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Sticky plants-those having glandular trichomes (hairs) that produce adhesive, viscous exudates-can impede the movement of, and entrap, generalist insects. Disparate arthropod groups have adapted to these widespread and taxonomically diverse plants, yet their interactions with glandular hosts rarely are incorporated into broad ecological theory. Ecologists and entomologists might be unaware of even well-documented examples of insects that are sticky-plant specialists. The hemipteran family Miridae (more specifically, the omnivorous Dicyphini: Dicyphina) is the best-known group of arthropods that specializes on sticky plants. In the first synthesis of relationships with glandular plants for any insect family, we review mirid interactions with sticky hosts, including their adaptations (behavioral, morphological, and physiological) and mutualisms with carnivorous plants, and the ecological and agricultural implications of mirid-sticky plant systems. We propose that mirid research applies generally to tritrophic interactions on trichome-defended plants, enhances an understanding of insect-plant interactions, and provides information useful in managing crop pests.

Can. ~n t . 109: 415-422 (1977) Of the three large ephydrid flies of Yellowstone's thermal springs, Ephydra thermophila numerically dominates acidic springs because only it can tolerate their water. Alkaline spring effluents are shared by Ephydra bruesi and Paracoenicz turbida. E. bruesi is excluded from alkaline high productivity springs, probably because its larval maturation time is long, relative to the short life of patches of larval habitat. Consequently, such springs support only P. turbida. Proportions of the two species in alkaline low-productivity springs are apparently determined by the proportions of available larval food occurring in still versus flowing water. P. turbida is superior in still water, and E. bruesi wins in flowing water. The analysis leads to predictions ( i ) that E. bruesi should be relatively abundant in low-productivity springs with pulsating flows, and (ii) that E. bruesi adults should prefer ovipositing in low-productivity effluents, while P. turbida adults should be less particular. Volume 109 THE CANADIAN ENTOMOLOGIST 417

Aphid parasite larvae in early stages of development are frequently destroyed when insect predators feed on active aphid prey. Stary (1966) discussed insect predators that may feed on living aphids, and thus destroy parasite eggs or larvae. He noted, however, only one case of direct attack on an aphid mummy: that of chrysopid larvae on Aphis fabae Scopoli parasitized by the braconid Lysiphlebus fabarum (Marshall). No observations were reported of direct attacks on mummified aphids by coccinellids, syrphids, or other aphidophagous insects.

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