首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 453 毫秒
1.
The aims of the present study were to investigate the effects of mariculture activities on inorganic mercury (Hg(2+)) adsorption/desorption on sediments and the distributions of newly adsorbed Hg(2+) on different chemical fractionations. The adsorption amount and binding energy of Hg(2+) on mariculture sediment (MS) were significantly higher (p<0.05) than reference sediment (RS). This may be explained by the strong complexation role that exists between Hg(2+) and organic matter (OM), which derived from unconsumed fish feed and fish metabolites. The reducible Hg(2+) in MS was significantly lower (p<0.01) than RS, which may have been caused by the decreasing amount of iron and manganese hydroxide in MS, lead to the decrease of Hg(2+) bound to them. On the contrary, the residual Hg(2+) was significantly higher (p<0.01) in MS than RS, which suggests that newly adsorbed Hg(2+) was more stable in MS than RS.  相似文献   

2.
Clay fractions in the non-calcareous surface sediments from the eastern Pacific were analyzed for clay minerals, REE and 143Nd/144Nd. Montmorillonite/illite ratio (M/I ratio), total REE contents ((REE), LREE/HREE ratio and cerium anomaly (бCe) may effectively indicate the genesis of clay minerals. Clay fractions with M/I ratio >1, бCe (0.85, (REE (400 μg/g, LREE/HREE ratio (4, and REE patterns similar to those of pelagic sediments are terrigenous and autogenetic mixed clay fractions and contain more autogenetic montmorillonite. Clay fractions with M/I ratio <1, бCe=0.86 to 1.5, ΣREE=200 to 350 μg/g, LREE/HREE ratio (6 and REE distribution patterns similar to that of China loess are identified as terrigenous clay fraction. The 143Nd/144Nd ratios or (э)Nd values of clay fractions inherit the features of terrigenous sources of clay minerals. Clay fractions are divided into 4 types according to (э)Nd values. Terrigenous clay minerals of type I with the (э)Nd values of -8 to -6 originate mainly from North American fluvial deposits. Those of type II with the (э)Nd values of -9 to -7 are mainly from the East Asia and North American fluvial deposits. Those of type III with (э)Nd values of -6 to -3 could come from the central and eastern Pacific volcanic islands. Those of type IV with (э)Nd values of -13 to -12 may be from East Asia eolian. The terrigenous and autogenetic mixed clay fractions show patchy distributions, indicating that there are volcanic or hot-spot activities in the eastern Pacific plate, while the terrigenous clay fractions cover a large part of the study area, proving that the terrigenous clay minerals are dominant in the eastern Pacific.  相似文献   

3.
A thick sequence of alkaline intrusions and volcanic rocks underlies a Quaternary caldera on Lihir Island. The sequence is host to a still-active subaerial hydrothermal system and associated epithermal gold mineralization. Chondrite-normalized (La/Lu)cn and (La/Sm)cn ratios progressively increase up the alteration sequence from the potassic alteration zone, to the argillic zone to the advanced argillic zone. (Tb/Lu)cn ratios only significantly increase in argillic and advanced argillic assemblages. Surface oxide alteration lithologies and acid sulphate water precipitates possess distinctly lower (La/Lu)cn and (Tb/Lu)cn ratios than the underlying subsurface alteration units. The changes in the REE, LREE and HREE fractionation trends from subsurface to surface alteration zones reflect the transition from a magmatic-hydrothermal, neutral chloride fluid regime at depth to acid sulphate meteoric waters in the upper portion of the alteration profile.Boiling of the LREE-Eu-enriched magmatic fluids occurred at a depth of at least 750 m. It is proposed that pronounced differential flow rates of the vapour and liquid phases and solution chemistry changes approximately above 300–350 m caused the incorporation of LREE and Eu into anhydrite-calcite veins and the deposition of LREE and HREE into wallrocks of upper parts of the potassic alteration unit. Condensation of the vapour phases into meteoric waters gave rise to low-temperature acid fluids that deposited large amounts of LREE within argillic and advanced argillic alteration units. This was also accompanied by HREE mobility due to large fluid volumes, acid fluid conditions and abundant sulphate complexes within the solutions. The HREE were either lost from the hydrothermal system or deposited in oxide assemblages and acid sulphate water precipitates.  相似文献   

