林丹、毒死蜱对淡水藻类毒性效应的比较研究

有机氯和有机磷农药是全球应用最广泛的两大类农药,以有机氯农药林丹以及有机磷农药毒死蜱为研究对象,比较了它们对长江中下游常见的3种淡水藻类包括铜绿微囊藻(Microcystis aeruginosa)、普通小球藻(Chlorella vulgaris)和梅尼小环藻(Cyclotella meneghiniana)的毒性效应。通过藻类生长抑制试验测定了林丹和毒死蜱对藻类的毒性效应,结果表明,林丹和毒死蜱对3种藻的生长存在不同程度的抑制效应,且质量浓度越高,抑制效应越强,其中低质量浓度的毒死蜱对铜绿微囊藻和普通小球藻具有一定的促进作用。实验还获得了两种农药对3种不同藻类的急慢性毒性数据,以96 h生物量计,林丹对铜绿微囊藻的EC50=442μg·L-1,LOEC=120μg·L-1,NOEC=60μg·L-1,MATC=85μg·L-1;对普通小球藻的EC50=524μg·L-1,LOEC=128μg·L-1,NOEC=61μg·L-1,MATC=88μg·L-1;对梅尼小环藻的EC50=11 849μg·L-1,LOEC=1 295μg·L-1,NOEC=406μg·L-1,MATC=725μg·L-1。毒死蜱对铜绿微囊藻的EC50=2 720μg·L-1,LOEC=1 026μg·L-1,NOEC=615μg·L-1,MATC=794μg·L-1;对普通小球藻的EC50=5 374μg·L-1,LOEC=1 978μg·L-1,NOEC=1 172μg·L-1,MATC=1 522μg·L-1;对梅尼小环藻的EC50=11 109μg·L-1,LOEC=2 792μg·L-1,NOEC=1 355μg·L-1,MATC=1 945μg·L-1。结果表明,林丹和毒死蜱对3种藻的生长存在不同程度的抑制效应。毒性数据显示相比于梅尼小环藻,铜绿微囊藻和普通小球藻对两种农药更为敏感。     

Cu2+和Cd2+对日本青鳉（Oryzias latipes）早期发育阶段的急性毒性效应研究

为探究并比较淡水鱼种日本青鳉早期发育阶段对Cu2和Cd2等重金属胁迫的响应,在实验室通过半静态方式,对日本青鳉受精卵和仔稚鱼分别进行了48 h和96 h急性毒性实验.结果表明:Cu2对日本青鳉胚胎24、48 h-LC50分别为8.164 mg·L-1和6.965 mg·L-1;Cd2+对日本青鳝胚胎24、48 h-LC50分别为63.084 mg· L-1和53.093 mg ·L-1;较低浓度组Cu2+(≤1.97 mg ·L-1)时日本青鳉胚胎的发育速率快于对照组,而较高浓度组(≥3.87 mg·L-1)胚胎的发育速率则慢于对照组;与Cu2略有不同,无论浓度高低Cd2对胚胎的孵化速率均产生抑制作用;Cu2+和Cd2质量浓度分别高于1.97 mg·Lq和19.68 mg· L-1时,两种重金属离子均显著降低胚胎的孵化率(P＜0.05).Cu2对日本青鳉初孵仔鱼24、48、72和96 h-LC50分别为5361 mg·L-1、2.844 mg·L-1、2.020 mg·L-1和1352 mg·L-1;Cd2+对日本青鳉初孵仔鱼24、48、72和96 h-LC50分别为15.907 mg·L-1、10550 mg·L-1、7.986 mg· L-1和6346 mg·L-1;Cu2+对日本青鳉稚鱼24、48、72和96 h-LC50分别为5.732 mg·L-1、4.037 mg· L-1、2A98 mg·L-1和1.955 mg·L-1;Cd2+对日本青鳉稚鱼的24、48、72和96 h-LC50分别为16A19 mg·L、11.745 mg· L-1、8516 mg·L-1和6.776 mg· L-1.与其它淡水水生生物相比,日本青鳉仔稚鱼对铜和镉离子较为敏感.     

