根表铁膜对水稻铅吸收转运的影响

通过温室土壤盆栽试验研究不同生育期水稻根表铁膜形成对水稻吸收和转运Pb的影响。结果表明,两种水稻根表铁膜形成量(以DCB-Fe含量计)及铁膜中吸附的Pb量均随着生育期的延长而减少。水稻根表铁膜Fe含量与铁膜吸附的Pb量呈显著的正相关关系(r=0.798,p0.01)。水稻根系和茎叶吸收积累Pb随着不同品种和不同生育期而变化。品种NK57籽粒Pb含量显著高于品种YD6,前者为后者的1.9倍。从富集系数和分配比率来看,Pb主要富集在水稻的铁膜和根系中,而积累在茎叶和籽粒中的比率较少。Pb从水稻根表铁膜、根系和茎叶向籽粒中的转运系数在两个水稻品种间差异均不显著。水稻分蘖期和孕穗期根表铁膜量与根系Pb含量均呈显著的正相关关系(p0.05),但是成熟期水稻根表铁膜量与根系、茎叶和籽粒中Pb含量相关性均不显著,说明根表铁膜形成对水稻分蘖期和孕穗期吸收积累Pb有一定影响,但对水稻成熟期根系、茎叶和籽粒吸收积累Pb影响不大。     

(N-[2-(2-氧-1-咪唑烷基)乙基]-N '-苯基脲(EDU)对环境臭氧胁迫下的水稻和小麦生长的影响

通过对作物定期喷施不同浓度(0、150、300和450 mg·L-1)的N-[2-(2-氧-1-咪唑烷基)乙基]-N'-苯基脲(ethy lenediurea,EDU)溶液,研究EDU对环境O3胁迫下水稻“粤晶丝苗2号”(Oryza sativa L.Yuejingsi 2)和小麦“北农9549”(Triticum a...     

水稻幼苗镉积累特征和离体叶片耐镉性的基因型差异

水稻根系对镉(Cd)的富集能力和向地上部的转运效率直接决定着水稻地上部的Cd积累量,是影响稻米中镉含量的关键因素。提高水稻根系对Cd的阻控能力有助于降低南方稻区大米镉含量超标的风险。以水稻核心种质资源中的高Cd积累品种‘齐头白谷’和低Cd积累品种‘27760’的幼苗和离体叶片为材料,对其Cd吸收转运特性和耐镉能力进行了比较研究。结果表明,根系细胞壁和原生质体的Cd吸收动力学特征都符合米氏方程,‘齐头白谷’的Cd最大吸收速率F_(max)显著大于‘27760’,Km值无显著差异。当根际环境中的Cd浓度高于0.89μmol·L~(-1)时,‘齐头白谷’的细胞壁和原生质体的Cd积累速率显著高于‘27760’。地上部细胞壁和原生质体的Cd吸收速率与根系可溶性组分中的Cd浓度呈显著的线性正相关。当根系可溶性组分中的Cd浓度相近时,‘齐头白谷’地上部细胞壁和原生质体的Cd积累速率显著高于‘27760’。在0.89~8.9μmol·L~(-1)的Cd溶液中,‘齐头白谷’离体叶片的失绿速度明显低于‘27760’。‘齐头白谷’具有耐Cd能力强、Cd积累速率快和转运效率高的特点。水稻离体叶片的耐Cd能力和幼苗根系的Cd积累能力以及幼苗的Cd转运能力高度相关,它们都可作为快速鉴定低Cd积累品种的生理指标。     

