Yolk utilization and growth to yolk-sac absorption in summer flounder (Paralichthys dentatus) larvae at constant and cyclic temperatures

Rates of development, growth and yolk conversion efficiency were determined in larvae of the summer flounder Paralichtys dentatus at constant temperatures of 21°, 16°, 12° and 5°C and in temperature cycles of 21°–16°, 16°–11°, and 11°–5°C. In constant incubation temperatures, development rate increased with increasing temperature. Larvae reared in the cyclic temperature regimes exhibited development rates intermediate to those at the temperature extremes of the cycle. All larvae reared at 5°C and in the 11°–5°C cycle regime died prior to total yolk-sac absorption. Although development rates were temperature dependent, no significant differences in notochord length ash-free dry weight or yolk utilization efficiency were found at the time of total yolk-sac absorption. The similarity in growth and yolk utilization efficiency for larvae reared under these various temperature regimes suggests that the physiological mechanisms involved are able to compensate for temperature changes encountered in nature.Contribution No. 195 from EPA, Environmental Research Laboratory, Narragansett, Rhode Island 02882, USA     

Effects of various temperature cycles on the larval development of the gastropod molluscCrepidula fornicata

Veligers ofCrepidula fornicata (L.) were reared for 12 days at constant temperatures of 15°, 20°, 25°, 30° and 35°C, and at 5 C° daily cycles of equal periodicity (COEP) over the temperature ranges 15° to 20°C, 20° to 25°C, 25° to 30°C and 30° to 35°C. COEP consisted of equal periods (6 h) of maximum temperature, minimum temperature, and uniformly increasing and decreasing temperature each 24 h period. Survival was high and not influenced by cyclic or constant temperature from 15° to 30°C. At 35°C and COEP 30° to 35°C, all larvae died before Day 6. Shell growth rate increased markedly over the range 15° to 25°C, and growth rates at cyclic temperatures in this range were intermediate between growth rates at the corresponding constant temperatures. Larvae reared at COEP 15° to 20°C and COEP 30° to 35°C had discontinuities in their shells due to inhibition of shell secretion during the adverse part of each temperature cycle. Groups ofc. fornicata veligers were exposed for 2 days to daily temperature cycles of equal and unequal periodicity in the critical 30° to 35°C range. [Cycles of unequal periodicity (COUP) consisted of unequal periods (varying between 3 and 15 h) of maximum and minimum temperature and uniformly increasing and decreasing temperature each 24 h period.] These veligers showed shell growth although their body tissue declined, as indicated by decreasing carbon content per larva. Least shell growth and most body tissue loss occurred in those cycles with the longest exposure to higher temperature. Larvae exposed for arious days to the mildest 30° to 35°C COUP (15 h at 30°C, 3 h increasing temperature, 3 h at 35°C and 3 h decreasing temperature) recovered and resumed normal growth when transferred to constant 30°C, but their growth was retarded in proportion to the number of days in the temperature cycle. Rates of shell growth of veligers in temperature cycles show an immediate effect of environmental temperature, while changes in carbon content per larva better reflect the effects of temperature on general metabolism and survival.     

Microbial activity, oxygen status and fermentation in the gut of the irregular sea urchin Echinocardium cordatum (Spatangoida: Echinodermata)

Microbial activity in the gut of the detrivore irregular sea urchin Echinocardium cordatum (Pennant) was studied by measurements of oxygen profiles, fermentation end products, C/N ratios, pH and concentrations of sulphide and sulphate in the gut segments, including the nodules of the intestinal caecum. The highest oxygen flux and consumption, and highest concentrations of short-chained fatty acids, and the lowest pH values occurred in the anterior stomach segments, including the anterior caecum. The C/N ratios indicate synthesis of microbial biomass in the caeca. The concentration of sulphate was high in the anterior stomach segments, whereas sulphide was only detectable in the nodules of the intestinal caecum. The anterior and intestinal caeca were the major sites for microbial activity, and oxidation of acetate and propionate produced in the two caeca corresponded to at least 9% of the total respiration of the sea urchin. Microbial fermentation, especially in the anterior caecum, seems to be important for the metabolism of E. cordatum, allowing the sea urchin to utilise refractile carbohydrates. The functions of the intestinal caecum are probably both residual fermentation and oxidation of accumulated sulphide. Received: 25 February 1998 / Accepted: 30 June 1998     

