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1.
The Lower Triassic succession of Barles, Alpes de Haute Provence, France, comprises an unconformable quartz arenite sand body of 90m thickness. The succession may be informally divided into (i) lower channellized cross-bedded member overlain by (ii) an upper fining upward member. The lower member comprises vertically stacked, subtidal channel units separated into five major sand bodies by thin developments of fine grained channel margin and shoal deposits. Subtidal channel fill deposits are dominated by varying scales of cross bedding. These scales vary systematically from the base to the top of the member, with large scale planar sets dominating the lowest channel sand body (sand body 1), medium scale planar and trough cross bedding characterizing sand bodies 2-4, the largest scale planar sets in the highest sand body (sand body 5). This upward change in cross bedding scale is concomitant with a decrease in both the relief of major channel sand body erosion surfaces, and the proportion of preserved interchannel shoal deposits. The succeeding fining upward member comprises small scale tidal channel units overlain by channel shoal and tidal flat deposits. Tidal flat sequences are characterized by parallel laminated, wave and current rippled sandstones separated by bioturbated, fine grained siltstones and mudstones. The vertical variation in facies of the Lower Triassic succession suggests two main periods of deposition. The lower member is considered to preserve successively more seaward components of a transgressive estuarine complex. The overlying upper member records the seaward progradation of tidal channel, shoal and tidal flat environments. The unconformity bounded nature of the lower member, combined with its systematic variation in facies, suggests it may represent an incised valley-estuarine fill developed in response to an early Triassic relative sea level fall and subsequent rise. Succeeding tidal channel and tidal flat deposits forming the upper fining upward member reflect a change in sediment supply and/or rate of relative sea level rise comparable with a progradational shoreline. It is unclear whether this final depositional episode represents a period of highstand progradation or a later lowstand shoreline system developed following a further period of relative sea level fall and rise.  相似文献   
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We present the results of a comprehensive major element, traceelement and Sr–Nd–Pb–O isotopic study of post-glacialvolcanic rocks from the Neovolcanic zones on Iceland. The rocksstudied range in composition from picrites and tholeiites, whichdominate in the main rift systems, to transitional and alkalicbasalts confined to the off-rift and propagating rift systems.There are good correlations of rock types with geochemical enrichmentparameters, such as La/Sm and La/Yb ratios, and with long-termradiogenic tracers, such as Sr–Nd–Pb isotope ratios,indicating a long-lived enrichment/depletion history of thesource region. 87Sr/86Sr vs 143Nd/144Nd defines a negative array.Pb isotopes define well-correlated positive arrays on both 206Pb/204Pbvs 207Pb/204Pb and 208Pb/204Pb diagrams, indicating mixing ofat least two major components: an enriched component representedby the alkali basalts and a depleted component represented bythe picrites. In combined Sr–Nd–Pb isotopic spacethe individual rift systems define coherent mixing arrays withslightly different compositions. The enriched component hasradiogenic Pb (206Pb/204Pb > 19·3) and very similargeochemistry to HIMU-type ocean island basalts (OIB). We ascribethis endmember to recycling of hydrothermally altered upperbasaltic oceanic crust. The depleted component that is sampledby the picrites has unradiogenic Pb (206Pb/204Pb < 17·8),but geochemical signatures distinct from that of normal mid-oceanridge basalt (N-MORB). Highly depleted tholeiites and picriteshave positive anomalies in mantle-normalized trace element diagramsfor Ba, Sr, and Eu (and in some cases also for K, Ti and P),negative anomalies for Hf and Zr, and low 18Oolivine values(4·6–5·0) below the normal mantle range.All of these features are internally correlated, and we, therefore,interpret them to reflect source characteristics and attributethem to recycled lower gabbroic oceanic crust. Regional compositionaldifferences exist for the depleted component. In SW Icelandit has distinctly higher Nb/U (68) and more radiogenic 206Pb/204Pbratios (18·28–18·88) compared with the NErift (Nb/U 47; 206Pb/204Pb = 18·07–18·47).These geochemical differences suggest that different packagesof recycled oceanic lithosphere exist beneath each rift. A thirdand minor component with relatively