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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Theoretical Population Biology 43 (1993), S. 337-367 
    ISSN: 0040-5809
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Animal Behaviour 31 (1983), S. 927-945 
    ISSN: 0003-3472
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Animal Behaviour 31 (1983), S. 927-945 
    ISSN: 0003-3472
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0003-3472
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Animal Behaviour 34 (1986), S. 302-303 
    ISSN: 0003-3472
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
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  • 6
    ISSN: 1432-1939
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Ovipositing females of the cynipid waspPseudeucoila bochei discriminate between parasitized and unparasitized hosts, which results in a far more uniform distribution of eggs over the hosts than would be obtained if oviposition were random (Fig. 1,a 0-f 0). For the description of the distributions a few models were worked out, which rest on the assumption that the hosts are probed at random. The total number of effective probes made in a larva during the experiment is a random variable with a Poisson distribution and an expectation λ. The chance that at a certain probe an egg will be laid (δ) is dependent on the number of eggs present (j); 1=δ0〈δ1≧δ2≧δ3.... In model I it was assumed that the female had only the ability to distinguish parasitized from unparasitized hosts. The chance that an egg will be laid in an unparasitized host when it is probed, δ0, is considered to be equal to 1, while δ1=δ2=...=δ n 〈1 (Fig. 2, 1,a 1-f 1). When the mean number of eggs present in a host was larger than about 1.1, this model did not describe the distribution of eggs satisfactorily (Fig. 3). It seemed that the ovipositing female is not only able to distinguish parasitized from unparasitized hosts, but also to distinguish thenumber of eggs present in a host. In model II it was assumed that the wasp could distinguish between hosts with 0, 1, and 2 or more eggs: the chance that an egg would be laid in a host containing 2, 3, 4, ... eggs was, hence, the same in this model δ1〈δ2=δ3=...=δ n (Fig. 2, 1,c 2,e 2,f 2). This model described the distributions of eggs much better (Figs. 4 and 5), but at mean numbers of eggs per host above 2 it was apparently inadequate. Two other models were then tried, in which the chance δ that an egg would be laid in a host decreased with the number of eggs already present (j). In model III (Fig. 2) the chance decreased according to the function δ j =δ/j (δ0=1, δ〈1). Fig. 1,d 3,e 3,f 3, gives some examples. In model IV the chance δ j =δ j (δ0=1, δ〈1) (see Fig. 1,d 4,e 4,f 4). From the comparison of Figs. 6 and 7 it is clear that model IV gives the best description of the distributions of eggs found. The value of these models is discussed, and plans for both an approach through experimental analysis and simulation models are given. In an Appendix the mathematical derivation of the models is presented.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Acta biotheoretica 34 (1985), S. 91-101 
    ISSN: 1572-8358
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Acta biotheoretica 31 (1982), S. 109-126 
    ISSN: 1572-8358
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A number of (insect) parasitoids have been found to avoid superparasitism, i.e., these parasitoids distribute their eggs more evenly over the available hosts than might be expected from chance only. By doing so each parasitoid individual ensures a greater probability of survival for its offspring as a result of a reduced within-host-competition. Recently a number of mathematical models have been developed, describing the distribution of the parasitoid eggs in the hosts. This paper gives a survey of these models, placing them within one and the same mathematical framework. An essential conceptual distinction, neglected up to now, emerges: parasitoids can either react to the number of previous visits to a particular host, or they can react to the number of eggs already present in that host. For each model the probability-generating function, the mean, the variance, and the probability distribution of the number of eggs are given, as well as a discussion of estimating and testing procedures. A few possibilities for generalizations of these models are discussed too.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Entomologia experimentalis et applicata 10 (1967), S. 295-311 
    ISSN: 1570-7458
