Effects of environmental factors on survival, growth, and production of American shad larvae

Episodic increases in temperature of 5°C above 20° C, over 48 h or declines in pH of 1·0 unit from pH 7·0 reduced survival of yolk-sac and feeding-stage larvae of American shad Alosa sapidissima . Over 16 days all measures of survival, growth, and production were more favourable at each higher temperature in the 15–25° C range. More favourable responses were also obtained at the higher prey level (500 v . 50 Artemia nauplii l^-1) and at the higher pH (7·5 v . 6·5). Combinations of high temperature and high prey levels, at pH 7·5, led to highest larval production. Little growth or production occurred at 15° C, regardless of pH or prey level. The effect of pH was strong with respect to survival, but weak with respect to growth. In attempts to restore American shad populations by larval stocking, release times and sites can be critical to optimize survival and eventual returns. Releases of larvae potentially will be most effective when made at temperatures >20° C, pH>7·0, and prey levels >50 1^-1. These conditions are most likely to occur in Maryland tributaries of Chesapeake Bay between mid-May and early June.     

Behaviour, growth and survival of redfish larvae in relation to prey availability

Growth, survival and condition of redfish larvae Sebastes spp., reared in the laboratory (0, 500 1500 and 4500 prey l^-1) were highest in the 1500 prey l^-1 treatment. Significantly lower larval growth and survival in the 4500 prey l^-1 treatment corresponded with lower prey bite: orient ratios in later weeks, suggesting that larvae were unable to forage efficiently at high prey densities. While these prey densities are higher than those reported in the field, naturally co-occurring Atlantic cod Gadus morhua larvae require higher prey densities when reared under similar conditions in the laboratory. These data suggest that prey availability may not be as limiting to redfish as for other commercially important marine species.     

Growth response of pikeperch larvae in relation to body size and zooplankton abundance

The most critical period at onset of feeding in pikeperch Stizostedion lucioperca is short (<5 days at 20° C). The larvae are sensitive to prey density during the first week of exogenous feeding. First-feeding larvae of 6.5 mm total length ( L_T ) needed prey densities of >585 prey l⁻¹ to maintain mass (C_maint), whereas 5 days older larvae of 7 mm L _T C_maint= 55 prey l⁻¹ and for 11 mm L _T larvae C_maint<10 prey 1⁻¹. Changes in specific growth rates for larvae of 7 and 11 mm were similar to a type-II functional response curve reaching a specific growth rate of 26 and 30% day⁻¹, respectively, at 1000 prey l⁻¹, whereas the 6·5 mm larvae showed a linear growth response reaching a specific growth rate of only 9% day ⁻¹ at 1000 prey l⁻¹. The results suggest that prey density is a limiting factor, which might contribute to the high variation between year-class Strengths.     

Nucleic acid contents and growth of first-feeding walleye pollock larvae in response to prey densities typical of sub-Arctic ecosystems

The growth, nucleic acid and protein contents of walleye pollock Theragra chalcogramma larvae reared at prey densities of 10, 30, 50, and 500 prey 1^-1 were measured for the first 9 days after the feeding initiation at 6° C. Incremental growth rates of larvae (mm day^-1) were low and variable for the first 7 days after feeding initiation. Growth rates and rates of RNA, DNA, and protein accumulation by larvae reared at 500 prey 1^-1 were positive while those of larvae reared at the lower prey levels did not differ significantly from zero. The RNA/DNA ratio was variable and exhibited no significant trend among food treatments. Estimates of instantaneous protein growth rates ranged from - 6·7 to 13·2% day^-1 at food densities of 10 and 500 prey 1^-1, respectively, and were moderately correlated with larval RNA/DNA ratios ( r = 0·628). The results suggest that in situ protein growth rates of first-feeding pollock larvae may be influenced by prey fields within the range of ambient food densities reported for sub-Arctic ecosystems.     