4.
Mineral and whole-rock REE abundances in garnet lherzolite and megacrystalline nodules from The Thumb display broad correlations with major element compositions. Lherzolites with > 12 modal % clinopyroxene plus garnet (“high-CaAl lherzolites”) have relatively flat chondrite-normalized whole-rock REE patterns. Lherzolites poor in clinopyroxene and garnet (“low-CaAl lherzolites”) have lower HREE in clinopyroxenes and garnets and higher whole-rock LREE/HREE. It is concluded that the low-CaAl lherzolites may have undergone LREE metasomatism after depletion of the major element compositions by partial melting and that much of the garnet now present was originally dissolved in aluminous orthopyroxene. The high-CaAl lherzolites may be interpreted either as primordial mantle samples or as products of equilibration with very LREE-enriched liquids. The “megacrystalline” nodules are medium- to ultracoarse-grained intergrowths and megacrysts with mineral compositions similar to discrete nodule suites in kimberlites. The REE abundances of the megacrystalline minerals are consistent with an origin as cumulates from magma with extremely fractionated REE, similar to minette or kimberlite.The patterns of correlation of REE and major elements in this inclusion suite are similar to the patterns observed in the garnet lherzolite and discrete nodule suites of southern African kimberlites. Both of the subcontinental mantle provinces represented by these suites contain three distinct petrogenetic components: refractory garnet lherzolite enriched in LREE and depleted in HREE, fertile garnet lherzolite with generally chondritic REE abundances, and a suite of ultracoarse minerals precipitated from magma with extremely fractionated REE generally similar to the host magmas.  相似文献   

5.
Clay fractions in the non-calcareous surface sediments from the eastern Pacific were analyzed for clay minerals, REE and 143Nd/144Nd. Montmorillonite/illite ratio (M/I ratio), total REE contents (ΣREE), LREE/HREE ratio and cerium anomaly (δCe) may effectively indicate the genesis of clay minerals. Clay fractions with M/I ratio <1, δCe >0.85, ΣREE <400 μg/g, LREE/HREE ratio ≈4, and REE patterns similar to those of pelagic sediments are terrigenous and autogenetic mixed clay fractions and contain more autogenetic montmorillonite. Clay fractions with M/I ratio >1, δCe=0.86 to 1.5, ΣREE=200 to 350 μg/g, LREE/HREE ratio ≈6 and REE distribution patterns similar to that of China loess are identified as terrigenous clay fraction. The 143Nd/144Nd ratios or ɛNd values of clay fractions inherit the features of terrigenous sources of clay minerals. Clay fractions are divided into 4 types according to ɛNd values. Terrigenous clay minerals of type I with the ɛNd values of ™8 to ™6 originate mainly from North American fluvial deposits. Those of type II with the ε Nd values of ™9 to ™7 are mainly from the East Asia and North American fluvial deposits. Those of type III with ε Nd values of ™6 to ™3 could come from the central and eastern Pacific volcanic islands. Those of type IV with ε Nd values of ™13 to ™12 may be from East Asia eolian. The terrigenous and autogenetic mixed clay fractions show patchy distributions, indicating that there are volcanic or hot-spot activities in the eastern Pacific plate, while the terrigenous clay fractions cover a large part of the study area, proving that the terrigenous clay minerals are dominant in the eastern Pacific.  相似文献   

6.
The distribution and anomalies of rare earth elements(REEs) of granitic regolith were studied in Inner Mongolia and Hainan Island, China. One profile showed slight REE enrichment of an upper layer and no obvious light REE/heavy REE(LREE/HREE) fractionation(La_N/Yb_N of 0.9). The second profile was significantly enriched in REEs and enriched in LREEs in the upper portion(La_N/Yb_N1.8). Eu, Ce, and Gd anomalies of the two profiles are different. Slightly negative Eu, Ce, and Gd anomalies in NMG-3-1 indicate slow dissolution of primary minerals and little secondary products; in contrast, a positive Eu anomaly in HN-2 suggests the vegetation cycle may contribute to soil. The Ce anomaly of HN-2 reflects oxidation of Ce and coprecipitation by Fe-and Mn-oxides and organic matter. Correlation between Ce and Gd anomalies in HN-2 suggests Ce and Gd are both influenced by redoxreduction.  相似文献   

