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Article

A Complete Assessment of Carbon Stocks in Above and Belowground Biomass Components of a Hybrid Eucalyptus Plantation in Southern Brazil

by
Márcio Viera
1,* and
Roque Rodríguez-Soalleiro
2
1
UFSM Polytechnic School, Federal University of Santa Maria (UFSM), Santa Maria 97105900, Brazil
2
Department of Vegetal Production, University of Santiago de Compostela (USC), 27154 Lugo, Spain
*
Author to whom correspondence should be addressed.
Forests 2019, 10(7), 536; https://doi.org/10.3390/f10070536
Submission received: 14 May 2019 / Revised: 24 June 2019 / Accepted: 26 June 2019 / Published: 27 June 2019
(This article belongs to the Special Issue Forest Carbon Inventories and Management)

Abstract

:
Hybrid eucalypt clones are grown for fiber production worldwide and to provide an ecosystem service that can store atmospheric carbon at a very fast rate. This study assessed the carbon stocks in the soil and various tree fractions in a 10-year-old plantation of Eucalyptus urophylla S.T. Blake × Eucalyptus globulus Labill. in Southern Brazil. Four experimental plots were established, and an inventory of Eucalyptus trees was conducted by considering five diametric classes. Three trees in each diametric class were harvested for biomass and carbon quantification. The understory biomass of native trees was quantified in five subplots and the litter was quantified in 16 subplots. Organic C was quantified in the soil (SOC) and roots (diameter ≤ 0.5 cm) to a depth of 100 cm. The C concentration in the different biomass fractions of the eucalyptus trees were 55.7% (±0.6), 50.4% (±0.4), 49.5% (±0.6) and 45.4 % (±0.9) for leaves, branches, wood and bark, respectively. The C concentrations in the understory fractions were 51.4% (±1.0) for the canopy and 50.0% (±0.9) for the stem. The carbon concentration in the fine root biomass was 45.7% (±1.4). Soil C concentrations were 1.23% (±0.32), 0.97% (±0.10), 0.45% (±0.14), and 0.24% (±0.10) for depths of 0–25, 25–50, 50–75, and 75–100 cm. C was allocated in: (a) the trees (aboveground fraction = 118.45 Mg ha−1 and belowground fraction = 30.06 Mg ha−1), (b) the understory = 1.44 Mg ha−1, (c) the litter = 8.34 Mg ha−1, and (d) the soil (without roots) = 99.7 Mg ha−1. The share of total C stock (a + b + c + d = 258.0 Mg ha−1) was similar in the aboveground (49.7%) and belowground (50.3%) fractions, thus indicating a very high rate of C sequestration in the biomass. Eucalyptus plantations in Brazil are fast growing (for this study = 36.7 m³ ha−1 year−1) and contribute to intense carbon sequestration in above and belowground biomass (14.8 Mg ha−1 year−1).

1. Introduction

Demand for wood products has grown strongly in recent years, thereby increasing interest in the use of land for fast-growing tree plantations. In Brazil, the total area covered by forest plantations in 2017 was about 9.8 M ha [1], yielding 91% of the wood destined for industrial purposes [2]. Eucalyptus was first introduced to Brazil more than 150 years ago. Plantations of the species now cover an area of 7.4 M ha and represent 75.2% of all forest plantations in the country [1] and yield on average 39 m3 ha−1 year−1 [2]. Eucalyptus has been planted extensively in Brazil in the past 10 years, with an increase of about 70% in plantations of the species in the period. Short rotations are used for pulpwood (6–7 years) and slightly longer rotations for solid timber (12–15 years). The main products are pulp, paper, wood panels, laminate flooring, plywood panels, furniture, other solid wood products, and charcoal and biomass for energy purposes [2].
Forest plantations play an important role in the global carbon cycle [3,4], as when forests grow, carbon is removed from the atmosphere and stored in the plants [5,6,7]. New forest establishment is of ecological, environmental, social, and economic value [6] and results in large amounts of C being sequestered [7,8,9], although trade-offs involving the impacts on hydrology and biogeochemistry should be taken into account [10]. Plantations can maximize carbon sequestration, but also have adverse side effects such as reduced stream flow [11] and decreased soil pH and base saturation [10].
Increasing the carbon stock depends on the biomass allocation of each species and the C concentrations in each component [12]. Biomass allocation depends on the resources available at the site as well as the type of management [13], stand age [3,9], and rotation length [14]. Likewise, the accumulation of soil carbon depends on the type of land use [15,16], soil chemical and physical properties [8], climatic conditions [7], net primary productivity, fertilization, site preparation, and soil drainage [17].
The transformation of the current fossil fuel-based energy generation systems to sustainable and renewable energy (RE)-based systems by ‘carbon-neutral’ alternatives has been reported to be essential [18]. Brazil is one of 97 developing countries that have included land use, land use change and forestry (LULUCF) in their nationally determined contributions (NDCs). However, the LULUCF sector requires scientific data to ensure that the national reports are consistent, complete, and comparable [19]. Several studies have estimated the carbon stocks in Eucalyptus stands (i.e., [20,21,22,23,24], but there is still a lack of studies considering all ecosystem components in the plantations including both above and belowground components such as the tree biomass and soil fraction. Accurate methods of estimating carbon stocks in forest stands are required for building and validating regional models [4]. In addition, the understory and the litter layer must be considered additional pools for estimating stand carbon sequestration [25]. Hybrid eucalypt clones in Brazil grow very quickly and thus have a high capacity to fix atmospheric carbon. Carbon stocks can be estimated in forestry plantations by biomass quantification, subsequent determination of C concentration, and fitting allometric equations.
The main goal of this study was to carry out a complete assessment of carbon stocks in a eucalypt plantation, close to the rotation age, and thus with stabilized C concentrations. An additional aim was to compare the carbon concentrations in above and belowground biomass components and the carbon stock in the soil of a 10-year-old hybrid plantation of Eucalyptus urophylla × Eucalyptus globulus in Southern Brazil.

