Long-term (≥20 years) application of fertilizers and straw return enhances soil carbon storage: a meta-analysis

Increasing soil carbon (C) storage is crucial to addressing climate change and ensuring food security. The C sequestration potential of the world’s cropland soil is 0.4–0.8 Pg soil C year^?1, which may be achieved through the adoption of recommended management practices (RMPs), including fertilizer management. This study aimed to quantitatively evaluate the influence of long-term application of different fertilizers and straw retention on soil organic carbon (SOC) storage, to compare the calculated response ratios with Intergovernmental Panel on Climate Change (IPCC)-recommended default relative stock change factors, and to propose recommendations for enhancing SOC sequestration. The meta-analysis indicated that the long-term application of chemical fertilizers (CF), organic fertilizers (OF), combined chemical and organic fertilizers (CFOF), and straw return (SR) significantly enhanced the SOC storage. Response ratios varied significantly (p < 0.05) across different fertilization measures and climatic zones, and was sensitive to the initial SOC content. The mean response ratio was 0.94 for no fertilizer (NF), 1.08 for CF, 1.48 for OF, 1.38 for CFOF, and 1.28 for SR. When IPCC default values for response ratios were applied, SOC storage with OF and CFOF treatments in warm temperate regions with a dry climate was underestimated by 26%, and in the cool temperate region with a moist climate was overestimated by 25% (p < 0.05). Analysis showed that sustained application of organic fertilizers and straw return could be a beneficial measures to mitigate climate change and ensure food security in China. Our findings highlight the importance of deriving SOC stock change factors for a detailed classification of cropland by fertilizer management, climate, and soil types in order to more accurately reflect the effects of policy measures.     

Synthesis of a novel humic acid-based polycarboxylic dispersant for coal water slurry

A novel humic acid-based polycarboxylic-type (HAP) dispersant for coal–water slurry (CWS) was successfully synthesized in aqueous solution from the copolymerization of HA, acrylic acid and maleic acid. The structure of HAP was characterized by Fourier transform infrared (FTIR), thermogravimetry (TG) and ¹H NMR. With HAP as a dispersant for Linfen coal slurry, the effects of the mass ratio of HA and monomer, initiator concentration, reaction temperature and reaction time on the HAP dispersant performance were discussed by examining the apparent viscosity of CWS. The results showed that CWS prepared withHAP dispersant performed excellent dispersity and stability. When the dosage of HAP was up to 0.5 wt.%, the apparent viscosity of CWS was 505 mPa·s. Experiments on the stability of CWS containing 0.5 wt.% HAP demonstrated that the penetration ratio reached 85.45 % after 96 h, which was higher by 12.87 % than that of CWS prepared with HA. And the CWS produced with HAP had lower dewatering rate within the storage time, which was less 1.85 % than that of CWS with HA when the storage time was 72 h. Furthermore, the maximum coal content of CWS with 0.5 wt.% HAP may reached 70 wt.%. This work found a new route for utilizing humic acid and enlarged the selecting range of the dispersant for CWS. It has a positive significance for protection of environment.     

Characterisation and seasonal variations of particles in the atmosphere of rural, urban and industrial areas: Organic compounds

Atmospheric aerosol samples(PM_(2.5–0.3), i.e., atmospheric particles ranging from 0.3 to2.5 μm) were collected during two periods: spring–summer 2008 and autumn–winter 2008–2009, using high volume samplers equipped with cascade impactors. Two sites located in the Northern France were compared in this study: a highly industrialised city(Dunkirk) and a rural site(Rubrouck). Physicochemical analysis of particulate matter(PM) was undertaken to propose parameters that could be used to distinguish the various sources and to exhibit seasonal variations but also to provide knowledge of chemical element composition for the interpretation of future toxicological studies. The study showed that PM2.5–0.3concentration in the atmosphere of the rural area remains stable along the year and was significantly lower than in the urban or industrial ones, for which concentrations increase during winter.High concentrations of polycyclic aromatic hydrocarbons(PAHs), dioxins, furans and dioxin like polychlorinated biphenyls(DL-PCBs), generated by industrial activities, traffic and municipal wastes incineration were detected in the samples. Specific criteria like Carbon Preference Index(CPI) and Combustion PAHs/Total PAHs ratio(CPAHs/TPAHs) were used to identify the possible sources of atmospheric pollution. They revealed that paraffins are mainly emitted by biogenic sources in spring–summer whereas as in the case of PAHs, they have numerous anthropogenic emission sources in autumn-winter(mainly from traffic and domestic heating).     

