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The release of Pb and rare earth elements (REE) during granitoid weathering was investigated through dissolution experiments of fresh granite and soil samples. Two aliquots of a granite sample from the El-Capitan Granite, Sierra Nevada, California, were leached several times using a dilute acid at pH = 1. The results of the experiment were compared with Pb and REE data from soils developed on the same rock. During the early stages of granitoid dissolution, Pb and REE were preferentially released from some of the accessory phases (i.e., allanite, sphene, and apatite). This caused higher 206Pb/207Pb and 208Pb/207Pb values and different REE patterns in solution compared with the rock values. Based on Pb isotopes and REE patterns, three stages of rock dissolution can be identified. In the first stage the dissolution of allanite dominates the release of Pb and REE from accessory phases, as 208Pb/207Pb, Ce/Pb, and chondrite-normalized Ce/Yb ratios in solution increase and approach the values of allanite. In the second stage, the dissolution of apatite and sphene become more significant. In the third stage, the isotopic ratios of Pb and the normalized-REE patterns reflect the depletion of accessory phases and the increase in the rate of feldspar dissolution. According to our estimate (based on Si release from the rock) all three stages account for the first 500 kyr of granitoid weathering.Using the isotopic ratios of Pb, major elemental compositions, and REE concentrations both in the experimental solutions and in the soil we were able to establish the following order of the weathering rates of accessory phases: allanite > apatite > sphene. In addition, we have demonstrated that biotite is significantly less resistant to weathering than hornblende under acidic conditions, and is probably dissolved completely after approximately 500 kyr of rock weathering. We also suggest that within 500 kyr of granitoid weathering K-feldspar accounts for 15% of the released K. 相似文献
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Flow-through dissolution experiments were carried out on crushed granitoid rock (the Elat Granite) and three mineral separates (plagioclase, perthite, and biotite + chlorite) from this rock at pH 1 and 25°C. Major element concentrations were combined with Pb and Sr isotopic analyses of starting materials and output solutions and together enabled us to elucidate several important mechanisms related to granitoid rock weathering. We observed an initial stage of rock dissolution (<200 hours of reaction) that was characterized by elemental release from traces of calcite and/or apatite and to a lesser extent from the interlayer sites of biotite. Dissolution in the interval of 200 to 400 h was dominated by the release of elements from the interlayer sites of biotite, and at 400 to 1000 h of reaction the chemistry of output solutions was dominated by the release of elements from tetrahedral and octahedral sites of biotite as well as from plagioclase. After 1000 h, the dissolution of plagioclase, and to a lesser extent biotite, dominated the composition of elements released by the rock. We demonstrate that Pb and Sr isotope ratios in the output solutions can be used to identify each of these stages of dissolution. By comparing our experimental results on the release of Pb and Sr isotopes with field measurements of Pb and Sr isotopes in soil chronosequences from the Wind River and the Sierra Nevada Mountains (USA), we are able to show that similar isotopic patterns appear in both the pH 1 experiments and in soils formed under natural conditions at higher pH. By combining these experimental results with previous field studies, we are able to estimate the duration of most of these stages of granitoid weathering under natural conditions in temperate climates. In soils older than a few hundred years and younger than 10,000 yr the release of elements from interlayer sites of biotite controls the weathering flux. Soils between 10,000 and 100,000 yr old are dominated by biotite and plagioclase weathering, with biotite weathering controlling the first part of this period and plagioclase dominating the later part. After more than 100,000 yr, plagioclase, and to a lesser degree biotite, dominate the weathering flux within these granitoid soils. 相似文献
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Causes of recent salinization of numerous plots in the Yizre'el Valley of Israel were examined through a detailed field study of two severely affected sites. in particular, the theory of artesian influence on salt build-up in the upper cultivated soil layer was investigated. Two piezometer nests and 12 wells were installed to study the subsurface hydraulic regime. Water samples and soil extracts were taken to characterize the chemical composition down to 10m. No significant head differences were measured at the lower site, while at the upper site 96 per cent of the head that existed at the deep (7.5 m) artesian layer was dissipated within the overlying thick clay layer. Slight head differences were noted in the shallow layers. the deep-lying, coarse-textured aquifer differs markedly from the upper confining layers and constitutes an independent water body that has little relevance to surface processes. Chemical and hydrological analyses indicate that applied low-quality irrigation waters May, be the primary cause of downward-moving salinity and alkalinity which, in turn, affect soil permeability and site productivity. 相似文献
