金属基工程纳米颗粒与水生高等植物的相互作用：研究现状综述

如今释放到水体环境中的工程纳米颗粒(ENP)数量与日俱增。为确保生态健康,需要进行相关的风险评估。本文综述了金属基ENP与水生高等植物之间的相互作用,找到了信息缺口并提出对未来研究的构想,为在该领域内的进一步探索提供了基础。本文讨论集中在以下3点：1. ENP的生物利用性;2. 生物对ENP的摄取、消化、转移以及生物累积;3. ENP对水生高等植物的毒性效果。由于ENP自身特性所带来的影响不明确以及水质状况记载情况不佳,ENP的摄取及相关动力学方面存在着很大的信息差距。分解似乎是驱动ENP生物累积的一种关键机制,然而纳米颗粒却常常被一些有着极少内化作用的植物的表面所吸收。然而,关于ENP在植物内的内化作用鲜有记载,因此纳米颗粒的内化作用对于生物累积及毒性的影响尚不明确。即使金属基ENP的纳米毒性已被报道,分解依然被认为是其毒性的主要机制。为推动该领域内的研究发展,未来的研究需结合ENP自身特性的影响、水体的理化参数以及它们之间的相互作用。相互作用对于ENP的生物利用性和对水生高等植物健康的风险都有重要影响。为了快速追踪类似数据的产生,我们建议测试方案趋向一致化。
精选自Melusi Thwala, Stephen J. Klaine, Ndeke Musee. Interactions of metal-based engineered nanoparticles with aquatic higher plants: a review of the state of current knowledge. Environmental Toxicology and Chemistry: Volume 35, Issue 7, pages 1677–1694, July 2016. DOI: 10.1002/etc.3364
详情请见http://onlinelibrary.wiley.com/doi/10.1002/etc.3364/full
     

Deposition of copper nanoparticles on multiwalled carbon nanotubes modified with poly (acrylic acid) and their antimicrobial application in water treatment

A novel hybrid material, Cu-PAA/MWCNTs (copper nanoparticles deposited multiwalled carbon nanotubes with poly (acrylic acid) as dispersant, was prepared and expected to obtain a more effective and well-dispersed disinfection material for water treatment. X-ray energy dispersive spectroscopy (EDS), transmission electron microscopy (TEM), the X-ray fluorescence (XRF), X-ray photoelectron spectra (XPS), Fourier transform infrared spectra (FT-IR), Raman spectroscopy, and thermal gravimetric analyzer (TGA) were used to characterize the Cu-PAA/MWCNTs. Escherichia coli (E. coil) was employed as the target bacteria. The cell viability determination and fluorescence imaging results demonstrated that Cu-PAA/MWCNTs possessed strong antimicrobial ability on E. coil. The deposited Cu was suggested to play an important role in the antimicrobial action of Cu-PAA/MWCNTs.     

Ecotoxicological effect of zinc oxide nanoparticles on soil microorganisms

The widespread production and use of zinc oxide nanoparticles (ZnO-NPs) in recent years have posed potential threat to the ecosystem. This study aimed to investigate the ecotoxicological effect of ZnO-NPs on soil microorganisms using laboratory microcosm test. Respiration, ammonification, dehydrogenase (DH) activity, and fluorescent diacetate hydrolase (FDAH) activity were used as ecotoxicological parameters. The results showed that in the neutral soil treated with 1 mg ZnO-NPs per g soil (fresh, neutral), ammonification was significantly inhibited during the study period of three months, but the inhibition rate decreased over increasing time. Inhibition in respiration was observed in the first month of the test. In various ZnO-NPs treatments (1 mg, 5 mg, and 10 mg ZnO-NPs per g soil), DH activity and FDAH activity were inhibited during the study period of one month. For both enzyme activities, there were positive dose–response relationships between the concentration of ZnO-NPs and the inhibition rates, but the curves changed over time due to changes of ZnO-NPs toxicity. Soil type affected the toxicity of ZnO-NPs in soil. The toxicity was highest in the acid soil, followed by the neutral soil. The toxicity was relatively low in the alkaline soil. The toxicity was not accounted for by the Zn²⁺ released from the ZnO-NPs. Direct interaction of ZnO-NPs with biologic targets might be one of the reasons. The adverse effect of ZnO-NPs on soil microorganisms in neutral and acid soils is worthy of attention.     

