Occurrence characteristics

发生特征
  • 文章类型: English Abstract
    微塑料是污水处理厂中最难去除的新污染物之一。为了探究其发生形式,大小分布,composition,去除效率,移民法,以及污水处理厂中微塑料颗粒的命运行为特征,以呼和浩特市的污水处理厂为例,总共设立了17个采样点。LASX软件计算了形状,丰度,和微塑料的尺寸,并进行了全过程分析。结果表明:纤维状微塑料丰度最高、分布最广,是其主要存在形式,占总丰度的61.8%;微塑料的大小主要在0到1.00mm之间,在四种尺寸中,中国微塑料的丰度为0.25至0.50毫米,占32.9%。在检测到的八种塑料成分中,聚酯物质(PET,PBT),纤维素,聚丙烯(PP)是主要成分,占25%,21%,17%,分别。污水厂进水丰度为(73±5)n·L-1,出水丰度为(14±2)n·L-1,总去除率为(80.8±12.1)%。在污水处理厂的三个处理阶段中,只有初级治疗起了去除的作用,在二次处理中,大量的微塑料激增。不同结构在微塑料去除中起主要作用的是细格(49.2±7.4)%和二级沉淀池(92.4±13.9)%。微塑料主要以纤维的形式存在,碎片,和电影。纤维的比例约为70%,碎片大小主要集中在0.50~5.00mm之间。大多数碎片在5.00毫米的范围内,占50%,使它们成为除了纤维以外的主要形式。膜状尺寸大多集中在小于0.50mm的范围内,占10%以上。因此,提高对小尺寸纤维状和膜状微塑料和大尺寸破碎微塑料颗粒的去除,可以有效降低污水厂排水对环境中微塑料的污染风险。
    Microplastics are among the most difficult new pollutants to remove in wastewater treatment plants. In order to explore the occurrence form, size distribution, composition, removal efficiency, migration law, and fate behavior characteristics of microplastic particles in sewage plants, taking a sewage treatment plant in Hohhot as an example, a total of 17 sampling sites were set up. The LAS X software counted the shape, abundance, and size of microplastics and conducted a full-process analysis. The results showed that: fibrous microplastics had the highest abundance and widest distribution and were the main form of existence, accounting for 61.8% of the total abundance; the size of microplastics ranged mainly between 0 and 1.00 mm, and among the four sizes, the abundance of microplastics 0.25 to 0.50 mm in China was the highest, accounting for 32.9%. Among the eight types of plastic components detected, polyester substances (PET, PBT), cellulose, and polypropylene (PP) were the main components, accounting for 25%, 21%, and 17%, respectively. The influent abundance of the sewage plant was (73 ±5) n·L-1, the effluent abundance was (14 ±2) n·L-1, and the overall removal rate was (80.8 ±12.1)%. Among the three treatment stages of the sewage plant, only the primary treatment played a role in removal, and the abundance of microplastics surged in the secondary treatment. Different structures playing a major role in the removal of microplastics were fine grids (49.2 ±7.4)% and secondary sedimentation tanks (92.4 ±13.9)%. Microplastics mainly existed in the form of fibers, fragments, and films. The proportion of fibers was approximately 70%, and the size of fragments was mainly concentrated between 0.50 and 5.00 mm. Most fragments were in the range of 5.00 mm, accounting for 50%, making them the main form apart from fibrous. The film-like size was mostly concentrated in the range of less than 0.50 mm, accounting for more than 10%. Therefore, improving the removal of small-sized fibrous and film-like microplastics and large-sized fragmented microplastic particles can effectively reduce the pollution risk of microplastics in the environment caused by sewage plant drainage.
