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1.
Atmospheric dust is an integral component of the Earth system with major implications for the climate, biosphere and public health. In this context, identifying and quantifying the provenance and the processes generating the various types of dust found in the atmosphere is paramount. Isotopic signatures of Pb, Nd, Sr, Zn, Cu and Fe are commonly used as sensitive geochemical tracers. However, their combined use is limited by the lack of (a) a dedicated chromatographic protocol to separate the six elements of interest for low‐mass samples and (b) specific reference materials for dust. Indeed, our work shows that USGS rock reference materials BHVO‐2, AGV‐2 and G‐2 are not applicable as substitute reference materials for dust. We characterised the isotopic signatures of these six elements in dust reference materials ATD and BCR‐723, representatives of natural and urban environments, respectively. To achieve this, we developed a specific procedure for dust, applicable in the 4–25 mg mass range, to separate the six elements using a multi‐column ion‐exchange chromatographic method and MC‐ICP‐MS measurements.  相似文献   
2.
In soils, mycorrhiza (microscopic fungal hypha) living in symbiosis with plant roots are the biological interface by which plants obtain, from rocks and organic matter, the nutrients necessary for their growth and maintenance. Despite their central role in soils, the mechanism and kinetics of mineral alteration by mycorrhiza are poorly constrained quantitatively. Here, we report in situ quantification of weathering rates from a mineral substrate, (0 0 1) basal plane of biotite, by a surface-bound hypha of Paxillus involutus, grown in association with the root system of a Scots pine, Pinus sylvestris. Four thin-sections were extracted by focused ion beam (FIB) milling along a single hypha grown over the biotite surface. Depth-profile of Si, O, K, Mg, Fe and Al concentrations were performed at the hypha-biotite interface by scanning transmission electron microscopy-energy dispersive X-ray spectroscopy (STEM-EDX). Large removals of K (50-65%), Mg (55-75%), Fe (80-85%) and Al (75-85%) were observed in the topmost 40 nm of biotite underneath the hypha while Si and O are preserved throughout the depth-profile. A quantitative model of alteration at the hypha-scale was developed based on solid-state diffusion fluxes of elements into the hypha and the break-down/mineralogical re-arrangement of biotite. A strong acidification was also observed with hypha bound to the biotite surface reaching pH < 4.6. When consistently compared with the abiotic biotite dissolution, we conclude that the surface-bound mycorrhiza accelerate the biotite alteration kinetics between pH 3.5 and 5.8 to ∼0.04 μmol biotite m−2 h−1. Our current work reaffirms that fungal mineral alteration is a process that combines our previously documented bio-mechanical forcing with the μm-scale acidification mediated by surface-bound hypha and a subsequent chemical element removal due to the fungal action. As such, our study presents a first kinetic framework for mycorrhizal alteration at the hypha-scale under close-to-natural experimental conditions.  相似文献   
3.
On December 4, 1983 an eruption started at vents located 1.5 km southwest of the summit of Piton de la Fournaise at the base of the central cone. After 31 months of quiescence this was one of the longest repose period in the last fifty years. The eruption had two phases: December 4 to January 18 and January 18 to February 18. Phase 1 produced about 8 × 106 m3 of lava and Phase II about 9 × 106 m3. The erupted lava is an aphyric basalt whose mineralogical and geochemical composition is close to that of other lavas emitted since 1977.The precursors of the December 4 outbreak were limited to two-week shallow (1.5–3 km) seismic crisis of fewer than 50 events. No long-term increase was noted in the local seismicity which is very quiet during repose periods and no long-term ground inflation preceded the eruption. Outbreaks of Phases I and II were preceded by short (2.5 hours and 1.5 hours) seismic swarms corresponding to the rise of magma toward the surface from a shallow reservoir. Large ground deformation explained by the emplacement of the shallow intrusions, was recorded during the seismic swarms. A summit inflation was observed in early January, before the phase II outbreak, while the phase I eruption was still continuing.Piton de la Fournaise volcanological observatory was installed in 1980. Seismic and ground deformation data now available for a period of 4 years including the 1981 and the 1983–1984 eruptions, allow us to describe the physical behavior of the volcano during this period. These observations lead us to propose that the magma transfer from deep levels to the shallow magma reservoir is not a continuous process but a periodic one and that the shallow magma reservoir was not resupplied before the 1981 and 1983–1984 eruptions. Considerations on the eruptive history and the composition of recent lavas indicate that the reservoir was refilled in 1977.  相似文献   
4.
