Biological degradation

生物降解
  • 文章类型: Journal Article
    通常发现氯化的挥发性有机化合物(CVOCs)与1,4-二恶烷组合,1,4-二恶烷用作溶剂稳定剂。分离这些化合物将是合乎需要的,因为1,4-二恶烷的生物降解遵循需氧途径,而需要厌氧条件来生物降解CVOCs。传统的吸附剂,如活性炭(AC)和碳质树脂对1,4-二恶烷和CVOCs具有很高的吸附能力,但缺乏选择性,限制它们用于分离(Liu等人。,2019)。在目前的工作中,两种大环吸附剂,β-CD-TFN和Res-TFN,检查了在1,4-二恶烷存在下氯化乙烯的选择性吸附。两种吸附剂均表现出CVOCs的快速吸附和1,4-二恶烷的最小吸附。Res-TFN对CVOCs的吸附能力高于β-CD-TFN(测得的线性分配系数,对于1,1,1,DCE,Kd2140-9750L·kg-1与192-918L·kg-1,顺式-1,2-DCE和TCE,分别),并且对CVOCs具有高度选择性(1,4-二恶烷的TCEKd〜117Kd)。相比之下,TCE和1,4-二恶烷在AC上的吸附在100µg·L-1处大约相等,TCE在Res-TFN上的吸附约为1/3。Res-TFN的更大吸附和选择性表明,它可以用作选择性吸附剂将CVOCs与1,4-二恶烷分离以允许单独的生物降解。
    Chlorinated volatile organic compounds (CVOCs) are often found in combination with 1,4-dioxane which has been used as a solvent stabilizer. It would be desirable to separate these compounds since biodegradation of 1,4-dioxane follows an aerobic pathway while anaerobic conditions are needed for biodegrading CVOCs. Conventional adsorbents such as activated carbon (AC) and carbonaceous resins have high adsorption capacities for 1,4-dioxane and CVOCs but lack selectivity, limiting their use for separation (Liu et al., 2019). In the current work, two macrocyclic adsorbents, β-CD-TFN and Res-TFN, were examined for selective adsorption of chlorinated ethenes in the presence of 1,4-dioxane. Both adsorbents exhibited rapid adsorption of the CVOCs and minimal adsorption of 1,4-dioxane. Res-TFN had a higher adsorption capacity for CVOCs than β-CD-TFN (measured linear partition coefficient, Kd 2140 -9750 L⋅kg-1 versus 192-918 L⋅kg-1 for 1,1, DCE, cis-1,2-DCE and TCE, respectively) and was highly selective for CVOCs(TCE Kd ~117 Kd for 1,4-dioxane). By comparison, TCE and 1,4-dioxane adsorption on AC was approximately equal at 100 µg⋅L-1 and approximately 1/3 of the adsorption of TCE on the Res-TFN. The greater adsorption and selectivity of Res-TFN suggest that it can be used as a selective adsorbent to separate CVOCs from 1,4-dioxane to allow separate biodegradation.
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  • 文章类型: Journal Article
    应对有害蓝藻水华(CyanoHAB)及其相关微囊藻毒素(MC)的威胁对于全球饮用水安全至关重要。在这次审查中,我们全面分析和比较了身体,化学,以及水生环境中MCs降解的生物学方法和基因工程。物理方法,如紫外线处理和光催化反应,在分解MC方面有很高的效率,具有进一步提高性能和减少危险副产品的潜力。使用二氧化氯和高锰酸钾的化学处理可以降低MC水平,但需要谨慎的剂量管理,以避免有毒副产物并保护水生生态系统。生物方法,包括微生物降解和植物修复技术,显示出MCs生物降解的希望,提供减少的环境影响和增加的可持续性。基因工程,例如微囊藻毒素酶A(MlrA)在大肠杆菌中的固定及其在集胞藻属中的表达。,已证明在分解MC如MC-LR方面是有效的。然而,与温度变化等特定环境条件相关的挑战,pH值,其他污染物的存在,营养可用性,氧气水平,和曝光,以及生物系统的可扩展性,需要进一步探索。我们提供了对MC降解技术的全面评估,深入研究它们的实用性,评估环境影响,并仔细检查它们的效率,以提供对这些方法在各种环境背景下的多面性的关键见解。整合各种方法以提高降解效率在水安全领域至关重要,强调持续创新的必要性。
    Addressing the threat of harmful cyanobacterial blooms (CyanoHABs) and their associated microcystins (MCs) is crucial for global drinking water safety. In this review, we comprehensively analyze and compares the physical, chemical, and biological methods and genetic engineering for MCs degradation in aquatic environments. Physical methods, such as UV treatments and photocatalytic reactions, have a high efficiency in breaking down MCs, with the potential for further enhancement in performance and reduction of hazardous byproducts. Chemical treatments using chlorine dioxide and potassium permanganate can reduce MC levels but require careful dosage management to avoid toxic by-products and protect aquatic ecosystems. Biological methods, including microbial degradation and phytoremediation techniques, show promise for the biodegradation of MCs, offering reduced environmental impact and increased sustainability. Genetic engineering, such as immobilization of microcystinase A (MlrA) in Escherichia coli and its expression in Synechocystis sp., has proven effective in decomposing MCs such as MC-LR. However, challenges related to specific environmental conditions such as temperature variations, pH levels, presence of other contaminants, nutrient availability, oxygen levels, and light exposure, as well as scalability of biological systems, necessitate further exploration. We provide a comprehensive evaluation of MCs degradation techniques, delving into their practicality, assessing the environmental impacts, and scrutinizing their efficiency to offer crucial insights into the multifaceted nature of these methods in various environmental contexts. The integration of various methodologies to enhance degradation efficiency is vital in the field of water safety, underscoring the need for ongoing innovation.