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  • 文章类型: Journal Article
    轮胎塑料和道路磨损颗粒(TPR-WP)是当前研究的重点,是微塑料的主要环境来源之一。我们选择了一个独特的土地利用类型——沙漠恢复区,收集玉井高速公路及其服务区的土壤和灰尘样品,并分析了TPR-WP丰度,type,通过激光直接红外(LDIR)的大小和形态。高速公路灰尘中TPR-WP的丰度(14,446.87±10,234.24n/kg)高于土壤中的TPR-WP的丰度(7500±3253.64n/kg)。随机森林模型表明,TPR-WP的来源与经济因素和自然气候高度相关。总的来说,中小型TPR-WP在粉尘中的比例高于土壤,超过一半的TPR-WP在20-50µm范围内。小粒径TPR-WP的比例随海拔升高而增加。污染负荷指数表明,调查区域总体处于I级风险带,而生态风险指数表明高速公路的污染水平为III和IV,服务区域是IV。总的来说,该研究对于阐明TPR-WP在高速公路和服务区土壤和灰尘中的分布和风险具有重要意义。
    Tire plastic and road-wear particles (TPR-WP) are a current research priority as one of the main environmental sources of microplastics. We selected a unique land use type - desert restoration area, collected soil and dust samples from the Yujing Expressway and its service areas, and analyzed TPR-WP abundance, type, size and morphology by laser direct infrared (LDIR). The abundance of TPR-WP in expressway dust (14,446.87 ± 10,234.24 n/kg) was higher than that in soil (7500 ± 3253.64 n/kg). Random forest model showed that the source of TPR-WP was highly correlated with economic factors and natural climate. Overall, the proportion of small and medium-sized TPR-WP in dust was higher than soil, more than half of the TPR-WP in dust were in 20 - 50 µm range. The proportion of small particle size TPR-WP increased with the rise of elevation. The pollution load index suggested that the survey region was generally at level I risk zone, while the ecological risk index indicated that the pollution level of expressway was III and IV, and the service area was IV. In general, the study was of great significance for clarifying the distribution and risk of TPR-WP in soil and dust of expressways and service areas.
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  • 文章类型: Journal Article
    污水污泥被认为是污水处理厂中多环芳烃(PAHs)的重要汇,土地利用过程中污泥被PAHs污染的潜在风险引起了人们的关注。为了确定优先控制的PAHs并增强其从污泥中的去除,发生特征,去除效率,并对中国各地污泥中的多环芳烃进行了风险评估分析。数据收集是从2001年到2023年。结果表明,在中国污泥中广泛检测到16种PAHs,总量(∑16PAHs)在0.06至34.93mgkgdw-1之间。化石燃料,煤炭,生物质燃烧是中国多环芳烃的主要人为来源。总的来说,菲(PHE),蒽(ANT),荧光素(FL),chrysene(CHR),芘(PYR),在中国,苯并[b]荧蒽(BbF)被认为是主要成分,3-5环多环芳烃占主导地位(84.01%-91.53%)。尽管好氧堆肥和厌氧处理显著提高了∑16PAHs的去除,污泥稳定化处理仅少量降低风险,特别是对于高分子量(HMW)多环芳烃。苯并[a]蒽(BaA),苯并[a]芘(BaP),和二苯并[a,h]蒽(DahA)被建议作为中国污水污泥的优先控制污染物,因为它们在污泥稳定之前和之后一直具有2.42-7.47、1.28-3.16、1.06-1.83的高风险商(RQ)值,分别。应该更加注意BaA,BbF,苯并[k]荧蒽(BkF),BaP,达哈,和北京的茚并[1,2,3-cd]芘(IcdP);ANT,BaA,上海的BaP;广州的BaA和BaP。尽管PAHs的毒性当量商(TEQ)满足国家标准的极限浓度要求,不能忽视长期暴露于HMWPAHs的潜在健康风险,因为终生癌症风险增量(ILCR)始终处于风险阈值范围(>1×10-6).提出了一些关于加强处理方法和土地使用标准的建议,以进一步减轻HMWPAHs的风险。
    Sewage sludge is considered to be an important sink for polycyclic aromatic hydrocarbons (PAHs) in wastewater treatment plants and the potential risks from sludge contaminated with PAHs during land application has attracted attention. To identify the priority PAHs for control and enhance their removal from sludge, the occurrence characteristics, removal efficiency, and risk assessment of PAHs in sewage sludges from across China were analyzed. Data collection was from 2001 to 2023. Results showed that 16 PAHs were widely detected in Chinese sewage sludge with total amounts (∑16PAHs) between 0.06 and 34.93 mg kg dw-1. Fossil fuel, coal, and biomass combustion are main anthropogenic sources of PAHs in China. In general, phenanthrene (PHE), anthracene (ANT), fluorescein (FL), chrysene (CHR), pyrene (PYR), and benzo[b]fluoranthene (BbF) are regarded as the main components and PAHs with 3-5 rings dominate (84.01%-91.53%) sewage sludge in China. Although aerobic composting and anaerobic treatment significantly improve ∑16PAHs removal, sludge stabilization treatment only reduced the risk by a small amount, especially for high-molecular-weight (HMW) PAHs. The benzo[a]anthracene (BaA), benzo[a]pyrene (BaP), and dibenzo[a,h]anthracene (DahA) are proposed as the priority control contaminants for sewage sludge in China because they have consistently high-risk quotient (RQ) values of 2.42-7.47, 1.28-3.16, 1.06-1.83 before and after sludge stabilization, respectively. More attention should be paid to BaA, BbF, benzo[k]fluoranthene (BkF), BaP, DahA, and indeno[1,2,3-cd]pyrene (IcdP) in Beijing; ANT, BaA, and BaP in Shanghai; and BaA and BaP in Guanghzou. Although the toxic equivalent quotient (TEQ) for PAHs met the limit concentration requirements of the national standard, the potential health risks due to long-term exposure to HMW PAHs cannot be ignored because the incremental lifetime cancer risk (ILCR) was consistently in the risk threshold range (>1 × 10-6). Some suggestions on enhanced treatment approaches and land use standards are proposed to further alleviate the risk from HMW PAHs.