2种杀虫剂对日本沼虾的急性毒性

研究了毒死蜱和硫丹对日本沼虾(Macrobrachium nipponense)的毒性作用.根据预试验确定2种杀虫剂对日本沼虾的急性毒性试验浓度,测定沼虾24和48 h的半致死浓度p(LC50),在0～48 h的ρ(LC50)值范围内设定6个浓度梯度,对日本沼虾进行24 h胁迫试验以测定耗氧量和排氨量.毒死蜱和硫丹对日本沼虾的24和48 hρ(LC50)分别为5.03、2.01和8.47、4.02 μg·L-1,其安全质量浓度分别为0.096和0.272 μg·L-1,表明日本沼虾对毒死蜱的敏感性明显高于硫丹.随着2种杀虫剂浓度的逐渐升高,日本沼虾的耗氧量和排氨量均呈现下降趋势,表明日本沼虾采用相同的适应方式来抵御2种杀虫剂对其基础代谢的胁迫,表现为被动的忍耐.     

超高压工程电缆绝缘油对海洋生物的生态毒性效应

随着超高压联网工程建设项目不断增多,取得巨大经济效益的同时,其电缆安全性日益受到关注。采用标准实验方法,研究电缆绝缘油对8种占据不同生态位的海洋生物(费氏弧菌(Vibrio fischeri)、牟氏角毛藻(Chaetoceros mueleri)、卤虫(Artemia sp.)、蒙古裸腹溞(Moina mongolica)、凡纳滨对虾(Litopenaeus vannamei)、裸项栉鰕虎鱼(Ctenogobius gymnauchen)、双齿围沙蚕(Perinereis aibuhitensis)、菲律宾蛤仔(Ruditapes philippinarum))的急性毒性,同时进行了电缆绝缘油对裸项栉鰕虎鱼14 d延长毒性实验和电缆绝缘油对蒙古裸腹溞的慢性毒性。结果表明,电缆绝缘油在50%饱和溶解浓度下未对费氏弧菌产生明显的发光抑制作用;对牟氏角毛藻、凡纳滨对虾、裸项栉鰕虎鱼、双齿围沙蚕和菲律宾蛤仔等5种生物未表现出急性毒性影响,其LC50均大于饱和浓度;对卤虫的96 h-LC50为17.07%,LOEC为12.5%,NOEC为6.25%;对蒙古裸腹溞96 h-LC50为29.75%,LOEC为25.0%,NOEC为12.5%;电缆绝缘油对卤虫和蒙古裸腹溞有剧毒。对裸项栉鰕虎鱼成鱼14 d延长毒性LC50大于500 000 mg·L~(-1);对蒙古裸腹溞母溞存活数的NOEC为625μg·L~(-1),LOEC为1 250μg·L~(-1);对母溞存活期的NOEC为312μg·L~(-1),LOEC为625μg·L~(-1);对产胎数的NOEC为625μg·L~(-1),LOEC为1 250μg·L~(-1);对产幼溞数的NOEC为625μg·L~(-1),LOEC为1 250μg·L~(-1)。     

硝基苯对3种中国土著水生生物的毒性

以中国林蛙(Rana chensinensis)蝌蚪、中华圆田螺(Cipangopaludina cahayensis)和日本沼虾(Macrobrachiumnipponense)3种我国代表性土著生物为对象,通过半静态试验研究了硝基苯暴露对这3种生物的急性毒性.采用美国环境保护局(USEPA)的Trimmed Spearman-Karver(TSK)法得到硝基苯的急性毒性p(96 h,LC50分别为:林蛙蝌蚪,117.04 mg·L-1;中华圆田螺,104.23 mg·L-1;日本沼虾,0.033 7 mg·L-1.基于p(96 h,LC50)值,取0.01为安全系数,安全浓度ps,分别为:林蛙蝌蚪,1.17 mg·L-1;中华圆田螺,1.04 mg·L-1;日本沼虾,0.34 μg·L-1.3种受试生物对硝基苯毒性反应的敏感性大小依次为:日本沼虾＞中华圆田螺＞林蛙蝌蚪.对照鱼类急性毒性实验的毒性分级标准,硝基苯对日本沼虾属于剧毒物质,而对林蛙蝌蚪和中华圆田螺则属于中等毒性物质.     

