Modeling in-situ uranium(VI) bioreduction by sulfate-reducing bacteria

We present a travel-time based reactive transport model to simulate an in-situ bioremediation experiment for demonstrating enhanced bioreduction of uranium(VI). The model considers aquatic equilibrium chemistry of uranium and other groundwater constituents, uranium sorption and precipitation, and the microbial reduction of nitrate, sulfate and U(VI). Kinetic sorption/desorption of U(VI) is characterized by mass transfer between stagnant micro-pores and mobile flow zones. The model describes the succession of terminal electron accepting processes and the growth and decay of sulfate-reducing bacteria, concurrent with the enzymatic reduction of aqueous U(VI) species. The effective U(VI) reduction rate and sorption site distributions are determined by fitting the model simulation to an in-situ experiment at Oak Ridge, TN. Results show that (1) the presence of nitrate inhibits U(VI) reduction at the site; (2) the fitted effective rate of in-situ U(VI) reduction is much smaller than the values reported for laboratory experiments; (3) U(VI) sorption/desorption, which affects U(VI) bioavailability at the site, is strongly controlled by kinetics; (4) both pH and bicarbonate concentration significantly influence the sorption/desorption of U(VI), which therefore cannot be characterized by empirical isotherms; and (5) calcium-uranyl-carbonate complexes significantly influence the model performance of U(VI) reduction.     

计算机模拟研究UO2+2在人体细胞液的形态分布

建立了由多种金属离子和小分子配体组成的多相细胞液热力学平衡模型.模拟研究了UO2 2在组织液和细胞液的形态分布及CO2-3、氨三乙酸（NTA）和乙二胺四乙酸（EDTA）浓度对细胞液中UO2 2形态分布的影响.在组织液中,正常生理pH下,当各形态UO2 2总摩尔浓度 [U]= 1.0×10-6 mol/L 或[U]=1.0×10-3 mol/L时,UO2 2均主要以[UO2(CO3)3]4-和[UO2(CO3)2]2-形态存在.在细胞液中,当[U]=1.0×10-6 mol/L时,UO2 2主要以[UO2(CO3)3]4-和[UO2(CO3)2]2-存在;当[U]=1.0×10-3 mol/L,pH为6.0～6.8时,细胞液中存在大量的固相(UO2)3(PO4)2·4H2O,当pH为6.8～7.4时,UO2 2主要以[UO2(CO3)3]4-、[UO2(CO3)2]2-和[(UO2)2CO3(OH)3]-存在.细胞液中(UO2)3(PO4)2·4H2O含量随[U]升高而增加.通过调节细胞液pH和增加细胞液CO2-3浓度均能降低其固相UO2 2配合物含量.在细胞液中增加NTA会增加(UO2)3(PO4)2·4H2O含量,当添加EDTA时会显著降低(UO2)3(PO4)2·4H2O含量.     

电磁辐射与电磁防护

本文讨论了电气进程带来的电磁辐射污染及其防护问题。从电磁辐射的来源、作用人群、对人体的影响方式阐述了电磁辐射防护的必要性。介绍了电磁辐射暴露限值标准、电磁辐射防护原理、防护装备标准及产品现状。提出了现有电磁辐射暴露限值标准及防护装备产品标准的不足,指出现阶段应进行的进一步工作：考虑非致热效应对人体的影响,完善统一电磁辐射暴露限值标准;增加电磁辐射防护装备标准覆盖面,以利加强监管,进一步规范产品市场。     

高温季节事故多发的原因分析及对策

以一个厂为例,分析认为5～8月份是事故多发期,总结出高温对神经系统影响、劳保用品穿戴不齐全、不规范和休息时间不能保证三点原因,同时提出提高安全意识,加强防暑降温工作、思想教育、强化安全生产监督机制四项措施。     

武汉市无公害蔬菜生产的问题与对策

介绍了我国部分城镇在粮食作物和蔬菜产品受化学农药等有害化学物污染简况和无公害蔬菜的研究进展。调查分析了武汉市目前蔬菜生产中农药污染的现状与问题，提出了在武汉市实施无公害蔬菜生产示范工程项目的建议和对策，并进行了讨论。     

长江上游攀西—六盘水地区资源开发与环境保护

长江上游攀西——六盘水地区是个资源富集的“金三角”。通过交通先行,加快资源开发,对增强21世纪经济发展后劲意义重大。但生态环境恶化,急需加强保护。     

我国的环境现状,类型与变化

本文结合区域的社会经济发展状况，通过采用一定的数学模型，分析了我国区域环境现状、类型及其变化，得出了一些有参考价值的结论。     

Distribution of radionuclides in the guano sediments of Xisha Islands, South China Sea and its implication

Several natural and anthropogenic radionuclides (²¹⁰Pb, ²²⁶Ra and ¹³⁷Cs) in guano-phosphatic coral sediments and pure guano particles collected from Ganquan, Guangjin, Jinqing and Jinyin Islands of the Xisha archipelago, South China Sea, were analyzed. The Constant Initial Concentration (CIC) model and the Constant Rate of Supply (CRS) model were applied for age calculation. The average supply rate of ²¹⁰Pb was 126 Bq m⁻² a⁻¹, very close to the flux of northern hemisphere average (125 Bq m⁻² a⁻¹). The activities of anthropogenic radionuclides in the sediments were very low, indicating that human nuclear tests did not notably impact this region. The main source of radionuclides in the sediments was from atmospheric precipitation, and the organic matter derived from plant and produced by nutrient-rich guano could further enhance them.     

Identification of close relationship between atmospheric oxidation and ozone formation regimes in a photochemically active region

Understanding ozone (O₃) formation regime is a prerequisite in formulating an effective O₃ pollution control strategy. Photochemical indicator is a simple and direct method in identifying O₃ formation regimes. Most used indicators are derived from observations, whereas the role of atmospheric oxidation is not in consideration, which is the core driver of O₃ formation. Thus, it may impact accuracy in signaling O₃ formation regimes. In this study, an advanced three-dimensional numerical modeling system was used to investigate the relationship between atmospheric oxidation and O₃ formation regimes during a long-lasting O₃ exceedance event in September 2017 over the Pearl River Delta (PRD) of China. We discovered a clear relationship between atmospheric oxidative capacity and O₃ formation regime. Over eastern PRD, O₃ formation was mainly in a NO_x-limited regime when HO₂/OH ratio was higher than 11, while in a VOC-limited regime when the ratio was lower than 9.5. Over central and western PRD, an HO₂/OH ratio higher than 5 and lower than 2 was indicative of NO_x-limited and VOC-limited regime, respectively. Physical contribution, including horizontal transport and vertical transport, may pose uncertainties on the indication of O₃ formation regime by HO₂/OH ratio. In comparison with other commonly used photochemical indicators, HO₂/OH ratio had the best performance in differentiating O₃ formation regimes. This study highlighted the necessities in using an atmospheric oxidative capacity-based indicator to infer O₃ formation regime, and underscored the importance of characterizing behaviors of radicals to gain insight in atmospheric processes leading to O₃ pollution over a photochemically active region.