磷浓度对海洋小球藻叶绿素荧光及生长的影响

海水富营养化影响微藻生长,引起海洋初级生产力变化.以海洋小球藻(Chlorella sp.)为研究对象,研究不同磷浓度对其叶绿素荧光、细胞密度和色素含量变化的影响,以期找到海洋小球藻最适生长的磷浓度,为富营养条件下微藻生长的研究提供基础资料.结果表明,在培养温度为(22±1) ℃、光照强度为4 000 lx、光暗比为12 h:12 h条件下,不同磷浓度对海洋小球藻叶绿素荧光、细胞密度及色素含量影响显著,最大光能转化效率(Fv/Fm)、潜在活性(Fv/Fo)、实际光能转化效率(ΦPSⅡ)和电子传递速率(ETR)均呈先升后降的趋势,3.62 μmol/L处理组显著低于其他各组,434.52 μmol/L处理组一直处在较高水平.说明海洋小球藻的光合作用对高磷的适应范围较广,但对低磷浓度培养反应敏感.非光化学淬灭(qN)的值,3.62 μmol/L处理组高于其他各组.从细胞密度和色素含量的变化可以看出,36.21 μmol/L处理组最高,434.52、3.62 μmol/L处理组均低于36.21 μmol/L处理组.海洋小球藻生长的最适磷摩尔浓度为36.21 μmol/L.     

铜、镉联合胁迫对羊角月牙藻的自由基氧化损伤影响研究

分析了铜和镉联合胁迫对羊角月牙藻(Selenastrum capricornutum)的影响,运用国内应用较少的新型技术——叶绿素荧光技术检测了胁迫下微藻的最大光能转化效率(Fv/Fm)受到的影响,并尝试通过膜脂过氧化损伤产物丙二醛(MDA)和其他指标在胁迫下的变化,对铜、镉联合胁迫机制进行初步探究。结果表明:(1)羊角月牙藻在铜、镉联合胁迫下生长受到抑制,表现出明显的浓度-效应关系。铜、镉的联合胁迫的相加指数为-1.63,表现为典型的拮抗作用。(2)通过叶绿素荧光技术的应用,探明Fv/Fm随毒性浓度的变化表现为浓度-效应关系,毒性浓度越大,羊角月牙藻的Fv/Fm越低,但在低毒性浓度刺激时随胁迫时间延长有回升迹象。(3)随毒性浓度的增加,羊角月牙藻的MDA增加,表现为显著的浓度-效应关系;可溶性蛋白质大体呈先升后降的趋势。(4)铜、镉联合胁迫下,MDA与羊角月牙藻生物量、Fv/Fm呈显著负相关。脂质过氧化是导致生物量下降和Fv/Fm受抑制的原因之一。(5)在微藻体内铜、镉发生拮抗作用的机制也可能与重金属的脂质过氧化作用由于拮抗受到抑制有关。     

2种苔藓的叶绿素荧光特性及耐受性对Pb2+浓度的响应

在不同pbz+质量浓度(0、25、50、100、200 mg/L)的人工条件下,利用叶绿素荧光动力学技术研究比较了狭叶扭口藓(Barbula subcontorta Broth.)和地钱(Marchantia polymorpha L.)的叶绿素荧光特性.结果表明:(1)总体上,随着Pb2+浓度的增加,狭叶扭口藓和地钱...     

锌污染对藻细胞膜电位和膜电阻的影响

运用细胞表面技术和电化学方法,构建一种非创伤性藻细胞膜电位传感系统,研究了Zn2+对大型轮藻(Nitella flexi-lis)膜电位和膜电阻的影响.结果表明,膜电位和膜电阻能快速而灵敏反映过量Zn2+对藻细胞的毒性影响,响应时间均控制在30min内,响应最低摩尔浓度为0.05 mmol/L.本实验浓度范围内.低摩尔浓度(0.05 mmol/L)Zn2+引起藻细胞膜电阻增大.膜电位无明显变化;而高摩尔浓度(0.10～1.00 mmol/L)Zn2+则导致藻细胞明显去极化,膜电阻减小.而且,低浓度Zn2+对藻细胞膜电位、膜电阻的影响具有可逆性;而高浓度Zn2+对其的影响不可逆.此外,藻细胞膜电位、膜电阻与时间呈显著的直线线性关系.上述特征不仅为水中Zn2+的快速生物检测提供了理论依据,亦为Zn2+的定量检测提供了新思路.     

