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1.
The clinopyroxenes and garnets from garnet lherzolite nodules in kimberlites were analyzed for the major and trace elements (Sc, Ti, V, Cr, Mn, Co, Sr, and Zr) with the secondary ion mass spectrometry (SIMS) techniques using an ion-microprobe. The concentration ranges for clinopyroxenes are: 12–90 ppm Sc, 60–2540 ppm Ti, 110–350 ppm V, 2400 ppm-1.68% Cr, 470–1100 ppm Mn, 18–70 ppm Co, 85–710 ppm Sr, and 6.3–120 ppm Zr. Those for garnets are: 71–180 ppm Sc, 140–6200 ppm Ti, 220–450 ppm V, 1.05–6.24% Cr, 1600–5220 ppm Mn, 33–92 ppm Co, and 66–250 ppm Zr.These data were used to assess a possible use of distribution of transition elements between clinopyroxene and garnet for geothermometry/geobarometry. The distribution coefficients of V and Mn show good correlations with (Ca/Ca+Mg+Fe)CPX, suggesting their potential usefulness.The abundances of these elements in minerals (and estimated whole-rocks) suggest that garnet lherzolite nodules in kimberlites can be classified into three groups. It is suggested that one of the groups (Group I) could be close to the pristine mantle on the basis of Ti and Zr abundances as well as REE systematics. Arguments on Ti/Zr ratios among different nodule types suggest that abundant granular garnet lherzolites could be cumulates crystallized from a residual liquid after ilmenite was extracted.IPG Contribution No. 281  相似文献   

2.
High indoor radon in approximately 30 percent of private dwellings in the Albuquerque, New Mexico area has been reported previously. The present study explains the areas of high indoor radon as a function of different soil and/or bedrock in the area. Soils were sampled during summer and winter periods using alpha track radon detectors. The values range from 40 to 890 pCi/I air at a depth of 38 cm. The gross mean average is 360 pCi/I for the area for summer readings and 200 pCi/I for winter readings; both values are well over the average U.S. soil radon values of approximately 100 pCi/I. Analyses of soil uranium show a range in values of 1–6 ppm, with a mean of 3.1 ppm. Thorium values range from 3.3 to 28.8 ppm, and Th/U ratios range from 2.9 to 4.6.These values for U, Th, and Th/U suggest that soil U and Th are close to the values reported for the Sandia granite, the source of most of the pediment on which Albuquerque is built. Soil infiltration rates range from ~6 × 10–4 to 4.5 × 10–3 cm/sec for the samples, and soil moisture content ranges from 1.4 to 7.2 percent. A fair correlation of summer soil radon with infiltration rate is noted. Correlation of soil radon with moisture content and/or with percent silt, silt + clay, clay size fraction material is not established by this study. Soil radon values do correlate with regions in the Albuquerque area where high indoor radon is common. A better correlation of high indoor radon values with soils developed immediately over bedrock is observed. Furthermore, all values of average soil and indoor radon increase significantly with proximity of the stations to the Sandia Mountains. Soil uranium also shows this trend. The data argue that regions of potentially high radon can thus be identified.  相似文献   

3.
Proton microprobe for chemical dating of monazite   总被引：1，自引：1，他引：0  
Although quantitative chemical analysis by proton microprobe has become an established technique, it has been rarely applied to problems in the earth sciences. The method, having lower detection limit (better than 10 ppm for U, Th and Pb) and higher spatial resolution than electron microprobe (typically 1 μm vs 3 μm), can be successfully used in geology. Here, we present a procedure for the chemical dating of monazite, (REE)PO4, by proton microprobe. The procedure is compared with electron probe microanalysis technique (EPMA).  相似文献   

