Introduction
⌅More than 40% of global terrestrial carbon is stored in primary tropical forests, although they only cover 6% of the world's terrestrial area (Ren et al., 2014Ren H, Li L, Liu Q, Wang X, Li Y, Hui D, et al., 2014. Spatial and temporal patterns of carbon storage in forest ecosystems on Hainan island, southern China. PLoS One 9(9): e108163. 10.1371/journal.pone.0108163). Most of the carbon of these primary forests stably accumulates in the soil (Zhou et al., 2006Zhou G, Liu S, Li Z, Zhang D, Tang X, Zhou C, et al., 2006. Old-growth forests can accumulate carbon in soils. Science 314: 1417. 10.1126/science.1130168). Worldwide, tropical primary forests are especially susceptible to global climate and land-use changes. In a global-scale meta-analysis, Zhou et al. (2018Zhou Z, Wang C, Luo Y, 2018. Effects of forest degradation on microbial communities and soil carbon cycling: a global meta-analysis. Glob Ecol Biogeogr 27: 110-124. 10.1111/geb.12663) found reduced soil organic carbon (SOC) content when converting this type of forests to other land uses. About one third of the global soil carbon budget is stored in tropical soils (Jackson et al., 2017Jackson RB, Lajtha K, Crow SE, Huggelius G, Kramer MG, Piñeiro G, 2017. The ecology of soil carbon: pools, vulnerabilities, and biotic and abiotic controls. Annu Rev Ecol Evol Syst 48: 419-445. 10.1146/annurev-ecolsys-112414-054234). Soil organic carbon would be relatively easily destabilized by the projected warming of tropical regions during the XXI century, which could accelerate global climate change by releasing more CO2. Soil organic carbon consists of different chemical moieties of different stability, which, in addition to spatial inaccessibility (occlusion and organo-mineral associations) constitute an important stabilization mechanism (Yang et al., 2020Yang J, Li A, Yang Y, Li G, Zhang F, 2020. Soil organic carbon stability under natural and anthropogenic-induced perturbations. Earth-Sci Rev 205: 103199. 10.1016/j.earscirev.2020.103199).
Different factors affect how SOC is horizontally and vertically distributed, including environmental factors and human activities, which usually results in a high heterogeneity at different spatial scales. Climate, soil texture (Yuan et al., 2022Yuan L, Kangning X, Ziqi L, Kaiping L, Ding L, 2022. Distribution and influencing factors of soil organic carbon in a typical karst catchment undergoing natural restoration. Catena 212: 106078. 10.1016/j.catena.2022.106078), land use, plant cover, and root traits (Cusack et al., 2021Cusack D, Kazanski AH, Chow K, Cordeiro, AL, Karpman J, and Ryals R, 2021. Reducing climate impacts of beef production: a synthesis of life cycle assessments across management systems and global regions. Glob. Change Biol. 27,1721-1736. 10.1111/gcb.15509) affect SOC content and spatial distribution through very specific inputs and outputs. Currently, the alarming tropical deforestation vastly decreases organic matter input into the soil, destabilizing soil organic matter, which ultimately alters soil carbon content of worldwide terrestrial ecosystems (Veldkamp et al., 2020Veldkamp E, Schmidt M, Powers JS, Corre MD, 2020. Deforestation and reforestation impacts on soils in the tropics. Nat Rev Earth Environ 1: 590-605. 10.1038/s43017-020-0091-5). This is particularly the case in the Peruvian Amazon, where many areas have significant losses of plant cover and above- and underground biomass. Peru has approximately 740,000 km2 of forests, most of them in the Amazon basin (MINAM, 2016). Annual deforestation in 2014 exceeded 1,770 km2 and it is estimated that by 2030 it will exceed 3,500 km2 (MINAM, 2016).
