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Factors influencing residual air saturation during consecutive imbibition processes in an air-water two-phase fine sandy medium – A laboratory-scale experimental study 影响气水两相细砂介质连续浸泡过程中残余空气饱和度的因素 - 实验室规模的实验研究
IF 3.5 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2024-09-01 DOI: 10.1016/j.jconhyd.2024.104416
Weile Huang , Yan Li , Yijin Du , Xinya He , Chengfeng Li , Jingya Xi , Yihang Yang , Xiaoyi Wu , Weiliang Liu

The residual air saturation plays a crucial role in modeling hydrological processes of groundwater and the migration and distribution of contaminants in subsurface environments. However, the influence of factors such as media properties, displacement history, and hydrodynamic conditions on the residual air saturation is not consistent across different displacement scenarios. We conducted consecutive drainage-imbibition cycles in sand-packed columns under hydraulic conditions resembling natural subsurface environments, to investigate the impact of wetting flow rate, initial fluid state, and number of imbibition rounds (NIR) on residual air saturation. The results indicate that residual air saturation changes throughout the imbibition process, with variations separated into three distinct stages, namely, unstable residual air saturation (Sgr-u), momentary residual air saturation (Sgr-m), and stable residual air saturation (Sgr). The results also suggest that the transition from Sgr-u to Sgr is driven by changes in hydraulic pressure and gradient; the calculated values followed the following trend: Sgr > Sgr-u > Sgr-m. An increase in capillary number, which ranged from 1.46 × 10−7 to 3.07 × 10−6, increased Sgr-u and Sgr-m in some columns. The increase in Sgr ranged from 0.034 to 0.117 across all the experimental columns; this consistent increase can be explained by water film expansion at the primary wetting front along with a strengthening of the hydraulic gradient during water injection. Both the pre-covered water film on the sand grain surface and a pore-to-throat aspect ratio of up to 4.42 were identified as important factors for the increased residual air saturation observed during the imbibition process. Initial air saturation (Sai) positively influenced all three types of residual air saturation, while initial capillary pressure (Pci) exhibited a more pronounced inhibitory effect on residual air saturation, as it can partly characterized the initial connectivity of the air phase generated under different drying flow rates. Under identical wetting flow rate conditions, Sgr was higher during the second imbibition than during the first imbibition due to variations in initial fluid state, involving both fluid distribution and the concentration of dissolved air in the pore water. In contrast, NIR did not have an obvious effect on the three types of residual air saturation. This work aims to provide empirical evidences and offer further insights into the capture of non-wetting phases in groundwater environments, as well as to put forward some potential suggestion for future investigations on the retention and migration of contaminants that involves multiphase interface interactions in subsurface environments.

残余空气饱和度在模拟地下水水文过程以及污染物在地下环境中的迁移和分布方面起着至关重要的作用。然而,介质性质、位移历史和水动力条件等因素对残余空气饱和度的影响在不同位移情况下并不一致。我们在类似于自然地下环境的水力条件下,在砂包柱中进行了连续的排水-浸润循环,以研究润湿流速、初始流体状态和浸润轮数(NIR)对残余空气饱和度的影响。结果表明,残余空气饱和度在整个浸润过程中都会发生变化,变化分为三个不同的阶段,即不稳定残余空气饱和度(Sgr-u)、瞬间残余空气饱和度(Sgr-m)和稳定残余空气饱和度(Sgr)。结果还表明,从 Sgr-u 到 Sgr 的过渡是由水压和梯度的变化驱动的;计算值遵循以下趋势:Sgr > Sgr-u > Sgr-m。毛细管数从 1.46 × 10-7 到 3.07 × 10-6,毛细管数的增加在某些色谱柱中增加了 Sgr-u 和 Sgr-m。在所有实验柱中,Sgr 的增加幅度从 0.034 到 0.117 不等;这种一致的增加可以解释为在注水过程中,水膜在主润湿前沿扩张,同时水力梯度增强。砂粒表面的预覆盖水膜和高达 4.42 的孔喉纵横比被认为是浸润过程中观察到的残余空气饱和度增加的重要因素。初始空气饱和度(Sai)对所有三种类型的残余空气饱和度都有积极影响,而初始毛细管压力(Pci)对残余空气饱和度有更明显的抑制作用,因为它可以部分描述不同干燥流速下产生的气相的初始连通性。在相同的润湿流速条件下,由于初始流体状态的变化(涉及流体分布和孔隙水中溶解空气的浓度),第二次浸泡时的 Sgr 比第一次浸泡时高。相比之下,近红外对三种残余空气饱和度的影响并不明显。这项工作旨在为地下水环境中非湿润相的捕获提供经验证据和进一步的见解,并为今后研究地下环境中涉及多相界面相互作用的污染物滞留和迁移问题提出一些潜在的建议。
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引用次数: 0
Sonoelectrochemical degradation of aspirin in aquatic medium using ozone and peroxymonosulfate activated with FeS2 nanoparticles 利用臭氧和过一硫酸盐活化的 FeS2 纳米粒子在水生介质中降解阿司匹林的声电化学方法
IF 3.5 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2024-09-01 DOI: 10.1016/j.jconhyd.2024.104419
Elham Aseman-Bashiz , Hossein Sayyaf

