A New Model for Size-Dependent Tree Growth in Forests

Masae Iwamoto Ishihara; Yasuo Konno; Kiyoshi Umeki; Yasuyuki Ohno; Kihachiro Kikuzawa

doi:10.1371/journal.pone.0152219

Abstract

Tree growth, especially diameter growth of tree stems, is an important issue for understanding the productivity and dynamics of forest stands. Metabolic scaling theory predicted that the 2/3 power of stem diameter at a certain time is a linear function of the 2/3 power of the initial diameter and that the diameter growth rate scales to the 1/3 power of the initial diameter. We tested these predictions of the metabolic scaling theory for 11 Japanese secondary forests at various growth stages. The predictions were not supported by the data, especially in younger stands. Alternatively, we proposed a new theoretical model for stem diameter growth on the basis of six assumptions. All these assumptions were supported by the data. The model produced a nearly linear to curvilinear relationship between the 2/3 power of stem diameters at two different times. It also fitted well to the curvilinear relationship between diameter growth rate and the initial diameter. Our model fitted better than the metabolic scaling theory, suggesting the importance of asymmetric competition among trees, which has not been incorporated in the metabolic scaling theory.

Citation: Ishihara MI, Konno Y, Umeki K, Ohno Y, Kikuzawa K (2016) A New Model for Size-Dependent Tree Growth in Forests. PLoS ONE 11(4): e0152219. https://doi.org/10.1371/journal.pone.0152219

Editor: Harald Auge, Helmholtz Centre for Environmental Research - UFZ, GERMANY

Received: September 16, 2015; Accepted: March 10, 2016; Published: April 1, 2016

Copyright: © 2016 Ishihara et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Data Availability: All relevant data are within the paper and its Supporting Information file.

Funding: MII was supported by the Environmental Research and Technology Development Fund (S-9-3) of the Ministry of the Environment, Japan.

Competing interests: The authors have declared that no competing interests exist.

Introduction

It is important to understand and predict tree growth because it is related to the productivity and dynamics of forest stands. Furthermore, tree growth rate is an important demographic parameter, together with mortality and recruitment rates [1]. Among various measurements of tree growth, diameter of tree stem has been most widely monitored because of the easiness and accuracy of the measurement compared to tree height.

There are several theoretical models to express stem diameter growth of individual tree. One of the simplest is a model based on the metabolic scaling theory. Enquist et al. [2] predicted that stem diameter growth rate scales to the 1/3 power of the diameter. This prediction was deduced from the assumption that growth rate of tree biomass is proportional to its gross photosynthetic rate, which in turn is determined by leaf biomass. This assumption means that both small and large trees have the same resource availability per unit leaf biomass.

However, resource availability may depend on tree size. In a closed forest stand, light is a limited resource and tree growth is governed mainly by light conditions [3–5]. Availability and competition for light is size-dependent and asymmetric [6–8]. Larger trees have an advantage over smaller trees, since the former shade the latter but the latter rarely do so [9]. In some extreme cases, competition is one-sided: larger tree suppress the growth of smaller trees but not vice versa [7,10,11]. Recent studies [6,12] extended the metabolic scaling theory to incorporate asymmetric competition. Their model fitted better to the data of natural forests than that of Enquist et al. [2], suggesting the importance of asymmetric competition.

Here, we propose a new theoretical model for tree diameter growth that implicitly considers asymmetric competition by extending the model of Kikuzawa [10]. Our model is based on a tree size distribution function. Frequency distribution of the tree biomass is often inverse J-shaped with many small trees and few larger trees. Small size differences among trees at the seedling or sapling stage due to genetic factors or slight differences in environmental conditions at the micro site will be amplified by competition among individuals. The initial normal frequency distribution in biomass becomes skewed to the right under asymmetric competition [7,11,13,14]. Such skewed size distribution can be expressed in Y-N curve: Y = N/(AN + B) [15] where Y is the cumulative tree biomass in the stand summed for the largest N trees and N is the rank of a tree ordered from the largest to the smallest tree. This relationship fitted to both even-aged plantation and uneven-aged natural forests [15,16]. Our model is based on this Y-N curve, which was later derived theoretically from a growth model assuming asymmetric competition [17]. We tested assumptions of our model and the fit of our model against tree growth data of multi-species secondary deciduous broadleaf forests in Hokkaido, northern Japan. We compared our model to the model by Enquist et al. [2].

Materials and Methods

Model of Enquist et al. (1999)

Enquist et al. [2] proposed a model for stem diameter growth on the basis of the metabolic scaling theory. They started from the assumption that whole plant biomass growth rate (dM/dt) is proportional to leaf biomass (L_B) (1) where M is whole plant biomass, t is time, C_G is a constant [18,19]. Here, leaf biomass L_B is proportional to the 3/4 power of individual tree volume V (= M/ρ; ρ being the density of tree body). On the other hand, stem diameter of a tree is proportional to the 3/8 power of the tree’s volume. By using these allometric correlations, Enquist et al. [2] obtained the following equation for stem diameter growth: (2) where C is the proportionality constant. By substitution and integration from t = 0 to t = T, they derived the following equation: (3)

The 2/3 power of stem diameter at time T (D_T) can be expressed as a linear function of the 2/3 power of the initial stem diameter (D₀), having a positive intercept and a slope of unity. Enquist et al. [2] argued that this equation was held in a secondary tropical forest.

Alternative new model

We developed an alternative tree growth model by extending that of Kikuzawa [10]. This model is based on six assumptions that will be described in the following parts:

Assumption 1: Y-N curve fits to the size frequency distribution of trees.
Assumption 2: A tree’s rank does not change with time.
Assumption 3: Stand biomass follows a power function of the height of the highest individual in the stand.
Assumption 4: Allometric relationship between tree biomass and tree height.
Assumption 5: Parameter B scales with parameter A of Y-N curve.
Assumption 6: Individual tree biomass scales with the 8/3 power of stem diameter.

Hozumi et al. [15] observed in natural forests and a plantation that the size frequency distribution of trees is inverse J-shaped, with many small trees and few larger trees. In many cases [15,16], such size hierarchy can be expressed by the following equation (assumption 1): (4) where Y is the cumulative biomass in the stand summed from the individual with largest biomass to the N-th largest tree, N is the rank of a tree ordered from the largest individual, and A and B are parameters that are constants but change with time. Later, this equation was derived theoretically from the tree growth model that assumed asymmetrical competition [17]. Therefore, this relationship stands on a firm ground.