Very fast changes in forest cover have been occurring in the Peruvian Amazon due to the increase of the agricultural frontier and extractive activities. Peruvian forests are among the world’s central carbon reserves of tropical forests, particularly in the Amazon. It is estimated that the Peruvian forests host a total of 6,928 PgC (only counting aerial carbon); from these, only 2.9 PgC are in protected areas (Csillik et al., 2019Csillik O, Kumar P, Mascaro J, O'Shea T, Asner GP, 2019. Monitoring tropical forest carbon stocks and emissions using Planet satellite data. Sci Rep 9: 17831. 10.1038/s41598-019-54386-6). According to reports from the National Forestry and Wildlife Inventory of Peru, carbon is mostly stored in the lowland forests, with carbon stocks of 138.8 t C ha-1 (SERFOR, 2021Servicio Nacional Forestal y de Fauna Silvestre, SERFOR. 2021. Cuenta de bosques del Perú, documento metodológico. Lima, Perú. pp 1-78. chrome-extension://efaidnbmnnnibpcajpcglclefindmkaj/https://www.inei.gob.pe/media/MenuRecursivo/publicaciones_digitales/Est/Lib1811/libro.pdf). However, these lowland forests generate 51.35% of all greenhouse gas emissions in Peru, with 97.393 GgCO2eq that come mainly from the conversion of forest or protected lands to agricultural land use and other human activities in the Peruvian Amazon (MINAM, 2021). It is estimated that between 2010 and 2019, Peru annually emitted an average of 75,774,039.55 t CO2e due to deforestation of Amazon forests (MINAM, 2021).
Soil organic carbon content plays a critical role in maintaining carbon balance and mitigating climate change, both nationally and globally. Soil organic carbon density is an important indicator of SOC content. Exploring the spatiotemporal dynamics of SOC density could allow policymakers to develop strategies to reduce carbon emissions (Chen et al., 2023Chen J, Biswas A, Su H, Cao J, Hong S, Wang H and Dong X, 2023. Quantifying changes in soil organic carbon density from 1982 to 2020 in Chinese grasslands using a random forest model. Front Plant Sci 14: 1076902. 10.3389/fpls.2023.1076902). Soil erodibility is affected by soil aggregation, which in turn is affected by the land use system (Wassie, 2020Wassie SB, 2020. Natural resource degradation tendencies in Ethiopia: a review. Environ. Syst. Res. 9, 1-29. 10.1186/s40068-020-00194-1). Therefore, erodibility has been considered in our study because soils in deforested sites have been evaluated for planting agricultural crops such as corn and rice, generating a strong change in land use. It is crucially important to carry out studies on carbon content of these dry forest soils. Thus, this study aimed to measure SOC content and SOC density, and soil erodibility, of the dry forest soils in the Peruvian Amazon with different plant covers, and at different soil depths.
Material and methods
⌅Site of study
⌅The study took place at two sites: i) “Ojos de Agua” forest, of 2,357.62 ha (6°50’50.99”S, 76°27’52.24”W; 382 m a.s.l.; mean annual temperature: 25.0°C; annual precipitation: 1167 mm; mean annual relative humidity: 73%; soil type: Eutric Cambisol), and ii) “El Quinillal” forest, of 10,557.07 ha (7°2’0.00”S, 76°19’52.42”W; 309 m a.s.l.; mean annual temperature: 25.5°C; annual precipitation: 1278 mm; mean annual relative humidity: 74%; soil type: Eutric Leptosol), which is located on the right bank of the Huallaga River (Fig. 1). Both forests are considered tropical dry forests and the tree species ‘Manchinga’ (Brosimum alicastrum (Swartz)) and Quinilla (Manilkara bidentata (A. DC.) Chev.) dominate. In recent years, they are affected by climate change and extensive corn crops (Vallejos-Torres et al., 2021Vallejos-Torres G, Ríos-Ramírez O, Saavedra H, Gaona-Jimenez, N, Mesén-Sequeira F, Marín C, 2021. Vegetative propagation of Manilkara bidentata (A.DC.) A.Chev. using mini-tunnels in the Peruvian Amazon region. For Syst 30: eRC01. 10.5424/fs/2021302-17971). Both forests had the three plant covers subject of this study: primary forest (trees of approximately 200 years), intervened forest (intervention done approximately 50 years ago), and deforested forest (trees were cut down 10 years ago) (Fig. 1) Both sites were approximately 50 km from each other, and within each site, each plant cover type was 500-1000 m apart from each other.