The catalytic performance of nano-FeS2 in the sonoelectrochemical activation of peroxymonosulfate (PMS) and ozone to remove aspirin (ASP) was studied for the first time. The crystal structure and Fe bonds in the catalyst were confirmed through XRD and FTIR analysis. Within 30 min, ASP (TOC) was removed by 99.2 % (81.6 %) and 98.6 % (77.4 %) in nano-FeS2/PMS and nano-FeS2/O3 sonoelectrochemical systems, respectively. Water anions, especiallyHCO3 (almost 50 %), had an inhibitory effect on ASP removal. The probes confirmed that SO4and HO were the key to ASP degradation in nano-FeS2/PMS and nano-FeS2/O3 systems, respectively. The effective activation of oxidants due to the ideal distribution of Fe2+ by catalyst was the main mechanism of ASP removal, in which electric current (EC) and ultrasound (US) played a crucial role through the recycling of Fe ions, dissolution and cleaning of the catalyst. LC-MS analysis identified thirteen byproducts in the ASP degradation pathways. The energy consumption of the proposed sonoelectrochemical systems was lower than previous similar systems. This study presented economic and sustainable hybrid systems for pharmaceutical wastewater remediation.

首次研究了纳米 FeS2 在过一硫酸盐(PMS)和臭氧的声电化学活化过程中去除阿司匹林(ASP)的催化性能。通过 XRD 和 FTIR 分析确认了催化剂中的晶体结构和铁键。在纳米 FeS2/PMS 和纳米 FeS2/O3 声电化学体系中,30 分钟内阿司匹林(TOC)的去除率分别为 99.2 %(81.6 %)和 98.6 %(77.4 %)。水阴离子,尤其是 HCO3-(接近 50%),对 ASP 的去除有抑制作用。探针证实,SO4-和 HO-分别是纳米 FeS2/PMS 和纳米 FeS2/O3 系统降解 ASP 的关键。催化剂理想的 Fe2+ 分布导致氧化剂的有效活化是去除 ASP 的主要机制,其中电流(EC)和超声波(US)通过回收铁离子、溶解和清洁催化剂发挥了关键作用。LC-MS 分析确定了 ASP 降解途径中的 13 种副产品。拟议的声电化学系统的能耗低于以前的类似系统。这项研究为制药废水修复提供了经济、可持续的混合系统。
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引用次数: 0
The value of simplified models of radionuclide transport for the safety assessment of nuclear waste repositories: A benchmark study 放射性核素迁移简化模型对核废料储存库安全评估的价值:基准研究
IF 3.5 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2024-08-26 DOI: 10.1016/j.jconhyd.2024.104417
Philipp Selzer , Haibing Shao , Christoph Behrens , Christoph Lehmann , Robert Seydewitz , Renchao Lu , Phillip Kreye , Wolfram Rühaak , Olaf Kolditz