我国实施流域水资源与水环境一体化管理构想

本文通过分析国外流域管理方面的经验和发展趋势 ,结合我国流域管理现状 ,提出我国在流域水资源与水环境一体化管理中实施方案的构想。     

Removal efficiency of a constructed wetland for wastewater treatment according to vegetation dominance

A free water surface wetland was built to treat wastewater containing metals (Cr, Ni and Zn) and nutrients from a tool factory in Santo Tomé, Santa Fe, Argentina. Eichhornia crassipes became dominant and covered about 80% of the surface throughout the first year, and decreased progressively until its disappearance. When water depth was lowered Typha domingensis steadily increased plant cover and attained 30% of the surface by the end of the study. While E. crassipes was dominant, the wetland retained 62% of the incoming Cr and 48% of the Ni. NO3- and NO2-, were also removed (65% and 78%, respectively), while dissolved inorganic phosphate (i-P(diss)) and NH4+ were not removed. Zn was below 50 microg l(-1) in both the influent and effluent. Metal concentration in the sediments did not increase and retention was mediated through macrophytes uptake. During the period of E. crassipes decline the wetland retained 49% of the incoming Cr, 45% of Ni, 58% NO3-, 94% NO2-, 58% NH4+ and 47% i-P(diss). Cr, Ni and Zn in the bottom sediment increased in the inlet but not in the outlet. Since T. domingensis became dominant, retention was 58% Cr, 48% Ni and 64% i-P(diss), while 79% NO3-, 84% NO2- and 13% NH4+ were removed. Metals in the bottom sediment increased in the inlet. In spite of the significant growth of E. crassipes at the beginning, T. domingensis remained after most of the transplanted macrophytes had disappeared. Macrophyte disappearance could be related to the overall toxicity of several environmental constrains as high pH and conductivity, metal concentration, and sulphide presence.     

Trace metal dynamics in an industrialized Brazilian river: A combined application of Zn isotopes, geochemical partitioning, and multivariate statistics

The Paraiba do Sul (PSR) and Guandu Rivers (GR) water diversion system (120 km long) is located in the main industrial pole of Brazil and supplies drinking water for 9.4 million people in the metropolitan region of Rio de Janeiro. This study aims to discern the trace metals dynamics in this complex aquatic system. We used a combined approach of geochemical tools such as geochemical partitioning, Zn isotopes signatures, and multivariate statistics. Zinc and Pb concentrations in Suspended Particulate Matter (SPM) and sediments were considerably higher in some sites. The sediment partition of As, Cr, and Cu revealed the residual fraction (F4) as the main fraction for these elements, indicating low mobility. Zinc and Pb were mostly associated with the exchangeable/carbonate (F1) and the reducible (F2) fractions, respectively, implying a higher susceptibility of these elements to being released from sediments. Zinc isotopic compositions of sediments and SPM fell in a binary mixing source process between lithogenic (δ^66/64Zn_JMC ≈ + 0.30‰) and anthropogenic (δ^66/64Zn_JMC ≈ + 0.15‰) end members. The lighter δ^66/64Zn_JMC values accompanied by high Zn concentrations in exchangeable/carbonate fraction (ZnF1) enable the tracking of Zn anthropogenic sources in the studied rivers. Overall, the results indicated that Hg, Pb, and Zn had a dominant anthropogenic origin linked to the industrial activities, while As, Cr, and Cu were mainly associated with lithogenic sources. This work demonstrates how integrating geochemical tools is valuable for assessing geochemical processes and mixing source effects in anthropized river watersheds.     

太湖饮用水源地金墅港、渔洋山水质综合评价

采用BP神经网络、内梅罗指数和综合营养状态指数评价了太湖金墅港、渔洋山饮用水源地水质及综合营养状态。结果表明,2012年金墅港和渔洋山的水质基本达到国家Ⅱ类水要求,其水质均处于中营养状态(31.43~47.66),不同水期对水源地营养状态影响较大,丰水期水质综合营养状态指数最低,且变化较小。渔洋山的年均富营养化状况(42.08)比金墅港(40.62)略重。     

Role of carbonyls and aromatics in the formation of tropospheric ozone in Rio de Janeiro,Brazil

The ozone in Rio de Janeiro has been in violation of national air quality standards. Among all of the monitoring stations, the Bangu neighbourhood has the most violations of the national standard of 160 μg m^?3 for the years 2012 and 2013. This study evaluated the reactivity of the carbonyls and aromatics in the tropospheric ozone formation processes. The samples were collected between July and October of 2013. Carbonyls were sampled using SiO₂ cartridges coated with C₁₈ and impregnated with 2,4-dinitrophenylhydrazine and were analysed by HPLC. Activated carbon cartridges and GC/MS were used to measure the concentration of monoaromatic hydrocarbons. An air quality monitoring station provided the concentrations of the criteria pollutants and the meteorological parameters. Cluster analysis and a Pearson correlation matrix were used to determine the formation of groups and the correlation of the variables. The evaluation of the volatile organic compounds (VOC) reaction with OH radicals and the MIR scale was used to extrapolate the reactivity of VOCs to the ozone formation. The average concentrations obtained were 19.7 and 51.9 μg m^?3 for formaldehyde and acetaldehyde, respectively. The mean concentrations obtained for aromatics were 1.5, 6.7, 1.5, 2.6 and 1.6 μg m^?3 for benzene, toluene, ethyl benzene, m+p-xylene and o-xylene, respectively. The cluster analysis indicated the presence of three similar groups, with one formed by gaseous criteria pollutants, another formed by the meteorological parameters, ozone and fine particles, and the last group formed by the aromatics. For the two reactivity scales evaluated, acetaldehyde and toluene were the main ozone precursors.