中国东部主要成矿时代磷块岩的组成

本文研究了我国震旦、寒武纪磷块岩的矿石岩石学,主要矿石矿物为碳氟磷灰石,重要伴生矿物为伊利石,白云石和自生石英。磷块岩的化学组成有三个显著特点,一是品位随矿石类型的不同而异;二是随成矿域不同而异;三是随成矿时代不同而异。成矿背景,成矿环境、磷块岩相以及矿石组成等因素的差异是导致上述矿石组成变化的主要原因。     

Uranium in supergene phosphorites

The distribution of uranium was studied in supergene phosphorites from the zones of the weathering of sedimentary and endogenous rocks, as well as in nonmarine coprolitic phosphorites and, to a lesser extent, phosphorites from ocean islands. These phosphorites show a diversity of the composition of their carbonate-apatite and structural characteristics. The uranium content ranges mostly from 5 to 100 ppm, with minimum and maximum values of 0.5 and 790 ppm. There is no correlation between the uranium content of a phosphorite and the type of rock with which it is connected. Lacustrine coprolitic phosphorites show elevated uranium contents (about 200 ppm). The maximum uranium content was detected in finely laminated phosphorite encrustations. The correlation analysis of the whole data set (63 samples) showed that uranium content is not correlated with any other component of phosphorites at a confidence level of 0.95. In contrast, there is a correlation between U and P₂O₅, CaO, and F for the combined set of samples from southern Siberian deposits. The significant correlation of U with Na₂O and CO₂ is variable both for southern Siberia on the whole and for particular deposits from this region.     

A comparative study of Pleistocene phosphorites from the continental slope off western India

Two types of phosphorite recovered from the continental slope off western India are described. The first type, phosphorite 1, comprises a hard, grey nodule composed of carbonate fluorapatite (CFA) and calcite as major minerals. The phosphorite consists of light‐brown microcrystalline apatite containing a few skeletal fragments and planktonic foraminifera. Scanning electron microscope (SEM) studies show evidence of dissolution of skeletal calcite and filling of the resulting cavities by phosphate composed of ovoid to rod‐shaped apatite microparticles. Apatite also occurs as coatings on these particles. The P₂O₅ content of the phosphorite is 29%, and the CO₂ content of the CFA is about 4·5%. The rare‐earth element (REE) abundance (ΣREE=2·02 μg g^–1) is lower than in other modern phosphorites. The ⁸⁷Sr/⁸⁶Sr ratio and ?Nd value of this sample are 0·70921 and –9·9 respectively. The ¹⁴C age found through accelerator mass spectrometry (AMS) dating (18 720 ± 120 years BP) is much younger than that determined by the U‐series method (100 ka). The second type, phosphorite 2, comprises a friable, light‐brown nodule consisting of CFA as the only major mineral, with a CO₂ content of the CFA of 4·5%. In thin section, the phosphate is light brown and homogeneous, and a few bone fragments are present. The P₂O₅ content is 33%, and REE contents (ΣREE = 0·18 μg g^–1) are lower than in phosphorite 1. The age of phosphorite 2 is >300 ka. Phosphorite 1 appears to have formed during the late Pleistocene through replacement of carbonate by phosphate; phosphorite 2 is also of Pleistocene age but is much older than phosphorite 1. The initial substrate for phosphorite 2 was a fish coprolite, which was subsequently phosphatized during slow sedimentation under low‐energy conditions. Microbial mediation is evident in both phosphorites. The colour, density and P₂O₅ content of the phosphorites are found to be dependent on the nature of the initial substrates and physico‐chemical conditions during phosphatization. The CO₂ content of the CFA is not related to the precursor carbonate phase. The nature of sediments, rates of sedimentation and the time spent undergoing phosphogenesis at the sediment–water interface may control REE concentrations in phosphorites.     

