一种简便快速检测涕灭威对DNA损伤的方法

介绍一种简便、快速检测涕灭威对DNA损伤的方法,并将这种方法与其他几种检测DNA损伤的方法进行了比较.这种方法直接把菌体或组织匀浆液放入琼脂糖凝胶的加样孔穴中,在原位裂解后,在较高pH环境下进行电泳,根据DNA的量和损伤程度评价涕灭威对生物个体或生态系统产生的影响.     

Culturable actinobacteria isolated from marine sponge <Emphasis Type="Italic">Iotrochota</Emphasis> sp.

The study describes the diversity of actinobacteria isolated from the marine sponge Iotrochota sp. collected in the South China Sea. Species and natural product diversity of isolates were analyzed, including screening for genes encoding polyketide synthases (PKS) and nonribosomal peptide synthetase (NRPS), and 16S rRNA gene restriction fragment length polymorphism (RFLP). PKS and NRPS sequences were detected in more than half of the isolates and the different “PKS-I–PKS-II–NRPS” combinations in different isolates belonging to the same species indicated a potential natural product diversity and divergent genetic evolution. The phylogenetic analysis based on 16S rRNA gene sequencing showed that the isolates belonged to genera Streptomyces, Cellulosimicrobium, and Nocardiopsis. The majority of the strains tested belonged to the genus Streptomyces and one of them may be a new species. To our knowledge, this is the first report of a bacterium classified as Cellulosimicrobium sp. isolated from a marine sponge. Key Laboratory of Marine Bio-recourses Sustainable Utilization (LMB-CAS), Guangdong Key Laboratory of Marine Materia Medica (LMMM-GD), South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, People’s Republic of China.     

长期单施NK肥条件下几种典型土壤磷的演化

为探讨我国典型土壤长期单施氮钾肥对土壤全磷和Olsen-P磷的影响,研究了不同气候条件、不同耕作制度下,7种典型土壤类型长期定位试验单施氮钾肥下土壤全磷和Olsen-P变化及其影响因素.结果表明,在长期单施氮钾肥条件下,除杭州水稻土全磷含量稳定在1.0g·kg-1左右外,其余6种耕作土壤全磷含量和土壤Olsen-P均呈显著下降趋势,全磷含量下降幅度在13.6%～44.9%之间;土壤Olsen-P下降速率比全磷高几倍,Olsen-P下降有一定阈值,这一阈值大约为5 mg·kg-1.土壤全磷含量与土壤Olsen-P含量呈极显著直线相关关系.因此,长期单施氮钾肥在很大程度上减少了土壤磷素养分库.     

利用稳定同位素202Hg稀释技术判定不同来源有机肥施用对外源汞在土壤中形态分布的影响

有机肥施入土壤后,是否会对土壤重金属的活性及植物吸收造成影响是人们关心的问题.本研究应用稳定同位素²⁰²Hg稀释技术,通过培养实验和改进的Tessier连续提取法,探索不同来源有机肥(秸秆、杨树叶、油枯、酒糟、猪粪、鸡粪)施用对外源汞在天津潮土中形态分布及有效性的影响.结果表明,在连续提取法中结合同位素²⁰²Hg稀释技术,通过同位素比值R_Hg(²⁰²Hg/²⁰⁰Hg)的变化对Hg进行形态分析,相比传统的对Hg形态直接进行含量测定,可以更精确直观地反映出Hg形态分布的变化.在潮土中加入外源²⁰²Hg和有机肥后,同位素比值R_Hg最为显著的变化集中在交换态(含水溶态)、胡敏酸结合态、富里酸结合态及有机质结合态,且不同来源有机肥对Hg形态的影响也主要集中在这部分形态,对碳酸盐结合态、铁锰氧化物结合态和残渣态的影响较小.与未加入有机肥的对照处理相比,猪粪及鸡粪的施用使外源示踪²⁰²Hg显著向活性较强的交换态(含水溶态)、富里酸结合态转移,而在胡敏酸结合态中比例降低,下降幅度约为55%(猪粪)和58%(鸡粪).油枯及酒糟的施用,使外源示踪²⁰²Hg显著向活性较低的胡敏酸结合态转移,其同位素比值R_Hg分别增长了约90%(酒糟)和85%(油枯),而在活性较高的交换态(含水溶态)和富里酸结合态中分布比例降低.秸秆和杨树叶对于污染土壤Hg形态分布的影响并不显著.研究结果表明,不同来源的有机肥对Hg污染潮土中Hg的形态分布有显著影响,因此,在Hg污染农田土壤上施用有机肥料需要格外谨慎.     

