Optimal size of storage for recovery after unpredictable disturbances

By Yoh Iwasa, T. Kubo. Evolutionary Ecology, 2004

234 citations recorded by the source corpus.

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

View Paper: https://www.semanticscholar.org/paper/bd8d44db68597b9f3206c4903d87f8ba5204302f

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Citations in the corpus

The Evolutionary Ecology of Sprouting in Woody Plants (2003, background): “Indeed, the only analytical model exploring optimal allocation patterns for sprouting has been developed in the context of temperate deciduous forests (Iwasa and Kubo 1997).”
Plant size and resprouting ability: trading tolerance and avoidance of damage? (2006, background): “Resprouting ability is under selection pressure not only from disturbance regimes but also from site productivity and climate (Specht 1981; Lamont & Markey 1995; Midgley 1996; Iwasa & Kubo 1997; Kruger et al. 1997; Ojeda 1998; Bellingham & Sparrow 2000; Clarke et al. 2005).”
Soil water availability effects on seed germination account for species segregation in semiarid roadslopes (2007, unknown): “the characteristic allocation of resources to storage (carbohydrates) in sprouting species which has an important cost on growth or reproduction (Iwasa and Kubo 1997; Bond and Midgley 2001; GuerreroCampo et al. 2006).”
The effects of mowing and fertilization on carbohydrate reserves and regrowth of grasses: do they promote plant coexistence in species-rich meadows? (2001, background): “Finally, we expect that fertilization is more beneficial for plants with large carbohydrate storage than for plants with a small storage because plants with specialized storage organs are able to utilize nutrientsmore efficiently (Iwasa and Kubo, 1997).”
Plant persistence traits in fire-prone ecosystems of the Mediterranean basin: a phylogenetic approach (2005, background): “If resprouters tend to allocate resources to belowground resources (Bell and Ojeda 1999, Schwilk 2002), then juveniles of resprouters should grow slower than juveniles of nonresprouters which lack resprouting structures (Chapin et al. 1990, Iwasa and Kubo 1997).”
To resprout or not to resprout: factors driving intraspecific variability in resprouting (2012, background): “of plants to quickly acquire resources for sustaining the maintenance costs and avoiding reserve depletion (Chapin III et al. 1990; Iwasa and Kubo 1997), and thus it should be positively correlated with the probability of plant survival (Moreno and Oechel 1991).”
Leaf area renewal, root retention and carbohydrate reserves in a clonal tree species following above‐ground disturbance (2002, background): “The resilience of the clone, in terms of renewal of above-ground stems and leaves, initially relies on reserves mobilized from below-ground organs that are protected from disturbance (Bowen & Pate 1993; Iwasa & Kubo 1997; Sakai et al .”
Seasonal changes in carbohydrate reserves in mature northern Populus tremuloides clones (2003, background): “Most studies on the seasonal movement and storage of carbohydrates in mature trees suggest that the root system is the main storage organ especially for species which grow in locations with frequent disturbances (Loescher et al. 1990; Iwasa and Kubo 1997).”
Leaf traits and resprouting ability in the Mediterranean basin (2006, background): “We can expect that the leaf performance of resprouters should permit enough carbon assimilation to meet the high metabolic demands of resprouting (Bloom, Chapin & Mooney 1985; Pate et al. 1990; Iwasa & Kubo 1997).”