不同价态铬在不同水分条件下的生物有效性及其对水稻的毒性

氧化还原过程在铬的形态转化中起了重要作用,而铬形态的转化能够影响其生物有效性及毒性。通过温室土培试验研究了六价铬(Cr(Ⅵ))与三价铬(Cr(Ⅲ))在淹水与不淹水条件下在土壤溶液中的动态变化及水稻对其吸收的变化。结果表明,土壤中添加Cr(Ⅲ)时,土壤溶液中检测不出Cr;而随着土壤中添加Cr(Ⅵ)浓度的增加,土壤溶液中Cr(Ⅵ)的浓度增加,但是溶液中检测不出Cr(Ⅲ);淹水处理总体上降低了土壤溶液中Cr(Ⅵ)的浓度。而土壤添加Cr(Ⅲ)、Cr(Ⅵ)和水分处理对土壤溶液p H没有显著影响,p H在7.08.0之间变动。土壤添加Cr(Ⅵ)处理的水稻中,只有90 mg·kg-1Cr(Ⅵ)淹水处理的水稻成活,而其余处理水稻没有成活。土壤中添加Cr(Ⅲ)处理,水稻幼苗生物量随Cr(Ⅲ)浓度的增加而显著降低;除了200mg·kg-1Cr(Ⅲ)处理外,其余淹水处理的水稻幼苗生物量明显高于不淹水处理的。土壤添加Cr(Ⅲ)处理的水稻,在不淹水条件下水稻空壳率比较高,淹水条件下,随着土壤中添加Cr(Ⅲ)浓度水平的增加,水稻各部位Cr含量有增加的趋势,但增加不显著,秸秆最高Cr含量达到33.80 mg·kg-1,籽粒中Cr含量最高0.30 mg·kg-1。土壤固定Cr(Ⅲ)的能力远强于Cr(Ⅵ),添加Cr(Ⅵ)处理的土壤溶液中Cr(Ⅵ)的浓度很高,对水稻表现出较强的生长抑制。     

A multi-integrated approach on toxicity effects of engineered TiO2 nanoparticles

The new properties of engineered nanoparticles drive the need for new knowledge on the safety, fate, behavior and biologic effects of these particles on organisms and ecosystems. Titanium dioxide nanoparticles have been used extensively for a wide range of applications, e.g, self-cleaning surface coatings, solar cells, water treatment agents, topical sunscreens. Within this scenario increased environmental exposure can be expected but data on the ecotoxicological evaluation of nanoparticles are still scarce. The main purpose of this work was the evaluation of effects of TiO₂ nanoparticles in several organisms, covering different trophic levels, using a battery of aquatic assays. Using fish as a vertebrate model organism tissue histological and ultrastructural observations and the stress enzyme activity were also studied. TiO₂ nanoparticles (Aeroxide® P25), two phase composition of anatase (65%) and rutile (35%) with an average particle size value of 27.6±11 nm were used. Results on the EC₅₀ for the tested aquatic organisms showed toxicity for the bacteria, the algae and the crustacean, being the algae the most sensitive tested organism. The aquatic plant Lemna minor showed no effect on growth. The fish Carassius auratus showed no effect on a 21 day survival test, though at a biochemical level the cytosolic Glutathione-S-Transferase total activity, in intestines, showed a general significant decrease (p<0.05) after 14 days of exposure for all tested concentrations. The presence of TiO₂ nanoparticles aggregates were observed in the intestine lumen but their internalization by intestine cells could not be confirmed.     

根表铁锰膜对不同生育期水稻吸收和转运As的影响

采用土壤盆栽试验法,研究不同生育期水稻根表铁锰膜形成及其对As吸收和转运的影响。结果表明,两个水稻品种YD6和NK57均在分蘖期形成的铁锰膜量最多,成熟期形成的铁锰膜量最少。水稻根系和茎叶吸收积累As随着水稻不同品种和不同生育期变化较大,As的吸收和积累与铁锰膜形成存在相关性。与分蘖期相比,YD6和NK57成熟期根系As含量分别减少81.6%和62.1%。孕穗期YD6和NK57茎叶As含量分别比分蘖期减少86.4%和65.5%,比成熟期减少87.8%和67.1%。分蘖期水稻根系和茎叶As含量与DCB-Fe或DCB-Mn浓度均呈显著的负相关关系,而孕穗期水稻根系和茎叶As含量与DCB-Fe浓度呈显著的正相关关系,说明不同生育期铁锰膜对水稻植株吸收和转运As的影响不同。两个水稻品种不同生育期,As均主要富集和分配在根表铁锰膜中,铁锰膜中As的分配比率达62.9%～84.9%。NK57从根表铁锰膜、根系和茎叶向籽粒转运As的能力比YD6强,籽粒中As含量是YD6的2.1倍。结果表明可以通过选育As低积累和低转运的水稻品种,来降低污染地区As对人体健康的威胁。     

