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Mineralogy of Pakkanadu carbonatites and associated rocks, South India: constraints on evolution and evidences for REE enrichment 南印度Pakkanadu碳酸盐岩和伴生岩石的矿物学:演化的制约因素和REE富集的证据
IF 1.8 4区 地球科学 Q2 Earth and Planetary Sciences Pub Date : 2023-08-17 DOI: 10.1007/s00710-023-00843-0
S. Mahapatro, T. Meshram, Mahesh Korakappa
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引用次数: 1
Mineral-scale insights into the petrogenesis of the 3.30 Ga rhyolite in the Contendas-Mirante region, northern São Francisco Craton, Brazil: implications from results of plagioclase and biotite analyses 巴西<s:1>圣弗朗西斯科克拉通北部Contendas-Mirante地区3.30 Ga流纹岩成因的矿物尺度研究:斜长石和黑云母分析结果的意义
IF 1.4 4区 地球科学 Q3 GEOCHEMISTRY & GEOPHYSICS Pub Date : 2023-08-04 DOI: 10.1007/s00710-023-00842-1
Eliana M. Branches Farias, Cristiano C. Lana, Stefano A. Zincone, Glaucia N. Queiroga, Leonardo M. Graça

The 3.30 Ga high-silica volcanic system of the Gavião Block, São Francisco Craton, represents the remnants of within-plate magmatism related to an intracontinental rift. However, the petrogenetic processes that may have taken place in the relatively shallow primitive continental crust has not been fully constrained due to a scarce record. Petrographic and chemical analyses in biotite, as well as in-situ Sr isotope ratios in plagioclase, were used to trace petrogenetic processes and physicochemical conditions of the magmatic system. The subvolcanic rock has a well-preserved primary volcanic feature represented by magma flow textures, euhedral to subhedral plagioclases, rapakivi microstructures, and glomerocrysts. Plagioclase populations formed at two distinct stages recorded by trace elements and Sr isotope. Plagioclase phenocrysts and rapakivi phenocrysts have a slight enrichment of light rare earth elements (LREE), Sr/Ba ratio, and slight variation of Sr isotopes composition. Meanwhile, other phenocrysts and rapakivi crystals have low LREE, Sr/Ba, and a limited variation of Sr isotope ratio. Mineral chemistry evidence points to country rock assimilation during plagioclase formation and a crustal source for primary biotites under oxidized conditions.

圣弗朗西斯科克拉通加维昂区块的 3.30 Ga 高矽卡岩火山系统是与大陆内部裂谷有关的板内岩浆活动的遗迹。然而,由于记录稀少,在相对较浅的原始大陆地壳中可能发生的岩石成岩过程还没有得到充分证实。通过对生物岩进行岩相学和化学分析,以及对斜长石进行原位锶同位素比值分析,可追溯岩浆系统的成岩过程和物理化学条件。次火山岩具有保存完好的原生火山岩特征,表现为岩浆流纹理、八面体至次八面体斜长石、拉帕基维微结构和团晶。根据痕量元素和锶同位素的记录,斜长石群形成于两个不同的阶段。斜长石表晶和rapakivi表晶的轻稀土元素(LREE)、Sr/Ba比值略有富集,Sr同位素组成略有变化。与此同时,其他表晶和rapakivi晶体的轻稀土元素(LREE)、Sr/Ba比值较低,Sr同位素比值变化有限。矿物化学证据表明,斜长石形成过程中存在乡村岩石同化现象,而在氧化条件下,原生生物岩则来源于地壳。
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引用次数: 0
Reply to the comment by S. Bouhlel 回复S. Bouhlel的评论
IF 1.4 4区 地球科学 Q3 GEOCHEMISTRY & GEOPHYSICS Pub Date : 2023-08-03 DOI: 10.1007/s00710-023-00838-x
Nejib Jemmali, Larbi Rddad, Marta Sośnicka, Emna Rahali, Fouad Souissi, Emmanuel John Carranza
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引用次数: 0
