Lichens as bioindicators in volcanic areas: Mt. Etna and Vulcano Island (Italy)

 The aim of this paper is to verify whether lichens have the capacity to accumulate atmospheric contaminators linked to volcanic activity. About 100 lichens were collected in 1994 and 1995 from two active volcanic areas in Italy: Mount Etna and Vulcano Island. Twenty-seven elements were analyzed for each individual lichen using Instrumental Neutronic Activation Analysis and Inductively Coupled Plasma-Mass Spectrometry. Lichen composition reflects the contribution of the volcanic particulate material, and the two areas investigated can be distinguished on the basis of the concentration of some lithophile elements. Moreover, the distribution in lichens of the elements (As, Sb, Br, Pb) – derived from gas emissions (plume, fumaroles) – also shows different geochemical trends on Mt. Etna and Vulcano. Received: 20 April 1998 · Accepted: 4 July 1998     

Trace element degassing and enrichment in the eruptive plume of the 2000 eruption of Hekla volcano, Iceland

During its last eruption in February 2000, Hekla volcano (Iceland) emitted a sub-Plinian plume that was condensed and scavenged down to the ground by heavy snowstorms, offering the unique opportunity to study the chemistry of the gaseous plume released during highly explosive eruptions. In this paper, we present results on trace element and minor volatile species (sulfates, chlorides, and fluorides) concentrations in snow samples collected shortly after the beginning of the eruption. The goal of this study is to better constrain the degassing and mobility of trace elements in gaseous emissions. Trace element volatility at Hekla is quantified by means of enrichment factors (EF) relative to Be. Well-known volatile trace elements (e.g., transition metals, heavy metals, and metalloids) are considerably enriched in the volcanic plume of Hekla. Their abundances are governed by the primary magmatic degassing of sulfate and/or halide compounds, which are gaseous at magmatic temperature. Their volatility is, however, slightly lower than in basaltic systems, most likely because of the lower magma temperature and higher magma viscosity at Hekla. More surprisingly, refractory elements (e.g., REE, Th, Ba, and Y) are also significantly enriched in the eruptive plume of Hekla where their apparent volatility is two orders of magnitude higher than in mafic systems. In addition, REE patterns normalized to the Hekla 2000 lava composition show a significant enrichment of HREE over LREE, suggesting the presence of REE fluorides in the volcanic plume. Such enrichments in the most refractory elements and REE fractionation are difficult to reconcile with primary degassing processes, since REE fluorides are not gaseous at magma temperature. REE enrichments at Hekla could be attributed to incongruent dissolution of tephra grains at low temperature by F-rich volcanic gases and aerosols within the eruptive plume. This view is supported by both leaching experiments performed on Hekla tephra and thermodynamic considerations on REE mobility in hydrothermal fluids and modeling of glass dissolution in F-rich aqueous solutions. Tephra dissolution may also explain the observed enrichments in other refractory elements (e.g., Th, Y, and Ba) and could contribute to the degassing mass balance of some volatile trace elements, provided they are mobile in F-rich fluids. It thus appears that both primary magmatic degassing and secondary tephra dissolution processes govern the chemistry of eruptive plumes released during explosive eruptions.     

BrO formation in volcanic plumes

Volcanoes have only recently been recognized as a potentially major source of reactive bromine species to the atmosphere, following from the detection of bromine monoxide (BrO) in the plume emitted by Soufrière Hills Volcano, Montserrat. However, BrO is not expected to be emitted in significant quantity from magma, presenting a puzzle regarding its formation. We report here new field measurements of the tropospheric plume emitted by Mt. Etna, Italy, which provide the first direct evidence of fast oxidation of halogen species in a volcanic plume, and lead to an explanation of how BrO is generated from magmatic HBr emissions. We show that the timescale of BrO formation (a few minutes after emission into the atmosphere) is consistent with rapid heterogeneous halogen chemistry involving sulphate aerosol in the plume. The model highlights considerable complexity to the oxidative chemistry of volcanic plumes.     