Under Eq (4), the biomass of an individual tree (M) that comprises the stand is expressed by the following equation [15]: (5)

This equation means that individual tree’s biomass is expressed as the function of N, the tree’s rank. Individual tree biomass of the same rank but different time (t = 0, T) will be expressed by the following equations: (5’) (5”)

Kikuzawa [10] suggested that under one-sided competition, individual tree’s rank changes little. Assuming that an individual tree’s rank does not change between two different times (assumption 2), we can eliminate N from Eqs (5’) and (5”) and obtain the following relationship between M₀ and M_T: (6)

Parameters A and B have biological meanings, and there is a relationship between parameters A and B [10]. Parameter A is a reciprocal of stand biomass (Y_max) [15]: (7)

Y_max was assumed to be expressed as follows (8) where d is stand biomass divided by the height of the highest individual in the stand (H_max). Kira and Shidei [20] define d as dry matter density and stated that d takes a constant value of 1–1.5 kg/m³, irrespective of stand height. By generalizing their findings, Kikuzawa [10] found that d is also a function of H_max: (9) where a is a parameter and K₁ is a constant. When a = 0, Eq (9) will be consistent with the statement of Kira and Shidei [20]. Substituting Eq (8) by Eq (9) will yield the following power function between stand biomass and the height of the highest individual in the stand (assumption 3): (10)

Substituting Eq (7) by Eq (10), we obtain (11)

Parameter B is the reciprocal of the maximum individual biomass of the stand (M_max) [15]: (12)

Kikuzawa [10] assumed that tree biomass M has an allometric relationship with tree height (H) (assumption 4) [21]: (13) where b is a parameter and K₂ is a constant. Applying this allometric relation to the maximum individual biomass (M_max), we obtain: (14)

By applying Eqs (14) to (12), we obtain: (15)

From Eqs (11) and (15), the scaling relationship between A and B is obtained (assumption 5) for full-density stands as follows: (16) where K₃ and c are constants.

Substitution of Eq (16)) in Eq (6) will yield the following: (17)

This equation shows the relationship between the biomass of the same ranked tree at a different time under the condition that Eq (4) is equally held at different times.

West et al. [22] and Enquist et al. [2] showed that the biomass of an individual tree is proportional to the 8/3 power of stem diameter D, M = K₄D^8/3 (assumption 6). Eq (17) can be rewritten considering this allometric relationship as follows: (18)

This equation expresses the relationship between the 2/3 power of stem diameter at t = T to the 2/3 power of the initial stem diameter (t = 0) and may be an alternative to the prediction of Enquist et al. (Eq 3).

Moreover, the diameter growth rate, dD/dt ≈ (D_T—D₀)/Δt, can be obtained using Eq (18): (19)

By using this equation, we can examine the relationship between diameter growth rate and initial size (D₀).

Data set

To test the six assumptions of our model and the fit of our model (Eqs 18 and 19) and the model of Enquist et al. [2], we used data sets of 11 secondary deciduous broadleaf forests in Hokkaido, northern Japan (Table 1). Mean annual temperature and annual precipitation during past 30 years at the nearest meteorological stations of 11 forests were 5.5–7.3°C and 887–1415 mm, respectively. Permanent plots between 25 m² and 2500 m² in area were set. The number of trees per hectare ranged from 2,000 to 200,000 (Table 1). Stand age and maximum stem diameter in each plot were highly correlated (r = 0.978, P<0.001). Therefore, we used stand age and the maximum stem diameter as a surrogate of stand maturity and named the plots in order of maturity: plot 1 the youngest and plot 11 the most mature.

Download:

Table 1. Description of plots used for analyses.

https://doi.org/10.1371/journal.pone.0152219.t001

Plots 1 to 5 were young forests that naturally regenerated after scarifications, dominated by birch trees (Betula ermanii and B. maximowiczii) [10,23,24] (S1 Table). Plot 5 was artificially thinned. Plots 6, 7, 8, 9, and 10 were relatively mature mixed forests of birches and some other tree species such as oak (Quercus crispula), maple (Acer mono and A. japonicum), and others that naturally regenerated after forest fires. Plot 11 was the most mature secondary forest that had been regenerated after fuel wood production and composed of oak, Carpinus laxiflora, Prunus sargentii, and other tree species. A few conifer trees (Abies sachalinensis) grew in plot 10 and 11.

Stem diameters at breast height (1.3 m aboveground) were measured using a measuring tape or a caliper for a 1- or 2-year interval for 7 to 15 years. The position of diameter measurement was marked with paint. Tree height was measured only in plots 1–5 for all censused years. All trees in each plot were analyzed together, regardless of species, but trees that died during the census were excluded from the analyses. When D_T < D₀, diameter growth (dD) was set as 0.

Analysis

To test the equation of Enquist et al. [2] (Eq 3), we conducted reduced major axis (RMA) regression of the 2/3 power of the initial stem diameter (D₀) to the 2/3 power of the diameter at final census t = T (D_T). RMA regression, one of model II regression methods, was used because the relationship between D₀ and D_T does not imply a direct causal relationship [25]. The lmodel2 function of R 2.15.3 was used to calculate the slope and intercept for RMA regression.

We tested the six assumptions used to derive our model. To test assumption 1 and 3–6, individual tree aboveground biomass was estimated by using an allometric equation. Although site- and species-specific allometric equations may give most accurate biomass estimates, we did not have an allometric equation for the studied forests and for each species. Recent studies [26,27] showed that generic multi-species equation created from compiled data is the best available choice when site-specific equation is not available. Thus, we decided to use a generic allometric equation created for natural forests in Japan [27]: where M is aboveground biomass of a tree, D is stem diameter at breast height, δ is species-specific wood density, and CF is the correction factor, which is 1.029 in this case. This equation was created from the compiled data of 1203 trees belonging to 102 species (60 deciduous angiosperm, 32 evergreen angiosperm, and 10 evergreen gymnosperm species) harvested from 70 natural forests all over Japan. This equation provided a similar biomass estimate as an allometric equation that had tree height as an additional predictive variable [27].

To test the assumption 1 (Y-N curve fits to the size-frequency distribution of trees), Eq (4) was fitted to the data by non-linear regression for each plot and each year via nls function of the R software.

To test the assumption 2 (a tree’s rank does not change with time), Spearman’s ρ was calculated between the rank at the initial census and that at the last census.

