Mineral systems,their types,and distribution in nature. I. Khibiny,Lovozero, and the Mont Saint-Hilaire

In accordance with the set of species-defining chemical elements in minerals, n-component systems (where n = 1, 2, 3, 4, 5, 6, 7, 8, 9, 10) for all mineral species (4952) known to 2014 inclusive were distinguished. Seventy chemical elements have been established to be species-defining, which are distributed by mineral systems as follows: 1 (29), 2 (62), 3 (68), 4 (61), 5 (61), 6 (55), 7 (49), 8 (38), 9 (28), and 10 (19). The number of mineral species in which certain chemical elements are species-defining has been specified. Oxygen (4041), hydrogen (2755), silicon (1448), calcium (1139), sulfur (1025), aluminum (960), iron (917), sodium (914), copper (616), phosphorous (580), arsenic (575), and magnesium (550) are the leading elements in minerals in the Earth’s crust. It has been found that the most species-defining elements are normally distributed by mineral systems. The distributions of mineral species in various systems from the Khibiny and Lovozero, Kola Peninsula, Russia; and Mont Saint-Hilaire, Quebec, Canada peralkaline plutons were compared and the characters of species-defining element distribution in these localities were compared. Si, Na, K, C, F, Ti, Ce, Zr, Nb, Sr, and Th are “excess” species-defining elements in minerals from the plutons compared to the total number of mineral species, whereas S, Cu, Pb, Cl, B, Te, Ag, Ni, and Be are “scarce” elements.     

Mineral Systems,Their Types,and Distribution in Nature: 2. Products of Contemporary Fumarole Activity at Tolbachik Volcano (Russia) and Vulcano (Italy)

The number of mineral species in which a certain chemical element is species-defining (according to statistical data up to 2015) has been specified. Seventy chemical elements are species-defining for 5044 minerals. The following chemical elements lead in the composition of minerals (number of mineral species in parentheses): oxygen (4115), hydrogen (2800), silicon (1471), calcium (1167), sulfur (1056), aluminium (985), sodium (949), iron (945), copper (636), phosphorus (597), arsenic (594), and magnesium (571). The distribution of mineral species by various systems in the products of contemporary fumarole activity at two volcanoes, Tolbachik in Kamchatka, Russia, and Vulcano in Sicily, Italy, has been compared. These locations were also compared for the distribution of species-defining elements. Thus, it has been determined that in fumaroles of both volcanoes, Tl, S, Cl, F and Na are “excessive,” present in minerals in elevated amounts, whereas H, Ca, Fe, and Mn are “deficient.” The abundance of Cu, Se, V, Mg, Zn, As, and F in minerals at Tolbachik is higher than the global mean values of these elements in the Earth’s crust, whereas the abundance is significantly lower at Vulcano. Sn, I, Br, K, Pb, Al, Fe, and Bi demonstrate the opposite behavior. Comparison of the Yadovitaya and Arsenatnaya fumaroles at the Tolbachik volcano showed that the products of the former are richer in H, Cl, Cu, S, K, O, Al, Fe, and Pb, and poorer in As, Ca, Mg, and Na as species-defining elements. In addition, V-and Mo-bearing minerals are found only at Yadovitaya, whereas minerals containing F, Ti, В, Те, and Zn are known only at Arsenatnaya.     

蒸发岩非传统稳定同位素研究综述

蒸发岩是海水/卤水蒸发浓缩的产物,不同的水化学环境下析出的蒸发岩类型不同,其在不同的地质历史时期都有分布,是重要的古海水和古环境记录载体。蒸发岩研究的主要问题包括:蒸发岩的物质来源、形成时代、蒸发盆地和卤水的演化历史、蒸发岩矿物所记录的环境变化。一些矿物、元素及同位素指标可用于解决这些问题,其中稳定同位素对于示踪蒸发岩的物质来源与形成过程具有不可替代的作用。近20年来,非传统稳定同位素地球化学获得快速发展,并在蒸发岩研究中获得成功应用,这些同位素体系包括阴离子元素B、Cl和Br,以及阳离子元素Mg、K和Ca。本文综述了多个非传统稳定同位素在蒸发岩领域的研究,主要包括:蒸发岩矿物与溶液之间的同位素分馏系数、蒸发岩的同位素信息重建古海水同位素组成及示踪蒸发岩成因和时代等。     

