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Parameter testing and application of the 3PG model for Eucalyptus grandis x Urophylla in subtropical conditions in South Africa

ABSTRACT

Background:

The productivity of the coastal Zululand region, which was known as the South African breadbasket for fibre is declining. Climate-related changes are a significant factor contributing to this decline. The 3PG (Physiological Processes Predicting Growth) model was calibrated for E. grandis x E. urophylla hybrids planted in this region to quantify the effect of climate variation x site on their growth and survival. Monthly weather data for the ungauged plantations were estimated using the Random Forest (RF) supervised learning algorithm. A dataset consisting of 17 permanent sample plots (PSPs) and published parameter values for this hybrid in various regions of Brazil were utilized for parameter estimation. Using a parsimonious optimization approach, we developed a novel method called extended Root Mean Square Error (eRMSE) to select the optimal parameter set.

Result:

The new parameter set yielded accurate predictions for three key variables; quadratic stem diameter (R2 = 0.85, E = 0.73), mean height (R2 = 0.84, E = 0.78), and basal area (R2 = 0.87, E = 0.78). Model performance at 15 independent sites allowed the comparison with three other Brazilian parameter sets for stand volume prediction at a specific age. The optimized parameter set provided a satisfactory, albeit slightly overestimated stand volume (V (m3ha-1), R2 = 0.65, E = -0.32) at the validation sites.

Conclusion:

The 3PG model can be adapted with parameter set from another region to characterize the growth of E.grandis x E.urophylla stands in South Africa.

Keywords:
Forest management; random forest; climate variation; process-based model.

HIGHLIGHTS

With local weather data, accurate estimates for ungauged plantations can be obtained. The 3PG parameters can easily be calibrated from previously published parameter set. Minimum ASW variable can be used to model growth on sites with groundwater access. 3PG model simulates tree growth dynamics in response to environmental changes.

INTRODUCTION

Global demand for wood continues to rise as the population grows (Brack, 2018BRACK, D. Sustainable consumption and production of forest products: Background analytical studies on the contribution of forests to the achievement of the Sustainable Development Goals. 2018. Available at: Available at: https://www.un.org/esa/forests/wp-content/uploads/2018/04/UNFF13_BkgdStudy_ForestsSCP.pdf . Accessed in: November 19th 2020.
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). To ensure a continued, sustainable supply, afforestation using fast-growing species in areas of optimal growth may be the most viable alternative approach (Elias; Boucher, 2014ELIAS, P.; BOUCHER, D. Planting for the Future: How Demand for Wood Products Could Be Friendly to Tropical Forests. Union of Concerned Scientists. 2014. Available at: Available at: https://www.ucsusa.org/sites/default/files/attach/2014/10/planting-for-the-future.pdf . Accessed in: November 19th 2020.
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). Clonal eucalypt forests have become important in this context due to their rapid growth rate, high wood quality, wide range of existing variability, and suitability to vegetative propagation (Rezende et al., 2014REZENDE, G. D. S.; DE RESENDE, M. D. V.; DE ASSIS, T. F. Eucalyptus Breeding for Clonal Forestry. In: Fenning, T. Challenges and opportunities for the world’s forests in the 21st century. Springer, 2014. p. 393-424.). The tropical E.grandis x E.urophylla hybrid has become an important plantation option and is widely planted in South Africa, as well as Australia, Brazil, China, India, Portugal, Spain, and Uruguay (Rezende et al., 2014REZENDE, G. D. S.; DE RESENDE, M. D. V.; DE ASSIS, T. F. Eucalyptus Breeding for Clonal Forestry. In: Fenning, T. Challenges and opportunities for the world’s forests in the 21st century. Springer, 2014. p. 393-424.).

In South Africa, this hybrid replaced E. grandis in the subtropical coastal Zululand region for commercial pulp production due to E. grandis’ vulnerability to diseases and pests (Van Den Berg, 2017VAN DEN BERG, G. J. A. Comparative Study of Two Eucalyptus Hybrid Breeding Strategies and the Genetic Gains of these Strategies. 2017. 168 p. PhD thesis University of Pretoria.). The hybrid offers high productivity, short rotation, good survival rate, and suitability for pulp and paper production, making it valuable to pulp growers (Melesse; Zewotir, 2017MELESSE, S. F.; ZEWOTIR, T. Variation in growth potential between hybrid clones of Eucalyptus trees in eastern South Africa. Journal of Forestry Research, v. 28, n. 6, p. 1157-1167, 2017. ). Furthermore, clonal forestry, including genetic and silvicultural improvements, was implemented in South Africa to increase the productivity of existing plantations and maintain low-cost wood production (Gardner, 2012GARDNER, R. A. W. Alternative eucalypt species for Zululand: Seven year results of site: species interaction trials in the region. The Southern African Forestry Journal, v. 190, n. 1, p. 79-88, 2012. ).

Despite yield gains, the unpredictability of climate change and productivity shifts continue to pose limitations for commercial forest managers in their planning horizons (Drew, 2021DREW, D. M. Exploring new frontiers in forecasting forest growth, yield and wood property variation. Annals of Forest Science, v. 78, n. 2, p. 1-2, 2021. ). Climate, unlike genetics and management, is the only factor foresters cannot directly control, yet it plays a significant role in determining the increased productivity levels in Eucalyptus plantations (Binkley et al., 2017BINKLEY, D.; CAMPOE, O. C; ALVARES, C.; CARNEIRO, R. L.; CEGATTA, I.; STAPE, J. L. The interactions of climate, spacing and genetics on clonal Eucalyptus plantations across Brazil and Uruguay. Forest Ecology and Management, v. 405, p. 271-283, 2017. ; Elli, 2020ELLI, E. F. Eucalyptus simulation models: understanding and mitigating the impacts of climate variability and change on forest productivity across Brazil. 2020. 261 p. PhD thesis University of Sao Paulo.). South Africa is inherently prone to drought (Baudoin et al., 2017BAUDOIN, M. A.; VOGEL, C.; NORTJE, K.; NAIK, M. Living with drought in South Africa: lessons learnt from the recent El Niño drought period. International Journal of Disaster Risk Reduction, v. 23, p. 128-137, 2017. ) and has a history of recurring dry periods (Xulu et al., 2018XULU, S.; PEERBHAY, K.; GEBRESLASIE, M.; ISMAIL, R. Drought influence on forest plantations in Zululand, South Africa, using MODIS time series and climate data. Forests, v. 9, n. 9, p. 528, 2018.). The coastal Zululand region experienced a severe drought combined with an extreme El Niño event in 2014 - 2015 (Baudoin et al., 2017). Climate-related changes have been a particular issue in the coastal Zululand region, likely tied to the region’s declining productivity. The commercial plantations in this region are intensively managed as short rotation forestry (8 - 12 years). Consequently, it becomes imperative to investigate the broad-scale impact of a rapidly changing environment on short rotation forestry.