Soil sampling
⌅Soil sampling took place in April 2023. It was carried out with a shovel and a metal bar. Pits were made that were 1 m deep and 1 m wide. Before making the pits, the site was cleaned of weeds and leaf litter. Samples were taken from 0 to 100 cm because several previous studies (Xie et al., 2023Xie M, Zhang T, Liu S, Liu Z and Wang Z, 2023. Profile soil organic and inorganic carbon sequestration in maize cropland after long-term straw return. Front. Environ. Sci. 11: 1095401. 10.3389/fenvs.2023.1095401; Ryzhova et al., 2023Ryzhova IM, Podvezennaya MA, Telesnina VM, et al., 2023. Assessment of Carbon Stock and CO2 Production Potential for Soils of Coniferous-Broadleaved Forests. Eurasian Soil Sc. 56, 1317-1326. 10.1134/S1064229323601166; Zhao et al., 2022Zhao X, Zhang W, Feng Y, Mo Q, Su Y, Njoroge B, Qu C, Gan X, Liu X, 2022. Soil organic carbon primarily control the soil moisture characteristic during forest restoration in subtropical China. Front Ecol Evol. 10: 1003532. 10.3389/fevo.2022.1003532), found significant C stock variation up to that depth. To study the vertical variation of SOC at the two sites, we selected a total of 24 plots (10 m × 10 m each), following the methodology of Yu et al. (2019Yu H, Zha T, Zhang X, Ma L, 2019. Vertical distribution and influencing factors of soil organic carbon in the Loess Plateau, China. Sci Total Environ 693: 133632. 10.1016/j.scitotenv.2019.133632) and distributed in three vegetation covers, these being primary forest, intervened forest, and deforested forest (Table 1). The distance between coverages was 221 m, 1298 m and 2551 m minimum, average and maximum, respectively. In each cover, 4 randomly distributed plots were installed, the distance between them was minimum, average and maximum of 76 m, 350 m and 882 m (Fig. 1). Pits were made for study and sample collection at five soil depths for each plot along 0–20, 20–40, 40–60, 60–80, and 80–100 cm, with a total of 120 soil samples analyzed.
Soil organic carbon estimation
⌅The cylinder (5.5 cm diameter, 5 cm height) method (Blake & Hartge, 1986Blake GR, Hartge K, 1986. Bulk density. In: Methods of Soil Analysis: Part 1 Physical and Mineralogical Methods; Klute A (ed). pp: 363-375. American Society of Agronomy, United States of America. 10.2136/sssabookser5.1.2ed.c13) was used to estimate soil bulk density (BD) (in g cm-3), as it follows:
BD: Wd/V…………….................................…..……(1)
where: Wd: weight of the (oven-dried) soil sample (g), and V: sampled soil volume (cm3). SOC concentration was estimated by wet oxidation following the Walkley & Black (1934Walkley A, Black IA, 1934. An examination of the Degtjareff method for determining soil organic matter and a proposed modification of the chromic acid titration method. Soil Sci 37: 29-38. 10.1097/00010694-193401000-00003) method; SOC stocks were calculated as it follows:
SOC (t ha-1) = OC × De × BD….….….….….….… (2)
where: OC: organic carbon content in the soil (%), De: sampling depth (cm), and BD: bulk density (g cm-3).
Estimation of soil erodibility and SOC density
⌅Soil erodibility (K) was estimated following Williams et al. (1984Williams JR, Jones CA, Dyke PT, 1984. A modeling approach to determining the relationsh ipbetween erosion and soil productivity. Transactions of the ASAE 27: 129-144. 10.13031/2013.32748) model, as it follows:
where: SAN: sand content (%); SIL: silt content (%); CLA: clay content (%); SOC: soil organic carbon (%); and =1-SAN/100.
Soil organic carbon density (SOCD) at each soil depth (0–20, 20–40, 40–60, 60–80, and 80–100 cm) was calculated using the following formula:
SOCD = Hha x BDha x SOCha x (1-Cha)/100
where: Hha: soil thickness (cm), BDha: soil bulk density (g cm-3), SOC: soil organic carbon (t ha-1), and Cha: percentage of the soil volume with a fraction >2mm. All values in this formula were transformed to hectares.
