Reply to: Comment on ‘A case example of near-surface correction for multicomponent VSPS’ by Gildas Omnes     

Colin MacBeth 《Geophysical Prospecting》1997,45(4):723-724

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Measurement of the spatial distribution of fluvial bedload transport velocity in both sand and gravel     

Colin D. Rennie  Robert G. Millar 《地球表面变化过程与地形》2004,29(10):1173-1193

Maps are presented of the spatial distribution of two‐dimensional bedload transport velocity vectors. Bedload velocity data were collected using the bottom tracking feature of an acoustic Doppler current pro?ler (aDcp) in both a gravel‐bed reach and a sand‐bed reach of Fraser River, British Columbia. Block‐averaged bedload velocity vectors, and bedload velocity vectors interpolated onto a uniform grid, revealed coherent patterns in the bedload velocity distribution. Concurrent Helley‐Smith bedload sampling in the sand‐bed reach corroborated the trends observed in the bedload velocity map. Contemporaneous 2D vector maps of near‐bed water velocity (velocity in bins centered between 25 cm and 50 cm from the bottom) and depth‐averaged water velocity were also generated from the aDcp data. Using a vector correlation coef?cient, which is independent of the choice of coordinate system, the bedload velocity distribution was signi?cantly correlated to the near‐bed and depth‐averaged water velocity distributions. The bedload velocity distribution also compared favorably with variations in depth and estimates of the spatial distribution of shear stress. Published in 2004 by John Wiley & Sons, Ltd.  相似文献   

Soft X-ray spectroscopic studies of the reaction of fractured pyrite surfaces with Cr(VI)-containing aqueous solutions     

Colin S. Doyle  Tom Kendelewicz  Gordon E. Brown Jr 《Geochimica et cosmochimica acta》2004,68(21):4287-4299

We have used synchrotron-based soft X-ray core-level photoemission and adsorption spectroscopies to study the reaction of aqueous sodium chromate solutions with freshly fractured pyrite surfaces. Pyrite surfaces were reacted with 50 μM sodium chromate solution at pH 7 for reaction times between 1 min and 37 hr. Additional experiments were performed at pH 2 and pH 4 with 50 μM sodium chromate solutions and at pH 7 with 5 mM solutions. At chromate concentrations of 50 μM, all chromium present on the pyrite surface was in the form of Cr(III), while at 5 mM, both Cr(III) and Cr(VI) were present at the pyrite surface. Minor quantities of oxidized sulfur species (sulfate, sulfite, and zero-valent sulfur) were identified as reaction products on the pyrite surface. The amount of oxidized sulfur species observed on the surface was greater when pyrite was reacted with 5 mM Cr(VI) solutions because the rate of chromium deposition exceeded the rate of dissolution of pyrite oxidation products, effectively trapping Cr(VI) and oxidized sulfur species in an overlayer of iron(III)-containing Cr(III)-hydroxide. This work shows that pyrite, an extremely cheap and readily available waste material, may be suitable for the removal of hexavalent chromium from acidic to circumneutral waste streams. The reduced chromium ultimately forms a coating on the pyrite surface, which passivates the pyrite surface towards further oxidation.  相似文献   

An experimental study of phase equilibria in the systems H2O–CO2–CaCl2 and H2O–CO2–NaCl at high pressures and temperatures (500–800?°C, 0.5–0.9?GPa): geological and geophysical applications     

Kirill I. Shmulovich  Colin M. Graham 《Contributions to Mineralogy and Petrology》2004,146(4):450-462

