Plant-provided foods for predatory arthropods such as extrafloral nectar and protein bodies provide indirect plant defence by attracting natural enemies of herbivores, enhancing top-down control. Recently, ecologists have also recognised the importance of carrion as a food source for predators. Sticky plants are widespread and often entrap and kill small insects, which we hypothesised would increase predator densities and potentially affect indirect defence. We manipulated the abundance of this entrapped insect carrion on tarweed (Asteraceae: Madia elegans) plants under natural field conditions, and found that carrion augmentation increased the abundance of a suite of predators, decreased herbivory and increased plant fitness. We suggest that entrapped insect carrion may function broadly as a plant-provided food for predators on sticky plants.

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.

Avoidance and tolerance of herbivory are important components of plant interactions with herbivores. Their relationship to each other and to plant defense is important in understanding how plants maximize fitness in the face of herbivore pressure. Various tarweed species have populations comprised of both early-season and late-season flowering individuals. Late-season flowering individuals employ a recently described indirect defense against herbivores in which the accumulation of dead insects on their sticky surfaces attracts predatory insects that eat herbivores. In two tarweed species (Hemizonia congesta and Madia elegans), we observed that key herbivores rarely interact with early-season individuals in the field, and early-season individuals did not invest in dense glandular trichomes that cause indirect defense. We conducted field and greenhouse bud-removal experiments to assess tolerance of M. elegans to herbivore damage. We found that lateseason individuals were more tolerant of simulated herbivory than early-season individuals in both the field and the greenhouse. Late-season individuals that were forced into an earlier phenology with a 24-h light cue lost their tolerance to simulated herbivory. One possible mechanism linking phenological avoidance of herbivores with decreased tolerance is that early-season individuals invested less in below-ground biomass than late-season individuals, which may accumulate belowground resources for regrowth at the expense of early flowering.

Many plants employ indirect defenses against herbivores; often plants provide a shelter or nutritional resource to predators, increasing predator abundance, and lessening herbivory to the plant. Often, predators on the same plant represent different life stages and different species. In these situations intraguild predation (IGP) may occur and may decrease the efficacy of that defense. Recently, several sticky plants have been found to increase indirect defense by provisioning predatory insects with entrapped insects (hereafter: carrion). We conducted observational studies and feeding trials with herbivores and predators on two sticky, insect‐entrapping asters, Hemizonia congesta and Madia elegans, to construct food webs for these species and determine the prevalence of IGP in these carrion‐provisioning systems. In both systems, intraguild predation was the most common interaction observed. To determine whether IGP was driven by resource abundance, whether it reduced efficacy of this indirect defense and whether stickiness or predator attraction was induced by damage, we performed field manipulations on H. congesta. Carrion supplementation led to an increase in predator abundance and IGP. IGP was asymmetric within the predator guild: assassin bugs and spiders preyed on small stilt bugs but not vice versa. Despite increased IGP, carrion provisions decreased the abundance of the two most common herbivores (a weevil and a mealybug). Overall seed set was driven by plant size, but number of seeds produced per fruit significantly increased with increasing carrion, likely because of the reduction in the density of a seed‐feeding weevil. Observationally and experimentally, we found that carrion‐mediated indirect defense of tarweeds led to much intraguild predation, though predators effectively reduced herbivore abundance despite the increase in IGP.

Avoidance and tolerance of herbivory are important components of plant interactions with herbivores. Their relationship to each other and to plant defense is important in understanding how plants maximize fitness in the face of herbivore pressure. Various tarweed species have populations comprised of both early-season and late-season flowering individuals. Late-season flowering individuals employ a recently described indirect defense against herbivores in which the accumulation of dead insects on their sticky surfaces attracts predatory insects that eat herbivores. In two tarweed species (Hemizonia congesta and Madia elegans), we observed that key herbivores rarely interact with early-season individuals in the field, and early-season individuals did not invest in dense glandular trichomes that cause indirect defense. We conducted field and greenhouse bud-removal experiments to assess tolerance of M. elegans to herbivore damage. We found that lateseason individuals were more tolerant of simulated herbivory than early-season individuals in both the field and the greenhouse. Late-season individuals that were forced into an earlier phenology with a 24-h light cue lost their tolerance to simulated herbivory. One possible mechanism linking phenological avoidance of herbivores with decreased tolerance is that early-season individuals invested less in below-ground biomass than late-season individuals, which may accumulate belowground resources for regrowth at the expense of early flowering.