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.

     

Population dynamics of a phytophagous lady-beetle,Epilachna vigintioctopunctata (Fabricius), living in spatio-temporally heterogeneous habitats. III. Effects of habitat structure on population dynamics

Temporal changes in the population size of a phytophagous lady-beetle were analyzed to identify mechanisms affecting lady-beetle population dynamics at different spatial scales. The study area (15 ha) included 18 habitat patches. The major host plants were potato for first generation larvae and eggplant for second generation larvae. The habitat patches were classified into three groups according to the major host plants in each patch: P-E patches (both host plants available), P patches (potato only), and E patches (eggplant only). The winter disappearance of adults in the whole study area, and larval mortality in E patches were apparently the most important factors disturbing the overall population density. Density-dependent movement of females appeared to have the greatest stabilizing effect on the yearly fluctuation of population density. Rate of increase of female adults from the first to the second generation,R, was generally higher on eggplants in E patches than in P-E patches because the adult density of the first generation was much higher in P-E patches. The yearly fluctuation of adult density in each generation tended to be less in patches with all habitat components necessary for the full life cycle (P-E patches). However, such patches were not favorable for first generation females, as indicated by the lower rate of increase from the first to the second generation. The density and stability of lady-beetle populations is discussed in relation to habitat structure.     

Biological studies upon Enchytraeus variatus Bouguenec & Giani 1987 in breeding cultures

The life history of an enchytraeid worm, Enchytraeus variatus, was studied under laboratory conditions at 18–22 °C. This species can reproduce simultaneously by asexual (architomy) or sexual reproduction. The number of ova per cocoon varies from 5 to 20 (x = 10.9). The generation period (from cocoon to next cocoon) varies from 14 to 39 days (x = 26.1) according to the period of the year. The number of generations per year is between 7.3 and 26.1 (x = 14). A mature worm can lay between 23.7 and 25.8 cocoons during its life (254 days as maximum observed) at a mean rate of 0.12 cocoon worm^–1 day^–1. Experimental cultures were carried out to determine the structure, density and biomass of the populations. A maximal density of 1 396 314 worms was recorded after 85 days of culture. Net production reached 21.48 g m^–2 day^–1 after 26 days in a culture initiated from cocoons.     

Effect of plant patch shape on the distribution and abundance of three lepidopteran species associated with Brassica oleracea

• 1 Plant patch shape may affect the abundance of herbivorous insects. Patches of the same size but longer or irregular have a higher perimeter/area relationship (P/A) than square or regular ones, which may determine the immigration, emigration and abundance of individuals in the patch.
• 2 Only specialist species should be affected by plant patch shape. Those species that are more abundant in smaller patches should be more abundant in patches with higher P/A, whereas those that are more abundant in larger patches should be more abundant in patches with lower P/A.
• 3 We studied the density of eggs, larvae and pupae of Pieris brassicae, Plutella xylostella and Trichoplusia ni in square (low P/A) and I‐shaped (high P/A) patches of 144 plants of Brassica oleracea. We also estimated their immigration to these patches, and the final plant weight.
• 4 Plant patch shape affected the abundance, but not the distribution, of the two specialist species. Whereas P. brassicae was denser in I‐shaped patches, P. xylostella was more abundant in square patches. The generalist T. ni was not affected by patch shape. Immigration of P. brassicae was higher in I‐shaped patches, but immigration of P. xylostella and T. ni was not affected by patch shape. Plants were heavier in the centre of square patches.
• 5 Our results suggest that plant patch shape affects the density of herbivorous insects and should be considered independently from other plant patch variables when studying the population dynamics of these organisms.

     

Reproductive potential of the earthworm Eisenia foetida

Summary Regression equations are provided for the earthworm Eisenia foetida with respect to age at which 50% of the population became clitellate at 25° C in relation to population density in activated sludge and in horse manure. Regression equations are provided for progeny per cocoon versus weight of cocoon, and weight of cocoon in relation to weight of parent; from these an equation is derived for progeny per cocoon relative to worm weight. Regression equations are given on (a) number of cocoons produced per adult in relation to age and population density from onset of adulthood to median peak production of cocoons, age 10 weeks, and from age 10 weeks to age 27 weeks, and (b) weight of worm in relation to population density and age between ages 5 and 27 weeks. From (a) and (b) a family of equations (c) are derived giving progeny per cocoon in relation to age of adult and population density. From equations (a) and (c) two families of equations are generated giving progeny per adult in relation to ascent to, and descent from, the median week of peak cocoon production in relation to population density. Data also are provided on age at which reproduction terminates in relation to population density, optimum population density for reproduction, and hatchability.     

