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.     

Effects of temperature and salinity on larval development ofNecora puber (Brachyura: Portunidae)

Temperature and salinity affected both length of larval development and mortality inNecora puber collected in the Ría de A Coruña during December 1984 and January 1985. Development time decreased considerably with increased temperature. This decrease was sharper when temperature increased from 15° to 20°C than when it increased from 20° to 25°C. At 35S, average development took 48, 32 and 28 d at 15°, 20° and 25°C, respectively. At the three salinities tested (25, 30 and 35), larval development was completed only at 15°C, at 20°C/30 and 35S, and at 25°C/35S. Development times at 15° and 20°C were highly significantly different at both 35 and 30S (P 0.01). However, there were no significant differences between development times at 20° and 25°C (P > 0.05). Within any one specific temperature series, no significant difference was observed between the salinity values tested (P > 0.05). The duration of each of the five zoeal stages was similar within each and the same temperature/salinity combination, whereas the duration of the megalop was twice as long as any of the zoeal stages. The combination of the lowest temperature (15°C) and the highest salinity (35) tested resulted in the greatest larval survival of 28%. Highest mortality occurred at 25°C, at which temperature development was completed only at 35S. A sharp drop in larval survival was observed in the transition period Zoea V — megalop in all combinations of temperature and salinity tested. Within the limits of tolerance to temperature and salinity, the former effected more pronounced differences in the duration of larval development, while salinity appeared to constitute a limiting factor for survival.     

Influence of salinity on embryonic development and the distribution ofSepia officinalis in the Delta Area (South Western part of The Netherlands)

The effect of salinity on embryonic development ofSepia officinalis (cuttlefish) in the Delta Area (South Western part of The Netherlands) was investigated in 1988/1989, and compared with data concerning the distribution ofS. officinalis in the three main parts of this area: Oosterschelde, Westerschelde and Grevelingen. Embryos hatched in water collected at Yerseke (Oosterschelde), Vlissingen (Western part of the Westerschelde) and Bommenede (Grevelingen), i.e., at salinity values above 28.1, but not in water sampled at Hoedekenskerke and Hansweert (Middle and Eastern part of the Westerschelde; salinities below 22.0). Under laboratory conditions, using diluted Oosterschelde water, the highest hatching percentages ofS. officinalis were found at salinities above 29.8. Some embryos hatched at a salinity value of 26.5 but no hatching occurred at salinities below 23.9. In embryos exposed to salinity changes during late embryonic development, the developmental rate decreased at salinity values of 28.7 or less. Below 22.4 embryos with morphological malformations were found. It can be concluded that salinity is an important factor limiting the distribution ofS. officinalis in most parts of the Delta Area, with the exception of the Western part of the Westerschelde and the Grevelingen.Contribution no. 489 of the Library of the Delta Institute for Hydrobiological Research     

Effects of salinity on respiration and nitrogen excretion in two species of echinoderms

The 30-d survival limit of Eupentacta quinquesemita and Strongylocentrotus droebachiensis is 12–13 S. The activity coefficient (1 000/righting time in seconds) of stepwise acclimated sea urchins declined from 16.3 at 30 S to 3.5 at 15 S. Oxygen consumption rates (QO₂) of both species held at 30 S and 13°C were highest in June and lowest in December. During the summer, when environmental salinity is most variable in southeastern Alaska, the QO₂ of both species held at 30, 20 and 15 S varied directly with salinity. Perivisceral fluid PO₂ varied directly with acclimation salinity in sea urchins, but not in sea cucumbers. Perivisceral fluid oxygen content of acclimated sea urchins was significantly lower at 15 and 20 S than at 30 S due to reduced PO₂ and extracellular fluid volume at the lower salinities. The QO₂ of both species varied directly with ambient salinity during a 30-10-30. semidiurnal pattern of fluctuating salinity. No change occurred in the average QO₂ of either species over a 15-30-15. semidiurnal pattern of fluctuating salinity. Sea urchin perivisceral fluid PO₂ declined as ambient salinity fluctuated away from the acclimation salinity in both cycles and increased as ambient salinity returned to the acclimation salinity. Total nitrogen excretion of stepwise acclimated sea cucumbers declined significantly from 30 to 15 S, but there was no salinity effect on total nitrogen excretion in sea urchins. Ammonia excretion varied directly with salinity in stepwise acclimated sea cucumbers (67–96% of total nitrogen excreted), but there was no salinity effect on ammonia excretion (89–95% of total nitrogen excreted) of sea urchins. Urea excretion did not vary with salinity in sea cucumbers (2–4% of total nitrogen excreted) or sea urchins (2–9% of total nitrogen excreted). Primary amines varied inversely with salinity in sea cucumbers (2–30% of total nitrogen excreted), but did not vary with salinity in sea urchins (2–4% of total nitrogen excreted). The oxygen: nitrogen ratio of both species indicated that carbohydrate and/or lipid form the primary catabolic substrate. The O:N ratio did not vary as a function of salinity. Both species are more tolerant to reduced salinity than previously reported, however, rates of oxygen consumption and/or nitrogen excretion are modified by salinity as well as season.     