双氯芬酸钠调控雨生红球藻生长的影响研究

研究不同质量浓度(0～200mg/L)双氯芬酸钠(DCF)对雨生红球藻(Haematococcus pluvialis)生物量、色素、虾青素、油脂和多糖等的影响。结果表明:(1)低浓度DCF有助于提高雨生红球藻生物量、叶绿素含量、类胡萝卜素含量、虾青素含量,高浓度时均起抑制作用。当DCF为50mg/L时,生物量干质量最高达到(1.93±0.04)g/L;当DCF为10mg/L时,叶绿素、类胡萝卜素、虾青素质量浓度最高分别达到(57.75±2.34)、(6.99±0.08)、(23.82±0.87)mg/L。(2)相较于对照组,10～100mg/L DCF有利于提高雨生红球藻多糖;50mg/L DCF促进油脂的合成,其他浓度均降低了油脂含量。     

PAC与粘土矿物混凝去除颤藻及残余铝形态研究

研究了PAC与不同粒径的天然粘土矿物复合混凝去除给水中的颤藻。结果表明，两者复合除藻效果显著优于单加PAC。当PAC浓度为12 mg/L，矿物浓度为24 mg/L，粒径为160目时，除藻效果最好，浊度和叶绿素a去除率分别为98.2%和100%。两者复合后PAC形态含量都发生了变化，悬浮态铝含量相对增加，溶解态铝含量相对减少，总残余铝量减小。     

氮浓度对小环藻、大型溞和金鱼藻相互作用的影响研究

以浮游植物小环藻(Cyclotella sp.)、浮游动物大型溞(Daphnia magna)和大型沉水植物金鱼藻(Ceratophyllum demersum)为研究对象,建立水生微宇宙模型,在1.5mg/L磷、2 600lx光强和25℃条件下,研究不同氮质量浓度(0.5、2.0、4.0、8.0、16.0mg/L)对生物操纵效果的影响。结果表明,小环藻单独培养时,氮浓度越高,小环藻增长率越大;小环藻和大型溞共培养、小环藻和金鱼藻共培养且氮为0.5～2.0mg/L时,小环藻生长受到明显抑制,大型溞和金鱼藻均生长良好;3者共培养且氮为0.5～16.0mg/L时,小环藻的生长均得到有效控制。总体而言,控藻效果表现为:小环藻、大型溞和金鱼藻共培养小环藻和金鱼藻共培养金鱼藻种植水对小环藻的化感作用小环藻和大型溞共培养,大型溞和金鱼藻的联合作用比其单独的控藻效果好,随着氮浓度增加,控制效果逐渐减弱,氮小于2.0mg/L最好。氮为0.5～2.0mg/L时,水中TN去除率相对较高,氮为16.0mg/L时,水中TP去除率相对较高。     

共振能量转移同步荧光猝灭法测定水体中孔雀石绿

采用L-半胱氨酸、巯基乙酸为稳定剂水相合成Cd Te量子点,且以Cd Te量子点为能量供体、孔雀石绿为能量受体建立荧光共振能量转移体系,从而实现孔雀石绿含量的同步荧光猝灭法测定。结果表明,当固定波长差为220 nm时,Cd Te量子点的同步荧光最大发射波长位于323 nm。在最优实验条件下,体系的同步荧光淬灭强度与孔雀石绿的浓度在0.5~10.0μmol/L范围内呈良好的线性关系,相关系数为0.9995,方法的检出限为10 nmol/L。该方法用于实际水样中孔雀石绿含量的测定,加标回收率为94%~105%。     