Optimal use of patches by parasitoids with a limited fecundity

1. a mathematical model is presented which predicts the expected optimal-patch-use strategy for solitary parasitoids with a limited fecundity.
2. The model predicts that the quality of the patches is determined by the proportion of unparasitized hosts and not by the density of those hosts, and that throughout the searching period the parasitoids should maintain the level of parasitism equal in all the patches irrespective of the host density per patch.
3. The spatial pattern of parasitism among field patches by a parasitoid with a low fecundity, Praestochrysis shanghaiensis, was in agreement with the prediction of the model, i.e., a similar level of parasitism in different patches was observed when the ratio of female parasitoids to hosts in the whole study area exceeded 0.07. When the ratio was less than 0.05, however, the level of parasitism per patch showed an inverse relation to the host density, and was positively correlated with the female parasitoid-host ratio.
4. The model assumes that the parasitoids move between patches without cost and have perfect information about patch quality. Consideration of the cost of moving and sampling bridges the gap between the observed and predicted rates of parasitism found when the female parasitoid-host ratio in the whole study area was low

     

Species responses of colonising beetles to variation in patch quality,number, and context in experimental aquatic landscapes

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Spatial variation in the magnitude and functional form of density‐dependent processes on the large skipper butterfly Ochlodes sylvanus

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Impact of cocoon predation and parasitism on endemic populations of the common pine sawfly, Diprion pini (L.) (Hymenoptera, Diprionidae) in different forest types

1 Predation and parasitism on litter‐buried cocoons of the common pine sawfly Diprion pini (L.) were compared in different forest types with endemic sawfly populations by field exposure of laboratory‐reared cocoons during three consecutive years (1993–1995). 2 The impact of cocoon predation was dependent on season and forest type. The highest predation (up to 95%) was found during autumn in forest stands with a dense understory vegetation. 3 Cocoon parasitism varied between year, season and forest type. The highest parasitoid attack was observed in pure pine forests with more or less barren soils, but did not exceed 24% of exposed cocoons. 4 Cocoons were exposed in small patches. Predators tended to exploit all cocoons of a patch, whereas parasitoids only attacked a few cocoons of a patch. Predation was similar on cocoons placed in the litter and those buried more deeply in the soil, whereas parasitism of soil‐buried cocoons was rare. 5 These results indicate that predators can have a remarkable potential for limiting endemic sawfly densities, if habitat conditions in a forest maintain their population and support their foraging behaviour. A notable effect of parasitoids on sawfly cocoons deposited in the litter is obviously restricted to typical pure and barren pine forests, but may play there a similar role as predation.     

Heterogeneity and density dependence in a field study of a tephritid-parasitoid interaction

Abstract.

• 1 The spatial distributions of two tephritid flies (Urophora stylata (Fabricius) and Terellia serratulae L.) attacking thistle flower heads and the levels of parasitism from their associated parasitoid guilds were studied over a 7-year period.
• 2 Using these data it is possible to seek both temporal, density dependent relationships between average levels of parasitism and host density per generation, and also any spatial patterns of parasitism contributing to stability that may be operating within the same field system.
• 3 Parasitism by the two most important generalist parasitoids of T.serratulae is a direct function of average T.serratulae density per year. There is little evidence of any stabilizing heterogeneity arising from the spatial distribution of parasitism within generations.
• 4 Temporal density dependence of Urophora stylata cannot be confirmed from the 7 years of study but there is evidence of spatial heterogeneity which may have an important effect on the dynamics of the host population.

     

The biology of Microctonus caudatus (Thomson), a braconid parasite of the ground beetle Harpalus rufipes (Degeer)

• 1 Microctonus caudatus parasitizes the adults of Harpalus rufipes. It is bivoltine, and its summer generation occurred in up to 27% of the study population of H.rufipes. The mean level of parasitism throughout both 1973 and 1974 was 8.4%.
• 2 Many larvae of M.caudatus are found in one host; the maximum number was 92, mean 20.8. There was indirect evidence of competition between larvae within the host, so that about sixty larvae, at most, were able to develop fully.
• 3 Larvae of the summer generation of M.caudatus emerged from host beetles between the end of July and mid September, invariably killing their host. The larvae pupated in the soil and adult parasites emerged from the pupal cocoons about 14 days later.
• 4 M.caudatus is parthenogenetic, and individuals oviposited readily in adult beetles in the laboratory. A culture of the parasite was maintained for almost a year at 15°C under artificial light of natural outdoor daylength, when four generations developed in the year. Time taken for development within the host was longest under short day conditions.