纳米水稳型C60（nC60）促进Zn2+和Cr6+ 在大型溞体内的吸收、抗氧化性和急性毒性

富勒烯(C60)作为一种被广泛使用的纳米工程材料,其环境行为和所造成的毒效应越来越引起人们的关注,特别是其与重金属的联合毒性.文章选取模式生物大型溞研究纳米水稳型富勒烯(nC60)与Zn+和Cr6+的联合毒性.按EPA 2024急性毒性试验结果,nC60对大型溞48 h-LC50为0.47 mg·L-1,最大无观察效应浓度(NOEC)为0.10 mg·L-1.NOEC浓度选定为nC60亚急性试验浓度,用于联合毒性试验.nC60增强了Zn2+和Cr6+对大型溞的毒性,Zn2和Cr6+对大型溞48 h-LC50分别由2.33mg·L-1和0.40mg·L-1降低为1.52 mg·L-1和033 mg·L-1;nC60增加了大型溞对Zn2+和Cr6+的摄入,暴露1440 min后体内Zn2+和Cr6+累积量分别由6.52 μg·g-1湿重和1.52 μg·g-1湿重增加到9.98 μg ·g-1湿重和3.01 μg·g-1湿重;nC60和Zn2+和Cr6+联合作用于大型潘后,大型溞SOD酶活性均呈现出增强的诱导现象,联合作用时诱导作用强于两种物质单独作用.此研究表明:在亚急性浓度下,nC60增强了Zn2+和Cr6+对大型溞的毒性,提高了大型潘体内Zn2+和Cr6+的积累,并提高大型溞体内自由基活性.     

丙烯酰胺对大型溞(Daphnia magna)的急性和慢性毒性

丙烯酰胺对大型(Daphniamagna)的急性试验表明,丙烯酰胺对大型的24h LC50、48h LC50值分别为173.21和89.59mg·L-1。21d生活周期试验结果表明,大型的生殖指标是对该种化合物最为敏感的慢性毒性参数。丙烯酰胺对大型生殖的无可见效应浓度(NOEC)为1.56mg·L-1,最低可见效应浓度(LOEC)为3.13mg·L-1,并据此计算出该毒物的最大允许浓度(MATC)为2.47mg·L-1。     

辛硫磷和敌百虫协同抑制斑马鱼乙酰胆碱酯酶(AChE)活性

以辛硫磷和敌百虫为供试毒物,研究其对斑马鱼的单一和联合毒性效应。结果显示,辛硫磷和敌百虫对斑马鱼的96 h半致死浓度(96 h-LC_(50))值分别为6.482 mg·L~(-1)和27.877 mg·L~(-1);按照农药毒性分级标准,辛硫磷对斑马鱼是高毒,敌百虫对斑马鱼是中毒。在辛硫磷和敌百虫联合急性毒性实验中,24、48、72和96 h的相加指数均大于0,表明辛硫磷和敌百虫对斑马鱼的联合毒性为协同效应。采用生化法测定乙酰胆碱酯酶活性发现,乙酰胆碱酯酶活性与辛硫磷、敌百虫以及辛硫磷+敌百虫之间有显著的剂量-效应关系,而且联合作用毒性均大于单一作用毒性。     