7.
Based on the concentration and distribution pattern analysis of the rare earth elements (REEs) at the Shell Bar section from Qaidam Basin, we studied the geochemical fractionations of REE in paleolake deposits and their paleo-environmental significance. Our results show that the REE concentration in AS (acid soluble) and AR (acid residual) fractions are 20.9 μg/g and 95.4 μg/g (except element Y) individually, showing a strong REE differentiation between AS and AR fractions. However, the two types of fractions (AS & AR) have similar REE distribution patterns, which are slightly rich in light earth rare elements (LREEs), with slightly right-tilting and negative Eu anomaly. The LREE of AR is richer than that of AS. There were no significant correlations between the REE in AS, AR and other proxies. It indicated that the lacustrine deposition had different material sources and experienced varying geochemical procedures. Correlation analysis between the REE and the content of fine grain-size (<4 μm) of the sediments, Rb/Sr ratio and Mn concentration showed high correlation coefficients. Our results demonstrated that the REE in acid soluble and residual fractions bear different environmental significances, which are strongly dependent on local environment. The REE of acid soluble fraction is closely related to the paleoclimatic changes in the lake catchment and the evolutionary processes of lake itself. Our results suggest that δCe and (La/Yb)n could be used as proxies of the reduction-oxidation conditions and furthermore the temperature change and the lake level fluctuations. Using these proxies, we reconstructed the paleoclimate and water level fluctuation history during the high lake level period lasting between 43.5 and 22.4 cal. ka BP.  相似文献   

8.
Sc, Y, Th, Cu and rare earth elements (REE) concentrations have been analyzed in 14 samples of surface sediments and in two gravity cores by means of ICP-MS. Mean concentrations of Sc, Y and Th in surface sediments are 6.23, 4.76 and 16.30 ppm, respectively, lower than those present in the Upper Continental Crust (UCC). Cu concentration in these sediments is very high, 1466 ppm, and is caused by inputs from the Odiel and Tinto rivers, affected by acid mine drainage. SigmaREE mean concentration is 106.8 ppm, lower than that observed in other rivers and estuaries. In the cores, Sc, Y and Th concentrations show a significant increase in the intermediate levels, between 10 and 40 cm depth. The same pattern exists with Cu, where concentrations of 4440 ppm can be reached. Vertical evolution patterns for Sc, Y, Cu and heavy REE (HREE) are similar, and contrary to those shown by Th, light REE (LREE) and middle REE (MREE). Plots of North American Shale Composite (NASC)-normalized REE data of surface sediments show a slight depletion in REE concentrations. Most samples present with middle REE enrichment relative to light REE and heavy REE. Conversely, samples of the intermediate levels of the cores show significant enrichment of REE relative to NASC and high values in the (La/Gd)NASC and (La/Yb)NASC ratios. These anomalies in the fractionation patterns caused by enrichments in LREE and MREE concentrations is related to the presence of high concentrations of Th. They were generated by effluents from fertilizer factories between 1968 and 1998 which used phosphorite as source material.  相似文献   

9.
C. K. Jain  I. Ali 《水文研究》2000,14(2):261-270
The effects of solution pH, sediment dose, contact time, and particle size on the adsorption of cadmium ions on bed sediments have been studied for a highly polluted river in western Uttar Pradesh, India. The role of the coarser sediment and the clay and silt fractions has been examined. The optimum contact time needed to reach equilibrium is of the order of 30 and 60 min for 0–75 μm and 210–250 μm sediment size, respectively. The extent of cadmium adsorption increases with increasing pH and adsorbent doses and decreases with adsorbent particle size. The important geochemical phases, iron and manganese oxide, provide the active support material for the adsorption of cadmium. The competitive experiments conducted in the presence of lead and zinc ions indicate that both the ions suppress the ability of cadmium to adsorb on to sediments. The Langmuir and Freundlich adsorption models were used to determine the mechanistic parameters associated with the adsorption process. Copyright © 2000 John Wiley & Sons, Ltd.  相似文献   