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  • 文章类型: Journal Article
    随着地膜覆盖农业的快速发展,大量的微塑料积累在农田土壤中。微塑料的富集危及农作物的生长和粮食安全,也带来了生态风险。在这项研究中,我们调查了延安市典型农业区的微塑料,在中国黄土丘陵区。微塑料的特性,包括它们的丰度,尺寸,和类型通过激光直接红外光谱仪进行测量。分析了微塑料的潜在来源,并评估了土壤微塑料污染的风险。阐述了土壤中微塑料的平均丰度,水,和肥料分别为4505±435n·kg-1、91±27n·L-1和39,629±10,114n·kg-1。粒径<100μm的微塑料占>90%。颗粒尺寸越小,微塑料的含量越高。前三种聚合物是聚乙烯(PE,37.4%),聚对苯二甲酸乙二醇酯(PET,15.0%),和乙烯醋酸乙烯酯(EVA,8.9%),分别。农业覆盖物,塑料薄膜,生活垃圾,地表水灌溉,有机堆肥可能是土壤微塑料的潜在来源。生态风险评价表明,总体采样点基于微塑料污染的丰度存在较小的生态风险,而聚合物类型对所研究的农业土壤显示出相对较高的生态风险。聚氯乙烯(PVC)和聚甲基丙烯酸甲酯(PMMA)对生态风险有很大贡献,应严格限制他们对农田环境的投入。对人类没有明显的致癌风险。该研究可为我国黄土丘陵沟陵区农田土壤微塑料污染现状及风险评价提供基础参考。
    Large amounts of microplastics accumulated in the soil of agricultural fields with the rapid development of mulch agriculture. The enrichment of microplastics endangered the growth of crops and food security, and it also posed ecological risks. In this study, we investigated microplastics in a typical agriculture area of Yan\' an City, in the loess hilly gully area of China. The characteristics of microplastics including their abundances, sizes, and types were measured through laser direct infrared spectrometer. The potential sources of microplastics were analyzed and the risk of soil microplastic pollution was evaluated. It was elaborated that the average abundances of microplastics in soil, water, and fertilizer were 4505 ± 435 n·kg-1, 91 ± 27 n·L-1, and 39,629 ± 10,114 n·kg-1, respectively. Microplastics with particle sizes < 100 μm accounted for >90 %. The smaller the particle size, the higher the content of microplastics. The top three polymers were polyethylene (PE, 37.4 %), polyethylene terephthalate (PET, 15.0 %), and ethylene vinyl acetate (EVA, 8.9 %), respectively. Agricultural mulch, plastic film, domestic waste, surface water irrigation, and organic compost were probably the potential sources of soil microplastics. The ecological risk evaluation showed that overall sampling sites had a minor ecological risk of microplastic pollution based on their abundance, while the polymer type showed a relatively high ecological risk for the investigated agricultural soils. Polyvinylchloride (PVC) and polymethylmethacrylate (PMMA) contribute considerably to the ecological risk, and their inputs to the farmland environment should be strictly limited. There was no significant carcinogenic risk to humans. This study would provide the basic reference for the current situation and risk assessment of farmland soil microplastics pollution in the loess hilly gully area of China.
