The influence of host intrapatch spatial distribution on parasitoid host acceptance behavior was investigated with Trichogramma principium parasitizing eggs of grain moth, Sitotroga cerealella. Single females were placed in Petri dishes, each containing 60 host eggs arranged either as a compact patch or partitioned into 60 or 12 clusters each consisting of 1 or 5 eggs, respectively. Partitioned patches provoked parasitization more often than compact patches. The percentage of ovipositing females (i.e., females parasitizing at least one of 60 host eggs) increased with the number of clusters, while it was independent of the intercluster distance over intervals of 2.5-15 mm. The mean number of eggs parasitized by ovipositing females during 48 h was almost independent of the host egg spatial pattern. As a result, the rate of parasitization was higher when the hosts were sparsely distributed within a patch than when they were aggregated., Nataliya D. Voinovich, Taisiya Ya. Umarova, Sergey Ya. Reznik, and Lit
We investigated the effects of genetic differences and host plant density on population development of the rose-grain aphid Sitobion avenae (F.) (Sternorrhyncha: Aphididae) in winter wheat stands. Aphid numbers on ears were recorded on 11 cultivars (6 years) and on plots where crop density was varied by thinning (12 years). Crop density significantly affected whole plant, tiller and ear mass, number of tillers, and leaf area and chlorophyll content. The duration and rate of aphid population growth, and the maximum numbers of aphids were ascertained by weekly counts. Maximum abundances increased with the length of time available for the growth of aphid populations while the rate of population growth was less important. Variation of maximum numbers of S. avenae on different cultivars was not significant, probably due to the small variation in the period available for the development of aphid populations. By contrast, there was a significant Variation of aphid performance associated with host plant density. Aphid populations on solitary plants persisted longer and became more abundant than in dense stands. The prolonged survival of aphid populations was probably caused by an extended period of tillering and lower average age of tillers of solitary plants. There was large annual variation in aphid abundance. It is likely that modifications of host plant development caused by differences in winter weather may contribute to this variation., Alois Honěk, Zdenka Martinková, and Lit
Most studies of responses of insects to elevated carbon dioxide have been made using short-term exposures to treated food plants and have involved measurements of responses in growth, reproduction, food consumption and efficiencies of conversion at specific stages in the life cycle. These will be reviewed in the light of longer-term studies recently published where whole generations have been reared in chambers with simultaneous treatment of plants and where insects have been free to select their food and microenvironment. Factors such as seasonal change in plants, choice of food plant, mode of feeding, timing of exposure, temperature, the role of natural enemies are considered and the whole placed in the context of other aspects of climate change.
It is concluded that in studies to date, the only feeding guild in which some species have shown increases in population density in elevated carbon dioxide are the phloem feeders. Chewing insects (both free-living,and mining) generally have shown no change or reduction in abundance, though relative abundance may be greatly affected. Compensatory feeding is common in these groups., John B. Whittaker, and Lit
Insect cold tolerance mechanisms are often divided into freezing tolerance and freeze intolerance. This division has been criticised in recent years; Bale (1996) established five categories of cold tolerance. In Bale's view, freezing tolerance is at the extreme end of the spectrum of cold tolerance, and represents insects which are most able to survive low temperatures. Data in the literature from 53 species of freezing tolerant insects suggest that the freezing tolerance strategies of these species are divisible into four groups according to supercooling point (SCP) and lower lethal temperature (LLT): (1) Partially Freezing Tolerant-species that survive a small proportion of their body water converted into ice, (2) Moderately Freezing Tolerant-species die less than ten degrees below their SCP, (3) Strongly Freezing Tolerant-insects with LLTs 20 degrees or more below their SCP, and (4) Freezing Tolerant Species with Low Supercooling Points which freeze at very low temperatures, and can survive a few degrees below their SCP. The last 3 groups can survive the conversion of body water into ice to an equilibrium at sub-lethal environmental temperatures. Statistical analyses of these groups are presented in this paper. However, the data set is small and biased, and there are many other aspects of freezing tolerance, for example proportion of body water frozen, and site of ice nucleation, so these categories may have to be revised in the future. It is concluded that freezing tolerance is not part of Bale's (1996) continuum, but rather a parallel, alternative strategy of cold tolerance., Brent J. Sinclair, and Lit
The intertidal collembolan Anurida maritima can endure periods of twice-daily submergence by seawater. The air-breathing terrestrial apterygote insect has developed specific adaptations to prevent respiratory failure during hypoxic stress. When submerged, the animal is initially enclosed by an air-bubble. This bubble lasts three times longer than the small amount of stored oxygen would allow. The air bubble acts not only as an oxygen store but also as a compressible gas gill. This was demonstrated by an O2-needle electrode technique which allowed recordings of pO2 changes in the watery medium close to the animal. Oxygen uptake in A. maritima follows an aerial mode of respiration during the first three hours of submergence. Oxygen consumption rate at decreasing ambient O2 partial pressures showed oxyregulating behaviour during severe hypoxia., Dietmar Zinkler, Raimund Rüssbeck, Marc Biefang, Horst Baumgärtl, and Lit