Effects of egg composition and prey density on the larval growth and survival of lake whitefish (Coregonus clupeaformis Mitchill)

Eggs were collected from two stocks of lake whitefish, Coregonus clupeaformis , in Lakes Michigan and Huron to assess the effect of egg composition and prey density on larval growth and survival. Egg composition parameters including wet weight (mg egg⁻¹), dry weight (mg egg⁻¹), percent water, total caloric content (cal egg⁻¹), caloric density (cal egg⁻¹), percent lipid content, and total lipidcontent (mg egg⁻¹) were measured. Fish hatched from six parental females in each stock were fed one of four rations (0, 18, 24, 50 brine shrimp larva⁻¹ day⁻¹) after yolk sac absorption. Length at hatch, endogenous growth, exogenous growth, and survival were measured during a 42-day laboratory experiment. Length at hatch of larvae was positively related to egg caloric content ( r ²=0.780). Endogenous growth for lake whitefish larvae was positively related to percent lipid content ( r ²=0.896) and total egg lipid content ( r ²=0.876) of parental females. Exogenous growth and survival of larval lake whitefish was positively related to prey availability. Larval fish growth was accurately modelled ( r ²=0.973) as a function of prey abundance using a threshold-corrected hyperbolic equation. These results indicate that both egg composition and prey availability have the potential to influence the growth and survival dynamics of larval lake whitefish significantly.     

Bile salt-dependent lipase in larval turbot, as influenced by density and lipid content of fed prey

Turbot larvae were fed three different densities of rotifers (1000, 3000 and 7500 rotifers 1⁻¹) with a low lipid level (< 15% of dry weight) or 7500 rotifers 1⁻¹ with a high lipid level (∼30% of dry weight). The larval consumption of rotifers increased with increasing prey densities and the content of bile salt-dependent lipase (BSDL) in larvae was correlated positively with the ingestion rate from days 6 to 8. This suggests that BSDL synthesis was stimulated by the amount of ingested prey in the early larval phase. However, growth was highest in larvae receiving the medium prey densities, which indicates that the larvae were not able to digest properly the ingested prey at the higher density. No significant effect on the BSDL content was seen in turbot larvae fed rotifers with a high or low lipid content.     

Nutritional condition and vertical distribution of Baltic cod larvae

Newly hatched Baltic cod Gadus morhua larvae are typically found at depths >60 m. This is a region of low light and prey availability, hence generating the hypothesis that larvae have to migrate from hatching depth to the surface layer to avoid starvation and improve their nutritional condition. To test this hypothesis, Baltic cod larvae were sampled during the spawning seasons of 1994 and 1995 with depth-resolving multiple opening/closing nets. Each larva was aged by otolith readings and its RNA/DNA ratio was determined as a measure of nutritional condition. The RNA/DNA ratios of these larvae aged 2-25 days (median 10 days) ranged from 0.4 to 6.2, corresponding to levels exhibited by starving and fast-growing larvae in laboratory calibration studies (starvation, protein growth rate, G_pi= -12.2% day⁻¹; fastgrowing larvae, G_pi=14.1%day⁻¹) respectively. Seventy per cent of the field caught larvae had RNA/DNA ratios between the mean values found for starving and fed laboratory larvae. Only larvae aged 8-11 days had higher mean RNA/DNA ratios above 45 m than below ( t -test, P<0.05). However, the instantaneous protein growth rates were significantly higher for all larval age groups in the surface layers ( t -test, P<0.05). Starving larvae were found in all depths sampled (10-85 m), whereas growing larvae (positive G_pi) were restricted to samples taken shallower than 45 m. These superior growth rates above 45 m corroborate the hypothesis and imply that migration to the shallow water layers is a prerequisite for good nutritional condition, growth and survival of Baltic cod larvae. The frequent occurrence of cod larvae older than 8 days in the deep water in poor condition suggests that a proportion of the larvae will die from Starvation in the deep layers of the Baltic Sea.     

Growth and physiological changes during metamorphosis of Senegal sole reared in the laboratory

