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排序方式: 共有497条查询结果,搜索用时 62 毫秒
81.
Veronika Gälman Johan Rydberg Andrei Shchukarev Staffan Sjöberg Antonio Martínez-Cortizas Richard Bindler Ingemar Renberg 《Journal of Paleolimnology》2009,42(1):141-153
Easily discernible sediment varves (annual laminations) may be formed in temperate zone lakes, and reflect seasonal changes in the composition of the accumulating material derived from the lake and its catchment (minerogenic and organic material). The appearance of varves may also be influenced by chemical processes. We assessed the role of iron (Fe) and sulfur (S) in the appearance of varves in sediments from Lake Nylandssjön in northern Sweden. We surveyed Fe in the lake water and established whether there is internal transport of Fe within the sediment. We used a unique collection of seven stored freeze cores of varved sediment from the lake, collected from 1979 to 2004. This suite of cores made it possible to follow long-term changes in Fe and S in the sediment caused by processes that occur in the lake bottom when the sediment is ageing. We compared Fe and S concentrations using X-ray fluorescence spectroscopy (XRF) in specific years in the different cores. No diagenetic front was found in the sediment and the data do not suggest that there is substantial vertical transport of Fe and S in the sediment. We also modeled Fe and S based on thermodynamic, limnological, and sediment data from the lake. The model was limited to the five components H+, e?, Fe3+, SO4 2?, H2CO3 and included the formation of solid phases such as Fe(OH)3 (amorphous), FeOOH (aged, microcrystalline), FeS and FeCO3. Modeling showed that there are pe (redox) ranges within which either FeS or Fe(OH)3/FeOOH is the only solid phase present and there are pe ranges within which the two solid phases co-exist, which supports the hypothesis that blackish and grey-brownish layers that occur in the varves were formed at the time of deposition. This creates new possibilities for deciphering high-temporal-resolution environmental information from varves. 相似文献
82.
海水中钢铁腐蚀与环境因素的灰关联分析 总被引:6,自引:0,他引:6
应用灰关联分析方法解析了海水环境因素与钢铁腐蚀的关系。根据灰关联度的计算 ,在诸海水环境因素中找出影响碳钢、低合金钢在海水中局部腐蚀深度及平均腐蚀率的主要影响因素 ,分析结果与现场试验结果较为吻合 相似文献
83.
84.
The significance of organic matter origin for carbon oxidation via sulfate and iron reduction in the sediments of three acid mine lakes is analyzed. Carbon reactivity was estimated by fitting first‐order expressions to measured rates. Carbon oxidation rates via sulfate and ferric iron reduction ranged from 3.4 to 4.7 mmol m–2 d–1 and resembled those reported for freshwater lakes. The estimated reaction constants increased from about 10–3 a–1 at the interface to the former mine grounds to 0.05 to 0.2 a–1 at the current sediment‐water interface. Aquatic organic matter accounted for an estimated 45...75% of total carbon oxidation rates while it amounted only to about 5...14% of the total organic matter that had been deposited. The results of this study suggest that in highly acidic mine lakes the reactivity of the deposited organic matter can rapidly increase after flooding, enhancing carbon oxidation and internal neutralization rates in the sediments. 相似文献
85.
