Carbon dioxide use by chemoautotrophic endosymbionts of hydrothermal vent vestimentiferans: affinities for carbon dioxide, absence of carboxysomes, and δ13C values

The hydrothermal vent vestimentiferans Riftia pachyptila Jones, 1981 and Ridgeia piscesae Jones, 1985 live in habitats with different abundances of external CO₂. R. pachyptila is found in areas with a high input of hydrothermal fluid, and therefore with a high [CO₂]. R. piscesae is found in a range of habitats with low to high levels of hydrothermal fluid input, with a correspondingly broad range of CO₂ concentrations. We examined the strategies for dissolved inorganic carbon (DIC) use by the symbionts from these two species. R. pachyptila were collected from the East Pacific Rise (9°50′N; 104°20′W) in March 1996, and R. piscesae were collected from the Juan de Fuca Ridge (47°57′N; 129°07′W) during September of 1996 and 1997. The differences in the hosts' habitats were reflected by the internal pools of DIC in these organisms. The concentrations of DIC in coelomic fluid from R. piscesae were 3.1 to 10.5 mM, lower than those previously reported for R. pachyptila, which often exceed 30 mM. When symbionts from both hosts were incubated at in situ pressures, their carbon fixation rates increased with the extracellular concentration of CO₂, and not HCO₃ ⁻, and symbionts from R. piscesae had a higher affinity for CO₂ than those from R. pachyptila (K _1/2 of 7.6 μM versus 49 μM). Transmission electron micrographs showed that symbionts from R. piscesae lack carboxysomes, irrespective of the coelomic fluid [DIC] of their host. This suggests that the higher affinity for CO₂ of R. piscesae symbionts may be their sole means of compensating for lower DIC concentrations. The δ¹³C values of tissues from R. piscesae with higher [DIC] in the coelomic fluid were more positive, opposite to the trend previously described for other autotrophs. Factors which may contribute to this trend are discussed. Received: 24 September 1998 / Accepted: 12 May 1999     

The use of RNA:DNA ratios to predict growth limitation of juvenile summer flounder (Paralichthys dentatus) from Delaware and North Carolina estuaries

Nutritional indices were used to develop biochemical correlates of feeding and growth rates for juvenile summer flounder, Paralichthys dentatus (Linnaeus), from North Carolina (NC) and Delaware (DE). Six parameters (Fulton's condition K=10⁴xweight/(length³), wet weight/dry weight, [protein], [RNA], [DNA], and RNA:DNA) were related to feeding and growth rates of fish from previously reported 10 to 14-d experiments at temperatures ranging from 2 to 20 °C with varying feeding levels (0 to 100% and libitum). RNA:DNA ratios were the best predictors of growth rates, but inclusion of a temperature term improved the relationship between RNA:DNA ratios and growth rate for Delaware fish. Feeding rates were poorly correlated with all parameters. RNA:DNA ratios of fish in the laboratory changed significantly within 1 d of starvation and refeeding at 16 °C. RNA:DNA of juvenile summer flounder collected from one site in Indian River Bay, DE and two sites in the Newport River Estuary, NC, between January and June 1992 were used to estimate in situ growth rates following settlement. Predicted growth rates in both estuaries were close to maximum (suggesting ad libitum feeding) until early May. Growth rates of juveniles from Delaware were <0% d^-1 from December through early March, and were higher (0.6 to 3% d^-1) from April through early June. However, growth rates of DE juveniles during May were <50% of maxinum. North Carolina juveniles had growth rates of 2 to 5% d^-1 from February through early April. Juveniles from one of the Newport River sites (a marsh habitat) were also severely growth limited (<20% of maximum) after April. Prolonged periods of sub-optimal growth may be important to survival and recruitment of juvenile summer flounder in northern mid-Atlantic estuaries. A model is presented which illustrates the potential impact that small changes in temperature and growth limitation can have on recruitment success in both delaware and North Carolina estuaries.     