The metamorphosis of Solea senegalensis was studied in larvae reared at 20° C and fed four different feeding regimes. A, Artemia (4 nauplii ml⁻¹); B, Artemia (2 nauplii ml⁻¹); C, mixed diet (2 nauplii ml⁻¹ and 3 mg ml⁻¹ microencapsulated diet); and D, microencapsulated diet (3·7 mg ml⁻¹). Rotifers were also supplied in all cases during the first days of feeding. These feeding regimes supported different growth rates during the pre-metamorphosis period (regime A, G=0·376 day⁻¹; regime B, G=0·253 day⁻¹; regime C, G=0·254 day⁻¹; regime D, G=0·162 day⁻¹). Larvae started metamorphosis 9 days after hatching (DAH) when fed the regime A, 13 DAH with regime B, 11 DAH with regime C and 15 DAH with regime D. A minimum 5·6–5·9 mm L_T was required under all feeding regimes to initiate the metamorphosis. Eye translocation was completed when the larvae reached 8·6–8·7 mm L_T (regimes A, B and C), but only 7·3 mm L_T with regime D. 4·4–6·2 days were required to complete eye migration under the regimes A, B and C, and 18·3 days under the regime D. This transformation is concomitant with changes in body reserves, and with the pattern of some digestive enzymes.     

The effect of light intensity and spectrum on the incidence of first feeding by larval haddock

Under full–spectrum white light, feeding success of haddock Melanogrammus aeglefinus first feeding larvae, as measured both by proportion of larvae feeding and mean prey consumed, peaked at 1·7-18 μmol s^-1 m^-2. Feeding was significantly reduced at lower and higher intensities. A similar result was observed for larvae feeding under blue (470 nm) light, with significantly greater feeding success at intermediate light intensity (1·8 μmol s^-1 m^-2). When different light qualities were compared, larvae had significantly greater feeding success when exposed to blue (470 nm) light than either full-spectrum white or green (530 nm) light. Haddock larvae were capable of prey capture under all light treatments tested, indicating a necessary degree of adaptive flexibility in feeding response. The results are consistent with predisposition of haddock larvae to optimal feeding in a visual environment comparable with open ocean nursery grounds. Information on the impact of light on haddock first feeding can be incorporated into models of larval growth, survival, year-class strength and recruitment, and assist in developing husbandry protocols to maximize larval survival in aquaculture.     

Particulate and filter feeding in threadfin shad, Dorosoma petenense, at different light intensities

Previous workers inferred from stomach analyses that threadfin shad ( Dorosoma petenense ) ate plankton by both filter and particulate feeding. These inferences were confirmed in this study by laboratory experiments in which both types of feeding were observed. Threadfin shad consumed relatively small food particles (≤ 0.39 mm) by filtration, while larger prey (7.5 mm) were eaten individually. The shad were able to filter feed on small foods (brine shrimp nauplii and phytoplankton) at all light intensities from 0 to 9 × 10¹ fL. These data indicate that under natural conditions shad can filter feed at any time of the 24 h period if food conditions are sufficient to trigger feeding. Filter feeding is probably induced by chemoreception rather than vision. The particulate feeding rate decreased as light intensity decreased, reaching a minimum between 9 × 10⁻⁴ and 9 × 10⁻⁵ fL. From these data it is inferred that particulate feeding is a visual process in this species, requiring intensities equivalent to bright moonlight or greater. Filter and particulate feeding abilities allow threadfin shad to consume most of the different types of plankton and to change their diet with seasonal changes in the composition of the plankton.     

The effect of starvation on RNA: DNA ratios and growth of larval striped bass, Morone saxatalis

Hatchery reared larval striped bass, Morone saxatilis , 8-days-post-hatching were subjected to various feeding/starvation regimes over a period of 14 days.
Batches of larvae from each treatment were sampled over the 14-day period and subdivided for determination of notochord length and RNA:DNA ratio. The best growth was found in fully fed F1000 larvae (exposed to 1000 Artermia nauplii l⁻¹), which reached 8.2 mm after 11 days and 9.6 mm after 14 days. Starved animals after 11 days had notochord lengths of 4.9 mm. Growth curves from feeding-delayed larvae indicated that animals fed after up to 5 days starvation were capable of complete recovery. F100 larvae (exposed to 100 Anemia nauplii 1^−l) had a slower growth rate than F1000 larvae, reaching a notochord length of 7.3 mm after 14 days. RNA:DNA ratios over time closely followed notochord growth curves, with clear differences between starved, F100 and F1000 larvae being established after only 2 days. Equilibrium RNA:DNA ratios of 3.0 and 2.25 were established in F1000 and F100 larvae, respectively, 6.8 days after the beginning of the experiment. The average lag time between a change from the starved to the fed condition and a change in RNA:DNA ratio as determined by the divergence of the nucleic acid curve from the starved condition was 0.66 days.
In treatments where starvation followed various periods of feeding, larvae regressed in notochord length such that the final length at 14 days reflected the degree of feeding. RNA:DNA ratios in these animals again closely followed growth curves with a lag time of 0.81 days.
It was concluded that RNA:DNA ratios provided very accurate indices of growth in striped bass larvae which were highly sensitive to feeding status.     