Laboratory study of survival and duration of individual zoeal stages as a function of temperature in the brachyuran crab Cancer magister

Larvae were hatched from ovigerous Dungeness crabs, Cancer magister, collected from Puget Sound Basin, Washington, USA, in April, 1986, and the effects of temperature on rates of survival and development were studied for each of the five zoeal stages both in small batch-culture and in individual culture. Culture method had little effect on the results at 10°, 15°, and 20°C. Increased mortality was measured at all stages at 20°C, with 100% mortality occurring during the terminal fifth stage. Fifth stage larvae may also show higher mortality at 15°C than at 10°C. Stage duration varied inversely with temperature at all stages, although differences between 10° and 15°C were greater than between 15° and 20°C. The results indicate that survival and stage duration are independent of the values for the previous and subsequent stages, that variability among larvae in instar duration increases with temperature, and that the terminal fifth zoeal stage is the most sensitive to temperature stress. Duration of a late zoeal instar is not related to its earlier development rate nor can early development rates be used to predict whether individual zoeae will successfully develop to the megalopa. Measurements of megalopa dry weights indicate no differences due either to previous culture temperatures or to total time to the megalopa. Predictive models of larval transport that require estimates of larval duration should account for both changes in temperature response that can affect individual stage duration, and variability among individuals in stage duration that can influence the degree of larval dispersion.     

Temperature influences muscle differentiation and the relative timing of organogenesis in herring (Clupea harengus) larvae

Eggs from spring spawning stocks of herring (Clupea harengus L.) were fertilized and reared at either 5, 8 or 12°C in 1991 and 1992. The differentiation of myotomal muscle fibres was investigated in relation to the development of other organs and tissues using light and electron microscopy. The gut, notochord, eyes and haemocoel appeared at the same relative point in development between fertilization and hatching at all temperatures. In contrast, the formation of the spinal cord, pronephros, pectoral fin buds and muscle fibres was relatively retarded at 5°C compared with 8 and 12°C. Myogenesis in the presumptive inner muscle mass occurred after 12 to 16 d at 5°C, 7 to 10 d at 8°C and 3.5 to 6 d at 12°C. Myoblasts aligned in orderly rows running from myosept to myosept prior to fusion to form myotubes. Actin and myosin filaments were synthesised throughout the cytoplasm in associated with presumptive Z-lines at the periphery of myotubes and immature muscle fibres. Differentiation of the superficial and inner muscle fibres types of larvae occurred at around the same time. Following this initial period of myogenesis, the number of myotomal muscle fibres remained constant until after hatching, so that increases in muscle bulk in the late embryo were entirely due to fibre hypertrophy. At hatching, the number of superficial muscle fibres present in myotomes just posterior to the yolk-sac was significantly less at 5°C (108±12) than at either 8°C (132±10) or 12°C (140±10) (mean±SD, 12 fish/temperature). In contrast, there were around 280 inner muscle fibres/myotome, comprising 90% of the trunk cross-sectional area, at all three temperatures. Myofibrillargenesis occurred relatively slowly at low temperatures, so that the volume density of myofibrils in the inner muscle fibres of larvae at hatching was significantly less at 5°C (39.2±9.0) than at either 8°C (49.6±8.8) or 12°C (50.2±9.8) (mean ±SD, 20 fibres/temperature from total of 5 fish). Undifferentiated myoblasts remained at hatching to form a population of presumptive myosatellite cells. The number of presumptive myosatellite cells per mm² cross-sectional area of muscle fibre was more than two times higher at 8°C (1493±335) than at either 5°C (478±102) or 12°C (924±233) (mean±SD, 5 fish/temperature). The results suggest that temperature can influence the commitment of myoblasts to differentiation at a critical stage in embryogenesis, thereby providing a potential mechanism for influencing future growth characteristics. Correspondence to: I.A. Johnston at Gatty Marine Laboratory     

Callus formation in seven species of agarophyte marine algae

Callus formation of seven species of the agarophyte marine algae Phyllophora nervosa, Gracilaria verrucosa, Furcellaria fastigiata, ceramium kondoi, Gelidium vagum, Laurencia paniculata, Rhodymenia pertusa was obtained from 1984 to 1986. A new sterile agent, chlorhexidin bigluconate, was used to get axenic explants from the algae thalli. The formation of callus from axenic explants depended on temperature of cultivation. In the case of F. fastigiata and G. vagum it occurred at 12° to 20°C, and with P. nervosa at 18° to 26°C. The exchange of sucrose with mannitol in the culture medium and the addition of some growth regulators stimulated the formation of callus. Mass formation of lumpy and warty extensions was observed in the explants from leaf blades of P. nervosa. The results might be useful for improving the aquaculture of agarophyte marine algae.     