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  • 文章类型: Journal Article
    目前,砷(As)和铅(Pb)污染日益严重。铅锌矿山As和Pb的释放造成的污染严重影响了水和土壤环境,威胁着人类的健康。有必要揭示As和Pb的释放特性。矿井排水(MD)和雨水(RW)浸出废岩的实际景象是As和Pb释放的主要缘由之一。然而,在MD和RW下,这些废岩中As和Pb的浸出行为缺乏深入研究。在这项研究中,我们通过使用X射线衍射(XRD)和飞行时间二次离子质谱(TOF-SIMS)研究了废石(S1-S6)中As和Pb的存在,然后,系统研究了浸出液中As和Pb浓度及水化学参数的变化。此外,还评估了As和Pb的释放与矿物组成之间的相关性。结果表明,这些废岩主要由碳酸盐和硫化物矿物组成。砷和铅主要与砷黄铁矿等硫化物矿物结合或缔合,黄铁矿,黄铜矿,这些废石中的方铅矿,少量的As和Pb被高岭石和绿泥石等粘土矿物吸收或包裹。在MD和RW浸出下,pH值,氧化还原电位(Eh),由于其缓冲能力,每种废石的电导率(EC)趋于一致;碳酸盐矿物较多的废石的渗滤液pH值高于硫化物矿物。与RW相比,在MD浸出下释放的As和Pb最多,达到6.57和60.32毫克/千克,分别,由于MD的低pH和高Eh值。然而,与废石一样,在碱性条件下释放更多,因为部分砷呈砷酸盐形式。As和Pb的释放主要与这些废岩中硫化物矿物的比例呈正相关。MD浸出显著促进了废石中As和Pb的释放,这将对周围环境造成巨大威胁,控制措施势在必行。本文不仅揭示了铅锌矿区周围As和Pb的污染机理,而且为今后的As和Pb污染防治提供了理论依据。
    At present, the pollution of arsenic (As) and lead (Pb) is becoming increasingly serious. The pollution caused by the release of As and Pb from lead-zinc mines has seriously affected the water and soil environment and threatened human health. It is necessary to reveal the release characteristics of As and Pb. The actual scene of mine drainage (MD) and rainwater (RW) leaching waste rocks is the one of the main reasons for the release of As and Pb. However, the leaching behavior of As and Pb in these waste rocks under MD and RW suffered from a lack of in-depth research. In this study, we investigated the occurrence of As and Pb in waste rocks (S1-S6) by using X-ray diffraction (XRD) and time-of-flight secondary ion mass spectrometry (TOF-SIMS), and then, the changes in As and Pb concentration and the hydrochemical parameter in leaching solution were systematically studied. Furthermore, the correlation between the release of As and Pb and mineral composition was also evaluated. Results showed that these waste rocks were mainly composed of carbonate and sulfide minerals. As and Pb were mainly bounded or associated with sulfide minerals such as arsenopyrite, pyrite, chalcopyrite, and galena in these waste rocks, and small parts of As and Pb were absorbed or encased by clay minerals such as kaolinite and chlorite. Under MD and RW leaching, the pH, redox potential (Eh), and electric conductivity (EC) of each waste rock tended to be consistent due to their buffering ability; the leachate pH of waste rocks with more carbonate minerals was higher than that of sulfide minerals. Both As and Pb were released most under MD leaching in comparison to RW, reaching 6.57 and 60.32 mg/kg, respectively, due to MD\'s low pH and high Eh value. However, As in waste rock released more under alkaline conditions because part of the arsenic was in the form of arsenate. As and Pb release were mainly positively correlated with the proportions of sulfide minerals in these waste rocks. MD leaching significantly promoted the release of As and Pb from waste rocks, which would cause a great threat to the surrounding environment, and control measures were imperative. This paper not only reveals the As and Pb pollution mechanism around the lead-zinc mining area but also provides a theoretical basis for the prevention and control of As and Pb pollution in the future.
