Effect of temperature on laboratory growth,reproduction and life span of Octopus bimaculoides

Laboratory culture of 40 Octopus bimaculoides from April 1982 to August 1983 through the full life cycle at 18°C vs 23°C provided information on the growth, reproductive biology and life span of this California littoral octopus. At 18°C, the cephalopods grew from a hatchling size of 0.07 g to a mean of 619 g in 404 d; the largest individual was 872 g. Octopuses cultured at 23°C reached their highest mean weight of 597 g in 370 d; the largest individual grown at this temperature was 848 g after 404 d. Growth data revealed a two-phase growth pattern: a 5 mo exponential phase followed by a slower logarithmic (power function) phase until spawning. At 5 mo octopuses grown at 23°C were over three times larger than their 18°C siblings. However, beyond 6.5 mo, growth rates were no higher at 23°C than at 18°C. At 13.5 mo, the mean weight of the 18°C group surpassed that of the 23°C group. The slope of the length/weight (L/W) relationship was significantly different for the two temperature regimes, with the 23°C octopuses weighing 18% less than their 18°C siblings at a mantle length of 100 mm. Females weighed more than males at any given mantle length. Males grew slightly larger and matured before females. The L/W relationship indicated isometric body growth throughout the life cycle. Higher temperature accelerated all aspects of reproductive biology and shortened life span by as much as 20% (from approximately 16 to 13 mo). O. bimaculoides has one of the longest life cycles among species with large eggs and benthic hatchlings. Extrapolations to field growth are made, and the possible effects of temperature anomalies such as El Niño are discussed.     

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.     

Effects of temperature on feeding and activity in the crab Scylla serrata

The effect of temperature on feeding, duration of emergence and movement by the crab Scylla serrata (Forskal) was measured under laboratory conditions using infrared time-lapse photography. Little difference was found between experiments carried out at 25° and 20°C. All parameters measured declined at 16°C. At 12°C emergence time and movement were 24 and 33% respectively of the level at 25°C. At 25°C, 65% of crabs fed, but none did so at 12°C. No statistically significant difference was found between male and female crabs in the parameters measured.     

Autecological investigation on marine diatoms 3. Thalassiosira nordenskioeldii and Chaetoceros diadema

The temperature range for the best competitive position by growth of Thalassiosira nordenskioeldii Cleve has been determined by comparing generation times. It ranges from-1.5° to 6°C. At these temperatures, especially at lower light intensities, it was one of the fastest growing species, whereas above 6°C many other species grew faster. High light intensities at increasing temperatures became damaging. A flowering of the cold oligo-eurytherm diatom T. nordenskioeldii occurs not only in the upper layers, but can also occur at greater depth simultaneously, because decreasing daylengths at 6°C had the least influence on its growth. Continuous light at 6°C had a positive influence on its growth. The start of the T. nordenskioeldii spring flowering under the Arctic Sea Ice is discussed in connection with the occurrence of enclosed marine diatoms in Polar Sea Ice. The influence of the winter temperature on the spring flowering of the North Sea, the southern border for flowerings of T. nordenskioeldii, is discussed. For Chaetoceros diadema (Ehrenberg) Gran the best competitive position by growth is reached at-1.5° to about 6°C. It has the best opportunity of reaching high cell numbers at the lowest temperatures of the range. The occurrence of the cold oligo-eurytherm diatom Ch. diadema in plankton samples at temperatures above 10°C need not be incorret, for the species did grow in cultures at 12° and 16°C. The wrong interpretation of the experimentally determined optimum temperature of e.g. T. nordenskioeldii caused a discrepancy between experimental results and field data that does not exist. The question is discussed whether ecologically it is relevant to talk about a temperature optimum. On account of the results of T. nordenskioeldii the question of the adaptation of diatom cultures for the start of the real experiments is discussed.     

Preliminary rearing experiments on the larvae of Sergestes lucens (Penaedia,Natantia, Decapoda)

Sergestes lucens Hansen, a mesopelagic shrimp fished commercially in Suruga Bay, Japan, was successfully reared from egg to post-larval stage V under laboratory conditions. Chaetoceros ceratosporum and Artemia nauplii were found to be satisfactory food in the laboratory during rearing. Growth, mortality, food preference, and feeding and swimming activities during the various developmental stages were investigated. Temperature changes greatly affected the speed of development and the mortality of the larvae. The optimum temperature range for larval development was 18° to 25°C. The growth rate (length) of larval stages was as rapid as 0.16mm/ day at 20 °C and 0.21 mm/day at 23 °C. The larvae first started feeding on phytoplankton at elaphocaris stage I, and then gradually became predators in the post-larval stages. It is suggested that the critical period for the species occurs in the elaphocaris stages. Environmental data, vertical distribution of the species, and data obtained from laboratory experiments suggest that the fluctuation in the abundance of S. lucens is greatly influenced by the water temperature at around 50 m from June to August. Feeding mechanisms observed in the post-larval stages are described.     

