Factors influencing the photodegradation of N-nitrosodimethylamine in drinking water

In order to provide basic data for practical application, photodegradation experiment of N-nitrosodimethylamine (NDMA) in aqueous solution was carried out with a low-pressure Hg lamp. Effects of the initial concentration of NDMA, solution pH, dissolved oxygen, and the presence of humic acid on NDMA photodegradation were investigated. NDMA at various initial concentrations selected in this study was almost completely photodegraded by UV irradiation within 20 min, except that at 1.07 mmol/L, NDMA could be photodegraded almost completely in the acidic and neutral solutions, while the removal efficiency decreased remarkably in the alkaline solution. Dissolved oxygen enhanced the NDMA photodegradation, and the presence of humic acid inhibited the degradation of NDMA. Depending on the initial concentration of NDMA, NDMA photodegradation by UV obeyed the pseudo-first-order kinetics. Dimethylamine, nitrite, and nitrate were detected as the photodegradation products of NDMA. ¹O₂ was found to be the reactive oxygen species present in the NDMA photodegradation process by UV, based on the inhibiting experiments using tert-butanol and sodium azide.     

Cleaning carcinogenic nitrosamines with zeolites

N-nitrosamines are characterized with an N-nitroso group N–NO. N-nitrosamines are strong carcinogens or potent carcinogens. Nitrosamines occur widely in the environment, e.g., as tobacco smoke that causes cancers of lungs, larynx, oral cavity and pharynx, pancreas, kidney and bladder. It is difficult to capture selectively N-nitrosamines in the environment. Therefore, zeolite, which is a molecular sieve, may help to sequester N-nitrosamines. Zeolites are a class of aluminosilicates, characterized by ordered microporous structures with acidic–basic sites on the surface and energetic field inside the pores. They have been widely applied in industry as adsorbents and catalysts because of their unique shape selectivity. Here, we review the latest research on adsorption and catalytic degradation of N-nitrosamines by zeolite materials. The efficiency of zeolite is increased using metal oxides. Removal of N-nitrosamines in smoke is discussed.     

砷浓度、形态及碳酸氢盐对蜈蚣草吸收砷的影响

为了探讨超富集植物蜈蚣草在处理高砷地下水方面的可行性,研究了水培条件下砷的浓度、形态和碳酸氢盐(HCO-3)对超富集植物蜈蚣草吸收砷的影响。实验中使用了浓度为0.1～100mg·L-1的As(III)和As(V)溶液。HCO-3处理中,HCO-3浓度范围为0.5～20mmol·L-1,As(III)或As(V)的浓度为5mg·L-1。结果表明,在水培条件下,蜈蚣草具有明显的耐高砷特征。当介质砷含量高达100mg·L-1时,砷的去除率可达到80%,且对As(III)的吸收效率高于As(V)。植物体内砷形态研究表明,蜈蚣草体内2种形态砷的含量与外源砷形态有一定的关系,As(V)处理条件下,植物体中的As(V)比例较As(III)处理高。高浓度的HCO-3(20mmol·L-1)处理对蜈蚣草地上部分生物量没有明显影响,但是抑制了地下部分的生长,并且对砷的吸收表现出明显的抑制作用。     

砷浓度、形态及碳酸氢盐对蜈蚣草吸收砷的影响

大同盆地是典型的高砷地下水分布区。利用从地方性砷中毒严重病区山阴县采集的高砷地下水样品,用稀释培养法实验研究了外加砷源对地下水中微生物数量的影响;同时基于生物学可培养法和16S rDNA序列比对法,选取代表性高砷水样,研究了耐砷菌的种群特征。结果表明,外加砷源对地下水中微生物数量影响显著,高浓度砷会抑制大部分微生物生长,使微生物数量减少;低浓度砷对微生物生长具有一定促进作用。通过多次分离、纯化从3个不同砷含量地下水样中分离到多株砷抗性菌,经鉴定属于主要为Bacillus、Pseudomonas、Paenibacillus、Aeromonas、Enterobacter5个属。从RDP(Ribosomal Database Project)分析显示3个水样可培养微生物组成不同,都有生存能力强能够耐低浓度NaAsO₂的Bacillales,优势耐砷菌是γ-proteobacteria,其中Enterbacter具有耐高浓度NaAsO₂的能力。     

Fate and removal of typical pharmaceutical and personal care products in a wastewater treatment plant from Beijing: a mass balance study