High-temperature tolerance of photosynthesis in the red alga Chondrus crispus

Chondrus crispus (Stackhouse) is a perennial red seaweed, common in intertidal and shallow sublittoral communities throughout the North Atlantic Ocean. In the intertidal zone, C. crispus may experience rapid temperature changes of 10 to 20C° during a single immerison-emerision cycle, and may be exposed to temperatures that exceed the thermal limits for long-term survival. C. crispus collected year-round at Long Cove Point, Chamberlain, Maine, USA, during 1989 and 1990, underwent phenotypic acclimation to growth temperature in the laboratory. This phenotypic acclimation enhanced its ability to withstand brief exposure to extreme temperature. Plants grown at summer seawater temperature (20°C) were able to maintain constant rates of lightsaturated photosynthesis at 30°C for 9 h. In contrast, light-saturated photosynthetic rates of plants grown at winter seawater temperature (5°C) declined rapidly following exposure to 30°C, reached 20 to 25% of initial values within 10 min, and then remained constant at this level for 9 h. The degree of inhibition of photosynthesis at 30°C was also dependent upon light intensity. Inhibition was greatest in plants exposed to 30°C in darkness or high light (600 mol photons m^-2s^-1) than in plants maintained under moderate light levels (70 to 100 mol photons m^-2s^-1). Photosynthesis of 20°C-acclimated plants was inhibited by exposure to 30°C in darkness or high light, but the degree of inhibition was less than that exhibited by 5°C-grown plants. Not only was light-saturated photosynthesis of 20°C plants less severely inhibited by exposure to 30°C than that of 5°C plants, but the former also recovered faster when they were returned to growth conditions. The mechanistic basis of this acclimation to growth temperature is not clear. Our results indicate that there were no differences between 5 and 20°C-grown plants in the thermal stability of respiration, electron transport associated with Photosystems I or II, Rubisco or energy transfer between the phycobilisomes and Photosystem II. Overall, our results suggest that phenotypic acclimation to seawater temperature allows plants to tolerate higher temperatures, and may play an important role in the success of C. crispus in the intertidal environment.     

The effect of microbial activity upon the sedimentary sulphur cycle

The sulphate content of an intertidal sediment at Anglesey (UK) was shown to vary during the year, the sulphate-reducing activity of the microbial population being limited by low temperature during winter, and by the low numbers of sulphate-reducing bacteria during May, 1969. A corresponding annual variation of the sedimentary sulphide could not be demonstrated, and the sulphide which was formed biologically during the course of the year was almost entirely lost from the sediment. This loss of sulphide was probably due to subsurface oxidation; and flushing, by water entering at the base of the sediment. It is suggested that sulphide was only precipitated within the sediment during summer when sulphate reduction was active, and even then only during part of the tidal cycle when flushing did not occur.     

Effect of temperature on the molting,growth and maturation of the antarctic krill Euphausia superba (Crustacea: Euphausiacea) under laboratory conditions

The effect of temperature on molting, growth, and maturation rates was studied on laboratory-maintained Euphausia superba. The length of intermolt periods (IMP's) was inversely proportional to temperature (20.10 d, SD=1.60, at 0.12°C; 16.87 d, SD=1.68, at 0.97°C; and 12.48 d, SD=0.90, at 4.48°C), and directly proportional to krill size at 0.12°C and 0.97°C. For individually maintained krill the maximum growth rate at 4.48°C (0.068 mm d^-1) was nearly twice that at 0.68°C (0.037 mm d^-1). There was no observable temperature effect on maturation rates. The maturation changes of juveniles at all temperatures indicated that more than two years are probably required to reach maturity. Mature males and females regressed to immature forms, suggesting that E. superba may reproduce in successive years. These results and previously reported field and laboratory data for E. superba and other euphausiid species suggest a 4+ year life span for this species.This work was supported by NSF grant DPP 76-23437     

Effects of constant and cyclic temperatures on the salinity tolerance of the estuarine sandhopper Orchestia chiliensis