Growth and moulting of Neomysis integer (Crustacea: Mysidacea)

The growth and moulting of Neomysis integer (Leach) was investigated in the field and the laboratory. In the Ythan estuary, Aberdeenshire, Scotland, monthly samples taken from November 1976 to October 1978 revealed that the summer generation juveniles and mature individuals grew at a rate of 4 to 5 mm and 1 to 2 mm monthly, respectively. The winter generation had a growth rate of 3 to 4 mm monthly for juveniles and about 1 mm for mature individuals; during the winter there was a period of 3 mo when growth was almost completely stopped. Mysids reared in the laboratory on Artemia sp. nauplii had an average daily growth rate of 0.06 mm at 9°C and 0.09 mm at 16°C. The growth factors of N. integer ranged from 3 to 17% for mature and immature individuals, respectively. Intermoult periods ranged from 3 to 7 d in immature mysids to 12 to 18 d in mature mysids. Average laboratory growth curves calculated from information on growth factors and intermoult periods indicate that at 9°C (winter generation) it takes N. integer 277 d to grow to be a 15 mm mature individual, whereas at 16°C (summer generation) it takes 188 d. N. integer moults 24 times as it grows from a juvenile to a mature individual.     

Effects of delayed feeding and temperature on the age of irreversible starvation and on the rates of growth and mortality of Pacific herring larvae

The time periods from exhausion of the yolk to the age of irreversible starvation for Pacific herring Clupea harengus pallasi larvae were 8.5, 7.0 and 6.0 d at 6°, 8° and 10°C, respectively. These periods are within the range perviously measured for Atlantic herring larvae and other temperature zone fish species; they are long compared to the periods for tropical species. The variation in the length of this period is due almost entirely to temperature; the natural logarithm of the time period from fertilization to irreversible starvation is highly correlated (r=0.91) with the mean rearing temperature for 25 species of pelagic marine fish larvae. The rates of growth and mortality, measured for 26 experimental populations of Pacific herring larvae reared at 6°, 8° and 10°C and ten ages of delayed first feeding, decreased and increased, respectively with increasing age of first feeding and increasing temperature. These rates, adjusted for the effects of rearing conditions, were compared with the rates for natural populations of herring larvae. Growth is generally faster in the sea than in experimental enclosures. Two of the eleven estimates of natural mortality rate were high enough to indicate possible catastrophic mass starvation. This is consistent with Hjort's critical period concept of year class formation and it suggests that mass starvation occurs in 18 to 36% of the natural populations of first feeding herring larvae.     

Autecology and clonal variability of the marine centric diatom Thalassiosira rotula (Bacillariophyceae) in response to light,temperature and salinity

The influence of 49 combinations of salinity (10–40 S, at 5 S intervals) and temperature (0°–30°C, at 5C° intervals) on the maximum daily division rate (K) and 18 combinations of light intensity (six levels) and temperature (5°, 15°, and 25°C) on photosynthesis, cell division, and chlorophyll a was examined using two clones of Thalassiosira rotula Meunier isolated from the upwelling area of Baja California (clone C8) and from Narragansett Bay, Rhode Islands (clone A8). Physiological differences appear to characterize these to clones with regard to their temperature tolerance (C8 5°–30°C, A8 0°–25°C), maximum growth rate (C8 K=2.9, A8 K=2.4), chlorophyll a content, and in the rates of growth and photosynthesis in response to light intensity and temperature. Optimum salinity for both clones (25–30 S) was generally independent of temperature, while chlorophyll a content decreased with temperature. T. rotula is a cosmopolitan paractic species; experimental studies indicate that it is eurythermal and moderately euryhaline. Comparison of five additional Narragansett Bay isolates of T. rotula reveal minimal spacial or temporal variability in genetically determined physiological characteristics within this local population.     

Influence of light and temperature on the growth rate of estuarine benthic diatoms in culture

Four species of estuarine benthic diatoms: Amphiprora c. f. paludosa W. Smith, Nitzschia c. f. dissipata (Kützing) Grunow, Navicula arenaria Donkin, and Nitzschia sigma (Kützing) W. Smith were grown in unialgal cultures. The growth rates of the diatoms were determined as the rate of increase of the chlorophyll a content of the cultures. The diatoms were cultured at different combinations of temperture, daylength, and quantum irradiance. The highest growth rates of Navicula arenaria occurred at 16° to 20°C; the other 3 species had their optimum at 25°C or higher. The small-celled species had higher growth rates at their optimum temperature, but at lower temperatures the growth rates of all 4 species became very similar. The minimum daily quantum irradiance that could effect light-saturated growth at 12° and 20°C ranged from 2.5 to 5.0 E.m^-2.day^-1. At 12°C, two species had their highest growth rates under an 8 h daily photoperiod. At 20°C, the three species tested all had highest growth rates under 16 h daily photoperiod. The growth response of the benthic diatoms is comparable to that of several cultures of planktonic diatoms, as described in the literature. The influence of temperature and quantum irradiance on the diatoms in the present investigation was comparable to the influence of temperature and light intensity on the ¹⁴C-fixation of marine benthic diatoms (Colijn and van Buurt, 1975).     