《地学前缘(英文版)》2020,11(4):1271-1287
The northern Xinjiang region is one of the most significant iron metallogenic provinces in China.Iron deposits are found mainly within three regions:the Altay,western Tianshan,and eastern Tianshan orogenic belts.Previous studies have elaborated on the genesis of Fe deposits in the Altay orogenic belt and western Tianshan.However,the geological characteristics and mineralization history of iron deposits in the eastern Tianshan are still poorly understood.In this paper I describe the geological characteristics of iron deposits in the eastern Tianshan,and discuss their genetic types as well as metallogenic-tectonic settings,Iron deposits are preferentially distributed in central and southern parts of the eastern Tianshan.The known iron deposits in the eastern Tianshan show characteristics of magmatic Fe-Ti-V(e.g.,Weiya and Niumaoquan),sedimentary-metamorphic type(e.g.,Tianhu),and iron skarn(e.g.,Hongyuntan).In addition to the abovementioned iron deposits,many iron deposits in the eastern Tianshan are hosted in submarine volcanic rocks with well-developed skarn mineral assemblages.Their geological characteristics and magnetite compositions suggest that they may belong to distal skarns.SIMS zircon U-Pb analyses suggest that the Fe-Ti oxide ores from Niumaoquan and Weiya deposits were formed at 307.7±1.3 Ma and 242.7±1.9 Ma,respectively.Combined with available isotopic age data,the timing of Fe mineralization in the eastern Tianshan can be divided into four broad intervals:Early Ordovician-Early Silurian(476-438 Ma),Carboniferous(335-303 Ma),Early Permian(295-282 Ma),and Triassic(ca.243 Ma).Each of these episodes corresponds to a period of subduction,post-collision,and intraplate tectonics during the Paleozoic and Mesozoic time. 相似文献
86.
87.
K. Urushibara-Yoshino 《Environmental Geology》1996,28(3):154-160
The properties of soils on previously dated sand dunes from Robe to Naracoorte in South Australia were examined. In these
areas younger sand dunes are composed of fresh sand, but older sand dunes are composed of calcarenited sand. The soils on
the sand dunes developed successionally by the age of sand dunes. The soil properties of these sand dunes differ depending
on the ages of the sand dunes. The properties of sand particles in soils are as follows:
(1) On the sand dunes of 4300 years B.P., A/C profile developed (Rendzina). On the sand dunes older than 125 000 years B.P.
and on the plateau of Tertiary limestone, soil profiles of A1/AB/B/C on the sand dunes of 83 000 years B.P. and A1/A3/B1/B2/C (Terra rossa) are well developed.
(2) Within the sand of A/C horizons of the sand dunes with the age of 4300 year B.P., the calcite grain content is about 64%,
and the quartz content is about 35%. Within the B horizons of soils on the dunes from 83 000 years B.P. to 347 000 years B.P.,
the calcite grain content is only 1–2%; however, the quartz grain content is about 92%. In the B2 horizons of soils on the dune of 690 000 years B.P. and on the Tertiary plateau, there are some calcite grains but the quartz
grain content is about 96%.
(3) The average size of quartz grains in the soils on the sand dunes from 4300 B.P. to 347 000 years B.P. is generally smaller,
but the average size of quartz on the sand dunes of 690 000 year B.P. becomes larger and the grains are well rounded. On the
Tertiary limestone plateau, the average quartz size becomes again smaller, and the grains are more rounded.
(4) Fet in B2 horizon of the soil profiles increases clearly corresponding to the age. Iron activity expressed by Feo/Fed also shows a close relation to the chronological sequence. The B horizon of the soil profiles shows a drastic decrease of
Feo/Fed according to the age. Iron crystalinity, (Fed-Feo)/Fet, has a tendency for a positive relation with increasing age.
Received: 1 June 1995 · Accepted: 4 December 1995 相似文献
88.
C. Neal S. Lofts C. D. Evans B. Reynolds E. Tipping M. Neal 《Aquatic Geochemistry》2008,14(3):263-288
Iron distributions in rainfall, streams, soils and groundwaters are described for the Upper River Severn catchment of mid-Wales.