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  • 文章类型: Journal Article
    抗生素对环境的生态危害已引起全球关注。在本文中,采用固相萃取和超高效液相色谱三重四极杆质谱(LC-MS/MS)分析了磺胺类抗生素(磺胺嘧啶,磺胺二甲嘧啶,磺胺嘧啶,磺胺噻唑,磺胺吡啶,磺胺甲恶唑)和四环素(四环素,土霉素,使用生态风险评估方法估算了长江口沿海水域和冲浪沉积物中的金霉素和强力霉素)以及水中抗生素的生态风险。结果表明,在水中检测到10种抗生素中的7种,总浓度为0.652至434.47ng/L在沉积物中检测到8种抗生素,总浓度范围为0.091至499.23ng/g。在沉积物和水中检测到的主要抗生素物种随季节变化。在河流交汇和人类活动影响较大的空间分布区域,浓度较高。春季和秋季的生态风险高于冬季和夏季。沉积物中单个微生物群落的空间变化不明显。抗生素与环境中微生物之间的关系主要为正。物理和化学因素与抗生素和微生物群落显着相关。本研究可为其他类型抗生素的应用提供研究思路,为抗菌药物耐药性(AMR)的预防提供依据。
    Antibiotics have attracted global attention due to the ecological risks to environment. In this paper, solid-phase extraction and ultra-performance liquid chromatography triple quadrupole mass spectrometry (LC-MS/MS) were utilized to analyze the fugitive characteristics of 10 antibiotics of sulfonamides (sulfadiazine, sulfamethazine, sulfadimidine, sulfathiazole, sulfapyridine, sulfamethoxazole) and tetracyclines (tetracycline, oxytetracycline, chlortetracycline and doxycycline) in the coastal waters and surfece sediments of the Yangtze River Estuary and the ecological risks of antibiotics in water were estimated using ecological risk assessment method. The results have showed that 7 of the 10 antibiotics were detected in the water, with total concentrations ranging from 0.652 to 434.47 ng/L. 8 antibiotics were detected in the sediment, with total concentrations ranging from 0.091 to 499.23 ng/g. The main antibiotic species detected in the sediment and water varied seasonally. Higher concentrations in spatially distributed areas where rivers meet and where human activities have a more significant impact. The ecological risks were found to be higher in spring and autumn than those in winter and summer. Spatial variation in individual microbial communities was not evident in the sediments. The relationship between antibiotics and microorganisms in the environment was predominantly positive. Physical and chemical factors were significantly correlated for both antibiotics and microbial communities. This study can provide research ideas for other types of antibiotics and provide a basis for the prevention of antimicrobial resistance (AMR).
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  • 文章类型: English Abstract
    通过现场采样分析了淮河流域安徽段水体和沉积物中微塑料的发生特征和生态风险水平,立体显微镜,扫描电子显微镜,傅里叶变换红外光谱(FTIR),风险指数(H),和污染负荷指数(PLI)模型。分析了流域水体和沉积物中微塑料的现状,进行了微塑料的生态风险评价。结果表明,流域内每个站点的微塑料检出率均为100%。地表水和沉积物中微塑料的平均丰度分别为(39800±3367)n·m-3和(5078±447)n·kg-1。下游微塑料的平均丰度高于上游和中游。水和沉积物中微塑料的粒径主要为20-150μm,占82.96%和80.77%,分别。微塑料主要是纤维(水76.05%,沉积物84.53%),薄膜(水21.83%,沉积物15.43%),和碎片(水2.12%,沉积物0.04%)。水和沉积物中的微塑料主要是透明的,占63.31%和83.69%,分别。聚乙烯(水中65.74%,沉积物80.62%)和聚丙烯(水中18.43%,沉积物9.71%)是水和沉积物的主要成分。微塑料主要来自农用薄膜,废弃的渔具和渔网,港口人工废弃的塑料袋。微塑性风险指数(H)模型评估显示,部分场地的风险指数较高,淮河流域安徽段微塑料风险等级为二级。污染负荷指数(PLI)模型评估表明,流域地表水和沉积物的生态风险总体较低。
    The occurrence characteristics and ecological risk level of microplastics in the water and sediments of the Anhui section of Huaihe River Basin were analyzed via field sampling, stereomicroscopy, scanning electron microscopy, Fourier transform infrared spectroscopy (FTIR), risk index (H), and pollution load index (PLI) model. The current situation of microplastics in the water and sediments of the basin was analyzed, and the ecological risk assessment of microplastics was conducted. The results showed that the detection rate of microplastics at each site in the basin was 100%. The average abundance of microplastics in surface water and sediments was (39800±3367) n·m-3 and (5078±447) n·kg-1, respectively. The average abundance of microplastics in the downstream was higher than that in the upstream and midstream. The particle size of microplastics in water and sediments was primarily 20-150 μm, accounting for 82.96% and 80.77%, respectively. The microplastics were primarily fiber (water 76.05%, sediment 84.53%), film (water 21.83%, sediment 15.43%), and debris (water 2.12%, sediment 0.04%). The microplastics in water and sediments were primarily transparent, accounting for 63.31% and 83.69%, respectively. Polyethylene (65.74% in water and 80.62% in sediment) and polypropylene (18.43% in water and 9.71% in sediment) were the major components of water and sediments. Microplastics were primarily derived from agricultural films, abandoned fishing gear and nets, and artificially abandoned plastic bags in ports. The microplastic risk index (H) model assessment revealed that the risk index of some sites was high, and the risk level of microplastics in the Anhui section of Huaihe River Basin was grade II. The pollution load index (PLI) model assessment revealed that the ecological risk of surface water and sediments in the basin was generally low.