Precambrian phosphorites in the Bijawar rocks of Hirapur-Bassia areas,sagar district,madhya pradesh,India

The Precambrian phosphorites of Bijawar Group of rocks show characteristics of a epicontinental sea with restricted and very shallow marine environment of formation along some shoals, which existed during the iron-rich Precambrian times. These phosphorite deposits located in the Hirapur-Bassia areas show extensive leaching of carbonate and phosphate minerals during episodes of weathering. X-ray diffraction studies indicated that carbonate-flourapatite is the major apatitic phase in these phosphorites while crandallite developed on the surface outcrops. There is a general tendency for the depletion of CO₂ in these apatites leading to formation of flourapatite. This CO₂ is an indicator of hidden weathering in the rocks. Major and trace element determinations of phosphorite have been used to indicate various correlation factors responsible for the concentration of elements in these Precambrian leached phosphorites.The paper is a contribution to the aims and objectives of IGCP Project 156The paper is dedicated to Prof. Dr. R. C. Misra, who as a teacher and guide had been a source of inspiration to the senior author for the last two decades     

Mineralogical and geochemical evidence for multi-stage origin of mineral veins hosted by teschenites at Tichá, Outer Western Carpathians,Czech Republic

Numerous mineral veins are hosted in a body of teschenite which is situated within the Lower Cretaceous flysch siliciclastics of the Silesian Unit at Tichá. Mineralogy, fluid inclusions, stable isotopes and trace elements have been studied in order to assess the origin of this mineralization. Three stages of vein cementation have been recognized, each of them being characterized by distinct mineral composition and genetic conditions. The first stage is composed of titanite, aegirine-augite to aegirine, annite, analcime and strontian apatite. These minerals originated from NaCl-rich, CaCl₂-poor magmatic brine (total fluid salinities range between 47 and 57 wt%), leaving after crystallization of host teschenite in low-pressure (<1 kbar) environment. Crystallization temperatures reached ～390–510 °C for early phases, titanite and aegirine-augite. The second stage is formed by calcite, chlorite, dolomite, siderite, strontianite, quartz, pyrite and sphalerite. The parent fluids were low-salinity (0.5–4.5 wt% NaCl eq.) aqueous solutions with low content of strong REE-complexing ligands, that were progressively cooled during mineral precipitation (up to ～190 °C at the beginning, ～90 °C at the end of crystallization). These fluids are interpreted to be predominantly of external origin, derived from surrounding sedimentary sequences during diagenetic dewatering of clay minerals. The highly positive δ¹⁸O and near-zero δ¹³C values indicate an interaction of fluids with sedimentary carbonates. The third stage is formed by a dense net of calcite veinlets, which probably originated during tectonic deformations connected with orogenetic movements during the Tertiary. The source of strontium for first stage mineralization was probably related to the special conditions of magmatic evolution of the host teschenite, whereas strontium for second stage minerals could have been remobilized during hydrothermal alteration from earlier teschenite-hosted mineral phases and/or limestone.     

Structural CO2 in the Apatite of the Late Cretaceous Phosphorite Resources in Egypt: Effect on the Crystal Chemistry and Geologic Implications

Abstract: Phosphorite deposits in Egypt, known as the Duwi Formation, are a part of the Middle East to North Africa phospho‐genic province of late Cretaceous to Paleogene age. Based on the petrographical observation, the phosphatic grains in the phosphorites are classified into phosphatic mudclasts and phosphatic bioclasts. Both of them are composed of francolite. The structural CO₂ contents in the francolite range from 3.3 to 7.2 % with an average of 5.3 %. Results indicated that the substitution with CO₃^2‐ of PO₄^3‐ in the francolite decreases the unit cell volume and a‐cell dimension, and increases the c/a ratio. Effect is more obvious in the a‐cell dimension; therefore, it is more significant in distinction between the different apatite species. Lack of covariance between structural CO₂ contents in the francolite and the carbonate minerals contents may render the supposition that the phosphorites formed as a result of replacement of preexisting calcareous sediments is doubtful. Similarity in CO₂ content in both weathered and fresh samples indicates that the structural CO₂ content in the phosphorites is not affected by weathering, and reflects the conditions and CO₂ concentration of the depositional environment. Similarity in mineralogy and CO₂ contents in the different phosphatic grains and higher CO₂ content in the Egyptian phosphorites compared with the authigenic phosphates of Peru margin, which formed by the same mechanism as the Duwi phosphorites, suggest that the phosphatic grains in the Duwi Formation were francolitized during diagenesis by introducing CO₂ from the surrounding pore water and diagenesis took place at an elevated temperature. Scattered values of structural CO₂ contents suggest the reworking origin of the phosphatic grains in the late Cretaceous phosphorites in Egypt.     