Influence of phosphate on deposition and detachment of TiO2 nanoparticles in soil

We examined influence of phosphate on transport of TiO₂ NPs in soil. Deposition was reduced at higher pH and by adsorption of phosphate in soil. Release was more for NPs initially deposited at higher pH. Release was more for NPs initially deposited in the presence of phosphate. Surface roughness and charge heterogeneity play a role in the deposition/ release. The widespread use of TiO₂ nanoparticles (NPs) makes inevitable their release into the soil. Phosphate is also widespread within soil, and is likely copresent with TiO₂ NPs. However, the influence of phosphate on deposition/release— and thereby on transport— of TiO₂ NPs in soil is yet to be elucidated. In this study we conducted saturated column experiments to systematically examine the transport of TiO₂ NPs in soil amended with phosphate at different ionic strengths (ISs) (1, 10, 100 mmol/L NaCl) and pHs (4 and 9). Results show that the deposition of TiO₂ NPs decreased with decreasing IS, increasing pH, and when soil absorbed phosphate. These observations are qualitatively in agreement with Derjaguin-Landau-Verwey-Overbeek (DLVO) interaction energy calculations, because the repulsive energy barrier is larger and secondary minimum depth is smaller at a lower IS, higher pH, and in the presence of phosphate. Accordingly, both primary- and secondary-minimum deposition were inhibited. Interestingly, although the deposition was less at higher pH and in the presence of phosphate, the subsequent spontaneous detachment and detachment by reduction of solution IS in these cases were greater. In addition, the presence of phosphate in the solution can cause a small quantity of attached TiO₂ NPs to detach, even without perturbations of physical and chemical conditions. Our study was the first to investigate the influence of phosphate on detachment of TiO₂ NPs and the results have important implication for accurate prediction of fate and transport of TiO₂ NPs in subsurface environments.     

Effects of iron oxide nanoparticles on phenotype and metabolite changes in hemp clones (Cannabis sativa L.)

● Fe₃O₄ NPs increased the biomass and chlorophyll content of hemp clones. ● Fe₃O₄ NPs penetrated and were internalized by root cells. ● Fe₃O₄ NPs induced the alteration of metabolite profiles in hemp leaves. ● The psychoactive compound THC in hemp leaves was significantly down-regulated. We investigated the effect of iron oxide nanoparticles (Fe₃O₄ NPs, ~17 nm in size) on the phenotype and metabolite changes in hemp (Cannabis sativa L.), an annual crop distributed worldwide. Hemp clones were grown in hydroponic cultures with Fe₃O₄ NPs (50, 100, 200, or 500 mg/L) for four weeks. TEM and ICP-MS were used to determine Fe₃O₄ NPs uptake and translocation. LC-MS-based metabolomics was employed to explore the deep insight into the effect of Fe₃O₄ NPs on hemp plants. The results revealed that plant growth enhanced gradually with increasing concentrations of given NPs up to 200 mg/L, which improved the fresh weight and dry weight by 36.13% and 74.68%, respectively, compared to the control. Even at a high dose (500 mg/L), Fe₃O₄ NPs promoted plant growth, including increased biomass and tissue length. NPs significantly increased the iron and chlorophyll content in plant tissues Increased catalase activity and reduced hydrogen peroxide content in hemp leaves suggested that the Fe₃O₄ NPs activated the defense system. TEM showed that NPs were abundantly attached to the cell wall and dispersed throughout the root cells. Metabolomics revealed that Fe₃O₄ NPs induced metabolic reprogramming in hemp leaves, including the up-regulation of carbohydrates and organic acids, and down-regulation of antioxidants, especially tetrahydrocannabinol (THC). The significantly up-regulated metabolites, including peonidin and 2-hydroxycinnamic acid, could be involved in photosynthesis in hemp plants. These results demonstrate the potential of Fe₃O₄ NPs for promoting hemp growth and decreasing the THC content at low doses.     

