The energetics of endotrophic development in the frog Geocrinia vitellina (Anura: Myobatrachinae).

The energetics of endotrophic development, where the nutrition required to complete metamorphosis is provided solely by yolk, has seldom been quantified. The energy cost of development to metamorphosis of the endotrophic Australian frog Geocrinia vitellina was measured using bomb calorimetry and closed-system respirometry. Dry yolk had an energy density of 26.4 J x mg(-1), and an average 2.8-mm-diameter ovum contained 144 J. Incubation at 15 degrees C produced a froglet of 5.8 mm snout-vent length, containing 88 J in 87 d, with 11% of residual yolk in the gut, which is markedly less than the 50% recorded in another endotroph, Eleutherodactylus coqui. Geocrinia vitellina lost 56 J of metabolic energy during development to metamorphosis at 15 degrees C, and the total production efficiency was 61.0%. A review of published egg energy densities found a mean for amphibians of 25.1 kJ x g(-1), significantly lower than the mean of 27.1 kJ x g(-1) for reptiles. Moreover, available amphibian data suggest that endotrophic species have high yolk energy densities and low mass-specific rates of oxygen consumption relative to exotrophic species (with feeding larvae); consequently, large ovum size may not necessarily be prerequisite for endotrophic development.     

The effects of nest temperature,nest substrate,and clutch size on the oxygenation of embryos and larvae of the Australian moss frog,Bryobatrachus nimbus

The jelly around amphibian eggs presents a formidable barrier to oxygen diffusion. Therefore, egg capsules must be thin enough, and the dimensions of globular egg masses small enough, to avoid oxygen limitation leading to developmental retardation or death. The eggs of the Australian moss frog, Bryobatrachus nimbus, have the thickest jelly capsule known for any anuran amphibian. Laboratory measurements of respirometric variables predict that single prehatching embryos should be normoxic between 5 degrees and 20 degrees C, with Po(2 in) maintained above critical levels (10.2-17.0 kPa). However, numerical models of embryos amid larger egg masses (13-20 eggs) predict hypoxia at temperatures above 5 degrees C. Contrary to model predictions, however, B. nimbus embryos rarely experience hypoxia in natural nests, because embryos occur in one or two layers and the moss substrate permits aeration of the lower surface while photosynthesis probably supplies oxygen directly. After hatching, larvae move to oxygen-rich regions of the jelly mass and disperse more widely within the mass as temperatures increase. Although nest characteristics relieve diffusive constraints, small clutch sizes, low rates of embryonic and larval respiration, and the cool climate occupied by B. nimbus are the main characteristics that prevent hypoxia.     

Maximum and actual field feeding-rates in larvae of the damselfly Pyrrhosoma nymphula (Sulzer) (Odonata: Zygoptera)

The paper presents information on factors influencing maximum feeding-rates (measured in the laboratory) in larvae of the damselfly Pyrrhosoma nymphula, and compares estimates of feeding rates in the field with maximum feeding-rates for larvae of the same size at the same temperature. Maximum feeding-rates in Pyrrhosoma larvae of different sizes were measured at 4, 5, 10 and 15°C. At low temperatures (4–5°C) maximum feeding-rate was depressed more than predicted either from the effects of temperature on the gut-clearance time of larvae or their respiratory rate. Maximum feeding-rate declined steadily throughout metamorphosis in the final instar and stopped completely prior to emergence of the adult. Feeding-rates in the field were calculated from ‘balanced’ energy equations, i.e. from the sum of larval growth, respiration and the production of faeces and exuviae. Feeding rates in the field were always much less than maximum feeding-rates for the same size of larva at the same temperature, and at the most were never more than 70% of the latter; they were closer to the maximum in summer than in winter, when they fell as low as 20% of the maximum. The relevance of these findings to studies on the efficiency with which carnivores utilize energy in the field, and the importance of Odonata larvae as predators in aquatic ecosystems is discussed.     