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Iron biogeochemical cycling and distribution between particulate, reactive (colloidal + dissolved, oxine-labile, Fe(II)) fractions were studied in the seasonally stratified, mesotrophic Lake Kinneret. This article presents various aspects of the Fe budget in the lake and relates them to the chemical reactivity of various physicochemical forms of Fe.The budget of Fe in Lake Kinneret is dominated by fluvial Fe load, rather than by internal recycling of Fe from the sediment, as shown by the fact that 75 to 94% of the variance in Fe concentrations in the lake can be explained by the fluctuation in the water discharge of the Jordan River. Iron associated with phytoplankton accounts for 9-16% of the bulk particulate Fe in the lake. However, within patches of the dominate algae, the dinoflagellate Peridinium gatunense, algal Fe accounts for more than 70% of the lake’s particulate Fe. The algal Fe is predominantly intracellular, and the Fe: chlorophyll a ratios were within the range of published values for dinoflagellates and cyanobacteria. Iron associated with particles larger than 0.025 μm (20-300 nM) accounts for 80-95% of total Fe in the epilimnion of Lake Kinneret throughout the year. In contrast, this fraction of Fe is dominant in the hypolimnion only during the period of lake mixing. Iron concentration of different size fractions (<0.025 μm, <0.2 μm and >0.025 μm) in the surface water covaried throughout the research period. These covariations suggest dynamic transformations of Fe between different size fractions, either due to partial dissolution/precipitation or desorption/adsorption. Oxine-labile Fe concentrations, the Fe fraction considered chemically labile and available for phytoplankton, ranged from 15 to 75 nM. In wintertime, the oxine-labile Fe accounts for only 10-20% of the total Fe, while in other seasons most of the Fe is oxine-labile. Oxine-labile Fe concentrations always exceed the 0.025 μm-filtered Fe, implying that some of the larger particles contain oxine labile-Fe, and therefore are reactive. The fraction of reactive particles in Lake Kinneret (10-80%) is high relative to that of the marine environments, and can most likely be attributed to its fluvial source, which contains a significant proportion of reactive Fe oxide and hydrous oxide particles.The annual variability in the epilimnetic concentrations of other trace elements and nutrients, such as Al, Mn, Cd, Zn, Pb, and P were studied and grouped according to their resemblance with river water discharge, redox processes, or biological uptake and scavenging. Distribution patterns of Al, Pb and Cd resembled that of Fe, suggesting that similar processes control the concentrations of these metals, namely significant contribution from the watershed, high affinity to particulate matter and little control of biota on their fate in the lake. Other elements such as Zn and P are more affected by biological uptake, while Mn is more affected by redox cycling within the lake. 相似文献
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Shear faults in Upper Cretaceous limestones of the central Negev desert adjacent to the Dead Sea Transform (DST) feature extensive ferruginous mineralization and dolomitization. This has been related to topographically driven flow of metalliferous groundwaters through an underlying clastic (Nubian Sandstone) aquifer and rise of the fluids up the fault zones. The present study combines Pb and Sr isotope measurements with detailed sampling and petrography at the eastern end of the Paran fault (Menuha Ridge) in order to identify the types of groundwater and the sources of enriched elements in this regional-scale sedimentary mineralization. Ferroan and non-ferroan dolomitization along the Paran fault caused significant enrichment of several elements (Mg, Cu, Mn, Ni, V, Zn, Pb, and U) and 87Sr/86Sr values that are significantly higher than the Upper Cretaceous limestone country rock. The non-ferroan dolomite and the ferroan dolomite sampled at three sites along the Menuha Ridge have similar 87Sr/86Sr values 0.7076-0.7089, and 0.7077-0.7086, respectively. Additionally, there is a positive correlation between Mg-content of the dolomites and their 87Sr/86Sr values. The isotopic composition of Sr and Pb of dolomite corresponds to the mineralogical type identified in the mineralized rock (non-ferroan dolomite, simple-zoned ferroan dolomite, and complex-zoned ferroan dolomite). The 207Pb/204Pb and 206Pb/204Pb ratios of Fe oxides and dolomites from the three sites plot on a straight line, where the simple-zoned ferroan dolomite values are at the non-radiogenic end of the line and the complex-zoned ferroan dolomites at the radiogenic end. Both 206Pb/204Pb and 207Pb/204Pb ratios in dolomites and to a lesser degree in Fe-oxides suggest that a mixing between two end-members controls the behavior of Pb in the mineralization products along the Paran fault. Rather than a single fluid source, the