The fate and removal of pharmaceuticals and personal care products (PPCPs) in wastewater treatment plants (WWTPs) has received great attention during the last decade. Numerous data concerning concentrations in the water phase can be found in the literature, however corresponding data from sludge as well as associated mass balance calculations are very limited. In the present study, the adsorbed and dissolved concentrations of 9 PPCPs were investigated in each unit of a WWTP in Beijing, China. Based on the calculation of mass balance, the relative mass distribution and removal efficiency of each target compound was obtained at each process. The amount of PPCPs entering into the WWTP ranged from 12 g·d^–1 to 3848 g·d^–1. Five target compounds (caffeine, chloramphenicol, bezafibrate, clofibric acid, and N,N-diethyl-meta-toluamide) were effectively removed, with rates of 57%–100%. Negative removal efficiencies were obtained for sulpiride, metoprolol, nalidixic acid, and carbamazepine, ranging from -19% to -79%. PPCPs mainly existed in dissolved form (≥92%) in both the raw influent and the final effluent. The sludge cake carried a much lower amount of PPCPs (17 g·d^–1) compared with the discharged effluent (402 g·d^–1). In A²/O treatment tanks, the anaerobic and anoxic tanks showed good performance for PPCPs removal, and the amount of adsorbed PPCPs was increased. The results reveal that both the dissolved and the adsorbed phases should be considered when assessing the removal capacity of each A²/O tank.     

桑沟湾溶解态汞的生物地球化学行为

作为一种毒性极强的重金属元素,汞在海洋中可以通过海洋生物的呼吸、摄食和吸附等过程被利用,并在沿食物链传递的过程中不断富集,最终危害人类的健康。利用冷原子荧光光度法(CV-AFS)对2011年4月、8月、10月和2012年1月桑沟湾溶解态无机汞(DIHg)和溶解态有机汞(DOHg)的含量进行了测定。结果表明,桑沟湾四个季节DIHg的浓度范围分别为52~865、131~359、31~134和22~119 pmol·L-1,DOHg的浓度范围分别为37~214、52~635、21~98和未检出~51 pmol·L-1。桑沟湾DIHg和DOHg具有相似的分布特征,均呈现出从近岸向外海逐渐降低的趋势,有明显的季节变化。桑沟湾DIHg和DOHg的周日变化与潮汐呈现出较好的负相关关系,且存在明显的昼夜差异。影响桑沟湾DIHg和DOHg分布的主要因素包括河流和地下水的输入、大气的干湿沉降、与黄海的交换、活性气态汞(Hg0)在海-气界面的交换、表层水体发生的光化学还原反应以及养殖生物的清除等。通过初步计算,桑沟湾溶解态汞(TDHg)的存留时间约为(1.27±0.53)年,远远低于大洋。根据美国国家环境保护局汞的质量标准和我国地表水环境质量标准,桑沟湾没有明显的汞污染。但海产品体内富集的汞可能会带来潜在的生态危机和食品安全问题,需要相关部门加以重视,确保桑沟湾养殖产业的平衡发展。     

北江流域抗生素污染水平和来源初探

北江是发源于湖南(武水)和江西(浈水),汇于广东韶关,流经广东全境并入海的三大河流之一。为了解整个北江抗生素污染情况,共设置44个采样点,并采集了河水及部分沉积物样品,较全面地分析了各样品中12种典型抗生素含量并初步探究了其污染来源。研究发现,包括北江源头在内的全河段均有抗生素的检出,5类抗生素在表层水和沉积物中的平均浓度分别为77.8 ng·L~(-1)和3.6 ng·g~(-1)。其中,大环内酯类污染最为严重,其含量范围为11.7~114.6 ng·L~(-1)和0~435.3 ng·g~(-1),远高于其他类抗生素。表层水中磺胺类的磺胺甲恶唑和氯霉素类的检出率达100%,其中以磺胺甲恶唑(14.7 ng·L~(-1))和阿奇霉素(25.0 ng·L~(-1))为主,而沉积物中以阿奇霉素(35.9 ng·g~(-1))、氧氟沙星(5.4 ng·g~(-1))和四环素(3.3 ng·g~(-1))为主。由于流域污染源种类和数量不同,各抗生素在北江中的分布也存在差异。表层水中抗生素含量水平表现为下游高于上中游,在沉积物中则主要集中于中、下游之间河段。这反映了人类活动强度对北江抗生素污染的直接影响。     

