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21.
1 INTRODUCTIONRecently ,thepollutionoftracemetalinseawaterhasbecomeincreasinglyevident.Researchershavefo cusedattentiontotracemetalpresentinvariousexistenceforms ,especiallyorganiccomplexingphases.Theexistencestatesandtransportmechanismofbaytracemetalswerethesubjectofstudybysomere searchers(Gu ,1 991 ;Florence ,1 998;Guo ,1 998;Wells,1 991 ,1 998a ,b ;Wellsetal.,1 998) .Whetherinfreshwaterorseawater,colloidsareclearlydominantfactorsaffectingtheexistencestatesandtransportmechanismoftrac…  相似文献   
22.
Dissolved organic matter(DOM) from freshwater, mid-salinity, and seawater endmember samples in the Jiulong River Estuary, China were fractionated using cross-flow ultrafiltration with a 10-kDa membrane. The colloidal organic matter(COM; 10 kDa–0.22 μm) retentate, low molecular weight(LMW) DOM(10 kDa) permeate, and bulk samples were analyzed using absorption spectroscopy and three-dimensional fluorescence excitation-emission-matrix spectroscopy. The UV-visible spectra of COM were very similar to those obtained for permeate and bulk samples, decreasing monotonically with increasing wavelength. Most of the chromophoric DOM(CDOM, expressed as the absorption coefficient a355) occurred in the LMW fraction, while the percentage of CDOM in the colloidal fraction was substantially higher in the freshwater endmember(13.4% of the total) than in the seawater endmember(6.8%). The bulk CDOM showed a conservative mixing behavior in the estuary, while there was removal of the COM fraction and a concurrent addition of the permeate fraction in the mid-salinity sample, implying that part of the colloidal CDOM was transformed into LMW CDOM. Two humic-like components(C1: 250, 325/402 nm; and C2: 265, 360/458 nm) and one protein-like component(C3: 275/334 nm) were identified using parallel factor analysis. The contributions of the C1, C2, and C3 components of the COM fraction to the bulk sample were 2.5%–8.7%, 4.8%–12.6%, and 7.4%–14.7%, respectively, revealing that fluorescent DOM occurred mainly in the LMW fraction in the Jiulong River Estuary. The C1 and C2 components in the retentate and permeate samples showed conservative mixing behavior, but the intensity ratio of C2/C1 was higher in the retentate than in the permeate fractions for all salinity samples, showing that the humic component was more enriched in the COM than the fulvic component. The intensity ratio of C3/(C1+C2) was much higher in the retentate than in the permeate fraction for mid-salinity and seawater samples, revealing that the protein-like component was relatively more enriched in COM than the humic-like component. The contribution of the protein-like component(C3) to the total fluorescence in the retentate increased from 14% in the freshwater endmember to 72% for the seawater endmember samples, clearly indicating the variation of dominance by the humic-like component compared to the protein-like component during the estuarine mixing process of COM.  相似文献   
23.
采用溶藻弧菌ATCC17749菌体作为抗原免疫新西兰大白兔,制备兔抗溶藻弧菌多克隆抗体;利用柠檬酸钠还原氯金酸法制备胶体金及胶体金-抗体结合物,并将其喷涂在玻璃纤维膜上冷冻干燥;在硝酸纤维素膜上包被兔抗溶藻弧菌多克隆抗体和羊抗兔IgG分别作为检测线和控制线;将处理后的玻璃纤维素膜、硝酸纤维膜、样品垫及吸水纸组装成双抗夹心试纸条,并对试纸条灵敏度、特异性、稳定性进行评价。结果表明,制备的兔抗溶藻弧菌多克隆抗体的效价可达1∶512 000;胶体金溶胶的最佳制备条件为:加入1.8 mL 10 mg/mL的柠檬酸三钠,500 W微波炉中火加热10 min;试纸条检测线和质控线的抗体最佳包被量分别为8.0 mg/mL和1.0 mg/mL;试纸条检测灵敏度为1×106cfu/mL,特异性试验显示,试纸条与哈氏弧菌、副溶血弧菌、霍乱弧菌、拟态弧菌、美人鱼弧菌、弗氏弧菌、河流弧菌、创伤弧菌等8株菌无交叉反应;稳定性试验表明,试纸在4℃干燥条件下能稳定保存5个月以上。制备的溶藻弧菌多克隆检测试纸条可灵敏、较特异地检测源自病鱼的溶藻弧菌,整个检测过程可在10 min内完成,适用于溶藻弧菌的快速检测。  相似文献   
24.