Porous FeOx/BiVO4-δS0.08：Highly efficient photocatalysts for the degradation of Methylene Blue under visible-light illumination

Porous S-doped bismuth vanadate with an olive-like morphology and its supported iron oxide （y wt.% FeOx/BiVO4-δS0.08, y = 0.06, 0.76, and 1.40） photocatalysts were fabricated using the dodecylamine-assisted alcohol-hydrothermal and incipient wetness impregnation methods, respectively. It is shown that the y wt.% FeOx/BiVO4-δS0.08 photocatalysts contained a monoclinic scheetlite BiVO4 phase with a porous olive-like morphology, a surface area of 8.8-9.2 m^2/g, and a bandgap energy of 2.38-2.42 eV. There was co-presence of surface Bi^5＋, Bi^3＋, V^5＋, V^3＋, Fe^3＋, and Fe^2＋ species in y wt.% FeOx/BiVO4-δS0.08. The 1.40 wt.% FeOx/BiVO4-δS0.08 sample performed the best for Methylene Blue degradation under visible-light illumination. The photocatalytic mechanism was also discussed. We believe that the sulfur and FeOx co-doping, higher oxygen adspecies concentration, and lower baudgap energy were responsible for the excellent visible-light-driven catalytic activity of 1.40 wt.% FeOx/BiVO4-δS0.08.     

风沙土对放射性核素的吸附与解吸

研究了采自新疆的风沙土对不同放射性核素的吸附与解吸情况。结果表明,风沙土对137Cs的吸附一解吸滞后作用明显,而对帅Sr的吸附一解吸滞后作用极微;风沙土对239Pu和238U的平衡吸附量分别为22．54cpm／mg和19．27cpm／mg,粒径为45μm的风沙土能牢固地吸附239Pu和238U。     

Health and ecotoxicological risk assessment for human and aquatic organism exposure to polycyclic aromatic hydrocarbons in the Baiyangdian Lake

Seasonal and regional distributions of 17 polycyclic aromatic hydrocarbons (PAHs) in surface waters from four different main water functional regions of the Baiyangdian Lake were analyzed through GC/MS/MS during spring and summer season. The aim was to identify their possible pollution sources and evaluate their health risk for human and ecotoxicological risk for aquatic organisms. Results showed that the range of total PAH concentration is 35.38–88.06 ng/L (average 46.57 ng/L) in spring and 25.64–301.41 ng/L (average 76.23 ng/L) in summer. PAH contamination was observed slightly lower in the summer season from the pollution characteristics of water bodies in most areas of the Baiyangdian Lake, and the levels of PAH pollution in the water body of urban residential regions and rural residential regions were relatively higher than those in tourist regions and low human disturbance regions. Source analysis based on diagnostic ratios confirmed that combustion sources and petroleum sources were two main sources for PAHs entering into the waters of the Baiyangdian Lake. Human health risk assessment showed that PAHs in surface waters from the Baiyangdian Lake will not cause a potential non-carcinogenic risk to local residents and the carcinogenic risk could mostly be accepted, but the potential lifetime carcinogenic risk for infants in rural residential regions should be concerned about. Urban residential regions and rural residential regions were subject to higher cumulative non-carcinogenic and carcinogenic risk when compared to the other functional regions. Ecotoxicological risk assessment found a moderate risk to aquatic organisms presented by individual PAH and a low risk by total PAHs, and PAHs in the water body of urban residential regions and rural residential regions also have relatively higher harm effects to aquatic organisms compared with the other two functional regions. This study revealed the pollution characteristics of PAHs and their possible sources in waters of the Baiyangdian Lake, clarified its correlation to regional anthropogenic activities, and provided corresponding risk management strategies for human and aquatic organisms.

     

Low-temperature (NO + O2) adsorption performance of alkaline earth metal-doped C-FDU-15

To improve the removal capacity of NO + O₂ effectively, the alkaline earth metal-doped order mesoporous carbon (A-C-FDU-15(0.001) (A = Mg, Ca, Sr and Ba)) and Mg-C-FDU-15(x) (x = 0.001?0.003) samples were prepared, and their physicochemical and NO + O₂ adsorption properties were determined by means of various techniques. The results show that the sequence in (NO + O₂) adsorption performance was as follows: Mg-C-FDU-15(0.001) (93.2 mg/g) > Ca-C-FDU-15(0.001) (82.2 mg/g) > Sr-C-FDU-15(0.001) (76.1 mg/g) > Ba-C-FDU-15(0.001) (72.9 mg/g) > C-FDU-15 (67.1 mg/g). Among all of the A-C-FDU-15(0.001) samples, Mg-C-FDU-15(0.001) possessed the highest (NO + O₂) adsorption capacity (106.2 mg/g). The species of alkaline earth metals and basic sites were important factors determining the adsorption of NO + O₂ on the A-C-FDU-15(x) samples, and (NO + O₂) adsorption on the samples was mainly chemical adsorption. Combined with the results of (NO + O₂)-temperature-programmed desorption ((NO + O₂)-TPD) and in situ diffused reflectance infrared Fourier transform spectroscopy (DRIFTS) characterization, we deduced that there were two main pathways of (NO + O₂) adsorption: one was first the conversion of NO and O₂ to NO₂ and then part of NO₂ was converted to NO₂^? and NO₃^?; and the other was the direct oxidation of NO to NO₂^? and NO₃^?.