Use of nucleic acids as indicators of growth in juvenile white shrimp,Penaeus vannamei

The use of nucleic acids to estimate crustacean growth is not well documented, and may be complicated by biochemical changes associated with their molt cycle. The objectives of this study were to assess the effects of molt stage on nucleic acid concentrations in abdominal muscle tissue of juvenile white shrimp,Penaeus vannamei, and to examine the relationship between nucleic acid concentrations and growth rates of shrimp exposed to different feeding regimes throughout a 12 d feeding experiment. RNA and DNA concentrations and RNA:DNA ratios were not significantly different among the five major molt stages early postmolt, late postmolt, intermolt, early premolt, and late premolt. In the feeding experiment, RNA concentrations and RNA:DNA ratios accounted for >70% of the variation in shrimp growth on three different sampling days. In addition, RNA concentrations and RNA:DNA ratios were used successfully to discriminate between unfed, moderately-fed, and well-fed shrimp. These variables exhibited significant treatment differences in <24 h after the initiation of the different feeding regimes, whereas significant changes in whole-body weight took longer to detect. Rapid detection of significant treatment effects can be useful in ecological studes, especially those concerned with food-web interactions.     

Vacuolate-attached filaments: highly productive Ridgeia piscesae epibionts at the Juan de Fuca hydrothermal vents

Vacuolate sulfur bacteria with high morphological similarity to vacuolate-attached filaments previously described from shallow hydrothermal vents (White Point, CA) were found at deep-sea hydrothermal vents. These filamentous bacteria grow in dense mats that cover surfaces and potentially provide a significant source of organic carbon where they occur. Vacuolate-attached filaments were collected near vents at the Clam Bed site of the Endeavour Segment of the Juan de Fuca Ridge and from the sediment surface at Escanaba Trough on the Gorda Ridge. A phylogenetic analysis comparing their 16S rRNA gene sequences to those collected from the shallow White Point site showed that all vacuolate-attached filament sequences form a monophyletic group within the vacuolate sulfur-oxidizing bacteria clade in the gamma proteobacteria. Abundance of the attached filaments was quantified over the length of the exterior surface of the tubes of Ridgeia piscesae worms collected from the Clam Bed site at Juan de Fuca yielding a per worm average of 0.070 ± 0.018 cm³ (n = 4). In agreement with previous results for White Point filaments, anion measurements by ion chromatography showed no detectable internal nitrate concentrations above ambient seawater (n = 9). For one R. piscesae tube worm “bush” at the Easter Island vent site, potential gross epibiont productivity is estimated to be 15 to 45× the net productivity of the worms.     

RNA:DNA ratio during the critical period and early larval growth of the red drum Sciaenops ocellatus

Eggs from two separate spawning stocks of the red drum Sciaenops ocellatus (Linnaeus) were hatched, and the larvae were reared in the laboratory for 2 wk under closely controlled conditions. Total RNA, DNA, and soluble protein were measured in each population daily in triplicate pooled samples of larvae from each of three tanks. Growth rate in mm d^-1 was determined for each population at 2 d intervals. Growth rate explained 72 and 95% of the variation in the RNA:DNA ratios of the two populations individually, and 86% of the variation in the RNA:DNA ratio when data from the two populations were combined. The RNA:DNA ratio appeared to be most effective as an indicator of growth in rapidly growing larvae, and to lose some resolution when growth was intermittent. The rates of deposition of RNA, DNA, and protein into tissue were all highly correlated with growth rate and with each other. Mean population RNA:DNA ratios of red drum yolk-sac larvae decreased from Day 1 post-hatch until larvae initiated successful feeding behavior, and then increased steadily throghout the remainder of the experimental period. This pattern of change in the RNA:DNA ratios during the yolk-sac stage appears to be an intrinsic developmental pattern of red drum ontogeny. The lowest values for the RNA:DNA ratio were observed just prior to the initiation of feeding or during the critical period, indicating that red drum larvae experience a decrease in capacity for protein synthesis as they initiate feeding. Intrinsic variation in the RNA:DNA ratio during development suggests that caution be used when comparing the RNA:DNA ratios of yolk-sac larvae to a critical ratio calculated from Buckley's general model.     