Comment on “Genesis of Zn‑Pb‑(Ba‑Sr) mineralization in the peridiapiric cover of Jebel El Akhouat, Ech Chehid salt dome, Northern Tunisia” (2022) by N. Jemmali, L. Rddad, M. Sośnicka, E. Rahali, F. Souissi and E. J. Carranza N.Jemmali、L.Rddad、M.Sośnicka、E.Rahali、F.Souissi和E.J.Carranza对“突尼斯北部Ech Chehid盐丘Jebel El Akhouat周皮覆盖层中Zn‑Pb‑(Ba‑Sr)矿化的成因”(2022)的评论
IF 1.4 4区 地球科学 Q3 GEOCHEMISTRY & GEOPHYSICS Pub Date : 2023-08-02 DOI: 10.1007/s00710-023-00839-w
Salah Bouhlel
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引用次数: 0
Apatite chemistry of Late Triassic granitic rocks from Yidun Terrane: Implications for petrogenesis and mineralization 益墩地体晚三叠世花岗质磷灰石化学:岩石成因和成矿意义
IF 1.4 4区 地球科学 Q3 GEOCHEMISTRY & GEOPHYSICS Pub Date : 2023-07-29 DOI: 10.1007/s00710-023-00836-z
Zhuanrong Sun, Guochen Dong, Jiahui Tang, Jianheng Guo, Zhongbao Wang

The Yidun Terrane hosts huge amounts of Late Triassic granitic plutons. While the southern Yidun Terrane, also referred to as the Zhongdian arc, mainly includes Late Triassic porphyry and related porphyry Cu-Au deposits, rare mineralization was found related to the contemporary granitic batholiths in the northern Yidun terrane (NYT). This paper has explored the chemical compositions of the apatite from these intrusions, which provide insights into the petrogenesis and the mineralization potential. The higher Mg and V concentrations and La/Sm ratios of the Zhongdian apatite than the Cuojiaoma and Daocheng apatite in the NYT suggestes that the Zhongdian porphyries were derived from a mixed source with both mantle and crustal contributions, while the Cuojiaoma and Daocheng granites are dominantly crustal derived. Compared with the Cuojiaoma and Daocheng apatite, the Zhongdian apatite are characterized by higher Sr, Eu/Eu* [EuN/(SmN×GdN)0.5], S and Cl, and low Mn and Y concentrations with adakitic affinity, indicating an environment with high oxygen fugacity and S and Cl contents for their parental magmas, which is favorable for the formation of porphyry Cu-Au deposits. By comparing the chemical characteristics of apatite from the ore-bearing porphyries and ore-barren granites in the Yidun Terrane, this study proposes that the apatite from the ore-bearing rocks commonly has relatively high Sr, S and Fe concentrations and low Mn, Y and Si/S ratio. These geochemical characteristics can be good indicators for predicting the metallogenic potential of the rocks.

宜墩地层蕴藏着大量的晚三叠世花岗岩柱岩。宜墩地层南部(又称中甸弧)主要包括晚三叠世斑岩型及相关斑岩型铜金矿床,而在宜墩地层北部(NYT)则发现了与当代花岗岩岩体有关的罕见矿化。本文探讨了这些侵入体中磷灰石的化学成分,为岩石成因和成矿潜力提供了启示。中甸岩磷灰石的镁和钒浓度以及la/Sm比值均高于聂拉山脉中的走马岩和稻城岩磷灰石,这表明中甸斑岩来源于地幔和地壳的混合来源,而走马岩和稻城花岗岩则主要来源于地壳。中甸斑岩的Sr、Eu/Eu* [EuN/(SmN×GdN)0.5]、S和Cl含量较高,而Mn和Y含量较低,且与赤铁矿亲和,表明其母岩具有高富氧环境和S、Cl含量,有利于斑岩型铜金矿床的形成。通过比较宜墩地层含矿斑岩和贫矿花岗岩中磷灰石的化学特征,本研究提出含矿岩石中的磷灰石通常具有相对较高的Sr、S和Fe浓度,以及较低的Mn、Y和Si/S比值。这些地球化学特征可作为预测岩石成矿潜力的良好指标。
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引用次数: 0
Rare native Ni, Fe, Cu, and Sn metals in Hemrin Basalt, northern Iraq: implications for mineral chemistry and ore genesis 伊拉克北部Hemrin玄武岩中稀有天然Ni、Fe、Cu和Sn金属:矿物化学和成矿意义
IF 1.4 4区 地球科学 Q3 GEOCHEMISTRY & GEOPHYSICS Pub Date : 2023-07-24 DOI: 10.1007/s00710-023-00840-3
Yawooz A. Kettanah

