Rates of oxygen consumption and ammonia excretion of juvenile Eurasian perch Perca fluviatilis L.

The impact of feeding, fish size (body weight from 18.5 to 56.5 g) and water temperature (20 and 23 °C) on oxygen consumption (OC, mg O₂ kg^–1 h^–1) and ammonia excretion (AE, mg TAN kg^–1 h^–1) was studied in Eurasian perch held in recirculation systems. OC for both fed and feed-deprived (3 days) fish was higher at 23 °C (278.5 and 150.1 mg O₂ kg^–1 h^–1) than at 20 °C (249.3 and 135.0 mg O₂ kg^–1 h^–1; P < 0.01). AEs for both fed and feed-deprived fish were also significantly higher at 23 °C than at 20 °C (P < 0.001). Water temperature and fish size had a significant impact on the oxygen:feed ratio (OFR, kg O₂ kg^–1 feed fed day^–1) and ammonia:feed ratio (AFR, kg TAN kg^–1 feed fed day^–1; P < 0.001). Their average values at temperatures of 20 and 23 °C were 0.17 and 0.19 kg O₂ kg^–1 feed fed day^–1 and 0.009 and 0.011 kg TAN kg^–1 feed fed day^–1, respectively.     

Low optimal temperatures for food conversion and growth in the big-headed turtle, Platysternon megacephalum

We held juvenile big-headed turtles, Platysternon megacephalum, from eastern China, at temperatures from 20 to 29.4 °C to determine effects on feeding, growth and food conversion. Food intake increased significantly from 20 to 22.4 °C, remained high until 27.1 °C, and then decreased dramatically at 29.4 °C. Digestive efficiency for energy decreased as temperature increased, whereas the digestive efficiency of protein increased from 20 to 25 °C, and decreased at higher temperatures. The relationships between specific growth rate (SGR), food conversion coefficient (C_c) and temperature (T) were curvilinear, and could be described by quadratic equations: SGR = −0.01 T² + 0.47 T − 5.24 and C_c = −0.37 T² + 17.20 T − 181.85. Maximum growth was estimated to occur at 23.9 °C, with 90% of the maximum being achieved within the range of 21.9–25.8 °C; maximal food conversion occurred at 23.2 °C, with a 90% range from 21.0 to 25.4 °C. The temperature range (22–25 °C) found to promote best growth and food conversion in juvenile P. megacephalum is lower than for many other freshwater turtles. Temperatures of 22–25 °C are recommended for use in culture of this species to maximize growth and food conversion.     

Biological performance of Octopus vulgaris in ‘integrated aquaculture’ models: effect of two potential fresh diets,sex and sexual maturation during the grow‐out phase

Two fresh diets were tested on the biological performance of males and females of Octopus vulgaris under industrial rearing conditions in floating cages. The presence of females could potentially release paralarvae to the natural environment (‘integrated aquaculture’). Octopuses were fed on a single diet of bogue (aquaculture by‐product), and on a mixed diet (60–40% crab‐bogue), in two trials. In Trial 1 (918 ± 125 g), growth was higher in octopuses fed on the mixed diet (1.9–2.0%d^?1) than in those fed on the bogue diet (1.8–1.9%d^?1) irrespective of sex, and mortality was 3% regardless of sex and diet. In Trial 2 (1483 ± 269 g), growth was higher in males fed on the mixed diet (1.8%d^?1) than in males fed on the bogue diet (1.4%d^?1), both higher than females (1.1–1.3%d^?1), and mortality was 22–28% regardless of sex and diet. Best biological performance in trial 1 was related to the lack of functional maturation in females, evidence by the low average gonadosomatic index (2.0–3.6%) in comparison with trial 2 (8.8–11.4%), regardless of diet. No correlations between final weight and sexual maturity indices were found, so the length of the rearing period to maximize biomass increment or to release paralarvae depends on functional maturation in females.     