In order to assess sites for a deep geological repository for storing high-level nuclear waste safely in Germany, various numerical models and tools will be in use. For their interaction within one workflow, their reproducibility, and reliability version-controlled open-source solutions and careful documentation of model setups, results and verifications are of special value. However, spatially fully resolved models including all relevant physical and chemical processes are neither computationally feasible for large domains nor is the data typically available to parameterize such models. Thus, simplified models are crucial for the pre-assessment of possible sites to narrow down the list of suitable candidates for which detailed site investigations and fully resolved models will be done at a later stage. Still, the accuracy of these simplified models is of importance as the pre-assessment of suitable sites will be based on them. In this study, we compare the modelling capabilities of TransPyREnd, a one-dimensional transport code based on finite differences, specifically developed for the fast estimation of radionuclide transport by the German federal company for radioactive waste disposal (BGE), with OpenGeoSys, which is a modelling platform based on finite elements in up to three spatial dimensions. Both codes are used in the site selection procedure for the German nuclear waste repository. The comparison of the model results of TransPyREnd and OpenGeoSys is augmented by comparisons with an analytical solution for a homogeneous material. For the purpose of numerical benchmarking, we consider a geological profile located in southern Germany as an example where the hypothetical repository is located in a clay-stone formation. TransPyREnd and OpenGeoSys yield overall similar results. However, both codes use different discretizations which impact is the highest for strongly sorbing compounds, while the difference gets negligible for less sorbing and more diffusive compounds as higher diffusion tends to blur the initial conditions. Overall, the OpenGeoSys model is more exact whereas the TransPyREnd model has considerable faster run times. We found in our example, that significant substance amounts are only leaving the host rock formation, if apparent diffusion is high, for which case both codes give similar results, while relative differences are considerable for strongly sorbing compounds. However, in the latter case no significant substance amount of radionuclides leaves the host-rock formation, thus deeming the differences in the model results minor for the overall safety assessments of sites.

为了评估德国安全储存高浓度核废料的深层地质处置库选址,将使用各种数值模型和工具。为了在一个工作流程中实现互动、可重现性和可靠性,版本控制的开源解决方案以及对模型设置、结果和验证的仔细记录具有特殊价值。然而,包括所有相关物理和化学过程在内的空间全解析模型,对于大面积区域来说,既不具备计算可行性,也不具备参数化此类模型的典型数据。因此,简化模型对于预先评估可能的场址至关重要,可缩小合适候选场址的范围,以便在稍后阶段进行详细的场址调查和建立完全解析的模型。不过,这些简化模型的准确性也很重要,因为对合适地点的预评估将以这些模型为基础。在本研究中,我们比较了 TransPyREnd 和 OpenGeoSys 的建模能力,前者是基于有限差分的一维传输代码,专门为德国联邦放射性废物处理公司(BGE)快速估算放射性核素传输而开发,后者则是基于有限元的三维建模平台。这两种代码都用于德国核废料处置库的选址程序。在对 TransPyREnd 和 OpenGeoSys 的模型结果进行比较的同时,还与均质材料的分析解决方案进行了比较。为了进行数值基准比较,我们以德国南部的一个地质剖面为例,假定处置库位于粘土石层中。TransPyREnd 和 OpenGeoSys 得出的结果总体类似。不过,这两种代码使用了不同的离散化方法,对于强吸附性化合物的影响最大,而对于吸附性较弱和扩散性较强的化合物,差异可以忽略不计,因为较高的扩散性往往会模糊初始条件。总体而言,OpenGeoSys 模型更为精确,而 TransPyREnd 模型的运行时间要快得多。我们在示例中发现,只有在表观扩散程度较高的情况下,才会有大量物质离开主岩层,在这种情况下,两种代码给出的结果相似,而对于吸附性较强的化合物来说,相对差异较大。不过,在后一种情况下,没有大量放射性核素离开主岩层,因此模型结果的差异对于场地的整体安全评估来说是微不足道的。
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引用次数: 0
Eco-toxicity assessment of polypropylene microplastics in juvenile zebrafish (Danio rerio) 聚丙烯微塑料对幼年斑马鱼(Danio rerio)的生态毒性评估。
IF 3.5 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2024-08-17 DOI: 10.1016/j.jconhyd.2024.104415
Suresh Priyadharshini , Jeyaraj Jeyavani , Khalid A. Al-Ghanim , Marimuthu Govindarajan , Sivashanmugam Karthikeyan , Baskaralingam Vaseeharan

