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31.
A new method for the direct determination of reduced and oxidized Mo species (Mo (V) and Mo (VI)) in seawater was developed and used for the first time. The method includes the complexation of Mo (V) with tartrate, solid phase extraction of the Mo (V)–tartrate complex by a XAD 7HP resin, followed by elution with acidic acetone. In this study, the eluted Mo (V) was quantified by graphite furnace atomic absorption spectrometry. The detection limit of this protocol was on the order of 0.2 nM. The analytical precision was 10% of ~ 10 nM. This method was successfully applied to the determination of Mo (V) and Mo (VI) in surface and bottom waters at the head of Peconic River Estuary. Total Mo (Mo (V) + Mo (VI)) ranged from 100–120 nM in most bottom saline waters, and 2.5–15 nM for surface fresher waters. Concentrations of Mo (V) in these environments ranged from 0 nM to ~ 15 nM, accounting for 0%–15% of the total dissolved Mo pool. The time series experiments showed that the Mo speciation changed within 1 h after the water collection, and therefore it is strongly suggested that speciation analysis be carried out within the first 15 min. However, since these are the first Mo speciation data in concentration ranges typical of normal marine and coastal waters, additional research may be required to optimize the methodology and further explore Mo cycling mechanisms.  相似文献   
32.
An interaction of dissolved natural organic matter (DNOM) with copper ions in the water column of the stratified Krka River estuary (Croatia) was studied. The experimental methodology was based on the differential pulse anodic stripping voltammetric (DPASV) determination of labile copper species by titrating the sample using increments of copper additions uniformly distributed on the logarithmic scale. A classical at-equilibrium approach (determination of copper complexing capacity, CuCC) and a kinetic approach (tracing of equilibrium reconstitution) of copper complexation were considered and compared. A model of discrete distribution of organic ligands forming inert copper complexes was applied. For both approaches, a home-written fitting program was used for the determination of apparent stability constants (Kiequ), total ligands concentration (LiT) and association/dissociation rate constants (ki1,ki- 1).A non-conservative behaviour of dissolved organic matter (DOC) and total copper concentration in a water column was registered. An enhanced biological activity at the freshwater–seawater interface (FSI) triggered an increase of total copper concentration and total ligand concentration in this water layer. The copper complexation in fresh water of Krka River was characterised by one type of binding ligands, while in most of the estuarine and marine samples two classes of ligands were identified. The distribution of apparent stability constants (log K1equ: 11.2–13.0, log K2equ:8.8–10.0) showed increasing trend towards higher salinities, indicating stronger copper complexation by autochthonous seawater organic matter.Copper complexation parameters (ligand concentrations and apparent stability constants) obtained by at-equilibrium model are in very good accordance with those of kinetic model. Calculated association rate constants (k11:6.1–20 × 103 (M s)− 1, k21: 1.3–6.3 × 103 (M s)− 1) indicate that copper complexation by DNOM takes place relatively slowly. The time needed to achieve a new pseudo-equilibrium induced by an increase of copper concentration (which is common for Krka River estuary during summer period due to the nautical traffic), is estimated to be from 2 to 4 h.It is found that in such oligotrophic environment (dissolved organic carbon content under 83 µMC, i.e. 1 mgCL− 1) an increase of the total copper concentration above 12 nM could enhance a free copper concentration exceeding the level considered as potentially toxic for microorganisms (10 pM).  相似文献   
33.
西北冰洋表层沉积物中重金属的赋存形态研究   总被引:1,自引:0,他引:1  
用连续提取法对选自西北冰洋的32个表层沉积物进行分析,测定了Cr、Cu、Pb在全样中及其在P1-2、P3、P4、P5中的含量.结果表明随着离岸距离增加,水深加深,Cr、Cu、Pb含量呈增高的趋势.研究区陆架沉积物中Cr、Cu、Pb含量分别为60.66、14.77、16.65μg/g;深海沉积物中Cr、Cu、Pb的含量分别为80.40、41.70、25.62μg/g.元素赋存形态分析表明,Cr、Cu、Pb主要赋存在残渣态,残渣态中三元素的含量平均值分别为64.97、19.67、17.56μg/g,占元素总量的比例分别为93.58%、75.02%和83.76%.三元素在各赋存形态中的含量分布是:Cu为残渣态>有机质和硫化物态>铁锰氧化态>可交换及碳酸盐态;Pb和Cr则为残渣态>铁锰氧化物态>有机质硫化物态>可交换态及碳酸盐态.研究区重金属元素在不同赋存形态中的含量分布与北太平洋深海沉积物中类似.  相似文献   
34.
研究长江口和浙江近岸海域的水团流向、缺氧程度、潮汐作用以及养殖活动对表层沉积物中颗粒磷赋存形式的影响,对东海生态环境的可持续发展有着重要的意义。长江口以北和浙江近岸泥质区各存在一个缺氧中心,杭州湾属于强潮区,而象山港遍布养殖场。2018年8—9月在上述4个海域分别采集表层沉积物,采用SEDEX方法进行了颗粒磷的形态划分和含量测定。研究结果表明:在长江口外北部缺氧区和浙江近岸泥质区的南部缺氧区,由于沉积物-水界面的还原环境可以活化铁结合态磷,使之转变为生物可以直接利用的弱吸附态无机磷,因此表现出沉积物中铁结合态磷的低值和弱吸附态无机磷的高值;前者的缺氧程度高于后者,因此其铁结合态磷的含量相应更低。杭州湾和象山港海域均受潮汐作用影响,两者沉积物中磷的分布比较均匀。象山港表层沉积物中铁结合态磷含量均较低,这可能是因为养殖活动造成的水体缺氧通过潮汐活动扩散到整个港底。象山港废弃养殖场沉积物中的碎屑磷和残余有机磷含量显著低于非养殖区,可能是由于养殖活动累积的生物沉积稀释了陆源输入的碎屑颗粒。  相似文献   
35.
