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We compared stand composition and structural attributes (i.e., snag and veteran tree densities, tree size variability, and maximum tree size) at sites found to be mixed-severity, as well as those found to be high-severity after recent (<150 years) and older (⩾150 years) stand-replacing fires.
A popular method of species grouping is "size-growth ordenation" which involves the simultaneous consideration of maximum tree size and average growth rate.
The maximum tree size was represented by the 95th percentile of the size distribution rather than the maximum observed size (King et al. 2006) to prevent bias from any errors or outliers.
Life-history traits tested are wood density (WD), maximum tree size (D950.1), and mortality rates for trees ≥ 10 cm DBH (MD10 and RGRD10, respectively).
One main disadvantage of CARTs is their tendency to grow huge trees by selecting splitting variables which lead to a maximum tree size.
We used principal components analysis (PCA) to examine the relationship between wood chemical traits (H, L, Cconv) and species' relative growth rate (RGR), mortality rates (M), WD and maximum tree size.
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In this analysis, the minimum tree sizes in mixed stands were smaller and the maximum tree sizes were greater, but the mean size was rather similar to monocultures.
Under a simplified multispecies coalescent model in which population sizes are assumed constant across populations, Liu et al. [ 32] have shown that the Maximum Tree, a species tree with the largest possible branch lengths under the constraint that gene coalescence times across loci always predate species divergence times, is the maximum likelihood estimate (MLE) of the species tree.
The peak in (g) at about 3150 BC followed by the maximum tree and site sample size suggest a major climatic event at this time.
In contrast to flower production (where small flowered species produce more flowers than larger flowered species), there was not a significant effect of flower size in any of the three most likely models analysing absolute values of maximum fruit production (Fig. 2c) or in the single most likely model of maximum fruit production scaled to tree size (Fig. 2d).
Additionally, we estimated the self-thinning line at this point in stand development and compared the size density relationship in this forest to the theorized (−1.605) log log slope of Reineke's Rule, which relates maximum stand density to average tree size.
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