The functional morphology of juvenile plants tolerant of strong summer drought in shaded forest understories in southern Spain

By L. Sack, P. Grubb, T. Marañón. Plant Ecology, 2003

145 citations recorded by the source corpus.

Subfields: Global and Planetary Change, Nature and Landscape Conservation, Plant Science

View Paper: https://www.semanticscholar.org/paper/63633ca3a451a5dd2c477b3ec17b552b2bf53dab

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Citations in the corpus

Responses of temperate woody seedlings to shade and drought: do trade‐offs limit potential niche differentiation? (2004, background): “…seen above, across species, Tshadefinal mass and T drought final mass were apparently linked with slow high-resource RGR, and with traits potentially conferring a reduced resource demand, such as low SLA and LAR, which are linked with long leaf lifespans (Walters and Reich 1999, Sack et al. 2003).”
Effects of the interaction between drought and shade on water relations, gas exchange and morphological traits in cork oak (Quercus suber L.) seedlings (2005, background): “Although the above-mentioned issue has been profusely studied in terms of changes in biomass allocation and relative growth rate (Burslem et al., 1996; Sack and Grubb, 2002; Sack et al., 2003), there is little information about the physiological response to the interaction of drought and shade (Abra”
New handbook for standardised measurement of plant functional traits worldwide (2013, background): “References on theory and significance: Rabotnov (1950); Schweingruber (1996); Fischer and Stöcklin (1997); Larson (2001); Schweingruber and Poschlod (2005); De Witte and Stöcklin (2010).”
Adjustment of structure and function of Hawaiian Metrosideros polymorpha at high vs. low precipitation (2007, background): “Leaf-specific hydraulic transport capacity facilitates the transport of water from the soil to the leaves, and thus permits a high stomatal conductance at a given water potential gradient (Carey, Callaway & Delucia 1998; Katul, Leuning & Oren 2003; Sack et al. 2003a; Sack & Holbrook 2006).”
Leaf plasticity in response to light of three evergreen species of the Mediterranean maquis (2006, methodology): “The existence of two kinds of leaves in the same plant can be considered as a special case of adaptation ( Rhizopoulou et al. 1991 ).”
Seedling growth and morphology of three oak species along field resource gradients and seed mass variation: a seedling age-dependent response (2010, unknown): “2000), including a reduced demand for resources (Sack et al. 2003).”
Variation in leaf chlorophyll concentration from tropical to cold-temperate forests: Association with gross primary productivity (2018, background): “, 1985), and in comparing sun versus shade adapted species (Johnson et al., 1993; Sack et al., 2003; Johnson et al., 1993).”
Ecological and evolutionary responses of Mediterranean plants to global change. (2014, unknown): “In fact, several studies have shown that certain Mediterranean plants growing under adverse conditions show a conservative strategy, with low plasticity and high phenotypic canalization of physiological and morphological traits (e.g. Valladares et al., 2000, 2002, 2005; Sack et al., 2003; Aranda et ”
Adaptive photosynthetic strategies of the Mediterranean maquis species according to their origin (2004, methodology): “SD [per mm2] was determined from nail varnish impressions of the abaxial lamina immediately to the right of the mid-vein, according to Sack et al. (2003).”
Plant Phenotypic Plasticity in Response to Environmental Factors (2014, unknown): “Phillyrea latifolia [41, 46]”
Structural determinants of leaf light-harvesting capacity and photosynthetic potentials (2006, background): “especially if they are related to plant size, or to developmental age ( Sack et al. 2002, 2003b ).”
Trade-offs in interspecific comparisons in plant ecology and how plants overcome proposed constraints (2016, background): “Six species were studied in detail in south-west Spain by Sack et al. (2003).”