Decolorization of azo dyes by a salt-tolerant Staphylococcus cohnii strain isolated from textile wastewater

The salt-tolerant Staphylococcus cohnii strain, isolated from textile wastewater, has been found effective on decolorizing several kinds of azo dyes with different structures. The optimal conditions for azo dye acid red B (ARB) decolorization by S. cohnii were determined to be pH = 7.0 and 30°C. The decolorization efficiency increased with the increase of the salinity concentration, and around 90% of ARB (100 mg·L^?1) could be decolorized in 24 h when the salinity concentration was up to 50 g·L^?1. Moreover, the strain could still decolorize 19% of ARB in 24 h even when the NaCl concentration was increased to 150 g·L^?1. Meanwhile, the dependence of the specific decolorization rate by S. cohnii on the ARB concentration could be described with Michaelis-Menten kinetics (K _m = 585.7mg·L^?1, V _max = 109.8 mg·g cell^?1·h^?1). The addition of quinone redox mediator, named 2-hydroxy-1,4-naphthoquinone and anthraquinone-2,6-disulfonate, significantly accelerated the decolorization performance of S. cohnii. Furtherly, the activities of azoreductase (0.55 ??mol·mg protein^?1·min^?1) and Nicotineamide adenine dinucleotide-dichlorophenol indophenol (NADH-DCIP) reductase (8.9 ??mol·mg protein^?1·min^?1) have been observed in the crude cell extracts of S. cohnii. The decolorization products of ARB were analyzed by HPLC-MS, and the results indicated the reductive pathway was responsible for azo dye decolorization by S. cohnii.     

Adsorption of fluoride on clay minerals and their mechanisms using X-ray photoelectron spectroscopy

This research investigates the adsorption mechanisms of fluoride (F) on four clay minerals (kaolinite, montmorillonite, chlorite, and illite) under different F^? concentrations and reaction times by probing their fluoride superficial layer binding energies and element compositions using X-ray photoelectron spectroscopy (XPS). At high F^? concentrations (C ₀ = 5?C1000 mg·L^?1), the amount of F^? adsorbed (Q _F), amount of hydroxide released by clay minerals, solution F^? concentration, and the pH increase with increasing C ₀. The increases are remarkable at C ₀>50 mg·L^?1. The QF increases significantly by continuously modifying the pH level. At C ₀<5?C100 mg·L^?1, clay minerals adsorb H⁺ to protonate aluminum-bound surface-active hydroxyl sites in the superficial layers and induce F^? binding. As the C ₀ increases, F^?, along with other cations, is adsorbed to form a quasi-cryolite structure. At C ₀>100 mg·L^?1, new minerals precipitate and the product depends on the critical Al³⁺ concentration. At [Al³⁺]>10^?11.94 mol·L^?1, cryolite forms, while at [Al³⁺]<10^?11.94 mol·L^?1, AlF₃ is formed. At low C ₀ (0.3?C1.5 mg·L^?1), proton transfer occurs, and the F^? adsorption capabilities of the clay minerals increase with time.     

贵州万山汞矿地区耐汞野生植物研究

在贵州万山地区废弃汞矿堆和矿山附近,受长期高剂量汞暴露的影响经过的自然选择,该地区出现了一些能耐受汞毒性的生态型植物。对汞耐受及汞富集植物的筛选对于汞污染土壤的植物修复具有一定的现实意义。通过对万山梅子溪地区汞污染土壤及汞耐受植物采样调查发现,该区域采样土壤中汞的含量均在50 mg·kg-1以上,达到重度汞污染水平。对该地区野生植物的采样分析发现,蔷薇科植物悬钩子不仅数量较多,单株植物生物量较大,表现出很强的耐汞毒性的能力,而且植株内可以很大程度地富集汞,在其植株中汞的含量可达20 mg·kg-1左右,属于汞富集植物,另外发现野蒿对汞也具有较强的富集能力,其植株中汞的含量可达10 mg·kg-1以上。该类型植物的发现将为植物的汞耐受以及汞富集机理研究提供新的素材,为汞污染土壤的植物修复技术提供新的植物类型,也为进一步开发汞污染土壤处理技术提供了一种可能。     