The primary objective of statistical growth and yield models in forest management has been to develop prediction tools that assist in decision-making (Burkhart and Tomé, 2012BURKHART, H. E.; TOMÉ, M. Modeling forest trees and stands. Springer Netherlands, 2012. 457p. ). These model’s relative simplicity and practicability have made them a default operational tool (Burkhart and Tomé, 2012BURKHART, H. E.; TOMÉ, M. Modeling forest trees and stands. Springer Netherlands, 2012. 457p. ). They have proven useful in providing quantitative insights for management and planning, predicting growth and yield, and providing product profile information (Landsberg; Sands, 2011LANDSBERG, J. J.; SANDS, P. Physiological Ecology of Forest Production: Principles, Processes and Models. In: JAMES, R. E.; JAMES, M.; MONICA, G. T. (Eds.). Terrestrial Ecology Series. Academic Press, Elsevier, 2011. v. 4, p. 342. ). However, the mechanistic approach in forest modelling, which utilizes process-based models (PBMs) alongside weather/climate data, has gained significant attention from forest scientists (Elli, 2020ELLI, E. F. Eucalyptus simulation models: understanding and mitigating the impacts of climate variability and change on forest productivity across Brazil. 2020. 261 p. PhD thesis University of Sao Paulo.). PBMs are structured to simulate stand growth based on the physiological processes driving growth and the impact of physical conditions on stands (Landsberg; Sands, 2011LANDSBERG, J. J.; SANDS, P. Physiological Ecology of Forest Production: Principles, Processes and Models. In: JAMES, R. E.; JAMES, M.; MONICA, G. T. (Eds.). Terrestrial Ecology Series. Academic Press, Elsevier, 2011. v. 4, p. 342. ).

The 3PG (Physiological Processes Predicting Growth) model (Landsberg; Waring, 1997LANDSBERG, J. J.; WARING, R. H. A generalised model of forest productivity using simplified concepts of radiation-use efficiency, carbon balance and partitioning. Forest Ecology and Management, v. 95, n. 3, p. 209-228, 1997. ) is an interesting case, and perhaps one of the popular PBMs in forest science. It finds a niche in the continuum so that it is more considered a “hybrid model” (incorporating elements of both process-based and empirical models). This model has been calibrated and tested for various species in diverse forest types and geographic locations. Its application extends widely as both a research and operational tool (Gupta; Sharma, 2019GUPTA, R.; SHARMA, L. K. The process-based forest growth model 3-PG for use in forest management: A review. Ecological Modelling, v. 397, p. 55-73, 2019. ). Specifically, the model has been calibrated and tested for E.grandis x E.urophylla hybrids in different regions in Brazil (Almeida et al., 2004ALMEIDA, A. C.; LANDSBERG, J. J.; SANDS, P. J. Parameterisation of 3-PG model for fast-growing Eucalyptus grandis plantations. Forest Ecology and Management, v. 193, n. 1-2, p. 179-195, 2004. ; Stape et al., 2004STAPE, J. L.; RYAN, M. G.; BINKLEY, D. Testing the utility of the 3-PG model for growth of Eucalyptus grandis x urophylla with natural and manipulated supplies of water and nutrients. Forest Ecology and Management, v. 193, n. 1-2, p. 219-234, 2004. ; Borges et al., 2012BORGES, J. S.; NEVES, J. C. L.; LOURENCO, H. M.; de BARROS, N. F.; DIAS, S. C. M. Parameterization of the 3PG model for Eucalypt in the region of Cerrado in Minas Gerais State. Ciência Florestal, Santa Maria, v. 22, n. 3, p. 567-578, 2012. ), but not under South African conditions. Despite the potential of the 3PG model to serve as a decision support tool for accurate growth prediction and risk management in short rotation forestry, its operational use in the South African forestry industry remains limited (Dye et al., 2004DYE, P. J.; JACOBS, S.; DREW, D. Verification of 3-PG growth and water-use predictions in twelve Eucalyptus plantation stands in Zululand, South Africa. Forest Ecology and Management, v. 193, p. 197-218, 2004. ; Esprey, 2006ESPREY, L. J. Assessment of a Process-Based Model to Predict the Growth and Yield of Eucalyptus grandis Plantations in South Africa. 2005. 221 p. PhD thesis University of KwaZulu-Natal, Durban. ).

In regions like South Africa, where weather stations are scarce and sparsely distributed (Lynch, 2004LYNCH, S. D. Development of a Raster Database of Annual, Monthly and Daily Rainfall for Southern Africa. Report to the Water Research Commission. 2004. Available at Available at https://www.wrc.org.za/wp-content/uploads/mdocs/1156-1-041.pdf . Accessed in: December 4th 2020.
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), process-based growth modelling will always be constrained by the availability of reliable meteorological data. The coastal Zululand has a steep climatic gradient (Louw et al., 2011LOUW, J. H.; GERMISHUIZEN, I.; SMITH, C. W. A stratification of the South African forestry landscape based on climatic parameters. Southern Forests, v. 73, n. 1, p. 51-62, 2011. ), and due to the inherent spatiotemporal variability of precipitation, high-resolution meteorological data is necessary to accurately capture environmental flunctuations. Unfortunately, no “off-the-shelf” products like the Australia’s SILO resources (https://www.longpaddock.qld.gov.au/silo/) exist for South Africa. Moreover, the globally available gridded datasets are generated at a low spatial resolution, insufficient to capture the high level of spatiotemporal variability of rainfall on a local scale (Cáceres et al., 2018). Thus improved point estimates of weather data are critical for making informed and effective management decisions.

The study had the following objectives (1) address challenges in obtaining accurate weather data for ungauged plantations in South Africa, (2) Assess the need for a new parameter set for running the 3PG model with E.grandis x E.urophylla under South African conditions, and (3) test the 3PG model in a key commercial region in South Africa.