The survival of Orchestia chiliensis (Milne Edwards, 1840) was investigated at salinities between 0.3 and 68 and constant or 10 C° cyclic temperatures between 5° and 25° C. Mortality increased with age, temperature and at salinity extremes. Small individuals show little seasonal acclimatisation apart from increased thermal tolerance at the highest exposure temperature. Larger individuals show a lateral shift in the mortality curve to the right in summer, giving increased survival at most salinities. Salinity had less effect on amphipods in cyclic regimes and survival was similar in 5° to 15° C and 10° to 20° C cycles. Mortality of larger individuals was higher in the 15° to 25° C cycle, but seasonal acclimatisation gave increased resistance at all fluctuating temperatures during the summer. Mortality in cyclic temperatures was higher than at similar constant temperatures. O. chiliensis does not actively evade immersion and diel temperature changes of 10 C° represent an important stress factor. This would affect all life stages and influence field populations both in the winter and the summer.     

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     

Intake and coversion of food in the fish Limanda limanda exposed to different temperatures

In the flat fish Limanda limanda L., feeding rate and conversion efficiency were studied as functions of body weight, sex, temperature and food quality. When offered herring meat at 13 °C (series I), females (live weights 1 to 150 g) consume more food than males; the magnitude of this difference is body weight-dependent. With increasing wieght, both females and males consume less food per unit body weight per day. Variations in daily ration are considerable; the range of deviation from mean feeding rate is about 60% for males and 40% for females. The range of deviation does not vary significantly among females and males of different body weights. At the same temperature level (13 °C; series II), females consume almost the same, or even less, cod meat than males. Among individuals of series I and II, there is a little difference in the feeding rate; however, herring-fed individuals obtain about 2 times more energy than cod-fed individuals. Each gram wet weight of herring meat yields 2001, each gram cod meat 1137, calories. Small individuals completely cease to feed at 3°C; they feed little at 8 °C. Larger females consume maximum amounts at 8 °C. Small individuals consume maximum amounts at higher temperatures. Thus, with increasing body weight (age), the temperature for maximum feeding shifts downwards. Feeding with cod or herring meat results in considerable changes in composition and calorific content of L. Limanda. The magnitude of these changes depends both on temperature and food quality. Food conversion efficiency values of herring-fed individuals are about 1 1/2 times higher than of cod-fed individuals. In series I and II, females are more efficient converters than males. In individuals weighing more than 50 g, conversion efficiency decreases in the order: 8°, 13°, 18° C; in smaller individuals this order is 13°, 18°, 8 °C. Conversion rate is about 2 to 5 times faster in individuals fed herring meat than those receiving cod meat. Conversion rate decreases in the order 13°, 8°, 18 °C in males, and in the order 18°, 13°, 8 °C in females; females of more than 80 g are exceptional in that they reach the maximum at 8 °C. From the data on food intake and food conversion, the biologically useful energy available for metabolism has been calculated for each test individual kept at 13° and 18 °C. At these temperature levels, the weight exponents are about 0.6; the a value or metabolic level for the 18 °C series is about 2 times higher than that at 13 °C. Thus, temperature affects metabolic rate but not the exponential value. The exponential value for the body weight-metabolism relation at 13 °C is for dab fed herring meat 0.9; the a value amounts to about half that for dab fed cod meat. Food quality, unlike temperature, alters not only the exponential value but also metabolic rate.     

Temperature adaptation in strains of the amphi-equatorial green alga Urospora penicilliformis (Acrosiphoniales): biogeographical implications

The temperature requirements for growth and the upper survival temperatures (UST's) of the amiphi-equatorial green alga Urospora penicilliformis collected from several localities within its distribution area between 1986 and 1991 were determined. Ecotypic variation, both with regard to growth ranges and optima and to survival temperatures, was demonstrated. In the polar strains of U. penicilliformis, temperature growth ranges were narrower and the growth optima and UST's were at lower temperatures compared to cold-temperate strains. In particular, the polar strains grew between 0 and 15°C with optimal growth at 0 or 5°C, whereas the cold-temperate isolates grew between 0 and (15) 20°C with almost equal growth rates or a growth optimum between 5 and 15°C. The Arctic strains survived 23 to 24°C, and the Antarctic isolate only 19°C, while the UST's of the cold-temperate isolates were between (24) 25 to 26°C. The data strongly indicate that a cold water history of ca. 3 million yr in the Arctic can be sufficient for changes in the temperature growth ranges and optima as well as for small changes of UST as shown in the Arctic populations of U. penicilliformis. For stronger reduction of upper survival temperatures, longer time periods are necessary as exemplified in the isolate from Antarctica, where low temperatures have existed for at least 14 million yr. The significantly lower UST of the Antarctic strain, points to an early contact of the alga with the cold water of the Antarctic region and may indicate an origin of U. penicilliformis in the Southern Hemisphere. The UST's of the cold-temperate isolates (24 to 26°C) would have allowed a migration across the equator during Pleistocene lowerings of the seawater temperatures in the tropics. Growth, however, would not have been possible during the passage across the equator due to the narrow temperature-growth window. The nature of the geographical boundaries and the control of seasonal development of U. penicilliformis by the temperature conditions in the various geographical regions are discussed in relation to the present local temperature regime.     

