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131.
Rock-weathering rates as functions of time 总被引:2,自引:0,他引:2
Steven M. Colman 《Quaternary Research》1981,15(3):250-264
The scarcity of documented numerical relations between rock weathering and time has led to a common assumption that rates of weathering are linear. This assumption has been strengthened by studies that have calculated long-term average rates. However, little theoretical or empirical evidence exists to support linear rates for most chemical-weathering processes, with the exception of congruent dissolution processes. The few previous studies of rock-weathering rates that contain quantitative documentation of the relation between chemical weathering and time suggest that the rates of most weathering processes decrease with time. Recent studies of weathering rinds on basaltic and andesitic stones in glacial deposits in the western United States also clearly demonstrate that rock-weathering processes slow with time. Some weathering processes appear to conform to exponential functions of time, such as the square-root time function for hydration of volcanic glass, which conforms to the theoretical predictions of diffusion kinetics. However, weathering of mineralogically heterogeneous rocks involves complex physical and chemical processes that generally can be expressed only empirically, commonly by way of logarithmic time functions. Incongruent dissolution and other weathering processes produce residues, which are commonly used as measures of weathering. These residues appear to slow movement of water to unaltered material and impede chemical transport away from it. If weathering residues impede weathering processes then rates of weathering and rates of residue production are inversely proportional to some function of the residue thickness. This results in simple mathematical analogs for weathering that imply nonlinear time functions. The rate of weathering becomes constant only when an equilibrium thickness of the residue is reached. Because weathering residues are relatively stable chemically, and because physical removal of residues below the ground surface is slight, many weathering features require considerable time to reach constant rates of change. For weathering rinds on volcanic stones in the western United States, this time is at least 0.5 my. 相似文献
132.
Age of amphibolites associated with alpine peridotites in the Dinaride ophiolite zone,Yugoslavia 总被引:1,自引:0,他引:1
Marvin A. Lanphere Robert G. Coleman Steven Karamata Jakob Pamić 《Earth and Planetary Science Letters》1975,26(3):271-276
Amphibolites associated with alpine peridotites in the Central Ophiolite zone in Yugoslavia have K-Ar ages of 160–170 m.y. These amphibolites and associated peridotites underwent deep-seated metamorphism prior to tectonic emplacement into the sedimentary-volcanic assemblage of the Dinarides. The alpine peridotites and associated local rocks of the ophiolite suite are interpreted as Jurassic oceanic crust and upper mantle. 相似文献
133.
Soil and stream sediment sampling have been the primary geochemical exploration tools in the Appalachian piedmont to date. However, the great thicknesses of soil and saprolite found in the region coupled with the dense vegetation frequently encountered favor biogeochemistry as an alternative or supplemental method since deep-rooted plants sample closer to bedrock. To evaluate this method, an orientation survey was performed in which soils and vegetation at 17 sites north of Mineral, Virginia, were sampled and analyzed for Ag, Cd, Cu, Pb and Zn. The traverse included stations over the host rocks of massive sulfide mineralization, as well as over apparent “barren” country rock. Samples were analyzed by atomic absorption spectrophotometry using standard digestion and analytical techniques.Both A- and B-horizon soil metals generally appear to be reliable indicators of mineralization, with soils developed over sulfides showing up to three-fold enrichment in metal content relative to the average soils developed on the country rock. Correlation of metal concentrations in vegetation to soil metal concentrations reveal plant concentrations expressed on a dry-weight basis correlate stronger and more frequently to soil metals than do ash-weight concentrations. Copper shows some promise in selected organs and species, Ag appears fair but data are limited to one organ of one species, and plant Pb seems totally unresponsive to soil metal concentrations perhaps because foliar absorption is an important plant uptake mechanism here. However, Zn and Cd in organs of the oak group, especially mature leaves and twigs of the current year's growth show the greatest promise as prospecting tools. They correlate well with soil metals and when compared directly to the geology they reliably reflect mineralization. Although results using White oak were slightly less profound than those obtained from the Black-Red oak group, White oak may be preferred as it is a single, more widespread, easily-identifiable species. Copper and especially Zn although essential elements to plants, do not appear to be “difficult” elements for biogeochemical prospecting in the Appalachian piedmont. 相似文献
134.
