Temperature tolerance of the polychaete worms Diopatra cuprea and Clymenella torquata

The resistance to high temperatures of two species of intertidal tube-dwelling polychaete worms has been tested to show seasonal and geographic variations. The summer 50% survival temperature at Beaufort, North Carolina, was 42.5 °C for Diopatra cuprea (Bosc) and 40.5 °C for Clymenella torquata (Leidy). Winter 50% survival temperatures for both species at Beaufort were approximately 4.0 C° lower. Both species showed a geographic difference in 50% survival temperature of more than 4.0 C° between North Carolina and Massachusetts in summer. D. cuprea from the Mississippi coast showed a lower survival temperature, probably due to combined temperature and salinity effects. Laboratory acclimation of C. torquata from Beaufort at low temperatures, during summer months, produced experimental results similar to those from winter animals. The seasonal differences in temperature tolerance are phenotypic expressions of a physiological response which can be related to environmental temperature patterns.     

Combined effects of temperature and salinity on the complete development ofEurytemora velox (Crustacea: Calanoidea)

The calanoid copepodEurytemora velox was collected from rock pools at Castletown, Isle of Man, UK. Its optimum environmental requirements, particularly temperature and salinity, were determined, with a view to its possible future use as living food in intensive fish and shellfish farming. The species was cultured in 21 different temperature and salinity combinations. Investigations covered a period of two years from December 1983 to December 1985. Complete development from hatching to adult stage was followed in 21 temperature and salinity combinations. Nauplii suffered relatively high mortalities, indicating the sensitivity of this development stage to variations in temperature and salinity. Highest nauplii survival was observed in the combinations 15°C with 25 and 20 S and 20°C with 20 S, the highest copepodite survival at 10°C and 20 S. Lower salinities were tolerated better at higher temperatures and higher salinities at lower temperatures. Development time varied with the temperature and salinity combinations. Lower salinities at the lower temperatures of 10° and 15°C and both lower and higher salinities at 20°C prolonged development, particularly of the naupliar stage. Highest Q₅ values (i.e., rate of change of development with a 5 C° increase in temperature) were recorded for the naupliar stage. Statistical analysis indicated that salinity influences the survival of both nauplii and copepodites; however, this effect is not linear.     

A response-surface approach to the combined effects of temperature and salinity on the larval development of Adula californiensis (Pelecypoda: Mytilidae). II. Long-term Larval survival and growth in relation to respiration

Larvae of the bivalve molluso Adula californiensis (Phillippi, 1847) were reared for 3 days, from fertilization to veliger stage, at optimum conditions (15°C, 32.2 S), and then transferred to experimental temperatures and salinities for 22 more days to determine the effects of these factors on survival and growth. For larvae surviving to 25 days, maximum survival was estimated, by response-surface techniques, to occur at temperatures below 10°C and at salinities above 25. A comparison of 60% survival response contours for 3, 15 and 25-day old larvae indicated a progressive shift in temperature and salinity tolerance with age of larvae. The older larvae became more tolerant to reduced salinity, but less tolerant to high temperatures. Growth of the larvae over 25 days of culture was slight, and relatively independent of temperature and salinity conditions found in the environment. Oxygen consumption of 3-day old veliger larvae measured at various combinations of temperature and salinity generally increased from 7° to 18°C, and then sharply decreased from 18° to 21°C. A plateau of oxygen consumption from 9° to 15°C at 32.9 S indicated that the larvae are adapted to oceanic rather than estuarine conditions. A comparison of 25-day larval survival, mean length, and growth, with oxygen consumption of 3-day old veliger larvae indicated that high temperatures (15°C, and above) coupled with reduced salinities (26.1, and below) were unfavorable for prolonged larval life. Because of the lack of larval adaptations to estuarine conditions, larva survival and, hence, successful recruitment of this species within Yaquina Bay (Oregon, USA) depends upon the essentially oceanic conditions found only during the summer in the lower part of the Bay.     