Cost of protein synthesis and energy allocation during development of antarctic sea urchin embryos and larvae

Cold environments represent a substantial volume of the biosphere. To study developmental physiology in subzero seawater temperatures typically found in the Southern Ocean, rates and costs of protein synthesis were measured in embryos and larvae of Sterechinus neumayeri, the Antarctic sea urchin. Our analysis of the "cost of living" in extreme cold for this species shows (1) that cost of protein synthesis is strikingly low during development, at 0.41 +/- 0.05 J (mg protein synthesized)(-1) (n = 16); (2) that synthesis cost is fixed and independent of synthesis rate; and (3) that a low synthesis cost permits high rates of protein turnover at -1 degrees C, at rates comparable to those of temperate species of sea urchin embryos developing at 15 degrees C. With a low synthesis cost, even at the highest synthesis rates measured (gastrulae), the proportion of total metabolism accounted for by protein synthesis in the Antarctic sea urchin was 54%-a value similar to that of temperate sea urchin embryos. In the Antarctic sea urchin, up to 87% of metabolic rate can be accounted for by the combined energy costs of protein synthesis and the sodium pump. We conclude that, in Antarctic sea urchin embryos, high rates of protein synthesis can be supported in extreme-cold environments while still maintaining low rates of respiration.     

The influence of temperature on growth rate and length of larval life of the gastropod, Crepidula plana Say

The relationship between rate of larval development and the potential to prolong larval life was examined for larvae of the marine prosobranch gastropod Crepidula plana Say. Larvae were maintained in clean glass dishes at constant temperatures ranging from 12–29°C and fed either Isochrysis galbana Parke (ISO) or a Tahitian strain of Isochrysis species (T-ISO). Under all conditions, larvae grew at constant rates, as determined by measurements of shell length and tissue biomass. Most larvae eventually underwent spontaneous metamorphosis. Regardless of temperature, faster growth was associated with a shorter planktonic stage prior to spontaneous metamorphosis. Within an experiment, higher temperatures generally accelerated growth rates and reduced the number of days from hatching to spontaneous metamorphosis. However, growth rates were independent of temperature for larvae fed ISO at 25 and 29°C and for larvae fed T-ISO at 20 and 25°C. Where growth rates were unaffected by temperature, time to spontaneous metamorphosis was similarly unaffected. Maximum durations of larval life at a given temperature were shorter for larvae of Crepidula plana than for those of the congener C. fornicata (L.), although both species grew at comparable rates. Interpretations of the ecological significance of these interspecific differences in delay capabilities will require additional data on adult distributions and larval dispersal patterns in the field.     

Temperature and the energetics of development in the house cricket (Acheta domesticus)

The influence of rearing temperature on the energetics of development was investigated in house crickets (Acheta domesticus). Crickets raised at 25 degrees C grew slower (0.51 mg d(-1), dry mass basis) and took longer to develop (119 d) but obtained a greater adult body mass (61 mg, dry mass) than crickets reared at 28 degrees C (0.99 mg d(-1), 49 d, 48 mg). Total metabolic energy consumed during development at 25 degrees C (1351 J) was twice that at 28 degrees C (580 J) primarily because of the longer development period, and as a consequence the specific net cost of growth was much greater for crickets reared at 25 degrees C (22.1 kJ g(-1)) than 28 degrees C (11.9 kJ g(-1)).     

The effects of low temperature on fertilized rabbit ova in vitro,and the normal development of ova kept at low temperature for several days

