988 in the Barents Sea. An increased rate of oxygen consumption vs temperature was observed for both species. In the range from 0° to 10 °CG. wilkitzkii andO. glacialis exhibit Q₁₀ values of 3.4 and 3.6, respectively. The results also indicate increased ammonia excretion rates forG. wilkitzkii andO. glacialis by an elevation of temperature from 0° to 10°C, with an overall Q₁₀ of 1.9 and 2.3, respectively. The present study demonstrates an increased O:N ratio with ambient temperature elevation from 0° to 10°C forG. wilkitzkii andO. glacialis, with overall Q₁₀ values of 2.0 and 1.6, respectively. This indicates a temperature-induced change in the metabolic substrate towards lipids.     

Oxygen consumption of midwater fishes and crustaceans from the eastern Gulf of Mexico

Oxygen consumption was measured as a function of temperature, oxygen partial-pressure (P_O2)and species depth of occurrence for twenty-three species of midwater fishes and crustaceans collected from the eastern Gulf of Mexico from June 1981 to July 1985. Q₁₀s (7° to 20°C) of 3.90 and 3.24 were recorded for myctophid and non-myctophid fish groups, respectively, while values of 2.22, 2.19, 2.19 and 2.54 were calculated for sergestid, penaeid, carid and euphausiid crustacean groups, respectively. Q₁₀s were consistent for species within each group. All of the species tested regulated their oxygen consumption to P_O2levels normally encountered within the eastern Gulf. Values of critical partial pressure (P_c) ranged from 20 to 40mm Hg and increased slightly with increasing temperature and respiration rate. Declining respiration with increasing minimum depth of occurrence was primarily a function of temperature alone. Changes in size, dry weight and water content contributed only a small fraction to the observed decrease. This finding contrasts with studies from the eastern Pacific Ocean, where temperature is a minor contributor to changes in respiration rate with depth.     

Metabolic maintenance costs of the suspension feeder Styela plicata

The bioenergetic basis of the biannual reproductive cycle of the solitary tunicate Styela plicata was investigated in order to evaluate hypotheses concerning the lack of larval settlement in summer. The rate of ingestion and absorption efficiency were measured in order to provide an estimate of the rate at which material was made available for maintenance, growth, and reproduction. At a given temperature the rate of ingestion was proportional to the 0.7 power of wet mass. the ingestion rate increased rapidly with increasing temperature between 12° and 18°C (Q₁₀3), but was independent of temperature between 18° and 28°C. Absorption efficiency was independent of temperature and body size and averaged approximately one-third for both carbon and nitrogen. Metabolic maintenance costs were estimated from measurements of oxygen consumption and excretion of ammonia and urea reported for s. plicata. These require only 18±11% of the carbon and 37±22% of the nitrogen absorbed from the gut of S. plicata over the temperature range 12° to 28°C. Metabolic maintenance makes no excessive demands on the material absorbed in the gut at a particular time of year, and a surplus of carbon and nitrogen substrate is available throughout the year for growth and reproduction. Predation on larvae and young adults may be responsible for the low rate of settlement observed in summer months.     

Influence of temperature changes on oxygen uptake and ammonia and phosphate excretion,in relation to body size and weight,in Oikopleura dioica (Appendicularia)

The relationship between the rates of oxygen consumption, ammonia and phosphate excretion of a pelagic tunicate, the larvacean Oikopleura dioica Fol, 1872 were assessed as a function of size, dry weight and ash-free dry weight at 15°, 20° and 24°C. O. dioica has higher respiration and excretion rates than copepods of similar weight, but the weight exponent of the allometric power function: Y=aX ^b is similar to that of other poikilotherms. Temperatures above 20°C have a depressing effect on respiration and ammonia excretion. 90% of the variance in metabolic rates is explainable by body mass and temperatures Q₁₀ values for oxygen consumption, ammonia and phosphate excretion, respectively, are 2.45, 1.86 and 1.75 between 15° and 20°C, and 3.75, 2.90 and 3.60 between 20° and 24°C. Metabolic quotients (O:N, O:P, N:P) indicate a protein-oriented diet. The results of this study suggest weak metabolic regulation in O. dioica, an energetic strategy which allows an immediate response to favourable changes in feeding conditions.     