贵州瓮安陡山沱组磷块岩稀土元素地球化学特征与沉积期后变化

贵州瓮安陡山沱组磷块岩保存了可能是全球最早的后生动物化石 (瓮安动物群 ),对于瓮安动物群出现过程中的古海洋环境重建具有重要科学意义。但必须对成岩后生作用对磷块岩中的稀土元素改造进行评估。通过对贵州瓮安陡山沱组磷块岩的磷质碎屑、磷质和白云质胶结物、磷条带和泥条带等的稀土元素地球化学特征研究,确定沉积期后变化对稀土元素的改造影响不大。上矿层磷块岩沉积期形成的磷质碎屑、成岩期形成的白云质和磷质胶结物具相同的稀土元素配分模式,暗示了沉积期后的改造作用对瓮安陡山沱组磷块岩保存的原生沉积信息影响不大。瓮安陡山沱组磷块岩具有显著的重稀土亏损特征。磷块岩的磷质和白云质胶结物、伴生磷质碎屑、强风化磷块岩相近的ErN/LuN 比值,表明沉积期后的改造作用不是重稀土元素亏损的主要原因。磷块岩的ErN/LuN、LaN/NdN 与Ce/Ce 间的相关性,表明越氧化的沉积环境中,轻和重稀土元素亏损越强。     

西垄玄武质岩石中的橄榄岩类包体、捕虏晶以及巨晶的矿物化学研究

浙江衢县西垄和金华龙游一带分布有许多第三纪的霞石玄武岩、玻基橄辉岩、橄辉玢岩和超基性火山角砾岩岩体和岩脉。它们富含橄榄岩类包体和来源于破碎的橄榄岩包体的各种捕虏晶(橄榄石、斜方辉石、透辉石和石榴石)。此外,还常含有富铝普通辉石、石榴石和钛铁矿巨晶。本文试图在大量的单矿物分析数据基础上,讨论橄榄岩类包体、捕虏晶以及巨晶的矿物化学及其形成条件。关于橄榄岩包体的主要元素和微量元素地球化学以及成因岩石学的研究,笔者已在另一篇论文中专门论述(从柏林和张儒瑗,1983),这里不再重复。     

Analcimic zones in the tertiary of anatolia and their geological positions

The Anatolian Tertiary and especially the Neogene have some geological series with analcime as the principal rock-forming mineral. Sedimentation basins receiving material in suspension and in solution permit the authigenesis of analcime dolomite, calcite and opal(C-T). Analcimes formed by hydrothermal alteration on the ocean floor, after the pillow lava and diabasic dyke complexes of ophiolites, can form a source of detrital analcime when they are on the continental medium. Continental alteration of the pillow lavas and diabasic dykes permits the formation of solutions suitable in composition for analcime authigenesis. Analcimes formed in these environments are particularly related to the silica content of these media.Principal clay minerals formed with analcimic formations are smectites and (14_s—14_c) mixed layers. Illite, chlorite and corrensite are also present in smaller quantities.     

Geochemistry of Cadmium in Mesozoic Phosphorites of the East European Platform

Cadmium is the most toxic admixture in mineral fertilizers. The Cd concentration in Mesozoic phosphorites, which are widespread in the East European Platform, has not been investigated. The present study was stimulated by the scanty and contradictory nature of the published data on this issue. We determined Cd concentration in 21 phosphorite samples from major deposits and checked the reliability of obtained results by external replicate analyses. It has been established that the Cd concentration in phosphorites varies from 5 ppm in the Late Jurassic–Early Cretaceous basin to 2 ppm in the Late Cretaceous basin. Cadmium does not enter the structure of phosphate and sulfide minerals. The Cd concentration is independent of the phosphorus abundance. However, all studied samples show a positive correlation of Cd with organic matter mainly contained in phosphates, supporting the biophilic nature of Cd. Mesozoic phosphorites of the East European Platform accumulated in epicontinental basins. They are significantly depleted in Cd relative to Mesozoic–Cenozoic phosphorites in pericontinental basins of the southern margin of the Tethys Ocean. The Cd concentration is more stable in Mesozoic phosphorites than in Mesozoic–Cenozoic deposits.     

