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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Industrial relations journal 20 (1989), S. 0 
    ISSN: 1468-2338
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Economics
    Notes: Here the authors use sample data to identify some of the major influences on why nurses choose to be a member of one union, as opposed to other unions, in the NHS
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial and engineering chemistry 24 (1985), S. 743-748 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 3
    ISSN: 1365-2427
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SUMMARY 1. The objective was to compare variations in egg hatching between the two species (interspecific variations) and between populations of the same species (intraspecific variations). There were significant interspecific, but not intraspecific, differences in female size, adult life-span, egg production, hatching success, incubation periods and hatching periods.2. The optimum temperature for hatching success within the range 3.8–22.1°C in the laboratory and the range over which at least 50% of the eggs hatched were lower for Chloroperia tripunctata (Scopoli) (8.5°C, 4.2–17.3°C) than for Siphonoperla torrentium (Pictet) (12.8°C, 6.1–19.4°C). Few eggs hatched at 22.r°C.3. The relationship between incubation period (d days) and water temperature (T°C) was given by: d=1219/T1.368 for S. torrentium, d=253/T0.459 for C. tripunctata. Both equations successfully predicted incubation periods for eggs placed in a stream. The period over which eggs hatched was much longer for C. tripunctata than for S. torrentium at all temperatures.4. The shorter incubation period (at r〉5.6°C) and shorter hatching period for S. torrentium ensure that larvae of this species are already growing when eggs of C. tripunctata start to hatch, but the prolonged hatching period of the latter species ensures a long period of larval recruitment to the population. These differences in egg hatching may reduce competition between the two closely-related species.
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  • 4
    ISSN: 1365-2427
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SUMMARY. 1. The chief objective was to determine the major environmental factors affecting the swimming activity of Hirudo medicinalis L. because the latter will affect the feeding and growth periods. 841 leeches were caught in samples taken every 2 weeks in 1982, 1983 and 1984.2. There were four major size groups, probably corresponding to year-classes. Only nine leeches were in their fourth year (Group IV), most leeches found on stones were in their first year (Group I) and most swimming leeches were in their second or third year (Groups II, and III). Size groups I-III overlapped considerably and could not be treated separately in subsequent analyses.3. Water temperature appeared to be the dominant factor affecting swimming activity, the threshold for activity being 7°C (range 5–9°C). A curvilinear regression provided the best description of the relationship between temperature and catches of swimming leeches; 62% (range 50–75%) of the catch variation could be explained by temperature.4. Atmospheric pressure at the time of sampling and its rate of change over 24 h preceding sampling had no significant effect on catches of swimming leeches, not even on the residuals of catches after the dominant effect of temperature had been removed. Similar analyses showed that there were no significant seasonal effects on swimming activity.5. From a discussion of the implications of this study, it is concluded that the absence of the medicinal leech from many water bodies may be due partially to the relatively high temperatures required for swimming activity in a large proportion of the population (11.9°C, 19.0°C, 22.7°C for 10%, 50%, 90% active respectively).
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Freshwater biology 18 (1987), S. 0 
    ISSN: 1365-2427
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: 1. The life cycle of Leuctra nigra (Olivier) took 2 years in a small stream in the English Lake District and the exponential growth of the larvae was scarcely affected by variations in water temperature (range 4.2-14.0°C). Mean growth rates for three year-classes were 0.43±0.01, 0.42±0.01, 0.39±0.05% body length day−1. There were thirteen or fourteen larval instars for males and fourteen or fifteen for females. The ratio between successive instars was a constant 1.20 (conformed with Dyar's rule).2. Larval growth and mortality were exponential at six constant temperatures (5.9, 8.2, 12.1, 15.8, 18.2, 19.8°C) in the laboratory. Mean growth rates (% body length day−1) increased directly with temperature from 0.37 (5.9°C) to 0.55 (19.8°C). Mean mortality rates (% day−1) increased directly with temperature from 0.20 (5.9°C) to 0.26 (12.1°C) and then markedly increased to 0.54-0.58 at the three higher temperatures. Only 7-10% of animals completed their life cycle at the three higher temperatures compared with 23–27% at the three lower temperatures. Egg production also decreased considerably at the higher temperatures.3. As growth rates in the stream and laboratory were similar at similar temperatures (〈14°C), the optimum conditions for growth in the laboratory were probably similar to those in the stream; therefore resources such as food and space were not restricting growth in the stream.4. The implications of the temperature-induced changes in growth and mortality are discussed and it is concluded that although the life cycle can change from semivoltine to univoltine with increasing temperature, the costs of a univoltine life cycle are high in terms of survival and egg production, both of which decreased markedly between 12.1 and 15.8°C. Therefore the optimum habitat for this species appears to be a summer cool stream (maximum temperature 〈14°C) and the optimal life cycle appears to be about 2 years from egg to adult.
