Detecting the effects of coal mining,acid rain,and natural gas extraction in Appalachian basin streams in Pennsylvania (USA) through analysis of barium and sulfate concentrations

To understand how extraction of different energy sources impacts water resources requires assessment of how water chemistry has changed in comparison with the background values of pristine streams. With such understanding, we can develop better water quality standards and ecological interpretations. However, determination of pristine background chemistry is difficult in areas with heavy human impact. To learn to do this, we compiled a master dataset of sulfate and barium concentrations ([SO₄], [Ba]) in Pennsylvania (PA, USA) streams from publically available sources. These elements were chosen because they can represent contamination related to oil/gas and coal, respectively. We applied changepoint analysis (i.e., likelihood ratio test) to identify pristine streams, which we defined as streams with a low variability in concentrations as measured over years. From these pristine streams, we estimated the baseline concentrations for major bedrock types in PA. Overall, we found that 48,471 data values are available for [SO₄] from 1904 to 2014 and 3243 data for [Ba] from 1963 to 2014. Statewide [SO₄] baseline was estimated to be 15.8 ± 9.6 mg/L, but values range from 12.4 to 26.7 mg/L for different bedrock types. The statewide [Ba] baseline is 27.7 ± 10.6 µg/L and values range from 25.8 to 38.7 µg/L. Results show that most increases in [SO₄] from the baseline occurred in areas with intensive coal mining activities, confirming previous studies. Sulfate inputs from acid rain were also documented. Slight increases in [Ba] since 2007 and higher [Ba] in areas with higher densities of gas wells when compared to other areas could document impacts from shale gas development, the prevalence of basin brines, or decreases in acid rain and its coupled effects on [Ba] related to barite solubility. The largest impacts on PA stream [Ba] and [SO₄] are related to releases from coal mining or burning rather than oil and gas development.

     

纳米氧化铝对斑马鱼幼鱼早期运动行为的影响

随着纳米技术的迅猛发展,纳米材料的安全性研究具有十分重要的意义。为探讨纳米氧化铝对斑马鱼幼鱼早期运动行为的影响,本研究将受精后6 h(6 hpf)的斑马鱼胚胎随机分成空白对照组(E3培养液)、纳米氧化铝组(12.5、25、50、100μg·mL~(-1))。采用6孔板染毒,每组160颗卵,共8个孔,每孔20颗卵/10 m L试液,染毒液更新周期为1 d。观察急性毒性和运动行为。结果显示,各纳米氧化铝组无明显的急性毒性;运动行为检测发现,25、50、100μg·m L~(-1)纳米氧化铝组受精后6 d幼鱼(6dpf)黑暗状态下的运动速度、运动距离、趋触性程度较空白对照组均显著下降(P0.05);在6 dpf幼鱼对强光刺激的惊恐逃避反射试验中发现,各组幼鱼在光照1 min内运动速度较光照前的黑暗期均明显下降(P0.05),但25μg·mL~(-1)和100μg·mL~(-1)浓度组在光照时速度下降得更慢(P0.05);关闭光源后,各组幼鱼的运动速度都会上升,但25μg·mL~(-1)和100μg·mL~(-1)浓度组在打开光源后速度上升得更慢(P0.05)。上述结果表明,纳米氧化铝可以影响斑马鱼幼鱼早期的运动行为。     

水污染源自动监控系统运行存在的问题及对策

为解决水环境污染问题,提升水污染源自动监控系统的运行效率,介绍了水污染源自动监控系统的基本情况,指出了其中存在的问题,提出了提升水污染源监控系统运行效果的对策:社会各方形成合力,共同展开源头保障工作,建设水污染源监控系统,规范化推广,提高运营效率,采取统一的业务专业化培训方式,严格规范相关设备的使用,定期进行业务考评,...     

