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.     

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.     

Effect of the hard clam Mercenaria mercenaria on benthic fluxes of inorganic nutrients and gases

The effect of the hard clam Mercenaria mercenaria (L.) on the exchange of dissolved nutrients (silicate, phosphate, ammonium, nitrate+nitrite) and gases (oxygen, carbon dioxide) across the sediment-water interface was examined in 1983 and 1984 using experimental mesocosms (13 m³), designed to simulate a shallow coastal ecosystem, that allow for reciprocal biogeochemical interactions between water column (5 m) and bottom sediments (30 cm deep). Benthic, fluxes, measured during a spring-summer warming period, were compared for mesocosms maintained either with added M. mercenaria (16 per m², treatment) or without M. mercenaria (control) as a component of the benthic community. Fluxes were within the range observed for the (control) community in situ in mid-Narragansett Bay and exhibited the pattern of increasing flux with increasing temperature observed in nature. For dissolved inorganic (DIN=ammonia+nitrate+nitrite), analytical problems allowed comparison of fluxes only at the higher temperatures (17° to 22°C); average DIN fluxes were 57% higher in mesocosms with clams. Fluxes of other nutrients and gases were modelled as exponential functions of temperature (9° to 22°C) using a linear regression of the natural logarithm of flux upon temperature in both treatment and control situations. Differences between regression slopes and intercepts for conditions with and without clams were assessed by analysis of covariance. Slopes of the linearized temperature-flux relationships were not significantly different between treatments for any flux measured, suggesting that presence of the clams did not alter the basic relationship of flux and temperature normally observed with this community. For oxygen consumption and silicate production, the regression intercepts were significantly higher in the clam treatment, suggesting that the level of flux was generally elevated in the presence of M. mercenaria by about 20% (oxygen) and 86% (silicate) at any given temperature. Data for carbon dioxide and phosphate showed similar trends to oxygen and silicate, but the variance in fluxes was larger and regression intercepts for the two treatments were not significantly different.     

Mantle protein excretion and calcification in the hardshell clam Mercenaria mercenaria. II. Protein synthesis and excretion by the isolated mantle

Sheets of mantle tissue from above the mantle line of Mercenaria mercenaria were incubated for 2, 6 and 20 h at 20°C in 50 Ci ³H-glycine in 50 ml artificial seawater. Incorporation of tritium into soluble proteins excreted by the mantle and into tissue proteins was followed. The excretion of soluble protein continued throughout the experiment; the proportion of incorporated label excreted reached 17% by 20 h. The initiation of excretion of labelled protein seemed to lag 60 to 70 min behind the initiation of protein synthesis. Protein synthesis by the mantle contributed to proteins of the extrapallium and mantle chambers and, thus, may be involved in synthesis and regulation of proteins involved in the shell-formation process.     

Oxygen consumption and ammonia excretion of<Emphasis Type="Italic"> Octopus vulgaris</Emphasis> (Cephalopoda) in relation to body mass and temperature

The common octopus, Octopus vulgaris Cuvier, is of great scientific and commercial importance and its culture is becoming an area of increasing interest. In this study, the combined effects of temperature (T) and body mass (M) on the routine oxygen consumption rate (R) and ammonia excretion rate (U) in O. vulgaris were quantified. The experiments were conducted in a closed seawater system, and great care was taken to reduce handling stress of the animals. Temperature, salinity, pH and ammonia, nitrite, nitrate and phosphate concentrations were monitored and controlled during the experiment. The following predictive equations were evaluated: at temperatures between 13°C and 28°C and at temperatures between 15.5°C and 26°C (T_a is degrees Kelvin and M in gram). O/N ratios showed that O. vulgaris has a protein-dominated metabolism. No significant relationship between the O/N ratio and body mass or temperature was found. Sex had no significant effect on the oxygen consumption rate or on the ammonia excretion rate. For other octopod species, the dependence of metabolic rate on temperature does not differ with that for O. vulgaris.Communicated by O. Kinne, Oldendorf/Luhe     

Nutrient uptake kinetics and growth of zooxanthellae maintained in laboratory culture

