The aquatic geochemistry of arsenic in volcanic groundwaters from southern Italy

This paper discusses the abundance, speciation and mobility of As in groundwater systems from active volcanic areas in Italy. Using literature data and new additional determinations, the main geochemical processes controlling the fate of As during gas–water–rock interaction in these systems are examined. Arsenic concentrations in the fluids range from 0.1 to 6940 μg/l, with wide differences observed among the different volcanoes and within each area. The dependence of As content on water temperature, pH, redox potential and major ions is investigated. Results demonstrate that As concentrations are highest where active hydrothermal circulation takes place at shallow levels, i.e. at Vulcano Island and the Phlegrean Fields. In both areas the dissolution of As-bearing sulphides is likely to be the main source of As. Mature Cl-rich groundwaters, representative of the discharge from the deep thermal reservoirs, are typically enriched in As with respect to SO₄-rich “steam heated groundwaters”. In the HCO₃⁻ groundwaters recovered at Vesuvius and Etna, aqueous As cycling is limited by the absence of high-temperature interactions and by high-Fe content of the host rocks, resulting in oxidative As adsorption. Thermodynamic modelling suggests that reducing H₂S-rich groundwaters are in equilibrium with realgar, whereas in oxidising environments over-saturation with respect to Fe oxy-hydroxides is indicated. Under these oxidising conditions, As solubility decreases controlled by As co-precipitation with, or adsorption on, Fe oxy-hydroxides. Consistent with thermodynamic considerations, As mobility in the studied areas is enhanced in intermediate redox environments, where both sulphides and Fe hydroxides are unstable.     

Uranium and potassium in calc-alkaline volcanic rocks from Sardinia

The U content of major rock-forming minerals in a suite of calc-alkaline volcanic rocks from Sardinia is very low and their partition coefficient of U (D^U = C^S/C^L) is smaller than 0.1. The values of D^U of the mineral phases decrease from basalt to dacite and, in all rocks, the bulk of U and K is present in the groundmass. The apparent close association between K and U in basic and intermediate rocks probably reflects the fact that most of their rock-forming minerals are relatively ‘inert’ with respect to both of these elements.     

Geochemical Features of the Two Early Paleozoic Ophiolitic Zones and Volcanic Rocks in the Central —Southern Tianshan Region ,Xinjiang

This paper deals with the geochemical features of the two Early Paleozoic ophiolite zones in the central-southem Tianshan region and the central Tianshan igneous rock belt between them.Study results suggest that the central Tianshan belt was an Ordovician volcanic arc with an affinity of continental crust, and the Kumux-Hongluhe ophiolitic zone that is located on the southern margin of central Tianshan has a crustal affinity to back-arc marginal sea.The Aqqikkudug-Weiya ophiolitic zone is an accretionary boundary between the Tuha continental block and the central Tianshan volcanic arc during Late Silurian to Devoniann;Ordovician ophi-olitic blocks,Silurian flysch sequence and HP metamorphic rock relics are distributed along the Aqqikkudug-Weiya zone.Geochemically,ophiolitic rocks in the Aqqikkudug-Weiya zone have an affinity to oceanic crust,reflecting a tectonic setting of paleo-trench or subduction zone .The Early Carboniferous red molasses were deposited unconformably on the pre-Carboniferous meta-mrophosed and ductile sheared volcanic and flysch rocks,providing an upper limit age of the central and southern Tianshan belts.     

The impact of dolomite and plagioclase weathering on the chemistry of shallow groundwaters circulating in a granodiorite-dominated catchment of the Sila Massif (Calabria,Southern Italy)

This work is aimed at investigating the weathering processes of the granodiorites cropping out in a small catchment of the Sila Massif. The mineral constituents in this granodiorite are plagioclase, often zoned with a Ca-rich core and a Na-rich rim, quartz, chlorite, K-feldspar, white mica and epidote. During this study, dolomite was discovered in local stream sediments, as separate monomineralic grains, probably resulting from erosion of veins cutting the crystalline rocks. Prevailing dissolution of foreign dolomite and a Ca-rich plagioclase is suggested by the Ca–Mg–HCO₃ chemical composition of local groundwaters and stream waters, which is rather unexpected for waters interacting with granitoid rocks. These qualitative observations are quantitatively confirmed by reaction path modelling of the weathering processes occurring in the study area, which was carried out using the EQ3/6 software package, version 8.0, and the Double Solid Reactant Method. Indeed, it was possible to ascertain that the release of both major dissolved constituents and several trace elements (Ba, Co, Cr, Fe, Mn, Ni, Pb, Sr, V and Zn), from rocks to waters, is chiefly controlled by the dissolution of foreign dolomite and the Ca-rich core of zoned plagioclases.     