Statistical analyses
⌅All statistical tests were run in R Studio (R Core Team, 2024R Core Team, 2024. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. http://www.R-project.org). The effects of vegetation cover in SOC at different depths were evaluated by analysis of variance (ANOVA) at a significance level of 5%, while means comparison was performed with Tukey's test using the agricolae package in R Studio (Mendiburu, 2010Mendiburu F De, 2010. Manual práctico para el uso de agricolae. Universidad Nacional Agraria La Molina. CRAN: https://cran.r-project.org/web/packages/agricolae/index.html). The categorical variable (cover type) was coded numerically following the methodology established by Yu et al. (2019Yu H, Zha T, Zhang X, Ma L, 2019. Vertical distribution and influencing factors of soil organic carbon in the Loess Plateau, China. Sci Total Environ 693: 133632. 10.1016/j.scitotenv.2019.133632): 0= Primary forest, 1= Intervened forest, and 2= Deforested forest. The correlation between SOC, vegetation cover type, and soil characteristics was evaluated by the Pearson’s correlation test (α = 0.05), using the base R cor function. To evaluate the response variables that helped explain SOC content at different depths, a principal component analysis (PCA) together with a multiple linear regression (MLR) analysis (Kaiser, 1960) were run.
Results
⌅Soil organic carbon content changes under different vegetation cover and soil depth
⌅Soil organic carbon content decreased with increasing soil depth (Fig. 2). The mean SOC content in the primary forest was 36.7±9.5 t ha-1, for the intervened forest was 29.5±7.6 t ha-1, and for the deforested forest, it was 22.8±7.6 t ha-1, decreasing with increasing soil depth. In the superficial soil layer (0-20 cm), SOC content in the primary forest had a value of 79.5±21.3 t ha-1, while in the deep layer (80-100 cm), it was 11.1±3.5 t ha-1. The SOC content of the superficial soil layer (0-20 cm) in the intervened forest was 58.5±11.8 t ha-1 and in the deep layer (80-100 cm) was 12.8±2.4 t ha-1. Meanwhile, the SOC of the superficial soil layer (0-20 cm) in the deforested forest had a value of 41.8±10 t ha-1, while in the deep layer (80-100 cm), it was 7.4±5.3t ha-1 (Fig. 3). The mean SOC value at the superficial (0-20 cm) layer was 59.9±21.3 ha-1 and decreased at greater depth with values of 10.4±4.3 ha-1 (80-100 cm). With increasing soil depth, it was observed that the coefficient of variation (CV) decreased from 35.6% in the 0-20 cm soil layer to 19.8% in the 80-100 cm soil layer (Fig. 2). The SOC content in the three forest canopies showed significant differences for the first and second soil depths, with the primary forest having the highest SOC. In general, in the first 0-40 cm, the SOC content decreased rapidly with soil depth, showing significant differences between plant covers, but below 40 cm, it did not show significant differences (Fig. 3).
Soil organic carbon correlation analyses
⌅The cover type and SOC had a significant, negative correlation at soil depths from 0 to 40 cm and 60 to 80 cm soil depth (Table 2). Overall, most tested variables were not correlated with SOC for the first 40 cm soil depth, but after this depth, variables like clay, silt, and soil erodilibity presented some significant correlations (Table 2).
| Variable/soil depth | 0-20 cm | 20-40 cm | 40-60 cm | 60-80 cm | 80-100 cm |
|---|---|---|---|---|---|
| Cover type | -0.742** | -0.559* | -0.284ns | -0.504* | -0.356ns |
| Sand (%) | 0.322ns | 0.181ns | 0.084ns | 0.324ns | -0.794** |
| Silt (%) | -0.346ns | 0.106ns | -0.628** | -0.528* | 0.531* |
| Clay (%) | -0.074ns | -0.287ns | 0.699** | 0.235ns | 0.685** |
| Soil density (g/cm3) | 0.013ns | -0.137ns | -0.182ns | -0.615** | -0.488* |
| Soil water content (%) | 0.203ns | -0.141ns | 0.314ns | 0.138ns | 0.431ns |
| Soil erodibility | -0.386ns | -0.043ns | -0.600** | -0.485** | 0.610** |
Factors contributing to SOC variation
⌅The main variables that contributed to explain the SOC in the superficial horizon (0-20 cm) were cover type, soil density, and soil erodibility with 13.8%, 13.4%, and 12.6%, respectively (Fig. 4). In the 20-40 cm horizon, the main variables were sand content, soil erodibility, and cover type with 14.9%, 13.5%, and 11.3%, respectively. In the 40 to 60 cm horizon, the main variables were soil erodibility, silt content, and clay content with 14.6%, 13.4%, and 13.1%, respectively. For the 60 to 80 cm horizon, the main variables were cover type and sand content with 13.2% and 12.9%, respectively. And for the 80 to 100 cm horizon, sand and silt content with 13.7% and 12.2%, respectively. It is generally evident that SOC was mostly explained by soil erodibility, followed by cover type and texture with an average of 12.8%, 11.53%, and 11.08%, respectively. Soil water content presented the lowest contribution, with an average of 7.3 % (Fig. 4).
