首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   55篇
  免费   1篇
  国内免费   3篇
地球物理   16篇
地质学   29篇
海洋学   3篇
天文学   1篇
综合类   2篇
自然地理   8篇
  2022年   2篇
  2021年   1篇
  2017年   1篇
  2016年   1篇
  2013年   1篇
  2012年   2篇
  2011年   4篇
  2010年   4篇
  2009年   3篇
  2008年   3篇
  2007年   5篇
  2005年   2篇
  2004年   3篇
  2002年   1篇
  2000年   3篇
  1996年   1篇
  1995年   2篇
  1993年   4篇
  1991年   1篇
  1986年   1篇
  1985年   1篇
  1982年   2篇
  1979年   1篇
  1977年   1篇
  1976年   1篇
  1974年   1篇
  1972年   1篇
  1965年   1篇
  1964年   2篇
  1963年   1篇
  1962年   1篇
  1956年   1篇
排序方式: 共有59条查询结果,搜索用时 15 毫秒
21.
We have studied cation ordering in dolomite in situ as a function of pressure, temperature, and experimental time using the multi-anvil apparatus and synchrotron radiation. Starting with ordered dolomite, we observe the onset of disordering taking place at 950°C, while complete disordering is achieved at 1,070 (±20)°C, for pressures ranging between 3.37 and 4.05 GPa. Pressure does not appear to have significant effect on the order/disorder transition over the investigated range. We find that dolomite can reach its equilibrium ordering state above 900°C within duration of laboratory experiment (few hours), both from disordered state and from ordered state. In addition, we have reversed the dolomite breakdown reaction [magnesite + aragonite = dolomite] between 4.5 and 5.5 GPa, by monitoring diffraction peak intensity. We also have determined that dolomite is stable up to 7.4 GPa at 1,100°C. We confirm some earlier studies where a change in slope (dP/dT) has been observed, but we find a non-zero slope in the low pressure range. Combining the values of entropy obtained from dolomite degree of ordering with enthalpy values deduced from our bracketing of [magnesite + aragonite = dolomite] equilibrium, we model the location of dolomite breakdown in the P–T space as a function of cation ordering. By comparing previous conflicting studies, we show that, although kinetics of order/disorder is fast, disequilibrium dolomite breakdown is possible. Our modeling shows that subducted disordered dolomite present in carbonated sediments could be decomposed to [magnesite + aragonite] at lower pressure (3.5 GPa) than usually considered (>5 GPa). This 2-GPa (60 km) difference is valid on a fast subduction path and is possible if disorder inherited from sedimentation is preserved. On a slow subduction path, however, dolomite breakdown is encountered at about 250 km depth, which is 100 km deeper than currently considered.  相似文献   
22.
As a first step toward describing water flow processes in bedrock, a coil‐type time domain reflectometry (TDR) probe capable of measuring volumetric water content, θ, in weathered bedrock at three depths was prepared. Because the coil‐type TDR probe is large in diameter (19 mm), it can be installed even in highly weathered bedrock more easily and appropriately than conventional TDR probes that consists of two or three rods of small diameter (5‐8 mm). The probe calibrations suggest that the values measured by the probe are very sensitive to changes in θ. Using the calibrated probe together with commercially available profile soil moisture sensors, the θ profile was monitored for 1 year. Even rainfall events with relatively small cumulative rainfall of 15 mm increased the bedrock θ, and the increments were comparable to those in the soil. After the end of the rainfall events, the bedrock θ displayed a more rapid drop than the soil, and varied little during the period of no rainfall. The water storage showed similar tendencies. These observations suggest that the bedrock θ is controlled by clearly distinguishable macropores and micropores within the bedrock. It is concluded that the coil‐type TDR probe is very effective in determining θ in weathered bedrock, and that bedrock, conventionally defined by conducting cone penetration tests and treated as impermeable, does conduct and hold substantial amounts of water, and therefore contribute greatly to hydrological processes in headwater catchments. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   
23.
24.