Atmospheric sources and sinks of volcanogenic elements in a basaltic volcano (Etna, Italy)

This study reports on the first quantitative assessment of the geochemical cycling of volcanogenic elements, from their atmospheric release to their deposition back to the ground. Etna’s emissions and atmospheric depositions were characterised for more than 2 years, providing data on major and trace element abundance in both volcanic aerosols and bulk depositions. Volcanic aerosols were collected from 2004 to 2007, at the summit vents by conventional filtration techniques. Precipitation was collected, from 2006 to 2007, in five rain gauges, at various altitudes around the summit craters. Analytical results for volcanic aerosols showed that the dominant anions were S, Cl, and F, and that the most abundant metals were K, Ca, Mg, Al, Fe, and Ti (1.5-50 μg m⁻³). Minor and trace element concentrations ranged from about 0.001 to 1 μg m⁻³. From such analysis, we derived an aerosol mass flux ranging from 3000 to 8000 t a⁻¹. Most analysed elements had higher concentrations close to the emission vent, confirming the prevailing volcanic contribution to bulk deposition. Calculated deposition rates were integrated over the whole Etna area, to provide a first estimate of the total deposition fluxes for several major and trace elements. These calculated deposition fluxes ranged from 20 to 80 t a⁻¹ (Al, Fe, Si) to 0.01-0.1 t a⁻¹ (Bi, Cs, Sc, Th, Tl, and U). Comparison between volcanic emissions and atmospheric deposition showed that the amount of trace elements scavenged from the plume in the surrounding of the volcano ranged from 0.1% to 1% for volatile elements such as As, Bi, Cd, Cs, Cu, Tl, and from 1% to 5% for refractory elements such as Al, Ba, Co, Fe, Ti, Th, U, and V. Consequently, more than 90% of volcanogenic trace elements were dispersed further away, and may cause a regional scale impact. Such a large difference between deposition and emission fluxes at Mt. Etna pointed to relatively high stability and long residence time of aerosols in the plume.     

Regional distribution of Al,B, Ba,Ca, K,La, Mg,Mn, Na,P, Rb,Si, Sr,Th, U and Y in terrestrial moss within a 188,000 km2 area of the central Barents region: influence of geology,seaspray and human activity

Five hundred and ninety-eight samples of terrestrial moss (Hylocomium splendens and Pleurozium schreberi) collected from a 188,000 km² area of the central Barents region (NE Norway, N Finland, NW Russia) were analysed by ICP-AES and ICP-MS. Analytical results for Al, B, Ba, Ca, K, La, Mg, Mn, Na, P, Rb, Si, Sr, Th, U and Y concentrations are reported here. Graphical methods of data analysis, such as geochemical maps, cumulative frequency diagrams, boxplots and scatterplots, are used to interpret the origin of the patterns for these elements. None of the elements reported here are emitted in significant amounts from the smelting industry on the Kola Peninsula. Despite the conventional view that moss chemistry reflects atmospheric element input, the nature of the underlying mineral substrate (regolith or bedrock) is found to have a considerable influence on moss composition for several elements. This influence of the chemistry of the mineral substrate can take place in a variety of ways. (1) It can be completely natural, reflecting the ability of higher plants to take up elements from deep soil horizons and shed them with litterfall onto the surface. (2) It can result from naturally increased soil dust input where vegetation is scarce due to harsh climatic conditions for instance. Alternatively, substrate influence can be enhanced by human activity, such as open-cast mining, creation of ‘technogenic deserts’, or handling, transport and storage of ore and ore products, all of which magnify the natural elemental flux from bedrock to ground vegetation. Seaspray is another natural process affecting moss composition in the area (Mg, Na), and this is most visible in the Norwegian part of the study area. Presence or absence of some plant species, e.g., lichens, seems to influence moss chemistry. This is shown by the low concentrations of B or K in moss on the Finnish and Norwegian side of the (fenced) border with Russia, contrasting with high concentrations on the other side (intensive reindeer husbandry west of the border has selectively depleted the lichen population).     

峨眉山玄武岩Sr、Nd、Pb同位素特征及其物源探讨

选择峨眉山玄武岩区2个出露最全的云南永胜大迪里剖面和宾川上仓剖面进行了Sr、Nd、Pb同位素地球化学研究.结果表明, 少数样品的Pb同位素与Hanan和Graham定义的C组分相似, 而大多数样品则不在C组分范围之内, 说明除地幔柱物质外, 有岩石圈物质的加入.在多元同位素图解上, 峨眉山玄武岩位于EMⅠ、EMⅡ和DMM三端元之间, 表明其源区可以由地幔柱、富集的岩石圈地幔和地壳不同程度的混合来解释.结合已有的微量元素资料分析, 其中的地壳组分主要为下地壳, 而早期玄武质岩浆在上升过程中由于通道不畅通, 有较多的上地壳组分的混染.岩石圈地幔的富集作用可能与地幔柱释放出的小体积富Na、P而贫K的流体交代作用有关.粗面岩的同位素组成和玄武岩接近, 说明粗面岩是玄武质岩浆分离结晶作用形成的.      