Temperature preference and tolerance,and oxygen consumption of the marbled rockfish,Sebastiscus marmoratus

Behavioral and metabolic responses of the marbled rockfish, Sebastiscus marmoratus (Cuvier), to temperature were measured to define optimal thermal habitat. Preferred temperature was determined by means of a newly developed horizontal temperature-gradient tank. Acclimation temperature had a direct positive effect on critical thermal maxima and minima and upper lethal temperatures but no effect on final preferred temperature. It was indicated that upper temperature tolerance and final preferred temperature of the marbled rockfish were closely connected. Oxygen consumption rate increased with temperature to 23°C but Q ₁₀ (the increase in rate caused by 10°C increase in temperature) declined above 20°C. The maximum Q ₁₀ (4.69) occurred between 15 and 20°C. The final preferred temperature of 20.7 ± 1.5 °C corresponded well to the temperature at which increase in oxygen consumption rate with temperature gradually lessened, approximately 20°C.     

Comparative studies on the metabolism of shallow-water and deep-sea marine fishes. II. Red-muscle metabolism in shallow-water fishes

Maximal rates of oxygen consumption in vitro have been measured under standardized conditions at three test temperatures (5°, 15°, 25°C) on minced preparations of red muscle from 10 species of shallow-water marine teleost fishes. These fishes came from three different geographic areas, two with cool average water temperatures (near 15°C: coastal southern California, Galápagos Islands) and one with warm average water temperatures (near 25°C: Hawaiian Islands). The group is made up of post-juvenile or adult epipelagic fishes, which are moderately or very active in terms of their locomotor activities. A large part of the range of phylogenetic diversity among the teleosts is represented, as is the body weight range from a few grams to several kilograms. The purpose of the work is to provide part of a set of tissue-metabolism data on shallow-water fishes for future comparison with similar results from deep-sea species. Of 8 complete curves for oxygen uptake rate versus temperature (R-T curves), 6 are normal in shape (Q₁₀1.5), 1 is normal but with a low Q₁₀, and 1 is partly flat, partly normal. The differences between the species in terms of both absolute positions and slopes of the R-T curves are not related in any consistent way to any of the three testable variables: phylogenetic position, long-term adaptation temperature, and body size. The red muscles of a variety of adult epipelagic fishes, at ecologically realistic temperatures, are shown to be exceptions to the general rule that tissues of ectothermous lower vertebrates have lower metabolic rates than comparable tissues of non-torpid endothermous higher vertebrates. This circumstance probably is a major factor in the great capacities for sustained high-speed swimming shown by most epipelagic fishes. Other physiological and ecological implications of the results are discussed.     

Daily energy requirements and trophic positioning of the sand shrimp<Emphasis Type="Italic"> Crangon septemspinosa</Emphasis>