4.
The Nickel Plate deposit, in which gold occurs as <25 μm blebs associated with arsenopyrite in garnet-pyroxene skarns, is in the subalpine zone near the southern limit of the Thompson Plateau. During the last glaciation the Cordilleran ice sheet moved south-southwest across the deposit and deposited a stony basal till. A dispersion train with anomalous concentrations of gold in tills and soils now extends 2 km down ice from the deposit.Gold contents of samples of humus (LFH horizon) and the −212 μm fraction of mineral soils (A, B and C horizons) was determined by instrumental neutron activation and fire assay-atomic absorption, respectively. Selected samples were examined in detail to determine distribution of gold between different size and density fractions.Despite erratic variability, Au contents of the −212 μm fraction generally decrease from 200–400 ppb close to the mine site to <50 ppb at distal sites. At most sites there is also a twofold increase of gold values down the soil profile. Within samples concentrations of Au in the −420 + 212 μm, −212 + 106 μm, −106 + 53 μm and −53 μm fractions are usually roughly constant. However, because of its abundance, the −53 μm fraction contains more than 70% of the gold. Amenability of gold in this fraction to cyanidation suggests that it is largely free gold. For size fractions > 53 μm the contribution of the heavy mineral (SG > 3.3) fraction to total gold content increases with decreasing grain size.Distribution of gold between size and density fractions is consistent with its release from the bedrock or pre-glacial regolith by glacial abrasion. The bulk of the gold was incorporated into the fine fractions of the till at or close to the source. However, differences between down ice dilution ratios for gold in different heavy mineral size fractions suggest that comminution of host minerals continued to transfer gold to the finer size fractions during glacial transport.For exploration purposes, B and C horizon samples provide the best anomaly contrast. Estimates of the abundance of gold particles in different size fractions indicate that the nugget effect, which causes erratic gold values in the −212 μm fraction, can be avoided by analysis of 30 g of −53 μm material.  相似文献   

5.
Regional-scale variations in soil geochemistry were investigated with special reference to differences among soil groups and lithology in an area of 9,699 km2 in Medak district, Andhra Pradesh, India. The concentrations of 29 elements (major: Si, Al, Fe, Mn, Mg, Ca, Na, K, Ti, P and trace: As, Ba, Cd, Co, Cr, Cu, F, Mo, Ni, Pb, Rb, Se, Sr, Th, U, V, Y, Zn, Zr) in 878 soil samples collected (557-topsoil, 321-subsoil) at a sampling density of 1 site/17 km2 from 557 sites representative of all the soil types present in studied area were determined, and their elemental composition are discussed. The baseline levels of these elements in soils are determined over different lithological units for the identification of anomalous values relative to these. For the first time, geochemical maps for Medak district are prepared on 1:50,000 scale and the lithogeochemical database generated provides information on the lateral and vertical distribution of elements in soil. The spatial variations in the distribution of elements reflect underlying geologic characteristics. Box-plots reveal that the concentration of most of the elements in soils were not strongly dependent on the soil group but the soil-geochemistry abruptly changes with the change in the soil parent materials indicating that the distribution of elements is mostly influenced by the bedrock lithology and other natural processes acting on them. For instance, the concentrations of Co, Cu, Fe, Mn, Ti, V and Zn are high in soils developed on basaltic terrain while the soils developed on granitic and gneissic terrain exhibit high elemental concentrations of K, Pb, Rb, Si, Th and Y. Alfisols had relatively high contents of elements while entisols had lower concentrations of most of the elements. The database can be used in the chemical characterisation of different geological units as well as applications in various environmental and agricultural fields. The results indicate that regional geology is an important determinant of soil geochemical baselines for soil pollution assessment and further emphasizes the importance of determining background levels locally. The defined baselines can be used to establish background values for future soil surveys.  相似文献   