Growth characteristics and nutrient uptake kinetics were determined for zooxanthellae (Gymnodinium microadriaticum) in laboratory culture. The maximum specific growth rate (_max) was 0.35 d^-1 at 27 °C, 12 hL:12 hD cycle, 45 E m^-2 s^-1. Anmmonium and nitrate uptake by G. microadriaticum in distinct growth phases exhibited Michaelis-Menten kinetics. Ammonium half-saturation constants (K_s) ranged from 0.4 to 2.0 M; those for nitrate ranged from 0.5 to 0.8 M. Ammonium maximum specific uptake rates (V_max) (0.75 to 1.74 d^-1) exceeded those for nitrate (0.14 to 0.39 d^-1) and were much greater than the maximum specific growth rate (0.35 d^-1), suggesting that ammonium is the more significant N source for cultured zooxanthellae. Ammonium and nitrate V_max values compare with those reported from freshly isolated zooxanthellae. Light enhanced ammonium and nitrate uptake; ammonium inhibited nitrate uptake which was not reported for freshly isolated zooxanthellae, suggesting that physiological differences exist between the two. Knowledge of growth and nutrient uptake kinetics for cultured zooxanthellae can provide insight into the mechanisms whereby nutrients are taken up in coral-zooxanthelae symbioses.Contribution No. 1515 from the University of Maryland Center for Environmental and Estuarine Studies, Chesapeake Biological Laboratory, Solomons, Maryland 20688-0038, USA     

Biological production of nitrite in seawater

The relative importance of 3 different sources for biological production of nitrite in seawater was studied. Decomposition of fecal pellets of the copepod Calanus helgolandicus (at a concentration of approximately 12 g-at N/l), in seawater medium, released small amounts of ammonia over a 6 week period. It nitrifying bacteria were added to the fecal pellets nitrite was barely detectable over the same period. Decomposition of phytoplankton (present at a concentration of about 8 g-at particulate plant N/l) with added heterotrophic bacteria, released moderate amounts of ammonia over a 12 week period. If the ammonia-oxidizing bacterium Nitrosocystis oceanus was added to the decomposing algae, nitrite was produced at a rate of 0.2 g-at N/l/week. Heterotrophic nitrification was not observed when 7 open-ocean bacteria were tested for their ability to oxidize ammonia. The diatom Skeletonema costatum, either non-starved or starved of nitrogen, produced nitrite when growing with 150 or 50 g-at NO ₂ ^- -N/l at a light intensity of about 0.01 ly/min. When nitrate in the medium was exhausted, S. costatum assimilated nitrite. If starved of vitamin B₁₂, both non-N-starved and N-starved cells of S. costatum produced nitrite in the medium with 150 g-at NO ₃ ^- -N/l. Nitrate was not exhausted and cell densities reached 2x10⁵/ml due to vitamin B₁₂ deficiency. If light intensity was reduced to 0.003 ly/min under otherwise similar conditions, cells did not grow due to insufficient light, and nitrite was not produced. In the sea, it appears that, in certain micro-environments, decomposition of particulate matter releases ammonia with its subsequent oxidation to nitrite. The amounts of these nutrients and the rate at which they are produced are dependent upon the nature of the materials undergoing decomposition and the associated bacteria. In certain other areas of the sea, where phytoplankton standing stock is high and nitrate is non-limiting, excretion by these organisms is a major source of nitrite.     

Kinetics of zinc uptake from solution,accumulation and excretion by the decapod crustacean<Emphasis Type="Italic"> Penaeus indicus</Emphasis>

Juveniles of the dendrobranchiate decapod Penaeus indicus take up radiolabelled zinc from solution at all exposure concentrations studied from 5.6 to 100 g l^–1, with an uptake rate constant of 0.045 l g^–1 day^–1 at 15 salinity and 25°C. Over the first 10 days of zinc exposure, the new zinc taken up is added to the existing zinc content of the prawn with no significant excretion; over this period the rate of accumulation of radiolabelled zinc is a measure of the absolute zinc uptake rate from solution. Over the next 10 days of zinc exposure to 10 g Zn l^–1, however, zinc is excreted at about half the rate of uptake resulting in a raised body concentration of zinc. Moulting had no significant effect on the accumulation of zinc. Newly accumulated zinc is distributed to all organs with the highest proportions of body content being found in the exoskeleton, followed by the muscle, the hepatopancreas and the antennal organs. Radiolabelled zinc is subsequently lost from all organs. Unlike caridean shrimps or prawns (pleocyemate decapods), therefore, penaeids (dendrobranchiate decapods) do not show regulation of zinc body concentrations to a constant level over a range of dissolved zinc bioavailabilities by matching zinc excretion to zinc uptake. Nevertheless, unlike amphipod crustaceans, P. indicus does excrete some of the zinc newly accumulated from solution after a time delay. Unlike their caridean counterparts, penaeid prawns inhabiting anthropogenically contaminated coastal waters with raised zinc bioavailabilities can be expected to contain raised body concentrations of zinc.Communicated by J.P. Thorpe, Port Erin     

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.     