Strontium isotope studies on young volcanic rocks from Germany and Italy

⁸⁷Sr/⁸⁶Sr ratios of Tertiary tholeiitic, basalts alkali olivine basalts and olivine nephelinites from Lower Saxony and Hessia and Quaternary leucite-nepheline tephrites from the Laacher See area are similar to those obtained from Hawaii and range from 0.7031 to 0.7054. Three trachytes and one phonolite from the Westerwald and one phonolite from the Laacher See area have higher values (0.7063 to 0.7093). Three Vesuvian lavas, three Somma lavas and two trachytes of the Phlegraic Fields show substantially higher ratios than the comparable basaltic rocks from N.W. Germany (0.7071 to 0.7102). Three peridotite nodules vary between 0.7048 and 0.7081. Three limestone composites of Paleozoic and Mesozoic age show values between 0.7129 and 0.7174.The ⁸⁷Sr/⁸⁶Sr ratios of the trachytes and phonolites from the Westerwald and Laacher See area are probably influenced by crustal material. Assimilation processes of limestones producing the olivine-nephelinites from N.W. Germany seem to be unlikely. A discussion of the origin of the Sr ratios in Vesuvian rocks and of mantle homogeneity is included.     

Oxygen isotope studies of potassic volcanic rocks of the Roman Province,Central Italy

The ¹⁸O/¹⁶O ratios of rocks and coexisting minerals were measured for 93 samples of leucite-bearing lavas, pyroclastics, and related volcanic rocks from the Quaternary Roman Co-Magmatic Province, Italy. The ¹⁸O values were found to generally increase northward in the sequence: Ischia (5.8 to 7.0); Somma-Vesuvius and Phlegrean Fields (7.3 to 8.3); Alban Hills (7.3 to 8.7); M. Sabatini (7.3 to 9.7); Vico Volcano (7.4 to 10.2); and M. Vulsini (8.1 to 11.7). The northward increase in ¹⁸O parallels a similar increase in ⁸⁷Sr/⁸⁶Sr, and these data indicate that the Roman magmas have interacted strongly with high-¹⁸O continental crust. A marked increase in ¹⁸O occurs just north of Rome where the Roman Province begins to overlap the calc-alkaline, oversaturated Tuscan Magmatic Province. Therefore, some of the observed ¹⁸O/¹⁶O and ⁸⁷Sr/⁸⁶Sr enrichments in the Roman magmas may have been facilitated by direct mixing with the high-¹⁸O Tuscan magmas or because the high-¹⁸O country rocks underwent widespread heating during a couple of million years of Tuscan igneous activity. Although many of the Roman magmas underwent fractional crystallization without appreciable change in ¹⁸O, contamination has produced a correlation between ¹⁸O and SiO₂ content at several of the volcanic centers; thus the trachytes are typically higher in ¹⁸O than the undersaturated rocks. The major features of the oxygen isotope data can be explained in terms of a simple two-component mixing model in which one end-member was a primary, strongly undersaturated magma derived from the upper mantle, with ¹⁸O+6, ⁸⁷Sr/⁸⁶Sr0.704 to 0.705, and SiO₂<44wt.%. However, none of the analyzed samples have these values, as they have all been contaminated to some extent. The closest approach is found in some of the leucitepyroxenite ejecta from the Alban Hills. The second end-member, derived from the continental crust, had a variable composition with ¹⁸O+12 to +20, ⁸⁷Sr/⁸⁶Sr0.712 to 0.720, and SiO₂65wt.%, and it mixed in much greater proportions in the volcanoes north of Rome than in those of the Alban Hills or the Naples area. The widespread interactions between the Roman magmas and the continental crust are probably due to (1) the fact that such low-SiO₂ magmas always have a very strong tendency to interact with quartz-bearing rocks of the continental crust, and (2) in Italy, these magmas were emplaced into a tectonically very active area containing poorly consolidated sedimentary rocks, and in the northern part of the belt there had been a prior history of extensive calc-alkaline igneous activity.Publication of the Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, California 91125, Contribution Number 2501.     