不同老化时间的TiO_2纳米颗粒对玉米生长的影响

为探讨老化时间对TiO_2纳米颗粒(nanoparticles,NPs)生物有效性的影响,研究了不同老化时间的Ti O_2NPs(0~120 d)对玉米幼苗生长的影响、在玉米体内的吸收及其在植株不同部位的存在位点等。研究发现,不同浓度的TiO_2NPs(1 000 mg·kg~(-1)和2 000 mg·kg~(-1))加入到土壤中,对玉米幼苗干鲜重没有明显的影响,但老化时间小于60 d时,对玉米幼苗株高有一定的抑制效应,老化60 d之后,随着老化时间的继续延长,毒性逐渐降低,最后趋于稳定。老化60 d时,TiO_2NPs处理的玉米幼苗根冠增大,玉米幼苗体内产生H2O_2的累积。在Ti O_2老化土壤中生长的玉米幼苗根系和地上部均有Ti的累积,1 000 mg·kg~(-1)的TiO_2NPs在玉米幼苗根部的生物累积系数达到35.4%,在地上部为13.6%,在玉米植株体内的转运系数为0.38;通过TEM观察,TiO_2NPs可以进入到玉米幼苗体内,并存在于根细胞的细胞质和叶绿体膜上,在叶片细胞的液泡和细胞核中也发现有TiO_2NPs的存在。上述研究结果为客观评价TiO_2NPs的生态风险提供了有用信息。     

Simultaneous removal of NOx and chlorobenzene on V2O5/TiO2 granular catalyst: Kinetic study and performance prediction

• A V₂O₅/TiO₂ granular catalyst for simultaneous removal of NO and chlorobenzene. • Catalyst synthesized by vanadyl acetylacetonate showed good activity and stability. • The kinetic model was established and the synergetic activity was predicted. • Both chlorobenzene oxidation and SCR of NO follow pseudo-first-order kinetics. • The work is of much value to design of multi-pollutants emission control system. The synergetic abatement of multi-pollutants is one of the development trends of flue gas pollution control technology, which is still in the initial stage and facing many challenges. We developed a V₂O₅/TiO₂ granular catalyst and established the kinetic model for the simultaneous removal of NO and chlorobenzene (i.e., an important precursor of dioxins). The granular catalyst synthesized using vanadyl acetylacetonate precursor showed good synergistic catalytic performance and stability. Although the SCR reaction of NO and the oxidation reaction of chlorobenzene mutually inhibited, the reaction order of each reaction was not considerably affected, and the pseudo-first-order reaction kinetics was still followed. The performance prediction of this work is of much value to the understanding and reasonable design of a catalytic system for multi-pollutants (i.e., NO and dioxins) emission control.     