Relationship between growth and biochemical indices in laboratory-reared juvenile Japanese flounder (Paralichthys olivaceus), and its application to wild fish

In order to estimate growth rates based on biochemical indices of the liver of wild Japanese flounder (Paralichthys olivaceus), juveniles were reared at six ration levels (0, 0.5, 2, 4, 6 and 8% body weight day⁻¹) in the laboratory for 14 days, and the relationship between their growth rates and biochemical indices (RNA/DNA, protein/DNA, triglyceride/DNA, phospholipid/DNA and cathepsin D activities) were determined. Positive and approximately linear relationships were seen between growth rates and the indices of RNA/DNA, protein/DNA and phospholipid/DNA. The triglyceride/DNA ratio decreased with increasing growth rates up to approximately 1% body weight day⁻¹, then increased linearly with increasing growth rates. There was no significant correlation between growth rates and cathepsin D activity, and the highest values were obtained in the starved fish. Compared with laboratory-reared specimens, wild specimens of similar sizes were found to have significantly larger livers. The RNA/DNA, protein/DNA and phospholipid/DNA ratios of wild specimens fell in a broad range between ration groups of reared juveniles. The protein/DNA ratios of wild specimens were low and outside the range of the reared juveniles at six ration levels. In contrast, the levels of cathepsin D activity of wild fish were highest compared to the reared fish. Estimated growth rates of wild fish from the RNA/DNA, protein/DNA and phospholipid/DNA regressions obtained from the rearing experiment were 1.66, −1.74 and 0.10% day⁻¹, respectively. Based on our results, the RNA/DNA index may be regarded as the most valid and reliable growth estimator. It is noted that the larger liver size, the lower liver protein/DNA ratio and the unexpectedly high level of cathepsin D activities of wild specimens found in this study may reflect the different metabolic conditions of fish reared in the laboratory compared to those collected in the field. Received: 29 February 2000 / Accepted: 26 August 2000     

Measuring RNA:DNA ratios in individual <Emphasis Type="Italic">Acartia tonsa</Emphasis> (Copepoda)

Acartia tonsa Dana is a dominant copepod in coastal waters and is therefore an important link in the food web between microplankton and higher trophic levels. RNA:DNA ratios have been used to describe growth and nutritional condition of field-collected copepods and to show strong correlation between RNA:DNA ratios and group egg production (EP). A method was developed using a sensitive, nucleic acid-specific fluorescent dye, and automated microplate fluorometer to measure DNA, RNA, and the RNA:DNA ratio of individual A. tonsa. DNA, RNA, and RNA:DNA ratios and EP were all significantly higher in copepods fed Thalassiosira sp. compared to starved copepods. There was a general trend toward an increase in RNA:DNA ratios with increase in EP, but due to the high degree of variation in both RNA:DNA ratios and EP among individual copepods there was no significant correlation between RNA:DNA ratios and EP. Significant differences in RNA:DNA ratios between fed (7.2) and starved (3.3) copepods were found after 2 days. This assay may be applied to other species of copepods sampled in the field to provide an index of the health of planktonic food webs.     

Response of hydrothermal vent vestimentiferan <Emphasis Type="Italic">Riftia pachyptila</Emphasis> to differences in habitat chemistry

Vestimentiferan tubeworms, which rely on intracellular sulfide-oxidizing autotrophic bacteria for organic carbon, flourish at deep-sea hydrothermal vents despite the erratic nature of their habitat. To assess the degree to which differences in habitat chemistry (sulfide, pH/CO₂) might impact host and symbiont metabolic activity, Riftia pachyptila tubeworms were collected from habitats with low (H₂S < 0.0001 mM) and high (up to 0.7 mM) sulfide concentrations. The elemental sulfur content of the symbiont-containing trophosome organ was lower in specimens collected from the low-sulfide site. Symbiont abundance, RubisCO activity, and trophosome carbon fixation rates were not significantly different for individuals collected from low- versus high-sulfide habitats. Carbonic anhydrase activities were higher in the anterior gas exchange organs of R. pachyptila from the low-sulfide habitat. Despite large differences in habitat chemistry, symbiont abundance and autotrophic potential were consistent, while the host appears to tailor carbonic anhydrase activity to environmental CO₂ availability.     