Combined effects of temperature and salinity on embryos and larvae of the northern bay scallop Argopecten irradians irradians

The combined effects of temperature and salinity on embryonic development and on larval survival and growth to setting size of the northerm bay scallop Argopecten irradians irradians (Lamarck) were studied in the laboratory. A 6x6 complete factorial design was used; temperatures ranged from 10° to 35°C, at 5C° intervals, and salinities ranged from 10 to 35S, at 5S intervals. Response-surface contour diagrams were generated to provide estimates of conditions for optimal responses. Normal development of embryos occurred over a very narrow range of temperature and salinity. Survival of larvae occurred over a wider range of temperature and salinity than did embryonic development or growth of larvae. Satisfactory growth (>70% of the maximum observed value) occurred only at high temperature-high salinity conditions; optimal conditions for survival occurred at similar salinities, but at slightly lower temperatures. Temperatures of 35°C or greater and/or salinities of 10S or less were lethal for all life stages studied. Both salinity and temperature exerted significant effects on development and survival, but temperature was clearly the dominant factor influencing growth. It is suggested that northern bay scallop embryos and larvae be reared at their respective optimal temperature-salinity levels so as to increase efficiency of aquaculture operations.This paper is adapted from a thesis submitted to the College of Fisheries, University of Washington, in partial fulfillment of the requirements for the MS degree. This study was conducted at the NMFS Laboratory in Milford, Connecticut, USA     

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.     

The significance of temperature,salinity and zinc as lethal factors for the mussel Mytilus edulis in a polluted estuary

Mussels, Mytilus edulis L., were subjected to high temperatures, low salinities and dissolved zinc in order to investigate possible environmental hazards of a discharge of heated effluent near Newport on the Yarra River estuary, Victoria, Australia. Exposure to zinc at 0.8 mg l^-1 for 14 d in otherwise favourable conditions significantly increased mortality resulting from subsequent exposure to temperatures between 29° to 31°C for 24 h without added zinc. Mussels collected from water of temporarily lowered salinity (8–16 S) showed significantly lower thermal resistance than controls collected from marine salinities (35 S). Mussels taken from a marine environment and exposed to 10 S died at a rate which increased with temperature. Mussels acclimated for 14 d to combinations of 10°, 16° and 22°C and 22 and 35 S, and subsequently exposed to increased zinc concentrations accumulated zinc to levels which were independent of temperature and salinity. The zinc was lethal more quickly at 22°C and 35 S than at the lower temperatures and salinities. The modes of toxic action of the salinity, zinc and temperature factors are discussed and it is argued that zinc which has been found accumulated in mussels near Newport could be reducing their resistance to raised temperatures and perhaps other stresses, probably as a result of effects on lysosomal functioning. The evidence suggests that the heated effluent will accelerate any toxic effects of zinc or low salinities which occur near Newport and so poses a hazard in winter as well as in summer.     

The combined effects of salinity and temperature on larvae of the mussel Mytilus edulis

The combined effects of salinity and temperature on survival and growth of larvae of the mussel Mytilus edulis (L.) were studied. The effects of salinity and temperature are significantly related only as the limits of tolerance of either factor are approached. Survival of larvae at salinities from 15 to 40 is uniformly good (70% or better) at temperatures from 5° to 20°C, but is reduced drastically at 25 °C, particularly at high (40) and low (20) salinities. Larval growth is rapid at a temperature of 15 °C in salinities from 25 to 35, at 20 °C in salinities from 20 to 35. Optimum growth occurs at 20 °C in salinities from 25 to 30. Growth decreases both at 25° and 10 °C; the decline is most drastic at high (40) and low (20) salinities.Part of a study completed at the Bureau of Commercial Fisheries, Biological Laboratory, Milford, Connecticut, USA, while on a UNESCO Fellowship.     