Palaeocene (c. 55–58 Ma) adakitic andesites from the Yanjiarea, NE China, are typically clinopyroxene-bearing sodic andesitescontaining 60· 9–62· 2% SiO2 and 4·02–4· 36% MgO, with high Mg-number [100 Mg/(Mg+ Fe) atomic ratio] from 65· 5 to 70· 1. Whole-rockgeochemical features include high Cr (128–161 ppm) andNi (86–117 ppm) concentrations, extremely high Sr (2013–2282ppm), low Y (10–11 ppm) and heavy rare earth elements(HREE; e.g. Yb = 0· 79–1· 01 ppm), and mid-oceanridge basalt (MORB)-like Sr–Nd–Pb isotopic compositions[e.g. 87Sr/ 86Sr(i) = 0· 70298–0· 70316,Nd(t) = +3· 8 to +6· 3 and 206Pb/ 204Pb = 17·98 – 18· 06], analogous to high-Mg adakites occurringin modern subduction zones. However, mineralogical evidencefrom clinopyroxene phenocrysts and microcrystalline plagioclaseclearly points to magma mixing during magma evolution. Iron-richclinopyroxene (augite) cores with low Sr, high Y and heavy REEcontents, slightly fractionated REE patterns and large negativeEu anomalies probably crystallized along with low-Ca plagioclasefrom a lower crustal felsic magma. In contrast, high Mg-numberclinopyroxene (diopside and endiopside) mantles and rims havehigher Sr and lower HREE and Y concentrations, highly fractionatedREE patterns (high La/Yb) and negligible Eu anomalies, similarto those found in adakites from subduction zones. The Yanjiadakitic andesites can be interpreted as a mixture between acrust-derived magma having low Mg-number and Sr, and high Yand HREE, and a mantle-derived high Mg-number adakite havinghigh Sr and low Y and HREE concentrations. During storage and/orascent, the mixed magma experienced further crustal contaminationto capture zircons, of a range of ages, from the wall rocks.The absence of coeval arc magmatism and an extensional tectonicregime in the Yanji area and surrounding regions suggest thatthese Palaeocene adakitic andesites were formed during post-subductionextension that followed the late Cretaceous Izanagi–Farallonridge subduction. Generation of these adakitic andesites doesnot require contemporaneous subduction of a young, hot oceanicridge or delamination of eclogitic lower crust as suggestedby previous models. KEY WORDS: magma mixing; adakitic andesites; Palaeocene; NE China  相似文献   
25.
Newly emerged landscapes above sea level are characterized by rapidly evolving geomorphic systems where the initial fluvial pattern adapts to a former submarine topography. Such an early formed fluvial system establishes drainage basins and unstable landforms that characterize high topographic asymmetry which are prone to fast removal or reorganization. Transitional landscapes might form depositional systems as lakes or ponds that subsequently are incised, captured and incorporated into drainage basins. In this study we focus on the recently emerged Hengchun Peninsula to survey its paleoenvironment evolution. Three drillings performed in the Gangkou basin with fieldwork revealed several indicators that reconstructed stages of the landscape reorganization. The major finding shows an ephemeral large lake in the central part of the Hengchun Peninsula that was drained to the Pacific c. 6000 bp . The lake belonged to an ephemeral lakeland that was created after the emergence of the peninsula. Currently, several areas as relict landforms indicate this stage of topography evolution that through high rates of incision and subsequent captures, transforms into drainage basins. Furthermore, two drillings show brackish waters at the present estuary of the Gangkou basin. These two different paleoenvironments today build one system – Gangkou catchment. Long-term uplift rates show that a hanging wall of the Hengchun Fault plays a significant role in the creation of a lakeland by tilting the peninsula's surface. The tilt impacts on asymmetrical emergence of the peninsula and catchment development. Our study shows that a new geomorphic system might create depositional ephemeral landforms (lakes) that represent phases of early topography evolution after emergence above a sea level that are subjected to instantaneous rearrangement and evolves through large-scale phases before it reaches a topographic steady-state.  相似文献   
26.
