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121.
Wilhelm Nümann 《Aquatic Sciences - Research Across Boundaries》1967,29(1):269-283
Nearly 900 tagged trouts (brown and rainbow trouts) have been exposed at a distance of 300 m and 1,5–4,5 km from the shore. In the first case the recapture was more favour-able. According to the series 6 to 20% brown trouts and only 1% rainbow trouts were recaptured. The greater part has been caught in the lake; only from October to May the reports came from the rivers. Brown and rainbow trouts lost in the lake their reddish spots or the rainbrowstripe and became silver. The growth is nearly as quick as in the lake trout. After a critical review of our own results and those found in literature we came to the conclusion that there are no morphological differences between brown and lake trouts. It may be that there are genetically fixed differences in the biological-physiological behaviour. But even in this case a classification inSalmo trutta morpha lacustris andS. t. m. fario could not be justifiable—for practical reasons only-because, independantly, in the single lakes the development of lake trouts from populations of brown trouts has happened polyphyletically. Also, for genetically different populations, normally no classifications in subspecies are made. Probably, the difference in the colour and growth-easily striking the eye-misdirects to assume the form ‘morpha lacustris’. 相似文献
122.
Günter Fries Friedrich Wilhelm Tesch 《Aquatic Sciences - Research Across Boundaries》1965,27(2):257-272
Ohne Zusammenfassung
Der Deutschen Forschungsgemeinschaft sei für die Unterstützung der Arbeit gedankt. 相似文献
123.
Torres MA Testa CP Gáspari C Masutti MB Panitz CM Curi-Pedrosa R de Almeida EA Di Mascio P Filho DW 《Marine pollution bulletin》2002,44(9):923-932
Digestive glands of the mangrove mussel Mytella guyanensis, collected at one non-polluted site (site 1) and two polluted sites (sites 2 and 3), were analysed for different antioxidant defenses, lipid peroxidation and DNA damage. Thiobarbituric acid-reactive substance (TBARS) and 8-oxo-7,8-dihydro-2'-deoxyguanosine levels were enhanced at the polluted sites. With the exception of superoxide dismutase, the activities of catalase and glutathione peroxidase were also higher at the polluted sites. Greater increases were observed in glutathione reductase, glutathione S-transferase and etoxyresorufine-O-deethylase activities at the polluted sites. Conversely, reduced glutathione content was higher at the control site. Trace metal contents in mussels collected at polluted sites were increased compared to the control site, and there were strong positive correlations between TBARS and Cu and Pb contents. M. guyanensis is routinely exposed to an oxidative stress condition at both polluted sites, and considering xenobiotic bioaccumulation in bivalve molluscs, the mangrove mussel represents an excellent bioindicator for environmental monitoring studies. 相似文献
124.
The behaviour of boron in a peraluminous granite-pegmatite system and associated hydrothermal solutions: a melt and fluid-inclusion study 总被引:1,自引:0,他引:1
Thomas Rainer Förster Hans-Jürgen Heinrich Wilhelm 《Contributions to Mineralogy and Petrology》2003,144(4):457-472
Detailed analyses of melt and fluid inclusions combined with an electron-microprobe survey of boron-bearing minerals reveal the evolution of boron in a highly evolved peraluminous granite-pegmatite complex and the associated high- and medium-temperature ore-forming hydrothermal fluids (Ehrenfriedersdorf, Erzgebirge, Germany). Melt inclusions in granite represent embryonic pegmatite-forming melts containing about 10 wt% H2O and 1.8 wt% B2O3. These melts are also enriched in F, P, and other incompatible elements such as Be, Sn, Rb, and Cs. Ongoing differentiation and volatile enrichment drove the system into a solvus, where two pegmatite-forming melts coexisted. The critical point is at about 712 °C, 100 MPa, 20 wt% H2O and 4.1 wt% B2O3. Cooling and concomitant fractional crystallisation from 700 to 500 °C induced development of two conjugate melts, an H2O-poor (A-melt) and an H2O-rich melt (B-melt) along the opening solvus. Boron is a major element in both melts and is preferentially partitioned into the H2O-rich melt. Temperature-dependent distribution coefficients DboronB - melt/A - melt D_{{\rm{boron}}}^{{\rm{B - melt/A - melt}}} are 1.3 at 650 °C, 1.5 at 600 °C, and 1.8 at 500 °C. In both melts, boron concentrations decreased during cooling because of exsolution of a boron-rich hypersaline brine throughout the pegmatitic stage. Boromuscovite containing up to 8.5 wt% was another sink for boron at this stage. The end of the melt-dominated pegmatitic stage was attained at a solidus temperature of around 490 °C. Fluid inclusions of the hydrothermal stage reveal trapping temperatures of 480 to 370 °C, along with varying densities and highly variable B2O3 contents ranging from 0.20 to 2.94 wt%. A boiling system evolved, indicating a complex interplay between closed- and open-system behaviour. Pressure switched from lithostatic to hydrostatic and back, generating hydrothermal convection cells where meteoric waters were introduced and mixed with magmatic fluids. Boron-rich solutions originated from magmatic fluids, whereas boron-depleted fluids were mainly of meteoric origin. This highlights the potential of boron for discriminating fluids of different origin. Tin is continuously enriched during the evolution because tin and boron are cross-linked by formation of boron-, fluorine- and tin-fluorine-bearing complexes and is finally deposited within quartz-cassiterite veins during the transition from closed- to open-system behaviour. Boron does not only trace the complex evolution of the Ehrenfriedersdorf complex but exerts, together with H2O, F and P, an important control on the physical and chemical properties of pegmatite-forming melts, and particularly on the formation of a two-melt solvus at low pressure. We discuss this with respect to experimental results on H2O solubility and the critical behaviour of the haplogranite-water system which contained variable concentrations of volatiles. 相似文献
125.
