Phosphorus mobility in dam reservoir affected by redox oscillations: An experimental study

The internal sedimentary phosphorus(P) load of aquatic systems is able to support eutrophication, especially in dam–reservoir systems where sedimentary P stock is high and where temporary anaerobic conditions occur. The aim of this study therefore is to examine the response of sedimentary P exposed to redox oscillations. Surface sediments collected in the Champsanglard dam–reservoir(on the Creuse River, France) were subjected to two aerobic phases(10 and 12 days) alternated with two anaerobic periods(21 and 27 days)through batch incubations. The studied sediment contained 77 ± 3 μmol/g DW of P, mainly associated with the ascorbate fraction(amorphous Fe/Mn oxyhydroxides). The used sediment was rich in organic matter(OM)(21% ± 1%) with primarily allochthone signature.Our results showed that redox oscillations enhance dissolved inorganic phosphorus release at sediment/water interface. During the first anaerobic stage, the P release was mainly controlled by the dissolution/precipitation of iron minerals. The more pronounced increase of P release during the second anaerobic stage(44%) was due to various mechanisms related to the change in quality of dissolved organic matter(DOM), namely a higher SUVA254 and humification indices. The release of more refractory DOM(rDOM) served to lower the microbial metabolism activity, possibly favored iron oxyhydroxide aggregation and thus limiting iron reduction. In addition, rDOM is able to compete for mineral P sorption sites,leading to a greater P release. In reservoir with predominant allochthone OM input, the release of more aromatic DOM therefore plays an important role in P mobility.     

Effect of environmental factors on the complexation of iron and humic acid

A method of size exclusion chromatography coupled with ultraviolet spectrophotometry and off-line graphite furnace atomic absorption spectrometry was developed to assess the complexation properties of iron (Fe) and humic acid (HA) in a water environment. The factors affecting the complexation of Fe and HA, such as ionic strength, pH, temperature and UV radiation, were investigated. The Fe-HA complex residence time was also studied. Experimental results showed that pH could influence the deprotonation of HA and hydrolysis of Fe, and thus affected the complexation of Fe and HA. The complexation was greatly disrupted by the presence of NaCl. Temperature had some influence on the complexation. The yield of Fe-HA complexes showed a small decrease at high levels of UV radiation, but the effect of UV radiation on Fe-HA complex formation at natural levels could be neglected. It took about 10 hr for the complexation to reach equilibrium, and the Fe-HA complex residence time was about 20 hr. Complexation of Fe and HA reached a maximum level under the conditions of pH 6, very low ionic strength, in the dark and at a water temperature of about 25°C, for 10 hr. It was suggested that the Fe-HA complex could form mainly in freshwater bodies and reach high levels in the warm season with mild sunlight radiation. With changing environmental parameters, such as at lower temperature in winter or higher pH and ionic strength in an estuary, the concentration of the Fe-HA complex would decrease.     

Accumulation and elimination of iron oxide nanomaterials in zebrafish (Danio rerio) upon chronic aqueous exposure

A 52-day continuous semi-static waterborne exposure (test media renewed daily) regimen was employed to investigate the accumulation and elimination profiles of two iron oxide nanomaterials (nano-Fe₂O₃ and nano-Fe₃O₄) in zebrafish (Danio rerio). Adult zebrafish were exposed to nanomaterial suspensions with initial concentrations of 4.0 and 10.0 mg/L for 28 days and then were moved to clean water for 24 days to perform the elimination experiment. Fe content was measured in fish body and feces to provide data on accumulation and elimination of the two iron oxide nanomaterials in zebrafish. The experiment revealed that: (1) high accumulation of nano-Fe₂O₃ and nano-Fe₃O₄ were found in zebrafish, with maximum Fe contents, respectively, of 1.32 and 1.25 mg/g for 4.0 mg/L treatment groups and 1.15 and 0.90 mg/g for 10.0 mg/L treatment groups; (2) accumulated nanoparticles in zebrafish can be eliminated efficiently (the decrease of body burden of Fe conforms to a first-order decay equation) when fish were moved to nanoparticle-free water, and the elimination rates ranged from 86% to 100% by 24 days post-exposure; and (3) according to analysis of Fe content in fish excrement in the elimination phase, iron oxide nanomaterials may be adsorbed via the gastrointestinal tract, and stored for more than 12 days.     

长江口近岸表层沉积物中基质结合态磷化氢的分布特征

利用气相色谱-脉冲火焰光度检测器(GC-PFPD)分析了长江口近岸表层沉积物中基质结合态磷化氢(MBP)的含量,并探讨了其潜在的影响因素.结果表明,5月沉积物中MBP的含量略高于11月,其含量变化范围分别为139～426 ng.kg-1和111～192 ng.kg-1,平均含量分别为224 ng.kg-1和158 ng.kg-1;并且,沉积物中MBP的含量存在显著的地理空间差异.此外,MBP含量与环境参数之间的相关分析显示,MBP与总磷(TP)、无机磷(IP)、有机磷(OP)有较好的线性关系(RTP=0.86,P<0.000 1;RIP=0.81,P<0.000 1;ROP=0.90,P<0.000 1),与碱性磷酸酶活性(APA)、pH的相关性较弱(RAPA=0.55,P=0.019;RpH=0.511,P=0.03),表明沉积物中MBP的含量与磷组分、APA及pH密切相关,但与有机碳、盐度等环境因子并无显著相关性.     