Phase equilibria in the ternary systems H₂O–CO₂–NaCl and H₂O–CO₂–CaCl₂ have been determined from the study of synthetic fluid inclusions in quartz at 500 and 800 °C, 0.5 and 0.9 GPa. The crystallographic control on rates of quartz overgrowth on synthetic quartz crystals was exploited to prevent trapping of fluid inclusions prior to attainment of run conditions. Two types of fluid inclusion were found with different density or CO₂ homogenisation temperature (T_h(CO₂)): a CO₂-rich phase with low T_h(CO₂), and a brine with relatively high T_h(CO₂). The density of CO₂ was calibrated using inclusions in the binary system H₂O–CO₂. Mass balance calculations constrain tie lines and the miscibility gap between brines and CO₂-rich fluids in the H₂O–CO₂–NaCl and H₂O–CO₂–CaCl₂ systems at 500 and 800 °C, and 0.5 and 0.9 GPa. The miscibility gap in the CaCl₂ system is larger than in the NaCl system, and solubilities of CO₂ are smaller. CaCl₂ demonstrates a larger salting-out effect than NaCl at the same P–T conditions. In ternary systems, homogeneous fluids are H₂O-rich and of extremely low salinity, but at medium to high concentrations of salts and non-polar gases fluids are unlikely to be homogeneous. The two-phase state of crustal fluids should be common. For low fluid-rock ratios the cation compositions of crustal fluids are buffered by major crustal minerals: feldspars and micas in pelites and granitic rocks, calcite (dolomite) in carbonates, and pyroxenes and amphiboles in metabasites. Fluids in pelitic and granitic rocks are Na-K rich, while for carbonate and metabasic rocks fluids are Ca-Mg-Fe rich. On lithological boundaries between silicate and carbonate rocks, or between pelites and metabasites, diffusive cation exchange of the salt components of the fluid will cause the surfaces of immiscibility to intersect, leading to unmixing in the fluid phase. Dispersion of acoustic energy at critical conditions of the fluid may amplify seismic reflections that result from different fluid densities on lithological boundaries.Editorial responsibility: I. Parsons  相似文献   

Nickel speciation in Sebertia acuminata,a plant growing on a lateritic soil of New Caledonia     

Nicolas Perrier  Fabrice Colin  Tanguy Jaffré  Jean-Paul Ambrosi  Jérôme Rose  Jean-Yves Bottero 《Comptes Rendus Geoscience》2004,336(6):567-577

Nickel speciation in a nickel hyperaccumulating plant (Sebertia acuminata) and its associated soil of southern New Caledonia was studied using various analytical methods. The soil is formed of iron oxides (goethite, hematite), which contain almost all the nickel. The available nickel is probably linked to the organic matter in the litter. Sebertia acuminata, acts as a nickel pump, and concentrates the metal in its leaves. It partitions nickel and silica; nickel is concentrated in the cells (probably in the vacuoles) as organometallic complexes, whereas silica forms the framework of the cells, and the phytolithes. A thorough study of these plants seems essential in order to define the soil–plant relations, and to propose appropriate ways for ecological restoration. To cite this article: N. Perrier et al., C. R. Geoscience 336 (2004).  相似文献   

A macroscale analysis of coastal steepening around the coast of England and Wales   总被引：1，自引：0，他引：1  

J A Taylor  A P Murdock  N I Pontee 《The Geographical journal》2004,170(3):179-188

Coastal steepening potentially presents an array of management issues in the form of financial implications of sea defence degradation, increased risk posed to the hinterland as wave attenuation is reduced, 'coastal squeeze' and statutory requirements in the light of the Habitats Directive. The extent to which coastal steepening has occurred throughout England and Wales has been investigated through use of a GIS and dataset based on historical Ordnance Survey map information. Data were collected along 1084 selected profile lines, positioned so as to be geomorphologically representative of the coast. Features recorded from each map year included the positions of mean high water (MHW) and mean low water (MLW), the relative movements of which infer changing intertidal gradients. The results presented in this paper are on a subject and scale not previously published. It is revealed that 61% of the coastline studied has experienced a tendency towards steepening. Of the remainder, 33% has flattened, and 6% has experienced no rotational movement. This tendency towards steepening has been the dominant movement on each of the west, south, and east coasts.  相似文献   

Re-examination of the magnetic lineations of the Gascoyne and Cuvier Abyssal Plains, off NW Australia     

Masako S. Robb  Brian Taylor  Andrew M. Goodliffe 《Geophysical Journal International》2005,163(1):42-55