6.
The interaction of organic compounds with the mineral phase is considered as one stabilization mechanism for organic carbon (OC) in soils. The objective of this study is to assess the role of mineral surfaces for the long-term stabilization of OC in arable soils, with special emphasis on iron oxides. Soil samples were taken from two contrasting treatment types, i.e. fertilized plots and C-depleted plots, in long-term agroecosystem experiments. The soil organic carbon pool of the C-depleted plots is considered to show a lower contribution of labile compounds and consequently to be relatively enriched in refractory compounds compared with the fertilized counterparts. In fractions <6 μm, OC was studied in relation to total mineral surface area, surface area contributed by oxides and silicates, and the content and type of iron oxides (dithionite and oxalate extractable iron, Fed and Feo). In two sandy soils, OC contents were linearly related to total mineral surface area and the content of the two iron oxide fractions (Fed and Feo). The surface area developed by the silicates was low and thus the surface area contribution from oxides was dominant in fractions <6 μm. In contrast to the sandy soils, in a loamy soil OC was not correlated with surface area or the iron oxide content. However, the different soils agreed with respect to the behavior of C in density fractions: losses of OC occurred mainly from the light fraction (2 g cm−3), whereas C in the heavy fraction (>2 g cm−3) proved to be stable. For the sandy soils, mineral surface area appears to control the storage of OC in fine fractions. Given the dominant surface area contribution from oxides, OC storage here primarily depends on the oxides. The C-depleted plots in particular show that surface area controls the accumulation of refractory C. The interaction of organic compounds with the mineral phase, mainly with the surface of oxides, seems to be a major mechanism for the long-term stabilization of OC in these sandy soils. An interaction with minerals seems to be important for stabilizing OC also in the loamy soil, although this is not reflected by a proportional relation between OC and surface area across the fractions.  相似文献   

7.
This contribution is a short history of the Zambian copper flower, Becium homblei (recently renamed B. centraliafricanum that has attracted attention as a plant associated with Cu-rich soils. It has a peculiar discontinuous distribution in Central Africa which has been explained in terms of biotype depletion. A field investigation into the ecology of the species shows that it is able to tolerate soil Cu concentrations of up to 15,000 μg/g (ppm), and soil nickel concentrations of nearly 5000 μg/g. B. homblei is also found on areas where soil metals are in trace quantities, and where soil bases, particularly Ca, are low. In spite of its tolerance to a wide range of edaphic conditions, the distribution of the species is very restricted in Zimbabwe, and this is almost certainly due to severe interspecific competition with a closely related species, B. obovatum, which is common on soils not unusually enriched in heavy metals. Pioneering work on geobotanical prospecting by use of Becium homblei was carried out by the late G. Woodward and others in the 1950s and 1960s. This species was used successfully for geobotanical prospecting for Cu. This present report is a brief history of these pioneering studies  相似文献   

8.
Refractory compounds are responsible for the long-term sequestration of organic matter in soil. The aim of this study is to assess the storage of refractory compounds, i.e. compounds with long turnover times, across size separates in arable soils. The contents and distribution of organic carbon (OC) and nitrogen (N) in size fractions were examined for two contrasting treatment types from long-term agroecosystem experiments, i.e. C-depleted and fertilized plots. The soil organic carbon (SOC) pool of the C-depleted plots is considered to be relatively enriched in refractory compounds compared with the SOC in the fertilized counterparts. In two of the three long-term experiments, the relative retention of OC in separates <20 μm was considerably higher than in separates 2000–20 μm (OC contents in depleted plots compared with fertilized plots). Highest residual contents of OC were found in fractions <6 μm. In the third experiment, additionally to the very fine fractions, separates 250–20 μm retained a high proportion of OC. The behavior of N was analogous to that of OC: the highest relative residues in the depleted plots were found in fine separates. These results indicate that in the investigated arable soils, C and N compounds associated with fine separates are most stable. Refractory OC in arable soils may be largely stored in fine particle-size fractions.  相似文献   

