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91.
章敏  韩晓华  潘永信 《岩石学报》2019,35(7):2206-2218
条带状铁建造(BIFs)中含有大量的亚铁磁性矿物,其组成及来源是认识BIF成因的重要依据。本文研究了南非巴伯顿绿岩带无花果树群(距今约32亿年)恩圭尼亚组的BIFs样品的磁学和矿物学特征。通过测量富铁层与富硅层的磁滞回线、等温剩磁获得曲线与退磁曲线、矫顽力谱分析、一阶反转曲线(FORC)、低温(20~300K)有场/无场冷却曲线以及k-T曲线、Lowrie三轴热退磁曲线,结合扫描电镜观测,揭示出研究样品中磁性矿物主要为赤铁矿和磁铁矿。基于矫顽力谱分析,富铁层中磁铁矿主要是多畴及假单畴颗粒,相对含量平均为2. 1%;赤铁矿的相对含量平均为97. 9%。富硅层中磁铁矿主要为假单畴及超顺磁性颗粒,相对含量平均为4. 6%;赤铁矿相对含量平均为95. 4%。测试样品具有Morin转变特征,转变温度介于250~260K,说明BIFs中主要为赤铁矿(0. 5~6mm)。富硅层样品出现~107K、~125K两个Verwey转变温度,表明其中可能存在生物成因和非生物成因两种类型磁铁矿。  相似文献   
92.
为了探讨生物硅对沉积物粒度测量结果的影响, 本文采用两种不同前处理方法对普里兹湾重力柱状样品进行了粒度测试。结果表明, 生物硅对沉积物的平均粒径以及黏土、粉砂、砂组分的影响较小, 而对沉积物的分选、偏态、峰态以及粒度频率分布的影响较显著。结合两组粒度组分相关性分析以及各粒级含量累积减小值, 认为生物硅对沉积物中砂、粉砂、黏土级组分含量的影响逐渐减小, 这也造成未去除生物硅的沉积物粒度测量结果偏粗。另外, 通过对比发现普里兹湾沉积物中生物硅粒径主要分布在<3Φ、5.25Φ—7.25Φ、8.75Φ—9.75Φ的粒径范围。极地研究中, 沉积物粒度结果为重建古环境变化提供重要参考, 本文研究认为在普里兹湾海域沉积物粒度研究中去除生物硅对研究结果有积极作用。  相似文献   
93.
《Sedimentology》2018,65(4):1390-1411
The earliest diagenetic post‐mortem exposure of biogenic carbonates at the sea floor and in the uppermost sediment column results in the colonization of hard‐part surfaces by bacterial communities. Some of the metabolic redox processes related to these communities have the potential to alter carbonate shell properties, and hence affect earliest diagenetic pathways with significant consequences for archive data. During a three‐month in vitro study, shell subsamples of the ocean quahog Arctica islandica (Linnaeus, 1767) were incubated in natural anoxic sediment slurries and bacterial culture medium of the heterotrophic Shewanella sediminis HAW ‐EB 3. Bulk analyses of the liquid media from the Shewanella sediminis incubation revealed an over ten‐fold increase in total alkalinity, dissolved inorganic carbon and ΩAragonite, and the alteration of the Mg/Ca, Mg/Sr and Sr/Ca ratios relative to control incubations without cultures. Ion ratios were most affected in the incubation with anoxic sediment, depicting a 25% decrease in Mg/Ca relative to the control. Shell sample surfaces that were exposed to both incubations displayed visible surface dissolution features, and an 8 wt% loss in calcium content. No such alteration features were detected in control shells. Apparently, alteration of shell carbonate properties was induced by microbially driven decomposition of shell intercrystalline organic constituents and subsequent opening of pathways for pore fluid–crystal exchange. This study illustrates the potential influence of benthic bacterial metabolism on biogenic carbonate archives during the initial stages of diagenetic alteration within a relatively short experimental duration of only three months. These results suggest that foremost the biological effect of bacterial cation adsorption on divalent cation ratios has the potential to complicate proxy interpretation. Results shown here highlight the necessity to consider bacterial metabolic activities in marine sediments for the interpretation of palaeo‐environmental proxies from shell carbonate archives.  相似文献   
94.