The profile distribution of SOC fractions
⌅The SOC obtained in this study was 7.6±5.1 t ha-1 in the primary forest, 6.2±3.6 t ha-1 in the intervened forest, and 4.7±2.7 t ha-1 in the deforested forest when evaluated between 0 to 100 cm depth. SOC density presented significant differences in the layers from 0 to 40 cm, but not from 40 to 100 cm (Fig. 5 A). The highest SOCD content was recorded in the surface layer from 0 to 20 cm with an average of 11.69 t ha-1, representing 40.4% of the total SOC stock in the entire profile (0–100 cm). In the 20 - 40 cm soil layers, the average SOCD was 7.2 t ha-1, representing 23.5% of the total SOC stock. In the 40 to 60-cm soil layers, the average SOCD was 5.7 t ha-1, representing 17.7% of the total SOC stock. In the 60 to 80-cm soil layers, the average SOCD was 3.8 t ha-1, representing 11.3% of the total SOC stock. In the 80–100 cm soil layers, the mean SOCD was 2.4 t ha-1, representing 7% of the total SOC stock in the entire 0–100 cm soil profile (Fig. 5 B).
Discussion
⌅Soil organic carbon characteristics in the soil profile
⌅The results found are close to those reported by Solis et al. (2020Solis R, Vallejos-Torres G, Arévalo L, et al., 2020. Carbon stocks and the use of shade trees in different coffee growing systems in the Peruvian Amazon. J Agric Sci 158: 450-460. 10.1017/S002185962000074X), who showed 87 t C ha-1 in a coffee system with Inga trees. Plant cover profoundly affects soil carbon stocks (Arasa-Gisbert et al., 2018Arasa-Gisbert R, Vayreda J, Román-Cuesta RM, Villela SA, Mayorga R, Retana J, 2018. Forest diversity plays a key role in determining the stand carbon stocks of Mexican forests. For Ecol Manag 415: 160-171. 10.1016/j.foreco.2018.02.023) and soil carbon sequestration, more precisely at the 0-15 cm layer (between 33.2 t ha-1 and 52.7 t ha-1) (Boulmane et al., 2010Boulmane M, Makhloufi M, Bouillet JP, Saint-André L, Satrani B, Halim M, et al., 2010. Estimation du stock de carbone organique dans la chênaie verte du Moyen Atlas marocain. Acta Bot Gall 157: 451-467. 10.1080/12538078.2010.10516222). A possible reason for this is the soil’s microbial communities – which differ among plant covers, and their influence in the cycling and accumulation of SOC (Weverka et al., 2023Weverka J, Runte GC, Porzig EL, Carey CJ, 2023. Exploring plant and soil microbial communities as indicators of soil organic carbon in a California rangeland. Soil Biol Biochem 178: 108952. 10.1016/j.soilbio.2023.108952).