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.     

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     

The respiratory metabolism of Tilapia mossambica (Teleostei)

In a series of experiments 174, 120 and 139 individuals of the teleost Tilapia mossambica (Peters), were acclimated to 30°C and to salinities of 0.4, 12.5 and 30.5, respectively. The effect of temperature and salinity upon oxygen consumption was studied by abruptly transferring fish of different wet weights to temperatures from 15° to 40°C at an average initial pO₂ of 250mm Hg. At each salinity, the proportionate response to temperature is size-independent. The metabolic rate increases as a function of temperature at 15° and 30°C but not at 40°C. Oxygen consumption is, however, salinity dependent; maximum rates are obtained at 12.5S. This salinity is isotonic in the 80 g fish and, to a lesser extent, in the 5 g fish. Reduction in osmotic load is suggested as the probable cause for a greater scope for activity and greater rate of oxygen consumption in 12.5 salinity.     

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.     

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.     

Salinity dependence of sexual and asexual reproduction in the rotifer Brachionus plicatilis

A salinity dependent mictic response was observed in a clone of Brachionus plicatilis cultured in the 2 to 4 salinity range. This response was related to asexual exponential reproduction rates (G) and could be divided into three categories: (a) no mixis occurred at a salinity of 35 S and above, where G values were lower than 0.30 d^-1, (b) low mictic levels in rotifers cultured at 2 and 30 S, where G values ranged between 0.40 to 0.50 d^-1, and (c) high mictic levels in rotifers cultured at salinities ranging between 4 and 20 S, where G values ranged between 0.50 to 0.85 d^-1. Fluctuations in mictic levels varied with time during the course of the experiments. Results suggest that salinity conditions leading to optimal parthenogenic reproduction also support mixis.     

Influence of salinity and temperature on the oxygen consumption in young juveniles of the Indian prawn Penaeus indicus

Routine oxygen consumption of very young juveniles (0.1 g) of Penaeus indicus H. Milne Edwards was significantly influenced by ambient temperature and weight of the animal, but not by ambient salinity, when tested at salinities (7, 21, and 35) to which they had been long-term (over 10 days) acclimated. Standard oxygen consumption of young juvenile prawns (1 to 3 g), subjected to step-wise changes in ambient salinity, from sea water to low salinity waters (2 to 6), and measured after short-term (24 h) salinity acclimation at each step, was lowest at salinities where prawns such as those tested occur naturally (10 to 15). The metabolic rates do not appear to have a direct relation to the osmotic gradient, even when the influence of interfering activity is eliminated. It appears that factors other than osmotic gradient will have to be sought in order to explain the metabolic patterns of P. indicus in relation to salinity.     

Stepwise acclimation—a method for estimating the potential euryhalinity of the gastropod Hydrobia ulvae

The White Sea gastropod Hydrobia ulvae (Pennant) was exposed to step-wise lowering or increase of the habitat salinity. The time allowed for acclimatization to the successive salinity levels was sufficient to complete non-genetic adaptation. In this way, the lower and upper salinity limits were extended. The tolerance limits obtained are assumed to be indicative of the capacity for non-genetic adaptation and to serve as a genotypical characteristic. The tolerance of specimens colleced from in situ conditions (mid littoral, 20 S) ranged between 14 and 34 S. After non-genetic adaptation, the lower tolerance value shifted to 6 S (adaptation limit), and the upper value to 76 S (final limit not reached). There is no reason for considering White Sea H. ulvae to represent a special physiological race of specimens from those on the coast of Great Britain.     

Effects of salinity on fasted rainbow trout,Salmo gairdneri

Rainbow trout (Salmo gairdneri Richardson) which had been maintained for 120 days in salinities of fresh water, 7.5, 15.0 and 32.5 at 10°C were fasted for up to 48 days under these same environmental conditions. Live weight loss between Days 7 and 48 of starvation could be described by a straight line, as could the decrease in condition factor . Trout maintained in 32.5% S showed a significantly greater weight loss than those in salinities of 15.0 and below. Muscle water content increased slightly during fasting in fresh water, 7.5 and 15.0 S. In 32.5 S, however, muscle water fell significantly between Days 19 and 37. Liver water content also increased slightly during fasting, except in 32.5 S, where water content again decreased between Days 19 and 37. The volume of the gall bladder contents increased during fasting.     