Condition of larval and juvenile red drum (Sciaenops ocellatus ) from estuarine nursery habitats

RNA:DNA ratios of larval and juvenile red drum (Sciaenops ocellatus) collected from nursery habitats in the Aransas Estuary, Texas, in 1994 were quantified using a highly sensitive ethidium-bromide fluorometric technique. RNA:DNA ratios of wild red drum were evaluated by comparing individual values to a linear regression model derived for starved laboratory-reared red drum. Wild red drum were in relatively good condition with <5% of the RNA:DNA ratios within or below the 95% prediction interval of 4 to 5 d starved red drum. A multiple-regression model explained 54% of the variability in the RNA:DNA ratio of wild red drum, and identified length and water temperature (midday) as significant factors. RNA:DNA ratios increased with fish length [≃1.1 mm⁻¹, over the size range investigated (5␣to 20 mm)]. The effect of temperature on the RNA: DNA ratio was assessed on different sampling trips, and ratios increased with increasing temperature. Abundance of larval and juvenile red drum in the Aransas Estuary varied as a function of both habitat (shoal grass Halodule wrightii, turtle grass Thalassia testudinum) and site (Aransas Bay, Redfish Bay); however, no differences in RNA:DNA ratios were detected between habitats or between sites. It is postulated that the nutritional condition of newly settled red drum from the Aransas Estuary in 1994 was relatively high, and that starvation was of minor importance. Received: 19 August 1996 / Accepted: 23 August 1996     

Nucleic acids and growth of larval and early juvenile spider crab,Hyas araneus

The spider crabHyas araneus (L.) was collected from the North Sea in winter 1986–1987 and reared in the laboratory from hatching of the Zoea I (ZI) through the first juvenile instar (CI). Within a given moult cycle, individuals of the same age were sampled in intervals of 2 (ZI, ZII, CI) or 3 d (megalopa) for analysis of dry weight (W), carbon (C), nitrogen (N), hydrogen (H), protein, DNA, and RNA. Lipid was calculated from C. Biomass, growth rate and nucleic acid contents showed high variability during each moult cycle and between instars. Instantaneous growth rates of C were high in postmoult and intermoult, and low in the premoult period of each moult cycle. A shift was observed from high rates of lipid accumulation in the postmoult and intermoult stages to proportionally increasing protein accumulation during late premoult (ZI), or throughout a major part of the remaining moult cycle (in all other instars). DNA was accumulated throughout the ZI and ZII instars, but decreased in late premoult megalopa. It increased again from late intermoult through intermediate premoult in juveniles. RNA increased continuously during ZI and ZII, and decreased in the megalopa, almost to levels that had been found immediately after hatching. In juveniles, variation in RNA followed closely those in DNA. Cell multiplication (expressed by DNA increase) dominated over increase in cell size (defined by the C/DNA ratio) during the zoeal instars and in postmoult through early intermoult in the megalopa and CI. When specific (C-related) RNA values and RNA/DNA ratios were compared with instantaneous growth rates in C and N, no general correspondence was detected. The only significant relationship between specific RNA values and instantaneous C or N growth rates was found in the megalopa. The same held for the relationship between the RNA/DNA ratio and growth. Here, in addition to the megalopa, a correspondence with C growth was also found in the CI instar. Our results suggest that variation in nucleic acids may provide useful insights into mechanisms of growth on the cellular level (cell multiplication vs cell enlargement). However, lack of general correlation with variation in growth rates ofH. araneus larvae shows that the use of nucleic acids as a measure of growth is probably based upon too simplistic assumptions; it may not yield reliable predictions, when growth is associated with developmental events.     