Response of gametophytes of Ecklonia radiata (Laminariales) to temperature in saturating light

Gametophytes of Ecklonia radiata (C.Ag.)J.Ag. from two New Zealand locations with different field temperature ranges were exposed to temperatures of 5° to 26°C in saturating light. Plants from Goat Island Bay (Lat. 36° 16S, Long. 174°48E) grew in 9.3° to 25°C and reproduced in 9.3° to 24°C. There was no growth at 8°C and plants died at 26°C. Plants from the cooler location, Houghton Bay (Lat. 41°20S, Long. 174°40E), grew from 8° to 24°C and reproduced up to 15°C but not at 21.5°C. The plants did not grow at 6°C and died at 26°C. The timing of the first cell division and subsequent growth rate were retarded close to the upper and lower tolerance limits. Reproduction was a broad optimum of roughly 12° to 20°C. Within this range, fertile female gametophytes grown at lower temperatures had fewer, larger cells and thus fewer potential ova than those grown at higher temperatures.     

Temperature and development in larvae of the turbot Scophthalmus maximus

Turbot (Scophthalmus maximus L.) were reared at 12 and 16°C until 26 d after hatching. At both temperatures, starting at the neural plate stage, somites were initially formed every 75 min. Expressed as a percentage of development time (DT, fertilisation to 90% larvae hatching) somite formation occurred relatively earlier during embryogenesis at 12°C (45% DT) than at 16°C (55% DT). At 12°C, after the 32-somite stage the rate of somite formation decreased to one every 300 min. The larvae hatched after 6 d at 12°C and 3 d at 16°C at a relatively primitive stage of development, prior to the opening of the mouth and anus, with unpigmented eyes, and a straight gut. Temperature altered the relative timing of organogenesis in the larval stages. At 12°C, the following characters appeared (in this order): swimbladder>loop in the gut (at the time of yolk exhaustion)>caudal fin. In contrast, at 16°C, the caudal fin appeared at the same time as the loop in the gut. At 16°C, spines formed on the head in the region of the otic capsule at the time the swimbladder formed and the yolk was exhausted, but were absent in 12°C larvae. At both temperatures, in 1 d-old larvae the myotomes just behind the yolk-sac contained 200 inner muscle fibres (presumptive white muscle). The initial growth of inner muscle was largely due to hypertrophy, but by 26 d at 12°C and 11 d at 16°C hyperplastic growth became important, as evidenced by a significant increase in the number of small fibres (<10 m²). By 26 d the average number of inner muscle fibres had increased to 341 at 12°C and 988 at 16°C. New muscle fibres were added in distinct germinal zones at the dorsal and ventral apices of the myotomes. Metamorphosis was associated with a thickening of the superficial (presumptive red) muscle layer and the appearance of tonic muscle fibres.     

Clearance rates of food suspension and food passage rates as a function of temperature in two north-sea bryozoans

The filtration rate has been determined for Electra pilosa and Conopeum reticulum, acclimated at 4 constant temperatures (6°, 12°, 18°, 22°C). Cryptomonas sp. was used as the test food-organism. Temperature affects filtration rate in both bryozoans. Clearance rate, measured at hourly intervals during the course of the experiment, was never uniform. Possibly, temporary reductions in ciliary activities were induced by the artificial conditions under which the experiments were carried out. The results obtained compare well with those reported by Bullivant (1968) on Bowerbankia imbricata, a cosmopolitan ctenostome. Rate of food passage through the alimentary canal is affected by temperature. The present study is the first to demonstrate the effect of temperature on the rate of filtration in bryozoans.     

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     

Metabolic maintenance costs of the suspension feeder Styela plicata

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

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.     

Feeding,conversion efficiencies,and growth of larval mummichogs,Fundulus heteroclitus

Feeding rates, conversion efficiencies and growth of larvae of the mummichog Fundulus heteroclitus, an extremely abundant estuarine fish, were measured at temperatures ranging from 18° to 30°C. The food used was Artemia salina nauplii. At the time of total yolk sac absorption (5 to 7 days after hatching), the feeding rate decreased for a short time, an indication of a shift in metabolism. Higher feeding rates and growth occurred at higher rearing temperatures. The highest conversion efficiency (gross growth efficiency) was 1.1%, at 22°C. Mummichog larvae may be energetically inefficient compared with other fish species, but efficiency might not be critical for this fish, which is an opportunistic omnivore in an energy-rich environment.Contribution No. 291 of the Belle W. Baruch Institute for Marine Biology and Coastal Research, supported by DOE contract No. EY-76-5-09-0869.     

