Out Of The Quagmire Of Plant Defense Hypotheses

By N. Stamp. The Quarterly review of biology, 2003

1,272 citations recorded by the source corpus.

Subfields: Ecology, Ecology, Evolution, Behavior and Systematics, Nature and Landscape Conservation

View Paper: https://www.semanticscholar.org/paper/76bd2ff2df2ac9ef734809f5d58a19226c2f1e67

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In Ecology, Evolution, Behavior and Systematics

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Citations in the corpus

Causes and implications of the correlation between forest productivity and tree mortality rates (2011, background): “…community-wide mortality rates by selecting for whole groups of species that, independent of their local shade tolerance, strike a particular balance in the trade-off between growth and persistence, particularly growth and defenses (Coley et al. 1985, Grime 2001, Stamp 2003, Endara and Coley 2011).”
Evolutionary ecology of plant defences against herbivores (2011, background): “Other problems remain unresolved: Such as why plant species vary so dramatically in their levels and effectiveness of defences (Stamp 2003; Endara & Coley 2011); whether plant volatiles have evolved as indirect defensive mechanisms (Dicke & Baldwin 2010; Kessler & Heil 2011); and the relative roles…”
Willow genotype, but not drought treatment, affects foliar phenolic concentrations and leaf‐beetle resistance (2004, background): “Models describing how resource availability affects plant allocation to growth and defence are developed with regard to all resources important for plants: light, and nutrient, as well as water (Herms & Mattson, 1992; Hartley & Jones, 1997; Stamp, 2003).”
Can allelopathically active submerged macrophytes stabilise clear-water states in shallow lakes? (2008, background): “The carbon–nutrient balance hypothesis (CNBH; Bryant, Chapin, & Klein, 1983) predicting that the concentration of defensive compounds depends on the availability of nitrogen and light has been vigorously debated over the past years (Stamp, 2003).”
Induced herbivore resistance in seaweeds: a meta‐analysis (2007, background): “We believe that marine studies should, from now on, address more advanced hypotheses, similar to those presented in the terrestrial literature (cf. Stamp 2003; Agrawal 2005).”
Grasses and the resource availability hypothesis: the importance of silica‐based defences (2007, background): “Although theories of defence allocation, of which the RAH is one (Hartley & Jones 1993), have been the subject of debate, the RAH has gained significant support (Stamp 2003).”
Do vigour of introduced populations and escape from specialist herbivores contribute to invasiveness? (2005, methodology): “An extension of the ERH hypothesis applies the assumption of a trade-off between growth and defence (Simms 1992; Stamp 2003) to provide an alternative mechanism for plant invasion.”
Arbuscular mycorrhizal fungi affect plant tolerance and chemical defences to herbivory through different mechanisms (2016, background): “Most theories of plant defence assume that resistance traits are costly for plants, resulting in trade-offs between plant growth rate and chemical defence (Stamp 2003; Agrawal 2011).”
Plant defence theory re‐examined: nonlinear expectations based on the costs and benefits of resource mutualisms (2011, background): “However, current general theories of plant defence are incomplete (Hamilton et al. 2001; Stamp 2003).”