We present an interpretation of gravity data acquired in 1984 by the French R/V Jean Charcot on the submarine part of the eastern flank of Piton de la Fournaise volcano. We comment on the Bouguer anomaly map and give a quantitative interpretation of three gravity profiles. The main results are that a gravity high over Grand Brûlé, the lower subaerial part of the eastern flank, does not extend far offshore and that an anomalous topographic feature, discovered in 1982 on the submarine eastern flank, is characterized by a large negative anomaly. We propose three hypotheses to explain the origin of this anomaly, i. e., it marks the site of a new volcano, or it is a consequence of lateral volcanism from a volcano older than Piton de la Fournaise, or more probably, it represents a great landslide deposit.  相似文献   
5.
A kinetic model for the microbial reduction of Fe(III) oxyhydroxide colloids in the presence of excess electron donor is presented. The model assumes a two-step mechanism: (1) attachment of Fe(III) colloids to the cell surface and (2) reduction of Fe(III) centers at the surface of attached colloids. The validity of the model is tested using Shewanella putrefaciens and nanohematite as model dissimilatory iron reducing bacteria and Fe(III) colloidal particles, respectively. Attachment of nanohematite to the bacteria is formally described by a Langmuir isotherm. Initial iron reduction rates are shown to correlate linearly with the relative coverage of the cell surface by nanohematite particles, hence supporting a direct electron transfer from membrane-bound reductases to mineral particles attached to the cells. Using internally consistent parameter values for the maximum attachment capacity of Fe(III) colloids to the cells, Mmax, the attachment constant, KP, and the first-order Fe(III) reduction rate constant, k, the model reproduces the initial reduction rates of a variety of fine-grained Fe(III) oxyhydroxides by S. putrefaciens. The model explains the observed dependency of the apparent Fe(III) half-saturation constant, , on the solid to cell ratio, and it predicts that initial iron reduction rates exhibit saturation with respect to both the cell density and the abundance of the Fe(III) oxyhydroxide substrate.  相似文献   
6.
7.
Evaporation of intercepted rain by a canopy is an important component of evapotranspiration, particularly in the humid boreal forest, which is subject to frequent precipitation and where conifers have a large surface water storage capacity. Unfortunately, our knowledge of interception processes for this type of environment is limited by the many challenges associated with experimental monitoring of the canopy water balance. The objective of this study is to observe and estimate canopy storage capacity and wet canopy evaporation at the sub-daily and seasonal time scales in a humid boreal forest. This study relies on field-based estimates of rainfall interception and evapotranspiration partitioning at the Montmorency Forest, Québec, Canada (mean annual precipitation: 1600 mm, mean annual evapotranspiration: 550 mm), in two balsam fir-white birch forest stands. Evapotranspiration was monitored using eddy covariance sensors and sap flow systems, whereas rainfall interception was measured using 12 sets of throughfall and six stemflow collectors randomly placed inside six 400-m2 plots. Changes in the amount of water stored on the canopy were also directly monitored using the stem compression method. The amount of water intercepted by the forest canopy was 11 ± 5% of the total rainfall during the snow-free (5 July–18 October) measurement periods of 2017 and 2018. The maximum canopy storage estimated from rainfall interception measurements was on average 1.6 ± 0.7 mm, though a higher value was found using the stem compression method (2.2 ± 1.6 mm). Taking the average of the two forest stands studied, evaporation of intercepted water represented 21 ± 8% of evapotranspiration, while the contribution of transpiration and understory evapotranspiration was 36 ± 9% and 18 ± 8%. The observations of each of the evapotranspiration terms underestimated the total evapotranspiration observed, so that 26 ± 12% of it was not attributed. These results highlight the importance to account for the evaporation of rain intercepted by humid boreal forests in hydrological models.  相似文献   
8.
Rates of reduction of Fe(III) oxyhydroxides by the bacterium Shewanella putrefaciens were measured as a function of the bacterial density and the Fe(III) substrate concentration. The results show that an earlier reported positive correlation between the solubility products (*Kso) and the maximum cell-specific reduction rates (vmax) of predominantly poorly crystalline Fe(III) oxyhydroxides also applies to insoluble and crystalline Fe(III) oxyhydroxides. The mineral solubilities were measured by a dialysis bag technique under acidic conditions (pH 1 up to 2.5) at 25 °C. Initial iron reduction rates by S. putrefaciens were determined in the presence of excess lactate as electron donor. In all cases, the microbial reduction rate exhibited saturation behavior with respect to the Fe(III) oxyhydroxide concentration. On a double logarithmic scale, the maximum rates vmax and the solubility products defined a single linear free energy relationship (LFER) for all the Fe(III) oxyhydroxides considered. The solubility provided a better predictor of vmax than the specific surface area of the mineral phase. A rate limitation by the electron transfer between an iron reductase and a Fe(III) center, or by the subsequent desorption of Fe2+ from the iron oxide mineral surface, are both consistent with the observed LFER.  相似文献   
9.