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  • 文章类型: Journal Article
    在这项研究中,海南岛三大河流49个抗生素抗性基因(ARGs)和两个整合酶基因(intl1、intl2)的发生与分布,中国,于2021年7月进行了调查,并探讨了目标基因在三条河流中的空间分布以及区域特征和环境因子等潜在影响因素。结果表明,在水体和沉积物中共检测到46个ARGs和2个整合酶基因,ARGs的绝对丰度范围为1.16×103至2.97×107拷贝/L和3.34×103-1.55×107拷贝/g。大环内酯类的ARGs,氨基糖苷类,磺胺类药物是本研究的主要ARGs类型。aadA2,tete,ermF,tetX,aac(6\')-Ib,tetW,qnrS基因是三条河流水体和沉积物中的主要ARGs。ARGs的相对丰度在中游和下游显示较高的丰度,在上游和河口显示较低的丰度。在进行相关分析后,发现在三个主要河流的水中检测到的ARGs之间存在显着正相关。然而,在沉积物中,tetC与tetQ呈负相关,macB与ermF和ereA呈负相关(p<0.05),其余ARGs呈正相关。具体来说,tetQ与tetC之间无显著正相关,macB和ereA,和沉积物中的ermF。在研究的九个环境因素中,发现pH是与水生环境中ARGs发生相关的主要因素,但它也仅与9种ARGs显著相关。在检测到的重金属中,在三条主要河流的水体中,只有Cd和Zn与两种ARGs表现出显著的相关性。结果表明,三大河流的ARGs污染处于起步阶段,检测丰度低,环境因素的影响很小,ARG之间的相互作用似乎是主要的驱动力。本研究为进一步了解热带海岛环境中ARGs的发生及其影响因素提供了科学依据。为后续管理奠定基础。
    In this study, the occurrence and distribution of 49 antibiotic resistance genes (ARGs) and two integrase genes (intl1, intl2) in three major rivers of Hainan Island, China, were investigated in July 2021, and to explore the spatial distribution of the target genes in the three rivers with the potential influencing factors such as regional characteristics and environmental factors. The results showed that a total of 46 ARGs and two integrase genes were detected in water and sediment, and the absolute abundance of ARGs ranged from 1.16 × 103 to 2.97 × 107 copies/L and 3.34 × 103-1.55 × 107 copies/g. ARGs of macrolides, aminoglycosides, and sulfonamides were this study\'s main types of ARGs. The aadA2, tetE, ermF, tetX, aac(6\')-Ib, tetW, and qnrS genes are predominant ARGs in the water and sediment of the three rivers. The relative abundance of ARGs shows higher abundance in the midstream and downstream and lower abundance in the upstream and estuarine. After conducting a correlation analysis, it was found that there was a significant positive correlation between the ARGs detected in the water of the three main rivers. However, in sediment, tetC was negatively correlated with tetQ, macB was negatively correlated with ermF and ereA (p < 0.05), while the remaining ARGs showed positive correlations. Specifically, there was no significant positive correlation between tetQ and tetC, macB and ereA, and ermF in the sediments. Among the nine environmental factors studied, pH was found to be the main factor associated with the occurrence of ARGs in the aquatic environment, but it was also significantly associated with only nine ARGs. Among the detected heavy metals, only Cd and Zn showed significant correlations with the two ARGs in the water bodies of the three main rivers. It indicated that the pollution of ARGs in the three major rivers was in the initial stage, the detection abundance was low, the influence of environmental factors was small, and the interaction between ARGs seemed to be the main driving force. This study provides a scientific basis for further understanding the occurrence of ARGs and their influencing factors in a tropical island environment, and lays a foundation for subsequent management.