study indicates that two types of metalliferous groundwaters were involved in the dolomitization and mineralization along the Paran fault. The first, and hitherto undocumented, fluid source is the Mg-rich Dead Sea Rift brine, migrating in the sub-surface before dolomitizing the carbonate bedrock. Migration of the brines took a deep path to the site of mineralization, with temperatures reaching 75 °C. Based on the geological history of the region, this probably took place in the Late Miocene-Early Pliocene interval. The second type of groundwater acquired its high solute concentrations from leaching igneous rocks and clastic sediments in the sub-surface, and infiltrated along the Paran fault, precipitating Fe-rich minerals and caused the first stage of dolomitization. This groundwater flowed at shallower depth than the DSR brines, and at lower temperatures (T ? 50 °C). The study shows that sedimentary mineralization in faults adjacent to active transform fault zones may arise from the combination of several different fluid flow regimes. 相似文献
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Rare earth element (REE) distributions and Pb isotope compositions were explored in soils varying in age from ca. 0.4 to ?300 ka, developed on moraines in the Wind River Mountains, Wyoming. Soil extracts (0.6 M HCl) were used to examine the soil labile pool while the major element distribution in soil profiles was used to determine the extent of weathering at different soil depths. The results show that the chondrite-normalized REE patterns of the deepest bulk soil within each profile reflects the composition of the moraine till, except for the oldest soil. Up to ca. 12 ka, the soil extract fraction is enriched in light REE, indicating early release of light REE to the soil labile pool while that of the two oldest soils are relatively enriched in heavy REE. In the soil extracts the La/Sm ratio normalized to the deepest soil (LaD/SmD) decreases systematically with soil age. Similarly, the Eu-anomaly in the deepest soil from each profile (EuD/EuD*) decreases slightly with soil age in the three young soils; however, EuD/EuD* increases with soil age in the older soils. The systematic trends of these two ratios indicate the depletion of light REE in young soils and the enrichment of Eu and heavy REE in the older soils. Based on the Pb isotope ratios, the relative contribution of Pb to the soil labile pool via mineral weathering of U- or Th-rich phases was assessed for the different stages of weathering. The whole-soil profile 208Pb/204Pb ratio was found to decrease with soil age and with LaD/SmD, whereas it increased with the EuD/EuD* ratio. In each horizon, Pb isotope ratios (206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb) ratio generally decrease with soil age. In order to overcome possible effects from parent material heterogeneity, the amount of radiogenic Pb as compared to the whole-soil composition was calculated and this was found to decrease systematically with soil age. 相似文献
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The daughter to parent (234U/238U) activity ratio in natural waters is often out of secular radioactive equilibrium. The major reason for this disequilibrium is related to the energetic α-decay of 238U and differential release of 234U relative to 238U. This disequilibrium originates from (1) preferential release of more loosely bound 234U from damaged mineral lattice sites or; (2) direct recoil of 234Th into surrounding media from near mineral surface boundaries, however, it is unclear which of the two mechanisms is most important in nature. To better quantify the effects of preferential release of 234U, two continuous laboratory granite leaching experiments conducted over 1100 h were performed. The leachates were characterized by declining U concentrations with time and (234U/238U) initially greater than unity (up to 1.15), which changed to below unity during leaching (∼0.95). The early elevated (234U/238U) suggests that additional 234U is released into solution by preferential release of 234U from mineral phases. However, the excess 234U constitutes a finite pool of easy leachable 234U and the (234U/238U) values become lower than unity when this pool is used up. A model based on first-order kinetics, dissolution rates and preferential release of 234U from damaged lattice sites was developed and is able to quantitatively predict the observed pattern of (234U/238U) values and U concentrations for the two granite leaching experiments. Extending the modeling to longer time scales more comparable to natural systems shows that the production of waters with high (234U/238U) ratios can be achieved in two distinct regimes (1) slow weathering where the rate of directly recoiled 234U near mineral surfaces into waters is high; (2) fast weathering where the role of incipient chemical weathering and preferential release of loosely bound 234U are important. The model is able to explain apparent opposite correlations between physical erosion rates and (234U/238U) in waters and it provides a new framework that will be useful for examining weathering regimes, their timescales and their coupling with physical erosion. 相似文献
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