Sand shrimp, Crangon septemspinosa Say, are important to the trophic dynamics of coastal systems in the northwestern Atlantic. To evaluate predatory impacts of sand shrimp, daily energy requirements (J ind.^–1 day^–1) were calculated for this species from laboratory estimates of energy losses due to routine (R_R), active (R_A), and feeding (R_SDA) oxygen consumption rates (J ind.^–1 h^–1), coupled with measurements of diel motile activity. Shrimp used in this study were collected biweekly from the Niantic River, Connecticut (41°33N; 72°19W) during late spring and summer of 2000 and 2001. The rates of shrimp energy loss due to R_R and R_A increased exponentially with increasing temperature, with the magnitude of increase greater between 6°C and 10°C (Q₁₀=3.01) than between 10°C and 14°C (Q₁₀=2.85). Rates of R_R doubled with a twofold increase in shrimp mass, and R_SDA was 0.130 J h^–1+R_R, irrespective of shrimp body size. Shrimp motile activity was significantly greater during dark periods relative to light periods, indicating nocturnal behavior. Nocturnal activity also increased significantly at higher temperatures, and at 20°C shifted from a unimodal to a bimodal pattern. Laboratory estimates of daily metabolic expenditures (1.7–307.4 J ind.^–1 day^–1 for 0.05 and 1.5 g wet weight shrimp, respectively, between 0°C and 20°C) were combined with results from previous investigations to construct a bioenergetic model and make inferences regarding the trophic positioning of C. septemspinosa. Bioenergetic model estimates indicated that juvenile and adult shrimp could meet daily energy demands via opportunistic omnivory, selectively preying upon items of high energy content (e.g. invertebrate and fish tissue) and compensating for limited prey availability by ingesting readily accessible lower energy food (e.g. detritus and plant material).Electronic Supplementary Material Supplementary material is available in the online version of this article at Communicated by J.P. Grassle, New Brunswick     

Temperature adaptation in sea anemones: Physiological and biochemical variability in geographically separate populations of Metridium senile

Latitudinally separate populations of the sea anemone Metridium senile (L.) are very similar genetically by electrophoretic criteria, yet respond differently to temperature. Anemones from southern and northern California (USA) have different oxygen consumption patterns in response to acclimatory and acute changes in temperature. Northern anemones show a pronounced increase in Q₁₀ at temperatures just above the normal environmental range, but southern anemones do not. The two populations also differed in the extent of metabolic compensation to temperature following several weeks of acclimation. This acclimation regime resulted in changes in the activities of several enzymes of intermediary metabolism, yet the extent and direction of these changes did not display a consistent trend with regard to acclimation temperature or population. The biochemical concomitants of acclimatory and acute temperature effects were studied further by measuring the concentrations of adenylates (ATP, ADP, and AMP) in anemones from the two populations exposed to different temperature regimes. During cold acclimation for several weeks, total adenylate concentrations (A_T) increased in both the southern and northern populations, possibly due to metabolic rate compensation, since A_T is positively correlated with tissue metabolic rate in many species. Moreover, the extremely low weight-specific oxygen consumption rates of M. senile are probably related to its very low A_T values. Acute temperature decreases had no effect on adenylate concentrations and adenylate energy charge (AEC); in contrast, acute temperature increases led to large changes in adenylate concentrations. The effects of starvation on adenylate concentrations are pronounced, and the effect is temperature-dependent. In starved individuals held at 20°C, AEC values fell to 50% of normal values after 8 d, while those held at 10°C maintained normal AEC values.     

Metabolic adaptation of Cancer irroratus developmental stages to cyclic temperatures

Metabolic-temperature responses of the developmental stages of the sublittoral crab Cancer irroratus cultured at 10° to 20°C daily cyclic and 15°C constant temperatures were determined. Generally, the metabolic rate increased with temperature in the lower range with Q₁₀'s (temperature coefficients) above 2, compensated in the midrange with Q₁₀'s between 1 and 2, and declined at the higher temperatures with Q₁₀ values less than 1. For the larvae cultured at a constant temperature of 15°C, the compensatory response range narrowed with development from first zoeae to the later zoeal stages. In contrast, the compensatory response of the first zoeae, megalops, and crab stages within the range 10° to 25°C was interrupted by a zone of thermal sensitivity between 15° and 20°C for those individuals cultured in the 10° to 20°C cyclic regime. The compensatory response range is narrower for the third stage zoeae and broader for the second, fourth, and fifth stage zoeae. Metabolic rate-temperature (M-T) patterns of C. irroratus developmental stages cultured under the cyclic regime varied from those held at constant temperature by increased respiration and metabolic rate compensation between 20° and 25°C, and by an extension of the metabolically active range towards higher temperatures.     

