Survival of largemouth bass, bluegill and channel catfish embryos after electroshocking

Survival to hatching was determined after electroshocking embryos of largemouth bass Micropterus salmoides , bluegill Lepomis macrochirus and channel catfish Ictalurus punctatus . Embryos at different developmental stages were exposed for 20 s to homogeneous electric fields (4–16 V cm⁻¹) of direct current (DC) or 60 or 120 Hz pulsed direct current (PDC) in water of 100 μS cm⁻¹ ambient conductivity. For all species, DC reduced survival of embryos at developmental stages before, during, or soon after epiboly; but survival did not differ from controls during later developmental stages. Survival of largemouth bass and bluegill was not reduced by 60 or 120 Hz PDC except for bluegill exposed at 12 h post‐fertilization. Channel catfish embryo survival was <5% when exposed to 60 or 120 Hz PDC at 8 h post‐fertilization, survival improved for embryos exposed at 67 h to 60 Hz but not to 120 Hz, and all embryos survived exposure to PDC at 150 h post‐fertilization. Exposure durations as short as 5 s resulted in <10% survival of largemouth bass during sensitive stages. All bluegill embryos aged 22 h post‐fertilization hatched prematurely after exposure to 16 V cm⁻¹ DC, but survival was not affected. The use of PDC for electroshocking near largemouth bass and bluegill nests could reduce the negative effects on survival of these species; however, PDC can reduce survival of channel catfish embryos.     

Individual variation in the rate of oxygen consumption by zebrafish embryos

A sensitive microsensor‐based method was used to measure oxygen consumption of individual zebrafish Danio rerio embryos at 6 h intervals from 24 to 75 h post‐fertilization. An increase in oxygen consumption rates from 4·54 to 8·29 nmol O₂ h⁻¹ was found during this period. At the individual level the differences in oxygen consumption rates caused the total oxygen consumption from 24 to 75 h post‐fertilization to vary between 0·261 and 0·462 μmol O₂ per individual with a mean of 0·379 μmol O₂ per individual. A separate carbon mass balance study corroborated the mean total oxygen consumption obtained by yielding a respiratory quotient of 0·80 for this period. These results suggest that there is significant intraspecific variation in the metabolic rate of developing zebrafish embryos, which may influence other early life‐history traits such as growth and starvation resistance.     

Survival and behaviour of post‐smolt Atlantic salmon in coastal habitat with extreme tides

The early marine migration of 55 Atlantic salmon post‐smolts tagged with acoustic transmitters was automatically monitored using 13 to 25 km long arrays of receivers deployed inside the Bay of Fundy, a coastal system on the east coast of Canada. The survival of post‐smolts from groups with short‐ and long‐term transmitters in coastal habitat up to 10 km from the river was 92 to 100%, indicating a successful transition to salt water and departure. Migration for 68 to 77% of post‐smolts followed a direct route and it was rapid (transit time usually <12 h). Post‐smolts initially migrated in a south to south‐west direction ( i.e . orientation towards the mouth of the bay) and they were aggregated near the coast. Post‐smolts with long‐term transmitters were monitored 20 km from the river where they continued to be aggregated, moving near the coast through a 'common corridor', and their survival to that point was at least 84%. Post‐smolts from both groups travelled heading out of the coastal system during ebb tides. Flood tides interrupted migration, and they caused changes in travel direction and delays in departure for post‐smolts not leaving by a direct route. Monitoring of coastal habitat inside the Bay of Fundy intercepted 62% of migrating post‐smolts with long‐term transmitters returning after an initial absence of 2 to 22 days. Returning post‐smolts displayed a resident behaviour, using the habitat monitored inside the Bay of Fundy during July and August.     

The development of haddock and Atlantic cod sperm cryopreservation techniques and the effect of sperm age on cryopreservation success