10.
This work reports a study on the rare-earth element (REE) behaviour in the high-sulfidation-type superficial alteration and in the phyllic and propylitic alteration in the subsurface of the island of Vulcano. The results of this study demonstrate notable differences in the REE behaviour in the different alteration facies. In silicic alteration, all REE are equally strongly depleted; in advanced argillic alteration, LREE are quite immobile whereas HREE are strongly depleted; in intermediate argillic, phyllic and propylitic alteration, REE patterns are almost unchanged compared with their fresh rock equivalents. These features indicate that the behaviour of REE in hydrothermal alteration facies at La Fossa is mainly controlled by pH, availability of complexing ions in the fluid (mainly SO42− and, in the silicic facies, F−) and the presence of secondary minerals able to host REE in their structures. The origin of the acid fluids is related to the hypogenic introduction of prevalently magmatic acid gases produced by the degassing of the shallow magmatic system of La Fossa volcano. In the active high-temperature fumarolic field of La Fossa, REE behaviour illustrates the transition from a dry vapor system, corresponding to the high-temperature fumaroles, to a wet condensing system in the surrounding area. The results of this research, carried out on an active high-sulfidation system, provide a useful tool for the study of high-sulfidation epithermal ore deposits and particularly help to understand the alteration processes during the main stage of hypogene wall rock alteration.  相似文献   

11.
Hroaki  Ishiga  Kotaro  Ishida  Kaori  Dozen Makoto  Musashino 《Island Arc》1996,5(2):180-180
Abstract Geochemical characteristics, mainly of major and trace elements and REE (rare earth elements) of bedded chert and shale/mudstone sequences, across the Permian/Triassic boundary in southwest Japan are examined. The boundary is characterized by the disappearance of bedded cherts, and the interval between the Upper Permian cherts and Lower Triassic (probably Smithian) cherts comprises siliceous shales and organic black mudstones. Bedded cherts are characterized by a gradual depletion of chemical elements from Middle to Upper Permian. However, overlying siliceous shales exhibit a clear enrichment in some elements, especially alkaline metals (such as K, Rb and Cs) and Ti, Th, Y, P2O5, and REE in comparison with elements of the PAAS (post Archean Australian shales). This indicates that average components of the upper continental crust were transported in the boundary interval, possibly caused by volcanic activity. Ce-negative shifting in NASC (North American Shales Composite)-normalized REE patterns is characteristic of this interval, and could be related to the deposition of siliceous rocks in Ce-depleted seawater. This was probably caused by an invasion of water mass with a Ce-negative anomaly into the previously existing water mass of the Paleo-Tethys. Weak negative Eu-anomalies in this interval are suggestive of plagioclase fractionation caused by acid volcanisms and the LREE/HREE ratios in the interval show a slightly light-REE enrichment. Organic black mudstones are characteristically intercalated in the interval. These rocks are usually regarded as a product of oceanic deterioration, but in pelagic conditions, organic materials were formed by high primary production that resulted from the active upwelling of ocean floor water currents with rich nutrients. This may have been caused by the inferred mixing of water masses of the Paleo-Tethys and of the Panthalassa in Early Triassic time which was regarded as an event synchronous with an increase in volcanic activity on highly matured island arcs and/or continents.  相似文献   