碘铈共掺杂纳米TiO_2的制备及可见光光催化性能

采用溶胶凝胶法制备了不同原料比例碘铈共掺杂纳米TiO2催化剂,运用X射线光电子能谱（XPS）,X射线衍射（XRD）,透射电镜（TEM）等检测手段对催化剂进行了初步表征.结果表明,经过450℃煅烧处理得到的TiO2、铈掺杂TiO2以及碘铈共掺杂TiO2催化剂均为锐钛矿相,掺杂的Ce和I原子可能以I—Ce—O及O—Ti—I等键合方式进入TiO2晶格内部,此外,I-Ce离子共掺杂能有效降低TiO2表面的电子-空穴对的复合.以染料罗丹明B（Rhodamine B,RhB）和无色小分子水杨酸（Salicylic acid,SA）为降解的目标化合物,发现碘铈共掺杂的最佳物质的量之比为nCe∶nI∶nTi=0.04∶0.05∶1,即I0.05Ce0.04TiO2催化剂在可见光照射下（λ〉420 nm）降解目标化合物其光化学活性明显优于单掺铈的TiO2催化剂和未掺杂的TiO2.该催化反应涉及到空穴氧化,并伴有羟基自由基（.OH）、超氧自由基（O2.-）及H2O2等氧化物种的产生.     

Enhanced 4-chlorophenol biodegradation by integrating Fe2O3 nanoparticles into an anaerobic reactor: Long-term performance and underlying mechanism

• 4-chlorophenol biodegradation could be enhanced in Fe₂O₃ coupled anaerobic system. • Metabolic activity and electron transport could be improved by Fe₂O₃ nanoparticles. • Functional microbial communities could be enriched in coupled anaerobic system. • Possible synergistic mechanism involved in enhanced dechlorination was proposed. Fe₂O₃ nanoparticles have been reported to enhance the dechlorination performance of anaerobic systems, but the underlying mechanism has not been clarified. This study evaluated the technical feasibility, system stability, microbial biodiversity and the underlying mechanism involved in a Fe₂O₃ nanoparticle-coupled anaerobic system treating 4-chlorophenol (4-CP) wastewater. The results demonstrated that the 4-CP and total organic carbon (TOC) removal efficiencies in the Fe₂O₃-coupled up-flow anaerobic sludge blanket (UASB) were always higher than 97% and 90% during long-term operation, verifying the long-term stability of the Fe₂O₃-coupled UASB. The 4-CP and TOC removal efficiencies in the coupled UASB increased by 42.9±0.4% and 27.5±0.7% compared to the control UASB system. Adding Fe₂O₃ nanoparticles promoted the enrichment of species involved in dechlorination, fermentation, electron transfer and acetoclastic methanogenesis, and significantly enhanced the extracellular electron transfer ability, electron transport activity and conductivity of anaerobic sludge, leading to enhanced 4-CP biodegradation performance. A possible synergistic mechanism involved in enhanced anaerobic 4-CP biodegradation by Fe₂O₃ nanoparticles was proposed.     

砷污染土壤中不同基因型水稻根表铁膜的形成及其对砷吸收和转运影响

采用土壤盆栽试验法,研究6个不同基因型水稻品种根表铁膜形成及其对As吸收、转运的影响。结果表明,水稻形成根表铁膜在不同基因型品种之间差异显著（p<0.001）,其中品种94D-22形成铁膜量（以Fe含量计）是品种圭630的1.5~1.8倍,添加As处理对水稻根表铁膜形成影响不显著。低As含量的对照土壤中,水稻根表铁膜量与根系As含量存在着显著的正相关关系（r=0.657,n=24,p<0.01）,与As转移系数呈显著的负相关关系(r=-0.612,n=24,p<0.01）。土壤添加As后,水稻根表铁膜量与茎叶As含量存在显著的正相关关系（r=0.653-0.673,n=24,p<0.01）,与As转运之间无显著相关性。比较生长于As污染土壤的不同水稻品种,科优1360茎叶积累As较少,且其根系转运As能力也较差,而品种94D-22正好相反。研究结果表明,在As含量较低的土壤中,水稻根表铁膜的存在可成为根系As的障碍层,阻止As向地上部转运;但在As含量较高的土壤,根表铁膜的存在却促进了水稻茎叶对As的积累,其对As的转运没有显著影响。人们可通过作物品种筛选来防治土壤As污染危害、降低As对人体健康的威胁。     