high 87Sr/86Sr and 207Pb/204Pbis found in a single volcano in SE Iceland (Öræfajökullvolcano), indicating the involvement of recycled sediments inthe source locally. The three plume components form an integralpart of ancient recycled oceanic lithosphere. The slope in theuranogenic Pb diagram indicates a recycling age of about 1·5Ga with time-integrated Th/U ratios of 3·01. Surprisingly,there is little evidence for the involvement of North AtlanticN-MORB source mantle, as would be expected from the interactionof the Iceland plume and the surrounding asthenosphere in formof plume–ridge interaction. The preferential samplingof the enriched and depleted components in the off-rift andmain rift systems, respectively, can be explained by differencesin the geometry of the melting regions. In the off-rift areas,melting columns are truncated deeper and thus are shorter, whichleads to preferential melting of the enriched component, asthis starts melting deeper than the depleted component. In contrast,melting proceeds to shallower depths beneath the main rifts.The longer melting columns also produce significant amountsof melt from the more refractory (lower crustal/lithospheric)component. KEY WORDS: basalts; trace element and Sr, Nd, Pb, O isotope geochemistry; Iceland plume; isotope ratios; oceanic crustal recycling; partial melting; plume–ridge interaction  相似文献   
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In order to constrain spatial variability in watermass conditions within the European Epicontinental Seaway prior to, during and after the Toarcian Oceanic Anoxic Event, carbon (δ13Cbel, δ13Ccarb) and oxygen (δ18Obel, δ18Ocarb) isotope records were obtained from three sections in the Grands Causses Basin (southern France). These data were then compared with similar records along a north–south transect across the European Epicontinental Seaway. As the conclusions reached here strongly depend on the reliability of belemnite calcites as archives of palaeoceanographic changes, an attempt was made to improve the understanding of isotope signals recorded in belemnite calcite. Intra‐rostral carbon and oxygen‐isotope data from six belemnite specimens belonging to the genus Passaloteuthis were collected. Intra‐rostral carbon‐isotopes are influenced by vital effects, whereas oxygen‐isotopes reflect relative changes in temperature and salinity. Palaeotemperatures calculated from δ18Obel‐isotope records from the Grands Causses Basin confirm relatively low temperatures throughout the Late Pliensbachian. Similar cool water conditions have previously been shown in Germany, England, Spain and Portugal. A temperature increase of up to 6 °C is observed across the Pliensbachian–Toarcian boundary. A pronounced negative shift of at least ?3‰ (Vienna‐Pee Dee Belemnite) is recorded in bulk carbonate carbon during the lower Harpoceras serpentinum zone, typical of the Toarcian Oceanic Anoxic Event. Before and after the Toarcian Oceanic Anoxic Event, a good correlation between δ13Ccarb and δ13Cbel exists, indicating well‐ventilated bottom‐waters and normal marine conditions. Instead, data for the Toarcian Oceanic Anoxic Event indicate the development of a strong north–south gradient in salinity stratification and surface‐water productivity for the Western Tethyan realm. This study thus lends further support to a pronounced regional overprint on carbon and oxygen‐isotope records in epicontinental seaways.  相似文献   
5.
Coincident observations made over the Moroccan desert during the Sahara mineral dust experiment (SAMUM) 2006 field campaign are used both to validate aerosol amount and type retrieved from multi-angle imaging spectroradiometer (MISR) observations, and to place the suborbital aerosol measurements into the satellite's larger regional context. On three moderately dusty days during which coincident observations were made, MISR mid-visible aerosol optical thickness (AOT) agrees with field measurements point-by-point to within 0.05–0.1. This is about as well as can be expected given spatial sampling differences; the space-based observations capture AOT trends and variability over an extended region. The field data also validate MISR's ability to distinguish and to map aerosol air masses, from the combination of retrieved constraints on particle size, shape and single-scattering albedo. For the three study days, the satellite observations (1) highlight regional gradients in the mix of dust and background spherical particles, (2) identify a dust plume most likely part of a density flow and (3) show an aerosol air mass containing a higher proportion of small, spherical particles than the surroundings, that appears to be aerosol pollution transported from several thousand kilometres away.  相似文献   
6.