12.
This study focuses on the trace and rare earth elements(REE) geochemistry of the Nkporo and Ekenkpon Shales of the Calabar Flank.The main aim is to infer their depositional environment and the degree of their metal enrichment.The shale samples were analyzed using inductively coupled plasma mass spectrometry.The results indicated that the mean concentrations of K,Na,and Fe in Nkporo and Ekenkpon Shales are 1.45,0.4,and 4.17 wt%,and 1.11,0.44,and 5.42 wt%;respectively.The Nkporo Shale is enriched with the following trace elements;PMn Sr Ba Zn Ce Rb Zr VCr Ni and depleted in the following trace elements;Ta GeSb Bi Cd Ag Te In Hg.While the Ekenkpon Shale is enriched with the following trace elements;P Mn Ba Sr VCe Zr Rb Cr Zn Ni and depleted in;Sb Ge Bi Ag Ce Te InHg.The concentration of redox-sensitive elements such as V,Ni,Mo,U,Cu,Cr,Re,Cd,Sb,Ti,Mn,and their ratio V/Mo and U/Mo in the black and grey shale samples show different patterns.The REE obtained from the Nkporo and Ekenkpon Shales were PAAS normalized.The Nkporo Shale showed a slightly flat light rare-earth element(LREE),middle rare-earth element(MREE),and heavy rare earth element(HREE) pattern enrichment.Ce/Ce*ranges from 0.95 to 1.09 in Nkporo Shale and 0.67 to 1.40 in Ekenkpon Shale.The Ekenkpon Shale showed a slight LREE,MREE enrichment,and depleted HREE patterns.The Mn contents and U/Mo ratio in Nkporo and Ekenkpon Shales suggests a poor oxygen transitional environment.The V/Mo and V/(V+Ni) ratios indicated that the Nkporo shales were deposited in an anoxic to suboxic conditions and Ekenkpon shales were also deposited under an anoxic to suboxic conditions.The V/Ni ratio indicated that the organic matter in the Nkporo shale is terrigenous while that of the Ekenkpon shales are both terrigenous and marine in origin.  相似文献   

13.
Effluents from brown coal mines are frequently rich in iron, the water being red-brown in colour and turbid. For several years a fish farm in the Lusatia (Brandenburg, Germany) has used such mine effluents for rearing rainbow trout. The total iron content of this water varies between 5 and 10 mg/l with pH ranging from 6.7 to 7.4. Water turbidity is high with a transparency of 10 to 40 cm at the most due to the substantial ferric hydroxide concentrations. Until 1989 trout have been reared in net cages within concrete settling basins destined for settling the ferric hydroxide mud. The cages were stocked with fingerlings in autumn, reaching portion size in the spring of the following year. Specific growth rate was 0.98% per day, comparable to that of trout in another farm unpolluted by iron but stocked at higher densities. The results show that fingerling rainbow trout may live in water containing more than 5 mg/l total iron but in the absence of Fe2+. These concentrations of water-borne iron seem to have only a limited detrimental effect on fish growth and feed conversion and do not prevent trout culture in principle.  相似文献   

14.
Modal composition and mineral composition of harzburgites from the southern Mariana fore-arc show that they are highly refractory. There are a few modals of clinopyroxene (0.7 vol %) in harzburgites. Two types of amphibole are found in these harzburgites: magnesiohornblende accompanied by clinopy-roxene with higher Al2O3 content (>7%) and lower Mg#; tremolite around orthopyroxene with lower Al2O3 content (< 2%) and higher Mg#. Trace element of clinopyroxene and two types of amphibole are ana-lyzed. Primitive mantle-normalised REE patterns for clinopyroxene and magnesio hornblende are very similar and both show HREE enrichment relative to LREE,while magnesiohornblende has higher con-tent of trace element than clinopyroxene. The contents of trace element of tremolite are much lower than those of magnesiohornblende. Clinopyroxene shows enrichment of most of the trace element except HREE and Ti relative to clinopyroxene in abyssal peridotites. Petrology and trace element characteristic of clinopyroxene and two types of amphibole indicate that southern Mariana fore-arc harzburgites underwent two stages of metasomatism. The percolation of a hydrous melt led to mobility of Al,Ca,Fe,Mg,Na,and large amounts of trace element. LILE and LREE can be more active in hydrous melt than HREE and Ti,and the activities of most of the trace element except some of LILE are influ-enced by temperature and pressure.  相似文献   

15.
The abundance and distribution of rare earth elements (REE) and their signatures in the Vigo Ria were studied from 50 samples of surface sediments and related to the geological formation in its watershed. The total amount of REE in the Ria is heterogeneous. It ranges from 220 mg kg−1 in the southern middle Ria margin in the vicinity of the Galiñeiro geological shore complex, which contains REE-enriched minerals, to 2 mg kg−1 near the Ria mouth due to dilution with high levels of carbonated biogenic particles (31% of Ca). Rare earth elements of the Ria sediments are considerably enriched in light-REE relative to heavy-REE (a LREE/HREE ratio of 9.7±1.6) and also show a slightly negative Eu-anomaly. Low European shale normalised REE patterns were distinguished in the innermost sediments of Vigo Ria, but were not correlated with Al. This suggests a minor contribution of REE from upstream freshwater inputs to the sediments in the middle Vigo Ria zone. Normalised REE ratios in the middle Ria imply that fine particles enriched in REE may be exported from the Ria to shelf mud patches and REE can be useful as sediment tracers of Ria input on the shelf.  相似文献   