Assumptions 3 and 4 were tested in plots 1–5 where tree height was measured. In plots 6–11, tree height was too high to be measured accurately and only assumption 5 that was derived from the assumption 3 and 4 was tested. To test the assumption 3 (stand biomass follows a power function of the height of the highest tree in the stand), we calculated stand biomass by summing aboveground biomass for all trees in each plot for each census year. Log-transformed stand biomass was regressed to the log-transformed height of the highest individuals by ordinary least square (OLS) regression. To test the assumption 4 (allometric relationship between tree biomass and tree height), log-transformed aboveground biomass was regressed to log-transformed tree height by OLS regression for each plot and census year. Note that the above generic allometric equation used to estimate aboveground biomass [27] did not include tree height as a predictive variable, so the relationship between tree biomass and tree height, if it does exist, is not an artifact.

We tested the assumption 5 about the relationship between A and B by fitting ln (B) = ln (K₃) + c × ln (A) to the parameter estimates of A and B obtained after fitting Y-N curve (assumption 1) by ordinary least square (OLS) regression and parameters K₃ and c were obtained.

To test the assumption 6 (individual tree biomass scales with the 8/3 power of stem diameter), ln (M) = ln (K₄) + e × ln (D) was fitted to log-transformed tree aboveground biomass (M) and log-transformed stem diameter (D) by RMA and OLS regressions. Because M was estimated from the allometric equation, which is the polynomial function of stem diameter, the scaling of M to D may be an artifact. Therefore, we also tested this assumption by using another dataset that had been used to create the generic allometric equation in Japan [27,28]. The dataset included measured aboveground biomass and stem diameter of 1203 trees destructively harvested from 70 boreal, temperate, and subtropical forests in Japan (hereafter called harvested dataset). This dataset was also used to additionally test assumption 4.

Using the estimates of parameters A₀, A_T, K₃, K₄ and c, we tested the fit of Eqs (18) and (19) to the 11 plots. We did not fit these equations directly to the data because these equations are highly flexible and can generate various curves depending on the five parameters. Thus, we first obtained the plot-specific estimates of A₀, A_T, K₃, and c through tests of assumptions 1 and 5 (S2 Table). For K₄, we did not use plot-specific estimate because it seemed to be affected by artifact (see previous paragraph). Instead, we used a common value that was estimated from harvested dataset by fitting ln (M) = ln (K₄) + 8/3 × ln (D). Then, we fitted Eqs (18) and (19) using these fixed parameter values.

Results

Evaluation of the model of Enquist et al. (1999)

Eq (3) proposed by Enquist et al. [2] fitted well only to some mature stands. Fig 1 shows the relationship between the 2/3 power of the initial diameter (D₀^2/3) and that of the final diameter (D_T^2/3). For example, in plot 11, the estimated slope of RMA regression was 1.03 (95% confidence interval [CI] = 1.02–1.04), which was almost identical to the unity expected by Eq (3). However, in younger stands, the relationship between D₀^2/3 and D_T^2/3 was not approximated well by a line. If we approximated by a line, for example in plot 4, the slope was obviously greater than unity and the intercept was negative (D_T^2/3 = -2.22 + 2.31D₀^2/3; r² = 0.89).

Download:

Fig 1. Relationship between the 2/3 power of initial stem diameter (D02/3) and final diameter (DT2/3) in 11 forests.

Gray lines are D_T^2/3 = a + bD₀^2/3 fitted by the reduced major axis regression. Estimated values of b are shown with the 95% confidence interval. Black curves show the relationship predicted by alternative model expressed in Eq (18) with adjusted r² values. For the values of parameters of alternative model, see S2 Table. Dashed lines show 1:1. Plot 1 is the youngest and plot 11 is the most mature forest.

https://doi.org/10.1371/journal.pone.0152219.g001

The value of slope b in the equation D_T^2/3 = a + bD₀^2/3 had a clear relationship with stand maturity. Slope b was near unity in the mature stands with large trees (plots 9–11, Fig 1), while it was greater than 1 and was near 2 in the younger stands with small trees (plots 1–5). Intermediate-aged stands (plots 6–8) showed intermediate b values between 1 and 2. Thus, the model of Enquist et al. [2] was not supported in small-sized young stands. The result did not change even when OLS regression was used instead of RMA regression (data not shown).

Assumption 1: Y-N curve fits to the size frequency distribution of trees

Y-N curve between cumulative biomass in the stand summed from the largest tree to the N-th largest tree (Y) and tree’s rank (N) fitted well to the actual size structure in all stands (Fig 2).

Download:

Fig 2. Fit of Y-N equation (Hozumi et al. 1968) in 11 forests.

Y is the cumulative aboveground biomass summed for N largest trees and N is the cumulative number of trees from the largest tree (i.e. tree’s rank). Curves are fitted Y-N equations, Y = N / (AN + B). Data and fitted Y-N curve of the first year census (black), those of last census (red), and the rests (gray). Plot 1 is the youngest and plot 11 is the most mature forest.

https://doi.org/10.1371/journal.pone.0152219.g002

Assumption 2: Tree’s rank does not change with time

Individual tree’s rank at the initial census and that at the final census were strongly correlated (Spearman’s ρ = 0.903–0.996, P<0.001). Therefore, we can assume no or few changes in a tree’s rank with time.

Assumption 3: Stand biomass follows a power function of the height of the highest individual in the stand

In plots 1–5 where tree height was measured, stand total biomass was well expressed by Y_max = K₁ H_max^a+1 (Eq 8, Fig 3, P < 0.002, adjusted r² = 0.74–0.95). The 95% CI for a + 1 was larger than 1 in all five plots. Therefore, assumption 3 was supported for all the five plots.

Download:

Fig 3. Relationship between stand biomass (Y_max) and the height of the highest individual in the stand (H_max).

Regression curves are Y_max = K₁ H_max ^a+1 fitted for 7–12 year-data in each plot. The estimated values of a+1 are shown in the legend (figures in parentheses). Plot 5 showed smaller biomass due to stand thinning.

https://doi.org/10.1371/journal.pone.0152219.g003

Assumption 4: Allometric relationship between tree biomass and tree height

Although the generic allometric equation used to estimate aboveground biomass did not have tree height as a predictive variable, estimated aboveground biomass showed an allometric relationship to tree height in plots 1–5 in each year, i.e., M = K₂ H^b, with b = 1.29–3.68 significantly different from 0 (Fig 4, P < 0.0001, adjusted r² = 0.56–0.95, except r² = 0.24 for 1 year in plot 1). Measured tree biomass of harvested dataset [27] also showed an allometric relationship to tree height (P < 0.0001, adjusted r² = 0.89, b = 3.28). Therefore, assumption 4 was supported for all five plots and for the compiled harvested dataset.

Download:

Fig 4. Allometric relationship between tree aboveground biomass (M) and tree height (H) in the last-year census.