Growth,food intake,protein retention and fatty acid profile in Octopus vulgaris (Cuvier, 1797) fed agglutinated moist diets containing fresh and dry raw materials based on aquaculture by‐products

The lack of specific compound diets for cephalopods is limiting the industrial development of some species. In this study, four agglutinated moist diets were tested in individually reared Octopus vulgaris (979 ± 151 g) for 8 weeks. All diets were based on bogue Boops boops, accidentally reared in fish farms (aquaculture by‐product), and agglutinated with alginate and calcium. One diet was based exclusively on bogue fillets, two on bogue fillets complemented with meat from two crab species (Portunus pelagicus, Grapsus grapsus) and the last one on bogue and G. grapsus meals. As a control diet, bogue and P. pelagicus were supplied fresh on alternate days. All diets induced similar feed intake (2.1–2.6% day^?1). However, the meal‐based diet induced negative growth in comparison with the control and the other agglutinated diets (0.80–0.85% day^?1). Higher lipid content in agglutinated diets (28–30% dw) in comparison with the control diet (16% dw) led to higher protein retention in muscle. These results underline the inadequacy of traditional meals in diets for cephalopods and that the inclusion of crab meat did not increase feeding rates and growth in O. vulgaris. The dietary fatty acid, with high levels of oleic and linoleic acid and low levels of ARA, clearly reflected in digestive gland, while only decreasing ARA and increasing EPA levels were observed in muscle, with no apparent negative effect on growth.     

The effects of temperature on growth rate and growth efficiency of juvenile common wolffish

The effects of temperature on the survival, growth rate and growth efficiency of larval and juvenile common wolffish, Anarhichas lupus L. were studied at 0–31 days and 9–12 months post-hatching, respectively. The influence of temperature regime during egg incubation on subsequent survival and growth was also examined. The fish were reared at constant water temperatures of 5, 8, 11 and 14°C, and all groups were fed dry pellets. At age 1 month, maximum growth rates were observed at 11 and 14°C. Growth rates and survival of early juveniles were dependent upon incubation history, high growth being obtained only if rearing temperature exceeded the temperature of egg incubation. In juveniles at age 9–12 months, the relationships between temperature and growth, and temperature and growth efficiency were parabolic: the optimum water temperatures for growth (Topt.G) and growth efficiency (Topt.GE) were 11°C and 9.7°C respectively. The growth rate and growth efficiency at these water temperatures were 0.9% day–1 and 0.45 g weight gain per g food offered, respectively. © Rapid Science Ltd. 1998     

Growth performance and physiological responses in striped knifejaw, Oplegnathus fasciatus, held under different photoperiods

The growth performance and stress response in striped knifejaw, Oplegnathus fasciatus (body weight 100–300 g) reared under four photoperiods (6L:6D, 12L:12D, 16L:8D and 24L:0D) were investigated. Fish were fed a commercial diet to apparent satiation, two times a day for 8 weeks. A trial of acute handling and confinement stress was also carried out to investigate the stress-induced levels of different stress indicators in O. fasciatus. Blood was also collected from undisturbed fish which was considered as control. Although there were no significant differences in weight gain, specific growth rate (SGR) and feed conversion efficiency (FCE) in fish exposed to 6L:6D, 16L:8D and 24L:0D photoperiods, all parameters in these photoperiods were significantly higher than those of 12L:12D photoperiod (P < 0.05). There was no significant difference in protein retention efficiency (PRE) between fish exposed to 16L:8D and 24L:0D photoperiods, but PRE in both photoperiods was significantly higher than that of 12L:12D photoperiod.Acute stress significantly increased the plasma levels of cortisol (110.3 ng ml^− 1) and glucose (195.4 mg dl^− 1), and decreased plasma levels of total protein (0.8 g dl^− 1); however, all parameters were returned back to the levels indistinguishable from those of control, undisturbed fish within 24 h. The levels of cortisol, glucose and total protein in fish exposed to different photoperiods during the study were far from the stress-induced levels (P < 0.05). The results demonstrated that the growth performance of O. fasciatus reared from 100 to 300 g can be stimulated significantly by using the manipulated photoperiods where feeding time may be playing an important role to increase food intake and feed conversion efficiency. It also revealed that the artificial photoperiods did not cause significant stress response in fish.     

