Tree species differentiation in growth, recruitment and allometry in relation to maximum height in a Bornean mixed dipterocarp forest

By T. Kohyama, E. Suzuki, T. Partomihardjo, Toshihiko Yamada, T. Kubo. 2003

215 citations recorded by the source corpus.

Subfields: Global and Planetary Change, Nature and Landscape Conservation

View Paper: https://www.semanticscholar.org/paper/f1b8d6e526837deb1000e0f0d4998d4c4ce5c237

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In Global and Planetary Change

In Nature and Landscape Conservation

Citations in the corpus

The contribution of interspecific variation in maximum tree height to tropical and temperate diversity (2005, methodology): “A number of methods have been used to estimate maximum height per species including asymptotic approaches (Thomas 1996) and the choice of the 95th percentile in height among all trees greater than 5 or 10 cm dbh (Kohyama et al. 2003, Poorter et al. 2003).”
Shedding light on shade: ecological perspectives of understorey plant life (2016, background): “A trade-off between growth rate and maximum height of adult plants has been shown to promote coexistence, because shorter species invest fewer resources in support and more in reproduction under shaded conditions (Kohyama et al. 2003).”
Interspecific Relationships among Growth, Mortality and Xylem Traits of Woody Species from New Zealand (2010, background): “Maximum height was an important axis of differentiation among tree species in New Zealand, as in Malaysian, Australian and neotropical rain forests (Thomas 1995; Kohyama et al. 2003; King, Davies & Supardi 2006a; Poorter et al. 2008).”
Tree size distributions in an old-growth temperate forest. (2009, methodology): “For example, reverse-J shape diameter distributions (Hough 1932, Robertson et al. 1978, Kohyama 1986, Niklas et al. 2003) and approximate negative exponential distributions (Meyer 1952, Goff and West 1975, Manion and Griffin 2001, Hitimana et al. 2004) have often been ascribed as an emergent prope”
Alternative height strategies among 45 dicot rain forest species from tropical Queensland, Australia (2005, background): “2b, King 1991; Thomas 1996; Kohyama et al. 2003), thicker stems, lower LMA (Fig.”
Definition and estimation of vital rates from repeated censuses: Choices, comparisons and bias corrections focusing on trees (2017, background): “…dependent mortality m(x) and absolute size- growth rate G(x), with recruitment rate r (or alternatively R or RGf) at minimum individual size xmin (Kohyama et al., 2003, 2015; cf. Equation 13); alternatively time- step models, such as transitionmatrices, require size- class dependent ma and…”
Causes and implications of the correlation between forest productivity and tree mortality rates (2011, background): “…of resources from growth toward reproduction (Silvertown November 2011 537TREE MORTALITY AND FOREST PRODUCTIVITY and Dodd 1999, Turner 2001, Kohyama et al. 2003), thereby slowing growth relative to canopy species of the same size (which may delay reproduction until they reach canopy…”
The role of wood density and stem support costs in the growth and mortality of tropical trees (2006, background): “…is augmented by additional tradeoffs between adult stature and a variety of architectural and photosynthetic characteristics (Thomas & Bazzaz 1999; Kohyama et al. 2003; Poorter et al. 2003) and between mean growth rate and the typical fertility of the soil on which a species occurs (Russo et al.…”
Linking functional traits and demographic rates in a subtropical tree community: the importance of size dependency (2014, background): “Thus, the trend that large-statured species grow faster at a given tree size (in this study, stem diameter) than small-statured species has been confirmed across a wide range of size classes and among several forest types (Kohyama et al. 2003; Poorter et al. 2008; Wright et al. 2010; Martinez-Vilalt”
Functional traits as predictors of vital rates across the life cycle of tropical trees (2016, background): “Extending this, we would expect large-statured species to become reproductive only when they attain a position in the forest canopy (Thomas 1996; Zuidema & Boot 2002), while smaller understorey species will likely reproduce when they obtain optimal crown depth (Kohyama et al. 2003) or foliage cover.”
Allometry, adult stature and regeneration requirement of 65 tree species on Barro Colorado Island, Panama (2006, background): “Again there is a wide range of results on this question (Aiba & Kohyama 1997, Alves & Santos 2002, King 1996; Kohyama et al. 2003, Poorter et al. 2003, Sterck & Bongers 1998, Sterck et al. 2001).”
Capturing diversity and interspecific variability in allometries: A hierarchical approach (2008, background): “The effects of the across-species covariates were generally intuitive and consistent with the literature (Aiba and Kohyama, 1997; Ackerly and Donoghue, 1998; Kohyama et al., 2003; Poorter et al., 2006; Sterck et al., 2001)—shade-tolerant species are generally shorter with broad and deep crowns.”