2. Materials and Methods

2.1. Site and Stand Description

The study was conducted in a 10-year-old Eucalyptus urophylla × E. globulus stand close to harvesting age (30°10′31.21′′ S and 51°36′17.85′′ W; elevation: 175 m a.s.l.). According to the Köppen system, the climate is classified as Cfa (humid subtropical). Average temperatures range from 13.4 °C in the coldest month to 24.3 °C in the hottest month, with an average annual rainfall of 1600 mm [26]. The soil is classified as an Acrisol, according to the Word Reference Base [27], and soil chemical and physical properties include a low cation exchange capacity, low base saturation, and acidic conditions (Table 1).
Eucalyptus seedlings were planted after minimum tillage in the planting line in July 2001. The stand was established with a spacing of 3.5 m × 2.5 m. Fertilizer was applied when the seedlings were planted, with 300 kg ha−1 of reactive phosphate and 100 g seedlings−1 of 06-30-06 (N-P2O5-K2O). After planting, fertilizer was applied twice, once in the third month and again in the twelfth month, with 15-05-30 (N-P2O5-K2O) 100 g plant−1.

2.2. Tree Sampling and Measurements

Four inventory plots (35 m × 20 m) were systematically established in a 10-year-old Eucalyptus urophylla × E. globulus stand. The diameter at breast height (DBH) and total height (H) were measured in all of the trees in each plot, and the density of live trees was calculated. The structure of the stand was very homogeneous in terms of density and tree size, with a coefficient of variation of tree height of only 9% (Table 2). Predictive equations were used to calculate stand variables such as basal area, standing volume, and leaf area index (LAI). The mean annual increment was 36.7 m3 ha−1 year−1, which is an intermediate level of productivity in the Brazilian context (Table 2). Based on the stand DBH distribution, trees were included in five diameter classes: 9.1–13.0; 13.1–17.0; 17.1–21.0; 21.1–25.0, and 25.1–29.0 cm, which corresponded to 5%, 18%, 32%, 37%, and 9% in relation to the total number of trees.
Three trees in each diameter class were harvested for the evaluation of the carbon stocks in aboveground Eucalyptus biomass. For each of the 15 trees harvested, the aboveground biomass was separated into four components: leaves, branches, bark, and commercial wood (smaller diameter use = 6.0 cm). Stems of diameter less than 6 cm were considered as branches.
The fresh weight of each tree component was measured and samples were taken to determine the dry weight and carbon contents. Wood and bark were sampled at three different points along the stem at relative heights of 0.25, 0.5, and 0.75. Branches and leaves were sampled randomly throughout the canopy, considering a sampling intensity of 5% of the total amount in each tree. The samples were transported to the laboratory and dried in a convection oven at 70 °C for 72 h to determine the dry weight and estimate the total carbon per tree and component.

2.3. Understory and Litter Sampling

Five 5 × 5 m square plots were systematically established in the Eucalyptus stand to estimate the understory biomass. The positions of the understory plots followed the same rectangular grid used for the inventory plots, leading to a 3 × 3 layout of the plots. In each understory plot, all plants except for the eucalyptus trees were cut and separated into two biomass components: leaves and stem. The understory was composed of more than 15 native tree species of the Atlantic Forest Biome (mainly Cupania vernalis Cambess.) with individuals less than 3 m in height and most plants at the initial stage of regeneration. The carbon accumulated in the litter layer was determined in four samples from each of the four plots used to measure Eucalyptus DBH and height. A square frame with an area of 0.0625 m2 was used for this purpose. All of the organic material inside the frame was sampled for biomass estimation. To calculate the total carbon accumulated in the litter layer, we considered that the carbon content represented 50% of the dry matter.

2.4. Root and Soil Sampling

Carbon was measured in the fine roots (diameter < 2 mm), medium roots with a diameter of 2–5 mm, medium roots of 5–10 mm, and soil. Nine sampling points were established in the middle of each of the nine aforementioned plots and the method of root sampling in soil pits was applied. A 1.3 m deep trench was manually excavated at each sample point for the collection of roots and soil. In each trench, four soil layers were demarcated for sampling: 0–25 cm, 25–50 cm, 50–75 cm, and 75–100 cm. A square frame with a side length of 10 cm was used to mark the area for excavating roots, yielding a volume of 2500 cm3 of soil for each sample at a 25 cm depth. The roots were separated from the soil by using water jets to wash the material through a set of sieves (2.0 mm and 0.34 mm meshes). The roots were dried and the dry mass was weighed on an analytical balance (accuracy 10−4 g). Soil samples were collected from the same trench for the analysis of organic carbon concentration and soil density.
The organic carbon in the different Eucalyptus components, understory, roots, and soil was determined on a dry weight basis in an element analyzer (Carlo Erba NA 1500, Milan, Italy).
As whole-tree excavation was not possible, the coarse root biomass was estimated for each inventoried tree by applying the model proposed by [28] for roots thicker than 10 mm in E. grandis × urophylla plantations of medium productivity including the stump:
Wcr = 0.0221 DBH2.6017 (n = 36)
where Wcr is the coarse root biomass (kg tree−1) and DBH is the tree diameter in cm. The C concentration determined for roots of 5–10 mm in this study was applied to the coarse roots.