大兴安岭中生代双峰式火山岩的地球化学特征

大兴安岭中生代火山岩的主要活动时期为晚侏罗世至早白垩世，由碱性系列玄武岩和亚碱性系列玄武岩以及伴生的中酸性火山岩组成。它们与邻区俄罗斯和蒙古同时期火山岩构成面形展布的巨型火山岩带。碱性系列玄武岩高度富集不相容元素，其富集程度类似于板内碱性系列玄武岩，但明显亏损Nb和Ta等高场强元素这一点又类似于活动大陆边缘火山弧或岛弧钙碱性玄武岩。亚碱性系列玄武岩适度富集不相容元素而强烈亏损高场强元素的特征类似于活动大陆边缘火山弧或岛弧火山岩，其中低钾玄武岩类似于拉斑玄武岩。大兴安岭酸性火山岩根据地球化学特征可划分为高Sr流纹岩类和低Sr流纹岩类。前者富集Ti、Ba、Sr、Co和Ni而贫Rb、Zr和Th等强不相容元素，类似于大陆溢流玄武岩省分异作用形成的流纹岩；后者明显富集不相容元素Rb、Zr和Th而亏损Ti、Ba、Sr和Co，它们与碱性系列玄武岩之间形成类似于大陆裂谷环境的双峰式火山岩组合。亚碱性系列玄武岩与高Sr流纹岩的成因关系类似于大陆伸张环境的双峰式火山岩，但前者形成从基性到酸性的连续演化系列，并没有形成Daly成分间断。这表明大兴安岭火山岩在源区及其原始岩浆的性质上明显区别于世界大陆溢流玄武岩省。也就是说，大陆溢流玄武岩省的双峰模式起源于干岩浆体系，这种岩浆分异形成的中性岩浆由于其教度大于玄武岩、挥发分含量低于流纹岩而未能喷出地表。大兴安岭富含水的原始岩浆使分异形成的中性熔岩被挥发分过饱和，导致中性熔岩的爆炸性喷发。     

Natural hexavalent chromium in groundwaters interacting with ophiolitic rocks

Thirty of the 58 groundwaters sampled in September-October 2000 in the study area (La Spezia Province, Italy) have Mg-HCO₃ to Ca-HCO₃ composition, undetectable Cr(III) contents, and virtually equal concentrations of total dissolved Cr and Cr(VI). Therefore, dissolved Cr is present in toto as Cr(VI), with concentrations of 5-73 ppb. These values are above the maximum permissible level for drinking waters (5 ppb). Local ophiolites, especially serpentinites and ultramafites, are Cr-rich and represent a Cr source for groundwaters. However, since Cr is present as Cr(III) in rock-forming minerals, its release to the aqueous solution requires oxidation of Cr(III) to Cr(VI). This can be performed by different electron acceptors, including Mn oxides, H₂O₂, gaseous O₂, and perhaps Fe(III) oxyhydroxides. Based on this evidence and due to the absence of anthropogenic Cr sources, the comparatively high Cr(VI) concentrations measured in the waters of the study area are attributed to natural pollution.     

Relationships between ultrapotassic and carbonate-rich volcanic rocks in central Italy: petrogenetic and geodynamic implications

The Pleistocene intra-Apennine volcanic (IAV) centres occurring east of the potassium-rich Roman comagmatic province show variable petrological and geochemical composition. Some rocks have a strongly undersaturated ultrapotassic kamafugitic affinity with K₂O/Na₂O=8–20, whereas the rocks from the southern center of Mt. Vulture are still strongly undersaturated in silica but are enriched in both Na₂O and K₂O with K/Na around unity. Carbonate-rich pyroclastic rocks, believed to represent carbonatitic magmas, are found in the IAV centers. Kamafugites have high abundances of LILE and high LILE/HFSE ratios, and their incompatible element patterns resemble closely those of ultrapotassic rocks from the adjoining Roman province. The Vulture volcanics also display high contents of LILE, but their LILE/HFSE ratios are intermediate between intraplate alkaline rocks and kamafugites. The carbonate-rich rocks exhibit an exotic mineralogy and high enrichments in LILE, which speaks for a carbonatitic affinity. However, they have similar incompatible element patterns but consistently lower abundances of almost all the elements than the associated silicate volcanics. These data favour the hypothesis that the IAV carbonate rocks may represent mixtures of silicate magmas and geochemically depleted carbonate material. The sedimentary carbonates that crop out extensively along the Apennine chain may be the source of barren carbonate material. Overall, geochemical data of IAV centres and of the rocks from the Roman province display strong geochemical and isotopic evidence of being generated in an upper mantle that was modified by addition of upper crustal material brought down by subduction processes. A possible exception is represented by Mt. Vulture which, however, occurs east of the main axis of the Apennines, on the western margin of the foreland Adria plate. The occurrence of strongly undersaturated alkaline rocks requires magma generation at high pressures and . This is in agreement with the hypothesis that subduction processes under the Apennines occurred by consumption of poorly hydrated thinned or delaminated continental crust.     