四氯丙烯对稀有鮈鲫的急性毒性及安全浓度评价

采用半静态试验方式测试了四氯丙烯对稀有鮈鲫(Gobiocypris rarus)的急性毒性,试验浓度分别设定为0.25 mg·L~(-1)、0.30mg·L~(-1)、0.36 mg·L~(-1)、0.42 mg·L~(-1)、0.50 mg·L~(-1)和0.60 mg·L~(-1),同时进行空白对照(试验用水)和分散剂对照(体积分数为0.006%的吐温-80水溶液)试验。采用气相色谱法对试验溶液进行浓度分析,实测浓度分别为0.19 mg·L~(-1)、0.25 mg·L~(-1)、0.34 mg·L~(-1)、0.40 mg·L~(-1)、0.51 mg·L~(-1)和0.64 mg·L~(-1),试验结果以实测浓度表示和统计。结果表明:四氯丙烯致稀有鮈鲫无死亡发生(EC0)的最高浓度为0.25 mg·L~(-1),导致稀有鮈鲫100%死亡(EC100)的最低浓度为0.51 mg·L~(-1)。根据实测浓度,用SPSS(17.0)概率单位法求得四氯丙烯对稀有鮈鲫的半数致死浓度96 h-LC50为0.347 mg·L~(-1),95%置信区间为0.328 mg·L~(-1)~0.361 mg·L~(-1)。     

Factors controlling N-nitrosodimethylamine (NDMA) formation from dissolved organic matter

The formation of cancinogenic nitrosamines, esp. N-nitrosodimethylamine (NDMA) in water and wastewater treatment plants has drawn much attention in recent years. Dissolved organic matter from the transported Luan River water as water source of Tianjin was fractionated with different XAD resins and a series of ultra-filtration membranes with molecular weight (MW) cut-offs of 5k Da, 3k Da, and 1k Da, respectively. The NDMA yields from the raw water and each fraction were measured to investigate their role in NDMAyield. Results indicated that the hydrophilic fraction had a higher NDMA yield than those of hydrophobic fraction and transphilic fraction. The fraction with MW below 1k Da had a higher NDMAyield than that with larger MW. NDMA formation increased as the dissolved organic carbon (DOC) to dissolved organic nitrogen (DON) ratio decreased, which indicated that DON might serve as the real important precursor for NDMA. The correlation between NDMA yield and specific ultraviolet absorbance at 254 nm (SUVA₂₅₄) suggested that the latter might not represent the specific precursors for NDMA in the water. Besides the water quality, the influences of pH, disinfectant dosage, and disinfection contact time on the formation of NDMA were also examined. These results will help water treatment plants establish measures to control this harmful disinfection by-product.     

Assessment of toxicity of two nitroaromatic compounds in the freshwater fish Cyprinus carpio

This study was conducted to evaluate the toxicological response of p-nitrotoluene and p-nitroaniline to the key fish species, Cyprinus carpio. A freshwater fish bioassay based on the 96 h LC ₅₀ was used to estimate the single and joint toxicity of the two chemicals. The toxicity of p-nitrotoluene was greater than that of p-nitroaniline based on 96 h LC ₅₀ values of 40.74 mg·L^?1 and 48.99 mg·L^?1, respectively. Both compounds had moderate toxicity toward Cyprinus carpio, and this toxicity increased with the exposure duration and concentration. Binary mixtures of the compounds were more toxic than the individual compounds at 96 h, and they acted upon partial addition. When the exposure time was longer, the toxicity increased for mixtures of compounds with the same concentration or toxicity. The results of this study suggest that exposure to a combination of these chemicals would result in a higher environmental risk in aquatic systems than exposure to either compound alone. Further research is needed to investigate the combined effects and sublethal toxicity of p-nitrotoluene and p-nitroaniline, since they are both still used in China.     