In recent years, everyone has recognized microplastics as an emerging contaminant in aquatic ecosystems. Polypropylene is one of the dominant pollutants. The purpose of this study was to examine the effects of exposing zebrafish (Danio rerio) to water with various concentrations of polypropylene microplastics (11.86 ± 44.62 μm), including control (0 mg/L), group 1 (1 mg/L), group 2 (10 mg/L), and group 3 (100 mg/L) for up to 28 days (chronic exposure). The bioaccumulation of microplastics in the tract was noted after 28 days. From the experimental groups, blood and detoxifying organs of the liver and brain were collected. Using liver tissues evaluated the toxic effects by crucial biomarkers such as reactive oxygen species, anti-oxidant parameters, oxidative effects in protein & lipids, total protein content and free amino acid level. The study revealed that the bioaccumulation of microplastics in the organisms is a reflection of the oxidative stress and liver tissue damage experienced by the group exposed to microplastics. Also, apoptosis of blood cells was observed in the treated group as well as increased the neurotransmitter enzyme acetylcholine esterase activity based on exposure concentration-dependent manner. The overall results indicated bioaccumulation of microplastics in the gut, which led to increased ROS levels. This consequently affected antioxidant biomarkers, ultimately causing oxidation of biomolecules and liver tissue injury, as evidenced by histological analysis. This study concludes that chronic ingestion of microplastics causes considerable effects on population fitness in the aquatic environment, as well as other ecological complications, and is also critical to understand the magnitude of these contaminants' influence on ichthyofauna.

近年来,大家都认识到微塑料是水生生态系统中新出现的污染物。聚丙烯是主要污染物之一。本研究的目的是考察将斑马鱼(Danio rerio)暴露在含有不同浓度聚丙烯微塑料(11.86 ± 44.62 μm)的水中长达 28 天(慢性暴露)的影响,包括对照组(0 mg/L)、第 1 组(1 mg/L)、第 2 组(10 mg/L)和第 3 组(100 mg/L)。28 天后,观察微塑料在肠道中的生物累积情况。收集了实验组的血液以及肝脏和大脑的解毒器官。利用肝脏组织,通过活性氧、抗氧化参数、蛋白质和脂质中的氧化作用、总蛋白质含量和游离氨基酸水平等关键生物标志物评估毒性效应。研究显示,微塑料在生物体内的生物累积反映了暴露于微塑料的群体所经历的氧化应激和肝组织损伤。此外,根据暴露浓度依赖性方式,在处理组中观察到血细胞凋亡以及神经递质酶乙酰胆碱酯酶活性增加。总体结果表明,微塑料在肠道中的生物累积导致了 ROS 水平的升高。组织学分析表明,这影响了抗氧化生物标志物,最终导致生物大分子氧化和肝组织损伤。这项研究的结论是,长期摄入微塑料会对水生环境中的种群适应性造成相当大的影响,并引发其他生态并发症,这对于了解这些污染物对鱼类的影响程度也至关重要。
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引用次数: 0
Urea-modified hazelnut shell biochar (N-HSB) for efficient Cr(VI) removal: Performance and mechanism insights 尿素改性榛子壳生物炭(N-HSB)用于高效去除六价铬:性能和机理研究。
IF 3.5 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2024-08-13 DOI: 10.1016/j.jconhyd.2024.104414
Yuting Zhang , Yuwei Tang , Baoming Jin , Ruiping Yan , Li Zhang , Yilong Li , Jinchunzi Li , Shuang Liang

Composite with a high specific surface area of 224.62 m2 g−1 was prepared by adding urea as a nitrogen source to hazelnut shell biochar (HSB). Nitrogen doping significantly enhanced the ability of biochar for Cr(VI) elimination, achieving twice the removal efficiency of unmodified biochar. The impacts of varying the pH and initial concentrations on Cr(VI) removal by urea-modified biochar (N-HSB) were investigated. The Cr(VI) removal by N-HSB was better described by intra particle diffusion model and pseudo-second order kinetic model under optimal conditions. Furthermore, XPS, FTIR, SEM, and BET analyses were used to verify the pivotal roles of oxygen- and nitrogen-containing functional groups. Electrostatic attraction, redox reaction, and complexation constituted the principal mechanisms facilitating Cr(VI) elimination by N-HSB. This study demonstrated that the modification of biochar with urea as a nitrogen source represented a promising strategy for enhancing the removal capacity of biochar for Cr(VI) in aqueous environments.

