ALBERT

Notes: Abstract  Growth and reproduction were compared among six geographically and genetically distinct intertidal populations of the annual, semelparous, dorid nudibranch Adalaria proxima (Alder & Hancock) to evaluate variation in fitness-related traits. The six populations spanned the geographic range in the northern British Isles: NE England (Cowling Scar), E Scotland (Kinkell Braes), NW Scotland (Loch Eriboll), W Scotland (Cuan Ferry), Northern Ireland (Portaferry), and N Wales (Menai Bridge). Nudibranchs from five sites were collected in July to August 1992 as post-metamorphic juveniles and were laboratory-reared under the same conditions of ambient temperature and photoperiod for up to 10 months and the completion of spawning. Individuals from the sixth site were added to the experiment in December 1992. Growth was monitored every 2 weeks, and reproductive performance was expressed as a weight-adjusted dimensionless index (ΣRI) of each individual's spawnings summed over the reproductive period. In general, larger nudibranchs produced larger first spawn masses and more total spawn than did smaller nudibranchs, but these size-related trends were observed only in some populations. The patterns of energy partitioning to spawnings varied significantly among populations, from allocations of a large number of eggs to few spawn masses (Loch Eriboll) to production of many small spawnings over a long spawning period (Portaferry). There was no relationship between maximum body size and the amount of spawn produced after the first spawning, nor to the length of the spawning period or the number of spawn produced. Both Menai Bridge and Kinkell Braes had low mean population ΣRI, reflecting a very poor reproductive performance, given their large maximum (pre-spawning) body sizes. By contrast, the Loch Eriboll, Cuan Ferry, and Portaferry populations all displayed high mean population ΣRI, albeit as a result of differing combinations of numbers and sizes of spawn masses and duration of the spawning period. This high variance of reproductive allocation among populations, and previous evidence of relatively stable among-population differences in allozyme frequencies, adult color, and embryo characteristics suggest very restricted larval transport of lecithotrophic larvae of A. proxima.

Notes: Abstract –  A model based on proximate considerations of life histories of Atlantic salmon, Salmo salar, was examined for its applicability to fit the variation in life-history of wild Arctic charr, Salvelinus alpinus, based on a qualitative assessment of information related to growth and lipid dynamics of Arctic charr. The original salmon model is discussed in context of modifications required to account for added complexities in the life history of Arctic charr in relation to anadromy versus residency. A study from North Norway shows that individual charr that emigrate from the lakes to the sea, maintain a high growth rate in the lake in late summer and early autumn compared with resident fish. Their relatively low lipid level in autumn combined with a high rate of change of lipid during winter was associated with postponement of maturation in the anadromous individuals. Individuals that remain resident in the lake arrested growth in autumn. Their high lipid level in autumn combined with a low rate of change of lipid during winter was associated with maturation the following summer, without emigration from freshwater. Results from this and other related studies show similarities with the model derived from lipid and growth dynamics of Atlantic salmon. The adjusted charr model illustrates possible proximate explanations for the high variation in life-history strategies of Arctic charr. However, the model does not account for the characteristic return migration of immature charr into freshwater several weeks after their entry to the sea. The proximate physiological stimulus for this movement of immature fish is not entirely clear.

Notes: Juvenile trout enter Loch Leven during autumn and winter from the nursery streams, spend their adolescent phase offshore until reaching a length of 0.30 cm, and then move to the littoral areas in early summer. There are two types of littoral area:‘favourable‘areas from which movement of individual fish in the summer is very restricted, and‘unfavourable‘areas used briefly in early summer from which movement away is pronounced. Trout are absent from the littoral areas in winter. In subsequent summers homing to previous feeding areas is characteristic of fish from‘favourable’areas, with a tendency for older fish to move to the south east area of the loch. Spawning runs occur simultaneously into the main inflows, chiefly between October and December. Emigration into the outflow occurs, but is probably unimportant.

Notes: The protected environment in culture permits fishes to reduce the proportion of energy normally channelled into the costs associated with competition for food, shelter and mates, avoidance of predators and counteracting parasites and diseases. The surplus energy so released is allocated to growth and reproduction, accelerating development through increased growth rate, earlier maturation and increased relative fecundity. Cultivators manipulate the rearing environment to remove seasonal variation in availability of resources, so that the fishes grow and develop through otherwise unproductive seasons. Such environmental manipulations exaggerate the basic accelerative effects. Since maturation deflects energy from growth, farmers also manipulate the fishes nutritionally, physiologically, hormonally and genetically to postpone maturation. As environmental regulators determine sex in many fish species, environmental manipulation in culture may have unintended effects on sex ratios. Mortality in culture should be very low, but survival of fishes released from culture is rarely as high as that of wild conspecifics. Finally, while short life-cycles and simplified population age-structures permit high rates of production in farms, they lead to ecological instability when the fishes are cultured for support of wild populations.

Notes: [Auszug] The liberation of gravitational energy as matter falls onto a supermassive black hole at the centre of a galaxy is believed to explain the high luminosity of quasars. The variability of this emission from quasars and other types of active galactic nuclei can provide information on the size of ...