Regression lines are ln(M) = ln(K₂) + b × ln(H) fitted for last-year data. The estimated values of b are shown.

https://doi.org/10.1371/journal.pone.0152219.g004

Assumption 5: Parameter B scales with A

Estimated parameters A and B of the Y-N curve followed the power function B = K₃A^c in all plots, with parameter c significantly different from 0 (Fig 5, P < 0.0001, adjusted r² = 0.98–1.00). Therefore, assumption 5 was supported.

Download:

Fig 5. Logarithmic relationship between parameters A and B of Y-N equation.

Regression lines are ln(B) = ln(K₃) + c ×ln(A) fitted for 7–15-year data censused in each of 11 plots. The estimated values of c are shown in the legend (figures in parentheses). Note that axes are in logarithmic scales. Plot 1 is the youngest and plot 11 is the most mature forest.

https://doi.org/10.1371/journal.pone.0152219.g005

Assumption 6: Individual tree biomass scales with the 8/3 power of stem diameter

Estimated tree aboveground biomass in the 11 forest plots showed a scaling relationship to stem diameter (Fig 6). However, the 95% CI of scaling exponent e of M = K₄D^e did not include 8/3, and the estimates were smaller than 8/3 (i.e., ≈2.67) in all years and plots (e = 1.71–2.54 by OLS regression, 1.74–2.55 by RMA regression). In particular, younger stands had a smaller scaling exponent (Fig 6; S1 Fig). Measured biomass of harvested dataset [27] also showed a scaling relationship to stem diameter. Again, the 95% CI of e was smaller than 8/3 (e = 2.33–2.36 by OLS regression, 2.35–2.38 by RMA regression). Therefore, assumption 6 was supported partially.

Download:

Fig 6. Allometric relationship between tree aboveground biomass (M) and tree stem diameter (D) in the last-year census.

Shown are ln(M) = ln(K₄) + e ×ln(D) fitted for the last year with estimated values of e. Plot 1 is the youngest and plot 11 is the most mature forest.

https://doi.org/10.1371/journal.pone.0152219.g006

Relationship between initial and final stem diameters

Eq (18) fitted well to the observed D₀^2/3 and D_T^2/3 data in both young and mature stands (Fig 1, black curve, parameter values are given in S2 Table). Eq (18) produced a curvilinear relationship between D₀^2/3 and D_T^2/3 from the obvious curve relationship in younger stands to the almost linear relationship in mature stands. The adjusted coefficient of determination was 0.64–0.99. In plots 1–7, Eq (18) explained 2–14% more variation in D_T^2/3 than Eq (3) by Enquist et al. [2] with a slope of unity. For plots 8–11, there was no difference in explained variation between two equations (0.0–0.8%).

Relationship between stem diameter growth rate and initial diameter

Eq (19) fitted to the observed convex relationship between the initial stem diameter and diameter growth rate in all plots (Fig 7, black curve, adjusted r² = 0.05–0.67, parameter values are given in S2 Table). The model of Enquist et al. [2] for tree growth rate (Eq 2) did not fit to the data (dashed line).

Download:

Fig 7. Relationship between initial stem diameter (D₀) and diameter growth rate, (D_T—D₀)/Δt.

Black curves are the proposed relationship expressed by Eq (19). Adjusted r² values are shown. Parameter values are given in S2 Table. Dashed gray lines show the model of Enquist et al. [2], dD/dt = βD₀^1/3, fitted by non-linear regression. Gray curves are the LOWESS smoothed curve using locally weighted polynomial regression by the lowess function of the R software. Plot 1 is the youngest and plot 11 is the most mature forest.

https://doi.org/10.1371/journal.pone.0152219.g007

Discussion

Our Eq (19) fitted to the observed convex relationship between growth rate of stem diameter and the initial stem diameter better than that of Enquist et al. [2] for all forests (Fig 7). Convex relationship between growth rate and size was shown to suggest asymmetric competition, while the linear-like relationship suggesting no competition or symmetric competition [7,29]. Indeed, asymmetric competition is the theoretical basis underpinning our model. Eq (18) was derived from Eq (4), which was mathematically derived from the growth model assuming asymmetric competition [17]. On the other hand, the model of Enquist et al. [2] is based on the assumption that tree growth is linear to leaf biomass. This means that both small and large trees have the same resource availability per unit leaf biomass. Such assumption may not be always true especially in closed forests where asymmetric competition for light is prominent than symmetric competition [6–8]. Smaller trees obtain less light resource per unit leaf biomass due to shading by larger trees resulting in reduced diameter growth than expected by the model of Enquist et al. (Fig 7). Thus, our results suggest that asymmetric competition is an important process in tree diameter growth.

The effect of asymmetric competition on tree growth can be seen in the difference between plots 4 and 5. Plot 5, which was adjacent to plot 4, was heavily thinned (95% of individual trees were thinned). The curve by Eq (19) was less convex in plot 5 than plot 4 (Fig 7). This suggests that smaller trees are less suppressed in their growth in plot 5 than those trees in plot 4, which may be the result of weakened asymmetric competition due to heavy thinning.

The model by Enquist et al. [2] and our model both fitted to the linear-like relationship beteween D_T^2/3 and D₀^2/3 in mature forests (Fig 1) even though two models are based on different ecological assumptions. This is because the linear-like relationship between D_T^2/3 and D₀^2/3 is a spurious trend resulting from autocorrelation. Since D_T = D₀ + T∙dD/dt, the correlation between D_T^2/3 and D₀^2/3 should include an autocorrelation of D₀ [30]. The degree of autocorrelation may be greater when the contribution of D₀ to D_T is greater. In other words, the autocorrelation is stronger in mature forests, as shown in Fig 1. To avoid artifact due to autocorrelation, it may be better to analyze the relationship between diameter growth rate (dD/dt) and initial diameter (D₀) rather than between D₀ and D_T. The theoretical relationship between ΔD/Δt and D₀ was easily obtained as Eq (19).

Our model is a non-spatial model that considers asymmetric competition. Various growth models that incorporated asymmetric competition have been proposed [6,8,12,31,32]. Some studies are based on sigmoid growth curve such as logistic model and Birch’s model [31,32]. However, there has been debate about the mathematical form of plant growth or even about sigmoid growth in trees [33–36]. Our model is not affected by the form of growth curve because we start from size frequency distribution (Y-N curve). Similarly, the growth model by Yokozawa & Hara [8] assumed no a priori growth function. Their model can evaluate the strength of symmetric and asymmetric competition from the field data. However, to apply to field data, spatial data of tree distribution was needed [37,38]. The models that extended the metabolic scaling theory [6,12] also required spatial data as well as data of light availability and crown area to parameterize the effect of asymmetric competition. Our model does not require these spatial, environmental, and morphological data and therefore may be applicable to various forest inventory data, which usually lack these detailed information.