MATERIAL AND METHODS

General study area

Due to its commercial importance, the ready availability of site and management information, the existence of a strong precipitation gradient, and similar genetics planted across sites, the Zululand region of KwaZulu-Natal province was chosen for this study. The province is situated in the southeastern part of South Africa, encompassing 7.7% of the nation’s total land area. The province exhibits a complex physiographic features resulting in a wide range of climatic conditions. The climate transitions from a subtropical climate near the coast to a temperate climate further inland. Notably, the Zululand region experiences an increase in precipitation from inland areas towards the coastal regions, as well as north to south (Louw et al., 2011LOUW, J. H.; GERMISHUIZEN, I.; SMITH, C. W. A stratification of the South African forestry landscape based on climatic parameters. Southern Forests, v. 73, n. 1, p. 51-62, 2011. ). The data were obtained from PSPs owned and managed by two forestry companies in South Africa: Mondi Forests (https://www.mondigroup.com) and Sappi (https://www.sappi.com) (Figure 1). Summary of the site and stand information is presented in Table 1. Also, 155 weather stations distributed across the KwaZulu-Natal province was used in the spatial interpolation of point estimate weather data for the unguaged plantations (Figure 2).

Figure 1:
Map showing the extent of the permanent sample plots.

Table 1:
Summary of site information used for model calibration and validation.

Figure 2:
Map displaying weather station locations across KwaZulu-Natal province.

Description of the 3PG Model

The 3PG model is a simple, process-based, stand-level model that was originally developed for monospecific, even-aged, and evergreen forest (Landsberg; Waring, 1997LANDSBERG, J. J.; WARING, R. H. A generalised model of forest productivity using simplified concepts of radiation-use efficiency, carbon balance and partitioning. Forest Ecology and Management, v. 95, n. 3, p. 209-228, 1997. ), but has since further developed for deciduous, uneven-aged and mixed-species forests (Forrester; Tang, 2016FORRESTER, D. I.; TANG, X. Analysing the spatial and temporal dynamics of species interactions in mixed-species forests and the effects of stand density using the 3-PG model. Ecological Modelling, v. 319, p. 233-254, 2016. ). The model runs on a monthly time-step, and the data required to run the 3PG model can be divided into four classes; weather data (temperature, solar radiation, precipitation, atmospheric VPD, number of frost days in a month), site information (latitude, soil texture, atmospheric CO2, and a simple fertility rating), stand initialization data (initial stocking, initial stem, root and foliage biomass, initial available soil water), and species-specific parameters (the main 3PG parameters consist of six major parameter classes which include biomass partitioning and turnover, Net Primary Productivity (NPP) & conductance modifiers, stem mortality, and stand characteristics). The output variables can be classified as follows: 1) State variables: biomass pools, stem number and plant-available soil water, 2) Stand-level outputs: stand basal area, stem volume, mean annual increment, and DBH, 3) Physiological and research-related variables: gross primary production, net primary production, stand evapotranspiration,and leaf area index, 4) Time-varying variables: growth modifiers, canopy quantum efficiency, light-use efficiency, etc.

Stand growth data

Tree-level diameter at breast height (DBH) and total height data for the study plots were obtained from two main sources. First from routine annual PSP re-measurements undertaken by the two forest companies involved in the study. Second, data for five plots were obtained from a set of band dendrometers installed in December 2013. In these five sites, DBH and stem number were measured every two weeks since the installation of the dendrometers, while total height measurements were taken annually. Height measurements were conducted on a subset of trees for each plot. The forestmangr package (Braga et al., 2021BRAGA, S. R.; OLIVEIRA, M. L. R. DE; GORGENS, E. B. forestmangr: Forest Mensuration and Management, 2021. Available at: Available at: https://cran.r-project.org/web/packages/forestmangr/forestmangr.pdf . Accessed in: August 01 2022.
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) was used to fit a Height-Diameter curve using the Weibull model (Equation 1) for estimating the height of non-measured trees. The data were grouped by site and age and the nls_table function was used to fit the H-D curve for all the sites at different age. In August 2018, a final set of measurements were taken at all sites. Where H is the height (m), D is the diameter at breast height, b 1 , b 2 , b 3 are the estimated model parameters.

H = 1.3 + b 1 ( 1 e ( b 2 D ( b 3 ) ) ) (1)

Mean height was calculated by substituting quadatic mean diameter into Equation 1. Stand basal area (BA, m2ha-1) was estimated using Equation 3, and stand volume (V, m3ha-1) using an estimator by Burkhart and Tomé (2012BURKHART, H. E.; TOMÉ, M. Modeling forest trees and stands. Springer Netherlands, 2012. 457p. ) (Equation 4). Where V is the utilizable volume (m3ha-1), BA is the basal area (m2ha-1), Dq is the quadratic mean DBH (cm), DBH is the stem diameter at breast height (cm), n is the number of observed trees per plot, TPH is the number of stems (trees/ha), Hmean is the mean height (m), and f the species-specific form factor.

D q = D B H 2 n (2)

B A = π * ( D q ) 2 * T P H ) 40000 (3)

V = B A H m e a n f (4)

Soil data

At the centre of each of the calibration sites, soil samples were collected from pits using a 1.2m manual steel auger at 10 cm intervals, until a soil depth of 1.2m was reached. Soil textural and chemical analysis was performed at the Institute for Commercial Forest Research (ICFR) (Table 2). Soil class was then determined based on sand, silt, and clay content. Soil class was relatively homogenous, as expected in this region. Available Soil Water (ASW) was estimated from the soil textural properties, using the soil water characteristics equation by Saxton and Rawls (2006SAXTON, K. E.; RAWLS, W. J. Soil Water Characteristic Estimates by Texture and Organic Matter for Hydrologic Solutions. Soil Science Society of America Journal, v. 70, n. 5, p. 1569-1578, 2006. ). Maximum ASW was calculated as the product of soil depth and derived available water capacity. In 3PG, the minimum available soil water (MinASW), which is used to account for water table access, is typically set to zero by default. However, if it is known that the plants have access to a deep permanent water source, this value can be set higher than zero. As a result, MinASW at five sites planted near perennial watercourses were increased to half of their ASW.

Table 2:
Average soil textural and chemical properties across the soil depths of the calibration sites.