Effects of varying irradiance on feeding in larval weakfish (Cynoscion regalis)

Weakfish larvae, Cynoscion regalis (Bloch and Schneider), were used in laboratory experiments, during May and June 1991–1993, to examine the effects of varying irradiance levels on capture and ingestion of Zooplankton prey (rotifers). Treatments consisted of six different irradiance levels: no light, 5, 11, 15, 20, and 500 × 10¹² quanta·cm⁻²·s⁻¹. These levels are typical of the irradiance range found in a 10-m water column during the late-spring, weakfish spawning season in Delaware Bay. Early-stage larvae (8 days post-hatching) did not feed in total darkness, and there was no difference in the incidence of feeding among the other treatment groups. Similarly, late-stage larvae (13 days post-hatching) showed no significant difference between the incidence of feeding in darkness and at 5 × 10¹² quanta·cm⁻² s⁻¹, though feeding within these two intensities was significantly lower than feeding in the other light levels. Results of a subsequent experiment indicated that the ability to feed in total darkness may depend on the abundance of available prey. Scanning electron microscope analysis of preserved weakfish larvae showed that neuromasts were not fully developed until larvae had reached at least 12 days post-hatching, and that younger larvae had only lateral line pores along the body trunk. There were no neuromasts evident on the head region, regardless of age. Thus, neuromasts may be involved in the capture of prey in darkness.     

Growth and survival of tench larvae fed under different feeding strategies

Two feeding experiments were conducted to evaluate the growth and survival rates of tench Tinca tinca L. larvae when initially fed with a combination of three different brands of Artemia nauplii under two conditions: (A) in the laboratory and (B) on a commercial farm. At the same time, a protozoan culture of the freshwater ciliate Colpoda cucullus was additionally tested in one of the experiments to possibly enhance the initial hunting behaviour of the larvae. The larvae were fed every 4 h from the onset of exogenous feeding up to 14 days of age. Three types of commercial Artemia products, mainly differing in size and high unsaturated fatty acid (HUFA) content, were used. One group was fed with C. cucullus as a starter. The different combinations of Artemia nauplii were used to evaluate possible effects on larval growth. The final growth at 26.3 °C, expressed in length and weight, did not show significant differences, suggesting the use of the most economically feasible Artemia strain studied. The experiments confirmed that using smaller prey during the first 2 days of feeding increases their survival rate, although the mean final survival rate was high (89%). In the experiment carried out at the commercial fish farm facilities, experimental groups were also fed with Artemia nauplii, using the EG type either enriched or not enriched with HUFA. Again, one of the groups was offered the ciliate C. cucullus as initial feed. Final growth showed significant differences when using Colpoda culture as a starter feed, although this test resulted in the lowest survival rate (69%), indicating that further studies on the management of its culture should be undertaken to improve the applicability of the technique. The mean final survival rate was 83%.     

Circadian rhythms in juvenile american shad, Alosa sapidissima

Swimming activity (in cm s⁻¹) of a school (55 individuals) of young-of-the-year ( total length=110 mm) American shad, Alosa sapidissima , was determined under a variety of photoperiod conditions. These included a normal (ambient), a shifted, and constant-light day. Swimming activity was measured over 4-day periods. During normal days swimming speeds followed periods of about 24 h, with fast speeds (up to 45 cm s⁻¹) and schooling occurring during the photoperiod. Under dark conditions speeds were slower (8 cm s⁻¹) with most fish swimming as individuals. During a shifted day swimming speeds and schooling corresponded to the imposed day. Under constant light (equivalent to bright moonlight) no schooling was evident, and a constant, but slow, swimming speed was observed in each 24-h period. These shad demonstrated an exogenous rhythm with respect to the imposed day length. It is hypothesized that an endogenous circadian rhythm would only be of use to a fish required to hunt or chase its prey. Shad, being plankton feeders, do not chase prey and therefore can exhibit an exogenous circadian rhythm with no detrimental feeding results.     

