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61.
Sarah A. S. Dare Sarah-Jane Barnes Hazel M. Prichard Peter C. Fisher 《Mineralium Deposita》2011,46(4):381-407
Magmatic sulfide deposits consist of pyrrhotite, pentlandite, chalcopyrite (± pyrite), and platinum-group minerals (PGM).
Understanding the distribution of the chalcophile and platinum-group element (PGE) concentrations among the base metal sulfide
phases and PGM is important both for the petrogenetic models of the ores and for the efficient extraction of the PGE. Typically,
pyrrhotite and pentlandite host much of the PGE, except Pt which forms Pt minerals. Chalcopyrite does not host PGE and the
role of pyrite has not been closely investigated. The Ni–Cu–PGE ores from the South Range of Sudbury are unusual in that sulfarsenide
PGM, rather than pyrrhotite and pentlandite, are the main carrier of PGE, probably as the result of arsenic contribution to
the sulfide liquid by the As-bearing metasedimentary footwall rocks. In comparison, the North Range deposits of Sudbury, such
as the McCreedy East deposit, have As-poor granites in the footwall, and the ores commonly contain pyrite. Our results show
that in the pyrrhotite-rich ores of the McCreedy East deposit Os, Ir, Ru, Rh (IPGE), and Re are concentrated in pyrrhotite,
pentlandite, and surprisingly in pyrite. This indicates that sulfarsenides, which are not present in the ores, were not important
in concentrating PGE in the North Range of Sudbury. Palladium is present in pentlandite and, together with Pt, form PGM such
as (PtPd)(TeBi)2. Platinum is also found in pyrite. Two generations of pyrite are present. One pyrite is primary and locally exsolved from
monosulfide solid solution (MSS) in small amounts (<2 wt.%) together with pyrrhotite and pentlandite. This pyrite is unexpectedly
enriched in IPGE, As (± Pt) and the concentrations of these elements are oscillatory zoned. The other pyrite is secondary
and formed by alteration of the MSS cumulates by late magmatic/hydrothermal fluids. This pyrite is unzoned and has inherited
the low concentrations of IPGE and Re from the pyrrhotite and pentlandite that it has replaced. 相似文献
62.
C.S. Brehme W.I. Boarman S.A. Hathaway A. Herring L. Lyren M. Mendelsohn K. Pease M. Rahn C. Rochester D. Stokes G. Turschak R.N. Fisher 《Journal of Arid Environments》2009,73(9):811-820
We documented changes in the abundance and composition of terrestrial flora and fauna with respect to distance from the sea edge and timing of large allochthonous inputs from the Salton Sea, California. We found significant effects that were most pronounced within 300 m of the shore, but extended 3 km inland via coyote scat deposition. The zone within 300 m of the sea had a higher density of vegetation with a distinctly different plant composition. The denser vegetation supported higher abundances of birds and reptiles. Coyotes exhibited spatial and temporal responses to marine subsidies of fish, while birds were likely subsidized by aquatic aerial insects. Top-down control, as well as dietary and habitat preferences, may have resulted in reduced number of ants, beetles, and small mammals near the sea. Species responses to the habitat edge appeared to be associated with life history, as the near shore habitat favored habitat generalists and shore specialists, while inland desert habitat favored many sand and open desert specialists. Ecosystem responses support current theories of allochthonous spatial subsidies and consumer-resource dynamics but were limited in scope, magnitude, and distance. 相似文献
63.
中国南京与美国德克萨斯稻田甲烷排放的比较 总被引:8,自引:0,他引:8
Field measurements of methane emission from rice paddies were made in Nanjing, China and in Texas, USA, respectively. Soil temperature at approximately 10 cm depth of the flooded soils was automatically recorded. Aboveground biomass of rice crop was measured approximately every 10 days in Nanjing and every other week in Texas. Seasonal variation of soil temperature in Nanjing was quite wide with a magnitude of 15.3℃ and that in Texas was narrow with a magnitude of 2.9℃. Analysis of methane emission fluxes against soil temperature and rice biomass production demonstrated that the seasonal course of methane emission in Nanjing was mostly attributed to soil temperature changes, while that in Texas was mainly related to rice biomass production. We concluded that under the permanent flooding condition, the seasonal trend of methane emission would be determined by the soil temperature where there was a wide variation of soil temperature, and the seasonal trend would be mainly determined by rice biomass production if there are no additional organic matter inputs and the variation of soil temperature over the rice growing season is small. 相似文献
64.
