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1.
Tony T. Gregg Amanda Dewees Drema Gross Bill Hoffman Dan Strub Matt Watson 《中国海洋大学学报(英文版)》2006,5(4):375-380
1Water LossInitiativesUnaccounted-for water(or unbilled water)has beenreceiving newscrutiny at both the state and nationallevels.For years,water conservationeffortsin Europehave emphasized reduction in water loss to a muchgreater extent thaninthe United S… 相似文献
2.
Amanda Albright Olsen 《Geochimica et cosmochimica acta》2008,72(7):1758-1766
We ran a series of 124 semi-batch reactor experiments to measure the dissolution rate of forsterite in solutions of nitric and oxalic acid solutions over a pH range of 0-7 and total oxalate concentrations between 0 and 0.35 m at 25 °C. We found that the empirical rate law for the dissolution of forsterite in these solutions is
3.
4.
The discharge of radioactive waste, from nuclear fuel reprocessing facilities, into the coastal waters of north-west Europe has resulted in a significant increase in the inventories of a number of artificial radionuclides in the North Atlantic. Radiocaesium, 90Sr and 99Tc, which behave conservatively in seawater, have been used widely as tracers of water movement through the North Sea, Norwegian Coastal Current, Barents Sea, Greenland Sea, Fram Strait, Eurasian Basin, East Greenland Current and Denmark Strait overflow. These studies are summarised in the present paper. It has been estimated that 22% of the 137Cs Sellafield discharge has passed into the Barents Sea, en route to the Nansen Basin, via the Bjomoya-Fugloya Section, with another 13% passing through the Fram Strait. This amounts to 14 PBq 137Cs. Quantifying the influx of other radionuclides has been more problematic. The inflowing Atlantic water now appears to be diluting waters in the Arctic Basin, which were contaminated in the late 1970s and early 1980s as a result of the substantial decrease in the discharge of reprocessing wastes. Sellafield (U.K.) has dominated the supply of 134Cs, 137Cs, 90Sr, 99Tc and Pu, whereas La Hague (France) has contributed a larger proportion of 129I and 125Sb. 相似文献
5.
6.
The conditional acid dissociation constants (pKa′) of two sulfonephthalein dyes, thymol blue (TB) and m-cresol purple (mCP), were assessed throughout the estuarine salinity range (0<S<40) using a tris/tris–HCl buffer and spectrophotometric measurement. The salinity dependence of the pKa′ of both dyes was fitted to the equations (25 °C, total proton pH scale, mol kg soln−1):The estimated accuracy of pH measurements using these calculated pKa′ values is considered to be comparable to that possible with careful use of a glass electrode (±0.01 pH unit) but spectrophotometric measurements in an estuary have the significant advantage that it is not necessary to calibrate an electrode at different salinities. pH was measured in an estuary over a tidal cycle with a precision of ±0.0005 pH unit at high (S>30) salinity, and ±0.002 pH unit at low (S<5) salinity. The pH increased rapidly in the lower salinity ranges (0<S<15) but less rapidly at higher salinities. 相似文献
7.
Shane M. Ohline Malcolm R. Reid Shamus L.G. Husheer Kim I. Currie Keith A. Hunter 《Marine Chemistry》2007
Accurate measurement of seawater pH has long been sought by marine chemists (for example: [Dickson, A.G. 1993a. The measurement of sea water pH. Marine Chemistry, 44, 131–142, Dickson, A.G. 1993b. pH buffers for sea water media based on the total hydrogen ion concentration scale. Deep-Sea Research, 40, 107–118; Zhang, 1996; Tapp, M., Hunter, K.A., Currie, K. and Macaskill, B. 2000. Apparatus of continuous-flow underway spectrophotometric measurement of surface water pH. Marine Chemistry 72(2–4), 193–202; Friis, K., Koetzinger, A., Wallace, D.W.R. 2004. Spectrophotometric pH measurement in the ocean: Requirements, design and testing of an autonomous charge-coupled device detector system. Limnology and Oceanography: Methods 2, 126–136]. Recently, such attempts have taken on greater significance as anthropogenic carbon dioxide emissions may create rapidly changing oceanic pH. Spectrophotometric techniques have been accepted generally as the best for determination of seawater pH. Here we report a new technique using thymol blue as the indicator dye and fitting the entire spectrum from 400 to 900 nm rather than measuring the absorbance values at only two or three points in the spectrum. This full-spectrum modelling enables a reduction in signal to noise over other techniques. In the laboratory, we find with seawater samples a pH precision increase of five-fold “within” a sample and seven-fold “between” samples when comparing the full spectrum to the three-point method of analysis [Zhang, H., Byrne, R.H. 1996. Spectrophotometric pH measurements of surface seawater at in-situ conditions: absorbance and protonation behaviour of thymol blue. Marine Chemistry 52, 17–25]. 相似文献
8.