Growth,protein retention and biochemical composition in Octopus vulgaris fed on different diets based on crustaceans and aquaculture by-products

The octopus, Octopus vulgaris, is one of the main targets for aquaculture diversification in Mediterranean countries. However, the development of octopus farming is limited by the lack of information regarding nutritional requirements of this species during its life cycle. In this study, five diets were tested on the biological performance (growth, protein retention and biochemical composition) of individually reared octopuses (n = 8 per diet), including three single diets constituted by: an endemic crab (the white crab, Plagusia depressa), a commercial crab imported frozen (the blue crab, Portunus pelagicus), and bogue (Boops boops) discarded from fish farms (aquaculture by-product), as well as two mixed diets, containing a 60–40% of blue crab-bogue and white crab-bogue, respectively. The rearing period lasted 8 weeks. Octopuses that fed on a mixed diet constituted by blue crab-bogue showed a higher growth than those feeding on bogue as a single food item. No significant differences in growth were observed among individuals feeding on single food items. Highest protein retention was observed in octopuses fed on diets containing discarded bogue, associated with a high lipid and monoenes content in this food item, underlying the use of lipid as energy source in O. vulgaris. However, discarded bogue was deficient in ARA in comparison with octopus tissues, which did not seem to affect growth during the experimental period. These findings underline the potential of aquaculture by-products, particularly bogue, as an adequate diet for culturing O. vulgaris.     

Feeding and growth of exercised and unexercised juvenile Atlantic salmon in freshwater,and performance after transfer to seawater

Juvenile Atlantic salmon (Salmo salar), selected from the upper modal group, were first held for 122 days (from December to May) in freshwater, and then for 49 days in seawater (34% salinity). In freshwater, the fish were exposed to either standing water or water currents corresponding to a swimming speed of 1 Bl s^–1. Natural light conditions prevailed throughout the whole experiment.In the freshwater phase, food intake, growth rate and condition factor of the fish increased with increasing daylength. Condition factors, however, decreased slightly during the last month of the freshwater period, suggesting that the fish underwent parr-smolt transformation. The growth rate and food intake of the fish subjected to standing water were approximately 15% lower than those of fish exposed to water currents.Transient suppression of appetite and growth, and an increase in plasma concentration of Cl^–, were seen after exposure of the fish to seawater. Within 28 days, all these parameters had been restored to pre-transfer levels. Previous exercise did not appear to have influenced the hypoosmoregulatory capacity of the fish. Growth rate and food intake observed during the seawater phase were similar, irrespective of the treatment experienced by the fish during freshwater rearing.     

Grass carp (Ctenopharyngodon idella) grazing on duckweed (Spirodela polyrhiza)

The aims of this experiment were (1) toquantify the ability of grass carp to processduckweed and (2) to assess indirect changes inwater chemistry and phytoplankton community,caused by grass carp feeding. Yearling grass carp sized 126 ± 7.7 mm (TL) and19.6 g in weight were kept in 9 laminate tanksof 1 m³ for 14 days. Two stockingdensities (2 and 6 fish per m³) anda control without fish were used. Standard growthrate (SGR) of grass carp fed exclusively onduckweed was 0.70% body weight (BW) d^–1and food conversion ratio (FCR) reached 2.0(average water temperature =21.1 ± 3.8 °C). Daily food intakewas 0.2 g of duckweed dry weight (DW), i.e.,1% of average BW of grass carp. SGR ofduckweed growing in 20 × 20 cm floatingenclosures, differed significantly[F(6,2) = 417.9; p = 0.002] between the twostocking densities of grass carp and thecontrol tanks (without fish). Mean SGR ofduckweed was 0.02 g g^–1 day^–1 and thehighest SGR was recorded in the control tanks.Both decrease in NH₄-N and increase inNO₂-N concentrations differedsignificantly between the treatments[F(2,2) = 45.3; p = 0.02 and F(2,2) = 19.2; p = 0.04 respectively]. Changes in other nitrogenand phosphorus components (NO₃-N, TN, TPand PO₄-P) caused by stocking of grasscarp were not significant. Biomass ofphytoplankton, dominated by filamentous algaeand blue-greens, increased proportionately tostocking density of grass carp. Althoughduckweed has a large potential for nutrientremoval, the most common pathway for thenutrients released through grass carp grazingif duckweed cover is loose is theirincorporation into phytoplankton biomass.     