Notes: The numbers of adult trout in Loch Leven were estimated in April each year 1968–71 by tagging fish caught by seine net, and estimating the proportion of the total stock tagged from examination of the angling catch during June-August. The vulnerability of tagged fish before June and after August was higher than that of untagged fish. Tag losses, estimated by double marking, were 2.15 % over a whole angling season. The reporting rate of tag recaptures varied within and between years from 0.43 to 0.71. Differential mortality of tagged and untagged fish was unimportant, except in two subsidiary experiments when fish were tagged in June and August, when handling losses reached 2.7%. With adjustment for these measured errors, the stock of trout beginning their third or more years in the loch in April, fell from 126 665 in 1968 to 52 337 in 1971.

Notes: The pathology and bacteriology of an aeromonad epidemic in the spawning population of brown trout (Salmo trutta L.) of the freshwater Loch Leven, Kinross, Scotland, is described, together with estimates of its quantitative effect on the stock of trout.

Notes: Abstract The application of genetic techniques to invertebrate fisheries is in many ways essentially similar to that in vertebrate (i.e. finfish) fisheries, for which there is already an extensive body of published data. However, there are also relative differences which lead to particular problems in the use of genetic data to study commercially important invertebrate species. The main role for genetics of both vertebrates and invertebrates has been, and is likely to continue to be, the identification of groups of interbreeding individuals as the basis for a fishery. It is in the identification of the breeding unit that the genetic differences between vertebrates and invertebrates can be of practical significance. The genetic breeding unit, usually called a 'stock' in fisheries biology, generally shows a certain uniformity of size in most marine fish which have been studied. Smaller or less mobile fish (e.g. flatfish) may only range a few tens of kilometres to their breeding grounds, whilst in more mobile, particularly migratory pelagic species (e.g. Scombridae), the area occupied by a stock is likely to be far greater and for a few (e.g. large pelagic elasmobranchs), a single unit of stock may be almost circumglobal. However, marine fish generally, particularly those large or plentiful enough to be of commercial interest, are likely to be fairly mobile and in many cases the order of mobility is likely to be in the region we might predict from our knowledge of the biology and habits of the species. In the genetic assessment of `stocks' for invertebrate fisheries, we face a number of additional problems, mostly related to the large evolutionary range of invertebrates exploited and their widely different biology. Although in Europe and North America marine invertebrate fisheries may be thought of as being mainly for decapod crustaceans and bivalve molluscs, globally commercially important marine invertebrate fisheries range from sponges to squid and include such diverse groups as sea cucumbers, barnacles, krill, octopuses, cuttlefish, sea anemones, ascidians, polychaetes, sea urchins, gastropods and jellyfish. An obvious feature of many of these invertebrates is that the adult (i.e. commercial) stage of the life cycle is sessile (e.g. barnacles, sponges, ascidians) or of very limited mobility (e.g. sea anemones, sea urchins, bivalves, gastropods), with the result that the dispersive phase of the life cycle is the larva. Other groups (e.g. krill, jellyfish) are planktonic or nektonic and may cover very large distances, but, unlike fish, have little control over the distance or direction of travel, whilst some of the open ocean pelagic squid are more mobile than most fish and may migrate thousands or kilometres to spawning grounds. The very low mobility of both larva and adult in some invertebrates indicates that dispersal, and hence stock size, is likely to be low and that, therefore, stocks are far more vulnerable to overfishing than in most fish species. An additional difficulty is that genetic studies to date indicate a remarkably high incidence of cryptic speciation in marine invertebrates, sometimes even in comparatively well studied commercially important species. Thus, although to date marine invertebrate fisheries have not received the same level of attention from geneticist as finfish fisheries, it is clear that for invertebrate fisheries genetic data are relatively far more important if a fishery is to be exploited without being endangered.

Notes: Abstract The spider crabs Inachus dorsettensis (Pennant) and Hyas coarctatus Leach are widespread in subtidal areas of muddy sand or gravel around western Europe. Both species have a life cycle with an obligatory planktonic larval phase of several weeks, which might be expected to cause widespread larval dispersal and consequent genetic homogeneity over considerable distances. However, earlier work on both taxa has indicated differences in growth pattern between populations separated by tens of kilometres. This study was undertaken to determine whether these differences were purely environmental or whether, despite the short distances involved, differences may have a genetic basis. A study of gene frequencies, as indicated by allozymes in samples of adults collected off the Isle of Man (northern Irish Sea), indicates significant genetic differentiation between populations over a geographical distance of only about 40 km in both Inachus dorsettensis (θ = 0.086 ± 0.048) and Hyas coarctatus (θ = 0.023 ± 0.017). Variability measures differed between species, showing I. dorsettensis to have a mean number of alleles per locus of 2.5–2.6 and a range of gene diversity of 0.216–0.241, while H. coarctatus showed lower values of mean number of alleles (1.9–2.0) and a range of gene diversity from 0.122 to 0.124. Given the high expected larval mobility of the two species the results are most surprising. Possible explanations are discussed in relation to population discontinuities and patterns of larval drift.