Cephalopod hatchling growth: the effects of initial size and seasonal temperatures

Temperature is known to have a strong influence on cephalopod growth during the early exponential growth phase. Most captive growth studies have used constant temperature regimes and assumed that populations are composed of identically sized individuals at hatching, overlooking the effects of seasonal temperature variation and individual hatchling size heterogeneity. This study investigated the relative roles of initial hatchling size and simulated natural seasonal temperature regimes on the growth of 64 captive Octopus pallidus over a 4-month period. Initial weights were recorded, and daily food consumption and fortnightly growth monitored. Two temperature treatments were applied replicating local seasonal water temperatures: spring/summer (14–18°C) and summer/autumn (18–14°C). Overall octopuses in the spring/summer treatment grew at a rate of 1.42% bwd⁻¹ (% body weight per day) compared to 1.72% bwd⁻¹ in the summer/autumn treatment. Initial size influenced growth rate in the summer/autumn treatment with smaller octopuses (<0.25 g) growing faster at 1.82% bwd⁻¹ compared to larger octopuses at 1.68% bwd⁻¹. This was opposite to individuals in the spring/summer treatment where smaller octopuses grew slower at 1.29% bwd⁻¹ compared to larger octopuses at 1.60% bwd⁻¹. Initial size influenced subsequent growth, however, this was dependent on feeding rate and appears to be secondary to the effects of temperature.     

Feeding of laboratory-reared larvae of the sea bream Archosargus rhomboidalis (Sparidae)

Feeding by larvae of the sea bream Archosargus rhomboidalis (Linnaeus) was investigated from late September, 1972 to early May, 1973 using laboratory-reared larvae. Fertilized eggs were collected from plankton tows in Biscayne Bay, and the larvae were reared on zooplankton also collected in plankton nets. Techniques were developed to estimate feeding rate, food selection, gross growth efficiency, and daily ration. Daily estimates of these were obtained through 16 days after hatching at rearing temperatures of 23°, 26°, and 29°C. Feeding rate increased exponentially as the larvae grew, and increased as temperature was raised. At 23°C larvae began feeding on Day 3, at 26° and 29°C larvae began feeding on Day 2. Feeding rates at initiation of feeding and on Day 16 were, respectively: 23°C, 7.16 food organisms per larva per hour (flh) and 53.78 flh; 26°C, 7.90 flh and 168.80 flh; 29°C, 17.62 flh and 142.07 flh. Sea bream larvae selected food organisms by size. At initiation of feeding they selected organisms less than 100 m in width. As larvae grew they selected larger organisms and rejected smaller ones. The major food (more than85% of the organisms ingested) was copepod nauplii, copepodites, and copepod adults. Minor food items were barnacle nauplii, tintinnids, invertebrate eggs, and polychaete larvae. Mean values for gross growth efficiency of sea bream larvae ranged from 30.6% at 23°C to 23.9% at 29°C. Mean values for daily ration, expressed as a percentage of larval weight, ranged from 84% at 23°C to 151% at 29°C and tended to decline as the larvae grew.This paper is a contribution from the Rosenstiel School of Marine and Atmospheric Science, University of Miami, Miami, Florida, USA     

Effect of temperature on specific dynamic action in the common octopus,<Emphasis Type="Italic"> Octopus vulgaris</Emphasis> (Cephalopoda)

Feeding causes an increase of metabolic rate, which initially escalates rapidly, reaches a peak value and then gradually declines to the pre-feeding rate. This phenomenon, termed specific dynamic action (SDA), reflects the energy requirements of the behavioral, physiological and biochemical processes that constitute feeding. The effect of temperature on SDA of the common octopus, Octopus vulgaris, was evaluated, by measuring the temporal pattern of the oxygen consumption rates of octopuses, after feeding, at two constant temperatures, 20°C and 28°C. At 20°C, the relative increase in the oxygen consumption rate after feeding (relative SDA) was significantly greater than at 28°C. The peak of the relative SDA occurred 1 h after feeding, and it was 64% at 20°C and 42% at 28°C. However, the SDA absolute peak, SDA duration (9.5 h) and SDA magnitude (the integrated postprandial increase in oxygen uptake) did not differ significantly between the two temperatures, indicating that the energetic cost of feeding was the same at both temperatures. The SDA response in O. vulgaris was much faster than it was in polar species, which have extended SDA responses due to low temperatures, and was also relatively fast in relation to the response in other temperate species, which is probably connected to the remarkably high growth rates of the species. A possible explanation of the observed summer migration of large octopuses from shallow to deeper areas is given, based on the effect of temperature on the energetic requirements of octopuses.     