通过在榛子壳生物炭(HSB)中添加尿素作为氮源,制备了具有 224.62 m2 g-1 高比表面积的复合材料。掺氮大大提高了生物炭去除六价铬的能力,去除效率是未改性生物炭的两倍。研究了改变 pH 值和初始浓度对尿素改性生物炭(N-HSB)去除六价铬的影响。在最佳条件下,N-HSB 的颗粒内扩散模型和伪二阶动力学模型能更好地描述其对六价铬的去除效果。此外,还利用 XPS、傅立叶变换红外光谱、扫描电镜和 BET 分析验证了含氧和含氮官能团的关键作用。静电吸引、氧化还原反应和络合作用构成了 N-HSB 消除六价铬的主要机制。这项研究表明,用尿素作为氮源对生物炭进行改性是提高生物炭在水环境中去除六价铬能力的一种有效策略。
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引用次数: 0
Study on the influence of different water and black shale content on the resistivity of loess 不同水分和黑页岩含量对黄土电阻率影响的研究
IF 3.5 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2024-08-08 DOI: 10.1016/j.jconhyd.2024.104413
Jishi Geng , Hao Huang , Qiang Sun , Jianjun Hu , Qingmin Shi , Chao Lyu

Soil degradation, characterized by the deterioration of soil physical and chemical properties, nutrient loss, and an increase in toxic substances, is a key ecological concern in mining activities. This study explores the use of waste black shale from mining development as an additive to loess to enhance soil properties for reclamation in mining areas. The research includes resistivity and organic carbon content tests on modified reclaimed loess with varying black shale and water contents. Additionally, the electrical properties of these modified soils are investigated across different AC frequencies. The results highlight the significance of soil plasticity and a 1.5% black shale content in influencing reclaimed loess's electrical properties. Moisture content and black shale influence changes in soil conductive paths and resistivity. The abundance of clay minerals in black shale plays a crucial role in altering soil electrical resistivity due to the adsorption of cations in water and the directional transport under an electric field. Considering soil's three-phase composition and diffuse bilayer structure, the study elucidates the mechanism behind changes in the electrical properties of improved reclaimed loess, accounting for water and black shale content. This research demonstrates the feasibility of using black shale as a soil additive and emphasizes the non-destructive assessment potential of electrical resistivity test (ERT) measurements for modified reclaimed soils.

土壤退化以土壤物理和化学性质恶化、养分流失和有毒物质增加为特征,是采矿活动中的一个主要生态问题。本研究探讨了如何利用矿业开发过程中产生的废弃黑页岩作为黄土添加剂,以增强矿区复垦的土壤特性。研究包括对不同黑页岩和水含量的改良复垦黄土进行电阻率和有机碳含量测试。此外,还研究了这些改良土壤在不同交流频率下的电特性。结果表明,土壤塑性和 1.5% 的黑页岩含量对改良黄土的电特性有重要影响。水分含量和黑页岩会影响土壤导电路径和电阻率的变化。由于阳离子在水中的吸附作用以及在电场作用下的定向传输,黑页岩中丰富的粘土矿物在改变土壤电阻率方面起着至关重要的作用。考虑到土壤的三相组成和弥散双层结构,该研究阐明了改良复垦黄土电特性变化背后的机理,并考虑了水和黑页岩的含量。这项研究证明了使用黑页岩作为土壤添加剂的可行性,并强调了电阻率测试(ERT)测量对改良再生土壤的无损评估潜力。
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引用次数: 0
Enhancing herbicide adsorption in low-fertility soil using sugarcane biochar: Insights from Imazapic dynamics 利用甘蔗生物炭增强低肥力土壤对除草剂的吸附:从 Imazapic 动力学中获得的启示。
IF 3.5 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2024-08-03 DOI: 10.1016/j.jconhyd.2024.104412
Jéssica Rafaelly Almeida Lopes , Zabele Laís Lyra Mendonça , João Paulo Siqueira da Silva , Ademir Amaral , André Maciel Netto