Laboratory study of effects of temperature and salinity on survival and larval development of a population of Rhithropanopeus harrisii from the Mondego River estuary,Portugal

Rhithropanopeus harrisii (Gould) is an introduced species in the estuary of the Mondego River (Portugal): it was first recorded from the Iberian Peninsula in 1989. The larval development of this population was studied under laboratory conditions at different temperatures and salinities, and showed a larval development pattern very similar to that reported for American estuarine populations of this species. Larval development was negatively correlated with temperature. Time to megalopa varied between 7 and 35 d; the first crab (C₁) was reached after a maximum of 11 to 43 d. Larval development was optimum at 25°C and 15S. Larval survival was maximum at 10, 15 and 20S at all three temperatures studied (20, 25 and 30°C). The percentage of abnormal megalopae increased with increasing salinity to a maximum (100%) at 30S; incidence of abnormality was not affected by temperature.     

Nitrite and Freshwater Fish

Nitrite occurs naturally in fresh waters as a result of nitrification of ammonia and denitrification of nitrate, and its concentration can be enhanced by partial oxidation of ammoniacal discharges. Nitrite is toxic to vertebrates including fish and a principal effect is the conversion of haemoglobin to methaemoglobin which is incapable of oxygen transport although there are circulatory and tissue effects as well. The toxic species is the nitrite ion (NO₂) which is believed to enter the blood via the branchial chloride/bicarbonate exchange and fish such as salmonids with high chloride uptake rates are more susceptible than those with low chloride uptake rates, for example carp. Nitrite toxicity is strongly aleviated by chloride and the concentration ratio of these ions is of great importance in assessing toxicity. Short term and long term toxicity data for a variety of fish species are presented. There are no field data on fish populations in waters where nitrite was the only pollutant. However extensive field surveys indicated that, waters with a mean chloride concentration of 25 mg l^-1 in good salmon fisheries were associated with concentrations of nitrite below 50 μg l^-1 N · NO₂, good coarse fisheries below 100 μg l^-1 N · NO₂.     

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.     

Adjustment of the components of energy balance in the gastropod Crepidula fornicata in response to thermal acclimation

Synchronous measurements were made of the routine rate of oxygen consumption and the clearance rate of Phaeodactylum tricornutum at different exposure temperatures by specimens of the suspension-feeding gastropod Crepidula fornicata which had been acclimated to temperatures between 10° and 25°C. The results show that the cost of activity (l O₂ consumed h^-1/ml seawater cleared h^-1) increases dramatically in individuals exposed to short-term increases of temperature up to 30°C, especially in limpets acclimated to 10°C. The process of thermal acclimation, however, results in two compensatory adjustments in energy expenditure and uptake which profoundly affect the energetics of water transport. Firstly, the routine oxygen consumption shows lateral translation of the rate-temperature curve which results in the maintenance of a relatively uniform energy expenditure despite an increase in acclimation temperature from 10° to 25°C. Secondly, because of the form of the rate-temperature curve for filtration by C. fornicata, lateral translation in response to warm acclimation results in an increase in the maximal clearance rate. Lateral translation of the rate-temperature curves for feeding rates and for oxygen consumption in response to thermal acclimation may thus be linked to maintain a balance between energy gain and expenditure. In this way, the greatly increased cost of activity which would occur with increase of temperature in the absence of acclimation is evaded. The minimal maintenance energy requirement, and hence the greatest scope for growth and reproduction, is then adjusted to coincide with temperatures prevailing in the environment.     

Glucose uptake in ocean profiles with special reference to temperature

Glucose uptake was measured at three different stations in the northwestern Pacific Ocean. The measurements were made at various temperatures (5° to 35°C) and glucose concentrations (3 to 100 g glucose/l). The uptake of almost all samples taken from the surface to 1,500 m was affected primarily by temperature. The temperature dependence of samples from near the transition region between the Kuroshio and the Oyashio current waters was twice as large as that of both current samples. Furthermore, the samples from the former, transition, region and the aphotic samples of the latter, current, regions showed an optimal temperature 15° to 30°C higher than the in situ temperature; the optimal temperature was only 5° to 10°C higher in the photic samples of the stable region. The average potential glucose uptake at/near the optimal temperature was 0.026 g glucose/l/h in the photic zone and 0.015 g glucose/l/h in the aphotic zone. However, after correction by the in situ temperature, the uptake was 0.024 and 0.003 g glucose/l/h, respectively.     

Effect of temperature and food on the heart beat,ventilation rate and oxygen uptake of Mytilus edulis

The heart beat, ventilation rate and oxygen uptake of Mytilus edulis L. were measured simultaneously, in response to changes in temperature and food level. There was no thermal acclimation of heart-beat frequency or amplitude to temperatures from 5° to 25°C. Oxygen consumption and ventilation rate acclimated to 10°, 15° and 20°C, but not to 25°C. Starvation reduced the rate of oxygen uptake and heart-beat frequency to a standard level and, in response to food, the ventilation rate and oxygen consumption immediately increased to an active level. Feeding was maintained after the initiation of active metabolism, and during the following 10 days the heart-beat frequency gradually increased to the level characteristic of fed individuals. There was no direct correlation between the rate of oxygen consumption and heart rate, and an apparent absence of a close nervous coupling between ventilation rate and heart rate in M. edulis.     