Three cryoprotectants [dimethyl sulphoxide (DMSO), propylene glycol (PG) and glycerol], two diluents (sucrose‐ and saline‐based), two sperm collection times, two freezing rates and three times between thaw and activation (0, 30 and 60 min) were tested in order to develop a protocol for the cryopreservation of sperm of haddock Melanogrammus aeglefinus and Atlantic cod Gadus morhua . The faster freezing rate resulted in extremely low post‐thaw motility in comparison to the slower freezing rate, which was successful for sperm from both gadids. In both cases, the use of PG resulted in significantly higher post‐thaw sperm motility‐recovery indices than with DMSO or glycerol, which did not differ significantly from one another. Diluent had no effect on post‐thaw sperm motility for Atlantic cod or haddock. Sperm collected at the end of the spawning season tended to have reduced post‐thaw motility compared to that collected 2 weeks after the start of spawning. A 30 min delay between thaw and activation of haddock and Atlantic cod sperm resulted in a significant decrease in sperm motility. When PG was used as cryoprotectant, sperm motility continued to decrease between 30 and 60 min post‐thaw. With DMSO or glycerol as cryoprotectant, motilities were already very low after 30 min post‐thaw and did not decrease any further after 60 min. Cryoprotectant, diluent and time between thaw and activation had no effect on mean or maximum sperm swimming speeds for either Atlantic cod or haddock sperm. Fertilization success for haddock eggs, like sperm motility, was higher with PG‐frozen sperm than DMSO‐ or glycerol‐frozen sperm. These results constitute the first reported successful cryopreservation of haddock sperm and improve on previous methods used to cryopreserve sperm from Atlantic cod.     

Reproductive biology of the milk shark Rhizoprionodon acutus and the bigeye houndshark Iago omanensis in the coastal waters of Oman

Female Rhizoprionodon acutus were found to mature between 62 and 74 cm total length ( L _T) whereas males matured between 63 and 71 cm L _T. The L _T at 50% maturity was 64·3 cm for females and 64·7 cm for males. Litter size varied from one to six embryos, and was positively correlated with maternal L _T. Female embryos outnumbered males by a ratio of 2·3:1. The size at birth was c . 37 cm L _T. Full‐term embryos and post‐partum females were observed during all seasons although their occurrence was highest in spring. Spermatozoa were rarely recorded in the oviducal gland, indicating that this species does not store sperm. It was not possible to generate maturity curves for Iago omanensis but it was evident that females matured by the time they reached 35 cm and males were mature by 31 cm L _T. This species displayed a clearly defined reproductive cycle with parturition occurring primarily in spring, after a gestation period of c . 1 year. Maximal embryo size was 19 cm L _T while maximal litter size was 24 embryos. The oviducal gland appeared to act as a seminal receptacle and it appeared that females may utilize these stores by not mating every year.     

The calpastatin/calpain system in trout Salmo trutta trutta muscle

Many recent reports suggest that the calpastatin/calpain system plays a role in cellular growth and differentiation. Defects of the calpastatin/calpain system have been linked to cellular dysfunctions, apoptosis, myocardial infarct, and dystrophies. The calpastatin/calpain system has also been implicated in post‐mortem tenderization of skeletal muscle through degradation of key myofibrillar and associated proteins, a process of key importance to meat quality. In the present study we investigate the presence and activity of the calpastatin/calpain system in trout muscle samples, collected at 0, 3, 18 and 28 h post‐mortem, by immunohistochemistry method. Calpastatin is a specific endogenous enzyme of cytosol, modulating the ubiquitous calpains. Calpastatin was found in samples obtained in vivo and immediately post‐mortem, but its concentration declined rapidly in samples obtained 3, 18 and 28 h post‐mortem. The ubiquitous m e m‐calpains, which are localized on Z line proteins and activated by intracellular Ca²⁺ increase, showed a rapid decline within 3 h post‐mortem. By contrast p94 calpain, which is specific to skeletal muscle, showed a slow decrease post‐mortem which was independent of intracellular Ca²⁺ increase. Our results suggest that the mechanism of activation and activity of the calpastatin/calpain system in trout is similar to that described in mammals.     

Geographical differences in marine feeding of Atlantic salmon post‐smolts in Norwegian fjords

Stomach content analyses were conducted on Atlantic salmon Salmo salar post‐smolt (average size, 119–154 mm fork length, L _F) caught in eight large Norwegian fjord systems along a north–south geographical axis during 1998–2001. In general, post‐smolts from southern Norway showed low feeding intensity in the fjords, whereas extensive feeding was observed in fjords in the northern and middle parts of Norway. The marine diet mainly included different crustaceans and in particular marine pelagic fish larvae (sand-eels Ammodytes spp., herring Clupea harengus and gadoids), but with a substantial spatial and annual variation in prey diversity and feeding intensity. Insects were most frequently taken in the estuary, although fishes often made a large contribution in mass. In contrast, fishes, and to some extent various crustaceans (particularly Hyperiidae, Gammaridae, Euphausiacea and Copepoda) dominated the diet in the middle and outer parts of the fjords, where post‐smolts also fed more extensively than in the inner part. The results indicate that extensive feeding immediately after sea entrance may be more common for post‐smolts in the northern and middle parts of Norway, than in the southern fjords. The observed differences in post‐smolt feeding may be due to spatial and temporal differences in prey availability within and between the different types of fjord systems, and this might influence post‐smolt growth and survival.     