不同培养介质中纳米氧化铜对小麦毒性的影响

采用琼脂培养和水培方法比较了纳米氧化铜(CuONPs)在不同暴露介质中的环境化学行为及其对小麦根生长的影响,并探讨了不同培养介质对CuONPs植物毒性的影响机制.结果表明,琼脂介质相对水相(营养液)环境可以减少CuONPs的团聚,增强其分散性.在琼脂和水相中Cu离子溶出随CuONPs浓度变化规律存在明显差异,在50～1000mg CuONPs·L-(1以Cu计)范围内,CuONPs在琼脂中无论是Cu2+的溶出浓度还是溶出比率均低于其在水相中的值.CuONPs在不同介质中表现出显著的小麦毒性差异.琼脂培养下小麦根生长半抑制效应浓度EC50(以CuONPs浓度表示)为108mg·L-1,而在水培方式下为9.0mg·L-1,说明琼脂介质极大缓解了CuONPs引起的植物毒性.分析表明,Cu2+溶出浓度较CuONPs投放量与小麦根生长抑制效应之间存在更好的指数相关关系,这说明该研究体系下CuONPs小麦毒性主要是由纳米颗粒释放Cu2+引起的.此结论较好地解释了当培养介质从水相变成琼脂时,Cu2+溶出减少,纳米毒性降低的现象.该研究结果认为,当前国内外使用水培法获得的纳米材料植物毒性研究结果在外推至实际土壤状况时将高估其环境安全性风险,推荐使用琼脂作为纳米材料土壤环境风险评价的模拟介质.     

The source and fate of sediment and mercury in the Tapajós River, Pará, Brazilian Amazon: Ground- and space-based evidence

We present results of mercury (Hg) in surface waters and soils and an analysis of satellite imagery from the Tapajós River basin, Brazilian Amazon, and the Reserva Garimpeira do Tapajós, the legal gold mining district of the basin. Hg bound to suspended sediment was roughly 600 and 200 times the concentration of dissolved Hg per litre of water, in impacted and pristine areas, respectively. Suspended sediments thus represent the major pathway of river-borne Hg. Median concentrations of Hg in suspended load from both impacted and pristine waters were 134 ppb, and 80% of samples were below 300ppb-in the range of naturally occurring surficial materials in the tropics. Regionally, riverine Hg fluxes were proportional to the concentration of total suspended solids. This shows that the dominant source of Hg is the sediment itself rather than anthropogenic mercury discharge from the small-scale mines. To independently test this conclusion, a mass balance was performed. A conservative calculation of the annual export of mercury (Hg) from the Creporí River (a minimum) was 1.6 tonnes for the year 1998-it could be significantly larger. This amount of Hg is difficult to account for by anthropogenic discharge alone, confirming that enhanced physical erosion caused by sluicing and dredging operations is the dominant source of Hg. We therefore conclude that gold mining operations are primarily responsible for elevated Hg concentrations. The dominant source of contamination is not, however, the loss of Hg in the gold amalgamation process. Rather, the disturbance and mobilization of large quantities of Hg-rich sediment and floodplain soil into the water column during mining operations is the source of contamination. These findings shift the focus of remediation and prevention efforts away from Hg control toward soil and sediment erosion control. The minimization or elimination of Hg losses in the mining process remains important for the health of local peoples and environments, but keeping basin soils and sediments in place would be a much more effective means of minimizing Hg fluxes to the region's rivers. To gain a spatial and historical perspective on the source and extent of emissions, satellite imagery was used. We were able to reconstruct historical mining activity, locate impacted areas, and estimate historical Hg fluxes with the imagery. To do so, the spectral characteristics of satellite images were calibrated to the concentration of suspended sediment in the rivers, which, in turn, is proportional to the Hg concentration. This analysis shows that mining-induced sediment plumes have been a dominant source of sediment to the Tapajós River system for decades. As well, the intensity and location of these emissions has varied through time. For example, sediment discharge from the Creporí River was greater in 1985 than in 1998; and the tributaries on the west bank of the Tapajós were actively being mined in 1985 but had been abandoned in 1998. This type of information should greatly assist in understanding original and ongoing sources of emissions, and in managing prevention and remediation efforts.     

