Beidou Xi

The evolution of water extractable organic matter and its association with microbial community dynamics during municipal solid waste composting

The humification of water extractable organic matter (WEOM) by microorganisms is widely used for assessing compost maturity and quality. However, the effect of bacterial and fungal community dynamics on humification of WEOM was not yet explored fully. Here, we used canonical correspondence analysis (CCA) and redundancy analysis (RDA) to investigate the link between bacterial and fungal community dynamics and humification process of WEOM, respectively. Results showed that water-soluble carbon (WSC), humification degree, molecule weight and abundance of aromatic carbon were significantly related to bacterial community (p<0.05), while the protein-like materials were statistically influenced by fungal community (p<0.05). Both bacterial and fungal communities significantly affected the abundance of oxygen-containing functional groups and humic-like materials (p<0.05). These humification parameters were most likely to be influenced by some of bacterial and fungal species at different composting stages. Lactobacillus, Aspergillus fumigatus and Galactomyces geotrichum can enhance the degradation of WSC and protein-like materials at the early composting. Bacteroidetes and Firmicutes could promote the increase of aromatic carbon, oxygen-containing functional groups, humification degree and molecular weight of WEOM during the initial fermentation stage. Cladosporium herbarum and Chaetomium globosum could be the dominant controllers at the second fermentation for acceleratingthe formation of oxygen-containing functional groups and humic-like materials of WEOM, respectively. Our results suggested that regulation for the dynamics of these special bacterial and fungal species at different composting stages might be a potential way to accelerate humification of municipal solid waste composting.

Contamination of Phthalate Esters (PAEs) in Typical Wastewater-Irrigated Agricultural Soils in Hebei, North China.

The Wangyang River (WYR) basin is a typical wastewater irrigation area in Hebei Province, North China. This study investigated the concentration and distribution of six priority phthalate esters (PAEs) in the agricultural soils in this area. Thirty-nine soil samples (0–20 cm) were collected along the WYR to assess the PAE residues in soils. Results showed that PAEs are ubiquitous environmental contaminants in the topsoil obtained from the irrigation area. The concentrations of Σ6PAEs range from 0.191 μg g−1 dw to 0.457 μg g−1 dw with an average value of 0.294 μg g−1 dw. Di(2-ethylhexyl) phthalate (DEHP) and di-n-butyl phthalate (DnBP) are the dominant PAE species in the agricultural soils. Among the DEHP concentrations, the highest DEHP concentration was found at the sites close to the villages; this result suggested that dense anthropogenic activities and random garbage disposal in the rural area are possible sources of PAEs. The PAE concentrations were weakly and positively correlated with soil organic carbon and soil enzyme activities; thus, these factors can affect the distribution of PAEs. This study further showed that only dimethyl phthalate (DMP) concentrations exceeded the recommended allowable concentrations; no remediation measures are necessary to control the PAEs in the WYR area. However, the PAEs in the topsoil may pose a potential risk to the ecosystem and human health in this area. Therefore, the exacerbating PAE pollution should be addressed.

Compost-derived humic acids as regulators for reductive degradation of nitrobenzene

Nitrobenzene (NB) is a major class of contaminants in soil and groundwater. The current methods involved in the reductive degradation of NB suffer either cost-ineffective or slow conversion rate. Here, we investigated the mechanisms regarding compost-derived humic acids (HAs) as cost-effective regulators to enhance the reduction of NB to aniline (AN). Our results show that the compost-derived HAs, which have been reduced by a Pd-H2 catalytic system, were able to reduce NB to AN, and their redox properties were the main factors governing the reduction of NB to AN. The decreasing reduction of NB was mainly caused by the decreasing phenol content of compost-derived HAs during composting. In addition, the results reveal that the increase in the generation content of AN was mainly attributed to the increase in the quinones, aromaticity and humic-like components of compost-derived HAs. The findings demonstrate that the HAs derived from compost are effective regulators to enhance the reduction of NB to AN, and that they exert a bright application prospect for the remediation of the NB-contaminated soil.

Insight into the composition and evolution of compost-derived dissolved organic matter using high-performance liquid chromatography combined with Fourier transform infrared and nuclear magnetic resonance spectra.

Size exclusion chromatography and reversed-phase high-performance liquid chromatography (RP-HPLC) were combined with Fourier transform infrared spectra (FTIR) and nuclear magnetic resonance (NMR) based on two dimensional (2D) hetero-spectral correlation spectra techniques to fractionate compost-derived dissolved organic matter (DOM) and determine how size- and hydrophobicity-distinguished fractions differ in the composition and evolution. The results showed that the compost-derived DOM was comprised of protein- and humic-like species. The low apparent molecule weight (AMW) protein-like components were enriched in C-C=H3 and N-C=O, and showed more bioreactivity compared with the high AMW counterpart. The hydrophobic and hydrophilic protein-like components both consisted of CCH3 and N-C=O. However, the relatively hydrophilic protein-like components were more easily consumed. As to the humic-like species, the relatively hydrophilic components were slightly larger than the relatively hydrophobic ones. The high AMW and relatively hydrophilic humic-like components were high in C-H, OCH3, N-C=O, N-H, COO, O-H and aromatic C. The low AMW and relatively hydrophobic humic-like components were enriched in CCH3 and N-C=O, and were easily biodegraded during composting. 2D hetero-spectral correlation spectra techniques enhance the characterization of DOM and provide a promising way to elucidate the environmental behaviors of DOM.