Fertilized rabbit ova at the 2-blastomere stage kept in rabbit serum were stored at low temperatures for various lengths of time. They were then cultured at 38 degrees C. for about 24 hours to determine their viability. A number of the viable ova were finally transplanted into recipient does. It was found that rapid cooling of ova to 5 degrees or to 0 degrees C. was more harmful to the subsequent viability of ova than slow cooling. Rapid cooling was not more lethal to the ova than slow cooling, but did prevent their future normal cleavage. There was no difference between those ova cooled rapidly or slowly to 10 degrees C. It was concluded that temperature shock has an adverse effect on ova, especially at the lower temperatures, though temperature shock can be remedied by acclimatization (slow cooling). Thus, the physiological significance of temperature shock would seem to be broadened. The optimal temperature for the storage of ova was investigated. It was found that 10 degrees C. was the best temperature; at this temperature viable ova were obtained after storage for 144 to 168 hours. At 0 degrees , 5 degrees , or 15 degrees C. the ova were viable for 96 to 120 hours, while at 22-24 degrees C., only for 24 to 48 hours. The percentage of dead ova was low at a favorable temperature, increasing only at the end of the storage period. At an unfavorable temperature, however, the rate of death increased steadily from beginning to end of storage. The percentage of abnormally cleaved ova (arrested cleavage and fragmentation) remained at a low level at first at a favorable temperature, but then increased just before or during death of the ova. A critical time for the viability, the abnormal cleavage, and the death of ova was characteristic of each temperature. About 24 to 28 per cent of the viable ova remaining after being stored at 0-15 degrees C. for 2 to 4 days and cultured at 38 degrees C. for 24 hours were capable of development into normal young. The compatibility of serum and ova, the absence of a correlation between the viability of the ova and the source of the fertilizing spermatozoa, and the fertilization of superovulated ova (i.e., the percentage of fertile does in follicular phase and in luteal phase, the percentage of unfertilized ova and of fertilized ova at different stages, the percentage of does that had produced a normal number of ova or had produced a large number of ova, etc.), are reported. The possibility of a more efficient utilization of the germ cells of valuable animals by means of the present techniques, and the possibility of a new approach to the experimental investigation of mammalian genetics and development, have been mentioned.     

The processes of methane formation and oxidation in the soils of the Russian arctic tundra

Methane emission from the following types of tundra soils was studied: coarse humic gleyey loamy cryo soil, peaty gley soil, and peaty gleyey midloamy cryo soil of the arctic tundra. All the soils studied were found to be potential sources of atmospheric methane. The highest values of methane emission were recorded in August at a soil temperature of 8-10 degrees C. Flooded parcels were the sources of atmospheric methane throughout the observation period. The rates of methane production and oxidation in tundra soils of various types at 5 and 15 degrees C were studied by the radioisotope method. Methane oxidation was found to occur in bog water, in the green part of peat moss, and in all the soil horizons studied. Methane formation was recorded in the horizons of peat, in clay with plant roots, and in peaty moss dust of the bogey parcels. At both temperatures, the methane oxidation rate exceeded the rate of methane formation in all the horizons of the mossy-lichen tundra and of the bumpy sinkhole complex. Methanogenesis prevailed only in a sedge-peat moss bog at 15 degrees C. Enrichment bacterial cultures oxidizing methane at 5 and 15 degrees C were obtained. Different types of methanotrophic bacteria were shown to be responsible for methane oxidation under these conditions. A representative of type I methylotrophs oxidized methane at 5 degrees C, and Methylocella tundrae, a psychroactive representative of an acidophilic methanotrophic genus Methylocella, at 15 degrees C.     

Temperature responses in larvae of Macoma balthica from a northerly and southerly population of the European distribution range

Planktonic marine invertebrate embryos and larvae experience high mortality rates. Processes during these early vulnerable stages of development are an important determinant of the dynamics of marine invertebrate populations. In order to evaluate possible specific local adaptations of the bivalve Macoma balthica (L.), larvae from parents living in Norway (Balsfjord) and France (Gironde Estuary) were reared in the laboratory at 10, 15 and 20 °C. The rate of growth and the time it took to develop a foot were measured. Larvae grew faster and developed quicker at higher temperatures. This was true for both origins tested. Within temperature treatments, the French larvae always developed and grew fastest. Size at metamorphosis (defined as the appearance of the foot) was 250 μm (SD=12.7) in five out of the six cases; the only exception was Norwegian larvae kept at the highest temperature that metamorphosed at a smaller size (229 μm, SD=6.4). Size at metamorphosis thus appears to be largely independent of temperature. In both populations, instantaneous survival rates declined with temperature with no effect of origin. Instantaneous survival declined faster with temperature than development rates increased, resulting in lower net survival of larvae to metamorphosis at the higher temperatures. Although the French larvae had a shorter development time at the same temperature than the Norwegian larvae, the total survival of larvae from the two origins was not significantly different. The larvae of M. balthica of both populations prove to be tolerant to considerably higher rearing temperatures than they will ever experience in their natural habitat.     