Zircon M127 – A Homogeneous Reference Material for SIMS U–Pb Geochronology Combined with Hafnium,Oxygen and,Potentially, Lithium Isotope Analysis
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Lutz Nasdala Fernando Corfu John W. Valley Michael J. Spicuzza Fu‐Yuan Wu Qiu‐Li Li Yue‐Heng Yang Chris Fisher Carsten Münker Allen K. Kennedy Peter W. Reiners Andreas Kronz Michael Wiedenbeck Richard Wirth Chutimun Chanmuang Manuela Zeug Tamás Váczi Nicholas Norberg Tobias Häger Alfred Kröner Wolfgang Hofmeister 《Geostandards and Geoanalytical Research》2016,40(4):457-475
In this article, we document a detailed analytical characterisation of zircon M127, a homogeneous 12.7 carat gemstone from Ratnapura, Sri Lanka. Zircon M127 has TIMS‐determined mean U–Pb radiogenic isotopic ratios of 0.084743 ± 0.000027 for 206Pb/238U and 0.67676 ± 0.00023 for 207Pb/235U (weighted means, 2s uncertainties). Its 206Pb/238U age of 524.36 ± 0.16 Ma (95% confidence uncertainty) is concordant within the uncertainties of decay constants. The δ18O value (determined by laser fluorination) is 8.26 ± 0.06‰ VSMOW (2s), and the mean 176Hf/177Hf ratio (determined by solution ICP‐MS) is 0.282396 ± 0.000004 (2s). The SIMS‐determined δ7Li value is ?0.6 ± 0.9‰ (2s), with a mean mass fraction of 1.0 ± 0.1 μg g?1 Li (2s). Zircon M127 contains ~ 923 μg g?1 U. The moderate degree of radiation damage corresponds well with the time‐integrated self‐irradiation dose of 1.82 × 1018 alpha events per gram. This observation, and the (U–Th)/He age of 426 ± 7 Ma (2s), which is typical of unheated Sri Lankan zircon, enable us to exclude any thermal treatment. Zircon M127 is proposed as a reference material for the determination of zircon U–Pb ages by means of SIMS in combination with hafnium and stable isotope (oxygen and potentially also lithium) determination. 相似文献
65.
MIKE WALKER Martin J. Head John Lowe Max Berkelhammer Svante Bj
rck Hai Cheng Les C. Cwynar David Fisher Vasileios Gkinis Antony Long Rewi Newnham Sune Olander Rasmussen Harvey Weiss 《第四纪科学杂志》2019,34(3):173-186
The Holocene, which currently spans ~11 700 years, is the shortest series/epoch within the geological time scale (GTS), yet it contains a rich archive of evidence in stratigraphical contexts that are frequently continuous and often preserved at high levels of resolution. On 14 June 2018, the Executive Committee of the International Union of Geological Sciences formally ratified a proposal to subdivide the Holocene into three stages/ages, along with their equivalent subseries/subepochs, each anchored by a Global boundary Stratotype Section and Point (GSSP). The new stages are the Greenlandian (Lower/Early Holocene Subseries/Subepoch) with its GSSP in the Greenland NGRIP2 ice core and dated at 11 700 a b2k (before 2000 CE); the Northgrippian (Middle Holocene Subseries/Subepoch) with its GSSP in the Greenland NGRIP1 ice core and dated at 8236 a b2k; and the Meghalayan (Upper/Late Holocene Subseries/Subepoch) with its GSSP in a speleothem from Mawmluh Cave, north‐eastern India, with a date of 4250 a b2k. We explain the nomenclature of the new divisions, describe the procedures involved in the ratification process, designate auxiliary stratotypes to support the GSSPs and consider the implications of the subdivision for defining the Anthropocene as a new unit within the GTS. 相似文献
66.
Efforts to measure the rate of nitrogen recycling in natural waters have depended on estimates of ammonium production using the 15N isotope dilution method. This technique requires the removal of dissolved ammonium from the water sample for analysis of the 15N content. Steam distillation or micro-diffusion methods have been most commonly used, but these techniques are labor intensive and time consuming. We have attempted to simplify the measurement of the planktonic regeneration of ammonium by presenting a mercury precipitation technique which is simple, practical, and easily used at sea. 相似文献
67.
68.