Woei-Lih Jeng   《Marine Chemistry》2006,102(3-4):242-251
The n-alkane average chain length (ACL) is the weight-averaged number of carbon atoms of the higher plant C25–C33 n-alkanes. The abundance of individual n-alkanes from higher plant sources generally increases with increasing carbon number in coastal marine sediments around Taiwan, but this trend is reversed for petrogenic hydrocarbons. The ACL would potentially be lowered if petrogenic hydrocarbons were added to sediments containing biogenic hydrocarbons alone. To test this idea, a marine environment off southwestern Taiwan known to contain both biogenic and petrogenic hydrocarbons and two nearby rivers were selected for investigating possible difference in ACL values between their sediments. The average CPI of C25–C33 n-alkanes was 4.08 ± 2.04 (range 1.90–8.96, n = 15) for the river sediments and 1.70 ± 0.16 (range 1.43–1.97, n = 15) for the marine sediments. The ACL of C25–C33 n-alkanes for river sediments ranged from 29.2 to 30.5 (average 29.9 ± 0.4), and for marine sediments from 28.4 to 29.3 (average 28.9 ± 0.3). The ACL difference between marine and river sediments was significant (Student's t test at 99% confidence) although it appeared small. It is suggested that the ACL can be an additional indicator for detection of petrogenic hydrocarbons in coastal marine sediments.  相似文献   
95.
碳酸钙-水体系氧同位素分馏系数的低温实验研究   总被引:4,自引:0,他引:4  
周根陶 《地学前缘》2000,7(2):321-338
碳酸钙是古气候和沉积岩稳定同位素地球化学研究中最常用的矿物 ,因此对碳酸钙水体系氧同位素分馏系数的实验校准已成为稳定同位素地球化学诞生以来的热点和前沿课题。但由于碳酸钙在自然界存在 3种同质多象变体 (方解石、文石和六方方解石 ) ,使人们对碳酸钙矿物与水之间氧同位素分馏系数的实验测定结果存在较大差别 ,当应用到同位素地质测温时 ,会给出显著不同的温度值。正确选用合理的方解石水或文石水体系分馏曲线 ,对低温和环境地球化学研究和应用具有重要价值。文章系统总结和评述了碳酸钙水体系氧同位素分馏系数实验校准的历史、方法和结果 ,对前人在表达方式上的不一致进行了统一 ,对氧同位素分馏的盐效应、动力氧同位素分馏效应和同质多象转变过程中的氧同位素继承性进行了讨论。通过对前人大量实验数据的系统处理并与理论计算相比较 ,推荐了热力学上平衡的方解石水体系氧同位素分馏方程 ,而对于文石水体系 ,理论计算结果尚有待于实验证实。  相似文献   
96.
Metal foil collection/flash desorption/flame photometric detection (MFC/FD/FPD) was one of the analytical methods used to measure emissions of gaseous, sulfur-containing compounds from several terrestrial natural sources during a cooperative field program in the summer of 1985. Nonspeciated, total sulfur gas emissions were determined by using the MFC/FD/FPD technique in combination with a Nafion Perma-Pure drying device to sample air from three designs of dynamic enclosure chambers. These enclosures were placed over various soil orders and vegetation in the vicinity of field sites in Iowa and Ohio previously examined during the 1977–80 SURE study of biogenic sulfur fluxes. Because of the sensitivity and detection characteristics of the MFC/FD/FPD technique, it was possible to obtain measurements on enclosure air samples that were collected for relatively short time periods,. e.g., 1 to 5 min. The magnitudes of these time-resolved, total sulfur gas emissions are correlated exponentially with internal enclosure air temperatures. Potential errors and uncertainties associated with this application of the MFC/FD/FPD methodology are assessed.The total sulfur gas flux values obtained from this study and the SURE program are compared. Unquantified sources of error in the current two parameter extrapolation model used to calculate regional and global terrestrial source strengths of biogenic sulfur emissions are also summarized and are shown to prevent a reliable estimate of overall uncertainty limits in the resultant inventory.  相似文献   
97.
为优化电感耦合等离子体发射光谱仪(ICP-OES)测试微量生物碳酸盐中元素含量的工作条件,在Thermo—Fisher公司生产的iCAP6300 Radial型ICP—OES上,对1050组仪器条件、32种不同组成的标准溶液、36个谱线对和两种仪器校正工作曲线进行了测试;借助开源科学计算软件Scilab数据插值和可视化...  相似文献   
98.