2.5. Data Calculation and Analysis

The Eucalyptus aboveground carbon stock was estimated by fitting individual tree carbon regression models. The carbon content in different aboveground components of the Eucalyptus trees (leaves = Cl, branches = Cbr, bark = Cb, and wood = Cw) were considered as dependent variables. Different combinations of log-transformed independent variables were used: tree diameter (DBH), tree height (H), and power combinations of these variables DBHx Hy. A logarithmic transformation enabled the reflection of the relationships between variables, with the assumption of an underlying power function with a multiplicative error structure. The SPSS 13.0 application for Windows [29] was used for modeling. The goodness of fit of the models was evaluated by considering the coefficient of determination (R2 adjusted), standard error of estimate (Syx), and by the graphic evaluation of the relationships between the observed and estimated values. The amount of carbon per hectare was estimated by the regression of the data from the forest inventory and extrapolation based on the area of the plot.
The accumulated understory carbon was estimated by multiplying the carbon content in the dry biomass of each component per plot and extrapolated to a per hectare basis. For the litter layer, the dry biomass of each subplot (n = 16) was multiplied by the carbon content (assuming a 50% content) and the amount was then extrapolated to a per hectare basis. For fine and medium roots, the biomass at each depth (n = 4) and at each point (n = 9) was multiplied by the corresponding carbon content, and extrapolated to a per hectare basis. For each soil sample, carbon stocks were calculated by multiplying soil carbon concentration by the bulk density (kg m−3) of each plot and by the depth of the soil layer. The bulk density was calculated by dividing the dry mass of soil (105 °C) by the volume of the sampling cylinder.
Duncan’s test was used to identify significant differences in the values. Analysis of variance (ANOVA) was used to test the effects of the tree components and soil depth on carbon concentration in the Eucalyptus fine roots and soil. All statistical tests were performed with the SPSS 13.0 application for Windows [29] after checking the ANOVA assumptions.

3. Results

3.1. Equations for Eucalyptus Aboveground Carbon Estimation

The equations selected for estimating the carbon amounts in the biomass components are shown in Table 3. The value of the adjusted coefficient of determination was high, the value of the standard error of estimate was low, and the residuals were normally distributed. This demonstrates that the equations obtained by the stepwise procedure performed well in relation to predicting the carbon content per component and tree (Figure 1).
All models were highly significant and the assumptions of normality and homogeneity of variances were met. The coefficient estimates were also significant (branches, p = 0.019; other components, p < 0.001). The equations for estimating the carbon contents of the wood components and total tree had a predictive power greater than 99.5% of the distribution of dependent variables and low standard error of estimation (0.0547 and 0.0490, respectively).

3.2. Aboveground Carbon Concentration and Contents

The Eucalyptus aboveground biomass contained different concentrations of organic carbon (p ≤ 0.05). The C concentration was higher in leaves, followed by branches, wood and bark (Table 4). The difference between the carbon concentration in leaves and bark was more than 100 g kg−1 biomass. Even for the highest concentration of organic carbon in leaves, the stock represented 1.6% of the total carbon stocked in the Eucalyptus aboveground biomass. The wood component accounted for more than 80% of the total carbon content of the trees, followed by the bark and branches.
The understory contributed 1.44 Mg ha−1 to the total carbon stock in the stand (Figure 2). The understory comprised herbs, shrubs, and small individuals of native tree species. The litter layer contained 8.34 Mg ha−1 carbon. Litter was composed of plant residues (Eucalyptus and understory) and represented 6.5% of the carbon stock in the aboveground biomass. Total carbon stock in aboveground biomass was 128.23 Mg ha−1, allocated in Eucalyptus biomass (92.4%), litter (6.5%), and understory (1.1%).

3.3. Belowground Carbon Concentration and Contents

The carbon concentration in the fine roots was higher (p ≤ 0.05) in the upper soil layer than at depths below 50 cm. The difference between the average carbon concentrations in the roots of the upper soil layer (0 to 25 cm in depth) and the deepest layer evaluated (75 to 100 cm) was more than 30 g kg−1. Almost 70% and 76% of the carbon stocks in the fine and medium roots, respectively, occurred in the upper soil layer (upper 25 cm) (Table 3 and Figure 3).
The sum of the C stocks in fine and medium roots was 0.95 Mg ha−1. The estimated C stock in the coarse roots was 29.11 Mg ha−1, with a small variation between the plots (Figure 2).
The soil organic carbon concentration was influenced by the soil depth (p ≤ 0.05). The carbon concentration in the upper layer was five times higher than in the deeper soil layer, directly reflecting the amount of carbon stocked in the soil. For a depth of 1 m, more than 43% of the soil carbon stock occurred in the upper layer (depth 25 cm). The total belowground carbon stock was 129.8 Mg ha−1 (roots + soil), corresponding to 50.3% of the carbon stocked in the Eucalyptus stand.

