Soil‐related habitat specialization in dipterocarp rain forest tree species in Borneo
By P. Palmiotto, Stuart Davies, K. Vogt, M. Ashton, D. Vogt, P. Ashton. 2004
208 citations recorded by the source corpus.
Subfields: Ecology, Evolution, Behavior and Systematics, Nature and Landscape Conservation
View Paper: https://www.semanticscholar.org/paper/71340d641ea52d518c5959e21f422d4d185a58da
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In Ecology, Evolution, Behavior and Systematics
- Jérôme Chave
- S. DeWalt
- C. Baraloto
- Stefan A. Schnitzer
- Charles D. Canham
- Kyle E. Harms
- Kalan Ickes
- Damien Bonal
In Nature and Landscape Conservation
- David A. Coomes
- Jérôme Chave
- Charles D. Canham
- S. DeWalt
- Stefan A. Schnitzer
- C. Baraloto
- G. Kunstler
- Sylvester Tan
Citations in the corpus
- Ectomycorrhizal Associations of the Dipterocarpaceae (2012, background): “In contrast, addition of P in various studies had no effect on % EcM on Shorea leprosula (Suhardi 2000), two species of Dryobalanops in two contrasting soil types (Palmiotto et al. 2004), or on Hopea nervosa and Shorea leprosula (Brearley et al. 2007).”
- A greater range of shade‐tolerance niches in nutrient‐rich forests: an explanation for positive richness–productivity relationships? (2009, background): “Yamada et al. (2007) explored whether the strong preference of Scaphium borneense for sandy ridge tops in a Malaysian tropical rain forest could be related to demographic rates, but found it had rather similar growth and mortality rates on sandy and loamy soils; concluding that its performance relat”
- Soil resource availability shapes community trait structure in a species‐rich dipterocarp forest (2012, background): “Dipterocarp species have spatially aggregated dispersions and habitat preferences in the FDP (Palmiotto et al. 2004; Davies et al. 2005).”
- Liana habitat associations and community structure in a Bornean lowland tropical forest (2006, background): “In addition, calcium, magnesium, and potassium concentrations were found to be greater in alluvial soils (udult) than sandstone hill (humult) soils in northwestern Borneo at Lambir Hills, Sarawak (Palmiotto et al. 2004), and total carbon, nitrogen, and phosphorus were greater on alluvium than sedime”
- Is tropical montane forest heterogeneity promoted by a resource-driven feedback cycle? Evidence from nutrient relations, herbivory and litter decomposition along a topographical gradient (2015, background): “Osono & Takeda 2004; Tateno & Takeda 2010), they are more likely to take large effects in tropical latitudes (including lowland forests with complex topographies such as Lambir, Borneo; Palmiotto et al. 2004).”
- Determinants of whole‐plant light requirements in Bornean rain forest tree saplings (2007, background): “Palmiotto et al . 2004 ) and may contribute to high Bornean tree species diversity (Potts et al . 2002).”
- PERFORMANCE TRADE-OFFS AMONG TROPICAL TREE SEEDLINGS IN CONTRASTING MICROHABITATS (2005, result): “In contrast with a recent field experiment in Malaysian forests that found differential species growth response to soil type (Palmiotto et al. 2004), we found little evidence for differential performance across soil types differing in soil moisture and phosphate availability.”
- EDAPHIC SPECIALIZATION IN TROPICAL TREES: PHYSIOLOGICAL CORRELATES AND RESPONSES TO RECIPROCAL TRANSPLANTATION (2005, background): “We focus on this hypothesis, as species responses to differences in both water and nutrient availability have been implicated in the strong edaphic associations observed in Northern Borneo (Baillie et al. 1987, Itoh 1995, Palmiotto et al. 2004), the location of the present study.”
- Soil‐related performance variation and distributions of tree species in a Bornean rain forest (2005, background): “Furthermore, a reciprocal seedling transplant experiment near Lambir found significantly higher growth rates for all species on clay, but only in gaps (Palmiotto et al. 2004).”
- Censusing and Measuring Lianas: A Quantitative Comparison of the Common Methods 1 (2006, background): “Lambir Hills is a 6800-ha National Park, composed mostly of wet tropical lowland, mixed dipterocarp forest, which receives on average around 3000 mm of precipitation per year with no marked seasonality (Lee et al. 2002, Palmiotto et al. 2004).”