9.
Concentrations of total and dissolved elements were determined in 35 water samples collected from rivers in Sardinia, a Mediterranean island in Italy. The overall composition did not change for waters sampled in both winter and summer (i.e., January at high-flow condition and June at low-flow condition), but the salinity and concentrations of the major ions increased in summer. Concentrations of elements such as Li, B, Mn, Rb, Sr, Mo, Ba and U were higher in summer with only small differences between total and dissolved (i.e., in the fraction <0.4 μm) concentrations. The fact that these elements are mostly dissolved during low flow periods appears to be related to the intensity of water–rock interaction processes that are enhanced when the contribution of rainwater to the rivers is low, that is during low-flow conditions. In contrast, the concentrations of Al and Fe were higher in winter during high flow with total concentrations significantly higher than dissolved concentrations, indicating that the total amount depends on the amount of suspended matter. In waters filtered through 0.015 μm pore-size filters, the concentrations of Al and Fe were much lower than in waters filtered through 0.4 μm pore-size filters, indicating that the dissolved fraction comprises very fine particles or colloids. Also, Co, Ni, Cu, Zn, Cd and Pb were generally higher in waters collected during the high-flow condition, with much lower concentrations in 0.015 μm pore-size filtered waters; this suggests aqueous transport via adsorption onto very fine particles. The rare earth elements (REE) and Th dissolved in the river waters display a wide range in concentrations (∑REE: 0.1–23 μg/L; Th: <0.005–0.58 μg/L). Higher REE and Th concentrations occurred at high flow. The positive correlation between ∑REE and Fe suggests that the REE are associated with very fine particles (>0.015 and <0.4 μm); the abundance of these particles in the river controls the partitioning of REE between solution and solid phases.Twenty percent of the water samples had dissolved Pb and total Hg concentrations that exceeded the Italian guidelines for drinking water (>10 μg/L Pb and >1 μg/L Hg). The highest concentrations of these heavy metals were observed at high-flow conditions and they were likely due to the weathering of mine wastes and to uncontrolled urban wastes discharged into the rivers.  相似文献   

10.
This paper discusses the mineralogy and geochemistry of the No. 6 Coal (Pennsylvanian) in the Junger Coalfield, Ordos Basin, China. The results show that the vitrinite reflectance (0.58%) is lowest and the proportions of inertinite and liptinite (37.4% and 7.1%, respectively) in the No. 6 Coal of the Junger Coalfield are highest among all of the Late Paleozoic coals in the Ordos Basin. The No. 6 Coal may be divided vertically into four sections based on their mineral compositions and elemental concentrations. A high boehmite content (mean 6.1%) was identified in the No. 6 Coal. The minerals associated with the boehmite in the coal include goyazite, rutile, zircon, and Pb-bearing minerals (galena, clausthalite, and selenio-galena). The boehmite is derived from weathered and oxidized bauxite in the weathered crust of the underlying Benxi Formation (Pennsylvanian). A high Pb-bearing mineral content of samples ZG6-2 and ZG6-3 is likely of hydrothermal origin. The No. 6 coal is enriched in Ga (44.8 μg/g), Se (8.2 μg/g), Sr (423 μg/g), Zr (234 μg/g), REEs (193.3 μg/g), Hg (0.35 μg/g), Pb (35.7 μg/g), and Th (17.8 μg/g). Gallium and Th in the No. 6 Coal mainly occur in boehmite, and the Pb-bearing selenide and sulfide minerals contribute not only to Se and Pb contents in the coal, but also probably to Hg content. A high Zr content is attributed to the presence of zircon, and Sr is related to goyazite. The REEs in the coal are supplied from the sediment-source region, and the REEs leached from the adjacent partings by groundwater.  相似文献   

11.
In order to reconstruct the past variations of the Southeast Asian monsoon intensity and estimate the sedimentary system reactivity to climatic changes in Southeast Asia over the last 450 kyr, mineralogical and sedimentological analyses have been performed on the terrigenous fraction of the South China Sea sediment. End-member modelling coupled with grain size data discriminates three end-members that determine the nature and intensity of the main sediment transport vectors. Low sea-level stands are characterized by sediment reworking that allows transportation of a coarse end-member (20–40 μm) to the deep-basin. By contrast, the other end-members (4–6 μm; 9–13 μm) are controlled by the shoreline position (sea level) and/or by changes of the rivers capacity transport (monsoon). Finally, aeolian input to the northern margin of the South China Sea can be considered negligible compared to the massive fluvial input and the reworking of the sediments.  相似文献   

