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Dorian M. Hatch Johanne I. Artman Juliana Boerio-Goates 《Physics and Chemistry of Minerals》1990,17(4):334-343
The transition from P213(T
4) to P212121(D
2
4
) in the langbeinite K2Cd2(SO4)3 has been analyzed using group theoretical methods and previously published structural data above and below the transition. We find that because the transition is strongly first-order, the primary-order parameter has relatively large values at the transition temperature, and higher order terms which involve the order parameter, the strain, and the coupling of the two must be included in the Landau expansion for the free energy. Complex displacements occur at the transition for all atoms of the unit cell, but these displacements can be resolved into contributions which can be shown from symmetry considerations to transform as the
2
3 irrep of P2
1 3(T
4) as well as contributions from symmetry-preserving displacements which transform under the irrep
1. Therefore, the transition is not a simple one and involves sulfate rotations and cadmium and potassium ion displacements. 相似文献
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Michael Gonsior Barrie M. Peake William T. Cooper David C. Podgorski Juliana D'Andrilli Thorsten Dittmar William J. Cooper 《Marine Chemistry》2011,123(1-4):99-110
Dissolved organic matter (DOM) was investigated along a gradient across the Subtropical Convergence (STC) off the South Island, New Zealand. Ultrahigh resolution electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS), excitation emission matrix fluorescence (EEM) spectroscopy, and molecular lignin analysis techniques were used to study this DOM. The analysis revealed a group of compounds found only in the coastal DOM samples, which were also characterized by an elevated terrestrial DOM fluorescence pattern and elevated lignin content if compared to the offshore samples. This group exhibited a high degree of carbon unsaturation, as evident from high double bond equivalence minus oxygen values (DBE-O > 9) and maximum fluorescence intensity. Sulfur-containing molecular formulae for summer DOM samples were much more abundant across the entire transect of the STC compared to winter and exhibited distinctly different hydrogen:carbon and oxygen:carbon elemental ratios, suggesting a possible correlation between biological activity and sulfur compounds. The molecular formulae common to all STC samples were compared with those calculated for DOM extracted from freshwater collected from a stream discharging into Doubtful Sound (West Coast, New Zealand). ESI-FT-ICR-MS measurements undertaken in negative electrospray ionization (ESI?) mode indicated that 30% of the molecular formulae were present in both types of DOM, while in positive ESI mode (ESI+) over 90% of the formulae were present in all samples. Hence, a significant portion of the molecular formulae assigned to the solid-phase extractable DOM pool (SPE-DOM) appear to be identical in oceanic and freshwater samples. 相似文献
6.
Wolf Uwe Reimold Alvaro Penteado Crsta Maximilian Hasch Astrid Kowitz Natalia Hauser Joana Paula Sanchez Luiz Sergio Amarante Simes Grace Juliana de Oliveira Patrice T. Zaag 《Meteoritics & planetary science》2019,54(10):2384-2397
Cerro do Jarau is a conspicuous, circular morpho‐structural feature in Rio Grande do Sul State (Brazil), with a central elevated core in the otherwise flat “Pampas” terrain typical for the border regions between Brazil and Uruguay. The structure has a diameter of approximately 13.5 km. It is centered at 30o12′S and 56o32′W and was formed on basaltic flows of the Cretaceous Serra Geral Formation, which is part of the Paraná‐Etendeka Large Igneous Province (LIP), and in sandstones of the Botucatu and Guará formations. The structure was first spotted on aerial photographs in the 1960s. Ever since, its origin has been debated, sometimes in terms of an endogenous (igneous) origin, sometimes as the result of an exogenous (meteorite impact) event. In recent years, a number of studies have been conducted in order to investigate its nature and origin. Although the results have indicated a possible impact origin, no conclusive evidence could be produced. The interpretation of an impact origin was mostly based on the morphological characteristics of the structure; geophysical data; as well as the occurrence of different breccia types; extensive deformation/silicification