Soil organic carbon variation with soil depth and plant cover
⌅Species-rich plant communities are more productive and exhibit more significant long-term SOC content. Soil microorganisms are essential for converting plant organic matter into SOC; consequently, the greater the canopy cover and height, the greater the SOC content (Siswo et al., 2023Siswo Kim, H, Lee J, Yun CW, 2023. Influence of Tree Vegetation and The Associated Environmental Factors on Soil Organic Carbon; Evidence from “Kulon Progo Community Forestry,” Yogyakarta, Indonesia. Forests 14: 365. 10.3390/f14020365). Overall, our findings were consistent with many previous studies showing that vegetation increases SOC (Saíz et al., 2012Saíz G, Pájaro MI, Domingues T, Schrodt F, Schwarz M, Feldpausch TR, Veenendaal E, Djagbletey G, Hien F, Compaore H, et al., 2012. Variation in soil carbon stocks and their determinants across a precipitation gradient in West Africa. Glob Change Biol 18: 1670-1683. 10.1111/j.1365-2486.2012.02657.x; Gruba et al., 2015Gruba P, Socha J, Błońska E, Lasota J, 2015. Effect of variable soil texture, metal saturation of soil organic matter (SOM) and tree species composition on spatial distribution of SOM in forest soils in Poland. Sci Total Environ 521-522: 90-100. 10.1016/j.scitotenv.2015.03.100). In our study, primary forests present Manchinga (B. alicastrum) and Quinilla (M. bidentata) trees as dominants with a larger diameter at breast height and greater height, while in intervened and deforested forests there are no trees of these species due to the massive extraction of wood, making M. bidentata a threatened species (Vallejos-Torres et al., 2021Vallejos-Torres G, Ríos-Ramírez O, Saavedra H, Gaona-Jimenez, N, Mesén-Sequeira F, Marín C, 2021. Vegetative propagation of Manilkara bidentata (A.DC.) A.Chev. using mini-tunnels in the Peruvian Amazon region. For Syst 30: eRC01. 10.5424/fs/2021302-17971). The distribution of C components in the soil surface is largely influenced by the chemical nature of the forest litter from which SOC originates. The species-specific litter quality determines the compositional characteristics of organic matter input to the soil and influences the magnitude of decomposition processes by microorganisms. Leaf litter introduces organic materials into the soil in different quantities and qualities, influencing the formation and stability of the soil C reserve. Dissolved organic matter in forest ecosystems significantly affects soil carbon cycling due to litter decomposition (Morffi-Mestre et al., 2023Morffi-Mestre H, Ángeles-Pérez G, Powers JS, Andrade JL, Feldman RE, May-Pat F, et al, 2023. Leaf litter decomposition rates: influence of successional age, topography and microenvironment on six dominant tree species in a tropical dry forest. Front For Glob Change 6: 1082233. 10.3389/ffgc.2023.1082233); therefore, litter-derived dissolved organic carbon is considered an important source of stabilized C in soil (Preusser et al., 2021Preusser S, Liebmann P, Stucke A, Wirsching J, Müller K, Mikutta R, et al., 2021. Microbial utilisation of aboveground litter-derived organic carbon within a sandy dystric cambisol profile. Front Soil Sci 1: 666950. 10.3389/fsoil.2021.666950). Vegetation type and soil depth affect soil carbon distribution by changing soil physical and chemical properties and microbial activity, as shown in previous research (Song et al., 2016Song BL, Yan MJ, Hou H, Guan JH, Shi WY, Li GQ, Du S, 2016. Distribution of soil carbon and nitrogen in two typical forests in the semiarid region of the Loess Plateau, China. Catena 143: 159-166. 10.1016/j.catena.2016.04.004). Soil organic carbon content was generally low in deforested forests with weeds due to sparse vegetation, shallower root systems, and lower root biomass, especially evidenced by fewer roots in deeper soils (Jia et al., 2017Jia XX, Yang Y, Zhang CC, Shao MA, Huang LM, 2017. A state-space analysis of soil organic carbon in China's loess plateau. Land Degrad Develop 28: 983-993. 10.1002/ldr.2675).