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  • 文章类型: Journal Article
    食品和饲料中的黄曲霉毒素B1(AFB1)污染是全球健康和经济威胁,需要立即制定有效的战略来减轻其负面影响。本研究的重点是屎肠球菌HB2-2(E.faeciumHB2-2)作为一种有效的AFB1降解微生物,利用形态学观察,生化分析,和16SrRNA序列分析。在pH为10的营养肉汤(NB)培养基中,在32°C下孵育E.faeciumHB2-296小时,对AFB1的降解率为90.0%。此外,屎肠球菌HB2-2在花生粕中表现出82.9%的AFB1降解率,将AFB1水平从105.1降低到17.9μg/kg。发现屎肠球菌HB2-2的AFB1降解能力取决于发酵上清液。通过液相色谱-质谱(LC-MS)分析了屎肠球菌HB2-2降解AFB1的产物,并根据确定的降解产物提出了可能的降解机理。此外,细胞毒性测定显示,与母体AFB1相比,降解产物的毒性显著降低。这些发现强调了屎肠球菌HB2-2作为减轻食品和饲料中AFB1污染的安全有效方法的潜力。
    Aflatoxin B1 (AFB1) contamination in food and feed is a global health and economic threat, necessitating the immediate development of effective strategies to mitigate its negative effects. This study focuses on the isolation and characterization of Enterococcus faecium HB2-2 (E. faecium HB2-2) as a potent AFB1-degrading microorganism, using morphological observation, biochemical profiling, and 16S rRNA sequence analysis. An incubation of E. faecium HB2-2 at 32 °C for 96 h in a pH 10 nutrient broth (NB) medium resulted in a remarkable degradation rate of 90.0% for AFB1. Furthermore, E. faecium HB2-2 demonstrated 82.9% AFB1 degradation rate in the peanut meal, reducing AFB1 levels from 105.1 to 17.9 μg/kg. The AFB1 degradation ability of E. faecium HB2-2 was found to be dependent on the fermentation supernatant. The products of AFB1 degradation by E. faecium HB2-2 were analyzed by liquid chromatography-mass spectrometry (LC-MS), and a possible degradation mechanism was proposed based on the identified degradation products. Additionally, cytotoxicity assays revealed a significant reduction in the toxicity of the degradation products compared to the parent AFB1. These findings highlight the potential of E. faecium HB2-2 as a safe and effective method for mitigating AFB1 contamination in food and feed.