Kinetics of nitrobenzene degradation coupled to indigenous microorganism dissimilatory iron reduction stimulated by emulsified vegetable oil

Widespread contamination by nitrobenzene(NB) in sediments and groundwater requires better understanding of the biogeochemical removal process of the pollutant. NB degradation, coupled with dissimilatory iron reduction, is one of the most efficient pollutant removal methods. However, research on NB degradation coupled to indigenous microorganism dissimilatory iron reduction stimulated by electron donors is still experimental. A model for remediation in an actual polluted site does not currently exist.Therefore, in this study, the dynamics was derived from the Michaelis–Menten model(when the mass ratio of emulsified vegetable oil and NB reached the critical value 91:1). The effect of SO_4~(2-), NO_3~-, Ca~(2+)/Mg~(2+), and the grain size of aquifer media on the dynamics were studied, and the NB degradation dynamic model was then modified based on the most significant factors. Utilizing the model, the remediation time could be calculated in a contaminated site.     

Mobilization of arsenic from contaminated sediment by anionic and nonionic surfactants

The increasing manufacture of surfactants and their wide application in industry,agriculture and household detergents have resulted in large amounts of surfactant residuals being discharged into water and distributed into sediment. Surfactants have the potential to enhance arsenic mobility, leading to risks to the environment and even human beings. In this study, batch and column experiments were conducted to investigate arsenic mobilization from contaminated sediment by the commercial anionic surfactants sodium dodecylbenzenesulfonate(SDBS), sodium dodecyl sulfate(SDS), sodium laureth sulfate(AES)and nonionic surfactants phenyl-polyethylene glycol(Triton X-100) and polyethylene glycol sorbitan monooleate(Tween-80). The ability of surfactants to mobilize arsenic followed the order AES SDBS SDS ≈ Triton X-100 Tween 80. Arsenic mobilization by AES and Triton X-100 increased greatly with the increase of surfactant concentration and p H, while arsenic release by SDBS, SDS and Tween-80 slightly increased. The divalent ion Ca~(2+) caused greater reduction of arsenic mobilization than Na~+. Sequential extraction experiments showed that the main fraction of arsenic mobilized was the specifically adsorbed fraction. Solid phase extraction showed that arsenate(As(V)) was the main species mobilized by surfactants,accounting for 65.05%–77.68% of the total mobilized arsenic. The mobilization of arsenic was positively correlated with the mobilization of iron species. The main fraction of mobilized arsenic was the dissolved fraction, accounting for 70% of total mobilized arsenic.     

Removal of Cs from water and soil by ammonium-pillared montmorillonite/Fe3O4 composite

To remove cesium ions from water and soil, a novel adsorbent was synthesized by following a one-step co-precipitation method and using non-toxic raw materials. By combining ammonium-pillared montmorillonite (MMT) and magnetic nanoparticles (Fe₃O₄), an MMT/Fe₃O₄ composite was prepared and characterized. The adsorbent exhibited high selectivity of Cs⁺ and could be rapidly separated from the mixed solution under an external magnetic field. Above all, the adsorbent had high removal efficiency in cesium-contaminated samples (water and soil) and also showed good recycling performance, indicating that the MMT/Fe₃O₄ composite could be widely applied to the remediation of cesium-contaminated environments. It was observed that the pH, solid/liquid ratio and initial concentration affected adsorption capacity. In the presence of coexisting ions, the adsorption capacity decreased in the order of Ca^2 + > Mg^2 + > K⁺ > Na⁺, which is consistent with our theoretical prediction. The adsorption behavior of this new adsorbent could be expressed by the pseudo-second-order model and Freundlich isotherm. In addition, the adsorption mechanism of Cs⁺ was NH₄⁺ ion exchange and surface hydroxyl group coordination, with the former being more predominant.     

Cobalt induced changes in immune response and adenosine triphosphatase activities in rats

Abstract

The immuno‐biochemical effects of cobaltous chloride in rats receiving iron‐sufficient and deficient diets were investigated. Rats receiving 100 ppm or more cobalt showed a significant reduction in thymus and body weights along with a marked decrease in hemoglobin, hematocrit, sheep agglutinins and plaque forming cells. These effects were more pronounced in rats receiving cobalt mixed with iron‐deficient diet than those fed on iron‐sufficient diet. The Na⁺‐K⁺ and mitochondrial (Oligomycin‐sensitive) Mg²+ATPase activities in brain and liver of rats fed with iron‐deficient diets were decreased significantly. However, the ATPase activities in these tissues from rats fed with cobalt mixed with iron‐sufficient diets were not altered.     

进一步保持和发扬我党的“真正优势”

本文在全面论述邓小平同志关于“共同的理想”和“铁的纪律”是我党“真正优势”光辉论断的基础上，指出目前我们在保持和发扬“真正优势”方面存在的不足，并认为中国共产党要顺利解决“两大历史性课题”，必须进一步保持和发扬自己的“真正优势”。     

铁水包底粘铁所引发的一起重伤事故分析

介绍了一起铁水包底粘铁所引发的事故经过,进行了事故原因分析,指出了事故教训和预防措施。