萼花臂尾轮虫毒性试验的方法学研究

为尝试以群体取代个体作为轮虫室内毒性试验目标物的可行性,本项研究以萼花臂尾轮虫(Brachionus calyciflorus)作为实验生物开展相关实验,建立生命表并确定接种密度对于种群生长率的影响,并且用3种农药(毒死蜱、丁草胺、三唑酮)开展了轮虫毒性试验。生命表实验结果表明,轮虫的平均寿命和世代周期分别为(78.76±33.08)h和(51.56±20.55)h。接种密度实验结果表明,随着接种密度的提高,轮虫种群增长率呈下降趋势。基于接种密度实验的结果,毒性试验以35个·(100 m L)-1作为受试种群的起始密度,试验周期定为144 h。毒性试验结果显示,毒死蜱对轮虫的96 h-EC50和120 h-EC50分别为0.6066 mg·L-1和0.7323mg·L-1;丁草胺对轮虫的96 h-EC50和120 h-EC50分别为1.851 mg·L-1和3.058 mg·L-1;三唑酮对轮虫的96 h-EC50和120 h-EC50分别为12.84 mg·L-1和11.63 mg·L-1。本项研究的结果肯定了以群体取代个体作为轮虫室内毒性试验目标物的可行性。     

纳米二氧化钛(nTiO_2)与双酚A对斜生栅藻(Scenedes-mus obliquus)的联合毒性效应

纳米二氧化钛(n Ti O2)在被人们广泛使用的同时,其潜在的环境影响也受到越来越多的关注。为深入探讨n Ti O2与环境中现有污染物的相互作用及生物效应,以斜生栅藻(Scenedesmus obliquus)为受试生物,按照毒性单位法、相加指数法和混合毒性指数法,研究了n Ti O2与双酚A(BPA,一种常见的环境类雌激素)的联合毒性效应。结果显示,n Ti O2与BPA对S.obliquus生长的72 h半抑制浓度(EC50)分别为28.7 mg·L-1与1.81 mg·L-1。而n Ti O2与BPA共存时,在不同毒性比(4:1,3:1,2:1,1:1,1:2和1:3)下,其联合毒性作用(以BPA计)的72 h EC50值分别为2.198,1.58,1.153,0.428,0.306和0.189 mg·L-1。两者的联合毒性作用不仅仅是简单的相加,而是随着两者毒性比的变化,由拮抗作用转变为相加作用,继而转变为协同作用。这表明,n Ti O2进入环境后与现有污染物的毒性比(浓度比)可能是其联合毒性作用模式的一个重要影响因素。     

Catalytic ozonation of organic compounds in water over the catalyst of RuO2/ZrO2-CeO2

This research investigates the performances of RuO₂/ZrO₂-CeO₂ in catalytic ozonation for water treatment. The results show that RuO₂/ZrO₂-CeO₂ was active for the catalytic ozonation of oxalic acid and possessed higher stability than RuO₂/Al₂O₃ and Ru/AC. In the catalytic ozonation of dimethyl phthalate (DMP), RuO₂/ZrO₂-CeO₂ did not enhance the DMP degradation rate but significantly improved the total organic carbon (TOC) removal rate. The TOC removal in catalytic ozonation was 56% more than that in noncatalytic ozonation. However this does not mean the catalyst was very active because the contribution of catalysis to the overall TOC removal was only 30%. The adsorption of the intermediates on RuO₂/ZrO₂-CeO₂ played an important role on the overall TOC removal while the adsorption of DMP on it was negligible. This adsorption difference was due to their different ozonation rates. In the catalytic ozonation of disinfection byproduct precursors with RuO₂/ZrO₂-CeO₂, the reductions of the haloacetic acid and trihalomethane formation potentials (HAAFPs and THMFPs) for the natural water samples were 38%–57% and 50%–64%, respectively. The catalyst significantly promoted the reduction of HAAFPs but insignificantly improved the reduction of THMFPs as ozone reacts fast with the THMs precursors. These results illustrate the good promise of RuO₂/ZrO₂-CeO₂ in catalytic ozonation for water treatment.     

