A field and experimental evaluation of the effect of data storage tags on the growth of cod

The effect of electronic data storage tags (DSTs) on the growth of cod Gadus morhua was evaluated in laboratory and field experiments. In the first laboratory experiment, large DSTs (60 × 18 mm, 3 g in water ) attached externally for 3 months did not have any effect ( anova , P  > 0·05) on the growth of adult cod (mean ±  s . d . 65 ± 4·5 cm total length) relative to untagged adult cod. In a second experiment, small DSTs (34 × 11 mm, 1·5 g in water) implanted into young cod (48·1 ± 4·4 cm) for an 8 month period did not have any effect upon the growth relative to untagged controls ( anova , P  > 0·05). Length data returned from tagging experiments conducted on adult cod (57·3 ± 7·5 cm) in the North Sea showed that the growth of fish tagged either externally or internally with large DSTs was not different ( t ‐test, P  > 0·05). Attachment wounds, however, provided evidence that external attachment of DSTs should be avoided unless sensor configuration requires access to the external environment, and that internal implantation should be preferred whenever possible.     

Ontogenetic changes in temperature preference of Atlantic cod

Final thermal preferendum ( T ) experiments were conducted in a horizontal thermal gradient tank from the beginning of August 2001 to mid‐November 2001 using Atlantic cod Gadus morhua from 6·5 to 79·0 cm fork length ( L _F). The value of T varied significantly ( P  < 0·005) with L _F( T  = 7·23–0·054 L _F), with smaller (younger) fish choosing higher temperatures than larger (older) fish. The preferendum varied from 6·9° C for fish of 6·5 cm to 3·0° C for those of 79·0 cm. Experiments comparing fish positions in the gradient tank between thermal gradients of 0·5–11·0 and 4·5–14·5° C demonstrated that fish positions were determined by temperature selection instead of undesirable tank effects. This study is the first to demonstrate the effect of ontogeny on temperature preferences of a marine fish species.     

Endurance swimming of diploid and triploid Atlantic salmon

When groups of diploid (mean ±  s . e . fork length, L _F) 33·0 ± 1·4 cm and triploid (35·3 ± 0·5 cm) Atlantic salmon Salmo salar were forced to swim at controlled speeds in a carefully monitored 10 m diameter 'annular' tank no significant difference was found between the maximum sustained swimming speeds ( U _ms, maintainable for 200 min) where the fish swam at the limit of their aerobic capability. Diploids achieved 2·99 body lengths per second (bl s⁻¹)(0·96 m s⁻¹) and triploids sustained 2·91 bl s⁻¹(1·02 m s⁻¹). The selection of fish for the trials was based on their ability to swim with a moving pattern projected from a gantry rotating at the radius of the tank and the selection procedure did not prove to be significant by ploidy. A significant difference was found between the anaerobic capabilities of the fish measured as endurance times at their prolonged swimming speeds. During the course of the experimentation the voluntary swimming speed selected by the fish increased and the schooling behaviour improved. The effect of the curvature of the tank on the fish speeds was calculated (removing the curved effect of the tank increased the speed in either ploidy by 5·5%). Implications of the endurance times and speeds are discussed with reference to the aquaculture of triploid Atlantic salmon.     

我国硅藻类的新记录属--微舟藻属及其一新种

利用透射电镜对采自东黄海海域典型站位的微型硅藻(nanodiatom,〈20μm)进行了研究.观察到我国微型硅藻类的一个新记录属:微舟藻属Nanoneis R.E.Norris以及该属的一个新种:长微舟藻Nanoneislongta sp.nov..该属的主要特征是:壳面两侧对称,具有不完全壳缝,壳面除中轴区外都有横肋纹或长室孔分布.本文描述该属的两个种,其中海斯微舟藻(Nanoneis hasleae R.E.Norris)为我国的新记录种,长微舟藻为新种,两种之间主要的区别特征是壳面外形、长宽比例以及壳面横肋纹的密度.并较详细地描述了该属种类的分类特征、生态习性和分布.     