Physioecology of zooplankton. II. Effects of phytoplankton concentration,temperature, and body size on the development and molting rates of Calanus pacificus and Pseudocalanus sp.

Developmental time and stage duration for Calanus pacificus Brodsky and Pseudocalanus sp. and the rate of loss of body carbon by molting for C. pacificus were estimated for copepodite stages cultured under various combinations of phytoplankton concentration and temperature. Mean development time and stage duration for C. pacificus decreased hyperbolically with increasing food concentration, and the minimum time required for reaching a given stage decreased logarithmically with a logarithmic increase in temperature. Low temperature retarded the development of early stages proportionally more than that of late stages, and stage duration increased logarithmically with increasing body weight. Therefore, copepodite development was not isochronal. The rate of loss of body carbon by molting was small, ranging from 0.2 to 2% day^-1. This rate increased hyperbolically with food concentration and was linearly related to the growth rate. The critical food concentration for the rates of development and molting increased with temperature and stage of development, but these rates were less dependent on food concentration than the growth rate. The development rate of Pseudocalanus sp. was higher than that of C. pacificus, and was less influenced by changes in food concentration and temperature. It is postulated that the inverse relationship between temperature and body size results from a differential effect of temperature and body size on the rates of growth and development. That is, with increasing body size the growth rate tends to become temperature-independent, but the development rate remains proportional to temperature. Thus, copepodites growing at low temperature can experience a greater weight increment between molting periods than individuals growing at high temperature, because the growth rate is similar at all temperatures but stage duration is longer at low temperature.Contribution No. 1128 from the Department of Oceanography, University of Washington, Seattle, Washington 98195, USA     

ATP content and adenylate energy charge of the mussel Mytilus edulis during the annual reproductive cycle in Lindåspollene,Western Norway

The oxygen consumption rates ( VO₂) of 6 specimens (6 to 13 kg) of the albacore tuna Thunnus alalunga were measured at sea, using specimens collected 300 km west of San Diego, California (USA) during July and August, 1981. Fish were tested in a closed continuous-flow respirometer, where they swam at about 1.3 body lengths s^-1 velocity in 15° to 19°C water. The albacore tuna is a temperate pelagic species experiencing water temperatures from about 10° to 20°C and attaining a maximum weight of 45 kg. The VO₂ ranged from 1 249 to 3 336 ml h^-1 (the mean VO₂ for the 6 fish was 2 228 ml h^-1); such values approach those of mammals of a similar size and are 3 to 4 times those of most active fishes (e.g. sockeye salmon). Among fishes, the only higher VO₂ values yet recorded were for the skipjack tuna Katsuwonus pelamis, a tropical species. The remarkably high metabolic rates of tunas are presumably correlated with their continuous swimming activity and the maintenance of endothermy. The exponent relating VO₂ to body weight (1.18), although large, is not statistically different from the exponents for most other active vertebrates.     

A comparative study of metabolic energy expenditure in the limpets Patella cochlear,P. oculus and P. granularis

Oxygen consumption of 3 species of Patella was measured in air and water at various temperatures. Measurements at constant temperature over a full tidal cycle showed no tidal or light-dark rhythms. Measurements under conditions simulating natural tidal, temperature and day-night cycles allowed calculation of daily respiratory energy budgets. P. cochlear occurs low on the shore, but experiences a food shortage due to intense intraspecific competition. Its rate of respiration is moderate, but metabolic expenditure is kept low because exposure to air is brief and body temperatures seldom rise above 23°C. P. cochlear has a respiratory rate-temperature (R-T) curve which peaks at 20°C and forms a plateau between 20° and 32.5°C. The midshore P. oculus has abundant food and adopts an exploitative strategy. Growth rate is very high, and this high turnover of energy is linked with a high metabolic rate, high Q10 (temperature coefficient) values, high body temperatures during the day-time low tide, and a respiratory R-T curve peaking at 32.5°C. Small P. oculus occur mainly in intertidal pools and respire faster in water, while larger individuals occur on bare rocks and respire faster in air over the upper temperature range. In contrast, the upper-shore P. granularis has little food, and conservation of energy is essential, particularly as its growth rate is moderate and its reprocurve output high. Respiratory losses are reduced by suppression of the R-T curve and low Q10 values, resulting in relative independence of temperature. Small P. granularis occur low on the shore and respire slower in water. Larger individuals occur at high levels due to migration, and respire slower in air. This further reduces respiratory energy losses. The patterns of respiration in these 3 species are thus related to food availability, resulting in exploitative or conservationist strategies.     