Ontogenetic changes of circulating erythroid cells and haemoglobin components in Esox lucius

Using light microscopy the morphology, the mitotic index and levels of erythroid cell types were detected from 48 h pike Esox lucius embryos before hatching to adult specimens. At the same developmental stages, the haemoglobins and globin chains expressed were electrophoretically characterized. The erythroid cells of the primitive generation were the most abundant from 48 h before hatching until 15–20 days after hatching, then their number decreased and only rare cells remained in the 3 month‐old juvenile specimens. These cells divided and differentiated in the blood and were substituted by the definitive erythrocyte series. As in other vertebrates, the immature cells of the two generations differed in morphological properties and in the synthetized haemoglobin. The circulating erythroid cells of the definitive population cell lineage were, at all differentiation stages, smaller than those of the primitive generation. The definitive erythrocytes appeared in blood smears of 7 days post‐hatching larvae, they increased rapidly and at 20 days they represented the predominant red blood cell population in the circulation of young pike. Electrophoretic analysis of haemolysates obtained from different developmental stages indicated the presence of distinct embryonic, larval and adult haemoglobins. The embryonic haemoglobins differed from those of the older larva and juvenile specimens and were detectable within the first week of post‐hatching development when only primitive erythrocytes were present in the blood.     

Changes in growth performance and proximate composition in Japanese flounder during metamorphosis

Morphological changes are described in Japanese flounder Paralichthys olivaceus larvae and juveniles with emphasis on growth during the period of metamorphosis. Ontogenetic changes in condition factor and lipid, glycogen and protein levels were also analysed to determine the utilization of stored energy. Fish grew from 6·6 to 20·3 mm L _T(1·15 to 84·4 mg in mass, M ) during the period from 11 to 40 days after hatching (DAH) at 19·3° C. Per cent specific growth rate per day (% G day⁻¹) for wet mass was lowest during the metamorphic phase (21–30 DAH) compared to pre‐(11–20 DAH) and post‐metamorphic (31–40 DAH) phases. When L _T and M were expressed as     , the b value was highest during the pre‐metamorphic phase and lowest during the metamorphic phase. These findings indicate that the developmental changes that occur during metamorphosis of Japanese flounder are closely related to the growth pattern. Moisture, lipid and glycogen contents were also at the lowest level during metamorphosis compared to pre‐ and post‐metamorphosis, which suggest that Japanese flounder use their energy reserves to accomplish metamorphosis due to an apparent decline in feeding during this period.     

Effects of temperature and delayed initial feeding on the survival and growth of Japanese flounder larvae

The effects of the timing of initial feeding (0, 1, 2, 3 and 4 days after yolk exhaustion) and temperature (15, 18 and 21° C) on the point‐of‐no‐return (PNR), survival and growth of laboratory‐reared Japanese flounder Paralichthys olivaceus larvae were studied under controlled conditions. The larvae reached PNR on 7·7, 5·2 and 4·2 days‐post‐hatching (dph) at 15, 18 and 21° C, respectively. At each temperature, larval growth did not differ significantly among the delayed initial feedings 1 day before PNR but decreased significantly in larvae first fed after that. In the treatments where initial feeding was equally delayed, larvae grew significantly faster at 18 and 21° C than at 15° C. The larvae survived apparently better at 15 and 18° C than at 21° C when initial feeding was equally delayed. At each temperature, survival of the larvae first fed before PNR did not differ noticeably, while delayed initial feeding after that apparently reduced their survival. These results indicated that there existed a negatively temperature‐dependent PNR in the Japanese flounder larvae. Survival and growth of the larvae strongly depended on temperature as well as the timing of initial feeding. High temperature accelerated the yolk exhaustion and growth of the larvae and thus reduced their starvation tolerance and survival. To avoid potential starvation mortality and obtain good growth, the Japanese flounder larvae must establish successful initial feeding within 2 days after yolk exhaustion at 15° C and within 1 day at both 18 and 21° C.     

Cell death caused by a combination of aluminum and iron in cultured tobacco cells

The inhibition of growth of tobacco cells ( Nicotiana tabacum L. cv. Samsun) after treatment with A1 in medium containing high concentrations of cations requires the presence of Fe (II or III) during the treatment. We examined whether the inhibition of the post‐treatment growth is due to cell death occurring during the treatment with A1 and Fe. In cells at the end of A1 treatment, the integrity of the plasma membrane and the integrity of the mitochondrial inner membrane were monitored by use of Evans blue staining and the cleavage of 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyl tetrazolium bromide (MTT), respectively. Time‐course and dose‐response experiments indicate that the inhibition of post‐treatment growth is strongly related to Evans blue uptake, but not to MTT cleavage. These results suggest that the loss of integrity of the plasma membrane caused by a combination of Al and Fe directly contributes to cell death and the inhibition of post‐treatment growth.     

