Jasmonate‐deficient plants have reduced direct and indirect defences against herbivores

By J. Thaler, M. Farag, Paul W. Pare, M. Dicke. 2002

246 citations recorded by the source corpus.

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

View Paper: https://www.semanticscholar.org/paper/49863c51053807813ad6901e56c7fe6bca836af2

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. M. Dicke
2. A. Janssen
3. R. Mumm
4. M. Sabelis
5. E. Pichersky
6. A. Agrawal
7. G. Howe
8. J. Stuefer

In Insect Science

1. M. Dicke
2. A. Agrawal
3. A. Janssen
4. R. Mumm
5. G. Howe
6. E. Pichersky
7. Martin Heil
8. Marc T. J. Johnson

Citations in the corpus

• Can plants betray the presence of multiple herbivore species to predators and parasitoids? The role of learning in phytochemical information networks (2005, background): “Although a role of prey-produced odours in this attraction cannot be fully excluded, evidence so far points at odour components that are of plant origin (Dicke et al. 1990a, b; Takabayashi et al. 1991; Dicke 1994; Thaler et al. 2002; Gols et al. 2003).”
• Variation in natural plant products and the attraction of bodyguards involved in indirect plant defense (2010, background): “Numerous mutants impaired in jasmonate biosynthesis or response, most in Arabidopsis thaliana but also other plant species such as tobacco and tomato, have been characterized (Baldwin et al. 2001; Thaler et al. 2002; Lorenzo and Solano 2005; Schaller and Stintzi 2008).”
• Signal signature and transcriptome changes of Arabidopsis during pathogen and insect attack. (2005, unknown): “Moreover, tomato plants affected in JA production or perception are more susceptible to caterpillar feeding than wild-type plants (Howe et al. 1996; Thaler et al. 2002a).”
• Effects of jasmonate‐induced defenses in tomato on the potato aphid, Macrosiphum euphorbiae (2005, unknown): “…JA-dependent defenses is known to attract the parasitoids and predators of caterpillars and leafminers (Turlings et al., 1990; Thaler et al., 2001; Thaler et al., 2002), and cis-jasmone has also been shown to attract the seven-spotted ladybird Coccinella septempunctata, and the aphid parasitoid…”
• The Tomato Homolog of CORONATINE-INSENSITIVE1 Is Required for the Maternal Control of Seed Maturation, Jasmonate-Signaled Defense Responses, and Glandular Trichome Development Online version contains Web-only data. Article, publication date, and citation information can be found at www.plantcell.org (2004, result): “This interpretation is in agreement with recent studies showing that terpene emission from tomato leaves is stimulated by exogenous MeJA and herbivore attacks that activate JA signaling (Farag and Paré, 2002; Thaler et al., 2002).”
• Current trends in the evolutionary ecology of plant defence (2011, background): “secondary metabolites, or physical barriers that slow herbivore growth) and indirect resistance (traits such as parasitoid-attracting volatiles) should evolve in concert? After all, these traits are often co-regulated at the physiological level (Thaler et al. 2002).”
• Clonal integration beyond resource sharing: implications for defence signalling and disease transmission in clonal plant networks (2004, background): “Nevertheless it seems clear that the jasmonic acid pathway and phloem-transmitted signals play a key role in the systemic induction of defence genes after herbivore damage (e.g. proteinase inhibitor genes in Solanaceae; Stastwick and Lehman, 1999; Thaler et al., 2002a, b; Stratmann, 2003).”