Petrogenesis of calc-alkaline,shoshonitic and associated ultrapotassic Oligocene volcanic rocks from the Northwestern Alps,Italy

Along the Western Alps there is geological evidence of late-Alpine (Oligocene) magmatic activity which clearly postdates the Lepontine (Eocene-early Oligocene) metamorphism and related deformation of the Alpine nappe pile. This magmatic activity was notably delayed in relation to the most important convergent processes and may be related to buoyancy of lithosphere, tensional tectonics and thermal updoming subsequent to the collision between the Eurasian and African plates. The geochemical features of the rocks and the geophysical characteristics of the Alpine chain, suggest that: (a) shoshonitic and calcalkaline melts may have been generated by partial melting of metasomatized peridotitic material and subsequent fractional crystallization and crustal contamination; silicic andesites and latites, however, could have been also derived from metasomatized eclogite or deep continental crust material; (b) the ultrapotassic lamprophyres with high K, P, LREE, Th, Zr, U and high ⁸⁷Sr/⁸⁶Sr ratios were generated by partial melting of strongly metasomatized mantle; the varied Sr-isotopic ratios may partially also reflect additional radiogenic component from the continental crust following magma segregation from the source.     

Saturation of groundwaters with respect to minerals of the host rocks

Calculations of the saturation of groundwaters with respect to minerals of the rocks hosting these waters indicate that most of the analyzed groundwaters were saturates with respect to calcite, dolomite, and quartz. Brines of chloride-calcic composition were determined to be saturated with respect to calcite, whereas brines of chloride-sodic composition are saturated with respect to dolomite and quartz. The solution was simultaneously saturated with respect to six minerals for the association ankerite-calcite-dolomite-pyrite-quartz-strontianite. An increase in the number of minerals with respect to which solution is saturated is correlated with an increase in the diversity of types of groundwaters and an increase in the runoff rate. The paper proposes possible avenues for searches for relations between hydrogeological and geochemical parameters that make it possible to adapt the thermodynamic models to real geological-hydrogeological conditions. The research was centered on the testing of groundwaters for their saturation with respect to minerals of the rocks hosting these waters. This parameter plays a significant part in forming the geochemical type of natural waters because it reflects the crystallization of a mineral from a solution and, consequently, the removal of an element from the aqueous solution.     

碧口群火山岩岩石成因研究

新元古代(846~776Ma)碧口群火山岩喷发于大陆板内裂谷环境。该火山岩系以基性火山岩为主,酸性火山岩次之,中性火山岩少见。根据岩石地球化学数据,碧口群裂谷基性熔岩总体上属于低Ti/Y(<500)岩浆类型。元素和同位素数据表明,碧口群基性熔岩的化学变化不是由一个共同的母岩浆的结晶分异作用所产生。它们极有可能是源于地幔柱源(εNd(t)≈+3,87Sr/86Sr(t)≈0.704,La/Nb≈0.7)。地壳混染作用对于碧口群裂谷基性熔岩的形成有重要贡献。我们的研究揭示,碧口群火山岩存在空间上的岩石地球化学变化。东部红岩沟和辛田坝—黑木林地区的碧口群基性熔岩以拉斑玄武岩为主,产生于幔源石榴子石稳定区的高度部分熔融。相反,西部白杨—碧口地区的碧口群基性熔岩的母岩浆则是形成于幔源的尖晶石-石榴子石过渡带:碱性熔岩是产生于部分熔融程度较低的条件下,拉斑玄武质熔岩则是产生于部分熔融条件较高的条件下。它们经受了浅层位辉长岩质(cpx+plag±ol)分离作用,化学变异较大。     

