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Chapter 2 Model Species

In this chapter, I looked for the best model to integrate species information based on quality of fit, cross-validation (LOO), and prediction (RMSEP). The result is summarised in Table 2.1.

2.1 Data

I used reduced data to explore the model form. I focused on trees at 20 meters from any plot edges for neighbourhood effect. I used only recruited trees in the censuses with at least 10 measurements of diameter at breast height (DBH, cm). I used only species with at least 10 trees following previous requirements. And, I randomly selected 10 trees among 9 species for lightweight training data. I further selected a random diameter measure for each individual as an evaluation data not used for model fitting (Fig. 2.1).

Tree diameter trajectories in training data. Color represent individuals and the red point the data used for evaluation.

Figure 2.1: Tree diameter trajectories in training data. Color represent individuals and the red point the data used for evaluation.

2.2 Individual fixed

We used the selected model, i.e. Gompertz model (Hérault et al. 2011), with all parameters as individual fixed effects:

\[ DBH_{t,i} \sim \mathcal N (10 + gmax_i \times \sum _{y=1|DBH_{t=0}} ^{y=t} exp(-\frac12.[\frac{log(\frac{DBH_{t,i}}{100.Dopt_i})}{Ks_i}]^2)), \sigma)\]

The model correctly converged (\(\hat R < 1.05\)) with an acceptable but marked correlation between \(dopt\) and \(ks\). \(gmax\) posteriors have logical uncertainty but are varying widely among individuals. Finally predictions of the diameter trajectories by the model are good and realistic. Nevertheless, some posteriors seems to show bimodality.

2.3 Individual random

We used the selected model, i.e. Gompertz model (Hérault et al. 2011), with \(gmax\) as individual fixed effects and \(Dopt\) and \(Ks\) as individual random effects centered on species fixed effects:

\[ DBH_{t,i,s} \sim \mathcal N (10 + gmax_i \times \sum _{y=1|DBH_{t=0}} ^{y=t} exp(-\frac12.[\frac{log(\frac{DBH_{t,i}}{100.Dopt_i})}{Ks_i}]^2)), \sigma) \\| Dopt_i \sim \mathcal N(Dopt_s,\sigma_D), Ks_i \sim \mathcal N(Ks_s,\sigma_K) \]

The model correctly converged (\(\hat R < 1.05\)) with an acceptable but marked correlation between \(dopt\) and \(ks\). \(gmax\) posteriors have logical uncertainty but are varying widely among individuals. Finally predictions of the diameter trajectories by the model are good and realistic.

2.4 Species fixed

We used the selected model, i.e. Gompertz model (Hérault et al. 2011), with \(gmax\) as individual fixed effects and \(Dopt\) and \(Ks\) as species fixed effects:

\[ DBH_{t,i,s} \sim \mathcal N (10 + gmax_i \times \sum _{y=1|DBH_{t=0}} ^{y=t} exp(-\frac12.[\frac{log(\frac{DBH_{t,i}}{100.Dopt_s})}{Ks_s}]^2)), \sigma)\]

The model correctly converged (\(\hat R < 1.05\)) with an acceptable but marked correlation between \(dopt\) and \(ks\). \(gmax\) posteriors have logical uncertainty but are varying widely among individuals. Finally predictions of the diameter trajectories by the model are good and realistic.

2.5 Species random

We used the selected model, i.e. Gompertz model (Hérault et al. 2011), with \(gmax\) as individual fixed effects and \(Dopt\) and \(Ks\) as species random effects centered on community fixed effects:

\[ DBH_{t,i,s} \sim \mathcal N (10 + gmax_i \times \sum _{y=1|DBH_{t=0}} ^{y=t} exp(-\frac12.[\frac{log(\frac{DBH_{t,i}}{100.Dopt_s})}{Ks_s}]^2)), \sigma) \\| Dopt_i \sim \mathcal N(Dopt,\sigma_K), Ks \sim \mathcal N(Ks,\sigma_D) \]

The model correctly converged (\(\hat R < 1.05\)) with an acceptable but marked correlation between \(dopt\) and \(ks\). \(gmax\) posteriors have logical uncertainty but are varying widely among individuals. Finally predictions of the diameter trajectories by the model are good and realistic.

2.6 Dmax

We used the selected model, i.e. Gompertz model (Hérault et al. 2011), with \(gmax\) as individual fixed effects and \(Dopt\) and \(Ks\) as individual random effects centered on species fixed effects:

\[ DBH_{t,i,s} \sim \mathcal N (10 + gmax_i \times \sum _{y=1|DBH_{t=0}} ^{y=t} exp(-\frac12.[\frac{log(\frac{DBH_{t,i}}{100.Dopt_i})}{Ks_i}]^2)), \sigma) \\| Dopt_i \sim \mathcal N(Dopt_s,\sigma_D), Ks_i \sim \mathcal N(Ks_s,\sigma_K) \]

But we constrained \(dopt\) fitting \(d=\frac{dopt}{DBH_{95}}\) with \(d\in[0,1]\). The model correctly converged (\(\hat R < 1.05\)) with an acceptable but marked correlation between \(dopt\) and \(ks\). \(gmax\) posteriors have logical uncertainty but are varying widely among individuals. Finally predictions of the diameter trajectories by the model are good and realistic.

2.7 Comparisons

The individual random model has the best prediction (lowest RMSEP) associated to the best evaluation (second lowest loo epld), and a decent computing time. Moreover, model using species level \(Dopt\) and \(Ks\) are underestimating \(Gmax\) absolute value while overestimating individual variation in \(Gmax\) (last figures). Moreover, constraining \(dopt\) fitting \(d=\frac{dopt}{DBH_{95}}\) with \(d\in[0,1]\) resolved maximum treedepth issues and have similar performances. This is the best model that I’ll use in next steps.

Table 2.1: Model choice summary with quality of prediciton (Root Mean Square Error of Prediction, RMSEP), cross-validation (Leave-One-Out Estimate of the expected Log pointwise Predictive Density, LOO ELDP), and speed (Elapsed yime).
Model RMSEP LOO ELDP Elapsed time
Individual fixed 0.5194675 -519.5235 1098.084
Individual random 0.5065365 -511.3851 467.245
Species fixed 0.7176675 -1131.3198 297.436
Species random 0.6995610 -1113.3024 405.419
Dmax 0.5031310 -511.7936 495.079

elpd_diff se_diff elpd_loo se_elpd_loo p_loo se_p_loo looic se_looic
Individual random 0.0000000 0.000000 -511.3851 66.12526 141.06429 19.340438 1022.770 132.25052
Dmax -0.4085308 5.008777 -511.7936 67.24839 148.77584 20.302966 1023.587 134.49677
Individual fixed -8.1383963 8.967316 -519.5235 63.32304 144.10479 17.511319 1039.047 126.64607
Species random -601.9172862 50.741055 -1113.3024 38.22549 91.71500 8.904312 2226.605 76.45097
Species fixed -619.9346413 51.696773 -1131.3198 37.95275 89.35234 8.624910 2262.640 75.90549

References

Hérault, B., Bachelot, B., Poorter, L., Rossi, V., Bongers, F., Chave, J., Paine, C.E.T., Wagner, F. & Baraloto, C. (2011). Functional traits shape ontogenetic growth trajectories of rain forest tree species. Journal of Ecology, 99, 1431–1440.