Increased winter temperature did not affect completion of smolting in Atlantic salmon

Four groups of 1+ year-old Atlantic salmon, Salmo salar, pre-smolts were reared under various temperature regimes: constant 10 °C from November onwards; ambient temperature until either 15 December or 1 February, then 10 °C; or ambient temperature throughout (control; 2–3 °C November–March). From 20 May onwards, temperature in all groups was ambient, increasing from 10 °C to 17 °C in late July. Rearing temperature had no significant effect on either the timing of completion of smolting, or the duration of the smolt-window. Mean gill Na⁺-K⁺ ATPase activity was not significantly affected by temperature regime; it increased in all groups from < 2.0 mol Pi mg protein^–1 h^–1 (units) in January to 5–7 units in mid-April, then back to < 2.0 units in July. Survival in 96 h, 37) salinity (S) tolerance tests was similar in all groups, increasing from < 10% in early March, to > 90% from mid-April to mid-June, then decreasing to < 20% by early July. Increased winter temperature significantly increased growth and condition factor compared with the control, but during April–May all four groups exhibited similar temporary decreases in condition factor in association with the completion of smolting.     

Efficient utilization of dietary lipids in Octopus vulgaris (Cuvier 1797) fed fresh and agglutinated moist diets based on aquaculture by‐products and low price trash species

The aim of this study was to evaluate growth, biochemical composition and dietary nutrients utilization in Octopus vulgaris fed on four diets based on bogue Boops boops, from different origin and in two presentations: fresh discarded bogue (aquaculture by‐product) (DB‐f), fresh wild bogue (low price trash species) (WB‐f), discarded bogue agglutinated moist diet (DB‐m) and wild bogue agglutinated moist diet (WB‐m). Diets based on DB showed higher lipid content (19–26% dw) than those based on WB (5–6% dw). Octopuses fed on DB‐based diets showed higher growth (1.5–1.9% day^?1) and higher protein efficiency ratio (0.64–0.69) than those fed on WB‐based diet (1.1–1.5% day^?1 and 0.36–0.37 respectively), which suggests good utilization of dietary lipids and also a possible protein sparing effect by lipids in O. vulgaris. Octopuses fed on diets presented fresh showed a higher growth (1.9–1.5% day^?1) and a higher feed efficiency (62–65%) than those fed on agglutinated diets (1.1–1.5% and 52–60% day^?1 respectively). Regarding fatty acids, the digestive gland clearly reflected dietary lipid and fatty acid profile, while muscle showed a more stable composition. Low dietary ARA content reflected in octopus tissues, especially in specimens fed on DB‐based diets, which did not seem to affect growth during the experimental period.     

The effect of temperature on the growth, survival and food consumption of the east coast rock lobster Panulirus homarus rubellus

The successful culture of the east coast rock lobster Panulirus homarus rubellus is reliant, among other factors, on the provision of optimal water quality for growth and survival. This study investigated the effect of temperature over a range of 9.7 °C (18.9 ± 0.7 °C to 28.6 ± 1.5 °C) on the growth and survival of juvenile (40.4 ± 9 mm CL; 63.64 ± 12.05 g) P. h. rubellus fed a diet of fresh mussel flesh. Specific growth rate (SGR) was significantly different between temperatures (p = 0.01), with the highest values recorded for the 24 and 28 °C treatments. There was no significant difference in moult increment (MI) between temperatures in terms of both an increase in weight (p = 0.83) and carapace length (p = 0.54). Intermoult period (IMP) differed significantly between temperatures (p = 0.0015) with mean IMP lowest at 24 °C, although not significantly different from the means of the 26 and 28 °C treatments. IMP was highest at 19 and 21 °C. Apparent feed intake was significantly different between treatments (p < 0.0001) and exhibited a strong positive correlation with increasing temperature (y = − 1.67 + 0.16x ; r² = 0.81). Food conversion ratio (FCR) differed significantly between temperatures (p = 0.02) with 24 °C exhibiting the most efficient FCR. Results indicate that efficient growout of juvenile P. h. rubellus, in terms of both growth and food conversion efficiency, is obtainable at 24 °C.     

