ELEVATED ATMOSPHERIC CO2 EFFECTS ON PHYTOCHEMISTRY, INSECT PERFORMANCE AND INSECT PARASITOID INTERACTIONS

被引:103
作者
ROTH, SK
LINDROTH, RL
机构
[1] Department of Entomology, University of Wisconsin, Madison, Wisconsin, 53706
关键词
COTESIA MELANOSCELA; ELEVATED CO2; GLOBAL CHANGE; LYMANTRIA DISPAR; TRITROPHIC INTERACTIONS;
D O I
10.1111/j.1365-2486.1995.tb00019.x
中图分类号
X176 [生物多样性保护];
学科分类号
090705 ;
摘要
This study was conducted to examine the effects of CO2-mediated changes in tree chemistry on the performance of the gypsy moth (Lymantria dispar L.) and the parasitoid Cotesia melanoscela (Ratz.). We used carbon-nutrient balance theory to develop hypotheses regarding changes in tree chemistry and the performance of both insects under elevated CO2. As predicted, levels of foliar nitrogen declined and concentrations of carbon-based compounds (e.g. starch and phenolics) increased under elevated CO2. Gypsy moth performance (e.g. growth, development) was altered by CO2-mediated changes in foliar chemistry, but the magnitude was small and varied across tree species. Larvae feeding on high CO2 aspen exhibited the largest reduction in performance, relative to larvae feeding on birch, oak, or maple. Parasitism by C. melanoscela significantly prolonged gypsy moth development and reduced growth rates. Overall, the effect of parasitism on gypsy moth performance did not differ between CO2 treatments. Altered gypsy moth performance on high CO2 foliage in turn affected parasitoid performance, but the response was variable: parasitoid mortality increased and adult female size declined slightly under high CO2, while development time and adult male size were unaffected. Our results suggest that CO2-induced changes in plant chemistry were buffered to the extent that effects on third trophic level interactions were weak to non-existent for the system examined in this study.
引用
收藏
页码:173 / 182
页数:10
相关论文
共 33 条
[1]  
Barbosa P, Saunders JA, Waldvogel MW, Plant‐mediated variation in herbivore suitability and parasitoid fitness, Proceedings of the 5th International Symposium on Insect‐Plant Relationships, pp. 63-71, (1982)
[2]  
Bazzaz FA, Chiariello NR, Coley PD, Pitelka LF, Allocating resources to reproduction and defense, BioScience, 37, pp. 58-67, (1987)
[3]  
Bradford MM, A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein‐dye binding, Analytical Biochemistry, 71, pp. 248-254, (1976)
[4]  
Bryant JP, Chapin FS, Klein DR, Carbon/nutrient balance of boreal plants in relation to vertebrate herbivory, Oikos, 40, pp. 357-368, (1983)
[5]  
Bryant JP, Chapin FS, Reichardt PB, Clausen TP, Response of winter chemical defense in Alaska paper birch and green alder to manipulation of plant carbon/nutrient balance, Oecologia, 72, pp. 510-514, (1987)
[6]  
Burgess AF, Crossman SS, Imported enemies of the gypsy moth and brown‐tail moth, USDA Technical Bulletin, 86, (1929)
[7]  
Coley PD, Bryant JP, Chapin FS, Resource availability and plant antiherbivore defense, Science, 230, pp. 895-899, (1985)
[8]  
Eamus D, Jarvis PC, The direct effects of increase in the global atmospheric CO2 concentration on natural and commercial temperate trees and forests, Advances in Ecological Research, 19, pp. 1-55, (1989)
[9]  
Godfray HCJ, Parasitoids, (1994)
[10]  
Greenblatt JA, Barbosa P, Montgomery ME, Host's diet effects on nitrogen utilization efficiency for two parasitoid species: Brachymeria intermedia and Coccygomimus turionellae, Physiological Entomology, 7, pp. 263-267, (1982)