Web(e.g. Baldwin et al. 2001), defence compound production (e.g. Bode, Halitschke & Kessler 2013) and VOC emission (e.g. Dicke & Baldwin 2010), as well as in bioassays mea-suring herbivore survival, performance and locomotion/ feeding behaviour (reviewed in Karban 2011). Although less well understood, plants’ responses to herbivore- Webinteractions (Dicke & Baldwin 2010). Other phytohormones, such as abscisic acid (ABA), gibb-erellins (GBs), auxins and cytokinins (hereafter CKs) have more recently emerged as important defence regulators as well (Robert-Seilaniantz et al. 2007; Robert-Seilaniantz, Grant & Jones 2011). Because the role of CKs in the modu-
REV ISS NPH 12886 204-2 315. - New Phytologist …
WebDicke 1992; Ozawa et al. 2000; Walling 2000; Leitner et al. 2005). These herbivore-specific volatile blends can provide foraging natural enemies of herbivores, such as predators … WebThe jasmonate-regulated sesquiterpene (E)-α-bergamotene and GLV components have been shown to reduce herbivore loads by attracting predators (Allmann & Baldwin, 2010; Halitschke et al., 2008; Kessler & Baldwin, 2001; Schuman et al., 2009, 2015) and predator attrac- tion by the GLV component can increase plant fitness (Schuman et al., 2012). high f number vs low f number
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WebPages 115-184 (March 2010) Download full issue. Previous vol/issue. Next vol/issue. Actions for selected articles. Select all / Deselect all. ... Marcel Dicke, Ian T. Baldwin. … WebDicke & Baldwin 2010; Lucas-Barbosa, van Loon & Dicke 2011). Herbivores can impact plant fitness directly by con-suming flowers and also indirectly through induced phyto-chemical changes that can result in shifts in biosynthetic pathways, and alter interactions between other antagonists and plant mutualists (Kessler, Halitschke & Poveda 2011). WebDicke 2005; Hopkins, van Dam & van Loon 2009; Dicke & Baldwin 2010). This direct form of resistance is effective against generalist herbivorous insects, but generally does high fly travel edison