Salinity tolerance,salinity preference and temperature tolerance in the high-shore harpacticoid copepod Tigriopus brevicornis

Tigriopus brevicornis (O. F. Müller) were collected in 1992 from rock pools close to U.M.B.S. Millport, Isle of Cumbrae, U.K. and acclimated to various combinations of salinity and temperature for at least 1 wk prior to laboratory experiments. Higher salinities of acclimation enhanced tolerance to high salinity stress, while tolerance of low salinities was hardly affected by acclimation salinity. Acclimation to low temperature (10°C) extended the survivable salinity range for T. brevicornis. High-salinity acclimation enhanced the survivable temperature range. Copepods acclimated to 60 survived significantly lower and higher temperatures than did 34-acclimated individuals. At high temperature, 75-acclimated female copepods had the highest median lethal temperature, 38.9°C. Females were significantly more resistant to high temperatures than males. The copepods were seen to have a very low median lethal temperature when frozen into solid ice for 2 h; 50% mortality occurred at-16.9°C in 10°C, 34-acclimated T. brevicornis. Salinity preference experiments demonstrated an ability to discriminate between salinities differing by as little as 3. Copepods acclimated to 34 chose salinities near their acclimation salinity; individuals acclimated to 5 favoured slightly higher salinities, while copepods acclimated to 60 chose rather lower salinities.     

Combined effects of temperature and salinity on fed and starved larvae of the mediterranean mussel Mytilus galloprovincialis and the Japanese oyster Crassostrea gigas

The combined effects of temperature, salinity and nutrition on survival and growth of larvae of the Mediterranean mussel Mytilus galloprovincialis and the Japanese oyster Crassostrea gigas were studied over a period of 7 d in the laboratory. Ripe adults, collected in spring and summer 1987 from natural populations in the Bay of Arcachon, France, were induced to spawn. Larvae of both species were cultured at four temperatures (15°, 20°, 25° and 30°C), four salinities (20, 25, 30 and 35S) per temperature, and two levels of nutrition (fed and unfed) per temperature/salinity combination. The fed larvae received a mixed algal diet of 50 cells each of Isochrysis galbana and Chaetoceros calcitrans forma pumilum per microlitre. In both bivalve species, larvae survived over a wide range of temperature and salinity, with the exception of mussel larvae, which died at 30°C. Statistical analysis indicated that nutrition had the greatest effect on larval development, explaining 64 to 75% of the variance in growth of M. galloprovincialis and 54 to 70% in growth of Crassostrea gigas. Unfed mussel larvae displayed little growth. Compared with temperature, the effect of salinity was very slight. M. galloprovincialis larvae exhibited best growth at 20°C and 35S and C. gigas at 30°C and 30S.     

The effect of salinity and cyclic temperature on larval development of the mud-crab Rhithropanopeus harrisii (Brachyura: Xanthidae) reared in the laboratory

Larvae of Rhithropanopeus harrisii (Gould) were reared from hatching to the first or second crab stages in 11 combinations of salinities and cyclic temperatures (5, 20, and 35 S at 20° to 25°C, 25° to 30°C, and 30° to 35°C; 25 S at 20° to 25°C and 30° to 35°C). The larvae survived to the megalops and first crab stages in all salinities and cycles of temperature other than 5 S at 30° to 35°C. The best survival to the megalops (94%) and first crab (90%) stages occurred in 20 S, 20° to 25°C. In all other combinations of salinities and temperatures there was a reduction in survival to the first crab stage. The duration of the larval stages was affected significantly by temperature, whereas the effect of salinity on the mean days from hatching to the first crab stage was not consistent at the different temperature cycles. Development to the first crab stage required the shortest time in 20 S, 30° to 35°C (mean 12.3 days), and the longest time in 5 and 35 S, 20° to 25°C (mean 22.6 days and 21.6 days, respectively). Megalops larvae reared in 35 S at all cycles of temperature, as well as larvae in 20 and 25 S, 30° to 35°C, showed a high percentage of abnormality, with the highest percentage occurring in 35 S, 30° to 35°C. It appears that larval development of R. harrisii is strongly influenced by environmental factors and not solely related to genetic differences.This research was supported by grants from the Nordic Council for Marine Biology and the U.S. Atomic Energy Commission [Grant No. At-(40-1)-4377].Contribution No. 116, Zoological Museum, University of Oslo, Norway.     

