The brine shrimp (Artemia parthenogenetica) as encapsulation organism for prophylactic chemotherapy of fish and prawn

Brine shrimp (Artemia parthenogenetica) which had ingested three water-insoluble antibacterial drugs i.e. sulfadiazine(SD), oxytetracycline (OTC) and erythromycin estolate (ERY-Es) were fed toTilapia and Mysis IIIof Penaeus orientalis K. The drug contents in the predators were then determined. After administration of drugs toTilapia and Mysis III, through the bio-encapsulation of the brine shrimp, efficacious therapeutical concentration of OTC and ERY-Es (but not SD) in the predators could be reached and maintained for more than 8 hours.     

Synthesis, Characterization and Antibacterial Activity of New Ln（Ⅲ ） Complexes with an Unsymmetrical Schiff Base Ligand

1Introduction SomeSchiffbasecomplexesderivedfromaminoacidsareparticularlyactiveinbiologycatalysisandmaterial.Thestudyofthemisfocusofthestudyof coordinationchemistry.Recently,studiesofsuchmetalcomplexesofmono Schiffbaseshavebeenre ported(Fanetal.,2003a,b;L…     

On the nature of the Galactic nebula We 1–12

In 1977, Weinberger published a list of 12 new extended possible planetary nebulae (PNe). Whereas, because of their characteristic morphology and/or the presence of a blue central star, almost all of them could easily be suspected to be genuine planetary nebulae, one object (No. 12) captivated because of its unusually bright central star. This find prompted Kaler & Feibelman to question the PN nature of this object (We 1–12) on the basis of IUE spectra. A definite conclusion could, however, not be drawn by them; thus, until now, the real nature of We 1–12 remained unsolved. For the first time, a spectral investigation of both the central star and the nebula is presented in this paper. It definitely shows that this intriguing object is an (isolated) H  ii region and its central star, as previously assumed, is an early B star which serves as the ionizing source. We 1–12, a part of which is coincident with a weak IRAS point source, is at a distance of 2–2.6 kpc and is reddened by E ( B − V )=0.6–0.8 mag.     

Evaluation of the spatial changes in seagrass cover in the lagoons of Lakshadweep islands,India, using IRS LISS III satellite images

A study was conducted in Lakshadweep islands to determine the feasibility of using Indian Remote Sensing (IRS) satellites for detecting changes in the seagrass from other coastal features. IRS ID and IRS P6 LISS III having spatial resolution of 23.5 m with lower cost compared to all other contemporary satellites with the same spatial resolution have not been widely used for monitoring the changes in seagrass cover. In this context, the present study attempted to explore the effectiveness of LISS III data for mapping seagrasses and to inform the international community about the usefulness of these low-cost imageries for coastal resource monitoring. Supervised classification and change detection studies found a significant decrease in seagrass cover of 73.03 ha in the Lakshadweep group of islands. An overall accuracy of 67.5% was obtained for the change maps, and seagrass cover and its changes vary at different islands.     

Transformation of Fe （Ⅱ） and Fe （Ⅲ） in Enclosures of Dongshan Bay

根据2008年8月与11月在东山湾海域获得的调查资料对表层水中溶解态Fe（II）和Fe（III）含量、浮游植物叶绿素a、营养元素及其浓度等环境参数进行分析。结果表明,夏、秋季海水中Fe（II）浓度及其在总溶解铁中所占比例均与浮游植物叶绿素a呈正相关,其相关系数分别为0.7959、0.9219。现场围隔实验表明,海水中总溶解态Fe含量在24 h内有较大的变化,最大减少量达到17.4%。DS2站点海水中Fe（II）浓度及其在总溶解铁中所占比例随光照强度增加而增加。最高值与初始值相比较,叶绿素a较高的DS2站点海水中Fe（II）浓度增加较叶绿素a较低的DS5号站点高0.053μg/L。Fe（II）和Fe（III）加富实验研究了溶解态的Fe（II）和Fe（III）在海水中相互转化。高浓度的Fe（II）在海水中被氧化成Fe（III）,海水中浮游植物也会引发光还原作用使Fe（III）还原成Fe（II）。     

On the pH-dependent formation constants of iron(III)-sulfur(IV) transient complexes