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  • 文章类型: Journal Article
    在这项研究中,分离了以黄曲霉毒素污染的玉米粒为食的水稻象鼻虫(SitophilusoryzaeL.)(鞘翅目:Curculionidae)肠道中的细菌,并评估了其抑制黄曲霉和去除/降解黄曲霉毒素B1(AFB1)的能力。分离出四种形态上不同的米曲霉肠道相关细菌分离株,并鉴定为枯草芽孢杆菌(RWGB1),海洋芽孢杆菌(RWGB2),坚定芽孢杆菌(RWGB3),基于16SrRNA基因序列分析的铜绿假单胞菌(RWGB4)。这些细菌分离物在双重培养试验中抑制黄曲霉的生长,并诱导真菌菌丝的形态畸形,如扫描电子显微镜所证实。所有四种细菌分离物均能够从营养肉汤培养基中去除AFB1。此外,这些细菌分离物的培养上清液降解了AFB1,并通过液相色谱-质谱证实了毒素分子的降解。细菌分离物,枯草芽孢杆菌RWGB1,大洋芽孢杆菌RWGB2和铜绿假单胞菌RWGB4能够产生抑制黄曲霉生长的抗真菌挥发性有机化合物。这些结果表明来自米曲霉肠的细菌分离物具有结合和/或降解AFB1的潜力。进一步研究它们在食品和饲料工业中的应用可以提高食品和饲料生产的安全性。
    In this study, bacteria residing in the gut of the rice weevils (Sitophilus oryzae L.) (Coleoptera: Curculionidae) feeding on aflatoxin-contaminated corn kernels were isolated and evaluated for their ability to suppress Aspergillus flavus and to remove/degrade aflatoxin B1 (AFB1). Four morphologically distinct S. oryzae gut-associated bacterial isolates were isolated and identified as Bacillus subtilis (RWGB1), Bacillus oceanisediminis (RWGB2), Bacillus firmus (RWGB3), and Pseudomonas aeruginosa (RWGB4) based on 16S rRNA gene sequence analysis. These bacterial isolates inhibited A. flavus growth in the dual culture assay and induced morphological deformities in the fungal hyphae, as confirmed by scanning electron microscopy. All four bacterial isolates were capable of removing AFB1 from the nutrient broth medium. In addition, culture supernatants of these bacterial isolates degraded AFB1, and the degradation of toxin molecules was confirmed by liquid chromatography-mass spectrometry. The bacterial isolates, B. subtilis RWGB1, B. oceanisediminis RWGB2, and P. aeruginosa RWGB4, were capable of producing antifungal volatile organic compounds that inhibited A. flavus growth. These results suggest that the bacterial isolates from S. oryzae gut have the potential to bind and/or degrade AFB1. Further research on their application in the food and feed industries could enhance the safety of food and feed production.
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  • 文章类型: Journal Article
    颗粒活性炭(GAC)过滤器中有机微污染物的去除可以归因于吸附和生物降解。这两个过程可以彼此交互或独立进行。为了说明他们互动的差异,选择了三种具有不同吸附和生物降解潜力的14C标记的有机微污染物,以研究它们在具有吸附(GAC)和非吸附(砂)过滤介质的色谱柱中的吸附和生物降解。使用14CO2的形成作为生物降解的标志,我们证明,与中度吸附双氯芬酸相比,吸附不良的N-亚硝基二甲胺(NDMA)的生物降解对空床接触时间(EBCT)的变化更敏感。Further,在缺氧条件下吸附的双氯芬酸可以在分子氧变得可用时降解,在GAC过滤器中进行15分钟的EBCT可以实现双氯芬酸的大量生物降解(≥60%)。这些发现表明,在GAC过滤器中保留的微污染物,通过吸附延长微污染物的停留时间,可以实现比液压保留时间允许的更长的降解时间段。对于生物顽固的化合物卡马西平,14C标记的化合物和非放射性标记的化合物之间的突破差异显示出通过连续吸附-解吸的大量保留,这可能对GAC滤波器性能的解释构成潜在的挑战。
    The removal of organic micropollutants in granular activated carbon (GAC) filters can be attributed to adsorption and biological degradation. These two processes can interact with each other or proceed independently. To illustrate the differences in their interaction, three 14C-labeled organic micropollutants with varying potentials for adsorption and biodegradation were selected to study their adsorption and biodegradation in columns with adsorbing (GAC) and non-adsorbing (sand) filter media. Using 14CO2 formation as a marker for biodegradation, we demonstrated that the biodegradation of poorly adsorbing N-nitrosodimethylamine (NDMA) was more sensitive to changes in the empty bed contact time (EBCT) compared with that of moderately adsorbing diclofenac. Further, diclofenac that had adsorbed under anoxic conditions could be degraded when molecular oxygen became available, and substantial biodegradation (≥60%) of diclofenac could be achieved with a 15 min EBCT in the GAC filter. These findings suggest that the retention of micropollutants in GAC filters, by prolonging the micropollutant residence time through adsorption, can enable longer time periods for degradations than what the hydraulic retention time would allow for. For the biologically recalcitrant compound carbamazepine, differences in breakthrough between the 14C-labeled and nonradiolabeled compounds revealed a substantial retention via successive adsorption-desorption, which could pose a potential challenge in the interpretation of GAC filter performance.