Climate features that influence life cycles, notably severity, seasonality, unpredictability and variability, are summarized for different polar zones. The zones differ widely in these factors and how they are combined. For example, seasonality is markedly reduced by oceanic influences in the Subantarctic. Information about the life cycles of Arctic and Antarctic arthropods is reviewed to assess the relative contributions of flexibility and programming to life cycles in polar regions. A wide range of life cycles occurs in polar arthropods and, when whole life cycles are considered, fixed or programmed elements are well represented, in contrast to some recent opinions that emphasize the prevalence of flexible or opportunistic responses. Programmed responses ale especially common for controlling the appearance of stages that are sensitive to adverse conditions, such as the reproductive adult. The relative contribution of flexibility and programming to different life cycles is correlated with taxonomic affinity (which establishes the general lifecycle framework for a species), and with climatic zone, the habitats of immature and adult stages, and food., Hugh V. Danks, and Lit
First stadium juveniles of P. angustus were reared under controlled seasonal conditions to maturity, reproduction and death. Individuals born in any one breeding season either had a 1-year or a 2-year life cycle (cohort-splitting). The life cycle was annual for individuals born in the first part of the breeding season (May-August), but became biennial for those born later (August-October). Two phenomena were involved: (1) Only individuals reaching the penultimate stadium (stadium VII) before a critical period at the end of spring could become adult in the breeding season following that of their birth. After this time, stadium VII individuals entered into aestivation and only became adult in the second autumn after their birth. (2) Females becoming adult in autumn entered reproductive dormancy and only laid eggs in the following spring. Overall, individuals born at the start of the breeding season easily reached stadium VII before the critical period and were able to breed at I year, whereas individuals born at the end of the breeding season reached stadium VII after the critical period, then had two consecutive periods of dormancy and only bred at 2 years age. Individuals from the same nest born in the middle of the breeding season (August) could have either annual or biennial life cycles, depending on whether they reached stadium VII before or during aestivation. The environmental factors capable of triggering aestivation in subadults and reproductive dormancy in autumn-maturing females are discussed., Jean-Francois David, Marie-Louise Celerier, Jean-Jacques Geoffroy, and Lit
Myrmica rubra is a northern, temperate Palaearctic ant species with a geographical range that extends from the Atlantic coast of Europe to central Asia. In Europe, its range covers > 25° of latitude where it lives under a variety of climates that vary from extreme oceanic in the west, to continental in the east. Colonies nest in the soil and their life cycles are known to be highly dependent on ambient temperature and soil moisture. We hypothesised that the brood-rearing behaviour of populations might be focally adapted to climate and that we might detect differences when the ants were reared under \"common-garden\" conditions. Brood-rearing behaviour was compared for 38 colonies of M. rubra drawn from 13 populations representing a range of 6 latitudes: all 6 were represented in eastern Europe and 2 in western Europe. A sample of ants from each colony was used to estimate respiration rate, body mass and fat content at the start of the experiment in spring (immediately post hibernation) and at the end of the experiment (mid summer). Respiration had a linear relationship with latitude, with northern populations having greater respiration rate in spring compared to southern populations. It is suggested that this is an adaptation to different seasonality over the species' range that results in the \"more active\" northern workers rearing fewer brood to maturity more quickly than southern workers. Fat content, a measure of worker \"quality\", had a parabolic relationship with latitude with mid latitude colonies having the fattest workers. Fatter workers appeared to rear heavier brood. This probably represented a functional response to environment with populations living at \"edge of range\" sites being physiologically more stressed and performing brood-rearing tasks less well than centre of range populations. We believe that this is the first demonstration of a consistent, intra-specific trend for Variation in the social physiology of an ant species over its geographic range., Graham W. Elmes, Judith C. Wardlaw, Mogens G. Nielsen, Vladilen E. Kipyatko, Elena B. Lopatina, Alexander G. Radchenko, Boyd Barr, and Lit
There is much current discussion about the factors that control the distribution and abundance of animal species, particularly at the edges of their range. The significance of temperature for survival and development is compared in two closely related psyllid species (Craspedolepta nebulosa and C. subpunctata) living on the same host plant (Chamerion angustifolium) (Onagraceae) but displaying different distributions along latitudinal and altitudinal gradients. The following measurements were made at critical periods during the life cycle (a) winter supercooling points (SCPs), (b) tolerance of short (1 min) and long term (1-25) days exposure to sub-zero temperatures above the SCP, (c) tolerance of short term exposure to high spring/summer temperatures and (d) comparative field development rates among species and sites during the early critical part of the growing season. Successful completion of the life cycle is related to heat availability during the growing season. This appears to limit the distribution of the Craspedolepta species, rather than their survival response to thermal extremes. No significant differences were found between the two species in the supercooling point or in their long and short term survival responses at low or high temperatures., Jeremy M. Bird, Ian D. Hodkinson, and Lit