The Hemrin Basalt (HB) is an abnormal occurrence because of its genesis, mineralogy, textures, rare native metals content, and odd geographic-geologic-tectonic setting. It occurs as a caprock for few NW/SE trending hills in a nearly flat-lying area. The HB is a high-K calc-alkaline, collision-related, continental-arc basalt and consists of diopside, labradorite and volcanic glass as the predominant constituents displaying rare firework and feathery textures. The accessory minerals in HB comprise small, discrete grains of native Ni, Fe, Cu, and Sn metals, and scattered grains of sulfides (pyrrhotite, pentlandite, molybdenite), oxides (magnetite, ilmenite, Cr-spinel), and apatite. These minerals occur as disseminated individual or composite grains of variable shapes within the groundmass of HB. Vesicle-filling secondary minerals are zeolite, calcite, anhydrite, and gypsum. The native metals were formed under reducing conditions. The reducing conditions were created as a result of assimilation of C- and S-rich sedimentary rocks by the ascending magma from the continental lithospheric mantle through the thick pile of sedimentary formations. The possible C- and S-rich rocks include the carbonates and evaporites of Fatha Formation and the Hemrin Coal Seam within the upper part of Injana Formation hosting the HB and overlying the Fatha Formation, and possibly the petroleum source, reservoir and caprocks forming the sedimentary column underlying the area. Assimilation of S from these rocks created sulfides, while assimilated C resulted in the formation of native metals.

海姆林玄武岩(HB)因其成因、矿物学、纹理、稀有原生金属含量以及奇特的地理-地质-构造环境而异常。它作为几座西北/东南走向山丘的盖岩出现在一个几乎平坦的地区。HB 是一种高 K 钙碱性、与碰撞有关的大陆弧玄武岩,主要成分为透辉石、拉长石和火山玻璃,具有罕见的烟花状和羽毛状纹理。HB 中的附属矿物包括原生镍、铁、铜和锡金属的离散小颗粒,以及硫化物(黄铁矿、戊铁矿、辉钼矿)、氧化物(磁铁矿、钛铁矿、铬尖晶石)和磷灰石的零散颗粒。这些矿物在 HB 的地层中以形状各异的单粒或复合粒的形式存在。填充囊泡的次生矿物有沸石、方解石、无水石膏和石膏。原生金属是在还原条件下形成的。这种还原条件是大陆岩石圈地幔中的岩浆通过厚厚的沉积地层上升同化富含 C 和 S 的沉积岩而形成的。可能富含 C 和 S 的岩石包括法塔地层的碳酸盐岩和蒸发岩,以及承载 HB 的 Injana 地层上部和法塔地层上覆的 Hemrin 煤层,还可能包括构成该地区底层沉积柱的石油源、储层和盖岩。从这些岩石中同化的 S 形成了硫化物,而同化的 C 则形成了原生金属。
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引用次数: 0
The Genesis of the Kenticha rare-metal granite-pegmatite, Southern Ethiopia 埃塞俄比亚南部Kenticha稀有金属花岗岩伟晶岩的成因
IF 1.4 4区 地球科学 Q3 GEOCHEMISTRY & GEOPHYSICS Pub Date : 2023-06-12 DOI: 10.1007/s00710-023-00835-0
Barsisa Bekele, Amit Kumar Sen

The Kenticha pegmatite field comprises suites of barren to fertile pegmatite swarms. It shows textural, mineralogical, and geochemical variations. The pegmatites are structurally controlled and emplaced in mafic–ultramafic belts during the Neoproterozoic. This study aims to constrain the genetic and tectonic setting of the Kenticha rare-metal (RM) pegmatite and the associated granite. The presence of minerals such as biotite, muscovite, spodumene, spessartine-almandine garnet, gahnite, beryl, tourmaline, cordierite, and topaz indicate the peraluminous nature of the granite and associated pegmatites. The Kenticha rare-metal granite-pegmatite shows ASI > 1.1, low V, Y, very low Sr, Ba, Th, Zr and REE, very high Be, Li, Rb, Cs, Ga, Nb, and Ta than the upper continental crust. The parental two-mica granite has higher Co, Rb, Ba, and Ce and lower