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  • 文章类型: Journal Article
    模块化木材产品作为具有成本效益和轻量化的组件的商业化产生了创新的工程产品,例如,胶合层压木材,层压单板木材,工字梁,交叉层压木材和实木与楔形接头连接。随着时间的流逝,木结构会变质,或需要新的结构元件来增加新建结构的刚度或承载能力,例如,大型玻璃或车库上的过梁,或减少横截面尺寸或节省昂贵的木材材料,同时仍然实现低重量。在这种情况下,需要修理或正确加固。在这项实验和数值研究中,预应力玄武岩BFRP加固的受弯木梁的静力性能,显示了玻璃GFRP和混合玻璃-玄武岩纤维棒。实验测试导致BFRP的承载能力增加(44%),GFRP(33%)和混合棒(43%)以及BFRP的刚度增加(28%),GFRP(24%)和混合棒(25%)。除此之外,用经过生物降解的预应力玄武岩棒加固的胶合层压木梁,7年的风化和长期暴露在各种环境条件下进行了检查,承载能力提高了27%,刚度提高了28%。此外,在现场研究了用预应力玄武岩钢筋加固的全尺寸层压木梁,作为高温下火灾条件下的探索性测试,并通过分析火灾后的物理机械性能来检查火灾期间的物理机械性能。此外,获得了数值模拟与实验研究的令人满意的相关性。差异在1.1%至5.5%之间。这种一致性是因为,在这项研究中,年轻的,确定了所有锯材质量等级的泊松和剪切模量。在火灾条件下暴露于火灾的梁的数值分析中,只有显着差异。实验,本研究中的理论和数值分析是探索性的,将作为未来研究的方向进行扩展。
    The commercialization of modular timber products as cost-effective and lightweight components has resulted in innovative engineering products, e.g., glued laminated timber, laminated veneer lumber, I-beams, cross-laminated timber and solid timber joined with wedge joints. With the passage of time, timber structures can deteriorate, or new structural elements are required to increase the stiffness or load-bearing capacity in newly built structures, e.g., lintels over large-scale glazing or garages, or to reduce cross-sectional dimensions or save costly timber material while still achieving low weight. It is in such cases that repair or correct reinforcement is required. In this experimental and numerical study, the static performance of flexural timber beams reinforced with prestressed basalt BFRP, glass GFRP and hybrid glass-basalt fiber bars is shown. The experimental tests resulted in an increase in the load-carrying capacity of BFRP (44%), GFRP (33%) and hybrid bars (43%) and an increase in the stiffness of BFRP (28%), GFRP (24%) and hybrid bars (25%). In addition to this, glued laminated timber beams reinforced with prestressed basalt rods subjected to biological degradation, 7 years of weathering and prolonged exposure to various environmental conditions were examined, and an increase in the load-bearing capacity of 27% and an increase in stiffness of 28% were obtained. In addition, full-size laminated timber beams reinforced with prestressed basalt bars were investigated in the field as an exploratory test under fire conditions at elevated temperatures, and the effect of the physical-mechanical properties during the fire was examined via an analysis of these properties after the fire. In addition, a satisfactory correlation of the numerical simulations with the experimental studies was obtained. The differences were between 1.1% and 5.5%. The concordance was due to the fact that, in this study, the Young, Poisson and shear moduli were determined for all quality classes of sawn timber. Only a significant difference resulted in the numerical analysis for the beams exposed to fire under fire conditions. The experimental, theoretical and numerical analyses in this research were exploratory and will be expanded as directions for future research.