Application of pyrite trace element chemistry to exploration for SEDEX style Zn-Pb deposits: McArthur Basin,Northern Territory,Australia

Sedimentary pyrites in black shales contain abundant trace elements that provide information on the chemistry of the seawater at the time of sedimentation. This study focuses on the Barney Creek Formation (~ 1640 Ma) in the McArthur Basin in the Northern Territory of Australia, which is host to one of the world's largest SEDEX Zn-Pb-Ag deposits, and several smaller deposits. Fine-grained sedimentary pyrite has been sampled from three drill holes through the Barney Creek Formation at various distances from SEDEX mineralisation. Samples were selected through the stratigraphy of each hole and analysed by LA-ICPMS for a suite of 14 trace elements. The data show that sedimentary pyrite at the base of the Barney Creek Formation, closest (within 1 km) to SEDEX mineralisation, is strongly enriched in Zn and Tl by one to two orders of magnitude compared to the global average for sedimentary pyrite. In contrast sedimentary pyrite from the hole furthest from SEDEX mineralisation (~ 60 km) contains mean Zn and Tl values equal to, or less than, the global average. Based on the three drill hole pyrite data sets it is concluded that trace elements that are contributed to the basin during hydrothermal exhalation, and adsorbed into contemporaneous sedimentary pyrite, are principally Zn, Tl, Cu, Pb, Ag and As. In contrast, trace elements that are adsorbed into sedimentary pyrite from background seawater are principally Mo, Ni, Co, Se and As. These differences have enabled the development of a SEDEX fertility diagram for sedimentary basins, based on the composition of sedimentary pyrite, that distinguish high Zn, but barren shales, from high zinc SEDEX-related shales. In parallel with the increase in Zn and Tl in sedimentary pyrite approaching mineralisation there is a decrease in Ni, Co and Mo. This means that the ratios Zn/Ni and Tl/Co are particularly good pyrite vectors to SEDEX mineralisation in the McArthur Basin, varying over 4 to 6 orders of magnitude from barren shales to mineralised shales. It is speculated that the reason for the reverse relationship between Ni, Co and Zn, Tl may be caused by hydrothermal exhalations into the water column that effect the ion-exchange pyrite surface complexation processes that alter the uptake of these elements into sedimentary pyrite.Another important conclusion of this study is that hydrothermal exhalations into a sedimentary basin may affect the redox sensitive trace element chemistry of sedimentary pyrite and therefore the trace element chemistry of pyritic black shales. Nickel, Co and Mo all decrease in proximity to hydrothermal vents that form SEDEX deposits, whereas Zn, Tl and Pb increase. Selenium and bismuth are the only redox sensitive trace elements that appear to be unaffected by hydrothermal activity in the McArthur Basin. This has implications on how trace element concentrations of black shales and pyrite are used to reflect past global ocean chemistry.     

Iron release in aqueous environment by fresh volcanic ash from Mount Etna (Italy) and Popocatépetl (Mexico) volcanoes

