Within-plant circulation of systemic elicitor of induced defence and release from roots of elicitor that affects neighbouring plants

By M. Dicke, H. Dijkman. 2001

83 citations recorded by the source corpus.

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

View Paper: https://www.semanticscholar.org/paper/cc783c6e49aab86f320d43c0fd98fd15778dac2a

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In Ecology, Evolution, Behavior and Systematics

In Insect Science

In Plant Science

Citations in the corpus

Resistance to insect pests: What do legumes have to offer? (2006, background): “These same volatile cues attract predators to neighbouring, conspecific plants due to passive and active accumulation of these volatiles cues (Dicke & Dijkman, 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).”
Chemical information transfer between plants: back to the future (2001, background): “, 2001) and among spider-mite infested and uninfested lima bean plants (Dicke and Dijkman, 2001).”
Linking aboveground and belowground interactions via induced plant defenses. (2005, background): “Moreover, compositional changes in leaf VOCs or root exudates might trigger neighbouring plants to induce their defenses [54, 55 ].”
The role of root exudates in rhizosphere interactions with plants and other organisms. (2006, background): “Roots infected with Meloidogyne incognita act as metabolic sinks, and symplastic transport of nutrients from the phloem to the feeding cell, and ultimately the nematode, results in increased leakage into the rhizosphere compared to healthy plants (42).”
Induction of two indirect defences benefits Lima bean (Phaseolus lunatus, Fabaceae) in nature (2004, background): “Although control subclusters produced both HIPVs (Fig. 2a) and EFN (Fig. 3) at low rates, treated subclusters produced both resistance compounds in much higher quantities (Figs 2b and 3). HIPV-release by Lima bean is generally assumed to be induced systemically (Dicke 1994; Dicke & Dijkman 2001 ).”
Do interactions between plant roots and the rhizosphere affect parasitoid behaviour? (2004, background): “Several studies show that the release of induced volatiles is not confined exclusively to the organ attacked but involves all the plant through the circulation of systemic elicitors (Mattiacci et al., 1995; Alborn et al., 1997; Guerrieri et al., 1999; Dicke & Dijkman, 2001).”
Clonal integration beyond resource sharing: implications for defence signalling and disease transmission in clonal plant networks (2004, background): “Experimental studies have shown that herbivores or parasitoid recruiting volatiles may not only be emitted from the site of damage, but systemic induction of volatile emission can lead to the release of gaseous infochemicals from undamaged parts of a plant (Dicke et al., 1993b; Takabayashi and Dicke”
Root-emitted volatile organic compounds: can they mediate belowground plant-plant interactions? (2016, background): “Similarly, Dicke and Dijkman (2001) observed that uninfested lima bean plants became more attractive to the predatory mite Phytoseiulus persimilis Athias-Henriot when they were incubated in a volume of distilled water that had previously contained the roots of a lima bean plant infested with spider…”