Root herbivore effects on above-ground herbivore, parasitoid and hyperparasitoid performance via changes in plant quality

By Roxina Soler, T. Martijn Bezemer, W. H. van der Putten, L. Vet, Jeffrey A. Harvey. 2005

251 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/73a2bf43cc4c92ab02ca437e0c2021bc8b35bdfe

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Citations in the corpus

Factors affecting the evolution of development strategies in parasitoid wasps: the importance of functional constraints and incorporating complexity (2005, background): “Similarly, Soler et al. (2005) reported that intermediate levels of root damage by cabbage root flies had varying effects on the development of an above-ground herbivore and associated parasitoid and hyperparasitoid species.”
Plant-mediated effects in the Brassicaceae on the performance and behaviour of parasitoids (2008, background): “…ze ); P M = p u p al m as s; O V = o v ip o si ti o n b y F 1 ; P A R = ra te s o f p ar as it is m ; S = su rv iv al to p u p at io n /a d u lt h o o d ; S R = se x ra ti o , fe m al e b ia s C. glomerata cocoons originating from plants exposed to root herbivory by D. radicum (Soler et al. 2005).”
Local and systemic induced responses to cabbage root fly larvae (Delia radicum) in Brassica nigra and B. oleracea (2006, background): “Moreover, higher levels of glucosinolates may reduce the effectiveness of natural enemies and higher trophic levels (Harvey et al. 2003; Soler et al. 2005).”
Root and shoot glucosinolates: a comparison of their diversity, function and interactions in natural and managed ecosystems (2008, background): “levels associated with plants (Soler et al. 2005; van Dam and Raaijmakers 2006).”
Root herbivores influence the behaviour of an aboveground parasitoid through changes in plant‐volatile signals (2007, unknown): “Mustard plants are also attacked by specialized root feeding herbivores, including the cabbage root fly, Delia radicum (Diptera: Anthomyiidae) (Coaker and Finch 1971).”
Trait plasticity in species interactions: a driving force of community dynamics (2010, background): “First, community ecology is short of general, mechanistic principles leading to quantitative predictions (Lawton 1999; Simberloff 2004; Lockwood 2008), presumably due to the multitude of direct and indirect interactions between the many species present.”
Herbivore induction of the glucosinolate–myrosinase defense system: major trends, biochemical bases and ecological significance (2008, background): “Attack of two specialist herbivores, one above ground and one below ground led to a 50–70% reduction in leaf glucosinolate content (Soler et al. 2005).”
Summer drought alters plant‐mediated competition between foliar‐ and root‐feeding insects (2007, background): “Parasitoids that developed on P. brassicae larvae feeding on plants subjected to root herbivory by the fly Delia radicum had an increased development time and a decreased cocoon weight (Soler et al., 2005).”
Variation in natural plant products and the attraction of bodyguards involved in indirect plant defense (2010, unknown): “primary and secondary parasitoids (Soler et al. 2005).”
Root-Secreted Malic Acid Recruits Beneficial Soil Bacteria1[C][W][OA] (2008, background): “Indeed, plant basal levels of shoot defenses were significantly altered following not only root herbivory, but also artificial damage and application of plant defense hormones (van Dam et al., 2003; Soler et al., 2005; Rasmann and Turlings, 2007).”
Multitrophic interactions below and above ground: en route to the next level (2011, background): “…be caused by changes in herbivore quality or quantity due to systemically induced resistance in infested plants, which may directly affect the abundance and performance of parasitoids feeding on these inferior hosts (Poveda et al. 2005; Soler et al. 2005; Jansen et al. 2009; Qiu 2011 The Authors.”