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%).     

Embryogenesis and larval biology of the ahermatypic scleractinian<Emphasis Type="Italic"> Oculina varicosa</Emphasis>

The ivory tree coral Oculina varicosa (Leseur, 1820) is an ahermatypic branching scleractinian that colonizes limestone ledges at depths of 6–100 m along the Atlantic coast of Florida. This paper describes the development of embryos and larvae from shallow-water O. varicosa, collected at 6–8 m depth in July 1999 off Fort Pierce, Florida (27°32.542 N; 79°58.732 W). The effect of temperature on embryogenesis, larval survival, and larval swimming speed were examined in the laboratory. Ontogenetic changes in geotaxis and phototaxis were also investigated. Embryos developed via spiral cleavage from small (100 µm), negatively buoyant eggs. Ciliated larvae developed after 6–9 h at 25°C. Embryogenesis ceased at 10°C, was inhibited at 17°C, and progressed normally at 25°C and 30°C. Larval survival, however, was high across the full range of experimental temperatures (11–31°C), although mortality increased in the warmest treatments (26°C and 31°C). Larval swimming speed was highest at 25°C, and lower at the temperature extremes (5°C and 35°C). An ontogenetic change in geotaxis was observed; newly ciliated larvae swam to the water surface and remained there for approximately 18 h, after which they swam briefly throughout the water column, then became demersal. Early larvae showed no response to light stimulation, but at 14 and 23 days larvae appeared to exhibit negatively phototactic behavior. Although low temperatures inhibited the development of O. varicosa embryos, the larvae survived temperature extremes for extended periods of time. Ontogenetic changes in larval behavior may ensure that competent larvae are close to the benthos to facilitate settlement. Previous experiments on survival, swimming speeds, and observations on behavior of O. varicosa larvae from deep-water adults indicate that there is no difference between larvae of the deep and shallow populations.Communicated by J.P. Grassle, New Brunswick     

Mass mortality of Strongylocentrotus droebachiensis (Echinodermata: Echinoidea) off Nova Scotia,Canada

A mass mortality of Strongylocentrotus droebachiensis, attributed to disease, was monitored in an echinoiddominated barren ground at Eagle Head on the south-western coast of Nova Scotia, Canada, in 1982. Mortality was 70% in a shallow (3 m) nearshore area, resulting in a loss of echinoid biomass of 2 042 g fresh weight m^-2, and 6% in deeper (7 m, 10 m) offshore areas. Echinoid density, size and nutritional condition (gonad index) were highest in the nearshore area. Survivorship was higher in juveniles (<15 mm diameter) than in adults resulting in the formation of a bimodal size distribution in the nearshore area. Mortality began around early October, near the peak of the annual cycle of seawater temperature (15°C), and was arrested by early December (seawater temperature 7°C) when morbid echinoids appeared to recover. In laboratory experiments, time to morbidity of S. droebachiensis exposed to morbid conspecifics increased exponentially with decreasing temperature (20° to 8°C). There was no survival at 20° and 16°C, 20% survival at 12°C and 100% survival at 8°C after 60 d; suggesting a lower temperature limit (between 12° and 8°C) for possible transmission of a pathogenic agent. Morbid laboratory echinoids from experiments at 16°C, and recovering echinoids collected in the nearshore area in early December, showed 100 and 85% survival respectively at <=8°C, and 0 and 15% survival respectively at 16°C, after 30 d. Time to morbidity was not affected significantly by nutritional condition and was similar for juvenile and adult echinoids. Time to morbidity was greater in echinoids exposed to one or three morbid individuals continuously, or seven morbid individuals for 1 h, relative to higher levels of exposure (up to seven morbid individuals continuously). Recent mass mortalities in S. droebachiensis have occurred in years of record high sea surface temperatures. The extent of mortality is correlated with the magnitude and duration of temperatures above a lower limit.     