Another characteristic of our model is that it deals with averaged growth rate for a given size. It cannot express the variation in individual tree growth due to local crowdedness as recent spatially explicit individual-based modeling can (eg. [39–41]). However, “macroscopic equation” like our model may be more useful for the future prediction of forest dynamics using dynamic global vegetation model [3].

Eq (19) described the curvelinear relationship of diameter growth rate to initial diameter (Fig 7). However, in some stands, the r² value was not high. There may be some reasons to dilute the size dependency of diameter growth. We used the assumption that tree biomass scales to the 8/3 of diameter, but this relationship was not fully supported as shown by previous studies [42,43]. The growth rate may be different among species or growth form even if their size is same [12,30,44]. Because our model is based on asymmetric competition, our model may not perform well in forests where symmetric competition predominates or where interaction among individuals is weak. Examples of such forests may be the forests that have low tree density and crowdedness [38] or forests developed at low-productivity or high-disturbance sites [6,45]. Future researches are needed to improve our model or test the generality of our model.

Supporting Information

S1 Fig. Estimated scaling exponent e of the allometric relationship between tree aboveground biomass (M) and tree stem diameter (D) for each plot.

Value of e in ln(M) = ln(K₄) + e ×ln(D) fitted by OLS regression for each year and plot is shown. Error bars show the maxima and minima of each forest. Edges of the box show the upper and lower quartiles. Bar shows the median.

https://doi.org/10.1371/journal.pone.0152219.s001

(TIF)

S1 Table. Species composition of 11 plots.

https://doi.org/10.1371/journal.pone.0152219.s002

(CSV)

S2 Table. Parameter values used to fit Eqs (18) and (19).

https://doi.org/10.1371/journal.pone.0152219.s003

(CSV)

S3 Table. Tree growth data of 11 plots.

Tree species name (Species), family name (Family), tree id (Tree.Number), diameter at breast height in year 19XY (DXY), tree height in year 19XY (HXY), and tree aboveground biomass in year 19XY (WAXY).

https://doi.org/10.1371/journal.pone.0152219.s004

(ZIP)

Acknowledgments

We thank the staff of Hokkaido Forestry Research Institute for the fieldwork and two anonymous reviewers, Takashi Kohyama and Eri Nabeshima for valuable comments.

Author Contributions

Conceived and designed the experiments: MII KK. Performed the experiments: KU YO KK. Analyzed the data: MII YK KU KK. Contributed reagents/materials/analysis tools: MII YK. Wrote the paper: MII YK KU KK.