MgSiO3 akimotoite is stable relative to majorite-garnet under low-temperature geotherms within steeply or rapidly subducting slabs. Two compositions of Mg–akimotoite were synthesized under similar conditions: Z674 (containing about 550 ppm wt H2O) was synthesized at 22 GPa and 1,500 °C and SH1101 (nominally anhydrous) was synthesized at 22 GPa and 1,250 °C. Crystal structures of both samples differ significantly from previous studies to give slightly smaller Si sites and larger Mg sites. The bulk thermal expansion coefficients of Z674 are (153–839 K) of a 1 = 20(3) × 10?9 K?2 and a 0 = 17(2) × 10?6 K?1, with an average of α 0 = 27.1(6) × 10?6 K?1. Compressibility at ambient temperature of Z674 was measured up to 34.6 GPa at Sector 13 (GSECARS) at Advanced Photon Source Argonne National Laboratory. The second-order Birch–Murnaghan equation of state (BM2 EoS) fitting yields: V 0 = 263.7(2) Å3, K T0 = 217(3) GPa (K′ fixed at 4). The anisotropies of axial thermal expansivities and compressibilities are similar: α a  = 8.2(3) and α c  = 10.68(9) (10?6 K?1); β a  = 11.4(3) and β c  = 15.9(3) (10?4 GPa). Hydration increases both the bulk thermal expansivity and compressibility, but decreases the anisotropy of structural expansion and compression. Complementary Raman and Fourier transform infrared (FTIR) spectroscopy shows multiple structural hydration sites. Low-temperature and high-pressure FTIR spectroscopy (15–300 K and 0–28 GPa) confirms that the multiple sites are structurally unique, with zero-pressure intrinsic anharmonic mode parameters between ?1.02 × 10?5 and +1.7 × 10?5 K?1, indicating both weak hydrogen bonds (O–H···O) and strong OH bonding due to long O···O distances.  相似文献   
27.
We studied the elemental and isotopic (Pb, B and Li isotopes) composition of melt inclusions hosted in highly forsteritic (Fo83–91) olivines that were collected from San Bartolo lava and pumice (ST79p, ST82p and ST531p) samples erupted by Stromboli in historical times. The studied melt inclusions have primitive calcalkaline to shoshonitic basaltic compositions. They cover a compositional range far wider than that exhibited by the whole-rocks and differ in key trace element ratios. San Bartolo melt inclusions are characterized by lower incompatible trace element abundances, higher ratios between fluid-mobile (B, Pb, U and LILE) and less fluid-mobile (REE, Th, HFSE) elements and lower La/Yb ratios relative to the pumice-hosted melt inclusions and pumiceous melts erupted during paroxysmal events. Trace elements, along with different Pb, B and Li isotopic signatures, attest to source heterogeneity on the small scale and provide new insights into subducted components beneath Stromboli. Results of a mixing model suggest that metasomatism of the mantle source of pumice-hosted melt inclusions was driven by solute-rich high-pressure fluids (<20%) expelled from the deep portion of the slab. Heterogeneous Pb isotopic composition together with light δ11B (−8.6 to −13.7‰) and δ7Li (+2.3 to −1.7‰) indicates that high-pressure liquids were released in variable proportions from highly dehydrated metabasalts and metasediments. On the other hand, the elemental and isotopic (δ11B ~ −1.9 to −5.9‰) composition of San Bartolo melt inclusions is better explained by the addition of a prevalent aqueous component (~2 to 4%) escaped at shallower depths from sediments and altered basaltic crust in almost equivalent proportions, with a smaller contribution by high-pressure fluids. Owing to the high-angle dip of the subducted cold Ionian slab, aqueous fluids and high-pressure fluids would rise through the mantle wedge and locally superimpose on each other, thus giving origin to variously metasomatized mantle domains.  相似文献   
28.