Effects of salinity fluctuations on the respiration rate of the southern oyster drill Thais haemastoma and the blue crab Callinectes sapidus

Respiration rates of Thais haemastoma and Callinectes sapidus were determined as a function of salinity with a flow-through respirometer at 20°C. Respiration rates were measured at 10, 20 and 30 S for acclimated animals. The effects of 10-5-10, 20-10-20, 30-10-30 and 10-30-10 S semidiurnal cycles (12 h) of fluctuating salinity on the rate of respiration of the oyster drill were studied. During each cycle, salinity was changed from the acclimation salinity over a 4 h interval, held at that salinity for 2 h, returned to the acclimation salinity over 4 h and held at that salinity for 2 h. The effects of diurnal (24.8 h) salinity cycles on respiration in the oyster drill and blue crab were also studied. Salinity was changed from the acclimation salinity over a 10.4 h interval, held at that salinity for 2 h, then returned to the acclimation salinity over 10.4 h and held at that salinity for 2 h. The respiration rate of 30 S acclimated oyster drills (679 l O₂ g dry weight^–1 h^–1) was significantly higher than for individuals acclimated to 10 S (534 l O₂ g dry weight^–1 h^–1). Blue crab respiration was 170 l O₂ g dry weight^–1 h^–1 at 30 S, and was significantly higher at 10 and 20 S than at 30 S. With the exception of the 20-10-20 S semidiurnal cycle, the respiration rate of oyster drills declined as salinity fluctuated in either direction from the acclimation salinity and increased as ambient salinity returned to the acclimation salinity. Semidiurnal cycles (12 h) of fluctuating salinity produced greater changes in the respiration rate of snails than analogous diurnal cycles (24.8 h). A 10-30-10 S pattern of fluctuation caused a greater percentage reduction in the steady state respiration rate of oyster drills than the 30-10-30 S pattern. The respiration rate of blue crabs varied inversely with fluctuating salinity. Relatively minor changes occurred in blue crab respiration rate with fluctuating salinity. Blue crab respiration rate characteristically dropped during the initial phase of declining salinity at a rate directly proportional to the rate of salinity decrease, perhaps representing a metabolic adjustment period by the blue crabs. The respiratory response of T. haemastoma to salinity is consistent with its incomplete volume regulation, while the response of C. sapidus is compatible with its ability to regulate extracellular fluid osmotic and ionic composition.     

Calcification in the maerl coralline alga Phymatolithon calcareum: Effects of salinity and temperature

The coralline alga Phymatolithon calcareum was dredged from 13 m in the Kattegatt, Baltic Sea, in December, 1980, and its rate of calcification was measured by ⁴⁵Ca⁺⁺-uptake methods. Light-saturated calcification rates at 5°C ranged from 15.8 g CaCO₃ g^-1 dry wt h^-1 for the basal parts of the plants to 38.7 g CaCO₃ g^-1 dry wt h^-1 for the tips. These age gradients were not apparent when calcification rates were expressed on the basis of surface area. Experiments with salinity (10, 20, 30) and temperature (0°, 5°, 10°, 20°C) indicated that optimum conditions for calcification were at 30 S and at temperatures above 10°C. Salinity had a greater influence on calcification rate than did temperature, and there was a positive relationship between salinity and calcification rate at all temperatures. In 6 mo old cultures, salinity was again the important factor, with all plants remaining healthy at 30 except those at the highest temperature (20°C). These trends, and the low calcification rates at 10S (4.6 g CaCO₃ g^-1 dry wt h^-1 at 5°C to 8.6 g CaCO₃g^-1 dry wt h^-1 at 20°C) suggest that low salinity may be the explanation for the general absence of P. calcareum from the brackish waters of the Baltic Sea. Short-term experiments in which salinity was kept constant while Ca⁺⁺ concentration was altered, and experiments in which salinity was varied and Ca⁺⁺ concentration kept constant, suggest that it is the calcium ion concentration and not salinity per se which affects calcification rates.     

