Indirect defence via tritrophic interactions.

By Martin Heil. New Phytologist, 2008

742 citations recorded by the source corpus.

Subfields: Ecology, Evolution, Behavior and Systematics, Insect Science

View Paper: https://www.semanticscholar.org/paper/5ee46365acddb5c8f3e30a17d03bdcf79a656331

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Ecology, Evolution, Behavior and Systematics

1. Martin Heil
2. M. Dicke
3. A. Agrawal
4. R. Karban
5. D. Cipollini
6. M. Maffei
7. T. C. Turlings
8. André Kessler

In Insect Science

1. Martin Heil
2. M. Dicke
3. A. Agrawal
4. R. Karban
5. M. Maffei
6. D. Cipollini
7. N. V. van Dam
8. T. C. Turlings

Citations in the corpus

• In the light of new greenhouse technologies: 1. Plant‐mediated effects of artificial lighting on arthropods and tritrophic interactions (2010, background): “Indirect defences, which allow the plant to offer food or shelter to predators and parasitoids that in return control herbivores (Heil, 2008), include the constitutive and induced secretion of extrafloral nectar, the production of cellular food bodies and (acaro-) domatia as well as the induced emis”
• Multitrophic interactions below and above ground: en route to the next level (2011, background): “Most commonly, plants attract members of the third trophic level to reduce herbivore pressure Dicke (1999), Heil (2008) Facilitation A positive effect of the presence of one species on the performance of another species (can, but does not need to be mutualistic) Bronstein (2009) Mutualism An…”
• Defence mechanisms of Brassicaceae: implications for plant-insect interactions and potential for integrated pest management. A review (2010, background): “The term indirect defence, that is generally used when plants attract, nour-ish or house other organisms to reduce pressure from their enemies, has been referred to in the literature only in the last 20 years (Dicke and Sabelis, 1989; see review by Heil, 2008).”
• Herbivore intoxication as a potential primary function of an inducible volatile plant signal (2016, background): “2012) and the absence of conclusive evidence regarding their benefits as tritrophic signals (Schuman, Barthel & Baldwin 2012; Heil 2014) adds to the current uncertainty regarding the evolutionary origin of HIPVs (van der Meijden & Klinkhamer 2000; Janssen, Sabelis & Bruin 2002; Heil 2008; Allison & ”
• Plastic defence expression in plants (2010, background): “…plants can make use of tritrophic interactions and produce traits such as extrafloral nectar (EFN) and volatile organic compounds (VOCs), which enhance the presence of carnivores, thereby reduce herbivore pressure and ultimately cause an ‘indirect defence’ (Price et al. 1980; Heil 2008).”
• Ecological and phytohormonal aspects of plant volatile emission in response to single and dual infestations with herbivores and phytopathogens (2013, background): “…that are produced in response to feeding damage as a navigational system for prey/host location, and much attention has been given to the roles of induced VOCs in mediating tritrophic interactions (Sabelis & Van De Baan 1983; Turlings et al. 1995; Heil 2008; Dicke & Baldwin 2010; Reddy 2012).”
• Defensive plant responses induced by Nesidiocoris tenuis (Hemiptera: Miridae) on tomato plants (2015, background): “Previous studies have demonstrated the role of JA in indirect defense mechanisms, which results in attraction of natural enemies to plants (Heil 2008; Dicke 2009).”
• Predicting novel herbivore–plant interactions (2013, background): “Numerous examples of plant-mediated tri-trophic interactions exist (Heil 2008).”
• Field parasitism rates of caterpillars on Brassica oleracea plants are reliably predicted by differential attraction of Cotesia parasitoids (2009, background): “Our analyses of the headspace of the three cultivars show that they differed most in the amount of terpenoids emitted, a ubiquitous class of HIPVs which are hypothesized to play a role in attracting parasitoids and predators (Takabayashi et al 1994; Kappers etal 2005; Schnee et al 2006; Heil 2008).”
• Trade‐offs between direct and indirect defences of lima bean (Phaseolus lunatus) (2008, background): “While traits such as cyanogenesis directly affect the herbivores, indirect defences generally act via the third trophic level (Paré & Tumlinson 1999; Heil 2008).”
• Sites of synthesis, biochemistry and functional role of plant volatiles (2010, background): “Wild Lima beans significantly benefited from induced increased nectar production in terms of less leaf damage, and higher growth rates and seed production, respectively (Kost and Heil, 2008).”
• Deciphering Chemical Language of Plant Communication (2016, background): “2013), recruit predators and parasitoids (Heil 2008) and mediate plant–plant communication (Heil and Ton 2008).”
• Current trends in the evolutionary ecology of plant defence (2011, background): “(c) Pseudomyrmex peperi workers consuming extrafloral nectar and serving as an indirect defence of Acacia collinsii (Photo by Martin Heil, modified from Heil 2008; with permission of New Phytologist).”
• Plant Defense against Insect Herbivores (2013, background): “Lectins Lectins are sugar-binding proteins found especially in storage organs and protective structures of some plants, particularly Leguminosae.”
• Latitudinal variation in herbivory: influences of climatic drivers, herbivore identity and natural enemies (2015, result): “Th ese results run counter to previous investigations reporting that top – down eff ects of the third trophic level on insect herbivores are greater in warmer, less seasonal climates, which are characteristic of lower latitudes (Coley and Aide 1991, Novotny et al. 1999, Heil 2008).”
• Direct and indirect root defences of milkweed (Asclepias syriaca): trophic cascades, trade‐offs and novel methods for studying subterranean herbivory (2011, background): “Indeed, the interplay between plant resistance and attraction of natural enemies of herbivores has been of long-standing interest (Price et al. 1980; Boethel & Eikenbary 1986; Thaler 1999; Heil 2008; Mooney et al. 2010).”
• Genetic and environmental interactions determine plant defences against herbivores (2011, methodology): “To date, a defensive function against herbivores could be unambiguously demonstrated for cyanogenesis (Ballhorn & Lieberei 2006; Ballhorn et al. 2009a) and EFN secretion (Kost & Heil 2008), but not for the release of VOCs (but see Heil 2004).”