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1.
双酚A及其类似物对斑马鱼胚胎及幼鱼的毒性效应   总被引:1,自引:0,他引:1  
为探讨双酚A及其类似物对鱼类早期生长发育的毒性效应,研究了双酚A及其7种类似物对斑马鱼胚胎及仔鱼的毒性效应。通过对胚胎的孵化率、心率、仔鱼体长等指标进行测定分析,结果显示:(1)双酚A及其7种类似物都可使斑马鱼胚胎出现心包水肿、卵黄囊肿、脊柱弯曲和尾部弯曲等症状。(2)综合考虑斑马鱼78 hpf胚胎心率、120 hpf胚胎孵化率及7 dpf仔鱼体长抑制率等指标,8种受试物中双酚P(BPP)的毒性最大,其次是双酚AP(BPAP)、双酚AF(BPAF)、双酚Z(BPZ),然后是双酚A(BPA)、双酚B(BPB)、双酚F(BPF),双酚S(BPS)的毒性最小,每种受试物的浓度与受精卵的孵化率、仔鱼心率呈明显负相关关系,与体长抑制率呈明显正相关关系。8种受试物毒性与辛醇-水分配系数(log K_(OW))呈正相关关系,log K_(OW)越大毒性则越大。  相似文献   
2.
以斑马鱼(Danio rerio)为研究对象,探讨铅(Pb)、得克隆(DP)及二者联合急性暴露对斑马鱼胚胎的神经毒性作用。结果表明,Pb(5、20μg·L~(-1))和DP(15、60μg·L~(-1))单独暴露均会引起斑马鱼自主运动频率增加,触摸反应能力和自由游泳活力下降,并且抑制初级运动神经元的生长,加剧尾部细胞凋亡。但与20μg·L~(-1)Pb单独暴露相比,高剂量联合暴露(20μg·L~(-1)Pb+60μg·L~(-1)DP)使斑马鱼的自主运动频率显著降低(P0.05),触摸反应能力和自由游泳活力显著增强(P0.05),初级运动神经元轴突长度显著增加(P0.05),尾部细胞凋亡减少。与5μg·L~(-1)Pb单独暴露相比,低剂量联合暴露(5μg·L~(-1)Pb+15μg·L~(-1)DP)也显著减少斑马鱼尾部的细胞凋亡(P0.05)。上述结果表明,Pb或DP单独暴露对斑马鱼均可引起神经毒性作用;但二者联合暴露对斑马鱼自主运动、触摸反应以及自由游泳活力的影响则表现为拮抗作用。  相似文献   
3.
刘迎  胡燕  姜蕾  潘波  秦涵淳  林勇 《生态毒理学报》2014,9(6):1091-1096
为评价六种常见农药表面活性剂对水生生物的风险,采用斑马鱼胚胎发育技术,研究其对斑马鱼胚胎的致死效应和致畸效应.结果表明,NP-10、OP-10、农乳700、农乳602、农乳1602、宁乳33对斑马鱼胚胎的致死中浓度分别为16.44、21.13、55.86、8446、109.90、120.08 mg·L-1,其中NP-10对斑马鱼胚胎急性毒性最大,宁乳33毒性最低;随着染毒剂量的增加,斑马鱼胚胎孵化率逐渐降低,致畸率逐渐提高,六种表面活性剂显示出相似的趋势,处理浓度与胚胎孵化率(致畸率)之间存在剂量-效应关系;NP-10、OP-10、农乳700处理组均诱导斑马鱼胚胎出现躯干侧翻、游囊关闭、躯干弯曲症状;农乳602、农乳1602、宁乳33处理组出现躯干侧翻、游囊关闭症状.  相似文献   
4.
水体突发性重金属污染胁迫下斑马鱼的行为反应分析   总被引:3,自引:0,他引:3  
研究了斑马鱼在不同程度突发性的Zn2+和Cr6+胁迫下的行为反应,采用计算机视觉技术量化研究斑马鱼游动行为数据。结果表明,在Zn2+和Cr6+的突发性胁迫中,斑马鱼的行为反应快速且敏感,游动行为与污染物种类、质量浓度和暴露时间直接相关,并表现出比较相似的行为变化规律;随着胁迫程度的增加,斑马鱼游动速度的变化幅度增大,反应时间缩短,且其变化曲线符合生物行为的环境压力模型。斑马鱼的行为变化远远提前于生物的病理损伤或死亡,可利用斑马鱼暴露于污染物时的行为变化实现在线水体突发性重金属污染事故的监测预警。  相似文献   
5.
为初步探讨农药对海胆胚胎的急性毒性效应,以虾夷马粪海胆(Strongylocentyotus internedius)为实验材料,研究了8种常见农药--草甘膦(Glyphosate)、百草枯(Paraquat)、异菌脲(Iprodione)、代森锰锌(Mancozeb)、三唑醇(Triadimenol)、霜霉威(Propamocarb)、百菌清(Chlorothalonil)和速克灵(Procymidone)对海胆胚胎各发育期(二细胞期、四细胞期、上浮囊胚期、原肠期、棱柱幼体期、四腕幼虫期)的半数效应浓度(EC50),并分析了正辛醇/水分配系数(LogP)与EC50的关系.结果显示:1)8种农药对海胆胚胎各发育期均具有一定的急性毒性,以四腕幼虫期为例,8种农药的EC50值分别为草甘膦(3.99mg·L-1)>百草枯(10.38mg·L-1)>代森锰锌(20.77mg·L-1)>速克灵(55.42mg·L-1)>霜霉威(56.09mg·L-1)>异菌脲(86.29mg·L-1)>三唑醇(273.20mg·L-1)>百菌清(647.38mg·L-1).2)LogP与EC50呈现一定的正相关性,即随着LogP的增加,各农药对海胆胚胎的抑制率逐渐降低.  相似文献   
6.