Biochar amendment has emerged as a potential solution for preventing, remediating, and mitigating agricultural compound pollution. This groundbreaking technique not only improves crucial soil properties like porosity, water retention capacity, cation exchange capacity, and pH, but also intricately impacts the interaction and retention mechanisms of polluting molecules. In this study, we investigate the dynamic of the herbicide Imazapic when subjected to applying pyrolyzed biochars, specifically at temperatures of 300 and 500 °C, within the context of a low-fertility soil characterized as dystrophic Yellow Ultisol (YUd) in a sugarcane cultivation area in Igarassu-PE, Brazil. The biochars were produced from sugarcane bagasse by pyrolysis process in a muffle furnace. In laboratory conditions, with saturated soil columns under steady-state, analyses of the mechanisms involved in interaction and transport and determining hydrodispersive parameters for Imazapic were performed by the two-site nonequilibrium transport model using the CXTFIT 2.0 program. Samples of YUd soil amended with biochar pyrolyzed at 300 °C presented a negligible interaction with Imazapic. However, adding biochar pyrolyzed at 500 °C (BC500) to the soil samples enhanced the adsorption coefficient and improved the interaction with Imazapic. This research points out that biochar produced from agricultural waste biomass, such as sugarcane bagasse specifically pyrolyzed at 500 °C, offers a potential means to adsorb herbicides, reducing their leaching to deeper layers of the amended soils and the risk of groundwater contamination and potential environmental negative impacts.

生物炭改良剂已成为预防、修复和减轻农业化合物污染的潜在解决方案。这一突破性技术不仅能改善土壤的孔隙度、保水能力、阳离子交换能力和 pH 值等重要特性,还能对污染分子的相互作用和滞留机制产生错综复杂的影响。在本研究中,我们研究了除草剂 Imazapic 在巴西 Igarassu-PE 甘蔗种植区的低肥力土壤--萎缩性黄色超土壤(YUd)--中应用热解生物炭(特别是在 300 和 500 °C 温度下)时的动态变化。生物炭是由甘蔗渣在马弗炉中通过热解工艺制成的。在实验室条件下,饱和土壤柱处于稳态,使用 CXTFIT 2.0 程序,通过两点非平衡迁移模型分析了伊马氮平的相互作用和迁移机制,并确定了伊马氮平的水分散参数。用 300 °C 高温分解的生物炭改良的裕德土壤样品与 Imazapic 的相互作用可以忽略不计。然而,在土壤样品中加入 500 °C 高温分解的生物炭(BC500)后,吸附系数提高了,与 Imazapic 的相互作用也有所改善。这项研究指出,由农业废弃生物质(如专门在 500 °C 高温下热解的甘蔗渣)制成的生物炭为吸附除草剂提供了一种潜在的方法,可减少除草剂向改良土壤深层的沥滤,降低地下水污染风险和潜在的环境负面影响。
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引用次数: 0
Microplastics and heavy metal contamination along a land-use gradient in a Himalayan foothill river: Prevalence and controlling factors 喜马拉雅山脚河流中沿土地利用梯度的微塑料和重金属污染:普遍性和控制因素
IF 3.5 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2024-07-30 DOI: 10.1016/j.jconhyd.2024.104411
Sunil Kumar , Diptimayee Behera , Kumar Ajay , Balasubramanian Karthick , Chetan Dharia , Ambili Anoop

The co-occurrence of microplastics (MPs) and heavy metals in aquatic systems has raised significant concerns, yet their relationship in freshwater ecosystems remains poorly understood. This study aims to evaluate the prevalence of MPs and factors controlling their distribution in both water and sediment in the Markanda River, Northwest India. MPs were extracted from sediment and water samples using density separation and classified through fluorescence microscopy and Raman spectroscopy. Metal concentrations in river water samples were analyzed using ICP-MS, and their correlation with MP abundance was explored. The results indicated the widespread occurrence of MP pollution across the Markanda River basin, with particle concentrations ranging from 10 to 530 particles L−1 in surface water and 1330–4330 particles kg−1 dry weight (dw) in sediment samples. The variability in MP abundance at sampling sites along the Markanda River courses results from factors such as the proximity of industrial establishments and human habitation, while the influence of grain size on MP distribution appears to be limited. Pellets (88.5 %) and fragments (8.5 %) were the most abundant types of MPs, with polyethylene (45.45 %) and polystyrene (30.9 %) being the dominant forms in water samples. The ICP-MS analysis of heavy metals in water samples indicated elevated levels of As (1.67 to 32.31 ppb) in downstream areas of the river system, influenced by human activities. While metals exhibited correlation with each other, there was a weak association, except for As, with the levels of MPs in the Markanda River. The SEM-EDX analyses to characterize chemical elements absorbed onto the surface of MP showed distinct variations in upstream and downstream sites, with the presence of elements such as Mn, Ni, Cr, Zn, As, Se, and Cu found in downstream areas. We conclude that MPs contaminated with heavy metals potentially threaten the ecological security of freshwater aquatic systems and highlight the importance of management action to reduce plastic pollution worldwide.