Geochemistry of banded iron formation of Orissa,India

Major and trace element analyses of representative samples of various types of banded iron-formation and its various minerals, associated sediments, iron ores and volcanic tuff from different localities of Orissa, India, are presented in this paper. The Orissa banded iron-formation is classified as Precambrian banded iron formation and is similar to the oxide facies iron formation of Lake Superior type. The Orissa iron formation consists only of iron oxide and silica with total absence of iron silicate, sulfide and carbonate minerals, and is devoid of terrigenous material. The trace element content suggests the source of the underlying quartzite to be a continental igneous rock mass, while the interbedded tuff are of undoubted volcanic origin. The overlying iron formation were chemically precipitated as oxidate sediments in which the principal iron mineral — magnetite — was formed at low temperature in a shallow marine environment. From the overwhelming similarity of major and trace element contents of all the samples from the different localities, it is postulated that these detached outcrops originated in the same continous basin.     

Indicator mineralogy of kimberlite boulders from eskers in the Kirkland Lake and Lake Timiskaming areas, Ontario, Canada

Sixteen kimberlite boulders were collected from three sites on the Munro and Misema River Eskers in the Kirkland Lake kimberlite field and one site on the Sharp Lake esker in the Lake Timiskaming kimberlite field. The boulders were processed for heavy-mineral concentrates from which grains of Mg-ilmenite, chromite, garnet, clinopyroxene and olivine were picked, counted and analyzed by electron microprobe. Based on relative abundances and composition of these mineral phases, the boulders could be assigned to six mineralogically different groups, five for the Kirkland Lake area and one for the Lake Timiskaming area. Their indicator mineral composition and abundances are compared to existing data for known kimberlites in both the Kirkland Lake and Lake Timiskaming areas. Six boulders from the Munro Esker form a compositionally homogeneous group (I) in which the Mg-ilmenite population is very similar to that of the A1 kimberlite, located 7–12 km N (up-ice), directly adjacent to the Munro esker in the Kirkland Lake kimberlite field. U–Pb perovskite ages of three of the group I boulders overlap with that of the A1 kimberlite. Three other boulders recovered from the same localities in the Munro Esker also show some broad similarities in Mg-ilmenite composition and age to the A1 kimberlite. However, they are sufficiently different in mineral abundances and composition from each other and from the A1 kimberlite to assign them to different groups (II–IV). Their sources could be different phases of the same kimberlite or—more likely—three different, hitherto unknown kimberlites up-ice of the sample localities along the Munro Esker in the Kirkland Lake kimberlite field. A single boulder from the Misema River esker, Kirkland Lake, has mineral compositions that do not match any of the known kimberlites from the Kirkland Lake field. This suggests another unknown kimberlite exists in the area up-ice of the Larder Lake pit along the Misema River esker. Six boulders from the Sharp Lake esker, within the Lake Timiskaming field, form a homogeneous group with distinct mineral compositions unmatched by any of the known kimberlites in the Lake Timiskaming field. U–Pb perovskite age determinations on two of these boulders support this notion. These boulders are likely derived from an unknown kimberlite source up-ice from the Seed kimberlite, 4 km NW of the Sharp Lake pit, since indicator minerals with identical compositions to those of the Sharp Lake boulders have been found in till samples collected down-ice from Seed. Based on abundance and composition of indicator minerals, most importantly Mg-ilmenite, and supported by U–Pb age dating of perovskite, we conclude that the sources of 10 of the 16 boulders must be several hitherto unknown kimberlite bodies in the Kirkland Lake and Lake Timiskaming kimberlite fields.     

