Jasmonate-Induced Responses of Nicotiana sylvestris Results in Fitness Costs Due to Impaired Competitive Ability for Nitrogen

By Ian T. Baldwin, William Hamilton. Journal of Chemical Ecology, 2000

91 citations recorded by the source corpus.

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

View Paper: https://www.semanticscholar.org/paper/58f91f32e050d2ad1bf075991fbd6b59306696ea

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Citations in the corpus

Trade‐offs in community ecology: linking spatial scales and species coexistence (2004, background): “…is common across terrestrial and aquatic systems (Leibold 1989; Balciunas & Lawler 1995; Kraajeveld & Godfray 1998; McPeek 1998; Schmitz 1998; Baldwin & Hamilton 2000; Bohannan & Lenski 2000a,b; Peacor & Werner 2001; Steiner 2003), and indirect evidence, in the response of different groups…”
Out Of The Quagmire Of Plant Defense Hypotheses (2003, background): “For instance, it appears that downregulation of growth rate, beyond that needed due to immediate resource requirements of activated defense, allows plants to reallocate resources, for example, to regrowth processes, which would increase tolerance to herbivory (Baldwin and Hamilton 2000).”
META-ANALYSIS OF SOURCES OF VARIATION IN FITNESS COSTS OF PLANT ANTIHERBIVORE DEFENSES (2002, background): “…were reported also for nitrogen-based defensive compounds such as alkaloids (e.g., Vrieling and van Wijk 1994, van Dam and Baldwin 1998, Baldwin and Hamilton 2000), which by the carbon–nutrient hypothesis are predicted to be produced mainly at high nutrient availability (Bryant et al.…”
Future directions in the study of induced plant responses to herbivory (2005, background): “: +1 607 254 4255; Fax: +1 607 255 8088; E-mail: aa337@cornell.edu 98 Agrawal mediated via changes in the community of carnivores (i.e., indirect defense) (Karban & Baldwin, 1997).”
The Ecological Concept of Costs of Induced Systemic Resistance (ISR) (2001, unknown): “For example, nitrogen supply can have strong influences of several inducible and constitutive defences of tomato (Stout et al., 1998a), and higher costs of induced nicotine production were found in plants growing on soils with lower nitrogen content (Baldwin et al., 1998) or under competitive condit”
Costs and benefits of induced resistance to herbivores and pathogens in plants (2010, background): “For example, the expression of JA-dependent resistance traits impairs the capacity of wild tobacco to compete for nitrogen [208, 229].”
Protozoa and plant growth: the microbial loop in soil revisited. (2004, background): “…(Kraffczyk et al., 1984; Jones & Darrah, 1995; Bonkowski et al., 2001b; Wamberg et al., 2003a,b), interactions with free-living bacteria (Mathesius et al., 2003; Joseph & Phillips, 2003) or production of secondary compounds to defend herbivores (Baldwin & Hamilton, 2000; Cipollini et al., 2003).”
Plant–soil feedbacks contribute to an intransitive competitive network that promotes both genetic and species diversity (2011, background): “However, costs of secondary compounds are often only detectable in competitive situations (i.e., an opportunity cost, Van Dam & Baldwin 1998; Baldwin & Hamilton 2000).”