A controlled-temperature plankton wheel

A controlled-temperature plankton wheel is described that is suitable for use on board a ship. The IMER plankton wheel system allows the use of various sizes of experimental bottles, up to 2.2 litres, the simulation of ambient light regimes and variable speed control for the rotation of the experimental bottles. The flexibility of the system was demonstrated by investigating the relationship between temperature and ingestion rate of an herbivorous copepod. Using four of the IMER plankton wheels simultaneously at four different temperatures (5°, 10°, 15° and 20° C), the ingestion rate of Calanus helgolandicus, feeding on Thalassiosira weissflogii, was shown to increase with increasing temperature; from a transformation of log_e (ingestion rate), this relationship was calculated as a Q₁₀ (10° to 20°C) for Copepodite Stage V (Q₁₀ 4.5) and adult female (Q₁₀ 2.7) C. helgolandicus. The possibility of damaging cells, by rotation at 2 rpm, was investigated using the spinose form of the diatom T. weissflogii. Such rotation did not cause any damage to the spines of T. weissflogii, but mixing this diatom with a magnetic stirrer bar did damage the spines to varying degrees, depending on the volume being mixed.     

Anaerobic heat production of bivalves (Polymesoda caroliniana andModiolus demissus) in relation to temperature,body size,and duration of anoxia

Anaerobic heat-production rates of two co-occurring species of estuarine bivalves (a clam and a mussel) were measured with double-twin heat-flow calorimeters, one at 20°C, the other at 30°C. There is no significant difference between the two species in metabolic rates. There is evidence of initial aerobic metabolism in some individuals, as shown by high initial rates exponentially decreasing with time, while others had fluctuating but stable average metabolic activity from the beginning. During aerobic as well as anaerobic metabolism, the bivalves showed rhythmic periods of activity and quiescence. The two species differed in their rhythmic pattern of active and resting metabolism. In the case ofPolymesoda caroliniana, periods of resting metabolism tend to be longer and periods of active metabolism shorter at 30°C than at 20°C. There is a similarity between thermograms ofModiolus demissus at 20° and 30°C. Following acute temperature changes from 5° to 20° and 30°C, the bivalves showed stable metabolic rates in a matter of hours. The stabilized average rates [pooled averages for both species of 1.34×10^-4 (standard error of the mean=0.17×10^-4) W g^-1 dry weight of tissue at 20°C and 2.10×10^-4 (SE=0.20×10^-4) W g^-1 at 30°C] signify a temperature coefficient (Q₁₀) of 1.56 between 20° and 30°C, or partial temperature acclimation. Subtracting heat production as a result of physical activity, i.e., considering only resting metabolism, the corresponding means and standard errors of the means are 1.24×10^-4 and 0.14×10^-4 W g^-1 at 20°C and 1.91×10^-4 and 0.077×10^-4 W g^-1 at 30°C. Anaerobic heat production rate at 20°C is proportional to body size (r=0.84, 9 degrees of freedom, DF). ForM. demissus, measured anaerobic heat production is on the order of 7.5% of the level of aerobic respiration reported in the literature.     