4. Discussion

The ability to measure the total amount of carbon in forest ecosystems accurately and precisely is required to evaluate the role of forests in the global carbon cycle [30]. In most forests, the largest C pools occurs in the aboveground live biomass and mineral soil organic matter, with smaller amounts in the roots and litter layer [31]. The most rapidly changing pool is usually the aboveground live biomass, with important differences between natural forests and forest plantations [32,33]. The size of the pool in the root biomass can be directly estimated by the average 0.26 root:shoot biomass ratio, but the soil pool is seldom related to the aboveground biomass or forest age [31].
In the present study, we determined the distribution of C stocks in a stand close to rotation age. Although variations in C stocks over time have not been studied, it is clear that land use change has led to an accumulation of aboveground C, resulting in a pool that is similar to that in the underground stock (including the roots and soil). Rapid accumulation of C stocks in the biomass of fast growing plantations has already been noted, with estimated rates of accumulation of 8.3–12.8 Mg C ha−1 year−1 in aboveground components reported [23]. The corresponding value determined in the present study was 11.8 Mg C ha−1 year−1. In the Eucalyptus aboveground biomass, the C was predominantly allocated in the wood, followed by the bark, branches, and leaves. This was consistent with previous findings in Eucalyptus plantations [3,9,23].
The C concentration determined in this study was highest in the leaves, followed by the branches, wood, roots, and bark. Although this gradient has previously been reported in other Eucalyptus plantations [24,34], the present study provides complementary information such as the increase in root C concentration with root diameter and the decrease in C concentration in fine roots with soil depth. Carbon budgets are usually calculated on the basis of the assumption that plant biomass is 50% C. For this study, the weighted average for Eucalyptus biomass was 48.9%. Thus, the general application of 50% C to all components would lead to a slight over-prediction of 3.4 Mg C ha−1 (relative error of 2.3%). Weighted averages of 47.7% for the aboveground biomass of E. globulus and E. nitens in Spain [12] and 49.77% for the above and belowground components of the same species in Tasmania [35] have previously been reported.
The understory biomass is not usually considered in studies of carbon fixation in fast-growing plantations. In the present study, we found that more than 1% of the total carbon stocked in the aboveground biomass was in the understory and that the C concentration in this ecosystem component was slightly higher than 50% (weighted average, 50.2%). In a study carried out in a E. urophylla × E. grandis stand of age 6–8 years in China, about 2% of the aboveground carbon was fixed in the understory biomass [3]. The relatively small amount of carbon found in the understory in the present study can be explained by the full canopy cover (leaf area index of 2.55 m2 m−2) of the plantation. Nonetheless, relative to the previous land use (pasture), afforestation has led to the presence of an understory of native trees.
Fine and medium roots thinner than 10 mm contributed 0.95 Mg ha−1 to the total C stock. More than 70% of the carbon stock in the fine and medium roots occurred in the topsoil (25 cm deep) where the highest C concentration in fine roots occurred. Considering the estimated amount of C in the coarse roots and stump, the root:shoot ratio for C stocks obtained in this study was 25.4, with a biomass root:shoot ratio of 26.5, a value close to that reported for allometric biomass relationships in angiosperms worldwide [36]. This indicates the importance of the accurate estimation of coarse root biomass for calculating the total ecosystem C budgets [35]. Tree root systems represent an important component of forest ecosystems because they absorb water and soil nutrients, thus supporting the arboreal structure and function as a store of nutrients and carbon [37,38]. Previous estimations of root C stocks in 8-year-old plantations in the same regions of this study provided values ≥10 Mg ha−1 [39].
In the present study, 38.6% of the total organic carbon in the Eucalyptus plantations occurred in the soil. In a study of other Eucalyptus plantations aged seven years, the ratio between the organic carbon in the soil (to a depth of 100 cm) and the total carbon was found to be greater (43%–63%) [40]. Soil organic matter comprises the largest C pool in many natural forests, but the aboveground biomass C pool is the predominant pool in forest plantations [31], as observed in the present study. Moreover, important losses of soil organic carbon occur in the upper mineral soils during the first decade after afforestation [41]. Such losses are common in afforested grassland soils under humid temperate climates [42] and occur as a consequence of mineralization of the labile fraction produced by soil disturbance during planting, even when minimum tillage is applied. Although we were not able to assess such losses in this study, this effect should be considered when land use changes are proposed.
The depth at which the soil is sampled is an important source of uncertainty in the determination of total C in forest ecosystems as forest soils are often very deep (several meters) [17]. The concentration of soil organic carbon (SOC) is influenced by the soil depth due to variations in organic matter. The carbon concentration in the upper soil layer found in this study was five times higher than in the deeper soil layers. Higher concentrations of carbon in the upper soil layers have generally been reported for other forest ecosystems, e.g., [3,6,40,43]. Most of the soil carbon in forest plantations (i.e., about 57% to 68%) has previously been detected in the upper 50 cm of soil [3,7,44]. This layer represented more than 75% of the soil carbon stock occurring within a depth of one meter in the present study. These results indicate the need to lengthen the rotations or make appropriate decisions at harvesting to prevent net soil C emissions due to soil disturbances during the operations.
The total C stored in the plantation under study was 258 Mg ha−1. This was much lower than the high biomass carbon densities found in native and older forests that are multi-aged, multilayered, and have been subjected to minimal human disturbance [45]. It is clear that protecting forests with large biomass stocks from deforestation and degradation (including transformation into plantations) prevents the release of significant carbon emissions into the atmosphere [46]. Plantations such as that considered in the present study are often established on former pasture land for the main purpose of the sustainable production of fiber, timber, and energy. The findings of the present and previous studies show that plantations, if adequately managed, can provide carbon sequestration as an important environmental service.