Spatial distribution of some elements and elemental contamination in the sediments of Köyceğiz Lake (SW Turkey)

Elemental accumulation, distribution and relationship profiles for sediment samples taken at 81 localities in the Köyce?iz Lake were investigated. Spatial distribution maps for ten elements (Cu, Pb, Zn, Ni, Cr, Co, Mn, Mo, Al, Fe) were created using the ordinary kriging interpolation method. Statistical tests revealed that the sediments taken from areas close to the Namnam (NamSM) and Karg?cak (KarSM) stream mouths have the highest element content. In addition, sediments close to NamSM have the highest contamination, according to contamination degree and modified contamination degree values. On the other hand, sediments close to KarSM have the highest value on the pollution load index. The enrichment factor and contamination factor values of Cr and Co, and especially Ni, close to NamSM are striking and have significantly higher values compared to the rest of the lake. There are strong correlations between these three elements, which were also confirmed by cluster analysis. Ni is the element having the highest value on the geoaccumulation index. In addition, according to the toxic unit results, it was found that 84–89% of the element-based toxic effect in the lake is due to Ni alone. According to the mean effect range median quotient values, the sediments of Köyce?iz Lake have a potential to show toxic effects of at least 76% in living organisms, which is due to the high levels of Ni. According to the mean probable effect low quotient value, it has been determined that Köyce?iz Lake is at a “highly impacted” level, which is the worst possible value on the quality scale.     

Modern Bottom Sediments of Lake Onega: Structure,Mineralogical Composition,and Systematization of Rare-Earth Elements

The results of studying the structure and mineral composition of the Upper Holocene bottom sediments of Lake Onega are presented. It is established that there are two types of columns of bottom sediments, for which stratification of layers and formation of Fe–Mn crusts are determined by the diagenesis processes occurring under physicochemical conditions of sediment accumulation according to two scenarios. The distribution spectra of rare-earth elements (REEs) are different in the indicated types of columns, which is apparently attributed to the differences in the oxidation–reduction conditions at the water–sediment interface during the formation of REEs and possibly to the influence of hydrothermal processes.     

和田软玉的化学成分和显微结构研究

采用场发射扫描电子显微镜（FE-SEM）系统对产自新疆和田的软玉样品的主要矿物组成、化学成分、显微结构等进行了较详细的研究,并与产自中国青海、辽宁、河南及韩国的软玉样品进行了比较。结果表明,各产地软玉样品的矿物组成、化学成分和显微结构有一定的差异。和田软玉样品中含有镁质绿泥石,而辽宁软玉样品中含有较多的闪锌矿,青海软玉样品中有含Zr元素矿物的颗粒,河南软玉样品中有含La与Ce元素较高矿物的颗粒;对纯度较高的软玉样品,仅依靠主成分很难区分其产地,但依靠其微量元素成分却能起到较好的鉴别作用;和田软玉样品中透闪石的显微结构较致密,纤维尺寸要小于其它产地软玉样品的。以上信息对确定软玉的产地具有较好的参考意义。     

Gold distribution and lithogeochemical discrimination of residual regolith and transported overburden,Minotaur gold deposit,Lake Lefroy,Western Australia

Abstract

The Yilgarn Craton of Western Australia hosts a number of Cenozoic paleochannels, which have been incised into the underlying Paleozoic and Precambrian rocks, filled with sediments and subsequently weathered. The paleochannels are of particular interest in mineral exploration as they may not only host placer-type deposits but also overlie significant supergene and primary mineralisation. Paleochannels also pose particular challenges during exploration as they mask underlying geochemical anomalies, including gold and pathfinder elements. This study investigates a method of distinguishing transported overburden from residual regolith utilising a combination of field and laboratory-based techniques. At the Minotaur deposit, the residual regolith and transported overburden are mineralogically similar, although the presence of biotite, chlorite and muscovite is more characteristic of the residual regolith. Geochemically, Zr, Ti, Co and Sc ratios form distinct groupings allowing more confident discrimination of transported overburden from the underlying residual regolith units. The presence of a distinct gold depletion zone at the redox front was also identified to be a feature of the Minotaur deposit, with Au enrichment occurring above (within transported overburden) and below (within saprolite) the redox front, similar to other gold deposits on Lake Lefroy. The lithological, stratigraphic and Au-enrichment characteristics at Minotaur have also been compared with regional studies and suggest the long-lived impact of paleovalleys on the depositional systems and Au distribution of Lake Lefroy. This work provides a basis for future studies of the region in particular the variation of depositional sequences within regional paleochannel networks.     