V, Zr, Y, Nb, Ni, La, Pb, Sr, and Th than the upper continental crust. The Ta/Nb value in the two-mica granite is nearly equal to the average upper crustal value. In both parental granite and pegmatites, the normative corundum (C) is greater than 1%. The P2O5 content is low in the assumed parental granite. However, in the main ore body, the P2O5 content increases towards the more fractionated pegmatite. Due to its peraluminous character and high content of Be, Cs, Li, Ta, and Rb, we can categorise the granite-pegmatite under the LCT subclass of the rare-element pegmatite. It's associated with S-type granite. HFSE and LIL elements show characteristics of bulk continental crust composition and syn-collisional felsic magmatism. Biotite composition suggests partial melting of the metasedimentary protolith as the source of the two-mica granite. The plots of Y vs. SO2, P2O5 vs. SiO2, % normative C vs. Rb, Y vs. Rb, and Th vs. Rb support the S-type magma source. Geochemical and mineralogical data show a nearly vertical evolutional trend of the granite-pegmatite. It varies from the basal granitic unit to the pegmatite core unit. The mineralization of rare metals in the granite-pegmatite was mainly controlled by genetic (processes).

肯蒂查伟晶岩区由贫瘠到肥沃的伟晶岩群组成。它显示出纹理、矿物学和地球化学方面的变化。伟晶岩受构造控制,在新近新生代期间位于黑云母-超黑云母带。本研究旨在确定肯蒂查稀有金属伟晶岩及相关花岗岩的成因和构造背景。生物橄榄石、白云母、榍石、锰铝石榴石、锰铝石榴石、绿柱石、电气石、堇青石和黄玉等矿物的存在表明了花岗岩和相关伟晶岩的过铝性质。肯蒂夏稀有金属花岗岩伟晶岩的 ASI 值为 1.1,V、Y 值较低,Sr、Ba、Th、Zr 和 REE 值极低,Be、Li、Rb、Cs、Ga、Nb 和 Ta 值极高,高于上部大陆地壳。与上部大陆地壳相比,母岩双云母花岗岩具有较高的钴、铷、钡和硒,较低的钒、锆、钇、铌、镍、镭、铅、锶和钍。双云母花岗岩中的Ta/Nb值几乎等于上地壳的平均值。在母体花岗岩和伟晶岩中,标准刚玉(C)含量均大于 1%。在假定的母体花岗岩中,P2O5 含量较低。不过,在主矿体中,P2O5 含量在分馏程度较高的伟晶岩中有所增加。由于花岗伟晶岩的过铝特性以及较高的 Be、Cs、Li、Ta 和 Rb 含量,我们可以将其归入稀有元素伟晶岩的 LCT 亚类。它与 S 型花岗岩有关。HFSE 和 LIL 元素显示了大块大陆地壳成分和同步碰撞熔融岩浆作用的特征。生物岩成分表明,双云母花岗岩的来源是元古代原岩的部分熔融。Y vs. SO2、P2O5 vs. SiO2、%规范C vs. Rb、Y vs. Rb和Th vs. Rb的曲线图支持S型岩浆源。地球化学和矿物学数据显示,花岗岩-伟晶岩几乎呈垂直演化趋势。从基底花岗岩单元到伟晶岩核心单元各不相同。花岗岩-伟晶岩中稀有金属的成矿主要受遗传(过程)控制。
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引用次数: 0
On the occasion of the 100th anniversary of Josef Zemann’s birthday: a tribute to his scientific oeuvre 在约瑟夫·泽曼诞辰100周年之际:向他的科学作品致敬
IF 1.8 4区 地球科学 Q2 Earth and Planetary Sciences Pub Date : 2023-06-09 DOI: 10.1007/s00710-023-00834-1
Gerald Giester, Thomas Armbruster, Tonci Balić-Žunić, Anton Beran, Herta Effenberger, Reinhard X. Fischer, Karen Friese, Eugen Libowitzky, Manfred Wildner, Lutz Nasdala
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引用次数: 0
Prachařite, CaSb5+2(As3+2O5)2O2·10H2O, a new mineral from Lavrion, Greece Prachařite, CaSb5+2(As3+2O5)2O2·10H2O,希腊Lavrion新矿物
IF 1.8 4区 地球科学 Q2 Earth and Planetary Sciences Pub Date : 2023-06-09 DOI: 10.1007/s00710-023-00830-5
Uwe Kolitsch, Jiří Sejkora, Dan Topa, Anthony R. Kampf, Jakub Plášil, Branko Rieck, Karl Heinz Fabritz

