The release of metal elements from litter decomposition in forest ecosystems is crucial for material cycling and ecosystem health, but the impact of future variations in rainfall due to climatic fluctuations on this release is unknown. This study conducted an outdoor rainfall variability simulation and an in situ litter decomposition experiment in a subtropical location, with a focus on pure Pinus massoniana (PM) and four PM mixed stands (PM+Bretschneidera sinensis, PM+Cercidiphyllum japonicum, PM+Taxus wallichiana, and PM+Nageia nagi). We studied the release of metal elements from litter after one year of decomposition under different rainfall conditions (30% increase, natural, and 30% decrease) and calculated the mixing effect on the litter. The results showed that K, Mg, Mn, Cu and Zn were released and Na, Ca and Fe were enriched after one year of litter decomposition. Increased rainfall promoted K, Na, Mg, Mn, and Zn release, reduced Fe and Cu release, enhanced the synergistic effect of Na and Mn release, and exacerbated the antagonistic effect of Cu. Decreased rainfall reduced the synergistic effect of mixed litter on the release of Na, Ca, Mg, and Fe, while enhancing the synergistic effect of Mn and Zn. The lower degree of metal element release from single PM litter resulted in the enrichment of metal elements in the litter of apoplasts. The effect of rainfall variability on metal element release was more significant compared to tree species characteristics. Overall, decreased rainfall inhibited metal element release and slowed down element cycling; increased rainfall promoted Na and Mn release and accelerated Cu enrichment. It is noteworthy that mixed litter effectively mitigated the effects of rainfall changes on metal element release by regulating elemental cycling. The findings of this study add to a better understanding of nutrient dynamics in forest ecosystems and offer techniques and insights for addressing future climate change.
Lignocellulosic composting has been widely promoted in the utilization of agricultural wastes, while few focus on orchard lignocellulosic wastes in the fruit industry. Peniophora is a laccase hyper-producer highly efficient in lignin degradation, yet its application in lignocellulosic composting has not been investigated. Here, an aerobic composting experiment was conducted to investigate the effects of inoculation with Peniophora crassitunicata and a commercial microbial inoculant (mainly Bacillus and Aspergillus) on grape (Vitis Vinifera L.) orchard lignocellulosic wastes degradation and the underlying mechanisms. The inoculation with P. crassitunicata, both individually (H) and in combination with the commercial microbial inoculant (HS), enhanced lignocellulose degradation efficiency. Notably, the co-inoculation exhibited higher lignocellulose degradation ratios and higher lignocellulosic enzyme activities compared to other treatments. The compost piles with co-inoculation experienced a more rapid temperature rise, a longer duration (15 days) of high temperatures, lower pH, and lower electrical conductivity (EC). Firmicutes (e.g. Bacillus, Paenibacillus) and Ascomycota (e.g. Aspergillus) along with Bacteroidota, Actinobacteriota, and Basidiomycota (e.g. Peniophora) dominated the microbial community in compost; carbohydrate metabolism dominated microbial metabolic pathways at the thermophilic phase, highlighting an active microbial community. As compost processed, highly mature and non-toxic compost products were finally obtained for the co-inoculation, with a pH of 7.87, C/N ratio of 13.5, NH4+-N/NO3‾-N ratio of 0.21-0.41, EC of 0.90 mS cm-1, and germination index of 149 %. The co-inoculation of P. crassitunicata with the commercial microbial inoculant effectively accelerated lignocellulose degradation and compost maturation, producing a friendly and non-toxic organic fertilizer for agricultural applications and thereby providing a new strategy for orchard wastes management and agricultural applications.
Using granulated blast furnace slag as raw material, chitosan and NaCl as modifier, chitosan modified granulated blast furnace slag based porous geopolymer (PCG) was prepared under the activation conditions of NaOH and sodium silicate. It was used to wrap different types of lightweight aggregates to obtain PCG-lightweight aggregate shell-core structure (PCG-L). PCG-L was used for the adsorption of Pb2+. Firstly, the influencing factors on the adsorption performance of the main component materials (PCG, lightweight aggregates) of PCG-L were studied. Then, the static adsorption properties and sustainable adsorption properties of Pb2+ by different shell-core structures were investigated. The relationship between the water absorption characteristics of the paste and the aggregate and the adsorption characteristics of PCG-L towards Pb2+ was established. The adsorption kinetics, adsorption isotherms and adsorption thermodynamics were analyzed. Finally, the adsorption mechanism of PCG-L was discussed by Zeta analyzer, FT-IR, EDS, XPS and MIP. The results indicate that as chitosan (0-2wt%) and NaCl (0-60wt%) increase, the saturated adsorption capacity of PCG for Pb2+ rises (98.57-159.93mg/g). The Pb2+ adsorption capacity of lightweight aggregate (0.34-1.21g/dm3) increases with its water absorption (0.2-15.0%). Under the premise that the water absorption rate of aggregate is greater than that of PCG, the higher the water absorption rate of the two, the stronger the adsorption capacity of the matching PCG-L, the maximum adsorption capacity of A2N30-H is 5.12g/dm3 and it can still maintain a high removal rate after 40 cycles of adsorption. PCG-L adsorption via ion exchange, electrostatic attraction, surface complexation, and pore fixation.
A novel method of S-scheme heterojunction photocatalyst assisted with plasma was proposed to degrade the methyl p-hydroxybenzoate (MeP) in wastewater. The two-dimensional MoS2/g-C3N4 composite was prepared by the thermal polycondensation method. The sheet-like morphologies and S-scheme heterogeneous structure were validated by XRD, XPS, EDS, FTIR, and TEM in the MoS2/g-C3N4 composite. The addition of MoS2/g-C3N4 increased the MeP degradation from 74.85% to 89.85% and the TOC removal rate from 25.16% to 40.12%. The MeP solution reduced the toxicity after treating the plasma/MoS2/g-C3N4 system. Quenching experiments and electron paramagnetic resonance (EPR) spectra showed that the UV light generated by the discharge is utilized by the catalyst, which increases the yield of O2-· and 1O2, enhancing the degradation efficiency of MeP. The absorption spectral range and electron transfer ability are improved by the interaction between MoS2 and g-C3N4. The proposed charge transfer mechanism is driven by the S-scheme heterojunction built-in electric field (IEF), thereby reducing the recombination of photogenerated electron-hole pairs. The production of free radicals is increased by the adsorption-reduction reaction on the surface of MoS2 and g-C3N4. In addition, the catalytic material has good photocatalytic performance after recycling. MoS2/g-C3N4 combined with plasma exhibits excellent photocatalytic performance and has a wide range of application prospects.