Occurrence and removal of N-nitrosodimethylamine and its precursors in wastewater treatment plants in and around Shanghai

Six wastewater treatment plants （WWTPs） were investigated to evaluate the occurrence and removal of N-nitrosodimethylamine （NDMA）, NDMA formation potential （FP） and four specific NDMA precursors, dimethylamine （DMA）, trimethylamine （TMA）, dimethyl- formamide （DMFA） and dimethylaminobenzene （DMAB）. DMA and tertiary amines with DMA functional group commonly existed in municipal wastewater. Chemically enhanced primary process （CEPP） had no effect on removal of either NDMA or NDMA FP. In WWTPs with secondary treatment processes, considerable variability was observed in the removal of NDMA （19%-85%） and NDMA FP （16%-76%）, moreover, there was no definite relationship between the removal of NDMA and NDMA FP. DMA was well removed in all the six surveyed WWTPs; its removal efficiency was greater than 97%. For the removal of tertiary amines, biologic treatment processes with nitrification and denitrification had better removal efficiency than conventional activated sludge process. The best removal efficiencies for TMA, DMFA and DMAB were 95%, 68% and 72%, respectively. CEPP could remove 73% of TMA, 23% of DMFA and 36% of DMAB. After UV disinfection, only 17% of NDMA was removed due to low dosage of UV was applied in WWTP. Although chlorination could reduce NDMA precursors, NDMA concentration was actually increased after chlorination.     

The role of root organic acids in the tolerance of Festuca rubra to zinc,lead and cadmium

Abstract

Festuca rubra L. plants are pseudometallophytes colonizing abandoned Pb/Zn mine areas, successfully employed in phytostabilization. To study the contribution of low-molecular weight organic acids to metal tolerance, F. rubra plants were grown for three months in hydroponics with Cd (1.8, 18 and 36 µmol?L^?1), Pb (50, 250 and 500?µmol?L^?1) and Zn (0.3, 3 and 6?mmol?L^?1), separately, and in ternary combination (18?µmol?L^?1 Cd + 250?µmol?L^?1 Pb + 0.3?mmol?L^?1 Zn). The roots retained most of the metals but their distribution from shoot to root was altered when the plants were treated with the ternary combination. The main organic acids in roots were citrate and malate. At the lowest concentrations, the metals caused small reductions in biomass, had no effects on photosynthetic pigments nor on malondialdehyde, but led to increases in root organic acids. At higher concentrations, phytotoxic responses were observed, associated with a decline of citrate and malate in the roots.     

邻苯二甲酸丁基苄酯致神经细胞氧化损伤

为探究邻苯二甲酸丁基苄酯(butyl benzyl phthalate,BBP)对小鼠神经的毒性作用,进行了小鼠体外毒理学研究。首先用不同浓度的邻苯二甲酸丁基苄酯染毒神经模型细胞—N2a神经瘤细胞,通过噻唑蓝比色法(MTT),Hoechst 33258染色实验评价邻苯二甲酸丁基苄酯的细胞毒效应;通过对染毒细胞氧自由基(ROS)、丙二醛(MDA)、还原型谷胱甘肽(GSH)含量的检测来探究BBP对小鼠神经瘤细胞的氧化损伤效应。随着BBP浓度的不断增高,细胞的MTT值逐渐变小,当BBP的浓度达到10 g·L-1时,MTT实验结果与对照组出现显著性差异;Hoechst 33258染色结果显示:高浓度的BBP导致细胞核呈现出不规则状态,出现了凋亡小体;随着BBP染毒浓度的升高N2a细胞中的ROS水平和MDA含量逐渐上升,分别在0.16 g·L-1和10 g·L-1开始与对照组相比出现了显著性的差异(p0.05);而GSH系数呈现下降趋势,在0.32 g·L-1时开始出现显著性差异(p0.05)。实验结果表明高浓度的邻苯二甲酸丁基苄酯可以导致神经瘤细胞的凋亡,并产生氧化损伤效应。     

Impact of solids on biphasic biodegradation of phenanthrene in the presence of hydroxypropyl-<Emphasis Type="Italic">β</Emphasis>-cyclodextrin (HPCD)

The consequence of polycyclic aromatic hydrocarbons (PAHs) in the environment is of great concern. The hydrophobic properties of PAHs significantly impact phase distribution causing limited bioavailability. Enhanced biodegradation has been extensively carried out by surfactants and the redeployment effect was recognized. However, the quantitative relationship concerning the impact of solids was rarely reported. A batch of biphasic tests were carried out by introducing Mycobacterium vanbaalenii PYR-1 and hydroxypropyl-β-cyclodextrin (HPCD) into a mixture of phenanthrene solution and various glass beads (GB37-63, GB105-125, and GB350-500). The comparative results demonstrated that HPCD had little effect on microbial growth and was not degradable by bacterium. A model was proposed to describe the biodegradation process. The regression results indicated that the partition coefficient k _d (1.234, 0.726 and 0.448 L·g^?1) and the degradation rate k (0 mmol·L^?1: 0.055, 0.094, and 0.112; 20 mmol·L^?1: 0.126, 0.141, and 0.156; 40 mmol·L^?1: 0.141, 0.156 and 0.184 d^?1) were positively and negatively correlated with the calculated total surface area (TSA) of solids, respectively. Degradation enhanced in the presence of HPCD, and the enhancing factor f was calculated (20 mmol·L^?1: 15.16, 40.01, and 145.5; 40 mmol·L^?1: 13.29, 37.97, and 138.4), indicating that the impact of solids was significant for the enhancement of biodegradation.     