In this study, we performed leaching experiments for timescales of hours-to-months in deionized water on fresh volcanic ash from Mt. Etna (Italy) and Popocatépetl (Mexico) volcanos to monitor Fe release as a function of ash mineral chemistry and size, with the aim of clarifying Fe release mechanisms and eventually evaluating the impact of volcanic ash on marine and lacustrine environments. To define sample mineralogy and Fe speciation, inclusive characterization was obtained by means of XRF, SEM, XRPD, EELS and Mössbauer spectroscopies. For Etna and Popocatépetl samples, glass proportions were quantified at 73 and 40%, Fe₂O₃ total contents at 11.6–13.2 and 5.8 wt%, and Fe³⁺/Fe_Tot ratios at 0.33 and 0.23, respectively. Leaching experiments showed that significant amounts of iron, ~?30 to 150 and ~?750 nmol g^?1 l^?1 for pristine Etna and Popocatépetl samples, respectively, are released within the first 30 min as a function of decreasing particle size (from 1 to 0.125 mm). The Popocatépetl sample showed a very sustained Fe release (up to 10 times Etna samples) all along the first week, with lowest values never below 400 nmol g^?1 l^?1 and a maximum of 1672 nmol g^?1 l^?1 recorded after 5 days. This sample, being composed of very small particles (average particle size 0.125 mm) with large surface area, likely accumulated large quantities of Fe-bearing sublimates that quickly dissolved during leaching tests, determining high Fe release and local pH decrease (that contributed to release more Fe from the glass) at short timescale (hours-to-days). The fractional Fe solubility (Fe_S) was 0.004–0.011 and 0.23% for Etna and Popocatépetl samples, respectively, but no correlation was found between Fe released in solution and either ash Fe content, glass/mineral ratio or mineral assemblage. Results obtained suggest that volcanic ash chemistry, mineralogy and particle size assume a relevant role on Fe release mostly in the medium-to-long timescale, while Fe release in the short timescale is dominated by dissolution of surface sublimates (formed by physicochemical processes occurring within the eruption plume and volcanic cloud) and the effects of such a dissolution on the local pH conditions. For all samples, a moderate to sustained Fe release occurred for leaching times comparable with their residence time within the euphotic zone of marine and lacustrine environments (variable from few minutes to few hours), revealing their possible contribution to increase Fe bioavailability.     

Environmental impact of the acid fumarolic plume of a passively degassing volcano (Vulcano Island,Italy)

This paper investigates the role played by the fumarolic plume of a passive degassing volcano in the genesis of rock coatings (RC) and in the introduction and re-distribution of metals and trace elements in the surficial environment. At La Fossa active volcano (Vulcano Island) and in the surrounding environment RC develop owing to exposure of the ground surface to the volcanic acid plume produced by the passive degassing of La Fossa. Significant positive anomalies of a wide variety of metals and trace elements (including Bi, Ag, Se, Te, Sb, Pb, As, Cu, Tl and Cd) were observed either in distal and proximal RC. Most of these anomalies are interpreted to be the result of the transport and subsequent deposition of trace elements, likely to form volatile compounds, in the fumarolic plume. Two main processes seem to control the geochemistry of RC: one is represented by the leaching and subsequent deposition of elements from the proximal toward the distal RC; the other is the direct input of trace elements carried by the emitted volcanic aerosol. The fact that most of the trace elements (particularly Pb, As, Tl, Bi, Te, Se, Cd) enriched in the RC of Vulcano are highly toxic and potentially dangerous to health in high concentration, indicates that the atmospheric metal injection by the quiescently degassing La Fossa volcano together with the subsequent deposition and remobilization by means of surficial waters may represent an environmental hazard that should be taken into account in evaluating the potential impact of volcanic air pollution on human health.     

Direct major- and trace-element analyses of rock varnish by high resolution laser ablation inductively-coupled plasma mass spectrometry (LA-ICPMS)

Laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS) was used to determine major and trace element concentrations in rock varnish samples from the Lahontan Range, near Fallon, NV and from a remote wilderness area near the San Juan River, in southeastern Utah. The data indicate that rapid LA-ICPMS analyses provide ample analytical resolution for semi-quantitative compositional determinations of both trace and major elements in the varnish despite the presence of a rock substrate component in most analyses. The overall major element contents of rock varnish from the two localities are grossly similar to rock varnish from other locations analyzed by solution ICPMS, electron microprobe, and energy dispersive scanning electron microscopy (SEM). Differences between microprobe and LA-ICPMS analyses may stem from different sampling scales and different degrees of substrate involvement. It was possible to detect significant variations in trace element contents in the rock varnish samples. The Lahontan Range is situated within a belt of W mineralization, and varnish from that locality contained significantly higher W and Mo contents than varnish from localities outside the W belt. Lead, Tl, Bi, Cd and As contents of varnish-coated pebbles from near the San Juan River in southeastern Utah, varied by an order of magnitude as a function of the position of the sampling site on the pebble. Elevated heavy element contents on the skyward-facing varnish surfaces indicate that heavy elements may be preferentially scavenged at the locations most likely to receive direct inputs of atmospherically-deposited airborne particulates. The source of metal-rich airborne particulates, in this case, is probably any one of several large coal-fired power plants in the Four Corners region, proximal to the San Juan study area. These patterns indicate that rock varnish chemistry is influenced by atmospherically-derived fluxes of both dissolved and particulate constituents, and that rock varnish can be used as a passive environmental indicator for a wide variety of elements, in much the same manner as moss and lichens.     