Fertility Rating

The 3PG model utilizes a Fertility Rating index (FR) to establish a correlation between soil fertility and stand productivity. The FR index assigns a ranking to soil fertility, ranging from 0 (extreme nutritional limitation) to 1 (no nutritional limitation). Although the empirical nature of the FR index has faced criticism, the assignment of FR to a specific site remains a challenging task (Landsberg; Sands, 2011LANDSBERG, J. J.; SANDS, P. Physiological Ecology of Forest Production: Principles, Processes and Models. In: JAMES, R. E.; JAMES, M.; MONICA, G. T. (Eds.). Terrestrial Ecology Series. Academic Press, Elsevier, 2011. v. 4, p. 342. ). In this study, we explored the likely variability in FR. We performed multiple 3PG model runs at 0.1 FR intervals to obtain the optimized values for each site (Supplementary material Fig. S1). Stepwise regression was performed using the optimized FR values as the independent variable. Soil physical and chemical properties, the total rainfall, ASW, and site index values were used as the explanatory variable (Table 3 for variables selected as the final model). The site index was the only explanatory variable that significantly contributed to the model (p < 0.01). Although the model from the stepwise regression gave a good R-squared, the relationship explained by the model was not statistically significant (p > 0.05). However, using only site index decreased the proportion of the explained variance (R2 = 0.36, p < 0.05). Consequently, and given that the region is characterized by relatively homogenous soils, FR was set to a constant value of 0.5 to run the 3PG model at both calibration and validation stages.

Table 3:
Variables selected in the stepwise regression. N - Nitrogen (%), S - Sulphur (%), P - Phosphorus (%), CN - Carbon-Nitrogen ratio, SI - Site Index.

Weather data

Estimates of meteorological data at the location of the study sites were generated by applying the Random Forest (RF) supervised learning algorithm developed by Breiman (2001BREIMAN, L. Random Forests. Machine Learning, v. 45, n. 1, p. 5-32, 2001. ), using the R package, randomForest (Liaw; Wiener, 2002LIAW, A.; WIENER, M. Classification and Regression by randomForest. R News, v. 2, n. 3, p. 18-22, 2002. Available at: https://www.r-project.org/doc/Rnews/Rnews_2002-3.pdf
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). Long-term daily weather data such as maximum and minimum temperature, precipitation, and solar radiation were obtained from the South African Sugarcane Research Institute (SASRI) and the South African Weather Services (SAWS) from January 2008 to December 2018. From these two databases, a total of 155 weather stations (Figure 2) were seleted to develop the regression model. In addition to latitude and longitude, the covariables used for modelling were aspect, elevation, slope, and distance from the ocean. Aspect and slope were derived from the GISCOE 20m Digital Elevation Model raster data. The distance from the ocean was calculated from the polyline of the African continent.

For evaluating the performance of the developed RF model, a subset of 6 out of the total 155 weather stations (Figure 2) was selected as validation stations. The RF model was applied to predict rainfall for these stations from 2008 to 2018. The performance analysis focused solely on precipitation data, considering its inherent spatiotemporal variability, which poses challenges for interpolation. A pair-wise comparison of model-predicted and observed monthly precipitation data was performed. The following statistical errors and indices from the Agricultural and Meteorological software (AgriMetSoft, 2019AGRIMETSOFT. Agricultural and Meteorological Software. Online Calculator. Available at Available at https://www.agrimetsoft.com/calculators/ . Accessed in: August 14th 2021.
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) were used to compare the predicted and observed data; Root Mean Square Error (RMSE), Mean Bias Error (MBE), Willmott index of agreement (d), coefficient of determination (R2), and Nash Sutcliffe model efficiency index (E) (Equation 5, 6, 7, 8 and 9). Where o i is the observed values, pi is the predicted values, o is the average observation value, and n is the number of observations.

R M S E i = 1 n o i p i 2 n (5)

M B E i = 1 n ( o i p i ) n (6)

d = 1 i = 1 n ( o i p i ) 2 i = 1 n ( | p i o | + | o i o | ) 2 (7)

R 2 ( n ( o i p i ) ( o i ) ( p i ) [ n o i 2 ( o i ) 2 ] [ n p i 2 ( p i ) 2 ] ) 2 (8)

E = 1 i = 1 n ( o i p i ) 2 i = 1 n ( | o i o | ) 2 (9)

Calibration of 3PG model

Following the parameterization guidelines presented by several authors (Sands, 2004bSANDS, P. Adaptation of 3-PG to novel species: guidelines for data collection and parameter assignment. CSIRO Forestry and Forest products, 2004. Available at: Available at: https://3pg.sites.olt.ubc.ca/files/2014/04/3-PG-guidelines.TR141.pdf . Accessed in: May 7th 2020.
https://3pg.sites.olt.ubc.ca/files/2014/...
; Esprey, 2006; Landsberg; Sands, 2011LANDSBERG, J. J.; SANDS, P. Physiological Ecology of Forest Production: Principles, Processes and Models. In: JAMES, R. E.; JAMES, M.; MONICA, G. T. (Eds.). Terrestrial Ecology Series. Academic Press, Elsevier, 2011. v. 4, p. 342. ), a base parameter set developed for E.grandis x E.urophylla hybrids in a different region by Borges et al. (2012BORGES, J. S.; NEVES, J. C. L.; LOURENCO, H. M.; de BARROS, N. F.; DIAS, S. C. M. Parameterization of the 3PG model for Eucalypt in the region of Cerrado in Minas Gerais State. Ciência Florestal, Santa Maria, v. 22, n. 3, p. 567-578, 2012. ) were used where parameters could not be calibrated due to lack of suitable data or showed low sensitivity ratings. Generic parameters, assigned values based on analogy with other species, such as solar radiation to Photosynthetically Active Radiation (molPAR_MJ = 2.3 mol/MJ), were chosen from Sands; Landsberg (2002)SANDS, P. J.; LANDSBERG, J. J. Parameterisation of 3-PG for plantation grown Eucalyptus globulus. Forest Ecology and Management, v. 163, n. 1-3, p. 273-292, 2002. as default parameters.AGRISA. A Raindrop in the Drought: Agri SA’s status report on the current drought crisis. Pretoria, South Africa. 2016. Available at: Available at: http://www.nstf.org.za/wp-content/uploads/2016/06/Agri-SA-Drought-Report_CS4.pdf . Accessed in: December 29th 2020.
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Allometric parameters for stem mass as a function of DBH

Biomass harvest data were measured from destructive samples taken in 2018 from the subset of five sites. Three trees representing the first quartile (Q1), third quartile (Q3), and the maximum in the diameter distribution were destructively harvested in each site. Measurements recorded were total height, DBH, aboveground biomass (stem wood, branch, and foliage). Parameters for the allometric (Equation 10) relationship between tree-level biomass (w s , kg/tree) and DBH were then estimated as defined by Sands; Landsberg (2002SANDS, P. J.; LANDSBERG, J. J. Parameterisation of 3-PG for plantation grown Eucalyptus globulus. Forest Ecology and Management, v. 163, n. 1-3, p. 273-292, 2002. ). Where B is stem diameter at breast height, a s is the coefficient, and n s is the power in the allometric relationship.DE CÁCERES, M.; MARTIN-STPAUL, N.; TURCO, M.; CABON, A.; GRANDA, V. Estimating daily meteorological data and downscaling climate models over landscapes. Environmental Modelling and Software, v. 108, p. 186-196, 2018.