12.
Lignin is preserved in the fine silt fraction of an arable Luvisol   总被引：1，自引：0，他引：1  
Knowledge about the fate of individual biomolecules during the decomposition process in soil is limited. We used the natural isotopic label introduced by 23 years of continuous maize cropping, together with compound specific 13C isotope analysis, to study lignin monomers in particle size fractions of a Luvisol. Isotope data indicated apparent decadal turnover times for lignin. A kinetic model suggests the existence of a fast and a slow decomposing lignin pool in the soil, reconciling a low stock-to-input ratio with decadal turnover times. We found new, maize-derived lignin primarily in the 63–2000 μm fraction, whereas old, C3-derived lignin from the pre-maize vegetation had accumulated mainly in the silt (2–20 μm) fraction. This distribution of lignin differed from that of total organic carbon, which was concentrated in the <2 μm fraction. Old, C3-derived carbon in all the soil fractions was depleted in lignin compared to new, maize-derived carbon. The observation that the 2–20 μm fraction was less depleted than the others indicates that lignin preservation is particle size specific, but the underlying mechanism controlling its preservation is not clear.  相似文献   

13.
In vitro bioaccessibility tests (IVBA) are inexpensive, physiologically-based extraction tests designed to estimate the bioaccessibility of elements along ingestion exposure pathways. Published IVBA protocols call for the testing to be done on the <250-μm fraction of soil, as these particles are most likely to adhere to the hands of children and be ingested. Most IVBA in the literature to date have been applied to soil samples from highly contaminated sites or to spiked samples, and relatively little work has been done to evaluate bioaccessibility of elements in a wide variety of uncontaminated ‘background’ soils.In 2004, the US Geological Survey and the Geological Survey of Canada sampled soils along north–south and east–west transects across the two countries to test and refine sampling and analytical protocols recommended for the planned soil geochemical survey of North America. Samples were collected at 220 sites selected randomly at approximately 40-km intervals. The focus of the investigation presented in this paper was twofold: (1) to begin to examine variations in bioaccessibility of As, Cd, Cr, Ni and Pb in a number of ‘background’ (i.e., unpolluted) soils from around North America and (2) to determine if there are significant differences that would preclude using the standard size fraction of <2 mm for extraction with a simulated gastric fluid as an expeditious and inexpensive bioaccessibility screening tool for the large numbers of future samples to be collected by this continental-scale project. A subset of 20 soil samples collected along the north–south transect at a depth of 0–5 cm was used for this study. Two separate size fractions (<2 mm and <250 μm) were extracted using a simulated human gastric fluid consisting of a solution of HCl and glycine adjusted to a pH of 1.5. In general, the leachate results for the <2-mm size fraction were not substantially different than those for the <250-μm size fraction for concentrations of As, Cd, Cr, Ni and Pb. Leachate concentrations for Cd, Ni and Pb appear to be controlled to some extent by the total concentration of the element in soil. Bioaccessibility of the elements in this study decreased in the order, Cd > Pb > Ni > As > Cr.  相似文献   