Do Norwegian Atlantic salmon feed in the northern Barents Sea? Tag recoveries from 70 to 78° N

Three tagged Atlantic salmon Salmo salar were recaptured as subadults or adults (1·4–3 kg) between 70·5 and 78° N in the western Barents Sea, two of which originated from the Alta Fjord region in northern Norway and one from the Drammen River, south-eastern Norway. An additional tag was recovered from the stomach of a Greenland halibut Reinhardtius hippoglossoides captured south-west of Bear Island at >600 m depth; this tag was from a smolt released in the River Alta 1 month earlier. These are the northernmost tag recoveries reported for Atlantic salmon, and indicate that Norwegian Atlantic salmon, especially the fish from northern populations, may use the northern Barents Sea as a feeding area during part of their life cycle.     

A new technique to gather 3‐D spatial information using a single camera

A new technique using a single camera and shadows to determine 3‐D spatial positions of fishes in the laboratory is described. The apparatus consisted of a large aquarium (2·0 × 1·5 × 0·4 m), a wide‐angle camera mounted above and two light sources to cast shadows to either side of the fish. Using image analysis and vector mathematics, aquarium objects were plotted within 1·5 cm of their actual location along the x ‐, y ‐ and z ‐axis. The technique was also successful in quantifying changes in 3‐D spatial pattern of juvenile fish, Atlantic cod Gadus morhua (7·4–8·6 cm standard length, L _S) and cohabitant piscivorous shorthorned sculpin Myoxocephalus scorpinus (12·0–25·8 cm L _S), at these same viewing fields. The new technique should have a wide application, largely because it is potentially less expensive, laborious and invasive than alternative methods for determining 3‐D positions of fishes.     

Age,growth, reproduction and feed of longnosed skate,Dipturus oxyrinchus (Linnaeus, 1758) in Saros Bay,the north Aegean Sea

The age, growth, reproduction, and feeding of longnosed skate (Dipturus oxyrinchus) were studied using 179 specimens from the Saros Bay (North Aegean Sea) between March 2005 and December 2007. Composition was 49.7% females and 50.3% males. Total length of females ranged from 14.9 to 100 cm (disc width, 9.8–65 cm), and of males from 15.2 to 86.5 cm (disc width, 10–57.5 cm). Total length‐weight and disc width‐weight relationships are described by the equations W = 0.0008*TL^3.35 and W = 0.0043*DW^3.29, respectively. The age data, derived from vertebrae readings, were used to estimate the growth parameters of the von Bertalanffy equation: L_∞ = 256.46 cm, K = 0.04 year^?1, t₀ = ?1.17year. The maximum age was 9 years. Males matured at 64–65 cm (disc width, 43.5 cm) and females at 82–83 cm TL (disc width, 53 cm). The stomach contained mainly Parapenaus longirostris, IRI: 93.47%.     

Growth, diet and metabolism of common wolf–fish in the North Sea, a fast–growing population

The von Bertalanffy growth parameters for common wolf–fish Anarhichas lupus in the North Sea were: male: L ∞=111·2 cm, t ₀=–0·43 and K =0·12; and female: L ∞=115·1 cm, t ₀=–0·39 and K =0·11, making this the fastest growing stock reported. Resting metabolic rates (RMR±S.E.) and maximum metabolic rates (MMR±S.E.) for six adult common wolf–fish (mean weight, 1·39 kg) at 5° C were 12·18±1·6 mg O₂ kg^–1 h^–1 and 70·65±7·63 mg O₂ kg^–1 h^–1 respectively, and at 10° C were 25·43±1·31 mg O₂ kg^–1 h^–1 and 113·84±16·26 mg O₂ kg^–1 h^–1. Absolute metabolic scope was 53% greater at 10° C than at 5° C. The diet was dominated by Decapoda (39% overall by relative occurrence), Bivalvia (20%) and Gastropoda (12%). Sea urchins, typically of low energy value, occupied only 7% of the diet. The fast growth probably resulted from summer temperatures approximating to the optimum for food processing and growth, but may have been influenced by diet, and reduced competition following high fishing intensity.     