二氧化钛纳米颗粒与重金属联合毒性研究进展

二氧化钛纳米颗粒(Ti O2-NPs)在广泛使用的同时也带来了潜在的环境污染、生态和健康风险。随着Ti O2-NPs的废弃量逐年上升,其与环境中重金属的联合毒性特别是对生态环境的影响逐渐引起国内外研究者重视。结合近几年国内外对二者相互作用的研究,重点综述Ti O2-NPs与铅(Pb)、镉(Cd)和砷(As)之间的联合毒性,并对存在的问题和今后的关注重点进行探讨。     

Photocatalytic degradation of the acetaminophen by nanocrystal-engineered TiO2 thin film in batch and continuous system

• Photocatalytic activity was improved in TiO₂ thin film by rapid thermal annealing. • Photoreactor was designed for TiO₂ thin film. • Considerable reusability and durability of prepared photocatalysts were studied. Un-biodegradable pharmaceuticals are one of the major growing threats in the wastewaters. In the current study, TiO₂ thin film photocatalysts were designed by nanocrystal engineering and fabricated for degradation of the acetaminophen (ACE) in a photocatalytic reaction under UV light irradiation in batch and continuous systems. The photocatalyst was prepared by sputtering and then engineered by thermal treatment (annealing at 300℃ (T300) and 650℃ (T650)). The annealing effects on the crystallinity and photocatalytic activity of the TiO₂ film were completely studied; it was found that annealing at higher temperatures increases the surface roughness and grain size which are favorable for photocatalytic activity due to the reduction in the recombination rate of photo-generated electron-hole pairs. For the continuous system, a flat plate reactor (FPR) was designed and manufactured. The photocatalytic performance was decreased with the increase of flow rate because the higher flow rate caused to form the thicker film of the liquid in the reactor and reduced the UV light received by photocatalyst. The reusability and durability of the samples after 6 h of photocatalytic reaction showed promising performance for the T650 sample (annealed samples in higher temperatures).     

过氧化氢和一氧化氮在小球藻抗阿特拉津胁迫中的作用

过氧化氢(H_2O_2)和一氧化氮(NO)作为信号分子,可调节植物生长、发育以及应对外源性胁迫。利用过氧化氢酶(CAT)以及NO清除剂(PTIO),研究了除草剂阿特拉津(atrazine,100μg·L~(-1))影响小球藻生长的机理,并分析内源性H_2O_2和NO在小球藻抗除草剂胁迫中的作用。研究结果表明,阿特拉津在诱发小球藻细胞死亡的过程中,不同程度促发了H_2O_2和NO生成;外源CAT可通过清除H_2O_2和诱导NO来缓解阿特拉津对小球藻的生长抑制;PTIO与阿特拉津的联合实验进一步证实,小球藻体内的NO诱导与H_2O_2的爆发无关,它们之间的合成没有相关性。因此,除草剂阿特拉津主要通过诱导小球藻体内的H_2O_2爆发来破坏藻细胞,抑制其生长,与NO的信号传递无关。     

Size and shape effects of MnFe2O4 nanoparticles as catalysts for reductive degradation of dye pollutants

• Size and shape-dependent MnFe₂O₄ NPs were prepared via a facile method. • Ligand-exchange chemistry was used to prepare the hydrophilic MnFe₂O₄ NPs. • The catalytic properties of MnFe₂O₄ NPs toward dye degradation were fully studied. • The catalytic activities of MnFe₂O₄ NPs followed Michaelis–Menten behavior. • All the MnFe₂O₄ NPs exhibit selective degradation to different dyes. The magnetic nanoparticles that are easy to recycle have tremendous potential as a suitable catalyst for environmental toxic dye pollutant degradation. Rationally engineering shapes and tailoring the size of nanocatalysts are regarded as an effective manner for enhancing performances. Herein, we successfully synthesized three kinds of MnFe₂O₄ NPs with distinctive sizes and shapes as catalysts for reductive degradation of methylene blue, rhodamine 6G, rhodamine B, and methylene orange. It was found that the catalytic activities were dependent on the size and shape of the MnFe₂O₄ NPs and highly related to the surface-to-volume ratio and atom arrangements. Besides, all these nanocatalysts exhibit selectivity to different organic dyes, which is beneficial for their practical application in dye pollutant treatment. Furthermore, the MnFe₂O₄ NPs could be readily recovered by a magnet and reused more than ten times without appreciable loss of activity. The size and shape effects of MnFe₂O₄ nanoparticles demonstrated in this work not only accelerate further understanding the nature of nanocatalysts but also contribute to the precise design of nanoparticles catalyst for pollutant degradation.     