微塑料(MPs)和重金属在水生系统中的共存引起了人们的极大关注,但人们对它们在淡水生态系统中的关系仍然知之甚少。本研究旨在评估印度西北部马尔康达河(Markanda River)水体和沉积物中微塑料(MPs)的普遍性及其分布控制因素。采用密度分离法从沉积物和水样中提取 MPs,并通过荧光显微镜和拉曼光谱进行分类。使用 ICP-MS 分析了河水样本中的金属浓度,并探讨了它们与 MP 丰度的相关性。结果表明,马坎达河流域普遍存在 MP 污染,地表水中的颗粒浓度为 10 至 530 微粒 L-1,沉积物样本中的颗粒浓度为 1330-4330 微粒 kg-1 干重(dw)。马坎达河河道沿岸采样点的 MP 丰度变化是由工业企业和人类居住地的邻近程度等因素造成的,而粒度对 MP 分布的影响似乎有限。颗粒(88.5%)和碎片(8.5%)是水样中含量最多的 MP 类型,聚乙烯(45.45%)和聚苯乙烯(30.9%)是水样中的主要形式。对水样中重金属的 ICP-MS 分析表明,受人类活动的影响,河流系统下游地区的砷含量升高(1.67 至 32.31 ppb)。虽然各种金属之间存在相关性,但除砷外,其他金属与马坎达河中的多孔介质含量关系不大。对 MP 表面吸收的化学元素进行的 SEM-EDX 分析表明,上游和下游地区存在明显差异,下游地区存在锰、镍、铬、锌、砷、硒和铜等元素。我们的结论是,受重金属污染的 MP 可能会威胁淡水水生系统的生态安全,并强调了在全球范围内采取管理行动减少塑料污染的重要性。
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引用次数: 0
Unveiling the ecotoxicological impact of microplastics on organisms - the persistent organic pollutant (POP): A comprehensive review 揭示微塑料对生物体的生态毒理学影响--持久性有机污染物(POP):全面综述。
IF 3.5 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2024-07-25 DOI: 10.1016/j.jconhyd.2024.104397
Sneha Siwach , Meghali Bharti , Sheetal Yadav , Padma Dolkar , Sonakshi Modeel , Pankaj Yadav , Tarana Negi , Ram Krishan Negi

Microplastics have been ubiquitous in our environment for decades, and numerous studies have revealed their extensive dispersion, reaching far beyond the surface of the land, soil, aquatic ecosystems. They have infiltrated the food-chain, the food web, even the air we breathe, as well as the water we drink. Microplastics have been detected in the food we consume, acting as vectors for hazardous chemicals that adhere to their hydrophobic surfaces. This can result in the transfer of these chemicals to the aquatic life, posing a threat to their well-being. The release of microplastics into different environmental settings can give rise to various eco-toxicological implications. The substantial body of literature has led scientists to the consensus that microplastic pollution is a global problem with the potential to impact virtually any type of ecosystem. This paper aims to discuss crucial information regarding the occurrence, accumulation, and ecological effects of microplastics on organisms. It also highlights the new and emerging disease named “Plasticosis” that is directly linked to microplastics and its toxicological effects like permanent scarring and long-term inflammation in the digestive system of the seabirds. By comprehending the behaviour of these microplastic pollutants in diverse habitats and evaluating their ecological consequences, it becomes possible to facilitate a better understanding of this toxicological issue.