Petrogenesis of Monte Vulture volcano (Italy): inferences from mineral chemistry,major and trace element data

The paper presents major and trace element data and mineral compositions for a series of foiditic-tephritic to phonolitic rocks coming from Monte Vulture, Southern Italy, and investigates their origin, evolution and relationship with the other centres of the Roman province.Major and trace element variation in the foiditic to tephritic suite agrees with a hypothesis of evolution by simple crystal/liquid fractionation, whereas the early erupted phonolitic trachytes and phonolites have geochemical characteristics which do not support their derivation from tephritic magma by crystal fractionation. Foiditic and phonolitic rocks have mineral compositions which are interpreted as indicating magma mixing. However geochemical evidence shows that this process did not play an important role during the magma evolution.The Vulture rocks have compositional peculiarities such as high abundance of Na₂O, CaO, Cl and S, when compared with other Roman volcanics. Instead, the distribution of incompatible elements is similar to those of Roman rocks, except for a lower content of Rb and K, higher P and lower Th/Ta and Th/Nb ratios which are still close to the values of arc volcanics.The high contents of Na, Ca and of volatile components are tentatively attributed to the interaction of magma with aqueous solutions, rich in calcium sulphate and sodium chloride, related to the Miocene or Triassic evaporites occurring within the sedimentary sequence underlying the volcano. The distribution pattern of the incompatible elements is interpreted as indicative of magma-forming in a subduction modified upper mantle and of the peculiar location of M. Vulture.     

山西省热矿水形成机制分析

本文以系统理论为指导，在深入研究地质北景的基础上，通过研究热矿水的含水介质，水动力场，水化学物和温度场的特征，划分了热矿水系统，探讨了热矿水的起源及形成机制，将山西热矿水的形成归纳为异常增温型和正常增温型两种基本模式，异常增温型又根据地质结构的不同，地下水径流条件的差异，列举了三种典型模式，最后指出了寻找热矿水的方向，开发利用热矿资源应注意的问题。     

Major element chemistry of the Huai River basin, China

The chemistry of major ions (Ca, Mg, Na, K, HCO₃, SO₄, Cl and Si) in the water of the Huai River basin was studied, based on samples from 52 sites from nine different water bodies in July 2008. Ions and total dissolved solids (TDS) displayed clear spatial patterns with lower concentrations in the south and higher in the north of the basin; the same conditions were also found in the East Line of South-North Water Transfer Project (SNWTP) in this region. The Huai River main channel and Hongze Lake have moderate ion concentrations relative to the whole basin. TDS concentrations versus the weight ratios of Na/(Na + Ca) and ternary ions demonstrate that the southern rivers (Shi R. and Pi R.) are mainly controlled by the weathering of carbonates, whereas the northern water systems (Guo R., Shaying R., Nansi Lake and its tributaries) are dominated by the weathering of evaporites. The Huai River main channel, Hongze Lake and the East Line of SNWTP are synergistically influenced by weathering of evaporites and carbonates, yet Hongze Lake and the East Line of SNWTP are mainly controlled by evaporation and crystallization processes. This study also confirmed that the Huai River is the geographic division between southern and northern China. Most rivers of this basin have very high ionic composition relative to the global median and other world rivers. The spatial patterns and ionic composition also suggest that intensive anthropogenic activities in northern areas of this basin are well characterized. A comparison with WHO and Chinese standards for drinking water indicates that the northern water systems of this basin are not suitable for use as drinking water sources, and pollution control should be improved and enhanced in northern areas of the basin.     

Formation and chemical evolution of magnesium chloride brines by evaporite dissolution processes—Implications for evaporite geochemistry