Energy source utilization by embryos and larvae of the muricid snail Chorus giganteus (Lesson, 1829)

The muricacean snail Chorus giganteus presents intracapsular development and the occurrence of nurse eggs that are ingested by the early encapsulated embryos indicate both that these snails develop through a lecitotrophic type of development and that reserves would be sufficient to support settlement and metamorphosis. In order to get more information about the use of energy resources, the dynamics of biochemical components throughout development at three temperatures (9, 12 and 15 °C) and the energetic cost of free-swimming life and metamorphosis are described. The uptake of ³H-alanine, as representative of dissolved organic matter, by embryo and larval stages is also investigated. While protein levels increased at all temperature conditions after ingestion of nurse eggs, lipids only increased when embryo and larvae were reared at 15 °C, and no change in carbohydrate levels was detected at any of the temperatures. The RNA/DNA indexes showed no significant differences with temperature at any stage of development but decreased along with the development of individuals. After hatching, organic matter and energy content of juveniles steadily decreased. Individuals at any of the developmental stage showed to be able to uptake alanine from seawater; the aminoacid uptake capacity increased along with intracapsular development. Uptake of alanine showed to be an active process and to follow Michaelis-Menten kinetics. This would be the first report about dissolved organic matter uptake by encapsulated development stages of any marine invertebrate species and let conclude that these larvae have the ability to obtain exogenous food in a dissolved form and to incorporate it into metabolizable compounds.     

Effect of delayed metamorphosis on larval competence, and post-larval survival and growth, in the abalone Haliotis iris Gmelin

Marine invertebrate species vary in their ability to delay metamorphosis, and in the degree to which delayed metamorphosis compromises juvenile performance. Abalone (Haliotis iris) larvae were deprived of metamorphosis cues and the effects of delayed metamorphosis on larval competence, and post-larval growth and survival were quantified. Larvae were exposed to a metamorphosis inducer (the coralline alga Phymatolithon repandum (Foslie) Wilks and Woelkerling) on Days 11, 18, 22, 26, 30 and 34 post-fertilisation (temperature 16-17 degrees C). Post-larvae were reared on diatoms (Nitzschia longissima Grunow) for 3-4 weeks post-metamorphosis. Delayed metamorphosis caused progressive negative effects on post-larval performance. Virtually all larvae initiated metamorphosis in response to P. repandum, regardless of larval age. The proportion of post-larvae that developed post-larval shell growth within 2 days of metamorphosis induction dropped only approximately 20% from Day 11 to Day 26 (P>0.05), but was significantly lower by Day 30 and Day 34 (P<0.001). Larvae that metamorphosed on Days 11, 18 and 22 showed high survival (>80%) and growth rates (means of 20-22 μm shell length per day). In contrast, larvae that metamorphosed on Day 26 and Day 30 had poor survival (30-40%) and lower (P<0.05) growth rates (15-16 μm/day). Of the larvae that metamorphosed on Day 34, only 7 (30%) survived their first week post-metamorphosis, and they grew only 2 μm/day on average. Only one of these post-larvae (4%) survived the second week. The visible yolk supply diminished over the life of the larvae and was near zero by Day 34. Nearly all larvae had died by Day 38. H. iris larvae remained competent to metamorphose for at least 3 weeks after they attained competence. Post-larval growth and survival were not reduced if metamorphosis occurred within 3 weeks of fertilisation. This extended period of larval competence implies that H. iris larvae can potentially disperse for up to several weeks before successful metamorphosis.     