The rheological properties of mantle materials are being investigated up to pressures of 16 GPa and temperatures of 1600°C for times up to 24 h, using a new sample assembly for the 6–8 multi-anvil apparatus. Al2O3 pistons, together with a liquid confining medium, are used to generate deviatoric stress in the specimen. Strain rates are estimated by monitoring the relative displacement of the guide blocks of the multi-anvil apparatus, scaled to the total axial strain of the sample. The applied stress on the sample is estimated using grain size piezometry. Strain rates and flow stresses of approximately 10–4 to 10–6 s–1 and 50 to 250 MPa respectively, are presently attainable.Preliminary results on San Carlos olivine single crystals, partially dynamically recrystallized to a grain size of 10 to 300 m, indicate that the effective viscosity of polycrystalline olivine is consistent with values obtained from olivine single crystal creep laws. Assuming a dislocation creep mechanism (n3.5) with (010)[001] as the dominant slip system, the data are best fit using a creep activation volume of 5 to 10×10–6 m3 mol–1.  相似文献   
29.
Pressure–temperature conditions of tourmaline breakdown in a metapelite were determined by high-pressure experiments at 700–900°C and 4–6 GPa. These experiments produced an eclogite–facies assemblage of garnet, clinopyroxene, phengite, coesite, kyanite and rare rutile. The modal proportions of tourmaline clearly decreased between 4.5 and 5 GPa at 700°C, between 4 and 4.5 GPa at 800°C, and between 800 and 850°C at 4 GPa, with tourmaline that survived the higher temperature conditions appearing corroded and thus metastable. Decreases in the modal abundance of tourmaline are accompanied by decreasing modal abundance of coesite, and increasing that of clinopyroxene, garnet and kyanite; the boron content of phengite increases significantly. These changes suggest that, with increasing pressure and temperature, tourmaline reacts with coesite to produce clinopyroxene, garnet, kyanite, and boron-bearing phengite and fluid. Our results suggest that: (1) tourmaline breakdown occurs at lower pressures and temperatures in SiO2-saturated systems than in SiO2-undersaturated systems. (2) In even cold subduction zones, subducting sediments should release boron-rich fluids by tourmaline breakdown before reaching depths of 150 km, and (3) even after tourmaline breakdown, a significant amount of boron partitioned into phengite could be stored in deeply subducted sediments.  相似文献   
30.
We report the first study of electrical conductivities of silicate melts at very high pressures (up to 10 GPa) and temperatures (up to 2,173 K). Impedance spectroscopy was applied to dry and hydrous albite (NaAlSi3O8) glasses and liquids (with 0.02–5.7 wt% H2O) at 473–1,773 K and 0.9–1.8 GPa in a piston-cylinder apparatus, using a coaxial cylindrical setup. Measurements were also taken at 473–2,173 K and 6–10 GPa in two multianvil presses, using simple plate geometry. The electrical conductivity of albite melts is found to increase with temperature and water content but to decrease with pressure. However, at 6 GPa, conductivity increases rapidly with temperature above 1,773 K, so that at temperatures beyond 2,200 K, conductivity may actually increase with pressure. Moreover, the effect of water in enhancing conductivity appears to be more pronounced at 6 GPa than at 1.8 GPa. These observations suggest that smaller fractions of partial melt than previously assumed may be sufficient to explain anomalously high conductivities, such as in the asthenosphere. For dry melt at 1.8 GPa, the activation energy at T > 1,073 K is higher than that at T < 1,073 K, and the inflection point coincides with the rheological glass transition. Upon heating at 6–10 GPa, dry albite glass often shows a conductivity depression starting from ~1,173 K (due to crystallization), followed by rapid conductivity enhancement when temperature approaches the albite liquidus. For hydrous melts at 0.9–1.8 GPa, the activation energies for conductivity at ≥1,373 K are lower than those at <973 K, with a complex transition pattern in between. Electrical conductivity and previously reported Na diffusivity in albite melt are consistent with the Nernst–Einstein relation, suggesting the dominance of Na transport for electrical conduction in albite melts.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号