Evidence of a shallow magma intrusion beneath the NE Rift system of Mt. Etna during 2013

Continuous GPS (CGPS) data, collected at Mt. Etna between April 2012 and October 2013, clearly define inflation/deflation processes typically observed before/after an eruption onset. During the inflationary process from May to October 2013, a particular deformation pattern localised in the upper North Eastern sector of the volcano suggests that a magma intrusion had occurred a few km away from the axis of the summit craters, beneath the NE Rift system. This is the first time that this pattern has been recorded by CGPS data at Mt. Etna. We believe that this inflation process might have taken place periodically at Mt. Etna and might be associated with the intrusion of batches of magma that are separate from the main feeding system. We provide a model to explain this unusual behaviour and the eruptive regime of this rift zone, which is characterised by long periods of quiescence followed by often dangerous eruptions in which vents can open at low elevation and thus threaten the villages in this sector of the volcano.     

Geochemistry and petrogenesis of the Fiskenaesset anorthosite complex,southern West Greenland: Nature of the parent magma

The petrogenesis of the Fiskenaesset anorthosite body has been investigated using major and trace element data for a large range of rock types from each zone of the complex. The chemistry of these ultramafic to anorthositic cumulates is interpreted in terms of crystal fractionation of a parental, trace element impoverished, tholeiitic magma, involving crystallisation of the cumulus phases olivine, orthopyroxene, clinopyroxene and (dominant) plagioclase feldspar. Amphibole appears not to have been a significant cumulus phase at any stage of crystallisation of the body, the abundant amphibole found in the rocks of the complex being produced by primary intercumulus crystallisation, supplemented by secondary metamorphic recrystallisation. Similarly, magnetite is unlikely to have been a significant early cumulus phase, although, together with chromite, it crystallised as a cumulus phase at high stratigraphic levels in the complex. The metamorphism appears to be largely isochemical, although sub-solidus metamorphic re-equilibration of the REE can be demonstrated on a grain-size scale.The spatial and temporal association between the anorthosite complex and the bordering metavolcanic amphibolites is matched by a strong similarity between the observed trace element chemistry of the amphibolites and the trace element chemistry of calculated successive liquids for the complex. This is taken to suggest a genetic relationship between the evolution of the anorthosite complex and enclosing amphibolites. The presence of trace element impoverished amphibolites (which are not cumulates) with trace element abundances comparable to those of the suggested parental liquid to the anorthosite complex, is used to derive a major element composition for the primary Fiskenasset magma. This composition approximates a moderately aluminous tholeiitic basalt, which may have been generated by hydrous fusion of previously depleted mantle. This primary magma underwent crystal fractionation under low pressure conditions, allowing the development of extensive plagioclase cumulates.The Fiskenaesset anorthosite, and similar bodies, cannot represent a cumulate residue complementary to the enclosing voluminous tonalitic gneisses, which have a calc-alkaline chemistry controlled by high pressure crystal liquid fractionation. Rather, the association between the cumulate layered complex and bordering supracrustal sequence may imply an ancient ocean crust analogue for the development of this component of Archaean high-grade terrains. It is suggested that slices of such Archaean ocean floor may be emplaced laterally into the base of the continental crust during subduction of oceanic lithosphere at Cordilleran type continental margins.     

藏北冈塘错地区OIB型和E-MORB型玄武岩组合及大地构造意义

通过对西藏羌塘中部冈塘错地区玄武岩地球化学特征研究,发现该区有OIB型和E-MORB型两类玄武岩.对两类玄武岩进行主量元素、稀土元素和微量元素地球化学图解分析及大地构造意义探讨,结合区域地质背景,认为冈塘错地区玄武岩形成于洋岛环境,可能受地幔柱岩浆活动影响,E-MORB型玄武岩的出现说明该区可能存在洋底高原.     