Interactions between light and temperature on the physiological ecology ofGracilaria tikvahiae (Gigartinales: Rhodophyta)

Main effects and interactions of light and temperature on rates of growth (), net photosynthesis (P_s), and dark respiration (R) of the red seaweedGracilaria tikvahiae were investigated in outdoor, nutrient-replete continuous-flow seawater culture chambers. Below 15°C,G. tikvahiae did not grow and between 15° and 30°C, both main effects and interactions of light and temperature on and P_s were significant, which explains the occurrence of this alga as a summer annual in its northern range. Temperature interacted with light (I) through its influence on the vs I and P_s vs I curves. The initial slope of the vs I curve, , the light saturation intensity, I_s, and maximum growth rate, _max, were all significantly lowerat 15°C compared to 20°, 25°, or 30°C. Maximum values of _max, the P_s:R ratio and the net photosynthesis:gross photosynthesis ratio (P_s:P_g) all occurred at 25°C, suggesting that this is the best temperature for growth ofG. tikvahiae. Values for P_max increased up to 30°C, indicating that the temperature for maximum growth and net photosynthesis are not the same forG. tikvahiae. Significant photoinhibition of growth and photosynthesis at full incident sunlight (I₀) occurred at 15°C but not at 20°, 25°, or 30°C. Steele's equation fit the 15°C vs I data best, whereas the hyperbolic tangent function fit the 20°, 25°, and 30°C data best. Main effects and interactionof light intensity and temperature on rates of R were also significant (P<0.001). R was highly intercorrelated with and P_s (0.86r0.94), indicating that R inG. tikvahiae is primarily regulated by growth rate and not temperatureper se. Environmental factors that regulate growth, such as light intensity, exert a great influence on R inG. tikvahiae.     

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     

Effect of temperature on the escape responses of larval herring,Clupea harengus

Herring (Clupea harengus L.) larvae from spring and autumn spawning stocks were reared at different constant temperatures from 5° to 17 °C. At equivalent developmental stages, the spring larvae were longer than the autumn larvae and the larvae reared at low temperatures were longer than those reared at high temperatures. At hatching and at the end of the yolk-sac stage, the larvae were induced, by a probe, to make C-start escape responses, which were recorded and analysed using a high-speed video recording at 400 frames s^-1. The response was rapid and of short duration. The tailbeat frequency and swimming speed were measured during the burst of swimming following the C-start at different test temperatures and in larvae with different temperature histories. The tail-beat frequency was strongly temperature-dependent, rising from 19 Hz at 5 °C to 37 Hz at 17 °C with no effect of temperature history, season or developmental stage. The burst-swimming speed ranged at hatching from 75 to 90 mm s^-1 at 5 °C to 110 to 160 mm s^-1 at 17 °C and at yolk resorption from 90–115 mm s^-1 at 5 °C to 175–190 mm s^-1 at 17 °C. The longer, spring-spawned larvae swam faster than the shorter autumn-spawned larvae. When the swimming speeds were expressed as body lengths (L) s^-1, these differences disappeared. Larvae swam from 7–9 L s^-1 at 5 °C to 15–20 L s^-1 at 17 °C at hatching, and from 8–9 L s^-1 at 5 °C to 15–17 L s^-1 at 17 °C at yolk resorption. There was, however, a significantly faster specific swimming speed by the larvae reared at 12 °C in spring 1991.Honorary Research Fellow of the Scottish Association for Marine ScienceUnfortunately, Karen Fretwell was drowned in an accident on 9 January 1993     

Nitrogen regeneration by the surf zone penaeid prawn Macropetasma africanus

Nitrogen excretion of individual Macropetasma africanus (Balss) from an exposed beach/surf zone in Algoa Bay, South Africa was monitored under laboratory and field conditions in relation to body mass, temperature and feeding during 1985. Excretion rate experiments were performed on starved prawns at 15°, 18°, 20° and 25°C, as well as on individuals fed on four different diets (mussel, fish, shrimp and natural diet) at 15° and 20°C. The ratios of the excreted compounds to total nitrogen excreted were similar for the four diets despite differences in their nitrogen content and in the amount of food consumed. At 15° and 20°C, ammonia excretion rates of fed individuals were four to seven times higher than in starved prawns. the excretion rates were not correlated with nitrogen content of diets. M. africanus recycles 1 557 g NH₄–N per metre strip per year or 1 832 g total nitrogen m^-1 yr^-1, which constitute 12 and 14%, respectively, of total phytoplankton requirements of the surf zone. This study indicates that large motile crustaceans, when abundant, can play an important role in nutrient recycling in turbulent marine environments.