Organic matter (OM) in mineral-organic associations (MOAs) represents a large fraction of carbon in terrestrial ecosystems which is considered stable against biodegradation. To assess the role of MOAs in carbon cycling, there is a need to better understand (i) the time-dependent biogeochemical evolution of MOAs in soil, (ii) the effect of the mineral composition on the physico-chemical properties of attached OM, and (iii) the resulting consequences for the stabilization of OM. We studied the development of MOAs across a mineralogical soil gradient (0.3-4100 kyr) at the Hawaiian Islands that derived from basaltic tephra under comparable climatic and hydrological regimes. Mineral-organic associations were characterized using biomarker analyses of OM with chemolytic methods (lignin phenols, non-cellulosic carbohydrates) and wet chemical extractions, surface area/porosity measurements (N2 at 77 K and CO2 at 273 K), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), and differential scanning calorimetry (DSC). The results show that in the initial weathering stage (0.3 kyr), MOAs are mainly composed of primary, low-surface area minerals (olivine, pyroxene, feldspar) with small amounts of attached OM and lignin phenols but a large contribution of microbial-derived carbohydrates. As high-surface area, poorly crystalline (PC) minerals increase in abundance during the second weathering stage (20-400 kyr), the content of mineral-associated OM increased sharply, up to 290 mg C/g MOA, with lignin phenols being favored over carbohydrates in the association with minerals. In the third and final weathering stage (1400-4100 kyr), metastable PC phases transformed into well crystalline secondary Fe and Al (hydr)oxides and kaolin minerals that were associated with less OM overall, and depleted in both lignin and carbohydrate as a fraction of total OM. XPS, the N2 pore volume data and OM-mineral volumetric ratios suggest that, in contrast to the endmember sites where OM accumulated at the surfaces of larger mineral grains, topsoil MOAs of the 20-400-kyr sites are composed of a homogeneous admixture of small-sized PC minerals and OM, which originated from both adsorption and precipitation processes. The chemical composition of OM in surface-horizon MOAs, however, was largely controlled by the uniform source vegetation irrespective of the substrate age whereas in subsoil horizons, aromatic and carboxylic C correlated positively with oxalate-extractable Al and Si and CuCl2-extractable Al concentrations representing PC aluminosilicates and Al-organic complexes (r2 > 0.85). Additionally, XPS depth profiles suggest a zonal structure of sorbed OM with aromatic carbons being enriched in the proximity of mineral surfaces and amide carbons (peptides/proteins) being located in outer regions of MOAs. Albeit the mineralogical and compositional changes of OM, the rigidity of mineral-associated OM as analyzed by DSC changed little over time. A significantly reduced side chain mobility of sorbed OM was, however, observed in subsoil MOAs, which likely arose from stronger mineral-organic bindings. In conclusion, our study shows that the properties of soil MOAs change substantially over time with different mineral assemblages favoring the association of different types of OM, which is further accentuated by a vertical gradient of OM composition on mineral surfaces. Factors supporting the stabilization of sorbed OM were (i) the surface area and reactivity of minerals (primary or secondary crystalline minerals versus PC secondary minerals), (ii) the association of OM with micropores of PC minerals (via ‘sterically’ enhanced adsorption), (iii) the effective embedding of OM in ‘well mixed’ arrays with PC minerals and monomeric/polymeric metal species, (iv) the inherent stability of acidic aromatic OM components, and (iv) an impaired segmental mobility of sorbed OM, which might increase its stability against desorption and microbial utilization.  相似文献   
10.
A high heat-flow (∼900 mW m−2) has been observed over a volcanic structure at the Ocean-Continent Transition in the Eastern Gulf of Aden (Oman margin). The anomaly is superposed to a progressive increase of heat-flow across the margin and can be interpreted either by (1) heat refraction, (2) fluid discharge or (3) cooling magma. The two first explanations cannot be ruled out definitely by modelling analysis, but require unlikely thermal conductivity or permeability values. The third one implies that the latest activity of the volcano was about 100 000 years old and therefore continued c. 18 Ma after the break-up of Africa and Arabia. This potential mechanism is consistent with other lines of evidence of post-rifting activity in the Gulf of Aden and could invalidate the conventional assumption that rifted-margins become passive after the break-up of continents.  相似文献   
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