w s = a s B n S (10)

The allometric parameter from the 15 harvested trees was used to calculate the individual tree mass for each tree measured at the 18 sites. Average w S and Dq were determined for each site. Combining these 18 pairs of w s and Dq, a single stand-based allometric relationship representing all sites was developed. This estimation followed Esprey (2006)ESPREY, L. J. Assessment of a Process-Based Model to Predict the Growth and Yield of Eucalyptus grandis Plantations in South Africa. 2005. 221 p. PhD thesis University of KwaZulu-Natal, Durban. recommendation to upscale the parameter values to stand level for consistency with 3PG calculations.DU PLESSIS, M.; ZWOLINSKI, J. Site and Stand analysis for growth prediction of Eucalyptus grandis on the Zululand Coastal plain. Southern African Forestry Journal, v. 198, p. 23-33, 2003.

Density-independent mortality coefficients

Some of the sites experienced mortality during the rotation. As a result, we fitted the parameter values for density-independent mortality. The Clutter and Jones mortality function (Equation 11) was used to estimate tree survival per year, then the data modelled was fitted using a Gaussian function with a non-zero asymptote (Landsberg; Sands, 2011LANDSBERG, J. J.; SANDS, P. Physiological Ecology of Forest Production: Principles, Processes and Models. In: JAMES, R. E.; JAMES, M.; MONICA, G. T. (Eds.). Terrestrial Ecology Series. Academic Press, Elsevier, 2011. v. 4, p. 342. ). Where, ɣNx = 0.60 (mortality rate for matured trees), ɣNo = 1.01 (the seedling mortality rate), and tɣN = 3.39 (age at which mortality has median value).

γ ( t ) = γ N x + ( γ N x γ N o ) e ( l n 2 ) t / t γ N (11)

Parameter estimation for Zululand E.grandis x E.urophylla

Eight parameters (test parameters) (Table 4) were selected from the list of 3PG parameters (base parameters). These parameters were selected because they could not be calibrated from the data available in this study, and 3PG outputs have shown sensitivity to them (Almeida et al., 2004ALMEIDA, A. C.; LANDSBERG, J. J.; SANDS, P. J. Parameterisation of 3-PG model for fast-growing Eucalyptus grandis plantations. Forest Ecology and Management, v. 193, n. 1-2, p. 179-195, 2004. ; Esprey et al., 2004ESPREY, L. J.; SANDS, P. J.; SMITH, C. W. Understanding 3-PG using a sensitivity analysis. Forest Ecology and Management, v. 193, p. 235-250, 2004. ; Forrester; Tang, 2016FORRESTER, D. I.; TANG, X. Analysing the spatial and temporal dynamics of species interactions in mixed-species forests and the effects of stand density using the 3-PG model. Ecological Modelling, v. 319, p. 233-254, 2016. ). Published parameter values for E.grandis x E.urophylla by Almeida et al. (2004)ALMEIDA, A. C.; LANDSBERG, J. J.; SANDS, P. J. Parameterisation of 3-PG model for fast-growing Eucalyptus grandis plantations. Forest Ecology and Management, v. 193, n. 1-2, p. 179-195, 2004. and Borges et al. (2012BORGES, J. S.; NEVES, J. C. L.; LOURENCO, H. M.; de BARROS, N. F.; DIAS, S. C. M. Parameterization of the 3PG model for Eucalypt in the region of Cerrado in Minas Gerais State. Ciência Florestal, Santa Maria, v. 22, n. 3, p. 567-578, 2012. ) were set as biologically plausible bounds (to give three test values: low, medium, high) in the estimation process. An algorithm was developed as part of an R3PG_Parameter_Testing pipeline using R software (R Core Team, 2021R CORE TEAM. R: A language and environment for statistical computing. Vienna, Austria.R foundation for statistical computing, 2021. Available at: https://www.r-project.org/.
https://www.r-project.org/...
) to generate all the possible combinations of the test parameter values. The R3PG calibration simulations utilized seventeen of the eighteen calibration sites listed in Table 1. One site (G22) was excluded due to tree theft at an early age, and the provided inventory data were from the adjacent compartment.

Table 4:
Test parameters and their values set as bound during parameter estimation.

No observed time-series data for the state variables (W F , W S , W R and θ S ) were available for parameter estimation in this study. We simulated growth from planting date (at age 0) and the initial biomass pools were set using default values (WF = 50%, WS = 25%, and WR = 25%) (Sands, 2010SANDS, P. J. 3PGPJS User Manual, 2010. Available at: Available at: https://3pg.sites.olt.ubc.ca/files/2014/04/3PGpjs_UserManual.pdf . Accessed in: May 18th 2020
https://3pg.sites.olt.ubc.ca/files/2014/...
). Therefore, parameter estimation was based on quadratic mean DBH, quadratic mean height, and basal area as surrogates for stem biomass. Basal area was selected because it is a function of stocking. The leaf area index (LAI) is a surrogate for foliage biomass. Though we lacked observed ground-based time-series LAI data for this study, we still evaluated the biological plausibility of the parameter and resulting 3PG predicted LAI values by qualitatively comparing them to the Landsat 8 Collection 1 Tier 1 Normalized Difference Vegetation Index (NDVI) product. We used the 8-Day NDVI composite dataset retrieved from Google Earth Engine (GEE) environment. The complete scripts and the template file for this algorithm are available on GitHub at https://github.com/EucXylo/R3PG_parameter_testing.

Selecting the optimized parameter set (pset)

All candidate psets generated were evaluated by matching their predicted Dq, Hmean, and BA values to corresponding observed data. To determine the best performing pset, a modified RMSE was used to account also for slope effects as defined in Equation 12. Where n is the number of observed values, SSE is the sum of square error, SSF is the sum of square fit (Figure 3).

e R M S E = S S E + S S F 2 n (12)

Figure 3:
A hypothetical graph explaining the eRMSE concept. Where SSE is the sum of square error (R3PG-predicted vs. observed values); SSF is the sum of square fit error (line of best fit prediction vs observed values); solid red line identity line; black dashed line is the line of best fit; blue squares are the R3PG-predicted vs. observed values data; black circles are the regression fit values; red circle represents a perfect model.