14.
Samples were collected near known gold mineralization from anomalous and background soils developed on glacial till in British Columbia and Ontario, and in residual soils in Nevada, Utah and the Yukon Territory. After wet sieving to five size fractions finer than 2000 mm, and separation of heavy minerals (S.G. > 3.3) for the − 212 + 106 μm and − 106 + 53 μm fractions, gold concentrations in each fraction were determined by fire assay-atomic absorption.In all cases more than 60% of the gold resides in the − 53 μm fraction. For the residual soils most of the remaining gold is associated with the light mineral fractions and only a negligible proportion resides in the heavy minerals. Estimates of the numbers of gold particles and subsampling variability suggest that gold, in both heavy and light mineral fractions, is largely present as inclusions of fine gold. For exploration purposes, optimum sample representativity would be obtained with the − 53 μm fraction. However, because this fraction is a major component of the soils, use of a coarser size fraction (e.g., − 212 μm) will only slightly reduce sample representativity. Also, because most of the gold is associated with the − 53 μm and light mineral fractions, use of heavy mineral concentrates offers no significant advantage and in some cases would result in anomalous conditions being overlooked.  相似文献   

15.
Blind ore bodies more than 200 m below the surface and ore-bearing faults are clearly indicated by soil-air Hg anomalies through an overburden 20–40 m thick over the Fankou Pb---Zn deposit. The background of soil-air mercury in this area is 50 ng m−3 and the highest value encountered is 2000 ng m−3. The maximum anomaly to background contrast is 40. The width of anomalies higher than 500 ng m−3 can be greater than 600 m. The background Hg in soils of the area is 0.06 ppm and increases to 0.15 ppm where there are soil-air anomalies. The contrast of Hg in soils is only 2.5. Mercury in the unconsolidated overburden is in the form of free gas and is absorbed onto soil colloids such as clay minerals and Fe-Mn oxides. The primary sulphides contain 14–320 ppm Hg where Hg is incorporated isomorphically in sulphide minerals, which is confirmed by microprobe analysis.Based on a systematic analysis of the materials from surface and underground workings for the mode of occurrence of Hg, the authors suggest that the Hg-vapour anomalies in soil-air are the oxidation products of the ore.  相似文献   

16.
The chemical status of ∼40 major and trace elements (TE) and organic carbon (OC) in pristine boreal rivers draining the basaltic plateau of Central Siberia (Putorana) and interstitial solutions of permafrost soils was investigated. Water samples were filtered in the field through progressively decreasing pore size (5 μm → 0.22 μm → 0.025 μm → 10 kDa → 1 kDa) using cascade frontal filtration technique. Most rivers and soil porewaters exhibit 2-5 times higher than the world average concentration of dissolved (i.e., <0.22 μm) iron (0.03-0.4 mg/L), aluminum (0.03-0.4 mg/L), OC (10-20 mg/L) and various trace elements that are usually considered as immobile in weathering processes (Ti, Zr, Ga, Y, REEs). Ultrafiltration revealed strong relationships between concentration of TE and that of colloidal Fe and Al. According to their partition during filtration and association with colloids, two groups of elements can be distinguished: (i) those weakly dependent on ultrafiltration and that are likely to be present as truly dissolved inorganic species (Li, Na, K, Si, Mn, Mo, Rb, Cs, As, Sb) or, partially (20-30%) associated with small size Fe- and Al-colloids (Ca, Mg, Sr, Ba) and to small (<1-10 kDa) organic complexes (Co, Ni, Cu, Zn), and (ii) elements strongly associated with colloidal iron and aluminum in all ultrafiltrates largely present in 1-100 kDa fraction (Ga, Y, REEs, Pb, V, Cr, Ti, Ge, Zr, Th, U). TE concentrations and partition coefficients did not show any detectable variations between different colloidal fractions for soil porewaters, suprapermafrost flow and surface streams. TE concentration measurements in river suspended particles demonstrated significant contribution (i.e., ?30%) of conventionally dissolved (<0.22 μm) forms for usually “immobile” elements such as divalent transition metals, Cd, Pb, V, Sn, Y, REEs, Zr, Hf, Th. The Al-normalized accumulation coefficients of TE in vegetation litter compared to basalts achieve 10-100 for B, Mn, Zn, As, Sr, Sn, Sb, and the larch litter degradation is able to provide the major contribution to the annual dissolved flux of most trace elements. It is hypothesized that the decomposition of plant litter in the topsoil horizon leads to Fe(III)-, Al-organic colloids formation and serves as an important source of elements in downward percolating fluids.  相似文献   