H_2O_2致大鼠RTE细胞系氧化应激作用及GSH保护作用的体外研究

许多具有氧化作用的空气污染物,均能使细胞产生氧化损伤,使胸腺基质淋巴生成素(thymic stromal lymphopoietin,TSLP)含量上升。而TSLP是一种启动过敏性炎症的重要因子,会导致哮喘等疾病发生率的上升。在本研究中用过氧化氢(H_2O_2)模拟具有氧化作用的空气污染物进行染毒,研究细胞氧化应激水平的变化,并讨论还原型谷胱甘肽(GSH)对细胞受氧化损伤的保护作用。将大鼠支气管上皮细胞(RTE)分组培养,每组设置6个平行实验,分别用低、中、高剂量H_2O_2染毒3 h;高剂量设置1个重复,作为保护组,在染毒前用GSH保护2 h。结果显示,高剂量组H_2O_2(3.2 mmol·L~(~(-1)))染毒的细胞,其细胞活力下降(P0.01),丙二醛(MDA)水平上升(P0.01),TSLP水平上升(P0.05),与之相比,用GSH保护后的同剂量染毒组,上述指标得到全面缓解(P0.01)。这表明高浓度的H_2O_2会损伤细胞活力,并使MDA及TSLP水平上升,而GSH对TSLP及MDA的升高有极显著的抑制作用,即对细胞有一定的保护作用。     

纳米TiO2与重金属Cd对铜绿微囊藻生物效应的影响

为了更全面地评价纳米TiO2的生物效应,尤其是纳米TiO2与其他环境污染物的联合作用,以铜绿微囊藻为受试生物,探讨了不同浓度的纳米TiO2,以及纳米TiO2与Cd联合作用对藻生长的影响。根据叶绿素a及藻胆蛋白的含量变化,低浓度的纳米TiO2溶液(0～50mg.L-1)可以促进藻的生长,当纳米TiO2的浓度大于50mg·L-1时,藻细胞的生长有所抑制,生长减慢,并呈剂量-效应关系;当纳米TiO2与Cd离子同时存在时,由于纳米TiO2对Cd离子的吸附作用,水中游离态Cd离子浓度降低,Cd离子对藻的毒性明显降低。因此,纳米TiO2的生态毒性和环境效应不容忽视,同时,应重视纳米材料及与其他环境污染物质共同作用后的生物效应。     

纳米二氧化硅对两性生殖和孤雌生殖卤虫无节幼体毒性影响的比较研究

研究了纳米二氧化硅(Nano-SiO_2)悬浮液对美国大盐湖两性生殖型卤虫(Artemia francisana,GSL)和渤海湾孤雌生殖型卤虫(Artemia parthenogenetica,BH)无节幼体的急性毒性和抗氧化酶系统的影响。研究结果表明,Nano-SiO_2对GSL和BH无节幼体24 h-LC50分别为23.02 mg·m L~(-1)和20.96 mg·m L~(-1),属低级毒性。Nano-SiO_2降低了GSL和BH无节幼体还原型谷胱甘肽(GSH)含量,抑制了过氧化氢酶(CAT)和超氧化物歧化酶(SOD)活性,致丙二醛(MDA)含量升高,表明氧化应激反应是导致Nano-SiO_2对卤虫无节幼体致死的作用机制之一。