Partial fusion of basic granulites at 5 to 15 kbar: implications for the origin of TTG magmas 总被引:24,自引:0,他引:24
Partial fusion experiments with basic granulites (S6, S37) believed to represent the lower crust beneath the Eifel region
(Germany) were performed at pressures from 5 to 15 kbar. Water-undersaturated experiments were carried out in the presence
of 1 wt% H2O plus 2.44 or 0.81 wt% CO2 equivalent to mole fractions of H2O/(H2O + CO2) of 0.5 and 0.75, respectively, of the volatile components added. At temperatures from 850 to 1100 °C the weight proportions
of melt range from 7 to 30 %. Melt compositions change from trondhjemitic over tonalitic to dioritic with increasing degree
of partial melting. Crystalline residua are plagioclase/pyroxene dominated at 5 kbar to garnet/pyroxene dominated at 15␣kbar.
Dehydration melting was studied in granulite S35 similar in composition to S6. The magmatic precursors of the granulite xenoliths
used in this study had geochemical characteristics of cumulate gabbro (metagabbro S37) and evolved melts (metabasalts S6,
S35), respectively. Melts from granulite S37 match the major element compositions of natural trondhjemites and tonalites.
At 5 kbar, their Al2O3 is relatively low, similar to tonalites from ophiolites. At 15 kbar, Al2O3 in the melts is high due to the near absence of plagioclase in the crystalline residua. The Al2O3 concentrations in 15 kbar melts from S6 (˜20 wt%) are higher than in natural tonalites. Depth constraints on the formation
of tonalitic magmas in the continental crust are provided by REE (rare earth element) patterns of the synthetic melts calculated
from the known REE abundances in metagabbro S37 and metabasalt S6 assuming batch melting and using partition coefficients
from the literature. The REE patterns of tonalites from active continental margins and Archean trondhjemite-tonalite-granodiorite␣associations
low in REE with LaN (chondrite normalised) from 10 to 30 and YbN from 1 to 2 are reproduced at pressures of 10 and 12.5 kbar from metagabbro S37 which displays a slightly L(light)REE enriched
pattern with LaN = 8 and YbN = 3. Natural tonalites with LaN from 30 to 100 require a source richer in REE than granulite S37. At 15 kbar, H(heavy)REEN in melts from granulite S37 are depressed below the level observed in natural tonalites due to the high proportion of garnet
(>30 wt%) in the residue. Melts from metabasalt S6 (enriched in REE with LaN = 38 and YbN = 16) do not match the REE characteristics of natural tonalites under any conditions.
Received: 1 July 1994 / Accepted: 11 September 1996 相似文献
126.
127.
128.
Wilhelm Heinrich Paul Metz Werner Bayh 《Contributions to Mineralogy and Petrology》1986,93(2):215-221
Stoichiometric mixtures of tremolite and dolomite were heated to 50° C above equilibrium temperatures to form forsterite and calcite. The pressure of the CO2-H2O fluid was 5 Kb and \(X_{{\text{CO}}_{\text{2}} }\) varied from 0.1 to 0.6. The extent of the conversion was determined by the amount of CO2 produced. The resulting mixtures of unreacted tremolite and dolomite and of newly-formed forsterite and calcite were examined with a scanning electron microscope. All tremolite and dolomite grains showed obvious signs of dissolution. At fluid compositions with \(X_{{\text{CO}}_{\text{2}} }\) less than about 0.4, the forsterite and calcite crystals are randomly distributed throughout the charges, indicating that surfaces of the reactants are not a controlling factor with respect to the sites of nucleation of the products. A change is observed when \(X_{{\text{CO}}_{\text{2}} }\) is greater than about 0.4; the forsterite and calcite crystals now nucleate and grow at the surface of the dolomite grains, thus indicating a change in mechanism at medium CO2 concentrations. As the reaction progresses, the dolomite grains become more and more surrounded by forsterite and calcite, finally forming armoured relics of dolomite. Under experimental conditions this characteristic texture can only be formed if the CO2-concentration is greater than about 40 mole %. These findings make it possible to estimate the CO2-concentration from the texture of the dolomite+tremolite+forsterite+calcite assemblage. The results suggest a dissolution-precipitation mechanism for the reaction investigated. In a simplified form it consists of the following 4 steps:
- Dissolution of the reactants tremolite and dolomite.
- Diffusion of the dissolved constituents in the fluid.
- Heterogeneous nucleation of the product minerals.
- Growth of forsterite and calcite from the fluid.
129.
The orientational ordering transition R \(R\bar 3m - R\bar 3c\) in NaNO3 near 552 K has been investigated using x-ray diffraction techniques. NaNO3 is a model system for CaCO3 and other minerals with orientational disorder of triangular molecules in a simple NaCl-type matrix. The temperature evolution of the integrated intensities of the superlattice reflection \(\bar 1\) 23 and the fundamental reflection 110 are discussed in terms of Landau theory of two coupled order parameters. It is shown that the known phenomenological critical exponent (Poon and Salje 1988) and the anomalous thermal expansion at T > T tr (Reeder et al. 1988) can be understood as the result of a Z point instability which mainly describes the NO 3 - disorder, and a second order parameter linked with the spontaneous strain of this phase transition. 相似文献
130.