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Freshwater biology 21 (1989), S. 0 
    ISSN: 1365-2427
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SUMMARY. 1. Brown trout were once given a variety of latin and common names, but are now regarded as belonging to only one polymorphic species, Salmo trutta L. A review of their geographical distribution shows that this species was originally native to Europe but has been successfully introduced in at least twenty-four countries outside Europe.2. Brown trout provide valuable commercial and sports fisheries, e.g. commercial and rod catches of sea-trout in England and Wales averaged 110,547 fish per year from 1983 to 1986 and the minimum value of these fisheries is estimated to be £55M.3. It is concluded from this brief review that the major objectives of scientific research on wild brown trout should be: (a) an assessment of the current status of stocks; (b) the maintenance of existing populations; (c) the development and improvement of mathematical models that can be used as tools for the conservation and management of this important national and international resource.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Freshwater biology 17 (1987), S. 0 
    ISSN: 1365-2427
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SUMMARY. 1. Field experiments were performed in the day and night at six modal water velocities (range 10–52cm s−1), using: (i) newly- emerged fry without neutral buoyancy; (ii) older fry in poor condition (weight well below that expected for resident fry); (iii) older fry in good condition (weight similar to that of resident fry); (iv) dead fry.2. An exponential model described the return rate of fry to the stream bottom; the mean distance travelled downstream varied considerably between the four fry categories, but always increased linearly with increasing water velocity.3. Results were similar for dead fry and newly-emerged fry released at night; 50% of the fry returned to the bottom in 10–11 s and nearly all returned in c. 70s, the maximum distance travelled ranging from c. 7 m at 10 cm s−1 to c. 37m at 52cm s−1, Newly-emerged fry released in the day returned slightly faster (54s for 99% return to bottom).4. Older fry in poor condition returned to the bottom slightly faster in the day than at night, but took about 2 min and travelled about twice the distance covered by dead fry. Older fry in good condition returned to the bottom at the fastest rate (3–6s for 50% and c. 30s for the rest), and travelled only about half (at night) or a third (in day) of the distance covered by dead fry.5. The implications of this investigation are discussed and it is concluded that, apart from water velocity, the age and condition of the fry were the two most important factors affecting their downstream movement.
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  • 8
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 26 (1987), S. 1686-1691 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of fish biology 35 (1989), S. 0 
    ISSN: 1095-8649
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: An example of density-dependent regulation is provided by a long-term investigation (1966-present) of a population of migratory trout (estuarine and sea trout), Salmo trutta L., in a Lake District stream. Evidence for the concept of a critical period for the survival of young fish is briefly reviewed and found to be rather equivocal. The concept is, however, relevant to the trout population. Loss rates were high before but low after a critical survival time (tc days after fry emergence) that varied between year-classes (range 33-70 days) and was inversely density-dependent on egg density. Survivor density and loss rates were strongly density-dependent on egg density before tc, but proportionate survival with stable loss-rates occurred after tc. Some trout established feeding territories soon after emergence and the number of fish without territories decreased from a high initial value to a negligible value at tc. Fish size at tc was not constant but increased as tc increased. The range of tc for the different year-classes was similar to that for survival times of unfed fry in the laboratory. A new stock-recruitment model, incorporating tc, has been developed for the trout population and shown to be related to the model (Ricker curve) used in the long-term study. The critical time can also be regarded as the critical age for survival in young trout; this concept may be relevant to other fish species.
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of fish biology 27 (1985), S. 0 
    ISSN: 1095-8649
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: A short review summarises the chief conclusions of an 18-year investigation of the population dynamics of migratory trout, Salmo trutta L., in a Lake District stream. The chief factors affecting growth, survival and production have been identified and their effects summarized in a series of mathematical models. The implications of this work are discussed in relation to long-term investigations, data analysis and modelling, and the scientific management of trout populations. It is shown that mathematical models, based on long-term investigations, can be used to assess the effects on a fish population of changes due to natural causes (e.g., droughts and spates) or human activities. One of the main objectives of future work should be the development and improvement of models that can be used as tools for the conservation and management of fish stocks.
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