Steven C. Schimmel James M. Patrick Linda F. Faas Jerry L. Oglesby Alfred J. Wilson 《Estuaries and Coasts》1979,2(1):9-15
Two long-term studies were conducted to determine toxicity, uptake and depuration of Kepone in blue crabs (Callinectes sapidus). In the first, Kepone was administered to crabs in seawater (0.03 or 0.3 μg Kepone/I) or food (eastern oyster,Crassostrea virginica, containing 0.25 μg/g Kepone). Uptake of Kepone in 28 days was primarily through the contaminated oysters. When these crabs were held in Kepone-free seawater and fed Kepone-free oysters for 28 days, no loss of the insecticide was evident. There were adverse effects on molting and survival in crabs fed oysters that contained 0.25 μg/g Kepone. A second study was conducted to determine: (1) the depuration of Kepone over a 90-day period in blue crabs fed oysters from the James River, Virginia (containing 0.15 μg/g Kepone); and (2) the effects of Kepone on molting and survival of blue crabs fed James River oysters or laboratory-contaminated oysters that contained 0.15 or 1.9 μg/g Kepone. Crabs fed Kepone-contaminated oysters followed by a diet of Kepone-free oysters for 90 days had detectable concentrations of the insecticide in tissues. Also, blue crabs that ate oysters containing Kepone in concentrations similar to those found in oysters from the James River, died or molted less frequently than crabs fed Kepone-free oysters meats. 相似文献
135.
The dissolved silica concentration in waters of Lake Superior probably is in a steady state because it is not influenced significantly by man, and the climate, topography and vegetation in the drainage area of the lake have been stable for the past 4000 years. Therefore the rate at which dissolved silica is introduced to the lake should equal the output rate.The primary inputs are: tributaries (4.1–4.6 × 108kgSiO2/yr), diffusion from sediment pore waters (0.21?0.78 × 108kgSiO2/yr) and atmospheric loading (0.26 × 108kgSiO2/yr). Silica is lost from the lake waters by: outflow through the St. Marys River, diatom deposition, adsorption onto particulates in the sediments, and authigenic formation of new silicate minerals. Tributary outflow accounts for less than one half the annual input of silica, and diatom deposition and silica adsorption withdraw less than 10% of the annual input. Therefore the formation of new silicate phases must be the dominant sink for dissolved silica in Lake Superior. The specific phases formed are not identified in the bottom sediments. X-ray diffraction studies suggest that smectite is one product, and amorphous ferroaluminum silicates may be another product.Mathematical modeling of the dissolved silica response to lake eutrophication suggests that the phosphate loading to Lake Superior would have to increase by about 250-fold to cause a silica depletion rate equal to that reported for Lake Michigan, assuming no change in the rate of upwelling of deep waters. 相似文献
136.
A number of experimental CO2 solubility data for silicate and aluminosilicate melts at a variety of P- T conditions are consistent with solution of CO2 in the melt by polymer condensation reactions such as SiO 4(m 4? +CO2(v)+Si n O 3n+1(m) (2n+1) ?Si n+1O 3n+4(m) (2n+4)? +CO 3(m )2? . For various metalsilicate systems the relative solubility of CO2 should depend markedly on the relative Gibbs free change of reaction. Experimental solubility data for the systems Li2O-SiO2, Na2O-SiO2, K2O-SiO2, CaO-SiO2, MgO-SiO2 and other aluminosilicate melts are in complete accord with predictions based on Gibbs Free energies of model polycondesation reactions. A rigorous thermodynamic treatment of published P- T-wt.% CO2 solubility data for a number of mineral and natural melts suggests that for the reaction CO2(m) ? CO2(v)
- CO2-melt mixing may be considered ideal (i.e., { \(a_{{\text{CO}}_{\text{2}} }^m = X_{{\text{CO}}_{\text{2}} }^m \) );
- \(\bar V_{{\text{CO}}_{\text{2}} }^m \) , the partial molal volume of CO2 in the melt, is approximately equal to 30 cm3 mole?1 and independent of P and T;
- Δ C p 0 is approximately equal to zero in the T range 1,400° to 1,650 °C and
- enthalpies and entropies of the dissolution reaction depend on the ratio of network modifiers to network builders in the melt. Analytic expressions which relate the CO2 content of a melt to P, T, and \(f_{{\text{CO}}_{\text{2}} } \) for andesite, tholeiite and olivine melilite melts of the form
137.
