An evaluation of the changes in soil properties as a consequence of forest planting is important, especially for fragile ecological areas [2]. Our results supported the hypothesis that bulk density, aggregates stability and the content of carbon were affected by tree species, and they also changed obviously among different soil layers. Additionally, water stable aggregates with bigger sizes had more soil organic matter content, but less calcium carbonate content. According to the Kyoto protocol, forest planting is an important action to build a soil carbon pool in terrestrial ecosystems [21]. The total carbon density was in the order of R. pseudoacacia > M.pumila > P. tabuliformis in all soil layers. Compared with M. pumila and P. tabuliformis plantations, P.tabuliformis plantation was more conducive to accumulation of soil organic carbon, decrease of soil inorganic carbon and bulk density, and then could improve the water stability of soil aggregates, which will facilitate the improvement of soil quality and protection of soil and water from loss.
Changes in soil properties among three plantations.
Soil aggregate stability is considered to be a property that provides information on soil quality [11]. In addition, many studied soil parameters aligned with SOC [8], especially such as aggregate water stability. It was observed that water stability of soil aggregates and SOC content both were in the order of P. tabuliformis > R. pseudoacacia > M.pumila, indicating that soil quality and related soil functions varied greatly among three plantations. Similarly, Chen et al. [13] found that soil organic carbon was higher in 10-year-old P. tabulaeformis than in 10-year-old R.pseudoacacia stands. In our study, it was demonstrated that P. tabuliformis would be more conducive to increase of SOC and improvement of aggregate stability compared with R. pseudoacacia and M.pumila. This is in agreement with results found by previous studies, which observed Pinus plantation could supply soil with considerably more organic material and improve water repellency of soil [3, 22]. Increase in SOC was mostly associated with an increase in soil hydrophobicity, especially under the wax/aromatic oil rich litter of the Pinus halepensis trees [9]. Moreover, the presence of water repellency can play an important role in the formation and stabilization of aggregates and can avoid high levels of soil degradation [11]. From this, it seemed logical that soil quality indicators including SOC and aggregate stability have been improved by P. tabuliformis plantation in the present study. Additionally, the fine root biomass (FRB) and fine root production (FRP) of P.tabulaeformis were greater than those of R. pseudoacacia [13]. Small and fine roots produced optimal conditions to form and stabilize aggregates due to the polysaccharides being produced by the microorganisms [1]. Meanwhile, BD was significantly related to most other soil parameters and it could be used as an indicator of soil structure [2]. The soil BD was in the order of P. tabuliformis < R. pseudoacacia < M.pumila, which indicated there was negative variation trend between BD and MWD or SOC. Our study demonstrated that the increase of SOC corresponded to the improvement of aggregate stability and decrease of BD, which was most significant in P. tabulaeformis plantation, and R. pseudoacacia plantation followed. At M. pumila plantation, MWD of water stable aggregates was the smallest (Fig. 2), which was similar with the lowest SOC (Fig. 3A). It was visible that M.pumila plantation had the lowest values of SOC and MWD, but the highest bulk density. This could be explained by long term cultivation management such as pruning and weed control resulting in the lower input and higher decomposition of organic substances. Lal [21] also believed that most soil under the managed ecosystems contained a lower SOC pool than their counterparts under natural ecosystems due to the depletion of the SOC pool in cultivated soil. Our findings also showed that soil organic matter was largest significantly in the surface layer (0–10 cm) compared to the other soil layers. This was in agreement with previous studies conducted in other forest ecosystems [24], and was a logical result as the surface layer is the main place of soil organic matter sources such as dry branches and fallen leaves.
Effects of tree species on soil carbon sequestration.