为了探讨长江口水体胶体有机碳含量的季节变化, 按季度采集长江口南支表层水样, 利用切向流超滤技术(TFF)分离水样中小胶体物质(1—5kD)、中胶体物质(5—500kD)和大胶体物质(500kD— 0.45μm), 测试分离后样品的有机碳浓度。结果表明: 长江口水体中总胶体有机碳浓度有明显的季节变化, 表现为冬季>夏季>秋季>春季, 其原因可能是冬季长江流域陆源输入增加, 水生生物生物量和生物活性减弱双方面的共同作用使得含量最高, 而春季流域陆源有机碳含量输入较少, 且流域内春汛雨量多水量大对水体中有机碳浓度具有稀释作用, 从而导致该季节胶体有机碳含量较少。总胶体有机碳在不同分子量的分配上季节差异不大, 中胶体有机碳浓度及其在总胶体有机碳中所占的比例均高于小胶体有机碳和大胶体有机碳。由于长江口胶体有机碳的含量较高, 并有明显的季节变化, 对有机碳的入海通量和生物地球化学循环发挥重要的作用。  相似文献   
25.
A HPLC-based protocol has been developed for the determination of zero-valent sulfur (ZVS) speciation, including solid, colloidal elemental sulfur and individual inorganic polysulfides in natural aquatic samples. The protocol includes four experimental procedures: (1) determination of polysulfide speciation by rapid single-phase derivatisation with methyl trifluoromethanesulfonate; (2) determination of the sum of polysulfide and colloidal sulfur by reaction with hydrogen cyanide (cyanolysis); (3) determination of total zero-valent sulfur by treatment with zinc chloride followed by extraction with chloroform; and (4) chromatographic determination of polythionates without sample pre-treatment. With proper sampling and preservation techniques in the field or on board ship, this combination of methods allowed the quantitative determination of: (a) individual polysulfide species; (b) dispersed colloidal sulfur; (c) dispersed solid elemental sulfur; and (d) tetra-, penta- and hexathionates. With minor modification, the method could be expanded to include other polythionates. Sixteen various wet chemical and liquid chromatographic methods were tested on nine synthetic reference samples (including solid elemental sulfur, colloidal elemental sulfur, inorganic polysulfides and polythionates) to establish the optimal protocol. The protocol was further evaluated by analysing the zero-valent sulfur content in microbially-produced sulfur and in sulfur from two natural samples of sulfide-rich seawater from tidal flats pools of the Wadden Sea (Germany).  相似文献   
26.
黔西织金矿区乐平世煤系中的菱铁矿以多种微观形态产出,基于镜下薄片观测、泥岩微量元素分析,探讨了菱铁矿 成因及演化。研究表明菱铁矿可划分为第一世代的胶状集合体、第二世代圈层结构发育不良的球粒及第三世代圈层结构发 育完好的鲕粒与菱面体三个成岩世代产物。菱铁矿胶状集合体是在成矿组分(Fe2+ 与CO32-) 浓度达到超饱和状态时快速结 晶形成的;圈层结构发育不良的菱铁矿球粒是成矿物质围绕第一世代形成的菱铁矿胶粒聚集而成;圈层结构发育完好的菱 铁矿鲕粒是大量放射状菱铁矿线晶以第二世代的球粒为核心连续共轴生长而成,晚二叠世脉动式的海侵可能是菱铁矿在结 晶非平衡态与平衡态与之间往复循环驱动因素,最终形成了同心圈层结构,而同心圈层发育完好的菱面体状菱铁矿可能是 成矿条件的变化促使鲕粒从放射状生长向自形菱面体生长而成。  相似文献   
27.