表面活性剂对Cd2+在沉积物上吸附行为的影响

以Cd2+为重金属代表,阴离子表面活性剂十二烷基苯磺酸钠(SDBS)、阳离子表面活性剂氯化十六烷基吡啶(CPC)、非离子表面活性剂辛基酚聚氧乙烯醚(TX-100)为表面活性剂代表,用实验模拟法研究了3种类型的表面活性剂对Cd2+在沉积物上吸附行为的影响.结果表明,不同种类的表面活性剂对Cd2+在沉积物上的吸附影响不同,SDBS对Cd2+的吸附影响可分为2个阶段,当SDBS初始质量浓度从0 mg/L增加到2 600 mg/L,Cd2+的吸附量从1.52 mg/g增至1.88 mg/g,增加了23.7%,随着SDBS初始浓度继续增加,Cd2+的吸附量开始下降,当SDBS初始质量浓度增至16 000 mg/L,Cd2+的吸附量降低至0.34 mg/g;CPC主要通过在溶液中电离出CP+,CP+与Cd2+竞争沉积物表面的吸附位从而抑制Cd2+的吸附,当CPC初始质量浓度从0 mg/L增加至16 000 mg/L,Cd2+的吸附量从1.50 mg/g降低至0.52 mg/g;TX-100能轻微抑制Cd2+在沉积物上的吸附,当TX-100初始质量浓度从0 mg/L增加到16 000 mg/L时,Cd2+吸附量从1.52 mg/g减少至1.35 mg/g.     

溶藻细菌L8的溶藻活性代谢产物对水华鱼腥藻光合特性的影响研究

从广州城区某富营养化池塘筛选出1株溶藻细菌L8(简称L8菌),研究了L8菌的溶藻活性代谢产物(简称L8菌溶藻产物)对水华鱼腥藻(Anabaena flos-aquae)光合特性的影响。结果表明,L8菌溶藻产物能够使水华鱼腥藻中的类胡萝卜素、藻蓝蛋白和别藻蓝蛋白的含量显著升高,经L8菌溶藻产物作用7d后,3者分别升高了35.7%、63.2%和185.7%,而叶绿素a含量下降了51.3%;经L8菌溶藻产物作用7d后,水华鱼腥藻的光系统Ⅱ(PSⅡ)的光化学效率、潜在活性以及光合电子产量均明显降低。低温(77K)荧光发射光谱的变化表明,光合色素相对含量的变化导致光能在水华鱼腥藻2个光系统之间的分配发生了变化,影响了光能在光系统Ⅰ(PSⅠ)、PSⅡ中的分配,进而影响了水华鱼腥藻的光合作用效率。     

Sources and fate of PCDD and PCDF

PCDD and PCDF were found in urban air particulates from St. Louis and Washington, D.C., and in sediments from the Great Lakes and Siskiwit Lake, Isle Royale. The similarity between the PCDD and PCDF found in air particulates and sediment samples and the presence of PCDD and PCDF in sediment from Siskiwit Lake (a location which can receive only atmospheric inputs) suggest that these compounds are emitted to the atmosphere from combustion sources. The historical input of PCDD and PCDF to dated sediment cores shows a strong increase since 1940, and this suggests that the incineration of chlorinated organic compounds is an important source of PCDD and PCDF to the environment.     

Meta-analysis of time-series studies of air pollution and mortality: effects of gases and particles and the influence of cause of death,age, and season

A comprehensive, systematic synthesis was conducted of daily time-series studies of air pollution and mortality from around the world. Estimates of effect sizes were extracted from 109 studies, from single- and multipollutant models, and by cause of death, age, and season. Random effects pooled estimates of excess all-cause mortality (single-pollutant models) associated with a change in pollutant concentration equal to the mean value among a representative group of cities were 2.0% (95% CI 1.5-2.4%) per 31.3 microg/m3 particulate matter (PM) of median diameter < or = 10 microm (PM10); 1.7% (1.2-2.2%) per 1.1 ppm CO; 2.8% (2.1-3.5%) per 24.0 ppb NO2; 1.6% (1.1-2.0%) per 31.2 ppb O3; and 0.9% (0.7-1.2%) per 9.4 ppb SO2 (daily maximum concentration for O3, daily average for others). Effect sizes were generally reduced in multipollutant models, but remained significantly different from zero for PM10 and SO2. Larger effect sizes were observed for respiratory mortality for all pollutants except O3. Heterogeneity among studies was partially accounted for by differences in variability of pollutant concentrations, and results were robust to alternative approaches to selecting estimates from the pool of available candidates. This synthesis leaves little doubt that acute air pollution exposure is a significant contributor to mortality.     