硫酸锰废渣浸出液对斑马鱼的毒性及抗氧化酶活性的影响

已有研究表明,堆积在湘西花垣河河岸的硫酸锰废渣含有多种重金属,可能是导致花垣河河水和沉积物重金属污染的主要原因.为了评价硫酸锰废渣的潜在生态风险和对水生动物的毒性,本研究分析了硫酸锰废渣浸出液中的主要重金属成分,用漫出液对斑马鱼进行了急性毒性实验,观察在急性胁迫下斑马鱼的体征变化,测定了斑马鱼在亚致死浓度下的生化指标的...     

Assessment of spatial distribution of soil loss over the upper basin of Miyun reservoir in China based on RS and GIS techniques

Soil conservation planning often requires estimates of the spatial distribution of soil erosion at a catchment or regional scale. This paper applied the Revised Universal Soil Loss Equation (RUSLE) to investigate the spatial distribution of annual soil loss over the upper basin of Miyun reservoir in China. Among the soil erosion factors, which are rainfall erosivity (R), soil erodibility (K), slope length (L), slope steepness (S), vegetation cover (C), and support practice factor (P), the vegetative cover or C factor, which represents the effects of vegetation canopy and ground covers in reducing soil loss, has been one of the most difficult to estimate over broad geographic areas. In this paper, the C factor was estimated based on back propagation neural network and the results were compared with the values measured in the field. The correlation coefficient (r) obtained was 0.929. Then the C factor and the other factors were used as the input to RUSLE model. By integrating the six factor maps in geographical information system (GIS) through pixel-based computing, the spatial distribution of soil loss over the upper basin of Miyun reservoir was obtained. The results showed that the annual average soil loss for the upper basin of Miyun reservoir was 9.86 t ha(-1) ya(-1) in 2005, and the area of 46.61 km(2) (0.3%) experiences extremely severe erosion risk, which needs suitable conservation measures to be adopted on a priority basis. The spatial distribution of erosion risk classes was 66.9% very low, 21.89% low, 6.18% moderate, 2.89% severe, and 1.84% very severe. Thus, by using RUSLE in a GIS environment, the spatial distribution of water erosion can be obtained and the regions which susceptible to water erosion and need immediate soil conservation planning and application over the upper watershed of Miyun reservoir in China can be identified.     

Comparing dark- and photo-Fenton-like degradation of emerging pollutant over photo-switchable Bi2WO6/CuFe2O4: Investigation on dominant reactive oxidation species

The extensive use of tetracycline hydrochloride (TCH) poses a threat to human health and the aquatic environment. Here, magnetic p-n Bi₂WO₆/CuFe₂O₄ catalyst was fabricated to efficiently remove TCH. The obtained Bi₂WO₆/CuFe₂O₄ exhibited 92.1% TCH degradation efficiency and 50.7% and 35.1% mineralization performance for TCH and raw secondary effluent from a wastewater treatment plant in a photo-Fenton-like system, respectively. The remarkable performance was attributed to the fact that photogenerated electrons accelerated the Fe(III)/Fe(II) and Cu(II)/Cu(I) conversion for the Fenton-like reaction between Fe(II)/Cu(I) and H₂O₂, thereby generating abundant ?OH for pollutant oxidation. Various environmental factors including H₂O₂ concentration, initial pH, catalyst dosage, TCH concentration and inorganic ions were explored. The reactive oxidation species (ROS) quenching results and electron spin resonance (ESR) spectra confirmed that ?O₂^? and ?OH were responsible for the dark and photo-Fenton-like systems, respectively. The degradation mechanisms and pathways of TCH were proposed, and the toxicity of products was evaluated. This work contributes a highly efficient and environmentally friendly catalyst and provides a clear mechanistic explanation for the removal of antibiotic pollutants in environmental remediation.     