16.
The organic matter-rich strata of the Yurtusi Formation of Lower Cambrian are wildly spread and steady in the Tarim Basin, in which cherts are developed, companied with phosphorite. Al/(Al+Fe+Mn) ratio and Si/(Si+Al+Fe) ratio of cherts range from 0.0023 to 0.0046 and 0.965 to 0.98, respectively, suggesting that cherts are formed in submarine hydrothermal activity and far away from terrestrial. Trace elements, such as As, Hg, Pb, Zn, Cu, Co, P, V, Ba, etc., are markedly rich in organic matter-rich sedimentary rocks of which Ba/Sr ratios are between 21.2 and 158.1. Compared with modern hydrothermal sediments, their Ba/Sr ratios are similar, it indicates that the organic matter-rich strata have the geochemical feature of submarine hydrothermal sediments. The total content of rare earth elements (ЕREE) in cherts is from 8.81 to 56.682 μg/g, on average 31.41 μg/g and the ΕREE of cherts is between continental margin chert's and abyssal chert's. The LREE/HREE ratio of cherts varies from 1.01 to 3.56, which reveals the characteristics of hydrothermal sediments. There is positive correlation between the total organic content (TOC) and Ba/Sr ratio which is geochemical index of submarine hydrothermal activity, which indicates that the submarine hydrothermal activity obviously influences the richness of organic matter in the Yurtusi Formation.  相似文献   

17.
Abstract The Isabela ophiolite, the Philippines, is characterized by a lherzolite‐dominant mantle section, which was probably formed beneath a slow‐spreading mid‐ocean ridge. Several podiform chromitites occur in the mantle section and grade into harzburgite to lherzolite. The chromitites show massive, nodular, layered and disseminated textures. Clinopyroxene (±orthopyroxene/amphibole) inclusions within chromian spinel (chromite hereafter) are commonly found in the massive‐type chromitites. Large chromitites are found in relatively depleted harzburgite hosts having high‐Cr? (Cr/(Cr + Al) atomic ratio = ～0.5) chromite. Light rare earth element (LREE) contents of clinopyroxenes in harzburgites near the chromitites are higher than those in lherzolite with low‐Cr? chromite, whereas heavy REE (HREE) contents of clinopyroxenes are lower in harzburgite than in lherzolite. The harzburgite near the chromitites is not a residual peridotite after simple melt extraction from lherzolite but is formed by open‐system melting (partial melting associated with influx of primitive basaltic melt of deeper origin). Clinopyroxene inclusions within chromite in chromitites exhibit convex‐shaped REE patterns with low HREE and high LREE (+Sr) abundances compared to the host peridotites. The chromitites were formed from a hybridized melt enriched with Cr, Si and incompatible elements (Na, LREE, Sr and H2O). The melt was produced by mixing of secondary melts after melt–rock interaction and the primitive basaltic melts in large melt conduits, probably coupled with a zone‐refining effect. The Cr? of chromites in the chromitites ranges from 0.65 to 0.75 and is similar to those of arc‐related magmas. The upper mantle section of the Isabela ophiolite was initially formed beneath a slow‐spreading mid‐ocean ridge, later introduced by arc‐related magmatisms in response to a switch in tectonic setting during its obduction at a convergent margin.  相似文献   

18.
悬浮物在自然水体（池塘、河流、湖泊等）中普遍存在,相较于上覆水,是微生物更为倾向的附着载体。相较于沉积物,更易获取硝酸盐,是水体反硝化发生的热点微区。悬浮物在水体中经历一系列碰撞、絮凝、溶解、离子交换、吸附解吸等物理化学过程,从而会引起颗粒物粒径、营养盐浓度等发生变化;悬浮物的沉降和再悬浮过程也会引起上覆水和沉积物之间的物质交换,并在好氧缺氧过渡过程中对氮转化造成影响,从而直接或者间接影响水体反硝化速率。本文概括了国内外关于悬浮物影响水体反硝化的研究进展和热点,总结了不同浓度、粒径、组成和种类的悬浮物对反硝化作用的影响,从溶解氧、功能微生物、无机氮、有机碳等环境因素重点归纳了悬浮物影响反硝化的过程,比较和分析了悬浮物反硝化的测定方法。结合当前悬浮物反硝化研究现状,建议未来可以从新兴污染物悬浮物、机理模型、测定方法等方面展开深入研究。  相似文献   

