Population fluctuation in the system of host-parasite interaction

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Contributions from the Entomological Laboratory, Kyoto University, No. 226.     

On the action of population density in the population fluctuation of the flour moth,Ephestia cautella

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Contributions from the Entomological Laboratory, Kyoto University, No. 228.     

Role of a parasitoid with a low fecundity,Praestochrysis shanghaiensis (Hymenoptera: Chrysididae), in the population dynamics of its host

1. Analysis of life tables of the oriental moth, Monema flavescens, obtained for 8 generations over 4 years, disclosed that the cocoon parasitoid, Praestochrysis shanghaiensis, acted as a density-disruptive factor.
2. The density of the host cocoon remained stable (max./min.=3.2), whereas that of the host adult varied (max./min.=14.3) although both showed similar fluctation patterns.
3. Stability of the host population was associated with the density-dependence in the ratio of first generation cocoons to overwintered generation moths, which was the key factor for the rate of change throughout the year. Chrysidid parasitism among the first generation cocoons ranged from 37.7 to 70.1%, and that among the second generation cocoons from 16.7 to 63.2%, each showing an inverse density-dependence and acting as the main determinant (key-factor) of the between-year variation in the density of the adult moths.
4. The density-dependence of the rate of change from overwintered generation adults to first generation cocoons was so strong that the parasitism on the second generation hosts had not effect on the cocoon density of the first generation. On the other hand, the density-dependence of the rate of change from first generation adults to second generation cocoons was weak, and the parasitism on the first generation hosts became the key factor for the between-year variation of the second generation cocoons.
5. It is suggested that the stability of the parasitoid-host system will be disrupted without three parasitism-restricting factors: asynchrony in the parasitoid attack on the second generation hosts, high mortality among parasitoid larvae of the second generation, and the high proportion of those first generation parasitoids that enter diapause. These factors are considered to be effective only in cooler parts of the distribution of the parasitoid.

     

A simple model of host-parasitoid interaction with host-feeding

Summary A simple mathematical model of host-parasitoid interaction with host-feeding was presented with special reference to the system of the greenhouse whitefly and the parasitoidEncarsia formosa. In the model, when a parasitoid encounters a host, it has a choice between feeding the host and ovipositing one egg in the host. It was shown that an intermediate value of the feeding ratio of all attacks gives the minimum equilibrium host density and the minimum amplitudes of fluctuation in the densities of the two species. Computer simulations of a modified model with time lags also gave the similar results. The model suggested for natural enemy introduction program that parasitoid species with host-feeding habits are promising agents for effective controls for pest insects and that the timing of introduction is very important. By an evolutionary analysis, it was shown that the feeding ratio evolves to minimize the host density under natural selection among parasitoids.     

Long-term population dynamics of two Carex curvula species in the Central Alps on native and alien soils

The demography of two closely related alpine sedges, Carex curvula subsp. curvula and Carex curvula subsp. rosae (=C. curvula and C. rosae) has been investigated on their typical sites in the Central Alps. Both species proliferate vegetatively and develop dense tussocks but they show different dominance behaviours in their respective grasslands. It was hypothesized that this may be caused by different growth abilities. The main aim of the study was to compare the vegetative growth of the species under field conditions, under competition-free conditions and under changed soil conditions. An attempt was also made to clarify whether vegetative growth is density dependent. Permanent plots were established in the respective grasslands of the two species and the ramet density was counted over 3 years. Groups of 10 and of 30 ramets of each species were grown in pots with typical and with alien substrate and their growth was observed for 5 years at the field site. The grassland populations of both species were very stable and the overall ramet growth rate (λ) was close to 1.0. Within the pots, both species reached a high ramet number. Only the group of 30 ramets of C. curvula on alien soil could not recover from the transplantation shock. Within the pots, C. rosae showed a greater ramet turnover and a higher increase in ramets than C. curvula. On their native substrate, both species had a significantly higher ramet increase than on the alien substrate. Ramet growth was found to be density dependent for both species, the increases recorded for the groups of 10 being significantly greater than for the groups of 30. Although C. curvula produced fewer ramets than C. rosae, the aboveground dry weight of the former was significantly higher. This may be decisive for its greater competitive success in closed grasslands. Received: 12 April 1997 / Accepted: 12 December 1997     

A numerical solution of theVolterra equation for the growth of an animal population accompanying an autotoxic effect

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Contribution from the Department of Fisheries, Faculty of Agriculture, Kyoto University.     

Long-term population trends in widespread British moths

The Rothamsted Insect Survey has operated a Great Britain-wide network of light-traps since 1968. From these data we estimated the first ever national abundance indices and 35-year population trends for 338 species of common macro-moths. Although the number of trap sites which run each year is not constant, there is a representative, well-distributed core of traps that have run for 15 years. The proportion of operating sites catching a species and the annual geometric mean catch of successful traps were used to provide estimates of species range and absolute abundance. T, an index of long-term population trends, was used to compare trends among species. T was not biased by trap site turnover. The percentage of species displaying significant decreases (54%) was more than double that displaying increases (22%). Species found throughout Great Britain are decreasing most rapidly in the south and especially the southeast but species with a southerly distribution are increasing. Results of a preliminary overview suggest habitat and climate change may both play a role in changing species dynamics. The existence of estimates of abundances and trends for such a large species pool opens the way for much further research, linking trends with land-use changes, climate change and inter-specific dynamics.     