Optimal growth and maximal survival temperatures of Atlantic Laminaria species (Phaeophyta) in culture

The effects of temperature on growth rate of rapidly-growing cultured macrosporophytes of 9 isolates of Atlantic Laminaria comprising 4 species have been investigated. No significant population variation was observed within species despite wide variations in temperature between the original collecting sites. L. saccharina showed a broad temperature optimum in the 10°–15°C range, whereas L. longicruris had a sharp optimum at 10°C. L. digitata and L. hyperborea grew more slowly, with only slightly sub-optimal growth over a wide temperature range, but with peaks at 10°C (L. digitata) and 15°C (L. hyperborea). The maximum survival temperatures of individual male and female vegetatively-growing gametophytes were ascertained for these species plus the Arctic L. solidungula, and were as follows: L. saccharina and L. longicruris, 23°C; L. digitata (male), 23°C; L. digitata (female), 22°C; L. hyperborea, 21°C; L. solidungula, 18°C. The lack of within-species differences demonstrates that the success of the genus in areas with different temperature regimes is brought about by phenotypic plasticity of individuals rather than the selection of temperature races or ecotypes.     

Growth rates of Corallina officinalis (Rhodophyta) at different temperatures

Specimens of Corallina officinalis L. were grown in the laboratory for 6 and 8 weeks at temperatures of 6°, 12°, 18°, and 25°C. After 6 weeks, the mean growth rates of main axes were 2.8 mm at 18°C, 2.9 mm at 12°C, and 0.2 mm at 5°C; no growth occurred at 25°C. At 6°C, growth increased with lower light intensities. The mean total increase in length of branchlets present when the plants were collected did not vary significantly at 12° and 18°C. At 12°C, axial intergenicula formed in culture produced more new branchlets than did field-grown intergenicula. Also, the production of these branchlets on cultured intergenicula was higher at 12°C than at 18°C.Based on a dissertation completed at Clark University in partial fulfillment of the requirements for a Master of Arts degree by B. J. Colthart.     

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.     

Laboratory rearing of Sepiolinae (Mollusca: Cephalopoda)

Five species of Sepiola and Sepictta were reared in the laboratory from egg to adult size. Spawning was achieved in 3 species of Sepiola after 5 to 7 months. The growth rate of the species reared did not depend upon temperature, which ranged from 12.5° to 20°C. A fairly constant size increase (2.5 mm mantle length/month) was observed in Sepiola during the 5 months after hatching. In Sepietta, the same growth rate was observed until the fourth month after hatching, when it increased to the rate of 5 mm mantle length/month.Laboratoire associé au C.N.R.S.     

Delayed growth of mussel (Mytilus edulis) and scallop (Pecten maximus) veligers at low temperatures

Veliger larvae of Mytilus edulis (L.) from Menai Straits, North Wales, were maintained for up to 2 mo during 1981 at 5°C and then grown on to metamorphosis at 17°C. Larvae so treated showed similar low mortality and equivalent spat production to control larvae. Growth rate at 17°C was less in treated larvae than in controls, but treated larvae grew a little during the period at low temperature. Larvae of Pecten maximus (L.) from the Irish Sea suffered high mortality at low temperature but larvae surviving 2 wk at 8°C could be grown on to spat at 17°C. The longevity of M. edulis larvae is discussed in relation to the genetic homogeneity of adult populations around the UK.     

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.     

Temperature adaptation in strains of the amphi-equatorial green alga Urospora penicilliformis (Acrosiphoniales): biogeographical implications

The temperature requirements for growth and the upper survival temperatures (UST's) of the amiphi-equatorial green alga Urospora penicilliformis collected from several localities within its distribution area between 1986 and 1991 were determined. Ecotypic variation, both with regard to growth ranges and optima and to survival temperatures, was demonstrated. In the polar strains of U. penicilliformis, temperature growth ranges were narrower and the growth optima and UST's were at lower temperatures compared to cold-temperate strains. In particular, the polar strains grew between 0 and 15°C with optimal growth at 0 or 5°C, whereas the cold-temperate isolates grew between 0 and (15) 20°C with almost equal growth rates or a growth optimum between 5 and 15°C. The Arctic strains survived 23 to 24°C, and the Antarctic isolate only 19°C, while the UST's of the cold-temperate isolates were between (24) 25 to 26°C. The data strongly indicate that a cold water history of ca. 3 million yr in the Arctic can be sufficient for changes in the temperature growth ranges and optima as well as for small changes of UST as shown in the Arctic populations of U. penicilliformis. For stronger reduction of upper survival temperatures, longer time periods are necessary as exemplified in the isolate from Antarctica, where low temperatures have existed for at least 14 million yr. The significantly lower UST of the Antarctic strain, points to an early contact of the alga with the cold water of the Antarctic region and may indicate an origin of U. penicilliformis in the Southern Hemisphere. The UST's of the cold-temperate isolates (24 to 26°C) would have allowed a migration across the equator during Pleistocene lowerings of the seawater temperatures in the tropics. Growth, however, would not have been possible during the passage across the equator due to the narrow temperature-growth window. The nature of the geographical boundaries and the control of seasonal development of U. penicilliformis by the temperature conditions in the various geographical regions are discussed in relation to the present local temperature regime.     