Dissolved (dialysis in situ) and total concentrations ofCu, Zn, Cd and Al in eight mining polluted rivers in the Røros area, central Norway, were determinedby atomic absorption spectrometry (flame and graphite furnace) and compared to pH, Caconcentration and alkalinity through seasonal variations in river discharge. Totalconcentrations of the metals were highest during early spring flood and during summer andautumn rain episodes. Dissolved concentrations also increased as the spring floodproceeded, but small discharge peaks within this 2 month period as well as a considerableautumn flood episode appeared to lower rather than to raise the dissolved metal concentrations.Consequently the dissolved fractions of Zn, Cd and Al showed a significant negative correlationwith river discharge, and were low at the discharge peaks. Possibly high sediment concentrationsoccurring at high flood conditions more than counteracted desorption induced by pHdecrease, and led to decreased dissolved fractions through adsorption. Cu speciationon the other hand seemed to be more closely linked to pH. Alkalinity and Ca concentration,both assumed to protect aquatic life from metal pollution, were significantly lowerduring episodes with high Cu and Al total concentrations.  相似文献   
36.
本文论述了高密度电阻率法在逊克县东安岩金矿床勘探中的应用效果;阐明了该方法在地质勘查中解决高阻脉状金矿体产状及埋深的技术手段.  相似文献   
37.
滇池水中铝的形态分布初探   总被引:2,自引:1,他引:2  
马莎  余定学等 《岩矿测试》2002,21(2):120-124
采用铬天青S光度法对滇池水中的总铝和各主要形态铝进行分析,并利用简单易行的紫外吸收表征水中有机物污染程度和颗粒物含量,初步探讨了各因素的变化对铝形态分布的影响。  相似文献   
38.
Introduction of species evolutionary sequence into the quantitative biostratigraphy is a significant work, either for studying biologic evolution or for making stratigraphic correlation and reconstructing geologic history. The quantitative biostratigraphy is to determine biostratigraphic event sequences by using probabilistic analysis. The evolutionary sequence systematics can efficiently ascertain species evolutionary sequences. Two methods have been proposed to determine the sequence of species-disappearance events: (1) species extinction events can be closed by last occurrence events using quantitative biostratigraphic analysis; (2) the duration of a species may be approximately replaced by the duration of its parent species. To combine these two methods for determining the sequence of species disappearance is the best way up to now. A consulting standard sequence that consists of the speciation sequence of Permian waagenophylloid corals and the biostratigraphic event sequence of other important fossils in Permian is used as an example. The group spearman rank-correlation test is used to test the consulting standard sequence by comparing four types of calculations and two kinds of sequences and to find abnormal events. Based on the found abnormal events in the test, the consulting standard sequence is revised to deal with different conditions. Sequences of speciation and species-disappearance, and species duration are determined. Application of species evolutionary sequence to quantitative biostratigraphy can largely improve the quality of biostratigraphic event sequence. In stratigraphic correlation, furthermore, event sequences have higher precision than range biozones.  相似文献   
39.
高峰100号矿体硫、铅同位素特征   总被引:1,自引:0,他引:1  
10 0号矿体的成矿物理化学环境为 :成矿温度 30 0± 30℃ ;成矿压力为 84.2× 10 5Pa ;LogfO2 =- 30 .4~- 35 .6 ,LogfCO2 =- 2 .5 5~ +0 .36 ,LogfS2 =- 8.3~ - 11.0 ,pH =4.2~ 4.9。同位素的分析结果 :硫化物的硫同位素为 6 4‰~ 12 .3‰ ,δ3 4 SΣS 值为 6 6~ 13 8;2 0 6Pb 2 0 4Pb值为 17 4 91~ 18 96 0 ,2 0 7Pb 2 0 4Pb值为 15 5 39~15 940 ,2 0 8Pb 2 0 4Pb值为 37 95 7~ 39 4 90。表明 10 0号矿体的硫源是混合硫 ,铅源是两种异常铅混合的结果。  相似文献   
40.
[Cu2+] and Cu complexation parameters in some selected freshwater systems in Switzerland were determined by the technique of ligand-exchange and DPCSV. Results from the water columns of some eutrophic and oligotrophic lakes are presented and compared to small acid lakes. Cu is strongly complexed by organic ligands which with very high stability constants at low concentrations are probably biologically produced, as indicated by the seasonal variations in the eutrophic lakes and by the relationship between Cu complexation and algal activity in the eutrophic (pCu=15–16), oligotrophic (pCu=13–14) and acidic (pCu=9–10) lakes. The extent of Cu complexation in river waters was generally lower than in the eutrophic lakes, at similar DOC levels. No obvious correlation between Cu complexation and DOC was observed, indicating that Cu complexing ligands are specific organic compounds.  相似文献   
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