Background Meadows and shrublands are two major vegetation types on the Qinghai-Tibetan Plateau, but little is known about biochemical characteristics and its relation to decomposability of soil organic carbon (OC) under these two vegetation types. The present study was designed to evaluate effects of aspectvegetation complex on biochemical characteristics and decomposability of soil OC. Methods Two hills were randomly selected; both with vegetation being naturally divided into southward meadows and northward shrublands by a ridge, and soils were sampled at depths of 0-15 and 15-30 cm, along contours traversing the meadow and shrubland sites. Particulate (particle size 2-0.05 mm) OC and nitrogen (N), microbial biomass C and N, non-cellulosic sugars, and CuO lignin were analyzed, and OC mineralization was measured for 49 days at 18 and 25°C under laboratory incubation, respectively. Results More than half of soil OC was present as particulate fraction across all samples, indicating the coarse nature of soil organic matter in the region. Averaging over depths, shrublands contained 87.7−114.1 g OC and 7.7−9.3 g N per kg soil, which were 63−78 and 26−31 % higher than those in meadows, respectively. Meanwhile the C/N ratio of soil organic matter was 11.4 −12.3 under shrublands, being 29−40 % higher than that under meadows. Soil OC under meadows was richer in noncellulosic carbohydrates and microbial biomass in the 0-15 and 15-30 cm depths but contained less lignin in the 15-30 cm depth. Ratios of microbiallyto plant-derived monosaccharides and between acid and aldehyde of the vanillyl units were greater in soils under shrublands, showing more abundant microbiallyderived sugars and microbially-transformed ligneous substances in OC as compared to meadow soils. By the end of 49 days' incubation, total CO 2 -C evolution from soils under meadows was 15.0-16.2 mg g −1 OC averaging over incubation temperatures and soil depths, being 27-55 % greater than that under shrublands.
A novel material named Fe/Mn-C layered double hydroxide composite (Fe/Mn-C-LDH) was synthesized to remove arsenic from an aqueous solution. The removal performance of the composite toward arsenic ions was studied through the batch experiments. The experiment results showed that Fe/Mn-C-LDH exhibited a high adsorption capacity of 46.47 mg/g for As(III) and 37.84 mg/g for As(V) at 318 K, respectively. In addition, the investigation of the release of Fe3+ and Mn2+ in the process of arsenic adsorption revealed that the Fe/Mn-C-LDH exhibited better stability than Fe/Mn-layer double hydroxide (Fe/Mn-LDH) with fewer Mn2+ and Fe3+ releasing under the same condition. The BET results showed that the specific surface area of Fe/Mn-C-LDH decreased after adsorption of As (III) and As (V). Furthermore, the Density Functional Theory (DFT) calculation results proved that the adsorbent combining arsenic by T-site to produce a better adsorption effect for arsenic. Possessing better stability and adsorption capacity, Fe/Mn-C-LDH could potentially serve as a perfect adsorbent for arsenic removal from an aqueous environment. It would provide a promising approach for removing heavy metal from the aquatic environment in the future.
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