Hatching time and growth of Nemurellapictetii (Plecoptera: Nemouridae) in the laboratory and a Lake District stream

SUMMARY. 1. Nemurella pictetii Klapæplek took 2 years to complete its life cycle in both the laboratory and a small stream in the English Lake District.
2. Hatching time (days after oviposition for 10%. 50% and 90% of the eggs to hatch) and hatching period (days between dates for 10% and 90% hatched) decreased with increasing water temperature in the laboratory, and the relationships were well described by a power-law. Estimates of the mean time for 50% hatching in the stream varied between 16 and 31 days after oviposition. depending on temperature.
3. Larval instars numbered fifteen for males and seventeen for females with a constant ratio of 1.18 between successive instars (conformed with Dyar's rule). Larval growth was exponential at four constant temperatures in the laboratory; mean instantaneous growth rates were 0.40±0.01% day⁻¹ at 5.9°C, 0.43±0.01% day⁻¹ at 8.2°C, 0.46±0.01% day⁻¹ at 12. 1°C. 0.56±0.02%day⁻¹ at 19.8°C. No larvae survived after instar XI at 19.8°C.
4. Larval growth was exponential in the stream and was scarcely affected by variations in water temperature (range 4.2 -14.0°C); mean growth rates for three year-classes were 0.41±0.02, 0.43±0.08, 0.54±0.05% day⁻¹. Their similarity to laboratory growth rates under optimum conditions suggests that the availability of resources, such as food and space, was not restricting growth in the stream.     

Critical involvement of dietary docosahexaenoic acid in the ontogeny of schooling behaviour in the yellowtail

To investigate involvement of the central nervous system in the ontogeny of behaviour, diets of differing quality were used to rear yellowtail Seriola quinqueradiata larvae and juveniles. Artemia nauplii enriched with oleic acid (OA), eicosapentaenoic acid (EPA), or two different concentration levels of docosahexaenoic acid (DHA) were fed to yellowtail larvae (L^T 7 mm; 13 days old) for 12 days, and their behavioural development was analysed together with growth, survival, activity and fatty acid composition. Yellowtail fed with DHA–enriched Artemia showed mutual attraction behaviour at 11 mm L^T, while those fed with OA– or EPA–enriched Artemia did not show this behaviour at the same size. While fish in the OA group showed poor growth, survival and activity index, fish in the EPA group were similar to the two DHA groups. In addition, most fish tested, including the OA group, showed clear optokinetic responses. Fatty acid composition of the diet was reflected in that of the fish body. Therefore, dietary DHA in the larval stage is considered to be essential for the development of schooling behaviour in the yellowtail.     

Assessment of rapid bioassays for detecting cyanobacterial toxicity

Simple and easy-to-use bioassays with Artemia salina (brine shrimp) larvae, luminescent bacteria and Pseudomonas putida were evaluated for the detection of toxicity due to cyanobacterial hepato-and neurotoxins. The hepatotoxins and a neurotoxin, anatoxin-a, were extracted from laboratory-grown cultures and natural bloom samples by the solid phase fractionation method and dissolved in diluent for different bioassays. The toxin concentration of cyanobacterial extracts was determined with HPLC. The Artemia biotest appeared to be quite sensitive to cyanobacterial hepatotoxins, with LC 50 values of 3–17 mg l^-1. The Artemia test was also shown to be of value for the detection of toxicity caused by anatoxin-a. The fractionated extract of anatoxin-a was not lethal to Artemia but it disturbed the ability of the larvae to move forwards. Filtered cyanobacterial cultures with anatoxin-a, on the other hand, caused mortality of Artemia larvae at concentrations of 2–14 mg l^-1. With the solid phase fractionation of cyanobacterial samples, no non-specific toxicity due to compounds other than hepato- and neurotoxins was observed. In the luminescent bacteria test, the inhibition of luminescence did not correlate with the abundance of hepatotoxins or anatoxin-a. The growth of Ps. putida was enhanced, rather than inhibited by cyanobacterial toxin fractions.     