17.
An orientation survey was conducted over the Quartz Mountain, Oregon, hot-spring type disseminated gold deposit to address three questions critical to successful exploration of the area: What is the relationship between bedrock geology and the trace-element content of trees and soils; do these relationships change seasonally; are these relationships similar in the two tree species which discontinuously blanket the area?Twig, needle and wood samples were collected four times during the year from both ponderosa pine (Pinus ponderosa) and white fir (Abies concolor). Soils were collected once. All samples were analyzed for Au and As and the wood samples were analyzed also for Sb.Arsenic was the best pathfinder element, having little analytical, spatial, or seasonal variation in the twig and needle samples. Anomalous levels were 150 μg/g (ppm) As in pine and 30 μg/g in fir. Gold showed analytical variation of 20–30%, sample duplicate variation up to 90%, spatial changes, and seasonal variation ranging from winter-summer background [10–20 ng/g (ppb) Au] to anomalies of 300–400 ng/g (ppb) Au in pine and 100 μg/g (ppb) Au in fir in the spring and fall. Antimony could not be completely evaluated as a pathfinder element because it was only determined in wood samples.Needles and twigs from both species proved to be viable sample media for exploration of the area. Wood was not a suitable medium because of low, erratic values, perhaps due in part to analytical technique. Needles had 2 to 20 times higher As concentrations than did twigs. Twigs had a slightly higher Au content [25 ng/g (ppb)] than did needles. The pine samples were higher in both elements than were the fir samples. The data, normalized by species, could be treated as one homogeneous data base.The soil Au and As data outlined the mineralization clearly with a central Au anomaly [100 ng/g (ppb) and greater] surrounded by As anomalies [100 μg/g (ppm) and greater] over a distance of 594 m. Neither spring nor fall tree Au anomalies were coincident with the soil Au anomaly. Consistent throughout the year, tree As anomalies coincided with the soil As anomalies, but covered a smaller area. Both the Au and As anomalies in trees appeared to be related to bedrock contact zones rather than to the soil the trees were growing in.  相似文献   

18.
Five Devonian plutons (West Charleston, Echo Pond, Nulhegan, Derby, and Willoughby) that constitute the Northeast Kingdom batholith in Vermont show wide ranges in elemental abundances and ratios consistent with major crustal contributions during their evolution. The batholith consists of metaluminous quartz gabbro, diorite and quartz monzodiorite, peraluminous granodiorite and granite, and strongly peraluminous leucogranite. Contents of major elements vary systematically with increasingSiO<2 (48 to 77 wt.%). The batholith has calc-alkaline features, for example a Peacock index of 57, and values for K<2O/Na2O (<1), K/Rb (60–350), Zr/Hf (30–50), Nb/Ta (2–22), Hf/Ta (up to 10), and Rb/Zr (<2) in the range of plutonic rocks found in continental magmatic ares. Wide diversity and high values of minor- and trace-element ratios, including Th/Ta (0.5–22), Th/Yb (0–27), Ba/La (0–80), etc., are attributed to intracrustal contributions. Chondrite-normalized REE patterns of metaluminous and relatively mafic intrusives have slightly negative slopes (La/Ybcn<10) and negative Eu anomalies are small orabsent. The metaluminous to peraluminous inter-mediate plutons are relatively enriched in the light REE (La/Ybcn>40) and have small negative Eu anomalies. The strongly peraluminous Willoughby leucogranite has unique trace-element abundances and ratios relative to the rest of the batholith, including low contents of Hf, Zr, Sr, and Ba, low values of K/Rb (80–164), Th/Ta (<9), Rb/Cs (7–40), K/Cs (0.1–0.5), Ce/Pb (0.5–4), high values of Rb/Sr (1–18) low to moderate REE contents and light-REE enriched patterns (with small negative Eu anomalies). Flat REE patterns (with large negative Eu anomalies) are found in a small, hydrothermally-altered area characterized by high abundances of Sn (up to 26 ppm), Rb (up to 670 ppm), Li (up to 310 ppm), Ta (up to 13.1 ppm), and U (up to 10 ppm). There is no single mixing trend, fractional crystallization assemblage, or assimilationscheme that accounts for all trace elementvariations from quartz gabbro to granite in the Northeast Kingdom batholith. The plutons originated by mixing mantle-derived components and crustal melts generated at different levels in the heterogeneous lithosphere in a continental collisional environment. Hybrid rocks in the batholith evolved by fractional crystallization and assimilation of country rocks (<50% by mass), and some of the leucogranitic rocks were subsequently disturbed by a mild hydrothermal event that resulted in the deposition of small amounts of sulfide minerals.  相似文献   