中国南方风化磷块岩研究

中国南方风化磷块岩中的风化磷矿的自然类型可分为两类七种型式，其中以“原位面型风化磷矿”和“位移溶洞砂砾磷矿”为主。风化磷矿是由其原矿的自身特性与外部适宜条件（水文地质条件为主导）综合作用的产物。根据碳酸盐、磷酸盐矿物分解、淋失程度可划分为弱风化、风化、强风化三个阶段。可用直接法、间接法和数学法３类共１３种方法加以判别     

Uranium (U) concentration and its genetic significance in the phosphorites of the Paleoproterozoic Bijawar Group of the Lalitpur district,Uttar Pradesh,India

The paper presents the uranium (U) concentration and distribution pattern in the Paleoproterozoic phosphorites of Lalitpur district of Uttar Pradesh. The study of thin sections, SEM and XRD reveal that apatite is the essential phosphate mineral while quartz and feldspars are the dominant gangue in the phosphorites of the investigated area. The collophane is observed to be mostly oolitic in form and microspherulitic in texture. The major element geochemistry indicated that the phosphorite samples are rich in P₂O₅, CaO, SiO₂ and Fe₂O₃ whereas depletion of MgO, MnO, K₂O and Al₂O₃ was observed. The CaO/P₂O₅ ratio ranges from 1.13 to 1.46 which is slightly lower than that of cations and anions substituted francolite (1.621) and close to that of carbonate-fluorapatite (1.318). The trace element geochemistry indicates that the phosphorites of Lalitpur have the significant range of U concentration (1.67 to 129.67 μg/g) which is more than that of Th (0.69 to 0.09 μg/g) among the analysed trace elements in the phosphorite samples of the area. The positive correlation of U with P₂O₅, CaO and U/P₂O₅ indicates a close association of U with phosphate minerals like collophane (apatite), whereas negative correlation of U with SiO₂ and Fe₂O₃ may be due to mutual replacement. The antipathetic relationship of U with Ni may be an indication of high oxidizing conditions, whereas sympathetic relationship of U with K₂O points towards higher alkaline conditions of the basin of deposition during phosphatization. The variable concentration of U and its relationship with significant major and trace elements in most of the phosphorite samples lead one to believe that the deposition of these phosphorites might have taken place in highly alkaline medium during fairly oxidizing to weakly reducing environmental conditions of geosynclinal basin.     

陕南天台山、茶店一带磷块岩的时代和成因特征

陕西南部汉中天台山、勉县茶店和略阳何家岩、金家河一带磷块岩的时代,目前有三种看法,即:泥盆纪、震旦纪和寒武纪。这一带磷块岩的成因也比较复杂。在磷酸盐沉积、成岩以后,又受到变质、褶皱、断裂和水溶液活动影响。本文对天台山、茶店一带的磷块岩的成矿时代和生成特点提出一些初步意见。     

Trace elements and REE in the Cevonian clastic complexes of the Magnitogorsk Megazone, Southern Urals

The first data on trace-element geochemistry, REEs included, of the Devonian clastic and volcanosedimentary complexes in the Magnitogorsk Megazone have been obtained with ICP-MS. The correlation links and the character of distribution indicate that many elements, including those readily passing into solutions during weathering, were transferred as mechanical suspensions. Therefore, minerals concentrating these elements were largely preserved, as also were the distribution and concentrations of elements inherent to the source rocks. Both accessory minerals (apatite, zircon, Ti-minerals, and magnetite) and rock-forming minerals (pyroxene, amphibole, biotite, serpentine, chlorite, and plagioclase) were found among mineral concentrators. Clay minerals also seem to have participated in the processes. The typical elements of various complexes were identified. The distribution of trace elements is correlated with the stratigraphic position of rocks and depends on the character of the petrographic provinces.     

Geochemistry of high-temperature coal ashes and the sedimentary environment of the New South Wales coals, Australia