Validation evaluation of 3PG performance

The predictive accuracy of the 3PG model was further tested by validating the model against data from 15 independent sites in the same region. Stand growth data at a specific age (ranging from 4 - 9 years) were made available. Summary of the site and stand information used is presented in Table 1. Weather data were obtained using the interpolation technique described. Plant available soil water was estimated from the South African soil classification map. However, ASW obtained from this map were overestimated (99 - 105mm) for sandy soil compared to the typical value (±80mm) for the region’s soil form specified by Olivier (2017)OLIVIER, F. Irrigation: Basics of Irrigation Scheduling: Information Sheets. Available at: Available at: https://www.sugar.org.za . Accessed in: September 30th 2021.
https://www.sugar.org.za...
and those derived from soil texture (34.7 - 60.7mm) used in model calibration. For this reason, the initial ASW was set as the mean ASW of the calibration sites. The optimized parameter set selected and three other Brazilian parameter sets by Borges et al. (2012BORGES, J. S.; NEVES, J. C. L.; LOURENCO, H. M.; de BARROS, N. F.; DIAS, S. C. M. Parameterization of the 3PG model for Eucalypt in the region of Cerrado in Minas Gerais State. Ciência Florestal, Santa Maria, v. 22, n. 3, p. 567-578, 2012. ) and Almeida et al. (2004ALMEIDA, A. C.; LANDSBERG, J. J.; SANDS, P. J. Parameterisation of 3-PG model for fast-growing Eucalyptus grandis plantations. Forest Ecology and Management, v. 193, n. 1-2, p. 179-195, 2004. ) were used to run the 3PG model.

Using these parameter sets, four sets of model predicted mean height and basal area were obtained and used to estimate stand volume using Equation 4; and these were compared with observed stand volume. The following statistical error and indices from AgriMetSoft (2019)AGRIMETSOFT. Agricultural and Meteorological Software. Online Calculator. Available at Available at https://www.agrimetsoft.com/calculators/ . Accessed in: August 14th 2021.
https://www.agrimetsoft.com/calculators/...
were used to evaluate the performance of the 3PG model: Root mean square error (RMSE), coefficient of determination (R2), and Nash Sutcliffe efficiency index (E).

Simulation software

For this study, simulation runs and optimization were performed using the 3PG package developed by Trotsiuk et al. (2020TROTSIUK, V.; HARTIG, F.; FORRESTER, D. I. r3PG - An r package for simulating forest growth using the 3-PG process-based model. Methods in Ecology and Evolution, v. 11, n. 11, p. 1470-1475, 2020. ) in the R system for statistical computing (R Core Team, 2021R CORE TEAM. R: A language and environment for statistical computing. Vienna, Austria.R foundation for statistical computing, 2021. Available at: https://www.r-project.org/.
https://www.r-project.org/...
). The package offers users a flexible switch between various options and submodules to use the original 3PGpjs (Landsberg; Waring, 1997LANDSBERG, J. J.; WARING, R. H. A generalised model of forest productivity using simplified concepts of radiation-use efficiency, carbon balance and partitioning. Forest Ecology and Management, v. 95, n. 3, p. 209-228, 1997. ) and 3PGmix (Forrester; Tang, 2016FORRESTER, D. I.; TANG, X. Analysing the spatial and temporal dynamics of species interactions in mixed-species forests and the effects of stand density using the 3-PG model. Ecological Modelling, v. 319, p. 233-254, 2016. ). To run the original 3PGpjs, we used settings = list(light_model = 1, transp_model = 1, phys_model = 1, height_model = 1, correct_bias = 0, calculate_d13c = 0). The function run_3PG was designed for SingleSite run type. As a result, we developed a for-loop function to run R3PG for MultiSite run type.

RESULTS

Interpolated precipitation data

The average annual rainfall variation for all study sites from 2008 - 2018 was compared to the long-term mean rainfall (1959 - 1999) (Figure 4). It is worth noting the exceptionally dry years of 2014 and 2015, which marked the region’s driest period on record. The very high dimensionless statistical indexes (> 0.80) used to evaluate the model’s performance demonstrated a strong agreement between the observed and predicted precipitation data (Figure 4). RF model-predicted rainfall closely matches observed rainfall for the study period (2008 - 2018) (Table 2). This indicates that the RF model has been adequately calibrated to generate reliable rainfall predictions across the range of measured precipitation. In terms of prediction errors, the RF model exhibited lower errors (Figure 5). Nonetheless, there were indications of bias caused by the model’s underestimation at the Oribi-flat Minnehaha weather station for a particular month (the square symbol in Figure 5). Given the excellent performance of the RF model, it was used to generate high-resolution weather data for growth modelling in this study.

Figure 4:
Mean annual rainfall for study sites (2008 - 2018) predicted by the Random Forest model. The black dash line indicates the long-term mean rainfall.

Figure 5:
Comparison of observed and model-predicted monthly rainfall for six validation stations using the Random Forest model. Shapes represent weather stations.

Allometric parameters aS and nS

The biomass equations, with aS = 0.099 and nS = 2.51, fitted the data well (R2 = 0.99; p < 0.001) (Figure 6). The standard errors for this parameter calibration are aS = 0.477 and nS = 0.005.

Figure 6:
Allometric relationship between mean single-tree stem biomass (wS) and Dq.

Parameter estimation

The parameter set with the lowest eRMSE was selected as the optimized parameter values for E.grandis x E.urophylla in the coastal Zululand region of South Africa. The list of parameter values for this study and Brazilian clones are presented in Table 5. Utilizing this parameter set enabled accurate predictions of mean height, basal area, quadratic diameter and stand volume during the calibration phase. The 3PG predictions explained over 80% of the variance for all output variables across the 17 calibration sites (Figure 7). The linear regression for all output variables were significantly different from zero (p < 0.001 ) (Figure 7). There was a low negative average bias for the output variables considered (-0.17 to -1.64), except for stand volume (-5.99) (Figure 7). This is as result of the model underprediction in most sites (Figure 7). The Nash Sutcliffe model efficiency index (E) indicated a strong match between 3PG prediction and observed data (E > 0.70, where E = 1 indicates a perfect match) (Figure 7).

Table 5:
List and source of parameters used in the calibration of 3PG, and the result of the 3PG calibration in this study.