Assessment of the performance of Pacific oyster (Crassostrea gigas) larvae fed with fresh and preserved Pavlova lutheri concentrates

The Prymnesiophycea Pavlova lutheriwas produced using a traditional technique (batch mode in carboys) and by an innovative technique (semi-continuous mode in alveolarphotobioreactor). Two experimental feedingtrials were carried out with Pacific oyster(Crassostrea gigas) larvae with freshand preserved (4 °C and 1 °C)P. lutheri concentrates used inmonospecific and bispecific diets, incombination with fresh Chaetoceroscalcitrans forma pumilum. Nodifferences in terms of gross composition andlarval performance were noticed between thefresh algae biomass produced by the twotechniques. The low temperatures allowedpreservation of the nutritionalcharacteristics of the P. lutheri freshculture for the time period considered (27days). The P. lutheri concentratespreserved at 4 °C or 1 °C didnot differ substantially in terms ofnutritional value. Larvae fed a monospecificdiet of P. lutheri, both fresh andpreserved, exhibited a modest growth rate (<2.1 µm day^–1), in some cases notsignificantly different from that observed inthe unfed larvae (the control), and a lowsurvival rate. In contrast, when Chaetoceros calcitrans forma pumilumwas used as a monospecific diet, good growthperformance (>4.5 µm day^–1) and ahigh survival rate (>86%) were observed inlarvae. A substitution of 50% (trial 1) or80% (trial 2) of fresh C. calcitransforma pumilum with the preserved P. lutheri concentrates did not adverselyaffect growth rate or survival of C.gigas larvae.     

Temperature influences on California rainbow trout physiological performance

Although thermal influences on the physiology of rainbow trout (Oncorhynchus mykiss) have been widely studied, there is little information about the responses of different genetic strains to temperatures. The effects of water temperature (10, 14, 19, 22, and 25 °C) on food consumption rate, growth rate, gross conversion efficiency, resting routine oxygen consumption rate, upper critical thermal tolerance and critical swimming velocity were investigated in juvenile rainbow trout of the Eagle Lake (O. m. aquilarum) subspecies and the Mt. Shasta strain. No strain-related differences in conversion efficiency, oxygen consumption rates, thermal tolerance or swimming performance were observed in 1995 (19, 22, and 25 °C) or 1996 (10, 14, and 19 °C), but Mt. Shasta strain trout grew faster at highest temperatures than did Eagle Lake trout. Food consumption rates, growth rates, conversion efficiency, and oxygen consumption rates declined at the extreme temperatures (10 and 25 °C) in both Eagle Lake and Mt. Shasta trout. Swimming performance was temperature-independent between 10 and 19 °C (overall mean: 5.43 body lengths s^–1).     

Natural carbon stable isotope ratios as indicators of the relative contribution of live and inert diets to growth in larval Senegalese sole (Solea senegalensis)