References

1. Condit R, Ashton P, Bunyavejchewin S, Dattaraja HS, Davies S, Esufali S, et al. The importance of demographic niches to tree diversity. Science. 2006;313: 98–101. pmid:16763113
- View Article
- PubMed/NCBI
- Google Scholar
2. Enquist B, West G, Charnov E, Brown J. Allometric scaling of production and life-history variation in vascular plants. Nature. 1999;88: 907–911.
- View Article
- Google Scholar
3. Purves D, Pacala S. Predictive models of forest dynamics. Science. 2008;320: 1452–1453. pmid:18556548
- View Article
- PubMed/NCBI
- Google Scholar
4. King DA. Influence of light level on the growth and morphology of saplings in a Panamianan forest. Am J Bot. 1994;81: 948–957.
- View Article
- Google Scholar
5. Kikuzawa K, Lechowicz MJ. Axiomatic plant ecology—Reflections toward a unified theory for plant production. In: Hikosaka K, Niinemets Ü, Anten N, editors. Canopy photosynthesis: from basics to applications. Netherlands: Springer; 2016. pp. 399–423.
6. Muller-Landau HC, Condit RS, Chave J, Thomas SC, Bohlman SA, Bunyavejchewin S, et al. Testing metabolic ecology theory for allometric scaling of tree size, growth and mortality in tropical forests. Ecol Lett. 2006;9: 575–88. pmid:16643303
- View Article
- PubMed/NCBI
- Google Scholar
7. Weiner J. Asymmetric competition in plant populations. Trends Ecol Evol. 1990;5: 360–364. pmid:21232393
- View Article
- PubMed/NCBI
- Google Scholar
8. Yokozawa M, Hara T. A canopy photosynthesis model for the dynamics of size structure and self-thinning in plant populations. Ann Bot. 1992;70: 305–316. Available: http://aob.oxfordjournals.org/cgi/content/abstract/70/4/305
- View Article
- Google Scholar
9. Kikuzawa K, Umeki K. Effect of canopy structure on degree of asymmetry of competition in two forest stands in northern Japan. Ann Bot. 1996;77: 565–571.
- View Article
- Google Scholar
10. Kikuzawa K. Theoretical relationships between mean plant size, size distribution and self thinning under one-sided competition. Ann Bot. 1999;83: 11–18.
- View Article
- Google Scholar
11. Hara T. Dynamics of size structure in plant populations. Trends Ecol Evol. 1988;3: 129–133. pmid:21227181
- View Article
- PubMed/NCBI
- Google Scholar
12. Coomes DA, Allen RB. Effects of size, competition and altitude on tree growth. J Ecol. 2007;95: 1084–1097.
- View Article
- Google Scholar
13. Koyama H, Kikuzawa K. Intraspecific competition among higher plants. VIII. Frequency distribution of individual plant weight as affected by the interaction between plants. J Inst Polytech Osaka City Univ. 1956;D7: 73–94.
- View Article
- Google Scholar
14. Weiner J, Thomas SC. Size variability and competition in plant monocultures. Oikos. 1986;47: 211–222.
- View Article
- Google Scholar
15. Hozumi K, Shinozaki K, Tadaki Y. Studies on the frequency distribution of the weight of individual trees in a forest stand I. A new approach toward the analysis of the distribution function and the -3/2th power distribution. Japanese J Ecol. 1968;18: 10–20.
- View Article
- Google Scholar
16. Kikuzawa K. Yield—Density diagram for natural deciduous broadleaved forest stands. For Ecol Manage. 1982;4: 341–358.
- View Article
- Google Scholar
17. Kobayashi Y, Kikuzawa K. A single theory explains two empirical laws applicable to plant populations. J Theor Biol. 2000;205: 253–260. pmid:10873436
- View Article
- PubMed/NCBI
- Google Scholar
18. Niklas KJ, Enquist BJ. Invariant scaling relationships for interspecific plant biomass production rates and body size. Proc Natl Acad Sci U S A. 2001;98: 2922–2927. pmid:11226342
- View Article
- PubMed/NCBI
- Google Scholar
19. Enquist BJ, Kerkhoff AJ, Stark SC, Swenson NG, McCarthy MC, Price CA. A general integrative model for scaling plant growth, carbon flux, and functional trait spectra. Nature. 2007;449: 218–222. pmid:17851525
- View Article
- PubMed/NCBI
- Google Scholar
20. Kira T, Shidei T. Primary production and turnover of organic matter in different forest ecosystems of the Western Pacific. Japanese J Ecol. 1967;
- View Article
- Google Scholar
21. Niklas KJ. Plant allometry. Chicago and London: The University of Chicago Press; 1994.
22. West G, Brown J, Enquist B. A general model for the structure and allometry of plant vascular systems. Nature. 1999;400: 664–667.
- View Article
- Google Scholar
23. Kikuzawa K. Intraspecific competition in a natural stand of Betula ermanii. Ann Bot. 1988;61: 727–734.
- View Article
- Google Scholar
24. Kikuzawa K. Self-thinning line and B-point line of the yield-density diagram in a young birch stand. For Ecol Manage. 1993;58: 287–298.
- View Article
- Google Scholar
25. White EP, Xiao X, Isaac NJ, Sibly RM. Methodological tools. In: Sibly RM, Brown JH, Kodric-Brown A, editors. Metabolic Ecology: A Scaling Approach. Oxford, UK: Wiley-Blackwell; 2012. pp. 9–20.
26. Chave J, Réjou-Méchain M, Búrquez A, Chidumayo E, Colgan MS, Delitti WBC, et al. Improved allometric models to estimate the aboveground biomass of tropical trees. Glob Chang Biol. 2014;20: 3177–3190. pmid:24817483
- View Article
- PubMed/NCBI
- Google Scholar
27. Ishihara MI, Usugi H, Tanouchi H, Aiba M, Kurokawa H, Onoda Y, et al. Efficacy of generic allometric equations for estimating biomass : a test in Japanese natural forests. Ecol Appl. 2015;25: 1433–1446. pmid:26485966
- View Article
- PubMed/NCBI
- Google Scholar
28. Falster DS, Duursma RA, Ishihara MI, Barneche DR, FitzJohn RG, Vårhammar A, et al. BAAD: a Biomass And Allometry Database for woody plants. Ecology. 2015;96: 1445.
- View Article
- Google Scholar
29. Hara T. Effects of the mode of competition on stationary size distribution in plant populations. Ann Bot. 1992;69: 509–513.
- View Article
- Google Scholar
30. Coomes DA, Allen RB. Testing the Metabolic Scaling Theory of tree growth. J Ecol. 2009;97: 1369–1373.
- View Article
- Google Scholar
31. Aikman DP, Watkinson AR. A model for growth and self-thining in even-aged monocultures of plants. Ann Bot. 1980;45: 419–427.
- View Article
- Google Scholar
32. Damgaard C, Weiner J. Modeling the growth of individuals in crowded plant populations. J Plant Ecol. 2008;1: 111–116.
- View Article
- Google Scholar
33. Sillett SC, Van Pelt R, Koch GW, Ambrose AR, Carroll AL, Antoine ME, et al. Increasing wood production through old age in tall trees. For Ecol Manage. 2010;259: 976–994.
- View Article
- Google Scholar
34. Stephenson NL, Das AJ, Condit R, Russo SE, Baker PJ, Beckman NG, et al. Rate of tree carbon accumulation increases continuously with tree size. Nature. 2014;507: 90–3. pmid:24429523
- View Article
- PubMed/NCBI
- Google Scholar
35. Sedmák R, Scheer L. Properties and prediction accuracy of a sigmoid function of time-determinate growth. iForest—Biogeosciences For. 2015; e1–e7.
- View Article
- Google Scholar
36. Tsoularis A, Wallace J. Analysis of logistic growth models. Math Biosci. 2002;179: 21–55. pmid:12047920
- View Article
- PubMed/NCBI
- Google Scholar
37. Umeki K. Growth characteristics of six tree species on Hokkaido Island, northern Japan. Ecol Res. 2001;16: 435–450.
- View Article
- Google Scholar
38. Kubota Y, Hara T. Tree Competition and Species Coexistence in a Sub-boreal Forest, Northern Japan. Ann Bot. 1995;76: 503–512.
- View Article
- Google Scholar
39. Uriarte M, Condit R, Canham CD, Hubbell SP. A spatially explicit model of sapling growth in a tropical forest: does the identity of neighbours matter? J Ecol. 2004;92: 348–360.
- View Article
- Google Scholar
40. Cheng X, Umeki K, Honjo T, Mizusaki D. Basal area growth rates of five major species in a Pinus–Cunninghamia forest in eastern China affected by asymmetric competition and spatial autocorrelation. J For Res. 2012;19: 86–96.
- View Article
- Google Scholar
41. Schneider MK, Law R, Illian JB. Quantification of neighbourhood-dependent plant growth by Bayesian hierarchical modelling. J Ecol. 2006;94: 310–321.
- View Article
- Google Scholar
42. Zianis D, Mencuccini M. On simplifying allometric analyses of forest biomass. For Ecol Manage. 2004;187: 311–332.
- View Article
- Google Scholar
43. Vieilledent G, Vaudry R, Andriamanohisoa SFD, Rakotonarivo OS, Randrianasolo HZ, Razafindrabe HN, et al. A universal approach to estimate biomass and carbon stock in tropical forests using generic allometric models. Ecol Appl. 2012;22: 572–583. pmid:22611855
- View Article
- PubMed/NCBI
- Google Scholar
44. Russo SE, Wiser SK, Coomes DA. Growth-size scaling relationships of woody plant species differ from predictions of the Metabolic Ecology Model. Ecol Lett. 2007;10: 889–901. pmid:17845289
- View Article
- PubMed/NCBI
- Google Scholar
45. Coomes DA, Lines ER, Allen RB. Moving on from Metabolic Scaling Theory: Hierarchical models of tree growth and asymmetric competition for light. J Ecol. 2011;99: 748–756.
- View Article
- Google Scholar

[ref1] 1. Condit R, Ashton P, Bunyavejchewin S, Dattaraja HS, Davies S, Esufali S, et al. The importance of demographic niches to tree diversity. Science. 2006;313: 98–101. pmid:16763113
View Article
PubMed/NCBI
Google Scholar

[2] View Article

[3] PubMed/NCBI

[4] Google Scholar

[ref2] 2. Enquist B, West G, Charnov E, Brown J. Allometric scaling of production and life-history variation in vascular plants. Nature. 1999;88: 907–911.
View Article
Google Scholar

[6] View Article

[7] Google Scholar

[ref3] 3. Purves D, Pacala S. Predictive models of forest dynamics. Science. 2008;320: 1452–1453. pmid:18556548
View Article
PubMed/NCBI
Google Scholar

[9] View Article

[10] PubMed/NCBI

[11] Google Scholar

[ref4] 4. King DA. Influence of light level on the growth and morphology of saplings in a Panamianan forest. Am J Bot. 1994;81: 948–957.
View Article
Google Scholar

[13] View Article

[14] Google Scholar

[ref5] 5. Kikuzawa K, Lechowicz MJ. Axiomatic plant ecology—Reflections toward a unified theory for plant production. In: Hikosaka K, Niinemets Ü, Anten N, editors. Canopy photosynthesis: from basics to applications. Netherlands: Springer; 2016. pp. 399–423.