根据物质呈纳米级状态时,其物理性质发生显著的变化,认为由其作为分散相分散于不同的分散介质(气体、液体和固体)中所构成的气溶胶、胶体溶液或固体溶胶,尤其是胶体溶液对运移成矿物质尤为重要,而对于被运移的胶粒来说,自身凝聚或被其他载体矿物或岩石的吸附富集将是一种重要的成矿作用,这特别有助于解释微细浸染型金矿、砂金矿及某些稀有及分散元素矿床的成因。  相似文献   
28.
In the Alps, debris flow deposits generally contain <5% clay‐size particles, and the role of the surface‐charged <2 μm particles is often neglected, although these particles may have a significant impact on the rheological properties of the interstitial fluid. The objective of this study was to compare debris flow deposits and parent materials from two neighbouring catchments of the Swiss Alps, with special emphasis on the colloidal constituents. The catchments are small in area (4 km2), 2·5 km long, similar in morphology, but different in geology. The average slopes are 35–40%. The catchments were monitored for debris flow events and mapped for surface aspect and erosion activity. Debris flow deposits and parent materials were sampled, the clay and silt fractions extracted and the bulk density, <2 mm fraction bulk density, particle size distribution, chemical composition, cation exchange capacity (CEC) and mineralogy analysed. The results show that the deposits are similar to the parent screes in terms of chemical composition, but differ in terms of: (i) particle size distribution; and (ii) mineralogy, reactivity and density of the <2 mm fraction. In this fraction, compared with the parent materials the deposits show dense materials enriched in coarse monocrystalline particles, of which the smallest and more reactive particles were leached. The results suggest that deposit samples should not be considered as representative of source or flow materials, particularly with respect to their physical properties.  相似文献   
29.
Material collected over a month on plates attached to the bed of the Afon Goch, Anglesey, a stream highly contaminated by acid mine drainage (AMD), was either examined intact by electron microscopy or suspended and cultured to reveal the presence of microbiota. Certain of the aerobic microbiota were identified, the genus Pseudomonas formed the commonest isolate and cultures of Serratia plymuthica were grown in order to compare the biofilms formed with the material collected in the Afon Goch. The material at the sediment–water interface of the Afon Goch was of similar underlying morphology to that of the cultured biofilms. However, the former had a superficial granular coating of equidimensional (60–100 nm) and evenly spaced iron rich particles (determined by X-ray microanalysis). The sediment–water interface of this AMD-contaminated stream is therefore best described as a highly contaminated biofilm. Evidence from previous work suggests that the streambed is active in iron removal from the water column. The intimate association of iron with microbiota at the streambed, therefore, implies that iron flux prediction may not be possible from physical and chemical data alone but requires knowledge of biofilm physiology and ecology. Microbially mediated metal precipitation, both by single bacteria and by biofilms, has been reported elsewhere but mass balance considerations suggest that this explanation cannot hold good for the large amounts of iron hydroxide depositing from waters of the prevalent pH and redox status. Filtered stream water analyses indicate the presence of colloidal iron hydroxide and also its removal downstream where ochreous (iron hydroxide rich) material accumulates. The process of iron immobilization is likely to be the attraction and physical trapping of colloidal iron hydroxide by extracellular polymeric substances (EPS) which constitute the matrix of biofilms. © 1997 John Wiley & Sons, Ltd.  相似文献   
30.
海洋有机质的光谱分析方法评述   总被引:1,自引:0,他引:1  
海洋有机质的光谱分析已成为海洋碳循环的研究热点之一。本文从天然有机质吸收光谱和荧光光谱分析的基本原理入手,系统梳理了有机质光谱分析中容易被忽视的基本概念,讨论了过滤与保存方式、p H值、荧光内滤效应等对有机质光谱分析的影响。结合色氨酸、酪氨酸、腐殖酸及大量现场样品的实验结果,对吸收光谱和三维荧光光谱的不同解析方法进行了系统的分析与对比。基于在南海、西菲律宾海获取的现场调查数据,对于文献中常用的荧光指数(FI)、腐殖化指数(HIX)、自生源指数(BIX)等光谱参数的内在含义及其在海洋环境中的适用性进行了评述。此外,还归纳和总结了胶体有机质和颗粒有机质荧光分析的最新进展,并对今后在光谱分析与观测领域有待完善和突破的一些关键领域进行了展望。  相似文献   
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