     

Patterns of parasitism by Trybliographa rapae, a cynipid parasitoid of the cabbage root fly, under laboratory and field conditions

ABSTRACT.

• 1 The spatial patterns of parasitism of the cabbage root fly caused by the cynipid parasitoid Trybliographa rapae (Westw.) have been studied in a laboratory system, within field cages and in a natural situation.
• 2 Continuous observations during the laboratory experiments showed the parasitoids to spend proportionately more time on the patches of high host density. This resulted in the per cent parasitism per patch being directly density dependent.
• 3 Similar patterns of parasitism were found from the field cage system, and also from experiments using the natural parasitoid population and either manipulated or natural host densities.
• 4 While mutual interference was marked in the laboratory experiments, there was little or no sign of it within the larger field cages.

     

The spatial patterns of parasitism of eumenid wasps,Anterhynchium flavomarginatum andOrancistrocerus drewseni by the miltogrammine flyAmobia distorta

1. Spatial patterns of parasitism of eumenid wasps Anterhynchium flavomarginatum and Orancistrocerus drewseni by the miltogrammine fly Amobia distorta were studied in Kyoto, Japan during 1980–1984.
2. In generations of low (<5%) and medium (5–20%) parasitism, percent parasitism per shed (the habitat of the hosts) increased as a function of host density. Conversely, in generations of high (>20%) parasitism, percent parasitism was rather constant over different host densities.
3. The spatial distributions of adult miltogrammine flies among sheds were censused in generations of low and medium parasitism. The frequency of observations of adult miltogrammine flies was higher at sheds of higher host density (aggregative behavioral response), but on the other hand, the adult miltogrammine flies distributed in an underdispersed (or regular) manner in relation to other conspecifics.
4. The spatially density independent relationship between host density and percent parasitism in generations of high parasitism was explained in relation to parasitoid dispersal from patches of high parasitoid density.

     

Patterns of density dependence in growth,reproduction and survival in the invasive freshwater snail Pomacea canaliculata in Japanese rice fields

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The frequency of detection of density dependence in insect orders

Abstract.

• 1 A priori, there are no obvious reasons why patterns should exist in the frequency of density dependence across insect orders. However, orders may reflect related factors which influence population regulation (e.g. life-history patterns and ecology) and are difficult to quantify. The frequency of occurrence of density dependence is compared in 171 time series (of ten or more generations) from Lepidoptera, Hemiptera, Diptera, Odonata, Hymenoptera and Coleoptera. A posteriori attempts are made to identify the cause of observed patterns.
• 2 Buhner's (1975) test found non-delayed density dependence more frequently in Odonata than Lepidoptera and Hymenoptera, which in turn showed non-delayed density dependence more frequently than Diptera, Hemiptera and Coleoptera. Similarly, detection was greater for Odonata than other orders using Dennis & Taper's (1993) test for density dependence and Crowley's (1992) test for attraction. Varley & Gradwell's (1960) test found density dependence less frequently in Hemiptera than other orders. These differences were independent of time series length, temporal trends and numbers of generations per year.
• 3 The reasons for observed patterns in detection of density dependence (and attraction) in insect orders are not clear; however, plausible explanations are differences in: (i) intrinsic growth rate, which is correlated with body size (although evidence to support this hypothesis is weak); (ii) the sampling method used; or (iii) whether individuals come from a single population or many populations.
• 4 Using Turchin's (1990) test, delayed (lag 2) density dependence was detected most frequently in Hymenoptera, which often show delayed diapause or are parasitoids.