An experimental study is described of Fe(III)-S(IV) formation constants measured as a function of pH (1–3), ionic strength (0.2–0.5 M) and [Fe(III)] _T (2.5–5.0×10^–4 M) using a continuous-flow spectrophotometric technique to make observations 160 ms after mixing. Preliminary experiments using pulse-accelerated-flow (PAF) spectrophotometry to measure rate constants on a microsecond timescale are also described. The conditional formation constant at 25 °C can be modeled with the following equation: {ie307-1} where {ie307-2}K ₇ andK ₈ can be interpreted as intrinsic constants for the coordination of HSO ₃ ^– by FeOH²⁺ and Fe³⁺, respectively, but until further evidence is obtained they should be regarded as fitting constants. PAF spectrophotometry showed that the initial reaction of Fe(III) with S(IV) (pH 2.0) is characterized by a second-order rate constant of 4×10⁶ M^–1 s^–1 which is comparable to rate of reaction of FeOH²⁺ with SO ₄ ^2– . However, the PAF results should be regarded as preliminary since unexpected features in the initial data indicate that the reaction may be more complex than expected.     

N1923-DA201大孔吸附树脂反相分配色层分离、偶氮胂Ⅲ比色测定矿石中钍

用N1923-二甲苯作固定相,AD201大孔聚二乙烯苯吸附树脂作裁体,研究了钍在硫酸介质中的反相分配色层分离条件。拟定了矿石中微量钍的测定方法。     

Kinetics of redox cycling of iron coupled with fulvic acid

The kinetics of conversion of iron(III) (hydr)oxides to ferrous iron mediated by fulvic acid have been investigated in order to improve the understanding of the redox cycling of iron at the oxic-anoxic boundary in natural waters. Under the conditions similar to natural waters, fulvic acid is able to reduce the iron(III) (hydr)oxide. The kinetics of the reaction depend on the reactivity of iron(III) (hydr)oxides and the reducing power of the fulvic acid. The rate of reaction is 60 nm/h obtained under following conditions: total concentration of Fe(III) 1.0 × 10^–4 M, pH 7.5, fulvic acid 5 mg/L. The rate is considered as a net result of reduction and oxidation in the > Fe^III-OH/Fe(II) wheel coupled with fulvic acid. In a real natural water system, reductants other than fulvic acid may be of importance. The results obtained in the laboratory, however, provide evidence that the Fe(OH)₃(s)/Fe(II) redox couple is able to act as an electron-transfer mediator for the oxidation of natural organic substances, such as fulvic acid by molecular oxygen either in the absence of microorganisms or as a supplement to microbial activity.     

Flotation Separation of Trace Elements from Alkaline-Earth Matrices by Co(III) Hexamethylenedithiocarbamate before ICP-AES Determination

A method for the selective separation of Ag, Cd, Cr, Cu, Ni, Pb and Zn in traces from solutions of calcite (CaCO₃), dolomite (CaMg(CO₃)₂) and gypsum (CaSO₄.2H₂O) before their determination by inductively coupled plasma-atomic emission spectrometry (ICP-AES) is presented. The expected interferences of Ca and Mg on intensities of trace analytes were removed by collecting the elements of interest with cobalt(III) hexamethylenedithiocar-bamate, Co(HMDTC)₃. The flotation of aqueous solutions (1 l) of calcite, dolomite and gypsum was performed at pH 6.0, by 1.5 mg l⁻¹ Co and 0.6 mmol l⁻¹ HMDTC⁻. To minimise the effect of the reaction between Ca/Mg, which restrains the function of the surfactant, careful selection of the most suitable foaming reagent was necessary. The accuracy of the method was established by analysing natural alkaline-earth minerals by the standard addition method as well as using the dolomite reference materials GBW 07114 and GSJ JDo-1. The ICP-AES limits of detection following flotation on different minerals were found to be 0.080 μg g⁻¹ for Cd, 0.105 μg g⁻¹ for Ag, 0.142 μg g⁻¹ for Cu, 0.195 μg g⁻¹ for Cr, 0.212 μg g⁻¹ for Ni, 0.235 μg g⁻¹ for Zn and 0.450 μg g⁻¹ for Pb.     

近30年来国外国家公园研究进展与启示

国家公园是自然保护和旅游研究领域的重要内容之一。本文以Web of Science数据库收录的近30年国外国家公园相关文献为基础,对筛选的451篇英文文献运用可视化软件CitespaceⅢ及系统综述的方法,从资源评估、环境影响、发展模式、规划、运营管理5个方面对国外国家公园研究主要内容进行述评,并对研究方法进行系统分析。最后,从国家公园立法、发展模式构建、管理内容与方法、社区参与模式与机制、环境监测与评估5个方面提出未来中国国家公园的研究方向。总体上看,国外有关国家公园的研究具有研究对象复杂、视角多元、方法综合的特征。在构建国家公园体制的大背景下,借鉴国际经验构建中国国家公园研究体系将对完善中国保护地相关研究、指导国家公园建设具有重要意义。