Average compositions of magmas and mantle sources of mid-ocean ridges and intraplate oceanic and continental settings estimated from the data on melt inclusions and quenched glasses of basalts

Based on the generalization of the compositions of melt inclusions and quenched glasses from basaltic rocks, the average compositions of magmas were estimated for mid-ocean ridges (MOR), intraplate continental environments (CR), and ocean islands and plateaus (OI). These compositions were used to constrain the average contents of trace and volatile elements in mantle sources. A procedure was developed for the estimation of the average contents of incompatible elements, including volatiles (H₂O, Cl, F, and S), in the mantle. A comparison of the obtained average contents for the depleted mantle (DM) with the available published estimates showed that the contents of most incompatible trace elements (H₂O, Cl, F, Be, B, Rb, Sr, Zr, Ba, La, Ce, Nd, Sm, Eu, Hf, Ta, Th, and U) can be reliably estimated from the ratio of K to the desired trace element in the MOR magmas and the average content of K in the DM. For Nb, Ti, P, S, Li, Y, and heavy REE, we used the ratios of their contents to an element with a similar degree of incompatibility in MOR magmas (U for Nb and Dy for the other elements). This approach was used to determine the average contents of incompatible elements in oceanic plume mantle (OPM) and the subcontinental mantle of intraplate settings or continental plume mantle (CPM). It was shown that the average composition of both suboceanic and subcontinental mantle plumes is moderately enriched compared with the DM in the most incompatible elements (K, U, Ba, and La) and volatile components (H₂O, Cl, and F). The extent of volatile component enrichment in the plume mantle (500–1500 ppm H₂O) is insufficient for a significant depression of the mantle solidus. Therefore, mantle plumes must be hotter than the ambient depleted mantle. The average contents of incompatible trace elements in the OPM are similar to those of the primitive mantle, which could be related either to the retention of primitive mantle material in the regions of plume generation or to DM fertilization at the expense of the deep mantle recycling of crustal materials. In the latter case, the negative anomaly of water in the trace-element distribution patterns of the OPM is explained by the participation of dehydrated crust in its formation. Variations in the compositions of magmas and their sources were considered for various geodynamic settings, and it was shown that the sources are heterogeneous with respect to trace and volatile components. The chemical heterogeneity of the magma sources and gradual transitions between them suggest that the mantle reservoirs interact with each other. Chemical variations in continental and oceanic plume magmas can be attributed to the existence of several interacting sources, including one depleted and at least two enriched reservoirs with different contents of volatiles. These variations are in agreement with the zoned structure of mantle plumes, which consist of a hot and relatively dry core, a colder outer shell with high contents of volatile components, and a zone of interaction between the plume and depleted mantle.     

湖北清江榨洞石笋中可溶硅的测定及其古气候意义研究

洞穴石笋蕴含着丰富的古气候信息，其正确解译有赖于各类古气候替代指标的开发，应用改进的硅钼兰分光光度法测定湖北清江榨洞石笋中痕量可溶硅，探讨其古气候指示意义。结果表明，石笋中可溶硅含量记录了岩溶地下水的硅酸组成，后进反映了气候控制下土壤的化学风化作用。因而，石笋可溶硅是一个潜在的古气候（特别是古湿度）替代指标。     

Oil and Gas Production in the Amu Dar'ya Basin of Western Uzbekistan and Eastern Turkmenistan

The Deccan flood basalt province of west-central India has been linked to the Reunion plume, and reconstructions suggest that the Kutch region was over the plume at the time of Deccan volcanism at 65-68 Ma. Field relations and isotopic data indicate that the alkaline basalts of Kutch, which occur to the NNW of the main Deccan tholeiitic province, preceded the main flood-basalt volcanism and are related to the limited plume incubation period. Several plugs of these alkali basalts contain small spinel peridotite xenoliths of mantle origin. The minerals of the spinel peridotites have been analyzed for their major, trace, and rare-earth element (REE) concentrations using electron micro-probe and LAM-ICPMS techniques. The modes and mineral chemistry, especially of the clinopyroxenes, indicate a fertile mantle; modeling of the clinopyroxene REE data is consistent with <5 to 15% of partial melting of a primitive mantle source material in the spinel peridotite field. Subsequent cryptic metasomatism introduced LREE, U, Th, and Zr. The xenoliths may represent: (1) young lithosphere generated during the lithospheric extension that preceded the main Deccan volcanism; or (2) material from the uppermost parts of the rising plume, brought to the surface by the first stages of the volcanism. Their low equilibration temperatures (≤900°C) and their textural and chemical similarity to xenolith suites from other Phanerozoic intraplate settings favor the first alternative. However, the extensive cryptic metasomatism may reflect the influence of the rising Deccan plume.     