The respiratory metabolism of Tilapia mossambica (Teleostei)

Tilapia mossambica (Teleostei) weighing 5 to 80 g were acclimated at 30°C to salinities of 0.4 (tap water), 12.5 (50% sea water) and 30.5 (100% sea water). Their respiration was measured at routine activity and the partial pressure of ambient oxygen gradually reduced from 250 to 50 mm Hg. Respiration is salinity-dependent; the proportionate ability to use oxygen in any one salinity is — above the critical pO₂ —the same in all experimental groups. This ability is a function of temperature and increases from 15° to 30°C, becoming temperature independent from 30° to 40°C as long as the pO₂ remains above 150 mm Hg. At 50 mm Hg pO₂, the limiting effect of oxygen causes a decrease in metabolic rate. This limiting effect is minimal in 80 g fish kept in an isotonic medium (12.5 S), allowing greater scope for activity and a higher rate of oxygen uptake.     

Effect of salinity on hemolymph calcium concentration during the molt cycle of the prawn Penaeus monodon

Prawns (Penaeus monodon) were obtained from ponds in Iloilo, Philippines, in 1984 and 1985 and maintained in salinities from 8 to 44. Total hemolymph calcium was largely affected by molt stage and less so by salinity. A sharp, transient increase in hemolymph calcium occurred 3 to 6 h postmolt, followed by an equally rapid decrease from 6 h postmolt to intermolt. This biphasis response was limited to prawns in 8, 20 and 32S; in 44S, hemolymph calcium remained the same throughout the sampling period. Peak concentrations of total calcium were greater in low (8 and 20S) than in high salinities. Salinity had no effect on the duration of molt cycle nor on time of occurrence of molt. Almost half of molting incidents occurred between 18.01 and 0.00 hrs, and one-third between 0.01 and 06.00 hrs.     

Copper effects on reproductive stages of Baltic Sea Fucus vesiculosus

Copper is an active ingredient in many antifouling products, and pleasure boats are estimated to be the major single source of copper pollution in Swedish coastal waters. For this reason, the effects of copper were studied on egg volume, fertilization, germination and development of apical hairs of Baltic Sea Fucus vesiculosus L. Germination was the most sensitive stage and was studied at different concentrations of copper, different salinities and different ages of zygotes. Low concentrations of copper, 2.5 g Cu l^-1, added to natural brackish water before fertilization, adversely affected germination at the ambient, suboptimal salinity of 6, suggesting that as little as a doubling of the copper levels in the studied area will severely affect the germination frequency of F. vesiculosus. The addition of 20 g Cu l^-1 caused about 70 to 80% decline in germination at 6S but also at 20S which is higher than optimum. At a salinity close to optimum (14S) no negative effect was noticed on germination when 20 g Cu l^-1 was added. The results suggest that the degree of salinity stress acting upon the zygotes is a more important factor for the response to copper than the influence of salinity on metal availability. When 2.5 to 60 g Cu l^-1 was added to the medium 24 h after fertilization, the zygotes were more resistant, resembling the response of adult marine fucoid tissue.     

Laboratory observations on spawning and embryonic development of a blue-ringed octopus

The infratidal zonation of animals in a 35 m deep fjord-like South African estuary is described. The barnacle Balanus amphitrite Darwin and the bivalve Musculus virgiliae Barnard form the uppermost zone and extend to a depth of 9 m. The oyster Crassostrea margaritacea (Lam.) forms a zone between 1 and 3 m depth while the sponge Grantessa ramosa (Haeckel) occurs between 3 and 7 m. The tubiculous polychaete Mercierella enigmatica Fauvel is the only species found below 10 m, and attains a depth of 33 m. In the wet season (summer) the surface salinity dropped to 2 and temperatures rose to 24°C. In the dry season (winter) surface salinity rose to 24 and temperatures dropped to 16°C. Salinity and temperature of deep water (6 to 33 m) were more stable and varied only between 32.5 and 35 and between 19.6° and 20.5°C, respectively. In June, water below 12 m was 50 to 60% saturated with oxygen but this declined to less than 5% saturation in January.     

The effect of temperature-salinity combinations on survival and growth of juvenile Patiriella pseudoexigua (Echinodermata: Asteroidea)

Adult Patiriella pseudoexigua were collected in October 1989 from Wanlitung, Taiwan and then induced to spawn in the laboratory. Post-metamorphosed juvenile P. pseudoexigua were reared on a diet of benthic algae Navicula sp. at 25°C and salinity (34). Six weeks after metamorphosis, juvenile P. pseudoexigua at ca. 400 m in radius were reared on a diet of benthic algae Navicula sp. at different combinations of temperatures (20, 25, 30°C) and salinities (26, 30, 34) for 40 d. Both temperature and salinity had a significant effect on juvenile survival and growth. Juveniles survived best (>90%) at 25°C and 34 and grew best (to ca. 750 m in radius) at 30°C and 34. Variation in juvenile size was small immediately after metamorphosis and increased with time.