Can aphid-induced plant signals be transmitted aerially and through the rhizosphere?

By K. Chamberlain, E. Guerrieri, F. Pennacchio, J. Pettersson, J. Pickett, G. Poppy, W. Powell, L. Wadhams, Christine Woodcock. 2001

85 citations recorded by the source corpus.

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

View Paper: https://www.semanticscholar.org/paper/fcdce532096631a7116e93c48e80a5c5bc403a45

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In Ecology, Evolution, Behavior and Systematics

In Insect Science

In Plant Science

Citations in the corpus

Clonal integration beyond resource sharing: implications for defence signalling and disease transmission in clonal plant networks (2004, background): “In these studies the distance between infested and control plants is normally about 15 cm or less (e.g. 15 cm for volatiles perception in Karban et al., 2000, less than 15 cm for root exudates perception in Chamberlain et al., 2001 and Guerrieri et al., 2002).”
Root-emitted volatile organic compounds: can they mediate belowground plant-plant interactions? (2016, background): “Positive intraspecific plant-plant interactions have been demonstrated in Vicia faba L. (Chamberlain et al. 2001; Guerrieri et al. 2002) and Phaseolus lunatus L. (Dicke and Dijkman 2001).”
Herbivore‐induced plant volatiles induce an indirect defence in neighbouring plants (2006, background): “…via a systemic signal within the same plant (Dicke & Dijkman 2001; Wäckers et al. 2001) or via the rhizosphere between two different individuals (Chamberlain et al. 2001; Pickett et al. 2003) was excluded in Experiment 3, because we used detached emitter tendrils to expose basifixed receiver…”
Chemical information transfer between plants: back to the future (2001, background): “Furthermore, information is presented on belowground communication among aphid-infested and uninfested faba bean plants (Chamberlain et al., 2001) and among spider-mite infested and uninfested lima bean plants (Dicke and Dijkman, 2001).”
The role of root exudates in rhizosphere interactions with plants and other organisms. (2006, background): “In addition to having direct effects on herbivore behavior, some root exudates induce defense responses in neighboring plants that reduce herbivore populations indirectly by attracting predators and parasites of the offending herbivore (30).”
Arbuscular mycorrhizal fungi and aphids interact by changing host plant quality and volatile emission (2014, unknown): “2012) and aphids (Chamberlain et al. 2001) regulate plant signalling leading to emission of VOCs, a further explanation relates to possible interactive effects of timing of AM fungal colonization with respect to aphid infestation (before AM fungi or after AM fungi) on plant signalling pathways.”
Mixing barley cultivars affects aphid host plant acceptance in field experiments (2002, background): “Recently, changes in aphid responses caused by allopathic interaction between damaged and undamaged plants have been studied (Pettersson et al., 1996; Chamberlain et al., 2001).”
Secondary Metabolites as Plant Traits: Current Assessment and Future Perspectives (2002, background): “They do not only occur above ground (Dicke and Bruin, 2001; Bruin and Dicke, 2001); recent results suggest such signal exchanges occur also below ground, in the rhizosphere (Chamberlain et al., 2001; Dicke and Dijkman, 2001).”
The use of push-pull strategies in integrated pest management. (2007, background): “Specific HIPVs such as methyl salicylate and (Z )-jasmone are attractive to predators and parasitoids and lead to the reduction of pest abundance in the field (17, 65).”
Fungal entomopathogens: new insights on their ecology (2009, background): “Plants also produce semiochemicals that are induced in response to herbivore- induced damage (Chamberlain et al. 2001).”