Effect of bacteria on the elemental composition of early diagenetic siderite: implications for palaeoenvironmental interpretations

Many ancient early diagenetic siderite concretions are thought to have been precipitated by microbially-mediated reactions, and their trace element chemistry has been used to infer palaeoenvironments of formation (e.g. marine versus freshwater). In this study, pure cultures of the microorganism Geobacter metallireducens were used to precipitate siderite in the laboratory at a range of temperatures (18–40°C). Magnesium and calcium, in three different ratios (3:1, as in seawater, 1:1, and 1:3 as in freshwater), or manganese were added to some cultures at each incubation temperature to study trace element incorporation. The siderite produced exhibited the rhombohedral crystal form typical of concretionary siderite. However, this microbial siderite did not simply retain the trace element chemistry of the water from which it precipitated, as is assumed in palaeoenvironmental interpretations. Instead, manganese and calcium incorporation were found to be inversely proportional to the rate of microbial activity, which itself is dependent upon the nutritional status of the microorganisms. Magnesium incorporation was found to be rate-independent, and at high Mg/Ca ratios, it caused inhibition of calcium incorporation. In short, the influence of microorganisms on the trace element composition of early diagenetic siderite must be taken into account in order to produce valid palaeoenvironmental interpretations.     

大火成岩省中苦橄岩的研究意义

苦橄岩是一种超镁铁质熔岩 ,它在大火成岩省中虽然只占很小的比例 ,但具有非常重要的意义。苦橄岩通常产于火山岩系的底部和下部 ,其中有的苦橄岩具有原始岩浆的特点 ,另有一些为堆积成因 ,也有少部分代表了演化岩浆。对它的岩石学、矿物学、元素和同位素地球化学以及橄榄石包裹体中挥发份的研究可以为研究大火成岩省和地幔柱的关系、地幔柱的热成分结构模式、大火成岩省和全球生物灭绝事件以及预测Cu Ni PGE硫化物矿床的成矿潜力提供重要约束。     

Evaluation of groundwater resources for drinking and agricultural purposes, Abar Al Mashi area, south Al Madinah Al Munawarah City, Saudi Arabia

A hydrogeochemical study was conducted on the groundwater of south Al Madinah Al Munawarah City, Saudi Arabia, to assess the quality of groundwater for drinking and irrigation uses. Groundwater samples have been collected and analyzed for major and some trace constituents from the study area. The nitrate concentration in most groundwater samples of the study area exceeded the safe limits for drinking purposes, whereas the concentrations of phosphate, boron, and trace constituents were below the maximum permissible limit for drinking purposes; Cr in two samples showed high content over the recommended limits of drinking purposes. Uncontrolled abstraction of groundwater in Abar Al Mashi area caused many environmental problems including water resource depletion and contamination. Correlations between chloride and major ions were positive and may be attributed to impact of agricultural activities on groundwater chemistry. Groundwater of the study area was classified into six water types. The chemical water types of groundwater in the study area contain CaHCO₃ in the eastern and southeastern parts and NaCl in western and northwestern parts, reflecting different land use characteristics and pollution sources. Piper diagram showed that almost all the samples fall in one zone, indicating similar chemical signature. Groundwater can be used safely for drinking with special treatments to eliminate the effect of increased concentrations of total dissolved solids, nitrate, and chromium. The groundwater of the study area can be used safely for irrigation on clay soil; however, specific crops should be selected according to their salt tolerance.     

滇西澜沧老厂地区玄武岩岩石成因与构造意义

对滇西澜沧老厂地区玄武岩进行了系统的主微量元素和Nd-Pb同位素地球化学研究,结果表明该玄武岩为典型的洋岛玄武岩(OIB)。Nd-Pb同位素研究表明,玄武岩浆含富集地幔组分。老厂地区玄武岩浆活动可能与地幔热柱有关,玄武岩可能为地幔热柱(软流圈)熔融产生的岩浆与富集的岩石圈地幔岩浆混合的产物。