5. Conclusions

The total C stock in a fast growing (36.7 m³ ha−1 year−1) Eucalyptus plantation aged 10 years (biomass + soil) was 258 Mg ha−1 and was distributed between the aboveground (49.7%) and belowground (50.3%) components. The above and belowground eucalypt biomass accounted for 57.6% of total C, whereas the share of the wood component alone was 40%. Soil represented an important component, accumulating 38.6% of the total C, mainly in the upper 25 cm. Litter and understory represented 3.2% and 0.6% of the total C, respectively. Plantations established for the sustainable production of goods can provide C accumulation as an important ecosystem service at a rate of 11.8 Mg ha−1 year−1 (eucalyptus aboveground biomass) or 14.8 Mg ha−1 year−1 (including the root system).

Author Contributions

M.V. devised the project, performed the experiments, analyzed the data and drafted the manuscript. R.R.-S. performed additional analysis of data and discussed the results. Both authors contributed to the final version of the manuscript.

Funding

The National Council of Technological and Scientific Development (CNPq—Brazil) awarded the first author with a research grant (Award Number 200589/2014-8) for a one-year stay at the USC in Spain.

Acknowledgments

We thank the CMPC pulp company for making the study area available and for their logistical support. We also thank Mauro Valdir Schumacher and Peter Trüby for helping with the carbon determination.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analysis or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