Karen L. Hunter Dewayne A. Fox Lori M. Brown Kenneth W. Able 《Estuaries and Coasts》2006,29(3):487-498
Modification of brackish marshes by nonindigenousPhragmites australis has occurred across a broad geographical area in eastern North America. Among its effects on marsh processes,Phragmites may be increasingly unfavorable to marsh surface fishes as its invasion progresses within an estuary. We assessed the effect
of thePhragmites invasion on resident marsh surface fishes by examining the population response ofFundulus heteroclitus (mummichog, 5–48 mm TL) andF. luciae (spotfin killifish, 5–41 mm TL) to four distinct invasion stages in three estuaries of the U.S. mid Atlantic region (New
Jersey, Delaware, and Maryland). We documented precipitous declines in mean catch per unit effort ofF. heteroclitus in pit traps from natural marsh (51.6), through initial (33.8), early (12.3), and late invasion stages (2.4) across all sites.
A similar pattern was documented forF. luciae, with mean catch per unit effort in pit traps declining from natural marsh (48.9), through initial (39.1), early (9.3), and
late invasion stages (2.7). Population structure of both species also changed somewhat across invasion stages such that we
collected a narrower size range of individuals of both species from late invasion stages. Patterns suggest that as thePhragmites invasion progresses, there is a decline in habitat function for larval and juvenileF. heteroclitus and an increased risk of extirpation ofF. luciae from brackish marshes along the east coast of the U.S. 相似文献
9.
Uranium co-precipitation with iron oxide minerals 总被引:2,自引:0,他引:2
Martine C. DuffJessica Urbanik Coughlin Douglas B. Hunter 《Geochimica et cosmochimica acta》2002,66(20):3533-3547
In oxidizing environments, the toxic and radioactive element uranium (U) is most soluble and mobile in the hexavalent oxidation state. Sorption of U(VI) on Fe-oxides minerals (such as hematite [α-Fe2O3] and goethite [α-FeOOH]) and occlusion of U(VI) by Fe-oxide coatings are processes that can retard U transport in environments. In aged U-contaminated geologic materials, the transport and the biological availability of U toward reduction may be limited by coprecipitation with Fe-oxide minerals. These processes also affect the biological availability of U(VI) species toward reduction and precipitation as the less soluble U(IV) species by metal-reducing bacteria.To examine the dynamics of interactions between U(VI) and Fe oxides during crystallization, Fe-oxide phases (containing 0.5 to 5.4 mol% U/(U + Fe)) were synthesized by means of solutions of U(VI) and Fe(III). Wet chemical (digestions and chemical extractions) and spectroscopic techniques were used to characterize the synthesized Fe oxide coprecipitates after rinsing in deionized water. Leaching the high mol% U solids with concentrated carbonate solution (for sorbed and solid-phase U(VI) species) typically removed most of the U, leaving, on average, about 0.6 mol% U. Oxalate leaching of solids with low mol% U contents (about 1 mol% U or less) indicated that almost all of the Fe in these solids was crystalline and that most of the U was associated with these crystalline Fe oxides. X-ray diffraction and Fourier-transform infrared (FT-IR) spectroscopic studies indicate that hematite formation is preferred over that of goethite when the amount of U in the Fe-oxides exceeds 1 mol% U (∼4 wt% U). FT-IR and room temperature continuous wave luminescence spectroscopic studies with unleached U/Fe solids indicate a relationship between the mol% U in the Fe oxide and the intensity or existence of the spectra features that can be assigned to UO22+ species (such as the IR asymmetric υ3 stretch for O = U = O for uranyl). These spectral features were undetectable in carbonate- or oxalate-leached solids, suggesting solid phase and sorbed U(VI)O22+ species are extracted by the leach solutions. Uranium L3-edge x-ray absorption spectroscopic (XAFS) analyses of the unleached