19.
In Adola, southern Ethiopia, mafic and ultramafic igneous rocks occur in narrow, 4–10 km wide, north-south-trending belts bounded by high-grade gneisses and migmatites. The mafic/ultramafic rocks are complexly deformed and metamorphosed in greenschist to lower amphibolite facies and are thought to be tectonically dismembered parts of an ophiolite complex. Preliminary geochemical and geochronological data highlight that the high-grade rocks in southern Ethiopia and northern Kenya include a significant portion of juvenile rocks that were accreted at the same time as ophiolitic rocks at 885-765 Ma. This is also the time of widespread oceanic magmatism and closure in the Arabian-Nubian Shield to the north.The Adola mafic rocks were previously described as island arc tholeiites and mid-ocean ridge basalts (MORB). New chemical analyses on the Megado belt rocks reveal the presence of boninites and related dacites interspersed with tholeiitic rocks. The Adola boninites are similar to the Cambrian boninites in western Tasmania in having relatively low Zr/Sm (≤32). Boninites with similarly low ratios have not been reported from elsewhere.The Adola tholeiites have high Ti/Zr (150–300). Mixing between tholeiite and boninite magmas may have resulted in elevated Ti/Zr (80–126) in some Adola boninites. Otherwise, Ti/Zr in the latter is low (20–40). Low Ti/Zr is characteristic of Tertiary boninites in the west Pacific. The fact that both Ti/Eu and Zr/Sm increase from the Adola and Tasmania type to the Tertiary boninites at constant Ti/Zr suggests that Ti might be an element that is also metasomatically added to the source of boninites and raises doubts about the role of amphibole in boninite petrogenesis.  相似文献   

20.
Several radioactive quartz-pebble conglomerate (QPC) occurrences at the western margin of Archaean Bonai granite and overlying Iron Ore Group (IOG) rocks have recently been located over a total strike length of 8–10 km intermittently in a NE-SW to E-W trend with steep dips due north-west to north in parts of Sundargarh district of Orissa. The QPC samples have analysed up to 0.039% U3O8 and 0.035% ThO2 with high concentration of Y (74 to 518 ppm), La(<100 to 880 ppm), Cr ( 126 to 633 ppm), Zr (137 to 1250 ppm) and Pb (31 to 581 ppm). Cellulose Nitrate (CN) film studies of few QPC samples indicated adsorbed uranium over goethite and infiltrated ferruginous material (limonite), secondary uranium as encrustation and fracture filling and discrete sub-rounded grains of monazite, zircon, allanite and rare xenotime in the matrix of QPC as radioactive phases. Higher content of Th over U, elevated concentration of Y and La in QPC eliminates the possibility of its low temperature product by epigenetic processes. Poor correlation of U with elements like Pb, Y, Zr, La and Cr can be explained due to surficial leaching of uranium from QPC after its deposition as reflected by adsorbed U over iron-oxides and low U/Th ratio in QPC in the area.  相似文献   

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