Trade‐offs between net assimilation rate and specific leaf area in determining relative growth rate: relationship with daily irradiance

By Bill Shipley. 2002

259 citations recorded by the source corpus.

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

View Paper: https://www.semanticscholar.org/paper/1c05cadba04cd5d97881633c93029c2ae42a7fb4

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In Global and Planetary Change

In Nature and Landscape Conservation

In Plant Science

Citations in the corpus

Causes and consequences of variation in leaf mass per area (LMA): a meta-analysis. (2009, result): “not equivocal, as some other reports show ULR to be much better correlated with RGR (Shipley, 2002).”
Specific Leaf Area and Leaf Dry Matter Content of Plants Growing in Sand Dunes (2005, result): “Values of SLA in this study were in the low to middle range compared to those found in plants growing in other field and laboratory conditions (Garnier et al., 1997; Poorter and de Jong, 1999; Meziane and Shipley, 1999; Shipley and Vu, 2002; Ackerly et al., 2002; Shipley, 2002).”
On the link between functional traits and growth rate: meta‐analysis shows effects change with plant size, as predicted (2016, background): “…1994 Huante et al 1995a Huante & Ricon 1997 Hoffman et al 2003 Huante et al 1995b Gleeson & Tilman 1994 Veneklaas et al 2002 Tomlinson et al 2014 Shipley 2002 Hunt & Cornelissen 1997 (a) Original stage: Seedling Juvenile Sapling Adult Mix * Flag: Reassigned Seedlings Saplings Adults Height…”
Seedling growth and morphology of three oak species along field resource gradients and seed mass variation: a seedling age-dependent response (2010, unknown): “The few studies that have explored these relationships under field conditions suggest that the physiological component (NAR) also plays an important role, especially in high light environments (Poorter 1999; Shipley 2002).”
The Ecology of Seeds: References (2005, background): “The predominance of SLA reported in many experiments may be due to the low irradiance that was used (Shipley, 2002).”
Linking growth strategies to long‐term population dynamics in a guild of desert annuals (2007, background): “NAR in determining RGR may be due to environmental conditions (McKenna & Shipley 1999; Meziane & Shipley 1999; Loveys et al. 2002; Shipley 2002) or the time-scale under consideration (Villar et al.”
The ‘hydrology’ of leaves: co‐ordination of structure and function in temperate woody species (2003, background): “However, Klamina may be orthogonal to traits that are also important in carbon economy, such as LMA, which can strongly influence photosynthetic rate per unit leaf mass (Evans 1972; Lichtenthaler 1985; Field & Mooney 1986; Koike 1988; Poorter & Van der Werf 1998; Reich et al. 1999; Wright et al. 200”
Differential responses of plant functional trait to grazing between two contrasting dominant C3 and C4 species in a typical steppe of Inner Mongolia, China (2011, background): “This is because leaf Pn is closely related to plant photosynthetic capacity and relative growth rate (Field and Mooney 1986; Shipley 2002, 2006), and plant stature and leaf size are directly associated with light interception for photosynthesis (Milla and Reich 2007; Poorter and Rozendaal 2008).”