Metabolism of epipelagic tropical ctenophores

Measurements of respiration and excretion at 25°C were made for five species of ctenophores collected during five cruises to the Bahamas (1982–1984). The mean element-specific respiration and ammonium excretion rates of freshly collected specimens of all species ranged from 4 to 16% d^-1, the mean atomic O:N ratios were 10 to 16, and ammonium averaged 60 to 90% of the total dissolved nitrogen excreted. For adult ctenophores, the carbon content ranged from 0.6% carbon (as percent of dry weight) for Bolinopsis vitrea to 3.7% carbon for Beroë ovata. There was a marked increase in the organic content (% carbon of dry weight) of small Bolinopsis vitrea with tentacles compared to fully lobate adults. B. vitrea had increasingly higher metabolic rates when held at food concentrations up to 100 copepods 1^-1 (about 250 g C 1^-1). The overall range between starved and well-fed B. vitrea was about two times for respiration and a factor of three for ammonium excretion. B. vitrea decreased from well-fed to a starved metabolic rate in about a day after removal from food. The metabolic rate of Eurhamphaea vexilligera was not measurably affected by short-term starvation or feeding (maximum 25 copepods 1^-1). In feeding experiments, E. vexilligera of 20 to 56 mm length fed at rates equivalent to clearance rates of 250 to 1 800 ml h^-1.     

Respiratory physiology in summer diapause embryos of the neustonic copepodAnomalocera patersoni

The respiratory physiology of summer diapausing eggs of the neustonic copepodAnomalocera patersoni, maintained under constant temperature (13 °C) and light (12 h light:12 h dark) conditions, was characterized by a bell-shaped curve, with low O₂ uptake levels at the beginning of dormancy. This was followed by a steady rise in O₂ consumption with maximum levels of 0.002 l O₂ embryo^–1 h^–1 70 d after spawning. A slow diminution in O₂ uptake then occurred until Day 150 when minimum values of 0.0003 l O₂ embryo^–1 h^–1 were recorded, coinciding with the hatching of the first embryos. Embryos continued to hatch asynchronously up to 360 d from the moment of egg laying. When eggs were subjected to 20 °C, the respiratory activity was almost three times higher than at 13 °C, even though both respiratory curves were similar. The elevated metabolism in eggs kept at 20 °C led to death of the embryos possibly due to a total depletion of metabolic reserves. ATP content also differed at the two temperatures. Diapause eggs kept at 20 °C showed no rapid rise in ATP content as opposed to those kept at 13 °C. The results of temperature shock experiments, in which eggs were first kept at winter temperatures for several weeks, after which the temperature was raised to 20 °C for another number of weeks prior to a second period of chilling at 13 °C, showed that as long as embryos were kept at 20 °C no hatching occurred. By contrast, hatching was observed after 10 d following the resumption of winter temperatures, suggesting that low environmental temperatures are an essential prerequisite for hatching of these eggs. The type of diapause inA. patersoni differs considerably from the one described in insects and in another neustonic copepod,Pontella mediterrana. In this case, there is a U-shaped respiratory curve with greatest O₂ consumption prior to the onset or upon breaking of diapause. Differences in the two types of diapause seem to involve not only differences in O₂ consumption levels but also in the sequence of metabolic changes with time and the metabolic requirements during sommer and winter dormancy.     

Nitrogen regeneration by two surf-zone mysids,Mesopodopsis slabberi andGastrosaccus psammodytes

Nitrogen regeneration by two surf zone mysids,Mesopodopsis slabberi andGastrosaccus psammodytes, was determined under laboratory conditions. The mysids were collected from the lower Sundays River estuary, South Africa, from early spring 1984 to late summer 1985. The forms of nitrogen excreted and the effects of mass, temperature and feeding on excretion rate were determined for each species at three experimental temperatures. Comparison of the forms of nitrogen excreted revealed only slight differences between species, with ammonia the major form and urea and amino acids the secondary excretory products in both cases. Mass significantly influenced the rate of ammonia excretion at all experimental temperatures, with no significant difference in slope (common b=0.602) detected between species. During the day sediment deprivation resulted in a 15% and 20% increase in mean ammonia excretion rates of juvenile and adultG. psammodytes respectively, whereas no significant differences were found at night. The mean ammonia excretion rates of fedM. slabberi andG. psammodytes were 2 and 2.5 times higher than starved excretion rates, respectively.G. psammodytes andM. slabberi recycle 139 to 150 g N per running meter of surf zone per year and 1 007 to 1 208 g N m^-1 yr^-1, respectively. Togehter this constitutes 10% of total phytoplankton nitrogen requirements in the surf zone.     

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.     

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.