Prachařite, ideally CaSb5+2(As3+2O5)2O2·10H2O, is a new mineral found in underground workings of the Plaka Mine No. 80, Plaka, Lavrion Mining District, Attica, Greece. It occurs as colourless to white, thin tabular hexagonal, in general sharp crystals up to 2.5 mm in diameter, and is associated with pharmacolite, sulphur and very rare smamite {Ca2Sb(OH)4[H(AsO4)2]·6H2O} on a matrix composed of sphalerite, galena and carbonate gangue. Prachařite is translucent to transparent, with a glassy lustre, white streak, a good cleavage parallel to {0001} and a distinct cleavage parallel to {10(overline{1 })0}. It is non-luminescent, brittle, and has an uneven fracture, a Mohs hardness of 2–2.5 and X-ray density Dx = 2.848 g/cm3, Dcalc. = 2.836–2.853 g/cm3 (for two measured compositions). Optically, it is uniaxial negative, with ω = 1.619(1) and ε = 1.553(1). Prachařite is trigonal, space group P(overline{3 })c1 (no. 165), with a = 13.951(2), c = 19.899(2) Å, V = 3354.1(10) Å3 and Z = 6. Strongest lines in the X-ray powder diffraction pattern are [d in Å (I) hkl]: 9.894 (100) 002; 6.045 (8) 200; 5.156 (10) 202; 4.946 (11) 004; 3.297 (19) 311, 006, 222; 2.988 (22) 400, 313, 116. Two sets of independent electron probe micro-analyses yielded (wt%): CaO 6.28/7.12, MgO 0.09/-, Zn -/0.01, Sb2O5 39.22/40.19, As2O3 47.59/47.39, SO3 -/0.02, H2O 21.65/22.04 (calculated on the basis of ideal composition derived from crystal-structure determination), total 114.83/116.77; the total is reproducibly high due to a loss of a third of all water molecules under the electron beam. The empirical formulae, based on O = 22 atoms per formula unit, for the two datasets are very similar, (Ca0.93Mg0.02)Σ0.95Sb2.02(AsO3)4.00·10H2O and Ca1.04Sb2.03(AsO3)3.92·10H2O. The ideal formula is CaSb5+2(As3+2O5)2O2·10H2O, determined with the help of a crystal-structure determination based on single-crystal X-ray diffraction datasets collected at room temperature (R1 = 2.3%). The atomic arrangement of prachařite is unusual; it is based on two different layers containing a six-membered ring of corner-sharing SbO6 octahedra, an eight-coordinated Ca1 atom in the centre of the ring, two non-equivalent AsO3 groups corner-linked to form a (As2O5)4− diarsenite group, and, on interlayer sites, a seven-coordination Ca2 atom and three water molecules (all only w

Prachařite,理想的CaSb5+2(As3+2O5)2O2·10H2O,是在希腊阿提卡Lavrion矿区Plaka第80号Plaka矿的地下工作中发现的一种新矿物。它呈无色至白色,薄板状六角形,一般为直径达2.5 mm的尖锐晶体,在闪锌矿、方铅矿和碳酸盐脉石组成的基体上与药辉石、硫和非常罕见的smamite {Ca2Sb(OH)4[H(AsO4)2]·6H2O}伴生。Prachařite半透明至透明,具有玻璃般的光泽,白色条纹,平行于{0001}的良好解理和平行于{10的明显解理(overline{1 }) 0}。不发光,脆性,断口不均匀,莫氏硬度为2-2.5,x射线密度Dx = 2.848 g/cm3, Dcalc = 2.836-2.853 g/cm3(两种测量成分)。光学上为单轴负,ω = 1.619(1), ε = 1.553(1)。Prachařite为三角形,P空间群(overline{3 }) c1 (a = 13.951(2), c = 19.899(2) Å, V = 3354.1(10) Å3, Z = 6。x射线粉末衍射图中最强谱线为[d] Å (I) hkl: 9.894 (100) 002;6.045 (8) 200;5.156 (10) 202;4.946 (11) 004;3.297 (19) 311, 006,222;[2988](22) 400, 313, 116。