Figure 7:
Statistics describing the relationship between observed and predicted variables at the calibration stage for (a) quadratic mean diameter (b) mean height (c) basal area, and (d) volume. Black dash lines are identity lines (1:1), solid black lines are fitted lines from the regression.

At the validation stage, the model-predicted basal area and mean height were used to estimate stand volume using Equation 4. All four parameter sets accounted for more than 60% of the variance in the observed stand volume (Figure 8), but the two parameter sets from Almeida et al. (2004ALMEIDA, A. C.; LANDSBERG, J. J.; SANDS, P. J. Parameterisation of 3-PG model for fast-growing Eucalyptus grandis plantations. Forest Ecology and Management, v. 193, n. 1-2, p. 179-195, 2004. ) significantly undestimated fast-growing sites (Figure 8). The parameter set developed by Borges et al. (2012BORGES, J. S.; NEVES, J. C. L.; LOURENCO, H. M.; de BARROS, N. F.; DIAS, S. C. M. Parameterization of the 3PG model for Eucalypt in the region of Cerrado in Minas Gerais State. Ciência Florestal, Santa Maria, v. 22, n. 3, p. 567-578, 2012. ) has slightly greater precision (R2 = 0.68) compared to this study (R2 = 0.65) but it showed poor performance in terms of slope (Figure 8). The low modelling efficiency index observed with the optimized parameters derived in this study was due to the overprediction by the 3PG model (Figure 8). Overall, the optimized parameter set accurately reproduced the time-course growth pattern of the E.grandis x E.urophylla hybrids growing in the coastal Zululand region (Figures 9 and 10).

Figure 8:
Statistics describing the relationship between observed and predicted stand volumes for the different parameter set (a) Borges et al. (2012BORGES, J. S.; NEVES, J. C. L.; LOURENCO, H. M.; de BARROS, N. F.; DIAS, S. C. M. Parameterization of the 3PG model for Eucalypt in the region of Cerrado in Minas Gerais State. Ciência Florestal, Santa Maria, v. 22, n. 3, p. 567-578, 2012. ), (b) This study, (c & d) Almeida et al. (2004ALMEIDA, A. C.; LANDSBERG, J. J.; SANDS, P. J. Parameterisation of 3-PG model for fast-growing Eucalyptus grandis plantations. Forest Ecology and Management, v. 193, n. 1-2, p. 179-195, 2004. ) used at the validation sites. Black dash lines are identity lines (1:1), solid black lines are fitted from the regression equation.

Figure 9:
Comparison of observed (line with dark circles) and predicted (line with white triangles) time series quadratic mean diameter (cm) for the calibration plots. The two black vertical lines represent drought years (2014 - 2015).

Figure 10:
Comparison of observed (line with dark circles) and predicted (line with white triangles) time series mean height (cm) for the calibration plots. The two black vertical lines represent drought years (2014 - 2015).

We observed realistic 3PG predicted LAI at some sites, particularly in the Northern (dry) region (E6a, B3a, B003, B032, and C15a). However, it is worth noting that within the Southern (wet) region, some sites (A017, B044, B35b, B38, C55, J006) exhibited remarkably high peak LAI values. The qualitatitive analysis of the predicted LAI in relation to the Landsat 8 NDVI values indicated a general decline in the NDVI values throughout the drought period from 2014 to 2015 (Figure 11).

Figure 11:
Comparison of 3PG predicted LAI values (line with dark circles) and Landsat 8 NDVI values (line with white triangles) across the 17 calibration sites. The two black vertical lines represent drought years (2014 - 2015).

DISCUSSION

This study findings suggest that 3PG model can be calibrated by estimating key parameters from a published parameter set developed in a different region. This aligns with the work of Fontes et al. (2006FONTES, L.; LANDSBERG, J.; TOMÉ, J.; TOMÉ, M.; PACHECO, C. A.; SOARES, P.; ARAUJO, C. Calibration and testing of a generalized process-based model for use in Portuguese eucalyptus plantations. Canadian Journal of Forest Research, v. 36, n. 12 p. 3209-3221, 2006. ), where they calibrated the 3PG model for Portuguese eucalypt plantations using parameter set developed in Austrialia by Sands and Landsberg (2002SANDS, P. J.; LANDSBERG, J. J. Parameterisation of 3-PG for plantation grown Eucalyptus globulus. Forest Ecology and Management, v. 163, n. 1-3, p. 273-292, 2002. ). The coefficient (a S ) in the allometric relationship between tree-level biomass and DBH was higher (0.099) compared to values obtained by Almeida et al. (2004ALMEIDA, A. C.; LANDSBERG, J. J.; SANDS, P. J. Parameterisation of 3-PG model for fast-growing Eucalyptus grandis plantations. Forest Ecology and Management, v. 193, n. 1-2, p. 179-195, 2004. ) and Borges et al. (2012BORGES, J. S.; NEVES, J. C. L.; LOURENCO, H. M.; de BARROS, N. F.; DIAS, S. C. M. Parameterization of the 3PG model for Eucalypt in the region of Cerrado in Minas Gerais State. Ciência Florestal, Santa Maria, v. 22, n. 3, p. 567-578, 2012. ), while the power (n S ) in the allometric relationship fell within the range of values reported by both authors. These parameters play a crucial role in predicting stem diameter and basal area using the 3PG model.

Of the eight parameters estimated in this study, two parameters differed from the reported Brazilian clone values used as references: biomass partitioning between the foliage and stem (pFS2) and the minimum temperature (Tmin). The optimum temperature (Topt) matched the value obtained by Esprey (2006), while the maximum fraction of NPP allocated to the roots (pRx) match those obtained by Almeida et al. (2004ALMEIDA, A. C.; LANDSBERG, J. J.; SANDS, P. J. Parameterisation of 3-PG model for fast-growing Eucalyptus grandis plantations. Forest Ecology and Management, v. 193, n. 1-2, p. 179-195, 2004. ). The soil water modifier (SWconst and SWpower) were different from the Brazilian parameters due to the soil type, while the remaining parameters matched values obtained by Borges et al. (2012BORGES, J. S.; NEVES, J. C. L.; LOURENCO, H. M.; de BARROS, N. F.; DIAS, S. C. M. Parameterization of the 3PG model for Eucalypt in the region of Cerrado in Minas Gerais State. Ciência Florestal, Santa Maria, v. 22, n. 3, p. 567-578, 2012. ).