Temperature acclimation of respiration and photosynthesis in the brown algaLaminaria saccharina

Sporophytes of the brown algaLaminaria saccharina (L.) Lamour grown at 15°C contained significantly more chlorophylla (chla) than did similar plants grown at 5°C. The increase in chla in 15°C plants was due to increased numbers of photosystem II reaction centes, and possibly to increased photosynthetic unit size, compared with 5°C plants. These changes were associated with increased values (photosynthetic efficiencies) in 15°C-grownL. saccharina relative to 5°C-grown plants. The changes in together with reduced respiration rates allowed 15°C-grownL. saccharina to achieve net photosynthesis and light-saturated photosynthesis at a lower photon fluence rate (PFR) than 5°C plants when both groups were assayed at the same temperature (15°C). The photon fluence rates necessary to reach the compensation point and achieve light-saturated photosynthesis (I _c andI _k , respectively) increased with increasing incubation temperature inL. saccharina grown at both 5 and 15°C. However, acclimation responses to growth temperature compensated for the short-term effect of temperature onI _c andI _k . Consequently, plants grown at 5 and 15°C were able to achieve similar rates of light-limited photosynthesis, and similarI _c andI _k values at their respective growth temperatures. These responses are undoubtedly important for perennial seaweeds such asL. saccharina, which frequently grow in light-limited habitats and experience pronounced seasonal changes in water temperature.Please address all correspondence and requests for reprints to I.R. Davison     

Comparative studies on the metabolism of shallow-water and deep-sea marine fishes. V. Effects of temperature and hydrostatic pressure on oxygen consumption in the mesopelagic zoarcid Melanostigma pammelas

Measurements have been made of routine oxygen consumption rates ( ) of the mesopelagic deep-sea zoarcid fish Melanostigma pammelas. Determinations were made over ecologically relevant ranges of 3 variables; temperature (3° to 10°C), hydrostatic pressure (1 to 170 atm), and oxygen partial pressure (1 to 160 mm Hg). Weight-specific s were uniformly low. Of the 3 test variables, only temperature had significant metabolic effects within the ranges studied. Q₁₀'s were 6.75 between 3° and 5°C. 1.47 between 5° and 7°C, and 17.4 between 7° and 10°C. These Q₁₀'s were constant over the hydrostatic pressure range studied. Between 3° and 7°C the fish regulated their rates of oxygen consumption down to PO₂'s comparable to those occurring in their natural environments (6 to 12 mm Hg). The showed no capacity to tolerate anoxic conditions. The physiological and ecological significance of these results is discussed, particularly with reference to thermal effects and to the basis of survival of this fish in the oxygen minimum layers of the eastern Pacific Ocean. Since it is possible to maintain M. pammelas in the laboratory for extended periods of time (over 12 months) it could serve as the basis for many interesting studies of deep-sea fish biology.     

Filter-feeding ethology of benthic invertebrates (ascidians). V. Influence of temperature on pumping,filtration and digestion rates and rhythms in Phallusia mamillata

