Leaf anatomy as a constraint for photosynthetic acclimation: differential responses in leaf anatomy to increasing growth irradiance among three deciduous trees

By Riichi Oguchi, K. Hikosaka, T. Hirose. 2005

293 citations recorded by the source corpus.

Subfields: Global and Planetary Change, Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/344c0a23f987ff87835d142e987c2fa3816218e2

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Global and Planetary Change

In Molecular Biology

In Plant Science

Citations in the corpus

The role of crown architecture, leaf phenology and photosynthetic activity in promoting complementary use of light among coexisting species in temperate forests (2010, background): “(e.g., Canham 1988; Niinemets 1998; Oguchi et al. 2005; Seino 2009; Sipe and Bazzaz 1994; Sterck 1999; VanPelt and Franklin 1999; Veres and Pickett 1982).”
Causes and consequences of variation in leaf mass per area (LMA): a meta-analysis. (2009, background): “In fully developed leaves, inflexible LVA is the primary factor constraining LMA and leaf photosynthetic adjustment to higher irradiance (Oguchi et al., 2005).”
Physiological and structural tradeoffs underlying the leaf economics spectrum. (2017, unknown): “…(2001), Miyazawa & Terashima (2001), Antonielli et al. (2002), Flexas et al. (2002, 2006a,b, 2007a,b), Slaton & Smith (2002), De Lucia et al. (2003), Oguchi et al. (2003, 2005), Bota et al. (2004), Ethier & Livingston (2004), Parida et al. (2004), Warren (2004, 2008a, 2011), Bernacchi et al.…”
A review of light interception in plant stands from leaf to canopy in different plant functional types and in species with varying shade tolerance (2010, background): “In some studies, the light-driven plasticity in MA has been observed to be larger in shade-intolerant than in shadetolerant species (Bloor and Grubb 2004; Groninger et al. 1996; Oguchi et al. 2005; Portsmuth and Niinemets 2007; Sánchez-Gómez et al. 2006).”
Mesophyll diffusion conductance to CO2: an unappreciated central player in photosynthesis. (2012, background): “Yet, recent studies have shown that the surface of expos d chloroplasts ( Sc) to leaf area ratio ( Sc/S) is generally smaller than Smes/S [15, 59-61], implying that the use of Smes/S as a substitute of Sc/S underestimates the anatomical constraints on diffus ion.”
Morpho-Anatomical Traits for Plant Adaptation to Drought (2012, background): “mesophyll thickness enhances the photosynthetic capacity if it is accompanied by an increase in the number of chloroplasts exposed near the surface area facing the intercellular spaces (Oguchi et al. 2005).”
Within-canopy variation in photosynthetic capacity, SLA and foliar N in temperate broad-leaved trees with contrasting shade tolerance (2014, background): “ORIGINAL PAPER Within-canopy variation in photosynthetic capacity, SLA and foliar N in temperate broad-leaved trees with contrasting shade tolerance”
Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, unknown): “, 2008) or light acclimation (Oguchi et al., 2005; Muller et al., 2009), but we are not aware of similar studies on plant acclimation to different [CO2] and temperature treatments (but see Smith et al.”