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Coevolution predator-prey

Payne, T.L., J.C. Dickens, and J.V. Richerson Insect Predator-Prey Coevolution Ada Enantiomeric Specificity in a Kairomone-Pheromone System. J. Chem. Ecol. 10, 487-492 (1984). [Pg.62]

Brodie, E. D., Jr., Ridenhour, B. J., and Brodie, E. D., III. (2002). The evolutionary response of predators to dangerous prey hotspots and coldspots in the geographic mosaic of coevolution between garter snakes and newts. Evolution 56,2067-2082. [Pg.439]

During the evolution of bark beetles, their hosts and associated fungi, parasites, predators and organisms, the composition of bark beetle pheromones will probably have been modified as other species evolved responses to components of the pheromone and exerted selection pressures on the beetle population. There is only circumstantial evidence that this might have happened. For example, in the experiments on widely separated populations of 7. pini (Lanier et al., 1972), California beetles attracted more local 7. pini than did New York beetles, and vice versa in New York. However, New York beetles in California attracted far more of the local predator E. lecontei than did the local 7. pini. California and New York 7. pini use different ratios of the enantiomers of ipsdienol as their pheromones. The high resolution of (-)ipsdienol in California populations versus the blend in New York supports the idea of coevolution of chemical systems of predator and prey production of and response to (+ )ipsdienol being eliminated in California by a predator which had evolved specific responses to it. Perhaps in the absence of E. lecontei in New York there was no pressure to resolve the blend. [Pg.347]


See other pages where Coevolution predator-prey is mentioned: [Pg.516]    [Pg.268]    [Pg.268]    [Pg.269]    [Pg.143]    [Pg.837]   
See also in sourсe #XX -- [ Pg.268 ]




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