It is also becoming increasingly clear that carbon accumulation in soil represents an important carbon stocks [24]. The quantitative relationship between the changes of SOC and SIC stocks in deep profiles following vegetation restoration should be further determined [30]. Our results showed SOCD ranged from 0.64–2.63 kg/m2 and SIOCD ranged from 0.37–4.08 kg/m2 over the 0–80 cm soil profiles. Compared with P. tabulaeformis, The STCD increased by 59%-100% and 3% -46% in R. pseudoacacia and M. pumila plantations respectively. SIOCD to STCD ratios in R. pseudoacacia and M. pumila plantations were 56–85% and 53–76%. Zethof et al. [8] and Wang et al. [29] also found inorganic carbon content was often much larger than that of organic carbon in semi-arid regions. SIOCD to STCD ratios were lower (12%-55%) under P. tabulaeformis plantation, which was due to coniferous trees having more acid exudate compared with broadleaf trees. And then, more carbonate would be dissolved [29]. In addition, higher organic matter accumulation under P. tabulaeformis plantation increased saturated hydraulic conductivity [2], which also increased carbonates leaching. The content of CaCO3 and SIOCD fluctuated with deepening soil layers, showing there was more inorganic carbon content in subsoils. Han et al. [30] also confirmed that the maximum soil in-organic carbon (SIC) values was at 60–100 cm soil layer. SIC content at subsoil increased significantly due to the dissolution and leaching of carbonates from topsoil and the subsequent precipitation in subsoils [6]. There was a lot more carbon in deep soil than we once thought, and the underlying processes inhibiting its turnover are still largely unknown [17].
Aggregate-CaCO 3 content decreased with increasing aggregate size.
In many semi-arid regions, where the presence of carbonates in soil is frequent, it is necessary to study the correlation between carbonates and aggregate stability. For example, Fernández-Ugalde et al. [19] thought carbonates must be considered when modelling soil structure formation. Calcium bridging is the dominant factor for the long-term positive effect of calcium addition on the structural stability of soil [10]. Chrenková et al. [11] found carbonate content had a positive influence in MWD for sandy soils. In semi-arid calcareous soils, Fernández-Ugalde et al. [19] found that the interaction of maize straw and carbonates resulted in a higher stability of macro-aggregates (> 250um) in carbonated soil than non-carbonated soil, then concluded the formation of secondary carbonates within and/or around macro-aggregate could explain this stability. In our case, the effect of carbonates in stabilization of aggregates showed two-sidedness. On the one hand, aggregate-inorganic carbon decreased with increasing aggregate size, except for the smallest size which had lower concentration than the next-bigger size. This occurred because the CaCO3 could make the soil particles consolidated in the dry state. But when soil was wetted by water, the CaCO3 could dissolve in water and make the soil particles separated and become dispersed. Therefore, the aggregates of calcareous soil were easily broken under the fast wetting condition. Our study also found that P. tabulaeformis could effectively decrease the content of CaCO3, which lead to the improvement of soil stability and reducing of soil erosion. On the other hand, there was a linear positive correlation between inorganic carbon content and MWD of water stable aggregates in the soil profile of P. tabulaeformis plantation, while a linear negative correlation was found in the soil profile of R. pseudoacacia plantation (Fig. 6). Therefore, this paper assumed that there was a threshold value of inorganic carbon content in soil. When it was higher than the threshold value, the aggregate structure would be destroyed with the dissolution of calcium carbonate in the process of rapid wetting; when it was lower than the critical value, calcium carbonate could be used as aggregate cement. Uddivira et al. [16] found that adding Ca2+ to the soil with Ca2+ concentration of 2.7 and 3.1cmol/kg increased the percentage content of water stable aggregates, on the contrary, adding Ca2+ in the soil with Ca2 + concentration of 13.9 cmol / kg would disperse more aggregates. Virto et al. [7] also believed that compared with the soil with 30% carbonate content, the carbonate in the soil with 15% carbonate content played a major cementation role in soil aggregates.
Aggregate-SOM content increased with increasing aggregate size.
Qiao et al. [33] suggested that micro-aggregates played key roles in protecting SOC based on more recalcitrant SOC stored in micro-aggregates. However, higher organic carbon content in the macro-aggregates (> 2 mm fraction) compared to the micro-aggregates (༜0.2 mm fraction) in our results, that was similar to previous studies [19], which observed that when organic inputs were increased in a calcareous soil, a greater proportion of stable macro-aggregate (> 250um) would be formed in comparison to a non-calcareous soil of similar characteristics. Gao et al. [18] also found the largest amount of organic carbon was stored in > 0.25 mm size aggregates. Elliott [4] observed more organic matter associated with macro-aggregates than with micro-aggregates in a temperature grassland soil. The conclusion also was line with the theory of aggregate hierarchy, which believes an increase in carbon concentration with increasing aggregates size class because that large aggregate-size classes are composed of small aggregate-size classes plus organic binding agents [4]. In general, there was a trade-off between SOC and CaCO3, which was similar to the conclusions of Yang et al. [6] and Han et al. [30].