Colonization of Vibrio pelagius and Aeromonas caviae in early developing turbot (Scophthalmus maximus L.) larvae

Polyclonal antisera made in rabbits against whole washed cells of Vibrio pelagius and Aeromonas caviae were used for detection of these bacterial species in the rearing water and gastrointestinal tract of healthy turbot ( Scophthalmus maximus ) larvae exposed to V. pelagius and/or Aer. caviae . The results demonstrated that this method is suitable for detection of V. pelagius and Aer. caviae in water samples and larvae at population levels higher than 10³ ml⁻¹ and 10³ larva⁻¹. Populations of aerobic heterotrophic bacteria present in the gastrointestinal tract of turbot larvae, estimated using the dilution plate technique, increased from approximately 4 × 10² bacteria larva⁻¹ on day 3 post-hatching to approximately 10⁵ bacteria fish⁻¹ 16 days post-hatching. Sixteen days after hatching, Vibrio spp. accounted for approximately 3 × 10⁴ cfu larva⁻¹ exposed to V. pelagius on days 2, 5 and 8 post-hatching. However, only 10³ of the Vibrio spp. belonged to V. pelagius . When larvae were exposed to Aer. caviae on day 2 post-hatching, the gut microbiota of 5-day old larvae was mainly colonized by Aeromonas spp. (10⁴ larva⁻¹), of which 9 × 10³ belonged to Aer. caviae . Later in the experiment, at the time when high mortality occurred, 9 × 10⁵ Aer. caviae were detected. Introduction of V. pelagius to the rearing water seemed to improve larval survival compared with fish exposed to Aer. caviae and with the control group. It was therefore concluded that it is beneficial with regard to larval survival to introduce bacteria ( V. pelagius ) to the rearing water.     

Toxic effects of zinc on fathead minnows Pimephales promelas in soft water

A fathead minnow life-cycle exposure to various zinc concentrations demonstrated that the most sensitive indicators of zinc toxicity were egg adhesiveness and fragility, which were significantly affected at 145 μg Zn 1⁻¹ and above, but were not affected at 78 μg Zn 1⁻¹ and below. These effects occurred shortly after the eggs were spawned (during water hardening) and therefore were not related to effects on the parental fish. Hatchability and survival of larvae were significantly reduced, and deformities at hatching were significantly increased at 295 ug Zn 1⁻¹ and above. Acclimated and unacclimated groups of larvae exposed to identical zinc concentrations for 8 weeks after hatch showed only slight differences in sensitivity.     

Growth and Grazing Rates of the Marine Planktonic Ciliate Strombidinopsis sp. on Red-Tide and Toxic Dinoflagellates

ABSTRACT We investigated growth and grazing rates of Strombidinopsis sp. when feeding on several species of red-tide and/or toxic dinoflagellates. Strombidinopsis sp. one of the largest aloricate choreotrichs so far reported, grew well on Lingulodinium polyedrum, Gymnodinium sanguineum, Scrippsiella trochoidea, Cochlodinium polykrikoides , and Prorocentrum minimum , but failed to grow on Amphidinium carterae. Specific growth rates of Strombidinopsis sp. increased rapidly with increasing prey density up to ca. 100 ng C ml^-1, but were saturated or increased slightly at higher concentrations. Maximum specific growth rates of Strombidinopsis sp. on various prey species were 1.38 day^-1 for C. polykrikoides , 1.27 for G. sanguineum , 1.06 for P. minimum , 0.83 for L. polyedrum , and 0.67 for S. trochoidea. Threshold prey concentrations (where net growth = 0) were 12–38 ng C ml^-1. Maximum ingestion and clearance rates of Strombidinopsis sp. were 353 ng C grazer^-1 day^-1 and 110 μ, l grazer^-1 h^-1, respectively. Strombidinopsis sp. exhibited higher maximum growth, ingestion, and clearance rates than the mixotrophic dinoflagellate Fragilidium cf. mexicanum or the heterotrophic dinoflagellates Protoperidinium cf. divergens and P. crassipes , when grown on the same prey species. In addition, the sequence of prey species arranged according to growth response of Strombidinopsis sp. differed considerably from those of Fragilidium cf. mexicanum, Protoperidinium cf. divergens , and P. crassipes.