Development of an immunochromatographic assay for the rapid detection of bromoxynil in water

A rapid immunochromatographic one-step strip test was developed to specifically determine bromoxynil in surface and drinking water by competitive inhibition with the nano colloidal gold-conjugated monoclonal antibody (mAb). Bromoxynil standard samples of 0.01–10 mg L⁻¹ in water were tested by this method and the visual limit was 0.06 mg L⁻¹. The assay only required 5 min and one-step by dispensing a drop of sample solution onto a strip. Parallel analysis of water samples with bromoxynil showed comparable results from one-step strip test and ELISA. Therefore, the one-step strip test is very useful as a screening method for qualitative detection of bromoxynil in water.     

零价铁纳米颗粒对硫酸盐还原菌的杀灭作用研究

在实验条件下通过混合振荡的方式,探究了零价铁纳米颗粒（NZVI）对硫酸盐还原菌（SRB）的杀灭能力和杀灭效果;并通过电镜扫描等手段观察零价纳米铁颗粒与硫酸还原菌形态变化,推测杀灭机制.结果表明,当向油田回注水中分别加入0、1、2、5和10mg/mL的零价铁时,该纳米粒子对硫酸还原菌的杀灭效率分别为0、75.6%、90....     

纳米氧化锌颗粒对大鼠气管上皮细胞动态变化的影响及毒性机理

纳米氧化锌(Zn O NPs)对呼吸道的毒性损伤作用备受关注,但有关其对呼吸道上皮细胞动态变化的影响机理还有待深入研究.因此,本研究通过将大鼠气管上皮细胞(RTE)暴露于不同浓度(1和10 mg·L~(-1))和不同粒径(50和200 nm)的Zn O NPs中,利用细胞电阻抗检测技术(ECIS)检测细胞动态变化,采用CCK8法检测细胞生长抑制效应,并通过胞内ROS和MDA含量变化探讨其影响机制.ECIS检测结果显示,Zn O NPs暴露下,RTE细胞生长和增殖受到明显抑制,且具有浓度依赖效应.当暴露浓度为1 mg·L~(-1)时,与对照组相比,50 nm暴露组细胞电阻抗值的下调幅度为18%,为200 nm暴露组的1.2倍.Zn O NPs诱导的RTE细胞增殖抑制率具有浓度依赖效应,当暴露浓度为10 mg·L~(-1)时,50和200 nm暴露组细胞增殖抑制率分别为暴露浓度为1 mg·L~(-1)时的2.9和1.4倍.Zn O NPs诱导的RTE细胞氧化应激结果显示,胞内ROS和MDA含量随着纳米颗粒暴露浓度的增加而增加,随着纳米颗粒粒径的减小而增加,具有显著的浓度-和剂量-依赖效应.当Zn O NPs浓度分别为1和10 mg·L~(-1)时,ROS含量分别是对照组的2.8和3.7倍;当暴露浓度为10 mg·L~(-1)时,50 nm暴露组细胞内ROS含量是200 nm暴露组的1.7倍;暴露浓度为1和10 mg·L~(-1)时,50 nm氧化锌处理组诱导的细胞内MDA含量分别是对照组的5.4和7.9倍.Zn O NPs能够影响呼吸道上皮细胞动态变化,从而破环RTE细胞屏障并进入细胞,诱导胞内ROS和MDA水平升高,进而抑制细胞的生长与增殖.研究表明,影响Zn O NPs诱导的RTE细胞动态变化和氧化应激的关键因素是颗粒粒径与暴露浓度.     

纳米颗粒在水环境中的团聚行为和毒性效应研究

随着纳米技术的快速发展,纳米颗粒以其特殊的物理化学性质在生产及生活的各个领域中被广泛使用。纳米颗粒具有较高的表面活性,会与环境中的物质发生相互作用造成表面结构的改变,从而对环境产生诸多影响。因此,纳米颗粒带来的健康风险及可能造成的环境危害,逐渐受到人们的关注。通过概述纳米颗粒的来源及性质,列举了几类应用较广的纳米颗粒的最新研究进展,总结了纳米颗粒在水环境中团聚的影响因素包括内部因素和外部环境因素,归纳了毒性效应及其检测技术,并探讨了纳米颗粒环境行为和毒性效应研究存在的问题。