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  • 文章类型: Journal Article
    目前的研究长期集中在土壤有机碳和土壤团聚体稳定性方面。然而,不同长期施肥对西南喀斯特地区黄壤团聚体组成和有机碳发生特征的影响尚不清楚。基于25年的黄壤长期定位试验,收集0-20厘米土壤层的土壤样品,并用不同的肥料处理(CK:未施肥对照;NPK:化学肥料;1/4M3/4NP:25%化学肥料替换为25%有机肥料;1/2M1/2NP:50%化学肥料替换为有机肥料;M:有机肥料)。在水稳定骨料中,土壤团聚体稳定性,总有机碳(TOC)易氧化有机碳(EOC),碳保存能力(CPC),并对碳库管理指数(CPMI)进行了分析。研究结果表明,平均重量直径(MWD)的顺序,几何平均直径(GWD),稳定水骨料的宏观骨料含量(R0.25)为M>CK>1/2M1/2NP>1/4M3/4NP>NPK。MWD,GWD,NPK处理的R0.25显著下降32.6%,43.2%,和7.0个百分点,分别,与CK治疗相比。不同粒径骨料中TOC和EOC含量的顺序为M>1/2M+1/2NP>1/4M+3/4NP>CK>NPK,随着有机肥用量的增加而增加。在宏观团聚体和散装土壤中,TOC(TOPC)和EOC(EOPC)的CPC,以及CPMI,排列为M>1/2M+1/2NP>1/4M+3/4NP>CK>NPK,但是微聚集体的情况恰恰相反。在用有机肥处理的散装土壤中,TOPC,EOPC,CPMI显著增加27.4%-53.8%,29.7%-78.1%,29.7-82.2个百分点,分别,与NPK治疗相比。冗余度分析和逐步回归分析表明,TOC是影响团聚体稳定性的主要理化因子,微骨料中的TOPC具有最直接的影响。总之,长期施用化肥导致SOC下降的主要原因是宏观聚集体中有机碳的损失。增加土壤养分供应和提高黄壤生产力的重要方法是施用有机肥以增加团聚体稳定性,宏观聚集体中SOC的存储和活动。
    Current research has long focused on soil organic carbon and soil aggregates stability. However, the effects of different long-term fertilization on the composition of yellow soil aggregates and the characteristics of the occurrence of organic carbon in the karst region of Southwest China are still unclear. Based on a 25-year long-term located experiment on yellow soil, soil samples from the 0-20 cm soil layer were collected and treated with different fertilizers (CK: unfertilized control; NPK: chemical fertilizer; 1/4 M + 3/4 NP: 25% chemical fertilizer replaced by 25% organic fertilizer; 1/2 M + 1/2 NP: 50% chemical fertilizer replaced by organic fertilizer; and M: organic fertilizer). In water-stable aggregates, soil aggregates stability, total organic carbon (TOC), easily oxidized organic carbon (EOC), carbon preservation capacity (CPC), and carbon pool management index (CPMI) were analyzed. The findings demonstrated that the order of the average weight diameter (MWD), geometric mean diameter (GWD), and macro-aggregate content (R0.25) of stable water aggregates was M > CK > 1/2M +1/2NP > 1/4M +3/4NP> NPK. The MWD, GWD, and R0.25 of NPK treatment significantly decreased by 32.6%, 43.2%, and 7.0 percentage points, respectively, compared to CK treatment. The order of TOC and EOC content in aggregates of different particle sizes was M > 1/2M +1/2NP > 1/4M +3/4NP> CK > NPK, and it increased as the rate of organic fertilizer increased. In macro-aggregates and bulk soil, the CPC of TOC (TOPC) and EOC (EOPC), as well as CPMI, were arranged as M > 1/2M +1/2NP > 1/4M +3/4NP> CK > NPK, but the opposite was true for micro-aggregates. In bulk soil treated with organic fertilizer, the TOPC, EOPC, and CPMI significantly increased by 27.4%-53.8%, 29.7%-78.1%, 29.7-82.2 percentage points, respectively, compared to NPK treatment. Redundancy analysis and stepwise regression analysis show that TOC was the main physical and chemical factor affecting the aggregates stability, and the TOPC in micro-aggregates has the most direct impact. In conclusion, the primary cause of the decrease in SOC caused by the long-term application of chemical fertilizer was the loss of organic carbon in macro-aggregates. An essential method to increase soil nutrient supply and improve yellow soil productivity was to apply an organic fertilizer to increase aggregates stability, storage and activity of SOC in macro-aggregates.