Heterogeneous interspecific interactions in a host-parasite system

Macroparasites of vertebrates usually occur in multi-species communities, producing infections whose outcome in individual hosts or host populations may depend on the dynamics of interactions amongst the different component species. Within a single co-infection, competition can occur between conspecific and heterospecific parasite individuals, either directly or via the host's physiological and immune responses. We studied a natural single-host, multi-parasite model infection system (polystomes in the anuran Xenopus laevis victorianus) in which the parasite species show total interspecific competitive exclusion as adults in host individuals. Multi-species infection experiments indicated that competitive outcomes were dependent on infection species composition and strongly influenced by the intraspecific genetic identity of the interacting organisms. Our results also demonstrate the special importance of temporal heterogeneity (the sequence of infection by different species) in competition and co-existence between parasite species and predict that developmental plasticity in inferior competitors, and the induction of species-specific host resistance, will partition the within-host-individual habitat over time. We emphasise that such local (within-host) context-dependent processes are likely to be a fundamental determinant of population dynamics in multi-species parasite assemblages.     

The effect of population density on the growth of an animal population

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Contribution from the Department of Fisheries, Kyoto University.

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Contribution from the Entomological Laboratory, Kyoto University, No. 201.     

Statistical characteristics of the density-independent population fluctuation and the evaluation of density-dependence and regulation in animal populations

In this study it was proved that the “density-independent population” shows the following characteristics if the analysis is made using time-series samples:

1. The slope b in the density-on-density regression between successive developmental stages has a general tendency to become smaller than 1, though the bias approaches zero if one or more of the following three conditions are satisfied: (a) the data cover a large number of generations, (b) the variance of the rate of population change for the period concerned is small relative to that for the residual period in a whole generation, and (c) the population has a distinct trend to either increase or decrease over generations.
2. The variance for the generation-to-generation population fluctuation increases continually as the number of generations is increased, even if the population has no inherent trend to increase or decrease. For a fixed number of generations, however, the variance remains constant among different developmental stages.

On the basis of these theoretical results, a modified method for detecting density-dependence from time-series samples was presented, together with a new, tentative technique of variance analysis to evaluate the regulation of numbers directly. The results of applying these methods to some sets of data from both hypothetical and actual populations illustrated their validity for use in population studies.     

Functional response to host density in a parasitic wasp,with reference to population regulation

1. The functional response to, and preference for, the host density in a parasite were examined experimentally using an icheumon wasp, Exidechthis canescens, and its host Cadra cautella under controlled conditions.
2. Wasps were more active in host-searching at higher than lower host densities. Percent parasitism increased rapidly with initial increments in host density and then tended to increase more slowly at higher host densities. A sigmoid functional response curve is indicated, which implies that the parasite is able to control its host even at low densities.
3. Wasps actively selected areas of high host density in which to concentrate host-searching behavior.
4. Host-searching by E. canescens is stimulated by the odor of the host when present, and by food in which hosts have developed but have been removed.
5. Both the functional response and the host-density preference of the parasite are mediated by its host-searching behavior. This relationship is discussed in the context of population regulation.

     

Regulatory processes and population cyclicity in laboratory populations ofAnagasta kühniella (Zeller) (Lepidoptera: Phycitidae)

AsMatsumoto andHuffaker (1973) concluded that their initial universe size was too small for the proper separation of the effects of host density and dispersion on parasite performance, a larger universe of 38 1/2″ (length) ×38 1/2″ (width) ×3″ (height) was used. When individual parasites were exposed to fixed densities and dispersion patterns of host, they displayed an overall decrease in the parasitization rate when compared to the small universe. In all cases aHolling -type response resulted. When a group of 10 parasites per test was employed a Nicholsonian type of response resulted. In an experimentally confined space, the parasites displayed a mutual behavioral interference resulting in emigration which accelerated as the parasite density increased.     

Regulatory processes and population cyclicity in laboratory populations ofAnagasta kühniella (Zeller) (lepidoptera: Phycitidae) V. Host finding and parasitization in a “small” universe by an entomophagous parasite,Venturia canescens (Gravenhorst) (Hymenoptera: Ichneumonidae)

Summary Host finding by the entomophagous parasite,Venturia canescens (Grav.), parasitizingAnagasta kühniella (Zeller) was studied. Studies utilizing fixed densities and dispersion patterns of the hosts where no choice of density groupings was offered showed that within the experimental conditions used, host density relationships were more important than dispersion. Decreasing the time hosts were exposed to a parasite from 72 hours to 24 hours did not alter the overall parasitization. In both cases progressively less hosts were parasitized as host density increased, which exemplified aHolling-type of response. However, when host densities were varied within the same universe, independent of dispersion patterns, and the parasites were given a “choice” of host densities to attack, an increasing percentage of hosts in the higher host density groups were parasitized; thus a density-dependent behavioral response was exhibited. These studies were conducted as a partial fulfillment in the Ph. D. program of one of us (B. M. Matsumoto) and form a part of a broad investigation into the processes operating in the dynamics of arthropod populations under grants toC. B. Huffaker from the U. S. Public Health Service, National Institutes of Health and the U. S. Department of Agriculture.     

The fitting of the logistic equation to the rate of increase of population density

Though there are many problems on the usefulness of the logistic curve, it may be necessary to examine before discussing these problems whether or not the actual data fit to the theoretical values. It has been clarified in this paper that the relation between the population density and its rate of increase per individual described by the differential equation (1) is represented by a straight line on a finite difference diagram on which N_i+1−N_i/N_i values are plotted against N_i+1. Utilizing this linear relation we may examine the fittness of the logistic curve to the actual data and when it is fitted we may estimate the parameters of the logistic equation by (5) and (6). The result of the application of this method to the experimental populations of azuki bean weevil indicates that the relation between parent and progeny densities fits well to the logistic type as has been proved byFujita andUtida (1953) who utilized the linear reltion between 1/R+2σ and parent density where R is the apparent rate of reproduction and σ is a constant dependent primarily upon the length of adult life (0≦σ≦1).