[ref6] 6. Muller-Landau HC, Condit RS, Chave J, Thomas SC, Bohlman SA, Bunyavejchewin S, et al. Testing metabolic ecology theory for allometric scaling of tree size, growth and mortality in tropical forests. Ecol Lett. 2006;9: 575–88. pmid:16643303
View Article
PubMed/NCBI
Google Scholar

[17] View Article

[18] PubMed/NCBI

[19] Google Scholar

[ref7] 7. Weiner J. Asymmetric competition in plant populations. Trends Ecol Evol. 1990;5: 360–364. pmid:21232393
View Article
PubMed/NCBI
Google Scholar

[21] View Article

[22] PubMed/NCBI

[23] Google Scholar

[ref8] 8. Yokozawa M, Hara T. A canopy photosynthesis model for the dynamics of size structure and self-thinning in plant populations. Ann Bot. 1992;70: 305–316. Available: http://aob.oxfordjournals.org/cgi/content/abstract/70/4/305
View Article
Google Scholar

[25] View Article

[26] Google Scholar

[ref9] 9. Kikuzawa K, Umeki K. Effect of canopy structure on degree of asymmetry of competition in two forest stands in northern Japan. Ann Bot. 1996;77: 565–571.
View Article
Google Scholar

[28] View Article

[29] Google Scholar

[ref10] 10. Kikuzawa K. Theoretical relationships between mean plant size, size distribution and self thinning under one-sided competition. Ann Bot. 1999;83: 11–18.
View Article
Google Scholar

[31] View Article

[32] Google Scholar

[ref11] 11. Hara T. Dynamics of size structure in plant populations. Trends Ecol Evol. 1988;3: 129–133. pmid:21227181
View Article
PubMed/NCBI
Google Scholar

[34] View Article

[35] PubMed/NCBI

[36] Google Scholar

[ref12] 12. Coomes DA, Allen RB. Effects of size, competition and altitude on tree growth. J Ecol. 2007;95: 1084–1097.
View Article
Google Scholar

[38] View Article

[39] Google Scholar

[ref13] 13. Koyama H, Kikuzawa K. Intraspecific competition among higher plants. VIII. Frequency distribution of individual plant weight as affected by the interaction between plants. J Inst Polytech Osaka City Univ. 1956;D7: 73–94.
View Article
Google Scholar

[41] View Article

[42] Google Scholar

[ref14] 14. Weiner J, Thomas SC. Size variability and competition in plant monocultures. Oikos. 1986;47: 211–222.
View Article
Google Scholar

[44] View Article

[45] Google Scholar

[ref15] 15. Hozumi K, Shinozaki K, Tadaki Y. Studies on the frequency distribution of the weight of individual trees in a forest stand I. A new approach toward the analysis of the distribution function and the -3/2th power distribution. Japanese J Ecol. 1968;18: 10–20.
View Article
Google Scholar

[47] View Article

[48] Google Scholar

[ref16] 16. Kikuzawa K. Yield—Density diagram for natural deciduous broadleaved forest stands. For Ecol Manage. 1982;4: 341–358.
View Article
Google Scholar

[50] View Article

[51] Google Scholar

[ref17] 17. Kobayashi Y, Kikuzawa K. A single theory explains two empirical laws applicable to plant populations. J Theor Biol. 2000;205: 253–260. pmid:10873436
View Article
PubMed/NCBI
Google Scholar

[53] View Article

[54] PubMed/NCBI

[55] Google Scholar

[ref18] 18. Niklas KJ, Enquist BJ. Invariant scaling relationships for interspecific plant biomass production rates and body size. Proc Natl Acad Sci U S A. 2001;98: 2922–2927. pmid:11226342
View Article
PubMed/NCBI
Google Scholar

[57] View Article

[58] PubMed/NCBI

[59] Google Scholar

[ref19] 19. Enquist BJ, Kerkhoff AJ, Stark SC, Swenson NG, McCarthy MC, Price CA. A general integrative model for scaling plant growth, carbon flux, and functional trait spectra. Nature. 2007;449: 218–222. pmid:17851525
View Article
PubMed/NCBI
Google Scholar

[61] View Article

[62] PubMed/NCBI

[63] Google Scholar

[ref20] 20. Kira T, Shidei T. Primary production and turnover of organic matter in different forest ecosystems of the Western Pacific. Japanese J Ecol. 1967;
View Article
Google Scholar

[65] View Article

[66] Google Scholar

[ref21] 21. Niklas KJ. Plant allometry. Chicago and London: The University of Chicago Press; 1994.

[ref22] 22. West G, Brown J, Enquist B. A general model for the structure and allometry of plant vascular systems. Nature. 1999;400: 664–667.
View Article
Google Scholar

[69] View Article

[70] Google Scholar

[ref23] 23. Kikuzawa K. Intraspecific competition in a natural stand of Betula ermanii. Ann Bot. 1988;61: 727–734.
View Article
Google Scholar

[72] View Article

[73] Google Scholar

[ref24] 24. Kikuzawa K. Self-thinning line and B-point line of the yield-density diagram in a young birch stand. For Ecol Manage. 1993;58: 287–298.
View Article
Google Scholar

[75] View Article

[76] Google Scholar

[ref25] 25. White EP, Xiao X, Isaac NJ, Sibly RM. Methodological tools. In: Sibly RM, Brown JH, Kodric-Brown A, editors. Metabolic Ecology: A Scaling Approach. Oxford, UK: Wiley-Blackwell; 2012. pp. 9–20.