Physico-chemical protection, rather than biochemical composition, governs the responses of soil organic carbon decomposition to nitrogen addition in a temperate agroecosystem

The heterogeneous responses of soil organic carbon (SOC) decomposition in different soil fractions to nitrogen (N) addition remain elusive. In this study, turnover rates of SOC in different aggregate fractions were quantified based on changes in δ13C following the conversion of C3 to C4 vegetation in a temperate agroecosystem. The turnover of both total organic matter and specific organic compound classes within each aggregate fraction was inhibited by N addition. Moreover, the intensity of inhibition increases with decreasing aggregate size and increasing N addition level, but does not vary among chemical compound classes within each aggregate fraction. Overall, the response of SOC decomposition to N addition is dependent on the physico-chemical protection of SOC by aggregates and minerals, rather than the biochemical composition of organic substrates. The results of this study could help to understand the fate of SOC in the context of increasing N deposition.

Distribution patterns of phthalic acid esters in soil particle-size fractions determine biouptake in soil-cereal crop systems.

The use of wastewater irrigation for food crops can lead to presence of bioavailable phthalic acid esters (PAEs) in soils, which increase the potential for human exposure and adverse carcinogenic and non-cancer health effects. This study presents the first investigation of the occurrence and distribution of PAEs in a maize-wheat double-cropping system in a wastewater-irrigated area in the North China Plain. PAE levels in maize and wheat were found to be mainly attributed to PAE stores in soil coarse (250–2000 μm) and fine sand (53–250 μm) fractions. Soil particle-size fractions with higher bioavailability (i.e., coarse and fine sands) showed greater influence on PAE congener bioconcentration factors compared to PAE molecular structures for both maize and wheat tissues. More PAEs were allocated to maize and wheat grains with increased soil PAE storages from wastewater irrigation. Additional findings showed that levels of both non-cancer and carcinogenic risk for PAE congeners in wheat were higher than those in maize, suggesting that wheat food security should be prioritized. In conclusion, increased soil PAE concentrations specifically in maize and wheat grains indicate that wastewater irrigation can pose a contamination threat to food resources.

Heterogeneity of the electron exchange capacity of kitchen waste compost-derived humic acids based on fluorescence components

AbstractComposting is widely used for recycling of kitchen waste to improve soil properties, which is mainly attributed to the nutrient and structural functions of compost-derived humic acids (HAs). However, the redox properties of compost-derived HAs are not fully explored. Here, a unique framework is employed to investigate the electron exchange capacity (EEC) of HAs during kitchen waste composting. Most components of compost-derived HAs hold EEC, but nearly two-thirds of them are found to be easily destroyed by Shewanella oneidensis MR-1 and thus result in an EEC lower than the electron - donating capacity in compost-derived HAs. Fortunately, a refractory component also existed within compost-derived HAs and could serve as a stable and effective electron shuttle to promote the MR-1 involved in Fe(III) reduction, and its EEC was significantly correlated with the aromaticity and the amount of quinones. Nevertheless, with the increase of composting time, the EEC of the refractory component did not show an increasing trend. These results implied that there was an optimal composting time to maximize the production of HAs with more refractory and redox molecules. Recognition of the heterogeneity of EEC of the compost-derived HAs enables an efficient utilization of the composts for a variety of environmental applications. Graphical abstractMicrobial reduction of compost-derived HAs

Response of humic-reducing microorganisms to the redox properties of humic substance during composting

Humic substance (HS) could be utilized by humus-reducing microorganisms (HRMs) as the terminal acceptors. Meanwhile, the reduction of HS can support the microbial growth. This process would greatly affect the redox conversion of inorganic and organic pollutants. However, whether the redox properties of HS lined with HRMs community during composting still remain unclear. This study aimed to assess the relationships between the redox capability of HS [i.e. humic acids (HA) and fulvic acids (FA)] and HRMs during composting. The results showed that the changing patterns of electron accepting capacity and electron donating capacity of HS were diverse during seven composting. Electron transfer capacities (ETC) of HA was significantly correlated with the functional groups (i.e. alkyl C, O-alkyl C, aryl C, carboxylic C, aromatic C), aromaticity and molecular weight of HA. Aromatic C, phenols, aryl C, carboxylic C, aromaticity and molecular weight of HS were the main structuralfeatures associated with the ETC of FA. Ten key genera of HRMs were found significantly determine these redox-active functional groups of HS during composting, thus influencing the ETC of HS in composts. In addition, a regulating method was suggested to enhance the ETC of HS during composting based on the relationships between the key HRMs and redox-active functional groups as well as environmental variables.