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  • 文章类型: Journal Article
    从非洲大象粪便中分离出一种能够降解黄曲霉毒素M1(AFM1)的细菌。经16srDNA测序鉴定为短小芽孢杆菌,命名为短小芽孢杆菌E-1-1-1。与物理和化学方法相比,生物学方法因其优点而备受关注,比如彻底排毒,高特异性,和环境友好。本工作旨在研究来自短小芽孢杆菌E-1-1-1的重组过氧化氢酶(rCAT)对模式溶液中AFM1降解的影响。进一步探索了降解机理,并将其应用于牛奶和啤酒。动态动量和虚拟机rCAT对AFM1的最大值分别为4.1μg/mL和2.5μg/mL/min,分别。rCAT介导的AFM1降解产物被鉴定为C15H14O3。分子对接模拟表明,氢键和π键在AFM1-rCAT的稳定性中起着重要作用。在其他工作中,与相同密度的AFM1相比,用过氧化氢酶产生的AFM1降解产物孵育的Hep-G2细胞的存活率提高了约3倍。此外,啤酒和牛奶的降解率分别为31.3%和47.2%,分别。因此,CAT可能是减少模式溶液中AFM1污染的潜在替代品,牛奶,啤酒,从而最大限度地减少其对人类健康的影响。
    A bacteria capable of degrading aflatoxin M1 (AFM1) was isolated from African elephant manure. It was identified as Bacillus pumilus by 16s rDNA sequencing and named B. pumilusE-1-1-1. Compared with physical and chemical methods, biological methods have attracted much attention due to their advantages, such as thorough detoxification, high specificity, and environmental friendliness. This work aimed to study the effects of a recombinant catalase (rCAT) from B. pumilusE-1-1-1 on the degradation of AFM1 in pattern solution. The degradation mechanism was further explored and applied to milk and beer. Kinetic Momentum and Virtual Machine Maximum values for rCAT toward AFM1 were 4.1 μg/mL and 2.5 μg/mL/min, respectively. The rCAT-mediated AFM1 degradation product was identified as C15H14O3. Molecular docking simulations suggested that hydrogen and pi bonds played major roles in the steadiness of AFM1-rCAT. In other work, compared with identical density of AFM1, survival rates of Hep-G2 cells incubated with catalase-produced AFM1 degradation products increased by about 3 times. In addition, degradation rates in lager beer and milk were 31.3% and 47.2%, respectively. Therefore, CAT may be a prospective substitute to decrease AFM1 contamination in pattern solution, milk, and beer, thereby minimizing its influence on human health.
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  • 文章类型: Journal Article
    在这项研究中,通过将微电场应用于好氧颗粒污泥(AGS)反应器,建立了好氧颗粒污泥电化学系统(AGES),用于降解磺胺甲恶唑(SMZ)。在微电场的刺激下,提高了污泥的颗粒化程度,提高了SMZ的降解率。通过扫描电子显微镜和X射线衍射对颗粒污泥的特征进行了表征。在电压为3V,有效电极面积为800mm2时,获得了SMZ的最佳降解率(88%)。动力学分析结果表明,AGES对SMZ的降解可以符合二级动力学方程,降解速率常数(k)为0.001Lmol-1·min-1。通过LC-MS检测SMZ在AGES系统中的降解产物,并阐明了其可能的降解途径。AGES系统中的微电场在微生物的富集和生长中起着选择性的作用,改变微生物群落的多样性。假单胞菌,Tolumonas,和Acidovorax是AGES系统中的优势细菌,这对减少SMZ和营养素负责。这项工作为改进AGS提供了一种绿色手段,并为将AGS工艺应用于现实世界的废水处理铺平了道路。
    In this study, an aerobic granular sludge electrochemical system (AGES) was established by applying the micro-electric field to an aerobic granular sludge (AGS) reactor for the degradation of sulfamethoxazole (SMZ). Under the stimulation of the micro-electric field, the granulation of sludge was improved and the degradation rate of SMZ was enhanced. The features of granular sludge were characterized by scanning electron microscopy and X-ray diffraction. The optimal degradation rate of SMZ (88%) was obtained at the voltage of 3 V and the effective electrode area of 800 mm2. The results of kinetics analyses revealed that the degradation of SMZ by AGES can be fitted with the second-order kinetic equation, showing a degradation rate constant (k) of 0.001 L mol-1·min-1. The degradation products of SMZ in the AGES system were detected by LC-MS and their possible degradation routes were elucidated. The micro-electric field in the AGES system played a selective role in microbes\' enrichment and growth, changing the diversity of the microbial community. Pseudomonas, Tolumonas, and Acidovorax were the dominant bacteria in the AGES system, which is accountable for the abatement of SMZ and nutrients. This work provides a green means for improving AGS and paves the way for applying the AGS process to real-world wastewater treatment.