Chemical analyses of high-temperature coal ashes were used to establish the distribution, association and relationship between major inorganic elements such as Si, Al, Ti, Fe, Mn, Mg, Ca, Na, K, P, S and CO₂ in a number of New South Wales economic coal seams and to study the composition and character of mineral matter in these coals. The methods used for the evaluation of the data were statistical analysis (univariate and bivariate), ratios, normative mineral composition and variation diagrams.The distribution of major and minor inorganic elements in coal appears to be related to the amount of mineral matter occurring in coal (determined as ash yield) and its mineralogical composition. The quantitative variations in levels of these elements can be classified as in-seam and inter-seam variations. In-seam variations are largely ash yield dependent, i.e. the levels of an element (wt.%) in coal increase along with the increase of its ash content (wt.%). The inter-seam variations are more complex and are related to both ash yield and to the mineralogical composition of mineral matter.The principal components of New South Wales coal ashes are silicon and aluminium. Silicon may be present as silica or combined with aluminium in different proportions to form clay minerals, such as kaolinite, illite, mixed-layer clay minerals, and smectite. Thus, the concentration levels of aluminium in relation to silicon in coal may give an indication about the character of clay minerals present in coal.Ratios and correlation coefficients of element pairs such as Al and Ti, Na and K, and Na and Al were used to determine differences in the chemical composition of high-temperature coal ashes of seams from various stratigraphic positions and provinces. In some seams the nature of associations of these elements is more significant than in others. This is interpreted as being a product of specific environmental conditions controlling the deposition of these seams.The nature of clay mineral content in coal is believed to be a major reason for chemical dissimilarities found between seams of various stratigraphic levels and geographic areas. For example, in some seams kaolinite, in others expandable clay minerals are dominant. The vertical distribution of these minerals has a stratigraphic significance. Within the Upper Permian Newcastle Coal Measures a trend from kaolinite-rich through to expandable minerals-rich and to kaolinite-rich assemblages can be observed from the bottom to the top. These changes are noticeably gradual.All significant variations in the clay mineral assemblages could relate to the long-term changes in the provenance of sedimentary material, weathering conditions in the source area and the rate of subsidence in the place of deposition. These changes are associated with major tectonic events controlling the history of sedimentation within the paralic Sydney and Gunnedah Basins during the Permian.     

Rare earth elements, yttrium and H, O, C, Sr, Nd and Pb isotope studies in mineral waters and corresponding rocks from NW-Bohemia, Czech Republic

The sparkling waters from the area of Kyselka near Karlovy Vary at the western slope of the Doupovske hory, Bohemia (Czech Republic), and CO₂-poor waters from two underground boreholes at Jachymov, Krusne hory, Bohemia, have been studied with the aim of characterizing the distribution of rare earth elements, yttrium, and H, O, C, Sr, Nd, Pb isotopes during the low-temperature alteration processes of the host rocks. Additionally, leaching experiments were performed at pH 3 on the granitic and basaltic host rocks from Kyselka and the granite of Jachymov. All REE patterns of the granite- and the basalt-derived waters from the Kyselka area are different from those of their source rocks and the leachates of the latter. This elucidates the inhomogeneous distribution of REE and Y among the solid phases in the altered magmatic rocks. The Eu and Ce anomalies in granite-derived waters are inherited, the Y anomaly is achieved by fluid migration. Yttrium is always preferentially leached by mineral waters, whereas Y/Ho ratios of rocks and their leachates are very similar. The REE abundances in waters from the wells in Jachymov are derived from rocks intensely leached and depleted in easily soluble REE-bearing minerals, whereas the granites and basalts from Kyselka still contain soluble, REE-bearing minerals. A comparison of REE/Ca patterns of the experimental leachates with those of the mineral waters elucidate the high retention of REE in rocks during water–rock interaction. In strongly altered rocks Sr isotope ratios of mineral waters and rocks differ widely, whereas the corresponding Nd isotope ratios are very similar. ²⁰⁷Pb/²⁰⁸Pb, ²⁰⁶Pb/²⁰⁸Pb and ²⁰⁶Pb/²⁰⁷Pb ratios in mineral waters are independent from U/Th ratios in the rocks. ²⁰⁶Pb/²⁰⁸Pb and ²⁰⁶Pb/²⁰⁷Pb are lower in mineral waters than in their source rocks and their leachates, which indicates that Pb is primarily derived from solid phases that do not contain significant contents of leachable U and Th. Thus, mineral waters, although CO₂ rich, only interact with surface films on minerals and not with the bulk of the minerals as in the leaching experiments.Calculation of mixing ratios of waters from the granitic and basaltic sources of the waters from the Kyselka area yield about 40% of water from the underlying granite in water recovered from the basalt, whereas the granite-derived water is mixed with only about 5% of the water from the basalt.     