Overall, the good agreement between the observed and predicted output variables (Figure 6) indicates adequate calibration of the 3PG parameters to predict forest growth in the study area. Furthermore, the eRMSE method demonstrated its ability to select optimized parameter with minimal residuals, low bias and a close alignment to the identity line (Figure 6). However, the 3PG model’s accuracy in simulating the four output variables considered during the calibration was lower than Borges et al. (2012BORGES, J. S.; NEVES, J. C. L.; LOURENCO, H. M.; de BARROS, N. F.; DIAS, S. C. M. Parameterization of the 3PG model for Eucalypt in the region of Cerrado in Minas Gerais State. Ciência Florestal, Santa Maria, v. 22, n. 3, p. 567-578, 2012. ) for E.grandis x E.urophylla, with BA (R2 = 0.98), Dq (R2 = 0.97), Hmean (R2 = 0.95), and stand volume (R2 = 0.92). Similarly, Almeida et al. (2004ALMEIDA, A. C.; LANDSBERG, J. J.; SANDS, P. J. Parameterisation of 3-PG model for fast-growing Eucalyptus grandis plantations. Forest Ecology and Management, v. 193, n. 1-2, p. 179-195, 2004. ) reported R2 = 0.96 for BA, R2 = 0.98 for Dq, and R2 = 0.98 for stand volume. In contrast, for Eucalyptus grandis in South Africa, Esprey (2006) reported R2 = 0.68 for Dq and R2 = 0.69 for Hmean which are lower than the one obtained in this study.

The 3PG model underpredicted early growth from age zero to about five years at certain sites during the calibration phase (Figures 8 and 9). According to Landsberg and Waring (1997LANDSBERG, J. J.; WARING, R. H. A generalised model of forest productivity using simplified concepts of radiation-use efficiency, carbon balance and partitioning. Forest Ecology and Management, v. 95, n. 3, p. 209-228, 1997. ), these systematic errors are expected due to the limitation of using Beer’s law to calculate absorbed photosynthetically active radiation. The model assumes a closed canopy which is not always true for young eucalypt plantations. In this study, some sites experienced mortality at post-planting, resulting in increased canopy gaps. This explains the bias reported in Figure 6. However, as the stand age, 3PG prediction tends to match with the observed values (Figures 8 and 9). This pattern was also observed by Esprey (2006)FONTES, L.; LANDSBERG, J.; TOMÉ, J.; TOMÉ, M.; PACHECO, C. A.; SOARES, P.; ARAUJO, C. Calibration and testing of a generalized process-based model for use in Portuguese eucalyptus plantations. Canadian Journal of Forest Research, v. 36, n. 12 p. 3209-3221, 2006. and Miehle et al. (2009MIEHLE, P.; BATTAGLIA, M.; SANDS, P. J. et al. A comparison of four process-based models and a statistical regression model to predict growth of Eucalyptus globulus plantations. Ecological Modelling, v. 220, n. 5, p. 734-746, 2009. ).

During the validation phase, the performance of the 3PG model indicated its capacity to forecast stand growth across a wide range of sites which were not previously calibrated. The optimized parameter set provided a reasonble prediction of the observed stand volume. However, the model tended to overpredict in most sites (Figure 7), possibly due to uniform values of ASW and FR used across the validation sites. Due to the lack of detailed information on soil properties at the validation sites, we used the mean ASW from the calibration sites. The weak correlation between FR and soil nutrients observed during the examination of FR variation across the sites can be attributed to the high leachabilty of nutrients from the well-drained, coarse-textured soils present in this region (Dye et al., 2004DYE, P. J.; JACOBS, S.; DREW, D. Verification of 3-PG growth and water-use predictions in twelve Eucalyptus plantation stands in Zululand, South Africa. Forest Ecology and Management, v. 193, p. 197-218, 2004. ). This emphasizes on the significance of a high-quality soil profile map for this region to obtain accurate soil information for tree growth modelling.

The 3PG model demonstrated its utility in identifying and quantifying the effects of the environmental factors affecting tree growth. This was illustrated using the 2014 - 2015 dry period (Figures 8 and 9). During the observed period, a noticeable decline in the growth rate of trees occurred across the majority of sites. However, we found that specific locations A017, B044, F011A, B35b, and C55 exhibited continuous growth even admist the dry period. It is important to emphasize that the decline in the Landsat 8 NDVI and 3PG predicted LAI values indicates an overall reduction in vegetation vigor (Figures 10). Nevertheless, the rate of decline and subsequent recovery varies across the different regions. These findings are consistent with the conclusions of Xulu et al. (2018XULU, S.; PEERBHAY, K.; GEBRESLASIE, M.; ISMAIL, R. Drought influence on forest plantations in Zululand, South Africa, using MODIS time series and climate data. Forests, v. 9, n. 9, p. 528, 2018.), who also noted that certain clones in central east region of KwaMbonambi showed stable NDVI values during the dry period, while others declined. Visually inspecting these sites from satellite imagery shows they were established adjacent to indigenous forest conservation zones, which almost invariably grow along perennial watercourses. Accordingly, it would seem very likely that these plots had higher-than-normal access to groundwater. As a result, we increased the minimum available soil water (MinASW), which indicates access to the water table, and the 3PG model effectively simulated the observed continuous growth in these sites.

The concurrence of these observations lends credibility to the biological plausibility of the 3PG model’s predictions and supports its effectiveness in capturing changes in vegetation dynamics in response to fluctuating environmental conditions such as droughts.

CONCLUSIONS

The random forest regression model offers an accurate and reliable approach for estimating long-term weather data for ungauged sites, enabling their use in process-based modelling. The R3PG package facilitated model parameterization by integrating several algorithms with the 3PG model. The study concluded that the 3PG model could be calibrated using parameter set from a different region to characterize Eucalyptus grandis x urophylla hybrid stands in South Africa. The MinASW variable enables accurate simulation of sites with access to ground water. The overprediction of stand volumes observed during the validation stage was due to the lack of soil water information at the validation sites, emphasizing the neccesity for accurate soil information in this area. Overall, the 3PG model demonstrated its potential in providing realistic predictions of stand growth over time in response to environmental and management changes, as well as exploring scenarios (“what if” questions).

ACKNOWLEDGEMENTS

We express our sincere gratitude to Mondi South Africa and Sappi South Africa for providing the PSPs data and funding. We also appreciate the South African Sugarcane Research Institute (SASRI) and South African Weather Services (SAWS) for providing the weather data.

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Publication Dates

  • Publication in this collection
    27 Nov 2023
  • Date of issue
    2023

History

  • Received
    01 Mar 2023
  • Accepted
    23 June 2023
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