Interspecific variation in sapling mortality in relation to growth and soil moisture
By John P. Caspersen, R. Kobe. 2001
115 citations recorded by the source corpus.
Subfields: Global and Planetary Change, Nature and Landscape Conservation
View Paper: https://www.semanticscholar.org/paper/c41d8e1d7b1666b5f3691aa031894b8706c9b30a
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In Global and Planetary Change
In Nature and Landscape Conservation
Citations in the corpus
- Sapling size influences shade tolerance ranking among southern boreal tree species (2006, background): “…change not only in relation to environmental conditions and variability (Kubota 479 Sapling size influences shade tolerance © 2006 British Ecological Society, Journal of Ecology 94, 471–480 et al. 1994; Clark et al. 1996; Caspersen & Kobe 2001), but also due to ontogenetically related constraints.”
- The functional morphology of juvenile plants tolerant of strong summer drought in shaded forest understories in southern Spain (2003, background): “Many plants around the world, however, do tolerate drought in deep shade (say Caspersen and Kobe (2001) , Sack and Grubb (2002)).”
- Factors predisposing episodic drought‐induced tree mortality in Nothofagus– site, climatic sensitivity and growth trends (2004, background): “These juveniles may have been susceptible because they were located in more exposed positions or had less access to more permanent ground water sources, due to less allocation to roots relative to shoots ( Caspersen & Kobe 2001 ).”
- Is drought the main decline factor at the rear edge of Europe? The case of southern Iberian pine plantations (2012, background): “The proposed trade-off is premised on the assumption that competition tolerance is achieved by maximizing low-light carbon gain (Smith and Huston, 1989; Caspersen and Kobe, 2001), which increases stomatal conductance of both carbon dioxide and water vapor; higher in P.”
- Effects of shade on growth and mortality of maple (Acer pseudoplatanus), ash (Fraxinus excelsior) and beech (Fagus sylvatica) saplings (2007, background): “Up to now, it is frequently used in investigations on shade tolerance of young trees ( Caspersen and Kobe, 2001 ; Lin et al. , 2002 ; Kunstler et al. , 2005 ; Kneeshaw et al. , 2006 ), sometimes with modifi - cations ( Wyckoff and Clark, 2000 , 2002 ; Delagrange et al. , 2004 ; Gratzer et al. ,…”
- Impact of the invasive shrub glossy buckthorn (Rhamnus frangula L.) on juvenile recruitment by canopy trees (2004, methodology): “We cannot estimate species differences in mortality with confidence because the parameters relating mortality to growth estimated by Kobe et al. (1995) and Caspersen and Kobe (2001) did not differ significantly among our study species.”
- Responses of temperate woody seedlings to shade and drought: do trade‐offs limit potential niche differentiation? (2004, background): “…differences in the responses of woody seedlings to shade and drought drive establishment patterns, especially in combination with variation in responses to nutrient supply and biotic factors (Streng et al. 1989, Burslem 1996, Grubb et al. 1996, Kollmann and Grubb 1999, Caspersen and Kobe 2001).”
- The impact of deer on relationships between tree growth and mortality in an old-growth beech-maple forest (2007, methodology): “relationships often determine which species persist within shaded understories (e.g., Kobe et al., 1995; Kobe, 1996, 1999; Pacala et al., 1996; Kobe and Coates, 1997; Caspersen and Kobe, 2001).”