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  • 文章类型: English Abstract
    这项研究的目的是评估发生水平,空间分布,污染源,陕北矿区苦野河多环芳烃(PAHs)的生态风险。总的来说,使用与荧光检测器串联的高效液相色谱-二极管阵列检测器,在59个采样点定量检测了16种优先PAHs。结果表明,Kuye河的ρ(ΣPAHs)范围为50.06至278.16ng·L-1,平均值为128.22ng·L-1。PAHs单体浓度范围为0~121.22ng·L-1,其中Chrysene浓度最高,平均值分别为36.58ng·L-1,其次是苯并(a)蒽和菲。各单体的检出率均在70%以上,其中12个单体的检出率为100%。此外,4环PAHs在59个样品中显示出最高的相对丰度,从38.59%到70.85%不等。Kuye河中PAHs的浓度显示出明显的空间变化。此外,最高的PAHs浓度主要在煤炭开采中观察到,工业,和人口稠密的地区。与中国和世界其他河流相比,Kuye河中的PAHs浓度显示为中等污染水平。另一方面,使用正定矩阵分解(PMF)和诊断比率来定量评估Kuye河中PAHs的来源分配。结果表明,焦化和石油排放,煤燃烧,燃料-木材燃烧,汽车尾气排放对上游工业区PAHs浓度的贡献为34.67%,30.62%,18.11%,和16.60%,和煤燃烧,燃料-木材燃烧,下游住宅区汽车尾气排放占64.93%,26.20%,8.86%。此外,生态风险评价结果表明,萘的生态风险较低,苯并(a)蒽的生态风险较高,分别,而其余单体显示出中等生态风险。在59个采样点中,只有12个属于低生态风险区,而其余采样点处于中等至高生态风险。此外,宁跳塔工业园区附近水域呈现接近高生态风险阈值的风险值。因此,迫切需要在研究区域制定预防和控制措施。
    The aim of this study was to assess the occurrence level, spatial distribution, pollution source, and ecological risk of polycyclic aromatic hydrocarbons (PAHs) in the Kuye River of the northern Shaanxi mining area. In total, 16 priority PAHs were quantitatively detected at 59 sampling sites using a high-performance liquid chromatography-diode array detector in series with a fluorescence detector. The results showed that the ρ(ΣPAHs) in the Kuye River ranged from 50.06 to 278.16 ng·L-1, with an average value of 128.22 ng·L-1. The PAHs monomer concentrations ranged from 0 to 121.22 ng·L-1, of which Chrysene had the highest concentration, with average values of 36.58 ng·L-1, respectively, followed by benzo(a)anthracene and phenanthrene. The detection rate of each monomer was more than 70%, of which 12 monomers revealed detection rates of 100%. In addition, the 4-ring PAHs showed the highest relative abundance in the 59 samples, ranging from 38.59% to 70.85%. The PAHs concentrations revealed significant spatial variation in the Kuye River. Moreover, the highest PAHs concentrations were mainly observed in coal mining, industrial, and densely populated areas. Compared with those in other rivers in China and worldwide, the PAHs concentrations in the Kuye River showed a medium pollution level. On the other hand, the positive definite matrix factorization (PMF) and diagnostic ratios were used to quantitatively assess the source apportionment of PAHs in the Kuye River. The results showed that coking and petroleum emissions, coal combustion, fuel-wood combustion, and automobile exhaust emissions contributed to the PAHs concentrations in the industrial areas of the upper reach by 34.67%, 30.62%, 18.11%, and 16.60%, and coal combustion, fuel-wood combustion, and automobile exhaust emissions contributed in the downstream residential areas by 64.93%, 26.20%, and 8.86%. In addition, the results of the ecological risk assessment showed low ecological risks of naphthalene and high ecological risks of benzo(a)anthracene, respectively, whereas the remaining monomers revealed medium ecological risk. Among the 59 sampling sites, only 12 belonged to low ecological risk areas, whereas the remaining sampling sites were at medium to high ecological risks. Moreover, the water area near the Ningtiaota Industrial Park showed a risk value close to the high ecological risk threshold. Therefore, it is urgent to formulate prevention and control measures in the study region.
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