Soil organic carbon correlation analyses
⌅Our land-use results showed a significant correlation at soil depths from 0-40 cm and from 60-80 cm depth and of soil erodibility with SOC between 0-80 cm depth, similar to the results found by Yu et al. (2019Yu H, Zha T, Zhang X, Ma L, 2019. Vertical distribution and influencing factors of soil organic carbon in the Loess Plateau, China. Sci Total Environ 693: 133632. 10.1016/j.scitotenv.2019.133632). The lower soil erodibility in the primary forest can be attributed to the greater amount of soil organic matter (SOM) compared to intervened and deforested forests. Land use type can affect soil properties and plant community characteristics, likely affecting soil erodibility (Chen et al., 2023Chen J, Biswas A, Su H, Cao J, Hong S, Wang H and Dong X, 2023. Quantifying changes in soil organic carbon density from 1982 to 2020 in Chinese grasslands using a random forest model. Front Plant Sci 14: 1076902. 10.3389/fpls.2023.1076902). In turn, soil erodibility is related to the granulometry, structure, and stability of soil aggregates, which indicates that soils with higher silt content are more erodible than clay soils. Meanwhile, SOM also plays a vital role in soil erodibility by maintaining the stability of soil aggregates (Deng et al., 2018Deng X, Chen X, Ma W, Ren Z, Zhang M, Grieneisen ML, Long W, Ni Z, Zhan Y, Lv X, 2018. Baseline map of organic carbon stock in farmland topsoil in East ChinaAgric Ecosyst Environ 254: 213-223. 10.1016/j.agee.2017.11.022). In our results, the clay fraction did not show a significant correlation with SOC. At the same time, there was a negative correlation of SOC with the sand fraction, results consistent with Zhong et al. (2018Zhong Z, Chen Z, Xu Y, Ren C, Yang G, Han X, Ren G, Feng Y, 2018. Relationship between Soil Organic Carbon Stocks and Clay Content under Different Climatic Conditions in Central China. Forests 9: 598. 10.3390/f9100598). The physicochemical properties of soil are interrelated and affected by land use and management activities (Thabit et al., 2023Thabit FN, El-Shater AH, Soliman W, 2023. Role of silt and clay fractions in organic carbon and nitrogen stabilization in soils of some old fruit orchards in the Nile floodplain, Sohag Governorate, Egypt. J Soil Sci Plant Nutr 23: 2525-2544. 10.1007/s42729-023-01209-3). Primary forests influence carbon contents due to the large amounts of organic matter associated with the thickest soil fraction.
Contributions of environmental factors to variations in SOC
⌅Soil organic carbon is affected by many related factors and is regulated in complex ways, with spatial differences both higher and lower in the soil column. Land use and soil factors significantly influenced SOC content. In this study, the effects of soil water content on SOC content also decreased with soil depth, influenced by the vegetation cover (Wang et al., 2022Wang L, Li Z, Wang D, Liao S, Nie X, Liu Y, 2022. Factors controlling soil organic carbon with depth at the basin scale. Catena 217: 106478. 10.1016/j.catena.2022.106478). The physicochemical properties of top soils and deep soils were significantly different. Therefore, the regulatory factors and mechanism of SOC varied between soil layers. Generally, the accumulation of SOC on the surface results from interactions between abiotic processes regulated by environmental factors and biotic processes regulated by microbes. Because the surface soil contains a large amount of plant litter, sufficient water and air on the surface are also conducive to increase soil microbial activity (Zhang et al., 2021Zhang CC, Wang YQ, Jia XX, Shao MA, 2021. Estimates and determinants of soil organic carbon and total nitrogen stocks up to 5 m depth across a long transect on the Loess Plateau of China. J Soils Sediments 21: 748-765. 10.1007/s11368-020-02861-3). The SOC changed significantly in the different forest types. This can be attributed to the increase in organic materials (litter and roots), as Xing et al. (2023) indicated that the highest SOC content found in the first soil horizons in primary forests is due to the presence of roots.
In this study we found a significant negative correlation between soil bulk density and SOC, indicating that bulk density does not influence the leaching of surface SOC to deep soil layers since low SOC in deep soils is related to the high density in tropical forests (Yang et al., 2016Yang XM, Drury CF, Reynolds WD, Yang JY, 2016. How do changes in bulk soil organic carbon content affect carbon concentrations in individual soil particle fractions?Sci Rep 6: 27173. 10.1038/srep27173). In our study we found some contrasting results with Jia et al. (2017Jia XX, Yang Y, Zhang CC, Shao MA, Huang LM, 2017. A state-space analysis of soil organic carbon in China's loess plateau. Land Degrad Develop 28: 983-993. 10.1002/ldr.2675), who investigated carbon stocks in different vegetation covers in deep soils and indicated that land use significantly affects deep SOC. In addition to land use type, soil factors also significantly impact the vertical distribution of SOC (Jiang et al., 2017). Soil moisture content positively correlated with SOC; therefore, SOC decomposition and soil C content were associated with changes in soil environment and soil microbial biomass due to soil moisture variation.