Correlation of bioluminescence emissions with ventral photophores in the mesopelagic squidAbralia veranyi (Cephalopoda: Enoploteuthidae)

Specimens of the squidAbralia veranyi were collected off the Bahamas in 1989. The bioluminescence of the ventral photophores was recorded on videotape at 11 to 12°C and 24°C, in conjunction with measurements of the spectral emission at the same temperatures. At 11 °C, the spectrum was unimodal, peaking at 490 nm with a narrow bandwidth. At the higher temperature a shoulder at about 440 nm appeared in the emission spectrum. The short, bright flashes from the subocular photophores had a broader bandwidth and a shorter wavelength emission maximum (475 nm) than that of the ventral photophores. Video recordings at the two temperatures showed no changes in either the identities of the luminescing photophores or their relative intensities. One structurally distinct type of photophore was not illuminated. We conclude that the observed spectral changes were produced within one group of photophores, and that recruitment of the unilluminated photophores would produce an additional spectral component, previously reported from another species ofAbralia (A. trigonura).     

Acquisition and loss of cold-tolerance in adult barnacles (Balanus balanoides) kept under laboratory conditions

In the laboratory, Balanus balanoides (L.) barnacles maintained without food at 5°C over the winter to summer period remained cold-tolerant. Winter animals maintained at 5°C and fed Artemia nauplii under a controlled light-dark regime until mid-summer lost this cold-tolerance. Summer animals, maintained without food at 5° or 15°C until midwinter, became cold-tolerant. Summer and winter animals subjected to increased (or decreased) ambient salinity for 48 h showed a small decrease (or increase) in their lower median lethal temperature (MLT—defined as the temperature at which 50% of the animals die after 18 h exposure to air). Summer animals subjected to desiccation for 48 h also showed a small decrease in their lower MLT. It is concluded that the seasonal changes in cold-tolerance of adult barnacles are probably induced by a combination of environmental factors including food availability, light intensity, day-length and changes in ambient sea-water temperatures. Development of cold-tolerance in the winter did not depend upon fertilisation. Changes in intra-cellular solute concentration which accompany adaptation to changes in ambient salinity or desiccation do not appear to be related to the seasonal changes in cold-tolerance.     

Influence of temperature on muscle-fibre development in larvae of the herringClupea harengus

The development of swimming (myotomal) muscles was studied in herring larvae (Clupea harengus L.) caught in the Firth of Clyde, Scotland, in spring 1990 and reared at either 5, 10 or 15°C. Two muscle-fibre types can be distinguished in the myotomes of herring larvae using ultrastructural criteria. A single layer of small-diameter muscle fibres, packed with mitochondria, is present beneath the entire surface of the skin (superficial muscle fibres). The remaining bulk of the muscle is composed of larger diameter fibres (inner muscle fibres) containing significantly more myofibrils than the superficial fibres. In 1 d-old larvae, the number of inner muscle fibres in myotomes immediately posterior to the yolk-sac was 311±41 at 15°C, 257±22 at 10°C and 187±22 at 5°C (mean±SD,n=6). The average diameter of inner muscle fibres increased with decreasing temperature, so that the total cross-sectional area of muscle was similar at each temperature. After 6 to 7 d, the number of muscle fibres had significantly increased at 15°C (383±25), but not at 10°C (281±32) or 5°C (192±17). In contrast, the average cross-sectional area of inner muscle fibres had increased by 19% at 15°C, 34% at 10°C, and 26% at 5°C. Temperature also influenced the relative proportions and spatial distributions of muscle-fibre organelles. For example, in 1 d-old larvae, the fraction of muscle-fibre volume (volume density) occupied by mitochondria in the superficial fibres was significantly higher at 15°C (46.0%) than at either 5°C (37.6%) or 10°C (38.8%). In the inner muscle fibres, the volume density of mitochondria was 26.1% at 15°C, 20.5% at 10°C and 15.9% at 5°C, whereas the volume density of myofibrils was similar at the three temperatures (33 to 38%). Typically, inner muscle fibres from 10°C larvae, but not from 5 or 15°C larvae contained a large central mitochondrion.     

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.