One-pot hydrothermal fabrication of BiVO4/Fe3O4/rGO composite photocatalyst for the simulated solar light-driven degradation of Rhodamine B

• BiVO₄/Fe₃O₄/rGO has excellent photocatalytic activity under solar light radiation. • It can be easily separated and collected from water in an external magnetic field. • BiVO₄/Fe₃O₄/0.5% rGO exhibited the highest RhB removal efficiency of over 99%. • Hole (h⁺) and superoxide radical (O₂^•−) dominate RhB photo-decomposition process. • The reusability of this composite was confirmed by five successive recycling runs. Fabrication of easily recyclable photocatalyst with excellent photocatalytic activity for degradation of organic pollutants in wastewater is highly desirable for practical application. In this study, a novel ternary magnetic photocatalyst BiVO₄/Fe₃O₄/reduced graphene oxide (BiVO₄/Fe₃O₄/rGO) was synthesized via a facile hydrothermal strategy. The BiVO₄/Fe₃O₄ with 0.5 wt% of rGO (BiVO₄/Fe₃O₄/0.5% rGO) exhibited superior activity, degrading greater than 99% Rhodamine B (RhB) after 120 min solar light radiation. The surface morphology and chemical composition of BiVO₄/Fe₃O₄/rGO were studied by scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, UV–visible diffuse reflectance spectroscopy, Fourier transform infrared spectroscopy, and Raman spectroscopy. The free radicals scavenging experiments demonstrated that hole (h⁺) and superoxide radical (O₂^•−) were the dominant species for RhB degradation over BiVO₄/Fe₃O₄/rGO under solar light. The reusability of this composite catalyst was also investigated after five successive runs under an external magnetic field. The BiVO₄/Fe₃O₄/rGO composite was easily separated, and the recycled catalyst retained high photocatalytic activity. This study demonstrates that catalyst BiVO₄/Fe₃O₄/rGO possessed high dye removal efficiency in water treatment with excellent recyclability from water after use. The current study provides a possibility for more practical and sustainable photocatalytic process.     

Combined effects of selenium/mercury and selenium/copper on the cell population of the alga Dunaliella minuta

The type of interaction of selenium and mercury, and selenium and copper on the cell growth of the planktonic alga Dunaliella minuta Lerche has been studied. The results for the various selenium/mercury and selenium/copper ratios showed that: (a) although mercury and selenium inhibited the growth of D. minuta when added to its cultures separately at levels greater than their respective threshold concentrations, they had antagonistic effects towards each other when added simulataneously at the beginning of growth; prior exposure of the culture to either metal for 2 d did not alter this antagonistic action; (b) similar antagonism was observed in combinations of selenium and copper for cultures with and without prior exposure to either metal. The reasons for the Se/Hg and Se/Cu antagonism are unknown; several hypotheses concerning possible detoxification mechanisms are proposed.     

Fe-C-H_2O_2协同催化氧化处理印染废水

用Fe-C-H2O2协同催化氧化体系对印染工业废水的降解脱色处理进行了研究。对影响印染废水降解的几种因素如铁屑/碳粒质量比、双氧水的质量分数、废水pH等进行考察。试验结果表明,对于色度为650度和ρ（COD）为468mg·L-1的印染废水,在废水pH=4.8的情况下,当铁屑/碳粒质量比为25∶1、H2O2用量为150mg·L-1、催化反应30min时,印染废水的脱色率达98%以上,CODCr去除率可达78%。与Fe-C微电解法相比,Fe-C-H2O2协同催化氧化方法对印染废水的脱色能力和去除COD,表现出了更好的处理效果。     

Computer simulation applied to the biological control of the insect Aphis gossypii for the parasitoid Lysiphlebus testaceipes

In integrated pest management (IPM), biological control is one of the possible options for the prevention or remediation of an unacceptable pest activity or damage. The success of forecast models in IPM depends, among other factors, on the knowledge of temperature effect over pests and its natural enemies. In this work, we simulated the effects of parasitism of Lysiphlebus testaceipes (Cresson, 1880) (Hymenoptera: Aphidiidae) on Aphis gossypii (Glover, 1877) (Hemiptera: Aphididae), a pest that is associated to crops of great economic importance in several parts of the world. We made use of experimental data relative to the host and its parasitoid at different temperatures. Age structure was incorporated into the dynamics through the Penna model. The results obtained showed that simulation, as a forecast model, can be a useful tool for biological control programs.     