The influence of temperature has been studied simultaneously on the pumping, filtration, and digestion rates of Phallusia mammillata (Cuvier, 1815). Eighteen experiments were made between 7° and 25°C on 5 individuals. The average velocities of the water current varied between 3.37 and 9.65 cm sec^-1 (maximum 34.90 cm sec^-1). No recognizable rhythm emerged; pumping was continuous except at 7°C, where it soon ceased. Above 20°C, the curves were irregular and reflected the high sensitivity of the ascidian. The pumping rate was highest at 15°C (mean=5,788 ml h^-1 g^-1 dry weight of organs). At 10°C, the mean was 3,560; at 20°C, 2,629 ml h^-1 g^-1 dry weight of organs. At 20°C, the coefficients of variation displayed higher values, indicating a more irregular pumping at this temperature. Although there was no filtration rhythm, the variability of the results was higher at 20°C and above. As for pumping, maximum values were observed at 15°C (mean=4,286 ml h^-1 g^-1 dry weight of organs) decreasing with lower and higher temperatures, such decreases being more marked at the higher temperatures. Means were 352 ml h^-1 g^-1 dry weight of organs at 7°C; 2,935 at 10°C; 1,995 at 20°C; 973 at 25°C. The mean temperature coefficients for the filtration rates were: Q₁₀ for 7° to 15°C=11.86, Q₁₀ for 10° to 20°C=0,66, Q₁₀ for 15° to 25°C=0.22. The filtering efficiency was fairly constant throughout an experiment; the pumping and filtration curves were in fact almost parallel. The filtering efficiency of the branchial sac was high (75 to 85%), with constant values at 10° and 15°C; it became smaller (59%) at 20°C, with a higher coefficient of variation. The digestion rate also displayed maximum values at 15°C (mean=5.47 mg of albumin equivalent 24 h^-1 g^-1 dry weight of organs). It was lower at 10°C (mean=3.60 mg) and reached its minimum at 20°C (mean=1.71 mg). The higher temperature affected the percentage of food utilization, which showed smaller values at 20°C (59%) than at 10°C (89%) and 15°C (87%).     

Rearing Pandalus borealis larvae in the laboratory

Larvae of the northern shrimp Pandalus borealis (Krøyer) are pelagic. In the Estuary and Gulf of St. Lawrence, Canada, the early stages are found in the upper 25-m of the water column in spring and early summer and are expected to experience a range of water temperatures from as low as 0°C to as high at 6°C. Little is known of the impact of water temperature on metabolic requirements of northern shrimp larvae. In this study, routine respiration (VO₂), maximum respiration (electron transport system activity, ETSA) and metabolic scope for growth (MS, ETSA–VO₂) of northern shrimp larvae were measured as a function of temperature (3, 5 and 8°C), developmental stage (I–V at 3°C, I–VII at 5°C and 8°C) and growth rate in dry mass. After logarithmic transformation, all three metabolic variables were linearly related to dry mass. The increase in VO₂ with body mass was faster at 5°C than at 3 or 8°C, whereas with ETSA this increase was slower. As a result, MS increased more slowly with dry mass at 5°C than at 3 and 8°C. However, MS did not limit growth in this study, since it explained only 39% of the variability in growth. All three metabolic variables as well as growth varied together as a function of temperature and ontogeny. Q₁₀ of all three metabolic variables ranged from 1.6 and 2.2 for stages I–V larvae, except for VO₂ at stage I (3.9) and stage III (2.9).     

Sensitivity of benthic community respiration and primary production to changes in temperature and light

In-situ measurements of benthic community respiration and primary production on an intertidal sandflat in Nova Scotia, Canada were used to test the hypothesis that community responses to light and temperature were similar within and between seasons. Multiple regression indicated that mean incubation temperature explained 57% of the variance in total sediment oxygen demand (TOD). The logarithmic relationship between TOD and temperature (Q₁₀=6.5) was not significantly different between fall and spring, suggesting no acclimation within season. Chemical oxygen demand measured in formalin-poisoned cores averaged 30% of TOD. Microalgal gross primary production (GROSS) was measured as oxygen production in light cores. Mean incubation temperature and sediment chlorophylla explained 56% of the variance. The linear relationship between GROSS and temperature had Q₁₀=2.0. When production was normalized to chlorophylla [GROSS(SP)], seasonal production-temperature curves were significantly different. The spring curve had Q₁₀=3.3; in the fall, production and temperature were not related. GROSS(SP)-light curves derived from Plexiglas shade experiments in the field were linear and not significantly different between fall and spring. Temperature alone was a better predictor of GROSS(SP) than light, even when P/I curves were adjusted for temperature. One can therefore model community respiration and photosynthesis at this site using daily averages in temperature, which are then summed over longer time scales to estimate monthly or seasonal rates.