Meta-Analysis of Time-Series Studies of Air Pollution and Mortality: Effects of Gases and Particles and the Influence of Cause of Death,Age, and Season

Abstract

A comprehensive, systematic synthesis was conducted of daily time-series studies of air pollution and mortality from around the world. Estimates of effect sizes were extracted from 109 studies, from single- and multipollutant models, and by cause of death, age, and season. Random effects pooled estimates of excess all-cause mortality (single-pollutant models) associated with a change in pollutant concentration equal to the mean value among a representative group of cities were 2.0% (95% CI 1.5-2.4%) per 31.3 μg/m³ particulate matter (PM) of median diameter <10 μm (PM₁₀); 1.7% (1.2-2.2%) per 1.1 ppm CO; 2.8% (2.1-3.5%) per 24.0 ppb NO₂; 1.6% (1.1-2.0%) per 31.2 ppb O₃; and 0.9% (0.7-1.2%) per 9.4 ppb SO₂ (daily maximum concentration for O₃, daily average for others). Effect sizes were generally reduced in multipollutant models, but remained significantly different from zero for PM₁₀ and SO₂. Larger effect sizes were observed for respiratory mortality for all pollutants except O₃. Heterogeneity among studies was partially accounted for by differences in variability of pollutant concentrations, and results were robust to alternative approaches to selecting estimates from the pool of available candidates. This synthesis leaves little doubt that acute air pollution exposure is a significant contributor to mortality.     

Field and laboratory studies of the fate and enantiomeric enrichment of venlafaxine and O-desmethylvenlafaxine under aerobic and anaerobic conditions

The stereoselectivity of R,S-venlafaxine and its metabolites R,S-O-desmethylvenlafaxine, N-desmethylvenlafaxine, O,N-didesmethylvenlafaxine, N,N-didesmethylvenlafaxine and tridesmethylvenlafaxine was studied in three processes: (i) anaerobic and aerobic laboratory scale tests; (ii) six wastewater treatment plants (WWTPs) operating under different conditions; and (iii) a variety of wastewater treatments including conventional activated sludge, natural attenuation along a receiving river stream and storage in operational and seasonal reservoirs. In the laboratory and field studies, the degradation of the venlafaxine yielded O-desmethylvenalfaxine as the dominant metabolite under aerobic and anaerobic conditions. Venlafaxine was almost exclusively converted to O-desmethylvenlafaxine under anaerobic conditions, but only a fraction of the drug was transformed to O-desmethylvenlafaxine under aerobic conditions. Degradation of venlafaxine involved only small stereoisomeric selectivity. In contrast, the degradation of O-desmethylvenlafaxine yielded remarkable S to R enrichment under aerobic conditions but none under anaerobic conditions. Determination of venlafaxine and its metabolites in the WWTPs agreed well with the stereoselectivity observed in the laboratory studies. Our results suggest that the levels of the drug and its metabolites and the stereoisomeric enrichment of the metabolite and its parent drug can be used for source tracking and for discrimination between domestic and nondomestic wastewater pollution. This was indeed demonstrated in the investigations carried out at the Jerusalem WWTP.     

Sorption and desorption of Cu and Cd by macroalgae and microalgae

The sorption and desorption of Cu and Cd by two species of brown macroalgae and five species of microalgae were studied. The two brown macroalgae, Laminaria japonica and Sargassum kjellmanianum, were found to have high capacities at pHs between 4.0 and 5.0 while for microalgae, optimum pH lay at 6.7. The presence of other cations in solution was found to reduce the sorption of the target cation, suggesting a competition for sorption sites on organisms. Sorption isotherms obeyed the Freundlich equation, suggesting involvement of a multiplicity of mechanisms and sorption sites. For the microalgae tested, Spirulina platensis had the highest capacity for Cd, followed by Nannochloropsis oculata, Phaeodactylum tricornutum, Platymonas cordifolia and Chaetoceros minutissimus. The reversibility of metal sorption by macroalgae was examined and the results show that both HCl and EDTA solutions were very effective in desorbing sorbed metal ions from macroalgae, with up to 99.5% of metals being recovered. The regenerated biomass showed undiminished sorption performance for the two metals studied, suggesting the potential of such material for use in water and wastewater treatment.     