The evolution of magnesium chloride brines with high bromide contents via a multistage reaction and dissolution process has been studied in brine seeps of a German potash mine. The observed chemical trends and phase equilibria can be modeled and interpreted in terms of a NaCl solution (cap rock brine) infiltrating into a potash zone characterized by the metamorphic mineral assemblage kieserite + sylvite + halite + anhydrite. Establishment of a persistent, stable equilibrium assemblage and constant fluid composition in the invariant point IP1 of the six component (Na-K-Mg-Ca-Cl-SO₄-H₂O) system of oceanic salts is prevented by the perpetually renewed input of NaCl-brine and by the intermittent exposure of incompatible kieserite. Instead, the solutions develop towards the metastable invariant point IP1(gy), with the mineral assemblage carnallite + polyhalite + sylvite + halite + gypsum, where gypsum takes the place of anhydrite (stage I). The temporary exposure of kieserite and the ensuing formation of polyhalite effectively buffer the solutions along the metastable polyhalite phase boundary during stages II and III. Eventually, in stage IV, polyhalite becomes depleted and admixture of more NaCl brine leads to low sulfate solution compositions, which are now only constrained by carnallite + sylvite + halite, and the once hexary system degenerates to a quaternary one (Na-K-Mg-Cl-H₂O) in point E. Bromide in brines shows equilibrium partitioning with respect to the wall rock minerals. The pattern of evolving brine compositions may serve as a model for similar brine occurrences, which in some cases may have been misinterpreted as remains of fossil, highly concentrated and chemically modified seawater. Similar magnesium chloride brines of salt lakes (e.g., Dead Sea, Dabusun Lake) show subtle differences and are constrained by fewer mineral equilibria (more degrees of freedom), and their low sulfate contents are due to gypsum precipitation, driven by calcium chloride input from dolomitization reactions. Finally, the observed reaction sequence is generalized, and a model for the formation of magnesium sulfate depleted, chloride-type potash salts and bischofite deposits by leaching of sulfate-type evaporites is proposed.     

中安第斯地区蒸发岩矿床成矿作用特征及构造背景

在中安第斯高原,包括玻利维亚西部、智利东部、阿根廷北部分布众多的盐湖,湖中含丰富的B、K、Li、Mg和其他蒸发盐类物质,封闭的盆地因蒸发作用使残留盐水中的成矿元素聚集并沉淀。这些矿床的形成与安第斯山的隆起和气侯变化关系密切。通过对该区蒸发岩型矿床的分布特征及成矿特征进行研究,讨论其形成的构造背景,分析成矿要素和找矿方向。     

The Distribution of Redox Sensitive Elements (U, As, Sb, V and Mo) along a River-Wetland-Lake System (Balaton Region, Hungary)

The distribution of redox sensitive elements (U, As,Sb, Mo and V) has been investigated in Lake Balatonand two man-made reservoirs (Lake Kis-Balaton-1 andKis-Balaton-2) built along the River Zala, the mainriver discharging into it. These elements underwentremoval in Lake Kis Balaton-2 (KB-2) during anoxicconditions (May and September).Similarities were found between the distributions ofdissolved As and Sb. Both elements had elevateddissolved concentrations in Lake Kis-Balaton-1 (KB-1)and in Lake Balaton in September. This increasedmobility could be due to a change of speciation (viareduction and the formation of methylated species).Such changes in speciation are well documented in theliterature and are generally enhanced during periodsof warmth and high primary productivity.Dissolved V and Mo distributions also showedsimilarities with higher concentrations in LakeBalaton than in other parts of the system.Although removal is not clearly detected from thedissolved concentrations, U, As, Sb and Mo aresignificantly enriched in the organic-rich sedimentsof Lake KB-1, while V is mainly associated with thealumino-silicate fraction. In Lake KB-1, theconcentrations of all elements in SPM (suspendedparticulate matter) are lower than in the depositedsediments (except for As) suggesting that enrichmentprocesses are occuring in the deposited sediments.Additionnally the cycling of As and Mo can be alsopartly controlled by uptake and scavenging processesin the water column, as suggested by the elevated Asand Mo concentrations observed in SPM seasonnally forAs in Lake KB-1 and at Z.mouth-1 station and for Mo atZ.mouth-1 station and Lake Balaton.     

西藏尼雄地区水系沉积物地球化学特征及异常分布规律

西藏尼雄地区位于拉达克—冈底斯拉萨—腾冲陆块,区内已发现尼雄特大型富磁铁矿、日阿中型铜多金属矿等矿床.文章以1：5万水系沉积物地球化学调查为基础,总结水系沉积物地球化学特征及分布规律.研究发现区内成矿作用与亲铜元素和铁族元素有关,二叠系昂杰组、拉噶组是区内金矿的有利地层,敌布错组是寻找银、锌、铅、镉矿产的最佳地层,所圈化探异常与已有矿（化）点区域套合较好.     