Migration of hatchery‐reared Atlantic salmon and wild anadromous brown trout post‐smolts in a Norwegian fjord system

Hatchery‐reared Atlantic salmon Salmo salar ( n  = 25) and wild anadromous brown trout (sea trout) Salmo trutta ( n  = 15) smolts were tagged with coded acoustic transmitters and released at the mouth of the River Eira on the west coast of Norway. Data logging receivers recorded the fish during their outward migration at 9, 32, 48 and 77 km from the release site. Seventeen Atlantic salmon (68%) and eight sea trout (53%) were recorded after release. Mean migratory speeds between different receiver sites ranged from 0·49 to 1·82 body lengths (total length) per second (bl s⁻¹) for Atlantic salmon and 0·11–2·60 bl s⁻¹ for sea trout. Atlantic salmon were recorded 9, 48 and 77 km from the river mouth on average 28, 65 and 83 h after release, respectively. Sea trout were recorded 9 km from the release site 438 h after release. Only four (23%) sea trout were detected in the outer part of the fjord system, while the rest of the fish seemed to stay in the inner fjord system. The Atlantic salmon stayed for a longer time in the inner part than in the outer parts of the fjord system, but distinct from sea trout, migrated through the whole fjord system into the ocean.     

Isolation by distance and selection effects on genetic structure of sardines Sardina pilchardus Walbaum

Allozyme data were used to analyse the genetic structure of Sardina pilchardus populations. Fifty samples from 15 locations between the North Sea and Mauritania, including samples from the Azores, Madeira and the Mediterranean Sea, were surveyed. A weak but significant structure was found between all samples ( F _ST= 0.057, P < 0·001). This structure results from a change in the most common allele of SOD* between the North African and the Azores populations separated by the greatest distance. This locus seemed to be under selective pressure according to the test of neutrality, and the variations in allele frequencies may be explained due to isolation by distance (IBD) of coastal populations (from Mauritania to the North Sea) ( r = 0·86, P < 0·001). When SOD* was removed from the analyses, IBD was not observed in coastal populations ( r = 0·236, P > 0·05) but was observed over the whole range ( r = 0·321, P = 0·05). The genetic structure of S. pilchardus is driven by both IBD and selective processes.     

Life‐history variation among local populations of Atlantic cod from the Norwegian Skagerrak coast

Small‐scale spatial variation in life history was found among genetically distinct local populations of Atlantic cod Gadus morhua from the Norwegian Skagerrak coast. Among populations, age at 50% maturity varied from 2·6 to 3·8 years, total ( L _T) length at 50% maturity from 35 to 60 cm, annual survival from 33 to 64%, mean L _T at age 4 years from 43 to 63 cm, and mean backcalculated L _T at age 1 year from 8 to 12 cm.     

Diet comparison between pelagic and demersal whiting in the North Sea

Pelagic North Sea whiting Merlangius merlangus preyed upon (pelagic) sprat and sandeel, while demersal whiting preyed upon (demersal) Norway pout and herring. Values of diet breadth were low for both feeding groups using Levin's index. Diet overlaps within layers were low ( D <0·25), while the between layer food overlap was moderate ( D =0·25–0·74) to high ( D >0·74) using Schoener's index. Selection of prey was density dependent. However, prey size also played an important role. The diet of whiting shifted from amphipods and mysids to fish with increasing predator length, and the length of prey consumed increased significantly with length of whiting. The fact that the stomach contents differed between the feeding groups demonstrates the need for a sampling design that includes both pelagic and demersal habitats when trying to quantify the diet of whiting.     

Age and growth of Mediterranean albacore

Estimated ages of 1136 individual albacore Thunnus alalunga (57–92 cm L F) from the Aegean and Ionian Sea ranged from 1⁺ to 9 years. Males grew faster and reached a greater size and age than females. No significant differences were found in the mean lengths at estimated ages between the two sampling areas. The von Bertalanffy growth model was fitted to mean lengths of estimated ages of individual fish and estimated growth parameters for the combined sexes were: L _∞=94·7 cm, K =0·258, to=–1·354 years. Significant differences were found when the Mediterranean albacore growth parameters were compared with those determined for Atlantic Ocean albacore. It is not possible to determine if the differences in growth rates for the two populations are phenotypic or genotypic at the present time.     