[ref26] 26. Chave J, Réjou-Méchain M, Búrquez A, Chidumayo E, Colgan MS, Delitti WBC, et al. Improved allometric models to estimate the aboveground biomass of tropical trees. Glob Chang Biol. 2014;20: 3177–3190. pmid:24817483
View Article
PubMed/NCBI
Google Scholar

[79] View Article

[80] PubMed/NCBI

[81] Google Scholar

[ref27] 27. Ishihara MI, Usugi H, Tanouchi H, Aiba M, Kurokawa H, Onoda Y, et al. Efficacy of generic allometric equations for estimating biomass : a test in Japanese natural forests. Ecol Appl. 2015;25: 1433–1446. pmid:26485966
View Article
PubMed/NCBI
Google Scholar

[83] View Article

[84] PubMed/NCBI

[85] Google Scholar

[ref28] 28. Falster DS, Duursma RA, Ishihara MI, Barneche DR, FitzJohn RG, Vårhammar A, et al. BAAD: a Biomass And Allometry Database for woody plants. Ecology. 2015;96: 1445.
View Article
Google Scholar

[87] View Article

[88] Google Scholar

[ref29] 29. Hara T. Effects of the mode of competition on stationary size distribution in plant populations. Ann Bot. 1992;69: 509–513.
View Article
Google Scholar

[90] View Article

[91] Google Scholar

[ref30] 30. Coomes DA, Allen RB. Testing the Metabolic Scaling Theory of tree growth. J Ecol. 2009;97: 1369–1373.
View Article
Google Scholar

[93] View Article

[94] Google Scholar

[ref31] 31. Aikman DP, Watkinson AR. A model for growth and self-thining in even-aged monocultures of plants. Ann Bot. 1980;45: 419–427.
View Article
Google Scholar

[96] View Article

[97] Google Scholar

[ref32] 32. Damgaard C, Weiner J. Modeling the growth of individuals in crowded plant populations. J Plant Ecol. 2008;1: 111–116.
View Article
Google Scholar

[99] View Article

[100] Google Scholar

[ref33] 33. Sillett SC, Van Pelt R, Koch GW, Ambrose AR, Carroll AL, Antoine ME, et al. Increasing wood production through old age in tall trees. For Ecol Manage. 2010;259: 976–994.
View Article
Google Scholar

[102] View Article

[103] Google Scholar

[ref34] 34. Stephenson NL, Das AJ, Condit R, Russo SE, Baker PJ, Beckman NG, et al. Rate of tree carbon accumulation increases continuously with tree size. Nature. 2014;507: 90–3. pmid:24429523
View Article
PubMed/NCBI
Google Scholar

[105] View Article

[106] PubMed/NCBI

[107] Google Scholar

[ref35] 35. Sedmák R, Scheer L. Properties and prediction accuracy of a sigmoid function of time-determinate growth. iForest—Biogeosciences For. 2015; e1–e7.
View Article
Google Scholar

[109] View Article

[110] Google Scholar

[ref36] 36. Tsoularis A, Wallace J. Analysis of logistic growth models. Math Biosci. 2002;179: 21–55. pmid:12047920
View Article
PubMed/NCBI
Google Scholar

[112] View Article

[113] PubMed/NCBI

[114] Google Scholar

[ref37] 37. Umeki K. Growth characteristics of six tree species on Hokkaido Island, northern Japan. Ecol Res. 2001;16: 435–450.
View Article
Google Scholar

[116] View Article

[117] Google Scholar

[ref38] 38. Kubota Y, Hara T. Tree Competition and Species Coexistence in a Sub-boreal Forest, Northern Japan. Ann Bot. 1995;76: 503–512.
View Article
Google Scholar

[119] View Article

[120] Google Scholar

[ref39] 39. Uriarte M, Condit R, Canham CD, Hubbell SP. A spatially explicit model of sapling growth in a tropical forest: does the identity of neighbours matter? J Ecol. 2004;92: 348–360.
View Article
Google Scholar

[122] View Article

[123] Google Scholar

[ref40] 40. Cheng X, Umeki K, Honjo T, Mizusaki D. Basal area growth rates of five major species in a Pinus–Cunninghamia forest in eastern China affected by asymmetric competition and spatial autocorrelation. J For Res. 2012;19: 86–96.
View Article
Google Scholar

[125] View Article

[126] Google Scholar

[ref41] 41. Schneider MK, Law R, Illian JB. Quantification of neighbourhood-dependent plant growth by Bayesian hierarchical modelling. J Ecol. 2006;94: 310–321.
View Article
Google Scholar

[128] View Article

[129] Google Scholar

[ref42] 42. Zianis D, Mencuccini M. On simplifying allometric analyses of forest biomass. For Ecol Manage. 2004;187: 311–332.
View Article
Google Scholar

[131] View Article

[132] Google Scholar

[ref43] 43. Vieilledent G, Vaudry R, Andriamanohisoa SFD, Rakotonarivo OS, Randrianasolo HZ, Razafindrabe HN, et al. A universal approach to estimate biomass and carbon stock in tropical forests using generic allometric models. Ecol Appl. 2012;22: 572–583. pmid:22611855
View Article
PubMed/NCBI
Google Scholar

[134] View Article

[135] PubMed/NCBI

[136] Google Scholar

[ref44] 44. Russo SE, Wiser SK, Coomes DA. Growth-size scaling relationships of woody plant species differ from predictions of the Metabolic Ecology Model. Ecol Lett. 2007;10: 889–901. pmid:17845289
View Article
PubMed/NCBI
Google Scholar

[138] View Article

[139] PubMed/NCBI

[140] Google Scholar

[ref45] 45. Coomes DA, Lines ER, Allen RB. Moving on from Metabolic Scaling Theory: Hierarchical models of tree growth and asymmetric competition for light. J Ecol. 2011;99: 748–756.
View Article
Google Scholar

[142] View Article

[143] Google Scholar

Figures

Abstract

Introduction

Materials and Methods

Model of Enquist et al. (1999)

Alternative new model

Data set

Analysis

Results

Evaluation of the model of Enquist et al. (1999)

Assumption 1: Y-N curve fits to the size frequency distribution of trees

Assumption 2: Tree’s rank does not change with time

Assumption 3: Stand biomass follows a power function of the height of the highest individual in the stand

Assumption 4: Allometric relationship between tree biomass and tree height

Assumption 5: Parameter B scales with A

Assumption 6: Individual tree biomass scales with the 8/3 power of stem diameter

Relationship between initial and final stem diameters

Relationship between stem diameter growth rate and initial diameter

Discussion

Supporting Information

S1 Fig. Estimated scaling exponent e of the allometric relationship between tree aboveground biomass (M) and tree stem diameter (D) for each plot.

S1 Table. Species composition of 11 plots.

S2 Table. Parameter values used to fit Eqs (18) and (19).

S3 Table. Tree growth data of 11 plots.

Acknowledgments

Author Contributions

References