Salinity-temperature relationships in the queen scallop Chalamys opercularis

The effects of reduced salinities on different size-ranges of Chlamys opercularis (L.) were studied at various temperatures using 3 methods of analysis: median lethal mortality over 24 h (LD₅₀, 24 h); surface-response analysis; time-mortality relationships. Reduced salinities ranging from 16 to 28 were lethal after a 24 h exposure, depending on the temperature and size of the scallop. Mortality increased at extremes of temperature, and spat appeared to have a slightly greater tolerance than larger individuals. Observations were also made on behavioural responses and byssus attachment at reduced salinities.     

Synergistic effects of cadmium and salinity combined with constant and cycling temperatures on the larval development of two estuarine crab species

The developmental stages from megalopa to third crab of the blue crab Callinectes sapidus Rathbun were tested in 12 combinations of cadmium (0, 50, and 150 ppb) and salinity (10, 20, 30, and 40) at 25°C. A reduction in survival and a significant delay in development from megalopa to third crab occurred within each salinity regime in 50 ppb compared with the control. Comparison of the delay in development within each salinity regime revealed that the sublethal effect of cadmium was most pronounced in the salinities normally preferred by C. sapidus. A similar comparison within each cadmium concentration, however, showed that the developmental time from megalopa to third crab was approximately the same irrespective of salinity. The developmental stages from hatch to first crab of the mud-crab Rhithropanopeus harrisii (Gould) were examined in 63 combinations of cadmium (0, 50, and 150 ppb), salinity (10, 20, and 30), constant temperature (20°, 25°, 30°, and 35°C) and cycling temperature (20° to 25°C, 25° to 30°C, and 30° to 35°C). The results indicated that cycling temperatures may have a stimulating effect on survival of the larvae compared to constant temperatures, both in the presence and in the absence of cadmium. Effects of cadmium and salinity and their interaction on the survival of the larvae from zoeae to megalopa were documented at most of the temperatures by analyses of variance. The zoeal larvae were more susceptible to cadmium than the megalopa. Effects of different combinations of cadmium and salinity on the duration of larval development were assessed by a t-test.     

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.     

Individual effects and interactions of salinity,temperature, and zinc on larval development of the grass shrimp Palaemonetes pugio. I. Survival and developmental duration through metamorphosis

Larvae of the estuarine grass shrimp Palaemonetes pugio (Holthuis) were reared from hatch through successful completion of metamorphosis in 80 combinations of salinity (3 to 31%), temperature (20° to 35°C), and zinc (0.00 to 1.00 ppm Zn⁺⁺). Response-surface methodology was employed to depict the individual effects and interactions of the three factors on survival and developmental duration through total larval development. Outside the optimal salinity-temperature conditions of 17 to 27 S and 20° to 27°C, viability of larvae was reduced by both the individual effects of salinity and temperature and interactions between the two factors. Survival capacity of larvae and resistance adaptations to salinity and temperature were progresively reduced by zinc concentrations from 0.25 to 1.00 ppm Zn⁺⁺. Response-surface analysis of the data suggested that the duration of total larval development of P. pugio was least at salinities from 18 to 23 and at temperatures from 30° to 32°C. At both higher and lower salinity-temperature conditions and in increasing zinc concentrations from 0.25 to 1.00 ppm Zn⁺⁺, developmental rates were retarded. A significant zinc-temperature interaction existed, whereby increasing zinc concentrations reduced both survival and developmental rates of larvae more at suboptimal temperatures. Larval resistance to zinc toxicity was least at supraoptimal salinities, indicative of a significant zinc-salinity interaction. The reduced viability, restricted euryplasticity, and retarded developmental rates of P. pugio larvae developing in media with low-level zinc contamination would limit the distributive properties of the pelagic phase in the life cycle of the species and reduce recruitment both into and out of the parent estuarine population.     