The relative contributions of live Artemia metanauplii and an inert diet for growth of Senegalese sole larvae and postlarvae were assessed through the analysis of carbon stable isotopes ratios (δ¹³C) in both diets and whole larval tissue. Larvae were reared on four dietary regimes: 100% live prey (rotifers and Artemia), 100% inert formulated diet and two co-feeding regimes of 70:30 and 30:70 ratios of Artemia and inert diet, respectively. Larvae from the live food regime and both co-feeding regimes showed a steep increase in δ¹³C from 10 days after hatching (DAH) as a result of the onset and continuation of Artemia consumption. From 12 DAH fish larvae from all the regimes showed significant isotopic differences as their δ¹³C increased to final asymptotic values of − 15.1, − 15.6 and − 16.3‰ in the live food, 70:30 and 30:70 regimes, respectively. Carbon turnover rates in larvae from both live food and co-feeding regimes were relatively high (0.071 to 0.116 d^− 1) but more than 90% of the observed change in fish tissue isotopic values was accounted for by the retention of carbon in new tissue growth. A two-source, one-isotope mixing model was applied to estimate the nutritional contribution of Artemia and inert diet to postlarvae growth in the co-feeding regimes. At 23 DAH, the relative contribution of live and inert diets to tissue growth in larvae was respectively, 88 and 12% for the 70:30 co-feeding regime and 73 and 27% for the 30:70 co-feeding regime. At 17 DAH, the estimated proportion of tissue carbon derived from the inert diet was higher at 23 and 38% for the 70:30 and 30:70 regimes, respectively. The results suggest that co-feeding regimes in Solea senegalensis larvae may be adjusted to meet ontogenetic changes in the capacity for larvae to utilise inert diets. The contrasting levels of carbon isotope discrimination between diet and tissue in larvae reared on either 100% live feed or 100% inert diet indicate relatively poor utilization of nutrients from the inert diet. The use of isotopic discrimination factors as potential indicators of the digestive physiological performance of a consuming organism in regards to its diet is discussed.     

Feed intake, growth rate and body composition of juvenile Baltic salmon exposed to different constant temperatures

Feed intake, specific growth rate and changes in body composition of age 1+ and 2+ Baltic salmon, Salmo salar L, were studied for fish held under constant temperature conditions. The 1+ fish (60 g) were reared for 6 weeks at 11, 15, 17, 19 or 23 °C and 2+ fish (250 g) were held at 15 °C. Feed intake of 1+ salmon increased from 176 kJ kg-1 day-1 at 11 °C to 275 kJ kg-1 day-1 at 17 °C and decreased to 229 kJ kg-1 day-1 at 23 °C. Specific growth rate increased from 1.18% day-1 at 11 °C to 1.59% day-1 at 15 °C and decreased to 0.56% day-1 at 23 °C. Optimum temperatures for feed intake and growth were estimated at 17.8 °C and 15.6 °C, respectively, and estimated upper thermal limits for feeding and growth were 29.0 °C and 24.1 °C, respectively. Models for feed intake and growth rate in relation to temperature and fish size are presented. The utilization efficiency of ingested energy decreased from 57% at 11 °C to 22% at 23 °C. For all groups of 1+ fish, most (approximately 86%) of the weight gain consisted of water. Lipid deposition accounted for about 52% of the body energy gain irrespective of rearing temperature.     

Quantifying the dietary biotin requirement of the catfish,Clarias batrachus

Asian catfish, Clarias batrachus, were fed semi-purified basaldiets containing 0, 0.1, 0.5, 1, 3 and 5 mg biotin kg^–1diet for 60 days. Fish fed the control diet (no biotin) showed(P < 0.05) higher mortality, lower weight gain, specificgrowth rate (SGR), feed efficiency ratio (FER) and protein efficiencyratio (PER) than in fish fed diets supplemented with biotin. The highestweight gain, SGR, FER and PER were noticed in fish fed 1 mg biotinkg^–1, followed by 0.5, 5, 3 and 0.1 mg biotinkg^–1, except for PER (followed by 0.5, 5, 0.1 and 3 mgbiotin kg^–1). Quadratic analysis showed that the optimumdietary biotin requirements for maximal weight gain, PER and PER were2.49, 2.54 and 2.52 mg kg^–1, respectively. Liver biotinconcentrations were influenced by levels of biotin in the diet.Concentration of liver biotin increased as level of dietarysupplementation increased and no biotin was detected in the liver of thecontrol fish. Liver pyruvate carboxylase and acetyl CoA carboxylaseactivities were higher in fish fed biotin-supplemented diets than incontrols. Biotin concentrations, pyruvate carboxylase and acetyl CoAcarboxylase activities in liver associated with normal growth rangedfrom 10.59 to 10.66 g g^–1, 147.97 to 148.18 units mgprotein^–1 and 12.76 to 12.78 units mg protein^–1, respectively. Biotin deficiency symptoms such as anorexia, darkskin colour and convulsions were observed in fish fed the control diet.The optimum dietary biotin requirement for maximal growth of C.batrachus is about 2.49 mg kg^–1 diet.     