U-Fe oxide solids with less than 1 mol% U reveal that U(VI) exists with four O atoms at radial distances of 2.19 and 2.36 Å and second shell Fe at a radial distance at 3.19 Å.Because of the large ionic radius of UO22+ (∼1.8 Å) relative to that of Fe3+ (0.65 Å), the UO22+ ion is unlikely to be incorporated in the place of Fe in Fe(III)-oxide structures. Solid-phase U(VI) can exist as the uranyl [U(VI)O22+] species with two axial U-O double bonds and four or more equatorial U-O bonds or as the uranate species (such as γ-UO3) without axial U-O bonds. Our findings indicate U6+ (with ionic radii of 0.72 to 0.8 Å, depending on the coordination environment) is incorporated in the Fe oxides as uranate (without axial O atoms) until a point of saturation is reached. Beyond this excess in U concentration, precipitating U(VI) forms discrete crystalline uranyl phases that resemble the uranyl oxide hydrate schoepite [UO2(OH)2·2H2O]. Molecular modeling studies reveal that U6+ species could bond with O atoms from distorted Fe octahedra in the hematite structure with an environment that is consistent with the results of the XAFS. The results provide compelling evidence of U incorporation within the hematite structure. 相似文献
10.
Gold mineralization at Hutti is confined to a series of nine parallel, N–S to NNW–SSE trending, steeply dipping shear zones.
The host rocks are amphibolites and meta-rhyolites metamorphosed at peak conditions of 660±40°C and 4±1 kbar. They are weakly
foliated (S1) and contain barren quartz extension veins. The auriferous shear zones (reefs) are typically characterized by four alteration
assemblages and laminated quartz veins, which, in places, occupy the entire reef width of 2–10 m, and contain the bulk of
gold mineralization. A <1.5 m wide distal chlorite-sericite (+biotite, calcite, plagioclase) alteration zone can be distinguished
from a 3–5 m wide proximal biotite-plagioclase (+quartz, muscovite, calcite) alteration zone. Gold is both spatially and temporally
associated with disseminated arsenopyrite and pyrite mineralization. An inner chlorite-K-feldspar (+quartz, calcite, scheelite,
tourmaline, sphene, epidote, sericite) alteration halo, which rims the laminated quartz veins, is characterized by a pyrrhotite,
chalcopyrite, sphalerite, ilmenite, rutile, and gold paragenesis. The distal chlorite-sericite and proximal biotite-plagioclase
alteration assemblages are developed in microlithons of the S2–S3 crenulation cleavage and are replaced along S3 by the inner chlorite-K-feldspar alteration, indicating a two-stage evolution for gold mineralization. Ductile D2 shearing, alteration, and gold mineralization formed the reefs during retrograde evolution and fluid infiltration under upper
greenschist to lower amphibolite facies conditions (560±60°C, 2±1 kbar). The reefs were reactivated in the D3 dextral strike-slip to oblique-slip environment by fault-valve behavior at lower greenschist facies conditions (ca. 300–350°C),
which formed the auriferous laminated quartz veins. Later D4 crosscutting veins and D5 faults overprint the gold mineralization. The alteration mineralogy and the structural control of the deposit clearly points
to an orogenic style of gold mineralization, which took place either during isobaric cooling or at different levels of the
Archean crust. From overlaps in the tectono-metamorphic history, it is concluded that gold mineralization occurred during
two tectonic events, affecting the eastern Dharwar craton in south India between ca. 2550 – 2530 Ma: (1) The assemblage of
various terranes of the eastern block, and (2) a tectono-magmatic event, which caused late- to posttectonic plutonism and
a thermal perturbation. It differs, however, from the pre-peak metamorphic gold mineralization at Kolar and the single-stage
mineralization at Ramagiri. Notably, greenschist facies gold mineralization occurred at Hutti 35–90 million years later than
in the western Dharwar craton.
Editorial handling: G. Beaudoin 相似文献