莱州湾近岸海域中典型抗生素与抗性细菌分布特征及其内在相关性

为了揭示海陆衔接区环境中抗生素与抗性细菌分布特征及其内在相关性,以莱州湾及其主要入海河流为研究区域,利用HPLC-MS/MS分析样品中15种磺胺类抗生素(SAs)和6种喹诺酮类抗生素(QNs)的浓度,并通过改良的Method 1604(US EPA)评估海水与沉积物中2种典型水传病原微生物大肠杆菌(E.coli)与金黄色葡萄球菌(S.aureus)的抗生素抗性水平,进而探讨该区域水体中抗性菌株的分布特点以及微生物抗性率与相应抗生素浓度的相关性。结果显示,莱州湾水体与沉积物中普遍存在磺胺与喹诺酮类抗生素残留及抗性污染问题。两大类抗生素在水体中平均残留浓度分别为3.89 ng·L~(-1)(SAs)和234.68ng·L~(-1)(QNs),在沉积物中分别为0.91 ng·g~(-1)(SAs)和49.37 ng·g~(-1)(QNs),且分布特征基本呈现自河流向海洋逐渐递减的趋势,说明河流输入是莱州湾抗生素污染的主要来源。在水体中,具有磺胺类抗性的E.coli和S.aureus平均检出量分别达到2 018和4 683 CFU·L~(-1),抗性率范围分别在0%~37.3%和10.6%~45.8%之间;而2种喹诺酮类抗性病原微生物的平均检出量则相对较低,分别为1 315 CFU·L~(-1)(E.coli)和1 461 CFU·L~(-1)(S.aureus),抗性率分别为0%~50.0%和0%~20.8%;此外,相比于E.coli,S.aureus为沉积物中的主要抗性病原微生物,磺胺与喹诺酮类抗性S.aureus检出率均高于80%,平均检出量分别为24CFU·g~(-1)和18 CFU·g~(-1)。相关性分析表明,莱州湾近岸海域水体中磺胺类抗生素浓度与磺胺类抗性微生物总量之间具有良好的线性关系,然而其与微生物抗性率之间并未表现出相似的规律,说明近岸海洋环境中抗生素的残留量不是影响抗性菌株丰度的唯一因素。     

新疆鸟类和哺乳动物物种丰富度空间异质性及其多尺度效应

基于新疆维吾尔自治区鸟类和哺乳动10km×10km物种空间分布数据及1km×1km土地利用数据,引入NDVI、海拔和地理纬度等辅助数据,分别对物种和土地利用数据进行尺度变换,计算分析了1～10km尺度下的景观指数,并进一步在生态系统层面进行尺度效应研究,以探究表征物种多样性空间异质性的合理尺度.结果表明:新疆总体的景观...     

Removal of Cr(VI) from water by in natura and magnetic nanomodified hydroponic lettuce roots

Environmental Science and Pollution Research - Biosorption is a viable and environmentally friendly process to remove pollutants and species of commercial interest. Biological materials are...     

Characteristics and removal mechanism of the precursors of N-chloro-2,2-dichloroacetamide in a drinking water treatment process at Taihu Lake

• N-Cl-DCAM, an emerging N-DBP in drinking water was investigated. • A new BAC has a better removal efficiency for N-Cl-DCAM precursors than an old BAC. • N-Cl-DCAM precursors are more of low molecular weight and non-polar. • Adsorption of GAC plays a major role in removal of N-Cl-DCAM precursors by an O₃-BAC. N-chloro-2,2-dichloroacetamide (N-Cl-DCAM) is an emerging nitrogenous disinfection by-product (N-DBP) which can occur in drinking water. In this study, an analytical method based on liquid chromatography with tandem mass spectrometry (LC-MS/MS) was developed to validate the concentration of N-Cl-DCAM, which was found to be 1.5 mg/L in the effluent of a waterworks receiving raw water from Taihu Lake, China. The changes of N-Cl-DCAM formation potential (N-Cl-DCAMFP) in the drinking water treatment process and the removal efficiency of its precursors in each unit were evaluated. Non-polar organics accounted for the majority of N-Cl-DCAM precursors, accounting for 70% of the N-Cl-DCAM FP. The effect of conventional water treatment processes on the removal of N-Cl-DCAM precursors was found to be unsatisfactory due to their poor performance in the removal of low molecular weight (MW) or non-polar organics. In the ozonation integrated with biological activated carbon (O₃-BAC) process, the ozonation had little influence on the decrease of N-Cl-DCAM FP. The removal efficiency of precursors by a new BAC filter, in which the granular activated carbon (GAC) had only been used for four months was higher than that achieved by an old BAC filter in which the GAC had been used for two years. The different removal efficiencies of precursors were mainly due to the different adsorption capacities of GAC for individual precursors. Low MW or non-polar organics were predominantly removed by GAC, rather than biodegradation by microorganisms attached to GAC particles.     

Cerebellar injury induced by cadmium via disrupting the heat-shock response

Environmental Science and Pollution Research - Cadmium (Cd) is a food contaminant that poses serious threats to animal health, including birds. It is also an air pollutant with well-known...     