RNA:DNA ratios and growth of herring (Clupea harengus) larvae reared in mesocosms

Autumn-spawned North Sea herring larvae (Clupea harengus L.) were released in two outdoor mesocosms of 2500 m³ (A) and 4000 m³ (B). The mesocosms were monitored for temperature, salinity, oxygen, chlorophyll a, zooplankton and herring larvae abundance. The density of suitable prey for first feeding larvae (mainly copepod nauplii) was initially low in Mesocosm A (<0.11^-1) compared to in Mesocosm B (>11^-1). Half-way through the experiment the situation was reversed, with higher densities of prey in Mesocosm A (>31^-1) as compared to Mesocosm B (11^-1). The average temperature declined steadily in both mesocosms from 18°C at release to 11–12°C by the end of the experiment 60 d later. The RNA:DNA values of individual herring larvae were related to protein growth rates and temperature adjusted according to Buckley (1984). A corresponding DNA growth index (Gdi) was given as: Gdi=0.68 TEMP+3.05 RNA:DNA-9.92. The RNA:DNA based growth indices were significantly correlated with other somatic growth estimates. The average estimated protein growth rate in the two mesocosms followed the same temporal pattern as the somatic growth rate, but with a lag of 2 d or more. Residual analysis of the regression of ln RNA versus ln DNA also showed the same temporal pattern as the RNA:DNA ratios, but the shift in condition as estimated by this method occurred more in synchrony with the other somatic growth measures. Larvae in Mesocosm A had RNA:DNA values similar to the starvation control kept in the laboratory the first days after release, confirming that larvae in Mesocosm A initially were in poor nutritional condition. On the other hand, the majority of the herring from Mesocosm B were characterised as starving or in poor nutritional condition towards the end of the experiment. The assessment of growth and nutritional condition were in accordance with independent survival estimates which suggested that the majority of the total mortality occurred during the first 15 d in Mesocosm A and there-after in Mesocosm B.     

Using growth band autofluorescence to investigate large-scale variation in growth of the abalone <Emphasis Type="Italic">Haliotis midae</Emphasis>

Growth of the abalone, Haliotis midae, was investigated at Port Alfred, on the south coast of South Africa, using both new and established techniques. A new method for aging animals is described, which makes use of shell autofluorescence under UV light to visualise internal growth bands. The deposition of growth bands was validated using measurements from shells of known age and, at one site, comparing growth estimates to those from cohort analysis undertaken at the same site. The new technique is far less time consuming and labour intensive than previously described methods; it is also non-destructive and proved to have potential for the reliable and rapid assessment of growth in large-scale studies. Growth of H. midae was also investigated at nine other sites, incorporating the full distribution range of the species. Systematic geographic variation in growth was observed along the South African coastline. Statistically significant differences existed among sites in growth rates for animals <4 years and between 4 and 6 years and in the mean maximum sizes attained. Generally, H. midae from the south/southeast coast were found to have faster growth rates, smaller mean maximum sizes and were assumed to attain sexual maturity (determined in previous studies) earlier than those along the southwest/west coast. The geographic differences in estimates of growth observed have significant implications for future modelling approaches and indicate that present national management strategies are not appropriate as they fail to take regional variability into account.     

Chemical composition and growth indices in leptocephalus larvae

 Leptocephali grow at extremely high rates (>1 mm d⁻¹), but, unlike most fish larvae, leptocephali may remain in the plankton as larvae for several months before metamorphosing into the juvenile form. During their planktonic phase, leptocephali accumulate energy reserves in the form of glycosaminoglycans which are then expended along with lipid reserves to fuel metamorphosis. Otolith growth rates were determined using scanning electron microscopy for four species of leptocephali common in the Gulf of Mexico, Paraconger caudilimbatus (Poey, 1867), Ariosoma balearicum (Delaroche, 1809), Gymnothorax saxicola (Jordan and Davis, 1891), and Ophichthus gomesii (Castelnou, 1855). Proximate composition, RNA:DNA ratios and protein growth rates were examined with respect to mass, length and age. The leptocephalus growth strategy was strongly reflected in the growth indices. Mass (Y) in all four species increased with increasing age (X) according to the equation Y = aX ^b , where a is a species-specific constant and 1.05 < b < 2.40. The accumulation of acellular mass was evident in protein growth rates and RNA:DNA ratios, and was observed as a shift in increasing size from rapid growth in length to a greater increase in mass with age. These results suggest that the proportion of actively metabolizing tissue declines with size and is replaced by the metabolically inert energy depot: the glycosaminoglycans. Leptocephali can thus grow to large size very rapidly with minimal metabolic penalty, an unusual and successful developmental strategy. Received: 27 December 1999 / Accepted: 8 June 2000     