Soil organic carbon fraction distribution
⌅In our study, 37.80% of SOCD and 40.37% of SOC were concentrated between 0-20 cm soil depth, and this decreased with soil depth in such a way that 7.88% of SOCD and 7.05% of SOC occurred in the 80-100 cm depth profile in the forests studied. This fraction distribution is controlled by factors such as humidity and bulk density along soil depths (Zhuo et al., 2022Zhuo Z, ChenQ, ZhangX, ChenS, GouY, et al., 2022. Soil organic carbon storage, distribution, and influencing factors at different depths in the dryland farming regions of Northeast and North China. Catena 210: 105934. 10.1016/j.catena.2021.105934). It is known that soils with high SOCD contain a high accumulation of organic matter (Arunrat et al., 2020Arunrat N, Pumijumnong N, Sereenonchai S, Chareonwong U, 2020. Factors Controlling Soil Organic Carbon Sequestration of Highland Agricultural Areas in the Mae Chaem Basin, Northern Thailand. Agronomy 10: 305. 10.3390/agronomy10020305) and, therefore, high carbon content, as found in our study. The vegetation cover type also influenced SOCD; primary forests with dense vegetation cover have the highest SOCD, followed by intervened forests, and forests deforested with cultivars (Zhu et al., 2021Zhu GF, Qiu DD, Zhang ZX, Sang LY, Liu YW, et al., 2021. Land-use changes lead to a decrease in carbon storage in arid region, China. Ecol Indic 127: 107770. 10.1016/j.ecolind.2021.107770). Studies have shown that an increase in vegetation cover, such as in a primary forest, could facilitate carbon accumulation in the soil and, therefore, increase SOCD (Gong et al., 2017). This can be attributed to (i) an increase in plant root productivity, (ii) a reduction in SOC loss by effectively blocking wind erosion, and (iii) the accumulation of litter on the soil surface. Generally, the increase in vegetation is followed by an increase in litter (Tian et al., 2022Tian HW, Zhang JH, Zhu LQ, Qin JT, Liu M, Shi JQ, et al., 2022. Revealing the scale- and location-specific relationship between soil organic carbon and environmental factors in China’s north-south transition zone. Geoderma 409: 115600. 10.1016/j.geoderma.2021.115600). Yu et al. (2019Yu H, Zha T, Zhang X, Ma L, 2019. Vertical distribution and influencing factors of soil organic carbon in the Loess Plateau, China. Sci Total Environ 693: 133632. 10.1016/j.scitotenv.2019.133632) found that the SOC content of each vegetation type ranged in the following order: forest land, cropland, and grassland. This is corroborated by Zhao et al. (2019Zhao W, Zhang R, Cao H, Tan W, 2019. Factor contribution to soil organic and inorganic carbon accumulation in the Loess Plateau: Structural equation modeling. Geoderma 352: 116-125. 10.1016/j.geoderma.2019.06.005), who found that humidity is one of the most critical factors that control the variations of SOCD studied between 0 cm to 100 cm soil depth.
In summary, this study of vertical variation of carbon at depths of 0-100 cm showed that vegetation cover significantly affects soil carbon stocks, more significantly at the 0-20 cm layer. Primary forests present Manchinga (B. alicastrum) and Quinilla (M. bidentata) trees as dominants with a larger diameter at chest height and greater height, while in the intervened and deforested forests, there are no trees of these species. The lower soil erodibility found in the primary forest can be attributed to a greater soil organic matter (SOM) content compared to intervened and deforested forests. Land use affects soil properties and plant community characteristics, which are likely to affect soil erodibility. In this study, the effects of soil water content on SOC content also decreased with soil depth, influenced by the vegetation cover index and soil bulk density. The types of vegetation cover also influenced SOC density. Above all, primary forests with dense vegetation cover have the highest SOC density, followed by intervened forests and forests deforested with cultivars.