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991.
厦门湾水体中铀、钍同位素及悬浮颗粒物的粒径谱--颗粒物采集方法的影响 总被引:2,自引:0,他引:2
运用增强型混合纤雏素(CN-CA)膜、聚碳酸酯膜和聚丙烯滤芯过滤3种不同的方法采集、研究厦门湾水体中悬浮颗粒物(SPM)及其U、Th同位素的粒径谱.发现3种方法所得SPM总浓度和U、Th各同位素的总比活度具有很好的一致性,但粒级分布存在差异.SPM的浓度随粒径的增大而增加,并且SPM的粒径谱控制着颗粒活性很强的4种钍同位素的拉径谱.对于所研究的3种方法,采用聚碳酸脂膜过滤是研究沿岸海域SPM及颗粒活性核素粒级分布比较理想的方法。 相似文献
992.
Hodaka Kawahata Mayuri Inoue Masato Nohara Atsushi Suzuki 《Journal of Oceanography》2006,62(4):405-412
The δ18O, δ13C and trace element composition of pearls collected from Ago Bay, Japan, were investigated in order to evaluate biomineralization
in the cultured pearl oyster (Pinctada fucata martensii). The oxygen isotopic data suggest that the pearls were produced around 23–24°C, mainly in June to early July, which is consistent
with their occurrence in the field. Therefore the pearls were produced under or close to isotopic equilibrium conditions,
although they showed high calcification rates (higher than 0.2–1.0 g cm− 2yr−1) under which, for example, coral skeletons (calcification rate ∼0.28 g cm− 2yr−1) often show non-equilibrium isotope partitioning. The δ13C values were ∼− 2.9‰ lower than those calculated for offshore waters under equilibrium conditions. This may be due to low-δ13C bottom waters resulting from the degradation of organic matter (OM) or to a contribution of low-δ 13C food. In the latter case, a simple mass balance calculation gives a respiration component of 14%. Twelve trace elements
of bulk pearl samples were classified into four groups on the basis of their enrichment/depletion patterns relative to seawater
and inter-element relationships: group 1, Co, Cr, Pb; group 2, Ba, Cs, U; group 3, Cu, Sn, V, and group 4, Mn, Rb, Mo. Comparison
with coral skeletons suggests that Ba and Mn (groups 2 and 4) were definitely much enriched in proteinaceous OM relative to
aragonite crystals in pearls and that V (group 3) in pearls showed only slight enrichment in the organicrich layer. By contrast,
the other elements showed small differences between both layers (enrichment factor of <3), suggesting that these elements
occur largely in aragonite crystals. 相似文献
993.
对冲绳海槽Jade热液区块状硫化物中流体包裹体的氦、氖和氩同位素组成进行了测定,流体包裹体的3He/4He比值为(6.2~10.1)Ra,均值为7.8Ra,与大洋中脊玄武岩一致[3He/4He≈(6~11)Ra],20Ne/22Ne比值为10.7~11.3,明显高于大气值(9.8),而40Ar/36Ar比值的变化范围在287~334之间,接近大气值(295.5),这些结果表明,块状硫化物中热液流体捕获的稀有气体是地幔和海水源组分混合的产物,且流体包裹体中的氦主要来自地幔,氖和氩主要来自海水。 相似文献
994.
Distribution and sources of organic carbon, nitrogen and their isotopes in sediments of the subtropical Pearl River estuary and adjacent shelf, Southern China 总被引:17,自引:1,他引:17
The isotopic composition (δ13C and δ15N) and organic carbon (OC) and total nitrogen (TN, organic plus inorganic) content of 37 carbonate-free surficial sediments of the subtropical Pearl River estuary and the adjacent shelf of South China Sea (SCS) was determined. The δ13C values indicate that the sediment organic material is a mixture from two sources, terrestrial and marine. Several of the sediments have extremely low (< 4) OC / TN ratios, which could be due to low OC contents and/or to a significant fraction of the TN present as inorganic nitrogen adsorbed on clays. In general, the spatial patterns of OC, TN, δ13C and δ15N are similar. Values are low at the river mouth and on the western coast, suggesting proportionally greater accumulation of terrestrial particulate organic matter relative to marine phytodetritus, which is limited by low productivity in the turbid plume of the Pearl River. Algal-derived organic carbon (al-OC) content is estimated to be low (≤ 0.06%) at the river mouth and higher (up to 0.57%) on the adjacent inner shelf based on a mixing model of end members. 相似文献
995.