References

  1. IBGE. Instituto Brasileiro de Geografia e Estatística. Produção da extração vegetal e da silvicultura. IBGE 2017, 32, 1–8. [Google Scholar]
  2. IBA. Brazilian Tree Industry; Report 2015; IBÁ: São Paulo, Brazil, 2015; 64p. [Google Scholar]
  3. Du, H.; Zeng, F.; Peng, W.; Wang, K.; Zhang, H.; Liu, L.; Song, T. Carbon storage in a Eucalyptus plantation chronosequence in Southern China. Forests 2015, 6, 1763–1778. [Google Scholar] [CrossRef]
  4. Volkova, L.; Bi, H.; Murphy, S.; Weston, C.J. Empirical estimates of aboveground carbon in open Eucalyptus forests of south-eastern Australia and its potential implication for national carbon accounting. Forests 2015, 6, 3395–3411. [Google Scholar] [CrossRef]
  5. Fialho, R.C.; Zinn, Y.L. Changes in soil organic carbon under Eucalyptus plantations in Brazil: A comparative analysis. Land Degrad. Dev. 2014, 25, 428–437. [Google Scholar] [CrossRef]
  6. Justine, M.F.; Yang, W.; Wu, F.; Tan, B.; Khan, M.N.; Zhao, Y. Biomass stock and carbon sequestration in a chronosequence of Pinus massoniana plantations in the upper reaches of the Yangtze River. Forests 2015, 6, 3665–3682. [Google Scholar] [CrossRef]
  7. Cook, R.L.; Binkley, D.; Stape, J.L. Eucalyptus plantation effects on soil carbon after 20 years and three rotations in Brazil. For. Ecol. Manag. 2016, 359, 92–98. [Google Scholar] [CrossRef]
  8. Sausen, T.L.; Schaefer, G.F.P.; Tomazi, M.; Santos, L.S.; Bayer, C.; Rosa, L.M.G. Clay content drives carbon stocks in soils under a plantation of Eucalyptus saligna Labill. in southern Brazil. Acta Bot. Bras. 2014, 28, 266–273. [Google Scholar] [CrossRef]
  9. Vallejos-Barra, O.; Daniluk-Mosquera, G.; Moras, G.; Ponce-Donoso, M.; Conteras, M.A. Above-ground carbon absorption in young Eucalyptus globulus plantations in Uruguay. Sci. For. 2014, 42, 9–19. [Google Scholar]
  10. Jackson, R.B.; Avissar, R.; Baidya, R.S.; Barrett, D.J.; Cook, C.W.; Farley, K.A.; LeMaitre, D.C.; McCarl, B.A.; Murray, B.C. Trading water for carbon with biological carbon sequestration. Science 2005, 310, 1944–1947. [Google Scholar] [CrossRef]
  11. Farley, K.A.; Jobbágy, E.G.; Jackson, R.B. Effects of afforestation on water yield: A global synthesis with implications for policy. Glob. Change Biol. 2005, 11, 1565–1576. [Google Scholar] [CrossRef]
  12. Rodríguez-Soalleiro, R.; Eimil-Fraga, C.; Gómez-García, E.; García-Villabrille, J.D.; Rojo-Alboreca, A.; Muñoz, F.; Oliveira, N.; Sixto, H. Exploring the factors affecting carbon and nutrient concentrations in tree biomass components in natural forests, forest plantations and short rotation forestry. For. Ecosyst. 2018, 5, 35. [Google Scholar] [CrossRef] [Green Version]
  13. Ryan, M.G.; Stape, J.L.; Binkley, D.; Fonseca, S.; Loos, R.A.; Takahashi, E.N.; Silva, C.R.; Silva, S.R.; Hakamada, R.E.; Ferreira, J.M.; et al. Factors controlling Eucalyptus productivity: How resource availability and stand structure alter production and carbon allocation. For. Ecol. Manag. 2010, 259, 1695–1703. [Google Scholar] [CrossRef]
  14. Liski, J.; Pussinen, A.; Pingoud, K.; Mäkipää, R.; Karjalainen, T. Which rotation length is favourable to carbon sequestration? Can. J. For. Res. 2001, 31, 2004–2013. [Google Scholar] [CrossRef]
  15. Maquere, V.; Laclau, J.P.; Bernoux, M.; Saint-Andre, L.; Gonçalves, J.L.M.; Cerri, C.C.; Piccolo, M.C.; Ranger, J. Influence of land use (savanna, pasture, Eucalyptus plantations) on soil carbon and nitrogen stocks in Brazil. Eur. J. Soil Sci. 2008, 59, 863–877. [Google Scholar] [CrossRef]
  16. Don, A.; Schumacher, J.; Freibauer, A. Impact of tropical land-use change on soil organic carbon stocks – a meta-analysis. Glob. Chang. Biol. 2010, 17, 1658–1670. [Google Scholar] [CrossRef]
  17. Lal, R. Forest soils and carbon sequestration. For. Ecol. Manag. 2005, 220, 242–258. [Google Scholar] [CrossRef]
  18. Karvonen, J.; Halder, P.; Kangas, J.; Leskinen, P. Indicators and tools for assessing sustainability impacts of the forest bioeconomy. For. Ecosyst. 2017, 4, 2. [Google Scholar] [CrossRef] [Green Version]
  19. Marasemi, T. Special Issue Information Forest Carbon Inventories and Management. 2019. Available online: https://www.mdpi.com/journal/forests/special_issues/Forest_Carbon_Inventories (accessed on 10 April 2019).
  20. Lima, A.M.N.; Silva, I.R.; Neves, J.C.L.; Novais, R.F.; Barros, N.F.; Mendonca, E.S.; Smyth, T.J.; Moreira, M.S.; Leite, F.P. Soil organic carbon dynamics following afforestation of degraded pastures with Eucalyptus in southeastern Brazil. For. Ecol. Manag. 2006, 235, 219–231. [Google Scholar] [CrossRef]
  21. Stape, J.L.; Bincley, D.; Ryan, M.G. Production and carbon allocation in a clonal Eucalyptus plantation with water and nutrient manipulations. For. Ecol. Manag. 2008, 255, 920–930. [Google Scholar] [CrossRef]
  22. Trugilho, P.F.; Arantes, M.D.C.; Pádua, F.A.; Almado, R.P.; Ana, E.R.B. Estimativa de carbono na madeira de um clone híbrido de Eucalyptus urophylla e Eucalyptus grandis. Cerne 2010, 16, 33–40. [Google Scholar]
  23. Gatto, A.; Barros, N.F.; Novais, R.F.; Silva, I.R.; Leite, H.G.; Villani, E.M.A. Estoque de carbono na biomassa de plantações de eucalipto na região centro-leste do estado de Minas Gerais. Rev. Árvore 2011, 35, 895–905. [Google Scholar] [CrossRef]
  24. Silva, C.A.; Klauberg, C.; Carvalho, S.P.C.; Piccolo, M.C.; Rodriguez, L.C.E. Estoque de carbono na biomassa aérea florestal em plantações comerciais de Eucalyptus spp. Sci. For. 2015, 43, 135–146. [Google Scholar]
  25. Yang, L.; Wang, J.; Huang, Y.; Hui, D.; Wen, M. Effects of the Interception of Litterfall by the Understory on Carbon Cycling in Eucalyptus Plantations of South China. PLoS ONE 2014, 9, e100464. [Google Scholar] [CrossRef] [PubMed]