Quantifying the metabolic cost to an Antarctic liverwort of responding to an abrupt increase in UVB radiation exposure

We quantified the metabolic cost to the Antarctic leafy liverwort Cephaloziella varians of responding to an abrupt increase in ultraviolet B (UVB) radiation exposure in the natural environment at Rothera Point on the western Antarctic Peninsula (67 °34'S, 68 °07'W). The liverwort was protected from exposure to UVB radiation for 44 days with screens containing Mylar polyester, after which time its thalli, which are normally black in colour, had become green owing to reduced concentrations of an anthocyanidin, identified here as riccionidin A, in thallus tips. Thalli were then exposed to an abrupt increase in UVB radiation by removing the screens. The thalli became visibly darker within 48 h of the screens being removed, resynthesizing riccionidin A to the same concentration as that present in thalli outside screens during this period. Chlorophyll fluorescence measurements indicated that nonphotochemical quenching was higher in the thalli formerly under the screens than in those not previously covered with screens, but that F _v/ F _m and photochemical quenching were the same in the two groups of thalli. We used data from aqueous phase oxygen electrode measurements to calculate an estimate for carbon fixation by C. varians during the 48 h after the screens were removed. Assuming a photosynthetic quotient for Antarctic bryophytes of 1, these analyses indicated that the minimum weight of carbon used to synthesize riccionidin A was equivalent to 1.85% of the carbon fixed by thalli during the 48 h after the abrupt increase in UVB radiation exposure.     

Effects of temperature on free‐embryonic diapause in the autumn‐spawning bitterling Acheilognathus rhombeus(Teleostei: Cyprinidae)

In bitterling Acheilognathus rhombeus , developmental arrest always occurred at stage D of the free‐embryonic phase, regardless of incubation temperature. Developmental arrest was terminated only by a cold treatment at 4° C for 60–90 days, initiated 10 days post‐hatching. After the termination of developmental arrest, free‐embryos became larvae c . 6 months after hatching, regardless of the time of initiation and duration of the cold treatment. In hybridization experiments between A. rhombeus and several species of spring‐spawning bitterlings, free‐embryos became free‐swimming larvae within 60 days after hatching in all experiments. Developmental arrest was not observed in any of the hybrids, regardless of parental sex. These results suggest that free‐embryonic diapause in A. rhombeus is not induced by environmental factors, such as cold, but by genetic factors, which are recessive to those in spring‐spawning bitterlings. Free‐embryonic diapause in A. rhombeus appears to be an adaptation to winter, which might have evolved with reproduction in autumn among autumn‐spawning bitterling species. This is the only report of free‐embryonic diapause after hatching in fishes, and only the second example of diapause in fishes, along with annual killifishes (Rivulidae).     

Differential responses to UVR by bacterioplankton and phytoplankton from the surface and the base of the mixed layer

SUMMARY 1. We tested the influence of ultraviolet radiation (UVR) and shallow stratification on phytoplankton and bacterioplankton from the surface and the base of the mixed layer in two boreal lakes in north-western Ontario, Canada.
2. We measured phytoplankton biomass and production, bacterioplankton production and plankton respiration after transplantation under three solar radiation treatments: ambient radiation (Photosynthetically active radiation (PAR) + ultraviolet-A (UVA) + ultraviolet-B (UVB)), minus UVB (PAR + UVA) and PAR only. We repeated this experiment on three occasions in each lake during the summer.
3. Solar stress (measured as reduced growth and photoinhibition) was generally only found in the 'base phytoplankton' (i.e. originating from the base of the mixed layer). No inhibition of photosynthesis by UVB exposure was found in near-surface phytoplankton. On the other hand, production of near-surface bacterioplankton was reduced following a 4-h UVR exposure but had increased after a 48-h exposure to both UVA and UVB compared with the PAR only treatment.
4. Negative effects of UVR on phytoplankton and bacterioplankton were not ubiquitous. We emphasise the importance of conducting experiments repeatedly, particularly those which test the effects of UVR on different community assemblages from different lakes.     