The lacustrine Peterson Limestone of western Wyoming and southeastern Idaho comprises six lithofacies throughout its 20,000 km2 aerial extent. These are: (1) calcareous sandstone and shale, (2) red nodular limestone, (3) pink sandy micrite, (4) biomicrite, (5) graded silty micrite, and (6) limestone conglomerate. The first two represent floodplain deposition and paleosols, whereas the remaining are shallow nearshore and deeper lacustrine sediments.This sequence was developed in a large fresh, hardwater lake surrounded by fluvial systems and associated flood plains in a warm temperate climate. Well-oxidized sandy terrigenous rocks, together with calcareous paleosol nodules, indicate that flood-plain deposition both preceded and was concurrent with lacustrine carbonate deposition. Micrite and biomicrite formed in deeper parts of the basin while sandy and silty carbonate accumulated in shallower lake-margin areas. Less-calcareous shale units which are interbedded with deeper-water carbonate were deposited either during rapid basin subsidence and deepening of the lake center or during periods of slower carbonate precipitation. Turbidity currents and subaqueous debris flows generated along steeper lake margins, resulted in the deposition of rhythmic layers of graded silty micrite and diamictic limestone conglomerate in the deepest part of the basin. The carbonate-rich sediments comprising these two lithofacies were originally deposited on shallow lake-margin benches and subsequently were transported downslope toward the lake center.Comparison with other carbonate-precipitating lacustrine systems indicates that this lake was not like modern playas. Although no known modern lacustrine system is precisely like Lake Peterson, the flora, fauna, composition, and distribution of facies within modern temperate-region lakes most closely resemble those of the Peterson Limestone. 相似文献
138.
This paper examines the effects of the mixing of dry air into a cloud top from the point of view of the droplet spectra. It is shown theoretically that the resulting cycling of the air up and down in the cloud, as seems to be the essential mechanism by which cumuli have been diluted to their observed liquid water mixing ratio, can double the largest drop radius and generate cloud parcels containing drops of all sizes up to this maximum. These changes in the droplet distribution with size occur by a process which is not greatly influenced by the cloud condensation nuclei or the details of droplet growth since maritime like spectra can develop in continental type cumuli. It shows that large numbers of cloud condensation nuclei should not have much effect in inhibiting the rainforming process by reducing coalescence growth. On the contrary, the controlling parameters which determine precipitation efficiency and times seem to be those which control the mixing. 相似文献
139.
Nicholas R. Golledge Derek Fabel Jeremy D. Everest Stewart Freeman Steven Binnie 《第四纪科学杂志》2007,22(8):785-791
We use cosmogenic 10Be surface exposure age techniques at a locality close to Rannoch Moor, western Scottish Highlands, in order to establish the age and chronology of its most recent glaciation. Glacial erratics and an in situ bedrock quartz vein sampled from this site—the summit of Beinn Inverveigh—have yielded zero‐erosion exposure ages of 12.9 ± 1.5 ka to 11.6 ± 1.0 ka, implying complete ice cover of the mountain during the Younger Dryas, or Loch Lomond Stadial. These results fit closely with published 14C dates that bracket the maximum (lateral) extent of ice cap outlet glaciers, and are the first internally consistent ages to specifically address this period of glaciation in Scotland. Furthermore, the dates imply that previous palaeoglaciological reconstructions for this area may have underestimated both the thickness of the former ice cap and, by implication, its volume. © British Geological Survey/Natural Environment Research Council copyright 2007. Reproduced with the permission of BGS/NERC. Published by John Wiley & Sons, Ltd. 相似文献
140.
Stream temperature will be subject to changes because of atmospheric warming in the future. We investigated the effects of the diurnal timing of air temperature changes – daytime warming versus nighttime warming – on stream temperature. Using the physically based model, Heat Source, we performed a sensitivity analysis of summer stream temperatures to three diurnal air temperature distributions of +4 °C mean air temperature: i) uniform increase over the whole day, ii) warmer daytime and iii) warmer nighttime. The stream temperature model was applied to a 37‐km section of the Middle Fork John Day River in northeastern Oregon, USA. The three diurnal air temperature distributions generated 7‐day average daily maximum stream temperatures increases of approximately +1.8 °C ± 0.1 °C at the downstream end of the study section. The three air temperature distributions, with the same daily mean, generated different ranges of stream temperatures, different 7‐day average daily maximum temperatures, different durations of stream temperature changes and different average daily temperatures in most parts of the reach. The stream temperature changes were out of phase with air temperature changes, and therefore in many places, the greatest daytime increase in stream temperature was caused by nighttime warming of air temperatures. Stream temperature changes tended to be more extreme and of longer duration when driven by air temperatures concentrated in either daytime or nighttime instead of uniformly distributed across the diurnal cycle. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献