Distribution and chemical speciation of arsenic in different sized atmospheric particulate matters

The distribution and chemical speciation of arsenic (As) in different sized atmospheric particulate matters (PMs), including total suspended particles (TSP), PM₁₀, and PM_2.5, collected from Baoding, China were analyzed. The average total mass concentrations of As in TSP, PM₁₀, and PM_2.5 were 31.5, 35.3, and 54.1 µg/g, respectively, with an order of PM_2.5 >PM ₁₀ > TSP, revealing that As is prone to accumulate on fine particles. Due to the divergent toxicities of different As species, speciation analysis of As in PMs is further conducted. Most of previous studies mainly focused on inorganic arsenite (iAs^III), inorganic arsenate (iAs^V), monomethylarsonate (MMA), and dimethylarsinate (DMA) in PMs, while the identification and sensitive quantification of trimethylarsine oxide (TMAO) were rarely reported. In this study, a high-performance liquid chromatography coupled to inductively coupled plasma mass spectrometry system was optimized for As speciation including TMAO in PMs. An anion exchange column was used to separate MMA, DMA and iAs^V, while a cation exchange column to separate TMAO and iAs^III. Results showed that iAs^V was the dominate component in all the samples, corresponding to a portion of 79.2% ± 9.3% of the total extractable species, while iAs^III, TMAO and DMA made up the remaining 21%. Our study demonstrated that iAs^III accounted for about 14.4% ± 11.4% of the total extracted species, with an average concentration of 1.7 ± 1.6 ng/m³. It is worth noting that TMAO was widely present in the samples (84 out of 97 samples), which supported the assumption that TMAO was ubiquitous in atmospheric particles.     

Hydroxyl, hydroperoxyl free radicals determination methods in atmosphere and troposphere

The hydroxyl radical (?OH) has a crucial function in the oxidation and removal of many atmospheric compounds that are harmful to health. Nevertheless, high reactivity, low atmospheric abundance, determination of hydroxyl, and hydroperoxyl radical's quantity is very difficult. In the atmosphere and troposphere, hydroperoxyl radicals (HO₂) are closely demanded in the chemical oxidation of the troposphere. But advances in technology have allowed researchers to improve the determination methods on the research of free radicals through some spectroscopic techniques. So far, several methods such as laser-induced fluorescence (LIF), high-performance liquid chromatography (HPLC), and chemical ionization mass spectroscopy have been identified and mostly used in determining the quantity of hydroxyl and hydroperoxyl radicals. In this systematic review, we have advised the use of scavenger as an advance for further researchers to circumvent some of these problems caused by free radicals. The primary goal of this review is to deepen our understanding of the functions of the most critical free radical (?OH, HO₂) and also understand the currently used methods to quantify them in the atmosphere and troposphere.     

负载稀土元素活性碳纤维在微型反应器中净化NO废气

以NH3为还原剂，以活性碳纤维（ACF）、HNO，浸渍的ACF、负载CuO的ACF和负载La2O3的ACF为催化剂，在微型反应器中考察各种催化剂对NO催化还原的活性，并进行了差热-热重、扫描电镜分析。实验结果表明，ACF负载La能有效地改善催化剂的活性，且催化活性中心为非晶态的氧化物；当ACF负载20％的La2O3时具有最好的低温活性，NO的去除率最高可达92％以上。     

生活垃圾填埋场封场后种植植物中重金属迁移研究

在上海老港生活垃圾填埋场填埋单元封场的覆盖土中掺混了矿化垃圾种植植物,分析Cd、Pb、Cu、Zn 4种重金属在土壤和植物中的迁移变化,研究表明:(1)覆盖土土质从一般耕作土变成肥沃土壤;覆盖土和种植混合土重金属Cd、Pb、Cu、Zn中Cd、Pb含量相近,但种植土的Cu含量略大于覆盖原土,Zn含量远大于覆盖原土;(2)植物能富集土壤和垃圾中的重金属,木本植物的根部富集重金属的能力强于草本植物,但重金属在草本植物根、茎、叶中的迁移速度大于木本植物;(3)植物根、茎、叶的Cu、Zn含量均远大于未受污染土壤种植植物相应部位的Cu、Zn含量,种植的植物不能供家养动物食用,以免通过食物链作用危及人体安全.