Suitability of estuarine nursery zones for juvenile weakfish (Cynoscion regalis): effects of temperature and salinity on feeding,growth and survival

Juvenile weakfish, Cynoscion regalis (Bloch and Schneider, 1801), exhibit significant spatial diffrences in growth rate and condition factor among estuarine nursery zones in Delaware Bay. The potential influence of temperature and salinity on the suitability of estuarine nursery areas for juvenile weakfish was investigated in laboratory experiments by measuring ad libitum feeding rate, growth rate and gross growth efficiency of juveniles collected in Delaware Bay in 1990 (40 to 50 mm standard length; 1.4 to 2.1 g) in 12 temperature/salinity treatments (temperatures: 20, 24, 28°C; salinities: 5, 12, 19, 26 ppt) representing conditions encountered in different estuarine zones during spring/summer. Feeding rates (FR) increased significantly with temperature at all salinities, ranging from 10 to 15% body wt d^-1 at 20°C to 33–39% body wt d^-1 at 28°C. Specific growth rates (SGR) ranged from 1.4 to 9.4% body wt d^-1 (0.3 to 1.5 mm d^-1) and gross growth efficiencies (K ₁) varied from 13.6 to 26.4% across temperature/salinity combinations. Based on nonlinear multiple regression models, predicted optimal temperatures for SGR and K ₁ were 29 and 27°C, respectively. Salinity effects on SGR and K ₁ were significant at 24 and 28°C where predicted optimal salinity was 20 ppt. At these warmer temperatures, SGR and K ₁ were significantly lower at 5 than at 19 ppt despite higher FR at 5 ppt. Therefore, maximum growth rate and growth efficiency occurred under conditions characteristic of mesohaline nurseries. This finding is consistent with spatial patterns of growth in Delaware Bay, implying that physicochemical gradients influence the value of particular estuarine zones as nurseries for juvenile weakfish by affecting the energetics of feeding and growth. Laboratory results indicate a seasonal shift in the location of physiologically optimal nurseries within estuaries. During late spring/early summer, warmer temperatures in oligohaline areas permit higher feeding rate and faster growth compared to mesohaline areas. By mid-late summer, spatial temperature gradients diminish and mesohaline areas provide more suitable physicochemical conditions for growth rate and growth efficiency whereas oligohaline areas become energetically stressful. Substantial mortality occurred at 5 ppt and 28°C, providing additional evidence that oligohaline conditions are stressful during late summer. Furthermore, juveniles provided a choice among salinities in laboratory trials preferred those salinities which promoted higher growth rates. The extensive use of oligohaline nurseries by juvenile weakfish despite the potential for reduced growth rate and growth efficiency suggests this estuarine zone may provide a substantial refuge from predation.     

A response-surface approach to the combined effects of temperature and salinity on the larval development of Adula californiensis (Pelecypoda: Mytilidae). I. Survival and growth of three and fifteen-day old larvae

Laboratory experiments of a factorial design were used to examine the combined effects of temperature and salinity on the survival and growth of early and late-stage larvae of Adula californiensis (Phillippi, 1847). Response-surface curves were generated to predict optimal conditions for survival and growth in order to better understand the successful recruitment of this species within the Yaquina Bay estuary (Oregon, USA). Three-day old cultured larvae were more sensitive to reduced salinity than were 15-day old larvae. However, the 15-day old larvae showed a narrower temperature tolerance than the 3-day old larvae. A. californiensis larvae survived over a wider range of temperatures near optimum salinities than at salinities near their lower tolerance limit, and conversely. Temperature and salinity ranges for maximum survival (10° to 15°C, 31 to 33) were narrower than the ranges which occur within the estuary where the adult populations exist. Larval size did not increase markedly during the 15-day rearing period, and was not greatly affected by temperature or salinity. No statistically significant temperature-salinity interaction was found for either survival or growth.     