Ernesto Medina Marta Francisco Leonel Sternberg William T. Anderson 《Estuarine, Coastal and Shelf Science》2005,63(4):527-536
The 87Sr, 13C, and 15N isotopic signatures of organic matter in sediments from the continental shelf facing the Orinoco Delta were measured to determine the contribution of sediments transported from the Amazon River by the coastal Guayana current and the sediments transported by the Orinoco River. Box core samples between 60 and 300 m water depth collected along 4 transects located eastwards to the Orinoco Delta were analyzed. Carbon and nitrogen concentrations decreased with depth under water on the shelf, and were strongly correlated indicating homogeneity of organic matter composition. Phosphorus content was also associated to organic matter in most samples, but some of them revealed deposition of P-enriched sediments. The 87Sr/86Sr ratios showed a strong continental signature averaging 0.7117, therefore, limiting the possible carbon and nitrogen sources associated with these sediments to C3 trees, C4 grasses, or freshwater phytoplankton. The δ13C values were relatively high averaging −21‰, above values reported for sediments on the Amapá shelf and the Amazon River in Brazil. Average δ13C values did not differ significantly among transects. High δ13C values point to the influence of organic matter transported from the C4-plants dominated savannas in the northern fringe of the Orinoco River. δ15N values were positive and averaged 5‰, being within the range of values measured in the Marajo island (Amazon River) and the estuary of the Pará River. The δ15N values differed significantly among transects (4.9–5.2‰), lowest values corresponding to the northernmost transect near the coast of Trinidad, and the highest values corresponding to the transect located at the southernmost position. 相似文献
996.
Tracing suspended organic nitrogen from the Yangtze River catchment into the East China Sea 总被引:2,自引:0,他引:2
Ying Wu Thorsten Dittmar Kai-Uwe Ludwichowski Gerhard Kattner Jing Zhang Zhuo Y. Zhu Boris P. Koch 《Marine Chemistry》2007
Total suspended matter was collected along the Yangtze River (Changjiang) and in the East China Sea in April to May and in September 2003, respectively, to study origin and fate of particulate organic nitrogen. Concentrations of particulate organic carbon (POC), nitrogen (PN) and hydrolyzable particulate amino acids (PAA; d- and l-enantiomers) were higher in the Yangtze Estuary than in the river and decreased offshore towards the shelf edge. In the coastal area, higher values of PAA were observed in the surface layer than in the bottom water. Stable carbon isotope ratios (δ13C) of POC increased from − 24.4‰ in the river to values around − 21‰ on the East China Sea Shelf. Dominant amino acids were aspartic acid + aspartine (Asx), glutamic acid + glutamine (Glx), glycine, alanine and serine. The proportions of Asx, Glx and isoleucine were higher in the marine than in the riverine samples contrary to the distributions of glycine, alanine, threonine and arginine. The proportions of d-amino acids were highest in the riverine suspended organic matter (6% of PAA) decreasing towards the shelf edge (1.5% of PAA). d-arginine, not reported in natural aquatic samples so far, was the most abundant d-amino acid in the river. The amino acid composition of the particulate organic matter (POM) in the Yangtze River indicates an advanced stage of degradation of POM. Highly degraded organic matter from soils is probably a main source of POM in the Yangtze River, but the relatively high δ13C values and low C/N ratios (7.7 ± 1.6) also indicate contribution from anthropogenic sources. The degraded riverine material was a dominant organic matter source in the estuary, where aquatic primary production had only a small overall contribution. In the East China Sea, gradual settling of riverine organic matter and the addition of fresher phytoplankton impacted the amino acid composition and δ13C values, and on the outer shelf relatively fresh phytoplankton-derived organic matter dominated. 相似文献
997.
南海沉积物中U,Th分布特征及其古环境意义 总被引:1,自引:0,他引:1
对采自南海深海中的两个柱样进行了分析。沉积速率分别为6.2cm·ka-1(317-82-25柱)和4.2cm·ka-1(90-37柱),均明显大于其他深海沉积速率,说明了南海这个边缘海的“放大效应”。此外,还分析了采自珠江口至外陆架的表层样,总结出从几元素在平面上的分布规律:从河口一陆架边缘~半深海,U,几含量的变化趋势均为多~少一多,Th/U比为小→大→小;而碳酸盐含量则显示出少→多→少的分布规律,即U,Th的含量与碳酸盐含量成反比,这可能是碳酸盐的所谓“稀释效应”所致。铀含量随柱样深度的变化曲线基本上与氧同位素曲线相吻合,其相关系数达0.67,证明U含量变化可能具有气候意义。Th的高含量点亦落在冷期之内。文中还探讨了水中铀的来源去向,说明了它能反映气候变化的原因。 相似文献
998.