几十年来,微塑料在我们的环境中无处不在,大量研究揭示了它们的广泛分布,远远超出了陆地、土壤和水生生态系统的表面。它们已经渗透到食物链、食物网,甚至我们呼吸的空气和饮用的水中。在我们食用的食物中发现了微塑料,它们是附着在疏水表面的有害化学物质的载体。这可能导致这些化学物质转移到水生生物中,对它们的健康造成威胁。微塑料释放到不同的环境中会产生各种生态毒理影响。大量文献已使科学家们达成共识,即微塑料污染是一个全球性问题,有可能影响几乎所有类型的生态系统。本文旨在讨论有关微塑料的发生、积累和对生物的生态影响的重要信息。它还强调了一种名为 "塑料病 "的新兴疾病,这种疾病与微塑料及其毒理效应(如海鸟消化系统中的永久性疤痕和长期炎症)直接相关。通过了解这些微塑料污染物在不同栖息地的行为并评估其生态后果,可以更好地了解这一毒理学问题。
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引用次数: 0
Dispersion of silica-encapsulated DNA magnetic particles in a homogeneous sand tank 硅胶包裹的 DNA 磁性颗粒在均质砂罐中的分散。
IF 3.5 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES Pub Date : 2024-07-23 DOI: 10.1016/j.jconhyd.2024.104410
Swagatam Chakraborty , Rayan Elhaj , Jan Willem Foppen , Jack F. Schijven

In this study, we focused on the 3D dispersion of colloids. To our knowledge, we were the first to do so. Thereto, we injected silica encapsulated DNA tagged superparamagnetic particles (SiDNAmag) in a homogeneous coarse grain sand tank. At four downstream locations, SiDNAmag concentrations were determined as a function of time. Longitudinal and transverse dispersivity values and associated uncertainties of SiDNAmag were determined using Monte Carlo modelling approach. The parameter associated uncertainties of hydraulic conductivity as well as of the effective porosity estimated from SiDNAmag breakthrough curves were statistically similar to those estimated from salt tracer breakthrough curves. Further, the SiDNAmag dispersivity uncertainty ranges were then statistically compared with the salt tracer (NaCl, and fluorescein) dispersivities. Our results indicated that time to rise, time of peak concentration and shape of the breakthrough curves of SiDNAmag were similar to those of the salt tracer breakthrough curves. Despite the size difference between the salt tracer molecules and SiDNAmag, size exclusion did not occur, probably due to the large pore throat diameter to SiDNAmag diameter ratio. The median longitudinal dispersivity (αL) of salt tracer and SiDNAmag were 4.9 and 5.8 × 10−4 m, respectively. The median ratio of horizontal and vertical transverse dispersivities to αL, (αTHL and αTVL, respectively), for salt tracer and SiDNAmag ranged between 0.52 and 0.56. Through the statistical tests, we concluded that the longitudinal and traverse dispersivities of SiDNAmag were not statistically significantly different from salt tracer in 3 dimensions and could be used to characterize the dispersive properties of the medium we used. Our work contributes to a better understanding of 3D dispersion of SiDNAmag in saturated porous media.

在这项研究中,我们的重点是胶体的三维分散。据我们所知,我们是第一个这样做的人。为此,我们在一个均质粗粒砂罐中注入了硅胶封装的 DNA 标记超顺磁性颗粒(SiDNAmag)。在四个下游位置,测定了 SiDNAmag 浓度与时间的函数关系。使用蒙特卡洛建模方法确定了 SiDNAmag 的纵向和横向分散值及相关不确定性。根据 SiDNAmag 突破曲线估算出的水力传导率和有效孔隙度的相关参数不确定性,与根据盐示踪剂突破曲线估算出的参数不确定性在统计上相似。此外,我们还将 SiDNAmag 分散性的不确定性范围与盐示踪剂(氯化钠和荧光素)的分散性进行了统计比较。结果表明,SiDNAmag 的上升时间、峰值浓度时间和突破曲线形状与盐示踪剂突破曲线相似。尽管盐示踪剂分子与 SiDNAmag 之间存在尺寸差异,但可能由于孔喉直径与 SiDNAmag 直径之比较大,因此没有发生尺寸排斥。盐示踪剂和 SiDNAmag 的纵向分散度中值(αL)分别为 4.9 和 5.8 × 10-4 m。盐示踪剂和 SiDNAmag 的水平和垂直横向扩散率与αL 的比值中位数(分别为 αTH /αL 和 αTV /αL)介于 0.52 和 0.56 之间。通过统计检验,我们得出结论:在三维空间中,SiDNAmag 的纵向分散度和横向分散度与盐示踪剂没有显著的统计差异,可用于描述我们所使用介质的分散特性。我们的工作有助于更好地理解 SiDNAmag 在饱和多孔介质中的三维分散。
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引用次数: 0
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Journal of contaminant hydrology
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