Temperature,salinity and ultraviolet irradiation effects on the growth of strains of Nitzschia ovalis

Three strains of Nitzschia ovalis Arnott grew at temperatures from 15°–36°C and at salinities from 5–40 S Optimum growth occurred at combinations of 25°, 27.5° and 30°C and 25, 30 and 35S. This estuarine benthic diatom tolerates wide salinity and temperature conditions while demonstrating resistance to ultraviolet irradiation at 350 nm.     

Distribution of the cladoceran Podon polyphemoides in the Chesapeake Bay

The distribution of the cladoceran Podon polyphemoides (Leuckart) in the Chesapeake Bay (USA) estuarine system was determined by a quantitative pump sampling method, and the patterns of abundance were correlated with temperature and salinity distributions. The species was seasonally recurrent, with distinct population maxima in the central portion of the bay. Population densities in excess of 60,000 podonids/m³ have been recorded. The podonids first appeared in the spring in the shallow tributaries, when water temperatures near the bottom reached 6°C. The vernal populations disappeared when summer temperatures exceeded 27°C, but reappeared in the fall as the water cooled. The species was euryhaline and eurythermal in its distribution, but the greatest concentrations were attained within relatively narrow zones of temperatures between 11^o and 26°C, and salinities between 8 and 18. The production of males, sexual females and sexual eggs occurred both in the spring and the fall between the thermal limits of 11^o and 17°C.     

Biological observations during rearing experiments with the garfish Belone belone

The garpike Belone belone enters the Wadden Sea in April, to spawn in May and June. The large eggs (3mm) bear numerous, long hair-like filaments. Embryonic and larval development were investigated during rearing experiments in 1970 and 1971. The development of the embryo is described, with special reference to the circulatory system and Kupffer's vesicles. The embryos display ventilation with pectoral fins and gill opercula when still in the egg. They hatch after 2 or 3 weeks at 20° and 16°C, respectively. Newly hatched larvae accept a wide variety of prey, including dry, aquarium fish food. Growth, feeding behaviour, swimming performance, and survival of the juveniles were investigated in the laboratory and in a small outdoor pond. Young garpikes (1 to 3 cm standard length) survive at temperatures ranging from 13° to 25°C, and salinities from 7 to 50%. They may reach 12 to 15 cm in their first summer. Their cruising speed is estimated to be 1 to 2 body lengths/sec. Garpikes disappear from The Wadden Sea in October, and probably migrate offshore. Observations on the behaviour of adults (40 to 70 cm total length) in a large indoor tank, indicate that they avoid high light intensities in winter. Adults display panic reactions when the water temperature drops below 6° to 7°C; this indicates that garpikes probably migrate in winter to greater depth (lower light intensity), to avoid water temperatures below 6°C and rough weather conditions in the upper water layers.     

Salinity and temperature tolerance of zoeae of the portunid crab Scylla serrata

The tolerances of the first zoeal stage of the crab Scylla serrata (Forskal) have been investigated in 64 different temperature-salinity combinations. Exposure to temperatures above 25°C or to salinities below 17.5 caused considerable mortality; therefore, zoeae are unsuited to estuarine conditions. The larvae can tolerate temperatures down to 5°C is they are inactive below 10°C. It is suggested that 10°C is probably a lower limit and that female crabs which migrate to sea to release their eggs do not enter water with a temperature below 12°C. Hydrological conditions along the south-east coast of Africa indicate that females would, therefore, migrate less than 10 km offshore.