Oxygen consumption and responses to hypoxia of ammocoetes of the southern hemisphere lampreyGeotria australis

The standard rate of oxygen consumption of ammocoetes (larvae) ofGeotria australis with a mean weight of c. 0.5 g was 9.6, 31.4 and 59.4l g^–1 h^–1 at 4.5, 15.5 and 25.0°C respectively, which gives an overall Q₁₀ of 2.4. The regression coefficient for the logarithmic relationship between oxygen consumption and body weight at 15.5°C was 0.704. The ammocoetes ofG. australis have a much lower rate of oxygen consumption at 15.5 and 25.0°C than those of holarctic lampreys. This presumably reflects the lower oxygen delivery pressure to their tissues and helps account for their slow growth rate. At 15.5°C, ammocoetes ofG. australis emerged from the substrate at 21–25 mm Hg and, unlike those of the Northern HemisphereIchthyomyzon greeleyi, died at 14–17 mm Hg. Thus, despite having a thinner water/blood barrier in the gills and blood with a higher oxygen affinity and capacity than holarctic ammocoetes, the larvae ofG. australis cannot survive very low dissolved oxygen tensions. This is apparently related to an inability of larvalG. australis to meet the high oxygen requirements of the respiratory pump at these oxygen tensions. During metamorphosis, oxygen consumption at 15.5°C rose from approximately 27l g^–1 h^–1 at the beginning of transformation to 33.2l g^–1 h^–1 by Stage 3 and then rapidly to 66l g^–1 h^–1 at Stage 6. It remained near this level in Stage 7 and the downstream migrant.     

Effect of temperature on the scope for growth in juvenile scallops Argopecten purpuratus (Lamark, 1819)

Theeffect of temperature on scope for growth was determined in juveniles of thenorthern scallop Argopecten purpuratus (Lamarck, 1819).This economically important species, has been introduced into the south ofChilegiven that large-scale cultivation within the natural distribution zone islimited. Nevertheless, the lower water temperatures that exist in the southcould restrict the growth rate. No difference in the scope for growth wasdetected in specimens kept at 10 ± 1 °C and 18 ±1 °C and fed with a mixed diet 1:1 of Chaetocerosgracilis and Tetraselmis suecica. Temperaturedid not affect the quantity of energy derived from food ingested, but energyloss through respiration, faeces and excretion was greater at 10 ± 1°C than at 18 ± 1 °C. The resultsindicate that the growth rates of A. purpuratus aremaintained between 10 ± 1 °C and 18 ± 1°C, which would favour large-scale cultivation over a widelatitudinal range.     

Growth and Chemical Composition of Spirulina Maxima and Spirulina Platensis Biomass at Different Temperatures

The influence of temperature on growth and biomass composition of two species of Spirulina, S. maxima and S. platensis used for food was studied. A 4L fermenter with temperature and agitation control was used to cultivate both species. Under continuous light, maximum cell production of 2.4 g l^–1 was verified for both cultures studied at temperatures above 25 °C: S. maxima (30 °C and 35 °C) and S. platensis (25 °C and 30 °C). An accentuated lag phase was observed for all cultures at lower temperatures (15–20 °C), and a maximum biomass production of 1.5 g l^–1 was achieved. It was also observed that an increase of temperature caused a marked decrease in protein content, while carbohydrate synthesis was stimulated. The concentration of -linolenic acid varied from 11–16% for S. maxima and from 12–14% for S. platensis, at the optimum growth temperatures. Greater culture volumes were also studied in order to compare the performance of glass and plastic containers. At optimum growth temperature, S. maxima produced the same cell growth and similar final biomass composition.