Ca-enrichment in olivines from volcanic rocks

Data are presented on the Ca-content of olivines in a range of volcanic rocks from a variety of suites. These include olivine basalts through to trachytes from Gough, St. Helena and Tristan da Cunha Islands; trachytes from central Victoria, Australia, and a leucitite and phonclitic-tephrite series from Bufumbira, Uganda. In olivine crystals from basaltic lavas the Ca- and Mn-contents are low and Fe shows the most significant zoning from core to rim. In Fe-rich olivines from trachytic differentiates Ca and Mn frequently show more significant variation than Fe. While the Mn-content is proportional to the Fe-content of these olivines, Ca-zoning, in many cases, is unrelated to Fe-content. The marked Ca-enrichment in olivines occurs with the absence of plagioclase in the host lavas. The Ca(Al  Na  K) ratio is shown to be related not only to the Ca-content of the olivines in the lava, but may be used to predict olivine stability in evolved compositions.     

Geochemical Characteristics and Metallogenesis of Volcanic Rocks as Exemplified by Volcanic Rocks in Ertix,Xinjiang

Volcanic rocks in Ertix,Xinjiang,occurring in the collision zone between the Siberia Plate and the Junggar Plate,are distributed along the Eritix River Valley in northern Xinjiang.The volcanic rocks were dated at Late Paleozoic and can be divided into the spilite-keratophyre series and the basalt-andesite series.The spilite-keratophyre series volcanic rocks occur in the Altay orogenic belt at the southwest margin of the Siberia Plate.In addition to sodic volcanic rocks.There are also associated potassic-sodic volcanic rocks and potassic volcanic rocks.The potassic-sodic volcanic rocks occur at the bottom of the eruption cycle and control the distribution of Pb and Zn deposits.The potassic volcanic rocks occur at the top of the eruption cycle and are associated with Au and Cu mineralizations.The sodic volcanic rocks occur in the middle stage of eruption cycle and control the occurrence of Cu(Zn) deposits.The basalt-andesite series volcanic rocks distributed in the North Junggar orogenic belt at the north margin of the Junggar-Kazakstan Plate belong to the potassic sodic volcain rocks.The volcanic rocks distributed along the Ulungur fault are relatively rich in sodium and poor in potassium and are predominated by Cu mineralization and associated with Au mineralization.Those volcanic rocks distributed along the Ertix fault are relatively rich in K and poor in Na,with Au mineralization being dominant.     

Tungsten abundances in some volcanic rocks

A radiochemical N.A.A. method was used to obtain new values on W distribution in some 125 volcanic rocks, mainly basalts and andesites, from different petrotectonic environments.These W data are below previously reported abundances. New median values in various types of rocks are suggested (ppm W). Basalts: ocean floor, 0.15; ocean islands subalkaline, 0.28; ocean islands alkaline, 0.60; island arc, 0.19: continental margin, 0.40; continental subalkaline, 0.30: continental alkaline, 1.35. Andesites: island arc, 0.23; continental margin, 1.05.Median values for all 91 basalts and all 20 andesites are 0.36 and 0.29 ppm respectively.     

Tin distribution in mid-Andean volcanic rocks

Volcanic rocks of the Rhyolite and Andesite Formations from the Central Andes (Chile, Argentina, Bolivia) have been analyzed for tin. Mean values of tin in rhyolitic rocks from Chile and Argentina are about 2 ppm, from the Bolivian Altiplano 3 ppm, and from the Bolivian Eastern Cordillera 4, 5 ppm. This means that an elemental increase of regional scale towards the Bolivian tin province exists.     

Clinoenstatite in volcanic rocks from the Bonin Islands

Multiply-twinned clinoenstatite has been found in andesitic rocks from Chichi-jima and Mukojima in the Bonin Islands.The clinoenstatite occurs as (1) reaction rims around olivine, (2) composite crystals with bronzite, and (3) anhedral phenocrysts rimmed or included by bronzite.The clinoenstatite is chemically characterized by low contents of Ca (less than 0.5 wt.% oxide), Fs (9.2–11.5) and Al (less than 0.6 wt.% oxide) relative to the coexisting bronzite. The partition coefficient, K _{D op} ^cp =(Mg/Fe²⁺)^cp/(Mg/Fe²⁺)^op between coexisting clinoenstatite and bronzite, ranges from 1.02 to 1.32 (average 1.17). The Fe²⁺/Mg+Fe²⁺ ratios of coexisting clinoenstatite and bronzite are different in different rock types, which suggests variable inversion temperatures of protoenstatite to orthopyroxene in boninite.Bronzite phenocrysts in a specimen, ranging from Fs15 to Fs30, coexist with augite phenocrysts, whereas those in the other specimens, ranging from Fs12 to Fs18, do not coexist with augite phenocrysts. These differences in petrographical nature and mineral chemistry among the specimens examined may be due to variations in their quenching stages.The boninite clinoenstatite and bronzite are relatively rich in Ca and Mg, compared with the Papuan and Mariana pyroxenes, which seems to depend upon the rock chemistry.     