  26. Alvares, C.A.; Stape, J.L.; Sentelhas, P.C.; Gonçalves, J.L.M.; Sparovek, G. Köppen’s climate classification map for Brazil. Meteorol. Z. 2013, 22, 711–728. [Google Scholar] [CrossRef]
  27. Food and Agriculture Organization of the United Nations. World Reference Base for Soil Resources: A Framework for International Classification, Correlation and Communication; FAO: Rome, Italy, 2014; 192p. [Google Scholar]
  28. Stape, J.L.; Binkley, D.; Ryan, M.G. Eucalyptus production and the supply, use and efficiency of use of water, light and nitrogen across a geographic gradient in Brazil. For. Ecol. Manag. 2004, 193, 17–31. [Google Scholar] [CrossRef]
  29. SPSS. Statistical Package for the Social Sciences: Programa de Computador, Ambiente Windows; Versão 7.5.1; IBM: Chicago, IL, USA, 1996. [Google Scholar]
  30. Brown, S. Measuring carbon in forests: current status and future challenges. Environ. Pollut. 2002, 116, 363–372. [Google Scholar] [CrossRef]
  31. Fahey, T.J.; Woodbury, P.B.; Battles, J.J.; Goodale, C.L.; Hamburg, S.P.; Ollinger, S.V.; Woodall, C.W. Forest carbon storage: Ecology, management, and policy. Front. Ecol. Environ. 2010, 8, 245–252. [Google Scholar] [CrossRef]
  32. IPCC. Forest Land. In Guidelines for National Greenhouse Gas Inventories. Volume 4: Agriculture, Forestry and Other Land Use; Cambridge University Press: Cambridge, UK; New York, NY, USA, 2006. [Google Scholar]
  33. Mancini, M.S.; Galli, A.; Niccolucci, V.; Lin, D.; Bastianoni, S.; Wackernagel, M.; Marchettini, N. Ecological Footprint: Refining the carbon Footprint calculation. Ecol. Indic. 2016, 61, 390–403. [Google Scholar] [CrossRef]
  34. Dallagnol, F.S.; Mognon, F.; Sanquetta, C.R.; Corte, A.P. Teores de carbono de cinco espécies florestais e seus compartimentos. Floresta Ambient. 2011, 18, 410–416. [Google Scholar] [CrossRef]
  35. Resh, S.C.; Battaglia, M.; Worledge, D.; Ladiges, S. Coarse root biomass for eucalypt plantations in Tasmania, Australia: Sources of variation and methods for assessment. Trees 2003, 17, 389–399. [Google Scholar] [CrossRef]
  36. Enquist, B.J.; Niklas, K.J. Global allocation rules for patterns of biomass partitioning in seed plants. Science 2002, 295, 1517–1520. [Google Scholar] [CrossRef]
  37. Tang, G.; Li, K.; Zhang, C.; Gao, C.; Li, B. Accelerated nutrient cycling via leaf litter, and not root interaction, increases growth of Eucalyptus in mixed-species plantations with Leucaena. For. Ecol. Manag. 2013, 310, 45–53. [Google Scholar] [CrossRef]
  38. Huang, X.; Liu, S.; Wang, H.; Hu, Z.; Li, Z.; You, Y. Changes of soil microbial biomass carbon and community composition through mixing nitrogen-fixing species with Eucalyptus urophylla in subtropical China. Soil Biol. Biochem. 2014, 73, 42–48. [Google Scholar] [CrossRef]
  39. Schumacher, M.V.; Witschoreck, R. Inventário de Carbono em Povoamentos de Eucalypus spp nas Propriedades fumageiras do sul do Brasil: “Um Estudo de caso”. In Fixação de Carbono: Atualidades, Projetos e Pesquisas; Sanquetta, C.R., Balbinot, R., Ziliotto, M.A.B., Eds.; AM Impressos: Curitiba, Brazil, 2004; pp. 111–124. [Google Scholar]
  40. Gatto, A.; Barros, N.F.; Novais, R.F.; Silva, I.R.; Leite, H.G.; Leite, F.P.; Villani, E.M.A. Estoques de carbono no solo e na biomassa em plantações de eucalipto. R. Bras. Ci. Solo 2010, 34, 1069–1079. [Google Scholar] [CrossRef]
  41. Pérez-Cruzado, C.; Mansilla, P.; Rodríguez-Soalleiro, R.; Merino, A. Influence of tree species on carbon sequestration in afforested pastures in a humid temperate region. Plant Soil 2002, 353, 333–353. [Google Scholar] [CrossRef]
  42. Kirschbaum, M.U.F.; Guo, L.B.; Gifford, R.M. Why does rainfall affect the trend in soil carbon after converting pastures to forests? A possible explanation based on nitrogen dynamics. For. Ecol. Manag. 2008, 255, 2990–3000. [Google Scholar] [CrossRef]
  43. De Koning, G.H.J.; Veldkamp, E.; López-Ulloa, M. Quantification of carbon sequestration in soils following pasture to forest conversion in northwestern Ecuador. Glob. Biogeochem. Cycles 2003, 17, 1098. [Google Scholar] [CrossRef]
  44. Madeira, M.V.; Fabião, A.; Pereira, J.S.; Araújo, M.C.; Ribeiro, C. Changes in carbon stocks in Eucalyptus globulus Labill, plantations induced by different water and nutrient availability. For. Ecol. Manag. 2002, 171, 75–85. [Google Scholar] [CrossRef]
  45. Keith, H.; MacKey, B.G.; Lindenmayer, D.B. Re-evaluation of forest biomass carbon stocks and lessons from the world’s most carbon-dense forests. Proc. Natl. Acad. Sci. 2009, 106, 11635–11640. [Google Scholar] [CrossRef]
  46. Canadell, J.G.; Raupach, M.R. Managing forests for climate change mitigation. Science 2008, 320, 1456–1457. [Google Scholar] [CrossRef]
Figure 1. Observed and estimated amounts of carbon in the 10-year-old Eucalyptus urophylla × Eucalyptus globulus stand.
Figure 1. Observed and estimated amounts of carbon in the 10-year-old Eucalyptus urophylla × Eucalyptus globulus stand.
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Figure 2. Illustrative carbon stock distributions (Mg ha−1) in the 10-year-old Eucalyptus urophylla × Eucalyptus globulus stand. F&M roots = Fine + Medium roots (Prepared by the authors).
Figure 2. Illustrative carbon stock distributions (Mg ha−1) in the 10-year-old Eucalyptus urophylla × Eucalyptus globulus stand. F&M roots = Fine + Medium roots (Prepared by the authors).
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Figure 3. Carbon concentrations in the fine roots (diameter < 2.0 mm) and soil and in the 10-year-old Eucalyptus urophylla × Eucalyptus globulus stand.