两组独立的电子探针显微分析得到(wt)%): CaO 6.28/7.12, MgO 0.09/-, Zn -/0.01, Sb2O5 39.22/40.19, As2O3 47.59/47.39, SO3 -/0.02, H2O 21.65/22.04 (calculated on the basis of ideal composition derived from crystal-structure determination), total 114.83/116.77; the total is reproducibly high due to a loss of a third of all water molecules under the electron beam. The empirical formulae, based on O = 22 atoms per formula unit, for the two datasets are very similar, (Ca0.93Mg0.02)Σ0.95Sb2.02(AsO3)4.00·10H2O and Ca1.04Sb2.03(AsO3)3.92·10H2O. The ideal formula is CaSb5+2(As3+2O5)2O2·10H2O, determined with the help of a crystal-structure determination based on single-crystal X-ray diffraction datasets collected at room temperature (R1 = 2.3%). The atomic arrangement of prachařite is unusual; it is based on two different layers containing a six-membered ring of corner-sharing SbO6 octahedra, an eight-coordinated Ca1 atom in the centre of the ring, two non-equivalent AsO3 groups corner-linked to form a (As2O5)4− diarsenite group, and, on interlayer sites, a seven-coordination Ca2 atom and three water molecules (all only weakly hydrogen-bonded), one of which is only partially occupied (split position). The mineral is named in honour of Dr Ivan Prachař, a long-term researcher of the mineralogy and underground workings of Lavrion.
{"title":"Prachařite, CaSb5+2(As3+2O5)2O2·10H2O, a new mineral from Lavrion, Greece","authors":"Uwe Kolitsch,&nbsp;Jiří Sejkora,&nbsp;Dan Topa,&nbsp;Anthony R. Kampf,&nbsp;Jakub Plášil,&nbsp;Branko Rieck,&nbsp;Karl Heinz Fabritz","doi":"10.1007/s00710-023-00830-5","DOIUrl":"10.1007/s00710-023-00830-5","url":null,"abstract":"<div><p>Prachařite, ideally CaSb<sup>5+</sup><sub>2</sub>(As<sup>3+</sup><sub>2</sub>O<sub>5</sub>)<sub>2</sub>O<sub>2</sub>·10H<sub>2</sub>O, is a new mineral found in underground workings of the Plaka Mine No. 80, Plaka, Lavrion Mining District, Attica, Greece. It occurs as colourless to white, thin tabular hexagonal, in general sharp crystals up to 2.5 mm in diameter, and is associated with pharmacolite, sulphur and very rare smamite {Ca<sub>2</sub>Sb(OH)<sub>4</sub>[H(AsO<sub>4</sub>)<sub>2</sub>]·6H<sub>2</sub>O} on a matrix composed of sphalerite, galena and carbonate gangue. Prachařite is translucent to transparent, with a glassy lustre, white streak, a good cleavage parallel to {0001} and a distinct cleavage parallel to {10<span>(overline{1 })</span>0}. It is non-luminescent, brittle, and has an uneven fracture, a Mohs hardness of 2–2.5 and X-ray density <i>D</i><sub>x</sub> = 2.848 g/cm<sup>3</sup>, <i>D</i><sub>calc.</sub> = 2.836–2.853 g/cm<sup>3</sup> (for two measured compositions). Optically, it is uniaxial negative, with ω = 1.619(1) and ε = 1.553(1). Prachařite is trigonal, space group <i>P</i><span>(overline{3 })</span><i>c</i>1 (no. 165), with <i>a</i> = 13.951(2), <i>c</i> = 19.899(2) Å, <i>V</i> = 3354.1(10) Å<sup>3</sup> and <i>Z</i> = 6. Strongest lines in the X-ray powder diffraction pattern are [<i>d</i> in Å (<i>I</i>) <i>hkl</i>]: 9.894 (100) 002; 6.045 (8) 200; 5.156 (10) 202; 4.946 (11) 004; 3.297 (19) 311, 006, 222; 2.988 (22) 400, 313, 116. Two sets of independent electron probe micro-analyses yielded (wt%): CaO 6.28/7.12, MgO 0.09/-, Zn -/0.01, Sb<sub>2</sub>O<sub>5</sub> 39.22/40.19, As<sub>2</sub>O<sub>3</sub> 47.59/47.39, SO<sub>3</sub> -/0.02, H<sub>2</sub>O 21.65/22.04 (calculated on the basis of ideal composition derived from crystal-structure determination), total 114.83/116.77; the total is reproducibly high due to a loss of a third of all