Genetically isolated stocks of orange roughy (Hoplostethus atlanticus), but not of hoki (Macruronus novaezelandiae), in the Tasman Sea and Southwest Pacific Ocean around New Zealand

Restriction fragment-length polymorphisms of mitochondrial (mt) DNA, generated by six-base restriction enzymes, were used to examine the stock structure of the two major commercial species in New Zealand fisheries, orange roughy (Hoplostethus atlanticus Collett) and hoki (Macruronus novaezelandiae Hector). Samples of orange roughy from six spawning sites around New Zealand and one site off Tasmania show significant genetic heterogeneity. Samples from two sites around the south of New Zealand were genetically similar to each other, but dissimilar to samples from all other sites. The common haplotype observed in northern sites was absent from the two southern sites. Low numbers of unique haplotypes were restricted to the Challenger Plateau in the Tasman Sea. There was no significant genetic heterogeneity in five samples of hoki from two spawning sites off New Zealand and one site off Tasmania.     

Relationships between nucleic acid concentrations and primary production in the Catalan Sea (Northwestern Mediterranean)

We explored the relationships between classical estimators of autotrophic biomass and primary production, such as chlorophyll a concentration and ¹⁴C-fixation rates, and biochemical indices based on DNA and RNA determinations, which have been proposed as indicators of physiological state in natural plankton populations. The measurements were made during two cruises across the Catalan Front, carried out in May 1989 and February 1990, corresponding respectively, to periods of stratification and moderate mixing. DNA and RNA concentrations (measured by a double-staining fluorimetric technique) were significantly correlated with chlorophyll a in February 1990, but not in May 1989, when a marked deep chlorophyll maximum was present. Significant positive correlations between RNA concentration and primary production and between RNA: DNA and primary production were found during both surveys, probably reflecting both higher RNA concentrations per cell and enhanced bacterial and microheterotrophic growth in high primary production situations. The results support the potential usefulness, in biological oceanography, of biochemical indicators based on DNA and RNA concentrations.     

Regional differences in duration of the planktonic larval stage of reef fishes in the eastern Pacific Ocean

Regional variation in the duration of the planktonic larval phase of three species of reef fishes, Thalassoma lucasanum (Labridae), Stegastes flavilatus, and Microspathodon dorsalis (Pomacentridae) was investigated between 1982 and 1991 at several sites in the tropical eastern Pacific over a distance of 3500 km, encompassing virtually their entire range of distribution. Durations of the larval phase, determined from counts of daily otolith increments, were significantly different (1.3 to 1.6 x) between sites. Populations of all three species had a consistently shorter larval life at the most northern site, Cabo San Lucas (Mexico) compared to Panamá and the offshore islands of Galápagos and Cocos. Analyses of otolith increment width over the precompetent period revealed that this disparity in larval duration primarily reflected differences in larval growth rates: faster growing fish spent less time in the plankton. In T. lucasanum, some of the variation in larval duration between Panamá and offshore sites (Galápagos Islands and Cocos Island) may be accounted for by a higher frequency of individuals delaying metamorphosis at the offshore sites. These data indicate that conditions in the planktonic environment are not homogeneous throughout the tropical eastern Pacific and may have a profound effect on aspects of the larval ecology of reef fishes in this region.     

Zooplankton growth rates: the influence of size and resources in tropical marine copepodites

Growth rates were determined for copepodites of the genera: Acartia, Centropages, Corycaeus, Oithona, Paracalanus, Parvocalanus and Temora in nearshore waters of Jamaica from in situ microcosm incubations. At these high local temperatures (∼28 °C), total copepodite development time was as short as 4 to 5 d. Mean instantaneous growth rates (g) ranged from as high as 1.2 d⁻¹ to as low as 0.1 d⁻¹. In general, cyclopoid copepods appeared to grow more slowly than calanoids of the same size. Enhancement of resources by nutrient addition caused a 32% increase in growth rates in experiments from a mesotrophic site, but only a 17% increase at a more eutrophic site. Additionally, copepodites at both sites showed faster development and generally larger size at stage in response to nutrient addition. Growth rates were positively related to chlorophyll concentration in the >2 μm size-fraction. A significant relationship of growth rate to body size (r ² = 0.45) emerged across a wide range of trophic status, but it was confounded with resource availability. It appears that growth in tropical copepod copepodites may be frequently limited by resources in a size-dependent manner. Received: 30 May 1997 / Accepted: 13 May 1998     