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Geology and Metal Contents of the Ruttan volcanogenic massive sulfide deposit, northern Manitoba, Canada     

C. Tucker. Barrie  Craig Taylor  Doreen E. Ames 《Mineralium Deposita》2005,39(8):795-812

The Paleoproterozoic Ruttan Cu–Zn volcanogenic massive-sulfide (VMS) deposit is a large, relatively low grade, bimodal-siliciclastic type deposit in the Rusty Lake volcanic belt of northern Manitoba. The deposit contained over 82.8 million tonnes of massive sulfide, of which 55.7 million tonnes were mined from 1973 to 2002. The deposit consists of a series of moderately to steeply dipping, south-facing lenses that extend along strike at the surface for 1.1 km and to a depth of 1.0 km. These lenses occur within a steeply dipping, bimodal volcanic, volcaniclastic and siliciclastic sequence. In the immediate mine area, transitional calc-alkalic to high-silica (tholeiitic), felsic, and intermediate volcanic/volcaniclastic rocks of the Mine Sequence are host to, and intercalated with, the massive-sulfide lenses. Transitional tholeiitic to calc-alkalic basalt and andesite are present in the footwall sequence, approximately 500 m down-section from the ore horizon. The overlying rocks are predominantly fine-grained volcaniclastics and siliciclastics, but include polyfragmental agglomerate that contains mafic bombs and scoriaceous felsic fragments. Syn-depositional felsic and mafic dikes, sills, and apophyses are ubiquitous throughout the Mine Sequence, including the ore lenses, indicating continued, near-vent magmatism, and volcanism during ore formation. Fabrics in altered hostrocks have consistent, down-plunge stretching lineations to the SSE that suggest the deposit has been elongated by a factor of ~1.2–1.5; otherwise, the deposit is remarkably undeformed. Syn- and post-depositional faults in the mine area have relatively minor displacements up to tens of meters. Proximal (within 200 m) footwall rocks exhibit moderate to strong chloritization, characterized by the upper greenschist to lower amphibolite facies assemblages that include cordierite–almandine–andalusite–sillimanite–biotite ± staurolite ± anthophyllite ± talc, and local silicification. The proximal hanging wall rocks are characterized by sericite ± gahnite alteration, which is restricted to within approximately 75 m of the uppermost lenses. Additional gangue minerals are anhydrite and carbonate minerals (siderite, dolomite, ankerite, and calcite), as well as chlorite, sericite, biotite, talc, and quartz. Carbonate (excluding siderite), potassium feldspar, silicification and epidotization are common distal alteration zones in the footwall to the Mine Sequence several kilometers to the northeast. There are three principal groups of massive sulfide lenses; the East lenses, the West lenses, and the Western Anomaly lenses to the far west. In general, Cu is relatively enriched at the stratigraphic base and in the center of the deposit, whereas Zn is enriched upsection and at the outer margins. Some of the Zn-rich ore exhibits primary mineralogical layering. Parts of the West and Western Anomaly lenses show two layers with Cu-rich bases and Zn-rich tops. The massive sulfide is typically 10–40-m thick; one area along the margin of the main lenses is over 130-m thick and may represent deposition adjacent to a syn-depositional fault. The main sulfide phases are pyrite, pyrrhotite, chalcopyrite, sphalerite, and galena, with tetrahedrite as the most abundant trace phase. Gahnite is ubiquitous in the chlorite-rich assemblages adjacent to the ore lenses. The average base, precious and trace metal contents estimated from Cu and Zn concentrates, and from millhead grades and recoveries. Metals easily transported as chloride and bisulfide complexes in hydrothermal fluids including: Pb, Ag, In, Cu, Cd, Au, and Zn are enriched by 1.5–2.5 orders of magnitude in comparison to the bulk continental crust. Other elements such as Sn, Mo, and As are at near-crustal concentrations, whereas Mn, Ga, and Co are significantly depleted in comparison to the crust. Calculated metal concentrations in the average hydrothermal fluid based on the average metal contents are comparable to, or higher than those measured at sediment covered ridge hydrothermal systems, which precipitate much of their metal budget in the subsurface. Average rare earth element contents for the sulfide are light rare earth element enriched (La_N/Yb_N=22) and range from 0.45 to 0.02x chondritic values, with a moderate negative Eu anomaly (Eu*=0.51). Metal and trace element contents in the Ruttan exhalite horizon, and in proximal (within 1–2 km) exhalites along strike from the 0.6 million tonne Dar-2 Cu–Zn deposit 12 km south of Ruttan, have positive Eu anomalies, whereas negative Eu anomalies are present at distance. The positive Eu anomalies reflect high temperature paleoseafloor hydrothermal venting and precipitation of Eu²⁺-enriched clays and possibly carbonates, and indicate proximity to base-metal deposits. Silver and lead are also enriched in the exhalites near the deposits, whereas Mn is enriched at ~1–3 km along strike, but not consistently. Editorial handling: B. Gemmel An erratum to this article is available at .  相似文献   

