THE INFLUENCE OF TEMPERATURE ON THE LIFE-HISTORY OF INSECTS

Author(s):  
ERNST JANISCH
1962 ◽  
Vol 94 (6) ◽  
pp. 667-671 ◽  
Author(s):  
C. A. Barlow

Life-history and development of Macrosiphum euphorbiae (Thomas) have been studied by Smith (1919), Patch (1925), and MacGillivray and Anderson (1958). In most of these studies, considerable variation in temperature was experienced. The effects of different constant temperatures have never been reported. The following experiments were conducted to determine the influence of temperature on development, survival, and fecundity of M. euphorbiae under closely controlled conditions.


1970 ◽  
Vol 15 ◽  
pp. 41-46 ◽  
Author(s):  
MM Rahman ◽  
W Islam ◽  
KN Ahmed

Xylocoris flavipes (Reuter) is one of the dominant predators of many stored product insect pest including Cryptolestes pusillus. The influence of temperature on predator development, survival and some selected life history parameters was determined. Eggs laid/female (27.27±2.52) and egg hatching rate (%) (88.25±2.19) were highest at 30°C and lowest at 20°C (5.43±1.19 and 30.79±4.63%) respectively but no eggs laid at 15°C. Mortality among immature stages (%) was highest (51.71±1.48) at 35°C and lowest (24.25c±1.14) at 25°C. Developmental times decreasing with the increasing of temperature. Maximum numbers of progeny/female/day (3.55±0.76) were produced at 25°C and minimum (0.83±0.04) were at 20°C.The sex ratios (% female) of X. flavipes were 47.04, 56.68, 51.66 and 50.07 for 20, 25, 30 and 35°C respectively. Survivorship of ovipositing females was highest at 25°C but lowest at 35°C respectively. Key words: Xylocoris flavipes, Cryptolestes pusillus, life history, temperature, developmental time   doi: 10.3329/jbs.v15i0.2201 J. bio-sci. 15: 41-46, 2007


Nematology ◽  
2004 ◽  
Vol 6 (6) ◽  
pp. 883-890 ◽  
Author(s):  
Russell Millar ◽  
David Wharton ◽  
Ian Brown

AbstractPanagrolaimus davidi is a free-living microbivore, associated with moss and algal patches in coastal regions around Ross Island, Antarctica. In laboratory experiments, temperature had a major influence on P. davidi life history parameters. The optimal temperature occurred between 25 and 30°C and the temperature at which population growth ceased was estimated at 6.8°C. Threshold temperatures for developmental processes were in the range 4.1°C (for egg incubation) to 7.6°C (for generation time). The life history strategy of P. davidi shows r-selected features and is more similar to temperate free-living nematodes than to other polar species, which show K-selected features. In the Antarctic, P. davidi is forced to remain dormant for long periods and growth occurs intermittently when conditions allow, suggesting A selection. The life history of P. davidi thus exhibits both A and r-selected features.


1966 ◽  
Vol 56 (4) ◽  
pp. 685-700 ◽  
Author(s):  
J. L. Readshaw

The life-history of Contarinia nasturtii (Kieff.), a gall-forming pest of swedes, was investigated in northern England in 1958–60, particular attention being paid to the influence of temperature and moisture on development in the soil. Most of the observations were made under controlled conditions in the laboratory, although much of the material came from the field.The adults emerge from the soil, mate, and live 1–3 days. In laboratory conditions, each female developed about 95 eggs, laid in batches of 2–50 on the young leaves of the host plant, and produced 78·7±11·4 unisexual larval progeny. The eggs require moist conditions, and hatched according to temperature after 1–10 days at 30–10°C. The larvae fed for 7–21 days at 25–15°C., producing a gall.The full-grown larvae burrow into the soil. It was found that they either pupated in oval-shaped cocoons just below the surface, producing adults 10–48 days later (at 25–12°C.) or become dormant in spherical cocoons. At 32·5°C. the pupae died, and below 32·5°C. males developed faster than females by about 24 hours.Dormancy is caused either by diapause, in which case the larvae require prolonged chilling before development can be resumed, or by drought, in which case development is resumed immediately in response to wetting.The incidence of diapause increased regularly during the summer generations, probably in response to decreasing day-length, and the larvae tended to avoid diapause when placed in high temperatures (e.g., 25°C.). The firmness of diapause appeared to vary according to the conditions experienced by the feeding and full-grown larvae, but, in general, the larvae completed diapause development after 100 days at 2–5°C. followed by 30 days at 20–25°C., i.e., after exposure to conditions similar to those experienced by the diapause larvae during winter and spring.Dormancy due to drought (quiescence) affected both non-diapause and post-diapause larvae; the former became quiescent on entering dry soil (pF>3·5–4·0), and the latter remained inactive if kept in dry or even in moist soil (pF 3·4) after completing diapause. In both cases, the termination of dormancy occurred immediately in response to a thorough wetting of the soil. The larvae left their spherical cocoons, moved to the surface, re-entered the ground and pupated in oval cocoons as if entering the soil for the first time.Factors that delay pupation of C. nasturtii similarly delay the development of its Hymenopterous parasites and hence synchronise the emergence of the adult parasites with the host's feeding stage.


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