Relationships between growth rate and RNA,DNA, protein and dry weight in Artemia salina and Euchaeta elongata

The concentrations of RNA, DNA and protein, and the dry weight in 3 cultures of the anostracan Artemia salina (L.) were measured to investigate the usefulness of the RNA-growth relationship in estimating growth or productivity. Similar analyses were performed on Copepodid stages III to VI of the calanoid copepod Euchaeta elongata Esterly collected periodically over 7 months in Haro Strait and over 4 months in Saanich Inlet, British Columbia, Canada. It was found that the RNA-growth relationship derived by Sutcliffe (1965) did not agree with that found for A. salina in this study. Also, neither equation accurately predicted growth rates for E. elongata copepodids. It is concluded that the general positive relationship between RNA concentration and growth rate lacks sufficient specificity to be used as a method for predicting growth rates in these species.     

Differential timing of larval starvation effects on filtration rate and growth in juvenile Crepidula onyx

This study demonstrates that the timing of larval starvation did not only determine the larval quality (shell length, lipid content, and RNA:DNA ratio) and the juvenile performance (growth and filtration rates), but also determine how the latent effects of larval starvation were mediated in Crepidula onyx. The juveniles developed from larvae that had experienced starvation in the first two days of larval life had reduced growth and lower filtration rates than those developed from larvae that had not been starved. Lower filtration rates explained the observed latent effects of early larval starvation on reduced juvenile growth. Starvation late in larval life caused a reduction in shell length, lipid content, and RNA:DNA ratio of larvae at metamorphosis; juveniles developed from these larvae performed poorly in terms of growth in shell length and total organic carbon content because of “depletion of energy reserves” at metamorphosis. Results of this study indicate that even exposure to the same kind of larval stress (starvation) for the same period of time (2 days) can cause different juvenile responses through different mechanisms if larvae are exposed to the stress at different stages of the larval life.     

RNA:DNA ratios and growth of herring (Clupea harengus) larvae reared in mesocosms

Autumn-spawned North Sea herring larvae (Clupea harengus L.) were released in two outdoor mesocosms of 2500 m³ (A) and 4000 m³ (B). The mesocosms were monitored for temperature, salinity, oxygen, chlorophyll a, zooplankton and herring larvae abundance. The density of suitable prey for first feeding larvae (mainly copepod nauplii) was initially low in Mesocosm A (<0.11^-1) compared to in Mesocosm B (>11^-1). Half-way through the experiment the situation was reversed, with higher densities of prey in Mesocosm A (>31^-1) as compared to Mesocosm B (～11^-1). The average temperature declined steadily in both mesocosms from 18°C at release to 11–12°C by the end of the experiment 60 d later. The RNA:DNA values of individual herring larvae were related to protein growth rates and temperature adjusted according to Buckley (1984). A corresponding DNA growth index (Gdi) was given as: Gdi=0.68 TEMP+3.05 RNA:DNA-9.92. The RNA:DNA based growth indices were significantly correlated with other somatic growth estimates. The average estimated protein growth rate in the two mesocosms followed the same temporal pattern as the somatic growth rate, but with a lag of 2 d or more. Residual analysis of the regression of ln RNA versus ln DNA also showed the same temporal pattern as the RNA:DNA ratios, but the shift in condition as estimated by this method occurred more in synchrony with the other somatic growth measures. Larvae in Mesocosm A had RNA:DNA values similar to the starvation control kept in the laboratory the first days after release, confirming that larvae in Mesocosm A initially were in poor nutritional condition. On the other hand, the majority of the herring from Mesocosm B were characterised as starving or in poor nutritional condition towards the end of the experiment. The assessment of growth and nutritional condition were in accordance with independent survival estimates which suggested that the majority of the total mortality occurred during the first 15 d in Mesocosm A and there-after in Mesocosm B.