Possible reasons for elevated fluorine concentrations in groundwaters of carbonate rocks

The concentration of dissolved F did not change in long-term (four months) experiments on the interaction of crushed limestone and marl with water (at R/W = 1) at room temperature. The comparison of the activity products and equilibrium constants of the mineral dissolution reactions indicates that the experimental solutions were undersaturated with respect to fluorite and oversaturated with respect to F-apatite. The long-term existence of such unequilibrated solutions is explained by the steady state of the system at which the primary F-bearing mineral (fluorite, mica, or palygorskite) is transformed into a secondary one (F-apatite). The dissolved F concentration is controlled under these conditions by the ratios of the dissolution reaction rates for the primary mineral and the precipitation rate of the secondary one. In the experiments with the association fluorite + calcite + dolomite (duration up to seven months), the solution was saturated with respect to these minerals. Their dissolution constants were utilized to derive dependences of the activity of the dissolved F ion on the activities of the Ca, Mg, and carbonate ions in the solutions. The experimental data are consistent with these dependences. If the solution is saturated with respect to gypsum, the activity of the dissolved F ion should also depend on one more parameter: the activity of the sulfate ion.     

Compositions of immiscible liquids in volcanic rocks

Immiscible liquids, preserved as chemically distinct, glassy globules, (Si-rich and Fe-rich) occur in many tholeiitic basalts and some alkaline and calcalkaline lavas. The glasses typically form part of a dark mesostasis containing skeletal magnetite crystals. In thick flows, the Si-rich liquid may crystallize to granophyric patches, and the Ferich one to aggregates of hedenbergite, magnetite, and accessory phases. The mesostases containing these immiscible phases constitute from 20% of a primitive olivine tholeiite (MgO=7.5%) to 50% of a highly fractionated quartz tholeiite (MgO=2.8%), but may be less if the rock is oxidized. Abundant ferric iron promotes early crystallization of magnetite and prevents the iron enrichment necessary to reach the immiscibility field; thus, aa flows rarely exhibit immiscibility, whereas the more reduced pahoehoe ones do.Alumina and alkalis are concentrated in the Si-rich liquid, whereas the remainder of the major elements are concentrated in the Fe-rich melt; but the partitioning of Fe, Mg, Ca, and P is less pronounced in alkaline rocks than in tholeiites. Conjugate liquids have compositions of granite and Fe-rich pyroxenite, though the Si-rich melt in alkaline rocks is more syenitic and the Fe-rich one contains considerable normative alkali feldspar. The liquids coexist with plagioclase and augite of, respectively, An₅₀ and Ca₃₄Mg₁₉Fe₄₇ compositions in tholeiites, and An₄₀ and Ca₄₂Mg₂₉Fe₂₉ in alkaline rocks. Immiscibility is not restricted to K-rich residual liquids, but the miscibility gap is narrower for Na-rich compositions. In tholeiitic basalts with 52% SiO₂, the Na₂O/K₂O ratios in conjugate liquids are equal, but at lower silica contents the Si-rich liquid is relatively more sodic, whereas at higher silica contents it is relatively more potassic. This may explain the association of sodic granites with mid ocean ridge basalts.Immiscible liquids are present in sufficient amounts in so many volcanic rocks that magma unmixing should be considered a viable means of differentiation during the late stages of fractionation of common magmas, at least at low pressures.     

下庄铀矿田火山岩的厘定及与周边同期火山岩的对比

本在系统分析下庄铀矿田火山岩的分布，火山岩系的旋回性，火山岩的岩石地球化学特征及火山岩的成岩时代等特征的基础上，较为详细地对下庄铀矿田的火山岩和赣南－粤北地区晚中生代武夷群火山岩各种特征进行了对比，厘定了下庄铀矿田火山夺为赣地－粤北地区晚中生代中火山岩系武夷群的组成部分；认为南岭铀成矿带今后寻找富矿，大矿的主要目标应该放在火山侵本和后火山侵入体的内外接触带上，以早期铀矿化（140－100Ma）为的主要目标类型。