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
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
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