of the rocks within the structure, in particular the sandstones; and also on the widespread occurrence of low‐pressure deformation features, including some planar fractures (PFs). A detailed optical microscopic analysis of samples collected during a number of field campaigns since 2007 resulted in the disclosure of a large number of quartz grains from sandstone and monomict arenite breccia from the central part of the structure with PFs and feather features (FFs), as well as a number of quartz grains exhibiting planar deformation features (PDFs). While most of these latter grains only carry a single set of PDFs, we have observed several with two sets, and one grain with three sets of PDFs. Consequently, we here propose Cerro do Jarau as the seventh confirmed impact structure in Brazil. Cerro do Jarau, together with Vargeão Dome (Santa Catalina state) and Vista Alegre (Paraná State), is one of very few impact structures on Earth formed in basaltic rocks. 相似文献
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Marine debris review for Latin America and the wider Caribbean region: from the 1970s until now, and where do we go from here? 总被引:1,自引:1,他引:0
The available literature on marine debris from Latin America and the Wider Caribbean Region was collected and linked, reviewing their methodologies and principal results (quantities, composition and spatial-temporal patterns). The study region comprises 52 coastal countries of which only 14 had registers of works on marine debris. A total of 70 works were available and 69 had their full contents accessed. Brazil dominated the available literature with 70% of the documents. Beaches were the most studied environment, and plastics the prevalent form of contamination in the whole region. The exposure of marine biota (species, type of contact, consequences) was highlighted. The studied region, although still little exploited by this sort of research, shows the same contamination patterns observed world-wide. We also contacted 40 researchers in the area, collecting scientific contributions, opinions and suggestions for improvement of this research field. Further advances and new (urgently needed) lines of research are also discussed. 相似文献
10.
Juraj Majzlan Peter Glasnák Robert A. Fisher Mary Anne White Michel B. Johnson Brian Woodfield Juliana Boerio-Goates 《Physics and Chemistry of Minerals》2010,37(9):635-651
Jarosite phases are common minerals in acidic, sulfate-rich environments. Here, we report heat capacities (C
p) and standard entropies (S°) for a number of jarosite samples. Most samples are close to the nominal composition AFe3(SO4)2(OH)6, where A = K, Na, Rb, and NH4. One of the samples has a significant number of defects on the Fe sites and is called the defect jarosite; others are referred
to as A-jarosite. The samples, their compositions, and the entropies at T = 298.15 K are:
There are additional configurational entropies of 13.14 and 8.23 J mol−1 K−1 in defect and NH4-jarosite, respectively. A detailed analysis of the synchrotron X-ray diffraction patterns showed a large anisotropic peak
broadening for defect and NH4-jarosite. The fits to the low-temperature (approx. <12 K) C
p data showed that our samples can be divided into two groups. The first group is populated by the K-, Na-, Rb-, and NH4-jarosite samples, antiferromagnetic at low temperatures. The second group contains the H3O-jarosite (studied previously) and the defect jarosite. H3O- and defect jarosite are spin glasses and their low-T
C
p was fit with the expression C
p = γT + ΣB
j
T
j
, where j = (3, 5, 7, 9). The linear term is typical for spin glasses and the sum represents the lattice contribution to C
p. Surprisingly, the C
p of the K-, Na-, Rb-, and NH4-jarosite samples, which are usually considered to be antiferromagnetic at low temperatures, also contains a large linear
term. This finding suggests that even these phases do not order completely, but have a partial spin-glass character below
their Néel transition temperature. 相似文献
Sample | Chemical composition | S o/(J mol−1 K−1) |
---|---|---|
K-jarosite | K0.92(H3O)0.08Fe2.97(SO4)2(OH)5.90(H2O)0.10 | 427.4 ± 0.7 |
Na-jarosite | Na0.95(H3O)0.05Fe3.00(SO4)2(OH)6.00 | 436.4 ± 4.4 |
Rb-jarosite | RbFe2.98(SO4)2(OH)5.95(H2O)0.05 | 411.9 ± 4.1 |
NH4-jarosite | (NH4)0.87(H3O)0.13Fe3.00(SO4)2(OH)6.00 | 447.2 ± 4.5 |
Defect jarosite | K0.94(H3O)0.06Fe2.34(SO4)2(OH)4.01(H2O)1.99 | 412.7 ± 4.1 |