Study on the reaction of 3-methyl-2-butenal and 3-methylbutanal with Cl atoms: kinetics and reaction mechanism

The reaction of Cl atoms with two C₅ aldehydes (3-methyl-2-butenal and 3-methylbutanal) were investigated by proton-transfer-reaction mass spectrum (PTR-MS) using smog chamber at 298 ± 1 K and 760 Torr. A relative rate method was used to determine the rate constants of the title reactions with m-xylene and trans-2-butene as reference compounds: (3.04 ± 0.18)  ×  10⁻¹⁰ and (2.07 ± 0.14)  ×  10⁻¹⁰ cm³/(molecule⋅sec) for 3-methyl-2-butenal and 3-methylbutanal, respectively. Additionally, the gas-phase products were also identified by PTR-MS, and the possible reaction mechanisms were proposed basing on the identified products. The detected gas-phase products are similar for two C₅ aldehydes reactions, mainly including small molecules of aldehydes, ketones and chlorinated aldehyde compounds. The atmospheric lifetimes (τ) calculated for 3-methyl-2-butenal (τ = 7.0 hr, marine boundary layer (MBL)) and 3-methylbutanal (τ = 10.3 hr, MBL) according to the obtained rate constants. The results indicate that Cl atoms at MBL are competitive with OH radicals for the degradation contribution of C₅ aldehyde compounds.     

Long-chain alkanes in the atmosphere: A review

As a representative species of intermediate volatile organic compounds (IVOCs), long-chain alkanes are considered to be important precursors of secondary organic aerosols (SOA) in the atmosphere. This work reviews the previous studies on long-chain alkanes in the atmosphere: (1) the detection methods and filed observations of long-chain alkanes in both gas and particle phases are summarized briefly; (2) the laboratory studies of long chain alkanes are reviewed, the kinetic data, reaction mechanism, SOA yields, and physicochemical properties of SOA are included in detail; (3) the research progress related to model simulations of long-chain alkanes are also discussed. In addition, based on available research results, several perspective contents are proposed that can be used as a guideline for future research plans.     

浅埋深黏土包气带氮迁移转化原位实验研究

通过原位实验,对浅埋深黏土包气带中氮的迁移转化开展研究.结果表明,实测地下水埋深介于145.9~173.6cm,地下水毛细上升高度计算值可达297.0cm,土壤含水率除表层外介于0.30~0.45cm³/cm³;NH₄⁺-N和NO₃^--N在地面以下155cm含量最高为1.43,23.00mg/kg,超出背景值1.13,21.05mg/kg;包气带含水率近饱和条件下,粘土对氮污染物迁移阻滞作用减弱,NH₄⁺-N和NO₃^--N在1d内自地表迁移至155cm.浅埋深地下水减弱了黏土对氮污染物运移的阻滞作用.浅埋深地下水减弱了黏土对氮污染物运移的阻滞作用.     

Sources of ambient non-methane hydrocarbon compounds and their impacts on O3 formation during autumn, Beijing

The field observation of 54 non-methane hydrocarbon compounds (NMHCs) was conducted from September 1 to October 20 in 2020 during autumn in Haidian District, Beijing. The mean concentration of total NMHCs was 29.81 ± 11.39 ppbv during this period, and alkanes were the major components. There were typical festival effects of NMHCs with lower concentration during the National Day. Alkenes and aromatics were the dominant groups in ozone formation potential (OFP) and OH radical loss rate (L_OH). The positive matrix factorization (PMF) running results revealed that vehicular exhaust became the biggest source in urban areas, followed by liquefied petroleum gas (LPG) usage, solvent usage, and fuel evaporation. The box model coupled with master chemical mechanism (MCM) was applied to study the impacts of different NMHCs sources on ozone (O₃) formation in an O₃ episode. The simulation results indicated that reducing NMHCs concentration could effectively suppress O₃ formation. Moreover, reducing traffic-related emissions of NMHCs was an effective way to control O₃ pollution at an urban site in Beijing.     

Pyrolysis characteristics of the mixture of printed circuit board scraps and coal powder

Thermogravimetric (TG) analysis and infrared spectroscopy were used to analyze the pyrolysis characteristics of printed circuit board scraps (PCBs), coal powder and their mixtures under nitrogen atmosphere. The experimental results show that there is a large difference between waste PCBs and coal powder in pyrolysis processing. The pyrolysis properties of the mixing samples are the result of interaction of the PCBs and coal powder, which is influenced by the content of mixture. The degree of pyrolysis and pyrolysis properties of the mixture are much better than that of the single component. The TG and the differential thermogravimetric (DTG) curves of the PCBs mixed with coal powder move towards the high-temperature zone with increasing amount of coal powder and subsequently the DTG peak also becomes wider. The Coats–Redfern integral method was used to determine the kinetic parameters of pyrolysis reaction mechanism with the different proportion of mixture. The gas of pyrolysis mainly composes of CO₂, CO, H₂O and some hydrocarbon. The bromide characteristic absorption peak has been detected obviously in the pyrolysis gas of PCBs. On the contrary, the absorption peak of the bromide is not obvious in pyrolysis gas of the PCBs samples adding 40% coal powder.