Iron is mainly supplied from within-catchment sources with highest concentrations occurring under reducing conditions. Iron
concentrations have doubled over the past 20 years (~5.0 μg yr−1 for the forest and ~3.7 μg yr−1 for the moorland). For the forested sites, the gradients are particularly high post-1993. UK rivers/lakes monitored by the
UK Acid Waters Monitoring Network show similar increases. Generally, Fe correlates with dissolved organic carbon (DOC). The
greatest rates of Fe increase coincide with those for DOC. Thermodynamic modelling using WHAM/Model VI indicates that Fe(III)
is mainly in microparticulate form (probably oxyhydroxides) apart from under reducing conditions. It is proposed that Fe increases
for surface waters are associated with increased microparticulate Fe(III) due to stabilisation against aggregation by binding
of DOM to its surface. The results relate to acidification declines and deforestation leading to land disturbance and wetter
conditions within the soil. There will be greater acidification reversal following tree harvesting due to lowering of atmospheric
SOx scavenging and this may have resulted in the greater increase in Fe in the later years of the study. 相似文献
89.
Je-Hun Jang Ryan Mathur Laura J. Liermann Shane Ruebush Susan L. Brantley 《Chemical Geology》2008,250(1-4):40-48
We measured the Fe isotope fractionation during the reactions of Fe(II) with goethite in the presence and absence of a strong Fe(III) chelator (desferrioxamine mesylate, DFAM). All experiments were completed in an O2-free glove box. The concentrations of aqueous Fe(II) ([Fe(II)aq]) decreased below the initial total dissolved Fe concentrations ([Fe(II)total], 2.15 mM) due to fast adsorption within 0.2 day. The concentration of adsorbed Fe(II) ([Fe(II)ads]) was determined as the difference between [Fe(II)aq] and the concentration of extracted Fe(II) in 0.5 M HCl ([Fe(II)extr]) (i.e., [Fe(II)ads] = [Fe(II)extr] − [Fe(II)aq]). [Fe(II)ads] also decreased with time in experiments with and without DFAM, documenting that fast adsorption was accompanied by a second, slower reaction. Interestingly, [Fe(II)extr] was always smaller than [Fe(II)total], indicating that some Fe(II) was sequestered into a pool that is not HCl-extractable. The difference was attributed to Fe(II) incorporated into goethite structure (i.e., [Fe(II)inc] = [Fe(II)total] −[Fe(II)extr]). More Fe(II) was incorporated in the presence of DFAM than in its absence at all time steps. Regardless of the presence of DFAM, both aqueous and extracted Fe(II) (δ56/54Fe(II)aq and δ56/54Fe(II)extr) became isotopically lighter than or similar to goethite (− 0.27‰) at day 7, implying that the isotope exchange occurred between bulk goethite and aqueous Fe. Consistently, the mass balance indicated that the incorporated Fe is isotopically heavier than extracted Fe. These observations suggested that (i) co-adsorption of Fe(II) with DFAM resulted in more pervasive electron transfer, (ii) the electron transfer from heavy Fe(II) in the adsorbed Fe(II) to light Fe(III) in goethite results in the fixation of heavy adsorbed Fe(III) on the surface and accumulation of Fe(II) within the goethite, and (iii) desorption of the reduced, light Fe from goethite does not necessarily occur at the same surface sites where adsorption occurred. 相似文献
90.
Mousa F. Attom 《Environmental Geology》2008,55(4):781-788
Iron filling and iron filling–cement mixture were used to improve the shear strength characteristics of Irbid clayey soil.
For this purpose, five types of Irbid clay soils were obtained and mixed with iron filling and iron filling–cement mixture
at different percentages. Two sets of prepared samples were mixed with the admixture. The first set was prepared by mixing
the soil samples with iron filling alone at 2.5, 5.0, 7.5, and 10% by dry weight of the soil. The second set was prepared
by mixing with iron filling–cement mixture at equal ratio of the same percentages of the first set. An unconfined compression
test was performed in this study to measure the shear strength properties of the soils. The test results showed that the increase
in the percentages of the iron filling and iron filling–cement mixture up to 10% will result in increasing the maximum dry
density of the soil and increase the unconfined compressive strength and the secant of modulus of elasticity of the clayey
soil. Also, the addition of iron filling–cement mixture increased the unconfined compressive strength and secant modulus of
elasticity of the clayey soil higher than the addition of iron filling alone. 相似文献