应用X射线衍射-扫描电镜-光学显微镜鉴定黑龙江石墨尾矿中的绢云母

石墨尾矿作为一类二次资源,当云母类矿物的含量在10%以上时,具有回收利用价值。黑龙江某地石墨尾矿中含有10%以上的云母类矿物,但其细度(500~800目)低于常规的云母矿,本文采用X射线衍射(XRD)分析矿物组成,再结合化学分析、扫描电镜-能谱、光学显微镜与纯矿物进行对比,由此鉴定云母类矿物种属。XRD研究初步表明石墨尾矿含有的云母族矿物属于白云母亚类或黑云母亚类。扫描电镜分析表明尾矿中的云母矿物与纯绢云母矿物均以片状和鳞片状为主要存在形态,而纯黑云母主要以片状形式存在。尾矿的Si O2含量为5%~13%,Al2O3含量为4%~8%,与纯绢云母接近。光学显微镜鉴定显示在正交偏光下石墨尾矿中的云母颜色和纯绢云母类似,而与纯黑云母截然不同。综合以上结果最终可确定该地石墨尾矿中的云母族矿物为白云母亚类中的绢云母。本研究为后续石墨尾矿的选矿工艺奠定了基础,也可应用于类似细度绢云母的鉴定。     

电子探针技术探究钪在白云鄂博矿床不同矿物中的赋存特征

随着对钪资源需求的不断增加,世界各国近年陆续开展钪成矿机理研究及找矿工作,核心内容之一是厘清钪的赋存特征.据前人研究,各类钪矿床中钪主要以类质同象、离子吸附形式存在,目前发现的含钪矿物种类已逾800种.对于白云鄂博矿床,钪资源储量较大,无独立钪矿物产出,钪以类质同象形式进入其他矿物,分布分散、含量低.囿于测试技术及取样...     

Uranium-enriched minerals in mesostasis areas of the Rhum layered pluton

The distribution of uranium in intercumulus minerals of the Rhum layered intrusion, Inner Hebrides, has been studied by the fission track technique. A striking feature was the frequent occurrence of intense fission track stars recorded on the organic solid state nuclear track detectors. The high uranium sources corresponding to such features were found to be small, discrete mineral phases, often not larger than 50 m in size. The phases were identified as the zirconium- or phosphorus-bearing minerals zirconolite (essentially (CaFe)(Zr)(Ti)₂O₇), baddeleyite, zircon and apatite. Although zirconolite and baddeleyite frequently coexist in mesostasis areas of lunar mare basalts, baddeleyite has been only rarely observed, and zirconolite not yet reported in terrestrial basalts, with this being the first recorded occurrence of zirconolite and baddeleyite from a terrestrial ultrabasic cumulate. From estimated uranium concentrations, all of which exceed 50 p.p.m., the uranium values decrease in the order zirconolite, baddeleyite, zircon, apatite. The mesostasis areas in which these minerals occur, are to a certain extent determined by the pre-existing cumulus mineral morphologies. Branching, or cup-shaped, olivines provide small scale hollows in which residual magmatic fluids become trapped. Such fluids clearly concentrate those elements not incorporated into the cumulus phases, e.g. uranium, phosphorus, zirconium, etc., and crystallise to give uranium-enriched minerals.     

塔里木盆地巴楚地区上泥盆统-下石炭统沉积-物源记录及其构造演化

泥盆纪-石炭纪是南天山洋-塔里木盆地北部陆缘构造演化的关键时期.选取塔里木盆地巴楚地区上泥盆统-下石炭统露头剖面,在沉积体系、碎屑组分、重矿物组合分析基础上,重点通过LA-ICP-MS分析砂岩样品.结果表明,上泥盆统-下石炭统砂岩碎屑颗粒以单晶石英为主,(变质) 结晶岩岩屑极少,物源构造属性主要指示陆块物源区;重矿物组合以锆石、电气石和TiO₂矿物等稳定重矿物为主,反映相对远距离的源汇体系和稳定的构造背景;2个年代学样品具有类似的碎屑锆石U-Pb年龄组成和Hf同位素特征,主要反映了383~479 Ma、710~932 Ma、1 752~1 936 Ma、2 419~2 597 Ma共4期构造热事件,并以前两期为主.对比研究显示,上述碎屑物源以塔里木盆地内古隆起为主,同时还可能有来自阿尔金造山带、西昆仑造山带的再旋回沉积.但并没有记录到来自盆地北侧造山带和岛弧的物源信息,说明该时期南天山洋盆并没有闭合,塔里木盆地北缘西部可能不存在洋盆的向南俯冲,晚泥盆世-早石炭世其可能为被动大陆边缘.