Reproduction, growth and mortality of the common bully, Gobiomorphus cotidianus McDowall, in a eutrophic New Zealand lake

Gobiomorphus cotidianus in Lake Waahi, North Island, New Zealand, (37° 34'S; 175° 08'E) spawned continuously between July 1976 and March 1977. Length frequency data indicated that two, and briefly, three year classes, were present, each made up of three groups which were the progeny from successive peaks in spawning activity. Scale examination revealed checks to growth associated with spawning and stressful midsummer conditions. These and length frequency data were used in growth estimates which indicated that bullies reached 3·5-4·0 cm after their first year, 5-6 cm after their second but did not survive a third year. Mortality was associated with spawning and midsummer stress.     

RETENTION AND EXCHANGE OF POTASSIUM IN A SYNAPTOSOMAL FRACTION OF MOUSE BRAIN

Abstract— Myelin, synaptosomal and mitochondrial fractions obtained from homogenates of whole mouse brain contain K⁺ which can exchange with ⁴²K⁺ at 2º in 0·32 m -sucrose. The content and rates of exchange of K⁺ were greater at pH 8·2 than at 6·1. In the synaptosomal preparations, the rates of exchange and content of ⁴²K⁺ and K⁺ declined progressively with decreasing pH.
Of the total synaptosomal K⁺, 95 per cent could exchange with external ⁴²K⁺. At pH 7·5, 20 per cent of the K⁺ and 78 per cent of the Na⁺ appeared to reside in osmotically insensitive pools. Synaptosomal K⁺ at 2º was slowly displaced by NaCl (0·18 m ) and the rate of exchange between ⁴²K⁺ and K⁺ was retarded. KCI (0·18 m ) did not readily displace endogenous Na⁺. Synaptosomal K⁺ exchanged with exogenous K⁺ more rapidly than with exogenous Na⁺.
These observations have been discussed in terms of possible roles for ion exchange as the principal means by which K⁺ traverses the plasma membrane at 2º.     

The influence of broad scale climatic phenomena on long term trends in Atlantic salmon population size: an example from the River Foyle, Ireland

The effect of marine climatic conditions in the North Atlantic on the abundance of returning migrant Atlantic salmon Salmo salar in the River Foyle, Ireland was examined. Catches of Atlantic salmon from commercial netting stations significantly predicted a measure of population size independent of catches over a 48 year period, thus commercial net catches were used as a measure of relative population size over a longer period in this study. The North Atlantic Oscillation index in winter (wNAOI) provides a generalized measure of climate variation for the northern hemisphere and between 1875 and 2001, the wNAOI was a highly significant predictor of the 5 year running mean of catches of migrant Atlantic salmon returning to the River Foyle. When the index was <0·151, the wNAOI correlated significantly and negatively with Atlantic salmon catches, with 70% of the variance in population size explained by variation in conditions in the marine environment between 1875 and 2001. When the wNAOI was >0·151, however, this relationship uncoupled. The probability of catches exceeding the long‐term median was 2·34 times lower in years where the wNAOI was above the 0·151 breakpoint than for years when it was <0·151. The wNAOI exceeded the 0·151 threshold on 8 out of the 10 years prior to 2001. Models of climate change indicated that the NAOI is likely to increase significantly with time. If these models are correct, this study would lead to the conclusion that a decoupling of these broad scale climate effects on Atlantic salmon population size will become the norm. Data presented here suggests two consequences of this. Firstly that the value of the NAOI as a predictive tool for forecasting adult Atlantic salmon population size will be limited and secondly that the median population size will become lower in the future.     

The survival of semi‐wild, wild and hatchery‐reared Atlantic salmon smolts of the Simojoki River in the Baltic Sea

The recapture rate and survival of hatchery‐reared Atlantic salmon Salmo salar stocked as 1 year‐old parr (semi‐wild) with that of hatchery‐reared Atlantic salmon stocked as 2 year‐old smolts and wild smolts of Atlantic salmon in the northern Baltic Sea were compared. This was done through tagging experiments carried out in 1986–1988 and 1992. The recapture rate of the semi‐wild groups varied from 1·0 to 13·1%, being similar in 3 tagging years and lower in 1 year than that of the wild groups (1·7–17·0%). The recapture rate of the semi‐wild groups was similar (in 2 years) or higher (in 2 years) than that of the hatchery‐reared groups stocked as smolts (1·3–6·3%). The survival of semi‐wild smolts during the sea migration was as high as that of wild Atlantic salmon of an equal size and two to three times higher than hatchery‐reared Atlantic salmon stocked as smolts. The survival rate was positively associated with smolt size. The suitability of hatchery‐reared parr and smolts in the management of reduced Atlantic salmon stocks is compared.     