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Description / Table of Contents: Zusammenfassung 1. Die Weibchen der Cynipide Pseudeucoila bochei legen ihre Eier in Larven verschiedener Drosophila-Arten. Obwohl bei Sektion der Wirtslarven manchmal mehr als ein Parasitenei gefunden wird, schlüpft aus einer Wirtspuppe immer nur eine Wespe. Überzählige Parasitenlarven gehen schon früh in der Entwicklung zugrunde. Die Frage lag vor, ob das Parasitenweibchen schon beim Ablegen ihrer Eier ein Unterschied machen kann zwischen bereits parasitierten und noch nicht parasitierten Wirtslarven. 2. Wenn parasitierte und nicht-parasitierte Wirtslarven zusammengebracht und den Parasitenweibchen ausgesetzt wurden, legten die Weibchen 75–79% ihrer Eier in die nicht-parasitierten Larven (Tabelle I). Damit wurde eindeutig ein gutes Unterscheidungsvermögen festgestellt. 3. Obwohl die Wespenweibchen parasitierte Wirte von nicht-parasitierten zu unterscheiden vermögen, wird nicht immer nur ein Ei pro Wirt abgelegt. Die Anzahl Parasiteneier pro Wirtslarve ist abhängig von der Anzahl der pro Wespe zur Verfügung stehenden Larven. Wird die Anzahl der Wirte niedriger, so wird die weitere Eiablage stark gehemmt (Abb. 1), und die Anzahl überparasitierter Wirte nimmt zu (Tabelle II). 4. Auch bei Überparasitierung ergibt sich noch eine deutliche Abweichung von einer Zufallsverteilung der Eier über die Wirtslarven (Tabelle IV). 5. Es wurde ein mathematisches Modell entwickelt, bei dem versucht wurde, ein quantitatives Maß für die Wirtsdiskriminierung zu finden. Die mathematischen Einzelheiten sind im Appendix dargelegt. Im Modell bedeutet λ die mittlere Anzahl der Besuche des eierlegenden Weibchen bei einer Wirtslarve, und δ die Wahrscheinlichkeit, daß bei einem zweiten, dritten, usw. Besuch ein zweites, drittes, usw. Ei gelegt wird. Es stellt sich heraus, daß δ bei höheren Parasitendichten zunimmt (Abb. 2). 6. Das Modell gibt eine gute Beschreibung der gefundenen Verteilungen von Parasiteneiern auf die Wirte (Tabelle V). 7. Die niedrige Anzahl der pro Wespe gelegten Eier bei höheren Parasitendichten wird nicht durch irgendeine ungünstige Wirkung der Wespendichte an sich verursacht, sondern durch die schnelle Abnahme der Anzahl geeigneter Wirtslarven während des Experimentes (Tabelle VI). 8. Die Weibchen machen bei der Eiablage keinen Unterschied zwischen Wirtslarven, die sie selber besucht haben und denjenigen, welche durch andere Weibchen besucht wurden (Tabelle VII). 9. Es ist naheliegend anzunehmen, daß die Vermeidung einer Überparasitierung adaptiv ist, weil sie unnötigen Verlust von Eiern verhütet.
    Notes: Abstract The cynipid wasp, Pseudeucoila bochei, lays her eggs in larvae of several species of the genus Drosophila. From one host pupa only one wasp emerges. It has been investigated whether this could be ascribed partly to discrimination between healthy and already parasitized hosts by the egg-laying female. This appeared to be the case. Discrimination is, however, not absolute: it depends strongly on the availability of healthy hosts. A mathematical model has been worked out in order to have some measure of the degree of discrimination under different conditions.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Environmental monitoring and assessment 61 (2000), S. 317-344 
    ISSN: 1573-2959
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Environmental and nature management can not operate effectivelywithout reliable information on changes in the environment andon the causes of those changes. Ecological monitoring canrepresent an important source of information. However, manyoperational monitoring programs are not very effective, i.e., not very useful for decision-making. We present a conceptualframework for the development and maintenance of effectiveecological monitoring programs. In the decision-making process,two main functions for monitoring can be recognized: an earlywarning and an early control function. Both these functionsrequire a high diagnostic power. This is used as a guideline forthe design process. The design consists of choices concerningmonitoring objectives, objects and variables to be monitored,sampling strategy and design, data collection, data handling, maintenance and organization. Arguments commonly put forward inliterature and in practice to support the various choices aresubjected to a critical analysis. The framework will be helpfulin the design of effective monitoring systems as it avoidsimportant components to be overlooked, clarifies the relationbetween the different components, maximizes the exploitation ofexisting possibilities and opportunities and identifiesshortcomings in advance. This will result in monitoring programsthat should be able to live up to their expectations.
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