骆马湖富营养化和生态状况调查与评价

为了了解骆马湖水质状况，在2005年对骆马湖富营养化状态和生态特性进行了调查，并结合“十五”期间的监测资料进行了分析。2005年骆马湖水体中总氮和总磷的平均值超《地表水环境质量标准》（GB3838-2002）中Ⅲ类，超标情况分别为0．78倍和0．54倍，达到湖库特定项目Ⅳ类水标准，骆马湖处于轻度富营养化状态。对骆马湖生态特征分析表明，由于该湖泊的形态以及“藻型浊水状态”和“泥沙型浊水状态”交替出现，遏制了湖水从高营养盐含量向全面富营养化状态演变，保障了底栖动物的良好生长环境，从而形成了骆马湖独特的环境生态平衡。     

Sources and distribution of polychlorinated-dibenzo-p-dioxins and -dibenzofurans in soil and sediment from the Yellow Sea region of China and Korea

Polychlorinated-dibenzo-p-dioxins and -dibenzofurans (PCDD/Fs) were measured in soils and sediments from the Yellow Sea region. Korean soils and sediments mostly contained detectable PCDD/Fs and showed a widespread distribution among locations. Soil and sedimentary PCDD/Fs from China were comparable to or less than those in Korea. The patterns of relative concentrations of individual congeners in soils were different between the two countries, but similar in sediments. Sources of PCDD/Fs in China and Korea were found to be independent of each other and their distributions reflected matrix-dependent accumulation. Spatial distribution indicated some point sources in Korea while Chinese sources were more widespread and diffuse. PCDD/Fs measured in the coastal areas of the Yellow Sea were comparable to or less than those previously reported in for eastern Asia. However, ∑TEQs in soils and sediments were near to or, in some cases exceeded environmental quality guidelines.     

Aerobic and anaerobic degradation of profluralin and trifluralin

Abstract

The degradation of profluralin [N‐(cyclopropylmethyl)‐α,α,α‐trifluoro‐2,6‐dinitro‐N‐propyl‐]p‐toluidine] and trifluralin (α,α,α‐trifluoro‐2,6‐dinitro‐N,N‐dipropyl‐p‐toluidine) was studied under aerobic and anaerobic soil conditions. Three soils (Goldsboro loamy sand, Cecil loamy sand, Drummer clay loam) were each treated with 1 ppmw herbicide; anaerobic conditions were maintained by flooding. Soil samples were extracted monthly and subjected to TLC analysis. No degradation was detected in sterile controls. Aerobic degradation of both herbicides was greatest in the Cecil loamy sand soil over the entire incubation period. Degradation of profluralin in Cecil soil under aerobic conditions was 86 percent after 4 months with three products detected; 83 percent of the trifluralin was degraded with two products detected. Anaerobic degradation accounted for 72 percent of the profluralin and 78 percent of the trifluralin after 4 months. Degradation of both herbicides increased with incubation time for the first 3 months and decreased slightly thereafter. Generally there was more extensive degradation (percent and in number of products formed) of profluralin than trifluralin under the conditions tested. More degradation products were detected for both herbicides under aerobic conditions than under anaerobic conditions.     

Copper-catalyzed chlorination and condensation of acetylene and dichloroacetylene

The chlorination and condensation of acetylene at low temperatures is demonstrated using copper chlorides as chlorinated agents coated to model borosilicate surfaces. Experiments with and without both a chlorine source and borosilicate surfaces indicate the absence of gas-phase and gas-surface reactions. Chlorination and condensation occur only in the presence of the copper catalyst. C₂ through C₈ organic products were observed in the effluent; PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed that is consistent with the observed product distributions. Similar experiments with dichloroacetylene indicate greater reactivity in the absence of the copper catalyst. Reaction is observed in the gas-phase and in the presence of borosilicate surfaces at low temperatures. The formation of hexachlorobenzene is only observed in the presence of a copper catalyst. PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed for the formation of hexachlorobenzene from dichloroacetylene.