Early and pervasive dolomitization by near-normal marine fluids: New lessons from an Eocene evaporative setting in Qatar

The upper Palaeocene–lower Eocene Umm er Radhuma Formation in the subsurface of Qatar is dominated by subtidal carbonate depositional packages overlain by bedded evaporites. In Saudi Arabia and Kuwait, peritidal carbonate depositional sequences with intercalated evaporites and carbonates in Umm er Radhuma have been previously interpreted to have been dolomitized via downward reflux of hypersaline brines. Here, textural, mineralogical and geochemical data from three research cores in Qatar are presented which, in contrast, are more consistent with dolomitization by near-normal marine fluids. Petrographic relationships support a paragenetic sequence whereby dolomitization occurred prior to the formation of all other diagenetic mineral phases, including chert, pyrite, palygorskite, gypsum, calcite and chalcedony, which suggests that dolomitization occurred very early. The dolomites occur as finely crystalline mimetic dolomites, relatively coarse planar-e dolomites, and coarser nonplanar dolomites, all of which are near-stoichiometric (50.3 mol% MgCO₃) and well-ordered (0.73). The dolomite stable isotope values (range −2.5‰ to +1‰; mean δ¹⁸O = −0.52‰) and trace element concentrations (Sr = 40 to 150 ppm and Na = 100 to 600 ppm) are compatible with dolomitization by near-normal seawater or mesohaline fluids. Comparisons between δ¹⁸O values from Umm er Radhuma dolomite and the overlying Rus Formation gypsum further suggest that dolomitization did not occur in fluids related to Rus evaporites. This study provides an example of early dolomitization of evaporite-related carbonates by near-normal seawater rather than by refluxing hypersaline brines from overlying bedded evaporites. Further, it adds to recent work suggesting that dolomitization by near-normal marine fluids in evaporite-associated settings may be more widespread than previously recognized.     

Evolution of the upper mantle beneath the southern Baikal rift zone: an Sr-Nd isotope study of xenoliths from the Bartoy volcanoes

Anhydrous and amphibole-bearing peridotite xenoliths occur in roughly equal quantitites in the Bartoy volcanic field about 100 km south of the southern tip of Lake Baikal in Siberia (Russia). Whole-rock samples and pure mineral separates from nine xenoliths have been analyzed for Sr and Nd isotopes in order to characterize the upper mantle beneath the southern Baikal rift zone. In an Sr-Nd isotope diagram both dry and hydrous xenoliths from Bartoy plot at the junction between the fields of MORB and ocean island basalts. This contrasts with data available on two other localities around Lake Baikal (Tariat and Vitim) where peridotites typically have Sr–Nd isotope compositions indicative of strong long-term depletion in incompatible elements. Our data indicate significant chemical and isotopic heterogeneity in the mantle beneath Bartoy that may be attributed to its position close to an ancient suture zone separating the Siberian Platform from the Mongol-Okhotsk mobile belt and occupied now by the Baikal rift. Two peridotites have clinopyroxenes depleted in light rare earth elements (LREE) with Sr and Nd model ages of about 2 Ga and seem to retain the trace element and isotopic signatures of old depleted lithospheric mantle, while all other xenoliths show different degrees of LREE-enrichment. Amphiboles and clinopyroxenes in the hydrous peridotites are in Sr–Nd isotopic disequilibrium. If this reflects in situ decay of ¹⁴⁷Sm and ⁸⁷Rb rather than heterogeneities produced by recent metasomatic formation of amphiboles then 300–400 Ma have passed since the minerals were last in equilibrium. This age range then indicates an old enrichment episode or repeated events during the Paleozoic in the lithospheric mantle initially depleted maybe 2 Ga ago. The Bartoy hydrous and enriched dry peridotites, therefore, are unlikely to represent fragments of a young asthenospheric bulge which, according to seismic reflection studies, reached the Moho at the axis of the Baikal rift zone a few Ma ago. By contrast, hydrous veins in peridotites may be associated with rift formation processes.     