Influence of environmental oxygen on development and hatching of aquatic eggs of the australian frog, Crinia georgiana

The effect of oxygen partial pressure (Po(2)) on development and hatching was investigated in aquatic embryos of the myobatrachid frog, Crinia georgiana, in the field and in the laboratory. Eggs from 29 field nests experienced widely variable Po(2) but similar temperatures. Mean Po(2) in different nests ranged between 2.9 and 19.3 kPa (grand mean 12.9 kPa), and mean temperature ranged between 11.9 degrees and 16.8 degrees C (grand mean 13.7 degrees C). There was no detectable effect of Po(2) or temperature on development rate or hatching time in the field, except in one nest at 2.9 kPa where the embryos died, presumably in association with hypoxia. Laboratory eggs were incubated at 15 degrees C at a range of Po(2) between 2 and 25 kPa. Between 5 and 25 kPa, there was almost no effect of Po(2) on development rate to stage 26, but the embryos hatched progressively earlier-at earlier stages and lower gut-free body mass-at lower Po(2). At 2 kPa, development was severely delayed, growth of the embryo slowed, and morphological anomalies appeared. A high tolerance to low Po(2) may be an adaptation to embryonic development in the potentially hypoxic, aquatic environment.     

The potential for cryopreserving larvae of the sea urchin, Evechinus chloroticus

Larvae of the sea urchin, Evechinus chloroticus, at varying stages of development, were assessed for their potential to survive cryopreservation. Ethylene glycol (EG) and dimethyl sulphoxide (Me2SO), at concentrations of 1-2 M, were evaluated as cryoprotectants (CPAs) in freezing regimes initially based on methods established for freezing larvae of other sea urchin species. Subsequent work varied cooling rate, holding temperature, holding time, and plunge temperature. Ethylene glycol was less toxic to larvae than Me2SO. However, no larvae survived freezing and thawing in EG. Larvae frozen in Me2SO at the gastrula stage and 4-armed pluteus stage regained motility post-thawing. The most successful freezing regime cooled straws containing larvae in 1.5 M Me2SO from 0 to -35 degrees C at 2.5 degrees C min(-1), held at -35 degrees C for 5 min, then plunged straws into liquid nitrogen. Motility was high 2-4 h post-thawing using this regime but decreased markedly within 24 h. Some 4-armed pluteus larvae that survived beyond this time developed through to metamorphosis and settled. Different Me2SO concentrations and supplementary trehalose did not improve long-term survival. Large variation in post-thaw survival was observed among batches of larvae produced from different females.     

Survival and development of horseshoe crab (Limulus polyphemus) embryos and larvae in hypersaline conditions

The horseshoe crab Limulus polyphemus spawns in the mid- to upper intertidal zone where females deposit eggs in nests below the sediment surface. Although adult crabs generally inhabit subtidal regions of estuaries with salinities from 5 to 34 ppt, developing embryos and larvae within nests are often exposed to more extreme conditions of salinity and temperature during summer spawning periods. To test whether these conditions have a negative impact on early development and survival, we determined development time, survival, and molt cycle duration for L. polyphemus embryos and larvae raised at 20 combinations of salinity (range: 30-60 ppt) and temperature (range: 25-40 degrees C). Additionally, the effect of hyperosmotic and hypoosmotic shock on the osmolarity of the perivitelline fluid of embryos was determined at salinities between 5 and 90 ppt. The embryos completed their development and molted at salinities below 60 ppt, yet failed to develop at temperatures of 35 degrees C or higher. Larval survival was high at salinities of 10-70 ppt but declined significantly at more extreme salinities (i.e., 5, 80, and 90 ppt). Perivitelline fluid remained nearly isoosmotic over the range of salinities tested. Results indicate that temperature and salinity influence the rate of crab development, but only the extremes of these conditions have an effect on survival.     