The role of food particle size in the growth of juvenile Atlantic salmon (Salmo salar L.)

The effect of particle size of a commercial pelleted feed on the growth of Atlantic salmon from first feeding alevins to first and second year smolts was investigated using 20-day feeding experiments. Ten experiments were performed over a two year period, each comprising six groups of fish separately selected from stock populations. Each group was presented with one of six sizes of food particle ranging from larger than the respective mean mouth breadth (100% feed size), through 50%, 25%, 12·5%, 6·25% to 3·125%. Experiments were performed in six radial flow/circumferential drain tanks under ambient photoperiod and water temperature. Growth rate was found to be closely related to feed size. Maximum growth in each case was shown only on one size of particle; larger and smaller sizes resulted in reduced growth. The particle size for maximum growth increased in direct proportion to fish length. Fish from 4·2 to 20·3 cm in length showed maximum growth on particle diameters 0·022 to 0·026 × fish fork length (PFR). First feeding alevins were found to show comparable growth rate on particle diameters 0·0115 to 0·090 PFR. Some seasonal variation in growth response was indicated. The results are discussed in relation to developmental and seasonal effects. Possible factors affecting the energetics of prey size related differential growth are discussed.     

Climate effects on size‐at‐age: growth in warming waters compensates for earlier maturity in an exploited marine fish

Over the past 3 decades, North Sea Atlantic cod (Gadus morhua) have exhibited variable length‐at‐age along with declines in spawning stock biomass and timing of maturity. Multiple factors affecting growth and development in fish acted on this economically important stock over the same period including warming waters and an intensive fishery. Here, we employ North Sea cod as a model population, exploring how a physiologically relevant temperature metric (the growing degree‐day, GDD; °C day) can be used to compare year‐classes on a physiologically relevant time‐scale, disentangling influences of climate (thermal history) on observed length‐at‐age trends. We conclude that the trends in North Sea cod length‐at‐age observed during the last three decades can be explained by a combination of temperature‐dependent growth increases and a trend toward earlier maturation, the latter likely induced by the intensive fishing pressure, and possibly evidence of fisheries‐induced evolution.     

Population structure in the pan-oceanic wreckfish, Polyprion americanus (Teleostei: Polyprionidae), as indicated by mtDNA variation

The wreckfish Polyprion americanus , a large [>1 m total length ( L _T)] demersal teleost, is distributed globally in temperate waters, including both sides of the North and South Atlantic Oceans, the Mediterranean, the western South Pacific, and the southern Indian Ocean. Wreckfish spawn off the south-eastern U.S. on an area of the Blake Plateau (the Charleston Bump) characterized by an extensive ridge having approximately 100 m relief, in 450–600 m depths. Juvenile wreckfish (<60 cm L _T) are pelagic and, in the North Atlantic, are not reported from the Blake Plateau fishing area, but occur in by-catch and fishery landings in the eastern Atlantic. Analysis of nine restriction fragment length profiles from a PCR-amplified fragment (∼1.5 kb) of the ND1 mitochondrial gene indicated no stock separation between eastern North Atlantic (Azores, Majorca, Madeira), and western North Atlantic (Blake Plateau) wreckfish. Restriction site differences separate western South Atlantic wreckfish from the North Atlantic; however, South Atlantic wreckfish share restriction-site similarities with western Pacific wreckfish that are not shared with North Atlantic wreckfish. North Atlantic circulation provides a mechanism for a long-lived pelagic stage to be dispersed from Blake Plateau spawning grounds to the eastern North Atlantic. Global circulation patterns may explain both the dispersal of mtDNA haplotypes and the disjunct distribution of wreckfish body lengths in a temperate, deep-water vagile species with an extended pelagic juvenile stage such as wreckfish.