water molecules under the electron beam. The empirical formulae, based on O = 22 atoms per formula unit, for the two datasets are very similar, (Ca<sub>0.93</sub>Mg<sub>0.02</sub>)<sub>Σ0.95</sub>Sb<sub>2.02</sub>(AsO<sub>3</sub>)<sub>4.00</sub>·10H<sub>2</sub>O and Ca<sub>1.04</sub>Sb<sub>2.03</sub>(AsO<sub>3</sub>)<sub>3.92</sub>·10H<sub>2</sub>O. The ideal formula is CaSb<sup>5+</sup><sub>2</sub>(As<sup>3+</sup><sub>2</sub>O<sub>5</sub>)<sub>2</sub>O<sub>2</sub>·10H<sub>2</sub>O, determined with the help of a crystal-structure determination based on single-crystal X-ray diffraction datasets collected at room temperature (<i>R</i>1 = 2.3%). The atomic arrangement of prachařite is unusual; it is based on two different layers containing a six-membered ring of corner-sharing SbO<sub>6</sub> octahedra, an eight-coordinated Ca1 atom in the centre of the ring, two non-equivalent AsO<sub>3</sub> groups corner-linked to form a (As<sub>2</sub>O<sub>5</sub>)<sup>4−</sup> diarsenite group, and, on interlayer sites, a seven-coordination Ca2 atom and three water molecules (all only w","PeriodicalId":18547,"journal":{"name":"Mineralogy and Petrology","volume":null,"pages":null},"PeriodicalIF":1.8,"publicationDate":"2023-06-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00710-023-00830-5.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"4389731","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The use of geochemical methods to pinpoint the origin of ancient white marbles 利用地球化学方法确定古代白色大理石的来源
IF 1.8 4区 地球科学 Q2 Earth and Planetary Sciences Pub Date : 2023-06-02 DOI: 10.1007/s00710-023-00833-2
Walter Prochaska

“Multi-method-approach” has now been for many years the buzzword in marble provenance analysis. Nevertheless a true combination of the results of different analytical methods is rarely applied in the sense of the combined simultaneous use of a large number of analytically obtained numerical variables. It is demonstrated here that the combination of data from isotope analysis, chemical data, and data from the chemical analysis of inclusion fluids of an artefact and of course in combination with a corresponding database enhances substantially the accuracy of marble provenance analysis. It is explicitly pointed out that the unchallenged collection of data of the chemical composition of marbles from different sources (and different analytical procedures) most probably implies severe differences in their comparability. Exemplarily presented is the nearly perfect discrimination of the most important fine-grained marbles and furthermore the possibility of the intra-site discrimination of the three Carrara districts and the assignment of two portrait heads to the Carrara Torano quarries.

多年来,“多方法分析”一直是大理石来源分析的流行语。然而,在同时使用大量解析得到的数值变量的意义上,很少应用不同分析方法的结果的真正组合。结果表明,同位素分析数据、化学分析数据、人工制品包裹体流体化学分析数据以及相应的数据库相结合,大大提高了大理石物源分析的准确性。有人明确指出,从不同来源(和不同的分析方法)收集的大理石化学成分数据很可能意味着它们的可比性存在严重差异。举个例子,对最重要的细粒大理石进行了近乎完美的识别,此外,对卡拉拉三个地区进行遗址内识别的可能性,以及将两个肖像头像分配给卡拉拉托拉诺采石场。
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引用次数: 1
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