The trade-off between maturation and growth during accelerated development in frogs

Developmental energetics are crucial to a species' life history and ecology but are poorly understood from a mechanistic perspective. Traditional energy and mass budgeting does not distinguish between costs of growth and maturation, making it difficult to account for accelerated development. We apply a metabolic theory that uniquely considers maturation costs (Dynamic Energy Budget theory, DEB) to interpret empirical data on the energetics of accelerated development in amphibians. We measured energy use until metamorphosis in two related frogs, Crinia georgiana and Pseudophryne bibronii. Mass and energy content of fresh ova were comparable between the species. However, development to metamorphosis was 1.7 times faster in C. georgiana while P. bibronii produced nine times the dry biomass at metamorphosis and had lower mass-specific oxygen requirements. DEB theory explained these patterns through differences in ontogenetic energy allocation to maturation. P. bibronii partitioned energy in the same (constant) way throughout development whereas C. georgiana increased the fraction of energy allocated to maturation over growth between hatching and the onset of feeding. DEB parameter estimation for additional, direct-developing taxa suggests that a change in energy allocation during development may result from a selective pressure to increase development rate, and not as a result of development mode.     

Early activation of adult organ differentiation during delay of metamorphosis in solitary ascidians, and consequences for juvenile growth

Abstract. Many animals have the ability to delay metamorphosis when conditions are unfavorable. This strategy carries obvious benefits, but may also result in severe consequences for lecithotrophic larvae that run low on time and energy. Precocious activation of postlarval developmental programs—so-called anticipatory development—may be adaptive and increase the survival of older, energy-depleted larvae by allowing more rapid metamorphosis. Three of six solitary ascidian species displayed extensive anticipatory development of postlarval structures, similar to heterochronies normally observed for colonial species. The capacity for anticipatory development may be linked to the length of competent period, taxonomic group, or both: members of suborder Phlebobranchia exhibited extensive anticipatory development and long competent periods, but members of suborder Stolidobranchia exhibited little or no anticipatory development and had shorter competent periods. Delay of metamorphosis of up to 3 d did not negatively impact postlarval and juvenile growth rates for any of three species tested, regardless of taxonomic group or length of competent period, although a longer, 7-d, delay resulted in slower postlarval growth in Ciona intestinalis . Anticipatory development of postlarval structures may ameliorate the negative consequences of delay of metamorphosis in C. intestinalis and Ascidiella aspersa , but Molgula socialis showed neither anticipatory development nor a negative impact of metamorphic delay on postlarval fitness. This is the first demonstration that anticipatory development of postlarval structures, normally associated only with colonial ascidians, can occur as a normal part of the development of solitary ascidians.     

Survival of indianmeal moth and navel orangeworm (Lepidoptera: Pyralidae) at low temperatures

Concerns over insect resistance, regulatory action, and the needs of organic processors have generated renewed interest in developing nonchemical alternative postharvest treatments to fumigants used on dried fruits and nuts. Low-temperature storage has been identified as one alternative for the Indianmeal moth, Plodia interpunctella (Hiibner), and navel orangeworm, Amyelois transitella (Walker) (Lepidoptera: Pyralidae), common postharvest pests in California dried fruits and nuts. The response of eggs, nondiapausing larvae, and pupae of both species to exposure to low temperatures (0, 5, and 10 degrees C) was evaluated. Eggs of both species were the least tolerant of low temperatures. At 0 and 5 degrees C, pupae were most tolerant, but at 10 degrees C, nondiapausing larvae of both species were most tolerant, with lethal time (LT)95 values of 127 and 100 d for Indianmeal moth and navel orangeworm, respectively. The response of diapausing Indianmeal moth larvae to subfreezing temperatures also was evaluated. Diapausing larvae were very cold tolerant at -10 degrees C, with LT95 values of 20 and 17 d for long-term laboratory and recently isolated cultures, respectively. Diapausing larvae were far less tolerant at lower temperatures. At -15 degrees C, LT95 values for both cultures were <23 h, and at -20 degrees C, LT95 values were <7 h. Refrigeration temperatures of 0-5 degrees C should be useful in disinfesting product contaminated with nondiapausing insects, with storage times of 3 wk needed for adequate control. Relatively brief storage in commercial freezers, provided that the temperature throughout the product was below -15 degrees C for at least 48 h, also shows potential as a disinfestation treatment, and it is necessary when diapausing Indianmeal moth larvae are present.     