纳米二氧化铈对蛋白核小球藻的生物学效应研究

纳米二氧化铈(CeO_2)在被广泛使用的同时,其潜在的环境效应也受到人们越来越多的关注。以蛋白核小球藻(Chlorella pyrenoidosa)为实验材料,研究纳米CeO_2的生物学效应,为探索纳米材料对微藻的生物学效应提供理论基础和数据支持。研究结果显示:1)纳米CeO_2在低浓度(≤80 mg·L~(-1))时可促进蛋白核小球藻的生长及色素、可溶性蛋白等的合成,但在高浓度(80 mg·L~(-1))下具有毒性效应;2)低浓度纳米CeO_2可诱导藻细胞合成超氧化物歧化酶(superoxide dismutase,SOD)等可溶性蛋白,以抵御纳米CeO_2的胁迫;但在高浓度时又会降低SOD活力;3)随着纳米CeO_2浓度的升高,藻细胞中丙二醛(malondialdehyde,MDA)含量显著增加,说明藻细胞中活性氧自由基(reactive oxygen species,ROS)过量积累,这将破坏藻细胞的膜结构与功能,使细胞遭受严重损伤。     

Crushing predation of the spiny star Marthasterias glacialis upon the sea urchin Paracentrotus lividus

Literature data report that only fish predators are able to crush sea urchin tests in Mediterranean rocky reefs. This experimental study showed that the spiny star Marthasterias glacialis is able to break Paracentrotus lividus tests and that the breaking event is more likely to occur for small-sized sea urchins than for big ones. Our results show that the role of M. glacialis in regulating P. lividus population density can be important in specific locations. They may have important implications, moreover, for the use of tethering techniques aimed at identifying predator types of sea urchins.     

响应面法优化O_3/H_2O_2/UV工艺降解1,2,4-三氯苯

研究了O3/H2O2/UV臭氧光催化工艺对水中TCB的降解效果,考察了TCB初始浓度、O3转化率、H2O2投加量及pH值对TCB降解效果的影响及其动力学分析,并通过响应面分析法对实验条件进行了优化组合.结果表明,O3/H2O2/UV对TCB的降解均遵循准一级反应动力学,其中条件优化组合后的反应动力学方程为y=0.0219x-0.0127,准一级反应速率常数为0.0219 min-1,所得线性相关系数为0.983.响应面分析结果表明,在TCB初始浓度0.3 mg.L-1、pH=10.1、H2O2投加量0.33 mmol.L-1、O3转化率99.75%的最优工艺组合条件下,TCB的3次平均去除率为94.2%,与预测值95.0%吻合度较高.     

Effect of short-term atrazine addition on the performance of an anaerobic/anoxic/oxic process

In this study, an anaerobic/anoxic/oxic (A²O) wastewater treatment process was implemented to treat domestic wastewater with short-term atrazine addition. The results provided an evaluation on the effects of an accidental pollution on the operation of a wastewater treatment plant (WWTP) in relation to Chemical Oxygen Demand (COD) and biological nutrient removal. Domestic wastewater with atrazine addition in 3 continuous days was treated when steady biological nutrient removal was achieved in the A²O process. The concentrations of atrazine were 15, 10, and 5 mg·L^?1 on days 1, 2 and 3, respectively. The results showed that atrazine addition did not affect the removal of COD. The specific NH₄ ⁺ oxidation rate and NO₃ ^? reduction rate decreased slightly due to the short-term atrazine addition. However, it did not affect the nitrogen removal due to the high nitrification and denitrification capacity of the system. Total nitrogen (TN) removal was steady, and more than 70% was removed during the period studied. The phosphorus removal rate was not affected by the short-term addition of atrazine under the applied experimental conditions. However, more poly-hydroxy-alkanoate (PHA) was generated and utilized during atrazine addition. The results of the oxygen uptake rate (OUR) showed that the respiration of nitrifiers decreased significantly, while the activity of carbon utilizers had no obvious change with the atrazine addition. Atrazine was not removed with the A²O process, even via absorption by the activated sludge in the process of the short-term addition of atrazine.