Inorganic aragonite occurs in a wide spectrum of depositional environments and its precipitation is controlled by complex physio-chemical factors. This study investigates diagenetic conditions that led to aragonite cement precipitation in Cenozoic glaciomarine deposits of McMurdo Sound, Antarctica. A total of 42 sandstones that host intergranular cement were collected from the CIROS-1 core, located proximal to the terminus of Ferrar Glacier. Standard petrography, Raman spectroscopy and electron microprobe analysis reveal a prominent aragonite cement phase that occurs as a pore-filling blocky fabric throughout the core. Oxygen isotope compositions (δ18O = −30·0 to −8·6‰ Vienna Pee-Dee Belemnite) and clumped isotope temperatures (TΔ47 = 13·1 to 31·5°C) determined from the aragonite cements provide precise constraints on isotopic compositions (δ18Ow) of the parent fluid, which mostly range from −10·8 to −7·2‰ Vienna Standard Mean Ocean Water. The fluid δ18Ow values are consistent with those of pore water, previously identified as cryogenic brine in the nearby AND-2A core. Petrographic and geochemical data suggest that aragonite cement in the CIROS-1 core precipitated from a similar brine. The brine likely formed and infiltrated sediments in flooded glacial valleys along the western margin of McMurdo Sound during the middle Miocene Climatic Transition, and subsequently flowed basinward in the subsurface. Consequently, the brine forms as a longstanding subsurface fluid that has saturated Cenozoic sediments below southern McMurdo Sound since at least the middle Miocene. Aragonite cementation in the CIROS-1 core is interpreted to reflect its proximal position to sites of brine formation and greater likelihood of experiencing brines with sustained high carbonate saturation states and Mg/Ca ratios. This unusual occurrence expands the range of known natural occurrences of aragonite cement. Given the potential for cryogenic brine formation in glaciomarine settings, blocky aragonite, as the end member of the spectrum of aragonite cement morphology, may be more widespread in glaciomarine sediments than currently thought.  相似文献   
99.
Biogenic opal content and mass accumulation rate (MAR) at IODP Expedition 323 Site U1343 were found to fluctuate consistently, generally being high under warm conditions and low under cold conditions during the last 2.4 Ma. Continuous wavelet transform analysis of the normalized biogenic opal content indicates that export production in the Bering Sea varied predominantly at 41-ka periodicity before 1.25 Ma, and shifted to 100-ka periodicity at the onset of the Mid-Pleistocene Transition (MPT; 1.25–0.7 Ma). The 100-ka cycles dominated until the Holocene. Export production in the Bering Sea decreased markedly in the Bering Sea two times during the MPT: the first occurred at the beginning of the MPT (1.25 Ma) and the second in the middle of the MPT (0.9 Ma). These decreases coincided with both increases in the relative abundance of sea-ice diatoms and decreases in the warm-water diatom species Neodenticula seminae, indicating that reductions in export production in the Bering Sea during the MPT were associated with climate cooling. Decreases in export production in the Bering Sea during the MPT were most likely associated with the increased influence of polar/Arctic domains on the high-latitude North Pacific.  相似文献   
100.
Musky Bay in Lac Courte Oreilles, Wisconsin, USA, is currently eutrophic. This large, shallow bay of an oligotrophic lake possesses the densest aquatic plant growth and a floating algal mat. Paleoecological reconstructions encompassing the last 130 years, were based on multiproxy analyses of sediment cores from three coring sites, two within the bay and one in the lake itself. These data were compared to historical records of the construction and expansion of two commercial cranberry bogs and shoreline residential homes to identify temporal and causal relations of eutrophication. The proxies investigated included: minor and trace elements; biogenic silica; and the diatom community. Post-depositional diagenesis of organic carbon, nitrogen, and phosphorus in the upper 30 cm of the core obscured records of historical ambient nutrient concentrations in the bay obviating their usefulness for this purpose. In contrast, calcium, magnesium, and potassium concentration profiles appeared to reflect runoff of soil amendments applied to the cranberry bogs and aerial fertilizer spraying over the eastern bog adjacent to Musky Bay. The increase in aluminum content since about 1930 coincided with the historical trend in shoreland development and construction of the original commercial cranberry farm. The biogenic silica profile recorded a steady increase of nutrients to Musky Bay over the last several decades. Stratigraphic changes in the diatom community indicated that nutrient input began to increase in the 1940s and accelerated in the mid-1990s with the onset of a noxious floating algal mat. The diatom community indicates the bay has possessed a significant macrophyte community for at least the last 200 years, but increased nutrient input was manifested by a change in the composition, and an increase in the density of the epiphytic diatom community. Cranberry farming appeared to be the major source of nutrients because the diatom community changes occurred prior to the significant increase in residential housing.  相似文献   
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