元素在不同自然体系的分布:偶数规则之后,还有一个普遍规律——以类地行星为例

在地球化学、天体化学乃至宇宙化学领域中,有一个应用十分广泛的著名的偶数规则(即Oddo-Harkins规律),该规律认为,元素在太阳系分布中,原子序数为偶数的元素丰度通常会比相邻的两个奇数元素丰度值高.通过研究发现,化学元素在宇宙不同自然体系中分布与分配,至少对非亲气元素而言,在统计上还呈周期性变化,而这种周期性变化恰好和元素周期律吻合.而偶数规则也和元素周期性变化规律存在着某种深刻的联系,实际上是同一地球化学现象不同侧面的反映.以地球和金星等自然体系的化学元素质量丰度的比值为例,说明任意两个自然体系,其形成与演化的历程、机制、程度、条件以及物质的来源和化学构成愈是接近,二者之间的元素比值的变化波形就愈符合元素周期律.定量地确定元素在自然体系中分布/分配曲线对元素周期性变化曲线的吻合程度.元素在自然体系分布上的元素周期性变化规律的发现及其量化描述的实现,为更科学地、精确地计算、校验和获取自然体系中化学元素的一些基础数据,提供了一个全新的思路.      

Evolution of late Triassic rift basin evaporites (Passaic Formation): Newark Basin, Eastern North America

The Passaic Formation of the late Triassic Newark Supergroup is 2700 m thick and was deposited in series of wide, deep to shallow lacustrine environments in the Newark rift basin (eastern North America). The Passaic Formation can be divided into lower, middle, and upper sections based on depositional structures, composition and the distribution and morphology of its evaporites. Evaporites formed as a result of syndiagenetic cementation and/or displacive processes. Evaporitive minerals now include gypsum and anhydrite, although other mineral species, such as glauberite, may have originally existed. Most of the evaporites of the Passaic Formation occur within massive red mudstone and siltstone lithologies in the form of diffuse cements, void-fillings, euhedral crystals, crystal clusters and nodules. These evaporites grew displacively within the fine siliciclastic matrix as a result of changes in the hydrochemical regimes of the rift basin. A well-developed upward increase in the amount of evaporite material is present in the Passaic Formation. This resulted from: (1) long-term, progressive increase in aridity, and (2) significant increase in evaporation surface area of the basin during its tectonic evolution. A nonmarine source for the evaporites is evident from the isotopic data. Sulphate δ³⁴S ranges from 11%. to 3.3%. CDT, while δ¹⁸O ranges from + 15.1%. to + 20.9%. SMOW, indicating derivation from early diagenetic oxidation of organic sulphur and pyrite within the organic-rich, lacustrine deposits. The ⁸⁷Sr/⁸⁶Sr ratios in sulphate are radiogenic (average 0.71211), showing the interaction of basin waters with detrital components and that the Newark Basin was isolated from the world ocean. Most of the original evaporites show evidence of diagenetic change to polycrystalline and polymineralic pseudomorphs now filled with recrystallized coarse-grained anhydrite (1–3 mm size) and low-temperature albite. Homogenization temperatures of fluid inclusions within the coarse-grained anhydrite indicate crystallization temperatures for anhydrite in the range of 150° to 280°C. Such elevated temperatures resulted from circulation of hot water in the basin. Later exhumation of these rocks caused partial to total replacement of anhydrite by gypsum in the upper part of the section. The resulting increase in volume due to hydration of anhydrite at shallow depths also emplaced non-evaporative satin-spar veins (fibrous gypsum) along bedding planes and in fractures. While the local geology of the Newark rift basin controlled the distribution of facies, the sedimentological development of the Passaic Formation evaporites resulted from the world-wide climatic aridity that prevailed during the late Triassic. because the Newark Basin sequence was only covered with about 3 km of sedimentary overburden that correspond to about 100°C and hence suggests that evaporites have experienced alteration by hot fluids. 5 As the Triassic marks the greatest evaporite formation world-wide and profound sense of parched continentality throughout the world existed before the final break-up of the Pangea, the Passaic Formation evaporites are an example of the influence of these palaeoclimatic conditions at the eastern margin of North America.