Figure 3. Carbon concentrations in the fine roots (diameter < 2.0 mm) and soil and in the 10-year-old Eucalyptus urophylla × Eucalyptus globulus stand.
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Table 1. Soil chemical and physical properties of the Eucalyptus urophylla × Eucalyptus globulus plantation (n = 9 repetitions), 10 years after establishment.
Table 1. Soil chemical and physical properties of the Eucalyptus urophylla × Eucalyptus globulus plantation (n = 9 repetitions), 10 years after establishment.
Depth (cm)O.M.NpH (H2O)CaMgAlNaCECeffect.BS
(%)cmolc dm−3%
0–252.460.084.640.340.414.130.287.4720.68
25–501.940.074.730.250.425.380.256.0921.56
50–750.900.034.810.240.384.830.224.7223.78
75–1000.480.024.870.240.304.450.308.0218.53
Depth (cm)PKSandSiltClayMicro PorosityMacro PorosityTotal PorositySDPD
ppm%%g cm−3
0–251.3252.1046.211.642.218.0630.1748.231.412.74
25–500.6454.0723.513.862.736.1616.4552.621.332.81
50–750.6140.3429.819.450.836.7915.0051.791.372.84
75–1000.5125.8949.925.724.436.9111.6348.541.462.84
Where O.M. = organic matter, CEC = cation exchange capacity, BS = base saturation, SD = soil density, and PD = particle density.
Table 2. Dendrometric variables in the 10-year-old Eucalyptus urophylla × Eucalyptus globulus stand.
Table 2. Dendrometric variables in the 10-year-old Eucalyptus urophylla × Eucalyptus globulus stand.
Variablesn (trees plot−1)N (trees ha−1)Basal Area (m2 ha−1)DBH (cm)H (m)V (m3 ha−1)LAI (m2 m−2)
µ73104334.5620.228.7366.92.55
σ3.042.92.614.12.636.20.15
µ = average; σ = standard deviation.
Table 3. Carbon equations for different components of the 10-year-old Eucalyptus urophylla × Eucalyptus globulus stand. Cw is carbon in wood (kg tree−1), Cb is carbon in bark (kg tree−1), Cbr is carbon in branches (kg tree−1), and Cl is carbon in leaves (kg tree−1). DBH is diameter at breast height (cm) and H is total tree height (m).
Table 3. Carbon equations for different components of the 10-year-old Eucalyptus urophylla × Eucalyptus globulus stand. Cw is carbon in wood (kg tree−1), Cb is carbon in bark (kg tree−1), Cbr is carbon in branches (kg tree−1), and Cl is carbon in leaves (kg tree−1). DBH is diameter at breast height (cm) and H is total tree height (m).
ComponentEquationProb > FR2 ajd.Syx
WoodLn Cw = −5.265 + 1.043 ln(DBH2 × H) <0.0010.9960.0547
BarkLn Cb = −4.855 + 2.299 lnDBH<0.0010.9650.1417
BranchesLn Cbr = −20.953 + 18.396 × (DBH × H−1) + 6.624 × (H × DBH−1)<0.0010.9060.1042
LeavesLn Cl = −0.446 + 0.075 × (DBH2 × H−1)<0.0010.8590.1502
Table 4. Soil, above and belowground carbon concentration, and stock in the 10-year-old Eucalyptus urophylla × Eucalyptus globulus stand. µ = average (proportion of components between brackets). σ = standard deviation. In rows, different letters indicate significant differences for the components (Eucalyptus) and depths (fine roots and soil) at p < 0.05 by Duncan’s test. * For litter, a carbon concentration of 50% was assumed.
Table 4. Soil, above and belowground carbon concentration, and stock in the 10-year-old Eucalyptus urophylla × Eucalyptus globulus stand. µ = average (proportion of components between brackets). σ = standard deviation. In rows, different letters indicate significant differences for the components (Eucalyptus) and depths (fine roots and soil) at p < 0.05 by Duncan’s test. * For litter, a carbon concentration of 50% was assumed.
ComponentsCarbon Concentration (%)Carbon Amount (Mg ha−1)
µLowerHigherσµσ
EucalyptusWood49.52 c48.6449.930.32103.40 (87.3)10.56
Bark45.45 d43.8846.230.718.57 (7.2)0.76
Branches50.41 b49.6050.890.404.46 (3.8)0.35
Leaves55.66 a54.4856.780.572.02 (1.7)0.13
Total--------118.45 (100)11.79
UnderstoryLeaves51.3849.7852.260.970.18 (12.7)0.22
Stem50.0248.7151.090.861.26 (87.3)1.35
Total--------1.44 (100)1.47
Litter50 *------8.34 (100)1.75
Fine roots (<2 mm)0–25 cm47.68 a46.9848.470.750.34 (69.9)0.01
25–50 cm46.31 ab44.7247.371.400.09 (18.3)0.04
50–75 cm44.56 b43.9145.741.020.032 (6.5)0.01
75–100 cm44.52 b43.4145.090.960.026 (5.3)0.02
0–100 cm--------0.48 (100)0.14
Medium roots (2–5 mm)0–25 cm46.3044.9147.281.240.22 (75.8)0.09
25–50 cm45.4544.1846.721.270.04 (13.4)0.03
50–75 cm45.48------0.02 (7.5)0.02
75–100 cm45.48------0.01 (3.4)0.02
0–100 cm--------0.29 (100)0.13
Medium roots (5–10 mm)0–100 cm47.2446.5847.900.660.170.12
Coarse roots (>10 mm)0–100 cm47.24 29.112.98
Soil0–25 cm1.23 a0.801.760.3243.1 (43.2)10.0
25–50 cm0.97 b0.811.200.1032.2 (32.3)3.9
50–75 cm0.45 c0.210.700.1415.5 (15.5)5.4
75–100 cm0.24 d0.120.410.108.9 (8.9)4.4
0–100 cm--------99.7 (100)12.1
Aboveground--------128.2 (49.7)--
Belowground--------129.8 (50.3)--
Total--------258.0 (100)--

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Viera, M.; Rodríguez-Soalleiro, R. A Complete Assessment of Carbon Stocks in Above and Belowground Biomass Components of a Hybrid Eucalyptus Plantation in Southern Brazil. Forests 2019, 10, 536. https://doi.org/10.3390/f10070536

AMA Style

Viera M, Rodríguez-Soalleiro R. A Complete Assessment of Carbon Stocks in Above and Belowground Biomass Components of a Hybrid Eucalyptus Plantation in Southern Brazil. Forests. 2019; 10(7):536. https://doi.org/10.3390/f10070536

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Viera, Márcio, and Roque Rodríguez-Soalleiro. 2019. "A Complete Assessment of Carbon Stocks in Above and Belowground Biomass Components of a Hybrid Eucalyptus Plantation in Southern Brazil" Forests 10, no. 7: 536. https://doi.org/10.3390/f10070536

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