Influence of delayed metamorphosis on postsettlement survival and growth in the sipunculan Apionsoma misakianum

Abstract. Certain stresses experienced by marine larvae from many groups can dramatically reduce aspects of juvenile performance. This study reports the effects of delayed metamorphosis and nutritional stress on survival and growth of the deposit-feeding sipunculan Apionsoma (= Golfingia ) misakianum . Approximately 600 larvae collected from the Florida Current plankton were distributed among 3 treatment groups. Ninety larvae (controls) were offered sediment and adult-conditioned seawater 4 d after collection, to induce metamorphosis; larvae of this species could not be induced to metamorphose by increasing the K⁺ concentration of seawater. The remaining 500 larvae were kept swimming for either 2 or 4 weeks, with or without phyto-plankton (clone T-ISO). At the end of the periods of prolonged larval swimming, subsampled larvae (360) were induced to metamorphose as in the controls. Surviving individuals were retrieved 6 weeks after the addition of excess sediment in all treatments, and weighed to document growth. Neither delayed metamorphosis nor starvation influenced juvenile survival. However, starving larvae for 2 weeks significantly reduced mean juvenile growth rates relative to the mean growth rate of control individuals (p<0.0001), while prolonging larval life by 4 weeks significantly reduced mean juvenile growth rates (p<0.05) whether or not larvae were fed. Reduced juvenile growth rates may have been caused by nutritional stress experienced by larvae in both the starved and fed treatments. The rapid response of freshly collected larvae to sediment indicates that competent larvae of this species routinely delay metamorphosis in the field. The extent to which they also experience food limitation is not yet clear. If competent larvae are food limited while delaying metamorphosis in the field, our results suggest that juveniles will grow more slowly and may thus exhibit reduced fitness.     

Effects of temperature on survival, development, growth and feeding of larvae of Yellowtail clownfish Amphiprion clarkii (Pisces: Perciformes)

To understand the physiological and ecological responses of marine fishes to the change of water temperature, newly-hatched larvae of Yellowtail clownfish Amphiprion clarkii were reared in captivity at water temperatures of 23, 26 and 29 °C till they completed the metamorphosis to juvenile phase, and larval survival, development, growth and feeding were evaluated during the experimental period. The results showed that water temperature influenced the physiological performance of larvae of A. clarkii significantly. The survival and growth rates of larvae of A. clarkii increased significantly with the increase of water temperature from 23 to 29 °C (P < 0.05). Water temperature also influenced larval development of A. clarkii significantly and larvae reared at 23 °C took longer time for post-larval development and metamorphosis compared to 26 and 29 °C (P < 0.05). Total length and body weight for post-larval development and metamorphosis decreased with the increase of water temperature from 23 to 29 °C (P < 0.05). Q₁₀ in developmental rate was higher than in daily growth rate at the same rearing temperature, indicating that at water temperature had greater influence on larval development than on growth. Water temperature also influenced larval feeding of A. clarkii significantly with feed ration (FR) and feed conversion efficiency (FCE) increased with the increase of water temperature from 23 to 29 °C (P < 0.05). There was a positive correlation between FR and specific growth rate (SGR) (P < 0.05) but not between FCE and SGR (P > 0.05), indicating that FR influenced growth rate significantly in larvae of A. clarkii. This study demonstrated that the physiological responses of larvae of A. clarkii to the change of water temperature and confirmed that water temperature influenced larval survival, development, growth and feeding significantly. This study suggests that the decline of larval survival and growth rates, extension of pelagic larval duration and reduction of larval feeding at lower temperature have ecological impacts on larval dispersal and metamorphosis, juvenile settlement and population replenishment in A. clarkii in the wild.