An Ecosystem Model Including Nitrogen Isotopes: Perspectives on a Study of the Marine Nitrogen Cycle
Chisato?YoshikawaEmail author Yasuhiro?Yamanaka Takeshi?Nakatsuka 《Journal of Oceanography》2005,61(5):921-942
We have developed an ecosystem model including two nitrogen isotopes (14N and 15N), and validated this model using an actual data set. A study of nitrogen isotopic ratios (δ15N) using a marine ecosystem model is thought to be most helpful in quantitatively understanding the marine nitrogen cycle.
Moreover, the model study may indicate a new potential of δ15N as a tracer. This model has six compartments: phytoplankton, zooplankton, particulate organic nitrogen, dissolved organic
nitrogen, nitrate and ammonium in a two-box model, and has biological processes with/without isotopic fractionation. We have
applied this model to the Sea of Okhotsk and successfully reproduced the δ15N of nitrate measured in seawater and the seasonal variations in δ15N of sinking particles obtained from sediment trap experiments. Simulated δ15N of phytoplankton are determined by δ 15N of nitrate and ammonium, and the nitrogen f-ratio, defined as the ratio of nitrate assimilation by phytoplankton to total nitrogenous nutrient assimilation. Detailed
considerations of biological processes in the spring and autumn blooms have demonstrated that there is a significant difference
between simulated δ15N values of phytoplankton, which assimilates only nitrate, and only ammonium, respectively. We suggest that observations of
δ 15N values of phytoplankton, nitrate and ammonium in the spring and autumn blooms may indicate the ratios of nutrient selectivity
by phytoplankton. In winter, most of the simulated biogeochemical fluxes decrease rapidly, but nitrification flux decreases
much more slowly than the other biogeochemical fluxes. Therefore, simulated δ15N values and concentrations of ammonium reflect almost only nitrification. We suggest that the nitrification rate can be parameterized
with observations of δ15N of ammonium in winter and a sensitive study varying the parameter of nitrification rate. 相似文献
999.
Ernesto Otero Randolph Culp John E. Noakes Robert E. Hodson 《Estuarine, Coastal and Shelf Science》2003,56(5-6):1187-1194
In this study, we examine the distribution and carbon stable isotope signature of dissolved organic carbon (DOC) and humic substances (HS) along a salinity gradient in the Altamaha and Satilla River estuaries. The maximum DOC concentrations in the Altamaha and Satilla were 10 and 29 mg C l−1, respectively, though concentrations were similar at the mouth of both estuaries. There was a decrease in HS content of DOC from 50 to 80% at the head of the estuaries to 10% at salinities higher than 30‰. The δ13C DOC varied between −25.5 and −19‰ and between −27 and −21‰ in the Altamaha and Satilla estuaries, respectively. The tendency towards more depleted δ13C DOC in the Satilla, especially in the lower salinity portion of this estuary, suggests greater terrestrial inputs in the Satilla than in the Altamaha. Seasonal fluctuations were observed in the form of increased (two to three times) range in DOC concentration, heavier δ13C DOC and increased proportion of estuarine–marine-derived DOC (average enrichment of δ13C DOC from +1 to +2) during low river flow (July–October). The δ13C HS in both rivers showed a similar trend, but was consistently more depleted than DOC, with an average range from −28 to −24.5‰. This suggests that HS have larger proportions of terrestrial components (a maximum of >60% at the mouth of the estuary) than DOC. The less depleted δ13C values of DOC in comparison with HS indicate a different source for the non-humic (non-HS) component of DOC (range in δ13C non-HS, −22 to −16‰). That source could either be the decomposition of detrital material derived from saltmarsh environments or microalgal-derived DOC of estuarine or marine origins. 相似文献
1000.
J. C. Bailey 《Australian Journal of Earth Sciences》2013,60(1):7-23
Hornblende‐bearing xenoliths in the I‐type Petford Granite, north‐east Queensland, show an abundance pattern suggesting redistribution in a convecting magma system and were probably carried up with the host magma. The Petford Granite and xenoliths are chemically cognate, but quartz monzodiorite‐granodiorite bodies (a potential source for the xenoliths) in the adjacent country rocks belong to an independent magma suite. The xenoliths are chemically similar to andesite lavas and dykes 90 km to the NW. They represent fragments of the parental andesite (diorite) of a calcalkaline suite, which fractionated to yield the Petford Granite. They are not source rocks for the granite melt, melt residua, or early cumulates. The fractionated granite melt broke through the earlier envelope of diorite and rose into the upper crust, carrying dioritic fragments with it. Interaction between magma and xenoliths was generally minimal. 相似文献