Mikrobiologische Volatilisierung von anorganischem Selen aus Deponiesickerwässern bei umweltrelevanten Konzentrationen

Background, aim, and scope Determination of the rates of microbial alkylation are of interest with respect to natural attenuation of harmful selenium concentrations or selenium charges in contaminated ecosystems. Materials and methods Landfill gas and the headspace of microbial microcosm incubation vessels were sampled in Tedlar^® bags. On-line hyphenation of an efficient enrichment method (cryotrapping-cryofocusing), a gaschromatographic separation technique, and the sensitive ICP-MS detection system was used for speciation of volatile organoselenium compounds. A detection limit at the ultra trace level (pg Se) was achieved with this CT-CF-GC-ICP-MS technique. Results Incubation of landfill leachate with Alternata alternata as an active methylating organism showed a production of volatile selenium compounds (DMSe, DMDSe, EMDSe, DEDSe) over the whole range of applied inorganic selenium concentrations (10?µg?L^–1 to 10?mg?L^–1), with volatilization rates of up to 10?mg m^–3?d^–1. For selenium concentrations of 1?mg?L^–1 in the nutrient broth, up to 7?% of the inorganic selenium was volatilized after one week. The same volatile selenium compounds were observed in landfill gas. Discussion The amount of volatilized selenium was comparable to that found in other studies with microbial pure cultures as well as isolates from waters or soils, but at much lower initial concentrations used in the incubations. Conclusions The alkylation of selenium in the enriched mixed culture from landfill leachate at environmentally relevant concentrations indicates that the organoselenium compounds of same species composition and distribution determined in landfill gas are produced by microorganisms. Recommendations and perspectives The microbial alkylation of toxic inorganic selenium species to less toxic or non-toxic, volatile compounds is an efficient method for bioremediation of contaminated sites even at relatively low Se concentrations.     

邻苯二甲酸二乙基己酯(DEHP)对马氏珠母贝(Pinctada martensi)血细胞免疫功能及氧化应激效应的影响

邻苯二甲酸二乙基己酯(DEHP)是一种持久性的有机污染物(POPs),具有潜在毒性、致癌性。选取马氏珠母贝(Pinctada martensi)为研究对象,研究DEHP对其血淋巴细胞免疫功能和脂质过氧化水平的影响。将成年马氏珠母贝暴露于不同浓度(0.5、2.0、8.0、16.0 mg·L-1)的DEHP中,暴露14 d后测定血细胞数目(THC)、吞噬能力(phagocytic activity)、细胞膜稳定性(cell membrane stability)、脂质过氧化程度(LPO)和总谷胱甘肽含量(T-GSH)的变化。结果显示,血细胞数目随DEHP浓度的升高而降低,呈明显的剂量-效应关系,最低可见效应浓度(LOEC)0.5 mg·L-1。细胞膜稳定性和吞噬活力均随DEHP浓度的升高,呈现先升高后降低的变化趋势,其LOEC值分别小于2和8 mg·L-1。细胞中丙二醛(MDA)含量随染毒浓度增加逐渐升高,在8 mg·L-1浓度组达到最高值,之后降低,与之相应的脂质过氧化水平也呈现先升高后降低的变化趋势,LOEC2 mg·L-1。8mg·L-1浓度组的总谷胱甘肽含量与对照组相比存在显著差异性(p0.05),LOEC8 mg·L-1。研究结果表明:DEHP染毒14 d对马氏珠母贝血淋巴细胞免疫功能有明显的影响,同时还会诱导机体产生氧化应激效应,在所测试的指标中,血细胞计数对DEHP的胁迫最敏感(LOEC0.5 mg·L-1),细胞膜稳定性和脂质过氧化水平的敏感性次之(LOEC2 mg·L-1)。