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.     

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.     

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.     

Energetics of Euphausia pacifica. II. Complete carbon and nitrogen budgets at 8° and 12° C throughout the life span

Complete carbon and nitrogen budgets at 8° and 12° C over the life span of Euphausia pacifica were constructed from data published in the foregoing publication. The relative magnitudes of physiological functions such as metabolism and growth for the different life history stages were compared. The carbon net growth efficiency (NGE) for E. pacifica increased to a maximum of 60 to 74% at Calyptopis 3 (a larval stage) and then decreased rapidly to a level of 10 to 12% for adults. The cumulative amount of assimilated carbon or nitrogen in reproductive products was equal to that in growth. The cumulative net production efficiency (tissue plus molts plus reproductive products) is 24 to 29%, and is slightly higher for nitrogen than for carbon. For juveniles and adults, the largest proportion (40 to 65%) of assimilated material is used in metabolism, and is about 10% higher at 8° than 12° C. The difference between measured and predicted ingestion (the sum of metabolism, leakage, defecation, growth, molting and reproduction) probably results from poorly understood aspects of zooplankton physiology (e.g. the effect of body weight on leakage). Nitrogen budgets at 8° C for furcilia bulanced the best, with deviations of less than 10%. In general, predicted ingestion was increasingly less than measured ingestion as body weight and temperature increased. Possible omissions or errors in assumptions or methods that may cause the imbalances are discussed.     

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

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

Effect of temperature on the egg and yolk-sac larval development of common pandora,<Emphasis Type="Italic"> Pagellus erythrinus</Emphasis>

Temperature is one of the most critical environmental factors for fish ontogeny, affecting the developmental rate, survival and phenotypic plasticity in both a species- and stage-specific way. In the present paper we studied the egg and yolk-sac larval development of Pagellus erythrinus under different water temperature conditions, 15°C, 18°C and 21°C for the egg stage and 16°C, 18°C and 21°C for the yolk-sac larval stage. The temperature-independent thermal sum of development was estimated as 555.6 degree-hours above the threshold temperature (the temperature below which development is arrested), i.e. 7°C for the egg and 12.1°C for the yolk-sac larval stage. Higher hatching and survival rates occurred at 18–21°C. At the end of the yolk-sac larval stage, body morphometry differed significantly (p<0.05) between the temperatures tested. The growth rate of the total length increased as temperature rose from 16°C to 18°C, while in the range of 18–21°C it stabilized and was independent of water temperature. The estimated Gompertz growth curve for the yolk-sac larvae of P. erythrinus was (r²=0.992) for the 16°C, (r²=0.991) for the 18°C and (r²=0.981) for the 21°C treatment. The efficiency of vitelline utilization during the yolk-sac larval stage was higher at 18°C.Communicated by O. Kinne, Oldendorf/Luhe     

Effect of temperature on the molting,growth and maturation of the antarctic krill Euphausia superba (Crustacea: Euphausiacea) under laboratory conditions

The effect of temperature on molting, growth, and maturation rates was studied on laboratory-maintained Euphausia superba. The length of intermolt periods (IMP's) was inversely proportional to temperature (20.10 d, SD=1.60, at 0.12°C; 16.87 d, SD=1.68, at 0.97°C; and 12.48 d, SD=0.90, at 4.48°C), and directly proportional to krill size at 0.12°C and 0.97°C. For individually maintained krill the maximum growth rate at 4.48°C (0.068 mm d^-1) was nearly twice that at 0.68°C (0.037 mm d^-1). There was no observable temperature effect on maturation rates. The maturation changes of juveniles at all temperatures indicated that more than two years are probably required to reach maturity. Mature males and females regressed to immature forms, suggesting that E. superba may reproduce in successive years. These results and previously reported field and laboratory data for E. superba and other euphausiid species suggest a 4+ year life span for this species.This work was supported by NSF grant DPP 76-23437     

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.     

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     

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.