Airborne signals prime plants against insect herbivore attack.

By Juergen Engelberth, H. Alborn, E. Schmelz, J. Tumlinson. Proceedings of the National Academy of Sciences of the United States of America, 2004

903 citations recorded by the source corpus.

Subfields: Ecology, Insect Science

View Paper: https://www.semanticscholar.org/paper/d9b37ec03d1845ae17dd491215fd6e5876efdd7e

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Citations in the corpus

Plant Volatiles: Recent Advances and Future Perspectives (2006, background): “…induce the expression of defense genes or emission of volatiles in neighboring plants (Arimura et al., 2000; Birkett et al., 2000; Ruther and Kleier, 2005; Farag et al., 2005) or prime these plants to respond faster to future herbivore attack (Engelberth et al., 2004; Kessler et al., 2006).”
Impact of chemical elicitor applications on greenhouse tomato plants and population growth of the green peach aphid, Myzus persicae (2006, background): “…resistance to herbivory or plant pathogens has been documented in over 100 plant systems (Karban & Baldwin, 1997; Heil & Bostock, 2002) including many cultivated crops (Gorlach et al., 1996; Korth & Dixon, 1997; Stout et al., 1998a; Kahl et al., 2000; Omer et al., 2001; Engelberth et al., 2004).”
Ecological and phytohormonal aspects of plant volatile emission in response to single and dual infestations with herbivores and phytopathogens (2013, background): “…they are involved in information transfer between and within plants, through the airborne transport of signals that lead to the priming or expression of defences in neighbouring plants or in distal parts of the emitting plant (Engelberth et al. 2004; Kessler et al. 2006; Frost et al. 2008).”
Stressful 'memories' of plants: evidence and possible mechanisms (2007, background): “Enhanced responses to biotic stresses come under the category of induced defence but in primed plants the defence response is only switched on when an attack occurs after the priming event [12].”
Herbivore‐induced plant volatiles: targets, perception and unanswered questions (2014, background): “This phenomenon was first reported for maize (Zea mays) seedlings that were exposed to HI-VOCs from neighbouring conspecific plants (Engelberth et al., 2004).”
Jasmonate Biosynthesis, Perception and Function in Plant Development and Stress Responses (2013, background): “In monocots, much less is known about the role of JAs, however, it has been shown they are required for sex determination, reproductive bud initiation and elongation, leaf senescence, pigmentation of tissues and responses to the attack by pathogens and insects (Engelberth et al., 2004; Tani et al., ”
Sites of synthesis, biochemistry and functional role of plant volatiles (2010, background): “Besides addressing organisms from other trophic levels, induced VOCs also act on neighbored leaves of other plants (Arimura et al., 2000; Engelberth et al., 2004; Heil and Silva Bueno, 2007).”