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  • 文章类型: Journal Article
    RNA在环境系统中的持久性是新兴应用的重要参数,包括生态调查,废水流行病学,和RNA干扰生物农药。RNA的持久性受其生物降解速率控制,特别是通过胞外酶,尽管决定这一比率的具体因素尚未得到表征。由于先前的工作表明核酸特异性DNA与溶解的有机物(DOM)相互作用,我们假设DOM可能结合RNA并阻碍其在自然系统中的生物降解。我们首先采用了先前用于评估RNA-蛋白质结合的技术,以区分DOM在所有位点结合的RNA与DOM未结合或部分结合的RNA。该技术的结果表明,腐殖酸比富里酸更广泛地结合RNA。浓度为8-10mgC/L时,还发现腐殖酸在抑制RNA的酶促降解方面比富里酸更有效。在含有DOM的地表水和土壤提取物中,相对于pH调节的对照,RNA降解被抑制了39-46%。由于DOM具有结合和抑制RNA酶降解的能力,在DOM浓度较高的环境系统中,RNA的生物降解可能会减慢,这可能会增加它的持久性。
    The persistence of RNA in environmental systems is an important parameter for emerging applications, including ecological surveys, wastewater-based epidemiology, and RNA interference biopesticides. RNA persistence is controlled by its rate of biodegradation, particularly by extracellular enzymes, although the specific factors determining this rate have not been characterized. Due to prior work suggesting that nucleic acids-specifically DNA-interact with dissolved organic matter (DOM), we hypothesized that DOM may bind RNA and impede its biodegradation in natural systems. We first adapted a technique previously used to assess RNA-protein binding to differentiate RNA that is bound at all sites by DOM from RNA that is unbound or partially bound by DOM. Results from this technique suggested that humic acids bound RNA more extensively than fulvic acids. At concentrations of 8-10 mgC/L, humic acids were also found to be more effective than fulvic acids at suppressing enzymatic degradation of RNA. In surface water and soil extract containing DOM, RNA degradation was suppressed by 39-46% relative to pH-adjusted controls. Due to the ability of DOM to both bind and suppress the enzymatic degradation of RNA, RNA biodegradation may be slowed in environmental systems with high DOM concentrations, which may increase its persistence.
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  • 文章类型: Journal Article
    溶解的有机物(DOM)可以通过光化学和生物过程去除或转化,产生将有机碳转化为无机碳的负面影响,在岩溶碳循环中起着至关重要的作用。然而,酸性矿井排水(AMD)会影响这一过程,因此,需要在这种背景下研究喀斯特河水(KRW)中DOM的退化。在这项研究中,为了揭示DOM在光化学和生物条件下的演化过程,在可见光照射(VL)条件下,AMD和KRW以不同比例混合,生物降解(BD),紫外线照射(UV)和紫外线照射+生物降解(UV+BD)。在UV+BD中以不同比例混合AMD和KRW后,样品中的平均DOC浓度显着降低(23%),比其他条件下高1.2-1.4倍,会导致无机碳的大量释放。通过平行因素分析(PARAFAC)对荧光参数的进一步分析显示,AMD中的DOM荧光成分主要包含源自自生成分的蛋白质样物质,而KRW中的DOM荧光成分主要是腐殖质样物质,既有原生来源,也有异源来源。因此,AMD可以促进喀斯特接收流中DOM的光化学和生物降解,导致DOC转化为无机碳。结果表明,UV+BD和AMD的协同作用加速了DOM的降解和KRW中无机碳的释放,从而影响岩溶碳循环的稳定性。
    Dissolved organic matter (DOM) can be removed or transformed by photochemical and biological processes, producing the negative effect of transforming organic carbon into inorganic carbon, which plays a vital role in the karst carbon cycle. However, acid mine drainage (AMD) will affect this process, so the degradation of DOM in karst river water (KRW) needs to be studied in this context. In this study, to reveal the evolution processes of DOM under photochemical and biological conditions in AMD-impacted KRW, AMD and KRW were mixed in different ratios under conditions of visible light irradiation (VL), biodegradation (BD), ultraviolet irradiation (UV) and ultraviolet irradiation + biodegradation (UV+BD). The average DOC concentrations in samples after mixing AMD and KRW in different proportions decreased significantly (by 23%) in UV+BD, which was 1.2-1.4 times higher than under the other conditions and would lead to a significant release of inorganic carbon. Further analysis of the fluorescence parameters via parallel factor analysis (PARAFAC) revealed that the DOM fluorescence components in AMD comprised mainly protein-like substances derived from autochthonous components, while the DOM fluorescence components in KRW were mainly humic-like substances with both autochthonous and allochthonous sources. Therefore, AMD could promote both the photochemical and biological degradation of DOM in karst receiving streams, resulting in the conversion of DOC to inorganic carbon. The results showed that the synergistic effects of UV+BD and AMD accelerated the degradation of DOM and the release of inorganic carbon in KRW, thus affecting the stability of the karst carbon cycle.
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