Early development of the head skeleton in Brycon moorei(Pisces, Ostariophysi, Characidae)

At hatching (15 h post fertilization), Brycon moorei possesses no skeletal structure. Thereafter, development is very rapid. The first oral teeth appear no later than 3 h post‐hatching, but they remain covered with epithelium until c . 45 h. At 7 h, the trabecular bars and part of the cartilaginous visceral arches are visible and at 15 h, the dentaries and premaxillaries are present. At 25 h, i.e . the onset of piscivory and cannibalism (the yolk sac is only fully resorbed after 36 h), the oral teeth are fully developed, the first pharyngeal teeth are formed, and some head movements already appear synchronized, but the mouth cavity is not completely isolated from the neurocranium by bony structures. Thereafter, no new buccal or pharyngeal bony structure is visible until 45 h, when the maxilla and opercula appear, along with a new type of cannibalistic behaviour. Cartilage resorptions also start at 45 h, but with no concomitant replacement by formation of calcified structures. Later, development gradually becomes similar to that of many previously studied teleosts. The developmental pattern of B. moorei is thus extremely rapid in comparison with other teleosts, i.e . it prioritizes feeding structures that permit the expression of piscivory at a very early age. The uniqueness of this pattern is discussed in relation to ecological constraints on early feeding and fast growth.     

Effects of handling and electrofishing on plasma glucose and whole blood lactate of Leuciscus cephalus

Chub Leuciscus cephalus exposed to simulated pulsed direct current electrofishing operations exhibited rapid elevations in plasma glucose and blood lactate levels. Plasma glucose levels were significantly higher 0·5 h after simulated electrofishing operations, and peaked 2 h after treatment. Glucose levels remained high for up to 4 h. No changes in plasma glucose were evident following handling. Simulated electrofishing operations and handling induced an immediate lactacidosis in chub. Initial responses to both treatments were similar except that blood lactate was significantly higher in fish exposed to simulated electrofishing operations than in handled fish 5 and 15 min after treatment. Blood lactate remained elevated in fish exposed to simulated electrofishing operations for 2 h, while blood lactate of handled fish returned to levels similar to those in the control fish within 0·5 h post‐treatment.     

Is rigor mortis the cause of post‐mortem shrinkage in juvenile Pagrus auratus?

An experiment demonstrated that post‐mortem shrinkage in fork length of juvenile pink snapper Pagrus auratus (179–262 mm) was the same in fish in which rigor mortis was surgically inhibited, as in intact fish, and averaged 5·5 ± 0·2 mm (mean ±  s.e ., range 2–9 mm) after 168 h.     

Diel activity patterns of juvenile Atlantic salmon in rivers with summer water temperature near the temperature‐dependent suppression of diurnal activity

Direct day and night underwater observations of juvenile Atlantic salmon Salmo salar during summer and autumn showed a duality in response to temperature between 7 and 11° C for young‐of‐the‐year (YOY) Atlantic salmon. They were predominantly diurnal in early summer and nocturnal in late summer although water temperatures were similar. Post‐YOY Atlantic salmon did not show a strong response to temperature as they were mostly nocturnal during the study period. It is suggested that the difference in activity patterns between YOY and post‐YOY Atlantic salmon can be explained by size‐dependent trade‐off between growth and predation risk.     

Does light intensity affect self‐feeding and food wastage in group‐held rainbow trout and white‐spotted charr?

The self‐feeding rhythms of rainbow trout Oncorhynchus mykiss and white‐spotted charr Salvelinus leucomaenis were studied when group‐held fishes ( n  = 10 per group) were fed using self‐feeders under two different light intensities (50 lx, 16 μW cm⁻² and 700 lx, 215 μW cm⁻²) during the light phase of the light‐dark cycle. Food wastage was also measured. At 50 lx, all groups of rainbow trout learned to operate the self‐feeder within 4 days, whereas it took up to 25 days for all groups at 700 lx. In contrast, all groups of white‐spotted charr learned self‐feeding within 17 days, irrespective of light intensity. These results, although non‐significant, suggest that lower light intensities can stimulate instrumental learning in rainbow trout, but not white‐spotted charr. In rainbow trout, the total number of trigger actuations for the entire experimental period was significantly higher at 50 rather than 700 lx, although this may have been related to delayed learning at 700 lx. There was no significant effect in white‐spotted charr. Growth rate (assessed using the thermal growth coefficient) was also higher in rainbow trout but not white‐spotted charr at 50 rather than 700 lx, although this difference was non‐significant. Light intensity had no significant effect on food wastage in either rainbow trout or white‐spotted charr, and it did not appear to affect the proportion of trigger actuations during the light phase. Clear diurnal feeding rhythms were observed in both species and these were classified into four categories: uniform, dawn, dusk and crepuscular. At 50 lx, fish from both species generally fed in temporally localized periods at either dawn and dusk, whilst feeding was predominantly uniform during the light phase at 700 lx.