Christina Yan Wang Hazel M. Prichard Mei-Fu Zhou Peter C. Fisher 《Mineralium Deposita》2008,43(7):791-803
The Jinbaoshan Pt–Pd deposit in Yunnan, SW China, is hosted in a wehrlite body, which is a member of the Permian (∼260 Ma)
Emeishan Large Igneous Province (ELIP). The deposit is reported to contain one million tonnes of Pt–Pd ore grading 0.21% Ni
and 0.16% Cu with 3.0 g/t (Pd + Pt). Platinum-group minerals (PGM) mostly are ∼10 μm in diameter, and are commonly Te-, Sn-
and As-bearing, including moncheite (PtTe2), atokite (Pd3Sn), kotulskite (PdTe), sperrylite (PtAs2), irarsite (IrAsS), cooperite (PtS), sudburyite (PdSb), and Pt–Fe alloy. Primary rock-forming minerals are olivine and clinopyroxene,
with clinopyroxene forming anhedral poikilitic crystals surrounding olivine. Primary chromite occurs either as euhedral grains
enclosed within olivine or as an interstitial phase to the olivine. However, the intrusion has undergone extensive hydrothermal
alteration. Most olivine grains have been altered to serpentine, and interstitial clinopyroxene is often altered to actinolite/tremolite
and locally biotite. Interstitial chromite grains are either partially or totally replaced by secondary magnetite. Base-metal
sulfides (BMS), such as pentlandite and chalcopyrite, are usually interstitial to the altered olivine. PGM are located with
the BMS and are therefore also interstitial to the serpentinized olivine grains, occurring within altered interstitial clinopyroxene
and chromite, or along the edges of these minerals, which predominantly altered to actinolite/tremolite, serpentine and magnetite.
Hydrothermal fluids were responsible for the release of the platinum-group elements (PGE) from the BMS to precipitate the
PGM at low temperature during pervasive alteration. A sequence of alteration of the PGM has been recognized. Initially moncheite
and atokite have been corroded and recrystallized during the formation of actinolite/tremolite, and then, cooperite and moncheite
were altered to Pt–Fe alloy where they are in contact with serpentine. Sudburyite occurs in veins indicating late Pd mobility.
However, textural evidence shows that the PGM are still in close proximity to the BMS. They occur in PGE-rich layers located
at specific igneous horizons in the intrusion, suggesting that PGE were originally magmatic concentrations that, within a
PGE-rich horizon, crystallized with BMS late in the olivine/clinopyroxene crystallization sequence and have not been significantly
transported during serpentinization and alteration. 相似文献
69.
Metamorphic fluid origins in the Osborne Fe oxide–Cu–Au deposit,Australia: evidence from noble gases and halogens 总被引:1,自引:1,他引:0
The Osborne iron oxide–copper–gold (IOCG) deposit is hosted by amphibolite facies metasedimentary rocks and associated with
pegmatite sheets formed by anatexis during peak metamorphism. Eleven samples of ore-related hydrothermal quartz and two pegmatitic
quartz–feldspar samples contain similarly complex fluid inclusion assemblages that include variably saline (<12–65 wt% salts)
aqueous and liquid carbon dioxide varieties that are typical of IOCG mineralisation. The diverse fluid inclusion types present
in each of these different samples have been investigated by neutron-activated noble gas analysis using a combination of semi-selective
thermal and mechanical decrepitation techniques. Ore-related quartz contains aqueous and carbonic fluid inclusions that have
similar 40Ar/36Ar values of between 300 and 2,200. The highest-salinity fluid inclusions (47–65 wt% salts) have calculated 36Ar concentrations of approximately 1–5 ppb, which are more variable than air-saturated water (ASW = 1.3–2.7 ppb). These fluid
inclusions have extremely variable Br/Cl values of between 3.8 × 10−3 and 0.3 × 10−3, and I/Cl values of between 27 × 10−6 and 2.4 × 10−6 (all ratios are molar). Fluid inclusions in the two pegmatite samples have similar 40Ar/36Ar values of ≤1,700 and an overlapping range of Br/Cl and I/Cl values. High-salinity fluid inclusions in the pegmatite samples
have 2.5–21 ppb 36Ar, that overlap the range determined for ore-related samples in only one case. The fluid inclusions in both sample groups
have 84Kr/36Ar and 129Xe/36Ar ratios that are mainly in the range of air and air-saturated water and are similar to mid-crustal rocks and fluids from
other settings. The uniformly low 40Ar/36Ar values (<2,200) and extremely variable Br/Cl and I/Cl values do not favour a singular or dominant fluid origin from basement-
or mantle-derived magmatic fluids related to A-type magmatism. Instead, the data are compatible with the involvement of metamorphic
fluids that have interacted with anatectic melts to variable extents. The ‘metamorphic’ fluids probably represent a mixture
of (1) inherited sedimentary pore fluids and (2) locally derived metamorphic volatilisation products. The lowest Br/Cl and
I/Cl values and the ultra-high salinities are most easily explained by the dissolution of evaporites. The data demonstrate
that externally derived magmatic fluids are not a ubiquitous component of IOCG ore-forming systems, but are compatible with
models in which IOCG mineralisation is localised at sites of mixing between fluids of different origin.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorised users. 相似文献