Severe problems of fragmented policies and uncoordinated implementation undermine natural resource management in Australia. There have been promising signs of progress through activities such as the National Forest Policy, Council of Australian Government water reforms, National Land and Water Resources Audit, the Murray‐Darling Basin initiative and the National Action Plan for Salinity and Water Quality to integrate resource policies. There have also been some notable successes at State and local level. But fragmentation endures. This paper provides evidence of the enduring problem of fragmentation and presents a framework to analyse Australia's experience in natural resource management. The analysis reveals the multi‐dimensional character of the problems and identifies a diverse set of actions that need to be taken to improve integration in policy and implementation. Particular attention is given to the potential for regional programs to contribute to improved integration and NRM.  相似文献   
7.
ABSTRACT. In the late 1980s more than 1 million Brazilians left Brazil without returning. Today an estimated 2 million Brazilians live abroad, 1.2 million of them in the United States. In this article I show that Brazilians migrate for a variety of reasons, including the geographical imagination. Why are so many Brazilians leaving for the United States? What are their geographical imaginations, and how are they described in their migration process? Using primary and secondary data and multiple methods, I address these questions by providing insights into Brazilian migrants' place perceptions, experiences, and reasons for migrating, focusing on the geographical imagination. Those migrants who end up returning to Brazil are more likely to cite financial and curiosity reasons for having migrated. A web of transnational religious and social networks sustains those immigrants who remain in the United States. Reasons for migrating are not economic alone; rather, they are based on interrelated and complex factors that range from adventure to curiosity, the cultural influence of the United States, family members, education, and escape.  相似文献   
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The Saharan Mineral Dust Experiment (SAMUM) was conducted in May/June 2006 in southern Morocco. As part of SAMUM, airborne in situ measurements of the particle size distribution in the diameter range 4 nm < D p < 100 μm were conducted. The aerosol mixing state was determined below D p < 2.5 μm. Furthermore, the vertical structure of the dust layers was investigated with a nadir-looking high spectral resolution lidar (HSRL). The desert dust aerosol exhibited two size regimes of different mixing states: below 0.5 μm, the particles had a non-volatile core and a volatile coating; larger particles above 0.5 μm consisted of non-volatile components and contained light absorbing material. In all cases, particles larger than 10 μm were present, and in 80% of the measurements no particles larger than 40 μm were present. The abundance of large particles showed almost no height dependence. The effective diameter D eff in the dust plumes investigated showed two main ranges: the first range of D eff peaked around 5 μm and the second range of D eff around 8 μm. The two ranges of D eff suggest that it may be inadequate to use one average effective diameter or one parametrization for a typical dust size distribution.  相似文献   
10.
Early diagenetic dolomite beds were sampled during the Ocean Drilling Programme (ODP) Leg 201 at four reoccupied ODP Leg 112 sites on the Peru continental margin (Sites 1227/684, 1228/680, 1229/681 and 1230/685) and analysed for petrography, mineralogy, δ13C, δ18O and 87Sr/86Sr values. The results are compared with the chemistry, and δ13C and 87Sr/86Sr values of the associated porewater. Petrographic relationships indicate that dolomite forms as a primary precipitate in porous diatom ooze and siliciclastic sediment and is not replacing the small amounts of precursor carbonate. Dolomite precipitation often pre‐dates the formation of framboidal pyrite. Most dolomite layers show 87Sr/86Sr‐ratios similar to the composition of Quaternary seawater and do not indicate a contribution from the hypersaline brine, which is present at a greater burial depth. Also, the δ13C values of the dolomite are not in equilibrium with the δ13C values of the dissolved inorganic carbon in the associated modern porewater. Both petrography and 87Sr/86Sr ratios suggest a shallow depth of dolomite formation in the uppermost sediment (<30 m below the seafloor). A significant depletion in the dissolved Mg and Ca in the porewater constrains the present site of dolomite precipitation, which co‐occurs with a sharp increase in alkalinity and microbial cell concentration at the sulphate–methane interface. It has been hypothesized that microbial ‘hot‐spots’, such as the sulphate–methane interface, may act as focused sites of dolomite precipitation. Varying δ13C values from −15‰ to +15‰ for the dolomite are consistent with precipitation at a dynamic sulphate–methane interface, where δ13C of the dissolved inorganic carbon would likewise be variable. A dynamic deep biosphere with upward and downward migration of the sulphate–methane interface can be simulated using a simple numerical diffusion model for sulphate concentration in a sedimentary sequence with variable input of organic matter. Thus, the study of dolomite layers in ancient organic carbon‐rich sedimentary sequences can provide a useful window into the palaeo‐dynamics of the deep biosphere.  相似文献   
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