Chemical and textural equilibration of garnet during amphibolite facies metamorphism: The influence of coupled dissolution–reprecipitation          下载免费PDF全文

Tim J Dempster  Julie La Piazza  Andrew G Taylor  Nicolas Beaudoin  Peter Chung 《Journal of Metamorphic Geology》2017,35(9):1111-1130

Metamorphic equilibration requires chemical communication between minerals and may be inhibited through sluggish volume diffusion and or slow rates of dissolution in a fluid phase. Relatively slow diffusion and the perceived robust nature of chemical growth zoning may preclude garnet porphyroblasts from readily participating in low‐temperature amphibolite facies metamorphic reactions. Garnet is widely assumed to be a reactant in staurolite‐isograd reactions, and the evidence for this has been assessed in the Late Proterozoic Dalradian pelitic schists of the Scottish Highlands. The 3D imaging of garnet porphyroblasts in staurolite‐bearing schists reveals a good crystal shape and little evidence of marginal dissolution; however, there is also lack of evidence for the involvement of either chlorite or chloritoid in the reaction. Staurolite forms directly adjacent to the garnet, and its nucleation is strongly associated with deformation of the muscovite‐rich fabrics around the porphyroblasts. “Cloudy” fluid inclusion‐rich garnet forms in both marginal and internal parts of the garnet porphyroblast and is linked both to the production of staurolite and to the introduction of abundant quartz inclusions within the garnet. Such cloudy garnet typically has a Mg‐rich, Mn‐poor composition and is interpreted to have formed during a coupled dissolution–reprecipitation process, triggered by a local influx of fluid. All garnet in the muscovite‐bearing schists present in this area is potentially reactive, irrespective of the garnet composition, but very few of the schists contain staurolite. The staurolite‐producing reaction appears to be substantially overstepped during the relatively high‐pressure Barrovian regional metamorphism reflecting the limited permeability of the schists in peak metamorphic conditions. Fluid influx and hence reaction progress appear to be strongly controlled by subtle differences in deformation history. The remaining garnet fails to achieve chemical equilibrium during the reaction creating distinctive patchy compositional zoning. Such zoning in metamorphic garnet created during coupled dissolution–reprecipitation reactions may be difficult to recognize in higher grade pelites due to subsequent diffusive re‐equilibration. Fundamental assumptions about metamorphic processes are questioned by the lack of chemical equilibrium during this reaction and the restricted permeability of the regional metamorphic pelitic schists. In addition, the partial loss of prograde chemical and textural information from the garnet porphyroblasts cautions against their routine use as a reliable monitor of metamorphic history. However, the partial re‐equilibration of the porphyroblasts during coupled dissolution–reprecipitation opens possibilities of mapping reaction progress in garnet as a means of assessing fluid access during peak metamorphic conditions.  相似文献   

Emplacement of the Cabezo María lamproite volcano (Miocene,SE Spain)     

Thomas M. Gernon  Samuel Spence  Clive N. Trueman  Rex N. Taylor  Eelco Rohling  Stuart J. Hatter  Ian C. Harding 《Bulletin of Volcanology》2015,77(6):1-13

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