19.
Zilong  Li  Yoshiaki  Tainosho  Jun-Ichi  Kimura  Kazuyuki  Shiraishi 《Island Arc》2005,14(4):636-652
Abstract The Mefjell plutonic complex consists of 500–550‐Ma Pan‐African plutonic rocks, which intrude into the Precambrian crystalline basement in the Sør Rondane Mountains, East Antarctica, and forms part of the Sør Rondane Suture Zone. The complex comprises syenitic and granitic (mostly monzogranitic) rocks, and is characterized by the presence of iron‐rich hydrous mafic minerals and primary ilmenite, both of which imply its formation at high temperature and under low oxygen fugacity conditions. The syenitic rocks are metaluminous, and are high in alkalis, K2O/Na2O, Al2O3, FeOt/(FeOt + MgO) (0.88–0.98), K/Rb (800–1000), Ga (18–28 p.p.m.), Zr (up to 2100 p.p.m.) and Ba. They also have a low Mg? (Mg/[Mg + Fe2+]), Rb, Sr, Nb, Y and F, low to moderate light rare earth element (LREE)/heavy rare earth element (HREE) ratios and positive Eu anomalies in their rare earth element (REE) patterns. The granitic rocks are metaluminous to peraluminous, and have a high Rb content, high Sr/Ba and LREE/HREE ratios, low K/Rb and negative Eu anomalies. Most of the syenitic and granitic rocks have Y/Nb ratios greater than 1.2, and are depleted in Nb, Ti and Sr on the primitive mantle‐normalized spider diagrams, indicating a crustal origin with subduction zone signatures. We interpret both the syenitic and granitic rocks to be derived from an iron‐rich lower crustal source by dehydration melting induced by the heat of mantle‐derived basaltic intrusion, after which they then underwent limited fractional crystallization. The Mefjell plutonic complex has a high Zr content and tectonic discrimination diagram signatures indicative of normal A‐type granitic rocks. Both rock suites may have been generated under the same postorogenic tectonic setting. The Mefjell syenitic rocks are chemically comparable to charnockites in the Gjelsvikjella and western Mühlig‐Hofmannfjella areas of East Antarctica, whereas the granitic rocks are comparable to aluminous A‐type granitic rocks in South India, which were emplaced during formation and evolution of the Gondwanaland supercontinent.  相似文献   

20.
Waste red mud and natural pumice/volcanic slag particles were surface modified and their selenium adsorption from waters was investigated. Acid activation/heat treatment of original red mud (ORM) particles significantly increased their micropore and external surface area and cumulative volume of pores. Iron oxide coating of pumice/slags and acid activation of ORM decreased their pHpzc values and increased surface acidity. Selenite/selenate adsorption on iron oxide surfaces and acid activated red mud (AARM) was very fast with approximately first‐order adsorption kinetics. Iron oxide coating of pumice/slag and acid activation of ORM particles significantly enhanced their selenite and selenate uptakes. Maximum Se adsorption capacities as high as 6.3 (mg Se/g adsorbent) were obtained by AARM. The extent of selenate uptakes by the surface modified particles was generally lower than those of selenite. Due to competition among Se species and other background water matrix for iron oxide adsorption sites, reduced selenite/selenate uptakes were found in natural water compared to single solute tests. Higher Se uptakes by iron oxide surfaces were found at pH 7.5 compared to pH 8.9, due to increased electrostatic repulsion among iron oxides and Se species at higher pH. The most effective adsorbents among the tested 17 different particles for Se uptake were AARM and iron oxide coated pumice. Se concentrations less than drinking water standards (5–10 µg/L) can be achieved by these particles. These low‐cost, natural, or recyclable waste particles appear to be promising adsorbents for Se removal after their surface modification.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号