     

Integrated control of apple pests in New Zealand 10. Population dynamics of codling moth in Nelson

Abstract

Sampling methods are described for estimating the population density, mortality, and natality of a univoltine population of codling moth attacking mature apple trees (cv. ‘Delicious’) at Nelson, New Zealand. These methods were used to construct life tables for the species over eight generations (1967–68 to 1974–75) on trees variously sprayed and not sprayed with ryania in an integrated control programme. Bait traps provided a sensitive measure of seasonal adult population density. Analysis of the life tables shows that migration of adults was the main key factor and that overwintering larval mortality (particularly that due to bird predation), fecundity, and ryania also made a major contribution to variation in generation mortality. In the absence of ryania the resident population usually increased between generations, whereas it usually decreased when ryania sprays were applied. The density dependence of overwintering larval mortality was due to bird predation, and the inverse density dependence of larval mortality from ryania was due to changes in the site of fruit entry with larval population density. Fecundity was density independent, and inconclusive evidence was obtained on the density dependence of migration. The wide variation in fecundity is attributed primarily to weather conditions. The impact on control strategy of the above key factors, density dependence, and total natural mortality is discussed. Ryania is found to be uneconomic, whereas the granulosis virus of codling moth and male removal with pheromone traps show promise as future control methods. The need to eliminate reservoirs of codling moth close to orchards under integrated pest control is emphasised. Regulation of codling moth populations at Nelson on neglected, unsprayed trees appears to result from intraspecific competition for fruits and cocooning sites, and weakly density-dependent mortality of mature larvae when seeking cocooning sites and while overwintering in their cocoons. Variation in fecundity also cohtributes to fluctuations in abundance of the species. In contrast, at low density in an integrated control programme no intraspecific competition was evident; migration, winter mortality, and fecundity were the main determinants of abundance. This illustrates the need to study pest populations at densities similar to those tolerable commercially.     

Reproductive phenology in Dendrocoelum lacteum (Turbellaria) in South Sweden

SUMMARY.

• 1 L 266 degree-days, above a threshold of 1.0°C, were required for cocoons from the triclad Dendrocoelum lacteum to hatch. The relation is described by ln D=6.12–1.17 1nr (D=number of days, T= temperature).
• 2 Laboratory and field cocoon deposition reached a maximum in late April; peaks of hatchling occurrence were 2 weeks later. The number of hatchlings per cocoon and eocoon viability declined as spring proceeded. Cocoon deposition ceased in June, coincident with regression of the reproductive organs of the adults.
• 3 Newly hatched triclads in the field are thought to avoid stones for their first weeks.
• 4 It is suggested that the earlier and more abundant offspring production in South Sweden than in Britain could be attributed to differences in spring temperature conditions.

     

Foraging strategy of a non-omniscient predator in a changing environment (I) model with a data window and absolute criterion

1. Almost all the models so far presented assume that predators are omniscient in the sense that they always have complete information about the spatial distribution of prey abundance and its change over time. But this type of model cannot cover the situation where the prey abundance in each patch changes over time due to factors other than predation. The model with a data window and absolute criterion (SAC) here enables us to treat such situations.
2. The strategy of non-omniscient predators can be generally devided into four procedures; collection of information, its memorization, decision of tactics and its execution. SAC involves only two tactics; to stay another time period in the patch the predator is staying presently or to move to another patch chosen at random. The choice of either one of the two tactics is made by comparing the profitability of the current patch estimated by the data window with a pre-determined absolute criterion.
3. Three changing patterns of prey abundance are considered. In the most general pattern good patches have a higher mean profitability than poor patches, but the profitability changes cyclically in each of patches.
4. There are only two possibilities for an optimal strategy; the “patch choice strategy” in which once the predator has taken a good patch, it tries to stay there even when the state becomes poor, and the ‘state choice strategy” in which the predator seeks for only good states in good patches. The condition for which either of the two foraging strategies is superior to the other is specified analytically.

     

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.     

Movement of the Apollo butterfly Parnassius apollo related to host plant and nectar plant patches

1. The movement of adults of the endangered Apollo butterfly, Parnassius apollo, was studied using mark–recapture data, within a population consisting of discrete patches of the species’ host plant (n = 43), which were segregated spatially from patches of the species’ main nectar plants (n = 14). 2. The Apollo routinely moved large distances (median 260 m, maximum 1840 m), and moved frequently between the two types of patches. Only 27% (28/105) of the recaptures were made on the same host plant patch as the release. 3. The population acts as a patchy population where the adults mix over the whole area, but successful reproduction can only take place in the discrete host plant patches. 4. Occurrence on a host plant patch was restricted by the area size of the host plant patch and the spatial configuration of nectar plant patches. Thus, although the Apollo is a good flyer, its movement over the patches is still constrained by the segregation of adult and larval resources.