本研究以稀有鮈鲫(Gobiocypris rarus)为对象,研究了不同浓度CdSe/ZnS量子点(QDs)暴露下,稀有鮈鲫胚胎发育过程中自主运动频率、内心率和体长的变化,以及利用体内超氧化物歧化酶(SOD)和丙二醛(MDA)作为毒性指标,反映CdSe/ZnS QDs暴露对稀有鮈鲫胚胎发育的氧化应激作用.结果显示:CdSe/ZnS QDs对稀有鮈鲫胚胎72 hpf(hours post fertilization)的半致死浓度(LC50)为319.629 nmol·L-1,96 hpf的半致畸浓度(EC50)为203.312 nmol·L-1.CdSe/ZnS QDs暴露不仅影响稀有鮈鲫胚胎死亡率、畸形率、自主运动频率、孵化时间和孵化率,而且使其内心率减缓、体长缩短,导致胚胎卵凝结,心包囊肿,出现脊椎弯曲等多种毒性现象.同时发现,CdSe/ZnS QDs暴露导致稀有鮈鲫体内MDA含量增加以及SOD活力的降低.这表明CdSe/ZnS QDs对稀有鮈鲫胚胎发育具有致畸、致死作用,而氧化应激可能是引起其胚胎致畸、致死的重要机制之一.  相似文献   
7.
In recent years, with the wide applications and mineral exploitation of rare earth elements, their potential environmental and health effects have caused increasing public concern. Effect of rare earth elements La and Yb on the morphological and functional development of zebrafish embryos were studied. The embryos were exposed to La3+ or Yb3+ at 0, 0.01, 0.1, 0.3, 0.5 and 1.0 mmol/L, respectively. Early life stage parameters such as egg and embryo mortality, gastrula development, tail detachment, eyes, somite formation, circulatory system, pigmentation, malformations, hatching rate, length of larvae and mortality were investigated. The results showed La3+ and Yb3+ delayed zebrafish embryo and larval development, decreased survival and hatching rates, and caused tail malformation in a concentration-dependent way. Moreover, heavy rare-earth ytterbium led to more severe acute toxicity of zebrafish embryo than light rare-earth lanthanum.  相似文献   
8.
Organic solvents, such as dimethylsulfoxide (DMSO) and methanol are widely used as vehicles to solubilise lipophilic test compounds in toxicity testing. However, the effects of such solvents upon innate detoxification processes in aquatic organisms are poorly understood. This study assessed the effect of solvent exposure upon cytochrome P450 (CYP)-mediated xenobiotic metabolism in Daphnia magna and zebrafish larvae (4 d post fertilisation). Adult D. magna were demonstrated to have a low, but detectable, metabolism of ethoxyresorufin in vivo and this activity was not modulated by pre-exposure to DMSO or methanol (24 h, up to 0.1% and 0.05% v/v, respectively). In contrast, the metabolism of ethoxyresorufin in zebrafish larvae was significantly reduced by both solvents (0.1% and 0.05% v/v, respectively) after 24 h of exposure. In zebrafish, these observed decreases in activity towards ethoxyresorufin were accompanied by decreased expression of a variety of genes coding for drug metabolising enzymes (corresponding to CYP1, CYP2, CYP3 and UDP-glucuronyl transferase [UGT] family enzymes), measured by quantitative PCR. Reduction of gene expression and CYP1 enzyme activities by methanol (0.05% v/v) in zebrafish larvae was partially reversed by co-exposure with Aroclor 1254 (100 μg L−1). Overall this study suggests that relatively low concentrations of organic solvents can impact upon the biotransformation of certain xenobiotics in zebrafish larvae, and that this warrants consideration when assessing compounds for metabolism and toxicity in this species.  相似文献   
9.
In the present investigation, hepatotoxic effect of a commercially available insecticide formulation of dicofol (Colonel–S® 18.5% emulsified concentrate) was studied in the developing chick embryo. Fertilized eggs of Gallus domesticus were immersed in three different dose concentrations, i.e. 250, 500, and 1000 mg L?1 of Colonel–S on “0” and fourth days of incubation for 60 min at 37 °C and incubated till embryonic day 16. Severe histopathological cellular lesions, such as extensive cell degeneration and necrosis with enlarged blood sinusoids, cytoplasmic vacuolization, and leucocyte infiltrations with congestion or dilation of central vein, appeared in dose-depended manner. Dicofol treatment also caused significant decrease in the levels of total protein, glycogen, and glutathione content and an increase in alkaline phosphatase activity of embryonic liver, whereas glutamic pyruvic transaminase activity showed mixed response.  相似文献   
10.
Actually, embryos can be cultured from the one‐cell stage up to the blastocyst stage, and their development can be easily monitored at any time: severe effects caused by toxic compounds are traduced by rapid embryonic death, less pronounced effects can be expressed by a lowered cleavage activity or by an arrest of the development from a particular stage. The system can be improved by transferring the embryos at the blastocyst stage in another more complete medium where they can “implant”; and form an inner cell mass with differentiated ectoderm and endoderm. Since last years, it has also become possible to culture postimplantation rodent embryos for short periods involving a number of particularly critical stages of organogenesis, such as the formation and closure of the anterior neuropore. Embryo‐culture also represents a useful system to study cytogenetic effects of chemicals which are often linked to lethal or teratogenic effects. These different possibilities are illustrated by examples of studies already performed with metals, and dealing with their teratogenic and/or cytogenetic effects on pre‐ and postimplantation rodents.  相似文献   
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